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PubMed2000

Exploring the genetic basis and proximate causes of female fertility advantage in gynodioecious Thymus vulgaris.

In many gynodioecous species, females produce more viable seeds than hermaphrodites. Knowledge of the relative contribution of inbreeding depression in hermaphrodites and maternal sex effects to the female fertility advantage and the genetic basis of variation in female fertility advantage is central to our understanding of the evolution of gender specialization. In this study we examine the relative contribution of inbreeding and maternal sex to the female fertility advantage in gynodioecious Thymus vulgaris and quantify whether there is genetically based variation in female fertility advantage for plants from four populations. Following controlled self and outcross (sib, within-population, and between-population) pollination, females had a more than twofold fertility advantage (based on the number of germinating seeds per fruit), regardless of the population of origin and the type of pollination. Inbreeding depression on viable seed production by hermaphrodites occurred in two populations, where inbreeding had been previously detected. Biparental inbreeding depression on viable seed production occurred in three of four populations for females, but in only one population for hermaphrodites. Whereas the maternal sex effect may consistently enhance female fertility advantage, inbreeding effects may be limited to particular population contexts where inbreeding may occur. A significant family x maternal sex interaction effect on viable seed production was observed, illustrating that the extent of female fertility advantage varies significantly among families. This result is due to greater variation in hermaphrodite (relative to female) seed fertility between families. Despite this genetic variation in female fertility advantage and the highly female biased sex ratios in populations of T. vulgaris, gynodioecy is a stable polymorphism, suggesting that strong genetic and/or ecological constraints influence the stability of this polymorphism.

Analysis of Variance↗
PubMed2005

Microbial indices of soil fertility.

AIMS: To find the new microbial parameters explaining the soil fertility from the microbial community viewpoint. METHODS AND RESULTS: Fatty acid methyl ester (FAME) analysis and terminal-restriction fragment length polymorphism (T-RFLP) analysis were carried out using 16 differently treated plots from the same field that had been kept under different fertilizer management systems since 1984. It was found that organic fertilizer application had small impact, whereas chemical fertilizer application, especially ammonium-nitrogen fertilizer, had strong impact on microbial community structures. Principal component analysis was conducted based on soil chemical and physical parameters, crop yields, FAMEs and terminal-restriction fragments (T-RFs) to provide 10 FAMEs and 10 T-RFs showing strong relation with soil fertility. CONCLUSION: We defined these 10 FAMEs and 10 T-RFs as 'keystone' biological parameters explaining soil fertility in the soil. SIGNIFICANCE AND IMPACT OF THE STUDY: This is the first report on the FAMEs and T-RFs related to soil fertility. Both analyses are rapid, inexpensive and reproducible means. As field assessment needs precise and rapid analysis, FAME and T-RFLP analyses and these new parameters are very useful to analyse soil fertility at biological viewpoint.

Agriculture↗
PubMed1997

The implications of a paternally derived centrosome during human fertilization: consequences for reproduction and the treatment of male factor infertility.

PROBLEM: Successful fertilization in humans follows a complex series of events, including the completion of meiotic maturation of the oocyte with the extrusion of the second polar body, the decondensation of the sperm nucleus and the maternal chromosomes into male and female pronuclei, the restoration of the sperm centrosome, and the nucleation of microtubule-mediated motility necessary to bring the male and female pronuclei into close apposition. These events occur after both fertilization in vitro and after intracytoplasmic sperm injection (ICSI), a new technique which is currently being applied in many clinics to overcome severe male infertility. Defects in any of the events leading to fertilization can be lethal to the zygote and may prove to be causes of infertility. METHODS: Imaging of inseminated human and rhesus oocytes using immunohistochemical techniques reveals several phases at which fertilization arrests. RESULTS: Oocytes from some infertile patients failed to complete fertilization due to failure of the sperm aster microtubules in uniting the sperm and egg nuclei. The rate of sperm aster formation, size, and organization during fertilization has been used as a measurement of bovine sperm quality. The development of an assay using Xenopus laevis oocyte extract can also be used to test sperm from various species for their ability to form esters and perform other centrosomal functions in vitro, as well as another indicator of sperm quality. Semen from men with questionable fertility was found to contain sperm which are generally incapable of producing sperm asters. In addition, the activity of centrosomal proteins such as gamma-tubulin and centrin have been detected in mammalian eggs and sperm. The levels of gamma-tubulin increase markedly after exposure to X. laevis egg extract. CONCLUSION: Defects in either male or female nucleus decondensation also resulted in the arrest of fertilization and was found to occur in both inseminated human oocytes and in rhesus oocytes fertilized by ICSI. These discoveries on the molecular basis of infertility in humans have important implications for infertility diagnosis and managing reproduction.

Animals↗
PubMed2000

Nitric oxide (NO) and interleukin-1beta (IL-1beta) in follicular fluid and their correlation with fertilization and embryo cleavage.

PROBLEM: Using an IVF model, the goal of the study was to investigate the relationship between follicular fluid (ff) NO and IL-1beta levels, as well as their correlation with fertilization of mature oocytes and embryo cleavage rates. METHOD OF STUDY: Follicular fluid was collected from 17 patients at the time of transvaginal oocyte retrieval following controlled ovarian stimulation. Oocytes harvested from these follicles were followed through fertilization and embryo cleavage. The NO metabolites nitrate/nitrite (NO3/NO2) were measured using the Griess reaction as an indirect assessment of NO activity. IL-1beta was measured using a high sensitivity ELISA system (Amersham, UK). The Student's t-test was utilized for unpaired data with the means considered significantly different when P < or = 0.05. RESULTS: Follicular fluid NO3/NO2 levels were significantly lower in follicles containing mature oocytes that fertilized (n = 30; 9.7 +/- 1.0 microM), versus those that did not fertilize (n = 23; 15.4 +/- 2.4 microM; P < 0.05). Follicles that contained oocytes that fertilized and went on to divide beyond the 6 cell stage had significantly lower ff levels of NO3/NO2 (n = 18; 7.5 +/- 0.9 microM), as compared to ff that contained oocytes that did not fertilize or failed to develop beyond the 5 cell stage (n = 35; 14.6 +/- 1.7 microM; P < 0.01). No correlation was found between ff NO3/NO2 levels (n = 28; 13.8 +/- 2.0 microM) and ff IL-1beta levels (n = 28; 0.5 +/- 0.08 pg/mL). An analysis of ff IL-1beta levels in relation to fertilization and embryo cleavage rates revealed no correlation. CONCLUSIONS: Lower ff NO3/NO2 levels at the time of oocyte retrieval are associated with adequate fertilization and embryo cleavage rates. In our IVF model, no correlation was found between ff IL-1beta levels and ff NO3/NO2, fertilization, or embryo cleavage rates.

Adult↗
PubMed2005

Does human semen contain a functional haemostatic system? A possible role for Tissue Factor Pathway Inhibitor in fertility through semen liquefaction.

There is already evidence that a few components of the haemostatic system exist in semen. If these comprise a functional system, they may have a role in seminal clotting and liquefaction processes and ultimately may influence fertility. What might be expected in semen as collected from fertility clinics i.e., after having both coagulated and subsequently liquefied is uncertain. It does however still contain significant amounts of Tissue Factor (TF) although its effect on semen quality remains poorly understood. The present study analyses semen for Tissue Factor Pathway Inhibitor (TFPI). Measurements were made in seminal plasma, swim-up sperm and prostasomes and its relationship with conventional fertility parameters assessed. TFPI antigen levels in seminal plasma were measured in a total of 176 subjects using an Enzyme-linked immunosorbent assay (ELISA). These include sub-fertile (n=37), normally fertile (n=40), fertile sperm donor (n=34), vasectomized subjects (n=65) and in a further group defined by normality in several parameters derived from the World Health Organization (WHO) fertility criteria and termed "pooled normal semen parameters" (PNSP). For characterization studies, both TFPI activity and antigen were measured on whole semen, swim-up sperm and prostasome-rich fraction (n=5). TFPI levels were significantly higher in normal men as compared to sub-fertile (P<0.01) or vasectomized subjects (P<0.001). TFPI levels were even higher in the donor quality semen and the PNSP group. TFPI levels also correlated with semen liquefaction time, normal semen viscosity, sperm progression, percentage of motile sperm and sperm counts (density). In conclusion, the present finding substantiates the concept of an active clotting system in human semen. TFPI could regulate the activity of abundant TF, as it does elsewhere. Given a functional set of coagulation factors in semen, the TF/TFPI balance might impinge on its liquefaction and hence on global fertility.

Adult↗
PubMed1982

Electrophoretic movement of fertilized sea-urchin eggs.

The eccentric shift of the sea-urchin egg within the fertilization membrane under an electric field was analysed by measuring the electrophoretic mobility of the isolated fertilization membrane and that of the egg deprived of the fertilization membrane. In addition, the migration speed of the egg proper was measured within the fertilization membrane under the conditions that: either (1) the movement of the whole egg was arrested, or (2) protamine sulphate was adsorbed on the fertilization membrane to reduce its mobility. The results led to conclusions that: (1) both the fertilization membrane and the egg cell with the hyaline layer are negatively charged; (2) movement of the normal fertilized eggs is due mainly to the surface charge of the fertilization membrane; and (3) the eccentric position of the egg within the fertilization membrane is due to migration of the egg proper, which is independent of the movement of the whole egg.

Animals↗
PubMed2004

Timing effects and the interpretation of period fertility.

Low fertility levels and later childbearing in many developed countries have reinvigorated the debate between period and cohort perspectives on fertility and on the meaningfulness of the period total fertility rate (TFR). Here, fertility-timing effects are defined as level changes in period fertility that do not reflect level changes in the completed fertility of cohorts. That definition leads to the average cohort fertility (ACF) as a measure of period fertility adjusted for timing effects. In an influential paper, Bongaarts and Feeney (1998) presented an alternative approach and a different measure, TFR*, to adjust for timing effects. Here, the two measures are compared. In the context of model populations, the ACF performs well, reflecting an average of the fertility of the active cohorts. The Bongaarts-Feeney TFR*, however, is frequently unreliable and can be erratic when there are cycles in period timing. When applied to twentieth-century U.S. experience, the TFR* behaves like a period measure and yields adjustments that are often wide of the mark. The ACF shows the stability associated with cohort measures and quantifies the substantial impact that timing effects had during the "birth dearth" of the 1970s. The period TFR reached a low of 1.74 in 1976, but the ACF never went below 2.06 during the 1970s.

Adult↗
PubMed1989

Fertilization and ovum recovery rates in superovulated ewes following cervical insemination or laparoscopic intrauterine insemination at different times after progestagen withdrawal and in one or both uterine horns.

In Exp. 1, 40 ewes were used in a 2 x 2 factorial design to investigate the effects of intrauterine versus cervical insemination and superovulation using pig FSH or PMSG and GnRH on egg recovery and fertilization rate. Cervical inseminations were carried out at 48 and 60 h (N = 20 ewes) and intrauterine insemination at 52 h (N = 20 ewes) after progestagen pessary withdrawal. Eggs were recovered on Day 3 of the oestrous cycle. Ovulation, egg recovery and fertilization rates were independent of the type of superovulatory hormone used. Fertilization rate was high irrespective of insemination site but intrauterine insemination at 52 h was associated with a significant (P less than 0.01) decrease in egg recovery of over 40% compared with cervically inseminated ewes. In Exp. 2 ewes were inseminated at 36 (N = 5), 48 (N = 6) or 60 (N = 6) h after pessary withdrawal to determine the optimum intrauterine insemination time to maximize both fertilization rate and egg recovery. Egg recovery per ewe flushed was 23, 59 and 67% after intrauterine insemination at 36, 48 and 60 h respectively. Correspondingly, 0, 85 and 100% of the eggs recovered were fertilized. The results of Exps 1 and 2 suggest that when intrauterine insemination occurs before or during ovulation it interferes with oocyte collection by the fimbria. In Exp. 3 egg recovery and fertilization rates were determined after cervical insemination at 48 and 60 h (N = 8) or intrauterine insemination at 48 (N = 9) or 60 (N = 8) h after progestagen withdrawal. Ewes in the last two groups were subdivided and inseminated unilaterally or bilaterally. Egg recovery was high after cervical insemination (95%) but only 36% of these eggs were fertilized. Unilateral intrauterine insemination was as effective as bilateral in ensuring high fertilization rates (100 versus 97%). Intrauterine insemination at 48 h compared with 60 h resulted in a significantly lower (P less than 0.05) percentage of eggs recovered (42 versus 90% respectively). However, reducing the degree of interference by adopting unilateral rather than bilateral insemination did not alleviate the detrimental effects of the 48-h insemination time on egg recovery. From these results we advocate the adoption of intrauterine insemination at 60 h after progestagen withdrawal to maximize fertilization rate and egg recovery in superovulated ewes.

Animals↗
PubMed2004

Determination of the rate of true fertility in duck breeds by the combination of two in vitro methods.

Embryonic mortality is a significant problem plaguing the hatching success. Its early forms are especially hardly distinguishable from true infertility. Propidium iodide (PI) staining of the germinal disc combined with outer perivitelline layer (OPVL) sperm counting was used for the determination of 'true' fertility of duck eggs in two different experiments: fertility investigation on fresh, unincubated eggs of Hungarian ducks and on incubated eggs of a crossbred, selected as 'infertile' at the 7th day of incubation. Examination of the relationship between OPVL sperm count and fertility seems to be an adequate tool for checking the effectiveness of insemination programmes and the fertilising capacity of poultry spermatozoa. The proportion of fertile eggs was around 50% when the number of OPVL sperm was between 0.1 and 0.2 spermatozoa/mm2. Ninety-nine percent of the eggs containing > 0.3 OPVL sperm/mm2 were fertile and all of the eggs containing < 0.05 sperm/mm2 were infertile. To assure the accuracy of fertility prediction by OPVL sperm counting, PI staining of the germinal disc was used to determine fertility in uncertain cases. Identification of very early embryonic mortality, i.e. that occurring before oviposition, is very difficult. The use of a dissecting microscope for the assessment of real fertility is suitable in most of the cases, while PI staining of the germinal discs proved to be more reliable for detecting very early embryonic death. The combination of the two methods proved to be a useful tool for detecting the 'true' fertility of duck eggs of different breeds.

Animals↗
PubMed2006

N fertilization effects on denitrification and N cycling in an aggrading forest.

We investigated N cycling and denitrification rates following five years of N and dolomite amendments to whole-tree harvested forest plots at the long-term soil productivity experiment in the Fernow Experimental Forest in West Virginia, USA. We hypothesized that changes in soil chemistry and nutrient cycling induced by N fertilization would increase denitrification rates and the N2O:N2 ratio. Soils from the fertilized plots had a lower pH (2.96) than control plots (3.22) and plots that received fertilizer and dolomite (3.41). There were no significant differences in soil %C or %N between treatments. Chloroform-labile microbial biomass carbon was lower in fertilized plots compared to control plots, though this trend was not significant. Extractable soil NO3- was elevated in fertilized plots on each sample date. Soil-extractable NH4+, NO3-, pH, microbial biomass carbon, and %C varied significantly by sample date suggesting important seasonal patterns in soil chemistry and N cycling. In particular, the steep decline in extractable NH4+ during the growing season is consistent with the high N demands of a regenerating forest. Net N mineralization and nitrification also varied by date but were not affected by the fertilization and dolomite treatments. In a laboratory experiment, denitrification was stimulated by NO3- additions in soils collected from all field plots, but this effect was stronger in soils from the unfertilized control plots, suggesting that chronic N fertilization has partially alleviated a NO3- limitation on denitrification rates. Dextrose stimulated denitrification only in the whole-tree-harvest soils. Denitrification enzyme activity varied by sample date and was elevated in fertilized plots for soil collected in July 2000 and June 2001. There were no detectable treatment effects on N2O or N2 flux from soils under anaerobic conditions, though there was strong temporal variation. These results suggest that whole-tree harvesting has altered the N status of these soils so they are less prone to N saturation than more mature forests. It is likely that N losses associated with the initial harvest and high N demand by aggrading vegetation is minimizing, at least temporarily, the amount of inorganic N available for nitrification and denitrification, even in the fertilized plots in this experiment.

Ammonium Sulfate↗
PubMed2006

Nitrous oxide fluxes in turfgrass: effects of nitrogen fertilization rates and types.

Urban ecosystems are rapidly expanding and their effects on atmospheric nitrous oxide (N2O) inventories are unknown. Our objectives were to: (i) measure the magnitude, seasonal patterns, and annual emissions of N2O in turfgrass; (ii) evaluate effects of fertilization with a high and low rate of urea N; and (iii) evaluate effects of urea and ammonium sulfate on N2O emissions in turfgrass. Nitrogen fertilizers were applied to turfgrass: (i) urea, high rate (UH; 250 kg N ha(-1) yr(-1)); (ii) urea, low rate (UL; 50 kg N ha(-1) yr(-1)); and (iii) ammonium sulfate, high rate (AS; 250 kg N ha(-1) y(-1)); high N rates were applied in five split applications. Soil fluxes of N2O were measured weekly for 1 yr using static surface chambers and analyzing N2O by gas chromatography. Fluxes of N2O ranged from -22 microg N2O-N m(-2) h(-1) during winter to 407 microg N2O-N m(-2) h(-1) after fall fertilization. Nitrogen fertilization increased N2O emissions by up to 15 times within 3 d, although the amount of increase differed after each fertilization. Increases were greater when significant precipitation occurred within 3 d after fertilization. Cumulative annual emissions of N2O-N were 1.65 kg ha(-1) in UH, 1.60 kg ha(-1) in AS, and 1.01 kg ha(-1) in UL. Thus, annual N2O emissions increased 63% in turfgrass fertilized at the high compared with the low rate of urea, but no significant effects were observed between the two fertilizer types. Results suggest that N fertilization rates may be managed to mitigate N2O emissions in turfgrass ecosystems.

Air Pollutants↗
PubMed2005

Identification of proteins in the accessory sex gland fluid associated with fertility indexes of dairy bulls: a proteomic approach.

We evaluated the expression of proteins in the accessory sex gland fluid (AGF) and their relationships with fertility indexes of dairy bulls. Fertility was normalized as the percentage point deviation of their nonreturn rates (PD) from the average fertility of all bulls from a given artificial insemination center. Services associated with each sire ranged from 269 to 77 321 and PD values from +7.7% to -18.1%. AGF, from 37 bulls, was obtained with an artificial vagina after cannulation of the vasa deferentia. Proteins from AGF were separated by 2-dimensional SDS-PAGE followed by staining with Coomassie blue and analysis of polypeptide maps using PDQuest software. Bulls were divided in groups based on PD values and the optical density of spots in the AGF gels used as independent variables to predict bull fertility. Proteins were identified by capillary liquid chromatography nanoelectrospray ionization tandem mass spectrometry (CapLC-MS/MS). An average of 52 +/- 5 spots was detected in the AGF gels, but there were no spots unique to groups of either high- (PD > or = 0) or low- (PD < 0) fertility sires. The former were neither less nor more homogeneous than the latter based on correlations of all matched spots between pairs of AGF maps. However, high fertility of dairy bulls was significantly associated with lower expression of 14-kDa spermadhesin Z13 isoforms and higher amounts of 55-kDa osteopontin and 58-kDa phospholipase A2 (PLA2) isoforms. The average intensity of 5 spots identified as BSP 30 kDa in the AGF gels had a quadratic association with fertility indexes (R2 = .18; P = .03). PD values of bulls were related (R2 = .56) to the quantity of spermadhesin, osteopontin, and BSP 30 kDa in the AGF polypeptide maps. Bull fertility was also determined by another equation (R2 = .53) with spermadhesin, BSP 30 kDa, and PLA2 as independent variables. We conclude that interactions among several proteins in accessory sex gland fluid explain a significant proportion of the variation in fertility scores of mature dairy sires.

Amino Acid Sequence↗
PubMed1996

Ewe fertility in the STAR accelerated lambing system.

Effects of environmental factors such as ewe age, season of exposure, and time from lambing to exposure on fertility were evaluated using records on 1,084 Dorset ewes in the STAR accelerated lambing system. The STAR program consisted of five 30-d concurrent breeding and lambing periods per year beginning on January 1, March 15, May 27, August 8, and October 20. Fertility in the flock changed in a cyclic and predictable fashion during the year. Changes in prolificacy were less consistent but also tended to show cyclic variation. Matings that occurred within the typical breeding season (August, October, and January) were more fertile than those occurring in March and June. However, fertility also varied with the age of the ewe and the time since the ewe's last lambing. Except in June, fertility at the first postpartum mating increased as ewes aged. In March and June matings, adult ewes that had just weaned lambs were less fertile than ewes that had failed to conceive in the previous season and therefore had longer postpartum intervals. However, in October and January, ewes that had just weaned lambs were more fertile. A matrix of expected pregnancy rates, or probabilities of fertility, was constructed using a mixed GLM to describe the combined effect of season, ewe age, and time since lambing on ewe fertility in accelerated lambing.

Aging↗
PubMed1986

Effect of sulfur fertilization on chemical composition, ensiling characteristics and utilization of corn silage by lambs.

Effects of S fertilization, 0 or 67 kg S/ha, as (NH4)2SO4, as a single or split application on chemical composition, ensiling characteristics and utilization of corn (Zea mays L.) silage by wether lambs was investigated. Corn forages were ensiled at hard-dent stage at 35% dry matter (DM). Sulfur fertilization increased (P less than .01) total S and SO4 but had no effect on N, Mg, Ca or fiber components in silages. Sulfur-fertilized corn silages (N:S = 42 and 43) and non-S fertilized silage (N:S = 62) were fed alone and supplemented with Na2SO4 at two rates to achieve N:S ratios of 12 (high) and 45 (low, to approximate S-fertilized silage), to 30 wether lambs (Suffolk and Dorset crosses) in metabolism and palatability trials. Both trials were randomized complete-block designs. Lambs weighed 36 and 41 kg, respectively. All silages were supplemented with 6.7 g urea/d. Digestibility of DM and cell wall components, and apparent absorption of S and N were increased (P less than .05) by S fertilization and supplementation. Nitrogen retention was increased (P less than .01) by S fertilization and supplementation. Retention was higher (P less than .001) for lambs that were fed S-fertilized silage, compared with supplementation to achieve a similar N:S ratio. It appears that S fertilization was more effective than S supplementation in improving efficiency of N utilization.

Ammonia↗
PubMed2006

Genetic correlations between milk production and health and fertility depending on herd environment.

High milk production in dairy cattle can have negative side effects on health and fertility traits. This paper explores the genetic relationship of milk yield with health and fertility depending on herd environment. A total of 71,720 lactations from heifers calving in 1997 to 1999 in the Netherlands were analyzed. Herd environment was described by 4 principal components: intensity, average fertility, farm size, and relative performance indicating whether herds had good (poor) health and fertility despite a high (low) production. Fertility was evaluated by days to first service and number of inseminations (NINS); somatic cell score was used as a measure of udder health. Data were analyzed with a multitrait reaction norm model. Genetic correlation within traits across environments ranged from 0.84 to unity. Genetic correlations of the 3 traits with milk yield were antagonistic but varied over environments. Genetic correlation of milk yield with days to first service varied from 0.30 in small herds to 0.48 in herds with low average fertility. Correlations with NINS varied from 0.18 in large herds to 0.64 in high fertility herds, and with somatic cell score from 0.25 in herds with a high fertility relative to production to 0.47 in herds with a relative low fertility. Selection in environments of average value resulted in different predicted responses over environments. For example, selection for a decrease of NINS of 0.1 in an average production environment decreased milk yield by 35 kg in low production herds, but by 178 kg in high production herds.

Analysis of Variance↗
PubMed2006

Effect of sire fertility and timing of artificial insemination in a Presynch + Ovsynch protocol on first-service pregnancy rates.

Sire fertility may influence pregnancy rate (PR) by differences in sperm survival in the female reproductive system and time required for capacitation and transport of sperm to site of fertilization. A predicted fertility index, Estimated Relative Conception Rate, was used to select 3 high-fertility artificial insemination (AI) sires (+3) and 3 average AI sires (-1). Ovulation can be predicted to occur at approximately 28 h following GnRH administration when used in an Ovsynch protocol. The objective of this study was to determine if AI at 2 times, 0 or 24 h after GnRH administration, in a Presynch + Ovsynch protocol resulted in different first-service PR when average or high-fertility sires were used. Lactating Holstein cows (n = 1,457) from 2 dairy herds located in the Piedmont region of North Carolina were utilized for 12 mo. Timing of AI did not affect first AI PR and no interaction of sire-fertility group and timing of AI was detected. First AI PR did not differ between sire-fertility groups (23.2 vs. 29.4%) for average and high-fertility groups, respectively. First-lactation cows were 53% more likely to conceive than older cows, and cows bred during April through June were 66% less likely to become pregnant compared with cows bred from October through January. No interactions were detected among parity, season, sire-fertility group, or time of AI. Using only 3 sires per group based on Estimated Relative Conception Rate estimates resulted in large variability of sire conception within groups, although group averages differed by 6 points.

Animals↗
PubMed1988

Genetic parameters for fertility of dairy bulls.

Genetic parameters for male fertility and fertility ratings of AI bulls were obtained by analyzing 298,013 service records of cows with successive calving records. Cows were mated to 746 service bulls, which were progeny of 126 sires. The model for variance component estimation accounted for fixed effects of herd-year-seasons, sire of the service bull, age of mates, and random effects of service bull and residual error. Estimates of variances of service bulls and residual error components for bull fertility indicated almost 10% of the phenotypic variation for fertility is among AI bulls. Best linear unbiased prediction of fertility ratings of individual bulls with inclusion of sire and maternal grandsire relationships on these data permitted the evaluation of 886 AI bulls for bull fertility. Heritability for bull fertility computed as twice the regression of son on sire was .158. Differences in fertility ratings of AI bulls ranged from -.29 to .19. Prediction of fertility of young AI bulls and more accurate rating of proven bulls might be useful to the industry.

Animals↗
PubMed1975

Fertility of turkey hens correlated with depth of insemination.

In a two year comparison of shallow insemination (two cm.) and deep insemination (seven cm.) involving both Large White and Bronze hens shallow insemination was superior to deep insemination for Large White hens. Shallow insemination of Large White hens resulted in a longer duration-of-fertility and a higher total fertility (P less than 0.01) than deep insemination. The mean fertiltity in a 51 day duration-of-fertility trial during early production was 56.1% following shallow insemination and 43.1% following deep insemination. Late in the breeding season the mean fertility was 39.7% and 27.4% for shallow and deep insemination, respectively. The mean duration-of-fetility was 40.4 days after shallow insemination and 31.2 days after deep insemination. Shallow insemination was superior to deep insemination whether hens were inseminated at 14 days or 28 day intervals. Fertility following shallow insemination of Bronze hens was not different from fertility following deep insemination. In a duration-of-fertility trial of Bronze hens, the mean fertility was 37.3% for shallow insemination and 39.8% for deep insemination. The mean duration-of-fertility were 51.2 days after shallow insemination and 47.0 days after deep insemination.

Animals↗