122 resultados para Lobsters


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Majority of the prawn catch of the Kerala coast comes from the inshore regions within the 10 fathom line. A bottom deposit formed of fine mud rich in humus is found to be the ideal condition for the penaeid prawns. Similarly the lobster is observed in large numbers at localised areas very near the coast in the crevices of rocks. Though it has been observed that prawns and lobsters exist in deep water as well under different conditions, our knowledge about these forms along the Indian coasts is very scanty, being restricted to the works of Spence Bate, Alcock, De Man and Ramadan. Recently, during the cruises of the University Research Vessel Conch off the Kerala Coast (1958-1963) two species of deep water prawns and one species of lobster were collected from depths 100 - 180 fathoms. Of these, Penaeopsis philippi is found in large numbers occupying an almost continuous bed extending from Anjengo to Mangalore, while P. rectacutus has a restricted appearance between Cochin and Calicut. However, some sort of year to year variation has also been observed regarding the abundance of the species at various stations. Peurulus sewelli has a more restricted distribution, the maximum number being found between Puvar and Cochin. Attempt has been made to correlate the occurrence of the species with the hydrological conditions at the bottom and the nature of the substratum. It is observed that Peurulus sewelli occupies a more or less hard bed formed of sand with shell fragments or stones and small percentage of silt, the bottom temperature at the stations varying from 11°C to l4°C. P. sewelli is a more or less permanent inhabitant of the edge of the continental shell off the Kerala Coast worthy of attention for detailed investigation with a view to explore the possibilities of commercial exploitation.

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Spiny lobsters of the family Palinuridae are known to exist in parts of Asia such as India, Japan, Indonesia and Malaya. In Ceylon spiny lobsters are caught chiefly by a primitive type of gear designed to catch these species and incidentally by nets set to catch fish. The limitations of these types of gear and the results of experimental fishing in Ceylon with different designs of lobster traps have been discussed earlier. As a result of these experiments a very effective trap for capturing spiny lobsters was developed and it was shown that spiny lobsters were present in large quantities (De Bruin 1960). This created great interest among skin-divers who found lobster fishing very remunerative.

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Six species of spiny lobsters of the genus Panulirus have been recorded in Ceylon waters. It is clear, therefore, that species dominance and ecological separation in the genus Panulirus is demonstrable and that the separation is dependent on the particular ecological preferences of the different species. In order to determine the factors governing the ecological separation, it was decided to make a detailed study of the environments in which the different species were found. Diving operations constituted the chief method of investigation. However, information was also obtained from commercial skin-divers, trap fishermen, bottom-set net fishermen and trawling operations. The period of investigations extended from 1962-1968.

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Investigations into the resources of spiny lobsters in Ceylon waters were first begun in 1958 and consisted initially of skin-diving surveys of sand-stone and rocky areas at night. The surveys revealed the presence of lobsters in appreciable quantities in these reefs. Experiments were then carried out to decide on the most effective method of capturing them. Lobster traps of different design were placed in the reefs and rocky areas and the most efficient design was selected for use. This design was used thereafter to assess the spiny lobster resources. However, traps proved ineffective on the east coast as the particular species present there did not enter traps. Where traps failed the resources were assessed using skin-divers. These operations revealed the presence of lobsters in large concentrations in particular areas around Ceylon, especially on the south-west, south and west coasts. (De Bruin, 1960 and 1962). This discontinuity in distribution is discussed in greater detail in a previous publication (De Bruin, 1969. The ecology of spiny lobsters, Panulirus spp., of Ceylon waters. Bulletin of the Fisheries Research Station, Ceylon, 20(2), pp. 171-189).

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Scores of publications on spiny lobsters and their fishing techniques are available from various parts of the world. A variety of fishing gears which vary in design and operation are employed for exploiting lobsters. A review of the work carried out on spiny lobsters with special reference to their distribution, fishing gear, fishing methods, baits and crafts in India, Sri Lanka, United States, Australia, South Africa, United Kingdom, Ireland and Portugal based on selected literature are considered and discussed.

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American lobsters (Homarus americanus H. Milne Edwards, 1837) are imported live to Europe and should according regulations be kept in land-based tanks until sold. In spite of the strict regulations aimed specifically at preventing the introduction of this species into the NE Atlantic, several specimens of H. americanus have been captured in the wild, especially in Oslofjord, Norway since 1999. One of the great concerns is interbreeding between the introduced American species and the local European lobster, H. gammarus (Linnaeus, 1758). For this reason an awareness campaign was launched in 2000 focusing on morphologically "unusual" lobsters caught in local waters. Morphological characters have been based on colour and sub-ventral spines on the rostrum. Two samples of H. americanus were used for comparisons, as well as samples of European lobster from Oslofjord collected in 1992. Previous genetic analyses (allozymes, mtDNA and microsatellite DNA) have demonstrated that the American lobster is distinct from its European counterpart, with several additional alleles at many loci in addition to different allelic frequency distribution of alleles of "shared" alleles. During the present study, thirteen microsatellite loci were tested in the initial screening, and the three most discriminating loci (Hgam98, Hgam197b and Hgam47b) were used in a detailed comparison between the two species. A total of 45 unusual lobsters were reported captured from Ålesund (west) to Oslofjord (southeast) from 2001 to 2005 and these were analysed for the three microsatellite loci. Nine specimens were identified as American lobsters. Comparisons between morphological and genetic characteristics revealed that morphological differences are not reliable in discrimination the two species, or to identify hybrids. Further, some loci display almost no overlapping in allele frequency distribution for the reference samples analysed, thus providing a reliable tool to identify hybrids.

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Munida is the most diverse and cosmopolitan genus of the galatheid squat lobsters. The group has attracted much attention in recent years from both systematic and evolutionary perspectives, yet information on the biology, ecology, and evolution of this genus is very limited. We investigated the genetic parentage of two North Atlantic species; Munida rugosa and M. sarsi sampled from the Clyde Sea on the west coast of Scotland. Microsatellite markers were used to establish the parental contribution from embryos of berried females (M. rugosa, n=25 and M. sarsi, n=5). The frequency of multiple paternity observed in both species (86% for M. rugosa and 100% for M. sarsi) is the highest ever reported for any marine crustaceans. Invariably more than two sires were involved in each case (minimum of two to three for M. rugosa and four for M. sarsi). Findings indicate that multiple paternity is likely to be the norm in both species. Within most multiply sired broods, sire contribution was highly skewed towards a single male (66% of broods for M. rugosa and 100% for M. sarsi). Furthermore, embryos from different sires were randomly distributed across the female's brood patch. This is the first report of multiple paternity in galatheids. While a number of theories can account for the high incidence of multiple paternity in these species (e.g. convenience polyandry as a result of cryptic female choice, forced copulations, the influence of fishing pressures), at present it is not possible to disentangle their individual and/or combined effects.