Variation in river water temperatures in an upland stream over a 30-year period.

Stream water temperature data from the Girnock burn, a 30-km2 catchment in Scotland were examined for systematic variation across 30 years of record (1968-1997). The data suggest that there has been no change in mean annual temperature with time, but at a seasonal level there is some indication of an increase in mean daily maximum temperatures during the winter (December to February) and spring (March to May) seasons. For the spring season, there is also evidence that mean temperature has increased. There are no apparent or obvious changes in stream flow to account for this. The strong relationship between air and stream temperatures (r2 = 0.96) implies that changes in the stream are the result of changes in the climate. It is possible that this may occur as a result of the effect of increasing air temperatures which may have also reduced the influence of snow and snowmelt on the catchment during the winter and spring seasons.

Distinguishing morphological features of the third larval stage of ovine Trichostrongylus spp.

In this paper we describe a procedure that enables the identification of species of infective third stage (L(3)) Trichostrongylus larvae. Lambs were infected with putatively monospecific infections of three species of Trichostrongylus commonly found in New Zealand (T. axei, T. colubriformis and T. vitrinus) and Teladorsagia (Ostertagia) circumcincta. After recovering L(3) from faecal cultures, the lambs were slaughtered and adult male worms recovered and examined for spicule morphology to verify identification. L(3) were examined for morphological features and measurement of their length. Further L(3) were exsheathed and examined under high power optics to observe posterior morphological features (tubercles). The posterior of T. colubriformis has a three-tubercle structure whereas T. vitrinus has a single tubercle and T. axei none. However, the tails of T. circumcincta also lack tubercles and thus T. axei cannot be readily distinguished from them on this feature. The range of lengths of L(3) of Trichostrongylus spp. (600-858 microm) and T. circumcincta (700-914 microm) were found to overlap considerably. The shape of the anterior end of these two species differs and this in combination with length provides an indication of the proportion of T. axei and T. circumcincta in a culture. A combination of tubercle number, with overall length and anterior morphology of L(3), can be used to differentiate nematode populations of T. axei, T. colubriformis, T. vitrinus and T. circumcincta.

Production and characterisation of monoclonal antibodies recognising ovine IgE.

Two monoclonal antibodies (mAbs), XB6 and YD3, which recognise ovine immunoglobulin E (IgE) were produced. Mast cells isolated from ovine intestinal mucosa were used as a source of IgE to immunize mice. Culture supernatants of hybridomas were screened by immunoassays on small-intestine tissue sections, isolated mucosal cells, and dot blots of lysed mast cell homogenate. Two mAbs were chosen for their specific binding to mast cells. Antigen bound by these mAbs was purified by immunoaffinity chromatography using XB6 mAb, and this produced two bands consistent with IgE heavy chain (86,000 Daltons) and immunoglobulin light chain (28,000 Daltons) when run under reducing conditions on SDS-PAGE gels. Purified IgE was shown on dot blots to react weakly with mAb to chimeric ovine IgE and strongly to polyclonal anti-sheep antibodies. The two mAbs induced an immediate hypersensitivity-like reaction when injected into the skin of sheep. The mAbs bound to mast cells and other mononuclear cells, presumably IgE-secreting B-cells in mesenteric lymph node sections. These mAbs proved useful for detecting IgE-bearing cells in various ovine tissues, for purifying mast cells from cell isolates by panning and immunomagnetic bead separation, for purifying serum IgE using immunoaffinity chromatography and for detecting IgE in an ELISA. Competitive binding assays showed that the two mAbs bind to different epitopes on IgE. These mAbs will be useful in research applications and in diagnostic assays.

Antibody responses of grazing alpacas (Lama pacos) in New Zealand to intestinal nematodes.

Alpaca (Lama pacos) were grazed for 10 months (October 1992-June 1993) on pasture with sheep or on pasture which had been recently grazed by sheep. The alpaca, of various age groups, totalled 94 at the beginning of the experiment and during the course of the experiment 32 progeny (cria) were born, 10 in spring 1992 and 22 in autumn 1993. Serum levels of specific antibodies to excretory/secretory antigens of the third larval stage (L3) of Cooperia curticei, Ostertagia circumcincta or Trichostrongylus colubriformis and somatic antigens from adult T. colubriformis were determined at monthly intervals by ELISA. Faecal egg count and live-weight were determined monthly and fleece-weight was measured at shearing. Three days after the birth of the cria, serum antibody levels ranged from 0.46-0.85 optical density units for the L3 antigens and averaged 0.22 for the adult T. colubriformis antigen. These levels declined to 0.1-0.24 and 0.06 respectively by 2-3 months of age. Subsequently, antibody levels increased steadily to reach maximal adult levels at approximately 23-26 months. Antibody levels were negatively correlated with FEC, but positively correlated with live-weight at 7 months although at 15 months antibodies and live-weight were negatively correlated. A positive correlation was found between weight and FEC. Fleece-weight showed no correlation with antibody level, a positive correlation with weight and a negative correlation with FEC. The relationships among antibody responses, FEC, live-weight and fleece-weight observed for alpaca in this experiment suggest that antibody responses might provide a useful indicator of alpaca immuno-responsiveness and has potential for use as a parameter for selection of alpaca with reduced FEC.