Linking Fish and Crustacean Taxonomic Composition With Seasonal Contrasts in The Soft-Bottom Intertidal Zone
Linking Fish and Crustacean Taxonomic Composition With Seasonal Contrasts in The Soft-Bottom Intertidal Zone
Linking Fish and Crustacean Taxonomic Composition With Seasonal Contrasts in The Soft-Bottom Intertidal Zone
234129
ISSN 1519-6984 (Print)
Original Article
ISSN 1678-4375 (Online)
b
Department of Fisheries and Aquaculture, University of Veterinary and Animal Sciences, Lahore, Pakistan
c
Department of Bioscience and Biotechnology, Chungnam National University, South Korea
Centre of Excellence in Marine Biology, University of Karachi, Pakistan
d
e
Government College Women University, Faisalabad, Pakistan
f
Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia
*e-mail: physioatique@gmail.com, shahidmahboob60@hotmail.com
Abstract
The primary objective of this study was to investigate the seasonal fish and crustacean variations concerning taxonomic
composition, species richness, and diversity in sandy beach habitat. For this purpose, we investigated the Sonmiani
Hor lagoon area during four distinct seasons, i.e., northeast (NE) monsoon, pre-monsoon, south-west (SW) monsoon,
and post-monsoon for one year. During each haul, the net was pulled about 100m along the beach in 0.5m depth. The
results showed a strong linear correlation between the diversity index and equitability in fishes (r = 0.978). The diversity
index was strong negatively correlated with the abundance and biomass (r = -0.978, -0.972, respectively). The physical
attributes like sea surface water temperature and salinity showed a strong negative effect on species assemblages
(r = -0.981 and -0.943, respectively). The mean air and water temperature illustrated approximately 3°C difference
during NE and pre-monsoon seasons. However, salinity, pH, and electrical conductivity did not show any significant
seasonal variabilities. Under the ecological indices, the fish species displayed higher diversity (H’ = 3.19) during SW
monsoon, whereas the lowest diversity was observed during pre-monsoon (H’ = 1.58). The equitability and species
richness, however, remained more noticeable during SW monsoon (J’ = 0.81). The total number of individuals of fish
and crustaceans reached 4799 with 3813 fish individuals and 986 individuals of crustaceans. A total of 27 families
of fish while five crustacean families comprising of 30 genera and 38 fish species while ten genera and 17 species
of crustaceans were recorded. Liza subviridis displayed the highest abundance among the sampled fish species. In
conclusion, fish species constituted a significant part of the coastal fauna in the study area. The seasonal variations
displayed distinct variations in fish species composition and diversity.
Keywords: seasonal variations, soft bottom, intertidal zone, Sonmiani Bay, species diversity, Mangroves.
Resumo
O objetivo principal deste estudo foi investigar as variações sazonais de peixes e crustáceos em relação à composição
taxonômica, riqueza de espécies e diversidade no habitat de praias arenosas. Para esse fim, investigamos a área da
lagoa Sonmiani Hor durante quatro estações distintas, ou seja, monção nordeste (NE), pré-monção, monção sudoeste
(SW) e pós-monção, por um ano. Durante cada transporte, a rede foi puxada cerca de 100 m ao longo da praia, a 0,5 m
de profundidade. Os resultados mostraram uma forte correlação linear entre o índice de diversidade e a equitabilidade
de peixes (r = 0,978). O índice de diversidade apresentou forte correlação negativa com a abundância e a biomassa
(r = -0,978 e -0,972, respectivamente). Os atributos físicos, como temperatura da água da superfície do mar e salinidade,
apresentaram forte efeito negativo sobre o conjunto de espécies (r = -0,981 e -0,943, respectivamente). A temperatura
média do ar e da água teve uma diferença de aproximadamente 3 °C durante a monção NE e a pré-monção. No
entanto, salinidade, pH e condutividade elétrica não apresentaram variabilidade sazonal significativa. A respeito dos
índices ecológicos, as espécies de peixes apresentaram maior diversidade (H’ = 3,19) durante a monção SW, enquanto
a menor diversidade observada foi na pré-monção (H’ = 1,58). A equitabilidade e a riqueza de espécies, no entanto,
1036 1036/1049 Braz. J. Biol., 2021 , vol. 81, no. 4 pp.1036-1049
Links between fish and crustacean composition with seasonal contrasts
permaneceram mais perceptíveis durante a monção SW (J’ = 0,81). O número total de peixes e crustáceos foi de 4.799,
com 3.813 peixes e 986 crustáceos. Foram registradas 27 famílias de peixes e 5 famílias de crustáceos, com 30 gêneros
e 38 espécies de peixes, além de 10 gêneros e 17 espécies de crustáceos. Liza subviridis apresentou a maior abundância
entre as espécies de peixes amostradas. Em conclusão, as espécies de peixes constituíram uma parte significativa da
fauna costeira na área de estudo. As variações sazonais apresentaram variações distintas na composição e diversidade
das espécies de peixes.
Palavras-chave: variações sazonais, fundo macio, zona entremarés, Baía de Sonmiani, diversidade de espécies,
Manguezais.
nested in a large mangrove area. The leading aims of this seasonal rivers enter the bay; the Porali River that drains
investigation included the study of fish and crustacean through the Bela region and empties into the central part of
species diversity, linking the species abundance with the the bay, and the Windor River that enters near the mouth.
hydrographic factors, taxonomic identification of fish and The total area of the bay is 125.5 km2 and is characterized
crustacean species, seasonal variations of hydrographic by the sandy beach, intertidal mudflats, and the muddy
observations, application of species diversity indices, fish beach adjacent to mangrove forests (Figure 1). Based on
and crustaceans assemblage structure and estimation of the seasonal precipitation intensity and related factors, we
biomass in Sonmiani Bay, Baluchistan, Pakistan. divided the study area climate into four distinct seasons:
northeastern (NE) monsoon, pre-monsoon, southwest
2. Material and Methods (SW) monsoon, post-monsoon.
Damb is a small coastal town with an estimated
2.1. Study area
population of 15,000 inhabitants, located along Miani Hor.
Pakistan falls in the subtropical zone, and its coastal Most of the inhabitants depend on the capture fisheries,
regions undergo mixed semidiurnal tides. Therefore, a either directly or indirectly. However, Damb is more
clear difference in tidal heights alternatively inundates the famous for its trash fish and shrimp production. There
intertidal zone twice a day. Consequently, the intertidal is an informal fishing jetty that entertains all sorts of
zone receives abundant and nutrient-laden waters with outboard fishing engines used in fishing boats. This part of
equal chances of squandering the salubrious nutrients the coastline is predominantly sandy with few patches of
to the open waters. On the other hand, fine sediments sandy cum muddy and sparse patches of black mangrove
get ensnared by mangrove trees that further stabilize the (Avicennia marina). The coastline area covered by Damb
coastline, along with nutrients that support the endemic is approximately five km long.
and visiting organisms in the intertidal zone.
The Miani Hor is a lagoon in Sonmiani Bay, situated 2.2. Field sampling
approximately 90 km from Karachi Metropolitan on the We identified two sampling stations on the sandy beach
easternmost coast of Baluchistan. The bay spreads on 60 km along the coast of Miani Hor. All the sampling events were
length and 7 km width with a tortuous and contorted body conducted by employing the seine net (10 m x 2.5 m and
of water and is connected to the sea on the southeastern 0.5 cm mesh size) operated by two persons in the shallow
end by a 4 km wide mouth. It takes a western turn by a surfing zone and covering 100 m of the beach in each haul.
short distance from its mouth. It then runs parallel to the The sampling events were conducted on a seasonal basis
shoreline in the shape of an arc, with an endpoint in the (northeast monsoon, pre-monsoon, south-west monsoon,
same line as its mouth (Rasool et al., 2002). The Hor is and post-monsoon) at each study station from January to
fed by Sonmiani bay lying outside in the Arabian Sea. Two December 2003.
the degree of displacement of EC in the SW monsoon and during pre-monsoon (H’ = 1.58). The other ecological
post-monsoon manifested higher variations as 68.37 and indices, e.g., equitability and species richness, remained
72.86 mS/cm, respectively. more noticeable during SW monsoon (J’ = 0.81) except for
a little increase in species richness of fish during the NW
3.2. Ecological indices
monsoon (S = 0.26). In the case of crustaceans, however,
There is a comparison of the percent abundance of the diversity was the highest in NE monsoon (H’ = 2.23),
fish and crustacean species in the study area in Figure 2, where equitability and species richness were more elevated
showing the diversity among the two animal groups in NW monsoon and post-monsoon (J’ = 0.70; S = 0.40,
varied throughout different seasons in the study period. respectively).
Fish species displayed higher diversity (H’ = 3.19) during The diversity and equitability indices displayed a
SW monsoon, whereas the lowest diversity was observed robust linear correlation displayed (r = 0.978) in the fish
species. The diversity index significantly correlated with the
abundance and biomass (r = -0.978, -0.972, respectively),
whereas the number of species exhibited significantly
higher species richness and biomass (r = -0.996, 0.954,
respectively). On the other hand, the physical attributes
such as sea surface WT and salinity displayed a strong
relationship with the fish assemblage (r = -0.981 and -0.943,
respectively; Table 2). However, most of the physical and
biological characteristics of crustacean assemblages did
not explain any significant correlation except for species
richness was found to be correlated with the number of
individuals of various species that occurred at the same
time (Table 2). Two-way ANOVA did not show any
significant differences in diversity index, equitability
between seasons, and groups except for species richness
within groups (p = 0.018) when α = 0.05.
3.3. Assemblage structure, number of species and
specimens
Figure 2. Seasonal comparison between percentage
abundance and biomass of fishes and crustaceans along the Over twelve months, the total number of individuals
coast of Miani Hor, (ABD = Abundance, BM = Biomass, (TNI) of collected amounted to 4,799 with fish TNI 3,813,
Crust = Crustacean, NEM = North-east monsoon, and crustaceans TNI 986 from Miani Hor intertidal sandy
PREM = Pre-monsoon, SWM = South-west monsoon, substratum. When we further breakdown the catch statistics
POSM = Post-monsoon). of our study, a total of 27 fish families and five crustacean
Table 2. Pearson correlation matrix showing the relationships between biotic and abiotic parameters of the Fish (A) and
Crustaceans (B) community structure.
Parameters D E SR % ABD % BM Species Ind TW
E 0.95* (A)
SR 0.61 0.53
% ABD -0.97* -0.88 -0.72
% BM -0.53 -0.51 -0.97* 0.61
Species -0.58 -0.48 0.99* 0.70 0.95*
Ind 0.02 0.18 0.58 -0.04 -0.75 -0.54
TW -0.006 -0.21 -0.45 -0.01 0.65 0.40 -0.98*
Salinity -0.001 0.06 0.71 -0.08 -0.83 -0.70 -.94* -0.86*
E 0.05 (B)
SR -0.79 -0.008
% ABD -0.46 0.33 -0.10
% BM 0.41 0.42 -0.80 0.61
Speceis 0.75 -0.25 -0.96* 0.01 0.66
Ind -0.26 0.44 -0.28 0.97* 0.76 0.15
TW -0.73 -0.71 0.61 0.01 -0.65 -0.41 -0.19
Sal 0.84 0.34 -0.93* 0.08 0.83 0.81 0.29 -0.86*
D = Diversity; E = Equability; SR = Species Richness; ABD = Abundance; BM = Biomass; Ind = Individuals; TW = Total Weight.
Asterix sign indicates very strong correlation.
families were sampled that further comprised of 30 genera There was a close link between the assemblage of various
and 38 fish species, and ten genera with 17 species of families representing the marine groups along the soft
crustaceans. Most of the samples were collected during bottom sandy coast in Miani Hor, and the fish species
the post-monsoon (27) and pre-monsoon (26), whereas constituted the significant number pelagic organisms shaping
SW monsoon and NE monsoon showed a lower number the underwater community of the shallow intertidal zone.
of individuals. We noticed an evident variation in fishes
3.4. Taxonomic abundance and biomass
over the study period. For instance, in NE monsoon and
pre-monsoon, 14 fish species were caught in each season, Here we give a detailed account of the taxonomic
while for SW monsoon and post-monsoon, 15 and 21 fish abundance and percent biomass of the crustaceans and
species were caught, respectively. However, we noticed a fish species in the study area in four distinct seasons,
different situation in the crustacean assemblage, where NE i.e., NE monsoon, premonsoon, SW monsoon and post-
monsoon and pre-monsoon revealed a higher number of monsoon. The total abundance of fish and crustaceans
species; nine and eight, respectively. The other two seasons, species recorded during NE monsoon was equal to 77.48%,
i.e., SW monsoon and post-monsoon, exhibited a lower out of which, the family Sillaginidae, represented by
number of species, seven and six, respectively (Table 3). Sillago sihama scored the highest abundance (23.64%)
A significant difference in the number of species and and constituted the most significant share (39.33%) of
specimens revealed among animal groups (p = 0.019 and the total biomass (2389.01 g), followed by Liza subviridis
p = 0.016), but no variation was detected between seasons. (21.15%) from family Mugilidae (Table 4). However,
Table 3. Presence dynamics of fish and crustacean species and families based on seasonal changes at Miani Hor (Sonmiani
Bay).
Fish Crustacea
Season
Family Species Family Species
NE monsoon 11 14 5 9
Pre-monsoon 18 14 4 8
SW monsoon 11 15 2 7
Post-monsoon 14 21 3 6
NE = Northeast, SW: Southwest.
Table 4. Abundance and biomass estimation of various intertidal soft-bottom taxonomic groups collected from Miani Hor
(Sonmiani Bay) during northeast monsoon season.
Family Species N Abundance (%) Biomass(g) Biomass (%)
Mugillidae L. subviridis 358 21.15 80.07 3.35
L. carinata 176 10.4 267.61 11.2
Sillaginidae S. sihama 400 23.64 939.81 39.33
Soleidae S. elongate 7 0.41 10.31 0.43
E. orientalis 1 0.05 3.32 0.13
Gobiidae B. dussumeiri 198 11.7 105.36 4.41
Scienidae Scienidae juveniles 55 3.25 25.47 1.06
O. cuverii 74 4.37 67.61 2.83
Platycephalidae P. indicus 1 0.05 0.31 0.01
Bothidae P. elevates 3 0.17 2.04 0.08
Scorpaenidae S. maculata 3 0.17 59.24 2.47
Teraponidae Terapon jarbua 7 0.41 2.08 0.087
Stegostomatidae S. commersonii 25 1.47 20.82 0.87
Leignathidae L. daura 3 0.17 9.1 0.38
Portunidae P. pelagicus 89 5.26 480.56 20.11
P. sanguinolentus 2 0.11 7.31 0.3
C. cruciata 1 0.05 3.26 0.13
Leucosiidae P. globosa 1 0.05 0.78 0.03
Calappidae A. lunaris 67 3.95 71.44 2.99
Penaeidae M. stebbingi 141 8.33 127.96 5.35
M. brevicornis 52 3.07 33.57 1.4
M. affinis 27 1.59 51.83 2.16
Diogenidae C. padavensis 1 0.05 19.15 0.8
Total 1692 2389.01
L. carinata contributed 11.20% of the total biomass as P. pelagicus contributed 4.66% in the overall biomass of
well. The mudskippers (Family: Gobiidae) were also the season as well (Table 5).
found in the same season with abundance and biomass of Linked with increasing sea surface WT and salinity, a
11.70% and 4.41%, respectively. The overall biomass of comparatively lowered abundance of fish species (61.21%)
fish species was more than double (66.68%) of the same and higher seasonal abundance of crustaceans (38.78%)
for crustaceans (33.27%). The crustacean species persisted indicated a paradigm shift in the species composition
lower in abundance (22.51%). However, crustaceans were during the SW monsoon season (Table 6), as compared to
represented by five families with Metapenaeus stebbingi the NE monsoon and pre-monsoon seasons. Further, the
abundance as 8.33% and Portunus pelagicus as 5.26%. species displayed even distribution with an overall smaller
However, concerning biomass, the Portunus pelagicus number of species sampled during this season (≤ 10% in
alone accounted for higher biomass (20.11%) in the abundance). For sample, only Secutor insidiator (10.31%)
shellfish group. was the most abundant as well as higher in sharing the
The ensuing season (pre-monsoon) revealed the highest 10.86% of the total seasonal biomass sampled, followed
abundance (96.05%) of fish species and the lowest for by Escualosa thoracata (8.61%) and juveniles of carangids
crustaceans (3.94%) during this investigation. Liza subviridis and Thryssa spp.(7.75% each), which constituted the central
(Family: Mugilidae), was the species showing the highest part of overall biomass of fish species (79.05%). However,
abundance (71.19%) with convincing share in biomass L. subviridis turned to be one of the dominant species
(40.98%) as well when compared with all other finfish in biomass contribution (13.05%) besides E. thoracata
catch (Table 5). However, Leiognathus berbis (5.80%) and (16.17%). An essential assemblage in the SW monsoon
Secutor insidiator (5.14%) were detected in relatively less existed in the abundance of post-larvae (PLs) of penaeid
abundance while other fish species even <1%. Although shrimps (31.10%). M. stebbingyi secured a higher place
crustaceans were much lower in abundance, Penaeus in biomass (11.32%) of the crustacean species on the
indicus (family: Penaeidae) abundance (2.19%) remained overall biomass distribution during the SW monsoon
the highest of all the crustaceans during pre-monsoon. The season (Table 6).
Table 5. Abundance and biomass estimation of various intertidal soft-bottom taxonomic groups collected from Miani Hor
(Sonmiani Bay) during premonsoon season.
Family Species N Abundance (%) Biomass Biomass (%)
Mugillidae L. subviridis 650 71.19 1177.37 40.98
Sillaginidae S. sihama 10 1.09 188.5 6.56
Soleidae S. elongata 3 0.32 25.26 0.87
Gobiidae B. dussueiri 2 0.21 1.63 0.56
Lactariidae L. lactarius 8 0.87 27.96 0.97
Leignathidae L. blochi 8 0.87 15.01 0.52
L. berbis 53 5.8 333.04 11.59
S. insidiator 47 5.14 60.36 2.1
Tetradontidae L. lagocephalus 1 0.1 7.87 0.27
Scatophagidae S. argus 2 0.21 627.25 21.83
Clupeidae E. thoracata 39 4.27 26.67 0.92
N. nasus 3 0.32 13.79 0.47
Carangidae A. melanoptera 2 0.21 15.55 0.54
C. talamproides 1 0.1 9.19 0.31
Belonidae S. strongylura 1 0.1 0.13 0.004
Engrualidae T. mystax 2 0.21 2.93 0.1
Serranidae E. fasciatus 44 4.81 24.49 0.85
Fistularidae F. commersonii 1 0.1 0.61 0.02
Portunidae P. pelagicus 1 0.1 134.04 4.66
C. cruciata 1 0.1 3.34 0.11
Calappidae A. lunaris 7 0.76 29.2 1.01
Penaeidae P. indicus 20 2.19 36.26 1.26
P. merguiensis 1 0.1 0.97 0.033
M. stebbingi 1 0.1 1.45 0.05
Diogenidae C. padavensis 4 0.43 88.43 3.07
C. avarus 1 0.1 21.67 0.75
Total 913 2872.97
Table 6. Abundance and biomass estimation of various intertidal soft-bottom taxonomic groups collected from Miani Hor
(Sonmiani Bay) during the southwest monsoon season.
Family Species N Abundance (%) Biomass Biomass (%)
Mugillidae L. subviridis 38 2.94 124.06 13.05
L. carinata 37 2.87 51.62 5.43
Sillaginidae S. sihama 5 0.38 14.91 1.56
Teraponidae T. jarboa 2 0.15 10.17 1.07
Leiognathidae S. insidiator 133 10.31 103.22 10.86
Hemiramphidae H. dussumerii 66 5.12 30.52 3.21
Carangidae Carangidae Juveniles 100 7.75 12.6 1.32
S. leptolepis 2 0.15 25.19 2.65
Engraulidae Thryssa Juveniles 100 7.75 34.69 3.65
S. gibbosa 4 0.31 9.89 2.65
Gerridae G. filamentosus 2 0.15 4.99 0.52
Lactaridae L. lactarius 88 6.82 83.58 8.79
Clupeidae Clupeide Juveniles 100 7.75 90.52 9.52
E. thoracata 111 8.61 153.7 16.17
Tetradontidae L. lagocephalus 1 0.07 1.42 0.14
Calappidae A. lunaris 2 0.15 20.54 2.16
M. planipes 23 1.78 12.52 1.31
Penaeidae M. stebbingi 58 4.49 107.57 11.32
M. brevicornis 13 1 8.16 0.85
P. penicillatus 2 0.15 7.86 0.82
P. merguiensis 1 0.07 2.94 0.3
PLs of Penaeidae 401 31.1 39.44 4.15
Total 1289 950.13
PLs = Post larvae.
Table 7. Abundance and biomass estimation of various intertidal soft-bottom taxonomic groups collected from Miani Hor
(Sonmiani Bay) during post monsoon season.
Serial No. Taxonomic Group N Abundance (%) Biomass Biomass (%)
Mugillidae L. subviridis 466 51.49 1167.89 35
L. carinata 43 4.75 38.42 1.15
L. vaigiensis 1 0.11 17.55 0.52
Sillaginidae S. sihama 176 19.44 447.58 13.41
Leiognathidae L. splendens 1 0.11 34.39 1.03
Teraponidae T. jarboa 10 1.1 81.03 2.42
Carangidae A. melanoptera 1 0.11 36.27 1.08
Engrualidae S. sindensis 1 0.11 1.74 0.05
Thryssa Juveniles 66 7.29 16.35 0.49
Engraulidae Juveniles 19 2.09 2.28 0.06
Mullidae U. vittatus 8 0.88 126.22 3.78
Hemiramphidae H. limbatus 30 3.31 66.55 1.99
H. dussumerii 1 0.11 25.14 0.75
Bothidae P. arsius 2 0.22 91.68 2.74
P. elevates 1 0.11 102 3.05
Stegostomidae S. commersonii 2 0.22 5.11 0.15
Lutjanidae L. fulviflammus 1 0.11 16.1 0..48
Pomadasydidae P. olivaceaum 1 0.11 8.14 0.24
Clupeidae I. melastoma 2 0.22 6.84 0.2
Platycephalidae C. crocodilla 1 0.11 64.63 1.93
P. indicus 2 0.22 926.41 27.76
Calappidae A. lunaris 2 0.22 8.72 0.26
Penaeidae P. sculptilis 3 0.33 0.28 0.008
PLs of shrimps 49 5.41 5.64 0.16
M.. monoceros 12 1.32 5.62 0.16
Diogenidae C. padavensis 2 0.22 22.15 0.66
D. diogenes 1 0.11 0.89 0.02
Total 905 3336.67
between the two locomotory animal groups (fish and frequent visitors and utilize the inshore areas as feeding
crustaceans (), by utilizing the beach seine net and beam and refuge grounds, as the low mid-tide circumstances
trawls. This research sampling resulted in the overall favor these opportunities. Moreover, the sea surface WT
presence of 27 families of fish comprising of 38 species. could be changing while the ebb tides generate turbulence
The seasonal variation in fish was not very characteristic as in the semi-enclosed lagoon stretch. Therefore, the species
a lower number of fish species were found in NE monsoon richness was higher as compared to the pre-monsoon
and pre-monsoon (14) in comparison with the highest and post-monsoon, corresponding to the diversity index.
fish variation during the post-monsoon (21) season. Few Silva et al. (2011), correlated the low species richness
ichthyofaunal families could be characterized as native of some benthic groups with specific environmental
and permanent residents, though one or more fish species parameters and physiological stress. According to Kinne
continued benefiting from the shallow coast of the Miani (1971), increased salinity worked as a favorable factor to
Hor. The salient examples incorporate family Mugilidae most macrofaunal taxa resulting in boosting their density
(Liza subviridis, L. carinata, and L. vaigiensis); family and diversity. Although the species abundance varied
Sillaginidae (Sillago sihama), family Leiognathidae (Secutor throughout this investigation, however, inter-seasonal
insidiator, Leiognathus daura, L.blochi, L.berbis), family species distribution prevailed for higher reflection.
Teraponidae (Terapon jarbua), Engraulidae (Thryssa mystax, The species abundance and variation could be a
Sardinella gibbosa, S. sindensis); Family Clupeidae (Ilisha function of sea WT. Generally, the estuarine benthic fauna
melastoma, Escualosa thoracata, Nematolosa nasus); belongs to Polychaeta, Crustacea, and Mollusca, which
family Bothidae (Pseudorhombus arsius, P. elevatus) and shows a higher tolerance to the environmental stress and
family Platycephalidae (Platycephalus indicus). substantial changes in the spatial and temporal structure of
The expanding diversity during NE monsoon and the community. Several studies hinted at the temperature as
SW monsoon implied that several fish species are the one of the most critical environmental variables that control
the marine life (Bhaud et al., 1995), especially during the determining that macrotidal dissipative beaches supported
reproduction and larval stages, recruitment patterns, and communities having higher richness, abundance, and biomass
metabolism are the essential elements that are directly than microtidal reflective beaches (McLachlan, 1990;
influenced by the WT (Sinclair, 1988; Bhaud and Cha, McLachlan et al., 1993). The distribution and abundance
1992). According to another research, predicting long term also vary in the intertidal zone affected by tidal phases and
changes in benthic communities is an elusive goal owing tidal states during distinct seasons. The physical structure
to the exceptionally long duration required to monitor such of the ecosystem belongs to the ocean and sandy beaches
confounding alterations that could have appeared because and is characterized by three variables: the sand grain size,
of temperature changes (Gray and Christie, 1983). The wave climate, and tidal regime. The resulting interactions
fish species were small-size and mostly at the juvenile among three factors feature an array of beach morpho-
and sub-adult life stages. As the surfing zone is a complex dynamics, that broadly range from microtidal reflective
habitat that equally serves as the shelter and feeding zone beaches (narrow and steep) to macrotidal dissipative
for several organisms. The higher density of juvenile and systems (broad and flat, with tidal flats) (Short, 1996).
small-sized fish species symbolizes that sandy beaches are Because beach ecosystems lack biological structures, the
rendering an alternative nursery habitat to estuaries for many intertidal macrofaunal communities have been physically
species. Lasiak (1984) proposed that the utilization of the controlled by the Autecological Hypothesis. The infaunal
surfing zone by large numbers of juveniles favor the use communities respond differently in the presence of
of shallow sandy beaches as a nursery ground due to the monsoon that occurs frequently, and its magnitude varies
abundant supply of food in the form of zooplankton and (Alongi, 1989). George et al. (2009) studied the benthic
avoidance from predation further encourages by shallow macroinvertebrate fauna and tried to develop its link with
waters coupled with higher turbidity and turbulence in the physicochemical parameters in the Niger Delta and
the zone. It is also imperative that habitats do not remain stated that many invertebrates play an essential role in
constant but vary regularly on a daily and seasonal basis. the circulation and recirculation of nutrients in aquatic
Therefore, we noticed a characteristic variation in the ecosystems. Besides, there are important links between
species distribution, abundance, and diversity in Miani Hor. unavailable nutrients held in detritus and useful protein
Species richness, abundance, and biomass are three materials in fish and shellfishes. Most benthic organisms
of the most frequently investigated ecological attributes feed on debris that settles on the bottom of the water and
of the sandy beach macrobenthic communities at the in turn, serves as a food source for the full range of fish
large-scale comparative studies. Fish species equally share species (Ajao and Fagade, 1990; Oke, 1990; Idowu and
this shallow intertidal zone, therefore, abundant diversity Ugwumba, 2005; Uwadiae, 2009).
and distribution lessen the equal chances of exploitation The literature survey could not provide any convincing
of resources available to benthic fauna. Consequently, arguments on the presence of various Molluscs, hermit
P. pelagicus, M. stebbingi, P. indicus, and A. lunaris were crabs, and other crab species along the coast of Miani Hor
detected to display a striking abundance and biomass in except fewer studies that investigated some commercial
crustacean species. Therefore, the species abundance shrimp and finfish species. Gondal et al. (2012) proclaimed
and biomass remain tightly linked with the density of a that 22 fish species belonged to 14 families, while eight
population. During the NE monsoon and pre-monsoon crustacean species represented one family (Penaeidae) in
seasons, relatively more families of crustaceans were Miani Hor. Similarly, Ahmed and Abbas, (1999) studied
recorded (5 and 4, respectively), which is higher than the the abundance of some finfish and shellfish juveniles in the
other two seasons (SE monsoon: 2, and post-monsoon: intertidal zone of Miani Hor and ranked some fish species
3). Accordingly, the increased values of diversity index like L. subviridis, Sillago sihama, Coilia dussumieria for
(H’) were found in NE monsoon and pre-monsoon (2.23 important commercial values. Moreover, the shellfish,
and 2.00, respectively). Though species richness did species, e.g. Penaeus merguiensis and Metapenaeus
not corroborate with the corresponding season, the SW stebbingyi were ranked as two important shrimp species
monsoon and post-monsoon showed an increased species in the coastal Miani Hor. Likewise, Hassan, (1989)
richness (S=0.37 and S=0.40, respectively). worked on the distribution and abundance of juveniles of
Among Crustacea, shrimps (Family: Penaeidae, e.g. Penaeid shrimp along the coast of Makran and observed
Metapenaeus stebbingi, Penaeus merguiensis), crabs M. stebbingi, P. semisulcatus, and P. stylifera as the most
(Family: Portunidae and Family: Calappidae e.g., Portunus abundant in the coastal waters. However, Ahmed et al.
pelagicus and Ashtoret lunaris) and hermit crabs (Family: (1982) surveyed the entire Makran coast for distribution
Diogenidae e.g., Clibanarius padavensis) were the essential and abundance of intertidal organisms on some beaches,
populations of intertidal animals discovered in the benthic but the macrofauna reported were more relevant to rocky
habitat. McLachlan et al. (1981) demonstrated that the intertidal zones.
species community features such as richness, density, The distribution of the lower number of intertidal benthic
and total abundance expanded from the steeper beaches fauna along the coast could be due to the narrow intertidal
with coarse sand to the flatter beaches with fine sands. zones, which also confirmed by the studies carried out by
Subsequent investigation covering a broad range of beaches Ahmed et al. (1982). Furthermore, demersal populations
and geographical areas validated these conclusions by tend to be higher because of the shallow sandy bottoms and
particular reference to the population dynamics of plaice and brown vol. 20, no. 1-2, pp. 91-104. http://dx.doi.org/10.1016/0306-
shrimp. Estuarine, Coastal and Shelf Science, vol. 56, no. 3-4, 4565(94)00031-D.
pp. 807-818. http://dx.doi.org/10.1016/S0272-7714(02)00315-3.
BIANCHI, G., 1985. FAO species identification sheets for fishery
ATIQUE, U. and AN, K.-G., 2018. Stream health evaluation purposes. Field guide to the commercial marine and brackish-water
using a combined approach of multi-metric chemical pollution species of Pakistan. Prepared with the support of PAK/77/033
and biological integrity models. Water, vol. 10, no. 5, pp. 661. and FAO (FIRM) Regular Programme. Rome: FAO.
http://dx.doi.org/10.3390/w10050661.
BLABER, S.J.M. and BLABER, T.G., 1980. Factors affecting
ATIQUE, U. and AN, K.-G., 2019. Reservoir Water Quality the distribution of juvenile estuarine and inshore fish. Journal
Assessment Based on Chemical Parameters and the Chlorophyll of Fish Biology, vol. 17, no. 2, pp. 143-162. http://dx.doi.
Dynamics in Relation to Nutrient Regime. Polish Journal of org/10.1111/j.1095-8649.1980.tb02749.x.
Environmental Studies, vol. 28, no. 3, pp. 1043-1061. http://
dx.doi.org/10.15244/pjoes/85675. BLABER, S.J.M. and WHITFIELD, A.K., 1977. The feeding
ecology of juvenile mullet (Mugilidae) in south-east African
ATIQUE, U. and AN, K.-G., 2020. Landscape heterogeneity impacts estuaries. Biological Journal of the Linnean Society. Linnean
water chemistry, nutrient regime, organic matter and chlorophyll Society of London, vol. 9, no. 3, pp. 277-284. http://dx.doi.
dynamics in agricultural reservoirs. Ecological Indicators, vol. org/10.1111/j.1095-8312.1977.tb00270.x.
110, pp. 105813. http://dx.doi.org/10.1016/j.ecolind.2019.105813.
BROWN, A.C. and MCLACHLAN, A., 1991. Ecology of sandy
ATIQUE, U., IQBAL, S., KHAN, N., QAZI, B., JAVEED, A., shores. Amsterdam: Elsevier.
ANJUM, K.M., HAIDER, M.S., KHAN, T.A., MAHMOOD, S.
and SHERZADA, S., 2020a. Multivariate assessment of water CHAOUTI, A. and BAYED, A., 2008. Spatial patterns of soft-
chemistry and metals in a river impacted by tanning industry. bottom macro-invertebrates and relationships with environmental
Fresenius Environmental Bulletin, vol. 29, pp. 3013-3025. conditions in a North African coastal lagoon (Smir lagoon,
Morocco). Vie et Milieu, vol. 58, pp. 25-35.
ATIQUE, U., KWON, S., and AN, K.-G., 2020b. Linking weir
imprints with riverine water chemistry, microhabitat alterations, CUÉLLAR-MERCADO, D.M., HERNÁNDEZ-ALCÁNTARA,
fish assemblages, chlorophyll-nutrient dynamics, and ecological P. and SOLÍS-WEISS, V., 2019. Composition, richness and
health assessments. Ecological Indicators, vol. 117, pp. 106652. taxonomic diversity of Polychaete assemblages from La Paz Bay
https://doi.org/10.1016/j.ecolind.2020.106652. and adjacent oceanic areas of the Southern Gulf of California.
Regional Studies in Marine Science, vol. 28, pp. 100576. http://
ATIQUE, U., LIM, B., YOON, J. and AN, K.-G., 2019. Biological
dx.doi.org/10.1016/j.rsma.2019.100576.
health assessments of lotic waters by biotic integrity indices and
their relations to water chemistry. Water, vol. 11, no. 3, pp. 436. DAUVIN, J.C., 2007. Paradox of estuarine quality: benthic
http://dx.doi.org/10.3390/w11030436. indicators and indices, consensus or debate for the future. Marine
Pollution Bulletin, vol. 55, no. 1-6, pp. 271-281. http://dx.doi.
AYUB, Z. and MIUZAMIMIIL, A., 2001. Species composition of
org/10.1016/j.marpolbul.2006.08.017. PMid:17007892.
the Jaira, Kalri and Kiddi groups of shrimps landing at the Karachi
Fish Harbour and in the near-shore waters of Karachi (Pakistan). DAVIS, T.L., 1988. Temporal changes in the fish fauna entering a
Pakistan Journal of Zoology, vol. 33, no. 3, pp. 179-187. tidal swamp system in tropical Australia. Environmental Biology
of Fishes, vol. 21, no. 3, pp. 161-172. http://dx.doi.org/10.1007/
BAE, D.-Y., ATIQUE, U., YOON, J., LIM, B. and AN, K.-G.,
2020. Ecological risk assessment of urban streams using fish BF00004860.
biomarkers of dna damages and physiological responses. Polish DAY, J., KEMP, W.M. and YANEZ-ARAN-CIBIA, A. (1989).
Journal of Environmental Studies, vol. 29, no. 2, pp. 1-10. http:// Estuarine ecology. New York: John Wiley and Sons.
dx.doi.org/10.15244/pjoes/104660.
EDWARDS, R. and STEELE, J.H., 1968. The ecology of 0-group
BAZAÏRI, H., BAYED, A., GLÉMAREC, M. and HILY, C., 2003. plaice and common dabs at Loch Ewe I. Population and food.
Spatial organisation of macrozoobenthic communities in response Journal of Experimental Marine Biology and Ecology, vol. 2, no.
to environmental factors in a coastal lagoon of the NW African 3, pp. 215-238. http://dx.doi.org/10.1016/0022-0981(68)90017-8.
coast (Merja Zerga, Morocco). Oceanologica Acta, vol. 26, no. 5-6,
pp. 457-471. http://dx.doi.org/10.1016/S0399-1784(03)00041-0. EL ASRI, F., ZIDANE, H., ERRHIF, A., TAMSOURI, M.,
MAANAN, M., MALOULI IDRISSI, M. and MARTIN, D.,
BERGHAHN, R., 2000. Response to extreme conditions in 2018. Polychaete diversity and assemblage structure in the
coastal areas: biological tags in flatfish otoliths. Marine Ecology Oualidia Lagoon, Moroccan Atlantic coast. Journal of the Marine
Progress Series, vol. 192, pp. 277-285. http://dx.doi.org/10.3354/ Biological Association of the United Kingdom, vol. 98, no. 6,
meps192277. pp. 1337-1346. http://dx.doi.org/10.1017/S0025315417000388.
BEUKEMA, J.J., 1992. Dynamics of juvenile shrimp Crangon EQUBAL, J., LAKRA, R.K., SAVURIRAJAN, M., SATYAM, K.
crangon in a tidal-flat nursery of the Wadden Sea after mild and
and THIRUCHITRAMBALAM, G., 2018. Testing performances
cold winters. Marine ecology progress series. Oldendorf, vol.
of marine benthic biotic indices under the strong seasonality in
83, no. 2, pp. 157-165. http://dx.doi.org/10.3354/meps083157.
the tropical intertidal habitats, South Andaman, India. Marine
BHAUD, M. and CHA, J.H., 1992. Sources de fluctuation et de Pollution Bulletin, vol. 135, pp. 266-282. http://dx.doi.org/10.1016/j.
stabilité dans le cycle de vie d’Eupolymnia nebulosa (Polychète) marpolbul.2018.07.034. PMid:30301038.
en Méditerranée. Annales de l’Institut Océanographique, vol. 68,
GEORGE, A.D.I., ABOWEI, J.F.N., DAKA, E.R. and JASPER,
no. 1-2, pp. 25-35. [). Institut océanographique.]
A., 2009. Benthic macro invertebrate fauna and physico-chemical
BHAUD, M., CHA, J.H., DUCHENE, J.C. and NOZAIS, C., parameters in Okpoka Creek sediments, Niger Delta, Nigeria.
1995. Influence of temperature on the marine fauna: what can International Journal of Animal and Veterinary Advances, vol.
be expected from a climatic change. Journal of Thermal Biology, 1, no. 2, pp. 59-65.
GIBSON, R.N., 1982. Recent studies on the biology of intertidal KHANOM, D.A., NESA, A., JEWEL, M.A.S., HAQUE, M.A.,
fishes. Oceanography and Marine Biology, vol. 20, pp. 363-414. PAUL, A.K., IQBAL, S., ATIQUE, U. and ALAM, L., 2020.
Muscular tissue bioaccumulation and health risk assessment of
GIBSON, R.N., ANSELL, A.D. and ROBB, L., 1993. Seasonal heavy metals in two edible fish species (Gudusia chapra and
and annual variations in abundance and species composition of Eutropiichthys vacha) in Padma River, Bangladesh. Punjab
fish and macrocrustacean communities on a Scottish sandy beach. University Journal of Zoology, vol. 35, no. 81-89, pp. 1-165.
Marine Ecology Progress Series, vol. 98, pp. 89-105. http://dx.doi. https://doi.org/10.17582/journal.pujz/2020.35.1.81.89.
org/10.3354/meps098089.
KIM, J.-J., ATIQUE, U. and AN, K.-G., 2019. Long-term ecological
GIBSON, R.N., ROBB, L., BURROWS, M.T. and ANSELL, health assessment of a restored urban stream based on chemical
A.D., 1996. Tidal, diel and longer term changes in the distribution water quality, physical habitat conditions and biological integrity.
of fishes on a Scottish sandy beach. Marine Ecology Progress Water, vol. 11, no. 1, pp. 114. http://dx.doi.org/10.3390/w11010114.
Series, vol. 130, pp. 1-17. http://dx.doi.org/10.3354/meps130001.
KINNE, O., 1971. Salinity. Marine Ecology (Berlin), vol. 1,
GONDAL, M.A., SAHER, N.U. and QURESHI, N.A., 2012. pp. 821-995.
Diversity and biomass distribution of intertidal fauna in sonmiani
bay (Miani Hor), balochistan (pakistan). Egyptian Journal of KOUADIO, K.N., DIOMANDÉ, D., OUATTARA, A., KONÉ,
Biological Science, vol. 4, no. 1, pp. 219-234. http://dx.doi. Y.J. and GOURÈNE, G., 2008. Taxonomic diversity and structure
org/10.21608/eajbsz.2012.14304. of benthic macroinvertebrates in Aby Lagoon (Ivory Coast, West
Africa). Pakistan Journal of Biological Sciences, vol. 11, no. 18,
GRAY, J.S. and CHRISTIE, H., 1983. Predicting long-term changes pp. 2224-2230. http://dx.doi.org/10.3923/pjbs.2008.2224.2230.
in marine benthic communities. Marine ecology progress series. PMid:19137831.
Oldendorf, vol. 13, no. 1, pp. 87-94. http://dx.doi.org/10.3354/
meps013087. LASIAK, T., 1984. Structural aspects of the surf-zone fish
assemblage at King’s Beach, Algoa Bay, South Africa: short-term
HAMPEL, H., CATTRIJSSE, A. and VINCX, M., 2003. Tidal, fluctuations. Estuarine, Coastal and Shelf Science, vol. 18, no. 3,
diel and semi-lunar changes in the faunal assemblage of an pp. 347-360. http://dx.doi.org/10.1016/0272-7714(84)90076-3.
intertidal salt marsh creek. Estuarine, Coastal and Shelf Science,
vol. 56, no. 3-4, pp. 795-805. http://dx.doi.org/10.1016/S0272- LEFRERE, L., OUASSAS, M., GUILLOIS, B., GILLET, P. and
7714(02)00296-2. MOUKRIM, A., 2015. Macrobenthic community structure of soft-
bottom sediments in the Khnifiss lagoon, South of Morocco. Journal
HAQUE, M.A., JEWEL, M.A.S., ATIQUE, U., PAUL, A.K., of Material and Environmental Science, vol. 6, pp. 2226-2236.
NAHER, N. and IQBAL, S., 2020. Seasonal and spatial variation
of flagellate communities in a tropical river. Limnologica, vol. MARCHAND, J., 1991. The influence of environmental conditions
85, pp. 125824. http://dx.doi.org/10.1016/j.limno.2020.125824. on settlement, distribution and growth of 0-group sole (Solea
solea (L.)) in a macrotidal estuary (Vilaine, France). Netherlands
HARA, J., ATIQUE, U. and AN, K.G., 2020. Multiyear links Journal of Sea Research, vol. 27, no. 3-4, pp. 307-316. http://
between water chemistry, algal chlorophyll, drought-flood dx.doi.org/10.1016/0077-7579(91)90033-W.
regime, and nutrient enrichment in a morphologically complex
reservoir. International Journal of Environmental Research and MARGALEF, R., 1958. Information theory in ecology. General
Public Health, vol. 17, no. 9, pp. 1-22. http://dx.doi.org/10.3390/ Systems, vol. 3, pp. 36-71.
ijerph17093139. PMid:32365942. MCLACHLAN, A., 1990. Dissipative beaches and macrofauna
HASSAN, H., 1989. Distribution and abundance of penaeid communities on exposed intertidal sands. Journal of Coastal
juveniles on Mekran and Sindh Coast. Pakistan Journal of Research, vol. 6, no. 1, pp. 57-71.
Zoology, vol. 21, no. 2, pp. 117-152. MCLACHLAN, A., JARAMILLO, E., DONN, T.E. and WESSELS,
HERNÁNDEZ-GUEVARA, N.A., PECH, D. and ARDISSON, F., 1993. Sandy beach macrofauna communities and their control
P., 2008. Temporal trends in benthic macrofauna composition by the physical environment: a geographical comparison. Journal
in response to seasonal variation in a tropical coastal lagoon, of Coastal Research, vol. 15, pp. 27-38.
Celestun, Gulf of Mexico. Marine and Freshwater Research, MCLACHLAN, A., WOOLDRIDGE, T. and DYE, A.H., 1981.
vol. 59, no. 9, pp. 772-779. http://dx.doi.org/10.1071/MF07189. The ecology of sandy beaches in southern Africa. African Zoology,
vol. 16, no. 4, pp. 219-231. http://dx.doi.org/10.1080/0254185
IDOWU, E.O. and UGWUMBA, A.A.A., 2005. Physical, chemical
8.1981.11447760.
and benthic faunal characteristics of a Southern Nigeria Reservoir.
The Zoologist, vol. 3, pp. 15-25. MOON, W.-K., ATIQUE, U. and AN, K.G., 2020. Ecological
risk assessments and eco-toxicity analyses using chemical,
IQBAL, S., ATIQUE, U., MAHBOOB, S., HAIDER, M.S.,
biological, physiological responses, DNA damages and gene-
IQBAL, H.S., AL-GHANIM, K.A., AL-MISNED, F., AHMED,
level biomarkers in Zebrafish (Danio rerio) in an urban stream.
Z. and MUGHAL, M.S., 2020. Effect of supplemental selenium
Chemosphere, vol. 239, pp. 124754. http://dx.doi.org/10.1016/j.
in fish feed boosts growth and gut enzyme activity in Juvenile
chemosphere.2019.124754. PMid:31726531.
Tilapia (Oreochromis niloticus). Journal of King Saud University -
Science, vol. 32, no. 5, pp. 2610-2616. http://dx.doi.org/10.1016/j. NICOLAIDOU, A., PETROU, K., KORMAS, K.A. and
jksus.2020.05.001. REIZOPOULOU, S., 2006a. Inter-annual variability of soft
bottom macrofaunal communities in two Ionian Sea lagoons.
IQBAL, S., ATIQUE, U., SHARIF MUGHAL, M., KHAN, N.,
Hydrobiologia, vol. 555, no. 1, pp. 89-98. http://dx.doi.org/10.1007/
SULTAN HAIDER, M., IQBAL, K.J. and AKMAL, M., 2017.
s10750-005-1108-2.
Effect of selenium incorporated in feed on the hematological
profile of tilapia (Oreochromis niloticus). Journal of Aquaculture NICOLAIDOU, A., PETROU, K., KORMAS, K.A. and
Research & Development, vol. 8, no. 10, pp. 1000513. http:// REIZOPOULOU, S., 2006b. Inter-annual variability of soft
dx.doi.org/10.4172/2155-9546.1000513. bottom macrofaunal communities in two Ionian Sea lagoons. In:
K. MARTENS, H. QUEIROGA, M. R. CUNHA, A. CUNHA, areas of the Galveston Bay Estuary, Texas (USA). Marine Ecology
M. H. MOREIRA, V. QUINTINO, A. M. RODRIGUES, J. Progress Series, vol. 193, pp. 217-239. http://dx.doi.org/10.3354/
SEROÔDIO and R. M. WARWICK, eds. Marine biodiversity. meps193217.
Developments in hydrobiology. Dordrecht: Springer, vol. 183.
http://dx.doi.org/10.1007/1-4020-4697-9_8 SAEED, F., IQBAL, K.J., ATIQUE, U., JAVID, A., KHAN,
N., IQBAL, S., MAJEED, H., AZMAT, H., KHAN, B.Y.A.,
OKE, O.O., 1990. Limnology and macrobenthos of owena BABOO, I., SHAHID, M.T. and AFZAL, G., 2020. Toxic trace
reservoir. Ibadan, Nigeria: University of Ibadan, 96 p. Doctoral metals assessment in selected organs of edible fish species,
dissertation, M. Phil. Thesis. sediment and water in Head Punjnad, Punjab, Pakistan. Punjab
OMENA, E.P., LAVRADO, H.P., PARANHOS, R. and SILVA, University Journal of Zoology, vol. 35, no. 1, pp. 43-50. https://
T.A., 2012. Spatial distribution of intertidal sandy beach polychaeta dx.doi.org/10.17582/journal.pujz/2020.35.1.43.50.
along an estuarine and morphodynamic gradient in an eutrophic
SELLESLAGH, J. and AMARA, R., 2007. Temporal variations
tropical bay. Marine Pollution Bulletin, vol. 64, no. 9, pp.
in abundance and species composition of fish and epibenthic
1861-1873. http://dx.doi.org/10.1016/j.marpolbul.2012.06.009.
crustaceans of an intertidal zone: environmental factor influence.
PMid:22818168.
Cybium, vol. 31, no. 2, pp. 155-162.
POST, A.L., WASSENBERG, T.J. and PASSLOW, V., 2006.
Physical surrogates for macrofaunal distributions and abundance SESHAPPA, G., 1953. Observations on the physical and biological
in a tropical gulf. Marine and Freshwater Research, vol. 57, no. features of the inshore sea bottom along the Malabar coast.
5, pp. 469-483. http://dx.doi.org/10.1071/MF05182. Proceedings of the Indian National Science Academy, vol. 19,
no. 2, pp. 257-279.
QUINN, N.J. and KOJIS, B.L., 1987. The influence of diel cycle,
tidal direction and trawl alignment on beam trawl catches in an SHANNON, C.E. and WEAVER, W., 1963. The mathematical theory
equatorial estuary. Environmental Biology of Fishes, vol. 19, no. of communication. 1949. Urbana, IL: University of Illinois Press.
4, pp. 297-308. http://dx.doi.org/10.1007/BF00003230.
SHORT, A.D., 1996. The role of wave height, period, slope, tide
RAHMAN, M.M., HAQUE, S.M., ISLAM, M.A., PAUL, A.K., range and embaymentisation in beach classifications: a review.
IQBAL, S., ATIQUE, U., WAHAB, A., EGNA, H. and BROWN, Revista Chilena de Historia Natural, vol. 69, no. 4, pp. 589-604.
C., 2020. Assessment of mud crab fattening and culture practices
in coastal Bangladesh: understanding the current technologies and SILVA, R.F., ROSA FILHO, J.S., SOUZA, S.R. and SOUZA-
development. Aquaculture, Aquarium, Conservation & Legislation FILHO, P.W., 2011. Spatial and temporal changes in the structure
(AACL) Bioflux, vol. 13, pp. 582-596. of soft-bottom benthic communities in an Amazon estuary (Caeté
estuary, Brazil). Journal of Coastal Research, vol. 64, pp. 440-444.
RASOOL, F., TUNIO, S., HASNAIN, S. and AHMAD, E., 2002.
Mangrove conservation along the coast of Sonmiani, Balochistan, SINCLAIR, M., 1988. Marine populations: an essay on population
Pakistan. Trees (Berlin), vol. 16, no. 2-3, pp. 213-217. http:// regulation. Seattle, WA: Washington Sea Grant.
dx.doi.org/10.1007/s00468-001-0151-5.
UWADIAE, R.E., 2009. Response of benthic macroinvertebrate
ROZAS, L.P. and ZIMMERMAN, R.J., 2000. Small-scale patterns community to salinity gradient in a sandwiched coastal lagoon.
of nekton use among marsh and adjacent shallow nonvegetated Report and Opinion, vol. 1, pp. 45-55.