Growth Per Moult of Tagged Lobsters (Homarus americanus) in Bonavista Bay, Newfoundland

1972 ◽  
Vol 29 (2) ◽  
pp. 143-148 ◽  
Author(s):  
G. P. Ennis

The suitability of the sphyrion tag for lobster growth studies is demonstrated by comparing growth of ferromagnetic- and sphyrion-tagged lobsters. Carapace length and total weight increments in one moult of 54 males (52–92-mm carapace length) tagged with sphyrion tags averaged 11.4 mm (15.7%) and 185.9 g (60.8%). For 56 females 57–89-mm carapace length they averaged 9.8 mm (13.3%) and 136.3 g (42.5%). Differences in growth per moult between sexes increased with size. For both sexes percent carapace length increment decreased with increase in carapace length but more rapidly for females. Carapace length increment increased with increasing carapace length for males, but for females there was no significant change over the size range considered. Incidence of moulting for sphyrion-tagged lobsters was 83.1% and comparable with an observed estimate (85.2%) from field samples obtained shortly after the moulting season.

1980 ◽  
Vol 37 (6) ◽  
pp. 945-956 ◽  
Author(s):  
G. P. Ennis

Female maturity ogives for five Newfoundland populations of the lobster (Homarus americanus) gave 50% maturities ranging from 71- to 76-mm carapace length. Sizes at which distinct inflections (indicating onset of maturity) and asymptotes (indicating 100% mature) are present in the abdomen width/carapace length ratio vs. carapace length relationships coincide with the smallest ovigerous and largest immature specimens, respectively, observed in those particular samples. Inflection in the crusher claw weight/whole weight ratio vs. carapace length relationships (used in this paper to indicate onset of maturity in males) occurred at larger sizes than inflections in the abdomen width/carapace length ratios of females.The percentage of nonovigerous females that spawn in a given year generally increases with increasing size. The highest percentage of nonovigerous females tagged with sphyrion tags prior to the spawning season that were ovigerous when recaptured 10–12 mo later was 83.8%. The percentage of ovigerous females with new shells (i.e. molted and spawned in same year) varied between areas and years and ranged from 0 to 38.5% of the total number of ovigerous females in fall samples. The percentage of ovigerous females in samples also varied between areas and years and ranged from 2.6 to 30.4% of the total number of females greater than the size at 50% maturity. In general a greater percentage of females was ovigerous at sizes between the size at 50% maturity and 80 mm (largest subcommercial size) than at commercial sizes.In a sample of nonovigerous females, the size range at which 50% were fertilized (76–80 mm) coincided closely with the size at 50% maturity (75 mm) for the area.At subcommercial sizes (< 81 mm) the sexes were approximately equally represented in fall trap-caught samples but females heavily outnumbered males in diver-caught samples taken over the same period. At commercial sizes, however, males heavily outnumbered females in the trap-caught samples while in diver-caught samples the sexes were equally represented.Key words: lobster (Homarus americanus), maturity ogives, maturity indices, percent ovigerous, sex ratios


2006 ◽  
Vol 63 (9) ◽  
pp. 1925-1933 ◽  
Author(s):  
M J Tremblay ◽  
S J Smith ◽  
D A Robichaud ◽  
P Lawton

Catchability (q) in traps was estimated for American lobsters (Homarus americanus) in Flagg Cove, off Grand Manan Island (New Brunswick, Canada), where large females (>100 mm carapace length (CL)) aggregate in late summer and early fall. In 2001 and 2002, diver surveys were used to estimate lobster density, and traps were then deployed to obtain catch rates. Bayesian generalized linear models were fit to the densities of different size groups (81–100, 101–130, 131–160, and >160 mm CL) of ovigerous females, non-ovigerous females, and males. Catchability was strongly affected by year. Differences in q due to sex and size for ovigerous females, non-ovigerous females, and males were apparent but were not consistent between years. Size was not an important factor for the catchability of lobsters between 81 and 160 mm CL. In comparison with lobsters of a similar size in other areas, Flagg Cove lobsters in the size range of 81–100 mm CL were less catchable. We hypothesize that this resulted from the high densities and larger sizes of lobsters in Flagg Cove, which likely lead to increased agonistic interactions and reduced entry of lobsters into traps.


1986 ◽  
Vol 43 (11) ◽  
pp. 2291-2294 ◽  
Author(s):  
S. L. Waddy ◽  
D. E. Aiken

Large female American lobsters, Homarus americanus (> 120 mm carapace length), maintained at nearshore Bay of Fundy temperatures often spawn twice without an intervening molt (consecutive spawning). Consecutive spawning occurs in two forms: successive-year (spawning in two successive summers, a molt in the first and fourth years) and alternate-year (spawning in alternate summers, a molt in the first and fifth years). In both types, females often are able to fertilize the two successive broods with the sperm from a single insemination (multiple fertilization). Twenty of 21 large females that were held for up to 13 yr displayed one of these types of consecutive spawning. Consecutive spawning and multiple fertilization enable large lobsters to spawn more frequently over the long term than their smaller counterparts. This, combined with the logarithmic relationship between body size and numbers of eggs produced, means that very large lobsters have a much greater relative fecundity than previously thought.


Author(s):  
Thomas Claverie ◽  
I. Philip Smith

Size at the onset of sexual maturity was determined in Munida rugosa based on allometric growth of chelipeds and abdomen, and on the proportion of ovigerous females. The variability of three different measurements of carapace length (CL) used previously for M. rugosa was also evaluated to minimize measurement error. Both sexes had symmetrical cheliped length and allometric cheliped growth over the size-range investigated, but males showed increased allometry beyond 22 mm CL. Females had greater positive allometry in abdomen width than males, but their size at maturity could not be precisely determined because sampled females were too large.


1970 ◽  
Vol 27 (2) ◽  
pp. 257-264 ◽  
Author(s):  
D. J. Scarratt

Mortalities of lobsters held in the laboratory and tagged with sphyrion tags inserted dorsally between the carapace and abdomen (subcarapace tag) and between the second and third abdominal segments (abdomen tag) did not differ significantly. Premoult tag loss was negligible. The subcarapace tag was retained significantly better through moulting.Returns of subcarapace-tagged and abdomen-tagged lobsters released on the fishing grounds in June, 11 weeks before the August 10 opening of the fishing season, were lower than returns of carapace-tagged lobsters released in early August. More subcarapace-tagged than abdomen-tagged lobsters were returned, and a higher proportion had moulted. Growth was comparable to that reported in the literature. Few lobsters were recaptured during the following fishing season, 14–16 months after liberation, and none subsequently. Returns from lobsters less than 63.5 mm carapace length (sublegal) when tagged were extremely low. Poor survival may be related in part to time of release. Some injury to internal organs may occur with both tags. The subcarapace tag is clearly superior but may be of limited value in the field for lobsters below 63.5 mm carapace length.


1989 ◽  
Vol 46 (6) ◽  
pp. 932-940 ◽  
Author(s):  
Gregory C. Jensen ◽  
David A. Armstrong

Pribilof Island blue king crab (BKC; Paralithodes platypus) were sampled by beam trawl in May and August of 1983 and April 1984 to determine timing of reproductive events. Biennial reproduction was found to be the result of slow ovarian growth in large, muciparous females, while smaller primiparous females are often able to spawn in two consecutive years. Mating and egg extrusion occur in late March to early May and eggs hatch in mid-April of the following year, consequently, the embryonic period and rate of development is approximately 12 mo, similar to that of its congener the red king crab (RKC; P. camtschatica). Comparison of the reproductive output of the two species revealed that despite the 2 yr ovarian cycle, BKC only produce 20–30% more dry egg mass at any carapace length than do RKC, a substantially smaller difference than previously calculated. One year after molt, females of both species are not significantly different in dry body weight over a size range of 100–140 mm carapace length, but RKC have produced about three times more dry ovarian weight than BKC of comparable size, suggesting that biennial reproduction in BKC may be the result of energetic limitations.


1997 ◽  
Vol 48 (8) ◽  
pp. 959 ◽  
Author(s):  
R. Melville-Smith ◽  
J. B. Jones ◽  
R. S. Brown

Laboratory and field trials were employed to examine the feasibility of using biological tags as moult indicators. Twenty-four animals were tagged with epidermal implants and held in aquaria for 2 years and 8 months before the tags were removed. Five tags failed to form useful cysts and one tag was damaged during processing. The remaining 18 lobsters moulted between three and six times, with this moulting record being accurately verified by 15 of the biological tags and incorrectly interpreted (by one moult) in one case. Two tags produced inconclusive results. Biological tags were tested in the field in the Fremantle area, with 132 animals being recaptured out of 1336 tagged. Eleven tags proved impossible to read, eight failed to form cysts, and the balance recorded up to six moults during the release period. Animals in the size range 60–80 mm carapace length (CL) recorded two moults per year, one in February–April and a second before the mid-November start to the fishing season. Females grew significantly less per moult than did males in the same size category (60–85 mm CL), and both sexes showed significantly smaller increments for animals ≥85 mm CL at release.


1990 ◽  
Vol 47 (12) ◽  
pp. 2402-2406 ◽  
Author(s):  
S. L. Waddy ◽  
D. E. Aiken

American lobster (Homarus americanus) have a dual mating strategy. Although most females mate when they are newly molted, mating can occur at any molt stage if necessary, in the laboratory, virtually all uninseminated preovigerous females mate prior to spawning. Male aggression is a major factor in the success of intermolt mating and males can discriminate between immature and mature females, and between inseminated and uninseminated females. Female receptivity is affected by both ovarian stage and the presence of stored sperm, but not by molt stage. Most females become unreceptive after insemination, but their receptivity returns once the supply of stored sperm is exhausted. Intermolt mating occurs in smaller lobster that for some reason did not mate at molt, and it is an important part of the reproductive strategy of larger lobster. Lobster s[Formula: see text] carapace length frequently spawn twice without molting and often fail to store sufficient sperm to fertilize consecutive spawnings. Intermolt mating ensures these females will produce fertile second broods.


1983 ◽  
Vol 40 (10) ◽  
pp. 1667-1675 ◽  
Author(s):  
Alan Campbell

Sphyrion-tagged lobsters recaptured in the Bay of Fundy during 1977–80 yielded mean annual molt increment and molt probability data for male and female lobsters of 60–171 mm carapace length from which growth curves were calculated. In addition, a multiple regression model was used to generate growth curves from premolt size, number of molt periods lobsters were exposed to, and growth increment data for 850 tagged lobsters at liberty for 1–5 yr. Von Bertalanffy parameters were calculated from these empirical growth curves, which suggest that lobsters take 20–35 yr from time of hatching to reach 200 mm carapace length in the Bay of Fundy. Analysis of pleopods indicated that the majority of lobsters molt during August–October each year. Growth per molt of immature (60–94 mm carapace length) and mature (95–170 mm carapace length) male and immature female lobsters was arithmetic (regression slope 1.04) but was regressive for mature females (slope 0.95). Mature lobsters molted less frequently than immature lobsters, but mature males grew more rapidly than mature females. Most mature females in the Bay of Fundy are on a 2-yr molt–reproductive cycle. About 20% of ovigerous females recaptured within 2 yr after release had extruded eggs a second time without molting, confirming that multiple egg extrusions between molts do occur naturally.


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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