Blood refractive index and ratio of weight to carapace length as indices of nutritional condition in juvenile rock lobsters (Jasus edwardsii)

2001 ◽  
Vol 52 (8) ◽  
pp. 1395 ◽  
Author(s):  
M. D. Oliver ◽  
M. D. Oliver ◽  
A. B. MacDiarmid ◽  
A. B. MacDiarmid

Nutritional condition reflects food quality and quantity and influences growth rate. Therefore, the ability to measure nutritional condition would be valuable in estimating the potential for growth of captive and wild lobsters. To assess potential indices of nutritional condition, we examined changes in blood refractive index and ratio of weight to carapace length of juvenile rock lobsters to treatments of varying food supply. Blood refractive index was strongly correlated with blood protein concentrations and was a reliable proxy for the circulating protein that is metabolized and diluted during periods of low food and starvation. The moult cycle imposes constraints on blood refractive index, however, so it is essential that the moult stage of the animal be assessed concurrently. Ratios of weight to carapace length were slower to respond to reduced food intake than was blood refractive index but were independent of the moult cycle and may, therefore, be a more direct reflection of nutritional health. These results showed that both blood refractive index and ratio of weight to carapace length are reliable and nondestructive indices of nutritional condition in juvenile rock lobsters.

1998 ◽  
Vol 49 (2) ◽  
pp. 151 ◽  
Author(s):  
Philip J. James ◽  
Lennard J. Tong

This paper describes a technique used by juvenile red rock lobsters, Jasus edwardsii, 20–70 mm carapace length, to open and feed on live mussels. This technique appears to be an innate behaviour. The maximum or critical size (shell length) of cultured and wild Mytilus galloprovincialis, and cultured Perna canaliculus, which J. edwardsiiis capable of opening, is strongly correlated with lobster carapace length. Jasus edwardsii is capable of opening significantly larger cultured than wild M. galloprovincialis; this is a reflection of the differences in shell morphology between wild and cultured mussels, and the vulnerability of different shapes to the opening technique employed. In replacement experiments, the greatest numbers of mussels were eaten from the smallest mussel sizes (6–20 mm shell length), whereas the greatest amount of dry flesh weight was consumed from the middle mussel sizes (11–40 mm shell length) for all three mussel types. Dry-weight consumption was considered the most appropriate indicator of preference, the amount of mussel flesh consumed being more relevant to a rock lobster farmer than the numbers of mussels eaten. The preferred mussel size was approximately half the critical size. The application of these results to rock lobster farming is discussed.


2014 ◽  
Vol 54 (2) ◽  
pp. 79-84 ◽  
Author(s):  
Bijan Bagchi ◽  
Subhrajit Modak ◽  
Prasanta K. Panigrahi

The relevance of parity and time reversal (PT)-symmetric structures in optical systems has been known for some time with the correspondence existing between the Schrödinger equation and the paraxial equation of diffraction, where the time parameter represents the propagating distance and the refractive index acts as the complex potential. In this paper, we systematically analyze a normalized form of the nonlinear Schrödinger system with two new families of PT-symmetric potentials in the presence of competing nonlinearities. We generate a class of localized eigenmodes and carry out a linear stability analysis on the solutions. In particular, we find an interesting feature of bifurcation characterized by the parameter of perturbative growth rate passing through zero, where a transition to imaginary eigenvalues occurs.


1992 ◽  
Vol 43 (4) ◽  
pp. 727 ◽  
Author(s):  
BJ Hill ◽  
TJ Wassenberg

Analysis of the natural diet of prawns over the moult cycle shows a preference for molluscan tissue at all stages, with an apparent greater preference in the stage immediately following the moult dropping in the intermoult stages and then increasing again before the next moult. A laboratory study was carried out to provide more information on feeding behaviour over the moult cycle. Adults of Penaeus esculentus (carapace length 25 to 30 mm, weight 15.5 to 25.2 g) held at 32 to 35 and 23 to 25°C did not feed on the night of ecdysis. On the following nights, feeding increased to peak at 2.7 g of penaeid tissue per day in moult Stage C. For the rest of the moult cycle, feeding was fairly steady at about 1.23 g of penaeid tissue per day but dropped sharply two nights before ecdysis. The prawns increased in weight by 0.7 to 6.1 g (mean 3.5 g) over a moult cycle. A stepwise linear-regression analysis showed that, within the range tested, the increase in weight was not a function of prawn weight, duration of moult cycle (range 14 to 34 days), or daily food consumption (0.95 to 2.33 g). They ate more crustacean tissue (Metapenaeus bennettae) than bivalve tissue (Perna canaliculatus) over the entire moult cycle, except for the night before and after ecdysis, when they ate bivalve tissue almost exclusively.


Aquaculture ◽  
2003 ◽  
Vol 220 (1-4) ◽  
pp. 667-682 ◽  
Author(s):  
D.J Johnston ◽  
K.A Calvert ◽  
B.J Crear ◽  
C.G Carter

Author(s):  
John B. Buchanan

Previous work on the biology and distribution of Calocaris is discussed briefly. The distribution in Northumberland waters is considered in relation to depth and bottom sediment.Quantitative monthly samples show that population numbers remain very stable throughout the year. A well marked egg-laying period occurs in January-February when relatively few eggs (average 38) are attached to the pleopods. Eggs are carried for 8–9 months and hatch in September-October. By a combination of size-frequency distribution and gonad-developmnt classification the age-groups in the population are interpreted. After passing through a phase of testes development and spermatophore formation individuals lay their first batch of eggs at the end of the 5th year. The ovaries regenerate over a 2-year period and a second egg-laying takes place at the end of the 7th year with a possible third at the end of the 9th year. The incidence of soft individuals in the samples together with observed changes in the coverage with epifaunistic growths indicate that after entering the 5th year a single annual moult cycle begins with a slowing down in growth rate.Population numbers, fecundity and larval survival are discussed. Both the survival curve and the apparent lack of serious predation suggest that the population reaches senescence


The giant tortoise of Aldabra, Geochelone gigantea , shows quite marked changes in proportions with age, although during growth the relations between the length of the carapace and various measurements of the plastron and scutes involve not only strong but also weak allometry. Certain scutes show a predisposition to split during growth. Accidental damage to the carapace is frequent. Males reach over 100 cm in carapace length but females are smaller, up to 80 cm. There is no segregation between the sexes in any single measurement investigated, except among the very largest animals. A general appraisal of carapace and tail shape is sufficient to sex only animals above 60 cm in carapace length. The number of annuli on each scute corresponds to the number of years of age at least up to the formation of the tenth to fifteenth annulus. A general assessment of the pattern of growth is made by plotting body measurements against number of annuli. Growth curves of individual tortoises are reconstructed by relating measurements of successively formed annuli to age. Growth rate is recorded by plotting the difference between successive pairs of annulus measurements against age. The growth rate of ageable tortoises varies between local populations on South Island and between populations of South and Middle Island. Growth rate declines with age, reaching asymptotes at mean values of between 20 and 30 years. Some individuals exhibit sudden increases in growth rate after several years of very slow growth. There is a well-marked daily cycle of activity, feeding being limited to the early morning and late evening. Agonistic behaviour is virtually absent. Breeding is seasonal and the males select partners from within a limited size range of tortoises. Most mating attempts are unsuccessful. On Aldabra, tortoises occur in a wide variety of habitats, in each of which they depend on a different plant species or vegetational association for food. On coastal plains the chief source of food is Sporobolus virginicus . A variety of small herbs is consumed on the barren stretches of coastal champignon. Distribution in these areas is profoundly affected by the availability of shade. Further inland, the tortoises browse heavily on Guettarda speciosa in woods dom inated by this tree. They take advantage of seasonal successions in the vegetation associated with freshwater pools, feeding on each community as it develops. Most of the woody plants near the pools are ignored. On the platin, browsing is selective and the regeneration of some trees is held in check. A very im portant food source here is the `tortoise turf’ (a sward in which Panicum sp. is often dominant) developed under conditions of heavy grazing and susceptible to erosion by wind and the tortoises themselves. On Middle Island, where the population is small, the tortoises exert very little effect on the vegetation. Associations with other animals are mostly casual, but along the south coast dunes Coenobita rugosus is dependent on tortoise faeces for food. Fossilized tortoise bones have been discovered at many points on Aldabra, deposited in brown limestone. They probably date from before the interstadial of about 30 000 years ago. Some adult tortoises range over 7 km or more, across a variety of habitats, but many individuals appear to be sedentary. The population of South Island is enormous of the order of 100 000 animals with a density of about 30 hm -2 on the platin. Higher densities are reached in Guellarda woodland. Local variation in numbers, size range and age structure depend on habitat preferences, differential movement of age classes and regional differences in growth rate. Attempts at assessing age class distribution are affected particularly by undersampling of the younger age classes, and the difficulty of counting the worn growth rings in animals with more than about 14. In the census sample, which may itself be an imperfect sample of the whole South Island population, at least 35 % of the animals are below 20 years of age and only about 20 % can have reached sexual maturity. More than 50 age classes may be present, but this and similar deductions are still speculative.


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