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21.
22.
Toby A. Gardner Jos Barlow Robin Chazdon Robert M. Ewers Celia A. Harvey Carlos A. Peres Navjot S. Sodhi 《Ecology letters》2009,12(6):561-582
The future of tropical forest biodiversity depends more than ever on the effective management of human-modified landscapes, presenting a daunting challenge to conservation practitioners and land use managers. We provide a critical synthesis of the scientific insights that guide our understanding of patterns and processes underpinning forest biodiversity in the human-modified tropics, and present a conceptual framework that integrates a broad range of social and ecological factors that define and contextualize the possible future of tropical forest species. A growing body of research demonstrates that spatial and temporal patterns of biodiversity are the dynamic product of interacting historical and contemporary human and ecological processes. These processes vary radically in their relative importance within and among regions, and have effects that may take years to become fully manifest. Interpreting biodiversity research findings is frequently made difficult by constrained study designs, low congruence in species responses to disturbance, shifting baselines and an over-dependence on comparative inferences from a small number of well studied localities. Spatial and temporal heterogeneity in the potential prospects for biodiversity conservation can be explained by regional differences in biotic vulnerability and anthropogenic legacies, an ever-tighter coupling of human-ecological systems and the influence of global environmental change. These differences provide both challenges and opportunities for biodiversity conservation. Building upon our synthesis we outline a simple adaptive-landscape planning framework that can help guide a new research agenda to enhance biodiversity conservation prospects in the human-modified tropics. 相似文献
23.
Marc A. Schlüter Catherine S. Pfarr Jay Pieczynski Eileen L. Whiteman Toby W. Hurd Shuling Fan Chia-Jen Liu Ben Margolis 《Molecular biology of the cell》2009,20(22):4652-4663
Although lumen generation has been extensively studied through so-called cyst-formation assays in Madin-Darby canine kidney (MDCK) cells, an underlying mechanism that leads to the initial appearance of a solitary lumen remains elusive. Lumen formation is thought to take place at early stages in aggregates containing only a few cells. Evolutionarily conserved polarity protein complexes, namely the Crumbs, Par, and Scribble complexes, establish apicobasal polarity in epithelial cells, and interference with their function impairs the regulated formation of solitary epithelial lumina. Here, we demonstrate that MDCK cells form solitary lumina during their first cell division. Before mitosis, Crumbs3a becomes internalized and concentrated in Rab11-positive recycling endosomes. These compartments become partitioned in both daughter cells and are delivered to the site of cytokinesis, thus forming the first apical membrane, which will eventually form a lumen. Endosome trafficking in this context appears to depend on the mitotic spindle apparatus and midzone microtubules. Furthermore, we show that this early lumen formation is regulated by the apical polarity complexes because Crumbs3 assists in the recruitment of aPKC to the forming apical membrane and interference with their function can lead to the formation of a no-lumen or multiple-lumen phenotype at the two-cell stage. 相似文献
24.
Allegra Via Cathryn M Gould Christine Gemünd Toby J Gibson Manuela Helmer-Citterich 《BMC bioinformatics》2009,10(1):351
Background
Many proteins are highly modular, being assembled from globular domains and segments of natively disordered polypeptides. Linear motifs, short sequence modules functioning independently of protein tertiary structure, are most abundant in natively disordered polypeptides but are also found in accessible parts of globular domains, such as exposed loops. The prediction of novel occurrences of known linear motifs attempts the difficult task of distinguishing functional matches from stochastically occurring non-functional matches. Although functionality can only be confirmed experimentally, confidence in a putative motif is increased if a motif exhibits attributes associated with functional instances such as occurrence in the correct taxonomic range, cellular compartment, conservation in homologues and accessibility to interacting partners. Several tools now use these attributes to classify putative motifs based on confidence of functionality. 相似文献25.
26.
Connectivity of larvae among metapopulations in open marine systems can be a double-edged sword, allowing for the colonization
and replenishment of both desirable and undesirable elements of interacting species-rich assemblages. This article studies
the effect of recruitment by coral and macroalgae on the resilience of grazed reef ecosystems. In particular, we focus on
how larval connectivity affects regime shifts between alternative assemblages that are dominated either by corals or by macroalgae.
Using a model with bistability dynamics, we show that recruitment of coral larvae erodes the resilience of a macroalgae-dominated
ecosystem when grazing is high, but has negligible effect when grazing is low. Conversely, recruitment by macroalgae erodes
the resilience of a coral-dominated ecosystem when grazing is low, leading to a regime shift to macroalgae. Thus, spillover
of coral recruits from highly protected areas will not restore coral cover or prevent flips to macroalgae in the surrounding
seascape if grazing levels in these areas are depleted, but may be pivotal for re-building coral populations if grazing is
high. Fishing restrictions and the re-introduction of herbivores should therefore be a prime conservation objective for preventing
undesirable regime shifts. Connectivity by some components of coral reef assemblages (e.g., macroalgae, pathogens, crown-of-thorns
starfish) may be detrimental to sustaining reefs, especially where overfishing and other drivers have eroded their resilience,
making them more vulnerable to a regime shift. 相似文献
27.
Background
Non-coding DNA sequences comprise a very large proportion of the total genomic content of mammals, most other vertebrates, many invertebrates, and most plants. Unraveling the functional significance of non-coding DNA depends on how well we are able to align non-coding DNA sequences. However, the alignment of non-coding DNA sequences is more difficult than aligning protein-coding sequences. 相似文献28.
Peter Burlinson David Studholme Joanna Cambray-Young Darren Heavens John Rathjen Jonathan Hodgkin Gail M Preston 《The ISME journal》2013,7(6):1126-1138
The bacteriovorous nematode Caenorhabditis elegans has been used to investigate many aspects of animal biology, including interactions with pathogenic bacteria. However, studies examining C. elegans interactions with bacteria isolated from environments in which it is found naturally are relatively scarce. C. elegans is frequently associated with cultivation of the edible mushroom Agaricus bisporus, and has been reported to increase the severity of bacterial blotch of mushrooms, a disease caused by bacteria from the Pseudomonas fluorescens complex. We observed that pseudomonads isolated from mushroom farms showed differential resistance to nematode predation. Under nutrient poor conditions, in which most pseudomonads were consumed, the mushroom pathogenic isolate P. fluorescens NZI7 was able to repel C. elegans without causing nematode death. A draft genome sequence of NZI7 showed it to be related to the biocontrol strain P. protegens Pf-5. To identify the genetic basis of nematode repellence in NZI7, we developed a grid-based screen for mutants that lacked the ability to repel C. elegans. The mutants isolated in this screen included strains with insertions in the global regulator GacS and in a previously undescribed GacS-regulated gene cluster, ‘EDB'' (‘edible''). Our results suggest that the product of the EDB cluster is a poorly diffusible or cell-associated factor that acts together with other features of NZI7 to provide a novel mechanism to deter nematode grazing. As nematodes interact with NZI7 colonies before being repelled, the EDB factor may enable NZI7 to come into contact with and be disseminated by C. elegans without being subject to intensive predation. 相似文献
29.
Toby R. Long 《Inorganica chimica acta》2005,358(6):2141-2145
The electrogenerated chemiluminescence (ECL) of platinum (II) octaethyl-porphyrin (PtOEP) in acetonitrile:methylene chloride (CH3CN:CH2Cl2, 50:50 v/v) and CH2Cl2 is reported. ECL was generated upon sweep to positive potentials using tri-n-propylamine (TPrA) as an oxidative-reductive coreactant. ECL efficiencies (?ecl) of 0.18 in CH3CN:CH2Cl2 (50:50 v/v) and 3.90 in methylene chloride were obtained using Ru(bpy)3(PF6)2 (bpy = 2,2′-bipyridine) as a relative standard (?ecl = 1). The ECL intensity peaks at a potential corresponding to oxidation of PtOEP and TPrA, and ECL emission spectra are nearly identical to photoluminescence emission spectra, indicating that emission is from the PtOEP triplet state. 相似文献
30.
Hua Jiang Yueqing Xie Andrew Burnette John Roach Steven L. Giardina Toby T. Hecht Stephen P. Creekmore Gautam Mitra Jianwei Zhu 《Applied microbiology and biotechnology》2013,97(2):621-632
Immunotoxins are rationally designed cancer targeting and killing agents. Disulfide stabilized antibody Fv portion—toxin conjugates (dsFv-toxin) are third generation immunotoxins containing only the antibody fragment variable portions and a toxin fused to the VH or VL. Pseudomonas exotoxin fragment (PE-38) is a commonly used toxin in immunotoxin clinical trials. dsFv-toxin purification was previously published, but the recovery was not satisfactory. This report describes the development of a cGMP production process of the dsFv-toxin that incorporated a novel purification method. The method has been successfully applied to the clinical manufacturing of two dsFv-PE38 immunotoxins, MR1-1 targeting EGFRvIII and HA22 targeting CD22. The two subunits, VL and VH PE-38 were expressed separately in Escherichia coli using recombinant technology. Following cell lysis, inclusion bodies were isolated from the biomass harvested from fermentation in animal source component-free media. The dsFv-toxin was formed after denaturation and refolding, and subsequently purified to homogeneity through ammonium sulfate precipitation, hydrophobic interaction and ion-exchange chromatography steps. It was shown, in a direct comparison experiment using MR1-1 as model protein, that the recovery from the new purification method was improved three times over that from previously published method. The improved recovery was also demonstrated during the clinical production of two dsFv-PE38 immunotoxins—MR1-1 and HA22. 相似文献