SURVIVAL OF FIVE SPECIES OF CAPTIVE MARINE MAMMALS

Survival in captivity was calculated for 1,707 bottlenose dolphins (BD), 72 killer whales (KW), 73 white whales (WW), 3,090 California sea lions (CSL), and 47 Steller sea lions (SSL) based on data in the Marine Mammal Inventory Report (MMIR) of the NMFS. Mean annual survival rates (ASRs) between 1988 and 1992 were 0.951, 0.937, and 0.954 for BD, KW, and WW, respectively, and 0.952 and 0.969 for CSL and SSL, respectively. These estimates represent significant increases in survival for both BD and CSL over the last 5 yr. Using all of the MMIR data (1940–1992), the ASR of BD calves (< 1 yr of age) was significantly less than the ASR of non-calves (0.666 vs .948, 0.001). Similarly, the ASR of CSL pups (< 1 yr of age) was significantly less than survival of non-pups (0.858 vs .962, 0.001). Survival of captive-born CSL was significantly higher than those born in the wild (0.962 vs .945, 0.003), but the difference was not significantly different for BD (0.948 vs .944, 0.60). For non-calf BD and KW, captive animals survived at a slightly lower rate (BD 0.944 vs .961, = 0.07; KW 0.938 vs .976, 0,001) than animals in the wild (BD: Wells and Scott 1990, KW: Olesiuk 1990). Survival of captive non-pup SSL was slightly higher (0.968 vs .930) than animals in the wild (York 1994, life-table analyses). Survival rates were significantly different among institutions for BD calves and non-calves, CSL pups and non-pups, and SSL non-pups.     

The effects of extended time in the laboratory on selected aspects of reproduction in the female rhesus monkey (Macaca mulatta)

Reproduction data from 60 wild-caught and 16 captive-born, hand-reared female rhesus monkeys (Macaca mulatta) were examined. Both groups had been maintained in a controlled laboratory environment, the wild-caught for a minimum of 10 years and the captive-born for a minimum of 5 years. All were bred to wild-caught males. Animals of both sexes were individually caged unless being bred. Data from 662 pregnancies indicated that, although seasonal breeding became attenuated in the laboratory, it did not disappear. Neither pregnancy outcome nor number of matings necessary for conception was affected by increasing parity or prior occurrence of fetal wastage or hysterotomy. Nor did hysterotomy affect the potential for a subsequent vaginal delivery. The number of matings necessary for conception were shown to be a useful predictor of animals that should be culled from the breeding colony. Birthweights of infants of wild-caught females, but only male infants of house-born females, increased with parity of the mother. Parity had only minimal effect on gestation length. Conception was shown to occur infrequently at less than 100 days postpartum even when animals were not lactating and were rebred begining as early as 56 days postpartum. Summary data were presented for pregnancy outcome, gestation length, infant birth weight, and sex for both groups of animals.     

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.     

GROWTH IN YOUNG GRAY WHALES (ESCHRICHTIUS ROBUSTUS)

Mean body lengths of gray whale calves were found to increase linearly from 4.6 m at birth to 7 m by weaning at six mo. After weaning, rates of length increase diminish, with calves reaching 8 m by one yr of age and 9 m by two yr. Evaluations of the weights of nine gray whales as functions of their measured lengths and girths reduce the emphasis placed on fast-induced seasonal variations in girth by Rice and Wolman (1971). From birth weights of just under one metric ton, calves double their weights by three mo of age and double again by weaning at six mo.     

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.     

Is Difference in Body Weight,Antler Length,Age or Dominance Rank related to the Number of Fights between Fallow Deer (Dama dama)?

Competitive interactions between mature male fallow deer were investigated to determine whether antler length, body weight, age or dominance rank were related to the number of fights between individuals. Four different hypotheses were tested; the first predicted that body weight and antler length indicate individual quality and, therefore, as the difference between competitors in body weight and antler length increases, there should be a corresponding decrease in fight rate. The second and third hypotheses predicted that, as difference in dominance rank increased there would be a decrease in fight rate between males either, as a risk reduction measure or because of inhibitory control by dominant males. A fourth hypothesis predicted that, where dominance rank does not mediate fight rate, that similarity between contestants based on age might be important. If this is the case, then as the difference in age between competitors increased there should be a decrease in fight rate. Our results show that when dominance rank is controlled for, there was no relation between body weight, antler length or age with fight rate. There was a negative relation between dominance rank difference and fight rate, a result that supports both the risk reduction and inhibitory hypotheses. There was an increasing tendency to fight with closely ranked males as cohorts reached peak reproductive age; males aged 5 yr fought with other 5‐yr‐old males based on rank difference and males aged 6 yr fought with other males aged six and across all age groups based on rank difference. This trend was not observed in 4 or 7‐yr‐old males. Our results suggest that males in prime breeding condition limit potential costs of fighting (such as time and energy) by only interacting with other males of similar rank.     

Mortality in Svalbard reindeer

Mortality rates in Svalbard reindeer followed the "U"-shaped pattern, with higher mortality rate among calves and old animals than in middle aged individuals. Assuming a stable population size, the mortality data predict a 16.2% annual mortality and recruitment rate among 6 months and older animals, and a male:female sex ratio of 48.5:51.5 among 1-yr old and older. Both predictions are supported by field data. Female mortality rate increased and differed from the male rate in the age interval 2-4 yr, while the male rate increased sharply and differed permanently from the female rate in the age interval above 6 yr. First and last breeding are thought to cause the increased mortality among 2–4 and 11–13 yr-old females. Increased involvement in rutting activities with age associated with lower grazing activity and depletion of fat reserves probably cause the increasing mortality rate among the 6+ yr males. Maximum life span was 17 yr in females and 12 yr in males. Apart from the unknown but possibly high neonatal calf-mortality, only few animals died during summer or during the rut in autumn. Death among calves, yearlings and most of the females occurred before antler-shedding in May-June. Most of the 2-yr and older males died after antler shedding, which occurs from December among the oldest and during April-May among the younger males. Hence, the major part of the mortality takes place in spring. The lack of visible subcutaneous and femur fat in most carcasses indicated starvation as the major mortality cause.     

Killer whale (Orcinus orca) reproduction at Sea World

Sea World has maintained killer whales (Orcinus orca) since 1965. The total killer whale inventory (1965–1993) has included 39 whales (25 females, 14 males); 28 were wild-caught and 11 captive-born, including one second-generation calf. As of September, 1993, there were 19 whales in the breeding program. Ten of these whales (53%) were captive-born, either at Sea World or other facilities in North America. The live wild-caught whales ranged in estimated age from 12–27 years (x? ± sd = 17.6 ± 4.2 years). The captive-born whales ranged in age from <1 to 8 years. In the Sea World breeding program (through September, 1993), there have been nine live births and one stillbirth, with eight calves part of the current inventory. Births occurred from July to February. Calving intervals ranged from 32–58 months. Female age at birth of first calves ranged from 8 years to an estimated 17 years (x? ± sd = 12.7 ± 3.0 years). Gestation, based on conception estimates from serum progesterone analysis, averaged 17 months (x? ± sd = 517 ± 20 days), but successful pregnancies with viable calves occurred from 15–18 months (468–539 days). Females, in the presence and absence of males, were polyestrus with periods of cycling interspersed with individually variable noncycling (presumed anestrous) periods ranging from 3–16 months. Mean serum progesterone levels (±se) were as follows: noncycling periods = 121 ± 20 pg/ml; peak elevations during nonconceptive ovulatory (estrous) cycles = 3,962 ± 2,280 pg/ml; first pregnancies = 14,592 ± 3,854 pg/ml; second pregnancies = 8,389 ± 395 pg/ml; and third pregnancy = 8,180 ± 4,556. © 1995 Wiley-Liss, Inc.     

AGE AND LENGTH AT WEANING AND DEVELOPMENT OF DIET OF PANTROPICAL SPOTTED DOLPHINS, STENELLA ATTENUATA, FROM THE EASTERN TROPICAL PACIFIC

Using stomach contents from 203 spotted dolphins ( Stenella attenuata ) killed in the yellowfin tuna fishery, we modeled the weaning process of calves. Spotted dolphins began to take solid food at approximately 6 mo of age, or 115 cm, but continued to suckle until they were nearly 2 yr old. Calves tended to feed more frequently on squid as they got older, which suggested there was a shift in diet during weaning. The average age and total body length at weaning was estimated to be 0.8 yr (approximately 9 mo) and 122 cm. The oldest suckling calf was almost 2 yr old, which suggests that some calves continued to suckle for more than a year after they could have been weaned. A better understanding of the weaning process, especially quantifying the period of time when calves are nutritionally dependent on their mothers may lead to a better evaluation of their potential vulnerability to the disturbance caused by the yellowfin tuna purse-seine fishery.     

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.     

Partitioning the effects of secular trend and ageing on adult stature

A group of 16 captive-born hairy-faced, white-lipped, black-mantled tamarins, Saguinus nigricollis, were observed from birth to maturity. The data for the parameters, body weight, head-body length, right foot length and dental eruption age was recorded at monthly intervals. Linear growth was complete at approximately 12 months of age. Body weight reached the level of the wild-caught parents at 16 to 17 months of age. Deciduous dentition was complete at eight weeks of age and all permanent teeth were present by 41 weeks of age. While this sampling is too small for statistical verification, the data provides guidelines on the parameters recorded.     

Age-dependent changes in sperm production, semen quality, and testicular volume in the black-footed ferret (Mustela nigripes)

The black-footed ferret (Mustela nigripes), which was extirpated from its native North American prairie habitat during the 1980s, is being reintroduced to the wild because of a successful captive-breeding program. To enhance propagation, the reproductive biology of this endangered species is being studied intensively. The typical life span of the black-footed ferret is approximately 7 yr. Female fecundity declines after 3 yr of age, but the influence of age on male reproduction is unknown. In this study, testis volume, seminal traits, sperm morphology, and serum testosterone were compared in 116 males from 1 to 7 yr of age living in captivity. Results demonstrated that testes volume during the peak breeding season was similar (P > 0.05) among males 1 to 5 yr of age, reduced (P < 0.05) among males 6 yr of age, and further reduced (P < 0.05) among males 7 yr of age. Motile sperm/ejaculate was similar in males 1 to 6 yr of age but diminished (P < 0.05) in those 7 yr of age. Males at 6 and 7 yr of age produced fewer (P < 0.05) structurally normal sperm than younger counterparts; however, serum testosterone concentrations were not reduced (P > 0.05) in older males. Histological comparison of testicular/epididymal tissue from 5- and 7-yr-old black-footed ferrets confirmed that the interval between these two ages may represent a transitional period to reproductive senescence. In summary, functional reproductive capacity of male black-footed ferrets exceeds that of females by at least 2 yr. Testes and seminal quality are indistinguishable among males 1 to 5 yr of age, with progressive reproductive aging occurring thereafter.     

Life history of the moose Alces alces: relationship between growth and reproduction

We studied the relationship between increase in body weight and reproductive performance in different populations of Norwegian moose to evaluate costs associated with early onset of reproduction, viz. whether early onset of reproduction was correlated with low adult body weight or reduced adult fecundity. The mean carcass weight of non-ovulating yearlings was significantly lower than for ovulating yearlings. However, those 2.5 yr old females that conceived as yearlings were lighter than non-reproducing females of the same age. Thus, to begin to reproduce as a yearling was assumed to be expensive because it reduces the possibilities for further growth. The cost associated with reproduction was further illustrated by the fact that the difference in mean carcass weight from age 2.5 to 3.5 yr of females that produced calves in both years, was less for the females from regions with lowest mean yearling weights, i.e. regions with probably the lowest resource availability. In populations with high mean yearling carcass weights, the proportion of cows with calf and the number of calves per pregnant female in the early reproductive phase (2.5 or 3.5 yr old) were higher than in populations in which the mean yearling weights were low. There was a negative correlation between growth rate in the population after 1.5 yr of age and the mean yearling carcass weight. Thus, low yearling weight was associated with a prolonged period of growth and thereby a reduced reproductive output during the first year of the female's life. For old females (≥ 9.5 yr old) the number of calves produced per pregnant female was highest in populations where yearling carcass weights were highest. Furthermore, mean yearling weight and the mean adult female weight were positively correlated in those regions. This relationship suggests that within this species early onset of reproduction is not related to retarded reproduction or lower weight later in life. We suggest that the moose has been selected for an early onset of reproduction.     

THE LIFE HISTORY OF FREE-RANGING ATLANTIC SPOTTED DOLPHINS (STENELLA FRONTALIS): AGE CLASSES, COLOR PHASES, AND FEMALE REPRODUCTION

Atlantic spotted dolphins (Stenella frontalis) were observed underwater and from the surface from 1985 to 1996 and photographed through successive years. Individuals were categorized into age classes by their degree of spotting and color phases. Dolphins spent an average of 3 yr in the two-tone color phase, 5 yr in the speckled phase, 7 yr in the mottled phase and up to 10 yr or more in the fused phase.
Sex ratios were close to parity, with old adults skewed towards females and juveniles and young adults skewed towards males. The average calving interval for 24 females was 2.96 years with a range of 1–5 yr. Females whose calves survived the first year had a significantly longer calving interval (3.56 years). The ages of first parturition for five females were estimated to be 10–12 yr. The age at sexual maturation was estimated to range from 8 to 15 yr.
Pregnancy rate fluctuated annually, with an average rate of 0.25 (range 0.07–0.57). Annual average birth rate was 0.08 (range 0.07–0.14), average calf production was 0.33 (range 0.06–0.52), average fecundity was 0.23 (range 0.13–0.30), and average recruitment was 0.06 (range 0.03–0.08). Most females who lost a calf conceived the same or following year.
Lactation lasted up to 5 yr, and 45% of visibly pregnant females were also lactating. Age of first parturition was associated with the mottled color phase. Average first-year mortality rate of calves was 0.24.     

The relative influence of age and weight on the reproductive behaviour of male grey seals Halichoerus grypus

The breeding behaviour of male grey seals Halichoerus grypus of known age and weight was studied on Sable Island, Nova Scotia. Branded males ranged in age from 8 to 16 years and although there was a positive relationship between age and weight, there was a large overlap between age classes. In general, there was an increase in length of tenure and rates of copulation with increasing male age but this was less marked among males between the ages of 13 and 16 years. Compared to older ones, males of 8 and 12 years were observed at more sites, travelled more extensively around the breeding colony, were transient more frequently and were unable to lie as close to females. There was no correlation between male body weight and either length of tenure or rates of copulation when males of age 8 (the smallest males) were excluded from the analysis. Most agonistic behaviour was made by larger, older males towards smaller, younger ones and appeared to be responsible for the short length of tenure and low reproductive rates of young bulls.     

Influence of level of nutrition during late pregnancy on reproductive productivity of red deer (2) Adult hinds gestating wapitixred deer crossbred calves

The present study aimed to relate feed intake of red deer hinds in the later stages of gestating wapitixred deer crossbred foetuses on dam body condition, gestation length, birth weight and calf growth. Multiparous hinds (N=18) conceiving at known dates to either wapiti (n=12) or red deer (n=6) sires were housed in individual pens from days 150-220 of pregnancy, during which time they were offered either ad libitum access to pelletised rations (n=6 crossbred-bearing hinds [HH] and n=6 red deer-bearing hinds [RH]) or a restricted offer (n=6 crossbred-bearing hinds [HL]) set at 70% of the average ad libitum intake of HH hind in the previous week. Hinds were returned to pasture at day 220 and calving was closely monitored. Liveweights, body condition score (BCS), and lactation score (LS) of hinds were recorded weekly from day 130 of pregnancy until calves were weaned at 12 weeks of age. Calves were tagged and weighed at birth, and subsequently weighed at 7 and 12 weeks of age. HH and RH hinds exhibited similar patterns and levels of MEI/kg0.75, which peaked at 7.8 MJME/kg0.75 at day 220. HL hinds peaked at approximately 5 MJME/kg0.75 and showed significantly lower rates of liveweight gain during pregnancy. Interestingly, both crossbred-bearing groups initiated mammary development in advance of the RH hinds. While there were significant effects of foetal genotype on mean gestation length (239 days versus 234 days for crossbred versus red deer) and mean birth weight (14.5 kg versus 10 kg), the nutritional contrast for gestation length of crossbred-bearing hinds (i.e. HH versus HL) was not significant but approached significance for birth weight (14.5 kg versus 11.9 kg; P=0.06). Regression analysis revealed weak relationships between changes in hind liveweight and gestation length (P>0.05) but a significant relationship with birth weight (P<0.05). However, change in hind BCS was significantly related to both gestation length and birth weight. Crossbred calves reared by HH hinds were 30% heavier at 7 and 12 weeks of age than the red deer calves. However, those reared by HL hinds were significantly lighter than their genotype contemporaries and only marginally heavier than the red deer calves. These results generally contrast with the previous studies on red deer hinds gestating red deer foetuses [Asher, G.W., Mulley, R.C., O'Neill, K.T., Scott, I.C., Jopson, N.B., Littlejohn, R. 2004. Influence of level of nutrition during late pregnancy on reproductive productivity of red deer, (1) Adult and primiparous hinds gestating red deer calves. Anim. Reprod. Sci., in press] and indicate that the genetically determined higher growth requirements of crossbred foetuses may override any mechanism of compensatory control of gestation length at the expense of calf birth weight. Furthermore, there were marked carryover effects of late gestational feeding on crossbred calf growth and their dam's BCS that highlight the high nutritional demands of lactation.     

ESTIMATING BODY LENGTH OF PYGMY RIGHT WHALES (CAPEREA MARGINATA) FROM MEASUREMENTS OF THE SKELETON AND BALEEN

Various parts of the skeleton and/or the longest baleen plate of 46 specimens of Caperea marginata from Australia and New Zealand were measured and related to body length. Of the 32 skull, postcranial and baleen-plate measurements available, eight were analysed and seven found to be good predictors of body length, by using a curvilinear model describing their relationship with body length. Greatest skull width, supraoccipital length and mandible length had the smallest prediction limits (± 0.28-0.33 m in small animals, ±0.44-0.58 m in large animals) when compared with postcranial measurements (scapula length, vertebra 7 centrum width). Baleen-plate length was also a useful predictor of body length (±0.32-0.77 m). There was a substantial increase in the arch of the skull as body length increased. Bulla length was not a good predictor of body length, because measurements were highly variable and because the bulla grew little during postnatal life. Physical maturity occurred at body lengths of at least 5.9 m, also the shortest length at which both epiphyses of the humerus and proximal epiphyses of the radius and ulna were fused. Weaning appears to occur at about 3-3.5 m. The following approximate relative age/length classes were erected: dependent calves, <3.6 m; subadults, 3.6-5.5 m; adults, >5.5 m. Females were significantly longer than males in the sample of 22 animals greater than 5.9 m, length of the smallest recorded physically mature animal.     

Characterization of male killer whale (Orcinus orca) sexual maturation and reproductive seasonality

Longitudinal serum testosterone concentrations (n=10 males) and semen production (n=2 males) in killer whales were evaluated to: (1) characterize fluctuations in serum testosterone concentrations with respect to reproductive maturity and season; (2) compare morphologic changes to estimated age of sexual maturity, based on changes in serum testosterone concentrations; and (3) evaluate seasonal changes in sperm production. Classification of reproductive status and age class was based on differences (P < 0.05) in serum testosterone concentrations according to age; juvenile males ranged from 1 to 7 years (mean+/-S.D. testosterone, 0.13+/-0.20 ng/mL), pubertal males from 8 to 12 years (2.88+/-3.20 ng/mL), and sexually mature animals were 13 years and older (5.57+/-2.90 ng/mL). For captive-born males, serum testosterone concentrations, total body length and height to width ratio of the dorsal fin were 0.7+/-0.7 ng/mL, 495.6+/-17.5 cm and 1.14+/-0.13c m, respectively, at puberty; at sexual maturity, these end points were 6.0+/-3.3 ng/mL, 548+/-20 cm and 1.36+/-0.1cm. Serum testosterone concentrations were higher (P<0.05) from March to June than from December to February in pubertal animals (4.2+/-3.4 ng/mL versus 1.4+/-2.6 ng/mL) and than from September to December in sexually mature animals (7.2+/-3.3 ng/mL versus 4.0+/-2.0 ng/mL). Ejaculates (n = 90) collected from two males had similar (P > 0.05) sperm concentrations across all months. These data represent the first comprehensive study on male testosterone concentrations during and after sexual maturation, and on reproductive seasonality in the killer whale.     

Life history of harbor porpoises (Phocoena phocoena) in Scottish (UK) waters

Life history parameters were determined for stranded and bycaught harbor porpoises (Phocoena phocoena) from Scottish (UK) waters (1992–2005). Fetal growth rate was 84.4 mm/mo and mean size at birth was 76.4 cm (range 65–88 cm). Males and females had a similar range of body lengths (65–170 cm and 66–173 cm, respectively), although asymptotic lengths were higher in females than males (approximately 158 cm and 147 cm, respectively). Nonpregnant females were significantly lighter, in relation to their length than males. Maximum estimated age was 20 yr for both sexes. Age at sexual maturity (ASM) was estimated as 4.35 yr in females and 5.00 yr in males. Conception occurred mainly in July and August although reproductively active males were recorded during April to July. Gestation lasted 10–11 mo, with calving mainly between May and July. Lactating females were recorded during June to November, while small calves with solid food in their stomachs were found mainly during February to May. Estimated pregnancy rate (0.34–0.40) is lower than recorded elsewhere, but is likely underestimated due to the prevalence of mature females of poor health status in the sample. Nevertheless, cetacean strandings can be an essential source of data on demographic parameters.     

Birth weight and birth rate of heavy calves conceived by transfer of in vitro or in vivo produced bovine embryos

The aim of this study was to evaluate the difference in birth weight and gestation length between Japanese Black calves obtained from transfer of bovine embryos produced in vitro (IVP) and those developed in vivo (IVD). An additional objective was to clarify the sire effect on birth weight and gestation length and to examine the birth rate of heavier calves. Two Japanese Black bulls breed at our experimental station were used as a semen source for production of IVP and IVD embryos. Thirty-eight Japanese Black heifers and cows of various genetic backgrounds were used as embryo donors for IVD embryos. Ovaries for IVP embryos were collected at random at a local slaughterhouse from Japanese Black cattle of various genetic backgrounds. IVP embryos were produced using co-culturing with cumulus cells in 5% CS+TCM 199. Both the IVD and IVP embryos were transferred non-surgically to Holstein recipients on day 7+/-1 of estrous cycle. In this study, the birth weights and gestation lengths of half-sib single calves for bull A and B were analyzed.The numbers of single calves born by transfer of IVP and IVD embryos for bull A and B were 133 and 121, 243 and 465, respectively. The birth weight of the IVP calves was significantly higher (P<0.01) than that of the IVD (bull A: 31.0+/-0.4 kg versus 27.2+/-0.4 kg and bull B: 29.9+/-0.6 kg versus 26.6+/-0.2 kg). Gestation length of the IVP calves for bull A was significantly longer (P<0.01) than that of the IVD (291.9+/-0.9 days versus 283.6+/-0.5 days). However, for bull B, there were no differences in gestation length between the IVP and IVD calves (285.9+/-0.7 days versus 286.2+/-0.3 days). These results clearly indicated that IVP calves had heavier birth weights than IVD calves but that the average gestation length of IVP calves was not always longer than that of IVD calves. Furthermore, the birth rate of heavier calves and the incidence of stillbirth and perinatal mortality up to 48 h post partum in IVP calves (bull A: 11.3%, bull B: 7.8%) were greater (P<0.05) than those in IVD calves from both bulls (bull A: 4.1%, bull B: 3.7%).