Numerical abundance of myxomycetes (myxogastrids) in soils in the West of England

Abstract A most-probable-number technique was used to quantify the abundance of myxomycetes (myxogastrids) in soil samples taken from 23 'Sites of Special Scientific Interest' and one other site in the West of England. Associated organisms and soil conditions were also recorded. Sixteen of the 24 sites yielded myxomycete plasmodium-forming units (PFUs) in numbers averaging 230 cm⁻³ fresh soil. Where detectable in samples of grassland soil, the numbers ranged from 20–2750 cm⁻³, in woodland soil from 20–800 cm⁻³, and in sand dunes from 80–400 cm⁻³. Repeated sampling revealed changing numbers at single sites. The abundance of PFUs was correlated positively with numbers of soil amoebae, ciliates and nematodes, and with levels of magnesium and soil density, and negatively with organic matter content and levels of NH₄-nitrogen and phosphate. Each PFU probably corresponded to one or several uninucleate cells in the soil rather than to a plasmodium.     

Biodiversity quality: A paradigm for biodiversity

This paper addresses the need for an internationally accepted definition of biodiversity the lack of which creates difficulty in measuring biodiversity difference and change. The authors suggest that well-sampled data can be used to generate a range of numerical indices reflecting species group characteristics/functionality that can be viewed in combination to create a picture of Biodiversity Quality. Examples of this approach demonstrate how to expand the currently accepted Convention on Biological Diversity definition, based on the “variability” of genes, species and ecosystems, since the numerical expression of the indices allows the probability of difference between biodiversity quality trends and values over time, and between sites or taxonomic groups, to be assessed for statistical inference of difference or similarity.     

Cellular trafficking of phospholamban and formation of functional sarcoplasmic reticulum during myocyte differentiation

Phospholamban (PLB) associates with the Ca²⁺-ATPase in sarcoplasmic reticulum (SR) membranes to permit the modulation of contraction in response to -adrenergic signaling. To understand how coordinated changes in the abundance and intracellular trafficking of PLB and the Ca²⁺-ATPase contribute to the maturation of functional muscle, we measured changes in abundance, location, and turnover of endogenous and tagged proteins in myoblasts and during their differentiation. We found that PLB is constitutively expressed in both myoblasts and differentiated myotubes, whereas abundance increases of the Ca²⁺-ATPase coincide with the formation of differentiated myotubes. We observed that PLB is primarily present in highly mobile vesicular structures outside the endoplasmic reticulum, irrespective of the expression of the Ca²⁺-ATPase, indicating that PLB targeting is regulated through vesicle trafficking. Moreover, using pulse-chase methods, we observed that in myoblasts, PLB is trafficked through directed transport through the Golgi to the plasma membrane before endosome-mediated internalization. The observed trafficking of PLB to the plasma membrane suggests an important role for PLB during muscle differentiation, which is distinct from its previously recognized role in the regulation of the Ca²⁺-ATPase. sarco(endo)plasmic reticulum calcium-adenosine triphosphatase; differentiation; C2C12 myocytes; vesicle trafficking     

Isolation of a high-affinity functional protein complex between OmcA and MtrC: Two outer membrane decaheme c-type cytochromes of Shewanella oneidensis MR-1

Shewanella oneidensis MR-1 is a facultatively anaerobic bacterium capable of using soluble and insoluble forms of manganese [Mn(III/IV)] and iron [Fe(III)] as terminal electron acceptors during anaerobic respiration. To assess the structural association of two outer membrane-associated c-type decaheme cytochromes (i.e., OmcA [SO1779] and MtrC [SO1778]) and their ability to reduce soluble Fe(III)-nitrilotriacetic acid (NTA), we expressed these proteins with a C-terminal tag in wild-type S. oneidensis and a mutant deficient in these genes (i.e., Delta omcA mtrC). Endogenous MtrC copurified with tagged OmcA in wild-type Shewanella, suggesting a direct association. To further evaluate their possible interaction, both proteins were purified to near homogeneity following the independent expression of OmcA and MtrC in the Delta omcA mtrC mutant. Each purified cytochrome was confirmed to contain 10 hemes and exhibited Fe(III)-NTA reductase activity. To measure binding, MtrC was labeled with the multiuse affinity probe 4',5'-bis(1,3,2-dithioarsolan-2-yl)fluorescein (1,2-ethanedithiol)2, which specifically associates with a tetracysteine motif engineered at the C terminus of MtrC. Upon titration with OmcA, there was a marked increase in fluorescence polarization indicating the formation of a high-affinity protein complex (Kd < 500 nM) between MtrC and OmcA whose binding was sensitive to changes in ionic strength. Following association, the OmcA-MtrC complex was observed to have enhanced Fe(III)-NTA reductase specific activity relative to either protein alone, demonstrating that OmcA and MtrC can interact directly with each other to form a stable complex that is consistent with their role in the electron transport pathway of S. oneidensis MR-1.     

Establishing Baseline Indices for the Quality of the Biodiversity of Restored Habitats Using a Standardized Sampling Process

The need for standardized biodiversity assessment methods to enable biodiversity quality to be measured is outlined. A general approach to sampling is suggested. The results of the use of this sampling process are given for two case studies of different taxonomic groups. The data assessment is made easier by the use of a bespoke computer program. Examples of the program output are presented. The advantage of this standardized measurement of biodiversity compared to species lists and the use of indicator species are outlined in the case studies macrofungi and butterflies. It was shown that the biodiversity quality of sites can be compared by the use of a range of measured biodiversity indices in a way that allows sites to be compared through time or between sites/treatments. In one case (butterflies), data that have been collected systematically in a recording scheme have been analyzed retrospectively and yielded valuable information on changes in biodiversity quality. The uses of this method in establishing baselines in restoration ecology are discussed. The importance of restoration ecology in the conservation of biodiversity could be underlined by the use of the methods presented in this article.     

An exchange of botanical information in the early contact situation: Wisakon of the Southeastern Algonquians

The termwisakon, recorded among Southeastern Algonquian Indians in the seventeenth and eighteenth centuries, frequently has been iden tified as one of several plant species. However, it appears thatwisakon referred not to any particular plant species but to a general category of substances that included both plant and nonplant materials. The misunderstanding illustrates some of the problems and procedures involved in the exchange and integration of botanical information by Europeans and Indians in the early culture contact situation.