Professional Documents
Culture Documents
R. PAWAR PRABHAKAR
Veer Wajekar Arts, Science and Commerce College,
Phunde - 400 702, Uran (Dist. –Raigad), Navi Mumbai, Maharashtra
E-mail: prabhakar_pawar1962@yahoo.co.in
ABSTRACT
105
R. PRABHAKAR PAWAR
and purse seines were operated as major fishing gears and the crustaceans, 31 species of gastropods, 11 species of bivalves,
catch is landed at Mora and Karanja, the major landing centers 3 species of cephalopods, 4 species of polychaetes and 1
at Uran. species of sponges. Numerous small sized species and
The coastal environment of Uran has been under considerable juveniles of commercially valuable species were represented
stress since the onset of Jawaharlal Nehru Port Trust (JNPT, an in the discards.
International port), Nhava-Seva International Container Fishes
Terminal (NSICT), Container Freight Stations (CFS) etc. These 29 species of fishes representing 28 genera and 23 families
activities affect the diversity of fin fish and shell fish resources. were recorded from the study sites (Table 1). Among all the
Entire region of Mora and Karanja landing centers is species of fishes recorded, abundance of ribbon fishes/spiny
considered as study area and sampling was conducted during hair tail (Lepturacanthus savala), croakers (Johnius soldado),
October-November 2009. dhoma (Sciaena dussumierii) and gold spotted grenadier
Sampling procedures anchovy (Coilia dussumierii) were recorded at both sites.
During present investigation, two stations namely Mora and Species like Bleeker’s whipray (Himantura bleekeri) and Sharp
Karanja were selected for qualitative and quantitative nose stingray (H. gerrardi) were rare whereas stripped mullet
assessment of species diversity from bycatch and discards. (Mugil cephalus), cat fish (Mystus seenghala), three stripped
From both the stations, ten samples were collected during tiger fish (Terapon jarbua) and mudskippers (Boleophthalmus
October-November 2009. Species representing the most boddarti) were very common.
common groups were collected from the bycatch and discards Crustaceans
and preserved in 10% buffered formaldehyde. The recorded 22 species of crustaceans representing 15 genera and 10
animals were identified up to species level as far as possible in families were recorded during present investigation (Table 2).
the laboratory. Among crustaceans, Prawns, shrimps and lobsters were
represented by 13 species of 7 genera and 4 families where as
RESULTS AND DISCUSSION crabs were represented by 9 species of 8 genera and 6 families.
Qualitative and quantitative assessment of species diversity At Karanja, the discard was dominated by Jawla Paste Shrimp
from the bycatch and discards at Mora and Karanja landing (Acetes indicus) and tonnes of juveniles of A. indicus and
centers have recorded 101 species of bycatch and were prawns of family Penaeidae were discarded back into the sea.
represented by 29 species of fin fishes, 22 species of Juveniles of edible crabs from family Portunidae and other
Table 1: Fishes identified from bycatch and discards at Mora and Karanja landing centers, Uran, Navi Mumbai, Maharashtra
Order Family Binomial Name Populations of bycatch
(Mean ± SD)
Carcharhiniformes Carcharhinidae Scoliodon sorrakowah (Maller and Henle, 1837) 7±2.64
Rajiformes Dasyatidae Himantura bleekeri (Blyth, 1860) 3 ± 1.63
Himantura gerrardi (Grey, 1851) 2 ± 1.17
Perciformes Sparidae Argyrops spinifer (Forsskal, 1775) 3 ± 0.89
Gobiidae Boleophthalmus boddarti (Pallas, 1770) 6 ± 1.83
Scombridae Euthynnus affinis (Cantor, 1849) 5 ± 1.34
Rastrelliger kanagurta (Cuvier, 1816) 4 ± 3.80
Gerreidae Gerres filamentosus (Cuvier, 1849) 3±1.10
Sciaenidae Johnius soldado (Lacepede, 1802) 7±4.15
Sciaena dussumierii Cuvier, 1830) 8±3.11
Centropomidae Lates calcarifer (Bloch, 1970) 6±1.66
Trichiuridae Lepturacanthus savala (Cuvier, 1829) 13±3.48
Carangidae Megalaspis cordyla (Linnaeus, 1758) 5±1.36
Parastromateus niger (Bloch, 1795) 5±1.85
Stromateidae Stromateus argenteus (Euphrasen, 1788) 6 ± 2.17
Polynemidae Polynemus tetradactylus (Shaw, 1804) 4 ± 1.83
Pricanthidae Priacanthus hamrur (Forsskal, 1775) 4 ± 1.66
Scatophagidae Scatophagus argus (Linnaeus, 1758) 5 ± 1.75
Terapontidae Terapon jarbua (Forsskål, 1775) 7 ± 1.83
Cichlidae Tilapia mosambica (Peters, 1852) 4 ± 1.45
Clupeiformes Engraulidae Coilia dussumieri (Valenciennes, 1848) 15 ± 2.25
Thryssa mystax (Bloch and Schneider, 1801) 4 ± 1.14
Clupeidae Tenualosa ilisha (Hamilton, 1822) 4 ± 1.63
Mugiliformes Mugilidae Mugil cephalus (Linnaeus, 1758) 11 ± 2.75
Chelon macrolepis (Smith, 1846) 11 ± 3.61
Siluriformes Bagridae Mystus seenghala (Sykes, 1839) 13 ± 3.39
Pleuronectiformes Cynoglossidae Cynoglossus macropepidotus (Bleeker, 1851) 4 ± 1.36
Anguilliformes Muraenidae Gymnothorax pseudothyrsoideus (Bleeker, 1852) 6 ± 2.17
Aulopiformes Synodontidae Harpadon nehereus (Hamilton, 1822) 13 ± 3.00
106
BYCATCH AND DISCARDS IN MARINE CAPTURE FISHERIES
Table 2: Crustaceans identified from bycatch and discards at Mora and Karanja landing centers, Uran, Navi Mumbai, Maharashtra
Order Family Binomial Name Populations of bycatch
(Mean ± SD)
Decapoda / Penaeidae Fenneropenaeus indicus (H. M.- Edwards,1837) 8 ± 2.06
Dendrobranchiata Penaeus monodon (Fabricius, 1798) 8 ± 1.57
Penaeus penicillatus (Alcock, 1905) 7 ± 1.14
Penaeus semisculatus (De Haan, 1844) 7 ± 1.81
Penaeus merguiensis (de Man, 1888) 5 ± 1.68
Metapenaeus affinis (H. Milne Edwards, 1837) 5 ± 1.36
Metapenaeus dobsoni (Miers, 1878) 5 ± 1.81
Metapenaeus stridulans (Alcock, 1905) 4 ± 1.08
Parapenaeopsis sculptilis (Heller, 1862) 3 ± 2.26
Parapenaeopsis stylifera (H. M.Edwards, 1837) 6 ± 1.47
Sergestidae Acetes indicus (H. Milne Edwards, 1830) 14 ± 2.65
Palinura Palinuridae Panulirus polyphagus (Herbst, 1793) 4 ± 1.40
Brachyura Portunidae Scylla serrata (Forsskål, 1775) 6 ± 1.34
Portunus sanguinolentus (Herbst, 1796) 4 ± 1.14
Portunus pelagicus (Linnaeus, 1758) 4 ± 0.98
Charybdis cruciata (Herbst, 1789) 4 ± 1.28
Matunidae Matuta lunaris (Forsskål, 1775) 3 ± 0.63
Xanthidae Leptodius exaratus (H. Milne Edwards, 1834) 4 ± 1.29
Eriphiidae Eriphia smithii (Macley, 1838) 4 ± 0.90
Ocypodidae Uca annulipes (H. Milne Edwards, 1837) 3 ± 0.49
Anomura Paguridae Pagurus prideaux (Leach, 1815) 3 ± 0.70
Stomatopoda Squillidae Squilla mantis (Linnaeus, 1758) 5 ± 1.02
Table 3 : Gastropods identified from bycatch and discards at Mora and Karanja (Uran)
Order Family Binomial name Populations of bycatch
(Mean ± SD)
Archaeogastropoda Trochidae Trochus stellatus (Gmelin, 1791) 3 ± 0.70
Trochus radiatus (Gmelin, 1791) 3 ± 0.70
Trochus tentorium (Gmelin, 1791) 2 ± 0.70
Euchelus asper (Gmelin, 1791) 3 ± 0.70
Clancules ceylonicus (Nevill, 1869) 2 ± 0.66
Neritimorpha Neritidae Nerita oryzarum (Recluz, 1841) 3 ± 0.66
Nerita crepidularia (Lamarck, 1816) 2 ± 0.63
Nerita albicilla (Linnaeus, 1758) 2 ± 0.89
Caenogastropoda Strombidae Tibia curta (Sowerby, 1842) 2 ± 0.70
Hypsogastropoda Bursidae Bursa lissostroma (Smith, 1914) 2 ± 0.64
Bursa spinosa (Lamarck, 1816) 2 ± 0.90
Bursa elegans (Sowerby, 1835) 2 ± 0.33
Bursa tuberculata (Brodrip, 1833) 3 ± 0.78
Naticidae Natica picta (Recluz, 1844) 2 ± 0.49
Natica maculosa (Lamarck, 1799) 2 ± 0.50
Planaxidae Planaxis sulcatus (Born, 1778) 4 ± 0.90
Potamididae Telescopium telescopium (Linnaeus, 1758) 3 ± 0.70
Potamides cingulatus (Gmelin, 1791) 4 ± 1.14
Neogastropoda Muricidae Murex adustus (Lamarck, 1799) 2 ± 0.60
Murex tribulus (Linnaeus, 1758) 2 ± 0.46
Ocinebra bombayana (Melvill, 1893) 2 ± 0.66
Thais carinifera (Lamarck, 1822) 3 ± 0.89
Turridae Surcula javana (Linnaeus, 1758) 2 ± 0.49
Surcula amicta (Smith, 1877) 2 ± 0.49
Clavus crassa (Smith, 1888) 2 ± 0.50
Buccinidae Babylonia spirata (Linnaeus, 1758) 2 ± 0.64
Cantharus spiralis (Gray, 1846) 2 ± 0.40
Cancellaridae Cancellaria costifera (Sowerby, 1835) 2 ± 0.66
Volemidae Hemifuus pugilinus (Born, 1778) 3 ± 0.75
Hemifuus cochlidium (Linnaeus, 1758) 2 ± 0.66
Onchidiidae Onchidium damelii (Samper, 1882) 3 ± 0.92
non-edible species of crabs were found common at both the representing 20 genera and 13 families were recorded at both
study stations. landing centers (Table 3). Species like Hemifusus pugilinus,
Gastropods H. cochlidium, Telescopium telescopium, Nerita crepidularia,
Juveniles and subadults of 31 species of gastropods Trochus radiatus, Bursa tuberculata, Tibia curta and Murex
107
R. PRABHAKAR PAWAR et al.,
Table 4: Pelecypods, Cephalopods, Polychaetes and Sponges identified from by catch and discards at Mora and Karanja landing centers, Uran,
Navi Mumbai, Maharashtra
Order Family Binomial Name Populations of bycatch
(Mean ± SD)
Pelecypods
Pteriomorpha Arcidae Arca granosa (Linnaeus, 1758) 3 ± 0.87
Veneroida Veneridae Callista erycina (Linnaeus, 1758) 2 ± 0.49
Katelysia opima (Gmelin, 1791) 3 ± 0.66
Dosinia cretacea (Reeve, 1850) 2 ± 0.78
Meretricinae Merettrix meretrix (Linnaeus, 1758) 3 ± 0.90
Merettrix casta (Chemnitz, 1782) 2 ± 0.75
Merettrix lyrata (Sowerby, 1851) 2 ± 0.64
Mactridae Mactre cornea (Poli, 1791) 2 ± 0.64
Dosiniiae Vellorita cyprinoids (Gray, 1825) 2 ± 0.68
Eulamellibranchiata Ostreidae Placenta placenta (Linnaeus, 1758) 4 ± 0.87
Pectinidae Chlamys singaporina (Sowerby, 1842) 2 ± 0.64
Cephalopods
Sepiida Sepiidae Sepia officinalis (Linnaeus, 1758) 7 ± 1.30
Teuthida Loligunidae Loligo vulgaris (Lamarck, 1798) 8 ± 1.25
Octopoda Octopodidae Octopus herdmani (Hoyle, 1904) 7 ± 1.22
Polychaetes
Aciculata Nereidae Perinereis cultrifera (Grube, 1840) 4 ± 1.03
Perinereis vancauria (Grube, 1840) 3 ± 0.75
Pseudonereis anamola (Gravier, 1901) 3 ± 0.78
Eunicida Eunicidae Marphysa sanguinea (Montagu, 1815) 2 ± 0.78
Sponges
Leucosoleniida Leucosoleniidae Leucosolenia complicata (Montagu, 1818) 4 ± 1.11
tribulus were recorded as common in discards at Karanja. were identified and Perinereis cultrifera, Pseudonereis anamola
and Marphysa sanguinea were abundant in discards at both
Pelecypods
sites (Table 4).
11 species of bivalves representing 9 genera and 7 families
were recorded in juvenile forms at both study sites (Table 4). Sponges
Abundantly recorded bivalve species in the discards were One species of sponge i.e. Leucosolenia complicata
Katelysia opima, Dosinia cretacea, Meretrix meretrix and representing the family Leucosolenidae was recorded in
Chlamys singaporina. fragmented form only at Karanja (Table 4).
Cephalopods Role of bycatch in degrading marine ecosystems has made it
Undersized cephalopods recorded include 3 species one of the most significant nature conservation issues in the
representing 3 genera and 3 families (Table 4). Juveniles of world (Harrington et al., 2006) with serious food-security
Sepia officinalis and Loligo vulgaris were common while implications for up to 1 billion people who depend on fish as
Octopus herdmani was rare in the bycatch. their principle source of protein (The World Bank, 2008).
Alverson et al. (1994) have provided an estimate of global
Polychaetes discards in commercial fisheries of 27.0 million mt with a
4 polychaete species representing 3 genera and 2 families range from 17.9 to 39.5 million mt.
Bycatch can alter biodiversity and ecosystem functions by
removing top predator and prey species at unsustainable levels
(Myers et al., 2007). Discarded bycatch raises a social issue
over waste and from 1992 – 2001, an average of 7.3 million
ton of fish were annually discarded, representing 8% of the
world catch (FAO, 2005). Davies et al. (2009) reported bycatch
as an insidious problem of invisible fishing resulting from
widespread unmanaged fisheries and enormous quantities of
biomass are being removed from the ocean without any form
of effective management. Even though bycatch is degrading
marine ecosystems, a consistent understanding of bycatch is
lacking due to several unresolved issues: definition,
measurement and quantification.
India is rich in natural resources and the annual harvestable
fishery potential of the country is estimated to be 3.48 million
ton (Verlecar et al., 2007). It is established that the fish biodiversity
of the country is diminishing at an alarming rate in all the aquatic
Figure 1: Legend general map of study area zones (Mahanta, 2004). Over-exploitation and indiscriminate
108
BYCATCH AND DISCARDS IN MARINE CAPTURE FISHERIES
killing of juveniles and brood fishes are the major cause for Research Institute, Cochin. pp. 96 – 99.
imperilment of fishes (Pandey and Das, 2004). CMFRI: Research Highlights 2007 – 2008. Central Marine Fisheries
From Indian waters, work of following investigators on bycatch Research Institute, Cochin. pp. 12.
and discards is worth to mention here. According to Menon Davies, R. W. D., Cripps, S. J., Nickson, A. and Porter, G. 2009.
(1996), the bycatch landings of trawlers in Karnataka, Kerala Defining and estimating global marine fisheries bycatch. Marine Policy,
and Tamil Nadu studied during 1985 – 90 represents 20 doi:10.1016/j.marpol.2009.01.003, 1-79.
genera of fishes, 26 crustaceans, 23 gastropods, 15 bivalves, FAO. 2005. Discards in the World’s Marine Fisheries: an update.
10 echinoderms, polychaetes, anemones, sponges, gorgonids, FAO Fisheries Technical Paper No 470. Rome: Food and Agricultural
ascidians and echiuroids along with large number of juvenile Organization of the United Nations.
young fishes and cephalopods. CMFRI (2002) recorded Harrington, J. M., Myers, R. A. and Rosenberg, A. A. 2006. Wasted
presence of 185 species as bycatch from the landings of fishery resources: discarded bycatch in the USA. Fish and fisheries. 6:
trawlers from Pak Bay and Gulf of Mannar and is represented 350 – 361.
by ground fish, stomatopods, undersized prawns, gastropods, Kurup, B. M., Premlal, P., Thomas, J. V. and Vijay, A. 2003. Bottom
bivalves, inedible crabs, echinoderms, sea weeds and sea trawl discards along Kerala coast: A case study. J. Mar. Biol. Assoc.
grasses. The discards of bottom trawlers from Kerala coast India. 45: 99 – 107.
have shown the presence of 103 species of fin fishes, 65 Lewison, R. L., Crowder, L. B., Read, A. J. and Freeman, S. A. 2004.
gastropods, 12 bivalves, 8 shrimps, 2 stomatopods, 12 crabs, Understanding impacts of fisheries bycatch on marine megafauna.
5 cephalopods, 3 echinoderms and 4 jelly fishes along with Trends in Ecology and Evolution. 19: 598 – 604
epifaunal species and juveniles of commercially valuable Mahanta, P. C. 2004. Species Survival Programme – A Need towards
species (Kurup et al., 2003). Biju and Deepthi (2006) recorded Protection of Threatened Fishes. Paper presented at the National
presence of 5 species of reptiles, 262 fin fishes, 12 Seminar on Biodiversity, Biotechnology and Environmental Toxicology
in the New Millennium. The Institute of Science, Mumbai on 22nd to
echinoderms, 140 molluscs, 4 prawns, 12 crabs, 5
24th Nov 2004, pp. 1 – 2.
stomatopods, 3 lobsters, 1 sipunculid worm, 1 bryozoan, 7
Menon, N. G. 1996. Impact of bottom trawling on exploited resources.
cnidarians, 3 sponges with many species of hermit crabs and
In Marine Biodiversity, Conservation and Management (Eds Menon
annelids in the trawl bycatch of Kerala coast. Bycatch and N G and Pillai C S S), Central Marine Fisheries Research Institute,
discards by trawlers at Mumbai have shown that 1671 tonnes Cochin. pp. 97 – 102.
of bycatch with a catch rate of 200 kg/hr was landed during
Menon, N. G., Nammalwar, P., Zachariah, P. U. and Jagadis, I.
January to December 2007, which formed 22% of the total 2000. Investigations on the impact of coastal bottom trawling on
catch. 73 species of fin fishes and shellfishes constituted the demersal fishes and macrobenthos. Central Marine Fisheries Research
Low Value Bycatch (LVB) and considering the size at maturity, Institute, Annual Report 1999 – 2000, Cochin. pp. 55 – 57.
all were juveniles (CMFRI, 2008). Myers, R. A., Baum, J. K., Shepherd, T. D., Powers, S. P. and Peterson,
C. H. 2007. Cascading effects of the loss of apex predatory sharks
ACKNOWLEDGEMENTS from a coastal ocean. Science. 315(Mar): 1846 – 1850.
Pandey, A. K. and Das, P. 2004. Fish Biodiversity Conservation:
Financial support provided by University Grants Commission,
Current Concepts and Future Directions. Paper presented at the
Western Regional Office, Pune is gratefully acknowledged [File National Seminar on Biodiversity, Biotechnology and Environmental
No: 47-599/08 (WRO) dated 2nd Feb 2009]. The author is Toxicology in the New Millennium. The Institute of Science, Mumbai
thankful to The Principal and Faculty Members, Dept. of on 22nd to 24th Nov 2004, pp. 1 – 2.
Zoology, Veer Wajekar Arts, Science and Commerce College, Rao, K. S. 1988. Ecological monitoring of trawling grounds. J. Indian
Phunde (Uran) for encouragement and support. Special thanks Fish. Assoc. 18: 239 – 244.
are due to Miss L. S. Patil for the critical reading of the The World Bank, The Sunken Billions, 2008. The Economic
manuscript. The author is thankful to the anonymous reviewer Justification for Fisheries Reform. Agricultural and Rural Development.
for valuable suggestions in the manuscript. The World Bank. Washington D. C.
Verlecar, X. N., Snigdha, Desai., S. R. and Dhargalkar, V. K. 2007.
REFERENCES Shark hunting – an indiscriminate trade endangering elasmobranches
to extinction. Curr. Sci. 92(8): 1078 – 1082.
Alverson, D. L., Freeberg, M. H., Murawaski, S. A. and Pope, J. G.
1994. A global assessment of fisheries bycatch and discards. FAO Worm, B., Barbier, E. B., Beaumont, N., Duffy, J. E, Folke, C,
Fisheries technical paper no. 339: 235. Halpern, B. S., Jackson, J. B. C., Lotze, H. K., Micheli, F., Palumbi,
S. R., Sala, E., Selkoe, K. A., Stachowicz, J. J. and Watson, R. 2006.
Biju, A. and Deepthi, G. R. 2006. Trawling and bycatch: Implications
Impacts of biodiversity loss on ocean ecosystem services. Science.
on marine ecosystem. Curr. Sci., 90 (7), 922 – 931.
314: 787–790. http://www.insideindonesia.org/edit73/
CMFRI: Annual Report 2001 – 2002. Central Marine Fisheries Fegan%20fishing.htm
109
INSTRUCTION TO AUTHORS
*Life Member will receive the journal for 15 years while other benefits will continues whole life
Note: 25% concession is given to all categories of subscriptions to contributors, students, researchers, scientists,
academic and research institutions and libraries on the above mention rates
Name: ....................................................................................................................................................
Address: .................................................................................................................................................
E-mail: ...................................................................................................................................................
NOTE: FOR MEMBERSHIP THE ABOVE INFORMATION CAN BE SENT ON SEPARATE SHEET
110