Open Access Open Access  Restricted Access Subscription Access

Food and Feeding Habits of Seahorse, Hippocampus kelloggi (Jordan and Snyder, 1902) in Cuddalore Coastal Water, Southeast Coast of India


Affiliations
1 Centre of Advanced Study in Marine Biology, Annamalai University, Parangipettai-608 502, Tamil Nadu, India
 

Background/Objectives: Seahorses might render them vulnerable to overfishing or other disruptions such as habitat damage. Different species of Hippocampus are harvested on a large-scale, and traded by at least 50 na-tions in high volumes and various product forms. The unsustainable exploitation has focused attention on the large gaps in our knowledge of wild seahorse biology and ecology. Hippocampus kelloggi is one the most widely held species in public aquaria and also used for traditional medicines.

Methods/Statistical analysis: Seahorse H. kelloggi samples were collected from Cuddalore coast during Oct. 2000 – Sept. 2001 for gut content analysis. The point’s method and percentage occurrence method have been adopted. The gut contents were estimated based on the frequency of occurrence of different food materials following the point’s method. The guts were considered ‘full’ when the gut was packed with food with thick wall and intact, ‘3/4 full’ when it was partly full ‘½ full’, ‘¼ full’, ‘trace’ and ‘empty’ according to the relative condition of the gut as indicated above.

Findings: The diet of H. kelloggi mainly considered of Acetes sp., copepods, mysids, tanaids, megalopa larvae, amphipods, shrimp larvae, polycheates , nematodes etc. Acetes sp. was dominant food item for adult and it was contributed 48.6 to 64.1% during different months. The other food items of amphipods (5.0 to 9.5%), tanaeids (2.4 to 9.1%), copepods (.33 to 0.7%), lucifer (2.8 to 10.0%), mysids (2.3 to 2.5%), shrimps (larvae and juveniles) (3.7 to 9.0%), polychaetes (5.3 to 12.5%), nematodes (1.2 to 6.3%) and the fish larvae (3.0 to 3.3%) were recorded. Copepods were the major food items in juveniles which contributed 15.4 to 29.8% for the whole year. The other food items were amphipods (11.3 to 18.5%), mysids (8.5 to 16.9%), tanaeids (6.4 to 17.4%), megalopa larvae (4.4 to 9.4%), Acetes sp. (4.3 to 16.6%), lucifer (2.2 to 8.5%), shrimps (larvae and juveniles) (2.5 to 4.3%), polychaetes (2.5 to 12.2%), and nematodes (4.4 to 16.0%). Active feeding was showed after spawning season in adult.

Application/Improvements: Through this work may hope to increase our understanding of seahorse feeding ecology, and to stimulate the development of sampling approaches that can help to balance the need to use specimens in research and the conservation needs.


Keywords

Hippocampus kelloggi, Adult, Juvenile, and Food Items, Percentage Occurrence, Dominant Food.
User
Notifications

  • S.J. Foster, A.C.J. Vincent. Life history and ecology of seahorses: implications for conservation and management. Journal of Fish Biology. 2004; 65(1), 1-61.
  • J. M. McPherson, A.C.J. Vincent. Assessing East African trade in seahorse species as a basis for conservation under international controls. Aquatic Conservation: Marine and Freshwater Ecosystems. 2004; 14(5), 521-538
  • B. S. Bhimachar, G. Venkataraman. A preliminary study of the fish populations along the Malabar Coast. Proceedings of the Indian Academy of Sciences. 1952; 18(6), 627-655.
  • C.M.C. Woods. Natural diet of the seahorse Hippocampus abdominalis. New Zealand Journal of Marine and Freshwater Research. 2002; 36, 655-660.
  • M.J. Wilson, A.C.J. Vincent. Preliminary success in closing the life cycle of exploited seahorse species, Hippocampus spp., in captivity. Aquarium Science and Conservation. 1998; 2(4), 179-196.
  • A.B. Bhunia, A. Choudhry. Some ecological considerations for zooplankton production in Chemaguri Creek, Sagar Island (south), Sundarbans. Mahasagar. 1982; 15(4), 247-252.
  • A.L.D.C. Castro, A.D.F. Diniz, I.Z. Martins, A.L. Vendel, T.P.R.D. Oliveira, I.M.D.L. Rosa. Assessing diet composition of seahorses in the wild using a non destructive method: Hippocampus reidi (Teleostei: Syngnathidae) as a study-case. Neotropical Ichthyology. 2008; 6 (4), 637-644.
  • A.C.J. Vincent. A role for daily greetings in maintaining seahorse pair bonds. Animal Behaviour. 1995; 49, 258-260.
  • M.Y. Yip, A.C.O. Lim, V.C. Chong, J.M. Lawson, S.J. Foster. Food and feeding habits of the seahorses Hippocampus spinosissimus and Hippocampus trimaculatus (Malasya). Journal of the Marine Biological Association of the United Kingdom. 2014; 95(5), 1-8.
  • P. Franzoi, R. Maccagnani R. Rossi, V.U. Ceccherelli. Life cycles and feeding habits of Syngnathus taenionotus and S. abaster (Pisces, Syngnathidae) in a brackish bay of the Po River Delta (Adriatic Sea). Marine Ecology Progress Series. 1993; 97(1), 71-81.
  • R.J. Livingston. Tropic organization of fishes in coastal sea grass system. Marine Ecology Progress Series.1982; 7(1), 1-12.
  • W.E. Frost. The natural history of the manew minnow, Phoxinus phoxinus. Journal of Animal Ecology. 1943; 12, 139-162.
  • M. Kennedy. P. Fitzmarice. Some aspects of biology of gudgeon Gobiogobio (L) in Irish water. Journal of Fish Biology. 1972; 4, 424-440.
  • R.M. Love. The chemical biology of fishes. London-New York: Academic Press. 1980, 2, pp. 1-943.
  • K. Tipton. S.S. Bell. Foraging patterns of two syngnthid fishes: importance of copepods. Marine Ecology Progress Series. 1988; 47, 31-43.
  • J. Alheit. Scheible W. Benthic harpacticoid copepods as a food source for fish. Marine Biology. 1982; 70, 141-147.
  • B.A. Bergret, P.C. Wainwrigth. Morphology and kinematics of prey capture in the syngnathid fishes Hippocampus erectus and Syngnathus floridae. Marine Biology. 1997; 127(4), 563-570.
  • B.C. Coull. Are members of the meiofauna food for higher trophic levels? Transactions of the American Microscopical Society. 1990; 109(3), 233-246.
  • J.M. Gee. An ecological and economic review of meiofauna as food for fish. Zoological Journal of the Linnean Society. 1989; 96, 243-261.
  • A.L.C. da Castro, A.F. de Diniz, I.Z. Martins, A.L. Vendel, T.P.R. de Oliveira, I.M.L. de Rosa. Assessing diet composition of seahorses in the wild using a non destructive method: Hippocampus reidi (Teleostei: Syngnathidae) as a study-case. Neotropical Ichthyology. 2008; 6(4), 637-644.
  • S. Mishra, R.C. Panigrahy. Zooplankton ecology of the Bahuda estuary (Orissa), east coast of India. Indian Journal of Geo-Marine Sciences.1999; 28, 297-301.
  • V. Santhakumari, M. Saraswathy. Zooplankton along the Tamil Nadu coast. Mahasagar. 1981; 14(4), 289-302.
  • K. Suresh, G. Durairaj. Harpacticoid copepod distribution on a sandy shore in the Vicinity of a power plant discharge, at Kalpakkam, along the east coast of India. Journal of Geo-Marine Sciences. 1996; 25, 307-311.
  • C.H. Ryer, R.J. Orth. Feeding ecology of the northern pipefish Syngnathus fuscus in a sea grass community of the lower Chesapeake Bay. Estuaries. 1987; 10(4), 330-336.
  • M.F. Payne, R.J. Rippingale. Rearing West Australian seahorse, Hippocampus subelongatus, and juveniles on copepod nauplii and enriched Artemia. Aquaculture. 2000, 188(3-4), 353-361.
  • R.L. Teixeira, J.A. Musick. Reproduction and food habits of the lined seahorse, Hippocampus erectus (Teleostei: Syngnathidae) of Chesapeake Bay, Virginia. RevistaBrasileira de Biologia. 2001; 61(1), 79-90.
  • K.L. Main.The influence of prey identifies and size on selection of prey by two marine fishes. Journal of Experimental Marine Biology and Ecology. 1985; 88, 145-152.
  • K.J. Mathew, G. Antony, T.S. Naomi, K. Solomon. On the quantitative abundance of Mysidacea collected from the eastern Arabian Sea and the Bay of Bengal. First workshop on the scientific results of FORV Sagar Sampada. 1989; 109-114.
  • P.P. Pillai. Heterogeneity in the distribution pattern of pelagic copepods collected on broad FORV Sagar Sampada in the Indian EEZ. In: Proceedings of the First workshop on scientific results of FORV Sagar Sampada. 1989; 95-108.
  • M. Prein. Aquaculture potential of seahorses and pipe fishes. Naga, the ICLARM Quarterly. 1995; 18(1), 20-21.
  • S. Rosama, H.K. Iyer. Species composition and coexistence of calanoid copepods in the shelf waters of Cochin. Mahasagar. 1979; 12(4), 227-238.
  • P.V. Sreenivasan. Observations on the food and feeding habits of the Tarpedo travelly and Megalapiscordyla (Linnaeus) from Vizhinjam Bay. Indian Journal of Fisheries. 1974; 21(1), 20-28.
  • S. Sivakami. On the food habits of the fishes of the family Carangidae – a review. The Marine Biological Association of India. 1996; 38(1&2), 118-123.
  • G.H. Swynnerton, E.B. Worthington. Note on the food of fish in Hawes water (West Morland). Journal of Animal Ecology. 1940; 9, 183-187.
  • G. Venkataraman. Studies on the food and feeding relationships of the inshore fishes of Calicut on the Malabar Coast. Indian Journal of Fisheries. 1960; 7(2), 275-307.
  • V.K. Venkataramani, R. Natarajan. Food and feeding habits of Selaroides leptolepis val. off Tuticorin coast. Matsya. 1998; 14, 53-62.
  • R.J. Wotton. Energy cost of egg production and environmental determinants of fecundity in teleost fishes. Symposia of the Zoological Society of London.1979; 44, 133-159.

Abstract Views: 549

PDF Views: 0




  • Food and Feeding Habits of Seahorse, Hippocampus kelloggi (Jordan and Snyder, 1902) in Cuddalore Coastal Water, Southeast Coast of India

Abstract Views: 549  |  PDF Views: 0

Authors

R. Balasubramanian
Centre of Advanced Study in Marine Biology, Annamalai University, Parangipettai-608 502, Tamil Nadu, India

Abstract


Background/Objectives: Seahorses might render them vulnerable to overfishing or other disruptions such as habitat damage. Different species of Hippocampus are harvested on a large-scale, and traded by at least 50 na-tions in high volumes and various product forms. The unsustainable exploitation has focused attention on the large gaps in our knowledge of wild seahorse biology and ecology. Hippocampus kelloggi is one the most widely held species in public aquaria and also used for traditional medicines.

Methods/Statistical analysis: Seahorse H. kelloggi samples were collected from Cuddalore coast during Oct. 2000 – Sept. 2001 for gut content analysis. The point’s method and percentage occurrence method have been adopted. The gut contents were estimated based on the frequency of occurrence of different food materials following the point’s method. The guts were considered ‘full’ when the gut was packed with food with thick wall and intact, ‘3/4 full’ when it was partly full ‘½ full’, ‘¼ full’, ‘trace’ and ‘empty’ according to the relative condition of the gut as indicated above.

Findings: The diet of H. kelloggi mainly considered of Acetes sp., copepods, mysids, tanaids, megalopa larvae, amphipods, shrimp larvae, polycheates , nematodes etc. Acetes sp. was dominant food item for adult and it was contributed 48.6 to 64.1% during different months. The other food items of amphipods (5.0 to 9.5%), tanaeids (2.4 to 9.1%), copepods (.33 to 0.7%), lucifer (2.8 to 10.0%), mysids (2.3 to 2.5%), shrimps (larvae and juveniles) (3.7 to 9.0%), polychaetes (5.3 to 12.5%), nematodes (1.2 to 6.3%) and the fish larvae (3.0 to 3.3%) were recorded. Copepods were the major food items in juveniles which contributed 15.4 to 29.8% for the whole year. The other food items were amphipods (11.3 to 18.5%), mysids (8.5 to 16.9%), tanaeids (6.4 to 17.4%), megalopa larvae (4.4 to 9.4%), Acetes sp. (4.3 to 16.6%), lucifer (2.2 to 8.5%), shrimps (larvae and juveniles) (2.5 to 4.3%), polychaetes (2.5 to 12.2%), and nematodes (4.4 to 16.0%). Active feeding was showed after spawning season in adult.

Application/Improvements: Through this work may hope to increase our understanding of seahorse feeding ecology, and to stimulate the development of sampling approaches that can help to balance the need to use specimens in research and the conservation needs.


Keywords


Hippocampus kelloggi, Adult, Juvenile, and Food Items, Percentage Occurrence, Dominant Food.

References