Ichnogenus Corophioides

Knox, Robert W. O'B.: Ichnogenus Corophioides.
A re-examination of syntypes and topotypes of the type species, Corophioides polyupsilon , shows that its structure is distinct from that of the other forms ascribed to the ichnogenus. An emended diagnosis of the ichnogenus is given, restricting it to forms which show a true U-within-U structure. Most of the species formerly included in Corophioides Smith 1893 can be referred to Diplocraterion Torell 1870, but in some cases a re-examination of the type material is necessary.     

Intercellular adhesion and cell separation in plants

Adhesion between plant cells is a fundamental feature of plant growth and development, and an essential part of the strategy by which growing plants achieve mechanical strength. Turgor pressure provides non‐woody plant tissues with mechanical rigidity and the driving force for growth, but at the same time it generates large forces tending to separate cells. These are resisted by reinforcing zones located precisely at the points of maximum stress. In dicots the reinforcing zones are occupied by networks of specific pectic polymers. The mechanisms by which these networks cohere vary and are not fully understood. In the Poaceae their place is taken by phenolic cross‐linking of arabinoxylans. Whatever the reinforcing polymers, a targeting mechanism is necessary to ensure that they become immobilized at the appropriate location, and there are secretory mutants that appear to have defects in this mechanism and hence are defective in cell adhesion. At the outer surface of most plant parts, the tendency of cells to cohere is blocked, apparently by the cuticle. Mutants with lesions in the biosynthesis of cuticular lipids show aberrant surface adhesion and other developmental abnormalities. When plant cells separate, the polymer networks that join them are locally dismantled with surgical precision. This occurs during the development of intercellular spaces; during the abscission of leaves and floral organs; during the release of seeds and pollen; during differentiation of root cap cells; and during fruit ripening. Each of these cell separation processes has its own distinctive features. Cell separation can also be induced during cooking or processing of fruit and vegetables, and the degree to which it occurs is a significant quality characteristic in potatoes, pulses, tomatoes, apples and other fruit. Control over these technological characteristics will be facilitated by understanding the role of cell adhesion and separation in the life of plants.     

Pollen-wall Proteins: 'Gametophytic' and 'Sporophytic' Fractions in the Pollen Walls of the Malvaceae

Proteins are stored in two sites in the pollen grain walls ofthe Malvaceae, (a) in the cellulosic intine, mainly in the vicinityof the circular apertures, and (b) in cavities in the sculpturedlayer of the exine. The intine-held materials are incorporatedduring the growth of the wall. The exine materials are derivedfrom the tapetum, which during dissolution releases cistemaewith a granular-fibrillar content bounded by ribosomal membranes.This fraction is injected into the exine cavities after thecompletion of wall growth through micropores in the tectum.PAS-reacting material is associated with the injected protein.Another tapetal fraction, lipid in nature and commonly containingcarotenoids, remains on the surface of the pollen grains toform the Pollenkitt. While protein can be detected cytochemically in both intineand exine sites, acid phosphatase and ribonuclease activitywas found to be associated only with the former. Immunofluorescencemethods using antiserum to total pollen leachates showed thatantigens are present in both sites. When the pollen grains are moistened, the exine-held proteinsbegin to pass out through the micro-pores in the tectum within30 s of moistening, while the main discharge from the aperturalintine follows in 4–5 min. These observations, together with evidence from other families,suggest that the intine-held proteins of angiosperm pollen grainsare always produced by the male gametophyte, while those heldin exine cavities are sporophytic in origin, being derived fromthe tapetum. As previously proposed, it seems probable thatin intraspecific incompatibility systems of the gametophytictype control is mediated through intine-held ‘recognitionsubstances’, whereas in sporophytic systems the exine-heldmaterials are concerned.     

Pollen Development and Quantitative Cytochemistry of Exine and Intine Enzymes in Sunflower, Helianthus annuus L

High resolution cytochemical methods have been used to characterizepollen development and pollen-wall structure in Helianthus annuus.Aniline-blue fluorescent material, presumably callose, was detectedin the nexine layer throughout its development. It was associatedwith acid phosphatase activity, while the outer sexine possessedintense esterase activity during the young spore period. Acidphosphatase and esterase were present in both intine and exinewall sites in contrast to their specific location in other pollentypes. Quantitative cytochemical estimates of enzyme activityduring development reveal esterase patterns typical of gametophyticsynthesis, while acid phosphatase patterns are characteristicof sporophytic origin suggesting tapetal transfer during thevacuolate period. Helianthus annuus L, sunflower, pollen development, exine enzymes, intine enzymes, quantitative cytochemistry