NOTES ON GEOGRAPHICAL VARIATION AND THE ANNUAL CYCLE IN PATAGONIAN POPULATIONS OF THE RUFOUS-COLLARED SPARROW ZONOTRICHIA CAPENSIS

Zonotrichia capensis australis inhabits Argentina from the northernmost limits of the Patagonian steppe south through Tierra del Fuego, and extends westward to the Pacific slope in southern Chile. At least part of the population has a north-south migration along the Andean foothills of Argentina as far north as southwestern Bolivia. The breeding range of australis is bounded on the north and northwest by subspecies of Z. capensis (chilensis, choraules , and possibly hypoleuca ) having conspicuous black lateral crown-stripes. Topotypical australis (Tierra del Fuego) have plain grey crowns, but the frequency of black nuchal markings and faint lateral crown-lines increases northward in the coastal populations. In inland populations (Andean piedmont) the frequency of black crown markings is apparently reversed, increasing southward. The size (wing-length, tarsus, bill, and probably body-weight) of australis decreases northward in both coastal and inland samples.
The nesting season of australis begins in late November and early December and extends to mid January and early February. Postnuptial moult begins from mid December to early January. Moult proceeds while the testes are apparently still functional. Postnuptial moult terminates from late January through mid March. There is no evidence in the current data of geographical trends in the chronology of nesting and postnuptial moult. The calendars appear to be about the same throughout the range of australis .
Postjuvenal moult begins about 4–5 weeks later than the onset of postnuptial moult and terminates in the latest birds in about mid March. Northward migration begins at about this time.     

Clinal variation at aspartate aminotransferase-2 in spotted seatrout,Cynoscion nebulosus (Cuvier), inhabiting the north-western Gulf of Mexico

Clinal variation was observed at the aspartate aminotransferase-2 (AAT-2) locus in the marine fish Cynoscion nebulosus (Cuvier) inhabiting the bays and estuaries of the Texas and northern Mexico Gulf coasts. Frequency of the AAT-2(80) allele increased from 0.9% at Sabine Lake, Texas to 17.1% at Rio Soto La Marina, Mexico. A statistically significant correlation existed in the frequency of this allele with degrees north latitude and west longitude. This information, if properly incorporated into a comprehensive enhancement programme, could facilitate supplemental stocking success.     

The fleas of a population of weasels in Wytham Woods, Oxford

Weasels were regularly livetrapped, anaesthetized and searched for fleas over two years, in Wytham Woods, near Oxford. Eleven species of fleas were identified among 262 collected. Seven normally occur on small rodents, one on rats, two on moles and one on birds. Fleas were collected on 103 of 338 occasions when an unconscious weasel was examined; on average males carried 0·6 fleas, females 1·5 fleas, but there was no significant difference between the proportion of males and females infested. The species distribution of the fleas on weasels in Wytham suggests that they acquire their fleas mainly from the nests and runways of their prey, which they have hunted through or taken over. Important prey, e.g. birds (22% of prey items identified) with uninviting nests contributed few fleas (2%); non-prey, e.g. moles (0–4% of items) with highly desirable nests, contributed disproportionately many, including 35 fleas (15%) of two species otherwise monoxenous on moles. A similar pattern is shown by the fleas carried by stoats in New Zealand.     

A comparison of two autoradiographic methods for detecting radiolabeled nucleic acids in embryos.

Two methods for preparing embryos for autoradiographic study of newly synthesized nucleic acids are described and compared. The first method consists of rapidly fixing radiolabeled embryos with acetic acid:methanol, spreading them on glass slides and exposing them for 8 days with a photographic emulsion. The second method consists of fixing, embedding in resin, and sectioning the embryos before their exposure with the emulsion for 3 weeks. Both techniques have many applications in studies of early embryonic activity, but the spread technique is very sensitive, simpler, and faster.     

Polymerization mechanism of polypeptide chain aggregation

The misfolding of polypeptide chains and aggregation into the insoluble inclusion body state is a serious problem for biotechnology and biomedical research. Developing a rational strategy to control aggregation requires understanding the mechanism of polymerization. We investigated the in vitro aggregation of P22 tailspike polypeptide chains by classical light scattering, nondenaturing gel electrophoresis, two-dimensional polyacrylamide gel electrophoresis (PAGE), and computer simulations. The aggregation of polypeptide chains during refolding occurred by multimeric polymerization, in which two multimers of any size could associate to form a larger aggregate and did not require a sequential addition of monomeric subunits. The cluster-cluster polymerization mechanism of aggregation is an important determinant in the kinetic competition between productive folding and inclusion body formation. (c) 1997 John Wiley & Sons, Inc. Biotechnol Bioeng 54: 333-343, 1997.