Skip to main content
Log in

Catch and bycatch captured by tropical tuna purse-seine fishery in whale and whale shark associated sets: comparison with free school and FAD sets

  • Original Paper
  • Published:
Biodiversity and Conservation Aims and scope Submit manuscript

Abstract

In an ecosystem approach to fisheries management (EAFM) framework of the tuna purse-seine fishery, the assessment of target species, but also that of bycatch species, is essential. In the Atlantic and Indian oceans, purse-seine nets are sometimes set around tuna schools associated with whale sharks and baleen whales, although less frequently than around free-swimming tuna schools or those associated with fish aggregating devices (FAD). However, knowledge on the targeted catch and bycatch in these megafauna associated fishing sets is still relatively limited. Therefore, the aims of this study were to assess species and size composition of the target tuna species, as well as the diversity of bycatch species in whale and whale shark associated sets. Whale associated sets were found to be very similar to free school sets in terms of tuna catch (large yellowfin tuna), bycatch occurrence (presence in half the sets) and species assemblage (alpha and beta diversity). Whale shark associated sets were intermediate between FAD and free school sets, with tuna catch (skipjack and juvenile yellowfin) closer to FAD than to free school sets. However, the presence of large yellowfin, the bycatch composition (with almost no finfish, abundantly captured in FAD sets) and the species assemblage showed similarity with free school sets. This study highlights the need for an EAFM in the tuna purse-seine fishery by providing knowledge on pelagic multi-specific catches and bycatches.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7

Similar content being viewed by others

References

  • Amandè MJ, Ariz J, Chassot E, Delgado de Molina A, Gaertner D, Murua H, Pianet R, Ruiz J, Chavance P (2010) Bycatch of the European purse seine tuna fishery in the Atlantic Ocean for the 2003-2007 period. Aquat Living Resour 23:353–362. https://doi.org/10.1051/alr/2011003

    Article  Google Scholar 

  • Amandè MJ, Chassot E, Chavance P, Murua H, de Molina AD, Bez N (2012) Precision in bycatch estimates: the case of tuna purse-seine fisheries in the Indian Ocean. ICES J Mar Sci 69:1501–1510. https://doi.org/10.1093/icesjms/fss106

    Article  Google Scholar 

  • Anderson MJ, Willis TJ (2003) Canonical analysis of principal coordinates: a useful method of constrained ordination for ecology. Ecology 84:511–525. https://doi.org/10.1890/0012-9658(2003)084%5b0511:CAOPCA%5d2.0.CO;2

    Article  Google Scholar 

  • Ariz J, Delgado A, Fonteneau A, Gonzales Costas F, Pallares P (1999) Logs and tunas in the Eastern Tropical Atlantic. A review of present knowledge and uncertainties. In: Proceedings of the international workshop on fishing for tunas associated with floating objects. IATTC Spec Rep 11:21–65

  • Bez N, Walker E, Gaertner D, Rivoirard J, Gaspar P (2011) Fishing activity of tuna purse seiners estimated from vessel monitoring system (VMS) data. Can J Fish Aquat Sci 68:1998–2010. https://doi.org/10.1139/f2011-114

    Article  Google Scholar 

  • Bonfil R (2008) The Biology and Ecology of the Silky Shark, Carcharhinus falciformis. In: Camhi MD, Pikitch EK, Babcock EA (eds) Sharks of the open ocean: biology, fisheries and conservation. Blackwell, Oxford, pp 114–127

    Chapter  Google Scholar 

  • Bourjea J, Clermont S, Delgado A, Murua H, Ruiz J, Ciccione S, Chavance P (2014) Marine turtle interaction with purse-seine fishery in the Atlantic and Indian oceans: lessons for management. Biol Conserv 178:74–87. https://doi.org/10.1016/j.biocon.2014.06.020

    Article  Google Scholar 

  • Capietto A, Escalle L, Chavance P, Dubroca L, Delgado de Molina A, Murua H, Floch L, Damiano A, Rowat D, Merigot B (2014) Mortality of marine megafauna induced by fisheries: insights from the whale shark, the world’s largest fish. Biol Conserv 174:147–151. https://doi.org/10.1016/j.biocon.2014.03.024

    Article  Google Scholar 

  • Cayré P (1984) Procédure suivie pour la révision de la composition spécifique des statistiques thonières FISM (France, Côte d’Ivoire, Sénégal et Maroc). Collect Vol Sci Pap ICCAT 21:102–107

    Google Scholar 

  • CDB (1992) Convention on biological diversity. www.cbd.int

  • Chao A (1987) Estimating the population size for capture-recapture data with unequal catchability. Biometrics 43:783–791

    Article  CAS  PubMed  Google Scholar 

  • Chassot E, Assan E, Soto M, Damiano A, Delgado De Molina A, Joachim LD, Cauquil P, Lesperance F, Curpen M, Lucas J, Floch L (2015a) Statistics of the European Union and associated flags purse seine fishing fleet targeting tropical tunas in the Indian Ocean 1981-2014. IOTC technical report. IOTC-2015-WPTT17-12

  • Chassot E, Floch L, Dewals P, Irié D, Tamegnon A, Cauquil P, Amande MJ, Chavance P (2015b) Statistics of the French purse-seine fishing fleet targeting tropical tunas in the Atlantic Ocean (1991-2013). Collect Vol Sci Pap ICCAT 71:540–572

    Google Scholar 

  • Colman JG (1997) A review of the biology and ecology of the whale shark. J Fish Biol 51:1219–1234. https://doi.org/10.1111/j.1095-8649.1997.tb01138.x

    Article  CAS  PubMed  Google Scholar 

  • Dagorn L, Holland KN, Restrepo V, Moreno G (2013) Is it good or bad to fish with FADs? What are the real impacts of the use of drifting FADs on pelagic marine ecosystems? Fish Fish 14:391–415. https://doi.org/10.1111/j.1467-2979.2012.00478.x

    Article  Google Scholar 

  • De Molina AD, Rojo V, Santana JC, Ariz J (2015) Estadísticas Españolas de la pesquería atunera tropical, en el océano Atlántico, hasta 2013. Collect Vol Sci Pap ICCAT 71:239–263

    Google Scholar 

  • Escalle L, Capietto A, Chavance P, Dubroca L, Delgado De Molina A, Murua H, Gaertner D, Romanov E, Spitz J, Kiszka JJ, Floch L, Damiano A, Merigot B (2015) Cetaceans and tuna purse seine fisheries in the Atlantic and Indian Oceans: interactions but few mortalities. Mar Ecol Prog Ser 522:255–268. https://doi.org/10.3354/meps11149

    Article  Google Scholar 

  • Escalle L, Pennino MG, Gaertner D, Chavance P, Delgado de Molina A, Demarcq H, Romanov E, Merigot B (2016) Environmental factors and megafauna spatio-temporal co-occurrence with purse-seine fisheries. Fish Oceanogr 25:433–447. https://doi.org/10.1111/fog.12163

    Article  Google Scholar 

  • Etienne RS, Olff H (2005) Confronting different models of community structure to species-abundance data: a Bayesian model comparison. Ecol Lett 8:493–504. https://doi.org/10.1111/j.1461-0248.2005.00745.x

    Article  PubMed  Google Scholar 

  • FAO (2003) Fisheries management. The ecosystem approach to fisheries. FAO technical guidelines for responsible fisheries, vol 4. FAO, Rome, pp 1–112

    Google Scholar 

  • Filmalter J, Capello M, Deneubourg JL, Cowley PD, Dagorn L (2013) Looking behind the curtain: quantifying massive shark mortality in fish aggregating devices. Front Ecol Environ 11:291–296. https://doi.org/10.1890/130045

    Article  Google Scholar 

  • Gaertner D, Menard F, Develter C, Ariz J (2002) Bycatch of billfishes by the European tuna purse-seine fishery in the Atlantic Ocean. Fish Bull 100:683–689

    Google Scholar 

  • Girard C, Benhamou S, Dagorn L (2004) FAD: fish aggregating device or fish attracting device? A new analysis of yellowfin tuna movements around floating objects. Anim Behav 67:319–326. https://doi.org/10.1016/j.anbehav.2003.07.007

    Article  Google Scholar 

  • Gleiss AC, Norman B, Wilson RP (2011) Moved by that sinking feeling: variable diving geometry underlies movement strategies in whale sharks. Funct Ecol 25:595–607. https://doi.org/10.1111/j.1365-2435.2010.01801.x

    Article  Google Scholar 

  • Goldbogen JA, Calambokidis J, Shadwick RE, Oleson EM, McDonald MA, Hildebrand JA (2006) Kinematics of foraging dives and lunge-feeding in fin whales. J Exp Biol 209:1231–1244. https://doi.org/10.1242/jeb.02135

    Article  PubMed  Google Scholar 

  • Goldbogen JA, Calambokidis J, Croll DA, Harvey JT, Newton KM, Oleson EM, Schorr G, Shadwick RE (2008) Foraging behavior of humpback whales: kinematic and respiratory patterns suggest a high cost for a lunge. J Exp Biol 211:3712–3719. https://doi.org/10.1242/jeb.023366

    Article  PubMed  Google Scholar 

  • Gotelli NJ, Colwell RK (2001) Quantifying biodiversity: procedures and pitfalls in the measurement and comparison of species richness. Ecol Lett 4:379–391. https://doi.org/10.1046/j.1461-0248.2001.00230.x

    Article  Google Scholar 

  • Hallier JP, Parajua JI (1999) Review of tuna fisheries on floating objects in the Indian Ocean. In: Proceedings of the international workshop on fishing for tunas associated with floating objects. IATTC spectrum report, vol 11, pp 195–221

  • Hampton J, Bailey K (1999) Fishing for tunas associated with floating objects: review of the western Pacific fishery. In: Proceedings of the international workshop on fishing for tunas associated with floating objects. IATTC spectrum report, vol 11, pp 222–284

  • Hurlbert SH (1971) The nonconcept of species diversity: a critique and alternative parameters. Ecology 52:577–586. https://doi.org/10.2307/1934145

    Article  PubMed  Google Scholar 

  • Kelleher K (2005) Discards in the world’s marine fisheries: an update. FAO fisheries technical paper, vol 470. Food and Agriculture Organization of the United Nations, Rome

    Google Scholar 

  • Lezama-Ochoa N, Murua H, Chust G, Ruiz J, Chavance P, de Molina AD, Caballero A, Sancristobal I (2015) Biodiversity in the by-catch communities of the pelagic ecosystem in the western Indian Ocean. Biodivers Conserv 24:2647–2671. https://doi.org/10.1007/s10531-015-0951-3

    Article  Google Scholar 

  • Marsac F, Fonteneau A, Menard F (2000) Drifting FADs used in tuna fisheries: an ecological trap? In: Le Gall JY, Cayré P, Taquet M (eds) Pêche thonière et dispositifs de concentration de poissons. Actes de colloques, vol 28. IFREMER, Issy-les-Moulineaux, pp 15–35

    Google Scholar 

  • Matsumoto T, Satoh K, Toyonaga M (2014) Behavior of skipjack tuna (Katsuwonus pelamis) associated with a drifting FAD monitored with ultrasonic transmitters in the equatorial central Pacific Ocean. Fish Res 157:78–85. https://doi.org/10.1016/j.fishres.2014.03.023

    Article  Google Scholar 

  • Meekan M, Fuiman L, Davis R, Berger Y, Thums M (2015) Swimming strategy and body plan of the world’s largest fish: implications for foraging efficiency and thermoregulation. Mar Megafauna. https://doi.org/10.3389/fmars.2015.00064

    Article  Google Scholar 

  • Pallarés P, Hallier JP (1997) Analyse du schéma d’échantillonnage multispécifique des thonidés tropicaux. Rapport scientifique. Program 95/37. IEO/ORSTOM

  • Pallarés P, Petit C (1998) Tropical tunas: new sampling and data processing strategy for estimating the composition of catches by species and sizes. Collect Vol Sci Pap ICCAT 48:230–246

    Google Scholar 

  • Pianet R (1999) Evolution du système de collecte et de traitement des données de la pêche thonière des senneurs européens et assimilés de 1981 à 1998. IOTC Proc. 1:74–96

    Google Scholar 

  • Pikitch EK, Santora C, Babcock EA, Bakun A, Bonfil R, Conover DO, Dayton P, Doukakis P, Fluharty D, Heneman B, Houde ED, Link J, Livingston PA, Mangel M, McAllister MK, Pope J, Sainsbury KJ (2004) Ecosystem-based fishery management. Science 80(305):346–347. https://doi.org/10.1126/science.1098222

    Article  Google Scholar 

  • R Development Core Team (2017) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna. Version 3.4.0

  • Romanov EV (2002) Bycatch in the tuna purse-seine fisheries of the western Indian Ocean. Fish Bull 100:90–105

    Google Scholar 

  • Rowat D, Brooks KS (2012) A review of the biology, fisheries and conservation of the whale shark Rhincodon typus. J Fish Biol 80:1019–1056. https://doi.org/10.1111/j.1095-8649.2012.03252.x

    Article  CAS  PubMed  Google Scholar 

  • Siegel S, Castellan NJ (1988) Nonparametric statistics for the behavioral sciences, 2nd edn. McGraw-Hill, New York, p 399

    Google Scholar 

  • Simpson EH (1949) Measurement of diversity. Nature 163:688. https://doi.org/10.1038/163688a0

    Article  Google Scholar 

  • Smith B, Wilson JB (1996) A consumer’s guide to evenness indices. Oikos 76:70–82. https://doi.org/10.2307/3545749

    Article  Google Scholar 

  • Torres-Irineo E, Amandè MJ, Gaertner D, de Molina AD, Murua H, Chavance P, Ariz J, Ruiz J, Lezama-Ochoa N (2014a) Bycatch species composition over time by tuna purse-seine fishery in the eastern tropical Atlantic Ocean. Biodivers Conserv 23:1157–1173. https://doi.org/10.1007/s10531-014-0655-0

    Article  Google Scholar 

  • Torres-Irineo E, Gaertner D, Chassot E, Dreyfus-León M (2014b) Changes in fishing power and fishing strategies driven by new technologies: the case of tropical tuna purse seiners in the eastern Atlantic Ocean. Fish Res 155:10–19. https://doi.org/10.1016/J.FISHRES.2014.02.017

    Article  Google Scholar 

  • Tyminski JP, de la Parra-Venegas R, Cano JG, Hueter RE (2015) Vertical movements and patterns in diving behavior of whale sharks as revealed by pop-up satellite tags in the Eastern Gulf of Mexico. PLoS ONE 10:e0142156. https://doi.org/10.1371/journal.pone.0142156

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Walters V, Fierstine HL (1964) Measurements of swimming speeds of yellowfin tuna and wahoo. Nature 202:208–209. https://doi.org/10.1038/202208b0

    Article  CAS  PubMed  Google Scholar 

  • Ward T, Tarte D, Hegerl E, Short K (2002) Ecosystem-based management of marine capture fisheries. World Wide Fund for Nature Australia, Ultimo

    Google Scholar 

  • Whittaker RH (1960) Vegetation of the Siskiyou mountains, Oregon and California. Ecol Monogr 30:279–338

    Article  Google Scholar 

  • Whittaker RH (1965) Dominance and diversity in land plant communities. Science 80(147):250–260. https://doi.org/10.1126/science.147.3655.250

    Article  Google Scholar 

  • Wilson JB (1991) Methods for fitting dominance/diversity curves. J Veg Sci 2:35–46. https://doi.org/10.2307/3235896

    Article  Google Scholar 

  • Yuen HSH (1966) Swimming speeds of yellowfin and skipjack tuna. Trans Am Fish Soc 95:203–209. https://doi.org/10.1577/1548-8659(1966)95%5b203:SSOYAS%5d2.0.CO;2

    Article  Google Scholar 

Download references

Acknowledgements

The authors are grateful to the skippers, the European purse-seiner associations (ORTHONGEL, OPAGAC and ANABAC) for their cooperation, and to Terres Australes et Antarctiques Françaises (TAAF) involved in the logbook data collection, which is supported by the French and Spanish National Fisheries agencies and research institutes (IRD/IEO/AZTI). We would also like to thank the teams of the ‘Observatoire Thonier’ (IRD), the ‘Centro Costero de Canarias’ (IEO) and AZTI Tecnalia for providing logbook and scientific observer data. L. Escalle was funded by a PhD grant from the University of Montpellier. This is contribution 888 from AZTI-Tecnalia Marine Research Division. The manuscript has been proof-read and the English corrected by Michael Paul. We thank two anonymous Reviewers for their constructive comments on an earlier version of the manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Lauriane Escalle.

Additional information

Communicated by Simon Ingram.

This article belongs to the Topical Collection: Coastal and marine biodiversity.

Appendix 1: Taxa list by taxonomic group, with their total abundance, occurrence, percentage of sets based on estimated abundance, ocean location (Atlantic (AO) and Indian (IO) Oceans), fishing mode where they occurred

Appendix 1: Taxa list by taxonomic group, with their total abundance, occurrence, percentage of sets based on estimated abundance, ocean location (Atlantic (AO) and Indian (IO) Oceans), fishing mode where they occurred

Taxonomic groups

Taxa

Abundance

Occurrence

% of set based on estimated Ab.a

Distribution

Fishing mode occurrence

FAD

FSC

WHA

WHS

Billfishes

Istiophoridaeb

376

268

1.1

AO & IO

X

X

X

X

 

Istiompax indica

593

400

4.3

AO & IO

X

X

X

X

 

Istiophorus albicans

4378

1378

3.3

AO

X

X

X

X

 

Istiophorus platypterus

154

95

1.1

IO

X

X

X

 
 

Makaira mazara

43

31

0.0

IO

X

   
 

Makaira nigricans

4621

2986

2.3

AO & IO

X

X

X

X

 

Kajikia albida

81

49

6.1

AO

X

X

  
 

Tetrapturus angustirostris

22

18

0.0

AO & IO

X

X

  
 

Kajikia audax

128

84

1.2

IO

X

X

X

 
 

Tetrapturus pfluegeri

76

43

0.0

AO

X

X

  
 

Xiphiidae

   

AO & IO

    
 

Xiphias gladius

190

137

0.0

AO & IO

X

X

X

X

Cephalopods

Cephalopoda

10

10

0.0

AO & IO

X

X

  

Other fishes

Balistidaeb

112,706

559

13.3

AO & IO

X

X

X

X

 

Abalistes stellaris

25,175

162

31.5

IO

X

X

X

 
 

Balistes capriscus

41,650

1086

13.4

AO

X

X

  
 

Balistes punctatus

8034

66

15.2

AO

X

   
 

Canthidermis maculata

2,173,585

8924

36.3

AO & IO

X

X

X

X

 

Canthidermis sufflamen

13,605

164

58.5

AO & IO

X

X

X

 
 

Belonidaeb

206

68

0.0

AO & IO

X

X

  
 

Ablennes hians

540

126

7.1

AO & IO

X

X

 

X

 

Tylosurus crocodilus crocodilus

261

47

0.0

AO & IO

X

X

  
 

Bramidaeb

125

19

0.0

AO & IO

X

X

  
 

Brama brama

10

6

0.0

AO & IO

X

   
 

Carangidaeb

45,970

301

14.6

AO & IO

X

X

  
 

Carangoides orthogrammus

321

39

2.6

IO

X

   
 

Caranx crysos

2,948,614

6151

48.8

AO

X

X

X

 
 

Caranx lugubris

72

46

2.2

AO & IO

X

X

  
 

Caranx sexfasciatus

4240

204

3.9

IO

X

X

  
 

Decapterus sp.b

44

6

0.0

AO & IO

X

   
 

Decapterus macarellus

104,881

967

16.2

AO & IO

X

X

  
 

Elagatis bipinnulata

1,011,942

9040

31.1

AO & IO

X

X

X

X

 

Naucrates ductor

561

195

1.5

AO & IO

X

X

X

X

 

Selene dorsalis

110

18

0.0

AO

X

X

  
 

Seriola rivoliana

83,219

2539

12.4

AO & IO

X

X

  
 

Uraspis sp.b

4992

251

12.4

AO & IO

X

   
 

Uraspis helvola

1706

88

2.3

AO & IO

X

   
 

Uraspis secunda

35,263

790

10.3

AO & IO

X

X

 

X

 

Uraspis uraspis

3788

61

23.0

IO

X

   
 

Coryphaenidaeb

5771

553

4.0

AO & IO

X

X

 

X

 

Coryphaena equiselis

8765

560

9.6

AO & IO

X

X

X

X

 

Coryphaena hippurus

145,891

8817

13.0

AO & IO

X

X

X

X

 

Diodontidaeb

753

125

0.0

AO & IO

X

X

X

 
 

Diodon eydouxii

1353

114

1.8

AO & IO

X

   
 

Diodon hystrix

697

154

2.6

AO & IO

X

X

X

X

 

Echeneidaeb

479

199

3.0

AO & IO

X

X

X

X

 

Echeneis naucrates

164

64

0.0

AO & IO

X

X

 

X

 

Phtheirichthys lineatus

206

7

0.0

AO & IO

X

  

X

 

Remora australis

1

1

0.0

AO & IO

 

X

  
 

Remora brachyptera

59

39

2.6

AO & IO

 

XX

  
 

Remora osteochir

52

34

0.0

AO & IO

X

X

X

X

 

Remora remora

1012

338

2.4

AO & IO

X

X

X

X

 

Remora albescens

23

19

5.3

AO & IO

 

X

X

 
 

Ephippidaeb

59

13

0.0

IO

X

   
 

Platax sp.b

851

78

1.3

IO

X

   
 

Platax teira

4411

286

2.4

IO

X

X

  
 

Exocoetidae

380

66

4.5

AO & IO

X

X

  
 

Fistulariidae

   

AO & IO

    
 

Fistularia sp.b

2

2

0.0

AO & IO

 

X

  
 

Gempylidae

   

AO & IO

X

X

  
 

Gempylus serpens

17

9

0.0

AO & IO

X

X

  
 

Ruvettus pretiosus

724

42

0.0

AO & IO

X

X

  
 

Hemiramphidae

   

AO

    
 

Euleptorhamphus velox

100

1

0.0

AO

    
 

Kyphosidae

   

AO & IO

    
 

Kyphosus sp.b

11,793

440

14.1

AO & IO

X

X

  
 

Kyphosus cinerascens

10,260

480

5.0

IO

X

X

  
 

Kyphosus sectatrix

17,073

388

18.4

AO

X

X

  
 

Kyphosus vaigiensis

9272

388

10.6

IO

X

X

  
 

Lampridae

   

AO & IO

    
 

Lampris guttatus

3

3

0.0

AO & IO

X

   
 

Lobotidae

   

AO & IO

    
 

Lobotes surinamensis

94,617

3966

7.6

AO & IO

X

X

X

X

 

Luvaridae

   

AO & IO

    
 

Luvarus imperialis

2

1

0.0

AO & IO

X

   
 

Molidaeb

14

11

1.6

AO & IO

X

   
 

Masturus lanceolatus

162

124

1.6

AO & IO

X

X

X

X

 

Mola mola

423

332

4.2

AO & IO

X

X

X

X

 

Ranzania laevis

780

45

8.9

AO & IO

X

X

  
 

Monacanthidaeb

2318

74

 

AO & IO

X

X

X

 
 

Aluterus monoceros

39,573

1110

7.2

AO & IO

X

X

X

 
 

Aluterus scriptus

2015

241

3.3

AO & IO

X

X

  
 

Cantherhines macrocerus

169

50

0.0

AO

 

X

  
 

Nomeidae

   

AO & IO

    
 

Cubiceps sp.b

1

1

0.0

AO & IO

 

X

  
 

Cubiceps capensis

4

3

0.0

AO & IO

X

X

  
 

Psenes cyanophrys

469

45

6.7

AO & IO

X

X

X

 
 

Pomacentridaeb

4

3

0.0

AO & IO

    
 

Abudefduf saxatilis

3

3

0.0

AO

 

X

  
 

Abudefduf vaigiensis

5

5

0.0

IO

X

X

  
 

Scombridaeb

269

29

0.0

AO & IO

X

X

  
 

Acanthocybium solandri

81,347

6552

12.0

AO & IO

X

X

X

X

 

Sarda sarda

8

2

0.0

AO

X

X

  
 

Scomber sp.b

43

3

0.0

AO & IO

X

X

  
 

Scomber japonicus

20

1

0.0

AO & IO

X

   
 

Scomber scombrus

20

5

0.0

AO

X

X

  
 

Serranidaeb

4146

21

19.0

AO & IO

X

   
 

Sphyraenidaeb

231

44

0.0

AO & IO

X

X

  
 

Sphyraena barracuda

12,036

1679

6.9

AO & IO

X

X

X

 
 

Tetraodontidaeb

74

6

0.0

AO & IO

X

X

 

X

 

Lagocephalus lagocephalus

1183

100

4.3

AO & IO

X

X

X

X

 

Zanclidae

   

AO & IO

    
 

Zanclus cornutus

2

2

0.0

AO & IO

X

X

  

Rays

Unidentified ray

33

22

0.0

AO & IO

X

X

X

 
 

Dasyatidaeb

68

58

0.0

AO & IO

X

X

X

 
 

Pteroplatytrygon violacea

580

480

0.8

AO & IO

X

X

X

X

 

Mobulidaeb

21

16

0.0

AO & IO

X

X

  
 

Manta sp.b

20

15

0.0

AO & IO

 

X

  
 

Mobula sp.b

263

167

2.4

AO & IO

X

X

X

X

 

Mobula alfredi

2

2

0.0

IO

 

X

  
 

Mobula birostris

175

124

0.0

AO & IO

X

X

X

X

 

Mobula japanica

623

290

2.1

AO & IO

X

X

X

X

 

Mobula mobular

290

153

1.3

AO

X

X

X

 
 

Mobula tarapacana

432

192

5.7

AO & IO

X

X

  
 

Mobula thurstoni

3

3

0.0

AO & IO

 

X

  
 

Myliobatidae

   

AO & IO

    
 

Aetobatus narinari

1

1

0.0

AO & IO

 

X

  
 

Rhinopteridae

2

2

0.0

AO & IO

X

X

  
 

Torpedinidae

3

3

0.0

AO & IO

X

X

  

Sharks

Unidentified shark

785

117

0.0

AO & IO

X

X

X

 
 

Carcharhiniformesb

341

74

0.0

AO & IO

X

X

  
 

Carcharhinidaeb

2151

427

4.2

AO & IO

X

X

X

X

 

Carcharhinus falciformis

42,296

7200

3.5

AO & IO

X

X

X

X

 

Carcharhinus leucas

93

7

0.0

AO & IO

X

X

  
 

Carcharhinus longimanus

1038

348

0.9

AO & IO

X

X

X

 
 

Carcharhinus obscurus

5

3

0.0

AO & IO

X

   
 

Galeocerdo cuvier

6

6

0.0

AO & IO

X

X

  
 

Prionace glauca

427

299

1.0

AO & IO

X

X

X

X

 

Sphyrnidaeb

234

97

7.2

AO & IO

X

X

X

 
 

Sphyrna lewini

3968

674

3.1

AO & IO

X

X

X

 
 

Sphyrna mokarran

627

87

0.0

AO & IO

X

X

  
 

Sphyrna zygaena

2694

527

1.7

AO & IO

X

X

X

X

 

Lamniformesb

3

3

0.0

AO & IO

 

X

  
 

Alopidaeb

24

10

0.0

AO & IO

X

   
 

Alopias superciliosus

54

23

4.3

AO & IO

X

   
 

Alopias vulpinus

4

3

0.0

AO & IO

X

   
 

Lamnidaeb

18

23

0.0

AO & IO

X

X

  
 

Carcharodon carcharias

3

3

0.0

AO & IO

X

   
 

Isurus sp.b

22

21

0.0

AO & IO

 

X

  
 

Isurus oxyrinchus

375

336

1.2

AO & IO

X

X

X

X

 

Lamna nasus

1

1

0.0

AO & IO

X

   
 

Megachasmidae

   

AO & IO

    
 

Megachasma pelagios

1

1

0.0

AO & IO

 

X

  
 

Squaliformesb

3

1

0.0

AO & IO

X

   
 

Etmopteridae

   

AO & IO

    
 

Etmopterus sp.

1

1

0.0

AO & IO

X

   

Turtles

Unidentified turtle

117

109

0.0

AO & IO

X

X

  
 

Cheloniidaeb

8

8

0.0

AO & IO

X

X

  
 

Caretta caretta

639

470

0.0

AO & IO

X

X

X

 
 

Chelonia mydas

164

150

1.3

AO & IO

X

X

X

X

 

Eretmochelys imbricata

46

45

0.0

AO & IO

X

X

X

 
 

Lepidochelys kempii

48

35

0.0

AO

X

X

X

 
 

Lepidochelys olivacea

1229

877

0.0

AO & IO

X

X

X

X

 

Dermochelyidae

   

AO & IO

    
 

Dermochelys coriacea

114

106

0.0

AO & IO

X

X

  
  1. FAD fish aggregating devices, FSC free school, WHA whale associated, WHS whale shark associated sets
  2. aPercentage of the sets with the taxa present, where the abundance was calculated based on the weight of the taxa captured. For the rest of the sets, the abundance was directly estimated (or counted when < 100 individuals) by the observer
  3. bThe abundance recorded for these taxa was redistributed among the lowest taxonomic level present per sub-region and fishing mode

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Escalle, L., Gaertner, D., Chavance, P. et al. Catch and bycatch captured by tropical tuna purse-seine fishery in whale and whale shark associated sets: comparison with free school and FAD sets. Biodivers Conserv 28, 467–499 (2019). https://doi.org/10.1007/s10531-018-1672-1

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10531-018-1672-1

Keywords

Navigation