Advances in pasture management for animal productivity and health

A wide range of management techniques is available to enhance quantity and quality of forage supply to grazing animals throughout the annual production cycle. Within broad limits, dry matter (DM) production is relatively insensitive to management of defoliation frequency, severity and duration. However defoliation management has effects on feed quality which can be enhanced, in particular, by control of pasture growth in the spring through maintenance of relatively low average pasture masses. Treading damage can have significant immediate and ongoing effects on pasture production and farmers can use a range of management techniques to minimise these.

Fertiliser application practices have a potent influence on pasture production and seasonality of that production. Available soil nitrogen is the primary nutrient deficiency limiting production in New Zealand's characteristically grass-dominant pastures. Nitrogen fertiliser usage has increased markedly in recent years, particularly to grow substantially greater amounts of forage during the cool season, and this trend looks set to continue. However, the use of nitrogen fertiliser has important environmental implications.

Pasture renewal and forage crop use has also increased in recent years. Care needs to be taken in conducting cost-benefit analyses, selecting the options that best meet the needs, and in establishment and subsequent management practices. Ryegrass (perennial and hybrids) and white clover remain the primary choice for permanent pasture renewal, the availability of safe endophytes having largely alleviated effects of endophyte toxicosis. Special-purpose mixtures are used, especially in dry environments. Italian ryegrasses, brassicas and chicory are common choices for forage crops. A range of management techniques can be used to alleviate deleterious effects of some forages, including ryegrass endophyte toxicosis, facial eczema, and toxins associated with Fusarium fungi. Generally these techniques are not totally effective. More research is required to increase our understanding of these disorders, and in order to develop more effective and reliable management practices.     

Development of New Stem Cell-based Technologies for Carnivore Reproduction Research

New reproductive technologies based on stem cells offer several potential benefits to carnivore species. For example, development of lines of embryonic stem cells in cats and dogs would allow for the generation of transgenic animal models, which could be used to advance both veterinary and human health. Techniques such as spermatogonial stem cell transplantation (SSCT) and testis xenografting offer new approaches to propagate genetically valuable individual males, even if they should die before producing sperm. These techniques might therefore have application to the conservation of endangered species of carnivores, as well as to biomedical research. Recently, our laboratory has successfully performed SSCT in the dog, with a recipient dog producing sperm of donor genetic origin. Testis xenografting has been used to produce sperm from pre-pubertal testis tissue from both cats and ferrets. These early steps reinforce the need not only for research on stem cell technologies, but also for additional research into complementary technologies of assisted reproduction in carnivores, so that the widest array of research and clinical benefits can be realized.     

Identification of Sperm-Head Morphometric Subpopulations in Iberian Red Deer Epididymal Sperm Samples

Computer-assisted sperm morphometry analysis (CASMA) was used in this study to identify sperm morphometric subpopulations in Iberian red deer epididymal sperm samples. Epididymal sperm samples were collected from 37 mature stags and were divided. One portion was diluted in a Tris–citrate–egg yolk medium. A microscope slide was prepared from single extended sperm samples prior to freezing. The remainder of each sample was frozen in nitrogen vapours using a conventional protocol. After thawing, sperm smears were prepared as described for extended samples. All slides were air-dried and stained with Hemacolor^®. The sperm-head dimensions for a minimum of 145 sperm-heads were analyzed from each sample by means of the Sperm-Class Analyser^®, and the mean measurements recorded. Each sperm-head was measured for four primary sperm-head parameters, and five parameters of head shape. All sperm morphometric parameters evaluated were placed in a statistical database and a multivariate cluster analysis was performed. The clustering analyses, based on 10 867 individual spermatozoa, revealed the existence of three subpopulations (SP₁, SP₂, SP₃) of spermatozoa with different morphometric characteristics (p  <  0.001). The proportion of spermatozoa present in any of the three subpopulations remained constant (p  >  0.05) through the cryopreservation process. Pre-freeze and post-thaw sperm quality was in vitro evaluated by microscopic assessments of individual sperm motility and of plasma membrane and acrosome integrities. In conclusion, our results show that applying the CASMA techniques and multivariate cluster analyses, it was possible to determine that three subtle subpopulations of spermatozoa with different morphometric characteristics coexist in red deer semen.     

Evaluation of dazomet as fumigant for the control of brown root rot disease

BACKGROUND: Brown root rot disease caused by Phellinus noxius is widespread in approximately 216 tree and plant species in tropical and subtropical countries. No direct means of protection against P. noxius infection have thus far been developed. Therefore, in this field survey, a method was developed for preventing and controlling brown root rot disease using fumigation with dazomet. RESULTS: Tracers were used to monitor the effect of dazomet fumigation. The results from field surveys and phytotoxicity tests showed that dazomet is able to kill P. noxius without any side effects on plants. CONCLUSION: The use of an environmentally friendly agent to control brown root rot disease is needed, and prevention of the disease is more important than treatment. Hence, chemical fumigation with 60 g m^?2 of 98% dazomet may be a possible means of preventing P. noxius incursion in agriculture, gardening and agroforestry. Copyright © 2012 Society of Chemical Industry     

Effects of Egg Yolk and Cooling Rate on the Survival of Refrigerated Red Deer (Cervus elaphus hispanicus) Epididymal Spermatozoa

Egg yolk is a common component to sperm refrigeration for most of the deer species, the role of which is to protect sperm membranes against cold shock. In addition, there have been many studies of conservation of ejaculated semen from stags, but few have been reported for epididymal spermatozoa. This work was designed to investigate the combined effects of cooling rates (slow: 0.23 degrees C/min vs rapid: 4.2 degrees C/min) from room temperature to 5 degrees C, and egg-yolk concentration (0, 5 or 20%) in the extender on the survival of Iberian red deer epididymal spermatozoa refrigerated at 5 degrees C. Heterospermic sperm samples were diluted to a final sperm concentration approximately 400x10(6) sperm/ml with a Tris-citrate-fructose (TCF)-egg-yolk diluent. Sperm quality was in vitro judged by microscopic assessments of individual sperm motility [sperm motility index (SMI)], and of plasma membrane (hypo-osmotic swelling test) and acrosome (NAR) integrities. Our results first showed that the presence of egg yolk in the extender significantly improves (p=0.01) the viability and sperm motility after sperm dilution. In addition, acrosome and plasma membrane integrities post-refrigeration did not differ significantly between cooling procedures; however, the SMI differed significantly between cooling procedures (slow: 46.6% vs rapid: 50.0%; p=0.01). Our results also showed that sperm quality was significantly (p<0.01) affected by the combined effects of egg-yolk concentration and cooling procedure, being rapid cooling with 20% of egg yolk the most suitable combination for epididymal sperm refrigeration. In conclusion, egg-yolk improved red deer epididymal spermatozoa characteristics after dilution. Rapid cooling protocol using TCF with 20% egg-yolk significantly improved sperm motility of red deer epididymal spermatozoa after cooling.