Solute Leakage from the Isolated Parenchyma of Allium cepa and Kalanchoe daigremontiana

Efflux of different solutes from leaf slices of Kalanchoëdaigremontiana and from slices of the onion bulb scale was reinvestigatedwith respect to (1) dependence on turgor, (2) selectivity, (3)integrity of protoplasts and cellular changes. In both materials efflux of solutes (electrolytes or sugars)is non-selective and strongly dependent on turgor. Treatmentof tissue slices with hypotonic solutions (below a criticalosmotic pressure) resulted in high leakage rates, an increasein free space and an increased number of damaged cells. Lowconcentrations of calcium did not prevent this loss of retentionand cell stability. Part of the surviving cells were found to have a strongly decreasedosmotic pressure of cell sap. Leakage did not occur simultaneouslyat all cells of the tissue slice. It can be concluded that effluxfrom parenchyma cells in hypotonic solutions results from irreversibleosmotic breakdown and reversible membrane defects both favouredby high turgor. Key words: Parenchyma cells, Allium cepa, Kalanchoé daigremontiana, Solute efflux, Viability, Permeability, Plasmoptysis     

Ribosomal RNA Sequencing of Members of the Crypthecodinium cohnii (Dinophyceae) Species Complex; Comparison with Soluble Enzyme Studies

ABSTRACT. Sixty-five members of the Ctypthecodinium cohnii species complex were analyzed for sequence differences within the D2 region of the 23S ribosomal RNA molecule. On the basis of 46 sequence differences the strains fell into 19 distinct ribosets (strains of identical sequence), some with many members. Members of four of the seven major sibling species (widespread breeding groups) were each found within single ribosets. Members of three other major sibling species were each, however, divided into two ribosets by a single sequence difference correlated with geographic separation and with previously reported electrophoretic polymorphisms of soluble enzymes within the sibling species. In addition to members of major sibling species, some ribosets include many minor sibling species (each represented by only one strain). Of 38 minor sibling species, 22 shared sequence with a major sibling species. Of these 22, 14 were identical in soluble enzymes to their related major sibling species or differed by only one of three enzymes. Other minor sibling species appear to have diverged extensively from any others in both rRNA sequence and electrophoretic profile. As a group, major sibling species differ markedly in the number of minor sibling species associated with them, suggesting differences in frequency of sexually isolating events in their past histories. These findings are discussed in the context of the previously proposed model of sympatric speciation.     

Size and function of ammonite aptychi in comparison with buccal masses of modern cephalopods

Morton, Nicol & Nixon, Marion 1987 07 15: Size and function of ammonite aptychi in comparison with buccal masses of modem cephalopods.
Previous impressions that the size of ammonite aptychi is unusually large, thereby posing a problem to their interpretation as part of the jaw apparatus, are shown to be incorrect. The relative length of the aptychus for at least the Jurassic ammonite groups studied, at approximately 15% of the length of the body chamber, is remarkably constant in different taxonomic groups and sizes. This is well within the range for buccal mass length as percentage of mantle length of living cephalopods, being most similar to Octopus and Sepia and much smaller than Nautilus. The height and width of aptychi relative to whorl height and width are larger but again ammonites are probably not significantly different from modern cephalopods. The size and design, with no obvious structures for biting or crushing, suggest that ammonites were adapted to a particular type of relatively unspecialised feeding in which mostly small animals were ingested, possibly with some external digestion. The large shovel-like lower jaw may have functioned like a scoop for collecting large quantities of water and small prey, and movement of the buccal complex with the upper jaw almost closed against the lower jaw could have expelled water while retaining captured prey. Calcification of aptychi may have been protective, but more likely acted to weight the buccal mass for nektobenthic feeding and to make it more rigid.     

Cuticular lipid differences between the malaria vector and non-vector forms of the Anopheles maculatus complex

Two chromosomal forms (E and F) of the Anopheles maculatus Theobald complex were distinguished by gas-liquid chromatographic (GC) analysis of cuticular lipids in association with a multivariate principal component analysis. The GC chromatogram obtained from n-hexane extracts of individual specimens showed no consistent qualitative differences in normalized peak areas between forms. Of the seventeen consistent peaks, five were found to be quantitatively different between forms at a high (99.5-99.95%) level of statistical confidence. Relative ratios of these five quantitatively different GC peaks were used as criteria to distinguish single specimens as either form E or form F. Chemical structures of the five GC peaks were assigned by both electron impact and chemical ionization gas chromatography/mass spectrometry analysis. The first three peaks, which were always doublets, were partially resolved saturated and mono-unsaturated free fatty acids; the other two peaks were n-alkanes. Principal component analysis substantiated that the vector form E has very similar cuticular lipid profiles and is well separated from the non-vector form F.