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ASSESSMENT OF BYCATCH AND DISCARDS IN MARINE CAPTURE


FISHERIES FROM URAN (RAIGAD), NAVI MUMBAI, MAHARASHTRA

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

INTRODUCTION The retained catch of non-targeted but


commercially viable species plus all discards in
Most fisheries are at least partially non-selective and they catch organisms that marine capture fisheries is referred to as
were not originally targeted. Bycatch is a catch that is either unused or unmanaged ‘bycatch’. At present, bycatch is a prominent
(Davies et al., 2009). The bycatch is an issue of critical ocean conservation and international issue raising ecological concerns
resource management concern. In global marine fisheries, bycatch represents as some of the bycatch species of marine
mammals, seabirds, sea turtles, elasmobranches
40.4% of marine catches, exposing systemic gaps in fishery policies and and fin fishes are vulnerable to overexploitation
management. The commercial fishing, especially the indiscriminate capture of and slow to recover from large population
non-target organisms is one of the most urgent threats to the world’s remaining declines. Bycatch alters biodiversity and
fish stocks (Worm et al., 2006). The unusable or unwanted sub-set of bycatch is ecosystem functions along with the behavior of
known as ‘discards’, which is subsequently thrown back to the sea, often dead or species that learn to take advantage of discards.
dying (Harrington et al., 2006). According to FAO, unused catch is that which is It also raises social issue over waste. During
not used for consumption, sold for any purpose, or reused by the fisher as bait. this study, a total of 101 species were recorded
The unmanaged catch refers to individual species or groups of different species from the marine capture fisheries bycatch and
discards at Karanja and Mora landing centers
that does not have specific management to ensure the take is sustainable (FAO, from Uran (Raigad), Navi Mumbai,
2005). Maharashtra. The recorded species have shown
Today, bycatch becomes one of the most significant nature conservation issues juveniles and subadults of commercially
in the world due to its role in degrading marine ecosystems. The bycatch is so valuable organisms and were represented by
pervasive that it affects the marine fauna including benthic invertebrates, juvenile 29 species of fin fishes, 22 species of crustaceans,
fishes, sharks, sea turtles, seabirds and marine mammals (Lewison et al., 2004). 31 species of gastropods, 11 species of bivalves,
Four major gear groups i. e. shrimp trawls, pelagic trawls, purse seines and the 3 species of cephalopods, 4 species of
high sea driftnets stand at the top in generating bycatch due to lack of selectivity polychaetes and 1 species of sponges. The species
recorded abundantly in bycatch includes
and results in capture of a huge quantity and diversity of non-target species Lepturacanthus savala, Johnius soldado,
(Alverson et al., 1994). Sciaena dussumierii, Coilia dussumierii and
Though bycatch and discards were degrading marine ecosystems, it also has Acetes indicus (Jawla Paste Shrimp). At present,
both direct and indirect impacts on marine biodiversity by killing huge amount of creeks from Navi Mumbai region were major
non-target species and young ones of commercially valuable species. Except few fishing grounds for fin fishes and shell fishes
reports (Rao, 1988; Menon, 1996; Menon et al., 2000; Kurup et al., 2003; Biju but in future, for conservation of marine
and Deepthi, 2006), meager information is available on quality and quantity of biodiversity resources, several principles and
marine fisheries bycatch and discards from Indian waters. The present study approaches require consideration when
developing measures to reduce bycatch through
aims at qualitative and quantitative assessment of bycatch and discards of marine changes in fishing gear and methods.
fishery landings at Uran coast (Raigad), Navi Mumbai, Maharashtra.

MATERIALS AND METHODS


KEY WORDS
Study area Bycatch, Discards
Juveniles, Marine ecosystem
Uran (Lat. 18º50’ 5" to 18º50’ 20" N and Long. 72º57’ 5" to 72º57’ 15" E) with
Navi Mumbai, Uran
the population of 23, 251 is located along the eastern shore of Mumbai Harbour
opposite to Coloba (Fig. 1) and is a major fishery landing center in Raigad district, Received : 25.06.2011
Navi Mumbai, Maharashtra, west coast of India. A creek called ‘Uran creek/
Revised : 23.07.2011
Sheva creek’ encircles Uran city on the north side and is continuous with the
Panvel creek and Thane creek joining Arabian Sea. Towards the south, Dharamtar Accepted : 12.09.2011
creek encircles Uran and the creek is continuous with the Karanja creek and Pen-
*Corresponding author
Khopoli creek. Along coast of Uran, trawl nets with a small cod end mesh size

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

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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

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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

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BYCATCH AND DISCARDS IN MARINE CAPTURE FISHERIES

killing of juveniles and brood fishes are the major cause for Research Institute, Cochin. pp. 96 – 99.
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109
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