Apoplastic Phloem Unloading in the Stem of Bean

Sucrose has been found in the apoplast of bean stems at a concentrationof 25–60 mM with an axial concentration gradient in theappropriate direction for Munch translocation. Removal of theepidermis from a 50 mm length of stem enabled the washout oflabelled photosynthate from the apoplast. The rate of labelwashout was strongly dependent on temperature, and the rateincreased on blockage of phloem pathways to the main sink forthat assimilate. Washout did not reduce when the bathed tissuewas plasmolyzed. We propose that sucrose is unloaded from thephloem into the apoplast, and a sucrose concentration is maintainedthere by a balance of sucrose uptake into sink tissue or reloadinginto the phloem. It is proposed that the apoplastic pool ofphotosynthate can act to buffer sudden changes in phloem contentswhen there are rapid changes in source-sink configuration. Key words: Sucrose, Phaseolus vulgaris, Apoplast, Phloem unloading     

Phloem Loading and Transport of Endogenously or Exogenously Labelled Photo-Assimilate in Bean, Beet, Maize and Cucurbit

Transport of carbon-11 labelled photo-assimilate was monitoredin Phaseolus vulgaris. Beta vulgaris, Zea mays, and Cucwbitopepo. The region of leaf to be labelled was first abraded anda solution passed over it to gain access to its apoplast andmonitor changes in label therein. With PCMBS in the bathingsolution the rate of washout of label into the bathing solutionincreased, but the effect of phloem loading was very variablefor each species: on some occasions transport was hardly affected,on others it was halted. This was true even for Cucurbito pepo,where a symplastic pathway of loading has been widely acceptedand suggests that PCMBS affects symplastic transport or thatthere is an apoplastic step in Cucurbito pepo. Apoplastic pHhad little effect on transport or label washout unless a veryacid (pH 40) buffer was introduced, contrary to notions of hydrogenion co-transport for sugar uptake. Anoxia caused phloem loadingto decrease immediately and label washout to increase in allspecies. It is suggested that both symplastic and apoplasticpathways can operate in all species but that their proportionvaries according to species and ambient and/or growth conditions. Key words: Phloem loading, photo-assimilate transport     

Interspecific relations of African crocidurine shrews (Mammalia: Soricidae) based on multivariate analysis of mandibular data

Eighteen graded non-metric characters and 30 measurements of the mandible and lower dentition were used to investigate the grouping of African species of the genera Crocidura, Suncus and Sylvisorex. Seventy-seven taxa (species, subspecies and synonyms), including four European species, were represented by one to nine mandibles (147 mandibles in all), and the means of four Pleistocene African species were also included. The metric data were subjected to principal component and canonical variate analyses, and the non-metric data to principal component analysis. Grouping was detected by comparing the results of the three analyses. Six groups are recognized within the genus Crocidura , typified by C. fumosa, C. turba, C. russula, C. fuscomurina, C. hirta and C. flavescens. Sylvisorex is divisible into two groups, typified by S. lunaris and S. granti. The African species of Suncus (but not the introduced species, S. murinus ) form a single group, which is linked to the Sylvisorex granti group. Suncus is closely related to, or convergent with, the Crocidura fuscomurina group. The first non-metric principal component, the second metric principal component and the second canonical variate are significantly correlated. It is considered that these together represent a general trend of evolutionary advance. Phylogenetic relations are discussed in the light of this; Crocidura may be diphylefic.     

Isoperoxidases in Epidermal Layers of Tobacco and Changes during Organ Formation in vitro

The content and pattern of soluble isoperoxidases were determined in epidermal explants taken from different internodes of tobacco plants in the vegetative and floral states. There were qualitative and quantitative differences in the isoperoxidases, with a decrease in content and fewer bands being observed acropetally, i.e., in going from the base of the stem towards the apex. Epidermal explants from floral branches were grown in in vitro culture, with various media moditications, to form de novo floral or vegetative buds, roots or callus. Changes in soluble isoperoxidases were followed electrophoretically in relation to these varying morphogenetic pathways. In each of them, the number of bands increased on both the anodic and cathodic sides with time in culture. Compared to each other these four morphogenetic programmes were different in their peroxidase zymograms, mainly through varying kinetics in the development of activity of the isoenzymes. The changes observed during root and vegetative bud formation agree with previously published data, and the changes during floral bud formation agree with those observed in vivo.     

Microevolution and taxonomy of European reptiles with particular reference to the grass snake Natrix natrix and the wall lizards Podarcis sicula and P. melisellensis

The grass snake Natrix natrix and the wall lizards Podarcis sicula and P. melisellensis are used as examples to compare the procedure and achievements of the conventional approach to naming subspecies with the use of multivariate morphometries to investigate racial differentiation.
The conventional procedure, which has changed little over the last 50 years, fails to take into account the appropriate evolutionary facts or refer to any abstracted levels of divergence necessary for subspecific recognition. Consequently, the patterns of population differentiation are obscured by the recognition of a large number of rather meaningless subspecies. There is a tendency to section clines into artificial categories and arbitrarily delimit subspecies by physiographic features.
On the other hand, the use of multivariate morphometries reveals the patterns of population differentiation which can be related to geological events and patterns of differentiation in other species and species groups. The nature of 'hybrid' zones and population differentiation enables the relative importance of evolutionary forces such as gene flow, selection and genetic drift to be discussed and provides evidence concerning speciation mechanisms. These techniques also contribute to the discussion regarding the nature of species and provide abstracted and operational criteria for taxonomic decisions.
The difference between the results of multivariate analysis and the conventional approach cannot be explained solely on the basis of choice of characters. Some of the advantages and disadvantages of using multivariate morphometries, as opposed to other modern techniques, for investigating racial affinities are discussed.     

BIOMETRIC ANALYSIS OF GEOGRAPHIC VARIATION AND RACIAL AFFINITIES

1. The study of geographic variation and the racial affinities between populations is of central importance to systematics and evolutionary theory. When using phenotypic variation to measure the similarity between the populations of a species one should analyse the variation in several characters simultaneously. This is a statistical procedure and is known as multivariate analysis. Multivariate analysis of phenotypic variation, unlike some other methods, has the advantage of not being dependent on living specimens. 2. To obtain an adequate sample at each locality, and an adequate distribution of localities within a given geographic area, can be a major problem. The pooling of data from adjacent localities is discussed. 3. There are several sources of phenotypic variation within a species, e.g. sexual and ontogenetic variation. Failure to eliminate the non-geographic sources of variation can confuse the assessment of the similarity between populations. 4. Correlation between characters can reflect similar genetic control and/or similar patterns of geographic variation, the biological interpretation being influenced by whether the data come from one locality or many. 5. The influences of environmental induction and genetic control cannot easily be separated. Also, some characters may not be entirely homologous throughout the range of the species. 6. Most studies rely on far too few characters of a too restricted type to give an ‘overall’ assessment of the phenotypic similarity. This is one of the most neglected aspects of the study of geographic variation. 7. The various forms of clinal and categorical variation, the precise nature and position of sharp transition (hybrid) zones, the relationship between non-adjacent as well as adjacent populations and the phenotypic divergence between island populations, etc., all come under the heading of geographic variation. The ideal technique should be able to elucidate all types of geographic variation but some techniques can only be used effectively with a few of them. Moreover, techniques may be limited in their application because they require the data to conform to certain models, e.g. normal distribution. 8. The degree of phenotypic similarity between populations can be measured by a wide range of similarity coefficients. Comparison between even a small series of populations produces a large set (or matrix) of similarity coefficients that is difficult to interpret. However, the relationships between populations can be summarized in several ways and these may be loosely grouped into four categories; (i) network diagrams, (ii) contours and isometric plots, (iii) hierarchical clusters, and (iv) ordination methods. These methods are explained and their advantages and limitations discussed. 9. The hierarchical (dendritic) model of cluster analysis is unsuitable for analysing all but a few types of geographic variation. 10. There are several types of ordination technique. They all aim to summarize the variation of many characters in a reduced number of axes. One can either emphasize the biological interpretation of each separate axis, or treat the analysis as a classifying technique and assess the grouping of the populations in the space defined by the axes. Considerable care is needed in interpreting the results of both of these approaches. If correctly applied, ordination techniques generally can be used to analyse all the forms of geographical variation and are therefore recommended. Contrary to current practice they can be used with a large number of characters. The advantages and limitations of the various ordination techniques are discussed. 11. Contours and their three-dimensional isometric plots can be used to portray geographic variations in the information obtained from a multivariate analysis. However, contours and isometric plots are limited in their applicability and the amount of information they can convey. 12. The sophistication of some multivariate methods should not be allowed to cloak the scientific inadequacies of a study. The use of more than one technique and variety in the choice of pertinent parameters may be of value in indicating the reliability of the results.     

Biochemical genetics and taxonomy in Plumatella fungosa and P. repens (Bryozoa: Phylactolaemata)

SUMMARY. Some authors have recently concluded that, using morphological criteria, the freshwater bryozoans Plumatella repens and P. fugosa cannot be separated and should be regarded as conspecific. To test this conclusion, electrophoretic techniques have been used to examine genetic differences between the two nominate species at several enzyme loci. Significant variation at a malate dehydrogenase locus and three aminopeptidase loci establish beyond doubt that P. repens and P. fugosa are separate but related species. No significant variation was found between two populations of P. repens . Morphological characters for the distinction of the two species are discussed and evaluated.