The bovine oviduct and its role in reproduction: a review of the literature

The bovine oviduct provides the environment for sperm transport and capacitation, oocyte transport and maturation, fertilization and early embryonic cleavage. Gamete interactions in the tube occur in contact with both the tubal epithelium and the oviduct fluid secreted by these cells. Current research continues to reveal the active role of the oviduct and its products play in normal fertilization and embryo development. This paper reviews the anatomy and physiology of the oviduct of the cow, including the specific events of reproduction which occur in this organ.     

Method for obtaining bovine zygotes produced in vivo

A superovulatory and surgical protocol was developed for recovery of bovine zygotes. Holstein cows and heifers were given follicle-stimulating hormone and cloprostenol to induce superovulation. Surgical cannulation and lavage of the uterine tube was performed 40 to 48 hours after the start of standing estrus. In general, cows had more corpora hemorrhagica than did heifers, but a higher percentage (P less than 0.05) of ova recovered from cows were infertile. Several heifers were subjected to the procedure twice, and embryo recovery rates were equivalent both times.     

Ultrastructural and ultracytochemical cyclic changes in the bovine uterine tube (oviduct) epithelium.

Ultrastructural and ultracytochemical features of the uterine tube (oviduct) infundibulum were studied in 8 Hereford cows, which were slaughtered in pairs on days 1 (estrus), 3, 9 or 10, and 18 of the estrous cycle. Fibrous granules (60 to 80 nm), which are supposedly related to basal body replication, were observed in the apical cytoplasm of ciliated cells. Close association between basal bodies and fibrous granules was apparent, especially during the follicular phase. Cilia were observed throughout of estrous cycle, although degeneration of cilia was not observed at any phase of the cycle. Prominent, striated rootlets were observed during both the follicular and luteal phases of the cycle. Maximum secretory cell differentiation was apparent during the follicular phase, at which time these cells were characterized by having a well-developed, rough endoplasmic reticulum with dilated cisternae, numerous ribosomes, and secretory granules of varied size and density. A prominent feature of the secretory granules was their membranous structure, consisting of concentric lamellae of equal dimensions. During the luteal phase, cytoplasmic protrusions were prominent, and extruded nuclei along with other cytoplasmic organelles were present in the tubal lumen. The presence of a well-developed, rough endoplasmic reticulum and numerous secretory granules during the follicular phase indicates that secretory activity of the uterine tube infundibulum may be stimulated by estrogen. During estrus, the cytoplasm of the stromal cells displayed abundant, rough endoplasmic reticulum with dilated cisternae. The increased and extensively dilated rough endoplasmic reticulum at the time of estrus probably indicates increased protein synthesis by the stromal cells. The presence of adenosine triphosphatase activity on the membrane of cilia suggests that this enzyme is involved in energy-forming reactions related to the vigorous action of cilia. The presence of acid phosphatase activity on the cell membrane of the epithelium, microvilli, and secretory granules may indicate involvement in the secretory mechanism of the cell.     

Mapping landscape connectivity for large spatial extents

Context

Mapping landscape connectivity across large spatial extents is an important component of ecological reserve network designs and species recovery plans. It can, however, be limited by computational power. One way to overcome this problem is to split the study area into smaller tiles, map landscape connectivity within each of those tiles, and then merge tiles back together to form composite connectivity maps.

Objectives

We tested the effects of landscape structure on the accuracy of composite landscape connectivity maps created from tiles and tested two methods to increase this accuracy.

Methods

We correlated replicate, composite current density maps with untiled maps. We tested whether our findings depended on the composition of the landscape by testing maps with corridors, barriers, different mixtures of high- and low-cost habitat, and road networks.

Results

We found that composite current density maps underestimated large-scale connectivity and overestimated the contribution of small habitat patches to overall connectivity. These biases became more pronounced as the tiles became relatively smaller. Landscapes with corridors or barriers were particularly sensitive. We increased the accuracy of tiled maps by increasing pixel size or by averaging several maps created using a “moving window” approach.

Conclusions

There is a trade-off between tile size and pixel size when modelling connectivity across large spatial extents. We suggest using the largest tile size possible when tiling is necessary, in conjunction with increased pixel size and a moving window method to increase accuracy of the composite current density maps.