Summary. Changes in the number and distribution of spermatozoa in the epididymis of the adult brown marsupial mouse were examined during July/August in mated and unmated males. The effects of mating on epididymal sperm populations were studied in 2 groups of males each mated 3 times and compared with the number and distribution of spermatozoa in the epididymides of 4 unmated control groups. One testis and epididymis were removed from each animal (hemicastration) either before or early in the mating season to provide information on initial sperm content and distribution. The contralateral side was removed later in the mating season to examine the effects of mating or sexual abstinence on epididymal sperm distribution.

Epididymal sperm number peaked in both the distal caput and distal corpus/proximal cauda epididymidis in late July. The total number of spermatozoa, including those remaining in the testis, available to each male at the beginning of the mating season in early August was ∼4·4 × 10⁶/side. Although recruitment of spermatozoa into the epididymis from the testis continued until mid-August, sperm content of the epididymis reached a peak of about 3·5 × 10⁶/epididymis in early August. At this time approximately 0·9 × 10⁶ spermatozoa remained in the testis which had ceased spermatogenic activity. Throughout the mating season, epididymal spermatozoa were concentrated in the distal corpus/proximal cauda regions of the epididymis and were replenished by spermatozoa from upper regions of the duct. Relatively few spermatozoa were found in the distal cauda epididymidis, confirming a low sperm storage capacity in this region.

A constant loss of spermatozoa from the epididymis, probably via spermatorrhoea, occurred throughout the mating season and very few spermatozoa remained in unmated males in late August before the annual male die-off. Mating studies showed that an average of 0·23 × 10⁶ spermatozoa/epididymis were delivered per mating in this species, but the number of spermatozoa released at each ejaculation may be as few as 0·04 × 10⁶/epididymis when sperm loss via spermatorrhoea is taken into account.

We suggest that the unusual structure of the cauda epididymidis, which has a very restricted sperm storage capacity, may function to limit the numbers of spermatozoa available at each ejaculation and thus conserve the dwindling epididymal sperm reserves in order to maximize the number of successful matings which are possible during the mating season.

Keywords: epididymis; spermatozoa; sperm storage; mating; marsupial; dasyurid

Summary. Female brown marsupial mice were mated and changes in the number and distribution of spermatozoa were assessed in several regions of the reproductive tract at 1, 2, 3, 7, 10, 14 and 18 days after mating. Approximately 40 × 10³ spermatozoa/side were present in the female reproductive tract between Days 1 and 7 after a single mating. This had decreased (to ∼9 × 10³ spermatozoa/side) by Days 10 and 14 after mating; by Day 18 no spermatozoa were recovered. The maximum number of spermatozoa recorded in a female tract was ∼72 × 10³ spermatozoa/side (Day 5 female, death in laboratory) and the minimum recorded was ∼2 × 10³ spermatozoa/side on Day 2 after mating.

Between Days 1 and 7 after mating most spermatozoa were located in the uterus and lower isthmus (isthmus 1) and spermatozoa were rarely found in the lateral vaginae. By 24 h after mating most spermatozoa (∼60%) were found in isthmus 1, but ∼35% were still present in the uterus. Histological observations of the lower isthmus at this time showed that large numbers of spermatozoa were present in both the lumen of the duct and the sperm storage crypts which are located in this region. By Day 7 after mating ∼91% of all spermatozoa in the female tract were in isthmus 1, most of these being confined to the sperm storage crypts. On Days 10 and 14 after mating almost all spermatozoa in the tract were in the crypt regions of isthmus 1 and on Day 18 degenerating spermatozoa were observed. No special orientation or association of spermatozoa in relation to crypt cells was observed.

These results show that, although the number of spermatozoa inseminated is low by mammalian standards sperm transport in this species is extremely efficient and a large proportion of spermatozoa reaches the isthmus before ovulation (∼1 in 1 to 1 in 7). Several observations may explain the remarkable success of these low numbers of spermatozoa, including specializations of the reproductive tract which may have a directing effect on sperm movement and the special relationship which exists between spermatozoa and the oviducal environment which results in viable sperm storage. Recent observations suggest that an unusual sinusoidal mode of progressive motility observed in this species, may also influence the success of the low numbers of ejaculated spermatozoa.

Keywords: marsupial; spermatozoa; sperm storage; oviduct; isthmus; ultrastructure

In vitro fertilization and early embryo culture was undertaken in the South American marsupial, the grey short-tailed opossum, Monodelphis domestica. Adult females were induced into oestrus by a system of pairing with an unfamiliar male and mature oocytes were recovered from the ovary 15–18 h after mating and placed in pre-warmed modified MEM medium at 33°C (basal body temperature) or 37°C. Spermatozoa recovered from the cauda epididymides of adult males were preincubated in medium for 2 h during which time paired spermatozoa separated and initiated hyperactivated motility. Oocytes were transferred to 0.4 ml drops of spermatozoa containing 0.5–1.0 × 10⁶ spermatozoa ml⁻¹. Only single spermatozoa bound to the zona pellucida, and fertilization occurred within 1–2 h as indicated by a breach in the zona and confirmed by electron microscopy. At 37°C, 95 of 152 (62.5%) oocytes were fertilized and 64 (67%) developed to two-cell stage or beyond. At 33°C, 5 of 28 (18%) oocytes were fertilized. This is the first report of complete in vitro fertilization in a marsupial.

The effect of different cryopreservation methods on the development and ultrastructure of preimplantation embryos of Sminthopsis crassicaudata, a small carnivorous marsupial and member of the family Dasyuridae, was investigated. Females were primed with 1 iu pregnant mares' serum gonadotrophin to induce oestrus and ovulation. Mating generally ensued and, approximately 6 days after priming, embryos were collected and cultured in 5% CO₂ in air at 35°C for 18–22 h in either Dulbecco's modified Eagles medium (DMEM) with high glucose or human tubal fluid medium (HTF), both supplemented with 10% fetal calf serum. Cleavage rates were higher in DMEM than in HTF. One slow and two ultrarapid freezing methods were used. Two out of 12 (17%) embryos cleaved in culture after freezing and thawing using the slow regimen, compared with six of 16 (38%) non-frozen controls. In addition, two of 11 (18%) embryos cleaved in culture following ultrarapid freezing and thawing by one of the two methods, compared to 31 of 41 (76%) non-frozen controls. Most of the embryos appeared morphologically normal under the light microscope after freezing and thawing by the slow regimen, but considerable variation in the degree of ultrastructural damage to the cellular organelles was evident with the transmission electron microscope. The rather low rate of cleavage after freezing and thawing was probably due, at least in part, to ultrastructural damage of the cells.

Changes in semen quality and morphology of the male reproductive tract were studied throughout the year in the highly promiscuous tammar wallaby. Body size, semen quality and gross morphology of the reproductive organs were assessed in adult males each month from January to November. The mean weight of males was similar in most periods sampled, but males were slightly heavier in the minor (P < 0.05) than the non-breeding season. Since body weight was correlated with weights of the testes, epididymides and accessory sex glands, organ weights were adjusted for body weight in subsequent analyses. In the major breeding season (late January/early February), when most females go through a brief, highly synchronized oestrus, the testes, prostate, Cowper’s glands, crus penis and urethral bulb were heaviest, volume and coagulation of ejaculates were greatest, and sperm motility had increased. Semen samples collected by electroejaculation at this time contained low numbers of spermatozoa, possibly as a result of dilution and entrapment by the seminal coagulum or depletion of epididymal stores during intense multiple mating activity. In the non-breeding season (late May–July), when mating does not normally occur in the wild, there was a significant decrease in the relative weight of nearly all male reproductive organs and a decline in most semen parameters. In the minor breeding season (September–November), when pubertal females undergo their first oestrus and mating, the weights of testes, epididymides and most accessory sex glands had significantly increased similar to those of males in the major breeding season. The total number and motility of ejaculated spermatozoa were highest during this period, but the volume and coagulation of ejaculates and weight of the prostate had only increased to levels that were intermediate between the major and non-breeding seasons. Ejaculate volume was strongly correlated with prostate weight, and % motile spermatozoa was strongly correlated with epididymis weight. Semen quality thus varied seasonally with changes in androgen-dependent reproductive organs in the male tammar wallaby and appeared to be influenced by the seasonal timing of oestrus in females. Semen quality may also improve in response to an increase in the number of available oestrous females.