A Bryophyte flora of Kent. II. Hepaticae

Abstract

The military training area on Salisbury Plain contains the largest area of chalk grassland in western Europe. The grassland swards, though relatively tall, are often rich in flowering plant species. The bryophyte flora of areas disturbed in five different ways (prehistoric earthworks, twentieth century rifle ranges, ant-hills, vehicle tracks and shell-holes) was compared to that of adjacent, relatively undisturbed grassland. There was no significant difference in bryophyte cover between quadrats on disturbed ground and the controls, but the disturbed sites supported more bryophyte species per quadrat. Of the 55 taxa recorded, 38 species were at least three times more frequent in the disturbed than the undisturbed sites, compared to four which were at least three times more frequent in the control sites. The species favouring disturbed conditions included several bryophytes characteristically associated with chalk soils in southern England, including some that fruit freely (e.g. Microbryum curvicollum, Tortula lanceola) and others that fruit very rarely (e.g. Abietinella abietina, Entodon concinnus). These results are discussed in relation to the conservation of bryophytes and other disturbance-tolerant and disturbance-dependent species on Salisbury Plain and in the wider context of the protection of the bryophytes of chalkland habitats.     

Identification of 5′-deoxypyridoxine-3-sulfate as the major urinary metabolite of 5′-deoxypyridoxine in rats with comments on the inhibition of arylsulfatase activity and manganese dioxide oxidation by neighboring groups

The major urinary metabolite of 5′-deoxypyridoxine in rats was shown to be identical to 5′-deoxypyridoxine-3-sulfate but different from 5′-deoxypyridoxine-4′-sulfate in its ultraviolet and infrared spectra, its migration in thin-layer chromatography, and its behavior in acid and base. Previous identification of the metabolite as 5′-deoxypyridoxine-4′-sulfate by other workers was based on its failure to be hydrolyzed by arylsulfatase and to be oxidized by manganese dioxide. We have now demonstrated that ortho-methyl groups inhibit arylsulfatase and that ortho-sulfate groups inhibit oxidation by manganese dioxide. Therefore, we conclude that under our conditions the major metabolite of 5′-deoxypyridoxine in the rat was the 3-sulfate.