USING CALLING ACTIVITY TO PREDICT CALLING ACTIVITY: A CASE STUDY WITH THE ENDANGERED HOUSTON TOAD (BUFO [ANAXYRUS] HOUSTONENSIS)

Understanding anuran calling activity patterns is important for maximizing efficiency and value of call survey data collection and analyses. Previous studies have primarily focused on identifying and quantifying abiotic variables that influence anuran calling activity, and investigating relationships between calling activity and population estimates. In this study we investigated the use of a predictor pond approach to guide call survey effort. In this approach, calling activity at a subset of breeding sites (e.g., ponds) is used as a predictor of calling activity at additional breeding sites, with the goal being to minimize sampling effort while simultaneously maximizing sampling efficiency. We explored the efficiency of this approach using call survey data collected on the endangered Houston Toad (Bufo [Anaxyrus] houstonensis) at 15 known breeding ponds over 9 survey years. We found that if calling activity at 3 predictor ponds was used to decide if additional call surveys would occur at the remaining 12 ponds, we would have hypothetically correctly assumed calling activity was not occurring at non-predictor ponds on 92.1% of survey nights, and we would have hypothetically detected 93.9% of the total number of detected individuals over the 9 survey years. We found the predictor pond approach performed well in our case study, and believe it could be a valuable tool for many anuran monitoring programs

Genetic and ultrastructural analysis reveals the key players and initial steps of bacterial magnetosome membrane biogenesis

Magnetosomes of magnetotactic bacteria contain well-ordered nanocrystals for magnetic navigation and have recently emerged as the most sophisticated model system to study the formation of membrane bounded organelles in prokaryotes. Magnetosome biosynthesis is thought to begin with the formation of a dedicated compartment, the magnetosome membrane (MM), in which the biosynthesis of a magnetic mineral is strictly controlled. While the biomineralization of magnetosomes and their subsequent assembly into linear chains recently have become increasingly well studied, the molecular mechanisms and early stages involved in MM formation remained poorly understood. In the Alphaproteobacterium Magnetospirillum gryphiswaldense, approximately 30 genes were found to control magnetosome biosynthesis. By cryo-electron tomography of several key mutant strains we identified the gene complement controlling MM formation in this model organism. Whereas the putative magnetosomal iron transporter MamB was most crucial for the process and caused the most severe MM phenotype upon elimination, MamM, MamQ and MamL were also required for the formation of wild-type-like MMs. A subset of seven genes (mamLQBIEMO) combined within a synthetic operon was sufficient to restore the formation of intracellular membranes in the absence of other genes from the key mamAB operon. Tracking of de novo magnetosome membrane formation by genetic induction revealed that magnetosomes originate from unspecific cytoplasmic membrane locations before alignment into coherent chains. Our results indicate that no single factor alone is essential for MM formation, which instead is orchestrated by the cumulative action of several magnetosome proteins

Volumetric rheology of polymers

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