Submit or Track your Manuscript LOG-IN

Skin Marks on the Indus River Dolphin (Platanista minor) and their Implications for Conservation

PJZ_54_5_2329-2336

Skin Marks on the Indus River Dolphin (Platanista minor) and their Implications for Conservation

Aamir Ibrahim1, Bingyao Chen1, Hassan Ali2, Imran Ali3, Yang Cao1 and Guang Yang1*

1Jiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Wenyuan Road 1, Qixia District, Nanjing 210023, China.

2Punjab Wildlife and Parks Department, Punjab, Pakistan.

3Center for GIS, University of the Punjab, Lahore 54000, Pakistan.

ABSTRACT

The Indus River dolphin (Platanista minor) is an endangered species found in the Indus River system of Pakistan including Beas River in India which is a part of Indus River system, enlisted in Appendix I of CITES Red List of threatened species. Currently, the whole population across the Indus River in Pakistan is divided into four subpopulations. Although photo-identification efforts on freshwater dolphins were successfully made on the Irrawady dolphin (Orcaella brevirostris) in South Asia, Baiji (Lipotes vexillifer) in the Yangtze River of China, and the Amazon River dolphin (Inia geoffrensis) in South America, it is very difficult to take photographs of Indus river dolphin. From March 1 to 9 in 2019, a survey was conducted in the area covered in a branch of approximately 70 km of the Indus River from Taunsa barrage (District Muzaffargarh, Tehsil Kott Addu) to just downstream of Ghazi Ghat near Samina (District Dera Ghazi Khan) in Punjab, Pakistan. We successfully photographed and first reported seven types of skin marks originated from their natural or social interactions and anthropogenic activities. Dead bodies of five calves were collected from two different subpopulations in the Punjab river section, two from the Chashma-Taunsa and three from the Taunsa-Guddu barrage. Illegal hunting of Indus river dolphin and utilization of blubber in upstream areas of Punjab is still in practice. Anthropogenic threats are needed to be evaluated for long-term conservation of this endangered species to reduce conflict and mortality in areas where fishing is under practice.


Article Information

Received: 28 August, 2021

Revised: 05 September, 2021

Accepted: 21 September, 2021

Available online 13 December 2021

(early access)

Published 20 June 2022

Authors’ Contribution

AI collected data and wrote the manuscript. IA made maps and HA, BC, YC and GY revised the final manuscript.

Key words

Anthropogenic effect, Calves, Indus river dolphin, Intraspecific interaction, Photo-identification

DOI: https://dx.doi.org/10.17582/journal.pjz/20210828090819

* Corresponding author: [email protected]

0030-9923/2022/0005-2329 $ 9.00/0

Copyright 2022 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

Freshwater ecosystems of Indian subcontinent are inhabited by two species of river dolphins, the Ganges river dolphin (Platanista gangetica) and the Indus river dolphin (P. minor) (Braulik et al., 2021). Both river dolphins are endangered species enlisted in Appendix I of CITES Red List of threatened species. The Indus river dolphin is distributed in the Indus River system of Pakistan including Beas River in India which is a tributary of the Indus River system, and legally protected by all wildlife legislations of Pakistan. Its distributional range has declined by 80%, and the habitat is severely fragmented by diversion of water, construction of dams and barrages for irrigation purposes (Braulik et al., 2004, 2014c; Smith et al., 2012). Currently, in Pakistan the whole population (n=1816) across the Indus river has been divided into four subpopulations, i.e., two subpopulations in the Punjab river section (n=741), one subpopulation (n=170) from Chashma Taunsa (C-T) barrage and another subpopulation (n=571) from Taunsa-Guddu (T-G) barrage (WWF, 2017). Freshwater dolphins are least known among cetaceans, although recent studies have provided valuable information such as abundance, distribution, habitat selection and phylogenetics of Indus river dolphin (Braulik et al., 2004).

Efforts are still needed to understand the basic ecological aspects of dolphin’s life, to evaluate the potential threats in the habitat for long term conservation of this endangered species (Braulik et al., 2004). All the freshwater cetaceans occur in developing countries. In the advancement of technology, a non-invasive process of photographic technique and tracking of individuals is helpful in providing explanation for a large range of basic ecological questions regarding social interaction, distribution, population size, migration, critical habitat, conflict with fisheries and negative anthropogenic effects (Whitehead et al., 1992).

Photo-identification efforts on freshwater dolphins were successfully made on the Irrawady dolphin (Orcaella brevirostris) (Smith et al.,1997), Baiji (Lipotes vexillifer) in the Yangtze river of China in South East Asia (Hua et al., 1990; Zhou et al., 1998), and the Amazon river dolphin (Inia geoffrensis) in South America (Parra and Corkeron, 2001; Kreb and Rahadi, 2004) targeted the natural marks such as nicks, scars, notches, white marks, distinctive shape of dorsal fin, white spots on the dorsal ridge and behind the blowhole.

But for the Indus river dolphin, it was very difficult to take photographs. The anomalous surfacing behavior of Indus river dolphin breaks surface unpredictably in different directions every time and surfaces alone without any synchronization in groups, they appear on the surface only for fraction of seconds and does not approach the boats. Further, only rudimentary dorsal fin is present and lack of any identifiable features for individual identification (Herald et al., 1969; Braulik et al., 2012a). Sporadic efforts were made in Pakistan however, without any success in identifying individuals. Concerted efforts were made to take photos of Ganges river dolphin in Nepal, out of 1200 photographs, not a single individual could be identified (Smith and Reeves, 2000). In 2012, another attempt was made on the Ganges river dolphin in river Ganges in the vicinity of Farakka barrage, India. Out of 1000 photographs, only three individuals were identified, two with lower broken jaws and one with a deep cut on dorsal fin (Sinha and Kannan, 2014).

Interactions with fisheries and mortality of cetaceans has been increasing in frequency and intensity during the last decades. This interaction occurs when fisheries and predators exploit the same areas to target the same species (Beverton, 1985; DeMaster et al., 2001). The photographs could provide some information on intraspecific interactions, such as an affiliated behavior (Herzing, 1997), copulation (Payne and Dorsey, 1983; Reynolds et al., 2000), aggression (Herzing, 1997; Connor et al., 1992), negative anthropogenic effects and fisheries interactions, such as visible marks of wounds or injuries, scarring due to entanglement in nets (Friedlaender et al., 2001; Robbins and Mattila, 2001; Romanov, 2001; Baird et al., 2002; Baird and Gorgone, 2005).

The present study was conducted with the following objectives: (1) photographical identification of Indus river dolphin based on natural marks such as tooth rakes, linear wounds or injuries, (2) analysis of different marks to highlight the social interaction, interaction with fisheries and negative anthropogenic effects. It was a successful attempt to prove the possibility of photo-ID in Indus river dolphin and unveil the new different aspects of Indus river dolphin’s life. Such information would be valuable for the conservation and management of Indus river dolphin.

MATERIALS AND METHODS

The study was conducted from March 1 to 9 in 2019, 70 km from Taunsa barrage (District, Muzaffargarh, Tehsil Kott Addu) to just downstream of Ghazi Ghat near Samina (District, Dera Ghazi Khan) in Punjab, Pakistan (Fig. 1). Weather permitting, a four m long, wooden boat equipped with 8 Horsepower (HP) engine was used for field survey. The boat moved downstream slowly (switched off engine) relying on the current flow of river. When a dolphin was sighted, boat moved and approached slowly; attempt was made to take photographs by Camera (Canon, EOS 70d) equipped with tele-photolens (Canon, 400 mm), and geographic positions were recorded with GPS Garmin 62s. We focused on taking photographs with visible marks of different types from various sources (Scott et al., 2005). All photographs were optically analyzed, any visible marks were identified, and classified in different categories (Fig. 2, Table I).

 

The dolphin’s carcasses were collected during routine patrolling by Punjab wildlife department staff. As corpses were recovered, initial examination such as morphometric measurements, gender identification was performed at the spot. Later these corpses were transported to nearby stations and stored at -20oCuntil the necropsy was performed.

RESULTS

A total of 14 groups of 44 cumulated individuals were sighted, the group size ranged from one to eight (Fig. 3), the average group size being 3.14±2.14. Fifteen individuals 34.09% were successfully photographed. Based on the quality of photographs, seven individuals 46.66% were categorized in class A, of good quality with higher visibility of identifiable marks, while eight individuals 53.33% in class B, of low quality with lower visibility of marks on their bodies. Based on the body marks on the dolphins, all photographs were divided into two categories, natural or intraspecific category (n=13) and anthropogenic category (n=2). All the marks were quantified as their origin and abundance details (Fig. 2, Table I).

 

 

Five dolphins were found dead from 2018 to 2020, two from Chashma-Taunsa (C-T) barrage were named as “Gabbar” and “Grey”, while other three were named as “Laila”, “Sultan” and “Naina” from Taunsa-Guddu (T-G) barrage sections (Figs. 4 and 6). The three dolphins from T-G barrage were transported to Lahore Zoo (Lahore, Punjab) and necropsy was performed there. A team of veterinarians confirmed the cause of death due to entanglement in nets (data will be published in a separate account).

 

 

DISCUSSION

Different skin marks have been reported globally on the bodies of different species of cetaceans (Connor et al., 2000). For Indus river dolphins, still no report is available to identify or analyze any skin marks. Here, for the first time we are reporting seven types of skin marks originated from their natural or social interactions and anthropogenic activities. All these marks were classified according to their nature (Fig. 2, Table I). Among all the skin marks 86.66% were originated from the natural or social interactions. The highest prevalence marks were fresh linear wounds and tooth rakes, other marks such as ring lesions and dark patches were moderately prevalent, while white patches and yellow spots prevalence was low. Leone et al. (2019) reported similar skin marks on bottlenose dolphins (Tursiops truncatus), by comparing couple of other studies suggested that, these marks were directly associated with natural different behavioral activities during social interactions among the individuals.

Some marks such as ring lesion, dark and white patches are the combination of social interactions and negative environmental effects. These marks are the healing of older injuries caused by repeated social interactions, later these injuries might have been caused by microorganisms (Thompson and Hammond, 1992; Wilson et al., 1999; Van et al., 2007; Hart et al., 2012; Luksenburg, 2014; Mariani et al., 2016) or parasites, pollution in the water or other associated negative environmental conditions (Bloom and Jager, 1994; Harzen and Brunnick, 1997; Wilson et al., 1999; Rowe and Dawson, 2009; Hart et al., 2012; Mariani et al., 2016). The major cause, overfishing in the habitat may have reduced the availability of food resources, resulting in the increase of the foraging cost and intense competition among organisms (Blasi et al., 2015). Bottlenose dolphins in aggression have been found chasing, ramming, body slamming, sideswipes, tail slaps and biting (Tyack and Clark, 2000). In the current study a dolphin was found rapid swimming and chasing other dolphins, lateral side slapping (Fig. 5) of the same dolphin was spotted in a group of six individuals. This behavior might be an indicator of aggression as a threat to other dolphins in similar area of habitat. Leone et al. (2019) are of the view that further histological analysis in future could provide information regarding etiology of these marks for evaluating dolphin’s health in the habitat.

Among all the skin marks 13.33% were originated by anthropogenic activities. In this study, 2 dolphins were found with traumatic injuries (open wounds), these wounds are characterized as clear sign of negative anthropogenic effects. During the dry season, water diverted into canals to support the agriculture, reduces the level of water in the river and the availability of space for dolphins and their prey. Conflict occurs when fishermen prefer to exploit areas for fishing in their habitat, resulting in negative anthropogenic outcome (Sinha et al., 2010; Braulik et al., 2012b) with most common external traumatic injuries such as parallel lines (entanglement in nets), deep wounds on skin, broken mandibles and teeth, lesions, notches and skin abrasions in different body regions (Kuiken et al., 1994; Siebert et al., 2001). These wounds make an individual more vulnerable to infection, which could limit the physiological activity, alter the behavior of dolphins, high energy demands, starvation and may lead to the death of the individual (Visser, 1999; Van et al., 2007; Bossart et al., 2017).

 

Table I. The origin, type of marks and their description reported in different studies on Bottlenose dolphins (Tursiops ssp.), and similar marks found in this study on the body of Indus River dolphin and their abundance (%) during 1-9 March in 2019.

Origin

Type of marks

Descriptions

References

ID

Abundance (%)

Natural or social interaction

Tooth rakes (TR)

Parallel linear skin wounds or scars

Connor et al., 1992

1, 2, 3, 4, 5, 14

40

Linear wounds (LW)

Laceration in the epidermis

Luksenburg, 2014

1, 4, 5, 6, 7, 8, 9, 10, 14

66.66

White patches (WP)

Small white patches of irregular shape

Wilson et al., 1997

1, 10

13.33

Ring lesion (RL)

Cream or white in center circled by normally colored skin

4, 6, 13

20

Dark Patches (DP)

Irregular shape of dark grey blemish

Thompson and Hammond, 1992; Harzen and Johnson,1997; Wilson et al.,1997

3, 4, 5

20

Yellow spot (YS)

Cluster of Cream or pale colored mass

Wilson et al.,1997

12

6.66

Anthropogenic

Open wounds (OW)

Deep cut-like wound, blubber visible

Lockyer and Morris, 1990

14, 15

13.33

 

Mortality in cetaceans is common due to incidental capture in fishing nets; this is a worldwide problem (Reeves et al., 2013). From 1993-2011, a total of 101 Indus dolphins were reported dead from Sindh Province due to incidental capture in fishing nets. While in the Punjab area only three dolphins (two mature and one calf) were reported dead in fishing nets in 2016 (WWF- Pakistan, 2011; Waqas et al., 2012; Braulik et al., 2015; Aisha et al., 2017). During 2018-2020, we have collected five dead bodies of calves from the two different subpopulations in the Punjab river section, two individuals from Chashma-Taunsa and three individuals from Taunsa-Guddu barrage (Fig. 6).

 

 

Incidental capture and mortality data of two marine dolphin species viz., harbor porpoise (Phocaena phocaena) and bottlenose dolphin (Tursiops truncatus), emphasized 65% death of calves in the former and 41% death of calves in the latter. Major causes for the higher mortality in calves might be that calves echolocate with higher frequencies than adults, hence they may not be able to detect nets as rapidly as detected by adults. Calves are playful, careless, active, and agile which increases the chances of entrapment (Au et al., 1999; Siebert et al., 2001; Silva and Sequeira, 2003). Most of the body parts from one corpse of dolphin (Gabbar 5) were absent, and it seems that illegal hunting of Indus river dolphin and utilization of blubber in upstream area of Punjab is still in practice. The negative impacts of fisheries besides capture in nets include increasing water pollution and other associated anthropogenic impacts across the habitat of Indus river dolphin. Turvey et al. (2007) are of the view that freshwater dolphins are at higher risk of extinction due to habitat loss and anthropogenic pressures, as evidenced by a recent extinction of the Baiji (Lipotes vexillifer) freshwater dolphin in China.

CONCLUSION

The study demonstrated photographs as a new efficient and cost-effective methodology for photo identification of river dolphins to study the free ranging Indus dolphins in the wild. It is an easy approach to document the behavior of Indus river dolphin and threats to them by analyzing different skin marks. The analysis of these marks showed the combination of natural social interaction, negative environmental effects, and anthropogenic effects of fisheries. Indus river dolphins survive under multiple anthropogenic pressures, most important of which are overfishing and increasing pollution. Reduction in the mortality and conflict with fisheries, is important to evaluate the effects of increasing pollution on the dolphin’s health and quality of the habitat. Capture-mark recapture (CMR) method is possible for population estimation of the Indus river dolphin. Some marks are short term such as tooth rakes and linear wounds, while some permanent marks such as ring lesion, dark patches, white patches and yellow spots are valuable for the CMR method.

ACKNOWLEDGEMENTS

This study was financially supported by the Key Project of the National Natural Science Foundation of China (NSFC) (grant no. 31630071 to G.Y), the National Key Program of Research and Development, Ministry of Science and Technology of China (grant no. 2016YFC0503200 to G.Y), and the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD). Authors are thankful to many people who have helped during field surveys, including Shahid Iqbal and Babar Bukhari.

Statement of conflict of interest

The authors have declared no conflict of interest.

REFERENCES

Aisha, H., Braulik, T.G., Khan, U., Leslie, A. and Nawaz, R., 2017. Indus river dolphin (Platanista gangetica minor) an update on the current population assessment and conservation challenges. Working paper SC/67A/SM/22 presented to the International Whaling Commission, Scientific Committee. 10.13140/RG.2.2.17025.56163.

Au, W.W.L., Kastelein, R.A., Rippe, T. and Schooneman, N.M., 1999. Transmission beam pattern and echolocation signals of a harbor porpoise (Phocoena phocoena). J. Acoust. Soc. Am., 106: 3699–3709. https://doi.org/10.1121/1.428221

Baird, R.W. and Gorgone, A.M., 2005. False killer whale dorsal fin disfigurements as a possible indicator of long-line fishery interactions in Hawaiian waters. Pac. Sci., 59: 593–601. https://doi.org/10.1353/psc.2005.0042

Baird, R.W., Stacey, P.J., Duffus, D.A. and Langelier, K.M., 2002. An evaluation of gray whale (Eschrichtius robustus) mortality incidental to fishing operations in British Columbia, Canada. Cet. Res. Manage., 4: 289–296.

Beverton, R.J.H., 1985. Analysis of marine mammal–fisheries interactions. In: Marine mammals and fisheries (eds. J.R. Beddington, R.J.H. Beverton and D.M. Lavigne). LDN, UK. pp. 3–33.

Blasi, M.F., Giuliani, A. and Boitani, L., 2015. Influence of trammel nets on the behaviour and spatial distribution of bottlenose dolphins (Tursiops truncatus) in the Aeolian Archipelago, Southern Italy. J. aquat. Mammal., 41: 295–310. https://doi.org/10.1578/AM.41.3.2015.295

Bloom, P. and Jager, M., 1994. The injury and subsequent healing of a serious propeller strike to a wild bottlenose dolphin (Tursiops truncatus) resident in cold waters of the Northumberland coast of England. J. aquat. Mammal., 20: 59–64.

Bossart, G.D., Fair, P., Schaefer, A.M. and Reif, J.S., 2017. Health and Environmental Risk Assessment Project for bottlenose dolphins (Tursiops truncatus) from the southeastern USA. J. aquat. Org., 125: 141–153. https://doi.org/10.3354/dao03142

Braulik, G.T., Frederick, I.A., Uzma, K., Mohammad, I., Ravindra, K.S., Thomas, A.J., Carl, D., Jeff, A.G., 2021. Taxonomi c revision of the South Asian River dolphins (Platanista): Indus and Ganges River dolphins are separate species. Mar. Mammal. Sci., 2021: 1–38.

Braulik, G.T., Smith, B.D. and Chaudhry, A.A., 2004. Platanista gangetica ssp. minor. 2004 IUCN red list of threatened species, IUCN, Gland, Switzerland and Cambridge, UK.

Braulik, T.G., Bhatti, I.Z., Ehsan, T., Hussain, B., Abdul, R.K., Khan, A., Khan, U., Kundi, U.K., Rajput, R., Reichert, P.A., Northridge, P.S., Bhagat, B.H. and Garstang, R., 2012a. Robust abundance estimate for endangered river dolphin subspecies in South Asia. Endanger. Sp. Res., 17: 201–215. https://doi.org/10.3354/esr00425

Braulik, G.T., Reichert, A.P., Ehsan, T., Khan, S., Northridge, S.P., Alexander J.S. and Garstang. R., 2012b. Habitat use by a freshwater dolphin in the low-water season. Aquat. Conserv. Mar. Freshw. Ecosyst., 22: 533–546. https://doi.org/10.1002/aqc.2246

Braulik, G.T., Barnett, R., Odon, V., Islas-Villanueva, V., Hoelzel, A.R. and Graves, J.A., 2014c. One species or two? Vicariance, lineage divergence and low mtDNA diversity in geographically isolated populations of South Asian River dolphin. J. Mammal. Evol., pp. 1 –10. https://doi.org/10.1007/s10914-014-9265-6

Braulik, G.T., Noureen, U., Arshad, M. and Reeves, R.R., 2015. Review of status, threats, and conservation management options for the endangered Indus River blind dolphin. Biol. Conserv., 192: 30–41. https://doi.org/10.1016/j.biocon.2015.09.008

Connor, R.C., Read, A.J. and Wrangham, R., 2000. Male reproductive strategies and social bonds. In: Cetacean societies: Field studies of dolphins and whales (eds. J. Mann, R.C. Connor, P.L. Tyack and H. Whitehead). pp. 247–269.

Connor, R.C., Smolker, R.A. and Richards, A.F., 1992. Two levels of alliance formation among male bottlenose dolphins (Tursiops sp.). Proc. natl. Acad. Sci. U.S.A., 89: 987–990. https://doi.org/10.1073/pnas.89.3.987

Demaster, D.P., Fowler, C.W., Perry, S.L. and Richlen, M.F., 2001. Predation and competition: the impact of fisheries on marine-mammal populations over the next one hundred years. J. Mammal., 82: 641–651. https://doi.org/10.1093/jmammal/82.3.641

Friedlaender, A.S., Mclellan, W.A. and Pabst, D.A., 2001. Characterizing an interaction between coastal bottlenose dolphins (Tursiops truncatus) and the spot gillnet fishery in south-eastern North Carolina, USA. J. Cet. Res. Manage., 3: 293–303.

Hart, L.B., Rotstein, D.S., Wells, R.S., Allen, J., Barleycorn, A. and Balmer, B.C., 2012. Skin lesions on common bottlenose dolphins (Tursiops truncatus) from three sites in the northwest Atlantic, USA. PLoS One, 7: e33081. https://doi.org/10.1371/journal.pone.0033081

Harzen, S. and Brunnick, B.J., 1997. Skin disorders in bottlenose dolphins (Tursiops truncatus), resident in the Sado estuary, Portugal. J. aquat. Mammal., 23: 59–68.

Herald, E.S., Brownell, J.R.L., Frye, F.L., Morris, E.J., Evans, W.E. and Scott, A.B., 1969. Blind river dolphin: First side-swimming cetacean. Science, 166: 1408–1410. https://doi.org/10.1126/science.166.3911.1408

Herzing, D.L. and Johnson, C.M., 1997. Interspecific interactions between Atlantic spotted dolphins (Stenella frontalis) and bottlenose dolphins (Tursiops truncatus) in the Bahamas, 1985–1995. J. aquat. Mammal., 23: 85–99.

Hua, Y.Y., Zhang, X., Wei, Z. and Wang, X., 1990. A note on the feasibility of using photo-identification techniques to study the Baiji, Lipotes vexillifer. Rep. Int. Whal. Commn., 12: 439–440.

Kreb, D. and Rahadi, K.D., 2004. Living under an aquatic freeway: Effects of boats on Irrawaddy dolphins (Orcaella brevirostris) in a coastal and riverine environment in Indonesia. J. aquat. Mammal., 30: 363–375. https://doi.org/10.1578/AM.30.3.2004.363

Kuiken, T., O’leary, M., Baker, J. and Kirkwood, J., 1994a. Pathology of harbor porpoises (Phocoena phocoena) from the coast of England and suspected bycatch. Eur. Cetacean Soc. Newsl., 26: 31–34.

Leone, A.B., Bonanno, F.G., Luigi, B. and Blasi, M.F., 2019. Skin marks in bottlenose dolphin (Tursiops truncatus) interacting with artisanal fishery in the central Mediterranean Sea. PLoS One, 14: e0211767. https://doi.org/10.1371/journal.pone.0211767

Lockyer, C.H., Morris, R.J., 1990. Some observations on wound healing and persistence of scars in Tursiops truncatus. Rep. Int. Whal. Commn., 12(Special issue): 113–118.

Luksenburg, J.A., 2014. Prevalence of external injuries in small cetaceans in Aruban waters, Southern Caribbean. PLoS One, 9: e88988. https://doi.org/10.1371/journal.pone.0088988

Mariani, M., Miragliuolo, A., Mussi, B., Russo, G.F., Ardizzone, G. and Pace, D.S., 2016. Analysis of the natural markings of Risk’s dolphins (Grampus griseus) in the central Mediterranean Sea. Mammals, 97: 1512–1524. https://doi.org/10.1093/jmammal/gyw109

Parra, G.J. and Corkeron, P., 2001. The feasibility of using photo-identification techniques to study the Irrawaddy dolphin (Orcaella brevirostris) (Owen in Gray 1866). J. aquat. Mammal., 27: 45-49.

Payne, R.S. and Dorsey, E., 1983. Sexual dimorphism and aggressive use of callosities in right whales (Eubalaena australis). In: Communication and behaviour of whales (ed. R.S. Payne). Westview Press, Boulder, CO. pp. 295–329.

Reeves, R.R., Mcclellan, K. and Werner, T.B., 2013. Marine mammal bycatch in gillnet and other entangling net fisheries, 1990 to 2011. Endanger. Sp. Res., 20: 71–97. https://doi.org/10.3354/esr00481

Reynolds, J.E., Wells, R.S. and Eide, S.D., 2000. The bottlenose dolphin: Biology and conservation. Gainesville, University Press of Florida.

Robbins, J. and Mattila, D.K., 2001. Monitoring entanglements of humpback whale (Megaptera novaeangliae) in the gulf of maine on the basis of peduncle scarring. Document SC/53/ NAH25 presented to the International Whaling Commission Scientifi Committee.

Romanov, E.V., 2001. Bycatch in the tuna purse-seine fishery in the western Indian Ocean. Fish. Bull., 100: 90–105.

Rowe, L.E. and Dawson, S.M., 2009. Determining the sex of bottlenose dolphins from Doubtful Sound using dorsal fin photographs. Mar. Mammal. Sci., 25: 19–34. https://doi.org/10.1111/j.1748-7692.2008.00235.x

Scott, E.M., Mann, J., Watson, J.J., Sargeant, B.L. and Connor, R.C., 2005. Aggression in bottlenose dolphins: evidence for sexual coercion, male-male competition, and female tolerance through analysis of tooth-rake marks and behavior. J. Behav., 21: 24–44. https://doi.org/10.1163/1568539053627712

Siebert, U., Wünschmann, A., Weiss, R., Frank, H., Benke, H. and Frese, K., 2001. Postmortem findings in harbour porpoises (Phocoena phocoena) from German North and Baltic seas. J. comp. Pathol., 124: 102–114. https://doi.org/10.1053/jcpa.2000.0436

Silva, M.A. and Sequeira, M., 2003. Patterns in the mortality of common dolphins (Delphinus delphis) on the Portuguese coast, using stranding records. J. aquat. Mammal., 29: 88–98. https://doi.org/10.1578/016754203101023924

Sinha, R.K. and Kannan, K., 2014. Ganges river dolphin: An overview of biology, ecology, and conservation status in India. AMBIO, 43: 1029–1046. https://doi.org/10.1007/s13280-014-0534-7

Smith, B.D. and Reeves, R.R., 2000. Report of the second meeting of the Asian River Dolphin Committee, Rajendrapur, Bangladesh, 22–24 February 1997. In: Biology and conservation of freshwater cetaceans in Asia (eds. R.R. Reeves, B.D. Smith and T. Kasuya). IUCN, Gland Switzerland.

Sinha, R.K., Behera, S.K. and Choudhury, B.C., 2010. Conservation action plan for the Gangetic dolphins. National Ganga River Basin Authority, Ministry of Environment and Forests, Govt. of India. pp. 44.

Smith, B.D., Braulik, G.T. and Ravindra, K.S., 2012. Platanista gangetica ssp. gangetica. IUCN Red List of Threatened Species.

Smith, B.D., Thant, U.H., Lwin, J.M. and Shaw, C.D., 1997. Investigation of cetaceans in the Ayeyarwady River and northern coastal waters of Myanmar. J. mar. Biol., 14: 173-194.

Thompson, P.M. and Hammond, P.S., 1992. The use of photography to monitor dermal disease in wild bottlenose dolphins. AMBIO., 21: 135–137.

Turvey, S.T., Pitman, R.L., Taylor, B.L., Barlow, J. and Akamatsu, T., 2007. First human-caused extinction of a cetacean species? Biol. Lett., 3: 537–540. https://doi.org/10.1098/rsbl.2007.0292

Tyack, P.L. and Clark, C.W., 2000. Communication and acoustic behavior of dolphins and whales. In: Hearing by whales and dolphins (eds. W.W.L. Au, A.N. Popper and R.R. Fay). Springer-Verlag. New York, USA. pp. 156-224. https://doi.org/10.1007/978-1-4612-1150-1_4

Van, B.M.F., Van, W.K., Reyes, J.C., Felix, F., Echegaray, M. and Siciliano, S., 2007. A preliminary overview of skin and skeletal diseases and traumata in small cetaceans from South American waters. Latin Am. J. aquat. Mammal., 6: 7–42. https://doi.org/10.5597/lajam00108

Visser, I. N., 1999. Propeller scars on and known home range of two Orca (Orcinus orca) in New Zealand waters. J. Mar. Freshw. Res., 33: 635–642. https://doi.org/10.1080/00288330.1999.9516906

Waqas, U., Malik, M.I. and Khokhar, L.A., 2012. Conservation of Indus River dolphin (Platanista gangetica minor) in the Indus River system, Pakistan: An overview. Zool. Sur. Pak., 21: 82-85.

Whitehead, H., Brennan, S. and Grover, D., 1992. Distribution and behaviour of male sperm whales on the Scotian Shelf, Canada. Can. J. Zool., 70: 912-918. https://doi.org/10.1139/z92-130

Wilson, B., Arnold, H., Bearzi, G., Fortuna, C.M., Gaspar, R. and Ingram, S., 1999. Epidermal diseases in bottlenose dolphins: Impacts of natural and anthropogenic factors. J. biol. Sci., 266: 1077– 1083. https://doi.org/10.1098/rspb.1999.0746

Wilson, B., Thompson, P.M. and Hammond, P, S., 1997. Skin lesions and physical deformities in bottlenose dolphins in the Moray Firth: Population prevalence and age-sex differences. AMBIO, 26: 243–245.

WWF-Pakistan, 2011. Report on Indus River dolphin mortality: Analysis of dead dolphin samples for pesticides. WWF-Pakistan, Lahore.

WWF-Pakistan, 2017. Signs of Hope for the endemic and endangered. Comprehensive population assessment of the Indus River dolphin (Platanista gangetica minor) in the Indus River. WWF-Pakistan, Lahore.

Zhou, K., Sun, J., Gao, A. and Würsig, B., 1998. Baiji (Lipotes vexillifer) in the lower Yangtze River: Movements, numbers, threats and conservation needs. J. aquat. Mammal., 24: 123-132.

To share on other social networks, click on any share button. What are these?

Pakistan Journal of Zoology

October

Pakistan J. Zool., Vol. 56, Iss. 5, pp. 2001-2500

Featuring

Click here for more

Subscribe Today

Receive free updates on new articles, opportunities and benefits


Subscribe Unsubscribe