Shark (Elasmobranchs) Fisheries Trend in Pakistan: Species Composition of Catch and their Conservation Status
Shark (Elasmobranchs) Fisheries Trend in Pakistan: Species Composition of Catch and their Conservation Status
Amir Javed1, Seema Shafique1, Shabir Ali Amir2 and Pirzada J.A. Siddiqui1,3*
1Centre of Excellence in Marine Biology, University of Karachi, Karachi, Pakistan
2Zoological Sciences Division, Pakistan Museum of Natural History, Garden Avenue,
Shakar-Parian, Islamabad-44000, Pakistan
3Iqra University Directorate of Advance Studies and Research Shaheed-e-Millat Rd, Phase 2 Defence View Housing Society, Karachi
ABSTRACT
Sharks are important group of marine and estuarine cartilaginous fishes and hold ecological and commercial importance. Studies on the diversity, life-history and species distribution in South-East Asian countries are limited. Here, we studied the number of sharks in landings, species composition, and status of shark fishery in four fish landing sites in Pakistan including Karachi Fish Harbor, Korangi Fish Harbor, Sonmiani Fish Harbor and Gawadar Fish Harborduring 2017-2018. A total of 1.99 million sharks belonging to 11 families and 41 species were recorded from these landing sites. Significantly, higher number of sharks landed at Karachi Fish Harbor (KFH) (86.9% of the total). Ninety-six percent of the sharks fall in three families (Carcharhinidae 45%, Triakidae 35%, Hemiscylliidae 16%). Species in Lamnidae had 2% contribution whereas each of the remaining families showed <2% representation. Carcharhinidae was the most species-rich family (23 spp.), all other families were represented by 1-3 species. Two peak periods of high catches were recorded during the months of March-April and September-October, the lowest catch was recorded in the summer. Size-range data suggests that juvenile and immature individuals of all shark species are being caught as a by-catch of other targeted fishery. Twenty-six years landing data of elasmobranchs in Pakistan during the period from 1993 to 2019 revealed decreasing trend in the catch, the highest being in 1999 (54,959 metric tonnes) and the lowest during 2019 (5,793 metric tons). Majority of the shark species (85% of total) in the landing are listed as CR, EN, NT or VU, and two species categorized as LC in the IUCN Red Data List. Similarly, nine species of sharks are listed in CITES Appendix II and of these 9 species, 8 species are also listed in CMS Appendix II. On the basis of our findings, it may be concluded that sharks inhabiting the North Arabian Sea are under considerable threats of overexploitation and fisheries by-catch.
Article Information
Received 12 June 2023
Revised 22 November 2023
Accepted 10 December 2023
Available online 02 February 2024
(early access)
Published 06 May 2025
Authors’ Contribution
AJ conducted the field work, analyzed the data and writing the manuscript. SS help in statistical analysis and format the manuscript. SAA help in data collection and analysis. PJAS conceived and designed the research, provide lab facilities, checking the manuscript and finally approved the manuscript for submission.
Key words
Sharks, Conservation, CITES, Fisheries, Elasmobranchs, Shark landing
DOI: https://dx.doi.org/10.17582/journal.pjz/20230612060631
* Corresponding author: [email protected]
0030-9923/2025/0003-1235 $ 9.00/00
Copyright 2025 by the authors. Licensee Zoological Society of Pakistan.
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
INTRODUCTION
Sharks, a group of cartilaginous fishes consisting of 250 species, are performing well in various ecosystems for over 400 million years (Compagno et al., 2005; Arai and Azri, 2019). Despite their evolutionary accomplishments, many species of shark are at the brink of extinction due to unmanaged fisheries where over-fishing to meet the high demand for their fins and meat, and by-catch are most prominent reasons (Musick et al., 2000; Ferretti, 2010; Dulvy et al., 2014; McClenachan et al., 2016). Moreover, having complex life history traits, overexploitation of this group tends to decline their population worldwide, and hence sharks are considered as extremely vulnerable group worldwide (IUCN, 2013). Their vulnerability is further compounded by the fact that sharks are slow grower and have low productivity with long gestation time (Arai and Azri, 2019). Similarly, environmental pollution and habitat destruction exert negative impact on their wellbeing (Hutching, 2000; Polidorro et al., 2012).
For the purpose of conservation and protection of threatened shark species and their trade control, several international legislations have been developed (Jabado and Spaet, 2017). In 2003, four shark species were initially categorized in the Appendix II of the CITES (Convention on International Trade in Endangered Species of Wild Fauna and Flora). In the last meeting of Parties in 2017, additional 12 species of shark were categorized in the Appendix II. Although these species are not threatened with extinction but their trade is prohibited to avoid the discordant utilization for their survival (cites.org). In addition, the convention on the migratory species (CMS) aims at conserving species that cross national boundaries or habitats beyond national jurisdiction. Migratory species of sharks at risk of extinction throughout their ranges are listed in CMS Appendix I and those with an unfavorable conservation status that would benefit the international corporation are listed Appendix II of the CMS (cms.int).
In Southeast Asian countries, scientific information regarding the shark landing is documented sporadically (Arai and Azri, 2019). A large knowledge gap still exists regarding the population of shark in the Southeast Asia, the main global consumer of shark products (Lam and Sadovy de Mitchenston, 2011). The main problem to the conservation and management of shark population in the world is the lack of information on their diversity, seasonal occurrence and fisheries in many areas (Arai and Azri, 2019).
Historically, Pakistan had no large-scale commercial shark fishery, which started gradually as artisanal small-scale activity and most of it was non-targeted by catch (Carpenter, 1997; Tesfamichael and Pauly, 2012; IOTC, 2013; Jabado and Spaet, 2017). Later on, a large-scale fishery targeting sharks has been developed involving some industrial boats (Jabado and Spaet, 2017). Fisheries reports and taxonomic checklists for sharks in Pakistan are limited (Psomadakis et al., 2015; Moazzam and Osmany, 2021, 2022; Osmany and Moazzam, 2022) no information is available on numbers, size ranges and sex of landed sharks. Similarly, seasonal variation in occurrence of sharks and their long-term landing trend have not been studied. Further research is inevitably required for proper management and conservation of shark fisheries in Pakistan. Here we assessed the species composition and seasonal occurrence of shark species in the commercial catch landed at various fish harbors particularly the major landing site at Karachi Fish Harbor. Long-term landing trends of sharks and rays over a period of 26 years (1994-2019) and conservation status of sharks is also presented.
MATERIALS AND METHODS
Study area and specimen
We observed the sharks at the landing sites in Pakistan during 2017-2018. The study sites included Karachi Fish Harbor (KFH; 24.8491° N, 66.9761° E) and Korangi Fish harbor (KoFH; 24.7937°N, E 67.1398°E) along Sindh coast, and Sonmiani Fish harbor (SFH; 25.4523° N, 66.5603° E) and Gwadar Fish Harbor (GFH; 25.1253°N, 62.3261°E) along Balochistan coast. The landing data, including total number of sharks species landed at each landing site per year and number of male and female sharks was acquired from Marine Fisheries Department and major traders where most of the landed sharks are processed for consumption and export. The landing sites were visited severally each month to note external morphological characteristics of at least 10 specimen of each species. Some rare species were found in less numbers. Measurements were made as per Irschick and Hammerschlag (2015) and used for identification of species according to Psomadakis et al. (2015) and Fishbase (https://www.fishbase.org 2023). The conservation status of all shark species was obtained from websites of IUCN Red List (https://www.iucnredlist.org) and CITES (Convention on International Trade in Endangered Species of wild flora and fauna - Appendix II; https://cites.org), and CMS (the memorandum of understanding for the Conservation of Migratory Sharks - Appendix II; https://www.cms.int).
Statistical analysis
The data were analyzed by using the PRIMER software package version 7.0 (Clarke and Gorely, 2006, 2015). Distributions of shark species at four locations were assessed using nMDS plot following Clarke and Gorely (2015). To investigate the relationships between season and number of each shark species recorded during landing, cluster analysis was conducted using the hierarchical method based on the Bray–Curtis similarity index (Bray and Curtis, 1957). Fishery landing trend was assessed using twenty-six year fisheries data (1993-2019) for shark landings retrieved from the Marine Fisheries Department. Polynomial regression by fitting highest degree (5) curves was employed.
RESULTS
Shark landings in Pakistan
A total of 1.991 million sharks landed at four fish landing sites situated in Sindh and Balochistan were recorded during 21 months study period (Table I). Forty-one species falling in 11 families were represented in the catch where species in 3 families constituting 96% of the catch (Carcharhinidae 45%, Triakidae 35%, Hemiscylliidae 16%). Species in Lamnidae had 2% contribution whereas each of the remaining families showed <2% representation (Fig. 1). Carcharhinidae was the most dominating family (23 spp.), followed by Hemiscyllidae (3 spp.), Trakaidae, Sphyrnidae, Lamnidae, Alopidae and Hemigalidae, the last five families were represented by 2 species each. Other four families had only one species each.
The landing data also depicts that significantly higher number sharks landed at KFH (86.9% of total) compared to other sites, KoFH (6.2%), GFH (5.1%), SFH (1.8%) (Fig. 2). Forty-one species of sharks were recorded from MoFH,
Table I. Number of shark species landed at four fish landing sites located in Sindh and Baluchistan: KFH, Karachi Fish Harbor; KoFH, Korangi Fish Harbor; SFH, Sonmiani Fish Harbor at Dam and GFH, Gawadar Fish Harbor. Conservation status of all 41 species was taken from IUCN Red List. Species included in Appendix-II of CITES (*Convention on International Trade in Endangered Species of wild flora and fauna) and CMS (+ the memorandum of understanding for the Conservation of Migratory Sharks) are also indicated.
Family |
Shark species |
Shark landing record |
Conser-vation Status (IUCN, CITES*, CMS+ |
|||||||
KFH |
KoFH |
SFH |
GFH |
Total sharks |
Male |
Female |
Size range TL (cm) |
|||
Alopiidae |
Alopias pelagicus |
4237 |
302 |
86 |
254 |
4879 |
2453 |
2426 |
134.7-142.3 |
EN*+ |
A. superciliosus |
1216 |
87 |
24 |
67 |
1394 |
654 |
740 |
169.1-331.3 |
VU*+ |
|
Carchar-hinidae |
Carcharhinus altimus |
15017 |
1072 |
312 |
883 |
17284 |
8632 |
8652 |
87.7-184.5 |
NT |
C. amblyrhynchoides |
12697 |
907 |
254 |
746 |
14604 |
7321 |
7283 |
76.3-125.7 |
VU |
|
C. amboinensis |
15648 |
1120 |
321 |
913 |
18002 |
9231 |
8771 |
96.1-168.9 |
VU |
|
C. brevipinna |
6851 |
490 |
134 |
412 |
7887 |
3876 |
4011 |
74-234.5 |
VU |
|
C. dussumieri |
12852 |
917 |
261 |
765 |
14795 |
7431 |
7364 |
84.5-141.9 |
EN |
|
C. falciformis |
64294 |
4592 |
1311 |
3765 |
73962 |
37541 |
36421 |
90.7-186.3 |
VU*+ |
|
C. hemiodon |
12430 |
889 |
254 |
734 |
14307 |
7231 |
7076 |
112-191.9 |
CR |
|
C. leucas |
16585 |
1185 |
337 |
976 |
19083 |
9563 |
9520 |
97-122.4 |
VU |
|
C. limbatus |
10866 |
776 |
221 |
639 |
12502 |
6231 |
6271 |
69.2-79.9 |
VU |
|
C. longimanus |
738 |
52 |
15 |
43 |
848 |
432 |
416 |
54.9-182.3 |
CR* |
|
C. macloti |
43044 |
3072 |
878 |
2532 |
49526 |
24764 |
24762 |
83-229.1 |
NT |
|
C. melanopterus |
12584 |
898 |
254 |
743 |
14479 |
7145 |
7334 |
95.4-180.4 |
VU |
|
C. plumbeus |
10323 |
737 |
210 |
607 |
11877 |
5976 |
5901 |
75.6-230.6 |
EN |
|
C. sorrah |
8874 |
634 |
181 |
522 |
10211 |
5132 |
5079 |
36.8-74.3 |
NT |
|
Galeocerdo cuvier |
2091 |
149 |
42 |
123 |
2405 |
1241 |
1164 |
69.8-343 |
NT |
|
Glyphis cf. gangeticus |
0 |
1 |
0 |
0 |
1 |
1 |
0 |
61.1-112.4 |
CR |
|
Lamiopsis temminckii |
0 |
1 |
0 |
0 |
1 |
1 |
0 |
70.1-90.8 |
EN |
|
Loxodon macrorhinus |
205393 |
14656 |
4123 |
12312 |
236484 |
115674 |
120810 |
61.8-92.1 |
NT |
|
Negaprion acutidens |
846 |
60 |
16 |
48 |
970 |
452 |
518 |
65-133.5 |
EN |
|
Prionace glauca |
371 |
25 |
6 |
22 |
424 |
231 |
193 |
74-169.9 |
NT |
|
Rhizoprionodon acutus |
125527 |
8963 |
2541 |
7383 |
144414 |
71451 |
72963 |
50.1-122.2 |
VU |
|
R. oligolinx |
94215 |
6745 |
1923 |
5543 |
108426 |
54321 |
54105 |
33-60.1 |
NT |
|
Scoliodon laticaudus |
105487 |
7543 |
2153 |
6251 |
121434 |
58751 |
62683 |
24.5-80.8 |
NT |
|
Triaenodon obesus |
77 |
5 |
2 |
4 |
88 |
37 |
51 |
84.3-100 |
VU |
|
Lamnidae |
Isurus oxyrinchus |
30696 |
2192 |
632 |
1876 |
35396 |
17643 |
17753 |
75.5-181.3 |
EN*+ |
I. paucus |
612 |
44 |
13 |
34 |
703 |
341 |
362 |
98.7-148.7 |
EN*+ |
|
Ginglymosto-matidae |
Nebrius ferrugineus |
1401 |
101 |
28 |
82 |
1612 |
821 |
791 |
71.9-121.4 |
VU |
Hemigaleidae |
Chaenogaleus macrostoma |
952 |
67 |
16 |
56 |
1091 |
531 |
560 |
44.5-90.9 |
VU |
Hemipristis elongata |
1436 |
101 |
23 |
83 |
1643 |
832 |
811 |
74.3-156.9 |
VU |
|
Hemis-cylliidae |
Chiloscyllium arabicum |
121885 |
8707 |
2431 |
7132 |
140155 |
71542 |
68613 |
28.4-72.4 |
NT |
C. griseum |
79238 |
5660 |
1613 |
4563 |
91074 |
45543 |
45531 |
65.7-109.8 |
VU |
|
C. indicum |
67321 |
7834 |
3411 |
3456 |
82022 |
41280 |
40742 |
38.6-82.4 |
VU |
|
Pseudocar-chariidae |
Pseudocarcharias kamoharai |
26 |
2 |
1 |
2 |
31 |
14 |
17 |
56.6-96.5 |
LC |
Rhinco-dontidae |
Rhincodon typus |
1 |
1 |
0 |
0 |
2 |
1 |
1 |
92-405.3 |
EN*+ |
Sphyrnidae |
Sphyrna lewini |
12589 |
897 |
254 |
743 |
14483 |
7143 |
7340 |
130.6-237.9 |
CR*+ |
Sphyrna mokarran |
17488 |
1241 |
356 |
1023 |
20108 |
11432 |
8676 |
77-265.5 |
CR*+ |
|
Stegosto-matidae |
Stegostoma tigrinum (fasciatum) |
11 |
1 |
1 |
1 |
14 |
6 |
8 |
115.7-205.3 |
EN |
Triakidae |
Iago omanensis |
275586 |
19681 |
5624 |
16210 |
317101 |
154356 |
162745 |
69.2-107.3 |
LC |
Mustelus mosis |
334477 |
23890 |
6832 |
19675 |
384874 |
194231 |
190643 |
64.7-73.5 |
NT |
whereas 39 spp. from KFH and 38 spp. from SFH and GFH were noted (Table II). Rhincodon typus only 1 specimen was recorded from each landing sites at KFH and KoFH, while one specimen each of the other two species (Glyphis cf. gangeticus and Lamiopsis temminckii) was recorded at KoFH only (Table I). A comparison was made using diversity and abundance data using non-metric MDS assessment tool which clearly demonstrated that KFH had only 20% similarity with other three sites. The other three sites had >60% similarity with each other in terms of species composition and their numbers appeared in the catches (Fig. 3).
Table II. Number of species in eleven families of sharks landed at four sites.
Family |
Number of species |
|||
KFH |
KoFH |
SFH |
GFH |
|
Pseudocarchariidae |
1 |
1 |
1 |
1 |
Alopiidae |
2 |
2 |
2 |
2 |
Lamnidae |
2 |
2 |
2 |
2 |
Hemiscylliidae |
3 |
3 |
3 |
3 |
Stegostomatidae |
1 |
1 |
1 |
1 |
Ginglymostomatidae |
1 |
1 |
1 |
1 |
Rhincodontidae |
1 |
1 |
0 |
0 |
Triakidae |
2 |
2 |
2 |
2 |
Hemigaleidae |
2 |
2 |
2 |
2 |
Carcharhinidae |
22 |
24 |
22 |
22 |
Sphyrnidae |
2 |
2 |
2 |
2 |
Total |
39 |
41 |
38 |
38 |
For abbreviations see Table I.
Sharks were landed in variable numbers. Most dominant species, with >0.1M individuals recorded in landings, included seven species in three families namely, Carchirhinidae (Loxodon macrorhinus, NT, 0.2364 M; Rhizoprionodon acutus, VU, 0.1444 M; R. oligolinx, NT, 0.1084 M; Scoliodon laticadus, NT, 0.1214 M), Hemiscyllidae (Chiloscyllium arabicum, NT, 0.1402 M) and Triakidae (Iago omanensis, LC, 0.3171 M; Mustelus mosis, NT, 0.3845 M) (Table I). This dominant group constitutes 73% of total individuals recorded during study period. Other 13 species were frequent (20-50 thousand), 07 species were occasional (1-20 thousand) and 10 species were rarely encountered (<1000) (Table I). Although these most contributing species are not in CITES Appendix II, but they are listed as VU, NT or LC in IUCN red-list. However, some nine species of sharks appeared in landings (Alopias pelagicus, A. supercilliosus, Isurus oxyrhinchus, I. paucus, Rhincodon typus, Carchrhinus falciformis, C. longimanus, Sphyrna lewini, S. mokkaran) are listed in CITES Appendix II and of these 9 species, 8 species are also listed in CMS Appendix II (Table I). Considering IUCN Red List, the landing data showed that 15 species were Vulnerable (VU), 10 species were Near-Threatened (NT), 9 species were Endangered (En), 5 species were Critical constituting 85% of catch. Only 2 species were listed as Least Concern (LC) (Table I).
Seasonal variation in shark catch landed at KFH
Seasonal landing data of sharks landed at KFH show monthly variations (Fig. 4). Sharks appeared in all landings throughout the year showing two peaks of high catches during March-April and September-October. Lower catch was recorded during summer (May-August). We pooled data for four seasonal periods with respect to monsoon, i.e., Summer Inter-monsoon (SIM, February-April), Southwest monsoon (SWM, May-July), Autumn Inter-monsoon (AIM, August-October) and Northeast monsoon (NEM, November-January). The cluster analysis of pooled data considering numbers of each species caught also showed that the periods of high catches were clustered together, i.e. SIM, AIM and NEM, and the summer season (SWM) with lower catches stand separately (Fig. 5).
Status of Elasmobranch fishery
Twenty-six years fisheries data (1993-2019) for total elasmobranch landings at KFH was retrieved from the Marine Fisheries Department. The data was assessed using polynomial regression by fitting highest degree (5) curves showing a declining trend (Fig. 6). The higher catches recorded during 1993-2010 followed a sharp decline to lower values and the continuous decreases in the catch were obvious during the next nine years up to 2019.
DISCUSSION
Like many other countries in the region, Pakistan also lacks significant data and required expertise, for example, to identify sharks properly and collect relevant data. Here we present information on shark landing, its seasonality and long-term trends in Pakistan which is in line with the Action 1 of Xiamen declaration (https://cites.org) emphasizing collection of shark fisheries data (catch, discards, effort), biological information, stock structure, nursery grounds and habitats of sharks. Xiamen declaration was adopted in the “Asian Regional Consultative Workshop on Capacity Assessments for the Implementation of new CITES Listing of Sharks and Manta Rays” (Xiamen, China, May 2014) where priority actions required for elasmobranchs management and conservation were highlighted including, data collection, strengthening legislation, enforcement and international cooperation, strengthening conservation and management measures and enhancing training to generate human resources with capacity to deal with existing issues and challenges.
We collected data on the species composition and numbers of sharks observed in landings at various fish landing sites in Pakistan during the study period. Although little is known about the movement and habitat use patterns of sharks in in the northern Arabian Sea bordering Balochistan and Sindh coasts of Pakistan, but the 41 species recorded here in the landings are known to be distributed in pelagic, oceanic, and demersal habitats. For example, two species of thresher sharks (Alopias pelagicus and A. supercilliosus) are generally found in the epipelagic zone in both neritic and oceanic waters over continental and insular slopes and shelves (Cartamil, 2009). Similarly, all the three species of bamboo sharks occurring in Pakistan are bottom dwellers (Last et al., 2010). Variable movement pattern are reported for sharks in family Carcharhinidae. They typically use restricted home-range which increases with the increasing body size of different species (Conrath and Musick, 2010). Carcharhinus sorrah (spot tail shark) can be found on shelve of continental and insular areas (Gambang, 1994), including coral reefs and moves relatively short distances of 50 km in near-shore waters but sometimes move large distances about 1000 km (Stevens et al., 2000). Species in Family Sphyrnidae, found in warm tropical to temperate waters (Compagno, 1984), are highly mobile with ability to migrate extensively and are generally found throughout the assortment of ecosystems including estuaries, bays, continental shelves and offshore waters (Wells et al., 2018).
Coastal catches are generally landed in respective landing sites along the coast of Pakistan. It may be noted that most of the large fishing trawlers and boats from Sind and Balochistan, particularly from offshore waters, call at KFH and hence higher diversity and numbers of sharks are recorded at this site. Therefore, the shark species landed at KFH would represent their seasonal distribution in Pakistan waters. Consequently, we study the seasonal variations in composition and abundance of sharks on the basis of landing data from KFH for which monthly data was available. The two peak seasons of high catches recorded here separated by a period of low catches which may be attributed to many factors. For example, reduced fishing efforts particularly during summer, high energy SW monsoon season, when fishing remains confined to the coastal waters only (Siddiqi, 1992). Water temperature and other environmental conditions are also known to regulate distribution of animals and their reproductive cycle (Arai and Azri, 2019). Upwelled cold water of low oxygen concentration in this area can change the distribution of many animals (Banse, 1968; Siddiqi, 1992). Migration may also result in variable catches and domination of certain species at different time of the year (Henderson et al., 2008). The differences between life-history and habitat among the species might change the seasonal occurrence and composition of species in the particular region (Arai and Azri, 2019). A variety of bottom feature, such as, sandy and muddy substrates, cliffs, rocky outcrops, bays and other low energy habitats are discretely available along Pakistan coast to support these animals throughout their life cycle (Psomadakis et al., 2015) and additional habitat use may benefit foraging success and promoting growth (Knip et al., 2010, 2012; Arai and Azri, 2019).
Shark fishery in Pakistan is mostly untargeted. Sharks are captured as bycatch during fishing operation to target other multiple commercial species including mackerel, scads, tuna and sardines using various fishing gears, such as, line-gears, drift gill-nets, bottom trawls nets, hooks and line and long-lines (Psomadakis et al., 2015) and also set-bag nets and purse seine (Personal observation). Artisanal fishery has also been involved in targeting sharks presumably in low numbers (data is not available). Similarly, most sharks are also caught as bycatch in India (Gupta et al., 2020) and elsewhere in other parts of the world (Bonfil, 1994). Legislations and ban on certain types of nets, such as, trawl and seine nets, are widely ignored in Pakistan and other regional countries.
Comparing known length at maturity (FishBase) with size data recorded here, it is alarming to note that juveniles and immature specimen are being caught of all landed shark species. A significant numbers of pregnant female sharks have been observed during surveys (personal observation). The indiscriminate fishing practice is a serious threat for the population of sharks particularly because of the fact that they are predominantly characterized as long-lived and slow growing animals producing few off-springs (Dulvy et al., 2017). Furthermore, the species identified in landings are categorized according to IUCN Red List where 39 species are listed as vulnerable (24%), endangered (4%), near-threatened (54%) or critical (3%) and their total represents 84% of the total catch. In addition, another 4% of the catch are either CITES Appendix II or CMS Appendix II species.
Information regarding catch of world’s shark and usage are often inadequate and regionally not even at the rudimentary level, despite the questions and arguments for the protection and sustainability of shark fisheries around the world (Rose, 1996; Baum and Myers, 2004; Lam et al., 2011). Like many other countries Pakistan is a data poor country. Twenty-six years data of fisheries landings in Pakistan clearly show a sharp decline in shark fisheries. The same has been reported for shark fisheries from different parts of the world such as Atlantic Ocean (Baum et al., 2003; Hutching and Baum, 2005), the Mediterranean Sea (Ferretti et al., 2008) and the Gulf of Mexico (Baum and Myers, 2004). Similarly, Southeast Asian countries are also known to have poor documentation of shark fisheries (Lam and Sadovy de Micheson, 2011). For example, India, a top shark harvesting country (Karnad et al., 2020), and Bangladesh (Bay of Bengal; Haque et al., 2022) are also reported have unmanaged and collapsing shark fishery. Further significant data collection, capacity building, awareness of the issue and biological data (such as, breeding behavior, feeding habitat, age at maturity, fecundity and migration) is required to understand the seasonal occurrence and movement pattern of sharks in Arabian Sea and surrounding waters and to make informed fishery management decisions in Pakistan.
ACKNOWLEDGMENT
Authors thankfully acknowledge the financial support to Amir Javed through Senior Research Fellowship from Center of Excellence in Marine Biology. We are indebted to Marine Fisheries Department, fishers and traders for help in data collection. Special thanks to Hamid Badar Osmany (Marine Fisheries Department) his assistance in the field observations.
Funding
The research was supported by the Center of Excellence in Marine Biology.
Ethical statement
The research work submitted here is Authors’ original work and all parties involved in the research are being given due credit. The data obtained from other sources is properly cited and acknowledged.
Statement of conflict of interest
The authors have declared no conflict of interest.
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