Morphology and innervation of the buccal glands of the Southern Hemisphere lamprey, Geotria australis.

The buccal glands of adults of the Southern Hemisphere lamprey Geotria australis consist of a pair of small, bean-shaped, hollow sacs, embedded within the basilaris muscle in the region below the eyes and to either side of the piston cartilage. Each gland, which is lined by a simple columnar epithelium and surrounded by an incomplete layer of skeletal muscle, discharges its contents into the oral cavity via a long, narrow duct. In downstream migrating young adults, the epithelial cells are low columnar, intermediate in electron density, and contain dark-staining inclusions and numerous lipid-like droplets. After saltwater acclimation, the epithelial cells become taller and the numbers of dark-staining inclusions increase whereas those of lipid-like droplets decline. By the end of the marine phase, the epithelium is more folded and now also contains dark and light cells. The ultrastructure of the epithelium shows the characteristics of both apocrine and merocrine secretion. Although intra-epithelial nerve endings were not observed, axons and occasional neurons are present in the lamina propria. Since the skeletal muscle capsule is also well innervated and contains neurons, a local feed-back mechanism may regulate the release of buccal gland fluid by monitoring the luminal pressure. Contractions of the skeletal muscle capsule and movements of the basilaris muscle during feeding would presumably assist the movement of secretion along the duct. The secretion possesses anticoagulating and haemolytic properties.     

Alteration of sea urchin embryo cell surface properties by mycostatin, a sterol binding antibiotic

Sea urchin embryos incubated in sea water containing mycostatin (MST), a polyene antibiotic, dissociate into single cells. Reaggregation of dissociated sea urchin embryo cells, and uptake of labeled precursors by these cells are also greatly inhibited although O₂ consumption is only slightly affected by this compound. It is known that mycostatin binds primarily to membrane sterols and affects only cells containing membrane sterols. Sea urchin cell membranes contain sterols. The effects of mycostatin on cell adhesion, reaggregation, and permeability seen in this study may be a result of an interaction with cell membrane sterols or sterol-associated molecules.     

Zinc efficiency of oilseed rape (t Brassica napus and t B. juncea) genotypes

Twenty five genotypes of oilseed rape (canola and mustard) were tested under varied supply of Zn (+Zn: 2 mg kg^–1 soil, -Zn: no Zn added) in two pot experiments in soil culture to determine the genotypic variation in tolerance to the Zn-deficient conditions, that is, to identify the Zn-efficient genotypes. On the basis of performance of genotypes in pot experiments, ten genotypes were tested in 1995 for their performance under varied supply of Zn (+Zn: 3.5 kg ha^–1, -Zn: no Zn added) on a Zn-deficient field in South Australia.Zn efficiency (ratio of shoot dry matter in -Zn to shoot dry matter in +Zn treatment and expressed in percentage) in pot Experiment 1 varied from 35% for 92-13 to 74% for Siren. Narendra, Dunkeld, Barossa, Oscar and Xinza 2 performed well under -Zn treatment. Zn efficiency in Experiment 2 varied from 32% for Wuyou 1 to 62% for Pusa Bold. Pusa Bold and CSIRO-1(mustard genotypes) were the most efficient in terms of dry matter production among all the oilseed rape genotypes tested. Root dry matter accumulation was significantly higher in Zn-efficient genotypes. Zn efficiency (ratio of seed yield in -Zn to seed yield in +Zn and expressed in percentage) in field experiment varied from 62% for Huashang 2 to 76% for Dunkeld. With few exceptions, the ranking of genotypes in pot and field experiments indicates similarity in their response to Zn deficiency. There looks to be genetic control over Zn concentration in tissues. Zn-efficient genotypes had lower Zn concentration in roots and higher Zn concentration in youngest fully opened leaf blades, indicating a better transport of Zn. This, together with a higher Zn uptake, appears to be the basis of expression of Zn efficiency.