Host gall size and oviposition success by the parasitoid Eurytoma gigantea

Abstract. 1. Eurytoma gigantea Walsh is a specialist parasitoid of the tephritid gallmaker Eurosta solidaginis (Fitch).
2. In the natural environment the incidence of parasitism by Eurytoma is greater in small galls than in large ones.
3. Laboratory experiments demonstrated that small galls are not more frequently discovered; however, oviposition attempts on small galls were more likely to be successful.
4. Eurytoma spends much time probing galls too big to penetrate; this leads to a decrease in foraging efficiency when many large galls are present.
5. The chance of successfully penetrating a gall depends on the thickness of the gall wall and the length of the parasitoid's ovipositor.
6. A simulation model was constructed which shows that a gallmak-er's chance of being parasitized depends on gall size, the number of parasitoids that discover the gall, and their ovipositor lengths.     

Integrated Analysis of Growth and Light Interception in Winter Lettuce II. Differences between Cultivars

‘Integrated growth analysis’ (emphasizing aspectsof crop and plant structure) and ‘light conversion analysis’(stressing the efficiency of interception and photosyntheticconversion of light) have been used to investigate the wintergrowth of different cultivars of butterhead and crisphead typesof glasshouse lettuce. Measurements from ‘Ambassador’ (large-framed butterhead),‘Renate’ (medium-sized butterhead) and ‘Cristallo’(crisphead) were made, statistical progressions were fittedto the primary data and hence estimates of all the analyticalcomponents were derived. Curves for crop growth rate, like those for most other components,followed a generally similar pattern for all three cultivars.In integrated growth analysis, the biomass curve for Ambassadorlay above the curves for the other cultivars. The weight advantagewas initially 60 per cent and it persisted with only a smallreduction (to 40 per cent) until the final harvest. Relativegrowth rate varied little between cultivars because differencesobserved in leaf area ratio were complementary to those seenin net assimilation rate. In light conversion analysis, differences in light interceptingefficiency between cultivars were not statistically significant,though Ambassador attained full interception 4 days earlierthan Renate and 6 days earlier than Cristallo. Differences inlight utilizing efficiency were small and non-significant exceptduring the post-rosette stage when the value for Renate waslower than that of either Ambassador or Cristallo. Deviationsaround the fitted curves were correlated with fluctuations inthe light regime. An assessment is made of the utility and limitations of thetwo procedures. It is concluded that both approaches can assistin analyzing the rate of dry matter production in crops or plantstands. Integrated growth analysis is advantageous when theneed arises to treat individual and population-based attributessimultaneously, while light conversion analysis provides a meansof explicitly incorporating the primary environmental variableinfluencing growth. Lactuca sativa L., lettuce cultivars, growth analysis, crop growth rate, relative growth rate, light interception, light utilization     

Cell Adhesion as a Basis of Pattern in Embryonic Development

The development of the modern methodologies of cell biologyin the fifties and sixties and of molecular biology in the seventiesand eighties has led to a reductionist view of embryonic developmentthat centers on the cell and the gene as the functional unitsof development. The functional units in most inductive and morphogeneticprocesses in the embryo are not single cells, however, but ratherare collectives of interacting cells that give rise to the tissuesand organs. Can these methodological developments reconcilea molecular analysis with the fact that form arises epigeneticallyfrom the increasing number of embryonic cells during development?To answer this question one must link genetic regulation tomechanochemical processes that coordinate cell division, cellmovement and cell death. Recent studies of cell adhesion suggestthat one such link is provided by cell adhesion molecules (CAMs)that mediate cell-cell binding. These studies suggest that CAMsare involved in defining cell collectives and their bordersas they interact during inductive events in morphogenesis. AlthoughCAMs cannot be considered the "cause" of induction, they playkey roles among the complex causal chains of inductive interactionsinvolving hormones and growth-factors, extracellular matrixcomponents and cellular receptors. We provide here a brief summaryof modern developments in the field centered about the functionof CAMs in morphogenesis and using recent experimental resultsin the developing feather as a paradigmatic example.     

EVALUATION OF THREE SCALING METHODS FOR HEDONICS

A collaborative study of twenty-three laboratories was conducted to compare the relative effectiveness of three scales: two forms of magnitude estimation scaling and one form of a category scale in the measurement of hedonic response to a controlled stimulus. Responses from 553 individual judges show that all scales yield hedonic measurements that are very similar in both direction and magnitude of difference between the stimuli. No scale showed any clear superiority in reliability, precision, or discrimination. Selection of a scale must be based on considerations other than the simple form of response.     

Coated Vesicles from the Protozoan Parasite Trypanosoma brucei: Purification and Characterization

ABSTRACT. A procedure was developed to purify a coated vesicle fraction from the protozoan parasite Trypanosoma brucei. Electron microscopy revealed a difference between T. brucei coated vesicles and clathrin-coated vesicles from other eukaryotes: trypanosome vesicles were larger (100 to ISO nm in diameter) and contained an inner coat of electron-dense material in addition to the external coat. Evidence suggests that the internal coat is the parasite's variant surface glycoprotein (VSG) coat. The SDS-PAGE analysis shows the major protein of T. brucei coated vesicles has a molecular mass of 61 kD, similar to VSG; this protein was recognized in an immunoblot by anti-VSG serum. Trypanosome coated vesicles also contain a protein which comigrates with the major protein (clathrin) of coated vesicles purified from rat brains. However, this protein is a minor component and it is not serologically cross-reactive with mammalian clathrin. Immunoblot analysis demonstrated that the parasite vesicles contained host IgG, IgM, and serum albumin.