Microsatellites and 16S sequences corroborate phenotypic evidence of trans-Andean variation in the parasitoid Microctonus hyperodae (Hymenoptera: Braconidae).

Eight South American geographical populations of the parasitoid Microctonus hyperodae Loan were collected in South America (Argentina, Brazil, Chile and Uruguay) and released in New Zealand for biological control of the weevil Listronotus bonariensis (Kuschel), a pest of pasture grasses and cereals. DNA sequencing (16S, COI, 28S, ITS1, beta-tubulin), RAPD, AFLP, microsatellite, SSCP and RFLP analyses were used to seek markers for discriminating between the South American populations. All of the South American populations were more homogeneous than expected. However, variation in microsatellites and 16S gene sequences corroborated morphological, allozyme and other phenotypic evidence of trans-Andes variation between the populations. The Chilean populations were the most genetically variable, while the variation present on the eastern side of the Andes mountains was a subset of that observed in Chile.

Wool growth rate in vitro is independent of host animal nutrition, season, and the potential mediators of photoperiod, melatonin and prolactin.

In most sheep breeds, wool growth varies seasonally and is correlated with changes in photoperiod, temperature, and nutrition. Wool growth regulation by these factors may result from systemic changes, or to a response localized at the wool follicle. Possible roles of systemic and local factors have been examined here by comparison of wool growth responses in vitro and in vitro. Wool follicles were isolated and maintained under conditions facilitating fibre growth for at least 4 days. The wool growth rate by follicles isolated regularly over a 10 month period was invariate (P > 0.10), in contrast to a seasonally varying wool growth rate by follicles from the same animals in vivo (P < 0.001). Although a high energy, high protein diet increased wool growth in vivo (P < 0.05), cultured follicles isolated from these animals showed no change in growth rate (P > 0.10). These observations suggest that the regulation of wool growth by environmental factors is extrafollicular and that there is no carryover of the in vivo growth rate when follicles are isolated and systemic signals are therefore removed. Additional work discussed here examined the regulation of pelage by prolactin and melatonin, potential endocrine mediators of photoperiod. The fibre production rate by isolated follicles maintained in control media was not different to that of prolactin or melatonin supplemented follicles (P > 0.10). It is concluded that selective breeding of domesticated sheep has suppressed the response of follicles to regulation by prolactin and melatonin. Studies currently underway using in situ RT-PCR will provide further characterization of this conclusion.