The relationship of infertility to antibody production in the uterovaginal sperm storage tubules of turkey breeder hens

1989 ◽  
Vol 31 (5) ◽  
pp. 955-961 ◽  
Author(s):  
T.A. Kirk ◽  
H.P. Van Krey ◽  
R.M. Hulet ◽  
E.A. Dunnington ◽  
D.M. Denbow
2020 ◽  
Vol 47 (3) ◽  
pp. 34-43
Author(s):  
E. O. Ewuola ◽  
K. T. Ogundeji ◽  
T. M. Osanyinlusi ◽  
D. M. Oyedele ◽  
K. A. Adebisi ◽  
...  

The biological basis of sustaining fertility in poultry is their ability to store sperm cells in the sperm storage tubules (SST) located in the uterovaginal junction. However, artificial insemination in poultry industry is haphazardly administered in Nigeria without regulation on semen dose and frequency of insemination for optimum fertility. The objective of this study was to establish a semen dosage and insemination interval for maximum fertility and embryonic survival in Nera black layer breeder chickens. A total of 80 breeder hens (52 weeks) were allotted to five (5) treatments with four (4) replicate per treatment. Semen was pooled from 10 matured breeder cocks and inseminated to four groups of hens at varied semen dose of 0.02mL (T1), 0.04mL (T2), 0.06mL (T3) and 0.08mL (T4) of undiluted semen while hens in T5 were mated naturally, both for two consecutive days. 0.02, 0.04, 0.06 and 0.08mL of pooled semen contained 20.43×10 , 40.87×106 , 61.30×106 and 81.74×106 motile spermatozoa. Eggs were collected, stored and artificially incubated weekly for 4 weeks. Fertility, embryo mortality and hatchability parameters were determined. Another 78 breeder hens were allocated into 4 treatments of 5 replicates per treatment with unequal number of hens and were inseminated with 0.02mL of raw semen containing 20.43 × 106 motile sperm cells at 3, 6, 9 and 12 days intervals. Fertility, hatchability and embryo mortality were determined. Data were analysed using descriptive statistics and ANOVA at &0.05 Hatch of fertile eggs in T5 at week 2 (65.36±13.28) was significantly higher (p<0.05) . than T1 (33.83±12.65), T2 (13.25±6.88), T3 (39.17±14.17) and T4 (28.21±11.37). At weeks 1 and 2, there was no significant different across the treatments. Fertility at 4 weeks in T1 (11.53±6.66) was significantly (p<0.05) different from treatments T2 (0.00±0.00), T3 (0.00±0.00), T4 (1.66±1.66) and T5 (0.00±0.00). Total and early embryo mortality in week 3 was significantly higher (p<0.05) in T1 (100.00±0.00, 95.00±5.00) than in treatments T2 (43.75±0.00, 43.75±25.77), T3 (66.67±23.57, 66.67±23.57), T4 (95.00±5.00, 85.00±15.00) and T5 (37.50±23.94, 22.92±15.73). Fertility was significantly (p<0.05) higher in 3 days insemination interval (52.65±7.25) compared with 6 days (39.87±4.70), 9 days (22.98±5.71) and 12 days (36.14±6.89). At weeks 1 and 3, the hatch of fertile eggs across the treatments was not significantly (p>0.05) different from one another. This study suggests that 6 inseminating semen dose of 0.02mL containing approximately 20.43×10 motile sperm cells in Nera black layer breeder chickens will give a maximum fertile period of 5 days, while insemination interval of 3 days using 0.02mLof semen gave highest fertility level.


Paleobiology ◽  
1980 ◽  
Vol 6 (02) ◽  
pp. 146-160 ◽  
Author(s):  
William A. Oliver

The Mesozoic-Cenozoic coral Order Scleractinia has been suggested to have originated or evolved (1) by direct descent from the Paleozoic Order Rugosa or (2) by the development of a skeleton in members of one of the anemone groups that probably have existed throughout Phanerozoic time. In spite of much work on the subject, advocates of the direct descent hypothesis have failed to find convincing evidence of this relationship. Critical points are:(1) Rugosan septal insertion is serial; Scleractinian insertion is cyclic; no intermediate stages have been demonstrated. Apparent intermediates are Scleractinia having bilateral cyclic insertion or teratological Rugosa.(2) There is convincing evidence that the skeletons of many Rugosa were calcitic and none are known to be or to have been aragonitic. In contrast, the skeletons of all living Scleractinia are aragonitic and there is evidence that fossil Scleractinia were aragonitic also. The mineralogic difference is almost certainly due to intrinsic biologic factors.(3) No early Triassic corals of either group are known. This fact is not compelling (by itself) but is important in connection with points 1 and 2, because, given direct descent, both changes took place during this only stage in the history of the two groups in which there are no known corals.


Author(s):  
D. F. Blake ◽  
L. F. Allard ◽  
D. R. Peacor

Echinodermata is a phylum of marine invertebrates which has been extant since Cambrian time (c.a. 500 m.y. before the present). Modern examples of echinoderms include sea urchins, sea stars, and sea lilies (crinoids). The endoskeletons of echinoderms are composed of plates or ossicles (Fig. 1) which are with few exceptions, porous, single crystals of high-magnesian calcite. Despite their single crystal nature, fracture surfaces do not exhibit the near-perfect {10.4} cleavage characteristic of inorganic calcite. This paradoxical mix of biogenic and inorganic features has prompted much recent work on echinoderm skeletal crystallography. Furthermore, fossil echinoderm hard parts comprise a volumetrically significant portion of some marine limestones sequences. The ultrastructural and microchemical characterization of modern skeletal material should lend insight into: 1). The nature of the biogenic processes involved, for example, the relationship of Mg heterogeneity to morphological and structural features in modern echinoderm material, and 2). The nature of the diagenetic changes undergone by their ancient, fossilized counterparts. In this study, high resolution TEM (HRTEM), high voltage TEM (HVTEM), and STEM microanalysis are used to characterize tha ultrastructural and microchemical composition of skeletal elements of the modern crinoid Neocrinus blakei.


Author(s):  
Leon Dmochowski

Electron microscopy has proved to be an invaluable discipline in studies on the relationship of viruses to the origin of leukemia, sarcoma, and other types of tumors in animals and man. The successful cell-free transmission of leukemia and sarcoma in mice, rats, hamsters, and cats, interpreted as due to a virus or viruses, was proved to be due to a virus on the basis of electron microscope studies. These studies demonstrated that all the types of neoplasia in animals of the species examined are produced by a virus of certain characteristic morphological properties similar, if not identical, in the mode of development in all types of neoplasia in animals, as shown in Fig. 1.


Author(s):  
J.R. Pfeiffer ◽  
J.C. Seagrave ◽  
C. Wofsy ◽  
J.M. Oliver

In RBL-2H3 rat leukemic mast cells, crosslinking IgE-receptor complexes with anti-IgE antibody leads to degranulation. Receptor crosslinking also stimulates the redistribution of receptors on the cell surface, a process that can be observed by labeling the anti-IgE with 15 nm protein A-gold particles as described in Stump et al. (1989), followed by back-scattered electron imaging (BEI) in the scanning electron microscope. We report that anti-IgE binding stimulates the redistribution of IgE-receptor complexes at 37“C from a dispersed topography (singlets and doublets; S/D) to distributions dominated sequentially by short chains, small clusters and large aggregates of crosslinked receptors. These patterns can be observed (Figure 1), quantified (Figure 2) and analyzed statistically. Cells incubated with 1 μg/ml anti-IgE, a concentration that stimulates maximum net secretion, redistribute receptors as far as chains and small clusters during a 15 min incubation period. At 3 and 10 μg/ml anti-IgE, net secretion is reduced and the majority of receptors redistribute rapidly into clusters and large aggregates.


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