ANNUAL REPRODUCTIVE CYCLE OF THE FEMALE HAWAIIAN MONK SEAL (MONACHUS SCHAUINSLANDI)

Abstract: The annual reproductive cycle is described for the adult female Hawaiian monk seal ( Monachus schauinslandi ) from data collected at Laysan Island (1982–1991) and Lisianski Island (1982–1983) in the Northwestern Hawaiian Islands. Pupping, lactation, weaning, and molting were directly observed, while mating was rarely observed and was, therefore, inferred from the occurrence of mounting injuries and from adult male and female association patterns. Pooled birth rates during the study period were 0.544 for all adult-sized females and 0.675 for females parous in earlier years. For parturient females, pupping peaked in late March and early April, weaning in May, mounting injuries in May and June, and molting in July. For non-parturient females, the median mounting injury and molting dates occurred 17 and 28 days earlier, respectively. Pupping date set the timing of subsequent events in the annual cycle, but the timing of those events was adjusted by loss of the pup or poor physical condition of the female. Individual pupping patterns varied widely. The mean interval for births in consecutive years was 381 days; females that pupped in consecutive years gave birth later each season. Conversely, females who skipped a year or more gave birth earlier their next pupping season.     

ANALYSIS OF CORPORA LUTEA TO ESTIMATE REPRODUCTIVE CYCLES OF WILD HAWAIIAN MONK SEALS (MONACHUS SCHAUINSLANDI)

Ovaries from 14 female Hawaiian monk seals, O-24 yr of age, collected from the northwestern Hawaiian Islands were analyzed by gross and histological examination for the presence of corpora hemorrhagica (CH), lutea (CL), albicantia (CA), and dominant follicles. Seven seals, 5-24 yr of age, were mature females, and another seven seals, O-5 yr of age, were immature based on the presence or absence of CL and CA in the ovaries. Two 5-yr-old seals did not have CL and CA, but one J-yr-old and both 6-yr-old seals had CL or CA. In addition, the weight of the more active ovary increased at 5 yr of age, indicating that puberty in these female Hawaiian monk seals occurred about 5 yr of age. The total number of CL and CA was significantly correlated to the ovarian weight, but not age of the seals, indicating that visible CA of Hawaiian monk seals probably degenerate within a year. If an ovulation resulted in pregnancy, we assumed that the resulting CL from that pregnancy persisted throughout gestation and regressed approximately 2 yr after ovulation. However, the CL of pregnancy were not easily differentiated from cyclic CL that did not result in pregnancy. Four of seven mature seals were clearly polyestrous from the analyses of their ovaries and reproductive histories. The remaining three seals were pregnant in previous consecutive years, and we could not positively determine whether they were also polyestrous. The ovaries from Hawaiian monk seals had unusually large, rounded granular cells containing the aging pigment, lipofuscin. These cells were located between loose fibrous tissues in all regressing CL and CA but were not present in any CH.