Sulfenylation of ENOLASE2 facilitates H2O2-conferred freezing tolerance in Arabidopsis

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Assessing Lead Risks at Non-Residential Hazardous Waste Sites

In 1996, the U.S. Environmental Protection Agency (USEPA) developed the Adult Lead Methodology (ALM) to provide an interim approach to assessing risks from non-residential exposures to lead. Because such exposures often involve occupational activities of adults, the ALM was directed at assessing soil-related lead risks to adults. Consistent with other approaches used in Superfund risk assessment, the ALM was designed to predict quasi-steady state blood lead concentrations (PbB) that might result from soil exposure. These predictions are converted to a risk estimate, expressed as the probability of exceeding a PbB level of concern. To examine the assumptions and variables in the ALM that have become available since 1996, a comparison was made of the attributes of seven alternative research models for which adequate documentation is available to understand and implement each approach. Several of these models have been used in regulatory decision-making; however, the USEPA has officially embraced none for general use. This analysis suggests that the ALM can continue to serve as a reasonable tool for assessing risks associated with non-residential exposures to soil. Under certain circumstances other models may be more applicable (i.e., for assessing acute or intensive exposures); however, the ALM is recommended for the majority of risk assessment applications.     

Preserving biodiversity under current and future climates: a case study

Aim The conservation of biological and genetic diversity is a major goal of reserve systems at local, regional, and national levels. The International Union for the Conservation of Nature and Natural Resources suggests a 12% threshold (area basis) for adequate protection of biological and genetic diversity of a plant community. However, thresholds based on area may protect only a small portion of the total diversity if the locations are chosen without regard to the variation within the community. The objectives of this study were to demonstrate methods to apply a coarse‐filter approach for identifying gaps in the current reserve system of the Psuedotsuga menziesii (Douglas‐fir) forest type group based on current climatic conditions and a global climate change scenario. Location Western United States. Method We used an ecological envelope approach that was based on seven bioclimatic factors, two topographic factors, and two edaphic factors. Multivariate factor analysis was then used to reduce the envelope to two dimensions. The relative density of habitat and protected areas were identified in each part of the envelope based on the current climate and potential future climate. We used this information to identify gaps in the reserve system. Results Although the protected areas occurred in all parts of the envelope, most existed in colder and drier areas. This was true for both the current climate and potential future climate. Main conclusion To protect more of the ecological envelope, future conservation efforts would be most effective in western Oregon, north‐western Washington, and north‐western California.     

Spatial variations in size, weight and condition factor of the females of Acartia clausi (Copepoda: Calanoida) along a salinity gradient in two contrasting estuaries of the Basque coast (Bay of Biscay)

Variations in prosome length and width, dry weight and condition factor of female Acartia clausi copepods were studied at three salinities (35, 34 and 33 psu) in the euhaline region of two estuaries (Bilbao and Urdaibai) of the Basque coast, with different level of anthropogenic impact. Effect of the environmental variables upon the morphology of A. clausi females on a small geographic scale is discussed. In general, biometric variables showed no significant differences between the two estuaries, but dry weight and condition factor were significantly higher in the estuary of Urdaibai at 35 and 34 psu, whilst at 33 psu they were higher in Bilbao. Body dimensions decreased significantly with decreasing salinity in both estuaries, however, no similar trends were observed for dry weight and condition factor. Temperature appeared the main variable to account size variations, but once eliminated seasonal effect of the temperature body size was related with oxygen concentration in the estuary of Bilbao and with salinity in Urdaibai. This study reveals that morphological characteristics of A. clausi not are only dependent on the temperature, but also, within a limited geographical zone, on local differences in environmental variables, mainly salinity and oxygen concentration.     

Fitness effects of parasite-mediated spatial heterogeneity within a swarm

The fitness consequences associated with the position an individualadopts within a dynamic group are not well understood. I investigatedmate acquisition by male chironomid midges using a simple swarmingmodel and empirically collected data on midge aerobatic ability.Previous work has suggested that the aerobatic ability of amale is an important predictor of his reproductive success,although there is contrary (and counterintuitive) evidence thatinfection with ectoparasitic mites increases a male's chanceof mating, despite having negative effects on flight speed.The model used here suggests that a male's location within theswarm, brought about passively through interindividual differencesin flight speed, may explain these contradictory results. Specifically,slower flying males (including those burdened with mites) adoptedpositions nearer the center of the swarm, whereas faster malestended to occupy the periphery. This in turn affected theiraccess to females because any mechanism that brought femalesnearer the swarm's center before capture (including high femaleflight speed and selective pairing by either males or females)significantly increased the relative reproductive success ofboth larger and parasitized males, with the benefits of parasitismpeaking at around 4 mites per host. There may be selective pressureon hosts and parasites to maintain this optimal mite densitybecause both are likely to benefit from the relationship: hostsenjoy an increased reproductive success, whereas only throughhost copulation can mites transfer to a female midge and returnto water (their next life-history stage) during host oviposition.     

Synthesis and structure-function study of artificial nucleases on the basis of hemin conjugates with peptide fragments of cell differentiation factor HLDF

A series of octa-hexapeptide fragments of HLDF and their conjugates with hemin were obtained by solid phase peptide synthesis. A relationship between the structure and the nuclease activity of the compounds was established. The effect of various factors (medium pH, the presence of metal ions, complexons, reducers, and buffer composition) on the DNA destruction with hemin peptides was studied. Preliminary information confirming an oxidative mechanism of this process was obtained. The cleavage of plasmid DNA under the action of hemin peptides was studied by the methods of electron microscopy, gel electrophoresis, and atomic force microscopy.     

Lymphatic Endothelial Differentiation in Pulmonary Lymphangioleiomyomatosis Cells

Pulmonary lymphangioleiomyomatosis (LAM) is a rare, low-grade neoplasm affecting almost exclusively women of childbearing age. LAM belongs to the family of perivascular epithelioid cell tumors, characterized by spindle and epithelioid cells with smooth muscle and melanocytic differentiation. LAM cells infiltrate the lungs, producing multiple, bilateral lesions rich in lymphatic channels and forming cysts, leading to respiratory insufficiency. Here we used antibodies against four lymphatic endothelial markers—podoplanin (detected by D2-40), prospero homeobox 1 (PROX1), vascular endothelial growth factor receptor 3 (VEGFR-3), and lymphatic vessel endothelial hyaluronan receptor 1 (LYVE1)—to determine whether LAM cells show lymphatic differentiation. Twelve of 12 diagnostic biopsy specimens (early-stage LAM) and 19 of 19 explants (late-stage LAM) showed immunopositivity for D2-40 in most neoplastic cells. PROX1, VEGFR-3, and LYVE1 immunoreactivity varied from scarce in the early stage to abundant in the late stage. Lymphatic endothelial, smooth muscle, and melanocytic markers were partially co-localized. These findings indicate that lymphatic endothelial differentiation is a feature of LAM and provide evidence of a previously unidentified third lineage of differentiation in this neoplasm. This study has implications for the histological diagnosis of LAM, the origin of the neoplastic cells, and potential future treatment with drugs targeting lymphangiogenesis.     

Growth Arrest Specific 1 (GAS1) Is Abundantly Expressed in the Adult Mouse Central Nervous System

Growth arrest specific 1 (GAS1) is a pleiotropic protein that induces apoptosis and cell arrest in different tumors, but it is also involved in the development of the nervous system and other tissues and organs. This dual ability is likely caused by its capacity to interact both by inhibiting the intracellular signaling cascade induced by glial cell-line derived neurotrophic factor and by facilitating the activity of the sonic hedgehog pathway. The presence of GAS1 mRNA has been described in adult mouse brain, and here we corroborated this observation. We then proceeded to determine the distribution of the protein in the adult central nervous system (CNS). We detected, by western blot analysis, expression of GAS1 in olfactory bulb, caudate-putamen, cerebral cortex, hippocampus, mesencephalon, medulla oblongata, cerebellum, and cervical spinal cord. To more carefully map the expression of GAS1, we performed double-label immunohistochemistry and noticed expression of GAS1 in neurons in all brain areas examined. We also observed expression of GAS1 in astroglial cells, albeit the pattern of expression was more restricted than that seen in neurons. Briefly, in the present article, we report the widespread distribution and cellular localization of the GAS1 native protein in adult mammalian CNS.