SHELL COLOUR IN CALLIOSTOMA ZIZYPHINUM (L.) FROM STRANGFORD LOUGH, N. IRELAND

Shells of Calliostoma zizyphinum taken from Strangford Lough,N. Ireland are divisible into three distinct colour forms: white(=var lyonsi) intermediate (a pale variegated form) and purple(a dark variegated form). The predominance of white and paleshelled individuals within and the absence of white Calliostomaoutside the lough was confirmed. The proportions of animalswith white and variegated shells at selected sites were almostidentical with those previously documented, suggesting a temporalstability of colour form ratios. No differences in shell thicknessand pedal adhesion were demonstrated between these forms. Snails with white shells reflect radiant heat better, have lightercoloured feet, move more rapidly, show a greater incidence ofshell repair and are more frequently exposed on weed at lowtide, than those with either intermediate or purple shells.Increased proportions of white individuals may be associatedwith high population densities. Under such circumstances, itis suggested that increased mobility may, by increasing dispersion,reduce intraspecific competition. In the event of exposure atlow tide a white shell would help minimize thermal stress. (Received 9 February 1987;     

The Generation of Non-Spherical Oat Protoplasts Indicates that Hyperpolarization is both Necessary and Sufficient for Stimulating Membrane Incorporation into the Plasma Membrane

We have devised conditions which produced isolated protoplastsof non-spherical shape and which, therefore, affected the mechanismsthat control the exchange of membrane material between the plasmamembrane and an intracellular membrane reservoir. Non-sphericalprotoplasts of Avena sativa were obtained if protoplasts weretreated with hypertonic shock in the presence of 1.0 mol m^–3LaCl₃ at pH 8.3. This indicated that their ability to removeplasma membrane material via endocytotic vesiculation was suppressed.Non-spherical protoplasts were obtained under isotonic conditionsif protoplasts were incubated with 1.0 mol m^-3 LaCl₃ at pH 8.3and the proton carrier CCCP (12 mmol m^–3) was added. Thenon-spherical protoplasts had intact membranes as judged bystaining with fluorescein diacetate. The loss of the sphericalshape was reversible. On addition of EDTA protoplasts resphericulatedimmediately. Incubation in isotonic solution at pH 8.3 containingeither only 1.0 mol m^–3 LaCl₃ or only CCCP did not influencethe protoplast shape. We conclude that the membrane hyperpolarizationinduced by CCCP at high pH acted to stimulate the incorporationof membrane material into the plasma membrane and, subsequently,produced nonspherical protoplasts if the removal of membranematerial was simultaneously suppressed. This demonstrates thatmembrane incorporation and removal are two largely independentprocesses.     

Tinopal AN as a selective agent for the differentiation of phytopathogenic and saprophytic Pseudomonas species

The selective toxicity of the respiratory inhibitor Tinopal AN (1,1-bis (3, N -5–dimethylbenzoxazol-2-yl) methine p -toluene sulphonate) towards phytopathogenic bacteria was investigated further and in general was confirmed using more than 160 additional strains of Pseudomonas spp. The mechanism(s) of the resistance shown by saprophytic fluorescent pseudomonads were studied to elucidate the differences between resistant saprophytic and sensitive phytopathogenic Pseudomonas species. Damage to, or partial removal of the cell wall of Tinopal AN-resistant Pseudomonas aeruginosa , resulted in a marked Tinopal AN-sensitivity, as judged by the ability of Tinopal AN to inhibit oxygen uptake. Furthermore, removal of part of the lipo-polysaccharide (LPS) component of the outer membrane also resulted in sensitivity. Mutants of Ps. aeruginosa with modified outer cell walls were tested for their reactions towards Tinopal AN, and two cell wall lipopolysaccharide (LPS) mutants of Escherichia coli (env Al) and Salmonella typhimurium (rfa) were, in contrast to the wild-type strains, found to be sensitive towards Tinopal AN. The results therefore suggest that the resistance of saprophytic pseudomonads towards Tinopal AN is due (at least in part) to the selectively permeable properties of the outer membrane of the cell wall. The usefulness of Tinopal AN for screening potentially phytopathogenic strains of Pseudomonas was confirmed.