Microbial growth efficiencies across a soil moisture gradient assessed using C-acetic acid vapor and N-ammonia gas

One integrative measurement of microbial activity in soils is the efficiency by which microbes convert assimilated carbon (C) into biomass C. This efficiency, called the microbial growth efficiency (Y), is a key physiological characteristic that regulates soil carbon sequestration, nutrient immobilization, and greenhouse gas emissions. Changes in rainfall patterns and soil water content as the result of global climate change have the potential to influence microbial activity and lead to changes in Y and thus, nutrient cycling at the ecosystem level. Unfortunately, little information is available on how environmental variables such as soil moisture influence Y. We have developed a new method for injecting ¹³C-labeled carbon as acetic acid vapor into soil that will allow measurement of microbial growth efficiency (as Y_C) without increasing soil moisture content. We compare Y determined with this new approach with an alternate method where injected ¹⁵N-labeled ammonia gas is used to quantify microbial N immobilization, and microbial growth efficiency is calculated based on microbial C:N and respiration rate (as Y_N). We also include injections of a solution containing labeled ammonium and acetate in our experiment to compare the results of our vapor methods with more commonly employed liquid-based methods. The ¹³C-acetic acid vapor, which was supplied to soils with soil moisture content ranging from 0.05 to 0.21 g H₂O g⁻¹ soil, was readily assimilated and respired by microbes. Between 0.10 and 0.21 g H₂O g⁻¹ soil (−0.60 to −0.04 MPa), values of Y_C averaged 0.46, and were significantly lower than values of Y_N, with average values of 0.58. Over this range, soil moisture content had no significant effect on either Y_C or Y_N. However, at the lowest soil moisture content (0.05 g H₂O g⁻¹ soil; <−6.0 MPa), Y_C and Y_N diverged substantially, suggesting that in very dry soils, constraints on microbial growth cause differential uptake of C and N resources.     

The effect of select seminal plasma proteins on endometrial mRNA cytokine expression in mares susceptible to persistent mating‐induced endometritis

In the horse, breeding induces a transient endometrial inflammation. A subset of mares are unable to resolve this inflammation, and they are considered susceptible to persistent mating‐induced endometritis PMIE Select seminal plasma proteins cysteine‐rich secretory protein‐3 (CRISP‐3) and lactoferrin have been shown to affect the innate immune response to sperm in vitro. The objective of this study was to determine whether the addition of CRISP‐3 and lactoferrin at the time of insemination had an effect on the mRNA expression of endometrial cytokines in susceptible mares after breeding. Six mares classified as susceptible to PMIE were inseminated during four consecutive oestrous cycles with treatments in randomized order of: 1 mg/ml CRISP‐3, 150 μg/ml lactoferrin, seminal plasma (positive control) or lactated Ringer's solution (LRS; negative control) to a total volume of 10 ml combined with 1 × 10⁹ spermatozoa pooled from two stallions. Six hours after treatment, an endometrial biopsy was obtained for qPCR analysis of selected genes associated with inflammation (pro‐inflammatory cytokines interleukin (IL)‐1β, IL‐8, tumour necrosis factor (TNF)‐α, interferon (INF)‐γ, anti‐inflammatory cytokines IL‐1RN and IL‐10, and inflammatory‐modulating cytokine IL‐6). Seminal plasma treatment increased the mRNA expression of IL‐1β (p = .019) and IL‐8 (p = .0068), while suppressing the mRNA expression of TNF (p = .0013). Lactoferrin also suppressed the mRNA expression of TNF (p = .0013). In conclusion, exogenous lactoferrin may be considered as one modulator of the complex series of events resulting in the poorly regulated pro‐inflammatory response seen in susceptible mares.     

Ovulation,Pregnancy Rate and Early Embryonic Development in Vernal Transitional Mares Treated with Equine‐ or Porcine‐FSH

The objective of this study was to compare the efficacy of purified equine‐ and porcine‐FSH treatment regimes in mares in early vernal transition. Mares (n = 22) kept under ambient light were examined ultrasonographically per‐rectum, starting January 30th. They were assigned to one of two treatment groups using a sequential alternating treatment design when a follicle ≥ 25 mm was detected. In the eFSH group, mares were treated twice daily with equine‐FSH, and in the pFSH group mares were treated twice daily with porcine‐FSH; treatments were continued until follicle(s) ≥ 35 mm, and 24 h later hCG was administered. Oestrous mares were inseminated with fresh semen and examined for pregnancy on days 11–20 post‐ovulation. In the eFSH group, 11/11 (100%) mares developed follicle(s) ≥ 35 mm, 8/11 (73%) ovulated and 6/8 (75%) conceived. In the pFSH group, 5/11 (45%) developed follicle(s) ≥ 35 mm, 4/11 (36%) ovulated and 3/4 (75%) conceived. Treatment with eFSH resulted in a greater ovarian stimulation; higher number of pre‐ovulatory‐sized follicles, higher number of ovulations and higher number of embryos (p < 0.05). Following ovulation, serum progesterone concentrations were correlated with the number of CLs and supported early embryonic development; maternal recognition of pregnancy occurred in all pregnant mares. We concluded that eFSH can be used to effectively induce follicular growth and ovulation in vernal transitional mares; however, if bred, diagnosis and management of twins’ pregnancies would be required prior to day 16 because of the increased risk of multiple embryos per pregnancy. Conversely, the current pFSH treatment regime cannot be recommended.     

Transplacental Transfer of Iron in the Water Buffalo (Bubalus bubalis): Uteroferrin and Erythrophagocytosis

The objectives of this investigation were to understand transplacental transport of iron by secreted uteroferrin (UF) and haemophagous areas of water buffalo placenta and clarify the role(s) of blood extravasation at the placental‐maternal interface. Placentomes and interplacentomal region of 51 placentae at various stages of gestation were fixed, processed for light and transmission electron microscopy, histochemistry and immunohistochemistry. Haemophagous areas were present in placentomes collected between 4 and 10 months of pregnancy. Perl’s reaction for ferric iron was negative in placentomes, but positive in endometrial glands. Positive staining for UF indicated areas in which it was being taken up by phagocytosis and/or fluid phase pinocytosis in areolae of the interplacentomal mesenchyme, with little staining in endometrial stroma. Imunohistochemistry detected UF in trophectoderm of haemophagous regions of placentomes and in other parts of the foetal villous tree, but the strongest immunostaining was in the epithelial cells and lumen of uterine glands. Ultrastructural analyses indicated that erythrophagocytosis was occurring and that erythrocytes were present inside cells of the chorion that also contained endocytic vesicles and caveolae. Results of this study indicate that both the haemophagous areas of placentomes and the areolae at the interface between chorion and endometrial glands are important sites for iron transfer from mother to foetal‐placental tissues in buffalo throughout pregnancy.     

Endothelin receptor subtype A blockade does not affect the haemodynamic recovery from haemorrhage during xenon/remifentanil or isoflurane/remifentanil anaesthesia in dogs

ObjectiveTo test the compensatory role of endothelin-1 when acute blood loss is superimposed on anaesthesia, by characterizing the effect of systemic endothelin receptor subtype A (ET_A) blockade on the haemodynamic and hormonal responses to haemorrhage in dogs anaesthetized with xenon/remifentanil (X/R) or isoflurane/remifentanil (I/R).Study designProspective experimental randomized controlled study.AnimalsSix female Beagle dogs, 13.4 ± 1.3 kg.MethodsAnimals were anaesthetized with remifentanil 0.5 μg kg^?1 minute^?1 plus either 0.8% isoflurane (I/R) or 63% xenon (X/R), with and without (Control) the systemic intravenous endothelin receptor subtype A antagonist atrasentan (four groups, n = 6 each). After 60 minutes of baseline anaesthesia, the dogs were bled (20 mL kg^?1) over 5 minutes and hypovolemia was maintained for 1 hour. Continuous haemodynamic monitoring was performed via femoral and pulmonary artery catheters; vasoactive hormones were measured before and after haemorrhage.ResultsIn Controls, systemic vascular resistance (SVR), vasopressin and catecholamine plasma concentrations were higher with X/R than with I/R anaesthesia at pre-haemorrhage baseline. The peak increase after haemorrhage was higher during X/R than during I/R anaesthesia (SVR 7420 ± 867 versus 5423 ± 547 dyne seconds cm^?5; vasopressin 104 ± 23 versus 44 ± 6 pg mL^?1; epinephrine 2956 ± 310 versus 177 ± 99 pg mL^?1; norepinephrine 862 ± 117 versus 195 ± 33 pg mL^?1, p < 0.05). Haemorrhage reduced central venous pressure from 3 ± 1 to 1 ± 1 cmH₂O (I/R, ns) and from 8 ± 1 to 5 ± 1 cmH₂O (X/R, p < 0.05), but did not reduce mean arterial pressure, nor cardiac output. Atrasentan did not alter the haemodynamic and hormonal response to haemorrhage during either anaesthetic protocol.Conclusions and clinical relevanceSelective ET_A receptor blockade with atrasentan did not impair the haemodynamic and hormonal compensation of acute haemorrhage during X/R or I/R anaesthesia in dogs.     

Factors contributing to the blackspot bruise potential of Idaho potato fields

Blackspot bruise is a major problem in the fresh market and frozen french fry industry. The blackspot bruise potential of Russet Burbank and Ranger Russet in Idaho potato fields was determined by surveying commercial fields during 1993 and 1994. Management factors were monitored to determine what practices were contributing to blackspot susceptibility in addition to mechanical damage. The survey included 17 Russet Burbank and 3 Ranger Russet fields in 1993, and 28 Russet Burbank and 8 Ranger Russet fields in 1994. The 1993 season was unusually cool and wet whereas 1994 was warmer than normal, resulting in a wide range of environmental conditions for the 2 year study. Blackspot bruise potential was determined at different stages of tuber physiological maturity by collecting samples several weeks prior to normal harvest, immediately before harvest, and after storing sub-samples for several months. The blackspot bruise potential was measured by both impact and abrasive peel tests. Field maturity was the factor most consistently related to blackspot potential both years. In 1994 a multiple regression of 3 independent variables — field maturity index, specific gravity, and percent available soil water at tuber sampling, compared with the blackspot potential as the dependent variable gave a correlation coefficient of r = 0.73 (p = 0.001). Due to the cool, wet growing season in 1993, there was not enough variability in specific gravity and available soil water among the fields sampled for these factors to correlate with the blackspot potential. The available fertility data, although not complete for all fields, indicated no direct relationship between N, P, or K fertilization and blackspot potential. Preharvest samples in late August had lower blackspot potential than harvest samples in mid September, and storage samples in February had the highest susceptibility. There was a consistent increase in blackspot severity when tubers were equilibrated at 4 C compared with 10 C prior to bruising.     

Effects on Grain and Malting Quality of Genes Altering Barley Starch Composition

In this study inbred barley lines carrying waxy and/or high amylose genes were obtained from a cross between Waxy Hector and a breeders» line BE285 (high amylose Glacier×Midas) and assessed for malting quality. Inbred lines were assayed and classified as having none, one or both genes. After malting, waxy lines had a slightly lower hot water extract than normal starch lines. Large effects were demonstrated for both grain nitrogen content and hot water extract in high amylose lines and, particularly, in lines with both genes. Endosperm modification during malting was reduced by both starch mutations. Electron microscopy showed that the phenotype with both genes was characterised by a highly compacted endosperm. During malting, this structure was extremely resistant to modification.     

The blood composition of different breeds of bulls undergoing beef performance tests

Blood samples taken on three occasions from each of 66 bulls undergoing beef performance tests were analysed for packed cell volume, blood glucose, haemoglobin, serum albumin, urea nitrogen, total protein, inorganic phosphate, Ca, Ca, Mg, K, Na, Cu, Fe and total iron binding capacity. The bulls were individually fed and situated at two centres, one accommodating Lincoln-Red, Devon and Sussex breeds and the other, Hereford. Significant differences between the Lincoln-Red, Devon and Sussex breeds were observed in concentrations of glucose, urea nitrogen, total iron binding capacity (P less than 0.001), Ca (P less than 0.01), Na and Cu (P less than 0.05). There were no significant correlations between the growth rates of individual bulls and their blood composition.