Life history parameters and diet of Risso's dolphins,Grampus griseus,from southeastern South Africa

The life history of Risso's dolphins (Grampus griseus) remains poorly known and data from strandings can help provide important information. Data from 126 Risso's dolphins stranded or bycaught along the southeastern coastline of South Africa between 1958 and 2017 were analyzed in relation to their sex, age structure, and diet. Mean estimated length at birth was 146.9 cm, while maximum length was 325 cm for males and 313 cm for females; small sample sizes precluded detailed examination of sexual dimorphism. Age estimates for 33 individuals (14 males, 17 females, 2 unknown sex) indicated a maximum age of 13 years (males) and 17 years (females), respectively; the oldest animal was 19 years (unknown sex). Mean length and age at attainment of sexual maturity were estimated at 280 cm and 7.1 years in males and at 282 cm and 7.7 years in females. Stomach contents from 27 individuals showed that diets of immature and mature males and females overlapped and consisted predominantly of cephalopods. Reported strandings decreased between 2000 and 2017, possibly due to a lack of reporting associated with a ban on driving on beaches or related to the collapse of the local “chokka” squid (Loligo reynaudii) fishery in 2014–2015.     

Greater silver smelt, Argentina silus in Icelandic waters

This paper presents results obtained from data on the greater silver smelt Argentina silus in Icelandic waters collected by the Marine Research Institute, Iceland, mainly since 1981. The greater silver smelt is most abundant in the waters off the south-east coast of Iceland clockwise to those off the west coast, but the species has also been observed off the north coast. Differences in the size composition in relation to area and depth are described. The preferred depth range of the greater silver smelt was found to be 300-600 m and the preferred temperature was about 6°C. Ageing is described showing a relatively fast growth up to the age of 8-9 years. The age/length and length/weight relations are given. Females grow faster than males. The 50% maturity point is reached by males at a length of 36-37 cm and at an age of approximately 8 years, and by females at a length of 37-38 cm and approximately 9 years. Spawning takes place to some extent year round but with one or two periods of greater intensity. Results from experimental fishing are described and problems in connection with a Commercial fishery are discussed.     

AGE,GROWTH, AND REPRODUCTIVE PATTERNS OF DALL'S PORPOISE (PHOCOENOIDES DALLI) IN THE CENTRAL NORTH PACIFIC OCEAN

Life history parameters were estimated for Dall's porpoise, Phocoenoides dalli, from biological specimens collected in the western Aleutian Islands, during 1981–1987. Of 2,033 males and 3,566 females examined, reproductive data were available for 1,941 males and 1,906 females; ages were determined for 813 males and 1,297 females. Female sexual maturity was based on the presence of one or more corpus on either ovary; 845 were sexually immature and 1,061 were sexually mature. Two estimates of female average age at sexual maturity (ASM) were 3.8 and 4.4 yr; average length at sexual maturity (LSM) was 172 cm. Males were considered sexually mature when evidence of spermatogenesis was detected; 1,136 were sexually immature and 805 were sexually mature. Two estimates of male ASM were 4.5 and 5.0 yr; LSM was 179.7 cm. Physical maturity was assessed for 246 males and 446 females by examining the degree of fusion in thoracic vertebral epiphyses. For both sexes, the average age at physical maturity was 7.2 yr. Average length at physical maturity was 202.6 cm for males and 192.7 cm for females. Average lengths of physically mature males (x?= 198.1 cm, SE = 0.8566) and females (x?= 189.7 cm, SE = 0.4002) were significantly different(P < 0.0001). Early postnatal growth was rapid in both sexes. A secondary growth spurt in both mass and length was characteristic for both sexes; the increase in length preceded the mass increase by 1–2 yr. Average length at birth (LOB) was approximately 100 cm; birth mass averaged 11.3 kg (SE = 0.0772). By the time the umbilicus had healed (<2 mo), the average length and mass had increased to 114.1 cm and 23.8 kg, respectively. Gestation period based on projections using LOB was 12 mo, but this was considered an overestimate. Calving was modal, centered in early July; an annual reproductive interval was indicated. Among the sexually mature females, 120 were pregnant, 55 were pregnant and lactating, 321 were pregnant with colostrum, and 33 were “resting.” By 3 July (95% CI =x? 1 d), 50% of births had occurred, during each of the seven years sampled. The ovulation rate was estimated at 0.914 ovulations per average reproductive year. Enlarged follicles and recent ovulations were observed in postpartum females in late July.     

Sexual maturation of cod (Gadus morhua L.) in the southern Baltic (1990–2006)

Baltic cod, like other species, is susceptible to inter‐annual fluctuations in sexual maturation, depending on the length, age, sex, extent of the habitat area, and stock abundance of the cod population. Maturity is one of the biological indicators used to detect changes in a stock that can be caused by fishing. To address these issues specifically for the eastern Baltic cod stock, long‐term data (1990–2006) from Polish research vessels in the southern Baltic were examined. To date, the ICES has used the same maturity ogives over extended periods and assumed invariant sex ratios for the assessment of eastern Baltic cod. The combined maturity ogives calculated in the present study were markedly lower, particularly for age groups 2–4 (5), in all periods, than those used in the ICES assessment. Moreover, the proportion of females increased with length and age, suggesting that annual verification of the sex ratio is needed. The present study also revealed that the total length (L_50%) and the age (mean age‐at‐maturity; MAM_50%) at which 50% achieved first sexual maturity were higher for females than for males in the study period. The long‐term mean L_50% and MAM_50% for females were 43.9 cm and 4.3 years, respectively, and for males 34.8 cm and 3.4 years. There was also a spatial difference between calculated maturity ogives, with slightly lower L_50% (range: 1.4–8.6 cm) in the Gdańsk Basin than in the Bornholm Basin. The increasing trend in fishing mortality observed in 1993–2004 (ICES data) did not translate into a temporal trend in calculated maturity ogives. However, changes in L_50% and MAM_50% reflected recruitment variations (ICES data). The significance of these findings is discussed in the context of the environment and recruits abundance.     

Growth, age at sexual maturity and condition in bearded seals (Erignathus barbatus) from Svalbard, Norway

The aim of this study was to describe growth, determine age at sexual maturity and investigate the condition of bearded seals (Erignathus barbatus) collected in the fjords of Spitsbergen, Svalbard, Norway. Morphometric data, teeth and sex organs were collected from 110 animals. Age was determined by reading the cementum layers in hard longitudinal sections of canine teeth. Sexual maturity in males was determined according to the size of the testes and bacula. Females were defined as being sexually mature according to findings of mature follicles or corpora lutea/albicantia. Von Bertalanffy growth curves were applied to both standard length and body mass, and asymptotic values for males and females were 231.1 ± 11.4 cm and 269.9 ± 26.2 kg, and 233.1 ± 7.5 cm and 275.3 ± 47.8 kg, respectively. Maximum recorded lengths and masses were 254 cm and 313 kg in males and 242 cm and 358 kg in females. All males older than 6 years were found to have been sexually mature. Females were found to attain sexual maturity at about 90% of the asymptotic length, corresponding to an age of 5 years. In males a significant decrease in condition was observed from June to August, with a subsequent increase in September. In adult females, condition decreased from May to June and increased again from June to September. The conditional changes seen are likely to be due to the extra energetic cost and reduced food intake associated with reproduction, lactation and molt. Accepted: 28 July 1998     

Grooming and resting of otters Lutra lutra in a marine habitat

The weight gain in lactating harbour seal pups and sex-specific growth curves are described. The relationship between body length, body weight and age were derived by regression analysis based on length and age data from 365 seals, and weight values from 136 seals. The asymptotic values of the curves describing body length were 148.0 cm and 147.2 cm in females and 153.9 cm and 155.5 cm in males using Gompertz and von Bertalanffy, respectively. The corresponding body weight values were 72.8 kg and 76.7 kg in females and 90.7 kg and 88.4 kg in males.     

Growth and age at sexual maturity of South American sea lions

The average age at sexual maturity (ASM) is an important parameter for evaluating the reproductive potential or status of a population. South American sea lions, Otaria flavescens in Patagonia (Argentina) were exploited and reduced to less than 10% of pre-exploitation numbers. At present, the population is recovering at a rate of 6%. In this paper, we studied growth and age at sexual maturity of South American sea lions in the south-western south Atlantic by examining 219 individuals (females and males) collected between 1989-2008. Individuals were aged by counting growth layer groups in tooth sections, standard body length was measured and male and female reproductive organs were examined macroscopically and histologically to establish individual sexual maturity. Maximum recorded length for males and females was 264 cm and 200 cm, respectively, and maximum ages 19 and 21 yrs. ASM defined as the age where 50% of females are mature, was estimated at 4.8±0.5 years old, corresponding to a mean SL of 147 cm, about 81% of their asymptotic length. First observed ovulation occurred during the 4th year, first birth may occur between 4 and 5 years old. Males physiologically mature between 4-6 years, but the size of the testes shows that all males became sexually mature by the age of 9 years when they reach a mean SL of 212 cm, about 86% of their asymptotic body length. The present information on ASM and growth of O. flavescens will improve the development of population dynamics models, to investigate the impact of recovering sea lions populations on its marine environment, as well as its trophic interactions with commercial fisheries.     

Life history of the orange-striped emperor <Emphasis Type="Italic">Lethrinus obsoletus</Emphasis> from the Mariana Islands

The present study investigated the age-based demography of the orange-striped emperor, Lethrinus obsoletus, from commercial samples in the Commonwealth of the Northern Mariana Islands (CNMI), spanning a 24-month market sampling period. Information on growth, life span, mortality, and reproduction was derived through analysis of sectioned sagittal otoliths and gonad material. The species had a moderate longevity of 13 years while females and males reached 50% sexual maturity at 3.8 years (22.9 cm fork length) and 2.8 years (19.9 cm fork length), respectively. Histological examination of gonads and sex-specific age frequency distributions suggest the sexual ontogeny of the species conforms to juvenile hermaphroditism, whereby sexual transition from female to male occurred prior to maturation. No annual spawning periods were identified, but the ubiquitous presence of post-ovulatory follicles in females and spermatogenic material in males coupled with a consistent lunar trend in gonadosomatic index patterns suggests the species spawns every lunar cycle throughout the year with spawning activity potentially increasing around the new moon. Ratios of natural to fishing mortality indicate a moderate level of exploitation (0.37); however, a large portion of harvested females had not reached reproductive maturity, suggesting that formal assessments of stock status are warranted to ensure the sustainable harvest of the species in CNMI.     

Reproductive biology and implications for management of the painted sweetlips Diagramma pictum in the southern Arabian Gulf

The reproductive biology of the painted sweetlips Diagramma pictum was determined from 487 individuals collected between January and December 2010 in the southern Arabian Gulf. There was no evidence of sex change and the combination of histological results with the sex composition of the size and age structures indicated a gonochoristic sexual pattern. There were peaks in gonado-somatic indices for females in March and October with spawning occurring during two seasons (April to May and November). The mean size and age at sexual maturity (L(m50) and A(m50) ) were 35·7 cm fork length (L(F) ) and 2·9 years for females and 26·7 cm L(F) and 0·5 years for males. The maximum recorded age (11 years) and small mean size and young age at sexual maturity for males may be a direct result of intensive demersal fishing in the southern Arabian Gulf. There was an exponential increase in the cumulative reproductive potential with size and a linear increase with age for both sexes. The mean L(F) (L(c50) ) at which D. pictum became vulnerable to capture was 33·3 cm, which corresponded to only 3 and 7% of the cumulative reproductive potential of males and females, respectively. Size-specific and age-specific reproductive potential indicated that conventional regulations that equate the mean size at first capture to sexual maturation are unsuitable for the management of D. pictum.     

Morphometrics,body condition,and growth of the ringed seal (Pusa hispida saimensis) in Lake Saimaa: Implications for conservation

Morphometrics and growth of the critically endangered Saimaa ringed seal (Pusa hispida saimensis), which inhabits a freshwater lake in Finland were studied using data from 344 carcasses. This study presents the first detailed information on ringed seal pup growth and body condition from birth to the age of one year. Newborn pups were on average 68 cm long and weighed 5 kg. Pups attained the majority of their first year growth during the nursing period. Body condition and growth declined after weaning, but pups recovered from postweaning nutritional deprivation at the age of 8 mo. The seals achieved their maximum body length, girth, and mandible size around the age of 4 yr, and asymptotic body mass two years later. Baculum growth indicated that males reached sexual maturity at age 5–6 yr. The Saimaa ringed seals' asymptotic body length and mass were 132 cm and 59 kg, respectively, which is similar to medium sized marine ringed seals. Saimaa ringed seals' survival to adulthood is extremely low due to high bycatch mortality; furthermore climate change may hamper pup growth and elevate mortality. Therefore we recommend continuation of fishing closures to improve pup survival.     

Age and Growth of Blue Antimora <Emphasis Type="Italic">Antimora rostrata</Emphasis> (Moridae) in Southwestern Greenland Waters

The results of determination of age and study on growth of blue antimora Antimora rostrata from the waters of Southwestern Greenland are presented. The results are based on the analysis of 200 fish otoliths. In the catches, we found specimens of antimora with total lengths of 18?70 cm, body weights of 23?2731 g, at the age of 7?38 years. Minimal age of males (not considering juvenile individuals) was 10 years at body length of 27?33 cm; maximal age was 18 years at 42 cm. Minimal age of females was 9 years at length of 21–27 cm; maximal age was 38 years at 70 cm. The rate of linear growth in blue antimora from Southwestern Greenland waters is comparable to that in the fish from New Zealand and Ross Sea waters but considerably lower than indicated earlier for fish from the waters of Iceland, Greenland, and the Mid-Atlantic Ridge. The age of reaching sexual maturity in males and females is preliminary determined as 15 and 19?20 years, respectively.     

External morphology of the short-beaked common dolphin, Delphinus delphis: growth, allometric relationships and sexual dimorphism

Growth, allometric relationships and sexual dimorphism are described from measurements of 105 male, 149 female and 38 unsexed specimens of short‐beaked common dolphin, Delphinus delphis, stranded along the Irish coastline (53.8% of the sample) or by‐caught in fisheries (46.2% of the sample), from 1990 to 2003. For each dolphin, 24 external body length measurements were recorded. Ages were determined for 183 dolphins by analysis of growth layer groups in the dentine. Males ranged in total body length (TBL) from 105 to 231 cm and females from 93 to 230 cm, with a maximum age of 25 years obtained for both sexes. Using a single Gompertz growth curve, asymptotic values obtained for TBL were 211.6 cm and 197.4 cm for males and females, respectively. Asymptotic lengths were attained at 11 years in males and 9 years in females. The gestation period was estimated to last approximately 11.5 months. Sexual size dimorphism (SSD) was evident, with males being significantly larger than females for 20 of the characters measured, and an SSD ratio of 1.06 was obtained. Sexual shape dimorphism was lacking, except for the presence of prominent postanal humps in mature males.     

Reproductive biology of brown trout, Salmo trutta macrostigma Dumeril 1858, in a tributary of the Ceyhan River which flows into the eastern Mediterranean Sea

The study describes some key elements of the reproductive biology, including spawning season, age at sexual maturity, fecundity and egg diameter of the native brown trout, Salmo trutta macrostigma, in a tributary of the Ceyhan River. A total of 197 brown trout (118 females and 79 males) were captured in 2000–2001 by electric fishing. In observations on monthly changes, the gonadosomatic index (GSI) and the monthly frequency distribution of egg diameter confirmed that spawning lasted from November to January. Some 27.7% of the females and 62.5% of the males attained sexual maturity in their second year. The smallest fork length (FL) of brown trout attaining sexual maturity was 17.4 cm for males and 17.8 cm for females. Mean fecundity in age groups II, III, IV and V were 360, 452, 693 and 1283 eggs per female, respectively. One 9‐year‐old female had a unique 3232 egg count. The mean fecundity of the sampled population was 554 eggs per fish, positively correlated with the FL (mm) (R = 0.8227 ) and body weight (R = 0.8130). The diameter of mature eggs in the spawning season ranged from 3.250 to 5.930 mm, with a 4.146 mm average. Mean egg diameter in age groups II, III, IV and V in the spawning season were 0.813, 3.799, 4.663 and 5.243 mm, respectively. Fecundity, egg weight and diameter were statistically different in all age groups.     

Variation in length and age at sexual maturity of Atlantic groundfish: a reply

Synopsis The assertion has been made by Halliday (1987) that trends in size and age at maturity of Atlantic groundfish published by Beacham (1983a, b, c, d, e, f) are artifacts induced by errors in determining the sex of an individual, distinguishing between immature and mature fish, sampling fish outside of the regular spawning season, and by nonrandom sampling of the population. In particular, Halliday asserts that for the Atlantic argentine,Argentina silus analysis, the conclusions of Beacham (1983a) that: (1) median length at sexual maturity declined over time; and (2) males matured at older ages than did females are invalid owing to biases in both sampling and analysis. In fact, if some of the biases indicated by Halliday were significant, then the decline in median length at sexual maturity is enhanced and the conclusions of Beacham (1983a) reinforced. Size and age at sexual maturity are dynamic characters in many vertebrate populations, and the fact that they should change for Atlantic groundfish should not be surprising given variable exploitation patterns in the fisheries since 1960.     

Reproductive aspects of male franciscana dolphins (Pontoporia blainvillei) off Argentina

As the first study to investigate reproductive aspects of male franciscana dolphin -Pontoporia blainvillei - in Argentine waters, the aim of this paper was to assess sexual maturity by using histological and morphometric methods. P. blainvillei was labeled as "Vulnerable" by the IUCN in 2008. The specimens analyzed were either incidentally caught in artisanal fishing nets (n=47) or found stranded on the beach (n=3). Testis weight and testicular index of maturity were reliable indicators of sexual maturity, being their values: MTW: 1.14 ± 0.60-4.49 ± 1.94; IM: 0.03 ± 0.01-0.09 ± 0.03, for immature and mature specimens' respectively. It was found that the hierarchical cluster analysis (HCA) might be appropriate for establishing sexual maturity stage, based on both the body morphometric measurements and age. The values for age, standard length and total weight at attainment sexual maturity were 2.92-3.54 years, 126.19-126.27 cm and 23.47-23.75 kg. Considering the extremely low relative testis weight, the reversed sexual length dimorphism, the absence of secondary sexual characteristics, and the lack of scars from intrasexual combats in males, the hypothesis that sperm competition does not occur in the species, and male combats for accessing female reproductive may be rare for P. blainvillei is reinforced. All these features fit the species within a serial monogamous mating system.     

Growth, size and age at maturity of the agile frog (Rana dalmatina) in an Iberian Peninsula population

The mean age of a population of agile frogs (Rana dalmatina) from the Iberian Peninsula was estimated using mark and recapture and skeletochronology. Life-history parameters, including growth rate, body length, age and size at maturity, sexual dimorphism and longevity, were studied. The regression between age and snout-vent length (SVL) was highly significant in both sexes. Males reached sexual maturity at two years of age, although sometimes they can reach it at only one year of age. The average SVL at maturity was 51.75 mm (standard error (SE) = 0.71; n = 45). Females reached sexual maturity at two years of age with an average SVL of 62.14 mm (SE = 2.20; n = 14). A subset of the female population reached sexual maturity at three years of age. Growth was rapid until sexual maturity was reached. There was an overlap of SVL between different age classes. Growth was continuous, fulfilling the conditions of Von Bertalanffy's model. The growth coefficient (K) was 0.840 in males and 0.625 in females. The maximum SVL was greater in females (73.00 mm) than in males (59.50 mm). Sexual dimorphism was significantly biased towards females in all age classes. The maximum longevity observed was 6 years in females and 8 years in males. Management strategies for agile frogs should take into account factors such as these life-history characteristics.     

Female-biased operational sex ratio of sexual host fish in a gynogenetic complex of Carassius auratus

To study the coexistence of sexual and gynogenetic forms, we examined the population structure of a gynogenetic complex of the Japanese crucian carp, Carassius auratus Temminck et Schlegel, during the April–June reproductive season by collecting 1225 mature fish that migrated from Lake Suwa to a tributary river for spawning. There were more sexual fish (about 80%) than gynogenetic fish in this complex, and the operational sex ratio in the sexual form was female biased (males were about 20%). Mean standard length and body weight of sexual females were larger than those of sexual males. Sex ratio was male biased in smaller fish (standard length, <8.5 cm) but female biased in larger fish (standard length, ≥8.5 cm). We determined age by scale ring marks; the average age of sexual females was higher than that of males, but there was no significant difference in the average age between sexual and gynogenetic females. Sex ratio in the sexual form was more female biased for old than for young fish, and the mean size of sexual females was larger than that of males of the same age. The clear female-biased sex ratio and age difference between sexual females and males can be explained either by (1) higher mortality of males or by (2) female-biased sex allocation. The latter process reduces the disadvantage of sex and contributes to the coexistence of sexual and gynogenetic forms. Received: November 24, 2000 / Accepted: March 6, 2001     

Life history of the Indo‐Pacific humpback dolphin in the Pearl River Estuary,southern China

We studied life history characteristics of the Hong Kong/Pearl River Estuary population of Indo‐Pacific humpback dolphins (Sousa chinensis), based on data from 120 specimens stranded between 1995 and 2009, 40 individuals biopsied at sea, and a long‐term (14+ yr) photo‐identification study. Ages were determined for 112 specimens by thin‐sectioning teeth and counting growth layer groups. Estimated length at birth was 101 cm. Longevity was at least 38 yr, and there was little difference in growth patterns of males and females. Growth was described by a Bayesian two‐phase Gompertz model; asymptotic length was reached at 249 cm. The tooth pulp cavity filled at an average of 18.5 yr of age. Physical maturity was reached at between 14 and 17 yr of age, apparently a few years after attainment of sexual maturity. Maximum lengths and weights of about 268 cm and 240 kg were attained. Females appear to lose all their spots by 30 yr, although males may retain some spotting throughout life. Calving occurred throughout the year, with a broad peak from March to June. Of 60 females monitored at sea for >14 yr of the study, none were documented to have more than three calves, suggestive of low reproductive output or low calf survival.     

A skeletochronological study of age, growth and longevity in a population of the frog Rana ridibunda from southern Europe

Age at sexual maturity and longevity in a population of Rana ridibunda from north-eastern Greece were studied by skeletochronology performed on the phalanges. Analysis of the age structure was based on counting the lines of arrested growth (LAGs). Sexual maturity for both sexes arises during the first year or after the first hibernation. Ages ranged from 1 to 5 years (mean=2.96) among 52 males and from 1 to 5 years (mean=3.73) among 56 females. The mean snout-vent length was 69.03+/-12.6mm in males and 82.38+/-13.27 mm in females. The difference between the sexes in age and size was significant. Growth of individuals was fitted on? The von Bertalanffy model. The growth coefficient (K) was 0.57 in males and 0.54 in females, mainly due to faster male growth between metamorphosis and maturation.     

The growth and maturation of the "tarantula", Avicularia avicularia L.

The growth of the theraphosid spider, Avicularia avicularia L. was studied principally by taking measurements of the fang length of exuviae and dead specimens. The relatic ships between fang length and increment at ecdysis and fang length and instar duration were investigated and used to construct a projected growth curve for the species. This suggests that males reach sexual maturity in approximately 13 instars and at a minimum age of about two and a half years. In males the adult instar is terminal and rarely lasts more than three months. Reproductive maturity in females is probably not reached earlier than the XIVth instar or three years from birth. The females continue to moult annually after maturity and have a longevity in excess of seven years. The pattern of colouration shows characteristic changes in early immature life and develops a slight sexual dimorphism in adults. Type II urticating hairs are present throughout life and occur in light and dark forms in the IInd instar. The mean length of the urticating hairs increases during the life cycle and a sexual dimorphism develops in the XIIth or XIIth instar. In adult males the urticating hairs are uniformly barbed whereas in the adult females the barbs are restricted to the proximal end.