PROPOSAL THESIS
Transcript of PROPOSAL THESIS
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CHAPTER I
INTRODUCTION
Taxonomy and conservation go hand-in-hand. We cannot
necessarily expect to conserve organisms that we cannot identify,
and our attempts to understand the consequences of environmental
change and degradation are compromised fatally if we cannot
recognize and describe the interacting components of natural
ecosystems. However, taxonomy and conservation clearly are not
the same thing. Describing the world’s species and their
relationships is not equivalent to saving them. Completed species
lists, regional taxonomies and guides on their own do nothing to
conserve species. But neither is it going to be possible to
develop the necessary plan1992; Samper 2004). It is very
important to know the living organisms around us, and careful and
accurate identification and classification are of vital
importance (Kapoor, 1998; Garcia et al., ‘2008).
Insects are important because of their diversity, ecological
role, and influence on agriculture, human health, and natural
resources (Foottit and Adler, 2009). Insects create the
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biological foundation for all terrestrial ecosystems. They cycle
nutrients, pollinate plants disperse seeds, maintain soil
structure and fertility, control populations of other organisms,
and provide a major food source for other taxa (Foottit and
Adler, 2009). According to Gullan and Cranston (2005), there are
insects that are considered keystone species because if they
became extinct, the 2 wider ecosystems might collapse. For
example, in tropical soils, termites convert cellulose which
suggests they are keystone species in tropical soil structuring.
Wasps are considered beneficial to man given its many aspect
in terms of its importance for understanding the evolution of
social behavior, these insects are an ecologically important
group. The high protein diet provides relevant ecological and
economic roles in the biological control of pests (Prezoto et al.,
2007). Some species are necrophagous, and play a considerable
role in nutrient cycling by accelerating this process (O’Donnell,
1995). The structure of social hymenopteran communities is
usually characterized by simple ecological indices (Santos &
Marques 1996, Aguiar & Martins 1997, Castro & Viana 1997). Due
to ecological importance of social wasps, various studies have
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been conducted in order to better understand the biology of this
group, involving aspects of preference for nesting habit,
seasonality and nest density (Diniz & Kitayama, 1994),
The family Vespidae includes some of the most common and
conspicuous of all wasps so that the word “wasp” is often used to
refer to common yellowjackets or paper wasps the social species
within the Vespidae rather than members of other, much more
diverse families of Hymenoptera.
About 5,000 species of Family Vespidae which belongs to
Class Insecta. Vespid wasps have been important subjects in
efforts to unravel the patterns and processes of the evolution of
eusocial behavior, as extant species of Vespids exhibit grades of
sociality ranging from solitary nesting to eusocial behavior
(Cowan D. 1991, Jeanne RL. 1980). Eusocial behavior in the
Vespidae is exhibited in the clade comprising the subfamilies
Stenogastrinae, Vespinae, and Polistinae. Some eusocial species
are independent founders: Females of one generation, either alone
or in cooperative groups, initiate new nests. Others are swarm-
founders: Females from more than one generation move to new sites
in a coordinated group and initiate nests (Jeanne RL. 1980).
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Forage for water, pulp, carbohydrates, and animal protein. When
hunting, social wasp are opportunistic generalist and use a
variety of mechanism to locate and choose prey. (Carpenter J.M.
1987).
As insects, wasps are characterized by three pairs of
jointed legs; an abdomen that is divided into 11 segments and
lacks any legs or wings; and a body separated into three parts
(head, thorax, and abdomen), with one pair of antennae on the
head. As true insects, they also have ectognathous, or exposed,
mouthparts. Wasps can be differentiated from bees as the latter
have a flattened hind basitarsus. Unlike bees, wasps generally
lack plumose hairs, in most wasps, it has two pairs of wings, an
ovipositor, or stinger which is only present in females because
it derives from the ovipositor, a female sex organ. Few or
no hairs in contrast to bees. Nearly all wasps are terrestrial;
only a few specialized parasitic groups are aquatic (Ross, 1991).
Although wasps are distributed world-wide, the greatest
diversity is to be found in the tropical regions of the globe.
Hymenoptera the order to which wasps belong, is one of the most
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diverse order of insects, nearly 100,000 species world-wide have
been recorded, the prospective number is certainly well over
300,000 (Archer, 1989). The exact number of described insect
species is uncertain due to synonyms and the lack of a global
list waiting to be discovered, (Groombridge 1992; Anon. 2003).
Morphometrics can be broadly defined as the quantitative
study of the size and shapes of organisms. Often only parts (e.g.
limbs) or organs of an organism are measured, and more general
conclusions are drawn about evolutionary relationships, for
example, from these measurements. What is now called traditional
morphometrics or multivariate morphometics, is the application of
multivariate statistical techniques (e.g. discriminate function
analysis) to morphological data sets (Adams et al., 2004).
Statement of the Problem
One of the problems that the agricultural industries faces
right now is the increase of pests in their plots or farm sites.
Wasps (Vespidae), as we all know it is a great pest killer since
it eats smaller insects particularly pests. In relation to this
problem, an assessment of the diversity of wasps (Vespidae) in
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specific sites in Mt. Malinao will be conducted for inventory
purposes.
A difference in every species is also a great and major
problem faced by researchers of wasps (Vespidae). Even debates
about this are organized in some countries. Having the important
and eligible ideas on differentiation of this organisms based on
wing morphometry is needed to comply with the said problem.
Objectives
The primary objective of the study is to focus on the taxonomy
and morphometry of different genera and species of wasps in
specific sites in Mt Malinao. The following objectives will be
observed in the experiment that will be conducted.
1.) Collect, describe and identify the Vespid wasps species
in Mt. Malinao up to at least genus level.
2.) Compare and distinguish similarities and differences
among the Vespid wasps in terms of external morphology and
morphometry.
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3.) To correlate microweather parameters (temperature, RH
and rainfall amount) with the occurrence and abundance of
vespid wasps.
Scope and Delimitation
The study focused only in the assessment of wasps (Vespidae)
found in Mt. Malinao. The sampling will be conducted in Mt.
Malinao only. The weather on the sampling dates will be observed
and will be recorded. Nests and juvenile wasps will not be
included in the gathering of samples. Sampling will be done from
August to October 2015
Significance of the Study
The success of the study is essential to giving basic
knowledge to the students and also professionals in the field of
insect taxonomic identification and classification. It will also
help the DENR (Department of Environment and Natural Resources)
to give information regarding the new and easier way of measuring
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the wing morphometry of Hymenoptera Vespidae and could provide
them the present information and condition of wasps (Vespidae) in
Mt. Malinao. It will also give information on the social and
behavioral characteristics of wasps (Vesipdae).
The data that will be gathered in this study can help the
farmers and localities on how Vespid wasps can help in pest
control in Mt. Malinao.
The survey and identification of genera and species of this
organism will contribute to the known data on specific areas
chosen. The abundance of these organisms also contributes to the
ecological aspects of the said areas.
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CHAPTER II
REVIEW OF RELATED LITERATURE AND STUDY
This chapter is a presentation of gathered literature and
studies, which are directly or indirectly related to the present.
That would help the researcher to simply understand, develop
concepts of the study by giving enough knowledge and background
that would clarify the essence of the study.
Vespid Wasps (Hymenoptera: Vespidae)
Social insects, such as termites, ants and
many bees and wasps, are the most familiar species
of eusocial animal (Gary 2008). They live together in large
well-organized colonies that may be so tightly integrated and
genetically similar that the colonies of some species are
sometimes considered super organisms. It is sometimes argued that
the various species of honey bee are the only invertebrates and
indeed one of the few non-human groups to have evolved a system
of abstract symbolic communication where a behavior is used
to represent and convey specific information about something in
the environment.
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Wasps are essential to the natural environment and function
at their highest level during the summer months. Wasps eat
arachnids and a lot of pest insects, such as ants or
caterpillars, sometimes by laying their eggs on or inside other
insects or spiders that are eaten by newly hatched wasp larvae.
Just like bees, wasps aid in the pollination of plants. In this
communication system, called dance language, the angle at which a
bee dances represents a direction relative to the sun, and the
length of the dance represents the distance to be flown. (Gullan,
P.J.; Cranston, P.S. 2005). Social wasps build nests and are
foragers (Spradbery 1973). For these reasons, social wasps can be
considered semi sessile organisms with some fidelity to their
environments, which makes them highly appropriate for community
structure studies (Heithaus 1979, Santos 2000).
Morphology
Wasps are characterized by jointed appendages,
an exoskeleton(hard, external covering), segmented body,
central nervous system, digestive system, open circulatory
system, and specialized sensory receptors. The term "jointed
appendages" refers to both legs and antennae.
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As insects, wasps are characterized by three pairs of
jointed legs; an abdomen that is divided into 11 segments and
lacks any legs or wings; and a body separated into three parts
(head, thorax, and abdomen), with one pair of antennae on the
head. As true insects, they also have ectognathous, or exposed,
mouthparts. Wasps can be differentiated from bees as the latter
have a flattened hind basitarsus. Unlike bees, wasps generally
lack plumose hairs, in most wasps, it has two pairs of wings, an
ovipositor, or stinger which is only present in females because
it derives from the ovipositor, a female sex organ. Few or
no hairs in contrast to bees. Nearly all wasps are terrestrial;
only a few specialized parasitic groups are aquatic (Ross, 1991).
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Figure 1. Basic morphology of wasp, the egg-laying ovipositor
that is modified into a stinger on female insects.
As male wasps don’t sting, in some cases be differentiated
from females by virtue of the fact that the upper region of the
male's mesosoma (called the tergum) consists of an additional
terga. The total number of terga is typically six. The difference
between sterile female worker wasps and queens also varies
between species but generally the queen is noticeably larger than
both males and other females.
Life cycle
The order Hymenoptera is the sister lineage of all other
holometabolous insects (Ishiwata
et al. 2011) insects that develop from an egg, through several
larval instars, to a pupa stage, and finally emerge as an adult
(Gauld and Bolton 1988). Vespidae, like all Hymenoptera have a
complete metamorphosis. From the egg hatches a larva, a legless,
eyeless grub whitish in colour, with well-developed mouth parts
provided with powerful muscles that occupy most of the head
capsule. Antennae are reduced to small orbits bearing one or
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several sensory cones. They have five growth stages called
instars. When the larva reaches the fifth stage, it continues to
feed for a short period of time and soon stops and starts
spinning a very fine lining on the cell walls whilst closing the
aperture with a silken cap of variable thickness, texture and
coloration interspecifically.
At this stage fecal matter is expelled from the larva, it is
pushed to the bottom of the cell or even extracted by workers (as
in the tribe Ropalidiini). The larva enters then a pre-pupal
stage that may last a few days after which it moults into the
pupal stage. About two to three weeks later the adult wasp
emerges biting through the cocoon cap. The emerging workers are
generally smaller than the queen and are responsible for all
aspects of nest construction and maintenance as well as foraging
activities (food and construction materials). The type of food
resource provided to larvae by the ovipositing female has been an
important biological trait throughout the evolution of
Hymenoptera and has resulted in a large variety of life histories
(Gauld and Bolton1988).
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Figure 2. General life cycle of a wasp.
History
Ancestral Hymenoptera fed on plant tissues, and the
transition from phytophagy to forms of 3 carnivory (parasitoids
and predators) has led to the greatest species diversity of the
order (Sharkey 2007, Heraty et al. 2011) The predominant
lifestyle in modern Hymenoptera is that of parasitoids where
larvae directly obtain nourishment from a single host individual
to complete their development, and in which death of the host
always results. As a rule and throughout the time, members of the
order Hymenoptera can be regarded as ecological specialists.
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Most species are rather narrowly adapted to specific habitats
and/or specific hosts.
Vespids are small to large wasps with wings folded
longitudinally at rest and all species are prompt fliers, often
encountered on sunny days. All but the Eumeninae form colonies of
various sizes, morphology and organization. Their remarkable
success as a taxon probably has more to do with their immense
range of behavioral adaptation rather than any physical or
biochemical characteristic. (Gauld and Bolton 1988, Eggleton and
Belshaw 1992, Godfray 1994, Quicke 1997). Approximately half the
species of Hymenoptera are parasitoids (Gauld and Bolton 1988,
Eggleton and Belshaw 1992, Godfray 1994, Quicke 1997, Grisssell
1999, Huber 2009).
Distribution
The order Hymenoptera contains over 115, 000 described
species and also selected groups of wasps are distributed
worldwide, and it is among the four most diverse groups of
insects along with the orders Coleoptera (beetles), Diptera
(flies), and Lepidoptera (butterflies and moths.) The Hymenoptera
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are major constituents of terrestrial habitats because of their
numerous interactions with other organisms via a diverse array of
ecological lifestyles. They are important as herbivores,
parasitoids, pollinators, predators, and scavengers (Sharkey
2007, Huber 2009).
About 5,000 species of Vespidae which belongs to Insecta and
this family is divided into 6 families including Vespinae (69
species), Eumeninae (3,579 species), Polistinae (958 species),
Stenogastrinae (58 species), Euparagiinae (10 species), and
Masarinae (344 species) (Carpenter, 1982). In Korea, taxonomic
studies of Vespidae have been conducted intermittently by Kim et
al. (1994, 2006), Kim and Yoon (1996), Kim (2001, 2011), Kim and
Kim (2011) and other researchers, but a complete list of domestic
species has not decided yet including whether some species
belonging to Dolichovespula, Vespula, Polistes live in Korea by
misidentified species and dealing with the synonym. However,
recently, according to Choi et al. (2012, submitted), it is
reported that it is valid to consider that domestic Vespidae has
2 subfamilies, 5 genera and 30 species (including 3 subspecies)
provisionally except Eumeninae. Vespidae are all eusocial and
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subsocial insects except the solitary type, and divided into 3
castes (gueen, worker or male).
Social wasps (Vespinae) are native to the Holarctic, but by
1945 the German wasp was accidentally imported to New Zealand
(Thomas 1960; Donovan 1978), and by 1983 the Common wasp was well
established in Dunedin although it was probably present in
Wellington several years previously (Donovan 1983a, b, 1984). The
German wasp now occurs throughout the country. In some areas
infestations adversely affect public health, tourism, apiculture,
silviculture, horticulture, and the environment.
The Common wasp appears to be spreading rapidly, and will
become probably as widely distributed (Donovan 1984). Arthropod
enemies of wasps have not been reported from New Zealand.
Spradbery (1973) listed approximately 150 insect species
associated with wasps in the Holarctic, and 400 plus organisms
were reported by Edwards (1980). Of these, the parasitoid
Sphecophaga vesparum (Hymenoptera: Ichneumonidae) appears to have
the greatest potential to reduce wasp numbers. Although males
infrequently occur, the species is parthenogenic and
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multivoltine, which suggests that a successful invasion could
eventually cause the demise of even large nests.
Ecology
Although pest insects attract the most attention, many
insects are beneficial to the environment and humans. Some
insects, like wasps,
bees, butterflies and ants, pollinate flowering plants.
Pollination is a mutualistic relationship between plants and
insects. As insects gather nectar from different plants of the
same species, they also spread pollen from plants on which they
have previously fed. This greatly increases plants' ability
to cross-pollinate, which maintains and possibly even improves
their evolutionary fitness. This ultimately affects humans since
ensuring healthy crops is critical to agriculture. As well as
pollination ants help with seed distribution of plants. This
helps to spread the plants which increases plant diversity. This
leads to an overall better environment (Wilson 1994). A serious
environmental problem is the decline insects, and a number of
species of insects are now cultured primarily for pollination
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management in order to have sufficient pollinators in the
field, orchard or greenhouse at bloom time (Deborah T 1991).
Besides the importance of social wasps for understanding
the evolution of social behavior, these insects are an
ecologically important group. The high protein diet provides
relevant ecological and economic roles in the biological control
of pests (Prezoto et al., 2007). Some species are necrophagous,
and play a considerable role in nutrient cycling by accelerating
this process (O’Donnell, 1995). Due to ecological importance of
social wasps, various studies have been conducted in order to
better understand the biology of this group, involving aspects of
preference for nesting habitat and nest density (Diniz &
Kitayama, 1994), seasonality (Diniz & Kitayama, 1998), nesting
habits (Lima et al., 2000) or inventories.
A significant number of species records have been carried
out in the Amazon region (Silveira, 2002; Silveira et al., 2005;
Silveira et al., 2008; Silva & Silveira, 2009), Atlantic forest
(Santos et al., 2007; Gomes & Noll, 2009) and Cerrado (Diniz &
Kitayama, 1994; Diniz & Kitayama, 1998; Souza & Prezoto, 2006;
Elpino-Campos et al., 2007; Prezoto & Clemente, 2010; Souza et
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al., 2010). In adition Wasps are important in food chains. Wasps
are critically important in natural biocontrol. Almost every pest
insect species has a wasp species that is a predator or parasite
upon it. Parasitic wasps are also increasingly used in
agricultural pest control as they have little impact on crops.
Inventorying an area is the first step towards its
conservation and rational use (Melo et al. 2005). By undertaking
a survey of species of social wasps, several aspects of their
biology and behavior must be considered, such as colony
seasonality, foraging activity, and nesting habits. Brazilian
rainforests represent a peak of biodiversity, and in this sense,
certain localities possess the greatest abundance and richness of
known species on the planet (Machado et al. 1998), including in
their diversity of social wasps (Richards 1978).
Studies on wasps Taxonomy and Diversity
Bingham (1897) and Das & Gupta (1989) made valuable
contributions on the taxonomy of Vespidae from India and its
adjacent countries. The knowledge on vespid fauna of Rajasthan is
very scanty and fragmentary. Fourteen genera and 20 species are
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recorded from Rajasthan till date in scattered literatures
(Nurse, 1903; van der Vecht, 1941; Chhotani & Ray, 1975; Giordani
Soika, 1982; Gusenleitner, 2006; Kojima et al., 2007; Girish
Kumar, 2010, 2011, 2012 a & b; Girish Kumar & Lambert Kishore,
2012; Girish Kumar & Carpenter, 2013; Girish Kumar et al., 2013).
An attempt has been made here to provide a consolidated account
on the fauna of the family Vespidae from the state of Rajasthan.
The social wasps of Brazil have the asynchronous colony
cycle. The pattern has been well-described for the genera
Mischocyttarus, Polistes and Polybia (Gobbi and Zucchi 1980;
Simões and Mecchi 1983; Gobbi 1984; Simões et al. 1985; Gobbi and
Simões 1988; Marques et al. 1992; Giannotti and Machado 1994;
Giannotti et al. 1995; Giannotti 1998). On the other hand, the
foraging activity of Polistinae are primarily limited by physical
factors (Spradbery 1973), such as light intensity, temperature,
air humidity, and wind speed, and some studies have shown that
individual wasps forage more intensively during the warmest and
least humid hours of the day (Giannotti et al. 1995; Andrade and
Prezoto 2001; Resende et al. 2001).
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Thirteen generations of S. v. vesparum were raised by July
1985, and all stages of the parasitoid were released into wasp
nests in Canterbury. Six of seven V. vulgaris nests and three of
six V. germanica nests were parasitized. Although releases
occurred late in the growth cycle of nests, at least one
generation of parasitoids emerged in four V. vulgaris nests and one
V. germanica nest. One of the V. vulgaris nests probably developed
two generations of parasitoids. Parasitoid numbers in this nest
increased approximately eight-fold. (B. J. Donovan & P. E. C.
Read 1987).
European paper wasps (Polistes Latreille, 1802) closely
related to P. gallicus. , as two distinct species can be
recognized in what has hitherto been considered Polistes
bischoffi Weyrauch, 1937. One species is almost as light coloured
as P. gallicus, and is mainly recorded from Southern Europe and
Western Asia. The other species is darker and has a more northern
distribution in Central Europe. Both species occur syntopically
in Switzerland. Given that the lost lectotype of P. bischoffi
originated from Sardinia, as a neotype. The northern species is
described as P. helveticus sp. n. here. We also provide a
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redescription of P. bischoffi rev. stat. and an identification
key including three more closely related species, P. biglumis, P.
gallicus and P. hellenicus. (Neumeyer R, Baur H, Guex G-D, Praz C
2014).
Records of 15 Palaearctic species of Vespidae are given. The
following taxa are newly recorded: Polistes rubellus
Gusenleitner, 2006, from Nepal, Dolichovespula adulterina (du
Buysson, 1905) and Katamenes tauricus (de Saussure, 1855) from
the Tuva Republic (Eastern Siberia, Russia), Vespula vulgaris
(Linnaeus, 1758) from Ciudad Real province (Spain), Ancistrocerus
gazelle (Panzer, 1798) from Gran Canaria (Spain, Canary Islands),
Hemipterochilus bicoloricornis (Giordani Soika, 1952) from Turkey
(Asian part), Microdynerus latro Blüthgen, 1955, from Syria, and
Leptochilus membranaceus (Morawitz, 1867) and Pseudepipona
tricolor Gusenleitner, 1976, both from Kazakhstan. Worldwide
distribution of each taxon is also summarized (Dvorak and Castro
2007)
Knowledge about taxonomy and biology of species of
Hymenoptera is hampered by the challenge of their identification
because of both intraspecific morphological plasticity and small
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body size (Godfray and Shimada 1999, Gariepy et al. 2007,
Grissell 1999, Stone et al. 2008,
Huber 2009). Studies of life history traits of Hymenoptera, such
as development time, are generally limited either by biology
(parasitoid: Mayhew and Blackburn 1999) and/or taxonomy
(Ichneumonoidea: Braconidae and Ichneumonidae: Harvey and Strand
2002) to facilitate the search for possible patterns. To support
broad scale comparisons of development time between interacting
species of Hymenoptera with different lifestyles and habitats, a
simple and efficient tool is required for rapid species
identification.
Morphometric Studies
Morphological measurements of insects, including Hymenoptera
and especially the eusocial species, have had a long history of
use (e.g. Huxley 1972) and have often been termed
morphometrics. This is not true multivariate morphometrics as
currently defined above and often only involves plots of two
variables, such as head width and antennal scape length to
describe allometric growth and caste differences in ants,
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although a combination of univariate and multivariate statistics
has sometimes been employed to determine caste differences (e.g.
Gelin et al., 2008). In other studies, such as those on bees,
multiple characters will be measured and used descriptively but
multivariate statistical analysis is not employed. I will refer
to this approach as classical morphometrics.
Wing morphometrics has been successfully used in taxonomic
studies of Hymenoptera to differentiate between closely related
taxa, and has also shown significant differences in wing shape,
size and mechanical properties between species (Aytekin et al.,
2007), however there are only a relatively few studies using wing
morphometrics to estimate fluctuating asymmetry.
Geometric morphometrics, a technique based on a rigorous
statistical assessment of shape, to compare the forewings of
fifteen species of Stenogastrinae wasps belonging to four
different genera. For the first time in this subfamily, we
propose a phylogenetic classification of the species based on
wing morphology that largely agrees with the cladistics data
available at genus level and reflects the differences among
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species in terms of nesting material and architecture of their
nest. (Baracchi, Dapporto and Turillazzi 2011).
Morphometric techniques to describe the venation patterns
typical of five populations of P. dominulus sampled at widely
separated geographic locations. Searched for significant
similarities and differences among the samples using the
technique of thin plate-splines (TPS) defined from landmarks
(specified points in the venation pattern). To test the
hypothesis that there might be a greater morphological similarity
between populations linked by the geographical routes easiest to
travel, we analysed the spatial organisation of shape changes and
compared shape similarities between the five conspecific
populations (Adams & Funk l997; Pavlinov 2001; Rohlf 1996).
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CHAPTER III
METHODOLOGY
This chapter consists of the description of the study site,
materials, research method, sources of data, and instrumentation
used in the study. These are vital for the collection and
accuracy of accumulated information.
Study Area
Malinao Volcano is situated between
the provinces of Albay and Camarines Sur in the southeastern
region of Luzon Island. The mountain is forested with an
elevation of 1,548 metres (5,079 ft) above sea level and a base
diameter of 22.5 kilometres (14.0 mi) as a large mass of land in
the midst of a forest and its crater has a wall that is breached
on the eastern side, located at 13°24′58″N 123°36′30″E .
(Knittel-Weber, 1990).
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Figure 3. Map of Bicol Peninsula and Mt. Malinao, Albay
Philippines
Securing Permits to Collect and Study Biological Specimens
Since the site is a protected area, permits needed from the
sites from Local Government Units and be presented to the
Department of Environment and Natural Resources (DENR) will be
secured first before conducting this study. The proposal will
also be presented to the DENR and the local council tasked to
monitor activities in the area.
Preliminary Activities
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There will be three sampling sites that will be chosen from
the study area. Each site will be visited first and inhabitants
of each site will be interviewed in order to determine the areas
where wasps colonies or individuals can be found. The Elevation
or altitude including exact coordinate of local site will be
measured using a GPS (Global Positioning System) device.
Collection of Wasps Specimens
Collection of insect specimen will be done from July to
October of 2015. The collection method will be aerial netting
which is done when insect is in flight. Aerial nets to be used
will come in wooden handles or long retractable handles for
obtaining representative specimens. Wasps, being diurnal insects
which is active during day time, will be captured from 8am until
11am of the day and from 1p.m. until 4 p.m. in the afternoon.
As an initial step for preservation of the specimen
gathered, the collected specimen will be placed on 70% Ethyl
Alcohol solution for 5-30 minutes.
Preservation and Identification of Collected Specimens
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The biological samples will be mounted with an insect pin
and will be dried inside a modified insect drier. Morphological
examination of the insect samples using magnifying lenses, and an
Olympus dissecting microscope. Photos of samples will be taken
using a camera mounted on the same microscope. The collected
specimen will be examined for morphometric analysis. Sorting of
species and sex determination will be done by comparison on the
differences and similarities of morphology. Taxonomic
identification of the species followed by the aid of the
dichotomous keys.
Statistical Analysis
Measuring of diversity
Shannon’s Index of General Diversity (H’) was used to
determine the diversity of species in the study site.
H'=−Pi(lnPi)
Where:
Pi = importance probability of each species (ni/N)
ni= number of individuals
N = total number of individuals
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ln = natural logarithm
Index of Dominance (C) was also be used to compare the
dominance of the same species in different area.
C=(¿/N)
Where:
N = total number of individuals of all species
ni = total number of individuals of species A
Measuring weather parameters
Temperature will be measured using a thermometer.
Temperature during sampling date and time will be noted. Relative
humidity will be measured using a psychrometer. Measurement will
be done during morning and dusk any relative values will be
recorded for data purposes. Amount of rainfall will be measured
using a container with calibration of centimeters. Measurement
will be done during dusk every day of sampling time. Analysis of
variance will be used for data analyses.
Statistical Analysis
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A t-test’s statistical significance indicates whether or not
the difference between two groups’ averages most likely reflects
a “real” difference in the population from which the groups were
sampled.
LITERATURE CITED
Adames DC, Funk DJ 1997. Morphometric inferences on siblingspecies and sexual dimorphism
in Neochlamisus bebbianae leaf beetles: multivariateapplications of the thin-plate spline. Systematic Biology46: 180–194.
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Adams, D.C., Rohlf, F.J. & Slice, D.E. (2004) Geometricmorphometrics: Ten years of progress following the‘revolution’. Italian Journal of Zoology, 71: 5-16.
Aguiar, C.M.L. & C.F. Martins. 1997.
Abundância relativa, diversidade e fenologia de abelhas(Hymenoptera, Apoidea) na caatinga, São João do Cariri,Paraíba, Brasil. Iheringia 83:151-163.
Andrade, F.R. and F. Prezoto. 2001. Horários de atividadeforrageadora e material coletado por
Polistes ferreri Saussure, 1853 (Hymenoptera, Vespidae), nasdiferentes fases de seu ciclo biológico. Revista Brasileirade Zoociências 3: 117–128.
Archer, M.E. 1989; a Key to the World Species of the Vespinae(Hymenoptera), College of
Ripon &York St John, the Academic Board research Committee.
Aytekin A., M., Terzo, M., Rasmont P. & Çağatay, N., (2007)Landmark Based Geometric
morphometric analysis of wing shape in Sibiricobombus Vogt(Hymenoptera: Apidae: Bombus Latreille). Annales de laSociété Entomologique de France, 43: 95-102.
Bingham CT. 1897. The Fauna of British India, including Ceylon and Burma,Hymenoptera,
Wasps and Bees: Taylor and Francis, London, 579+ i- xxix.
B. J. Donovan & P. E. C. Read (1987) Attempted biological controlof social wasps, Vespula
spp., (Hymenoptera: Vespidae) with Sphecophaga vesparum(Curtis) (Hymenoptera: Ichneumonidae) in New Zealand, NewZealand Journal of Zoology, 14:3, 329-335, DOI:10.1080/03014223.1987.10423002.
Brewer, Gary. "Social insects". North Dakota State University.Archived from the original on 21
March 2008. Retrieved 6 May 2009.
34
Brown Rafe M. & Gonzales Juan Carlos. 2007. A New Forest Frog ofthe Genus Platymantis
(Amphibia: Anura: Ranidae) from the Bicol Peninsula of LuzonIsland, Philippines.
Carpenter, J.M. & O.M. Marques. 2001. Contribuição ao estudodos vespídeos do Brasil
(Insecta, Hymenoptera, Vespoidae, Vespidae). Cruzdas Almas, Universidade Federal da Bahia. Publicações
digitais, vol.2.
Carpenter, J.M. 1991. Phylogenetic relationship in the Vespidae,pp. 7-32.
In Ross, K.G. and R.W. Mathews Eds. The Social Biology ofWasps. Ithca: Cornell University Press.
Carpenter J.M. 1987. Phylogenetic relationship and classificationOf Vespidae
(Hymenotera:Vespidae) Systematic Entomology 12:431-431.
Carpenter, J.M. (1982) the phylogenetic relationships and naturalclassification of the Vespoidea
(Hymenoptera). Syst. Entomol. 7:11-38.
Castro, M.S. & B.F.Viana. 1997. Bees visiting coconutinflorescences in Bahia, Northeast Brazil.
J. Apic. Res. 36: 180-181.
Chhotani OB and Ray KK. 1975. Fauna of Rajasthan, India.Hymenoptera. Rec Zool Surv India
71: 13-49.
Cowan D. 1991. The solitary and prosocial Vespidae. See Ref. 94a,pp. 33–73
Das BP and Gupta VK. 1989. The social wasps of India and theadjacent countries
(Hymenoptera: Vespidae). Oriental Ins. Monograph 11: 1-292.
35
Diniz, I. R. & Kitayama, K. 1994. Colony densities andpreferences for nest habitats of some social
wasps in Mato Grosso State, Brasil (Hymenoptera: Vespidae).Journal of Hymenoptera Research 3:133-143.
Donovan, B. J. 1978: The German wasp. Vespula germanica (F.)(Hymenoptera: Vespidae) in
New Zealand. In: Papers presented at honeydew seminar.Christchurch. Ministry of Agriculture and Fisheries,Advisory Services Division. pp. 49-63.
DVOŘÁK and CASTRO (2007) Šumava National Park Administration,Department of Science
and Research, Sušická 399, CZ-341 92 Kašperské Hory, CzechRepublic; e-mail: [email protected] Av. Sanz Gadea9, E-44002 Teruel, Spain; e-mail:[email protected]
Erwin, T. L. 1982 Tropical forests: their richness in Coleopteraand other arthropod species.
Coleopts. Bull. 36, 74–75.
Eggleton P, Belshaw R (1992) Insect parasitoids: an evolutionaryoverview. Philosophical
Transactions of the Royal Society of London Series B 337: 1-20.
Foottit, R.G. and Adler, P.H. (2009). Insect Biodiversity:Science and Society. Blackwell
Publishing Ltd.
Gauld ID, Bolton B (1988) the Hymenoptera. British Museum(Natural History)/Oxford
University Press, London. 332 ppGariepy T, Kuhlmann U, Gillott C, Erlandson M (2008) A large-scale comparison of conventional
and molecular methods for the evaluation of host-parasitoidassociations in
36
nontarget risk-assessment studies. Journal Applied ofEcology 45: 708-715.
Gelin, L.F.F., Da Cruz, J.D., Noll, F.B., Giiannotti, E., DemSantos, G.M., & Bichara-Filho,
C.C. (2008) Morphological Caste Studies In the NeotropicalSwarm-FoundingPolistinae Wasp Angiopolybia pallens(Lepeletier) (Hymenoptera: Vespidae) Neotropical Entomology37: 691-701
Grissell EE (1999) Hymenopteran biodiversity: some alien notions.American Entomologist 45:
235-244.
Giordani Soika A. 1982. Revisione delle specie orientali delgenere Antepipona Sauss. Boll Mus
civ Stor nat Venezia 32: 205-257.
Girish Kumar P. 2014 (2013). A study on the genus Anterhynchium deSaussure (Hymenoptera:
Vespidae: Eumeninae) from Indian subcontinent. Rec Zool SurvIndia 113(Part- 4): 139-158.
Girish Kumar P.and Carpenter JM. 2013. A taxonomic review of thegenus Antodynerusde
Saussure, 1855 (Hymenoptera: Vespidae: Eumeninae) from theIndian subcontinent.
Zootaxa 3731(2): 267-278.
Gusenleitner J. 2006. Über Aufsammlungen von Faltenwespen inIndien (Hymenoptera,
Vespidae). Linzer boil Beitr 38(1): 677-695.
Godfray HCJ, Shimada M. (1999) Parasitoids: a model system toanswer questions in
behavioural, evolutionary and population ecology. ResearchPopulation Ecology 41: 3-10.
Gobbi, N. and R. Zucchi. 1980. On the ecology of Polistesversicolor versicolor (Olivier) in
37
Southern Brazil (Hymenoptera, Vespidae, Polistini). I.Phenological account. Naturalia 5: 97–104.
Groombridge, B., 1992 Global biodiversity: status of the Earth’sliving resources. London:
Chapman and Hall.
Gess, F.W. 1981. Some aspects of an ethological study of theaculeate wasps and the bees of a
Karroid area in the Vicinity of Grahamstown, South Africa.Ann. Cape Provincial Museum (Natural History) 14: 1-80.
Gerais. Experientae 28: 67-94. Santos, G. M.de M., V.P.G.Santana-Reis, J. J. Resende, P. De
Giannotti, E. and V.L.L. Machado. 1994. The seasonal variation ofbrood stages duration of
Polistes lanio (Fabricius, 1775) (Hymenoptera, Vespidae).Naturalia 19: 97–102.
Gullan, P.J.; Cranston, P.S. (2005). The Insects: An Outline ofEntomology (3 ed.). Oxford:
Blackwell Publishing. ISBN 1-4051-1113-5.
Harvey JA, Strand MR (2002) the developmental strategies ofendoparasitoid wasps vary with host
feeding ecology. Ecology 83: 2439-2451.
Heithaus, E.R. 1979. Community structure of neotropical flowervisiting bees and wasps:
Diversity and phenology. Ecology 60: 190-202.
Holldobler, Wilson (1994). Journey to the ants: a story ofscientific exploration. Westminster
college McGill Library: Cambridge, Mass.:Belknap Press ofHaravard University Press, 1994. pp. 196–199. ISBN 0-674-48525-4.
38
Huber JT (2009) Biodiversity of Hymenoptera. In: RG Foottit, PHAdler (eds), Insect
Biodiversity: Science and Society. Blackwell Publishing,London. pp 303-323.Huxley, J. (1972) Problems of Relative Growth 2nd edition, DoverPublications Inc., New York.
Ishiwata K, Sasaki Go, Ogawac J, Miyata T, Su Z-H (2011)Phylogenetic relationships among
Insect orders based on three nuclear protein-coding genesequences. Molecular Phylogenetics and Evolution 58: 169-180.
Jeanne RL. 1980. Evolution of social behavior in the Vespidae.Annu. Rev. Entomol. 25:371–96
Kim, J.K. (2001) A new species of genus Polistes Latreille(Pilistinae, Vespidae, Hymenoptera)
from Korea. Korean J. Entomol. 31(1):59-62.
Kim, J.K. (2011) Dolichovespula kuami (Vespidae: Hymenoptera)taxonomic compliment with
newly found specimens. Sociobiology. 57(1):11-18.
Kim, J.K. and I.B. Yoon (1996) A new species of Dolichovespula(Insecta: Hymenoptera: Vespidae) from Korea. Korean J. Syst. Zool. 12(3):199-202.
Kim, J.K. and I.K. Kim (2011) Discovery of Vespa binghami(Vespidae: Hymenoptera) in
Korea. Korean J. Syst. Zool. 27(1):105-107.
Kim, J.K., M. Choi and T.Y. Moon (2006) Occurrence of Vespavelutina Lepeletier from Korea,
and a revised key for Korean Vespa species (Hymenoptera:Vespidae). Entomol.
Res. 36:112-115.
39
Knittel-Weber, C. And Knittel, U. Petrology and Genesis of theVolcanic Rocks on the Eastern
Flank of Mount Malinao, Bicol Arc (Southern Luzon,Philippines). J. Southeast Asian Earh Sci., 1990; 4 (4): 267 – 280
Kojima J, Lambert K., Nguyen LTP and Saito F. 2007. Taxonomicnotes on the paper wasps of
the genus Ropalidia in the Indian subcontinent (Hymenoptera:Vespidae). Entomol Sc 10: 373-393.
Lima, M. A. P., Lima, J. R. & Prezoto, F. 2000. Levantamento dosgêneros de vespas sociais
(Hymenoptera, Vespidae), flutuação das colônias e hábitos denidificação no campus da UFJF, Juiz de Fora, MG. RevistaBrasileira de Zoociências 2(1):69-80.
Machado, A.B.M., G.A.B. Fonseca, R.B. Machado, L.M.S. Aguiar andL.V. Lins. 1998. Livro
vermelho das espécies ameaçadas de extinção da fauna deMinas Gerais. Belo Horizonte: Biodiversitas. 605 pp.
Mayhew PJ, Blackburn TM (1999) Does parasitoid development modeorganise life-history traits
in the parasitoid Hymenoptera? Journal of Animal Ecology 68:906-916.
Marques, O.M., C.A.L. Carvalho & J.M. Costam. 1993. Levantamentodas espécies de vespas
sociais (Hymenoptera: Vespidae) no município de Cruz dasAlmas – Estado da Bahia. Insecta 2: 1-9.
Marques, O.M., C.a.L. Carvalho and J.M. Costa. 1992. Fenologia dePolistes canadensis
canadensis (L., 1758) (Hymenoptera, Vespidae) em Cruz dasAlmas - Bahia. Insecta 1: 18.
May, R. M. 1974 Biological populations with No overlappinggenerations: stable points, stable
40
cycles and chaos. Science 186, 645–647.
May, R. M., Lawton, J. H. & Stork, N. E. 1995 Assessing rates.In Extinction rates (ed. J. H.
Lawton & R. M. May), pp. 1–24. Oxford: Oxford UniversityPress.
Marco & C.C. Bichara Filho. 2000. Flying capacity of swarmfounding wasp Polybia occidental
is Olivier, 1971(Hymenoptera, Vespidae). Rev. Bras.
Melo, A.C., G.M.M. Santos, J.D. Cruz and O.M. Marques. 2005.Vespas Sociais (Vespidae); pp.
244–257, in: F.A. Juncá, L. Funch and W. Rocha (ed.).Biodiversidade e conservação da Chapada Diamantina.Brasília: Ministério do Meio Ambiente.
Neumeyer R, Baur H, Guex G-D, Praz C (2014) A new species of thepaper wasp genus Polistes
(Hymenoptera, Vespidae, Polistinae) in Europe revealed bymorphometrics and molecular analyses. ZooKeys 400: 67–118.doi: 10.3897/ zookeys.400.6611
Nurse CG. 1903. New species of Indian aculeate Hymenoptera. AnnMag Nat Hist (7)71: 530-
534.
O’Donnell, S. 1995. Necrophagy by Neotropical Swarm-FoundingWasps (Hymenoptera:
Vespidae, Epiponini). Biotropica 27(1):133-136.
Pavlinov IY 2001. Geometric morphometries, a new analyticalapproach to comparison of
digitized images. Zoological Journal of Moscow 79: 1–27.
Prezoto, F.; Ribeiro-Júnior, C.; Oliveira, S. A. & Elisei, T.2007. Manejo de vespas e marimbondos
em ambientes urbanos. In: Pinto, A. S.; Rossi, M. M. &Salmeron, E. orgs. Manejo de pragas urbanas. Piracicaba, Ed.Piracicaba. p. 125-130.
41
Prezoto, F. & Clemente, M. A. 2010. Vespas sociais do ParqueEstadual do Ibitipoca, Minas
Gerais, Brasil. MG Biota 3(4)22-32.
Quicke DLJ, Laurenne NM, Fitton MG, Broad GR (2009) A thousandand one wasps: a 28S
rDNA and morphological phylogeny of the Ichneumonidae(Insecta: Hymenoptera) withan investigation into alignment parameter space and elision.Journal of Natural History43: 1305-1421.
Resende, J.J., G.M.M. Santos, C.C. Bichara-Filho and M. Gimenes.2001. Atividade diária de
busca de recursos pela vespa social Polybia occidentalis(Olivier, 1791) (Hymenoptera, Vespidae). Revista Brasileirade Zoociências 3: 105–115.
Richards, O.W. 1978. The social wasps of the Americas excludingthe Vespinae. London: British
Museum (Natural History). 580 pp.
Rojas, M. 1992 the species problem and conservation: what are weprotecting? Conserv. Biol. 6, 170–178.
Rohlf FJ, Marcus LF 1993. A revolution in morphometries. Trendsin Ecology and Evolution 3: 129–132
Ross, K. G., and R. W. Matthews. 1991. The Social Biology of Wasps.Ithaca: Comstock Pub.
Associates.
Santos, G. M. M.; Bichara Filho, C. C.; Resende, J. J.; Cruz, J.D. &. Marques, O. M. 2007.
Diversity and Community Structure of Social Wasps(Hymenoptera:Vespidae) in three Ecosystems in Itaparica
42
Island, Bahia State, Brazil. Neotropical Entomology36(2):180-185.
Samper, C. 2004 Taxonomy and environmental policy. Phil. Trans.R. Soc. Lond. B 359, 721 728.
(DOI 10.1098/ rstb.2004.1476.)
Sharkey MJ (2007) Phylogeny and classification of Hymenoptera.Zootaxa 1668: 521-548.
Sharkey MJ, Carpenter JM, Vilhelmsen L, Heraty J, Liljeblad J,Dowling APG, Schulmeister S,
Murray D, Deans AR, Ronquist F, Krogmann L, Wheeler WC(2011) Phylogeneticrelationships among superfamilies of Hymenoptera. Cladistics
27: 1-33.Silveira, O. T. 2002. Surveying Neotropical Social Wasps. Anevaluation of methods in the
“Ferreira Penna” research station (ECFPN), in Caxiuanã, PA,Brazil (Hym., Vespidae, Polistinae). Papéis Avulsos deZoologia 42(12):299-323.
Spradbery, J. P. 1973: Wasps. London, Sidgwick & Jackson; andSeattle, University of
Washington Press. 408 p.
Stone GN, Atkinson RJ, Rokas A, Nieves-Aldrey JL, Melika G, AcsZ, Csoka G, Hayward A,
Bailey R, Buckee C, McVean GAT (2008) Evidence forwidespread cryptic sexual generations in apparently purelyasexual Andricus gallwasps. Molecular Ecology 17:652–665
Spradbery, J.P. 1973. Wasps. An account of the biology andnaturalhistory of social and solitary
wasps. Seattle, UniversityWashignton Press, 408p
Santos, G.M. de M. & O.M. Marques. 1996. Análise faunística decomunidades de formigas
43
epigéias (Hymenoptera Formicidae) em dois agroecossistemasem Cruz das Almas - Bahia. Insecta 5: 1-17.
Santos, G.M. de M. 2000. Comunidades de vespas sociais(Hymenoptera-Polistinae) em três
ecossistemas do estado da Bahia, com ênfase na estrutura daguilda de vespas visitantes de flores de Caatinga. Tese dedoutorado, Faculdade de Filosofia, Ciências e Letras deRibeirão Preto/USP, 129p.
Simões, D. and M.R. Mecchi. 1983. Estudo sobre a fenologia dePolybia (Myrapetra) paulista
Ihering, 1896 (Hymenoptera, Vespidae). Naturalia 8: 185–191.
Smith, Deborah T (1991). Agriculture and the Environment: The1991 Yearbook of
Agriculture (1991 ed.). United States GovernmentPrinting. ISBN 0-16-034144-2.
Thomas, C. R. 1960: The European wasp (Vespula germanica Fab.) inNew Zealand. New
Zealand DS1R information series no. 27: 74 p.
Vecht J van der 1941. The Indo-Australian species of the genusRopalidia (=Icaria) (Hym.,
Vespidae) (first part). Treubia 18: 103-190.
Zoociên. 2: 33-39. Pleasants, J.M. 1983. Structure of plant andpollinator communities, P.375-393.
In G.E. Jones & R.J. Little (eds.), Handbook ofexperimental and pollination biology. New York, Van NostrandReinhold, 558p.