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.     

AGE STRUCTURE AND GROWTH OF THE BOTTLENOSE DOLPHIN (TURSIOPS TRUNCATUS) FROM STRANDINGS IN THE MISSISSIPPI SOUND REGION OF THE NORTH-CENTRAL GULF OF MEXICO FROM 1986 TO 2003

Despite their high abundance and wide distribution, little is known about the historical or current growth and age structure of coastal bottlenose dolphins ( Tursiops truncatus ) in the north-central Gulf of Mexico. Between 1986 and 2003, teeth were collected from bottlenose dolphins stranded on the mainland coast of Mississippi and the adjacent barrier islands. Bottlenose dolphin strandings occurred year round, peaking in March and April. Neonate strandings also peaked during these 2 mo. Age estimates were obtained from 111 animals by reading the growth layer groups in the dentine layer of the teeth. The ages ranged from <1 yr to 30 yr of age. The two-stage Laird–Gompertz growth model was fitted to the total length and age data. On the basis of this model, the asymptotic lengths were estimated at 250 cm for females and 255 cm for males. The length at birth estimates were 98–103 cm for females and 100–107 cm for males. These lengths are similar to those of bottlenose dolphin populations from other Gulf of Mexico areas and from the North Atlantic Ocean along the southeastern United States.     

AGE, GROWTH, AND REPRODUCTION OF THE FINLESS PORPOISE, NEOPHOCAENA PHOCAENOIDES, IN THE COASTAL WATERS OF WESTERN KYUSHU, JAPAN

Abstract: In the coastal waters of western Kyushu, Japan, a total of 97 incidentally taken or stranded finless porpoises, Neophocaena phocaenoides , was collected for studying age, growth and reproduction. An additional 17 specimens from the Inland Sea were used for a comparison of life history. Mean neonatal body length was 78.2 cm. Both males and females grew to around 140 cm by 5 yr of age. The maximum body lengths of males and females in western Kyushu were 174.5 cm and 165.0 cm, respectively, which were smaller than those recorded in other Japanese waters. Females probably attain sexual maturity at ages of 6–9 yr and at body lengths of 135–145 cm. Males probably mature sexually at ages of 4–6 yr, at body lengths of 135–140 cm and at weight of testis of 40–150 g. The lack of females aged 5–6 yr and males aged 4–5 yr precluded firm conclusions on ages at sexual maturity. Parturition in western Kyushu was estimated to be prolonged from autumn to spring, whereas in the Inland Sea and Pacific waters it was restricted from spring to summer with a peak in April. These geographical differences and available information on distribution implies that the finless porpoises in western Kyushu constitute a local population.     

Reproduction in Bagre marinus (Ariidae) off Pernambuco, northeastern Brazil

Throughout 1997, the catches of artisanal gillnetters working off the coast of northeastern Brazil were sampled monthly for Bagre marinus (Mitchill 1815). Significantly more females (n = 207) than males (n = 82) were caught, although there was no significant difference in their size compositions (21–47 cm fork length, FL). All males sampled (21–40 cm FL) had developed gonads and were classified as sexually mature. According to macroscopic and microscopic examination of their reproductive tract, females were separated into four reproductive stages (immature, maturing, mature, and resting). Size at 50% sexual maturity for females was estimated to be 33 cm FL. A positive linear relationship was detected between the size of mature females and their fecundity (between 11 and 32 oocytes). Clear reproductive progress indicated a spawning period between March and May. We conclude that further fishery‐independent data are required to determine patterns of male abundances and distributions.     

Spawning seasonality and body sizes at sexual maturity in the bluespine unicornfish,Naso unicornis (Acanthuridae)

We herein evaluate several reproductive metrics of Hawaiian Archipelagic populations of the bluespine unicornfish (Naso unicornis), an economically and ecologically important, broadly distributed tropical Pacific reef fish, based on multi-year, fishery-dependent and fishery-independent collections. Sex-specific spawning seasonality was characterized for fish collected mostly from Oahu (Main Hawaiian Islands, MHI) using a gonadosomatic index. Histological slides preparations were used to score gonad developmental phase and to classify individuals of either sex as immature or mature. Sex-specific median body lengths at maturity (L₅₀) were estimated by logistic fits of proportion mature versus length class. Spawning was highly seasonal in Hawaii, with a single brief (May–June) peak spawning period. Proportionate gonad-to-body weight values were relatively low, averaging only about 0.1 % and 0.6 % across all months of year and 0.16 % and 1.03 % during May–June for males and females, respectively. Median lengths at sexual maturity differed between the sexes. L₅₀ values for fish collected throughout all months of year were 30.1 ± 0.5 (standard error) cm Fork Length (FL) for males and 35.5 ± 0.7 cm FL for females. Spawning seasonality and L₅₀ estimates for bluespine unicornfish in Hawaii suggest that the species spawns several months earlier in the calendar year and matures at larger body lengths in Hawaii versus Guam, the Northern Mariana Islands, and Pohnpei in the Federated States of Micronesia. Estimated lengths at sexual maturity are compared to the minimum length (14 inches or 35.6 cm FL) mandated for this species in Hawaii: median size at maturity occurs at a length appreciably less than (males) or approximately equal to (females) minimum legal size. A likely disproportionately large contribution of old females to population replenishment is discussed relative to the minimum size limit.     

Age and growth of yellow eels, Anguilla anguilla, in the estuary of the Guadalquivir river (south-west Spain)

A total of 1068 eels were examined from a population located in the Guadalquivir river estuary (37°N, 6°25'W). Maximum ages recorded were 4 + (males) and 7+ (females), and maximum lengths were 39-1 cm (males) and 54.1 cm (females). No growth was recorded between November and April, most occurring in May and, to a lesser extent, in June-October. Females grew to be larger than males. A classification analysis, based on 17 different European eel populations revealed that populations in brackish waters grew faster than those in fresh waters, but latitude also had an influence. Length-weight relationships obtained for three eel categories (males, females and undifferentiated) were used to estimate relative condition: condition cycles were similar between sexes, with increases in autumn and decreases in winter. There were monthly fluctuations in the sex ratio, and females dominated significantly in the combined catch (234 males/276 females).     

Sexual maturity and estimated fecundity in female Indo‐Pacific bottlenose dolphins (Tursiops aduncus) from South Australia: Combining field observations and postmortem results

Knowledge of life history of bottlenose dolphins in Australia is limited, with no studies comparing field and postmortem data from the same region. Carcasses of 88 opportunistically collected females (1987–2015) were studied, including eight observed for up to 23 yr before death. Ovaries were weighed and number of corpora determined grossly. Nineteen mammary glands were examined histologically. Relative age was determined using developmental features and body length, estimated age by tooth incremental lines, and physical maturity by epiphyseal fusion. Age at sexual maturation was 7.17 yr (6–>14 yr) at body lengths of 191–209 cm. Physical maturation occurred at 12–17 yr, and body lengths of 195–233 cm. An Exponential model provided the best fit for age at body length, with an asymptote at 214 cm. Combined ovary weight increased between birth and sexual maturation, with significantly more corpora in the left ovary. Corpora increased with age and appeared to persist throughout life. For mature females, 95% had ≤ 11 corpora. Number of corpora was consistent with number of calves for females with known life histories. Estimated interbirth period was about 4 yr. Three females with abnormal reproductive features were either chronically diseased and/or had high heavy metal burdens.     

Sexual size dimorphism,growth, and maturity of the fluvial eight-barbel loach in the Kako River,Japan

The maturation and growth pattern of the fluvial eight-barbel loach Lefua sp. (Japanese name: nagare-hotoke-dojo), an endangered species, was investigated using an individual identification-recapture method from 1995 to 1998 in an upper reach of a headwater tributary of the Kako River, Hyogo Prefecture, Japan. Based on observations of the gonads through the abdominal skin, the loach was estimated to breed mostly from May to July. All the males matured by age 1⁺, and all the females matured by age 2⁺. Gamete release in all individuals of both males and females was predicted from recaptured loaches during each breeding season. The standard length of mature females was significantly larger than that of males, showing sexual size dimorphism (SSD). The maximum sizes recorded were 75.4 mm SL for females and 61.2 mm SL for males. Both males and females of immature specimens grew mainly from May to November, including the breeding season, with no significant differences in growth rates between them. After sexual maturity, both males and females grew mainly from July to October (or November), after the breeding season, and the females exhibited higher growth rates than males. Therefore, SSD of the species seems to be attributable to the different growth rates after maturity. The longevity of the loach was estimated to exceed ten years based on individual growth patterns of various sizes during the survey period. It is likely that the loach has an iteroparous life history, breeding every year, and moderate growth rates after maturity.     

Reproductive biology of common snook Centropomus undecimalis (Perciformes: Centropomidae) in two tropical habitats

In Southeastern Mexico, Centropomus undecimalis is an important fish species of sport and commercial fisheries for coastal and riverine communities. Fisheries along rivers and coasts depend on migratory habits of this species, and these movements are probably related to reproduction. In spite of its economic importance, few studies have been conducted focusing on its reproductive biology, and this research aims to analyze these habits. Samples (fork length, somatic and gonads weight, and macroscopic maturity stages) were obtained from organisms collected by fishermen from the largest fishing cooperatives along the coastal and riverine areas of Tabasco, from July 2006 to March 2008. Fish size ranged from 34 to 112 cm fork length, with an average age of 6.42 years for males and 9.12 years for females. In riverine areas, fish sizes ranged from 30 to 85 cm and the average age was 5.5 years for males and 6.6 years for females. Significant differences were recorded between lengths of males and females from the two areas (Kruskal-Wallis, p < 0.05). The male:female ratio was 1:0.68 in the coast, and 1:0.16 in riverine areas. The length-weight relationship did not vary between both sexes among areas (ANCOVA, p > 0.05). A curve for eviscerated weight was calculated for both sexes, for coastal fishes SW = 0.0059 (FL)3.07, and the riverine ones SW = 0.0086 (FL) 2.98, with an isometric growth (b = 3). The period of maximum reproduction was from July to August, with temperatures of 28 to 30 degrees C. A significant correlation between the gonadosomatic index (GSI) and rainfall was recorded for samples of both males and females from coastal areas (r = 0.63, r = 0.70) whereas only one positive correlation was recorded for riverine females (r = 0.57). The size at first maturity (L50) was estimated at 60 cm and 80 cm (FL), corresponding to 5.5 and 8.5 years of age, for males and females, respectively. An important proportion of mature females of eight years and older, suggests that these ages contribute significantly to the reproductive biomass. The results indicate that due to changes in the exploitation period, we recommend to protect populations of the common snook.     

LIFE HISTORY OF FRASER'S DOLPHIN, LAGENODELPHIS HOSEI, BASED ON A SCHOOL CAPTURED OFF THE PACIFIC COAST OF JAPAN

Life history of Fraser's dolphin, a little known delphinid species, was examined based on 108 specimens from a school captured by the driving fishing method in Japan. The sex ratio was approximately 1:1, and mature dolphins of both sexes formed the bulk of the school. The oldest animals were two males and a female of 17.5 yr. Age and body length at sexual maturity were estimated at 7–10 yr and 220–230 cm in males and 5–8 yr and 210–220 cm in females. Mature males were larger in body length than mature females and showed apparent secondary sexual features: deepening of the tail stock and widening and darkening of the lateral dark stripe. The annual ovulation rate was 0.49. The estimated neonatal length (110 cm) predicts a gestation period of about 12.5 mo and calving peaks in spring and probably also in fall. The calving interval was estimated to be about 2 yr. These life history parameters are similar to those of the striped and pantropical spotted dolphins, except for longevity. The reproductive rate of this species may be lower than that of other pelagic delphinids, if the observed shorter longevity is real.     

Reproductive biology of the prawn Melicertus kerathurus (Decapoda: Penaeidae) in Thermaikos Gulf (N. Aegean Sea)

The reproductive biology including insemination frequency, ovarian maturation, gonadosomatic index (GSI), size at first maturity, and fecundity of Melicertus kerathurus were investigated using monthly samples from Thermaikos Gulf. Insemination was recorded by the presence of a spermatophore in the thelycum, and ovarian development was based on macroscopic ovarian staging (ST1–ST5). Inseminated females were found throughout the year with high percentages recorded from April to July. Although all ovarian stages were represented in mated females, insemination increased with size and ovarian maturation. High percentages of vitellogenic or mature ovarian stages were observed from May to July, while immature and developing ovaries were predominant mainly in winter. Spawned ovaries occurred from May to October. Carapace length at first maturity based on the presence of a spermatophore (CL_50sp) was estimated at 39.20 mm, while that based on the presence of vitellogenic and mature ovaries (CL_50ov) at 40.70 mm. The seasonal peak in the proportion of mature females (ST4) varied with size. Inseminated females at ST4 and GSI peaked in June–July. GSI varied in relation to insemination status and ovarian stage. In large females (>50 mm CL), the decline in mature ovaries and GSI increment with size indicates a relative reduction in the reproductive output. The number of oocytes ranged from 62,742 to 602,947 (mean ± SD: 268,000 ± 113,000). As the prawns are targeted during the spawning season, mainly by the artisanal fishery, and female size at first maturity is selected by artisanal net size, managerial measures toward artisanal fishery should be implemented.     

Reproduction of the long-tongued nectar bat Macroglossus minimus (Pteropodidae) in Brunei, Borneo

The long‐tongued nectar bat Macroglossus minimus lagochilus (Megachiroptera, Pteropodidae) is a small fruit bat inhabiting South‐east Asia. Its reproduction was studied in Brunei, Borneo, where individuals were usually captured in rainforest (Ulu Temburong). Adult females (n = 23) had body masses of 13.0–19.0 g, with forelimbs 3.83–4.33 cm in length. All adult females were pregnant, with pregnancies observed during every month except May, September and November when no adult females were captured. Female M. minimus in Brunei have a reproductive cycle that is consistent with a pattern of seasonal bimodal polyoestry. Most births appear to occur from November to May, during which time females experience two births: the first centred around November and December, and the second centred around April and May. These two birth seasons appear correlated to the two seasons of greater rainfall in Brunei: October to December, and April to July. Oestrous and mating apparently occur soon after each birth; however, there appears to be a 2‐ to 3‐month period of delayed embryonic development following the births centred around April and May. The data are consistent with embryonic development commencing around July and August (after a delay) for the births centred around November and December, and around December and January for the births centred around April and May. The data suggest that all adult females participate in each breeding season. Adult males (n = 20) had body masses of 12.5–18.0 g, with forelimbs 3.91–4.26 cm in length.     

Sexuality, sex change and maturation patterns in the yellowfin seabream, Acanthopagrus latus (Teleostei: Sparidae) (Houttuyn, 1782)

Macroscopic and histological studies were carried out to describe the reproductive styles and sex reversal and to follow gonadal changes in captive yellowfin seabream during the second year of life. Four reproductive styles are found in Acanthopagrus latus (Houttuyn, 1782): (i) males and females (gonochorism), (ii) functional males, (iii) transitionals and (iv) functional females. The species is a protandric hermaphrodite and begins life as a functional male with testicular zone undergoing active spermatogenesis, while the ovarian zone is arrested at the primary growth (perinucleolar) phase. Males and females were encountered in virtually all size‐classes. Functional males outnumbered the functional females in all size‐classes in which they were encountered. Sex reversal begins in the transitionals from July to August, after spawning in the functional males, at 14.9–20.2 cm standard length (SL) and, by November, maturation of the ovarian tissue begins. A. latus in cages in Kuwait waters spawns from January to April with a peak in February for males, and a peak in March for females and transitionals. Spawning begins in the 18.3–20.2 cm size‐range fish, peaking in the 20.3–22.2 cm size‐range in both males and females and also in the transitionals, although a few of the latter spawn from 14.9 cm SL. In relation to age, spawning begins at 20 months in males and peaks at 21 months. Females begin to spawn at 21 months with a peak at 22 months, while transitionals generally begin to spawn at 20 months, although a few 14–15‐month‐old sex‐changing individuals were encountered. Temperature, either alone or in combination with other unknown factors, triggers spawning in A. latus.     

Age, growth and mortality of picarel, Spicara smaris L. (Pisces: Centracanthidae), from the eastern Adriatic (Croatian coast)

Age, growth and mortality of picarel Spicara smaris L. collected in the eastern middle Adriatic during April and May in 1999 were studied. The total lengths of individuals ranged from 6.3 to 19.8 cm, and the weight from 2.2 to 78.3 g. The slopes ( b values) of the total length–weight regressions indicated negative allometric growth for females ( b =2.8± 0.03) and isometric growth for males ( b =3.08±0.04). The oldest female and male were 4 and 6 years, respectively. The von Bertalanffy growth parameters for the sexes combined were ( L _∞=22.76 cm, K =0.277, t ₀=−0.793). The overall sex ratio was 1 : 4.1 in favour of females. Individuals larger than 17.9 cm were all males.     

Growth and reproduction of Chelidonichthys lucerna (Linnaeus) (Pisces: Triglidae) in the Gulf of Gabès,Tunisia

Growth and reproduction of Chelidonichthys lucerna is reported from Tunisian waters. A total of 286 specimens was collected from landings of bottom trawlers between January 2003 and November 2004. The total length ranged from 16 to 36 cm in females and from 17 to 26 cm in males. Marginal increment analysis of otoliths showed that the translucent zone was laid from October to May and the opaque zone laid from June to September. Females were from 0.5 to 9 years and males from 1 to 7 years old. Growth parameters of the von Bertalanffy growth function were TL_∞ = 40.26; K = 0.06 and t₀ = ?3.03 in females and TL_∞ = 46.16; K = 0.059 and t₀ = ?1.32 in males. The coefficient of the allometric length–weight relationships differed significantly by sex. Females with mature gonads were observed between October and May, with peaks in January and February. Length at which 50% of specimens were mature was 21.6 cm TL (estimated age about 3 years) in females and 19.2 cm TL (estimated age about 1.5 years) in males.     

Seasonal changes in serum metabolites in free-ranging alpine marmots (<Emphasis Type="Italic">Marmota marmota</Emphasis>)

Circannual changes in serum parameters and body mass were studied in free-ranging Marmota marmota that had been shot in Switzerland (Grisons) for management reasons in May, July, and September of 1995, 1996, and 1997; and in April 1996. Markers of lipid (triglycerides, cholesterol), protein (total protein, urea-nitrogen) and mineral (calcium, inorganic phosphate) metabolism were evaluated in 111 haemolysis-free serum samples; the effects of sex, age, reproductive status, season and year were tested. Mean body mass was higher in adult males than in adult females in July and September, and serum cholesterol concentrations were lower in adult males in May. Pregnant females had lower concentrations of total protein than non-pregnant females, and triglyceride concentrations were negatively correlated with the number of uterine ampullae. Inorganic phosphate decreased and total protein increased with age. In adults, triglycerides, cholesterol and urea-nitrogen increased mainly from May to July and decreased between September and May. Total protein, calcium and phosphate did not change throughout the year. This suggests that, during the active season, ingested lipids and amino acids were utilised for metabolic needs or lipid storage, while in winter, lipids were catabolised and protein was spared. Quantitative differences between years, observed for triglycerides and total protein during the active season, were probably due to different climatic conditions in each year.     

Elk survival and mortality causes in the Blue Mountains of Washington

We studied survival of elk (Cervus elaphus) ≥1 yr old and quantified mortality sources in the Blue Mountains of Washington, 2003–2006, following a period of extensive poaching. The population was managed under a spike-only general hunting season, with limited permits for larger males and for females. We radiomarked 190 elk (82 males and 39 females >1 yr old and 65 males 11 months old), most with rumen transmitters and neck radiocollars; 60 elk only received rumen transmitters. We estimated annual survival using known fate models and explored survival differences among sex and age classes and in 2 potentially different vulnerability zones for males. We found little support for differences in survival between younger (2–3-yr old) and older (≥4-yr old) branch-antlered males or zone differences for yearling males. A model with zone differences for branch-antlered males was the second ranked model and accounted for 14% of the available model weight. From the best-supported models, we estimated annual survival for yearling males at 0.41 (95% CI: 0.29–0.53). We estimated pooled adult female survival at 0.80 (95% CI: 0.64–0.93); when an age-class effect was included, point estimates were higher for prime-aged females (2–11 yr: S = 0.81 [0.70–0.88]) than for older females (≥12 yr: S = 0.72 [0.56–0.83]), but confidence intervals broadly overlapped. Only 1 of 7 models with a female age effect on survival was among the competitive models. For branch-antlered males, survival ranged 0.80–0.85, depending on whether zone variation was modeled. We recorded 78 deaths of radiomarked elk. Human-caused deaths (n = 55) predominated among causes and most were of yearling males killed during state-sanctioned hunts (n = 28). Most subadult male deaths were from tribal hunting (n = 5), and most mature males died from natural causes (n = 6) and tribal hunting (n = 5). We detected few illegal kills (n = 4). Our results suggest that increased enforcement effectively reduced poaching, that unreported tribal harvest was not a trivial source of mortality, and that spike-only general seasons were effective in recruiting branch-antlered males. © 2011 The Wildlife Society.     

Seasonal changes in glomerular filtration rate in Antechinus stuartii (Marsupialia: Dasyuridae)

The small marsupial Antechinus stuartii experiences a synchronised life cycle that culminates in complete male mortality (within 3 weeks) following the 1 week mating period in mid-August (late winter). There are pronounced physiological changes in male A. stuartii over the life cycle and renal function was assessed for correlation with these changes. Glomerular filtration rate and urine and plasma electrolytes were determined in male and female A. stuartii in February, May, July and August. Females showed little change in glomerular filtration rate, except for pre-mating values in August which decreased. In contrast, glomerular filtration rate of males decreased significantly in July and August. Plasma sodium and chloride levels were higher in males than females and were higher in animals in July and August than in February and May. Plasma potassium levels dropped in both males and females in July and August. Plasma osmolality was higher in animals in February compared to animals from May and August. However, there were no significant sex or seasonal differences in urine electrolytes, although urea concentration was higher in females than males. Urine osmolality was higher in both sexes in July and August. There were no significant differences in total excretory rates of sodium, potassium or chloride between sexes or between seasons. Many of the alterations in renal function are correlated with known physiological and hormonal profiles in A. stuartii. This is the first observation of seasonal changes in glomerular filtration rate that are unrelated to dietary and water stresses. Accepted: 8 September 1997     

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