DOI: 10.22120/jwb.2020.131461.1164
Special issue 41-49 (2020)
Challenges for Biodiversity and Conservation in the Mediterranean Region
(http://www.wildlife-biodiversity.com/)
Research Article
Crustacean diversity of Ildırı Bay (Izmir, Turkey)
Murat Ozaydinli1*, Kemal Can Bizsel2
1
Ordu University, Fatsa Faculty of Marine
Science, Department of Fisheries Technology
Engineering, 52400, Ordu, Turkey,
2
Dokuz Eylül University, Institute of Marine
Sciences and Technology, 35340, Izmir, Turkey
*Email: muratozaydinli@gmail.com
Received: 22 July 2020 / Revised: 16 September 2020 / Accepted:
22 September 2020 / Published online: 21 October 2020. Ministry
of Sciences, Research, and Technology, Arak University, Iran.
Abstract
In this study, the crustacean diversity in Ildırı
Bay, which is characterized by a high density of
aquaculture activity and tourism, was
investigated. Sampling was carried out by boxcorer during four seasonal cruises (April, July,
November 2010, and February 2011) at eight
stations. Based on the analyzed samples,
Crustacea has been represented with two
classes, five orders, 25 families, and 40 species
in the study area. Amphipods were the dominant
taxon in terms of species richness (15 species),
followed by both tanaids (8 species) and
decapods (8 species). Although tanaids were the
most abundant taxon, decapods had the highest
biomass. The most abundant tanaid species was
Chondrochelia savignyi (Kroyer, 1842).
Crustacea abundance was negatively correlated
with depth.
Keywords: Amphipod, Benthic, Semi-enclosed
water, The Aegean Sea
Introduction
Crustaceans are a critical element of the marine
benthic ecosystem in terms of macrofauna
diversity and impact assessment. Many studies
have been conducted on crustacean species in
the Aegean Sea (Geldiay and Kocataş 1970,
Geldiay and Kocataş 1973, Katağan 1982,
Ergen et al. 1988, Kırkım 1998, Katağan et al.
2001, Koçak et al. 2001, Ateş 2003, Sezgin
2003, Yokeş et al. 2007, Anastasiadou et al.
2020). These studies and more have been
compiled by Bakır et al. (2014), who has given
a checklist. A total of 1028 Crustacean species
was reported along the Aegean Sea coast of
Turkey Bakır et al. (2014).
The Ildırı Bay is characterized by a high
intensity of aquaculture and tourism activities
(Demirel 2010, Bengil and Bizsel 2014). The
data from The Provincial Agriculture
Directorate (TIM) show that 15,690 tonnes of
aquaculture fish (sea bream, seabass, and
bluefin tuna) are produced by 20 facilities in
Ildırı Bay per year (Demirel 2010). There are
some studies that investigated the impact of
aquaculture on water quality (Basaran et al.
2007) and microplankton (Yurga et al. 2005) in
Ildırı Bay. Apart from research on aquaculture
impacts, studies on macrobenthos diversity of
the bay are very scarce. The molluscan fauna of
Ildırı Bay has been reported by Culha et al.
(2019) and Dogan et al. (2007). Additionally, a
new crustacean species (Ampithoe bizseli) was
reported by Özaydinli and Coleman (2012)
during sampling from a floating aquaculture
cage in Ildırı Bay. Although no study focuses
42| Journal of Wildlife and Biodiversity 4 (Special issue): 41-49 (2020)
on the crustacean diversity of Ildırı Bay, there
are some studies carried out as complementary
of the neighboring areas. Kocataş et al. (2001)
sampled only one station in Ildırı Bay in his
study on the benthic amphipods of Çeşme
Peninsula coasts. Mantıkçı (2009) investigated
the impact of aquaculture on the
macrozoobenthos in Gerence Bay, which is a
semi-enclosed marine region as an adjacent site
to Ildırı Bay.
The study aims to provide an understanding of
the crustacean fauna in Ildırı Bay, which is
intensely under the anthropogenic impact. This
is the first detailed study on the species
composition and diversity of the crustacean
fauna of Ildırı Bay.
Material and methods
Study Area
The Ildırı Bay is located at the middle-Western
coasts of the Anatolia Peninsula in Turkey. The
Çeşme and Karaburun peninsulas surround it.
At the bay entrance, some islands separate the
bay from Sakız (Chios) Strait (Fig. 1).
Sampling was carried out during four seasonal
cruises (April, July, November 2010 and
February 2011) aboard the ‘R/V DokuzEylül 1’
and ‘R/V K. Piri Reis’, at seven stations (St1St7) and one reference station (StR). St5 and
St7 were closed around the fish cages, while St6
was relatively distant away. The other four
stations, St1, St2, St3, and St4, were in the
shallower zone where the fish cages were
moored previously until the year that the study
began (Fig. 1). The bottom substrate
characteristics of the study stations were given
in Table 1.
Figure 1. Location of the study area (box on the left) and the stations (box on the right) (map produced
based on Schlitzer 2020)
A sampling of macrobenthic fauna
Sediment samples for analyzing macrobenthic
fauna were collected using Box Corer with a
sampling area of 0.25 m2. Three subsamples
from each sample were collected randomly by
using plexiglass sampling cores with 4.5 cm
internal diameter. Each subsample was
preserved in a plastic vial containing a 4%
formalin solution until the microscopic analysis
in the laboratory.
Before microscopic analysis, each sample was
sieved through a 0.5 mm mesh sieve and stored
in a plastic vial in 4% formaldehyde. The
samples were then sorted and analyzed under a
stereo-microscope. Crustacea specimens were
identified to lowest possible taxon level by
following the many different monographs,
papers, and guides (Bellan-Santini et al. 1982,
1989, 1993, 1998, Carpenter and Niem 1998
Kırkım 1998) and current taxonomic status
43 | Journal of Wildlife and Biodiversity 4 (Special issue): 41-49 (2020)
were checked by the World Register of Marine
Species (WoRMS Editorial Board 2020). Their
wet weight obtained rapidly after blotting the
excessive liquids on absorbent paper. The
number of individuals per unit area for each
taxa (ind. m–2) and their biomass per unit area
(g m–2) were determined.
Table 1. Characteristics of sampling stations
Stations
Biotope
Depth
St1
Fine sand, Silt-Clay, Posidonia
15
St2
Fine sand, Silt-Clay, Posidonia
10
St3
Fine sand, Silt-Clay, Posidonia
15
St4
Fine sand, Silt-Clay, Posidonia
20
St5
Coarse and Fine sand, Silt-Clay
50
St6
Coarse and Fine sand, Silt-Clay
50
St7
Fine sand, Silt-Clay
70
StR
Fine sand, Silt-Clay
60
Data analysis
The community parameters of the species were
calculated for each station and sampling period.
Diversity was calculated using the (log-based)
Shannon-Wiener index (H’) (Shannon and
Weaver 1949), and evenness index (J’) was
calculated following Pielou (1977).
Cluster analysis was performed using the BrayCurtis similarity index values (Bray and Curtis
1957) to obtain the degree of similarity in
species composition of crustaceans among
sampling stations. Prior to this analysis, the data
have been transformed (log x+1), according to
the procedure described in Clarke and Warwick
(2001), for minimizing the influence of
dominant and rare taxa. Calculations and
analyses were done using the PRIMER v.5
software package. Spearman Rank Order
Correlation between crustacean abundance and
depth was done using the STATISTICA 8.0
software package.
Results
In the study area, the crustaceans were
represented by two classes, five orders, 25
families, and 40 species. Even though
Ostracoda are classified as members of
meiofauna, they were also included in the
analysis, as they retained on the sieves.
Systematics of the species found at the study
site are presented in Table 2.
Amphipods were the dominant taxon in terms
of species richness (15 species), followed by
both tanaids (8 species) and decapods (8
species). Cumaceans and isopods were
represented by 4 and 3 species, respectively.
Although tanaids were the most abundant taxon
with 6,180 and./m2 in total, decapods had the
highest biomass (5.73 g/m2, 42 % of total).
Nevertheless, amphipods have the highest
species number, which have ranked them as the
secondary taxon in terms of both abundance
and biomass.
The most abundant tanaid species was
Chondrochelia savignyi (Krøyer, 1842), with
4,236 and./m2 in total (Fig. 2). Chondrochelia
savignyi was found in every sampling periods
at St1 and St2, but rarely at St3 and St4. This
species was never found at stations that closed
to the floating cages offshore.
Three species, Harpinia dellavallei Chevreux,
1910, Perioculodes longimanus angustipes
Ledoyer, 1983, and Agathotanaidae (sp.) were
only found in StR. Besides, Achaeus cranchii
Leach. 1817 was the species found at St7 only
in a single sampling period.
45 | Journal of Wildlife and Biodiversity 4 (Special issue): 41-49 (2020)
Table 2. Systematic of the Crustacea species at the study site
Class
Malacostraca
Order
Amphipoda
Family
Ampeliscidae
Phoxocephalida
e
Leucothoidae
Corophiidae
Maeridae
Aoridae
Oedicerotidae
Tanaidacea
Agathotanaidae
Apseudidae
Leptocheliidae
Leptognathiida
e
Cumacea
Tanaidae
Paratanaoidea
Nannastacidae
Isopoda
Leuconidae
Bodotriidae
Gnathiidae
Decapoda
Inachidae
Paguridae
Callianassidae
Ethusidae
Galatheidae
Diogenidae
Processidae
Ostracoda
Species
Ampelisca sp.
Ampelisca jaffaensis (Bellan-Santini & Kaim-Malka, 1977)
Ampelisca sarsi (Chevreux 1888)
Ampelisca truncata Bellan-Santini & Kaim-Malka, 1977
Ampelisca typica (Bate 1856)
Harpinia dellavallei Chevreux 1910
Leucothoe sp.
Leucothoe oboa Karaman 1971
Leucothoe venetiarum Giordani-Soika 1950
Leptocheirus longimanus Ledoyer 1973
Maera sp.
Microprotopus cf. maculatus Norman 1867
Perioculodesa equimanus (Korssman 1880)
Perioculodes longimanus angustipes Ledoyer 1983
Synchelidium longidigitatum Ruffo 1947
Agathotanaidae (sp.) 1
Apseudes latreillii (Milne-Edwards 1828)
Heterotanais oerstedii (Kroyer 1842)
Chondrochelia savignyi (Kroyer 1842)
Araphura brevimanus (Lilljeborg 1864)
Akanthophoreus gracilis (Krøyer 1842)
Tanais dulongii (Audouin 1826)
Pseudoparatanais batei (Sars 1882)
Campylaspis sp.
Cumacea (sp.)
Eudorella truncatula (Bate 1856)
Iphinoe sp.
Gnathia sp.
Gnathia vorax (Lucas 1849)
Gnathia oxyuraea (Lilljeborg 1855)
Achaeus cranchii Leach 1817
Anapagurus sp.
Callianassa subterranea (Montagu 1808)
Ethusa mascarone (Herbst 1785)
Galathea intermedia Liljeborg 1851
Paguridae (sp)
Paguristes syrtensis De Saint Laurent 1971
Processa cf. canaliculata Leach 1815
Ostracoda (sp.) 1
Ostracoda (sp.) 2
46| Journal of Wildlife and Biodiversity 4 (Special issue): 41-49 (2020)
Figure 2. Dominance of species (left); Abundance and composition of the species (right) in Ildırı Bay
Results of Shannon-Wiener diversity and
Pielou’s evenness indices were presented in
Table 3. St2 was the richest station in terms of
Crustacea species for all sampling periods
except April 2010. Hence, the highest diversity
values were obtained in this station, i.e.,
H’=1.83 and H’=1.67 in July and November
2010, respectively. As a consequence of higher
abundance of C. savignyi (Kroyer, 1842), the
highest abundance values were found at St2 and
St4 in July 2010 and February 2011,
respectively. No species were detected at
stations: N'10-St3, J'10-St7, N'10-St7.
When seasonal data were pooled for each
station, St2 had the highest species number (19
species), while St4 had the highest number of
individuals (Fig. 2). According to correlation
analysis, Crustacea abundance was negatively
correlated with depth (r=-0.5054, p<0.05).
A dendrogram for hierarchical clustering of the
Crustacea abundances at the study site, using
group-average clustering of Bray-Curtis
similarities, is shown in Fig. 3. As seen in this
dendrogram, the outer stations (St5, St6, St7
and StR) differentiated from the inner stations
(St1, St2, St3, and St4), in terms of abundance
of Crustacea species. The similarity between
these two groups was lower than 20 %. C.
savignyi (Kroyer, 1842), Ostracoda (sp.) 1 and
Eudorella truncatula (Bate, 1856) were mainly
responsible for the dissimilarity between the
inner and the outer stations. StR differentiated
from the other stations in all sampling periods
except in July 2010 (J_R) due to presence of C.
savignyi (Kroyer, 1842).
Figure 3. A dendrogram for hierarchical clustering of the crustacean abundances at the study site
46| Journal of Wildlife and Biodiversity 4 (Special issue): 41-49 (2020)
Table 3. Community parameters of crustacean species
Stations
Number of
Species
Total
Individual
Pielou
Evenness
Shannon-Wiener
Diversity
St
S
N(ind./m2)
J'
H'(loge)
1
5
3
1
3
2
1
1
1
2
9
2
3
4
3
3
4
7
1
2
2
1
3
10
3
5
1
5
1
1
700
839
419
629
419
210
210
210
419
1205
419
301
231
208
629
693
372
210
419
72
210
839
432
60
1779
210
165
140
210
0.89
0.95
0.00
1.00
1.00
0.00
0.00
0.00
1.00
0.83
1.00
0.95
1.00
0.95
1.00
0.68
0.86
0.00
1.00
1.00
0.00
0.95
0.62
0.95
0.70
0.00
0.93
0.00
0.00
1.43
1.04
0.00
1.10
0.69
0.00
0.00
0.00
0.69
1.83
0.69
1.04
1.39
1.04
1.10
0.94
1.67
0.00
0.69
0.69
0.00
1.04
1.43
1.04
1.12
0.00
1.49
0.00
0.00
April' 10
2
3
4
5
6
7
R
1
July' 10
2
3
4
5
6
November' 10
R
1
2
4
5
6
R
1
February' 11
2
3
4
5
6
7
R
Discussion
In this study, 40 crustacean species were
recorded, and amphipods were the dominant
taxon in species numbers (15 species). Kocataş
et al. (2001), in his study investigating the
benthic amphipods of the coast of the Çeşme
Peninsula, identified four amphipod species in
one station located in Ildırı Bay.
According to Bakır et al. (2014), 484 Crustacea
species were recorded in the soft substrate in the
Aegean Sea in a depth range of 0–100 m. In the
same study, the distribution of the Arthropoda
species was mapped along the coast of Turkey.
According to this map, there are between 60–79
arthropod species in the coastal areas of Ildırı
Bay and between 14–24 species in the more
exposed areas.
Mantıkçı (2009) found 13 crustacean species in
his study investigating fish-farm impact in
Gerence Bay, which is adjacent to Ildırı Bay.
Only two species, Tanais dulongii (Audouin,
1826) and Callianassa cf. subterranean
(Montagu, 1808)were in common with our
study.
Aslan-Cihangir and Panucci-Papadopoulou
(2011) reported that depth is an essential factor
in peracarid distribution patterns (Robertson et
al. 1989, Corbera and Cardell 1995, Lourido et
47 | Journal of Wildlife and Biodiversity 4 (Special issue): 41-49 (2020)
al. 2008) and they found negative correlation
(r=-0.4424, p<0.05) between peracarid
abundance and depth. As well as in our study,
Crustacea abundance was negatively correlated
with depth (r=-0.5054, p<0.05).
Despite limited knowledge on the bay's
biodiversity obtained from the scarce previous
study, the contribution of this study, as being
the first systematical study, indicated the
potential of the region in terms of area.
Acknowledgments
This work forms part of the MSc thesis of the
first author. This study was funded by The
Scientific and Technological Research Council
of Turkey (TUBITAK, Project no: 107Y225).
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