Atlantic reef fish biogeography and evolution

SPECIALPAPER

Atlantic reef fish biogeography andevolution

S. R. Floeter1,2*, L. A. Rocha3, D. R. Robertson4, J. C. Joyeux5, W. F. Smith-

Vaniz6, P. Wirtz7, A. J. Edwards8, J. P. Barreiros9, C. E. L. Ferreira10,

J. L. Gasparini5, A. Brito11, J. M. Falcon11, B. W. Bowen3 and G. Bernardi12

1National Center for Ecological Analysis and

Synthesis, University of California, 735 State

St., 300, Santa Barbara, CA, 93101, USA,2Departamento de Ecologia e Zoologia, Lab. de

Biogeografia e Macroecologia Marinha,

Universidade Federal de Santa Catarina,

Florianopolis, SC 88010-970, Brazil, 3Hawaii

Institute of Marine Biology, University of

Hawaii, Kaneohe, HI, 96744, USA,4Smithsonian Tropical Research Institute,

Balboa, Unit 0948, APO AA 34002, Panama,5Departamento de Ecologia e Recursos

Naturais, Universidade Federal do Espırito

Santo, Vitoria, ES, 29060-900, Brazil, 6US

Geological Survey, Florida Integrated Science

Center, Gainesville, FL, 32653, USA, 7Centro

de Ciencias do Mar, Universidade do Algarve,

Faro, P-8000-117, Portugal, 8School of Biology,

Newcastle University, Newcastle upon Tyne,

NE1 7RU, UK, 9Departamento de Ciencias

Agrarias, Universidade dos Acores, 9701-851,

Portugal, 10Departamento de Biologia

Marinha, Universidade Federal Fluminense,

Niteroi, RJ, 24001-970, Brazil, 11Dpto. Biologıa

Animal (Ciencias Marinas), Universidad de La

Laguna, La Laguna, Tenerife, Islas Canarias,

38206, Spain, 12Department of Ecology and

Evolutionary Biology, University of California,

Santa Cruz, CA, 95060, USA

*Correspondence: S. R. Floeter, Departamento

de Ecologia e Zoologia, Lab. de Biogeografia e

Macroecologia Marinha, Universidade Federal

de Santa Catarina, Florianopolis, SC 88010-970,

Brazil.

E-mail: [email protected]

ABSTRACT

Aim To understand why and when areas of endemism (provinces) of the tropical

Atlantic Ocean were formed, how they relate to each other, and what processes

have contributed to faunal enrichment.

Location Atlantic Ocean.

Methods The distributions of 2605 species of reef fishes were compiled for

25 areas of the Atlantic and southern Africa. Maximum-parsimony and distance

analyses were employed to investigate biogeographical relationships among those

areas. A collection of 26 phylogenies of various Atlantic reef fish taxa was used to

assess patterns of origin and diversification relative to evolutionary scenarios

based on spatio-temporal sequences of species splitting produced by geological

and palaeoceanographic events. We present data on faunal (species and genera)

richness, endemism patterns, diversity buildup (i.e. speciation processes), and

evaluate the operation of the main biogeographical barriers and/or filters.

Results Phylogenetic (proportion of sister species) and distributional (number

of shared species) patterns are generally concordant with recognized

biogeographical provinces in the Atlantic. The highly uneven distribution of

species in certain genera appears to be related to their origin, with highest species

richness in areas with the greatest phylogenetic depth. Diversity buildup in

Atlantic reef fishes involved (1) diversification within each province, (2) isolation

as a result of biogeographical barriers, and (3) stochastic accretion by means of

dispersal between provinces. The timing of divergence events is not concordant

among taxonomic groups. The three soft (non-terrestrial) inter-regional barriers

(mid-Atlantic, Amazon, and Benguela) clearly act as ‘filters’ by restricting

dispersal but at the same time allowing occasional crossings that apparently lead

to the establishment of new populations and species. Fluctuations in the

effectiveness of the filters, combined with ecological differences among provinces,

apparently provide a mechanism for much of the recent diversification of reef

fishes in the Atlantic.

Main conclusions Our data set indicates that both historical events (e.g. Tethys

closure) and relatively recent dispersal (with or without further speciation) have

had a strong influence on Atlantic tropical marine biodiversity and have

contributed to the biogeographical patterns we observe today; however, examples

of the latter process outnumber those of the former.

Keywords

Atlantic Ocean, biodiversity, biogeographical barriers, biogeographical prov-

inces, historical biogeography, marine biogeography, phylogeography, specia-

tion, Tethys Sea.

Journal of Biogeography (J. Biogeogr.) (2008) 35, 22–47

22 www.blackwellpublishing.com/jbi ª 2007 The Authorsdoi:10.1111/j.1365-2699.2007.01790.x Journal compilation ª 2007 Blackwell Publishing Ltd

‘To some scholars, the search for patterns is a fishing

expedition, an unworthy exercise… To me, however, it

provides the critical raw data that enable us to propose and

to constrain possible explanations. Patterns help us to

identify… critical circumstances of events that could affect

diversity’. (Vermeij, 1996).

INTRODUCTION

Marine biogeographers have used the geography of endemism

to divide the biosphere into major provinces/regions (Ekman,

1953; Briggs, 1974; Vermeij, 1978), each of which is charac-

terized by a number of species found only in limited

geographical areas, known as areas of endemism. For simplic-

ity we will use the term ‘province’ to identify major areas of

endemism (Briggs, 1974, 1995). In characterizing biogeo-

graphical provinces, it is necessary to recognize the types of

barriers or boundaries that separate them (Briggs, 1973, 1974;

Floeter & Gasparini, 2000; Joyeux et al., 2001; Rocha, 2003). It

is also a general aim to understand why and when these

provinces were formed, and how they relate to each other

(Vermeij, 2001). In order to achieve these goals we need to

learn more about richness and endemism patterns, diversity

buildup (i.e. speciation processes), ecological and palaeoeco-

logical settings, and the operation of biogeographical barriers

or filters.

Here we discuss the geographic distribution and evolution of

Atlantic ‘reef fishes’, a group that includes any shallow

(< 100 m) tropical/subtropical benthic or benthopelagic fishes

that consistently associate with hard substrates of coral, algal, or

rocky ‘reefs’ or occupy adjacent sand substrate. The distribu-

tion of the great majority of reef fishes is dependent on the

dispersal of eggs and larvae in ocean currents, since these fishes

are relatively sedentary during adult stages (Leis, 1991; Victor,

1991). Reef fishes are highly diverse; they are not limited to

tropical reef areas (like reef-building corals) and thus are ideal

for comparisons involving centres of high diversity and

peripheral, lower-diversity areas; they are relatively easy to

identify compared with other groups (e.g. sponges, ascidians);

and, finally, a number of reef fish phylogenies (mainly

molecular) have been published in the last decade, providing

insights into speciation patterns within a geographic context.

The tropical Atlantic reef fauna encompasses four primary

provinces: Brazil, the ‘Greater’ Caribbean, the Mid-Atlantic

Ridge, and the Eastern Atlantic (Table 1; Briggs, 1974). Five

major barriers define these regions. The first is the > 3500-km-

wide Atlantic itself, which gradually began to form as a deep

ocean barrier (the mid-Atlantic Barrier, MAB) following the

separation of Africa and South America c. 84 Ma (Pittman

et al., 1993). The second barrier emerged c. 12–18 Ma with the

uplift of the Red Sea land bridge, separating the tropical faunas

of the Atlantic from the Indian Ocean and closing the Tethys

Seaway in the Terminal Tethyan Event (TTE; Steininger & Rogl,

1984; Bellwood & Wainwright, 2002). The third barrier is the

freshwater outflow from the Orinoco and Amazon rivers, which

spans 2300 km of the NE coast of South America, separating

Brazilian and Caribbean reef habitats, and which was estab-

lished c. 11 Ma (Hoorn et al., 1995). The final closure of the

Isthmus of Panama (IOP) c. 3.1 Ma (Coates & Obando, 1996)

separated the Caribbean from the Tropical Eastern Pacific.

Finally, the tropical reef fauna of the Atlantic has been isolated

from the southern Indian Ocean by the cold Benguela Current

for at least 2 Myr (the Benguela barrier; Shannon, 1985; Marlow

et al., 2000). These geographic and oceanographic features are

regarded as the primary barriers or filters producing diver-

gences and speciation among the regional faunas of the Atlantic.

The Atlantic provinces proposed by Briggs (1974) were

based on fewer (and less reliable) species distributional data,

and he did not have access to modern statistical methods. Here

we assemble the first comprehensive distribution data base for

the entire tropical and subtropical Atlantic, including the

southwestern Indian Ocean. Recent field and taxonomic

research in understudied areas, such as tropical West Africa

(e.g. Afonso et al., 1999; Edwards et al., 2003; Wirtz et al.,

2007), the Brazilian coast (e.g. Floeter et al., 2001; Rocha &

Rosa, 2001; Menezes et al., 2003; Dutra et al., 2005), and

associated oceanic islands (e.g. Santos et al., 1997; Gasparini &

Floeter, 2001; Feitoza et al., 2003), revealed new species (e.g.

Sazima et al., 1998; Rocha & Rosa, 1999; Heiser et al., 2000;

Gasparini et al., 2003), and greatly advanced the knowledge of

geographical distributions of tropical reef fishes. Concurrently,

new data were made available on the palaeoceanographic

characteristics of the tropical Atlantic (e.g. Stramma & Schott,

1999; Marlow et al., 2000; Peeters et al., 2004). Many mor-

phological and molecular phylogenies of Atlantic reef fishes

(see Methods) have recently been published and can help to

elucidate historical affinities among endemism areas, as well as

the origins and diversification patterns of Atlantic reef fishes.

This paper has a number of purposes, namely: (1) to

summarize current information on diversity and endemism in

Atlantic reef fishes; (2) to evaluate relationships among the

main Atlantic biogeographical regions, analysing the effect of

the various barriers or filters on these relationships; and (3) to

review published phylogenies (mainly derived from recent

molecular studies) and assess origins and diversification

patterns of Atlantic reef fishes by addressing the following

questions: (a) what is the geographical pattern of sister taxa

among provinces? (b) are area relationships based on phylo-

genetic and distributional patterns concordant? (c) is there a

congruent pattern of divergences resulting from historical

events? (d) what is the relative importance of vicariant events

and dispersal across soft barriers on contemporary biodiversity?

METHODS

Atlantic reef fish data base

Species lists were compiled for 25 areas of the Atlantic Ocean

through literature searches of peer-reviewed checklists and

published field guides, and from extensive observations by the

authors (see Table 1 for area definition and references used).

This data base represents the most exhaustive data set on the

Atlantic reef fish biogeography and evolution

Journal of Biogeography 35, 22–47 23ª 2007 The Authors. Journal compilation ª 2007 Blackwell Publishing Ltd

Table 1 Definitions of the studied areas of the Atlantic Ocean and references of checklists used to compile the data set. Regions were based

on the results of the maximum-parsimony analysis. Entries in italics signify two or more areas pertaining to the same geographic group.

Province Area Geographical definition References

Northwestern Atlantic (NWA)

Carolinian Carolinian From Cape Kennedy to

North Carolina

Smith-Vaniz et al. (1999),

Quattrini et al. (2004)

Greater Caribbean Bermuda Smith-Vaniz et al. (1999)

Western Caribbean Continental area from

Florida to Tobago and

Venezuela (including

Gulf of Mexico)

Cervigon (1982), Smith-Vaniz et al. (1999),

Smith (1997), Randall (1996),

Schmitter-Soto et al. (2000),

Smith et al. (2002, 2003)

Eastern Caribbean Insular area from

Bahamas, Cuba to

Dominica and Barbados

Bohlke & Chaplin (1993),

Smith-Vaniz et al. (1999),

Claro & Parenti (2001),

Smith et al. (2002),

Smith-Vaniz et al. (2006)

Southwestern Atlantic (SWA)

Brazilian Northeastern Brazil From the Mouth of the

Amazon to southern Bahia

Carvalho-Filho (1999), Rocha et al. (1998),

Feitoza (2001), Rocha & Rosa (2001),

Menezes et al. (2003), Feitoza et al. (2005),

Dutra et al. (2005), S.R. Rosa, C.R.R. Nunes &

L.A. Rocha (unpublished manuscript)

Southeastern Brazil From Espırito Santo to

Santa Catarina

Menezes et al. (2003), Floeter et al. (2007),

Hostim-Silva et al. (2006)

Atol das Rocas Fernando de Noronha Ridge Rosa & Moura (1997), Menezes et al. (2003),

Sampaio et al. (2006)

Fernando de Noronha Fernando de Noronha Ridge Menezes et al. (2003), Sampaio et al. (2006)

St Paul’s Rocks Lubbock & Edwards (1981),

Feitoza et al. (2003), Sampaio et al. (2006)

Trindade Is. Gasparini & Floeter (2001),

Menezes et al. (2003), Sampaio et al. (2006)

Eastern South America ‘Argentina’ From Uruguay to

Patagonia

Menni et al. (1984),

Cousseau & Perrota (2004)

Mid-Atlantic Ridge (MAR) Ascension Lubbock (1980), D.R. Robertson

(personal observation)

St Helena Edwards & Glass (1987a,b), Edwards (1990),

D.R. Robertson (personal observation)

Northeastern Atlantic (NEA) Western Mediterranean Gibraltar to the Strait

of Messina

Jennings (2000), Hureau (1998)

Eastern Mediterranean Levant to the Strait

of Messina

Jennings (2000), Hureau (1998)

Azores Macaronesia Santos et al. (1997)

Madeira Macaronesia Quero et al. (1990), Wirtz (2001),

Wirtz (unpublished data)

Canaries Macaronesia Brito et al. (2002)

Tropical Eastern Atlantic (TEA) Northwest Africa Gibraltar to Cape

Verde (Senegal)

Quero et al. (1990), Almada et al. (2001),

Falcon et al. (2002)

Cape Verde Is. Reiner (1996), Brito et al. (1999),

Menezes et al. (2004)

Sao Tome & Prıncipe Includes Annobon Afonso et al. (1999), Wirtz et al. (2007)

Tropical West Africa Cape Verde to

Mocamedes (Angola)

Quero et al. (1990), Reiner (2001),

Edwards et al. (2003)

S. R. Floeter et al.

24 Journal of Biogeography 35, 22–47ª 2007 The Authors. Journal compilation ª 2007 Blackwell Publishing Ltd

distributions of Atlantic reef fishes compiled to date (Table S1,

Supplementary Material).

Atlantic reef fish phylogenies

The following phylogenies were used for analysis and infer-

ences: Abudefduf (Quenouille et al., 2004), Acanthostracion/

Lactophrys (Klassen, 1995), Acanthurus (Rocha et al., 2002),

Alphestes (Craig et al., 2004, 2006), Anisotremus (Bernardi &

Lape, 2005), Aulostomus (Bowen et al., 2001), Centropyge

‘xiphipops’ complex (Bowen et al., 2006a), chaenopsids (Has-

tings, 2000), Chromis (Quenouille et al., 2004; C. chromis clade

– Domingues et al., 2005; C. ‘multilineata’ complex – L.A.

Rocha, D.R. Robertson, A.J. Edwards & B.W. Bowen, in

preparation), Clepticus (Heiser et al., 2000), Dermatolepis

(Craig et al., 2004), Diplodus (Summerer et al., 2001), Elac-

atinus (Taylor & Hellberg, 2005), Gnatholepis (Rocha et al.,

2005a), Gobiesocinae (Briggs, 1955), Hippocampus (Casey

et al., 2004), Halichoeres (Rocha, 2004; Barber & Bellwood,

2005), Holacanthus (Bellwood et al., 2004; G. Bernardi,

S.R. Floeter & D.R. Robertson, in preparation), Lethrinus

(Galbo et al., 2002), Ophioblennius (Muss et al., 2001),

Pomacanthus (Bellwood et al., 2004), Rypticus (Guimaraes,

1999; Carlin et al., 2003), Sparisoma/Nicholsina (Robertson

et al., 2006), Sparidae (Orrell et al., 2002), Strongylura (Ban-

ford et al., 2004), and Thalassoma (Costagliola et al., 2004).

When interpreting the phylogenies we assumed that no

extinctions have occurred, and followed estimates (and

associated errors) of the timing of speciation events provided

and discussed in the original publications. A minimum age of

3.1 Ma was assumed for splits related to the closure of the

Isthmus of Panama.

Data analyses

Maximum-parsimony (MP) analyses of 25 geographical areas

in the Atlantic Ocean were performed using paup* (Swofford,

2002). Geographical areas were characterized by the presence/

absence of 2605 reef fish taxa. MP analyses were performed

with heuristic searches having starting trees obtained by means

of the tree-bisection-reconnection (TBR) branch-swapping

algorithm. Support for each node from the majority consensus

tree from the data set was investigated with 1000 bootstrap

pseudo-replicates (Felsenstein, 2004).

To evaluate relationships among areas based on reef fish

phylogenies, we calculated the ratio (proportion; given in each

arrow) between the number of nodes in which two areas form a

sister pair in a given phylogeny (when the terminal clade was a

polytomy, the relationships were counted for all the areas

involved, i.e. overlap) and the number of times the same pairs

of areas were available for evaluation in the studied phyloge-

nies. The number of studied pairs (possibilities of interactions)

was around 300 for the seven areas in the studied phylogenies. It

is important to note that not all phylogenies include taxa

present in all the areas, and some have more than one pair of

sister areas; we thus worked with proportions of the areas in

question (to avoid bias related to unequal coverage of areas).

In order to summarize the relationships among the areas,

cluster analyses (Bray-Curtis dissimilarity index and UPGMA

method) were performed using mvsp software based on: (1)

the number of reef fish species (or genera) common to the

pairs of areas, and (2) the matrix of ratios indicating the

importance of the phylogenetic connections. Varying the

clustering routine had no effect on the grouping of the sites,

except when indicated in the figure legend.

RESULTS AND DISCUSSION

Geographical distributions

Diversity and endemism

In total, our data base covers 1720 teleost reef fish species from

465 genera and 69 families from the Atlantic, plus another 885

Table 1 continued.

Province Area Geographical definition References

Southwest Africa (SA) Benguela From Mocamedes

(Angola) to the

Cape of Good Hope

Smith & Heemstra (1995), Heemstra &

Heemstra (2004), L.E. Beckley, P.A. Hulley, &

P.H. Skelton (unpublished manuscript),

D. Polack (personal communication)

Agulhas From the Cape of

Good Hope to

Kei River

Smith & Heemstra (1995),

Heemstra & Heemstra (2004), L.E. Beckley,

P.A. Hulley, & P.H. Skelton

(unpublished manuscript),


Southwestern Indian

Ocean (SWIO)

South Africa’s

Indian Ocean

From Kei River to

Kosi Bay

Smith & Heemstra (1995),

Heemstra & Heemstra (2004), L.E. Beckley,

P.A. Hulley & P.H. Skelton

(unpublished manuscript),




species from South Africa’s tropical Indian Ocean, resulting in

a total of 2605 species. Encompassing the Greater Caribbean,

the Northwestern Atlantic (NWA) has the highest number of

species and genera in the Atlantic (831 species – Table 2 and

Fig. 1; 150 genera – Table 3, based on selected speciose

families). This number is dominated by Caribbean species with

tropical affinities (814). The endemism figures are high for

these areas (species: 57% NWA and 33% Caribbean; genera:

16% for both the Caribbean and the NWA). When considered

separately, the western Caribbean plus Florida (‘Caribbean

Province’ sensu Briggs, 1974) and the eastern Caribbean (‘West

Indian Province’ sensu Briggs, 1974) have essentially identical

levels of endemism, each with c. 50 (or c. 7%) endemic species.

This is much lower than the 19% endemism rate of the ‘West

Indian Province’ found back in 1974 (Briggs, 1974).

The Southwestern Atlantic (SWA; Brazilian oceanic islands

and Argentina included) has slightly over half (471) of the

species richness of its northwest counterpart, and a some-

what lower, but still substantial, rate of endemism (25%).

This endemism rate of the Brazilian coast plus its oceanic

islands provides the basis for distinguishing the ‘Brazilian

Province’, first proposed by Briggs (1974, 1995; see also

Floeter & Gasparini, 2000; Joyeux et al., 2001). When only

the Brazilian coast is considered, the endemism level drops

to c. 10% (see also Rocha, 2003). Within coastal Brazil, the

northeast coast has nine endemic species (2.3% of the total

richness), and the southeast coast has eight endemics (2.1%).

The SWA contains 117 genera, 78% of the Caribbean

number, with only three endemic genera (2.6%), vs. 16% of

endemic genera in the Caribbean.

The Mid-Atlantic Ridge (MAR) islands of Ascension and

St Helena harbour 111 reef fish species, with 29 (26.1%)

endemics, justifying the province proposed by Briggs (1974,

1995).

The Eastern Atlantic (EA; from the Mediterranean to the

Benguela region) has 551 species (124 genera), with 64% of

these species (31.5% of genera) restricted to this side of the

Atlantic (Tables 2 and 3). The tropical area of the EA (Cape

Verde Islands, Sao Tome, and the West African coast from

Cape Verde in Senegal to Mocamedes in Angola) includes 388

species (106 genera), and the endemism rate is c. 30% for

species (3.8% for genera). Thus, the species and genera

richness in the tropical EA (TEA) is considerably lower than

that of the tropical Western Atlantic (WA), which is consistent

with earlier literature (e.g. Briggs, 1974, 1995; Paulay, 1997).

In comparison, the species richness of the tropical Eastern

Pacific (TEP) is approximately 89% of the richness of the

Caribbean (Robertson, 1998; Fig. 1). The number of species of

reef fishes found in tropical South Africa is about 1140, but

only 20% of these are also found in the Atlantic Ocean, mainly

in the Agulhas area. Approximately 5% are found in tropical

areas of the Atlantic.

The relative impoverishment of the Atlantic fauna compared

with that of the Indo-West Pacific (Paulay, 1997; Bellwood &

Wainwright, 2002) probably reflects the much smaller geo-

graphical scale of the region and the historical changes that

have impacted reefs, especially in the wider Caribbean

(Vermeij, 2001, 2005; Johnson et al., 2007). There is no doubt

that the reef biota of this region has been subject to wide-scale

disturbances and episodic extinctions, with the consequence

that the present-day assemblages are less diverse than those of

the Miocene (Budd, 2000). Based on skeletonized groups, it

seems that Pliocene extinctions were severe in the Western

Atlantic, where many groups underwent 20 to 30% genus-level

extinction (Vermeij, 2001, 2005). The closure of the Isthmus

also modified the oceanographic regime of the western

Caribbean, with a change from cooler upwelling to a warmer

oligotrophic regime (Johnson et al., 2007). Moreover, Pleisto-

cene glaciations that squeezed the tropical regions and the area

of shallow-water habitats (Bellwood & Wainwright, 2002) are

also thought to be related to the relative paucity of species in

the tropical Atlantic provinces, even when compared with the

south-western Indian Ocean (Table 2). However, in the

Table 2 Species richness, number of endemics and endemism

(%) of Atlantic areas and South Africa’s Indian Ocean*.

Richness Endemics Percentage

Western Atlantic (WA) 1023 881 86.1

Northwestern Atlantic (NWA) 831 473 56.9

Caribbean 814 272 33.4

Southwestern Atlantic (SWA) 471 118 25.1

Brazilian coast 437 46 10.5

Mid-Atlantic Ridge (MAR) 111 29 26.1

Eastern Atlantic (EA) 551 352 63.9

Tropical Eastern Atlantic (TEA) 388 117 30.6

Southwestern Indian Ocean (SWIO) 1141 – –

*See Table 1 for definitions of the areas.

Figure 1 Reef fish richness patterns in the Atlantic Ocean and

adjacent areas. Circle diameters are sized in proportion to the

number of species in each area. The largest circle inside the

Atlantic represents 750 species in the Western Caribbean plus

Florida.



absence of a good fossil record, there is almost no direct

evidence of extinction in reef fishes.

Apart from the high endemism of Ascension and St Helena

(Table 4), endemism rates on oceanic islands vary from zero in

Madeira (although there are two endemic species shared with

the Canaries and one with the Azores), to 1.1% in the Azores,

1.8% in Bermuda, 1.6% in the Canaries, c. 3% in Sao Tome

and Prıncipe (plus Annobon), 5% in Atol das Rocas plus

Fernando de Noronha, 5.7% at Trindade Island, 8.3% in the

Cape Verde Islands, and 9.3% at St Paul’s Rocks.

Various combinations of island age, geographic isolation,

area of available habitat and patterns of oceanic currents

connecting these islands to potential source areas are probably

involved in producing the relatively low endemism in the

non-MAR islands (Table 4; Briggs, 1966; Smith-Vaniz et al.,

1999; Gasparini & Floeter, 2001; Rocha, 2003; Wirtz et al.,

2007). The low level of endemism at Bermuda, the Canaries,

and other high-latitude locations seems to indicate extirpation

during Pleistocene glacial periods and recent recolonization

(Briggs, 1966; Smith-Vaniz et al., 1999; Rocha, 2004; Domin-

gues et al., 2006, 2007), with little time for subsequent

speciation. In the Tropics, the intermediate endemism rates of

3–6% at Sao Tome and Prıncipe, Fernando de Noronha Ridge

and Trindade Island probably result from the proximity

(< 1000 km) to continental margins, and/or connections to

mainland areas via seamounts. In contrast, the high ende-

mism at the Cape Verde Islands may be related to: (1) greater

isolation (from the mainland and between islands), (2) high

heterogeneity of habitats (Perez-Ruzafa et al., 2005), and (3)

maintenance of warm tropical waters in glacial periods. The

genus Diplodus is thought to have originated in this

archipelago (Summerer et al., 2001), as well as the only

endemic Atlantic damselfish genus (Similiparma) and the

monotypic genus Virididentex (Sparidae). The Cape Verde

Islands are also known for high diversity and endemism in

tropical marine invertebrates, including several endemic

species in the gastropod genus Conus (Cunha et al., 2005;

Duda & Rolan, 2005). The high endemism of St Paul’s Rocks

is related to geographic isolation and overall low species

richness (five of the 54 species are endemics, whereas 17 of

the 205 Cape Verde species are endemics). Despite having

three species shared only with Ascension and St Helena on the

Table 3 Selected speciose families – total number of genera per family and genera restricted to single regions (in parentheses). NW, New

World (TEP + WA); TEP, Tropical Eastern Pacific; WA, Western Atlantic; Braz., Brazil; Carib., Caribbean; EA, Eastern Atlantic; Med,

Mediterranean; Cape + SWIO, South African’s Cape + Indian Ocean. Indones., Indonesia (based on Allen & Adrim, 2003) is included for

comparison purposes.

Family NW TEP1 WA2 Braz.3 Carib. EA4 TEA Med Cape+IO* Indones.�

Apogonidae 3 (1) 1 3 (1) 3 3 2 2 1 12 (11) 14

Balistidae 6 6 4 4 4 4 4 1 12 (6) 10

Batrachoididae 7 (7) 3 (2) 5 (5) 5 (1) 5 (1) 2 2 1 5 (2) 2

Blenniidae 10 (4) 7 (2) 7 (1) 6 7 (1) 13 (3) 10 (1) 9 21 (18) 28

Carangidae 10 (1) 9 10 (1) 10 (1) 8 11 (1) 9 7 9 (1) 14

Chaenopsidae 13 (13) 10 (3) 10 (3) 3 10 (2) – – – – –

Dactyloscopidae 8 (8) 6 (1) 7 (2) 4 (1) 6 (1) – – – – –

Gobiesocidae 6 (6) 3 6 (6) 5 6 (1) 5 (3) 5 (1) 5 (1) 6 (3) 5

Gobiidae 26 (14) 13 25 (14) 15 25 (8) 19 (16) 14 19 (8) 50 (43) 50

Haemulidae 3 3 3 3 3 3 (1) 3 2 2 (1) 2

Labridae 8 (2) 7 8 (2) 7 8 (1) 11 (5) 9 8 29 (25) 35

Labrisomidae 7 (3) 6 (2) 5 (1) 4 5 (1) 2 2 – – –

Lutjanidae 7 (3) 2 6 (3) 5 6 3 3 – 7 (4) 8

Muraenidae 11 (1) 9 (1) 8 7 8 8 7 4 12 (6) 12

Pomacentridae 7 (3) 7 (3) 4 4 4 5 (1) 5 (1) 1 13 (10) 19

Pseudochromidae – – – – – – – – 6 (6) 11

Scaridae 4 (1) 3 4 (1) 4 4 3 3 1 6 (4) 7

Serranidae 27 (16) 15 27 (15) 15 23 (7) 12 (1) 11 5 25 (15) 21

Sparidae 6 (3) 2 6 (1) 4 5 12 (4) 12 (1) 10 21 (13) –

Syngnathidae 10 (3) 5 9 8 9 (1) 8 (3) 4 4 15 (10) 18

Tripterygiidae 4 (3) 4 (3) 1 1 1 1 (1) 1 1 5 (5) 5

No. genera (endemic) 183 (92) 121 (17) 158 (56) 117 (3) 150 (24) 124 (39) 106 (4) 79 (9) 256 (177*) 261�Percent endemic genera 50.3 14.0 35.4 2.6 16.0 31.5 3.8 11.4 69.1* –

1: Eastward-migrant tropical transpacific Pacific genera that occur in the TEP but not the WA or SWIO are not counted as TEP genera.

2: Genera known only from southern Brazil are included in counts of TWA-restricted genera.

3: Including Argentina.

4: Including Macaronesian and Mediterranean (some extending north in the Northeastern Atlantic) genera, except endemic Mediterranean genera.

*Numbers in parentheses do not represent strict endemism, but genera not found in the Atlantic and the TEP.

�Coral reef fishes only.



MAR, all the other components of St Paul’s Rocks are shared

with the Brazilian coast or the Fernando de Noronha Ridge

(Feitoza et al., 2003). Thus, all the Brazilian oceanic islands

are considered here as impoverished outposts of the Brazilian

Province (Fig. 4; Edwards & Lubbock, 1983; Floeter &

Gasparini, 2000).

Composition of the faunas

Species richness varies greatly among biogeographical regions,

not only in terms of total numbers, but also in the relative

contributions from each taxonomic family (Fig. 2). Some

features are immediately apparent.

(1) Overall patterns of species richness per family in the

NWA and SWA are similar but each family is consistently

more diverse in the NWA, especially families of small

cryptobenthic fishes. Three of the most speciose families of

Neotropical reef fishes have far more species in the NWA than

in the SWA (Gobiidae with 91 vs. 27; Labrisomidae with 46 vs.

16; and Chaenopsidae with 51 vs. 4). This is not the case with

other species-rich groups that are not restricted to the

Neotropics: the Labridae, Scorpaenidae, Haemulidae and

Carangidae have comparable numbers in both areas, and

Pinguipedidae has more species in the SWA.

(2) The EA areas (TEA and NEA) have very similar patterns

but differ greatly from the WA areas. Two speciose families,

Sparidae and Blenniidae, are markedly more speciose in both

parts of the EA than in the WA (40 vs. 21 and 43 vs. 24).

However, two of the four most speciose families in the WA are

absent or very poorly represented in the EA (Chaenopsidae is

absent; and Labrisomidae has only two species). The MAR

islands are more similar to the EA than to the WA. Two

pantropical families are relatively (percentage of the total

fauna) more speciose in the MAR than elsewhere in the

Atlantic, namely Muraenidae and Carangidae.

(3) The southwestern Indian Ocean (SWIO) exhibits a

highly distinctive pattern, with several families being more

important there than in the Atlantic areas (e.g. Acanthuridae,

Apogonidae, Clinidae, Labridae, Pomacentridae); several

families are unrecorded in the Atlantic (e.g. Caesionidae,

Nemipteridae, Pseudochromidae, Siganidae); and some fam-

ilies that are important in the Atlantic faunas are lacking in

the SWIO (Chaenopsidae, Dactyloscopidae, Grammatidae,

Labrisomidae).

Some genera have highly skewed distributions (Fig. 3). For

example, 156 genera occur in the New World (NW - both sides

of tropical America) but not in the EA (e.g. Anisotremus,

Calamus, Elacatinus, Haemulon, Halichoeres (‘Iridio’ clade),

Lythrypnus, Ogcocephalus, and Opistognathus). Other genera,

such as Malacoctenus, Mycteroperca, Sparisoma and Stegastes

(Fig. 3), are much more diverse in the WA (and the TEP) than

in the EA. However, Diplodus, Parablennius and Scartella are

more speciose in the EA than in the WA. Eighty-four genera

occurring in the EA (not considering southern Africa) are not

found in the WA (e.g. Gobius, Lipophrys, Pagellus, Spicara,

Symphodus, Thorogobius, Wheelerigobius). Eighteen EA genera

occur in the Indo-Pacific but not in the WA or TEP (e.g.

Branchiostegus, Callionymus, Coris, Lethrinus, Periophthalmus,

Plectorhinchus), indicating a historical connection via southern

Africa or Tethys relicts.

Table 4 Endemism rates of reef fishes and characteristics of the oceanic islands of the Atlantic Ocean.

Island

Endemism

(%)

Richness

(n species) Latitude

Distance

from

mainland

(km)

Isolation

from

nearest reef

habitat (km)

Maximum

distance inside

the archipelago

(km)

Shelf

surface

(km2)

Age

(Ma)

Ice age

effects*

Diversity

of

habitats

St Helena 13.2 76 16� S 1870 1290� – 156 10 No Low

Ascension 11.0 82 8� S 1536 1290� – 106 1.5 No Low

St. Paul’s Rocks 9.3 52 1� N 1010 630§ – 1? 9.3 No Low

Cape Verde Is. 8.3 207 16� N 560 Mainland 365 13,991 10.3 No High

Trindade Is. 5.7 85 20� S 1160 300– 47 32 3.6 No Low

F. de Noronha Ridge 5.0 120 4� S 350 Mainland 150 27** 12 No Interm.

Sao Tome & Prıncipe 3.0 221 1� N 250 210�� 140 860 31 No High

Bermuda 1.6 280 32� N 1049 Mainland – 1204 60 Yes High

Canaries 1.6 182 28� N 100 Mainland 490 8027 20.5 Yes High

Azores 1.1 95 38� N 1300 740�� 675 5363 0.2–7 Yes High

Madeira 0.0 133 33� N 630 285§§ 96 810 15 Yes? Interm.

*Only temperature effects.

�To Ascension.

�To St Helena.

§To F. de Noronha.

–To seamounts of the Vitoria-Trindade Chain.

**Noronha only.

��To Fernando Poo (=Bioko).

��To Madeira.

§§To Selvagem Islands.



A few genera show disjunct distributions that indicate either

extinction in the WA or colonization of the EA from the IO. For

example, Cirrhitus, Girella and Prionurus are found in the EA,

Indo-West Pacific and TEP but not in the WA. Tyler (1997)

reported a Caribbean fossil of the putative sister taxon of the

surgeonfish genus Naso, providing direct evidence for the

extinction scenario (today, no member of the Naso lineage is

found in the Atlantic). The relationship between these patterns

of diversity and the origin of genera will be discussed later.

Relationships among areas and biogeographical

barriers/filters

The maximum-parsimony analysis using the presence/absence

species distribution data base illustrates relationships among

the WA (further subdivided into the NWA and SWA), the EA

(further subdivided into the NEA, TEA, Benguela, MAR and

Cape) and the South African Indian Ocean (Fig. 4). Despite

the Amazon filter, the SWA and NWA have the greatest

number of species and genera in common (348 and 201,

respectively, including a total of 55 families; Fig. 5). These

species represent 42% of the NWA total reef fish fauna and

74% of the SWA fauna (Fig. 5). If closely related species pairs

(n = 30; Table S2) are included in the calculations, their

representation increases to 45% and 82%, respectively (Fig. 6).

Another way to look at the effectiveness of Atlantic

biogeographical barriers/filters is to examine the proportional

representation of trans-barrier species within each family

(Figs 6–8). Notably, families Serranidae and Carangidae have

the greatest number of species crossing the Amazon filter. With

the exception of gobiids, the families containing trans-Ama-

zonian species are mostly pelagic spawners with medium to

large body sizes. Demersal-spawning and brooder families with

small-bodied cryptobenthic species seem to be the most

affected by the Amazon freshwater and sediment discharge

(e.g. Chaenopsidae, Gobiidae). Most of these families are

disproportionately more diverse on Caribbean coral reefs than

in the SWA (Floeter & Gasparini, 2000; Moura & Sazima,

2003; Rocha, 2003). The second highest exchange is between

the EA and the WA (NWA and SWA areas with c. 106 species

in each link). In total, we recorded 112 species with trans-

Atlantic distributions (Fig. 7). This corresponds to approxi-

Figure 2 Species richness, by family, for the five major Atlantic

biogeographical regions and the Southwestern Indian Ocean.

NWA: Northwestern Atlantic, SWA: Southwestern Atlantic, MAR:

Mid-Atlantic Ridge (Ascension + St Helena), EA: Eastern Atlan-

tic, TEA: Tropical Eastern Atlantic, NEA: Northeastern Atlantic,

SWIO: South Africa’s tropical Indian Ocean (from Kei River to

Kosi Bay). The ordering of families in each region follows the

ranking of those families in the NWA. Coloured bars (and bold

below) indicate families that are disproportionally more impor-

tant in one or more specific regions. Families: 1, Gobiidae; 2,

Serranidae; 3, Chaenopsidae; 4, Labrisomidae; 5, Paralichthyidae;

6, Apogonidae; 7, Gobiesocidae; 8, Labridae; 9, Muraenidae; 10,

Syngnathidae; 11, Carangidae; 12, Scorpaenidae, 13, Sparidae; 14,

Haemulidae; 15, Lutjanidae; 16, Opistognathidae; 17, Pomacen-

tridae; 18, Blenniidae; 19, Dactyloscopidae; 20, Batrachoididae,

21, Ophidiidae; 22, Scaridae; 23, Bothidae; 24, Grammatidae; 25,

Holocentridae; 26, Ogcocephalidae; 27, Ophichthidae; 28, Mal-

acanthidae; 29, Monacanthidae; 30, Synodontidae; 31, Tetra-

odontidae; 32, Tripterygiidae; 33, Antennariidae; 34, Bythitidae;

35, Chaetodontidae; 36, Diodontidae; 37, Pomacanthidae; 38,

Balistidae; 39, Congridae; 40, Sciaenidae; 41, Callionymidae; 42,

Microdesmidae; 43, Ostraciidae; 44, Chlopsidae; 45, Mullidae; 46,

Priacanthidae; 47, Acanthuridae; 48, Ptereleotridae; 49, Carapi-

dae; 50, Fistulariidae; 51, Kyphosidae; 52, Moringuidae; 53,

Pempheridae; 54, Uranoscopidae; 55, Aulostomidae; 56, Cirrhiti-

dae; 57, Dactylopteridae; 58, Caesionidae; 59, Caracanthidae; 60,

Centracanthidae; 61, Chanidae; 62, Cheilodactylidae; 63, Clinidae;

64, Kuhliidae; 65, Lethrinidae; 66, Myrocongridae; 67, Nemip-

teridae; 68, Pentacerotidae; 69, Pinguipedidae; 70, Platycephali-

dae; 71, Plesiopidae; 72, Pseudochromidae; 73, Siganidae; 74,

Synanceiidae; 75, Trichonotidae; 76, Xenisthmidae; 77, Zanclidae.



mately three times fewer trans-Atlantic species than trans-

Amazon species (n = 348). Relative to the total fauna, these

species comprise 11.8% of the WA fauna (23% of the SWA and

13% of the NWA), 20% of the EA, and 45% of the MAR

islands fish fauna.

When the TEA is considered separately, the proportion of

trans-Atlantics rises to 27% of the fauna. If putative sister

species are included as trans-Atlantic units (species that have

their closest relatives on the other side of the Atlantic Ocean;

Table S2), the proportion of trans-Atlantic fish taxa in the TEA

increases to 38% of the fauna, a proportion close to that of the

MAR. The number of reef fish species common to the MAR

(Ascension + St Helena) and the EA (n = 64) or common to

the MAR and the SWA (n = 71) constitute c. 60% of the MAR

fish fauna (Fig. 5).

The majority of trans-Atlantic species belong to families of

pelagic-spawners with long pelagic larval durations (PLDs; e.g.

Muraenidae, Serranidae; Victor, 1991) and/or fishes that are

known rafters (e.g. Balistidae, Carangidae, Diodontidae,

Monacanthidae). Entire families in the MAR and TEA are

composed of trans-Atlantic species (e.g. Diodontidae, Holo-

centridae, Priacanthidae, Synodontidae). If trans-Atlantic sister

species are considered, 16 families in the TEA are composed

only of these wide-ranging taxa (Fig. 7). Detailed statistical

analyses involving several biological attributes of reef fishes

crossing barriers in the Atlantic will be published elsewhere.

The weakest connection across a soft barrier corresponds to

the Benguela Current filter, represented by 47 species (38

shared with the TEA – plus 22 putative sister species, and 9

shared with the SWA). Relative to the total fauna of each side,

the 60 species and sister species in common comprise 16% of

TEA fishes but only 5% of SWIO. These numbers indicate that

the strength of the connection between the Indo-Pacific and

the EA has previously been underestimated (Briggs, 1974,

1995). Examples from other taxonomic groups with a good

fossil record reinforcing the relationships between the IO (and/

or the IWP) and the TEA include gastropods, bivalves, and

opisthobranch molluscs (Edmunds, 1977; Oliver and von

Cosel, 1992; Vermeij & Rosenberg, 1993).

The link between the IO and SWA has been under-

appreciated in previous analyses (but see Vermeij & Snyder,

2003 for gastropod examples). The nine shared species are few

in comparison to the total number of species in each area, but

reveal a possible connection across the South Atlantic. The

Figure 3 Richness patterns of six selected

genera in the Atlantic Ocean and adjacent

areas. Circle diameters are sized proportion-

ally to the number of species in each area.

The maximum number of species is given (in

the largest circle) for comparison.



Figure 4 Relationships of 25 areas in the Atlantic Ocean based on maximum-parsimony analysis using the presence/absence distribution

data base of 2605 reef fish species. Values at nodes represent bootstrap support (1000 replicates). Consistency index = 0.499, homoplasy

index = 0.501 and retention index = 0.620.

MAR

WT

V

IV

III

II

I

ET

NWA

SWA

TEA348

71

10516%

10%

27%

74%

15%

64%

4%

13%

58%

42%

64

38

47

107

923%

28%

0.8%3%

2%

SWIO

SWIO

TEAMARSWANWA

0.16

0.32

0.48

0.64

0.8

0

Figure 5 Biogeographical barriers and relationships among areas based on the number of reef fish species common to each pair of

areas. Hard barriers: (I) Isthmus of Panama, 3.1–3.5 Ma (II) Terminal Tethyan Event (Red Sea land bridge), 12–18 Ma. Soft barriers:

(III) Amazon discharge, 6–10 Ma; (IV) Mid-Atlantic Barrier, 0–60 Ma; (V) Benguela Barrier, 2 Ma. Areas/provinces: WT, West Tethys;

ET, East Tethys. NWA, Northwestern Atlantic (Caribbean + Bermuda + Carolinian); SWA, Southwestern Atlantic (Brazil + Brazilian

oceanic islands + Argentina); MAR, Mid-Atlantic Ridge (Ascension + St Helena); EA, Eastern Atlantic (Macaronesia + Gulf of Guinea);

SA, South Africa (tropical Indian Ocean). Arrow widths are sized proportionally to the number of species common to the areas. The

proportion of the number of species common to a pair of areas relative to its entire reef fish fauna is given at each end of the arrows.

In order to summarize the relationships among the areas, a cluster analysis (Bray-Curtis dissimilarity index; UPGMA method) based on

the matrix of the number of shared species among areas indicating the importance of the biogeographical connections is shown at the

bottom. Varying the clustering routine has no effect on the grouping of the sites. The link between the SWIO and the Atlantic (47 species)

is further divided into two: 38 with the TEP and 9 with the SWA.



recent record of the starry toadfish Arothron firmamentum in

Argentinian waters (Dıaz de Astarloa et al., 2003) and at St

Paul’s Rocks (L. Fritzsche, personal communication) exempli-

fies this route via the South Atlantic gyre. Two recent

population genetic surveys support the direct recent (post

Benguela-establishment) colonization of the SWA by an IO

goby (genus Gnatholepis, Rocha et al., 2005a) and angelfish

(genus Centropyge, Bowen et al., 2006a). There are also

examples of an IO genus found at St Helena and Ascension

but nowhere else in the Atlantic (Helcogramma sp.; Hadley-

Hansen, 1986; Heemstra & Heemstra, 2004), and there is an

assumed invasion of the Atlantic by Chaetodon sedentarius

from the western IO C. dolosus clade at around 1.6 Ma (Fessler

& Westneat, 2007).

A cluster analysis based on the shared species synthesized the

overall pattern closely linking the NWA to the SWA, and the

MAR to the EA (Fig. 5), in a similar fashion to the maximum-

parsimony analysis (Fig. 4).

The number of species shared only between the NWA and

the SWA (n = 225) is the highest among all pairwise compari-

sons; these species are proportionately more dominant in the

SWA than in the NWA (48% vs. 27%). Eleven species are found

only in the EA and the MAR (e.g. Acanthostracion notacanthus,

Gymnothorax unicolor, Myroconger compressus, Xyrichtys sanc-

taehelenae), comprising 10% of the total MAR fauna.

The SWIO and the TEA share 15 species (plus 11 putative

sister-species pairs totalling c. 10% of the EA fauna), for

example Gymnothorax margaritophorus and Rhabdosargus

globiceps (both with wider distributions in the Indo-Pacific),

and Lithognathus mormyrus and Sarpa salpa (with a putative

EA origin owing to their wider distributions in this area). An

additional 52 species with subtropical affinities are distributed

Brazilian Coast

Caribbean

Nu

mb

er o

f sp

ecie

s

Car

angi

dae

Mur

aeni

dae

Ser

rani

dae

Mon

acan

thid

ae

Bal

istid

ae

Con

grid

ae

Dio

dont

idae

Syn

odon

tidae

Ant

enna

riida

e

Hol

ocen

trid

ae

Labr

idae

Lutja

nida

e

Pria

cant

hida

e

Aca

nthu

ridae

Apo

goni

dae

Ble

nniid

ae

Bot

hida

e

Chl

opsi

dae

Sca

ridae

Sci

aeni

dae

Gob

iidae

Gob

ieso

cida

e

Cha

etod

ontid

ae

Kyp

hosi

dae

Ops

togn

athi

dae

Dac

tylo

pter

idae

Dac

tylo

scop

idae

Labr

isom

idae

Oph

idiid

ae

Mic

rode

smid

ae

Cal

liony

mid

ae

Ura

nosc

opid

aeT

ripte

rygi

idae

Pte

rele

otrid

aeP

emph

erid

ae

Cirr

hitid

ae

Byt

hitid

aeC

haen

opsi

dae

Fis

tula

riida

e

Mor

ingu

idae

Mal

acan

thid

ae

Ogc

ocep

halid

ae

Bat

rach

oidi

dae

Mul

lidae

Oph

icht

hida

e

Car

apid

ae

Pom

acan

thid

ae

Sco

rpae

nida

eH

aem

ulid

ae

Spa

ridae

Syn

gnat

hida

e

Tet

raod

ontid

ae

Par

alic

hthy

dae

Ost

raci

idae

Pom

acen

trid

ae

0

10

20

30

40

0

Others

Sister-species

Brazil + Caribbean

10

20

30

40

5090 5180

Gobiidae

Syn

gnat

hida

e

Pom

acen

trid

ae

Apo

goni

dae

Ops

togn

athi

dae

Bat

rach

oidi

dae

Byt

hitid

ae

Mic

rode

smid

ae

Trip

tery

giid

ae

Ble

nniid

ae

Labrisomidae

Gobiesocidae

Chaenopsidae

Figure 6 Distributions of species in families of fishes across the Amazon Barrier: numbers of species found on both sides of the

barrier (Brazil + Caribbean); numbers of species that have their closest relative on the other side of the barrier (sisters); and numbers of

species found on one side that have no known sisters on the other side of the barrier (other). Demersal-spawning and brooder families are

indicated with arrows.



along the South African coast from the Agulhas to the

Benguela region (Namibia and southern Angola). However,

these species do not reach tropical waters. A few are also found

in the NEA and/or the Mediterranean, thus representing anti-

tropical distributions (e.g. Sparidae). A cluster analysis sum-

marizing the overall pattern of shared-only taxa (not shown)

closely linked the NWA to the SWA as in Fig. 5, but with the

IO and the EA closely related, and the MAR between the two

clusters.

A cluster analysis of genera (Fig. 9) revealed a pattern

similar to that of the species cluster analysis (Fig. 4). At this

taxonomic level, however, we were able to include the TEP,

which clustered with the WA as expected. The TEP and the

NWA have 155 genera in common, the NWA and the SWA

have 144, the TEA and WA have 110, and the TEA and South

Africa’s Indian Ocean have 94. The generic endemism rate is

very high (50.3%) in the New World (TEP + WA) and in the

EA as a whole (31.5%; Table 3). Within these major regions,

16% of the Caribbean genera are endemic, followed by 14% in

the TEP, 11.4% in the Mediterranean, 3.8% in the TEA, and

2.6% in the SWA.

Subtropical and temperate areas

The subtropical and warm-temperate areas included in our

analysis are impoverished outposts of adjacent tropical areas.

For example, the Carolinian Province (sensu Smith-Vaniz

et al., 1999) and Argentina (see Irigoyen et al., 2005) clustered

with oceanic islands of the nearest contiguous tropical region

(Fig. 4). Despite some recognized endemism (although taxo-

nomically restricted to eight Gobiidae genera plus one

Gobiesocidae genus; Table 3), the Mediterranean Sea has a

marine fauna related to the Macaronesian Islands and the

northeastern Atlantic coast (Goncalves et al., 1993, 2005;

Briggs, 1995; Almada et al., 2001). South Africa’s Benguela (the

‘Southwest Africa’ province of Briggs, 1974) and Agulhas

provinces grouped with Ascension and St Helena, possibly as a

result of their common low diversity rather than of their

Mid-Atlantic Ridge

Tropical Eastern Atlantic

Tropical Western Atlantic

88 98 59

Nu

mb

er o

f sp

ecie

s

Car

angi

dae

Mur

aeni

dae

Ser

rani

dae

Mon

acan

thid

aeB

alis

tidae

Con

grid

aeD

iodo

ntid

aeS

ynod

ontid

aeA

nten

narii

dae

Hol

ocen

trid

aeLa

brid

aeLu

tjani

dae

Pria

cant

hida

eA

cant

hurid

aeA

pogo

nida

e

Ble

nniid

aeB

othi

dae

Chl

opsi

dae

Sca

ridae

Gob

iidae

Aul

osto

mid

aeC

allio

nym

idae

Kyp

hosi

dae

Cha

etod

ontid

ae

Dac

tylo

pter

idae

Labr

isom

idae

Mic

rode

smid

aeM

ullid

ae

Oph

icht

hida

eO

phid

iidae

Pom

acan

thid

aeS

corp

aeni

dae

Spa

ridae

Syn

gnat

hida

e

Tetr

aodo

ntid

ae

Pin

guip

edid

aeO

stra

ciid

ae

Pom

acen

trid

ae

0

5

Others

Sister-species

Amphiatlantic

5

0

10

35

30

25

20

15

5

0

10

10

30

25

20

15

Figure 7 Distributions of species in fami-

lies of fishes across the Mid-Atlantic Barrier,

and at the Mid-Atlantic Ridge islands

(Ascension and St Helena): numbers of spe-

cies found on both sides of the barrier

(Amphiatlantic); numbers of species that

have their closest relative on the other side of

the barrier or on the Mid-Atlantic Ridge

Islands (sisters); and numbers of species

found on one side that have no known sisters

on the other side of the barrier (other).

Species recorded as vagrants were also

included.



biogeographical affinities (i.e. long-branch attraction; Felsens-

tein, 2004). These areas are a mix of EA and IO species, as

expected from their geographic locations. Notwithstanding

this, there are a number of endemics in southwestern Africa

(38 species representing 12% of the fauna), such as the genus

Clinus with 10 endemic species.

Patterns of historical relationships using phylogenies

Origins and diversification of Atlantic reef fishes

Owing to the rarity of reef fish fossils from studied areas (the

Mediterranean being the exception; e.g. Carnevale, 2006),

historical relationships are recovered from published

phylogenetic hypotheses (morphological or molecular-based).

Although controversial (cf. Bromham & Penny, 2003; Pulque-

rio & Nichols, 2007), molecular phylogenies can provide some

idea of the age of cladogenic events through the use of

‘molecular clocks’ (Avise, 2000). With a collection of 26

available phylogenies involving Atlantic reef fish taxa (refer-

ences in Methods), we assess the origins and diversification

(i.e. faunal enrichment) patterns of Atlantic reef fishes using

the evolutionary scenarios shown in Fig. 10. These scenarios

are based on the expected timing and sequence of cladogenic

events from geological and palaeoceanographic records.

What is the geographical pattern of distributions of sister taxa

among provinces?

The three strongest sister-species relationships among regions

(Fig. 11) are: (1) the TEA and MAR, with 86% of the species

being sisters (e.g. Thalassoma sanctaehelenae/ascensionis –

newtoni (Fig. 12), Sparisoma strigatum – cretense); (2) NWA

and SWA [78%; e.g. Thalassoma bifasciatum – noronhanum,

Sparisoma griseorubra – frondosum, Diplodus argenteus –

holbrooki/bermudensis, Halichoeres (Fig. 12), Acanthurus ‘bahi-

anus’ clades]; and (3) the TEP and NWA [69%; e.g. Abudefduf

taurus – concolor, Anisotremus virginicus – taeniatus (Fig. 13)].

While outside the domain of this study, we also observed

strong relationships between the IO and WP [75%; e.g.

Hippocampus ‘kuda’ complex, Pomacanthus (Fig. 12)].

The relatively recent formation of the Isthmus of Panama is

reflected in the number of endemic genera (Fig. 9) and sister

taxa shared between the WA and the TEP (e.g. Rosenblatt,

1967; Knowlton & Weigt, 1998; Bernardi & Lape, 2005). Many

Caribbean reef fishes are phylogenetically related to the EP

[69%; e.g. Abudefduf taurus – concolor, Anisotremus virginicus –

taeniatus (Fig. 13)]. However, it is important to note that

Robertson et al. (2004) reviewed the literature and showed that

10 out of 16 EP species (0.63 ratio) are more closely related to

Indo-Pacific than to NWA lineages. Thus, the relationship

South AfricaIndian Ocean

Tropical Eastern Atlantic

Nu

mb

er o

f sp

ecie

s

Car

angi

dae

Mur

aeni

dae

Ser

rani

dae

Mon

acan

thid

ae

Bal

istid

ae

Dio

dont

idae

Syn

odon

tidae

Ant

enna

riida

e

Labr

idae

Aca

nthu

ridae

Ble

nniid

ae

Bot

hida

e

Spa

ridae

Sci

aeni

dae

Gob

iidae

Gob

ieso

cida

e

Kyp

hosi

dae

Cen

trac

anth

idae

Cal

liony

mid

ae

Cirr

hitid

ae

Fis

tula

riida

e

Mal

acan

thid

ae

Bat

rach

oidi

dae

Leth

rinid

ae

Sco

rpae

nida

e

Hae

mul

idae

Syn

gnat

hida

e

Tet

raod

ontid

ae

Par

alic

hthy

dae

121

0

10

20

30Others

Sister-species

Indian Ocean + TEA

0

15

30

45

60

75

90

Figure 8 Distributions of species in families

of fishes across the Benguela Barrier: num-

bers of species found on both sides of the

barrier (Indian Ocean + Tropical Eastern

Atlantic); numbers of species that have their

closest relative on the other side of the barrier

(sisters); and numbers of species found on

one side that have no known sisters on the

other side of the barrier (other).



between the EP and the NWA (69%) is about the same as its

relation to the WP (63%; e.g. Thalassoma lucasanum; Aulo-

stomus). The Caribbean reef fishes are more closely related to

the TEP (69%) than to the EA [47%; e.g. Hippocampus erectus

– hippocampus (Fig. 12)].

The Mid-Atlantic Barrier seems quite permeable, at least in

terms of the relationship between Brazil and the Gulf of

Guinea. Brazilian species are sisters to EA species in 67% of the

cases [e.g. Clepticus brasiliensis – africanus, Hippocampus reidi –

algiricus (Fig. 12)]. The percentage of sisters between the

Caribbean and the EA is lower (47% of cases) than the Brazil-

EA link, and the same pattern applies to the MAR (63% Brazil-

MAR and 44% Caribbean-MAR). It is interesting that

Abudefduf taurus is found in the Caribbean and in the TEA,

but not in Brazil; however, Muraena melanotis is found in St

Paul’s Rocks and in the TEA, but not in the Caribbean. Recent

records of strays of Sargocentron hastatum in the Caribbean

(Wilk et al., 2005) and Acanthurus monroviae in Brazil (Luiz

et al., 2004) indicate that this barrier is breached occasionally.

Relationships between the Atlantic reef fish fauna and that

of the Indian Ocean are also strong, 67% of the nodes being

sisters in comparisons with the TEA (e.g. Aulostomus chinensis

– strigosus (Fig. 12); Lethrinus atlanticus), and 50% with the

Caribbean, Brazil and the MAR [e.g. Dermatolepis inermis –

striolata, Gnatholepis, Centropyge (Fig. 12)]. Craig & Hastings

(2007) showed that two EA Cephalopholis species (taeniops and

nigri) are closely related to species present in the IO, instead of

in the WA. Other examples of putative sistership between the

IO and the EA are the Anthiinae Meganthias carpenteri (EA)

and M. natalensis (IO) (Anderson, 2006), the butterflyfishes

Figure 10 Evolutionary scenarios for

Atlantic reef fishes based on expected timing

and sequence of cladogenetic events derived

from geological and palaeoceanographic

records. Colour coding represents geograph-

ical areas: magenta, New World (NW); blue,

Eastern Pacific (EP); red, Western Atlantic

(WA); green, Caribbean (CA); brown, Brazil

(BR); orange, Eastern Atlantic (EA); pink,

mid-Atlantic Ridge (MAR); black: Indo-West

Pacific (IWP) origin or splits of unknown

geography. IP, Indo-Pacific; IO, Indian

Ocean. Splits resulting from the Amazon

Barrier are also responsible for faunal

enrichment within the Atlantic Basin (see

scenarios discussed in Rocha, 2003). These

splits result in trans-Amazon sister species

(see Figs 6, 12 & 14 for examples).

Tro

pica

l E P

acifi

c

Car

ibbe

an

Dis

sim

ilarit

y in

dex

SW

Atla

ntic

Car

olin

ian

Tro

pica

l E A

tlant

ic

Mac

aron

esia

Med

iterr

anea

n

S A

fric

a B

engu

ela

S A

fric

a A

gulh

as

SW

Indi

an O

cean

0.80

0.64

0.48

0.32

0.16

0

18

187

19

185

3320

64

12265

270

287

2039

10

6 00 509

15

3

NW

WANEA

EA

Figure 9 Cluster analysis based on the presence/absence of

genera in different areas of the Atlantic and Southern Africa and

the number of endemic genera in each area (Bray-Curtis, UP-

GMA). Horizontal lines show disjunct distributions (or distribu-

tions not related to the cluster analysis) of the genera. Numbers

opposite the horizontal lines represent the total number of genera

related to each distribution. Line thickness is proportional to

the number of genera. Bold numbers represent endemism. Itali-

cized numbers do not represent strict endemism, but genera found

in the assigned areas plus the IWP. NW: New World; WA:

Western Atlantic; NEA: Northeastern Atlantic; EA: Eastern

Atlantic.



Chaetodon hoefleri (EA) and C. marleyi (IO), and the

Drepanidae Drepane africana (EA) and D. longimana (IO)

(Heemstra & Heemstra, 2004). All these cases indicate a clear

phylogenetic connection of the TEA to (sub)tropical southern

Africa.

Another interesting aspect among sister species is the

percentage of putative sympatric (or microallopatric) vs.

allopatric speciation. From a total of 50 sister pairs in the

available phylogenies we found only nine examples (18%) of

range overlap (i.e. where sympatric speciation might be

inferred). Williams & Reid (2004) reported five examples of

range overlap between sister species among 19 studied pairs in

snails of the genus Echinolittorina. Among these cases, we

could not be sure that sympatric speciation occurred because

they could also reflect secondary contact after allopatric split,

and thus although sympatric speciation may have occurred it

seems to be of less importance in marine faunal enrichment.

Are phylogenetic and distributional patterns concordant with

‘traditionally’ accepted provinces?

The overall picture is that phylogenetic and distributional

patterns are concordant. In spite of the Amazon filter (Floeter

& Gasparini, 2000; Joyeux et al., 2001; Rocha, 2003), a strong

relationship between the NWA and the SWA exists in terms of

both shared species (Fig. 5) and sister species (Figs 6 & 11). It

is interesting to note that many ‘Brazilian’ fishes were recently

discovered in the southern tip of the Caribbean (e.g. St.

Vincent, Venezuela and Tobago; see Joyeux et al., 2001; Rocha,

2003; Robertson et al., 2006). New genetic evidence has also

MAR

WP

WP

V

IV

III

II

I

EP

NWA

SWA

EA

0.69

0.63*

0.780.63

0.47

0.86

0.67

IO0.75

WPNWA SWA MAR EA IO0

0.12

0.24

0.36

0.48

0.6

0.50

0.67

Figure 11 Biogeographical barriers and relationships among areas based on reef fish phylogenies. Legends of the barriers are the same as

in Fig. 1. Areas/Provinces: WT, West Tethys; ET, East Tethys. WP, West Pacific; EP, Eastern Pacific; NWA, Northwestern Atlantic

(Caribbean + Bermuda + Carolinian); SWA, Southwestern Atlantic (Brazil + Brazilian oceanic islands + Argentina); MAR, Mid-Atlantic

Ridge (Ascension + St Helena); EA, Eastern Atlantic (Mediterranean + Macaronesia + Gulf of Guinea + Benguela); IO, Indian Ocean.

Arrow width is sized proportionally to the ratio (proportion; numbers are given in each arrow) between the number of nodes in which two

areas form a sister pair in a given phylogeny and the number of times the same pair of areas are available for evaluation in the studied

phylogenies (see Methods). In order to summarize the relationships among the areas, a cluster analysis (Bray-Curtis; UPGMA) based on

the matrix of ratios indicating the importance of the phylogenetic connections is shown at the bottom. Varying the clustering routine

has no effect on the grouping of the sites, except for the EP, which was further excluded from the analysis owing to its inconsistent

position in the dendrogram with different routines (sometimes grouping with the Western Atlantic sites and sometimes grouping with

the Western Pacific). *: ratio based on the compilation of genetic studies by Robertson et al. (2004). The arrows connecting to the IO

represent separate numbers for the EA-IO and WA-IO relationships.



revealed examples of closer evolutionary links between ‘Bra-

zilian’ and Venezuelan fishes rather than between Brazil and

other areas of the NWA [e.g. Sparisoma griseorubra –

frondosum (Robertson et al., 2006); samples of Nicholsina usta

(Brazil) closer to Venezuela than to Florida (Fig. 12)].

The link between the EA and MAR is found both in

phylogenetic and in distributional patterns (Figs 5 & 11). The

links between the WA and EA and between the Atlantic basin

and Indian Ocean are also concordant. It was not possible to

assess the relationships between the TEP and the Atlantic by

Figure 12 Phylogenies related to Tethys

relicts, recent invasions from the Indian

Ocean, and diversification within the Atlantic

scenarios. Colour coding represents geo-

graphic ranges: blue, Eastern Pacific (EP);

red, Western Atlantic (WA); green, Carib-

bean (CA); brown, Brazil (BR); orange,

Eastern Atlantic (EA); pink, mid-Atlantic

Ridge (MAR); black, IWP origin or splits of

unknown geography. Numbers (or confi-

dence intervals) represent the estimated

timing of speciation events in Ma as given in

the original publications. The minimum age

of 3.1 Ma for the splits related to the final

closure of the Isthmus of Panama is assumed.

Age estimates for Pomacanthidae were cali-

brated using fossil evidence (see Bellwood

et al., 2004). Coalescence analysis was used to

estimate divergence times in Centropyge and

Gnatholepis (Rocha et al., 2005a; Bowen

et al., 2006a). The complete phylogeny for

the genus Sparisoma is given in Fig. 14.

Figure 13 Phylogenies related to the origin

in the New World scenario. See Fig. 12 leg-

end for colour codes and inferred timing of

speciation events.



species distributions (they share only a few species), but the

relationships at the genus level (Fig. 9) and sister-species

numbers reflect this historical connection (e.g. Rosenblatt,

1967; Knowlton & Weigt, 1998; Fig. 13).

A general agreement with the biogeographical provinces

described by Briggs (1974, 1995) was observed in all analyses.

Both the maximum-parsimony (Fig. 4) and the distance

(Figs 5 & 10) analysis largely agreed with earlier proposed

provinces (Briggs, 1974, 1995; Vermeij, 1978). The relationship

of the Brazilian oceanic islands with the Brazilian Province also

supported Briggs (1974, 1995), Lubbock & Edwards (1981),

Gasparini & Floeter (2001), Rocha (2003) and Feitoza et al.

(2003) in that these islands are impoverished outposts of the

Brazilian Province. However, the Brazilian Province

should be extended to Santa Catarina at 28� S (Floeter et al.,

2001).

Briggs (1974) divided the Greater Caribbean into the

western Caribbean plus Florida (Caribbean Province) and

the eastern Caribbean (West Indian Province). Recent genetic

and biogeographical surveys have demonstrated an important

partition at the Mona Passage – between Puerto Rico and

Hispaniola (Baums et al., 2005; Dennis et al., 2005; Taylor &

Hellberg, 2006), while others found genetic breaks between

Florida and the Bahamas (Carlin et al., 2003; Rocha et al.,

2005b). Vermeij (2005), working with fossils, also found a deep

split between Florida and the Caribbean for molluscs. There is

thus some justification for partitioning within the NWA (e.g.

Gilbert, 1972). However, genetic analyses of wide-ranging fish

species in the NWA revealed no significant partitions in most

cases (Shulman & Bermingham, 1995; Muss et al., 2001; Rocha

et al., 2002; Bowen et al., 2006b). Using the 10% endemism

level proposed by Briggs (1974) as well as similarity and

parsimony analyses (Figs 4 & 5), the recognition of a ‘Greater

Caribbean’ Province including the eastern and western Carib-

bean plus Florida and Bermuda is supported (Burgess et al.,

1994; Smith-Vaniz et al., 1999).

As expected, the mid-Atlantic islands of Ascension and

St Helena are intermediate in faunal composition between

the WA and EA, consistent with their intermediate location.

Seventy-one species are shared with the west and 64 with the

east, but, as a result of the greater similarity of their total

richness with the EA (7.5% of the WA fauna vs. 16% for the

EA), they clustered with the EA in Figs 5 & 11 and with south-

west Africa and the EA in Fig. 4. A reinforcement of this

pattern is the stronger phylogenetic relationship of Ascension

and St Helena and the EA [Fig. 11; e.g. Ophioblennius and

Thalassoma (Fig. 13)]. However, genetic analyses of the genera

Acanthurus and Centropyge in the Atlantic support a close

relationship between the MAR and the SWA (Rocha et al.,

2002; Bowen et al., 2006a).

The division of the EA into three sub-areas (the TEA, the

warm-temperate NEA, and southwestern Africa – Fig. 4) was

predicted by sea-surface-temperature isotherm bunching at

capes along the African coast. The difference between our

analysis and that of Briggs (1974, 1995; i.e. ‘Lusitania’

Province) is that the northwest African coast is more closely

related to the TEA in overall diversity than to the Macarone-

sian Islands or the Mediterranean. In an analysis of the

blenniid fauna, Almada et al. (2001) found that Mauritania

clustered with the TEA, but Morocco grouped with the NEA.

Avila (2000) found that Moroccan molluscs were affiliated

with both the Cape Verde Islands and the NEA. In addition,

there is recent genetic evidence for both endemism in the

Mediterranean (e.g. Aurelle et al., 2003; Bargelloni et al., 2003;

Table 3) and genetic continuity along the Mediterranean and

the Atlantic coastline (e.g. Bargelloni et al., 2003; Costagliola

et al., 2004), as well as cases where one of two sister species are

present in the Mediterranean and adjacent Atlantic, while the

other is found in tropical west Africa and the Macaronesian

islands (e.g. Chromis chromis – limbata, Domingues et al.,

2005; Parablennius sanguinolentus – parvicornis, Almada et al.,

2005).

Is there a general relationship between diversity and origin

of clades?

The uneven distribution of species in selected genera in

different provinces (Fig. 3) seems to be related to their putative

origin. For example, the genera Anisotremus, Elacatinus,

Rypticus, Serranus, and Sparisoma all have several species in

the NW (New World, i.e. both sides of tropical America) and

are now thought to have originated and diversified in the NW

(Fig. 13; Guimaraes, 1999; Bernardi & Lape, 2005; Taylor &

Hellberg, 2005; Robertson et al., 2006), some with subsequent

invasion of the EA (Fig. 13; Carlin et al., 2003; Serranus – M.

Kochzius & A. Dominici-Arosemena, personal communica-

tion). In contrast, the genus Diplodus is more speciose in the

EA than in the WA, and its molecular phylogeny indicates an

EA origin (Fig. 12; Summerer et al., 2001). Distributional data

indicate that the same pattern should be expected for

Parablennius and Scartella. (Both lack molecular phylogenies;

however, these groups are currently being analysed by

V. Almada and collaborators.)

The link between species richness and area of origin is found in

the genus Lethrinus, which occurs in the EA and the Indo-Pacific

but not in the WA. The only Atlantic species (L. atlanticus) is

nested deeply within the Indo-Pacific Lethrinus (Galbo et al.,

2002), indicating that this genus originated and diversified in the

Indo-Pacific, and that the Atlantic species is the result of an

invasion around 5–6 Ma, assuming the standard divergence of

2% per million years for cytochrome b (Avise, 2000). Even

considering a divergence rate of 1% per million years, this

invasion probably occurred via southern Africa well after the

Tethyan Terminal Event (c.12–18 Ma).

In summary, it seems that the greatest species richness for

reef fish genera is found at their locations of origin.

Is there a congruent pattern linked to historical events? Is the

timing of divergence consistent among the various taxa?

It is clear from the phylogenies that all major biogeographical

barriers/filters left their marks (Figs 12–14). Nevertheless,



speciation events are not simply predicted by geological

or oceanographic events. Both episodic extinction and

cladogenic events influence patterns of faunal richness. Owing

to the lack of a fossil record for reef fishes, we could

not infer extinctions; instead, we could only explore

relationships between speciation and large-scale historical

events.

The timing of cladogenic events is not concordant among

genera (Figs 12 & 13). For example, trans-Atlantic divergence

times range from c. 5.5 Ma (Fig. 13; Thalassoma, Costagliola

et al., 2004; Nicholsina usta clade, Robertson et al., 2006) to

c. 3 Ma (Fig. 13; Sparisoma ‘rubripinne’ clade, Robertson et al.,

2006; Hippocampus ‘erectus’ clade, Casey et al., 2004), as well as

£ 1 Ma (Fig. 13; Hippocampus reidi – algiricus, Casey et al.,

Figure 14 Comparative chronogram of

cladogenic events based on seven distinct reef

fish phylogenies (references in Methods).

Time-scales are based on conventional rates

of divergence for fish cytochrome b

sequences (1% per Ma at the top and 2.5%

per Ma at the bottom). The grey band

highlights the diversification that occurred

during the late Miocene to the Pliocene

(peaking from 8 to 2 Ma if the 2.5% per Ma

time-scale is assumed). Colour coding rep-

resents geographic ranges as in Figs 12 and

13.



2004) to a few tens of thousands of years (Gnatholepis, Rocha

et al., 2005a). The relatively recent time frame of partitions

(e.g. Robertson et al., 2006) eliminates vicariance following the

opening the Atlantic (65 Ma), and there is no suggestion of

simultaneous interruptions of gene flow among species

resulting from a single palaeoceanographic event.

The lack of congruent divergences is also found across the

Amazon barrier [Figs 13 & 14: from 6 Ma in Ophioblennius

macclurei – trindadensis (Muss et al., 2001); to 4 Ma in

Thalassoma bifasciatum – noronhanum (Costagliola et al.,

2004); to c. 1 Ma in Acanthurus bahianus (Rocha et al.,

2002), Halichoeres radiatus – brasiliensis (Rocha, 2004) and

Sparisoma atomarium – tuiupiranga (Robertson et al., 2006);

to very recent in Acanthurus coeruleus (Rocha et al., 2002) and

Sparisoma viride – amplum (Robertson et al., 2006)]. Likewise,

the dispersal events from the Indian Ocean to the Atlantic vary

widely through time (Fig. 13; from 4.6 Ma in the Chromis

‘chromis’ clade to 0.13 Ma in Gnatholepis, Rocha et al., 2005a).

These invasions seem to have occurred both before the

Benguela upwelling c. 2 Ma and relatively recently (Bowen

et al., 2001, 2006a; Rocha et al., 2005a).

In summary, the Benguela, mid-Atlantic, and Amazon filters

have restricted dispersal but also allowed occasional crossings

that resulted in the establishment of new populations and

species. Ocean-current dynamics, which are likely to affect

dispersal across these barriers, have varied considerably with

changing sea-levels over the past 10 Myr (Kaneps, 1979;

Rocha, 2003; Robertson et al., 2006). The effectiveness of the

Amazon barrier, in particular, is thought to have been strongly

influenced by changing sea-levels not only through variation in

current speeds (Kaneps, 1979), which affect larval transit times,

but also through variations in the salinity of that barrier and

the availability of marine habitats beneath the freshwater

plume (Rocha, 2003). Fluctuations in the effectiveness of the

three filters provide a mechanism for much of the recent

diversification of reef fishes in the Atlantic.

Despite the lack of a consistent temporal signal for

speciation events, an important diversification occurred during

the late Miocene to the Pliocene (peaking from 8 to 2 Ma;

Fig. 14). This phenomenon is probably related to the closing of

the Isthmus of Panama and its effects on the direction and

speed of the Atlantic currents (see Muss et al., 2001 and

references therein). A second burst of speciation events

occurred well after the Isthmus closure (Figs 13 & 14), many

of them £ 1.5 Ma and possibly related to fluctuations in the

effectiveness of the three filters or recent diversification across

ecological gradients (Rocha, 2004; Rocha et al., 2005a,b; Taylor

& Hellberg, 2005; Robertson et al., 2006). For example, some

Caribbean species are present in the Brazilian offshore islands

of Fernando de Noronha and Atol das Rocas (South of the

Amazon barrier) but do not occur on the adjacent Brazilian

continental shoreline, which imposes very different ecological

conditions (high sediment loads, low water transparence,

continental freshwater runoff, etc.). In some cases, these

species are replaced by closely related sister taxa along the

coast. This observation led Rocha et al. (2005b) to propose

ecological speciation in the genus Halichoeres, and a very

similar pattern was observed in gobies of the genus Bathygobius

(Lima et al., 2005).

What is the relative importance of vicariant persistence and

dispersal routes on contemporary biodiversity?

Our data indicate that both vicariant events, such as the

closure of the Isthmus of Panama, and dispersal events across

the three primary Atlantic biogeographical filters have con-

tributed to the distribution patterns that we observe today.

Theories concerning the origins of the NW reef biota

involve two primary hypotheses: relicts of Tethyan fauna vs.

colonization from the IWP (Veron, 1995; Barber & Bellwood,

2005). The relict hypothesis is based on the separation of the

western Atlantic from the eastern Indian and Pacific oceans,

resulting in two isolated reef systems after the final closure of

the Red Sea land bridge c. 12–18 Ma (Steininger & Rogl,

1984). The alternative hypothesis is colonization from the

Pacific across the East Pacific Barrier (EPB) and into the

Caribbean prior to the closure of the Isthmus of Panama,

and/or colonization of the Atlantic from the Indian Ocean via

southern Africa.

These theories yield clear predictions. The relict theory

predicts that the age of the Atlantic/East Pacific fauna must

exceed 12 Myr, with origins derived from IO lineages (Fig. 10,

scenario A). Colonization via the opened Isthmus predicts that

NW species must be older than 3.1 Myr (Coates & Obando,

1996), and that they will have sister taxa with central and

eastern Pacific distributions (Fig. 10, scenario B). Recent

invasions via South Africa predict that Atlantic species must

be younger than 3.1 Myr and will have Indian Ocean sister

species (Fig. 10, scenario C1). A vicariant scenario (C2)

involving the closure of the Isthmus of Panama and the

intensification of the Benguela upwelling system could involve

the following steps: (1) an original large geographical range

encompassing the IO, WA and TEP; (2) isolation of the TEP

population with the rise of the Isthmus (c. 3.1 Ma); and (3)

isolation of the WA and the IO by the Benguela Barrier (c.

2 Ma).

Other possible scenarios for the origins and diversification

of the Atlantic reef fauna would be origin in the NW,

probably after W-E Tethys separation deep in the phylo-

genies – i.e. ‘sister-genera’ relationships (Fig. 10, scenario D),

and/or dispersal within the Atlantic basin (Fig. 10, scenarios

E and F).

From our compilation of phylogenies (Figs 12–14), Atlantic

reef fishes fit all of the proposed scenarios. Supporting the

Tethys relict scenario, we have examples of the 18-Ma major

split in the Halichoeres phylogeny (Figs 12 & 14), and the

c. 20-Ma splits in Holacanthus and Pomacanthus, all dividing

the NW and IWP clades. Moreover, there is the morphological

phylogeny of Scaridae (Bellwood, 1994), where Sparisoma is

thought to be a Tethyan relict (Streelman et al., 2002).

A similar case is the 20-Ma split of the EA clade Chaetodon

robustus-hoefleri (Chaetodontidae) from IWP clades (Fessler &



Westneat, 2007). Orrell et al. (2002) also suggested a clear

Tethyan partition within the sparid evolution.

Supporting colonization via the opened Isthmus hypothesis

(Fig. 10, scenario B), we have the diversification of a NWA

clade within Halichoeres (Barber & Bellwood, 2005) and

Thalassoma (Costagliola et al., 2004) (Fig. 14). Bellwood

(1994) and Gomon (1997) discuss similar cases for Scarus

and Bodianus, respectively.

In recent years, there has been mounting evidence that late

Pliocene or Pleistocene (< 3 Ma) invasions via southern Africa

(Fig. 10, scenario C1) contribute to diversity in the Atlantic.

Examples in Fig. 12 include the genera Aulostomus, Centropyge,

Gnatholepis, and the Hippocampus ‘kuda’ clade (see Casey

et al., 2004; Rocha et al., 2005a; Bowen et al., 2006a). The

evolution of the genus Dermatolepis fits with scenario C2.

Relatively recent diversification within the NW (Fig. 10,

scenario D – with or without ancient separation of clades

related to Tethys) is found in the Abudefduf ‘declivifrons’ clade,

Alphestes, Anisotremus, Chaenopsidae, Chromis ‘cyanea’ clade,

Elacatinus, Gobiescocinae, and Rypticus. It is interesting to

note that the number of geminate pairs separated by the

Isthmus of Panama is relatively low, compared with the total

number of species in the Neotropical clades. Speciation events

within the EP or the WA are much more common than

previously expected, and may correspond to instances of

sympatric and ecological speciation.

Within the Atlantic basin, the available phylogenies indicate

invasions from the WA to the EA in most cases: Clepticus,

Hippocampus ‘erectus’ clade, Nicholsina, Ophioblennius, Spari-

soma ‘rubripinne’ clade, and Thalassoma (Fig. 10, scenario E).

Invasions from the EA to the WA are rare (e.g. Diplodus).

However, further studies of other genera with distribution

patterns like that of the genus Parablennius (see Fig. 3) may

reveal more cases of westward migrants (see Luiz et al., 2004;

Fig. 10, scenario F).

In summary, historical relationships among Atlantic prov-

inces are complex and reticulated (sensu Brooks, 2004), with

provinces comprising a mixture of residents (species that

evolved within province boundaries – after the closure of the

Tethys seaway) and colonizers (species that evolved outside the

province and dispersed across a variety of time frames).

Moreover, this work provides additional evidence for the

importance of founder speciation by means of dispersal in the

evolution of reef fishes (see also Paulay & Meyer, 2002 and

Queiroz, 2005).

Conclusions and future prospects

Here we have attempted to elucidate the role of biogeograph-

ical hard barriers (Tethys and Panama) as well as of more

porous biogeographical filters (Benguela, mid-Atlantic, and

Amazon barriers) in generating and maintaining Atlantic

biodiversity. Most of the contemporary reef fish families were

established by the lower Eocene (50 Ma), and most modern

genera were present by the mid-Miocene (10 Ma) (Bellwood &

Wainwright, 2002). As a consequence, the closure of the Tethys

Sea must have affected the evolution of Atlantic reef biota.

Some elements of the Atlantic reef fauna pre-date this event,

including corals (Veron, 1995), the endemic lineages of

parrotfishes (Bellwood, 1994; Streelman et al., 2002), some

wrasses (Barber & Bellwood, 2005), and angelfishes (Bellwood

et al., 2004). The three soft barriers or filters have clearly

restricted dispersal and have promoted the development of

new species in allopatry and/or parapatry. Since habitat

characteristics vary greatly among regions, ecological specia-

tion may also have been important in diversification. Fluctu-

ations in the effectiveness of the soft barriers provide a

mechanism for much of the recent faunal exchanges in the

Atlantic. Thus, vicariant events (e.g. the closure of the Isthmus

of Panama), relatively recent dispersal (with further speciation

or not), and adaptation to novel habitats seem to have

combined to regulate Atlantic tropical marine biodiversity, all

having contributed to the biogeographical patterns we observe

today. Processes originating from dispersal across barriers or

colonization of novel habitats seem to outnumber vicariant

events. However, it will be necessary to analyse additional

higher-level phylogenies (family and genus levels; e.g. Orrell

et al., 2002), when they become available, to separate out the

relative importance of Tethys relicts vs. later colonization. The

plurality of biogeographical histories and speciation patterns in

the marine tropics found here agrees with the recent findings

of Rocha (2003) for fishes, Meyer (2003) for cowries, and

Williams & Reid (2004) for littorinid snails.

Finally, there are undeniable roles for humanity in contem-

porary biogeographical processes. These include three obvious

factors involving the transport and introduction of exotic

species, and probably several others that elude our grasp. First,

the aquarium trade has introduced Indo-Pacific species into

the Atlantic, most notably the Pacific lionfishes in the NWA

(Whitfield et al., 2002). Second, ballast water in cargo vessels is

considered a primary threat; however, the screens on ballast

tanks mostly exclude fish larvae, and the smaller invertebrate

larvae are a much greater hazard (Wonham et al., 2000).

Third, the Suez Canal has essentially reopened the Tethys Sea

connection between the Red Sea and the Mediterranean. The

invasions to date have been for the most part limited by the

cooler subtropical conditions in the Mediterranean [but see

Edwards (1987) for examples of some species that have spread

their distribution ranges since 1902 and Bariche & Saad (2005)

for a recent example], but this may change if predictions of

global warming are accurate (see Brito et al., 2005 and Bianchi,

2007 on the recent tropicalization of the littoral ichthyofauna

of the Canary Islands and the Mediterranean). Both the Suez

connection and the southern African connection may be

enhanced by global warming, and the consequences for inter-

ocean faunal exchanges are uncertain.

ACKNOWLEDGEMENTS

We thank the following people for helping us cross-check

data, allowing us to use unpublished data, and/or sharing

their expert knowledge in their study families: L. Beckley,



P.A. Hulley, P.H. Skelton, D. Polack, J.L. Van Tassell, J. Leis,

R. Fricke, J.E. Randall, W.N. Eschmeyer, G.R. Allen, P. Lobel,

M. Biscoito, A.G. Floeter, R. Reeves, O.J. Luiz Jr, J.C. Briggs,

R.R. Warner, A. Carvalho-Filho, J. Williams and K. Matsu-

ura. We also thank colleagues who reviewed earlier versions

of the manuscript: G.J. Vermeij, J.C. Briggs, V. Faria,

V. Almada, V. Domingues and H. Choat. Essential financial

support was provided by the Smithsonian Tropical Research

Institute (STV grants to S.R.F. and C.E.L.F.), the National

Geographic Society (grants 7937-05 to S.R.F. and 7708-04 to

L.A.R.), and the Universidade Federal de Santa Catarina. This

work was partly conducted while S.R.F. was a postdoctoral

associate at the National Center for Ecological Analysis and

Synthesis, a center funded by the NSF (grant DEB-0072909)

and the University of California, Santa Barbara. We also

acknowledge the access to many institutional ichthyological

collections and the cooperation of their curatorial staffs –

without their help the distributional data for this study would

have been inadequate.

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SUPPLEMENTARY MATERIAL

The following supplementary material is available for this

article online:

Table S1 Atlantic reef fish data base.

Table S2 Sister-species table and references.

This material is available as part of the online article

from: http://www.blackwell-synergy.com/doi/abs/10.1111/j.

1365-2699.2007.01790.x

Please note: Blackwell Publishing is not responsible for the

content or functionality of any supplementary materials

supplied by the authors. Any queries (other than missing

material) should be directed to the corresponding author for

the article.

BIOSKETCH

Sergio R. Floeter has held a position as professor in

vertebrate zoology at the Universidade Federal de Santa

Catarina in southern Brazil since 2006. His main research

interests are reef fish macroecology, biogeography, evolution,

and conservation. He also plays the guitar.

Editor: David Bellwood



Table S1 Atlantic reef fish database - Floeter et al.

Family Genus Species Authority & Year CA

RO

LIN

IAN

BE

RM

UD

A

W_C

AR

IBB

EA

N_F

LOR

IDA

E_C

AR

IBB

EA

N

NE

_BR

AZI

L

SE

_BR

AZI

L

AR

GE

NTI

NA

_UR

UG

UA

Y

ATO

L_R

OC

AS

F_N

OR

ON

HA

ST_

PA

ULS

_RO

CK

S

TRIN

DA

DE

AS

CE

NS

ION

ST_

HE

LEN

A

AZO

RE

S

MA

DE

IRA

CA

NA

RIE

S

W_M

ED

ITE

RR

AN

EA

N

E_M

ED

ITE

RR

AN

EA

N

CA

BO

_VE

RD

E

SÃ

O_T

OM

É

TRO

PIC

AL_

WE

ST_

AFR

ICA

NO

RTH

_WE

ST_

AFR

ICA

SA

FRIC

A_B

EN

GU

ELA

SA

FRIC

A_C

AP

E

SA

FRIC

A_I

ndia

n O

cean

ACANTHURIDAE Acanthurus bahianus Castelnau, 1855 1 1 1 1 1 1 1 1 1 1 1ACANTHURIDAE Acanthurus chirurgus (Bloch, 1787) 1 1 1 1 1 1 1 1 1 1ACANTHURIDAE Acanthurus coeruleus Bloch & Schneider, 1801 1 1 1 1 1 1 1 1 1 1ACANTHURIDAE Acanthurus dussumieri Valenciennes, 1835 1 1ACANTHURIDAE Acanthurus monroviae Steindachner, 1876 1 1 1 1 1 1 1 1 1ACANTHURIDAE Acanthurus triostegus (Linnaeus, 1758) 1 1ACANTHURIDAE Naso brevirostris (Cuvier, 1829) 1 1ACANTHURIDAE Prionurus biafraensis (Blache & Rossignol, 1961) 1 1ACANTHURIDAE Zebrasoma gemmatum (Valenciennes, 1835) 1 1ANTENNARIIDAE Antennarius bermudensis Schultz, 1957 1 1 1ANTENNARIIDAE Antennarius hispidus (Bloch & Schneider, 1801) 1 1ANTENNARIIDAE Antennarius multiocellatus (Valenciennes, 1837) 1 1 1 1 1 1 1 1 1 1ANTENNARIIDAE Antennarius nummifer (Cuvier, 1817) 1 1 1 1 1 1ANTENNARIIDAE Antennarius ocellatus (Bloch & Schneider, 1801) 1 1 1 1ANTENNARIIDAE Antennarius pardalis (Valenciennes, 1837) 1 1 1ANTENNARIIDAE Antennarius pauciradiatus Schultz, 1957 1 1 1 1ANTENNARIIDAE Antennarius radiosus Garman, 1896 1 1 1 1ANTENNARIIDAE Antennarius senegalensis Cadenat, 1959 1 1 1 1 1 1ANTENNARIIDAE Antennarius striatus (Shaw, 1794) 1 1 1 1 1 1 1 1 1 1 1 1 1 1ANTENNARIIDAE Histrio histrio (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1 1APOGONIDAE Apogon affinis (Poey, 1875) 1 1 1 1 1 1 1APOGONIDAE Apogon americanus Castelnau, 1855 1 1 1 1 1 1APOGONIDAE Apogon anisolepis Böhlke & Randall, 1968 1APOGONIDAE Apogon aurolineatus (Mowbray, 1927) 1 1 1 1APOGONIDAE Apogon axillaris Valenciennes, 1832 1 1APOGONIDAE Apogon binotatus (Poey, 1867) 1 1 1APOGONIDAE Apogon gouldi Smith-Vaniz, 1977 1 1 1 1APOGONIDAE Apogon imberbis (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1APOGONIDAE Apogon kallopterus Bleeker, 1856 1 1APOGONIDAE Apogon lachneri Böhlke, 1959 1 1APOGONIDAE Apogon leptocaulus Gilbert, 1972 1 1APOGONIDAE Apogon maculatus (Poey, 1860) 1 1 1 1APOGONIDAE Apogon mosavi Dale, 1977 1 1APOGONIDAE Apogon phenax Böhlke & Randall, 1968 1 1APOGONIDAE Apogon pillionatus Böhlke & Randall, 1968 1 1APOGONIDAE Apogon planifrons Longley & Hildebrand, 1940 1 1 1 1 1 1APOGONIDAE Apogon pseudomaculatus Longley, 1932 1 1 1 1 1 1 1APOGONIDAE Apogon quadrisquamatus Longley, 1934 1 1 1 1APOGONIDAE Apogon robbyi Gilbert & Tyler, 1997 1 1 1 1APOGONIDAE Apogon robinsi Böhlke & Randall, 1968 1 1 1APOGONIDAE Apogon townsendi (Breder, 1927) 1 1 1APOGONIDAE Astrapogon alutus (Jordan & Gilbert, 1882) 1 1 1APOGONIDAE Astrapogon puncticulatus (Poey, 1867) 1 1 1 1 1 1APOGONIDAE Astrapogon stellatus (Cope, 1867) 1 1 1 1 1 1 1 1APOGONIDAE Phaeoptyx conklini (Silvester, 1915) 1 1 1 1APOGONIDAE Phaeoptyx pigmentaria (Poey, 1860) 1 1 1 1 1 1 1 1 1 1APOGONIDAE Phaeoptyx xenus (Böhlke & Randall, 1968) 1 1 1AULOSTOMIDAE Aulostomus chinensis (Linnaeus, 1766) 1 1AULOSTOMIDAE Aulostomus maculatus Valenciennes, 1837 1 1 1AULOSTOMIDAE Aulostomus strigosus Wheeler, 1955 1 1 1 1 1 1 1 1 1 1 1 1 1BALISTIDAE Abalistes stellatus (Anonymous, 1798) 1 1BALISTIDAE Balistes capriscus Gmelin, 1789 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1BALISTIDAE Balistes punctatus Gmelin, 1789 1 1 1 1 1 1 1BALISTIDAE Balistes vetula Linnaeus, 1758 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1BALISTIDAE Canthidermis maculata (Bloch, 1786) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1BALISTIDAE Canthidermis sufflamen (Mitchill, 1815) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1BALISTIDAE Melichthys niger (Bloch, 1786) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1BALISTIDAE Odonus niger (Rüppell, 1836) 1 1BALISTIDAE Rhinecanthus aculeatus (Linnaeus, 1758) 1 1BALISTIDAE Rhinecanthus rectangulus (Bloch & Schneider, 1801) 1 1BALISTIDAE Xanthichthys lineopunctatus (Hollard, 1854) 1 1BALISTIDAE Xanthichthys ringens (Linnaeus, 1758) 1 1 1 1 1BALISTIDAE Xenobalistes punctatus Heemstra & Smith, 1983 1 1BATRACHOIDIDAE Amphichthys cryptocentrus (Valenciennes, 1837) 1 1BATRACHOIDIDAE Austrobatrachus foedus (Smith, 1947) 1 1BATRACHOIDIDAE Batrichthys albofasciatus Smith, 1934 1BATRACHOIDIDAE Batrichthys apiatus (Valenciennes, 1837) 1 1 1BATRACHOIDIDAE Batrichthys felinus Smith, 1952 1 1BATRACHOIDIDAE Chatrabus hendersoni (Smith, 1952) 1BATRACHOIDIDAE Chatrabus melanurus (Barnard, 1927) 1 1BATRACHOIDIDAE Halobatrachus didactylus (Bloch & Schneider, 1801) 1 1 1BATRACHOIDIDAE Opsanus beta (Goode & Bean, 1880) 1 1BATRACHOIDIDAE Opsanus dichrostomus Collette, 2001 1

BATRACHOIDIDAE Opsanus pardus (Goode & Bean, 1880) 1 1BATRACHOIDIDAE Opsanus phobetron Walters & Robins, 1961 1 1BATRACHOIDIDAE Opsanus tau (Linnaeus, 1766) 1BATRACHOIDIDAE Perulibatrachus elminensis (Bleeker, 1863) 1 1 1BATRACHOIDIDAE Perulibatrachus rossignoli (Roux, 1957) 1 1BATRACHOIDIDAE Porichthys kymosemeum Gilbert, 1968 1 1BATRACHOIDIDAE Porichthys oculofrenum Gilbert, 1968 1 1 1BATRACHOIDIDAE Porichthys pauciradiatus Caldwell & Caldwell, 1963 1 1BATRACHOIDIDAE Porichthys plectrodon Jordan & Gilbert, 1882 1 1 1 1BATRACHOIDIDAE Porichthys porosissimus (Cuvier, 1829) 1 1BATRACHOIDIDAE Sanopus astrifer (Robins & Starck, 1965) 1BATRACHOIDIDAE Sanopus barbatus (Meek & Hildebrand, 1928) 1BATRACHOIDIDAE Sanopus greenfieldorum Collette, 1983 1BATRACHOIDIDAE Sanopus johnsoni Collette & Starck, 1974 1BATRACHOIDIDAE Sanopus reticulatus Collette, 1983 1BATRACHOIDIDAE Sanopus splendidus (Berg, 1893) 1BATRACHOIDIDAE Thalassophryne montevidensis (Berg, 1893) 1BATRACHOIDIDAE Thalassophryne nattereri Steindachner, 1876 1 1BATRACHOIDIDAE Thalassophryne punctata Steindachner, 1876 1 1BATRACHOIDIDAE Triathalassothia argentina (Berg, 1897) 1BATRACHOIDIDAE Triathalassothia gloverensis Greenfield & Greenfield, 1973 1BATRACHOIDIDAE Triathalassothia lambaloti Menezes & de Figueiredo, 1998 1BLENNIIDAE Aidablennius sphynx (Valenciennes, 1836) 1 1 1BLENNIIDAE Antennablennius australis Fraser-Brunner, 1951 1 1BLENNIIDAE Antennablennius bifilum (Günther, 1861) 1 1BLENNIIDAE Aspidontus dussumieri (Valenciennes, 1836) 1 1BLENNIIDAE Bathyblennius antholops (Springer & Smith-Vaniz, 1970) 1BLENNIIDAE Blennius normani Poll, 1949 1 1BLENNIIDAE Blennius ocellaris Linnaeus, 1758 1 1 1 1BLENNIIDAE Chalaroderma capito (Valenciennes, 1836) 1 1BLENNIIDAE Chalaroderma ocellata (Gilchrist & Thompson, 1908) 1BLENNIIDAE Chasmodes bosquianus (Lacepède, 1800) 1BLENNIIDAE Chasmodes longimaxilla Williams, 1983 1BLENNIIDAE Chasmodes saburrae Jordan & Gilbert, 1882 1BLENNIIDAE Coryphoblennius galerita (Linnaeus, 1758) 1 1 1 1 1 1BLENNIIDAE Entomacrodus cadenati Springer, 1967 1 1 1 1BLENNIIDAE Entomacrodus nigricans Gill, 1859 1 1 1 1 1BLENNIIDAE Entomacrodus sp.n. 1BLENNIIDAE Entomacrodus textilis (Valenciennes, 1836) 1 1BLENNIIDAE Entomacrodus vomerinus (Valenciennes, 1836) 1 1 1 1BLENNIIDAE Hypleurochilus aequipinnis (Günther, 1861) 1 1 1BLENNIIDAE Hypleurochilus bananensis (Poll, 1959) 1 1 1 1 1BLENNIIDAE Hypleurochilus bermudensis Beebe & Tee-Van, 1933 1 1 1 1BLENNIIDAE Hypleurochilus caudovittatus Bath, 1994 1BLENNIIDAE Hypleurochilus fissicornis (Quoy & Gaimard, 1824) 1 1 1BLENNIIDAE Hypleurochilus geminatus (Wood, 1825) 1 1 1BLENNIIDAE Hypleurochilus langi (Fowler, 1923) 1 1BLENNIIDAE Hypleurochilus multifilis (Girard, 1858) 1BLENNIIDAE Hypleurochilus pseudoaequipinnis Bath, 1994 1 1 1 1 1 1BLENNIIDAE Hypleurochilus springeri Randall, 1966 1 1BLENNIIDAE Hypsoblennius exstochilus Böhlke, 1959 1BLENNIIDAE Hypsoblennius hentz (Lesueur, 1825) 1 1BLENNIIDAE Hypsoblennius invemar Smith-Vaniz & Acero P., 1980 1 1 1 1BLENNIIDAE Hypsoblennius ionthas (Jordan & Gilbert, 1882) 1 1BLENNIIDAE Istiblennius edentulus (Forster & Schneider, 1801) 1 1BLENNIIDAE Lipophrys trigloides (Valenciennes, 1836) 1 1 1 1 1 1 1BLENNIIDAE Microlipophrys adriaticus (Steindachner & Kolombatovic, 1883) 1BLENNIIDAE Microlipophrys basiliscus (Valenciennes, 1836) 1 1BLENNIIDAE Microlipophrys bauchotae (Wirtz & Bath, 1982) 1BLENNIIDAE Microlipophrys caboverdensis (Wirtz & Bath, 1989) 1BLENNIIDAE Microlipophrys canevae (Vinciguerra, 1880) 1 1BLENNIIDAE Microlipophrys dalmatinus (Steindachner & Kolombatovic, 1883) 1 1BLENNIIDAE Microlipophrys nigriceps (Vinciguerra, 1883) 1 1BLENNIIDAE Microlipophrys pholis (Linnaeus, 1758) 1 1 1 1 1BLENNIIDAE Microlipophrys velifer (Norman, 1935) 1 1 1 1BLENNIIDAE Omobranchus woodi (Gilchrist & Thompson, 1908) 1 1BLENNIIDAE Ophioblennius atlanticus (Valenciennes, 1836) 1 1 1 1BLENNIIDAE Ophioblennius macclurei (Silvester, 1915) 1 1 1 1BLENNIIDAE Ophioblennius sp. 1 1BLENNIIDAE Ophioblennius sp.EA 1 1 1BLENNIIDAE Ophioblennius trinitatis Miranda-Ribeiro, 1919 1 1 1 1 1 1BLENNIIDAE Parablennius cornutus (Linnaeus, 1758) 1 1 1 1BLENNIIDAE Parablennius dialloi Bath, 1990 1BLENNIIDAE Parablennius gattorugine (Linnaeus, 1758) 1 1 1BLENNIIDAE Parablennius goreensis (Valenciennes, 1836) 1 1BLENNIIDAE Parablennius incognitus (Bath, 1968) 1 1 1 1 1 1 1BLENNIIDAE Parablennius marmoreus (Poey, 1876) 1 1 1 1 1 1BLENNIIDAE Parablennius parvicornis (Valenciennes, 1836) 1 1 1 1 1 1BLENNIIDAE Parablennius pilicornis (Cuvier, 1829) 1 1 1 1 1 1 1 1 1BLENNIIDAE Parablennius rouxi (Cocco, 1833) 1 1BLENNIIDAE Parablennius ruber (Valenciennes, 1836) 1 1BLENNIIDAE Parablennius salensis Bath, 1990 1BLENNIIDAE Parablennius sanguinolentus (Pallas, 1814) 1 1 1BLENNIIDAE Parablennius sierraensis Bath, 1990 1

BLENNIIDAE Parablennius tentacularis (Brünnich, 1768) 1 1BLENNIIDAE Parablennius verryckeni (Poll, 1959) 1 1BLENNIIDAE Parablennius zvonimiri (Kolombatovic, 1892) 1 1BLENNIIDAE Plagiotremus rhinorhynchos (Bleeker, 1852) 1 1BLENNIIDAE Plagiotremus tapeinosoma (Bleeker, 1857) 1 1BLENNIIDAE Salaria basilisca (Valenciennes, 1836) 1 1BLENNIIDAE Salaria pavo (Risso, 1810) 1 1 1 1BLENNIIDAE Scartella caboverdiana Bath, 1990 1BLENNIIDAE Scartella cristata (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1 1BLENNIIDAE Scartella emarginata (Günther, 1861) 1 1 1 1BLENNIIDAE Scartella nuchifilis (Valenciennes, 1836) 1BLENNIIDAE Scartella poiti Rangel, Gasparini & Guimarães, 2004 1BLENNIIDAE Scartella sp.n. 1 1BLENNIIDAE Scartella springeri (Bauchot, 1967) 1BLENNIIDAE Spaniblennius clandestinus Bath & Wirtz, 1989 1BLENNIIDAE Spaniblennius riodourensis (Metzelaar, 1919) 1BLENNIIDAE Xiphasia matsubarai Okada & Suzuki, 1952 1 1BLENNIIDAE Xiphasia setifer Swainson, 1839 1 1BOTHIDAE Arnoglossus capensis Boulenger, 1898 1 1 1 1 1 1 1 1BOTHIDAE Arnoglossus imperialis (Rafinesque, 1810) 1 1 1 1 1 1 1BOTHIDAE Arnoglossus laterna (Walbaum, 1792) 1 1 1BOTHIDAE Arnoglossus thori Kyle, 1913 1 1 1 1 1 1BOTHIDAE Bothus guibei Stauch, 1966 1 1BOTHIDAE Bothus lunatus (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1BOTHIDAE Bothus maculiferus (Poey, 1860) 1 1 1 1 1 1BOTHIDAE Bothus mellissi Norman, 1931 1 1BOTHIDAE Bothus ocellatus (Agassiz, 1831) 1 1 1 1 1 1 1BOTHIDAE Bothus pantherinus (Rüppell, 1830) 1 1BOTHIDAE Bothus podas_maderensis (Lowe, 1834) 1 1 1 1BOTHIDAE Bothus podas_podas (Delaroche, 1809) 1 1 1 1 1BOTHIDAE Bothus robinsi Topp & Hoff, 1972 1 1 1 1 1 1BOTHIDAE Chascanopsetta lugubris Alcock, 1894 1 1 1 1 1 1 1 1BOTHIDAE Chascanopsetta valderostratus (Alcock, 1890) 1 1BOTHIDAE Engyophrys senta Ginsburg, 1933 1 1 1 1BOTHIDAE Monolene antillarum Norman, 1933 1 1 1 1 1 1BOTHIDAE Monolene atrimana Goode & Bean, 1886 1 1 1BOTHIDAE Monolene megalepis Woods, 1961 1 1BOTHIDAE Monolene mertensi (Poll, 1959) 1 1BOTHIDAE Monolene microstoma Cadenat, 1937 1BOTHIDAE Monolene sessilicauda Goode, 1880 1 1BOTHIDAE Pseudorhombus arsius (Hamilton, 1822) 1 1BOTHIDAE Pseudorhombus elevatus Ogilby, 1912 1 1BOTHIDAE Trichopsetta caribbaea Anderson & Gutherz, 1967 1 1BOTHIDAE Trichopsetta melasma Anderson & Gutherz, 1967 1 1BOTHIDAE Trichopsetta orbisulcus Anderson & Gutherz, 1967 1 1BOTHIDAE Trichopsetta ventralis (Goode & Bean, 1885) 1 1BYTHITIDAE Bidenichthys capensis Barnard, 1934 1 1BYTHITIDAE Calamopteryx goslinei Böhlke & Cohen, 1966 1 1BYTHITIDAE Calamopteryx robinsorum Cohen, 1973 1 1BYTHITIDAE Dermatopsoides kasougae (Smith, 1943) 1BYTHITIDAE Dermatopsoides talboti Cohen, 1966 1 1BYTHITIDAE Dinematichthys minyomma Sedor & Cohen, 1987 1 1BYTHITIDAE Grammonoides opisthodon (Smith, 1934) 1BYTHITIDAE Grammonus ater (Risso, 1810) 1 1BYTHITIDAE Grammonus claudei (de la Torre y Huerta, 1930) 1 1 1BYTHITIDAE Grammonus longhursti (Cohen, 1964) 1 1 1BYTHITIDAE Ogilbia boehlkei Møller, Schwarzhans & Nielsen, 2005 1 1BYTHITIDAE Ogilbia cayorum Møller, Schwarzhans & Nielsen, 20051 1BYTHITIDAE Ogilbia jeffwilliamsi Møller, Schwarzhans & Nielsen, 2005 1 1BYTHITIDAE Ogilbia mccoskeri Møller, Schwarzhans & Nielsen, 2005 1BYTHITIDAE Ogilbia sabaji Møller, Schwarzhans & Nielsen, 2005 1 1BYTHITIDAE Ogilbia sp.1(Abrolhos) 1BYTHITIDAE Ogilbia sp.2 (Panama, Torro Pt.) 1BYTHITIDAE Ogilbia suarezae Møller, Schwarzhans & Nielsen, 2005 1 1BYTHITIDAE Ogilbia tyleri Møller, Schwarzhans & Nielsen, 2005 1BYTHITIDAE Ogilbichthys ferocis Møller, Schwarzhans & Nielsen, 2004 1BYTHITIDAE Ogilbichthys haitiensis Møller, Schwarzhans & Nielsen, 2004 1BYTHITIDAE Ogilbichthys kakuki Møller, Schwarzhans & Nielsen, 2004 1 1BYTHITIDAE Ogilbichthys longimanus Møller, Schwarzhans & Nielsen, 2004 1 1BYTHITIDAE Ogilbichthys microphthalmus Møller, Schwarzhans & Nielsen, 2004 1 1BYTHITIDAE Ogilbichthys puertoricoensis Møller, Schwarzhans & Nielsen, 2004 1BYTHITIDAE Ogilbichthys tobagoensis Møller, Schwarzhans & Nielsen, 2004 1BYTHITIDAE Petrotyx sanguineus (Meek & Hildebrand, 1928) 1 1BYTHITIDAE Pseudogilbia sanblasensis Møller, Schwarzhans & Nielsen, 2004 1BYTHITIDAE Stygnobrotula latebricola Böhlke, 1957 1 1 1 1CAESIONIDAE Caesio caerulaurea Lacepède, 1801 1 1CALLIONYMIDAE Callionymus lyra Linnaeus, 1758 1 1 1CALLIONYMIDAE Callionymus maculatus Rafinesque, 1810 1CALLIONYMIDAE Callionymus marleyi Regan, 1919 1 1CALLIONYMIDAE Callionymus sanctaehelenae Fricke, 1983 1CALLIONYMIDAE Diplogrammus pauciradiatus (Gill, 1865) 1 1 1 1CALLIONYMIDAE Draculo celetus (Smith, 1963) 1 1CALLIONYMIDAE Draculo shango (Davis & Robins, 1966) 1CALLIONYMIDAE Foetorepus agassizii (Goode & Bean, 1888) 1 1 1

CALLIONYMIDAE Foetorepus dagmarae (Fricke, 1985) 1 1CALLIONYMIDAE Foetorepus goodenbeani Nakabo & Hartel, 1999 1 1CALLIONYMIDAE Paracallionymus costatus (Boulenger, 1898) 1 1 1CALLIONYMIDAE Paradiplogrammus bairdi (Jordan, 1888) 1 1 1 1 1 1 1 1 1CALLIONYMIDAE Synchiropus monacanthus Smith, 1935 1 1CALLIONYMIDAE Synchiropus phaeton (Günther, 1861) 1 1 1 1 1 1CARANGIDAE Alectis alexandrina (Geoffroy Saint-Hilaire, 1817) 1 1 1 1 1CARANGIDAE Alectis ciliaris (Bloch, 1787) 1 1 1 1 1 1 1 1 1 1 1CARANGIDAE Campogramma glaycos (Lacepède, 1801) 1 1 1 1CARANGIDAE Carangoides bartholomaei (Cuvier, 1833) 1 1 1 1 1 1 1 1 1 1 1CARANGIDAE Carangoides chrysophrys (Cuvier, 1833) 1 1CARANGIDAE Carangoides equula (Temminck & Schlegel, 1844) 1 1CARANGIDAE Carangoides ferdau (Forsskål, 1775) 1 1CARANGIDAE Carangoides gymnostethus (Cuvier, 1833) 1 1CARANGIDAE Carangoides ruber (Bloch, 1793) 1 1 1 1 1 1 1 1 1 1CARANGIDAE Caranx crysos (Mitchill, 1815) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1CARANGIDAE Caranx hippos (Linnaeus, 1766) 1 1 1 1 1 1 1 1 1CARANGIDAE Caranx latus Agassiz, 1831 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1CARANGIDAE Caranx lugubris Poey, 1860 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1CARANGIDAE Caranx senegallus Cuvier, 1833 1 1 1CARANGIDAE Caranx fischeri Smith-Vaniz & Carpenter, 2007 1 1 1 1 1CARANGIDAE Chloroscombrus chrysurus (Linnaeus, 1766) 1 1 1 1 1 1 1 1 1 1CARANGIDAE Hemicaranx amblyrhynchus (Cuvier, 1833) 1 1 1 1CARANGIDAE Hemicaranx bicolor (Günther, 1860) 1CARANGIDAE Lichia amia (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1CARANGIDAE Oligoplites palometa (Cuvier, 1832) 1 1 1CARANGIDAE Oligoplites saliens (Bloch, 1793) 1 1 1 1CARANGIDAE Oligoplites saurus saurus (Bloch & Schneider, 1801) 1 1 1 1 1CARANGIDAE Parona signata (Jenyns, 1841) 1 1CARANGIDAE Pseudocaranx dentex (Bloch & Schneider, 1801) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1CARANGIDAE Scomberoides commersonnianus Lacepède, 1801 1 1CARANGIDAE Selene brownii (Cuvier, 1816) 1 1 1 1CARANGIDAE Selene dorsalis (Gill, 1863) 1 1CARANGIDAE Selene vomer (Linnaeus, 1758) 1 1 1 1 1 1CARANGIDAE Selene setapinnis (Mitchill, 1815) 1 1 1 1 1 1CARANGIDAE Seriola carpenteri Mather, 1971 1 1 1 1 1 1 1CARANGIDAE Seriola dumerili (Risso, 1810) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1CARANGIDAE Seriola fasciata (Bloch, 1793) 1 1 1 1 1 1 1 1 1 1 1CARANGIDAE Seriola lalandi Valenciennes, 1833 1 1 1 1 1 1 1CARANGIDAE Seriola rivoliana Valenciennes, 1833 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1CARANGIDAE Seriola zonata (Mitchill, 1815) 1 1 1 1CARANGIDAE Trachinotus africanus Smith, 1967 1 1CARANGIDAE Trachinotus botla (Shaw, 1803) 1 1CARANGIDAE Trachinotus carolinus (Linnaeus, 1766) 1 1 1 1 1CARANGIDAE Trachinotus cayennensis Cuvier, 1832 1 1CARANGIDAE Trachinotus falcatus (Linnaeus, 1758) 1 1 1 1 1 1 1CARANGIDAE Trachinotus goodei Jordan & Evermann, 1896 1 1 1 1 1 1 1CARANGIDAE Trachinotus goreensis Cuvier, 1832 1 1 1 1CARANGIDAE Trachinotus marginatus Cuvier, 1832 1 1CARANGIDAE Trachinotus maxillosus Cuvier, 1832 1 1 1 1CARANGIDAE Trachinotus ovatus (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1CARANGIDAE Trachinotus teraia Cuvier, 1832 1 1CARAPIDAE Carapus acus (Brünnich, 1768) 1 1 1 1 1CARAPIDAE Carapus bermudensis (Jones, 1874) 1 1 1 1 1 1CARAPIDAE Echiodon dawsoni Williams & Shipp, 1982 1 1 1 1CARAPIDAE Echiodon dentatus (Cuvier, 1829) 1CENTRACANTHIDAE Centracanthus cirrus Rafinesque, 1810 1 1 1 1 1 1CENTRACANTHIDAE Spicara alta (Osório, 1917) 1CENTRACANTHIDAE Spicara australis (Regan, 1921) 1 1 1CENTRACANTHIDAE Spicara axillaris (Boulenger, 1900) 1 1 1CENTRACANTHIDAE Spicara maena (Linnaeus, 1758) 1 1CENTRACANTHIDAE Spicara melanurus (Valenciennes, 1830) 1 1CENTRACANTHIDAE Spicara nigricauda (Norman, 1931) 1 1CENTRACANTHIDAE Spicara smaris (Linnaeus, 1758) 1 1 1CHAENOPSIDAE Acanthemblemaria aspera (Longley, 1927) 1 1CHAENOPSIDAE Acanthemblemaria betinensis Smith-Vaniz & Palacio, 1974 1CHAENOPSIDAE Acanthemblemaria chaplini Böhlke, 1957 1 1CHAENOPSIDAE Acanthemblemaria greenfieldi Smith-Vaniz & Palacio, 1974 1CHAENOPSIDAE Acanthemblemaria harpeza Williams, 2002 1CHAENOPSIDAE Acanthemblemaria johnsoni Almany & Baldwin, 1996 1 1CHAENOPSIDAE Acanthemblemaria maria Böhlke, 1961 1 1CHAENOPSIDAE Acanthemblemaria medusa Smith-Vaniz & Palacio, 1974 1 1CHAENOPSIDAE Acanthemblemaria paula Johnson & Brothers, 1989 1CHAENOPSIDAE Acanthemblemaria rivasi Stephens, 1970 1CHAENOPSIDAE Acanthemblemaria spinosa Metzelaar, 1919 1 1CHAENOPSIDAE Chaenopsis cf._stephensi Robins & Randall, 1965 1CHAENOPSIDAE Chaenopsis limbaughi Robins & Randall, 1965 1 1 1CHAENOPSIDAE Chaenopsis megalops Smith-Vaniz, 2000 1CHAENOPSIDAE Chaenopsis ocellata Gill, 1865 1 1CHAENOPSIDAE Chaenopsis resh Robins & Randall, 1965 1 1CHAENOPSIDAE Chaenopsis roseola Hastings & Shipp, 1981 1 1CHAENOPSIDAE Chaenopsis stephensi Robins & Randall, 1965 1 1CHAENOPSIDAE Coralliozetus cardonae Evermann & Marsh, 1899 1 1CHAENOPSIDAE Ekemblemaria nigra (Meek & Hildebrand, 1928) 1

CHAENOPSIDAE Emblemaria atlantica Jordan & Evermann, 1898 1 1 1 1CHAENOPSIDAE Emblemaria australis Ramos, Rocha & Rocha, 2003 1 1CHAENOPSIDAE Emblemaria biocellata Stephens, 1970 1 1CHAENOPSIDAE Emblemaria caldwelli Stephens, 1970 1 1CHAENOPSIDAE Emblemaria caycedoi Acero P., 1984 1CHAENOPSIDAE Emblemaria culmenis Stephens, 1970 1 1CHAENOPSIDAE Emblemaria diphyodontis Stephens & Cervigón, 1970 1 1CHAENOPSIDAE Emblemaria hyltoni Johnson & Greenfield, 1976 1CHAENOPSIDAE Emblemaria pandionis Evermann & Marsh, 1900 1 1 1CHAENOPSIDAE Emblemaria piratula Ginsburg & Reid, 1942 1 1CHAENOPSIDAE Emblemaria sp.n. 1 1CHAENOPSIDAE Emblemaria vitta Williams, 2002 1 1CHAENOPSIDAE Emblemariopsis bahamensis Stephens, 1961 1 1CHAENOPSIDAE Emblemariopsis bottomei Stephens, 1961 1 1CHAENOPSIDAE Emblemariopsis dianae Tyler & Hastings, 2004 1CHAENOPSIDAE Emblemariopsis diaphanus Longley, 1927 1CHAENOPSIDAE Emblemariopsis leptocirris Stephens, 1970 1 1CHAENOPSIDAE Emblemariopsis occidentalis Stephens, 1970 1 1CHAENOPSIDAE Emblemariopsis pricei Greenfield, 1975 1CHAENOPSIDAE Emblemariopsis ramirezi (Cervigón, 1999) 1 1CHAENOPSIDAE Emblemariopsis randalli Cervigón, 1965 1 1CHAENOPSIDAE Emblemariopsis ruetzleri Tyler & Tyler, 1997 1 1CHAENOPSIDAE Emblemariopsis signifera (Ginsburg, 1942) 1 1 1 1CHAENOPSIDAE Emblemariopsis sp.n.1 1 1CHAENOPSIDAE Emblemariopsis sp.n.2 1CHAENOPSIDAE Emblemariopsis sp.n.3 1 1CHAENOPSIDAE Emblemariopsis tayrona (Acero P., 1987) 1CHAENOPSIDAE Hemiemblemaria simulus Longley & Hildebrand, 1940 1 1CHAENOPSIDAE Lucayablennius zingaro (Böhlke, 1957) 1 1CHAENOPSIDAE Protemblemaria punctata Cervigón, 1966 1 1CHAENOPSIDAE Stathmonotus gymnodermis Springer, 1955 1 1CHAENOPSIDAE Stathmonotus hemphillii Bean, 1885 1 1 1CHAENOPSIDAE Stathmonotus sp. 1CHAENOPSIDAE Stathmonotus stahli_stahli (Evermann & Marsh, 1899) 1 1CHAENOPSIDAE Stathmonotus stahli_tekla Nichols, 1910 1 1CHAETODONTIDAE Chaetodon auriga Forsskål, 1775 1 1CHAETODONTIDAE Chaetodon capistratus Linnaeus, 1758 1 1 1 1CHAETODONTIDAE Chaetodon hoefleri Steindachner, 1881 1 1 1 1 1 1CHAETODONTIDAE Chaetodon interruptus Ahl, 1923 1 1CHAETODONTIDAE Chaetodon madagaskariensis Ahl, 1923 1 1CHAETODONTIDAE Chaetodon marleyi Regan, 1921 1 1 1CHAETODONTIDAE Chaetodon ocellatus Bloch, 1787 1 1 1 1 1 1 1 1CHAETODONTIDAE Chaetodon robustus Günther, 1860 1 1 1 1CHAETODONTIDAE Chaetodon sanctaehelenae Günther, 1868 1 1 1CHAETODONTIDAE Chaetodon sedentarius Poey, 1860 1 1 1 1 1 1 1 1CHAETODONTIDAE Chaetodon striatus Linnaeus, 1758 1 1 1 1 1 1 1 1 1 1CHAETODONTIDAE Chaetodon unimaculatus Bloch, 1787 1 1CHAETODONTIDAE Chaetodon vagabundus Linnaeus, 1758 1 1CHAETODONTIDAE Prognathodes aculeatus (Poey, 1860) 1 1 1 1CHAETODONTIDAE Prognathodes aya (Jordan, 1886) 1 1CHAETODONTIDAE Prognathodes brasiliensis Burgess, 2001 1 1 1CHAETODONTIDAE Prognathodes dichrous (Günther, 1869) 1 1CHAETODONTIDAE Prognathodes guyanensis (Durand, 1960) 1 1 1 1 1CHAETODONTIDAE Prognathodes marcellae (Poll, 1950) 1 1 1 1 1CHAETODONTIDAE Prognathodes obliquus (Lubbock & Edwards, 1980) 1CHANIDAE Chanos chanos (Forsskål, 1775) 1 1CHEILODACTYLIDAE Cheilodactylus fasciatus Lacepède, 1803 1 1 1CHEILODACTYLIDAE Cheilodactylus pixi Smith, 1980 1 1CHEILODACTYLIDAE Chirodactylus brachydactylus (Cuvier, 1830) 1 1 1CHEILODACTYLIDAE Chirodactylus grandis (Günther, 1860) 1 1 1CHEILODACTYLIDAE Nemadactylus bergi (Norman, 1937) 1 1CHLOPSIDAE Catesbya pseudomuraena Böhlke & Smith, 1968 1CHLOPSIDAE Chilorhinus suensonii Lütken, 1852 1 1 1 1CHLOPSIDAE Chlopsis bicolor Rafinesque, 1810 1 1 1 1 1 1 1 1CHLOPSIDAE Chlopsis dentatus (Seale, 1917) 1 1 1 1 1 1CHLOPSIDAE Kaupichthys hyoproroides (Strömman, 1896) 1 1 1 1 1CHLOPSIDAE Kaupichthys nuchalis Böhlke, 1967 1 1 1CIRRHITIDAE Amblycirrhitus earnshawi Lubbock, 1978 1CIRRHITIDAE Amblycirrhitus pinos (Mowbray, 1927) 1 1 1 1 1 1 1 1CIRRHITIDAE Cirrhitus atlanticus Osório, 1893 1 1 1CIRRHITIDAE Cirrhitus pinnulatus (Forster, 1801) 1 1CIRRHITIDAE Cyprinocirrhites polyactis (Bleeker, 1874) 1 1CLINIDAE Blennioclinus brachycephalus (Valenciennes, 1836) 1 1 1CLINIDAE Blennioclinus stella Smith, 1946 1 1CLINIDAE Blennophis anguillaris (Valenciennes, 1836) 1 1 1CLINIDAE Blennophis striatus (Gilchrist & Thompson, 1908) 1 1 1CLINIDAE Calliclinus geniguttatus (Valenciennes, 1836) 1CLINIDAE Cancelloxus burrelli Smith, 1961 1 1CLINIDAE Cancelloxus elongatus Heemstra & Wright, 1986 1CLINIDAE Cirrhibarbis capensis Valenciennes, 1836 1 1 1CLINIDAE Climacoporus navalis Barnard, 1935 1 1CLINIDAE Clinitrachus argentatus (Risso, 1810) 1 1CLINIDAE Clinoporus biporosus (Gilchrist & Thompson, 1908) 1 1CLINIDAE Clinus acuminatus (Bloch & Schneider, 1801) 1 1

CLINIDAE Clinus agilis Smith, 1931 1 1CLINIDAE Clinus berrisfordi Penrith, 1967 1 1CLINIDAE Clinus brevicristatus Gilchrist & Thompson, 1908 1 1CLINIDAE Clinus cottoides Valenciennes, 1836 1 1 1CLINIDAE Clinus helenae (Smith, 1946) 1 1CLINIDAE Clinus heterodon Valenciennes, 1836 1 1CLINIDAE Clinus latipennis Valenciennes, 1836 1 1CLINIDAE Clinus navalis (Barnard, 1935) 1 1 1CLINIDAE Clinus nematopterus Günther, 1861 1CLINIDAE Clinus robustus Gilchrist & Thompson, 1908 1 1CLINIDAE Clinus rotundifrons Barnard, 1937 1 1CLINIDAE Clinus spatulatus Bennett, 1983 1CLINIDAE Clinus superciliosus (Linnaeus, 1758) 1 1 1CLINIDAE Clinus taurus Gilchrist & Thompson, 1908 1 1CLINIDAE Clinus venustris Gilchrist & Thompson, 1908 1 1CLINIDAE Clinus woodi (Smith, 1946) 1 1CLINIDAE Fucomimus mus (Gilchrist & Thompson, 1908) 1 1CLINIDAE Muraenoclinus dorsalis (Bleeker, 1860) 1 1 1CLINIDAE Pavoclinus graminis (Gilchrist & Thompson, 1908) 1 1CLINIDAE Pavoclinus laurentii (Gilchrist & Thompson, 1908) 1 1CLINIDAE Pavoclinus litorafontis Penrith, 1965 1CLINIDAE Pavoclinus mentalis (Gilchrist & Thompson, 1908) 1 1CLINIDAE Pavoclinus myae Christensen, 1978 1 1CLINIDAE Pavoclinus pavo (Gilchrist & Thompson, 1908) 1 1 1CLINIDAE Pavoclinus profundus Smith, 1961 1CLINIDAE Pavoclinus smalei Heemstra & Wright, 1986 1CLINIDAE Ribeiroclinus eigenmanni (Jordan, 1888) 1 1 1CLINIDAE Smithichthys fucorum (Gilchrist & Thompson, 1908) 1 1CLINIDAE Xenopoclinus kochi Smith, 1948 1 1CLINIDAE Xenopoclinus leprosus Smith, 1961 1 1CONGRIDAE Ariosoma anale (Poey, 1860) 1 1 1 1 1CONGRIDAE Ariosoma balearicum (Delaroche, 1809) 1 1 1 1 1 1 1 1 1 1 1 1 1CONGRIDAE Bassanago albescens (Barnard, 1923) 1CONGRIDAE Conger cinereus Rüppell, 1830 1 1CONGRIDAE Conger conger (Linnaeus, 1758) 1 1 1 1 1 1 1CONGRIDAE Conger orbignianus Valenciennes, 1842 1 1 1 1CONGRIDAE Conger triporiceps Kanazawa, 1958 1 1 1 1CONGRIDAE Conger wilsoni (Bloch & Schneider, 1801) 1 1CONGRIDAE Gorgasia inferomaculata (Blache, 1977) 1 1CONGRIDAE Heteroconger camelopardalis (Lubbock, 1980) 1 1 1 1 1 1CONGRIDAE Heteroconger longissimus Günther, 1870 1 1 1 1 1 1 1 1 1 1 1CONGRIDAE Heteroconger luteolus Smith, 1989 1 1CONGRIDAE Paraconger caudilimbatus (Poey, 1867) 1 1 1CONGRIDAE Paraconger guianensis Kanazawa, 1961 1CONGRIDAE Paraconger macrops (Günther, 1870) 1 1CONGRIDAE Paraconger notialis Kanazawa, 1961 1 1 1 1DACTYLOPTERIDAE Dactyloptena orientalis (Cuvier, 1829) 1 1DACTYLOPTERIDAE Dactylopterus volitans (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1DACTYLOSCOPIDAE Dactylagnus peratikos Böhlke & Caldwell, 1961 1DACTYLOSCOPIDAE Dactyloscopus boehlkei Dawson, 1982 1DACTYLOSCOPIDAE Dactyloscopus comptus Dawson, 1982 1DACTYLOSCOPIDAE Dactyloscopus crossotus Starks, 1913 1 1 1 1 1DACTYLOSCOPIDAE Dactyloscopus foraminosus Dawson, 1982 1 1 1DACTYLOSCOPIDAE Dactyloscopus moorei (Fowler, 1906) 1 1 1DACTYLOSCOPIDAE Dactyloscopus poeyi Gill, 1861 1 1DACTYLOSCOPIDAE Dactyloscopus tridigitatus Gill, 1859 1 1 1 1 1 1 1 1DACTYLOSCOPIDAE Gillellus greyae Kanazawa, 1952 1 1 1 1 1 1DACTYLOSCOPIDAE Gillellus healae Dawson, 1982 1 1 1DACTYLOSCOPIDAE Gillellus inescatus Williams, 2002 1DACTYLOSCOPIDAE Gillellus jacksoni Dawson, 1982 1DACTYLOSCOPIDAE Gillellus uranidea Böhlke, 1968 1 1 1DACTYLOSCOPIDAE Gillelus sp.n. 1 1DACTYLOSCOPIDAE Leurochilus acon Böhlke, 1968 1DACTYLOSCOPIDAE Myxodagnus belone Böhlke, 1968 1DACTYLOSCOPIDAE Platygillellus brasiliensis Feitoza, 2002 1DACTYLOSCOPIDAE Platygillellus rubrocinctus (Longley, 1934) 1 1 1DACTYLOSCOPIDAE Platygillellus smithi Dawson, 1982 1DACTYLOSCOPIDAE Storrsia olsoni Dawson, 1982 1 1DIODONTIDAE Chilomycterus antennatus (Cuvier, 1816) 1 1 1 1DIODONTIDAE Chilomycterus antillarum Jordan & Rutter, 1897 1 1 1 1 1 1DIODONTIDAE Chilomycterus reticulatus (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1DIODONTIDAE Chilomycterus schoepfii (Walbaum, 1792) 1 1 1DIODONTIDAE Chilomycterus spinosus_mauretanicus(Le Danois, 1954) 1 1 1 1DIODONTIDAE Chilomycterus spinosus_spinosus (Linnaeus, 1758) 1 1 1DIODONTIDAE Cyclichthys orbicularis (Bloch, 1785) 1 1DIODONTIDAE Cyclichthys spilostylus (Leis & Randall, 1982) 1 1DIODONTIDAE Diodon eydouxii Brisout de Barneville, 1846 1 1 1 1 1 1 1 1DIODONTIDAE Diodon holocanthus Linnaeus, 1758 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1DIODONTIDAE Diodon hystrix Linnaeus, 1758 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1DIODONTIDAE Diodon liturosus Shaw, 1804 1 1DIODONTIDAE Lophodiodon calori (Bianconi, 1854) 1 1FISTULARIIDAE Fistularia commersonii Rüppell, 1838 1 1FISTULARIIDAE Fistularia petimba Lacepède, 1803 1 1 1 1 1 1 1 1 1 1 1 1 1FISTULARIIDAE Fistularia tabacaria Linnaeus, 1758 1 1 1 1 1 1 1 1 1 1

GOBIESOCIDAE Acyrtops amplicirrus Briggs, 1955 1GOBIESOCIDAE Acyrtops beryllinus (Hildebrand & Ginsburg, 1926) 1 1 1 1GOBIESOCIDAE Acyrtops sp. 1 1 1GOBIESOCIDAE Acyrtus artius Briggs, 1955 1 1 1 1GOBIESOCIDAE Acyrtus pauciradiatus Sampaio, de Anchieta, Nunes & Mendes, 2004 1GOBIESOCIDAE Acyrtus rubiginosus (Poey, 1868) 1 1GOBIESOCIDAE Apletodon dentatus (Facciolà, 1887) 1 1 1 1GOBIESOCIDAE Apletodon incognitus Hofrichter & Patzner, 1997 1 1 1 1 1GOBIESOCIDAE Apletodon pellegrini (Chabanaud, 1925) 1 1 1 1 1GOBIESOCIDAE Apletodon wirtzi Fricke, 2007 1GOBIESOCIDAE Arcos macrophthalmus (Günther, 1861) 1 1 1GOBIESOCIDAE Chorisochismus dentex (Pallas, 1769) 1 1 1GOBIESOCIDAE Derilissus altifrons Smith-Vaniz, 1971 1 1GOBIESOCIDAE Derilissus kremnobates Fraser, 1970 1GOBIESOCIDAE Derilissus nanus Briggs, 1969 1GOBIESOCIDAE Derilissus vittiger Fraser, 1970 1GOBIESOCIDAE Diplecogaster

bimaculata bimaculata (Bonnaterre, 1788) 1 1 1

GOBIESOCIDAE Diplecogasterbimaculata pectoralis Briggs, 1955 1 1 1 1

GOBIESOCIDAE Diplecogaster ctenocrypta Briggs, 1955 1GOBIESOCIDAE Diplecogaster megalops Briggs, 1955 1 1 1GOBIESOCIDAE Eckloniaichthys scylliorhiniceps Smith, 1943 1 1 1GOBIESOCIDAE Gobiesox barbatulus Starks, 1913 1 1 1 1GOBIESOCIDAE Gobiesox lucayanus Briggs, 1963 1GOBIESOCIDAE Gobiesox marmoratus Jenyns, 1842 1GOBIESOCIDAE Gobiesox nigripinnis (Peters, 1860) 1 1GOBIESOCIDAE Gobiesox punctulatus (Poey, 1876) 1 1 1GOBIESOCIDAE Gobiesox strumosus Cope, 1870 1 1 1 1 1 1GOBIESOCIDAE Gouania willdenowi (Risso, 1810) 1 1GOBIESOCIDAE Lecanogaster chrysea Briggs, 1957 1GOBIESOCIDAE Lepadogaster candolii Risso, 1810 1 1 1 1 1GOBIESOCIDAE Lepadogaster lepadogaster (Bonnaterre, 1788) 1 1 1 1 1 1GOBIESOCIDAE Lepadogaster purpurea (Bonnaterre, 1788) 1 1 1 1GOBIESOCIDAE Opeatogenys cadenati Briggs, 1957 1 1 1 1GOBIESOCIDAE Opeatogenys gracilis (Canestrini, 1864) 1 1GOBIESOCIDAE Tomicodon australis Briggs, 1955 1 1 1GOBIESOCIDAE Tomicodon briggsi Williams & Tyler, 2003 1 1GOBIESOCIDAE Tomicodon clarkei Williams & Tyler, 2003 1GOBIESOCIDAE Tomicodon cryptus Williams & Tyler, 2003 1 1GOBIESOCIDAE Tomicodon fasciatus (Peters, 1859) 1 1GOBIESOCIDAE Tomicodon lavettsmithi Williams & Tyler, 2003 1GOBIESOCIDAE Tomicodon leurodiscus Williams & Tyler, 2003 1 1GOBIESOCIDAE Tomicodon reitzae Briggs, 2001 1 1GOBIESOCIDAE Tomicodon rhabdotus Smith-Vaniz, 1969 1GOBIESOCIDAE Tomicodon rupestris (Poey, 1860) 1 1GOBIIDAE Barbulifer antennatus Böhlke & Robins, 1968 1GOBIIDAE Barbulifer ceuthoecus (Jordan & Gilbert, 1884) 1 1 1 1GOBIIDAE Bathygobius burtoni (O'Shaughnessy, 1875) 1 1 1GOBIIDAE Bathygobius casamancus (Rochebrune, 1880) 1 1 1 1GOBIIDAE Bathygobius curacao (Metzelaar, 1919) 1 1 1 1GOBIIDAE Bathygobius mystacium Ginsburg, 1947 1 1 1 1GOBIIDAE Bathygobius soporator (Valenciennes, 1837) 1 1 1 1 1 1 1 1 1 1 1 1 1GOBIIDAE Bollmannia boqueronensis Evermann & Marsh, 1899 1 1GOBIIDAE Bollmannia communis Ginsburg, 1942 1 1GOBIIDAE Bollmannia eigenmanni (Garman, 1896) 1GOBIIDAE Bollmannia litura Ginsburg, 1935 1GOBIIDAE Bollmannia sp. n. 1 1GOBIIDAE Buenia affinis Iljin, 1930 1 1GOBIIDAE Buenia jeffreysii (Günther, 1867) 1GOBIIDAE Buenia sp.n.(Canaries) 1 1GOBIIDAE Caffrogobius agulhensis (Barnard, 1927) 1 1GOBIIDAE Caffrogobius caffer (Günther, 1874) 1 1GOBIIDAE Caffrogobius multifasciatus (Smith, 1959) 1 1GOBIIDAE Caffrogobius natalensis (Günther, 1874) 1 1GOBIIDAE Caffrogobius nudiceps (Valenciennes, 1837) 1 1 1GOBIIDAE Caffrogobius saldanha (Barnard, 1927) 1 1 1GOBIIDAE Chriolepis benthonis Ginsburg, 1953 1GOBIIDAE Chriolepis fisheri Herre, 1942 1 1 1GOBIIDAE Chriolepis vespa Hastings & Bortone, 1981 1 1GOBIIDAE Chriolepsis sp.n. 1 1GOBIIDAE Chromogobius britoi Van Tassell, 2001 1 1GOBIIDAE Chromogobius quadrivittatus (Steindachner, 1863) 1 1GOBIIDAE Chromogobius zebratus (Kolombatovic, 1891) 1 1GOBIIDAE Corcyrogobius liechtensteini (Kolombatovic, 1891) 1 1GOBIIDAE Corcyrogobius lubbocki Miller, 1988 1 1GOBIIDAE Coryphopterus alloides Böhlke & Robins, 1960 1 1GOBIIDAE Coryphopterus dicrus Böhlke & Robins, 1960 1 1 1 1 1GOBIIDAE Coryphopterus eidolon Böhlke & Robins, 1960 1 1 1GOBIIDAE Coryphopterus glaucofraenum Gill, 1863 1 1 1 1 1 1 1 1GOBIIDAE Coryphopterus hyalinus Böhlke & Robins, 1962 1 1 1GOBIIDAE Coryphopterus lipernes Böhlke & Robins, 1962 1 1GOBIIDAE Coryphopterus personatus (Jordan & Thompson, 1905) 1 1 1 1GOBIIDAE Coryphopterus punctipectophorus Springer, 1960 1 1GOBIIDAE Coryphopterus thrix Böhlke & Robins, 1960 1 1 1 1GOBIIDAE Coryphopterus venezuelae Cervigón, 1966 1 1

GOBIIDAE Ctenogobius saepepallens (Gilbert & Randall, 1968) 1 1 1 1 1GOBIIDAE Deltentosteus collonianus (Risso, 1820) 1 1GOBIIDAE Deltentosteus quadrimaculatus (Valenciennes, 1837) 1 1GOBIIDAE Didogobius bentuvii Miller, 1966 1GOBIIDAE Didogobius kochi Van Tassell, 1988 1 1GOBIIDAE Didogobius schlieweni Miller, 1993 1 1GOBIIDAE Didogobius sp.n. 1GOBIIDAE Didogobius splechtnai Ahnelt & Patzner, 1995 1 1GOBIIDAE Elacatinus atronasus (Böhlke & Robins, 1968) 1 1GOBIIDAE Elacatinus chancei (Beebe & Hollister, 1933) 1 1GOBIIDAE Elacatinus dilepis (Robins & Böhlke, 1964) 1 1GOBIIDAE Elacatinus evelynae (Böhlke & Robins, 1968) 1 1GOBIIDAE Elacatinus figaro Sazima, Moura & Rosa, 1997 1 1GOBIIDAE Elacatinus gemmatus (Ginsburg, 1939) 1 1GOBIIDAE Elacatinus genie (Böhlke & Robins, 1968) 1 1GOBIIDAE Elacatinus horsti (Metzelaar, 1922) 1 1GOBIIDAE Elacatinus illecebrosus (Böhlke & Robins, 1968) 1GOBIIDAE Elacatinus lori Colin, 2002 1GOBIIDAE Elacatinus louisae (Böhlke & Robins, 1968) 1 1GOBIIDAE Elacatinus macrodon (Beebe & Tee-Van, 1928) 1 1 1GOBIIDAE Elacatinus multifasciatus (Steindachner, 1876) 1 1GOBIIDAE Elacatinus oceanops Jordan, 1904 1 1 1GOBIIDAE Elacatinus pallens (Ginsburg, 1939) 1 1GOBIIDAE Elacatinus pridisi Guimarães, Gasparini & Rocha, 2004 1GOBIIDAE Elacatinus prochilos (Böhlke & Robins, 1968) 1 1GOBIIDAE Elacatinus randalli (Böhlke & Robins, 1968) 1 1GOBIIDAE Elacatinus saucrus (Robins, 1960) 1 1GOBIIDAE Elacatinus sp.n.(Noronha) 1 1GOBIIDAE Elacatinus tenox (Böhlke & Robins, 1968) 1 1GOBIIDAE Elacatinus xanthiprora (Böhlke & Robins, 1968) 1 1 1GOBIIDAE Elacatinus zebrellus (Robins, 1958) 1 1GOBIIDAE Evermannichthys bicolor Thacker, 2001 1GOBIIDAE Evermannichthys convictor Böhlke & Robins, 1969 1GOBIIDAE Evermannichthys metzelaari Hubbs, 1923 1 1GOBIIDAE Evermannichthys spilus Böhlke & Robins, 1969 1GOBIIDAE Evermannichthys spongicola (Radcliffe, 1917) 1 1 1GOBIIDAE Gammogobius steinitzi Bath, 1971 1 1GOBIIDAE Ginsburgellus novemlineatus (Fowler, 1950) 1 1GOBIIDAE Glossogobius callidus (Smith, 1937) 1 1GOBIIDAE Gnatholepis thompsoni Jordan, 1904 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1GOBIIDAE Gobiosoma grosvenori (Robins, 1964) 1 1GOBIIDAE Gobiosoma hemigymnum (Eigenmann & Eigenmann, 1888) 1 1 1GOBIIDAE Gobiosoma hildebrandi (Ginsburg, 1939) 1GOBIIDAE Gobiosoma longipala Ginsburg, 1933 1 1GOBIIDAE Gobiosoma parri Ginsburg, 1933 1GOBIIDAE Gobiosoma robustum Ginsburg, 1933 1 1 1GOBIIDAE Gobiosoma spes (Ginsburg, 1939) 1 1GOBIIDAE Gobiosoma spilotum (Ginsburg, 1939) 1 1GOBIIDAE Gobiosoma yucatanum Dawson, 1971 1GOBIIDAE Gobius ater Bellotti, 1888 1 1GOBIIDAE Gobius ateriformis Brito & Miller, 2001 1GOBIIDAE Gobius auratus Risso, 1810 1 1GOBIIDAE Gobius bucchichi Steindachner, 1870 1 1 1GOBIIDAE Gobius cobitis Pallas, 1814 1 1 1GOBIIDAE Gobius cruentatus Gmelin, 1789 1 1 1 1GOBIIDAE Gobius fallax Sarato, 1889 1 1GOBIIDAE Gobius gasteveni Miller, 1974 1 1 1GOBIIDAE Gobius geniporus Valenciennes, 1837 1 1GOBIIDAE Gobius kolombatovici Kovacic & Miller, 2000 1GOBIIDAE Gobius niger Linnaeus, 1758 1 1 1 1 1GOBIIDAE Gobius paganellus Linnaeus, 1758 1 1 1 1 1 1 1GOBIIDAE Gobius roulei de Buen, 1928 1 1 1GOBIIDAE Gobius rubropunctatus Delais, 1951 1 1GOBIIDAE Gobius senegambiensis Metzelaar, 1919 1 1 1GOBIIDAE Gobius strictus Fage, 1907 1 1GOBIIDAE Gobius tetrophthalmus Brito & Miller, 2001 1GOBIIDAE Gobius vittatus Vinciguerra, 1883 1 1GOBIIDAE Gobius xanthocephalus Heymer & Zander, 1992 1 1 1GOBIIDAE Gobulus myersi Ginsburg, 1939 1 1 1 1GOBIIDAE Gorogobius nigricinctus (Delais, 1951) 1 1 1GOBIIDAE Hetereleotris zonata (Fowler, 1934) 1 1GOBIIDAE Knipowitschia caucasica (Berg, 1916) 1GOBIIDAE Knipowitschia panizzae (Verga, 1841) 1GOBIIDAE Lebetus guilleti (Le Danois, 1913) 1 1GOBIIDAE Lebetus scorpioides (Collett, 1874) 1 1GOBIIDAE Lesueurigobius friesii (Malm, 1874) 1 1GOBIIDAE Lesueurigobius heterofasciatus Maul, 1971 1 1 1GOBIIDAE Lesueurigobius koumansi (Norman, 1935) 1 1GOBIIDAE Lesueurigobius sanzi (de Buen, 1918) 1GOBIIDAE Lesueurigobius suerii (Risso, 1810) 1 1 1 1 1GOBIIDAE Lythrypnus brasiliensis Greenfield, 1988 1 1GOBIIDAE Lythrypnus crocodilus (Beebe & Tee-Van, 1928) 1 1 1GOBIIDAE Lythrypnus elasson Böhlke & Robins, 1960 1 1GOBIIDAE Lythrypnus heterochroma Ginsburg, 1939 1 1

GOBIIDAE Lythrypnus minimus Garzón & Acero P., 1988 1 1GOBIIDAE Lythrypnus mowbrayi (Bean, 1906) 1GOBIIDAE Lythrypnus nesiotes Böhlke & Robins, 1960 1 1GOBIIDAE Lythrypnus okapia Robins & Böhlke, 1964 1 1 1GOBIIDAE Lythrypnus phorellus Böhlke & Robins, 1960 1 1 1 1GOBIIDAE Lythrypnus sp.1(Noronha) 1 1GOBIIDAE Lythrypnus sp.2(Trindade) 1GOBIIDAE Lythrypnus spilus Böhlke & Robins, 1960 1 1 1 1GOBIIDAE Mauligobius maderensis (Valenciennes, 1837) 1 1GOBIIDAE Mauligobius nigri (Günther, 1861) 1GOBIIDAE Microgobius carri Fowler, 1945 1 1 1 1 1GOBIIDAE Microgobius microlepis Longley & Hildebrand, 1940 1 1 1GOBIIDAE Microgobius signatus Poey, 1876 1 1GOBIIDAE Millerigobius macrocephalus (Smith, 1948) 1 1GOBIIDAE Monishia william (Smith, 1948) 1 1GOBIIDAE Nematogobius brachynemus Pfaff, 1933 1 1 1GOBIIDAE Nematogobius maindroni (Sauvage, 1880) 1 1 1 1GOBIIDAE Nes longus (Nichols, 1914) 1 1 1 1GOBIIDAE Odondebuenia balearica (Pellegrin & Fage, 1907) 1 1GOBIIDAE Oligolepis acutipennis (Valenciennes, 1837) 1 1GOBIIDAE Oligolepis keiensis (Smith, 1938) 1 1GOBIIDAE Ophiogobius ophicephalus (Jenyns, 1842) 1GOBIIDAE Palatogobius paradoxus Gilbert, 1971 1 1GOBIIDAE Pariah scotius Böhlke, 1969 1GOBIIDAE Parrella macropteryx Ginsburg, 1939 1 1 1GOBIIDAE Periophthalmus barbarus (Linnaeus, 1766) 1 1GOBIIDAE Pomatoschistus bathi Miller, 1982 1 1GOBIIDAE Pomatoschistus canestrinii (Ninni, 1883) 1GOBIIDAE Pomatoschistus knerii (Steindachner, 1861) 1 1GOBIIDAE Pomatoschistus marmoratus (Risso, 1810) 1 1GOBIIDAE Pomatoschistus microps (Krøyer, 1838) 1 1 1GOBIIDAE Pomatoschistus minutus (Pallas, 1770) 1 1 1GOBIIDAE Pomatoschistus norvegicus (Collett, 1902) 1 1GOBIIDAE Pomatoschistus pictus (Malm, 1865) 1 1 1 1GOBIIDAE Pomatoschistus quagga (Heckel, 1837) 1 1GOBIIDAE Pomatoschistus tortonesei Miller, 1969 1GOBIIDAE Porogobius schlegelii (Günther, 1861) 1 1 1 1GOBIIDAE Priolepis ascensionis (Dawson & Edwards, 1987) 1 1GOBIIDAE Priolepis dawsoni Greenfield, 1989 1 1 1 1 1GOBIIDAE Priolepis hipoliti (Metzelaar, 1922) 1 1 1 1GOBIIDAE Priolepis robinsi Garzón-Ferreira & Acero P., 1991 1GOBIIDAE Priolepis sp.n. 1 1GOBIIDAE Psammogobius knysnaensis Smith, 1935 1 1 1GOBIIDAE Pseudaphya ferreri (de Buen & Fage, 1908) 1 1GOBIIDAE Psilotris alepis Ginsburg, 1953 1 1GOBIIDAE Psilotris amblyrhynchus Smith & Baldwin, 1999 1GOBIIDAE Psilotris batrachodes Böhlke, 1963 1 1GOBIIDAE Psilotris boehlkei Greenfield, 1993 1GOBIIDAE Psilotris celsus Böhlke, 1963 1 1 1 1 1GOBIIDAE Psilotris kaufmani Greenfield, Findley & Johnson, 1993 1 1GOBIIDAE Pycnomma roosevelti Ginsburg, 1939 1 1GOBIIDAE Redigobius dewaali (Weber, 1897) 1 1GOBIIDAE Risor ruber (Rosén, 1911) 1 1 1 1 1GOBIIDAE Speleogobius trigloides Zander & Jelinek, 1976 1GOBIIDAE Thorogobius angolensis (Norman, 1935) 1 1GOBIIDAE Thorogobius ephippiatus (Lowe, 1839) 1 1 1 1 1GOBIIDAE Thorogobius macrolepis (Kolombatovic, 1891) 1 1GOBIIDAE Thorogobius rofeni Miller, 1988 1GOBIIDAE Vanneaugobius canariensis Van Tassell, Miller & Brito, 1988 1 1 1 1 1GOBIIDAE Vanneaugobius dollfusi Brownell, 1978 1 1GOBIIDAE Vanneaugobius pruvoti (Fage, 1907) 1 1GOBIIDAE Varicus bucca Robins & Böhlke, 1961 1GOBIIDAE Varicus imswe Greenfield, 1981 1GOBIIDAE Varicus marilynae Gilmore, 1979 1 1GOBIIDAE Vomerogobius flavus Gilbert, 1971 1 1GOBIIDAE Wheelerigobius maltzani (Steindachner, 1881) 1 1 1GOBIIDAE Wheelerigobius wirtzi Miller, 1988 1 1GOBIIDAE Zebrus zebrus (Risso, 1827) 1 1GOBIIDAE Zosterisessor ophiocephalus (Pallas, 1814) 1 1GRAMMATIDAE Gramma brasiliensis Sazima, Gasparini & Moura, 1998 1 1 1GRAMMATIDAE Gramma linki Starck & Colin, 1978 1 1GRAMMATIDAE Gramma loreto Poey, 1868 1 1GRAMMATIDAE Gramma melacara Böhlke & Randall, 1963 1 1GRAMMATIDAE Lipogramma anabantoides Böhlke, 1960 1 1GRAMMATIDAE Lipogramma evides Robins & Colin, 1979 1 1GRAMMATIDAE Lipogramma flavescens Gilmore & Jones, 1988 1 1GRAMMATIDAE Lipogramma klayi Randall, 1963 1 1GRAMMATIDAE Lipogramma regium Robins & Colin, 1979 1 1 1GRAMMATIDAE Lipogramma robinsi Gilmore, 1997 1 1GRAMMATIDAE Lipogramma roseum Gilbert, 1979 1 1GRAMMATIDAE Lipogramma trilineatum Randall, 1963 1 1HAEMULIDAE Anisotremus moricandi (Ranzani, 1842) 1 1 1 1HAEMULIDAE Anisotremus surinamensis (Bloch, 1791) 1 1 1 1 1 1 1 1 1HAEMULIDAE Anisotremus virginicus (Linnaeus, 1758) 1 1 1 1 1

HAEMULIDAE Haemulon album Cuvier, 1830 1 1 1 1 1HAEMULIDAE Haemulon aurolineatum Cuvier, 1830 1 1 1 1 1 1HAEMULIDAE Haemulon steindachneri (Jordan & Gilbert, 1882) 1 1 1 1 1HAEMULIDAE Haemulon boschmae (Metzelaar, 1919) 1 1HAEMULIDAE Haemulon bonariense Cuvier, 1830 1 1HAEMULIDAE Haemulon carbonarium Poey, 1860 1 1 1 1HAEMULIDAE Haemulon chrysargyreum Günther, 1859 1 1 1 1 1HAEMULIDAE Haemulon flavolineatum (Desmarest, 1823) 1 1 1 1HAEMULIDAE Haemulon macrostomum Günther, 1859 1 1 1HAEMULIDAE Haemulon melanurum (Linnaeus, 1758) 1 1 1 1 1HAEMULIDAE Haemulon parra (Desmarest, 1823) 1 1 1 1 1 1 1HAEMULIDAE Haemulon plumieri (Lacepède, 1801) 1 1 1 1 1HAEMULIDAE Haemulon sciurus (Lacepède, 1801) 1 1 1 1HAEMULIDAE Haemulon squamipinna Rocha & Rosa, 1999 1 1HAEMULIDAE Haemulon striatum (Linnaeus, 1758) 1 1 1 1 1HAEMULIDAE Orthopristis chrysoptera (Linnaeus, 1766) 1 1 1 1HAEMULIDAE Orthopristis ruber (Cuvier, 1830) 1 1 1 1HAEMULIDAE Parapristipoma humile (Bowdich, 1825) 1 1 1HAEMULIDAE Parapristipoma octolineatum (Valenciennes, 1833) 1 1 1 1 1 1 1HAEMULIDAE Plectorhinchus chubbi (Regan, 1919) 1 1HAEMULIDAE Plectorhinchus macrolepis (Boulenger, 1899) 1 1 1HAEMULIDAE Plectorhinchus mediterraneus (Guichenot, 1850) 1 1 1 1 1 1 1HAEMULIDAE Pomadasys commersonnii (Lacepède, 1801) 1 1HAEMULIDAE Pomadasys corvinaeformis (Steindachner, 1868) 1 1 1HAEMULIDAE Pomadasys crocro (Cuvier, 1830) 1 1HAEMULIDAE Pomadasys incisus (Bowdich, 1825) 1 1 1 1 1 1 1 1HAEMULIDAE Pomadasys jubelini (Cuvier, 1830) 1 1 1 1HAEMULIDAE Pomadasys multimaculatum (Playfair, 1867) 1 1HAEMULIDAE Pomadasys olivaceus (Day, 1875) 1 1 1HAEMULIDAE Pomadasys perotaei (Cuvier, 1830) 1 1 1 1HAEMULIDAE Pomadasys rogerii (Cuvier, 1830) 1 1 1 1HAEMULIDAE Pomadasys striatus (Gilchrist & Thompson, 1908) 1 1HAEMULIDAE Pomadasys stridens (Forsskål, 1775) 1HAEMULIDAE Pomadasys suillus (Valenciennes, 1833) 1 1HOLOCENTRIDAE Corniger spinosus Agassiz, 1831 1 1 1 1 1 1 1HOLOCENTRIDAE Holocentrus adscensionis (Osbeck, 1765) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1HOLOCENTRIDAE Holocentrus rufus (Walbaum, 1792) 1 1 1 1 1 1HOLOCENTRIDAE Myripristis jacobus Cuvier, 1829 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1HOLOCENTRIDAE Neoniphon marianus (Cuvier, 1829) 1 1 1HOLOCENTRIDAE Ostichthys trachypoma (Günther, 1859) 1 1 1HOLOCENTRIDAE Plectrypops retrospinis (Guichenot, 1853) 1 1 1 1 1 1 1 1HOLOCENTRIDAE Sargocentron bullisi (Cuvier, 1829) 1 1 1 1 1 1HOLOCENTRIDAE Sargocentron coruscum (Poey, 1860) 1 1 1HOLOCENTRIDAE Sargocentron hastatum (Cuvier, 1829) 1 1 1 1 1 1HOLOCENTRIDAE Sargocentron poco (Woods, 1965) 1 1 1HOLOCENTRIDAE Sargocentron punctatissimum (Cuvier, 1829) 1 1HOLOCENTRIDAE Sargocentron vexillarium (Poey, 1860) 1 1 1 1KUHLIIDAE Kuhlia mugil (Forster, 1801) 1 1KUHLIIDAE Parakuhlia macrophthalmus (Osório, 1893) 1KYPHOSIDAE Girella stuebeli Troschel, 1866 1KYPHOSIDAE Kyphosus bigibbus Lacepède, 1801 1 1KYPHOSIDAE Kyphosus incisor (Cuvier, 1831) 1 1 1 1 1 1 1 1 1 1 1 1 1KYPHOSIDAE Kyphosus sectatrix (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1KYPHOSIDAE Kyphosus vaigiensis (Quoy & Gaimard, 1825) 1 1LABRIDAE Acantholabrus palloni (Risso, 1810) 1 1 1 1 1 1 1 1 1LABRIDAE Anampses caeruleopunctatus Rüppell, 1829 1 1LABRIDAE Bodianus insularis Gomon & Lubbock, 1980 1 1 1LABRIDAE Bodianus pulchellus (Poey, 1860) 1 1 1 1 1 1 1 1 1 1LABRIDAE Bodianus rufus (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1LABRIDAE Bodianus scrofa (Valenciennes, 1839) 1 1 1 1LABRIDAE Bodianus speciosus (Bowdich, 1825) 1 1 1 1LABRIDAE Clepticus africanus Heiser, Moura & Robertson, 2000 1LABRIDAE Clepticus brasiliensis Heiser, Moura & Robertson, 2000 1 1 1 1 1LABRIDAE Clepticus parrae (Bloch & Schneider, 1801) 1 1 1 1LABRIDAE Coris atlantica Günther, 1862 1 1 1 1LABRIDAE Coris julis (Linnaeus, 1758) 1 1 1 1 1 1LABRIDAE Ctenolabrus rupestris (Linnaeus, 1758) 1 1 1LABRIDAE Decodon puellaris (Poey, 1860) 1 1 1 1 1 1LABRIDAE Doratonotus megalepis Günther, 1862 1 1 1 1 1 1 1 1 1 1LABRIDAE Halichoeres bathyphilus (Beebe & Tee-Van, 1932) 1 1 1 1 1LABRIDAE Halichoeres bivittatus (Bloch, 1791) 1 1 1 1 1LABRIDAE Halichoeres brasiliensis (Bloch, 1791) 1 1 1LABRIDAE Halichoeres caudalis (Poey, 1860) 1 1 1LABRIDAE Halichoeres cyanocephalus (Bloch, 1791) 1 1 1LABRIDAE Halichoeres dimidiatus (Agassiz, 1831) 1 1 1 1LABRIDAE Halichoeres garnoti (Valenciennes, 1839) 1 1 1 1LABRIDAE Halichoeres maculipinna (Müller & Troschel, 1848) 1 1 1 1LABRIDAE Halichoeres nebulosus (Valenciennes, 1839) 1 1LABRIDAE Halichoeres penrosei Starks, 1913 1 1 1LABRIDAE Halichoeres pictus (Poey, 1860) 1 1 1 1LABRIDAE Halichoeres poeyi (Steindachner, 1867) 1 1 1 1 1 1LABRIDAE Halichoeres radiatus (Linnaeus, 1758) 1 1 1 1 1 1 1LABRIDAE Halichoeres socialis Randall & Lobel, 2003 1LABRIDAE Halichoeres sp.n. (G.of Mexico) 1

LABRIDAE Labroides dimidiatus (Valenciennes, 1839) 1 1LABRIDAE Labrus bergylta Ascanius, 1767 1 1 1 1 1LABRIDAE Labrus bimaculatus Linnaeus, 1758 1 1 1 1 1 1LABRIDAE Labrus merula Linnaeus, 1758 1 1 1LABRIDAE Labrus viridis Linnaeus, 1758 1 1LABRIDAE Lachnolaimus maximus (Walbaum, 1792) 1 1 1 1 1LABRIDAE Lappanella fasciata (Cocco, 1833) 1 1 1 1LABRIDAE Lappanella guineensis Bauchot, 1969 1LABRIDAE Stethojulis interrupta (Bleeker, 1851) 1 1LABRIDAE Stethojulis strigiventer (Bennett, 1833) 1 1LABRIDAE Symphodus bailloni (Valenciennes, 1839) 1 1LABRIDAE Symphodus cinereus (Bonnaterre, 1788) 1 1LABRIDAE Symphodus caeruleus (Azevedo, 1999) 1LABRIDAE Symphodus doderleini Jordan, 1890 1 1LABRIDAE Symphodus mediterraneus (Linnaeus, 1758) 1 1 1 1 1 1LABRIDAE Symphodus melanocercus (Risso, 1810) 1 1LABRIDAE Symphodus melops (Linnaeus, 1758) 1 1 1LABRIDAE Symphodus ocellatus (Forsskål, 1775) 1 1LABRIDAE Symphodus roissali (Risso, 1810) 1 1LABRIDAE Symphodus rostratus (Bloch, 1791) 1 1LABRIDAE Symphodus staitii (Nordmann, 1840) 1LABRIDAE Symphodus tinca (Linnaeus, 1758) 1 1 1LABRIDAE Symphodus trutta (Lowe, 1834) 1 1 1LABRIDAE Thalassoma ascensionis (Quoy & Gaimard, 1834) 1LABRIDAE Thalassoma bifasciatum (Bloch, 1791) 1 1 1 1LABRIDAE Thalassoma hebraicum (Lacepède, 1801) 1 1LABRIDAE Thalassoma lunare (Linnaeus, 1758) 1 1LABRIDAE Thalassoma newtoni (Osório, 1891) 1LABRIDAE Thalassoma noronhanum (Boulenger, 1890) 1 1 1 1 1 1LABRIDAE Thalassoma pavo (Linnaeus, 1758) 1 1 1 1 1 1 1 1LABRIDAE Thalassoma purpureum (Forsskål, 1775) 1 1LABRIDAE Thalassoma sanctaehelenae (Valenciennes, 1839) 1LABRIDAE Xyrichtys blanchardi (Cadenat & Marchal, 1963) 1 1LABRIDAE Xyrichtys incandescens Edwards & Lubbock, 1981 1 1 1LABRIDAE Xyrichtys martinicensis Valenciennes, 1840 1 1 1 1 1LABRIDAE Xyrichtys novacula (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1LABRIDAE Xyrichtys sanctaehelenae (Günther, 1868) 1 1 1LABRIDAE Xyrichtys splendens Castelnau, 1855 1 1 1 1 1 1LABRISOMIDAE Labrisomus albigenys Beebe & Tee-Van, 1928 1 1LABRISOMIDAE Labrisomus bucciferus (Poey, 1868) 1 1LABRISOMIDAE Labrisomus cricota Sazima, Gasparini & Moura, 2002 1 1LABRISOMIDAE Labrisomus filamentosus Springer, 1960 1 1 1LABRISOMIDAE Labrisomus gobio (Valenciennes, 1836) 1 1LABRISOMIDAE Labrisomus guppyi (Norman, 1922) 1 1LABRISOMIDAE Labrisomus haitiensis Beebe & Tee-Van, 1928 1 1 1LABRISOMIDAE Labrisomus kalisherae (Jordan, 1904) 1 1 1 1 1 1LABRISOMIDAE Labrisomus nigricinctus Howell Rivero, 1936 1 1LABRISOMIDAE Labrisomus nuchipinnis (Quoy & Gaimard, 1824) 1 1 1 1 1 1 1 1 1 1 1 1 1LABRISOMIDAE Labrisomus sp.n. 1 1LABRISOMIDAE Malacoctenus africanus Cadenat, 1951 1 1LABRISOMIDAE Malacoctenus aurolineatus Smith, 1957 1 1LABRISOMIDAE Malacoctenus boehlkei Springer, 1959 1 1LABRISOMIDAE Malacoctenus delalandii (Valenciennes, 1836) 1 1 1 1LABRISOMIDAE Malacoctenus erdmani Smith, 1957 1 1LABRISOMIDAE Malacoctenus gilli (Steindachner, 1867) 1 1LABRISOMIDAE Malacoctenus macropus (Poey, 1868) 1 1 1LABRISOMIDAE Malacoctenus sp.1(aff.triangulatus) 1 1LABRISOMIDAE Malacoctenus sp.2(Trindade) 1LABRISOMIDAE Malacoctenus sp.3(St_Pauls) 1LABRISOMIDAE Malacoctenus sp.4(Noronha) 1 1LABRISOMIDAE Malacoctenus triangulatus Springer, 1959 1 1 1LABRISOMIDAE Malacoctenus versicolor (Poey, 1876) 1 1LABRISOMIDAE Nemaclinus atelestos Böhlke & Springer, 1975 1 1 1LABRISOMIDAE Paraclinus arcanus Guimarães & Bacellar, 2002 1 1LABRISOMIDAE Paraclinus barbatus Springer, 1955 1 1LABRISOMIDAE Paraclinus cingulatus (Evermann & Marsh, 1899) 1 1LABRISOMIDAE Paraclinus fasciatus (Steindachner, 1876) 1 1 1LABRISOMIDAE Paraclinus grandicomis (Rosén, 1911) 1 1LABRISOMIDAE Paraclinus infrons Böhlke, 1960 1 1LABRISOMIDAE Paraclinus marmoratus (Steindachner, 1876) 1 1LABRISOMIDAE Paraclinus naeorhegmis Böhlke, 1960 1 1LABRISOMIDAE Paraclinus nigripinnis (Steindachner, 1867) 1 1 1LABRISOMIDAE Paraclinus rubicundus (Starks, 1913) 1 1LABRISOMIDAE Paraclinus spectator Guimarães & Bacellar, 2002 1LABRISOMIDAE Starksia atlantica Longley, 1934 1 1LABRISOMIDAE Starksia brasiliensis (Gilbert, 1900) 1 1LABRISOMIDAE Starksia culebrae (Evermann & Marsh, 1899) 1LABRISOMIDAE Starksia elongata Gilbert, 1971 1 1LABRISOMIDAE Starksia fasciata (Longley, 1934) 1LABRISOMIDAE Starksia guttata (Fowler, 1931) 1 1LABRISOMIDAE Starksia hassi Klausewitz, 1958 1 1LABRISOMIDAE Starksia lepicoelia Böhlke & Springer, 1961 1 1LABRISOMIDAE Starksia leucovitta Williams & Mounts, 2003 1LABRISOMIDAE Starksia melasma Williams & Mounts, 2003 1

LABRISOMIDAE Starksia multilepis Williams & Mounts, 2003 1 1LABRISOMIDAE Starksia nanodes Böhlke & Springer, 1961 1 1LABRISOMIDAE Starksia occidentalis Greenfield, 1979 1LABRISOMIDAE Starksia ocellata (Steindachner, 1876) 1 1 1LABRISOMIDAE Starksia rava Williams & Mounts, 2003 1 1LABRISOMIDAE Starksia sella Williams & Mounts, 2003 1 1LABRISOMIDAE Starksia sluiteri (Metzelaar, 1919) 1 1LABRISOMIDAE Starksia smithvanizi Williams & Mounts, 2003 1LABRISOMIDAE Starksia sp.n.5(Trindade) 1LABRISOMIDAE Starksia sp.n.6(LA_Rocha) 1LABRISOMIDAE Starksia starcki Gilbert, 1971 1 1LABRISOMIDAE Starksia variabilis Greenfield, 1979 1LABRISOMIDAE Starksia y-lineata Gilbert, 1965 1LETHRINIDAE Lethrinus atlanticus Goode & Bean, 1879 1 1 1LETHRINIDAE Lethrinus nebulosus Linnaeus, 1758 1 1LUTJANIDAE Aphareus rutilans (Peters, 1877) 1 1LUTJANIDAE Apsilus dentatus (Kaup, 1856) 1 1 1LUTJANIDAE Apsilus fuscus Valenciennes, 1830 1 1 1 1LUTJANIDAE Etelis oculatus (Valenciennes, 1828) 1 1 1 1 1 1LUTJANIDAE Lutjanus agennes Bleeker, 1863 1 1 1LUTJANIDAE Lutjanus alexandrei Moura & Lindeman, 2007 1 1LUTJANIDAE Lutjanus analis (Cuvier, 1828) 1 1 1 1 1 1LUTJANIDAE Lutjanus apodus (Walbaum, 1792) 1 1 1 1 1LUTJANIDAE Lutjanus buccanella (Cuvier, 1828) 1 1 1 1 1 1LUTJANIDAE Lutjanus campechanus (Poey, 1860) 1 1 1LUTJANIDAE Lutjanus cyanopterus (Cuvier, 1828) 1 1 1 1 1 1LUTJANIDAE Lutjanus dentatus (Duméril, 1861) 1 1 1LUTJANIDAE Lutjanus endecacanthus Bleeker, 1863 1 1LUTJANIDAE Lutjanus fulgens (Valenciennes, 1830) 1 1 1 1LUTJANIDAE Lutjanus goreensis (Valenciennes, 1830) 1 1 1 1 1 1LUTJANIDAE Lutjanus griseus (Linnaeus, 1758) 1 1 1 1 1 1 1LUTJANIDAE Lutjanus jocu (Bloch & Schneider, 1801) 1 1 1 1 1 1 1 1 1LUTJANIDAE Lutjanus mahogoni (Cuvier, 1828) 1 1LUTJANIDAE Lutjanus purpureus Poey, 1876 1 1 1 1 1 1LUTJANIDAE Lutjanus sanguineus (Cuvier, 1828) 1 1LUTJANIDAE Lutjanus synagris (Linnaeus, 1758) 1 1 1 1 1 1LUTJANIDAE Lutjanus vivanus (Cuvier, 1828) 1 1 1 1 1 1 1LUTJANIDAE Ocyurus chrysurus (Bloch, 1791) 1 1 1 1 1 1 1 1LUTJANIDAE Pristipomoides aquilonaris (Goode & Bean, 1896) 1 1 1 1 1LUTJANIDAE Pristipomoides freemani Anderson, 1966 1 1 1 1 1 1 1LUTJANIDAE Pristipomoides macrophthalmus (Müller & Troschel, 1848) 1 1 1LUTJANIDAE Rhomboplites aurorubens (Cuvier, 1829) 1 1 1 1 1 1 1MALACANTHIDAE Branchiostegus semifasciatus (Norman, 1931) 1 1 1MALACANTHIDAE Caulolatilus bermudensis Dooley, 1981 1MALACANTHIDAE Caulolatilus chrysops (Valenciennes, 1833) 1 1 1 1 1MALACANTHIDAE Caulolatilus cyanops Poey, 1866 1 1 1MALACANTHIDAE Caulolatilus dooleyi Berry, 1978 1MALACANTHIDAE Caulolatilus guppyi Beebe & Tee-Van, 1937 1MALACANTHIDAE Caulolatilus intermedius Howell Rivero, 1936 1 1MALACANTHIDAE Caulolatilus microps Goode & Bean, 1878 1 1 1MALACANTHIDAE Caulolatilus williamsi Dooley & Berry, 1977 1MALACANTHIDAE Lopholatilus chamaeleonticeps Goode & Bean, 1879 1 1 1MALACANTHIDAE Lopholatilus villarii Miranda-Ribeiro, 1915 1 1MALACANTHIDAE Malacanthus plumieri (Bloch, 1786) 1 1 1 1 1 1 1 1 1 1MICRODESMIDAE Cerdale fasciata Dawson, 1974 1MICRODESMIDAE Cerdale floridana Longley, 1934 1 1 1 1MICRODESMIDAE Microdesmus aethiopicus (Chabanaud, 1927) 1 1MICRODESMIDAE Microdesmus africanus Dawson, 1979 1MICRODESMIDAE Microdesmus bahianus Dawson, 1973 1 1 1MICRODESMIDAE Microdesmus carri Gilbert, 1966 1MICRODESMIDAE Microdesmus lanceolatus Dawson, 1962 1MICRODESMIDAE Microdesmus longipinnis (Weymouth, 1910) 1 1 1 1 1 1 1MICRODESMIDAE Microdesmus luscus Dawson, 1977 1 1MONACANTHIDAE Aluterus heudelotii Hollard, 1855 1 1 1 1 1 1 1 1 1 1MONACANTHIDAE Aluterus monoceros (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1MONACANTHIDAE Aluterus schoepfii (Walbaum, 1792) 1 1 1 1 1 1 1 1 1MONACANTHIDAE Aluterus scriptus (Osbeck, 1765) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1MONACANTHIDAE Cantherhines dumerilii (Hollard, 1854) 1 1MONACANTHIDAE Cantherhines fronticinctus (Günther, 1867) 1 1MONACANTHIDAE Cantherhines macrocerus (Hollard, 1853) 1 1 1 1 1 1 1 1 1 1 1MONACANTHIDAE Cantherhines pardalis (Rüppell, 1837) 1 1 1MONACANTHIDAE Cantherhines pullus (Ranzani, 1842) 1 1 1 1 1 1 1 1 1 1 1MONACANTHIDAE Monacanthus ciliatus (Mitchill, 1818) 1 1 1 1 1 1 1 1MONACANTHIDAE Monacanthus tuckeri Bean, 1906 1 1 1 1MONACANTHIDAE Pervagor janthinosoma (Bleeker, 1854) 1 1MONACANTHIDAE Pseudalutarius nasicornis (Temminck & Schlegel, 1850) 1 1MONACANTHIDAE Stephanolepis auratus (Castelnau, 1861) 1 1MONACANTHIDAE Stephanolepis hispidus (Linnaeus, 1766) 1 1 1 1 1 1 1 1 1 1 1 1 1 1MONACANTHIDAE Stephanolepis setifer (Bennett, 1831) 1 1 1 1 1 1MONACANTHIDAE Thamnaconus modestoides (Barnard, 1927) 1 1MORINGUIDAE Moringua edwardsi (Jordan & Bollman, 1889) 1 1 1 1 1 1MORINGUIDAE Neoconger mucronatus Girard, 1858 1 1 1 1MULLIDAE Mulloidichthys flavolineatus (Lacepède, 1801) 1 1MULLIDAE Mulloidichthys martinicus (Cuvier, 1829) 1 1 1 1 1 1 1 1 1 1 1 1 1 1

MULLIDAE Mullus argentinae Hubbs & Marini, 1933 1 1MULLIDAE Mullus auratus Jordan & Gilbert, 1882 1 1 1MULLIDAE Mullus barbatus Linnaeus, 1758 1 1 1MULLIDAE Mullus surmuletus (Peters, 1877) 1 1 1 1 1 1 1MULLIDAE Parupeneus barberinus (Kaup, 1856) 1 1MULLIDAE Parupeneus indicus (Shaw, 1803) 1 1MULLIDAE Parupeneus rubescens (Lacepède, 1801) 1 1MULLIDAE Pseudupeneus maculatus (Bloch, 1793) 1 1 1 1 1 1 1 1 1MULLIDAE Pseudupeneus prayensis (Cuvier, 1829) 1 1 1 1 1 1MULLIDAE Upeneus parvus Poey, 1852 1 1 1 1 1MURAENIDAE Anarchias longicaudis (Peters, 1877) 1 1 1 1 1MURAENIDAE Anarchias similis (Lea, 1913) 1 1 1 1 1 1 1MURAENIDAE Channomuraena vittata (Richardson, 1845) 1 1 1 1 1 1 1 1 1MURAENIDAE Echidna catenata (Bloch, 1795) 1 1 1 1 1 1 1 1 1 1MURAENIDAE Echidna peli (Kaup, 1856) 1 1 1 1MURAENIDAE Enchelycore anatina (Lowe, 1838) 1 1 1 1 1 1 1 1 1 1 1 1 1MURAENIDAE Enchelycore carychroa Böhlke & Böhlke, 1976 1 1 1 1 1 1 1 1 1 1MURAENIDAE Enchelycore nigricans (Bonnaterre, 1788) 1 1 1 1 1 1 1 1 1 1 1 1 1 1MURAENIDAE Gymnothorax afer Bloch, 1795 1 1 1 1MURAENIDAE Gymnothorax bacalladoi Böhlke & Brito, 1987 1 1 1MURAENIDAE Gymnothorax conspersus Poey, 1867 1 1 1 1 1MURAENIDAE Gymnothorax favagineus Bloch & Schneider, 1801 1 1MURAENIDAE Gymnothorax funebris Ranzani, 1840 1 1 1 1 1 1 1 1 1MURAENIDAE Gymnothorax hubbsi Böhlke & Böhlke, 1977 1 1 1MURAENIDAE Gymnothorax johnsoni (Smith, 1962) 1 1MURAENIDAE Gymnothorax kolpos Böhlke & Böhlke, 1980 1 1 1MURAENIDAE Gymnothorax maderensis (Johnson, 1862) 1 1 1 1 1 1 1 1 1MURAENIDAE Gymnothorax mareei Poll, 1953 1 1 1MURAENIDAE Gymnothorax meleagris (Shaw, 1795) 1 1MURAENIDAE Gymnothorax miliaris (Kaup, 1856) 1 1 1 1 1 1 1 1 1 1 1 1 1 1MURAENIDAE Gymnothorax moringa (Cuvier, 1829) 1 1 1 1 1 1 1 1 1 1 1MURAENIDAE Gymnothorax nigromarginatus (Girard, 1858) 1 1MURAENIDAE Gymnothorax ocellatus Agassiz, 1831 1 1 1 1 1MURAENIDAE Gymnothorax polygonius Poey, 1875 1 1 1 1 1 1 1 1 1 1MURAENIDAE Gymnothorax saxicola Jordan & Davis, 1891 1 1 1 1MURAENIDAE Gymnothorax undulatus (Lacepède, 1803) 1 1MURAENIDAE Gymnothorax unicolor (Delaroche, 1809) 1 1 1 1 1 1 1 1MURAENIDAE Gymnothorax vicinus (Castelnau, 1855) 1 1 1 1 1 1 1 1 1 1 1 1 1MURAENIDAE Monopenchelys acuta (Parr, 1930) 1 1 1 1MURAENIDAE Muraena augusti (Kaup, 1856) 1 1 1 1MURAENIDAE Muraena helena Linnaeus, 1758 1 1 1 1 1 1 1 1MURAENIDAE Muraena melanotis (Kaup, 1860) 1 1 1 1 1MURAENIDAE Muraena pavonina Richardson, 1845 1 1 1 1 1MURAENIDAE Muraena retifera Goode & Bean, 1882 1 1 1 1MURAENIDAE Muraena robusta Osório, 1911 1 1 1 1 1 1MURAENIDAE Uropterygius macularius (Lesueur, 1825) 1 1 1 1 1 1 1 1MURAENIDAE Uropterygius wheeleri Blache, 1967 1 1 1 1MYROCONGRIDAE Myroconger compressus Günther, 1870 1 1 1 1OGCOCEPHALIDAE Halieutaea fitzsimonsi (Gilchrist & Thompson, 1916) 1 1OGCOCEPHALIDAE Halieutichthys aculeatus (Mitchill, 1818) 1 1 1 1 1OGCOCEPHALIDAE Ogcocephalus corniger Bradbury, 1980 1 1 1OGCOCEPHALIDAE Ogcocephalus cubifrons (Richardson, 1836) 1OGCOCEPHALIDAE Ogcocephalus declivirostris Bradbury, 1980 1 1 1OGCOCEPHALIDAE Ogcocephalus nasutus (Cuvier, 1829) 1 1 1OGCOCEPHALIDAE Ogcocephalus notatus (Valenciennes, 1837) 1 1 1 1OGCOCEPHALIDAE Ogcocephalus pantostictus Bradbury, 1980 1 1OGCOCEPHALIDAE Ogcocephalus parvus Longley & Hildebrand, 1940 1 1 1 1OGCOCEPHALIDAE Ogcocephalus pumilus Bradbury, 1980 1 1OGCOCEPHALIDAE Ogcocephalus radiatus (Mitchill, 1818) 1 1 1OGCOCEPHALIDAE Ogcocephalus rostellum Bradbury, 1980 1 1 1OGCOCEPHALIDAE Ogcocephalus vespertilio (Linnaeus, 1758) 1 1 1 1OPHICHTHIDAE Ahlia egmontis (Jordan, 1884) 1 1 1 1 1 1OPHICHTHIDAE Aplatophis chauliodus Böhlke, 1956 1 1OPHICHTHIDAE Aprognathodon platyventris Böhlke, 1967 1 1OPHICHTHIDAE Apterichtus anguiformis (Peters, 1877) 1 1 1 1OPHICHTHIDAE Apterichtus ansp (Böhlke, 1968) 1 1 1 1 1OPHICHTHIDAE Apterichtus caecus (Linnaeus, 1758) 1 1 1 1 1OPHICHTHIDAE Apterichtus gracilis (Kaup, 1856) 1OPHICHTHIDAE Apterichtus kendalli (Gilbert, 1891) 1 1 1OPHICHTHIDAE Bascanichthys bascanium (Jordan, 1884) 1 1 1OPHICHTHIDAE Bascanichthys ceciliae Blache & Cadenat, 1971 1OPHICHTHIDAE Bascanichthys inopinatus McCosker, Böhlke & Böhlke, 1989 1OPHICHTHIDAE Bascanichthys paulensis Storey, 1939 1 1 1OPHICHTHIDAE Bascanichthys scuticaris (Goode & Bean, 1880) 1 1 1OPHICHTHIDAE Callechelys bilinearis Kanazawa, 1952 1 1 1 1OPHICHTHIDAE Callechelys guineensis (Osório, 1893) 1 1 1 1 1OPHICHTHIDAE Callechelys leucoptera (Cadenat, 1954) 1OPHICHTHIDAE Callechelys muraena Jordan & Evermann, 1887 1 1OPHICHTHIDAE Callechelys springeri (Ginsburg, 1951) 1 1OPHICHTHIDAE Caralophia loxochila Böhlke, 1955 1 1 1OPHICHTHIDAE Echelus myrus (Linnaeus, 1758) 1 1 1 1 1OPHICHTHIDAE Echiophis foresti (Cadenat & Roux, 1964) 1OPHICHTHIDAE Echiophis intertinctus (Richardson, 1848) 1 1 1 1OPHICHTHIDAE Echiophis punctifer (Kaup, 1860) 1 1 1 1 1

OPHICHTHIDAE Ethadophis akkistikos McCosker & Böhlke, 1984 1OPHICHTHIDAE Gordiichthys ergodes McCosker, Böhlke & Böhlke, 1989 1OPHICHTHIDAE Gordiichthys irretitus Jordan & Davis, 1891 1 1OPHICHTHIDAE Gordiichthys randalli McCosker & Böhlke, 1984 1OPHICHTHIDAE Hemerorhinus opici Blache & Bauchot, 1972 1OPHICHTHIDAE Herpetiochthys regius (Richardson, 1848) 1 1OPHICHTHIDAE Ichthyapus insularis McCosker, 2004 1OPHICHTHIDAE Ichthyapus ophioneus (Bleeker, 1857) 1 1 1 1 1 1 1 1OPHICHTHIDAE Leiuranus semicinctus (Lay & Bennett, 1839) 1 1OPHICHTHIDAE Letharchus aliculatus McCosker, 1974 1OPHICHTHIDAE Letharchus velifer Goode & Bean, 1882 1 1OPHICHTHIDAE Myrichthys breviceps (Richardson, 1848) 1 1 1 1 1 1 1 1OPHICHTHIDAE Myrichthys ocellatus (Lesueur, 1825) 1 1 1 1 1 1 1 1OPHICHTHIDAE Myrichthys pardalis (Valenciennes, 1839) 1 1 1 1OPHICHTHIDAE Myrophis anterodorsalis McCosker, Böhlke & Böhlke, 1989 1OPHICHTHIDAE Myrophis platyrhynchus Breder, 1927 1 1 1 1OPHICHTHIDAE Mystriophis crosnieri Blache, 1971 1 1 1 1OPHICHTHIDAE Mystriophis rostellatus (Richardson, 1848) 1 1 1OPHICHTHIDAE Ophichthus apicalis (Anonymous [Bennett], 1830) 1 1OPHICHTHIDAE Ophichthus brasiliensis (Kaup, 1856) 1OPHICHTHIDAE Ophichthus cruentifer (Goode & Bean, 1896) 1 1OPHICHTHIDAE Ophichthus cylindroideus (Ranzani, 1840) 1 1 1 1OPHICHTHIDAE Ophichthus gomesii (Castelnau, 1855) 1 1 1 1 1 1OPHICHTHIDAE Ophichthus hyposagmatus McCosker & Böhlke, 1984 1 1OPHICHTHIDAE Ophichthus melanoporus Kanazawa, 1963 1 1OPHICHTHIDAE Ophichthus menezesi McCosker & Böhlke, 1984 1 1OPHICHTHIDAE Ophichthus ophis (Linnaeus, 1758) 1 1 1 1 1 1 1 1OPHICHTHIDAE Ophichthus puncticeps (Kaup, 1860) 1 1 1OPHICHTHIDAE Ophichthus regius (Richardson, 1848) 1 1OPHICHTHIDAE Ophichthus rex Böhlke & Caruso, 1980 1OPHICHTHIDAE Ophichthus rufus (Rafinesque, 1810) 1 1 1OPHICHTHIDAE Ophichthus unicolor Regan, 1908 1 1OPHICHTHIDAE Ophisurus serpens (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1OPHICHTHIDAE Phaenomonas longissima (Cadenat & Marchal, 1963) 1 1 1OPHICHTHIDAE Pisodonophis boro (Hamilton, 1822) 1 1OPHICHTHIDAE Pisodonophis cancrivorus (Richardson, 1848) 1 1OPHICHTHIDAE Pisodonophis semicinctus (Richardson, 1848) 1 1 1 1 1OPHICHTHIDAE Pseudomyrophis atlanticus Blache, 1975 1OPHICHTHIDAE Quassiremus ascensionis (Studer, 1889) 1 1 1 1 1OPHICHTHIDAE Scolecenchelys gymnotus (Bleeker, 1857) 1 1OPHICHTHIDAE Scolecenchelys laticaudata (Ogilby, 1897) 1 1OPHICHTHIDAE Asarcenchelys longimanus McCosker, 1985 1OPHICHTHIDAE Brachysomophis atlanticus Blache & Saldanha, 1972 1OPHIDIIDAE Brotula barbata (Bloch & Schneider, 1801) 1 1 1 1 1 1 1 1OPHIDIIDAE Brotula sp.n. 1OPHIDIIDAE Genypterus blacodes (Forster, 1801) 1 1OPHIDIIDAE Genypterus brasiliensis Regan, 1903 1 1OPHIDIIDAE Ophidion barbatum Linnaeus, 1758 1 1 1OPHIDIIDAE Ophidion beani Jordan & Gilbert, 1883 1 1OPHIDIIDAE Ophidion grayi (Fowler, 1948) 1 1OPHIDIIDAE Ophidion holbrookii (Putnam, 1874) 1 1 1 1OPHIDIIDAE Ophidion lagochila (Böhlke & Robins, 1959) 1 1OPHIDIIDAE Ophidion lozanoi Matallanas, 1990 1 1OPHIDIIDAE Ophidion marginatum (DeKay, 1842) 1 1OPHIDIIDAE Ophidion nocomis Robins & Böhlke, 1959 1OPHIDIIDAE Ophidion robinsi Fahay, 1992 1OPHIDIIDAE Ophidion saldanhai Matallanas & Brito, 1999 1 1OPHIDIIDAE Ophidion selenops Robins & Böhlke, 1959 1 1OPHIDIIDAE Ophidion sp. 1OPHIDIIDAE Ophidion welshi (Nichols & Breder, 1922) 1 1OPHIDIIDAE Otophidium chickcharney Böhlke & Robins, 1959 1 1 1OPHIDIIDAE Otophidium dormitator Böhlke & Robins, 1959 1 1 1OPHIDIIDAE Otophidium omostigmum (Jordan & Gilbert, 1882) 1 1 1OPHIDIIDAE Parophidion schmidti (Miranda Ribeiro, 1903) 1 1 1 1OPHIDIIDAE Parophidion vassali (Risso, 1810) 1 1 1 1OPHIDIIDAE Petrotyx sanguineus (Meek & Hildebrand, 1928) 1 1OPHIDIIDAE Raneya fluminensis (Miranda Ribeiro, 1903) 1 1OPISTOGNATHIDAE Lonchopisthus higmani Mead, 1959 1 1OPISTOGNATHIDAE Lonchopisthus lemur (Myers, 1935) 1 1 1OPISTOGNATHIDAE Lonchopisthus micrognathus (Poey, 1860) 1 1OPISTOGNATHIDAE Lonchopisthus sp.n. 1 1OPISTOGNATHIDAE Opistognathus aurifrons (Jordan & Thompson, 1905) 1 1 1 1OPISTOGNATHIDAE Opistognathus brasiliensis Smith-Vaniz, 1997 1OPISTOGNATHIDAE Opistognathus cuvieri Valenciennes, 1836 1 1OPISTOGNATHIDAE Opistognathus gilberti Böhlke, 1967 1 1OPISTOGNATHIDAE Opistognathus leprocarus Smith-Vaniz, 1997 1OPISTOGNATHIDAE Opistognathus lonchurus Jordan & Gilbert, 1882 1 1 1 1OPISTOGNATHIDAE Opistognathus macrognathus Poey, 1860 1 1 1 1OPISTOGNATHIDAE Opistognathus maxillosus Poey, 1860 1 1OPISTOGNATHIDAE Opistognathus megalepis Smith-Vaniz, 1972 1OPISTOGNATHIDAE Opistognathus melachasme Smith-Vaniz, 1972 1OPISTOGNATHIDAE Opistognathus nothus Smith-Vaniz, 1997 1 1 1OPISTOGNATHIDAE Opistognathus robinsi Smith-Vaniz, 1997 1 1 1OPISTOGNATHIDAE Opistognathus signatus Smith-Vaniz, 1997 1 1

OPISTOGNATHIDAE Opistognathus sp.n.(aff.aurifrons) 1 1 1 1OPISTOGNATHIDAE Opistognathus whitehursti (Longley, 1927) 1 1 1 1OSTRACIIDAE Acanthostracion guineensis (Bleeker, 1865) 1 1OSTRACIIDAE Acanthostracion notacanthus (Bleeker, 1863) 1 1 1 1 1OSTRACIIDAE Acanthostracion polygonius Poey, 1876 1 1 1 1 1 1 1 1 1OSTRACIIDAE Acanthostracion quadricornis (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1 1OSTRACIIDAE Anoplocapros robustus (Fraser-Brunner, 1941) 1OSTRACIIDAE Lactophrys bicaudalis Linnaeus, 1758 1 1 1 1OSTRACIIDAE Lactophrys trigonus (Linnaeus, 1758) 1 1 1 1 1 1 1 1OSTRACIIDAE Lactophrys triqueter (Linnaeus, 1758) 1 1 1 1 1 1OSTRACIIDAE Lactoria cornuta (Linnaeus, 1758) 1 1OSTRACIIDAE Lactoria diaphana (Bloch & Schneider, 1801) 1 1OSTRACIIDAE Lactoria fornasini (Bianconi, 1846) 1 1OSTRACIIDAE Ostracion cubicus Linnaeus, 1758 1 1OSTRACIIDAE Ostracion meleagris Shaw, 1796 1 1OSTRACIIDAE Tetrosomus concatenatus (Bloch, 1785) 1 1PARALICHTHYIDAE Ancylopsetta cycloidea Tyler, 1959 1 1PARALICHTHYIDAE Ancylopsetta dilecta (Goode & Bean, 1883) 1 1PARALICHTHYIDAE Ancylopsetta kumperae Tyler, 1959 1 1PARALICHTHYIDAE Ancylopsetta microctenus Gutherz, 1966 1PARALICHTHYIDAE Ancylopsetta quadrocellata Gill, 1864 1 1PARALICHTHYIDAE Citharichthys arctifrons (Mitchill, 1815) 1 1PARALICHTHYIDAE Citharichthys arenaceus Evermann & Marsh, 1900 1 1 1 1 1PARALICHTHYIDAE Citharichthys cornutus (Günther, 1880) 1 1 1 1 1 1PARALICHTHYIDAE Citharichthys dinoceros Goode & Bean, 1886 1 1 1 1PARALICHTHYIDAE Citharichthys gymnorhinus Gutherz & Blackman, 1970 1 1 1PARALICHTHYIDAE Citharichthys macrops Dresel, 1885 1 1 1 1 1PARALICHTHYIDAE Citharichthys minutus Cervigón, 1982 1 1PARALICHTHYIDAE Citharichthys spilopterus Günther, 1862 1 1 1 1 1PARALICHTHYIDAE Citharichthys stampflii (Steindachner, 1894) 1 1 1PARALICHTHYIDAE Citharichthys valdezi Cervigón, 1986 1 1PARALICHTHYIDAE Cyclopsetta chittendeni Bean, 1895 1 1 1 1PARALICHTHYIDAE Cyclopsetta decussata Gunter, 1946 1PARALICHTHYIDAE Cyclopsetta fimbriata (Goode & Bean, 1885) 1 1 1 1 1PARALICHTHYIDAE Etropus crossotus Jordan & Gilbert, 1882 1 1 1 1 1PARALICHTHYIDAE Etropus cyclosquamus Leslie & Stewart, 1986 1PARALICHTHYIDAE Etropus intermedius Norman, 1933 1 1 1PARALICHTHYIDAE Etropus longimanus Norman, 1933 1 1PARALICHTHYIDAE Etropus microstomus (Gill, 1864) 1 1PARALICHTHYIDAE Etropus rimosus Goode & Bean, 1885 1 1PARALICHTHYIDAE Gastropsetta frontalis Bean, 1895 1 1 1PARALICHTHYIDAE Paralichthys albigutta Jordan & Gilbert, 1882 1 1 1PARALICHTHYIDAE Paralichthys brasiliensis (Ranzani, 1842) 1 1 1PARALICHTHYIDAE Paralichthys dentatus (Linnaeus, 1766) 1PARALICHTHYIDAE Paralichthys isosceles Jordan, 1891 1 1PARALICHTHYIDAE Paralichthys lethostigma Jordan & Gilbert, 1884 1 1PARALICHTHYIDAE Paralichthys oblongus (Mitchill, 1815) 1 1PARALICHTHYIDAE Paralichthys orbignyanus (Valenciennes, 1842) 1 1PARALICHTHYIDAE Paralichthys patagonicus Jordan, 1889 1 1PARALICHTHYIDAE Paralichthys squamilentus Jordan & Gilbert, 1882 1 1PARALICHTHYIDAE Paralichthys triocellatus Miranda-Ribeiro, 1903 1 1PARALICHTHYIDAE Paralichthys tropicus Ginsburg, 1933 1 1PARALICHTHYIDAE Pseudorhombus elevatus Ogilby, 1912 1 1PARALICHTHYIDAE Syacium guineensis (Bleeker, 1862) 1 1 1 1 1PARALICHTHYIDAE Syacium gunteri Ginsburg, 1933 1 1 1PARALICHTHYIDAE Syacium micrurum Ranzani, 1842 1 1 1 1PARALICHTHYIDAE Syacium papillosum (Linnaeus, 1758) 1 1 1 1 1 1 1PARALICHTHYIDAE Xystreurys rasile (Jordan, 1891) 1 1PEMPHERIDAE Pempheris poeyi Bean, 1885 1 1 1PEMPHERIDAE Pempheris schomburgki Müller & Troschel, 1848 1 1 1 1 1 1 1PINGUIPEDIDAE Parapercis atlantica (Vaillant, 1887) 1PINGUIPEDIDAE Parapercis fasciatus? (Jenyns, 1840) 1PINGUIPEDIDAE Parapercis maritzi Anderson, 1992 1 1PINGUIPEDIDAE Parapercis multifasciata Döderlein, 1884 1 1 1PINGUIPEDIDAE Parapercis robinsoni Fowler, 1929 1 1PINGUIPEDIDAE Pinguipes brasilianus Cuvier, 1829 1 1PINGUIPEDIDAE Pseudopercis numida Miranda-Ribeiro, 1903 1 1 1PINGUIPEDIDAE Pseudopercis semifasciata (Cuvier, 1829) 1 1PLATYCEPHALIDAE Platycephalus indicus (Linnaeus, 1758) 1 1PLATYCEPHALIDAE Solitas gruveli (Pellegrin, 1905) 1 1POMACANTHIDAE Centropyge acanthops (Norman, 1922) 1 1POMACANTHIDAE Centropyge argi Woods & Kanazawa, 1951 1 1 1 1POMACANTHIDAE Centropyge aurantonotus Burgess, 1974 1 1 1 1 1 1 1POMACANTHIDAE Centropyge resplendens Lubbock & Sankey, 1975 1POMACANTHIDAE Holacanthus africanus Cadenat, 1951 1 1 1 1POMACANTHIDAE Holacanthus bermudensis Goode, 1876 1 1 1 1POMACANTHIDAE Holacanthus ciliaris (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1POMACANTHIDAE Holacanthus tricolor (Bloch, 1795) 1 1 1 1 1 1 1 1POMACANTHIDAE Pomacanthus arcuatus (Linnaeus, 1758) 1 1 1 1 1 1POMACANTHIDAE Pomacanthus paru (Bloch, 1787) 1 1 1 1 1 1 1 1 1 1POMACANTHIDAE Pomacanthus rhomboides (Gilchrist & Thompson, 1908) 1 1POMACANTHIDAE Pomacanthus semicirculatus (Cuvier, 1831) 1 1POMACENTRIDAE Abudefduf hoefleri (Steindachner, 1881) 1 1POMACENTRIDAE Abudefduf luridus (Cuvier, 1830) 1 1 1 1

POMACENTRIDAE Abudefduf saxatilis (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1POMACENTRIDAE Abudefduf sordidus (Forsskål, 1775) 1 1POMACENTRIDAE Abudefduf taurus (Müller & Troschel, 1848) 1 1 1 1 1 1 1POMACENTRIDAE Abudefduf vaigiensis (Quoy & Gaimard, 1825) 1 1POMACENTRIDAE Chromis bermudae Nichols, 1920 1POMACENTRIDAE Chromis cadenati Whitley, 1951 1 1POMACENTRIDAE Chromis chromis (Linnaeus, 1758) 1 1POMACENTRIDAE Chromis cyanea (Poey, 1860) 1 1 1POMACENTRIDAE Chromis enchrysura Jordan & Gilbert, 1882 1 1 1 1 1 1 1POMACENTRIDAE Chromis flavicauda (Günther, 1880) 1 1 1 1POMACENTRIDAE Chromis insolata (Cuvier, 1830) 1 1 1 1POMACENTRIDAE Chromis jubauna Moura, 1995 1 1 1 1POMACENTRIDAE Chromis limbata (Valenciennes, 1833) 1 1 1 1 1POMACENTRIDAE Chromis lubbocki Edwards, 1986 1POMACENTRIDAE Chromis multilineata (Guichenot, 1853) 1 1 1 1 1 1 1 1 1 1 1 1 1 1POMACENTRIDAE Chromis sanctaehelenae Edwards, 1987 1POMACENTRIDAE Chromis scotti Emery, 1968 1 1 1 1 1POMACENTRIDAE Dascyllus trimaculatus (Rüppell, 1829) 1 1POMACENTRIDAE Microspathodon chrysurus (Cuvier, 1830) 1 1 1 1 1 1 1POMACENTRIDAE Microspathodon frontatus Emery, 1970 1 1POMACENTRIDAE Similiparma hermani (Steindachner, 1887) 1POMACENTRIDAE Stegastes adustus (Troschel, 1865) 1 1 1 1POMACENTRIDAE Stegastes diencaeus (Jordan & Rutter, 1897) 1 1POMACENTRIDAE Stegastes fuscus (Cuvier, 1830) 1 1 1POMACENTRIDAE Stegastes imbricatus Jenyns, 1840 1 1 1 1POMACENTRIDAE Stegastes leucostictus (Müller & Troschel, 1848) 1 1 1 1POMACENTRIDAE Stegastes lubbocki Allen & Smith, 1992 1POMACENTRIDAE Stegastes otophorus (Poey, 1860) 1POMACENTRIDAE Stegastes partitus (Poey, 1868) 1 1 1 1POMACENTRIDAE Stegastes pictus (Castelnau, 1855) 1 1 1 1 1 1POMACENTRIDAE Stegastes planifrons (Cuvier, 1830) 1 1 1 1POMACENTRIDAE Stegastes rocasensis (Emery, 1972) 1 1 1POMACENTRIDAE Stegastes sanctaehelenae (Sauvage, 1879) 1POMACENTRIDAE Stegastes sanctipauli Lubbock & Edwards, 1981 1 1POMACENTRIDAE Stegastes sp.(aff_variabilis) 1 1 1 1 1POMACENTRIDAE Stegastes uenfi Novelli, Nunan & Lima, 2000 1 1POMACENTRIDAE Stegastes variabilis (Castelnau, 1855) 1 1PRIACANTHIDAE Cookeolus japonicus (Cuvier, 1829) 1 1 1 1 1 1 1 1 1 1 1PRIACANTHIDAE Heteropriacanthus cruentatus (Lacepède, 1801) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1PRIACANTHIDAE Priacanthus arenatus Cuvier, 1829 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1PRIACANTHIDAE Priacanthus hamrur (Forsskål, 1775) 1 1PRIACANTHIDAE Pristigenys alta (Gill, 1862) 1 1 1 1 1 1PRIACANTHIDAE Pristigenys niphonia (Cuvier, 1829) 1 1PSEUDOCHROMIDAEHalidesmus scapularis Günther, 1872 1 1PTERELEOTRIDAE Ptereleotris calliura (Jordan & Gilbert, 1882) 1 1PTERELEOTRIDAE Ptereleotris helenae (Randall, 1967) 1 1PTERELEOTRIDAE Ptereleotris randalli Gasparini, Rocha & Floeter, 2001 1 1 1 1SCARIDAE Cryptotomus roseus Cope, 1871 1 1 1 1 1 1 1 1 1SCARIDAE Nicholsina usta_collettei Schultz, 1968 1 1 1SCARIDAE Nicholsina usta_usta (Valenciennes, 1840) 1 1 1 1 1SCARIDAE Scarus coelestinus Valenciennes, 1840 1 1 1 1SCARIDAE Scarus coeruleus (Bloch, 1786) 1 1 1 1SCARIDAE Scarus ghobban Forsskål, 1775 1 1SCARIDAE Scarus guacamaia Cuvier, 1829 1 1 1 1 1 1SCARIDAE Scarus hoefleri (Steindachner, 1881) 1 1 1 1SCARIDAE Scarus iserti (Bloch, 1789) 1 1 1 1SCARIDAE Scarus taeniopterus Desmarest, 1831 1 1 1 1SCARIDAE Scarus trispinosus Valenciennes, 1840 1 1SCARIDAE Scarus vetula Bloch & Schneider, 1801 1 1 1SCARIDAE Scarus zelindae Moura, Figueiredo & Sazima, 2001 1 1SCARIDAE Sparisoma amplum (Ranzani, 1842) 1 1 1 1 1 1SCARIDAE Sparisoma atomarium (Poey, 1861) 1 1 1 1SCARIDAE Sparisoma aurofrenatum (Valenciennes, 1840) 1 1 1SCARIDAE Sparisoma axillare (Steindachner, 1878) 1 1 1 1 1 1SCARIDAE Sparisoma chrysopterum (Bloch & Schneider, 1801) 1 1 1 1SCARIDAE Sparisoma cretense (Linnaeus, 1758) 1 1 1 1 1 1 1 1SCARIDAE Sparisoma frondosum (Agassiz, 1831) 1 1 1 1 1SCARIDAE Sparisoma griseorubra Cervigón, 1982 1SCARIDAE Sparisoma radians (Valenciennes, 1840) 1 1 1 1 1 1SCARIDAE Sparisoma rubripinne (Valenciennes, 1840) 1 1 1 1SCARIDAE Sparisoma sp.(aff_rubripinne) 1 1 1SCARIDAE Sparisoma strigatum (Günther, 1862) 1 1SCARIDAE Sparisoma tuiupiranga Gasparini, Joyeux & Floeter, 2003 1 1 1SCARIDAE Sparisoma viride (Bonnaterre, 1788) 1 1 1 1SCIAENIDAE Argyrosomus regius (Asso, 1801) 1 1 1 1 1SCIAENIDAE Equetus lanceolatus (Linnaeus, 1758) 1 1 1 1 1 1 1SCIAENIDAE Equetus punctatus (Bloch & Schneider, 1801) 1 1 1SCIAENIDAE Odontoscion dentex (Cuvier, 1830) 1 1 1 1 1SCIAENIDAE Pareques acuminatus (Bloch & Schneider, 1801) 1 1 1 1 1SCIAENIDAE Pareques iwamotoi Miller & Woods, 1988 1 1 1 1SCIAENIDAE Pareques umbrosus (Gmelin, 1789) 1 1 1 1 1SCIAENIDAE Sciaena umbra (Schultz, 1958) 1 1 1 1 1 1SCIAENIDAE Umbrina canariensis (Rafinesque, 1810) 1 1 1 1 1 1 1 1 1SCIAENIDAE Umbrina cirrosa Cuvier, 1829 1 1 1 1

SCIAENIDAE Umbrina ronchus (Longley, 1935) 1 1 1 1 1 1 1 1 1SCIAENIDAE Umbrina steindachneri (Ginsburg, 1952) 1SCORPAENIDAE Neomerinthe beanorum (Jordan & Swain, 1885) 1 1SCORPAENIDAE Neomerinthe folgori Günther, 1868 1 1 1SCORPAENIDAE Neomerinthe hemingwayi Fowler, 1935 1 1 1SCORPAENIDAE Phenacoscorpius nebris Eschmeyer, 1965 1SCORPAENIDAE Pontinus accraensis Norman, 1935 1 1 1 1SCORPAENIDAE Pontinus castor Poey, 1860 1 1 1SCORPAENIDAE Pontinus corallinus Miranda-Ribeiro, 1903 1SCORPAENIDAE Pontinus kuhlii (Bowdich, 1825) 1 1 1 1 1 1 1SCORPAENIDAE Pontinus leda Eschmeyer, 1969 1 1SCORPAENIDAE Pontinus longispinis Goode & Bean, 1896 1 1 1 1 1SCORPAENIDAE Pontinus nematophthalmus (Günther, 1860) 1 1 1SCORPAENIDAE Pontinus nigropunctatus (Günther, 1868) 1SCORPAENIDAE Pontinus rathbuni Goode & Bean, 1896 1 1 1 1 1SCORPAENIDAE Pterois miles (Bennett, 1828) 1 1SCORPAENIDAE Scorpaena agassizii Goode & Bean, 1896 1 1 1 1SCORPAENIDAE Scorpaena albifimbria Evermann & Marsh, 1900 1 1 1SCORPAENIDAE Scorpaena angolensis Norman, 1935 1 1 1 1SCORPAENIDAE Scorpaena annobonae Eschmeyer, 1969 1SCORPAENIDAE Scorpaena ascensionis Eschmeyer, 1971 1SCORPAENIDAE Scorpaena azorica Eschmeyer, 1969 1 1SCORPAENIDAE Scorpaena bergii Evermann & Marsh, 1900 1 1 1 1SCORPAENIDAE Scorpaena brachyptera Eschmeyer, 1965 1 1SCORPAENIDAE Scorpaena brasiliensis Cuvier, 1829 1 1 1 1 1 1SCORPAENIDAE Scorpaena calcarata Goode & Bean, 1882 1 1 1 1 1SCORPAENIDAE Scorpaena canariensis (Sauvage, 1878) 1 1 1SCORPAENIDAE Scorpaena dispar Longley & Hildebrand, 1940 1 1 1 1 1SCORPAENIDAE Scorpaena elachys Eschmeyer, 1965 1 1SCORPAENIDAE Scorpaena elongata Cadenat, 1943 1 1 1 1 1SCORPAENIDAE Scorpaena grandicornis Cuvier, 1829 1 1 1 1 1 1SCORPAENIDAE Scorpaena inermis Cuvier, 1829 1 1 1SCORPAENIDAE Scorpaena isthmensis Meek & Hildebrand, 1928 1 1 1 1 1 1SCORPAENIDAE Scorpaena laevis Troschel, 1866 1 1 1 1SCORPAENIDAE Scorpaena loppei Cadenat, 1943 1 1 1SCORPAENIDAE Scorpaena maderensis Valenciennes, 1833 1 1 1 1 1 1 1SCORPAENIDAE Scorpaena melasma Eschmeyer, 1965 1SCORPAENIDAE Scorpaena mellissii Günther, 1868 1SCORPAENIDAE Scorpaena normani Cadenat, 1943 1 1 1SCORPAENIDAE Scorpaena notata Rafinesque, 1810 1 1 1 1 1 1 1 1SCORPAENIDAE Scorpaena petricola Eschmeyer, 1965 1SCORPAENIDAE Scorpaena plumieri Bloch, 1789 1 1 1 1 1 1 1 1 1SCORPAENIDAE Scorpaena porcus Linnaeus, 1758 1 1 1 1 1 1SCORPAENIDAE Scorpaena scrofa Linnaeus, 1758 1 1 1 1 1 1 1 1 1 1SCORPAENIDAE Scorpaena stephanica Cadenat, 1943 1 1 1SCORPAENIDAE Scorpaenodes africanus Pfaff, 1933 1 1SCORPAENIDAE Scorpaenodes arenai Torchio, 1962 1 1SCORPAENIDAE Scorpaenodes caribbaeus Meek & Hildebrand, 1928 1 1 1 1 1SCORPAENIDAE Scorpaenodes elongatus Cadenat, 1950 1SCORPAENIDAE Scorpaenodes insularis Eschmeyer, 1971 1 1 1SCORPAENIDAE Scorpaenodes tredecimspinosus (Metzelaar, 1919) 1 1 1 1 1SCORPAENIDAE Sebastapistes cyanostigma (Bleeker, 1856) 1 1SCORPAENIDAE Sebastes capensis (Gmelin, 1789) 1 1SERRANIDAE Acanthistius brasilianus (Cuvier, 1828) 1 1SERRANIDAE Acanthistius patachonicus (Jenyns, 1840) 1 1 1SERRANIDAE Acanthistius sebastoides (Castelnau, 1861) 1 1SERRANIDAE Alphestes afer (Bloch, 1793) 1 1 1 1 1 1 1 1SERRANIDAE Anthias anthias (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1SERRANIDAE Anthias asperilinguis Günther, 1859 1 1 1SERRANIDAE Anthias cyprinoides (Katayama & Amaoka, 1986) 1SERRANIDAE Anthias helenensis Katayama & Amaoka, 1986 1SERRANIDAE Anthias menezesi Anderson & Heemstra, 1980 1 1 1SERRANIDAE Anthias nicholsi Firth, 1933 1 1 1 1SERRANIDAE Anthias salmopunctatus Lubbock & Edwards, 1981 1SERRANIDAE Anthias tenuis Nichols, 1920 1 1 1 1SERRANIDAE Anthias woodsi Anderson & Heemstra, 1980 1 1SERRANIDAE Bathyanthias cubensis (Schultz, 1958) 1SERRANIDAE Bathyanthias mexicanus (Schultz, 1958) 1SERRANIDAE Bathyanthias roseus Günther, 1880 1SERRANIDAE Bullisichthys caribbaeus Rivas, 1971 1 1SERRANIDAE Callanthias ruber (Rafinesque, 1810) 1 1 1 1 1 1SERRANIDAE Centropristis fuscula Poey, 1861 1 1 1SERRANIDAE Centropristis ocyurus (Jordan & Evermann, 1887) 1 1SERRANIDAE Centropristis philadelphica (Linnaeus, 1758) 1 1SERRANIDAE Centropristis striata (Linnaeus, 1758) 1 1SERRANIDAE Cephalopholis cruentata (Lacepède, 1802) 1 1 1 1SERRANIDAE Cephalopholis fulva (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1SERRANIDAE Cephalopholis furcifer (Valenciennes, 1828) 1 1 1 1 1 1 1 1 1 1 1SERRANIDAE Cephalopholis nigri (Günther, 1859) 1 1 1 1SERRANIDAE Cephalopholis taeniops (Valenciennes, 1828) 1 1 1 1SERRANIDAE Dermatolepis inermis (Valenciennes, 1833) 1 1 1 1 1 1 1 1SERRANIDAE Diplectrum bivittatum (Valenciennes, 1828) 1 1 1 1SERRANIDAE Diplectrum formosum (Linnaeus, 1766) 1 1 1 1 1 1 1 1SERRANIDAE Diplectrum radiale (Quoy & Gaimard, 1824) 1 1 1 1 1 1

SERRANIDAE Dules auriga Cuvier, 1829 1 1 1SERRANIDAE Epinephelus adscensionis (Osbeck, 1765) 1 1 1 1 1 1 1 1 1 1SERRANIDAE Epinephelus aeneus (Geoffroy Saint-Hilaire, 1817) 1 1 1 1 1 1SERRANIDAE Epinephelus andersoni Boulenger, 1903 1 1SERRANIDAE Epinephelus caninus (Valenciennes, 1843) 1 1 1 1SERRANIDAE Epinephelus chabaudi (Castelnau, 1861) 1 1SERRANIDAE Epinephelus costae (Steindachner, 1878) 1 1 1 1 1 1 1SERRANIDAE Epinephelus drummondhayi Goode & Bean, 1878 1 1 1SERRANIDAE Epinephelus fasciatus (Forsskål, 1775) 1 1 1SERRANIDAE Epinephelus flavocaeruleus (Lacepède, 1802) 1 1SERRANIDAE Epinephelus flavolimbatus Poey, 1865 1 1 1 1 1SERRANIDAE Epinephelus goreensis (Valenciennes, 1830) 1 1 1SERRANIDAE Epinephelus guttatus (Linnaeus, 1758) 1 1 1 1SERRANIDAE Epinephelus haifensis Ben-Tuvia, 1953 1 1 1 1SERRANIDAE Epinephelus itajara (Lichtenstein, 1822) 1 1 1 1 1 1 1 1 1 1 1 1 1 1SERRANIDAE Epinephelus lanceolatus (Bloch, 1790) 1 1SERRANIDAE Epinephelus marginatus (Lowe, 1834) 1 1 1 1 1 1 1 1 1 1 1 1 1 1SERRANIDAE Epinephelus morio (Valenciennes, 1828) 1 1 1 1 1 1SERRANIDAE Epinephelus mystacinus (Poey, 1852) 1 1 1 1 1SERRANIDAE Epinephelus nigritus (Holbrook, 1855) 1 1 1 1 1 1 1SERRANIDAE Epinephelus niveatus (Valenciennes, 1828) 1 1 1 1 1 1SERRANIDAE Epinephelus poecilonotus (Temminck & Schlegel, 1842) 1 1SERRANIDAE Epinephelus rivulatus (Valenciennes, 1830) 1 1SERRANIDAE Epinephelus striatus (Bloch, 1792) 1 1 1 1SERRANIDAE Gonioplectrus hispanus (Cuvier, 1828) 1 1 1 1 1 1SERRANIDAE Hemanthias aureorubens (Longley, 1935) 1 1SERRANIDAE Hemanthias leptus (Ginsburg, 1952) 1 1SERRANIDAE Hemanthias vivanus (Jordan & Swain, 1885) 1 1 1 1SERRANIDAE Holanthias caudalis Trunov, 1976 1SERRANIDAE Holanthias fronticinctus Günther, 1868 1SERRANIDAE Hypoplectrus aberrans Poey, 1868 1 1SERRANIDAE Hypoplectrus chlorurus (Cuvier, 1828) 1 1SERRANIDAE Hypoplectrus gemma Goode & Bean, 1882 1 1 1SERRANIDAE Hypoplectrus gummigutta (Poey, 1851) 1 1SERRANIDAE Hypoplectrus guttavarius (Poey, 1852) 1 1SERRANIDAE Hypoplectrus indigo (Poey, 1851) 1 1SERRANIDAE Hypoplectrus nigricans (Poey, 1852) 1 1 1SERRANIDAE Hypoplectrus providencianus Acero P. & Garzón-Ferreira, 1994 1SERRANIDAE Hypoplectrus puella (Cuvier, 1828) 1 1 1 1SERRANIDAE Hypoplectrus sp.(Mayan_hamlet) 1SERRANIDAE Hypoplectrus sp.(tan_hamlet) 1 1SERRANIDAE Hypoplectrus unicolor (Walbaum, 1792) 1 1 1SERRANIDAE Jeboehlkia gladifer Robins, 1967 1 1SERRANIDAE Liopropoma aberrans (Poey, 1860) 1 1 1SERRANIDAE Liopropoma carmabi (Randall, 1963) 1 1 1 1SERRANIDAE Liopropoma eukrines (Starck & Courtenay, 1962) 1 1SERRANIDAE Liopropoma mowbrayi Woods & Kanazawa, 1951 1 1 1 1SERRANIDAE Liopropoma rubre Poey, 1861 1 1 1SERRANIDAE Liopropoma sp.n.(Bahia) 1SERRANIDAE Liopropoma sp.n.(Stome) 1SERRANIDAE Meganthias carpenteri Anderson, 2006 1SERRANIDAE Meganthias natalensis (Fowler, 1925) 1 1SERRANIDAE Mycteroperca acutirostris (Valenciennes, 1828) 1 1 1 1 1SERRANIDAE Mycteroperca bonaci (Poey, 1860) 1 1 1 1 1 1 1 1 1SERRANIDAE Mycteroperca cidi Cervigón, 1966 1 1SERRANIDAE Mycteroperca fusca (Lowe, 1838) 1 1 1 1SERRANIDAE Mycteroperca interstitialis (Poey, 1860) 1 1 1 1 1 1 1SERRANIDAE Mycteroperca microlepis (Goode & Bean, 1879) 1 1 1 1 1SERRANIDAE Mycteroperca phenax Jordan & Swain, 1884 1 1 1SERRANIDAE Mycteroperca rubra (Bloch, 1793) 1 1 1 1SERRANIDAE Mycteroperca tigris (Valenciennes, 1833) 1 1 1 1 1SERRANIDAE Mycteroperca venenosa (Linnaeus, 1758) 1 1 1 1 1 1 1SERRANIDAE Nemanthias carberryi Smith, 1954 1 1SERRANIDAE Paralabrax dewegeri (Metzelaar, 1919) 1 1SERRANIDAE Parasphyraenops atrimanus Bean, 1912 1 1SERRANIDAE Parasphyraenops incisus (Colin, 1978) 1 1SERRANIDAE Plectranthias garrupellus Robins & Starck, 1961 1 1SERRANIDAE Pronotogrammus martinicensis (Guichenot, 1868) 1 1 1 1 1SERRANIDAE Pseudogramma gregoryi (Breder, 1927) 1 1 1 1SERRANIDAE Pseudogramma guineensis (Norman, 1935) 1 1 1SERRANIDAE Rypticus bistrispinus (Mitchill, 1818) 1 1 1 1 1 1SERRANIDAE Rypticus bornoi Beebe & Tee-Van, 1928 1 1SERRANIDAE Rypticus maculatus Holbrook, 1855 1 1SERRANIDAE Rypticus saponaceus (Bloch & Schneider, 1801) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1SERRANIDAE Rypticus subbifrenatus Gill, 1861 1 1 1 1 1 1 1 1 1SERRANIDAE Schultzea beta (Hildebrand, 1940) 1 1 1SERRANIDAE Serraniculus pumilio Ginsburg, 1952 1 1 1SERRANIDAE Serranus accraensis (Norman, 1931) 1SERRANIDAE Chelidoperca africana Cadenat, 1960 1 1SERRANIDAE Serranus annularis (Günther, 1880) 1 1 1 1 1SERRANIDAE Serranus atricauda Günther, 1874 1 1 1 1 1 1 1SERRANIDAE Serranus atrobranchus (Cuvier, 1829) 1 1 1 1 1SERRANIDAE Serranus baldwini (Evermann & Marsh, 1899) 1 1 1 1 1 1SERRANIDAE Serranus cabrilla (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1

SERRANIDAE Serranus chionaraia Robins & Starck, 1961 1 1 1SERRANIDAE Serranus dewegeri Metzelaar, 1919 1 1 1SERRANIDAE Serranus flaviventris Gilchrist, 1904 1 1 1 1 1SERRANIDAE Serranus hepatus (Linnaeus, 1758) 1 1 1SERRANIDAE Serranus heterurus (Cadenat, 1937) 1 1SERRANIDAE Serranus knysnaensis Gilchrist, 1904 1 1 1SERRANIDAE Serranus luciopercanus Poey, 1852 1SERRANIDAE Serranus maytagi Robins & Starck, 1961 1 1SERRANIDAE Serranus notospilus Longley, 1935 1 1 1SERRANIDAE Serranus phoebe Poey, 1851 1 1 1 1 1 1 1SERRANIDAE Serranus sanctaehelenae Boulenger, 1895 1 1SERRANIDAE Serranus scriba (Linnaeus, 1758) 1 1 1 1 1 1SERRANIDAE Serranus sp.n. (Cabo Verde) 1SERRANIDAE Serranus sp.n. (Stome) 1SERRANIDAE Serranus sp.n.(cf_notospilus) 1 1SERRANIDAE Serranus subligarius (Cope, 1870) 1 1 1SERRANIDAE Serranus tabacarius (Cuvier, 1829) 1 1 1 1SERRANIDAE Serranus tigrinus (Bloch, 1790) 1 1 1SERRANIDAE Serranus tortugarum Longley, 1935 1 1SIGANIDAE Siganus sutor (Valenciennes, 1835) 1 1SPARIDAE Archosargus probatocephalus (Walbaum, 1792) 1 1 1 1SPARIDAE Archosargus rhomboidalis (Linnaeus, 1758) 1 1 1 1 1 1SPARIDAE Argyrops spinifer (Forsskål, 1775) 1 1SPARIDAE Argyrozona argyrozona (Valenciennes, 1830) 1 1 1SPARIDAE Boops boops (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1SPARIDAE Boopsoidea inornata Castelnau, 1861 1 1SPARIDAE Calamus arctifrons Goode & Bean, 1882 1 1SPARIDAE Calamus bajonado (Bloch & Schneider, 1801) 1 1 1 1 1 1SPARIDAE Calamus calamus (Valenciennes, 1830) 1 1 1 1 1 1SPARIDAE Calamus campechanus Randall & Caldwell, 1966 1SPARIDAE Calamus cervigoni Randall & Caldwell, 1966 1 1SPARIDAE Calamus leucosteus Jordan & Gilbert, 1885 1 1SPARIDAE Calamus mu Randall & Caldwell, 1966 1SPARIDAE Calamus nodosus Randall & Caldwell, 1966 1 1SPARIDAE Calamus penna (Valenciennes, 1830) 1 1 1 1 1SPARIDAE Calamus pennatula Guichenot, 1868 1 1 1 1SPARIDAE Calamus proridens Jordan & Gilbert, 1884 1 1 1SPARIDAE Cheimerius nufar (Valenciennes, 1830) 1 1SPARIDAE Chrysoblephus anglicus (Gilchrist & Thompson, 1908) 1 1SPARIDAE Chrysoblephus cristiceps (Valenciennes, 1830) 1 1SPARIDAE Chrysoblephus gibbiceps (Valenciennes, 1830) 1 1SPARIDAE Chrysoblephus laticeps (Valenciennes, 1830) 1 1SPARIDAE Chrysoblephus puniceus (Gilchrist & Thompson, 1908) 1 1SPARIDAE Cymatoceps nasutus (Castelnau, 1861) 1 1SPARIDAE Dentex angolensis Poll & Maul, 1953 1 1 1 1SPARIDAE Dentex barnardi Cadenat, 1970 1 1SPARIDAE Dentex canariensis Steindachner, 1881 1 1 1 1 1SPARIDAE Dentex congoensis Poll, 1954 1 1SPARIDAE Dentex dentex (Linnaeus, 1758) 1 1 1 1 1SPARIDAE Dentex gibbosus (Rafinesque, 1810) 1 1 1 1 1 1 1 1SPARIDAE Dentex macrophthalmus (Bloch, 1791) 1 1 1 1 1 1 1SPARIDAE Dentex maroccanus Valenciennes, 1830 1 1 1 1 1SPARIDAE Diplodus annularis (Linnaeus, 1758) 1 1 1SPARIDAE Diplodus argenteus_argenteus(Valenciennes, 1830) 1 1 1 1SPARIDAE Diplodus argenteus_caudimacula(Poey, 1860) 1 1 1SPARIDAE Diplodus bellottii (Steindachner, 1882) 1 1 1 1SPARIDAE Diplodus bermudensis Caldwell, 1965 1SPARIDAE Diplodus cervinus_cervinus (Lowe, 1838) 1 1 1 1 1 1SPARIDAE Diplodus cervinus_hottentotus (Smith, 1844) 1 1SPARIDAE Diplodus fasciatus (Valenciennes, 1830) 1SPARIDAE Diplodus holbrooki (Bean, 1878) 1 1 1SPARIDAE Diplodus prayensis (Smith, 1844) 1SPARIDAE Diplodus puntazzo Steindachner, 1882 1 1 1 1 1 1 1SPARIDAE Diplodus sargus_ascensionis Steindachner, 1903 1SPARIDAE Diplodus sargus_cadenati de la Paz, Bauchot & Daget, 1974 1 1 1 1 1SPARIDAE Diplodus sargus_capensis (Smith, 1844) 1 1 1 1SPARIDAE Diplodus sargus_helenae (Sauvage, 1879) 1SPARIDAE Diplodus sargus_lineatus (Valenciennes, 1830) 1SPARIDAE Diplodus sargus_sargus (Linnaeus, 1758) 1 1SPARIDAE Diplodus vulgaris (Geoffroy Saint-Hilaire, 1817) 1 1 1 1 1 1 1 1SPARIDAE Gymnocrotaphus curvidens Günther, 1859 1 1SPARIDAE Lagodon rhomboides (Linnaeus, 1766) 1 1 1 1SPARIDAE Lithognathus aureti Smith, 1962 1 1SPARIDAE Lithognathus lithognathus (Cuvier, 1829) 1 1 1SPARIDAE Lithognathus mormyrus (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1SPARIDAE Oblada melanura (Linnaeus, 1758) 1 1 1 1 1 1 1 1SPARIDAE Pachymetopon aeneum (Gilchrist & Thompson, 1908) 1 1SPARIDAE Pachymetopon blochii (Valenciennes, 1830) 1 1SPARIDAE Pachymetopon grande Günther, 1859 1 1SPARIDAE Pagellus acarne (Risso, 1827) 1 1 1 1 1 1 1SPARIDAE Pagellus bellottii_bellottii Steindachner, 1882 1 1 1 1 1 1SPARIDAE Pagellus bellottii_natalensis Steindachner, 1903 1 1SPARIDAE Pagellus bogaraveo (Brünnich, 1768) 1 1 1 1 1SPARIDAE Pagellus erythrinus (Linnaeus, 1758) 1 1 1 1 1 1 1

SPARIDAE Pagrus africanus Akazaki, 1962 1 1 1 1 1SPARIDAE Pagrus auriga Valenciennes, 1843 1 1 1 1 1 1 1 1SPARIDAE Pagrus caeruleostictus (Valenciennes, 1830) 1 1 1 1 1SPARIDAE Pagrus pagrus (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1 1 1 1SPARIDAE Petrus rupestris (Valenciennes, 1830) 1 1SPARIDAE Polysteganus praeorbitalis (Günther, 1859) 1 1SPARIDAE Polysteganus undulosus (Regan, 1908) 1 1SPARIDAE Porcostoma dentata (Gilchrist & Thompson, 1908) 1 1SPARIDAE Pterogymnus laniarius (Valenciennes, 1830) 1 1SPARIDAE Rhabdosargus globiceps (Valenciennes, 1830) 1 1 1 1 1SPARIDAE Rhabdosargus holubi (Steindachner, 1881) 1 1SPARIDAE Rhabdosargus sarba (Forsskål, 1775) 1 1SPARIDAE Sarpa salpa (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1SPARIDAE Sparodon durbanensis (Castelnau, 1861) 1 1SPARIDAE Sparus aurata Linnaeus, 1758 1 1 1 1 1SPARIDAE Spondyliosoma cantharus (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1SPARIDAE Spondyliosoma emarginatum (Valenciennes, 1830) 1 1 1SPARIDAE Stenotomus caprinus Jordan & Gilbert, 1882 1 1SPARIDAE Stenotomus chrysops (Linnaeus, 1766) 1SPARIDAE Virididentex acromegalus (Osório, 1911) 1SYNGNATHIDAE Acentronura dendritica (Barbour, 1905) 1 1 1 1 1 1SYNGNATHIDAE Anarchopterus criniger (Bean & Dresel, 1884) 1 1 1 1SYNGNATHIDAE Anarchopterus tectus (Dawson, 1978) 1 1 1 1 1SYNGNATHIDAE Bryx dunckeri (Metzelaar, 1919) 1 1 1 1 1 1SYNGNATHIDAE Bryx randalli (Herald, 1965) 1 1SYNGNATHIDAE Bryx sp.n. 1SYNGNATHIDAE Cosmocampus albirostris (Kaup, 1856) 1 1 1 1 1SYNGNATHIDAE Cosmocampus brachycephalus (Poey, 1868) 1 1 1SYNGNATHIDAE Cosmocampus elucens (Poey, 1868) 1 1 1 1 1 1SYNGNATHIDAE Cosmocampus hildebrandi (Herald, 1965) 1 1SYNGNATHIDAE Cosmocampus profundus (Herald, 1965) 1 1SYNGNATHIDAE Cosmocampus retropinnis Dawson, 1982 1 1SYNGNATHIDAE Enneacampus ansorgii (Boulenger, 1910) 1 1 1SYNGNATHIDAE Enneacampus kaupi (Bleeker, 1863) 1 1SYNGNATHIDAE Entelurus aequoreus (Linnaeus, 1758) 1SYNGNATHIDAE Halicampus crinitus (Jenyns, 1842) 1 1 1 1 1 1 1 1 1SYNGNATHIDAE Hippocampus aff._reidi 1 1 1SYNGNATHIDAE Hippocampus algiricus Kaup, 1856 1 1 1 1 1SYNGNATHIDAE Hippocampus capensis Boulenger, 1900 1SYNGNATHIDAE Hippocampus erectus Perry, 1810 1 1 1 1 1 1 1 1SYNGNATHIDAE Hippocampus guttulatus Cuvier, 1829 1 1SYNGNATHIDAE Hippocampus hippocampus (Linnaeus, 1758) 1 1 1 1 1 1 1 1SYNGNATHIDAE Hippocampus reidi Ginsburg, 1933 1 1 1 1SYNGNATHIDAE Hippocampus zosterae Jordan & Gilbert, 1882 1 1 1 1SYNGNATHIDAE Micrognathus andersonii (Bleeker, 1858) 1 1SYNGNATHIDAE Micrognathus erugatus Herald & Dawson, 1974 1 1SYNGNATHIDAE Minyichthys inusitatus Dawson, 1983 1 1SYNGNATHIDAE Minyichthys sentus Dawson, 1982 1 1SYNGNATHIDAE Minyichthys sp.n. 1SYNGNATHIDAE Nannocampus elegans Smith, 1961 1 1SYNGNATHIDAE Nerophis lumbriciformis (Jenyns, 1835) 1SYNGNATHIDAE Nerophis maculatus Rafinesque, 1810 1 1 1SYNGNATHIDAE Nerophis ophidion (Linnaeus, 1758) 1 1 1 1 1SYNGNATHIDAE Penetopteryx nanus (Rosén, 1911) 1 1SYNGNATHIDAE Syngnathoides biaculeatus (Bloch, 1785) 1 1SYNGNATHIDAE Syngnathus abaster Risso, 1827 1 1SYNGNATHIDAE Syngnathus acus Linnaeus, 1758 1 1 1 1 1 1 1 1 1 1SYNGNATHIDAE Syngnathus floridae (Jordan & Gilbert, 1882) 1 1 1 1SYNGNATHIDAE Syngnathus folletti Herald, 1942 1 1 1SYNGNATHIDAE Syngnathus fuscus Storer, 1839 1 1 1SYNGNATHIDAE Syngnathus louisianae Günther, 1870 1 1 1SYNGNATHIDAE Syngnathus phlegon Risso, 1827 1 1SYNGNATHIDAE Syngnathus scovelli (Evermann & Kendall, 1896) 1 1 1 1SYNGNATHIDAE Syngnathus springeri Herald, 1942 1 1 1SYNGNATHIDAE Syngnathus taenionotus Canestrini, 1871 1SYNGNATHIDAE Syngnathus tenuirostris Rathke, 1837 1SYNGNATHIDAE Syngnathus typhle Linnaeus, 1758 1 1 1 1 1 1SYNGNATHIDAE Syngnathus watermeyeri Smith, 1963 1SYNODONTIDAE Saurida brasiliensis Norman, 1935 1 1 1 1 1 1 1 1SYNODONTIDAE Saurida caribbaea Breder, 1927 1 1 1 1 1 1SYNODONTIDAE Saurida gracilis (Quoy & Gaimard, 1824) 1 1SYNODONTIDAE Saurida normani Longley, 1935 1 1 1SYNODONTIDAE Saurida suspicio Breder, 1927 1 1SYNODONTIDAE Saurida undosquamis (Richardson, 1848) 1 1SYNODONTIDAE Synodus foetens (Linnaeus, 1766) 1 1 1 1 1 1SYNODONTIDAE Synodus indicus (Day, 1873) 1 1SYNODONTIDAE Synodus intermedius (Spix & Agassiz, 1829) 1 1 1 1 1 1SYNODONTIDAE Synodus poeyi Jordan, 1887 1 1 1 1SYNODONTIDAE Synodus saurus (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1SYNODONTIDAE Synodus synodus (Linnaeus, 1758) 1 1 1 1 1 1 1 1 1 1 1 1 1 1SYNODONTIDAE Trachinocephalus myops (Forster, 1801) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1TETRAODONTIDAE Amblyrhynchotes honckenii (Bloch, 1785) 1 1TETRAODONTIDAE Arothron firmamentum (Temminck & Schlegel, 1850) 1 1 1TETRAODONTIDAE Arothron hispidus (Linnaeus, 1758) 1 1

TETRAODONTIDAE Arothron immaculatus (Bloch & Schneider, 1801) 1 1TETRAODONTIDAE Arothron inconditus Smith, 1958 1 1TETRAODONTIDAE Arothron nigropunctatus (Bloch & Schneider, 1801) 1 1TETRAODONTIDAE Arothron stellatus (Bloch & Schneider, 1801) 1 1TETRAODONTIDAE Canthigaster bennetti (Bleeker, 1854) 1 1TETRAODONTIDAE Canthigaster capistrata (Lowe, 1839) 1 1 1 1 1TETRAODONTIDAE Canthigaster figueiredoi Moura & Castro, 2002 1 1 1 1 1TETRAODONTIDAE Canthigaster jamestyleri Moura & Castro, 2002 1 1TETRAODONTIDAE Canthigaster rivulata (Temminck & Schlegel, 1850) 1 1TETRAODONTIDAE Canthigaster rostrata (Bloch, 1786) 1 1 1 1TETRAODONTIDAE Canthigaster sanctaehelenae (Günther, 1870) 1 1TETRAODONTIDAE Canthigaster solandri (Richardson, 1845) 1 1TETRAODONTIDAE Canthigaster supramacula Moura & Castro, 2002 1 1TETRAODONTIDAE Chelonodon patoca (Hamilton, 1822) 1 1TETRAODONTIDAE Ephippion guttifer (Bennett, 1831) 1 1 1 1 1TETRAODONTIDAE Sphoeroides dorsalis Longley, 1934 1 1 1 1 1TETRAODONTIDAE Sphoeroides maculatus (Bloch & Schneider, 1801) 1 1TETRAODONTIDAE Sphoeroides marmoratus (Lowe, 1838) 1 1 1 1 1 1 1TETRAODONTIDAE Sphoeroides nephelus (Goode & Bean, 1882) 1 1 1 1TETRAODONTIDAE Sphoeroides pachygaster (Müller & Troschel, 1848) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1TETRAODONTIDAE Sphoeroides spengleri (Bloch, 1785) 1 1 1 1 1 1 1 1TETRAODONTIDAE Sphoeroides testudineus (Linnaeus, 1758) 1 1 1 1 1TETRAODONTIDAE Torquigener balteatus Hardy, 1989 1 1TRIPTERYGIIDAE Acanthanectes hystrix Holleman & Buxton, 1993 1TRIPTERYGIIDAE Acanthanectes rufus Holleman & Buxton, 1993 1TRIPTERYGIIDAE Cremnochorites capensis (Gilchrist & Thompson, 1908) 1TRIPTERYGIIDAE Enneanectes altivelis Rosenblatt, 1960 1 1 1 1 1 1 1 1TRIPTERYGIIDAE Enneanectes atrorus Rosenblatt, 1960 1 1TRIPTERYGIIDAE Enneanectes boehlkei Rosenblatt, 1960 1 1TRIPTERYGIIDAE Enneanectes jordani (Evermann & Marsh, 1899) 1 1TRIPTERYGIIDAE Enneanectes n.sp.1 1TRIPTERYGIIDAE Enneanectes n.sp.2 1TRIPTERYGIIDAE Enneanectes n.sp.3 1TRIPTERYGIIDAE Enneanectes pectoralis (Fowler, 1941) 1 1 1TRIPTERYGIIDAE Enneanectes smithi Lubbock & Edwards, 1981 1TRIPTERYGIIDAE Helcogramma obtusirostre (Klunzinger, 1871) 1 1 1TRIPTERYGIIDAE Helcogrammoides cunninghami (Smitt, 1898) 1TRIPTERYGIIDAE Tripterygion delaisi delaisi Cadenat & Blache, 1970 1 1 1 1TRIPTERYGIIDAE Tripterygion delaisi xanthosoma Zander & Heymer, 1970 1 1 1TRIPTERYGIIDAE Tripterygion melanurus Guichenot, 1850 1 1TRIPTERYGIIDAE Tripterygion tripteronotus (Risso, 1810) 1 1 1URANOSCOPIDAE Astroscopus guttatus Abbott, 1860 1URANOSCOPIDAE Astroscopus sexspinosus (Steindachner, 1876) 1 1URANOSCOPIDAE Astroscopus ygraecum (Cuvier, 1829) 1 1 1 1 1URANOSCOPIDAE Uranoscopus albesca Günther, 1861 1 1URANOSCOPIDAE Uranoscopus cadenati Smith, 1966 1 1URANOSCOPIDAE Uranoscopus polli (Latreille, 1804) 1 1URANOSCOPIDAE Uranoscopus scaber Linnaeus, 1758 1 1 1 1 1

452 280 810 757 396 382 83 101 117 52 85 82 76 95 133 182 213 172 207 221 282 250 88 296 260

Table S2 APPENDIX – Sister-species table and references (Floeter et al.) Legends: WA = (North + South) West Atlantic; NWA = Northwestern Atlantic; SWA = Southwestern Atlantic; EA = Eastern Atlantic; TEA = Tropical Eastern Atlantic; MAR = mid-Atlantic Ridge; ASC = Ascension; SHE = St. Helena; CV = Cape Verde Is.; MAC = Macaronesia; IO = Indian Ocean; IWP = Indo-West Pacific.

Family Genus Species Reference Type Figure (ms)

ANTENNARIIDAE Antennarius multiocellatus (WA)/pardalis (EA) Pietsch & Grobecker (1987)

WA-EA

Antennarius ocellatus (NWA)/senegalensis (EA) Pietsch & Grobecker (1987)

WA-EA

APOGONIDAE Apogon maculatus (NWA)/americanus (SWA)

Look alike NWA-SWA

AULOSTOMIDAE Aulostomus strigosus (SWA-EA)/chinensis (IP) Bowen et al. (2001) IWP-EA 12

BLENNIIDAE Hypleurochilus pseudoaequipinnis (WA)/ aequipinnis (EA)

Look alike WA-EA

Ophioblennius atlanticus (EA)/ sp1 (ASC), sp2 (CV)/macclurei (NWA)

Muss et al. (2001) EA-MAR 12

CARANGIDAE Hemicaranx amblyrhynchus (WA)/bicolor (EA) Smith-Vaniz, pers obs.

WA-EA

Trachinotus marginatus (WA)/goreensis (EA) Smith-Vaniz, pers obs.

WA-EA

CARAPIDAE Carapus bermudensis (WA)/acus (EA) Look alike WA-EA

CHAETODONTIDAE Prognathodes aculeatus (NWA)/brasiliensis (SWA)

Hubbs (1963) NWA-SWA

Prognathodes aya (WA)/marcellae (EA) Hubbs (1963) WA-EA

Prognathodes dichrous (MAR)/obliquus (St Paul's Rocks)

Look alike WA-MAR

CIRRHITIDAE Amblycirrhitus pinos (WA)/earnshawi (ASC) Look alike WA-MAR

Cirrhitus atlanticus (EA)/pinnulatus (IWP) Look alike IWP-EA

DACTYLOSCOPIDAE Platygillellus rubrocinctus (NWA)/brasiliensis (SWA)

Feitoza (2002) NWA-SWA

DIODONTIDAE Chilomycterus spinosus (WA)/mauretanicus (EA) Leis (2006) WA-EA

DREPANIDAE Drepane africana (EA)/ longimana (IWP) Heemstra & Heemstra (2004)

IWP-EA

GOBIESOCIDAE Tomicodon fasciatus (NWA)/australis (SWA) Briggs, pers com NWA-SWA

GOBIIDAE Elacatinus figaro (SWA)/randalli (NWA) Sazima et al. (1998); Taylor & Hellberg (2005)

NWA-SWA 13

GRAMMATIDAE Gramma loreto (NWA)/brasiliensis (SWA) Sazima et al. (1998) NWA-SWA

LABRIDAE Bodianus pulchellus/rufus (WA)/insularis (MAR)

Gomon & Lubbock (1980)

WA-MAR

Clepticus parrae (NWA)/brasiliensis (SWA)/africanus (TEA)

Heiser et al. (2000) WA-EA 12

Coris julis (MED+NEA+MAC)/atlantica (TEA)

Aurelle et al. (2003) other

Halichoeres cyanocephalus (NWA)/dimidiatus (SWA)

Rocha (2004) NWA-SWA

Halichoeres maculipinna (NWA)/penrosei (SWA)

Rocha (2004) NWA-SWA

Halichoeres radiatus (WA)/brasiliensis (SWA) Rocha et al. (2005) WA-SWA

Thalassoma ascensionis (ASC), sanctahelenae (SHE)/newtoni (EA)

Costagliola et al. (2005)

EA-MAR 12

Thalassoma bifasciatum (NWA)/noronhanum (SWA)

Costagliola et al. (2004)

NWA-SWA 12

LABRISOMIDAE Malacoctenus triangulatus (WA)/africanus (EA) Look alike WA-EA

Paraclinus fasciatus (NWA)/arcanus (SWA) Guimarães & Bacellar (2002)

NWA-SWA

Paraclinus marmoratus (NWA)/spectator (SWA)

Guimarães & Bacellar (2002)

NWA-SWA

Paraclinus nigripinnis (NWA)/rubicundus (SWA)

Guimarães & Bacellar (2002)

NWA-SWA

Starksia ocellata (NWA)/brasiliensis (SWA) Look alike NWA-SWA

LUTJANIDAE Lutjanus apodus (WA)/goreensis (EA) Look alike WA-EA

Lutjanus cyanopterus (WA)/agennes (EA) Look alike WA-EA

Lutjanus mahogony (WA)/fulgens (EA) Look alike WA-EA

MULLIDAE Mullus auratus (NWA)/argentinae (SWA)/ barbatus (NEA)/surmuletus (EA)

Look alike WA-EA

Pseudupeneus maculatus (WA)/prayensis (EA) Look alike WA-EA

OPHICHTHIDAE Myrichthys ocellatus (WA)/pardalis (EA) Look alike WA-EA

OPHIDIIDAE Ophidion holbrookii (WA)/barbatum (EA) Look alike WA-EA

OPISTOGNATHIDAE Opistognathus aurifrons (NWA)/spn (SWA-southern NWA)

Smith-Vaniz, pers obs.

NWA-SWA

Opistognathus macrognathus (NWA)/brasiliensis (SWA)

Smith-Vaniz, pers obs.

NWA-SWA

OSTRACIIDAE Acanthostracion polygonius-quadricornis (WA)/ guineensis-notacanthus (EA)

Klassen (1995) WA-EA 12

POMACANTHIDAE Centropyge argi (NWA)/aurantonotus (NWA-SWA-EA)/resplendens (ASC)

Bowen et al. (2006) WA-MAR 12

POMACENTRIDAE Abudefduf saxatilis (WA-EA)/hoefleri (EA) Look alike WA-EA

Chromis chromis (MED)/limbata (MAC+TEA)

Domingues et al. (2005)

other 12

Microspathodon chrysurus (WA)/frontatus (EA) Look alike WA-EA

Stegastes aff variabilis (NWA)/variabilis (SWA)

Robertson, unpublished data

NWA-SWA

Stegastes rocasensis (RC-FN)/sanctipauli (SPR)


others

Stegastes fuscus (SWA)/imbricatus (EA) Robertson, unpublished data

WA-EA

Stegastes partitus (CA)/pictus (SWA-Venez)/lubbocki (AS)/sanctahelenae (SH)


WA-MAR

PTERELEOTRIDAE Ptereleotris helenae (NWA)/randalli (SWA) Gasparini et al. (2003)

NWA-SWA

SCARIDAE Nicholsina usta (WA)/collettei (EA) Robertson et al. (2006)

WA-EA 12

Scarus coelestinus (NWA)/trispinosus (SWA)/guacamaia (WA)

Choat, pers com NWA-SWA

Scarus taeniopterus (NWA)/zelindae (SWA)

Choat, pers com NWA-SWA

Sparisoma cretense (EA)/strigatum (MAR) Robertson et al. (2006)

EA-MAR 14

Sparisoma atomarium (NWA)/tuiupiranga (SWA)

Robertson et al. (2006)

NWA-SWA 14

Sparisoma griseorubra (Venez)/frondosum (SWA)/chrysopterum (NWA)


NWA-SWA 14

Sparisoma rubripinne (NWA)/axillare (SWA-Venez)/spn (EA)


NWA-SWA 12, 14

Sparisoma viride (NWA)/amplum (SWA) Robertson et al. (2006)

NWA-SWA 14

SERRANIDAE Dermatolepis inermis (WA)/striolata(IO) Craig et al. (2004) others 12, 14

Meganthias carpenteri (EA)/natalensis (SWIO) Anderson (2006) IWP-EA

Rypticus saponaceus (WA)/ sp.n. (EA) Carlin et al. (2003) WA-EA

Cephalopholis nigri (EA)/ argus (IWP) Craig & Hastings IWP-EA

(2007)

Mycteroperca acutirostris (WA)/ rubra (EA, coast)/ fusca (MAC+CV)

Heemstra (1991); Heemstra & Randall (1993)

WA-EA

SYNGNATHIDAE Hippocampus reidi (WA)/algiricus (EA) Casey et al. (2004) WA-EA 12

TETRAODONTIDAE Canthigaster rostrata (NWA)/figueiredoi (SWA)/capistrata (MAC+CV)/ supramacula (EA)

Moura & Castro (2002)

WA-EA

Sphoeroides spengleri (WA)/marmoratus (EA) Moura & Castro (2002)

WA-EA

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Atlantic reef fish biogeography and evolution

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