Ecology shapes metabolic and life history scalings in termites

1. Metabolic rate (B) is a fundamental property of organisms, and scales with body mass (M) as B = αM^β. There has been much debate on whether scaling parameters should be viewed as constants or variables. However, there is increasing evidence that ecological differentiation can affect both α and β. 2. In colonial organisms such as social insects, individual metabolism is integrated at the colony level. Theory and data suggest that whole‐colony metabolism partly reflects individual‐level metabolic and life‐history scalings, but whether these have been affected by ecological diversification is little known. 3. Here, this issue was addressed using termites. Data from the literature were assembled to assess the interspecific scalings of individual metabolic rate with individual mass, and of individual mass with colony mass. Concurrently, it was tested whether such scalings were affected by two key ecological traits: lifestyle and diet. 4. Individual‐level metabolic scaling was affected by diet, with β = 1.02 in wood feeders and 0.60 in soil feeders. However, there was no difference in α. Further, individual mass scaled to the 0.25 power with colony mass, but forager species had larger colonies and smaller individuals relative to wood‐dwelling, sedentary ones, thus producing a grade shift. 5. Our results show that ecological diversification has affected fundamental metabolic and life‐history scalings in termites. Thus, theory on the energetics and evolution of colonial life should account for this variability.     

Ecological interpretation of multiple population size structures in trees: The case of Araucaria angustifolia in South America

Abstract In this paper I examined the usefulness of tree population size distributions in evaluating the conservation status of populations of an endangered tree species. I set expectations derived from two complimentary views of the ecology of rainforest trees and examined whether they were met by size distributions of populations of the South American dominant conifer Araucaria angustifolia and its relationship with forest structural characteristics. Specifically, I evaluated the expectations that (i) A. angustifolia trees have larger diameter than average angiosperm trees and form a higher monospecific canopy layer above the shorter angiosperm canopies; (ii) A. angustifolia populations are characterized by size distributions with many large individuals and a long tail of relatively rare, small individuals (have symmetry coefficient <0); (iii) the symmetry of the size distribution of A. angustifolia populations is negatively related to the abundance of large (d.b.h. ≥ 10.0 cm) individuals in the population; and (iv) the abundance of A. angustifolia trees is negatively related to the abundance of angiosperm trees, as the successional accumulation of angiosperm stems would not be accompanied by the recruitment of new A. angustifolia. These expectations were evaluated using data on 25 populations of A. angustifolia sampled in the Rio Grande do Sul State in southern Brazil. The first, third and fourth expectations were met, while the second one was only partially met. This was because populations showed a bimodal distribution regarding symmetry in size distribution, with most populations showing normal or negative symmetry, and those logged, adult‐depleted populations showing positive skewness.     

Climate change effects on plant biomass alter dominance patterns and community evenness in an experimental old‐field ecosystem

Atmospheric and climatic change can alter plant biomass production and plant community composition. However, we know little about how climate change‐induced alterations in biomass production affect plant species composition. To better understand how climate change will alter both individual plant species and community biomass, we manipulated atmospheric [CO₂], air temperature, and precipitation in a constructed old‐field ecosystem. Specifically, we compared the responses of dominant and subdominant species to our climatic treatments, and explored how changes in plant dominance patterns alter community evenness over 2 years. Our study resulted in four major findings: (1) all treatments, elevated [CO₂], warming, and increased precipitation increased plant community biomass and the effects were additive rather than interactive, (2) plant species differed in their response to the treatments, resulting in shifts in the proportional biomass of individual species, which altered the plant community composition; however, the plant community response was largely driven by the positive precipitation response of Lespedeza, the most dominant species in the community, (3) precipitation explained most of the variation in plant community composition among treatments, and (4) changes in precipitation caused a shift in the dominant species proportional biomass that resulted in lower community evenness in the wet relative to dry treatments. Interestingly, compositional and evenness responses of the subdominant community to the treatments did not always follow the responses of the whole plant community. Our data suggest that changes in plant dominance patterns and community evenness are an important part of community responses to climatic change, and generally, that such compositional shifts can alter ecosystem biomass production and nutrient inputs.     

Cytochemical Localization of Plasma Membrane Enzyme Markers During Interiorization of Tachyzoites of Toxoplasma gondii by Macrophages

The enzyme activity of Mg-ATPase, Na⁺-K⁺-ATPase, 5'-nucleotidase and NAD(P)H-oxidase was cytochemically detected at the ultrastructural level in mouse peritoneal macrophages infected with untreated and with specific antibody-coated Toxoplasma gondii tachyzoites. The Mg⁺⁺-ATPase and 5'-nucleotidase were distributed throughout the macrophages'plasma membrane but were not observed in the membrane lining endocytic vacuoles containing ingested parasites; however, Na⁺-K⁺-ATPase activity was detected in the macrophages'plasma membrane as well as in the parasitophorous vacuoles that contained untreated or specific antibody-coated parasites. Reaction product, indicative of NAD(P)H-oxidase, was detected in the parasitophorous vacuoles that contained only-specific antibody-coated parasites.     

Surface Anionic Groups in Symbiote-Bearing and Symbiote-Free Strains of Crithidia deanei1

The surface anionic groups of symbiote-bearing and symbiote-free strains of Crithidia deanei were compared by determining cellular electrophoretic mobility, by ultrastructural cytochemistry, and by identification of sialic acids by thin-layer and gasliquid chromatography. Symbiote-free Crithidia deanei has a highly negative surface charge (-0.9984 μm?s^-1? V^-1? cm), which is slightly reduced (-0.8527 μm?s^-1? V^-1? cm) by the presence of the endosymbiote. Treatment of both strains of C. deanei with neuraminidase decreased significantly the electrophoretic mobility of cells toward the cathodic pole, indicating the existence of exposed sialic acid residues responsible for the negative charge on the protozoan cell surface. Thin-layer and gas-liquid chromatography showed that N-glycolyl- and N-acetylneuraminic acids were present in both strains of C. deanei.     

Mechanism of Acquired Immunity Induced by “Leptomonas pessoai” against Trypanosoma cruzi in Mice*

Living culture forms of “Leptomonas pessoai” cross protected mice against T. cruzi challenge infection. Circulating antibodies have been detected in the immunized mice by immunodiffusion analysis, passive hemagglutination, complement fixation test and antibody binding assay; these antibodies cross reacted with T. cruzi extracts. A cellular immune response was indicated by leucocyte migration inhibition using L. pessoai and T. cruzi antigens, strongly suggesting a role for cell-mediated immunity in the mechanism of protection induced by L. pessoai.     

Fine Structure and Cytochemistry of the Nucleus and the Kinetoplast of Epimastigotes of Trypanosoma cruzi1

ABSTRACT. Ultrastructural cytochemical techniques were used to analyze the nucleus and the kinetoplast of epimastigotes of Trypanosoma cruzi. With the use of ethanolic phosphotungstic acid, which detects basic proteins, reaction product was seen in the chromatin and at the periphery of the kinetoplast. Thallium alcoholate, which interacts with DNA, stained strongly the whole kinetoplast and the chromatin. With the use of a silver impregnation method that detects acidic nucleolar proteins, silver granules were seen preferentially located in the central region of the nucleolus. With the EDTA method, which reveals the presence of ribonucleoproteins, staining was observed in the nuclear pores. Also 6–8 nm fibrils, 25 nm and 40 nm granules, which correspond to the perichromatin fibers, interchromatin granules and the perichromatin granules, respectively, were identified in the nucleus. The EDTA method also revealed the presence of 40 nm granules in the kinetoplast. These granules were seen mainly at the two extremities of the kinetoplast. Freeze-fracture images indicate that the nuclear membrane contains ca. 9 pores/μm² of nuclear surface area. The mean diameter of the pores was 80 nm. All these results suggest that epimastigotes of T. cruzi have a very active nucleus and a high rate of nucleocytoplasmic interchange.