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M. R. Saseendranath
Kerala Veterinary and Animal Science University, Mannuthy, Thrissur, INDIA
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Feeding Ecology of Red Spotted Swimming Crab, Portunus Sanguinolentus (Herbst, 1783) along Mangaluru Coast, Karnataka

Chandrappa Hadadi Aishwarya1, S.R. Somashekara1, U.A. Suryawanshi2, P. Nayana1, H.N. Anjanayappa1, J.G.K. Pathan2,*
1College of Fisheries, Mangaluru, Karnataka Veterinary, Animal and Fisheries Sciences University, Bidar-585 401, Karnataka, India.
2College of Fishery Science, Maharashtra Animal and Fishery Sciences University, Nagpur-440 002, Maharashtra, India.

Background: Crabs are one of the major marine fisheries resources in India and they are among the most valuable seafood species due to their delicious taste, nutritional value and economic importance. The knowledge of the feeding ecology of these crabs is particularly important to understand their ecological interactions, since the abundance of preferred prey organisms strongly affects their distribution, growth, reproduction, behavior and migration.

Methods: The study was conducted along the Mangaluru coast, with fortnightly crab samples gathered from the Mangaluru fish landing centre from March 2021 - February 2022. Random sampling ensured the inclusion of all size categories and samples were analyzed for weight, morphometric measurements, sex and food and feeding habits. The level of stomach fullness was assessed visually and the contents were examined using Point’s volumetric method, identifying food items at the lowest taxonomic level and grouping them into dietary categories.  The vacuity index and Gastro-somatic index (GaSI) were calculated to describe the trophic behaviour of Portunus sanguinolentus.

Result: Gut content analysis revealed that P. sanguinolentus fed predominantly on crustaceans (31.45%), fish (22.84%), molluscs (18.70%) and larger quantities of sand and debris (20.29%) and unidentified matters (6.68%). The presence of debris and unidentified matter in the foregut suggests that P. sanguinolentus is a bottom-feeding omnivore which feeds on fresh and decaying matter. Size-wise analysis of gut contents revealed that juveniles (<80mm CW) preferred miscellaneous items followed by crustacean remains as their diet, sub-adults (80-100mm CW) crustaceans (42.65%) and miscellaneous (50.07%) and adults (>100mm CW) had a solid preference for crustaceans and molluscs.

Marine crabs are valuable seafood animals because of their esteemed delicacy, nutritive content and the significance of the fishery they support (Sudhakar et al. 2012). Crabs play a significant role as a marine fishery resource in India, accounting for an average of 9.6% of the overall crustacean landings between 1975 and 2020 (Madhubala and Selvamohan, 2023). Portunus pelagicus formed the dominant species in Karnataka, followed by P. sanguinolentus (Josileen et al. 2019). The various authors investigate the crab’s food and feeding habits, its status and potential (Dana et al., 2024), the physico-chemical environment and management strategies (Mandal et al., 2017), as well as the carapace (Sanjay et al., 2024).
       
Red-spotted swimming crabs, Portunus sanguinolentus, are found throughout the Indo-Pacific region, from the eastern coast of South Africa to the coasts of Hawaii. They usually live on muddy or sandy bottoms that are between 10 and 30 meters deep. Compared to male, female crabs prefer higher salinities. For this reason, they frequently live in deeper waters (Campbell and Fielder, 1986).
       
Understanding a species dietary habits is crucial to comprehending their ecological interactions, according to Biswass (1993). The availability of preferred prey organisms has a significant impact on crab distribution, growth, reproduction, behaviour and migration rate (Sánchez-Paz et al., 2006; Vinagre et al., 2007). The present study aims to study food composition, feeding behaviour and variation among the different size groups of P. sanguinolentus.
The current research was conducted along the Mangaluru coast. Fortnightly samples were gathered from the commercial catch at Mangaluru fish landing centre (12.9141oN, 74.8560oE) from March 2021 to February 2022 as a result of the fishing prohibition period (June 1st to July 31st 2021) on the West coast; collecting samples in June and July was not feasible. Random sampling was undertaken to ensure the inclusion of all size categories in the study. Samples were brought to the laboratory for recording weight, morphometric measurements (carapace width and carapace length), sex and to study food and feeding habits (Sukumaran and Neelakantan, 1997, Dineshbabu, et al., 2007).
       
Only foregut was used to study the dietary patterns and consumption behaviors of P. sanguinolentus. The degree of stomach fullness was visually evaluated based on categories including full, three-quarters full, half full, one-quarter full and empty, following the method outlined by Muthiah (1994). Crabs with full and ¾ full were considered active feeders and ½ were considered moderate feeders. Similarly, stomachs with ¼ and empty full were supposed to denote poor feeding.
       
The frequency of food items’ occurrence was accomplished by counting every foregut containing at least one specimen or part of the specific item (taxon) (Manooch and Mason, 1983; Williams, 1982). The contents of the stomach were transferred to a Petri dish and analyzed using Point’s volumetric method, taking into account the level of fullness, following the approach described by Hynes (1950). A qualitative analysis identified all the food organisms present in the stomach. Food items were identified to the most specific taxonomic level possible and subsequently categorized into five dietary groups: crustaceans, fish, molluscan remains, sand and debris and miscellaneous.
       
Since a predator’s diet cannot be fully described by a single technique for analyzing stomach contents (Hyslop, 1980), the trophic behavior of the species was described by the calculation of the vacuity index and the gastro-somatic index (GaSI).


Vacuity index, the number of empty stomachs encountered during the study period was calculated by vacuity index (Biswass, 1993).
 
Five hundred ninety-six (596) specimens of P. sanguinolentus, ranging in size from 77.3 mm to 165.2 mm carapace width (CW), comprising 294 males and 302 females, were assessed.
 
Diet composition
 
Gut contents analysis by points method revealed that crustaceans 31.45% was the top food preference of P. sanguinolentus (which included appendages, telson, other body parts of prawn, chelipid of crabs, stomatopods), fish(scales, bones, eyeball, vertebrae) formed the secondary preferred food 22.84%, subsequently by mollusc remains (squid tentacles, bivalves, gastropods)18.70%  and a large quantities of sand and debris (sand, mud, mesh and plastics)20.29% and miscellaneous items (algae filaments and unidentified matters) 6.68% (Fig 1, 2, 3, 4).
 

Fig 1: Mollusc remains (Gastropod).



Fig 2: Crustaceans remnants(crabs chilipids).



Fig 3: Debris (Mesh).


       
According to the occurrence method, the top food preference was crustaceans, which contributed the most in January (24.76%), followed by November (24.28%) and the least in August (10.71%). Fish remains were recorded maximum in December (19.45%), March followed subsequently (19.393%) and minimum in August (11.6%). Mollusc presence was significantly elevated in quantity during May (22.52%) and less in October (12.65%). Substantial amounts of sand and debris were detected throughout the study period, forming the highest in September (28.04%), followed by August (26.78%) and most down during December (17.64%). Miscellaneous food groups practically occurred in all the stomachs with food particles, with a peak in August (33.03%) and the lowest in May (12.61%) (Fig 5).

Fig 4: Percentage points of food groups during different months for P. sanguinolentus.



Fig 5: Percentage frequency of occurrence of major food groups during different months for P. sanguinolentus.


 
Food items in relation to size group
 
It was observed that juveniles (<80 mm CW) favoured miscellaneous items, with crustacean remains as the next most common component of their diet. In sub-adults (80-100 mm CW), the primary food source categories were crustaceans and miscellaneous. Adults (>100 mm CW) strongly preferred crustaceans and molluscs (Fig 6).

Fig 6: Percentage frequency of occurrence of major food groups during different size groups of P. sanguinolentus.


 
Feeding intensity
 
Based on the condition of the foregut, crabs were categorized into three groups. Crabs with full and ¾ full were considered active feeders and ½ were considered moderate feeders. Similarly, stomachs with ¼ and empty full were considered to denote poor feeding. Out of 596 stomachs (21.94%) were in full condition, (13.82%) were in 3/4th full, (19.59%) were in ½ full, (18.13%) were in 1/4th full and (26.50%) were in empty stomach. The majority of the actively fed crabs (full stomach) were recorded as being highest during December (24.59%), followed by September (22.72%) and least in August (8.46%). Moderately fed crabs were found maximum during October (32.25%), November (22.03%) and minimum in December (11.47%). Poorly fed crabs were recorded highest in August (33.07%), followed by March (30.90%) and lowest during October (16.12%) (Fig 7).

Fig 7: Feeding intensity in different months of P. sanguinolentus.


 
Feeding intensity in relation to size
 
Actively fed crabs (Highest feeding intensity) were discovered in the size group of 70-80 mm (49.9%) followed by 80-90 mm (26.47%) and least in 160-170 mm (11.53%). Moderately fed crabs were observed maximum in the size group of 100-110 mm (21.25%),140-150 mm (18.18%) and minimum in 150-160 mm. Crabs with empty stomachs were observed across all size groups except the 70-80 mm range, with the majorly occurred in the 130-140 mm (39.68%) and 160-170 mm size group (Fig 8).

Fig 8: Feeding intensity in different size groups of P. sanguinolentus.



Gastro-somatic Index
 
Gastro-somatic index of P. sanguinolentus varied from 1.708 to 2.617. The highest value was observed in May (2.617) and minimum in August (1.708) (Fig 9).

Fig 9: Gastrosomatic index in different months of P. sanguinolentus.


 
Vacuity index
 
Out of 596 stomachs examined, 159 had empty stomachs (27.10%). The frequency of stomachs being empty was also analysed every month, where August had the most elevated number of empty stomachs (43.07%), followed by November (33.89%), April (32.25%) and May (30.43%) and the most downward was observed in December (14.75%) (Fig 10).

Fig 10: Vacuity index in different months of P. sanguinolentus.


       
A comprehensive study of aquatic animals’ habits of food and feeding is important to understand their biology, such as growth, reproduction, migration patterns, etc. An organism’s diets vary considerably at different stages of life and the habitat they live in (Khan et al., 2018). Based on qualitative and quantitative analyses, this research confirmed that P. sanguinolentus (Fig 11 and 12) is a predator of faunal slow-moving benthic macroinvertebrates like crustaceans and molluscs, miscellaneous items consisting of algal filaments, polychaetes, fish remains and other items such as sand and debris. These findings in this study support those of Rasheed and Mustaquim, (2018). The most common food items found in their study were crustaceans (small crabs) and fish. Molluscs (gastropods and bivalves) remains were found to be a minor food in this study. Comparable findings have been noted by Chande and Mgaya (2004) for P. segnis in Tanzania. The occurrence of fish remains in the gut load  of portunids confirms that they exhibit scavenging behaviour that feeds on dead fish (Prasad and Neelakantan 1988; Cannicci et al., 1996). 

Fig 11: Portunus sanguinolentus.



Fig 12: Samples of P.sanguinolentus.


       
Pooled data revealed the percentage occurrence of feeding habits across various months; crustacean remains formed major food items (20.22%), subsequently by fishre mains (16.93%) and large quantities of sand and debris (23.3%) and mollusc remains (16.5%) and miscellaneous items (22.96%). These observations agree with the study of Prasad and Neelakantan (1988) on Scylla serrata from the Karwar region, which showed that portunid crabs mainly fed on crustaceans, detritus, molluscs, fishes and miscellaneous items from Karwar waters (Prasad and Neelakantan 1988). 
       
Josileen (2011) observed that crustaceans constituted a prominent food group, molluscs constituted the second dominant group and teleost fish were the 3rd most significant food item for P. pelagicus from the Mandapam coast in India. Portunus segnis’s diet mainly depends on local food availability, making it an opportunistic predator. Hamida (2019) stated that the biological aspects of an organism, such as growth and reproduction, largely depend on the presence of favourite food items or prey organisms.
       
The blue crab Portunus segnis’s dietary makeup was observed by Tadi Beni et al., (2019) from Iran, who reported 34.4% of empty stomachs. They concluded that the frequency of empty stomachs varied throughout the study period. In this study, the prevalence of an empty stomach fluctuated across different months, averaging 27.10% overall. The dietary patterns of portunid crabs have been previously studied (Ropes, 1968; Patel et al., 1979; Williams, 1982) and they reported that portunid crabs are opportunistic omnivores and rarely feed on motile forms like fish and shrimp species in their diets.
       
This study noticed fluctuations in dietary patterns concerning different size groups  and juveniles strongly preferred miscellaneous and crustaceans. In subadults, crustaceans and other miscellaneous items were the predominant components. Adults showed a clear inclination for crustaceans and molluscs. This conforms to reports of Sukumaran and Neelakantan (1997) in P. sanguinolentus. 
       
Khongngain et al. (2017) and Sarkar et al. (2017) noted that feeding activity varies seasonally due to changes in the availability of preferred food items, maturity stages and spawning seasons. In this investigation also, feeding intensity varied among different months; crabs with full stomachs were observed highest in September (33.33%), 3/4 stomach in December (27.86%), ½ full in October (32.25%), 1/4 full in January (26.75%) and empty stomachs in August (43.07%). Same outcomes have been reported by Khan et al. (2018), where the feeding intensity was less during the spawning season in S. serrata.
               
Whereas in size groups, full stomachs were dominant in the size group of 70-80 mm CW (66.66%) and empty stomachs were highest in the size group 130-140mm CW (39.68%), followed by 160-170 mm CW (38.46%). These observations agree with Wenner et al. (1974), who noticed that the preying utility is less in adults and relatively more among juveniles. Freier et al., (1996) state that the impact of larger chela size and muscle mass is probably responsible for the variance in the propensity for food items among crab sizes.
The study confirmed that P. sanguinolentus predominantly preys on infaunal, slow-moving benthic macroinvertebrates  like crustaceans and molluscs, with the occasional inclusion of fish remains, sand and debris, indicating a scavenging behaviour. The diet composition varied across different size groups, with juveniles preferring miscellaneous items and crustaceans, sub-adults favouring crustaceans and miscellaneous items and adults strongly preferring crustaceans and molluscs. Feeding effort was also seasonal and size-related; the highest feeding intensity was observed in juveniles and lower feeding activity during breeding season. These results add to our understanding of the ecological role and especially the trophic importance, of this crab. This function concerning the crab combining with other species to interact in the ecosystem deserves more attention and to be studied in a wider range about ecological equilibrium.
The authors thank the Department of Fisheries Resources and Management and the Dean, College of Fisheries, Mangaluru, Karnataka Veterinary, Animal and Fisheries Sciences University, Bidar, for providing the necessary facilities to conduct the research. 
Authors declare no competing or conflicting interests.

  1. Biswass, S.P. (1993). Manual of Methods in Fish Biology. New Delhi: South Asia Publishers PVT Ltd.157.

  2. Campbell, G.R. and Fielder, D.R. (1986). Size at sexual maturity and occurrence of ovigerous females in three species of commercially exploited portunid crabs in S.E. Queensland. Proceedings of the Royal Society Queensland. 97: 79-87.

  3. Cannicci, S., Guebas, F.D., Anyona, D. and Vannini, M. (1996). Natural diet and feeding habits of Thalamitacrenata (Decapoda, Portunidae). J. Crust. Biol. 16(4): 678-83.

  4. Chande, A.I. and Mgaya, Y.D. (2004). Food habits of the blue swimming crab Portunuspelagicusalong the Coast of Dar es Salaam, Tanzania. West. Indian Ocean J. Mar. Sci. 3: 37-42.

  5. Dana, S.S., Mazumder, C., Sau, S., Karjee, R., Sarkar Ray, M. (2024). Present status, constraints and potentials of mud-crab culture in West Bengal . Bhartiya Krishi Anusandhan Patrika. 38(4): 413-416. doi: 10.18805/BKAP616.

  6. Dineshbabu, A.P., Sreedhara, B. And Muniyappa, Y. (2007). Fishery and stock assessment of Portunus sanguinolentus (Herbst) from south Karnataka coast, India. J. Mar. Biol. Assoc. India. 49(2): 134-140.

  7. Freier, J. and Sampedro, M.P. and Gonzales-Gurriaran, E. (1996). Influence of morphometry and biomechanics on diet selection in three portunid crabs. Mar. Ecol. Prog. Ser. 137: 111-121.

  8. Hamida, O.B.A.B.H., Hamida, N.B.H., Ammar, R., Chaouch, H. and Missaoui, H. (2019). Feeding habits of the swimming blue crab Portunussegnis (Forskål, 1775) (Brachyura: Portunidae) in the Mediterranean. J. Mar. Biolog. Assoc. U.K. 99(6): 1343-1351.

  9. Hynes, H.B.N. (1950). The food of freshwater sticklebacks (Gasterosteus aculeatus and Pygosteus pungitius) with a review of methods used in studies of the food of fishes. J. Anim. Ecol. 17: 36-58.

  10. Hyslop, E.J. (1980). Stomach contents analysis: A review of methods and their application. J. Fish Biol. 17: 411-529.

  11. Josileen, J. (2011). Food and feeding of the blue swimmer crab, Portunuspelagicus(Linnaeus, 1758) (Decapoda, Brachyura) along the coast of Mandapam, Tamil Nadu, India. Crustaceana. 84(10): 1169-1180.

  12. Josileen, J., Maheswarudu, G., Padua, S., Sasikumar, G., Varghese, E. and Mohamed, K.S. (2019). CMFRI Marine Fisheries Policy Series No. 15; Fishery Management Plan for Palk Bay Blue Swimming Crab. 

  13. Khan, M.A, Das, S.K. and Bhakta, D. (2018). Food and feeding habits, gastrosomatic index and gonado-somatic index of Scylla serrata from Hooghly-matlah estuary of West Bengal, India. J. Mar. Biol. Ass. India. 60(1): 14.

  14. Khongngain, O., Das, S.K. and Bhakta D. (2017). Study on food and feeding biology of Trichogasterfasciata bloch and schneider, 1801 from a wetland of Nadia district of West Bengal. J. Inland Fish. Soc. India. 49(2): 03-09.

  15. Madhubala, K. and Selvamohan, T. (2023). Gut-isolated bacteria and biochemical composition of edible crab species in Manapad, India. J. Food, Agri. Environ. 21(1): 81-86.

  16. Mandal Amit, Das S.K. Dr., Majumder, A. (2017). Studies on physico- chemical environment and management of crab (Scylla serrata) farming in 24 Parganas (West Bengal). Indian Journal of Animal Research. 52(12): 1782-1789. doi: 10. 18805/ijar.B-3423.

  17. Muthiah, C. (1994). Some of the Fishery Biology of lizardfish Saurida spp. from the Karnataka Coast. Ph.D. Thesis, Karnataka University, Karwar.185.

  18. Manooch, III C.S. and Mason, D.L. (1983). Comparative food studies of yellowfin in tuna, Thunnusalbacares and blackfin tuna, Thunnusatlanticus, (Pisces: Scombridae) from the southeastern and gulf coast of the United States. ActaIchthyol Piscat. 13(2: 25-46.

  19. Patel, N.M.,Chhaya, N.D. and Bhaskaran, M. (1979). Stomach contents of Portunus pelagicus (L.) from AD net catches. Indian J. Mar. Sci. l8: 48-49.

  20. Prasad, P.N. and Neelakantan, B. (1988). Food and feeding of the mud crab Scylla serrata (Forskal) (Decapoda: Portunidae) from Karwar waters. Indian J. Fish. 35(3): 164-170.

  21. Rasheed, S. andMustaquim, J. (2018). Natural diet of two commercial crab species, Portunussegnis (Forskål, 1775) and P. sang- uino-lentus (Herbst, 1783), in the Coastal Waters of Karachi. Vet. Anim. Sci. 6(3): 35-42.

  22. Ropes, J.W. (1968). The feeding habits of the green crab Carcinus maenas. Fish. Bull. 67(2): 183-203.

  23. Sánchez-Paz, A.,García-Carreño, F.,Muhlia-Almazán, A., Peregrino- Uriarte, A.B., Hernández-López, J. and Yepiz-Plascencia, G. (2006). Usage of energy reserves in crustaceans during starvation: Status and future directions. Insect Biochemistry and Molecular Biology. 36(4): 241-249.

  24. Sanjay, C., Mogalekar,  H.S., Sahu, A., Kashyap, N., Dhurve4, D., Narsale, S., Kadam,  R., Debbarma, S. (2024).  Carapace length-weight, carapace width-weight relationships, condition factor and sex ratio of freshwater crab sartoriana spinigera (Wood-Mason, 1971) from the River Burhi Gandak, North Bihar, India. Indian Journal of Animal Research. 1-7. doi: 10.18805/IJAR.B-5232.

  25. Sarkar, S., Das, S.K. and Bhakta, D. (2017). Length weight relationship and relative condition factor of Indian shad, Tenualosailisha from Hooghly estuary system, West Bengal. J. Inland Fish. Soc. India. 49(1): 22-26.

  26. Sudhakar, M., Raja, K., Anathan, G. and Sampathkumar, P. (2012). Compositional characteristics and nutritional quality Podopthalmus vigil (Fabricius). Asian J. Biol. Sci. 4: 166-174.

  27. Sukumaran, K.K. and Neelakantan, B. (1997). Food and feeding of Portunus (Portunus) sanguinolentus (Herbst) and Portunus (Portunus) pelagicus (Linnaeus) (Brachyura: Portunidae) along the Karnataka coast. Indian J. Mar Sci. 26(1): 35-38.

  28. Tadi Beni, F., Pazooki, J. and Safaei, M. (2019). Dietary ecology of the Portunussegnis (Forskal, 1775) in the coastal waters of Hormozgan Province, Iran. Iran. J. Fish. Sci. 18(4): 646-655.

  29. Vinagre, A.S., Do Amaral, A.P.N., Ribarcki, F.P., Da Silveira, E.F. and Perico E. (2007). Seasonal variation of energy metabolism in ghost crab O. quadrata at Siriu Beach (Brazil). Comp. Biochem. Physiol. 146(4): 514-519.

  30. Wenner, A.M., Fusaro, C. and Oaten, A. (1974). Size at onset of sexual maturity and growth rate in crustacean populations.  Can. J. Zool. 52(9): 1095-1106.

  31. Williams, M.J. (1982). Natural food and feeding in the commercial sand crab Portunuspelagicus linnaeus, 1766 (Crustacea: Decapoda: Portunidae) in the Moreton Bay, Queensland. J. Exp. Mar. Biol. Ecol. 59(2-3): 165-176.

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