141 research outputs found
Habitat structure: a fundamental concept and framework for urban soil ecology
Habitat structure is defined as the composition and arrangement of physical matter at a location. Although habitat structure is the physical template underlying ecological patterns and processes, the concept is relatively unappreciated and underdeveloped in ecology. However, it provides a fundamental concept for urban ecology because human activities in urban ecosystems are often targeted toward management of habitat structure. In addition, the concept emphasizes the fine-scale, on-the-ground perspective needed in the study of urban soil ecology. To illustrate this, urban soil ecology research is summarized from the perspective of habitat structure effects. Among the key conclusions emerging from the literature review are: (1) habitat structure provides a unifying theme for multivariate research about urban soil ecology; (2) heterogeneous urban habitat structures influence soil ecological variables in different ways; (3) more research is needed to understand relationships among sociological variables, habitat structure patterns and urban soil ecology. To stimulate urban soil ecology research, a conceptual framework is presented to show the direct and indirect relationships among habitat structure and ecological variables. Because habitat structure serves as a physical link between sociocultural and ecological systems, it can be used as a focus for interdisciplinary and applied research (e.g., pest management) about the multiple, interactive effects of urbanization on the ecology of soils
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Influenza Research Database: An integrated bioinformatics resource for influenza virus research
The Influenza Research Database (IRD) is a U.S. National Institute of Allergy and Infectious Diseases (NIAID)-sponsored Bioinformatics Resource Center dedicated to providing bioinformatics support for influenza virus research. IRD facilitates the research and development of vaccines, diagnostics and therapeutics against influenza virus by providing a comprehensive collection of influenza-related data integrated from various sources, a growing suite of analysis and visualization tools for data mining and hypothesis generation, personal workbench spaces for data storage and sharing, and active user community support. Here, we describe the recent improvements in IRD including the use of cloud and high performance computing resources, analysis and visualization of user-provided sequence data with associated metadata, predictions of novel variant proteins, annotations of phenotype-associated sequence markers and their predicted phenotypic effects, hemagglutinin (HA) clade classifications, an automated tool for HA subtype numbering conversion, linkouts to disease event data and the addition of host factor and antiviral drug components. All data and tools are freely available without restriction from the IRD website at https://www.fludb.org.National Institutes of Health/National Institute for Allergy and Infectious Diseases [HHSN272201400028C]. Funding for open access charge: J. Craig Venter Institute
Analysis of the genomic homologous recombination in Theilovirus based on complete genomes
At present, Theilovirus is considered to comprise four distinct serotypes, including Theiler's murine encephalomyelitis virus, Vilyuisk human encephalomyelitis virus, Thera virus, and Saffold virus. So far, there is no systematical study that investigated the genomic recombination of Theilovirus. The present study performed the phylogenetic and recombination analysis of Theilovirus over the complete genomes. Seven potentially significant recombination events were identified. However, according to the strains information and references related to the recombinants and their parental strains, four of the recombination events might happen non-naturally. These results will provide valuable hints for future research on evolution and antigenic variability of Theilovirus
Disturbance and stress - different meanings in ecological dynamics?
There is an increasing frequency of papers
addressing disturbance and stress in ecology without
clear delimitation of their meaning. Some authors
use the terms disturbance and stress exclusively as
impacts, while others use them for the entire process,
including both causes and effects. In some studies, the
disturbance is considered as a result of a temporary
impact, which is positive for the ecosystem, while
stress is a negative, debilitating impact. By developing
and testing simple theoretical models, the authors
propose to differentiate disturbance and stress by
frequency. If the frequency of the event enables the
variable to reach a dynamic equilibrium which might
be exhibited without this event, then the event (plus its
responses) is a disturbance for the system. If frequency
prevents the variable’s return to similar pre-event
dynamics and drives or shifts it to a new trajectory,
then we are facing stress. The authors propose that
changes triggered by the given stimuli can be evaluated
on an absolute scale, therefore, direction of change of the variable must not be used to choose one
term or the other, i.e. to choose between stress and
disturbance
Rapid and sensitive real-time assay for the detection of respiratory syncytial virus using RT-SIBA®
Type II Heat-Labile Enterotoxins from 50 Diverse Escherichia coli Isolates Belong Almost Exclusively to the LT-IIc Family and May Be Prophage Encoded
Some enterotoxigenic Escherichia coli (ETEC) produce a type II heat-labile enterotoxin (LT-II) that activates adenylate cyclase in susceptible cells but is not neutralized by antisera against cholera toxin or type I heat-labile enterotoxin (LT-I). LT-I variants encoded by plasmids in ETEC from humans and pigs have amino acid sequences that are ≥95% identical. In contrast, LT-II toxins are chromosomally encoded and are much more diverse. Early studies characterized LT-IIa and LT-IIb variants, but a novel LT-IIc was reported recently. Here we characterized the LT-II encoding loci from 48 additional ETEC isolates. Two encoded LT-IIa, none encoded LT-IIb, and 46 encoded highly related variants of LT-IIc. Phylogenetic analysis indicated that the predicted LT-IIc toxins encoded by these loci could be assigned to 6 subgroups. The loci corresponding to individual toxins within each subgroup had DNA sequences that were more than 99% identical. The LT-IIc subgroups appear to have arisen by multiple recombinational events between progenitor loci encoding LT-IIc1- and LT-IIc3-like variants. All loci from representative isolates encoding the LT-IIa, LT-IIb, and each subgroup of LT-IIc enterotoxins are preceded by highly-related genes that are between 80 and 93% identical to predicted phage lysozyme genes. DNA sequences immediately following the B genes differ considerably between toxin subgroups, but all are most closely related to genomic sequences found in predicted prophages. Together these data suggest that the LT-II loci are inserted into lambdoid type prophages that may or may not be infectious. These findings raise the possibility that production of LT-II enterotoxins by ETEC may be determined by phage conversion and may be activated by induction of prophage, in a manner similar to control of production of Shiga-like toxins by converting phages in isolates of enterohemmorhagic E. coli
Young off-axis volcanism along the ultraslow-spreading Southwest Indian Ridge
Author Posting. © The Authors, 2010. This is the author's version of the work. It is posted here by permission of Nature Publishing Group for personal use, not for redistribution. The definitive version was published in Nature Geoscience 3 (2010): 286-292, doi:10.1038/ngeo824.Mid-ocean ridge crustal accretion occurs continuously at all spreading rates
through a combination of magmatic and tectonic processes. Fast to slow spreading
ridges are largely built by adding magma to narrowly focused neovolcanic zones. In
contrast, ultraslow spreading ridge construction significantly relies on tectonic
accretion, which is characterized by thin volcanic crust, emplacement of mantle
peridotite directly to the seafloor, and unique seafloor fabrics with variable
segmentation patterns. While advances in remote imaging have enhanced our
observational understanding of crustal accretion at all spreading rates, temporal
information is required in order to quantitatively understand mid-ocean ridge
construction. However, temporal information does not exist for ultraslow spreading
environments. Here, we utilize U-series eruption ages to investigate crustal
accretion at an ultraslow spreading ridge for the first time. Unexpectedly young
eruption ages throughout the Southwest Indian ridge rift valley indicate that
neovolcanic activity is not confined to the spreading axis, and that magmatic crustal
accretion occurs over a wider zone than at faster spreading ridges. These
observations not only suggest that crustal accretion at ultraslow spreading ridges is
distinct from faster spreading ridges, but also that the magma transport
mechanisms may differ as a function of spreading rate.This work was supported by
the following NSF grants: NSF-OCE 0137325; NSF-OCE 060383800; and NSF-OCE
062705300
High diversity of picornaviruses in rats from different continents revealed by deep sequencing
Outbreaks of zoonotic diseases in humans and livestock are not uncommon, and an important component in containment of such emerging viral diseases is rapid and reliable diagnostics. Such methods are often PCR-based and hence require the availability of sequence data from the pathogen. Rattus norvegicus (R. norvegicus) is a known reservoir for important zoonotic pathogens. Transmission may be direct via contact with the animal, for example, through exposure to its faecal matter, or indirectly mediated by arthropod vectors. Here we investigated the viral content in rat faecal matter (n=29) collected from two continents by analyzing 2.2 billion next-generation sequencing reads derived from both DNA and RNA. Among other virus families, we found sequences from members of the Picornaviridae to be abundant in the microbiome of all the samples. Here we describe the diversity of the picornavirus-like contigs including near-full-length genomes closely related to the Boone cardiovirus and Theiler's encephalomyelitis virus. From this study, we conclude that picornaviruses within R. norvegicus are more diverse than previously recognized. The virome of R. norvegicus should be investigated further to assess the full potential for zoonotic virus transmission
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