Bio-economical and ethical impacts of alien finfish culture in European inland waters

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Bio-economical and ethical impacts of alien finfish culture in European inland waters Giovanni M. Turchini Sena S. De Silva Received: 5 October 2006 / Accepted: 5 October 2007 / Published online: 27 October 2007 Ó Springer Science+Business Media B.V. 2007 Abstract Since 1989, and in comparison to the global trend, inland aquaculture production of European finfish has declined. To date, the yearly European freshwater aquaculture production is 371,727 tons, valued at over US$1 billion. Indigenous species accounted for less than one-third of the production, whereas alien species (a species that has been moved beyond its natural range of distribution) accounts for the remainder. However, in general, indigenous species command a higher market price. Currently, food quality and food safety are leading concerns of consumers, and European consumers are also becoming alert to environmentally detrimental practices. Therefore, to aim at economic sustainability, the sector needs to satisfy consumer expectations of environmentally friendly practices. It is believed that farming alien finfish species can threaten local biodiversity through escapes, and this represents a current environmental concern relative to aquaculture. In this context, an attempt is made in this paper to understand and quantify the impacts of alien finfish cultivation in European inland waters, and to suggest remedial measures. Keywords Alien species Á Biodiversity Á Ethical quality Á European aquaculture Á Organic aquaculture Á Sustainability Introduction In spite of a recent decrease in the rate of growth in aquaculture in most continents, it is still the fastest growing primary production sector in the world, having recorded an average annual growth rate of 11.1%, 8.8% and 6.3% per year over the 5 year-periods of 1990– 1994, 1995–1999 and 2000–2004, respectively (FAO 2006). Of all cultured aquatic G. M. Turchini (&) Á S. S. De Silva School of Life and Environmental Sciences, Deakin University, Warrnambool, VIC 3280, Australia e-mail: [email protected] S. S. De Silva Network of Aquaculture Centres in Asia-Pacific, PO Box 1040, Kasetsart Post Office, Bangkok 10903, Thailand 123 Aquacult Int (2008) 16:243–272 DOI 10.1007/s10499-007-9141-y

Transcript of Bio-economical and ethical impacts of alien finfish culture in European inland waters

Bio-economical and ethical impacts of alien finfishculture in European inland waters

Giovanni M. Turchini Æ Sena S. De Silva

Received: 5 October 2006 / Accepted: 5 October 2007 / Published online: 27 October 2007� Springer Science+Business Media B.V. 2007

Abstract Since 1989, and in comparison to the global trend, inland aquaculture

production of European finfish has declined. To date, the yearly European freshwater

aquaculture production is 371,727 tons, valued at over US$1 billion. Indigenous species

accounted for less than one-third of the production, whereas alien species (a species that has

been moved beyond its natural range of distribution) accounts for the remainder. However,

in general, indigenous species command a higher market price. Currently, food quality and

food safety are leading concerns of consumers, and European consumers are also becoming

alert to environmentally detrimental practices. Therefore, to aim at economic sustainability,

the sector needs to satisfy consumer expectations of environmentally friendly practices. It is

believed that farming alien finfish species can threaten local biodiversity through escapes,

and this represents a current environmental concern relative to aquaculture. In this context,

an attempt is made in this paper to understand and quantify the impacts of alien finfish

cultivation in European inland waters, and to suggest remedial measures.

Keywords Alien species � Biodiversity � Ethical quality � European aquaculture �Organic aquaculture � Sustainability

Introduction

In spite of a recent decrease in the rate of growth in aquaculture in most continents, it is

still the fastest growing primary production sector in the world, having recorded an average

annual growth rate of 11.1%, 8.8% and 6.3% per year over the 5 year-periods of 1990–

1994, 1995–1999 and 2000–2004, respectively (FAO 2006). Of all cultured aquatic

G. M. Turchini (&) � S. S. De SilvaSchool of Life and Environmental Sciences, Deakin University,Warrnambool, VIC 3280, Australiae-mail: [email protected]

S. S. De SilvaNetwork of Aquaculture Centres in Asia-Pacific, PO Box 1040,Kasetsart Post Office, Bangkok 10903, Thailand

123

Aquacult Int (2008) 16:243–272DOI 10.1007/s10499-007-9141-y

organisms, finfish accounts for 47.4% of a global production of 59.4 million tons, valued at

US$70.3 billion (FAO 2006).

The share of European finfish aquaculture in world aquaculture production has declined

from 11% in 1990 to 5.2% in 2004 as a result of greater expansion in other continents.

Nevertheless, in absolute terms European aquaculture is still growing and in 2004 it

reached a total production of 1,473,905 tons. This increase has been supported by the fast

growth of marine aquaculture, while on the other hand, inland finfish production in Europe

has declined. Since 1989, when the European inland finfish production (excluding the

Russian federation) recorded its highest production of 477,714 tons, valued at over

US$1.28 billion, a sharp reduction in production was recorded by 2004, when the levels

were 358,336 tons and US$1 billion, respectively (FAO 2006).

Thus, the potential growth for global aquaculture and European mariculture is prom-

ising, but the opposite holds for the European inland sector. In inland waters, competition

for freshwater resources will increase further, and the success of aquaculture will depend

largely on the sector’s ability to cope with new challenges through technology advance,

market development and active involvement in integrating a sustainable resource man-

agement (Varadi 2001).

In spite of the growth in global aquaculture, the sector has recently had to face heavy

criticism of the negative environmental influences resulting from some of its practices, in

particular its increasing dependence on wild fish for feed production (Naylor et al. 2000;

Tacon 2004), discharge of nutrients, chemicals, antibiotics and other therapeutants to the

environment (Black 2001; Pillay 2004), and influences on biodiversity (IUCN 2000;

Kapuscinski and Brister 2001; Nguyen and De Silva 2007). In general, alien species are

considered to pose a major threat to biodiversity in respect of all habitats (IUCN 2000), and

inland aquatic habitats can be considered even more susceptible to such threats

(Leppakoski et al. 2002). The increasing dependence of aquaculture on alien species

(De Silva et al. 2006; Nguyen and De Silva 2007) poses a major hazard to biodiversity and

hence its sustainability.

It is evident that the history of introduction of non-indigenous (alien) species into

European water dates back to pre-historic times (Leppakoski et al. 2002). The ancient

history of European inland aquaculture is directly linked to the introduction of common

carp (Cyprinus carpio L.) culture in monastic houses in the Middle Ages, and subsequently

of brown trout (Salmo trutta L.) in France in the fourteenth century (Pillay and Kutty

2005). Even now, European inland aquaculture is still dominated by common carp, which

have been spread from the original native countries into the entire continent, and by trout

culture. However, the leading trout species cultured at present is the rainbow trout

(Oncorhynchus mykiss W.), a species native to North America and introduced into Europe

in the nineteenth century to establish populations both for recreational angling and for

aquacultural purposes (Fausch et al. 2001).

European inland aquaculture is nowadays dominated by alien species (Anonymous

1995) and, in relation to its historical developments, it can be considered as an advanced

sub-model of global aquaculture sector. However, high production levels achieved at the

expense of social and environmental damage/perturbations are no longer acceptable to the

community or by the markets.

Food quality and food safety are leading concerns for the consumers (Johnsen 1991;

Moretti et al. 2003) and European consumers are also becoming concerned about and alert

to environmentally detrimental practices (Jaffry et al. 2004; Rohr et al. 2005; Vermeir and

Verbeke 2006), such as the impacts on biodiversity of alien species (Naylor et al. 2001).

The future success of the European inland aquaculture sector will, as for global

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aquaculture, be increasingly market driven (Josupeit et al. 2001) and principally dependent

on its ability to conform to increasing consumer expectation for environmentally friendly

and sustainable culture practices (Pettinger et al. 2004; Focardi et al. 2005; Vermeir and

Verbeke 2006). Thus, in assessing the success of finfish cultivation, a more holistic

approach is needed, not only in respect of the bio-economical aspects but also of the ethical

aspects aimed at delivering a final product to meet consumer and public expectations and

aspirations. In this rather complex context, an attempt is made in this paper to understand

and quantify the impacts of alien finfish cultivation in European inland waters, and to

suggest remedial measures.

Database, classification and analysis

The present study has been based on the database of the FAO, Fishery Department, Fishery

Information, Data and Statistics Unit. FISHSTAT PLUS: Universal software for fishery

statistical time series, Version 2.3. Databases: Aquaculture production: quantities 1950–

2004; Aquaculture production: values 1984–2004 (FAO 2006). The values reported are

expressed in US$ as the nominal value, therefore not inflation adjusted. In the present

treatise, only finfish species cultured in freshwater have been included. A detailed list of

the selected countries is reported in the Appendix.

The natural distribution of the species in question was determined with reference to the

sites http://www.fishbase.org (Froese and Pauly 2006) and also checked against the Catalog

of Fishes of the California Academy of Sciences, commonly referred to as the Eschmeyer

Catalog, and the database of invasive species (http://www.issg.org/database/welcome/)

from the Invasive Species Specialist Group (ISSG) which is part of the Species Survival

Commission (SSC) of the World Conservation Union (IUCN).

The origin of the common carp is a widely debated issue. Its origin was considered by

Balon (1995) who concluded that the wild ancestor of the common carp originated in the

Black, Caspian and Aral Seas drainages and dispersed east into Siberia and China and west

as far as the Danube River.

For some species entries in the FAO databases, the full scientific names are not provided

and are reported as ‘‘nei’’ (not elsewhere identified). In such cases, entries were considered

indigenous if there was a reasonable probability that they were European native species

(i.e., freshwater breams nei, mullets nei, roachs nei, chubs nei). On the other hand, if the

named group can aggregate well known species which can be alien or indigenous (i.e.,

cyprinids nei, catfishes nei, chars nei, salmonids nei, sturgeons nei, trouts nei, whitefishes

nei) then these were considered as ‘‘not specified’’, treated separately and not included in

the indigenous/alien computations. The total values (quantity and value) reported for these

not specified species were relatively small and therefore only a slight underestimation of

alien species is expected.

The European inland freshwater finfish culture

European inland freshwater aquaculture is a diverse and complex industry, showing a great

diversity in terms of technologies, resources, size and intensity of operations. In addition to

geographical diversity, there are also significant socio-economic differences between the

western and eastern parts of Europe (Varadi 2001). Amongst the most common culture

systems employed in Europe there are extensive and semi-intensive common carp, other

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cyprinids and catfish farming in ponds, land-based intensive flow-through farming systems

mainly of trout or other salmonids, and recirculating farming systems for eels or other high

valued species (Anonymous 1995).

The yearly European freshwater aquaculture production in the 5-year period from 2000

to 2004 was 371,727 tons, valued at over US$1 billion. Indigenous species accounted for

120,780 tons, alien species for 245,879 tons and ‘‘not specified’’ species for 5.698 tons

(Table 1).

Total value of cultured alien species was almost double that of indigenous species,

although the average value per unit (expressed as US$ kg–1) was higher for the latter. The

‘‘not specified’’ species recorded the highest value per unit which was mainly due to the

entry production of ‘‘Sturgeon nei’’ in different countries.

In the analysis of the origin of farmed species in Europe, it is important to underline that

the same species were considered either indigenous or alien in relation to the country of

production. For example, Atlantic salmon (Salmo salar) recorded in Greece was consid-

ered to be alien, while common carp was considered as indigenous to, for example,

Germany and other eastern European countries, but alien to France and other western

European countries.

Within the indigenous species farmed in Europe (Table 2), common carp accounted for

the highest production with more than 93,900 tons valued over US$225 million. The

second species in order of production was the European eel (Anguilla anguilla) with only

8,684 tons, followed by brown trout (Salmo trutta) with 2,489 tons. However, the unitary

value of brown trout and European eel compared to common carp were double and triple,

respectively. Other indigenous species farmed in Europe with an yearly production above

1,000 tons were two other cyprinids species: roach (Rutilus rutilus) and tench (Tincatinca).

The group of alien farmed fish in the inland European aquaculture was dominated by

rainbow trout (Oncorhynchus mykiss) which is the most cultured finfish in Europe,

accounting for a total production of more than 210,186 tons (Table 3). Nearly 1.5% of the

total European freshwater culture production in the last 5 years was reported for species

the origin of which it was impossible to ascertain. The two most important groups from a

production viewpoint were Cyprinids nei accounting for 2,834 tons and Sturgeons nei for

1,382 tons (Table 4).

Sturgeons nei showed the highest total value with more than US$9 million and a rel-

atively higher unitary value in term of US$ kg–1. This production ([1,100 tons) of highly

valued sturgeons nei occurred mainly in Italy. It is possible to speculate that the majority of

this production is the North American species Acipenser transmontanus and hybrids of

indigenous and alien species (Williot et al. 2001).

Table 1 The yearly European aquaculture production and value of freshwater finfish (average of 2000–2004), subdivided by species origin

Production (·1,000 tons) Value (millions US$) Value per unit (US$ kg–1)

Indigenous species 120.8 341.0 2.82

Alien species 245.6 640.6 2.61

Not specified 5.7 21.8 3.83

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Overall status of alien species in European inland aquaculture

The European freshwater aquaculture production increased steadily from a little more than

32,000 tons/year in the early 1950s to more than 418,000 tons/year during the first 5 years

of the 1990s (Fig. 1). It is important to underline that, in the database used, a sharp increase

of production in 1988 has been recorded when former USSR countries were included. The

alien species accounted for less than 20% of the total production in the 1950s and their

contribution increased to more than 65% in recent years.

Table 2 The yearly European aquaculture production and value of indigenous freshwater finfish (averageof 2000–2004)

Common name Scientific name Production(tons)

Value(thousands US$)

Value per unit(US$ kg–1)

Common carpa Cyprinus carpio 93,900.8 225,485.6 2.40

Freshwater fishes neib Osteichthyes 9,172.0 18,979.5 2.07

European eel Anguilla anguilla 8,684.4 66,961.2 7.71

Brown trout Salmo trutta 2,489.6 11,434.0 4.59

Roach Rutilus rutilus 2,250.8 5,300.0 2.35

Tench Tinca tinca 1,395.2 3,579.6 2.57

Crucian carp Carassius carassius 988.6 2,566.1 2.60

Arctic char Salvelinus alpinus 404.2 2,084.8 5.16

Northern pike Esox lucius 373.8 1,358.8 3.64

Wels catfish Silurus glanis 283.4 1,137.1 4.01

Pike-percha Stizostedion lucioperca 184.2 534.5 2.90

Freshwater bream Abramis brama 148.6 278.1 1.87

Rudd Scardinius erythrophthalmus 123.0 264.8 2.15

Huchen Hucho hucho 90.2 202.9 2.25

European perch Perca fluviatilis 89.8 311.4 3.47

Flathead grey mullet Mugil cephalus 39.2 149.0 3.80

Bleak Alburnus alburnus 38.8 73.8 1.90

Roaches nei Rutilus spp. 32.8 26.2 0.80

Atlantic salmon Salmo salar 30.4 130.6 4.29

Mullets nei Mugilidae 15.2 45.2 2.97

Freshwater gobies nei Gobiidae 12.8 27.2 2.13

Whitefishes nei Coregonus spp 11.4 29.1 2.55

Danube sturgeon Acipenser gueldenstaedtii 8.6 34.0 3.95

Chubs nei Leuciscus spp. 3.4 13.6 4.00

Freshwater breams nei Abramis spp. 2.8 7.6 2.70

Grayling Thymallus thymallus 2.2 6.4 2.90

Peled Coregonus peled 1.6 5.0 3.11

Sturgeon Acipenser sturio 1.2 10.6 8.85

Sterlet sturgeon Acipenser ruthenus 0.6 2.9 4.80

Orfe Leuciscus idus 0.2 0.3 1.50

a Production in European countries where considered indigenousb nei: not elsewhere identified

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Since the early 1990s, the European freshwater aquaculture production showed a

negative trend, in particular in respect of the value (Fig. 2), when it declined from more

than US$1,200 million/year in 1988 to US$1,000 million/year in 2004. Alien species

contributed approximately 65% to the total value of European freshwater aquaculture.

Table 3 The yearly European aquaculture production and value of alien freshwater finfish (average of2000–2004)

Common name Scientific name Production(tons)

Value(thousandsUS$)

Valueper unit(US$ kg–1)

Rainbow trout Oncorhynchus mykiss 210,186.8 572,781.0 2.73

Silver carp Hypophthalmichthys molitrix 13,862.2 25,400.3 1.83

Common carpa Cyprinus carpio 6,068.2 8,868.1 1.46

Bighead carp Hypophthalmichthys nobilis 5,508.8 10,612.4 1.93

North African catfish Clarias gariepinus 3,879.8 6,340.5 1.63

Goldfish Carassius auratus 1,998.2 3,031.7 1.52

Grass carp Ctenopharyngodon idellus 1,612.8 3,453.0 2.14

Brook trout Salvelinus fontinalis 727.8 3,042.9 4.18

Black bullhead Ameiurus melas 473.4 1,770.7 3.74

Wels catfish Silurus glanis 373 1,115.6 2.99

Tilapias neib Oreochromis spp. 264 1,059.9 4.01

Torpedo-shaped catfishes nei Clarias spp. 212 649.1 3.06

Siberian sturgeona Acipenser baerii 118.6 732.0 6.17

Pike-percha Stizostedion lucioperca 92 683.0 7.42

Striped bass, hybrid Morone chrysops · M. saxatilis 86.8 444.6 5.12

Nile tilapia Oreochromis niloticus 71 194.0 2.73

European whitefisha Coregonus lavaretus 65.2 258.5 3.96

Atlantic salmona Salmo salar 16.8 140.1 8.34

Largemouth black bass Micropterus salmoides 3.6 25.4 7.06

Buffalofishes nei Ictiobus spp. 0.4 1.0 2.50

a Production in European countries where considered alienb nei: not elsewhere identified

Table 4 The yearly European aquaculture production and value of not specified freshwater finfish groups(average of 2000–2004)

Common name Scientific name Production(tons)

Value(thousands US$)

Value per unit(US$ kg–1)

Cyprinids neia Cyprinidae 2,834.2 5,672.7 2.0

Sturgeons nei Acipenseridae 1,382.2 9,392.7 6.8

Trouts nei Salmo spp. 637.2 2,758.6 4.3

Chars nei Salvelinus spp. 470.4 2,175.5 4.6

Salmonoids nei Salmonoidei 372.6 1,830.7 4.9

Catfishes nei Ictalurus spp. 1.6 2.4 1.5

Freshwater siluroids nei Siluroidei 0.2 3.3 16.7

a nei: not elsewhere identified

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Alien species percent contribution to total inland aquaculture value in Germany and

Central Europe (62.7 and 34.2%, respectively) was higher then the relative contribution to

production (55.7 and 24.1%, respectively) (Table 5). It is therefore evident that the culture

of alien species has a positive effect on the sector value in these areas. On the other hand,

in all other instances the opposite was evident, showing that the culture of indigenous

species has a positive impact on the value of aquaculture production.

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250 Aquacult Int (2008) 16:243–272

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Moreover, it is interesting to point out that the contribution of alien species to the total

inland finfish production is extremely high (\88%) in the western regions (France, Italy,

Iberian peninsula, Denmark, and the British Isles) independent of latitude, while on the

other hand, in the eastern region the percentage contribution of alien species is consistently

lower (\47%). In Germany and Northern Europe, which can be considered as the longi-

tudinal center of Europe, the contribution of alien species is 55–63%. This geographical

western to eastern trend can be clearly related to the different roles that rainbow trout and

cyprinids have in the relative markets. Generally, in the western regions the production is

dominated by the alien rainbow trout while native cyprinids are more important in the

eastern regions (Varadi 2001).

Alien species of intra-continental origin

In European inland aquaculture, there are a number of finfish species that have been

translocated within the continent across nations and watersheds. In year 2004, a total

production of 6,898 tons of farmed European finfish species were outside their natural

range of distribution, which is mainly ascribable to common carp (5,063 tons), while in its

natural range of distribution its production in 2004 was 94,282 tons. There is conflicting

evidence with regard to the ancestry of common carp, and in the present analysis the

suggestion of Balon (1995), who reported that common carp dispersed towards European

countries as far as the Danube River, was adopted. Accordingly, common carp is alien to

Belgium, France, Greece, Italy, Sweden, Switzerland and the United Kingdom. Another

species, the wels catfish (Silurus glanis) originally from Eastern Europe and Asia, has been

translocated within Europe and is currently farmed in Croatia and France.

The situation with the European whitefish (Coregonus lavaretus) is controversial,

especially in respect of its still debated taxonomic status, consequently making it com-

plicated to determine its native range of distribution. It is farmed on a small scale in the

Czech Republic and in Finland, where its native status has been questioned, and can be

considered to be alien (Welcomme 1988). Other intra-continent translocations of farmed

fish are pike-perch (Stizostedion lucioperca) farmed in Croatia, Denmark, France and

Slovenia, the Atlantic salmon (Salmo salar) in Greece, and the Siberian sturgeon

(Acipenser baerii) in France. The FAO database reports an increasing production of

sturgeon nei which is dealt with in detail by Williot et al. (2001).

Alien species of American origin

Alien rainbow trout (Oncorhynchus mykiss), originating from the Pacific coast of North

America, is the most cultured species in European freshwater . In the period 2000–2004,

the yearly average total production of rainbow trout in European inland waters was

210,187 tons, accounting for US$572.8 million (Fig. 3a, b). It is also cultured in brackish

and marine water and a sharp increase in production has been observed in Europe (Fig. 3c).

European trout production can be divided into two sub-sectors which differ not only in the

environment but also in the final product size: namely ‘portion-size’ and ‘large’ trout

exceeding 1 kg, produced in fresh water and in marine conditions, respectively (Varadi

et al. 2001). The unit value of trout cultured in fresh, brackish and marine waters was

US$2.73, US$3.15 and US$2.48, respectively.

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Fig. 3 Mean yearly production (a) and the average unit value (b) of rainbow trout cultured in freshwater inEurope. Mean yearly production of rainbow trout in different environments in Europe (c). Data representaverage of 5-year periods from 1985 to 2004

252 Aquacult Int (2008) 16:243–272

123

In Europe, inland trout production is typically carried out in intensive and environ-

ment-controlled systems, mostly flow-through raceways (Anonymous 1995). Trout

culture is likely to be constrained in the future by the rising price of water and by costs

associated with effluent treatment (Varadi 2001; Wedekind et al. 2001). Industry esti-

mates advocate that this sector’s expansion will be possible mainly in Spain or in some

eastern European countries, through increased capital investment and adoption of more

up-to-date technology. However, the potential growth of the trout culture sector will be

counterbalanced by a drastic decline in countries such as Denmark and Germany, where

environmental controls are becoming increasingly restrictive (Anonymous 1995; Varadi

2001; Wedekind et al. 2001), and the gradual decline in market price (Josupeit et al.

2001).

Other salmonids native to the Pacific coast of North America (Oncorhynchus spp.) are

also farmed in European waters, mainly in Spain and France. Recent increases in brook

trout (Salvelinus fontinalis) production has been reported from Belgium, Bosnia and

Herzegovina, Bulgaria, Czech Republic, Denmark, France, Romania, Slovakia, Slovenia

and the United Kingdom.

In European inland aquaculture, there are other American native finfish species sup-

porting a relatively good production (1,292 tons/year in the 5-year period 2000–2004). The

Italian production (1,118 tons in 2004) of the not specified sturgeons which is mainly

ascribable to the North American species Acipenser transmontanus (Williot et al. 2001)

could be added. Other Central or North American finfish species which are currently farmed

in European inland waters are the black bullhead (Ameiurus melas), the buffalofishes nei

(Ictiobus spp.), the channel catfish (Ictalurus punctatus), the largemouth black bass

(Micropterus salmoides) and the hybrid striped bass (Morone chrysops · M. saxatilis).

Alien species of Asian origin

Alien species of Asian origin form the second largest group of non indigenous fish farmed

in European waters accounting for more than 5% of the European freshwater production.

Five Asian cyprinid species are commonly farmed in central and eastern European

countries: the grass carp (Ctenopharyngodon idellus), the bighead carp (Hypophthal-michthys nobilis), the black carp (Mylopharyngodon piceus), the goldfish (Carassiusauratus) and the silver carp (Hypophthalmichthys molitrix).

Alien species of African origin

Until 1983, African finfish species were not farmed in Europe. In 1984, an initial pro-

duction of 20 tons of the North African catfish (Clarias gariepinus) was recorded in the

Netherlands. Thereafter, an increase in the production of African finfish was recorded at a

rate of more than 65% per year. Apart from the North African catfish, other African species

such as the Mozambique tilapia (Oreochromis mossambicus), the Nile tilapia (O. niloticus)

and other unspecified tilapias are now farmed in Belgium, Greece, Hungary, Italy,

Netherlands, Slovakia, Spain, Switzerland and the United Kingdom. In 2004, the total

production of African finfish in the European waters was 5,859 tons/year with a total value

of over US$8 million.

Aquacult Int (2008) 16:243–272 253

123

Country perspectives

In the previous sections, a synthesis of the role of indigenous versus alien species in

European aquaculture was attempted. It is also important to consider the extent to which

alien species are utilized in inland aquaculture of individual European nations, particularly

in view of the fact that decisions pertaining to agricultural–primary production sectors are

common to most nations of the European Union, and therefore may impact future

developments and trends of the sector. However, in the following section no attempt is

made to evaluate the farming systems per se.

France

France is the biggest European freshwater aquaculture producer accounting for more than

14.2% of that of Europe. The bulk of French production is represented by two alien

species, rainbow trout (41,346 tons/year) and common carp (5,042 tons/year) (Table 6).

The production of two alien species, wels catfish and Siberian sturgeon, have increased

sharply, probably backed by the high market value (US$3.13 kg–1 and US$6.17 kg–1,

respectively). The culture of alien species in France accounts for 88.3% of the national

production but only for 81.7% of the total value (Table 5). Three indigenous species are

farmed in French freshwaters: roach, brown trout and tench. While roach and tench pro-

duction fluctuates, brown trout production has recently increased steadily. The market

price of brown trout is considerably higher than its alien counterparts (US$4.49 kg–1 and

US$2.03 kg–1, respectively).

Germany

Germany is the second largest producer of farmed freshwater finfish in Europe amounting

to 43,033 tons/year or 11.5% of the European production (Table 5). As in France, German

production (Table 6) is dominated by rainbow trout (23,884 tons/year) followed by

common carp (12,928 tons/year). The main difference between the two countries is that

common carp is considered to be indigenous to Germany (Balon 1995). Therefore, alien

species culture accounts for little more than half of the entire German inland finfish

production, while in monetary terms it represents 62% of the value (Table 5).

German aquaculture, as well as the inland fishery, changed drastically after reunification

in 1990. The collapse of the infrastructure (i.e., large co-operative production and mar-

keting structure) in East Germany led to a dramatic decline in production from lake

fisheries and aquaculture (Wedekind et al. 2001).

The difficult situation which is facing the German inland aquaculture sector is exac-

erbated by different constraints. Carp farming is mainly limited by imposed production

limits and by the seasonal nature and unreliability of the market, while trout farming seems

to be mainly limited by pathological issues, lack of adequate technologies and investments,

and a number of obstacles derived from bureaucracy, which make fish production difficult

and increase costs (Wedekind et al. 2001). However, there is a growing interest in the

potential culture of two native salmonids, brown trout and arctic char, which are high

valued and can compensate for the encountered difficulties. In the last 5 years, European

eel and wels catfish production have also been recorded for this country (Table 6). In 2004,

254 Aquacult Int (2008) 16:243–272

123

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Aquacult Int (2008) 16:243–272 255

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256 Aquacult Int (2008) 16:243–272

123

a production of 37 tons of not specified sturgeons (at US$8.08 kg–1) has been recorded,

likely to be Siberian sturgeons and hybrids (Williot et al. 2001).

Italy

Italy is historically considered as one of the world leaders in rainbow trout production.

However, in recent years, a contraction of its production has been recorded, and in the

period from 2000 to 2004 the average yearly production was 38,099 tons (Table 6).

Simultaneously, a downward phase in the indigenous eel production has also been

recorded, probably because of the continuing increasing price of elvers. The black bull-

head, which is sometime erroneously considered as an indigenous Italian catfish

(considered naturalized in 1908: Froese and Pauly 2006), is a North American native

species. Its production is declining and attributed to the outbreak of a viral epizootic

disease termed ‘‘iridovirosis’’ in the early 1990s (Favero et al. 2001), which compromised

the Italian catfish farm industry. During the last 5 years, interesting new production has

been recorded: the tench (Tinca tinca) (which is usually considered to be an indigenous

species, but it seems that it has been introduced and naturalized during the 17th century:

Froese and Pauly 2006), and three alien species, the hybrid striped bass, the North African

catfish and tilapia. The not specified sturgeon production has increased to 1,100 tons/year

in 2004. As mentioned previously, the majority of this production is of alien species; in

particular the North American species and hybrids of indigenous and alien species (Williot

et al. 2001). The unitary value of sturgeons is the highest at US$7.89 kg–1, second only to

the value recorded for eels (US$11.28 kg–1).

Iberian peninsula

Rainbow trout dominates inland aquaculture of Spain and Portugal and represents almost

the entire production (Tables 5 and 6). A fluctuating production of the indigenous tench

and brown trout and a recent production of tilapia have been recorded in Spain. Here, an

increasing production (225 tons in 2004) of not specified sturgeons has also been reported.

The sturgeons farmed in the Iberian peninsula are likely to be the Siberian sturgeon and the

Adriatic sturgeon (Acipenser naccarii) (Williot et al. 2001), and the two species can be

considered as aliens to Iberian inland freshwaters.

Eel production in Portugal was a well established industry until 1994, where an inland

production of 976 tons in freshwater was recorded. In spite of its high market value, eel

production decreased dramatically due to the high price of wild juveniles and the inca-

pability of the local eel industry to cope with competing countries (Bernardino 2000). The

major inland production in Portugal is represented by rainbow trout, but as seen in many

other European countries the production is declining.

Denmark

In spite of the relatively small size of Denmark territory, it supports 8.7% of the total

European freshwater finfish production. The indigenous species farmed in the Danish

freshwater are the European eel (1,885 tons/year), brown trout (235 tons/year) and

Atlantic salmon (9.2 tons/year), while the farmed alien species are rainbow trout

Aquacult Int (2008) 16:243–272 257

123

(30,430 tons/year), brook trout (126 tons/year) and pike-perch (3.2 tons/year). Alien

species culture account for more than 93% of the entire national inland production and

83% in monetary terms (Table 5). The highest unitary value has been reported for the

indigenous European eel with more than US$8.84 kg–1, the lowest (US$2.97 kg–1) for

rainbow trout (Table 7).

British Isles

As in the majority of the western European countries, the freshwater production in the

British Isles is dominated by rainbow trout (Table 7). An oscillating but increasing pro-

duction of brown trout, with a high unitary value (US$6.57 kg–1), has been recorded.

Interestingly, in the last 5 years in the United Kingdom, novel productions of many

indigenous species have appeared, likely due to diversification activities of farmers

searching for alternative, better value species. On the other hand, in Ireland the only

species farmed is the rainbow trout.

Northern Europe

In the northern European countries (Belgium, Finland, Iceland, Netherlands and Sweden; there

is no entry for Norway, while Denmark has already been treated separately) freshwater

aquaculture is equally distributed between one native and two alien species. In the last 5 years,

rainbow trout accounted for 5,249 tons/year, European eel for 4,247 tons/year and the North

African catfish for 3,032 tons/year. Rainbow trout production is declining, while the pro-

duction of the European eel and the North African catfish are sharply increasing, reaching

more than 10-fold increments since the late 1980s to the beginning of the millennium. Sur-

prisingly, the two species receive a very different appreciation from the market: European eel

is valued at US$7.48 kg–1 while the North African catfish is only US$1.46 kg –1.

Central Europe

In central Europe, as defined in Table 5, 75.9% of the total inland finfish production is

supported by indigenous species. The bulk of the production is represented by common

carp (25,840 tons/year) followed by a small but steadily increasing production of another

native cyprinid (tench, 214 tons/year) and the wels catfish (180 tons/year). Within the

group of native cultured freshwater finfish, brown trout and arctic char command the

highest market prices of US$5.92 kg–1 and US$6.00 kg–1, respectively. As regards farmed

alien species, rainbow trout is the most dominant (4,202 tons/year) followed by silver carp,

bighead carp and grass carp. A recent increase in the production of other alien species, such

as the North African catfish, brook trout and Nile tilapia has been recorded (Table 8).

Balkan peninsula

The Balkan peninsula (Table 5) is a heterogeneous area including countries with consid-

erable geographical and geophysical differences and different river systems draining into

the Mediterranean and Black Seas.

258 Aquacult Int (2008) 16:243–272

123

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Aquacult Int (2008) 16:243–272 259

123

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Aquacult Int (2008) 16:243–272 261

123

In some countries, such as Croatia and Greece, mariculture is the principal aquaculture

industry, while in other countries the bulk of the production is mainly ascribable to inland

farming. Within this diverse group, the dominant farmed freshwater finfish is indigenous

common carp (9,595 tons/year), but its production is declining (Table 9). The second

largest production is represented by alien rainbow trout (7,258 tons/year) which recorded a

2-fold increase in the last 5 years. Simultaneously, a reduction of brown trout has been

recorded even if, compared to rainbow trout, the unitary value is considerably higher.

The farming of the indigenous European eel and wels catfish are two fast growing

inland aquaculture industries in this region and similar positive trends are shown for alien

brook trout and pike-perch. Alien cyprinids, such as the silver carp, the bighead carp, the

grass carp and the goldfish are abundant, but their production is declining. An interesting

small production of Atlantic salmon is well established in Greece. In the last 5 years, in the

Balkan region, a small production of many indigenous species has also been recorded

(Table 9).

Poland and Eastern Europe

Polish production accounts for over 9.3% of the entire European inland aquaculture pro-

duction and is almost completely based on two species: indigenous common carp

(20,480 tons/year) and alien rainbow trout (11,899 tons/year) (Table 10).

Eastern Europe is the European region where alien species are less important and

account for only 32.8% of the total production (28% in monetary terms). Rainbow trout

production is limited, while a bigger role is taken by other alien finfish, mainly cyprinids

(Table 10). The bulk of the local production is represented by indigenous common carp

(25,172 tons/year), followed by another indigenous cyprinid, the crucian carp (975 tons/

year). There are other emerging farmed indigenous species such as freshwater bream,

northern pike, pike-perch, European perch, roach, European eel, rudd and tench.

Environmental impacts of cultured alien finfish farming in Europe

Problems associated with the practice of culturing non-native (alien) fish can be varying.

These can be categorized according to the time frame of impact, immediate or on long-

term or the typology of the effect, direct and indirect. Introduction of new species across

non-native geographical areas has been a common practice worldwide and primarily done

for aquaculture purposes (Welcomme 1988; De Silva et al. 2006). The diffusion of alien

finfish from farms into natural environments is mainly due to the unavoidable event of fish

escape (Pillay 2004). A representative example of such occurrence is the recorded well

established fisheries of rainbow trout in the Loch Fad (Scotland) dependent on the escaped

trout from local cage farms (Phillips et al. 1985).

Among the immediate impacts of fish translocations is the potential spread of new

pathogens. For example, the unintentional diffusion of the cestode Bothriocephalusacheilognathi has been ascribed to the introduction of grass carp from Asia to Europe

(Ivasik et al. 1969). The bacterial disease furunculosis (caused by Aeromonas salmonicida)

has been introduced probably from Denmark into United Kingdom waters with the

translocation of brown trout, and successively from the United Kongdom to Norway with

infected salmon smolts (Pillay 2004). An example of the introduction of a parasite asso-

ciated with finfish translocation is that of the nematodes parasite (Anguillicola) which is

262 Aquacult Int (2008) 16:243–272

123

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Aquacult Int (2008) 16:243–272 263

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264 Aquacult Int (2008) 16:243–272

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Aquacult Int (2008) 16:243–272 265

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266 Aquacult Int (2008) 16:243–272

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endemic to Australian and Asian eels. The parasite is believed to have been introduced into

Europe together with imported oriental eels and has since spread rapidly through northern

Europe (Lehtonen 2002) and central Europe (Barus 1995). In addition to the direct

introduction of diseases, fish translocations can also have a catalytic effect as in the case of

viral hemorrhagic septicemia in brown trout in the British Isles after the introduction of the

North American rainbow trout, which were very susceptible to the disease (Mills 1982).

Besides disease-related problems, the introduction of alien species can impact the

indigenous flora and fauna directly through predation or competition and indirectly by

reducing the local biodiversity. The introduction of new diseases, increased pathogenicity

of local bacteria or virus strains, the competition for food, the habitat disruption, or direct

predation derived by introduction of alien fish, can obviously affect the local fauna, modify

the natural selection processes and reduce population size, or even be responsible for the

extinction of local population/species (Kapuscinski and Brister 2001; Pillay 2004; De Silva

et al. 2006; Nguyen and De Silva 2007). In a nutshell, the introduction of alien species can

dramatically affect biodiversity. The problem can be exacerbated by decreased population

size and the subsequent risk of inbreeding depression (Kapuscinski and Brister 2001).

Another direct assault on biodiversity can be borne out by the potential outbreeding

depression or even worse by hybridization and introgression (Kapuscinski and Brister

2001; Nguyen and De Silva 2007).

The impacts of aquaculture on biodiversity and particularly the utilization of alien

species for culture purposes are of current and increasing concern (Beardmore et al. 1997),

and the consequences of decreasing or changing biodiversity are well known to be

potentially devastating (Chapin et al. 2000). More than a decade ago, 134 non-native fish

species had already been reported to have been introduced into European freshwaters

(Holcik 1991), of which 76 were non-European. More than 50 finfish species were reported

to be successfully introduced to at least one European country (Lehtonen 2002). It has been

speculated that the presence of alien fish can be a reliable indicator of river health

(Kennard et al. 2005), and therefore the wellbeing of European inland waters can be

considered to be at high risk (Leppakoski et al. 2002).

Economic impacts of alien species

Variable results have been accomplished by species introductions, depending on the

species and geographic area. Only a few finfish species are generally recognized as ben-

eficial from a socio-economic viewpoint, usually by improving fishing or aquaculture

opportunities (Lehtonen 2002; De Silva et al. 2006). In natural waters, the introductions

have resulted in many cases in economically profitable fisheries, although most intro-

ductions have failed or led to unwanted consequences in the form of reduced or collapsed

native fish stocks (Lehtonen 2002).

It is evident, from the data discussed earlier, that European aquaculture has, in the past,

gained large benefits from the cultivation of rainbow trout, common carp and other Asian

carps. In the eastern European countries, inland aquaculture is historically dominated by

carp culture, while alien finfish cultivation (mainly rainbow trout) is responsible for a

limited (\50%) contribution. In western European countries, inland aquaculture is totally

dominated (*90%) by alien finfish (almost entirely rainbow trout). In both areas, either

carp or rainbow trout farming are today directly involved in the dramatic collapse of the

European inland aquaculture now showing the lowest market prices. On the other hand,

many European native species are in recent years supporting small but fast growing

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industries. In particular, European eel, brown trout, arctic char, tench, wels catfish,

northern pike, European perch and native sturgeons seem to be able to gain market

recognition and a higher value. As such, these species represent an alternative to the

almost unprofitable rainbow trout and carp farming. At the same time, in recent years, in

the complex panorama of European inland aquaculture, the appearance of new exotic

species for culture purposes should be considered with concern. Wels catfish is increas-

ingly farmed outside its native range even if the market price is considerably lower

(US$2.99 kg–1) relative to that in the native countries (US$4.01 kg–1). Alien species from

Africa such as the North African catfish and tilapias are now increasingly farmed, com-

monly in indoor facilities, in different European countries. The utilization of alien

sturgeons from intra- and inter-continent origins is another worrying concern. An appro-

priate cost–benefit analysis from economic, social and environmental points of view should

be undertaken sooner rather than later.

Towards sustainable development of European inland aquaculture

The European Union strategies for sustainable development of the aquaculture industry

aspire at creating long-term economic viability and secure employment (Focardi et al.

2005). To achieve these goals, the assurance of product quality (Moretti et al. 2003; Valfre

et al. 2003; Myhr and Dalm 2005; Rohr et al. 2005), promotion of high animal health and

welfare standards (Huntingford et al. 2006) and ensuring an environmentally sound

industry (Jaffry et al. 2004; Pillay 2004) are essential.

In this complex and multifactorial context the role of alien finfish farming need to be

carefully considered. At present, it is almost impossible to predict how a non-indigenous

species will behave in a new environment. Therefore, treating all introduced species as

‘‘guilty until proven innocent’’ appears to be the only environmentally acceptable approach

(Leppakoski et al. 2002). The eradication of established alien finfish is a considerably

difficult exercise, possibly successful only in restricted areas (Britton and Brazier 2006),

and almost impossible, so far, in open waters (Leppakoski et al. 2002). Avoiding new

occurrences is today imperative for sustainable development of aquaculture (Black 2001).

Organic aquaculture

In recent years, growing interest has been given, particularly from European rainbow trout

farmers, to the development of certified organic aquaculture products mainly as a tool to

increase product value and therefore increase economic viability. However, it seems

essential to point out that the term ‘organic aquaculture’, or more generally ‘organic

agriculture’, refers to a process that uses methods respectful of the environment from the

production stages through handling and processing. Organic production is not merely

concerned with a product, but also with the whole production system and processes

(Scialabba and Hattam 2002). The quantities and diversity of certified organic aquaculture

produce remain small, partly due to the absence of universally accepted standards and

accreditation criteria for organic aquaculture (Scialabba and Hattam 2002). At the

European Community level, organic agriculture is regulated by Council Regulations (EEC)

No.2092/91 of 24 June 1991 and (EC) No.1804/1999 of 19 July 1999 which do not apply to

aquaculture. In fact, harmonization is not feasible until individual nations develop relevant

national legislation. Italy may become the leading country in Europe for the development

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of organic aquaculture. Indeed, two draft laws, aiming to establish a national quality

trademark, a system of certification authorities and control regulations, are currently being

discussed in Parliament (D’Andrea 2006). The proposed regulations include only marine

species endemic to the Mediterranean Sea, while in freshwater aquaculture some alien

salmonids, catfishes and sturgeons are permitted. In Denmark in 2004, a new regulation on

organic aquaculture came into force for a voluntary ‘Organic’ label. Farmed fish for

organic labeling may be treated with antibiotics only once, and no genetically modified or

biologically treated fish are permitted on the farm. The ‘organic’ label can only be used for

European eel and fish from the family Salmonidae (salmon and trout, independent of their

origin) (Larsen 2006). In Germany, guidelines have been developed for eco-fish farming in

ponds by the Biokreis Association, and there are additional general guidelines for organic

farming that have to be observed. These guidelines address different issues and the only

mention of species is that they should be ‘‘preferably regional species’’ (Barg 2006). In the

draft of general principles concerning organic aquaculture production by IFOAM (Inter-

national Federation of Organic Agriculture Movements), a basic principle is that ‘‘when

introducing non-native species, special care must be taken to avoid permanent disruption to

natural ecosystems’’ (Scialabba and Hattam 2002).

In consideration of the aforementioned environmental impacts of alien finfish farming, a

fundamental criterion which needs to be considered as mandatory in developing ‘organic’

aquaculture is to restrict the eligibility to such qualifying attribution to indigenous species

only.

Ethical quality

During the last decade, many studies and surveys have highlighted the increasing concern

of most of the European actors involved in food production systems about health and safety

issues (Botonaki et al. 2006). Even though public interest in sustainability is increasing and

consumer attitudes are positive, behavioral patterns are not always consistent. The domi-

nant attribute to which consumers pay more attention in decision making seems to be the

price followed by others, such as the brand, convenience, packaging, ingredients, taste, and

at times the presence of credence attributes like sustainability (Vermeir and Verbeke

2006). However, it has also been reported that environmental, organic and ethical issues

are increasingly important factors influencing consumer food choices in different European

countries (Torjusen et al. 2001; Pettinger et al. 2004).

Concerns about utilization of alien finfish species can be compared to the globally

debated concerns about the utilization of genetically modified organisms (GMOs) in the

food industry. Some of the thoughts and considerations about ethical issues relative to

GMOs can be transferred to the context of alien finfish cultivation.

If one were to compare consumer health to the environmental status of an inland water

body, the unpredictable effects on human health of the introduction of new genetic material

from GMOs is comparable to the unpredictable effect on the environmental equilibrium of

the introduction of new genetic material from an alien species. Consequently, as the theory

of the ‘‘substantial equivalence’’ (chemically similarity to its natural counterpart) of a

genetically modified food is limited and misguided (Millstone et al. 1999) and an ‘‘ethical

equivalence’’ should be included (Pouteau 2000), similarly in the context of alien finfish

farming an ethical assurance needs to be developed. Continuing the parallel, we can

cogitate that a rainbow trout and a brown trout can be substantially considered equivalent

both from an eco-biological and a nutritional point of view. However, considering the

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numerous environmental hazards of farming non-indigenous species (Kapuscinski and

Brister 2001; Pillay 2004; Kennard et al. 2005; Nguyen and De Silva 2007), in Europe

rainbow trout fails the test of ethical equivalence. On the other hand, in measuring the

‘‘ethical equivalence’’ the context is of a paramount importance (Pouteau 2002). As such,

while the utilization of alien species can be ethically acceptable in some developing

countries where there is an inadequate food production and there are no native species

available with favorable farming attributes (De Silva et al. 2006), it seems that in European

inland aquaculture the farming of alien fish is unjustifiable.

Conclusions

While in other regions of the world, mainly in developing countries, the benefits of alien

finfish farming can outweigh the potential negative environmental impacts of such prac-

tices, in the European context the situation is different. To aim at economic sustainability,

the sector needs to satisfy consumer expectations of environmentally friendly practices.

Moreover, the local finfish fauna is considerably rich in species with optimal cultural

potential and the market is already showing positive appraisal of such products. It is known

that the aquaculture sector is constantly and increasingly market driven and therefore it is

logical and advisable to farm native species. In the desirable evolution of food ethical

assurance, the origin of farmed species needs to be considered as a standard requirement.

Acknowledgement Giovanni M. Turchini’s contribution to this study was made whilst holding an APDDiscovery, Post Doctoral Fellowship from the Australian Research Council (ARC) for the projectDP0772271 and the latter support is gratefully acknowledged.

Appendix

The European countries selected in the present treatise were: Albania, Austria, Belgium,

Bulgaria, Channel Islands, Denmark, Faeroe Islands, Finland, France, Germany, Greece,

Hungary, Iceland, Ireland, Italy, Malta, Netherlands, Norway, Poland, Portugal, Romania,

Spain, Sweden, Switzerland, United Kingdom, Yugoslavia SFR (until 1991), Bosnia and

Herzegovina (from 1992), Croatia (from 1992), Macedonia (from 1992), Serbia and

Montenegro (from 1992), Slovenia (from 1992), Czechoslovakia (until 1992), Czech

Republic (from 1993), Slovakia (from 1993), Belarus (from 1988), Estonia (from 1988),

Latvia (from 1988), Lithuania (from 1988), Moldova (from 1988), Ukraine (from 1988).

The Russian Federation was excluded because of much overlap to the Asian continent,

and no entries were recorded for finfish culture in freshwater environments for the Channel

Islands, Faeroe Islands, Malta and Norway.

The selected European nations have been aggregated according to total production and

main geographical areas and therefore eleven major nation groups were considered divided

into the five individual largest European producers (Denmark, France, Germany, Italy and

Poland) and six main geographical areas: Balkan peninsula (Albania, Bosnia and

Herzegovina, Bulgaria, Croatia, Greece, Macedonia, Romania, Serbia and Montenegro,

Slovenia), British Isles (Ireland, United Kingdom), Central Europe (Austria, Czech

Republic, Hungary, Slovakia, Switzerland), Eastern Europe (Belarus, Estonia, Latvia,

Lithuania, Moldova, Ukraine), Iberian peninsula (Spain, Portugal) and Northern Europe

(Belgium, Finland, Iceland, Netherlands, Sweden).

270 Aquacult Int (2008) 16:243–272

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References

Anonymous (1995) Aquaculture and the environment in the European Community. European Commission,Directorate-general for fisheries, Luxembourg

Balon EK (1995) Origin and domestication of the wild carp, Cyprinus carpio: from Roman gourmets to theswimming flowers. Aquaculture 129:3–48

Barg U (2006) National aquaculture legislation overview—Germany. In: National aquaculture legislationoverview fact sheets. FAO Inland Water Resources and Aquaculture Service (FIRI), Rome

Barus V (1995) First record of Anguillicola crassus (Nematoda) in the Morava River drainage basin.Helminthologia (Bratislava) 32:89

Beardmore JA Mair GC Lewis RI (1997) Biodiversity in aquatic systems in relation to aquaculture.Aquacult Res 28:829–839

Bernardino FNV (2000) Review of aquaculture development in Portugal. J Appl Ichthyol 16:196–199Black KD (2001) Sustainability of aquaculture. In: Black KD (ed) Environmental impacts of aquaculture.

Sheffield Academic Press, Sheffield, pp 199–212Botonaki A, Polymeros K, Tsakiridou E, Mattas K (2006) The role of food quality certification on

consumers’ food choices. Br Food J 108:77–90Britton JR, Brazier M (2006) Eradicating the invasive topmouth gudgeon, Pseudorasbora parva, from a

recreational fishery in northern England. Fish Manag Ecol 13:329–335Chapin FSI, Zavaleta ES, Eviner VT, Naylor RL, Vitousek PM, Reynolds HL, Hooper DU, Lavorel S, Sala

OE, Hobbie SE, Mack MC, Dıaz S (2000) Consequences of changing biodiversity. Nature 405:234–242D’Andrea A (2006) National aquaculture legislation overview—Italy. In: National aquaculture legislation

overview fact sheets. FAO Inland Water Resources and Aquaculture Service (FIRI), RomeDe Silva SS, Nguyen TTT, Abery NW, Amarasinghe US (2006) An evaluation of the role and impacts of

alien finfish in Asian inland aquaculture. Aquac Res 37:1–17FAO (2006) Food and Agriculture Organization of the United Nation, Fishery Department, Fishery Infor-

mation, Data and Statistics Unit. FISHSTAT Plus: Universal software for fishery statistical time series.Version 2.3 2000

Fausch KD, Taniguchi Y, Nakano S, Grossman GD, Townsende CR (2001) Flood disturbance regimesinfluence rainbow trout invasion success among five holarctic regions. Ecol Appl 11:1438–1455

Favero L, Bovo G, Borghesan F, Mutinelli F, Manfrin A, Selli L, Cappellozza E, Giacometti P, Ormelli S(2001) Iridovirosis in catfish (Ictalurus melas): aetiopathogenetic and anatomo-histopathologicalaspects. Boll Soc It Patol Ittica 13:39–48

Focardi S, Corsi I, Franchi E (2005) Safety issues and sustainability development of European aquaculture:new tools for environmentally sound aquaculture. Aquac Int 13:3–17

Froese R, Pauly D (2006) Fishbase, World Wide Web electronic publication. http://www.fishbase.org,version (07/2006)

Holcik J (1991) Fish introductions in Europe with particular reference to its central and eastern part. Can JFish Aquat Sci 48:13–23

Huntingford FA, Adams C, Braithwaite VA, Kadri S, Pottinger TG, Sandøe P, Turnbull JF (2006) Currentissues in fish welfare. J Fish Biol 68:332–372

IUCN (2000) Guidelines for the prevention of biodiversity loss caused by alien invasive species. InvasiveSpecies Specialist Group (ISSG), Species Survival Commission (SSC) of the World Conservation Union(IUCN). IUCN, Gland, Switzerland (also see http://www.issg.org/database/welcome/)

Ivasik VM, Kulakovskaya OP, Vorona NI (1969) Parasite exchange of herbivorous fish species and carps inponds of the western Ukraine. Hydrobiol J 5:68–71

Jaffry S, Pickering H, Ghulam Y, Whitmarsh D, Wattage P (2004) Consumer choices for quality andsustainability labelled seafood products in the UK. Food Policy 29:215–228

Johnsen PB (1991) Aquaculture product quality issues—Market position opportunities under mandatoryseafood inspection regulations. J Anim Sci 69:4209–4215

Josupeit H. Lem A, Lupin H (2001) Aquaculture products: quality, safety, marketing and trade. In:Subasinghe RP, Bueno P, Phillips MJ, Hough C, McGladdery SE, Artur JR (eds) Aquaculture in thethird millennium. Technical proceedings of the conference on aquaculture in the third millennium,Bangkok, Thailand, 20–25 February 2000. NACA, Bangkok and FAO, Rome, pp 249–257

Kapuscinski AR, Brister DJ (2001) Genetic impacts of aquaculture. In: Black KD (ed) Environmentalimpacts of aquaculture. Sheffield Academic Press, Sheffield, pp 128–153

Kennard MJ, Arthington AH, Pusey BJ, Harch BD (2005) Are alien fish a reliable indicator of river health?Freshw Biol 50:174–193

Larsen K (2006) National aquaculture sector overview—Denmark. In: National aquaculture sector overviewfact sheets. FAO Inland Water Resources and Aquaculture Service (FIRI), Rome

Aquacult Int (2008) 16:243–272 271

123

Lehtonen H (2002) Alien freshwater fishes of Europe. In: Leppakoski E, Gollasch S, Olenin S (eds) Invasiveaquatic species of Europe. Distribution, impacts and management. Kluwer, Dordrecht, pp 153–162

Leppakoski E, Gollasch S, Olenin S (2002) Alien species in European waters. In: Leppakoski E, Gollasch S,Olenin S (eds) Invasive aquatic species of Europe. Distribution, impacts and management. Kluwer,Dordrecht, pp 1–6

Mills S (1982) Britain’s native trout is floundering. New Sci 96:498–501Millstone E, Brunner E, Mayer S (1999) Beyond ‘substantial equivalence’. Nature 401:525–526Moretti VM, Turchini GM, Bellagamba F, Caprino F (2003) Traceability issues in fishery and aquaculture

products. Vet Res Commun 27:497–505Myhr AI, Dalm RA (2005) Introduction of genetic engineering in aquaculture: ecological and ethical

implications for science and governance. Aquaculture 250:542–554Naylor RL, Williams SL, Strong DR (2001) Aquaculture—a gateway for exotic species. Science 294:

1655–1656Naylor RL, Goldburg RJ, Primavera J, Kautsky N, Beveridge MCM, Clay J, Folkes C, Lubchence J,

Mooney H, Troell M (2000) Effects of aquaculture on world food supplies. Nature 405:1017–1024Nguyen TTT, De Silva SS (2007, in press) Freshwater finfish biodiversity and conservation: an Asian

perspective. Biod Cons, doi:10.1007/s10531-005-0312-8Pettinger C, Holdsworth M, Gerber M (2004) Psycho-social influences on food choice in Southern France

and Central England. Appetite 42:307–316Phillips MJ, Beveridge MCM, Ross LG (1985) The environmental impact of salmonid cage culture in inland

fisheries: present status and future trends. J Fish Biol 27:123–137Pillay TVR (2004) Aquaculture and the environment. Blackwell, OxfordPillay TVR, Kutty MN (2005) Aquaculture, principles and practices. Blackwell Publishing, OxfordPouteau S (2000) Beyond substantial equivalence: ethical equivalence. J Agric Environ Ethics 13:273–291Pouteau S (2002) The food debate: ethical versus substantial equivalence. J Agric Environ Ethics 15:

291–303Rohr A, Luddecke K, Drusch S, Muller MJ, Alvensleben RV (2005) Food quality and safety—consumer

perception and public health concern. Food Control 16:649–655Scialabba NEH, Hattam C (2002) Organic agriculture, environment and food security. FAO, Food and

Agriculture Organization of the United Nations, RomeTacon AGJ (2004) Use of fish meal and fish oil in aquaculture: a global perspective. Aquat Resour Cult Dev

1:3–14Torjusen H, Lieblein G, Wandel M, Francis CA (2001) Food system orientation and quality perception

among consumers and producers of organic food in Hedmark County, Norway. Food Qual Pref 12:207–216

Valfre F, Caprino F, Turchini GM (2003) The health benefit of seafood. Vet Res Commun 27:507–512Varadi L (2001) Review of trends in the development of European inland aquaculture linkages with

fisheries. Fish Manag Ecol 8:453–462Varadi L, Szucs I, Pekar F, Blokhin S, Csavas I (2001) Aquaculture Development Trends in Europe. In:

Subasinghe RP, Bueno P, Phillips MJ, Hough C, McGladdery SE, Artur JR (eds) Aquaculture in thethird millennium. Technical proceedings of the conference on aquaculture in the third millennium,Bangkok, Thailand, 20–25 February 2000. NACA, Bangkok and FAO, Rome, pp 397–416

Vermeir I, Verbeke W (2006) Sustainable food consumption: exploring the consumer ‘‘attitude—behavioralintention’’ gap. J Agric Environ Ethics 19:169–194

Wedekind H, Hilge V, Steffens W (2001) Present status, and social and economic significance of inlandfisheries in Germany. Fish Manag Ecol 8:405–414

Welcomme RL (1988) International introductions of inland aquatic species. FAO Fisheries TechnicalPaper 294

Williot P, Sabeau L, Gessner J, Arlati G, Bronzi P, Gulyas T, Berni P (2001) Sturgeon farming in WesternEurope: recent developments and perspectives. Aquat Living Resour 14:367–374

272 Aquacult Int (2008) 16:243–272

123