A Space-time Model of Carbon Translocation along a Shoot Bearing Fruits

A carbon-based model is described of the source-sink relationshipsof a stem bearing fruits in space and time and focusing on growthvariability along the branch. The novelty of the model comesfrom the aggregation of physiological processes taking intoaccount spatial aspects. The stem is represented as a set ofcompartments (metamers) connected to source (leafy shoots) andsink (fruits) compartments. Each leafy shoot forms one compartment.The fruit consists of three compartments involved in translocation(cytoplasm), structure (cell wall) and storage (vacuole). Physiologicalprocesses considered are photosynthesis, respiration of fruitsand leaves, translocation of assimilates and fruit growth. Assimilateproduction is regulated by sink strength. Carbon translocationbetween two compartments depends on the gradient of assimilateconcentration. The gradient induces carbon translocation fromthe most to the least concentrated compartment, except for thevacuole compartment into which translocation is possible whateverthe concentration gradient. Fruit growth, in terms of freshweight, results from the phloem water supplied to the fruitaccording to the concentration gradient between the fruit andthe stem. The model is calibrated for peach trees by comparingobserved and simulated fruit dry and fresh weights for a shootwith normal fruit load. The model simulates variability betweenpeach fruits and the effect of contrasting fruit loads. Accordingto this model, photosynthesis increases and assimilate concentrationsin leaves and phloem decrease with decreasing leaf:fruit ratioas reported in the literature. Simulated concentrations of assimilatesin the phloem range from 2 to 14%. Simulated concentration gradientsand specific mass transfer for peach trees range from 0.05 to0.17 g cm^-3m^-1and from 0 to 3 g cm^-2h^-1, respectively, and areof the same order of magnitude as those reported for variousother tree species. The model is used to analyse the effectof fruit position relative to the leaves. Copyright 1999 Annalsof Botany Company Peach tree, Prunus persica (L.) Batsch, model, carbohydrates, translocation, source-sink, fruit.     

The interaction of soil biota and soil structure under global change

The structural framework of soil mediates all soil processes, at all relevant scales. The spatio-temporal heterogeneity prevalent in most soils underpins the majority of biological diversity in soil, providing refuge sites for prey against predator, flow paths for biota to move, or be moved, and localized pools of substrate for biota to multiply. Just as importantly, soil biota play a crucial role in mediating soil structure: bacteria and fungi aggregate and stabilize structure at small scales (μm–cm) and earthworms and termites stabilize and create larger-scale structures (mm–m). The stability of this two-way interaction of structure and biota relations is crucial to the sustainability of the ecosystem. Soil is constantly reacting to changes in microclimates, and many of the soil–plant–microbe processes rely on the functioning of subtle chemical and physical gradients. The effect of global change on soil structure–biota interactions may be significant, through alterations in precipitation, temperature events, or land-use. Nonetheless, because of the complexity and the ubiquitous heterogeneity of these interactions, it is difficult to extrapolate from general qualitative predictions of the effects of perturbations to specific reactions. This paper reviews some of the main soil structure–biota interactions, particularly focusing on soil stability, and the role of biota mediating soil structures. The effect of alterations in climate and land-use on these interactions is investigated. Several case studies of the effect of land-use change are presented.     

A Comparative Study of 14 Strains of Naegleria australiensis Demonstrates the Existence of a Highly Virulent Subspecies: N. australiensis italica n. spp.1

Fourteen strains of Naegleria australiensis, including the type strain, were compared for virulence for mice, maximum growth temperature, lectin agglutination, isoenzyme pattern, and total protein banding pattern. Their relation to other species of Naegleria also was compared by immunoelectrophoretic analysis. Strains with high virulence, comparable to that of N. fowleri, were found to be different in concanavalin A agglutination as well as with regard to zymograms and total protein patterns. Although serologically different from N. fowleri and reacting with N. australiensis antiserum in the fluorescent antibody test, these high-virulence strains differed in number of immunoelectrophoretic precipitin bands. Because of these results, the high-virulence strains are considered to be a subspecies of N. australiensis. The low-virulence strains showed minor differences from the type strain. Thus, N. australiensis does not appear to be as homogenous a species as N. fowleri. Pathogenic N. australiensis also seems to be more widespread than previously thought.     

Sexual behaviour and evolution of sexual dimorphism in body size in Jaera (Isopoda Asellota)

Individuals of the genus Jaera do not mate at random. In the species from the Mediterranean group, J. italica and. J. nordmanni, large males and medium sized females are at an advantage and their sizes are positively assorted. These effects are attributable to sexual competition between males. In the Ponlo-caspian species J. istri, no advantage of large males exists, but sexual selection could be the cause for a long passive phase prior to copulation and for normalizing selection upon female size at pairing. In the Atlantic species, J. albifrons, no selection can be ascertained.
Differential mating success in males appears as one of the causes of the evolution of sexual dimorphism in body size, which makes males larger, of equal size, or smaller than females according to the species. The reason for this reversal in dimorphism seems to differ in the two sexes. Sexual selection provides an explanation for the evolution of male size, while the interspecific changes in female length are more likely due to ecological factors.     

Effect of a Purified Initiation Factor F3 (B) on the Selection of Ribosomal Binding Sites on Phage MS2 RNA

STUDIES with T4 mRNA showed that initiation factor F2 (C) promotes the attachment of ribosomes to mRNA¹. On the 30S ribosomal subunit this effect is independent of the function of F2 in the binding of formylmethionyl tRNA², whereas formation of a 70S-mRNA complex depends on the binding of fMet-tRNA³. Template competition experiments⁴ showed that, with F2 (C), the ribosome seems to have the same affinity for synthetic polynucleotides as for natural mRNA. Addition of initiation factor F3 (B), however, leads to preferential binding of ribosomes to the natural mRNA. This suggests⁴ that while factor F2 (C) binds the ribosome to any site on the mRNA, the function of factor F3 (B) is to recognize some specific signal in natural mRNA corresponding, perhaps, to the beginning of a cistron. Fractionation of initiation factor F3 (B) into several species differing in their specificity for different mRNA templates⁵ gave further support to the hypothesis that this protein can select binding sites. An excellent system to demonstrate this effect of F3 (B) would be the binding of ribosomes to RNA from E. coli RNA bacteriophages, since Steitz⁶ has analysed and determined the nucleotide sequence of the three binding sites corresponding to the three cistrons of R17 mRNA. Experiments were thus undertaken to study the effect of a purified fraction of F3 (B) on the binding of ribosomes to the different sites of such a phage RNA.