Classification of Vegetation and Analysis of its Recent Trends at Camp Williams, Utah Using Remote Sensing and Geographic Information System Techniques

Current vegetation classes were generated from remotely sensed data to provide coarse-level information for an ecosystem management plan developed at Camp Williams, Utah. Vegetation trend from 1973 - 1993 was also examined via satellite imagery. The data set consisted of Landsat Multispectral Scanner (MSS) and Thematic Mapper (TM) images from July or August of 1973, 1975, 1980, 1988, and 1993. Two approaches were used to detect vegetation change. The first approach determined overall and cover type trend from standard digital image differencing of soil-adjusted vegetation index (SAVI) images. The second approach used an unsupervised classification of a composite SAVI image of all dates. The first approach defined areas of increase, decrease, and no significant change in SAVI and differences in trend for tree versus shrub cover types. The second approach resulted in an ecological classification that defined new environmental patterns based on vegetation trend

Assessing the accuracy of blending Landsat-MODIS surface reflectances in two landscapes with contrasting spatial and temporal dynamics: A framework for algorithm selection

Blending algorithms model land cover change by using highly resolved spatial data from one sensor and highly resolved temporal data from another. Because the data are not usually observed concurrently, unaccounted spatial and temporal variances cause error in blending algorithms, yet, to date, there has been no definitive assessment of algorithm performance against spatial and temporal variances. Our objectives were to: (i) evaluate the accuracy of two advanced blending algorithms (STARFM and ESTARFM) and two simple benchmarking algorithms in two landscapes with contrasting spatial and temporal variances; and (ii) synthesise the spatial and temporal conditions under which the algorithms performed best. Landsat-like images were simulated on 27 dates in total using the nearest temporal cloud-free Landsat-MODIS pairs to the simulation date, one before and one after. RMSD, bias, and r2 estimates between simulated and observed Landsat images were calculated, and overall variance of Landsat and MODIS datasets were partitioned into spatial and temporal components. Assessment was performed over the whole study site, and for specific land covers. Results addressing objective (i) were that: ESTARFM did not always produce lower errors than STARFM; STARFM and ESTARFM did not always produce lower errors than simple benchmarking algorithms; and land cover spatial and temporal variances were strongly associated with algorithm performance. Results addressing objective (ii) indicated ESTARFM was superior where/when spatial variance was dominant; and STARFM was superior where/when temporal variance was dominant. We proposed a framework for selecting blending algorithms based on partitioning variance into the spatial and temporal components and suggested that comparing Landsat and MODIS spatial and temporal variances was a practical method to determine if, and when, MODIS could add value for blending

Blending Landsat and MODIS Data to Generate Multispectral Indices: A Comparison of “Index-then-Blend” and “Blend-then-Index” Approaches

The objective of this paper was to evaluate the accuracy of two advanced blending algorithms, Spatial and Temporal Adaptive Reflectance Fusion Model (STARFM) and Enhanced Spatial and Temporal Adaptive Reflectance Fusion Model (ESTARFM) to downscale Moderate Resolution Imaging Spectroradiometer (MODIS) indices to the spatial resolution of Landsat. We tested two approaches: (i) "Index-then-Blend" (IB); and (ii) "Blend-then-Index" (BI) when simulating nine indices, which are widely used for vegetation studies, environmental moisture assessment and standing water identification. Landsat-like indices, generated using both IB and BI, were simulated on 45 dates in total from three sites. The outputs were then compared with indices calculated from observed Landsat data and pixel-to-pixel accuracy of each simulation was assessed by calculating the: (i) bias; (ii) R; and (iii) Root Mean Square Deviation (RMSD). The IB approach produced higher accuracies than the BI approach for both blending algorithms for all nine indices at all three sites. We also found that the relative performance of the STARFM and ESTARFM algorithms depended on the spatial and temporal variances of the Landsat-MODIS input indices. Our study suggests that the IB approach should be implemented for blending of environmental indices, as it was: (i) less computationally expensive due to blending single indices rather than multiple bands; (ii) more accurate due to less error propagation; and (iii) less sensitive to the choice of algorithm

Monoubiquitination of syntaxin 3 leads to retrieval from the basolateral plasma membrane and facilitates cargo recruitment to exosomes

Syntaxin 3 (Stx3), a SNARE protein located and functioning at the apical plasma membrane of epithelial cells, is required for epithelial polarity. A fraction of Stx3 is localized to late endosomes/lysosomes, although how it traffics there and its function in these organelles is unknown. Here we report that Stx3 undergoes monoubiquitination in a conserved polybasic domain. Stx3 present at the basolateral—but not the apical—plasma membrane is rapidly endocytosed, targeted to endosomes, internalized into intraluminal vesicles (ILVs), and excreted in exosomes. A nonubiquitinatable mutant of Stx3 (Stx3-5R) fails to enter this pathway and leads to the inability of the apical exosomal cargo protein GPRC5B to enter the ILV/exosomal pathway. This suggests that ubiquitination of Stx3 leads to removal from the basolateral membrane to achieve apical polarity, that Stx3 plays a role in the recruitment of cargo to exosomes, and that the Stx3-5R mutant acts as a dominant-negative inhibitor. Human cytomegalovirus (HCMV) acquires its membrane in an intracellular compartment and we show that Stx3-5R strongly reduces the number of excreted infectious viral particles. Altogether these results suggest that Stx3 functions in the transport of specific proteins to apical exosomes and that HCMV exploits this pathway for virion excretion

Single-nanoparticle phase transitions visualized by four-dimensional electron microscopy

The advancement of techniques that can probe the behaviour of individual nanoscopic objects is of paramount importance in various disciplines, including photonics and electronics. As it provides images with a spatiotemporal resolution, four-dimensional electron microscopy, in principle, should enable the visualization of single-nanoparticle structural dynamics in real and reciprocal space. Here, we demonstrate the selectivity and sensitivity of the technique by visualizing the spin crossover dynamics of single, isolated metal–organic framework nanocrystals. By introducing a small aperture in the microscope, it was possible to follow the phase transition and the associated structural dynamics within a single particle. Its behaviour was observed to be distinct from that imaged by averaging over ensembles of heterogeneous nanoparticles. The approach reported here has potential applications in other nanosystems and those that undergo (bio)chemical transformations

Differential Association between HERG and KCNE1 or KCNE2

The small proteins encoded by KCNE1 and KCNE2 have both been proposed as accessory subunits for the HERG channel. Here we report our investigation into the cell biology of the KCNE-HERG interaction. In a co-expression system, KCNE1 was more readily co-precipitated with co-expressed HERG than was KCNE2. When forward protein trafficking was prevented (either by Brefeldin A or engineering an ER-retention/retrieval signal onto KCNE cDNA) the intracellular abundance of KCNE2 and its association with HERG markedly increased relative to KCNE1. HERG co-localized more completely with KCNE1 than with KCNE2 in all the membrane-processing compartments of the cell (ER, Golgi and plasma membrane). By surface labeling and confocal immunofluorescence, KCNE2 appeared more abundant at the cell surface compared to KCNE1, which exhibited greater co-localization with the ER-marker calnexin. Examination of the extracellular culture media showed that a significant amount of KCNE2 was extracellular (both soluble and membrane-vesicle-associated). Taken together, these results suggest that during biogenesis of channels HERG is more likely to assemble with KCNE1 than KCNE2 due to distinctly different trafficking rates and retention in the cell rather than differences in relative affinity. The final channel subunit constitution, in vivo, is likely to be determined by a combination of relative cell-to-cell expression rates and differential protein processing and trafficking

Use of Cross-Taxon Congruence for Hotspot Identification at a Regional Scale

One of the most debated problems in conservation biology is the use of indicator (surrogate) taxa to predict spatial patterns in other taxa. Cross-taxon congruence in species richness patterns is of paramount importance at regional scales to disclose areas of high conservation value that are significant in a broader biogeographical context but yet placed in the finer, more practical, political context of decision making. We analysed spatial patterns of diversity in six arthropod taxa from the Turkish fauna as a regional case study relevant to global conservation of the Mediterranean basin. Although we found high congruence in cross-taxon comparisons of species richness (0.241<r<0.645), hotspots of different groups show limited overlap, generally less than 50 per cent. The ability of a given taxon to capture diversity of other taxa was usually modest (on average, 50 percent of diversity of non-target taxa), limiting the use of hotspots for effective conservation of non-target groups. Nevertheless, our study demonstrates that a given group may partially stand in for another with similar ecological needs and biogeographical histories. We therefore advocate the use of multiple sets of taxa, chosen so as to be representative of animals with different ecological needs and biogeographical histories

Detection of microRNA Expression in Human Peripheral Blood Microvesicles

MicroRNAs (miRNA) are small non-coding RNAs that regulate translation of mRNA and protein. Loss or enhanced expression of miRNAs is associated with several diseases, including cancer. However, the identification of circulating miRNA in healthy donors is not well characterized. Microvesicles, also known as exosomes or microparticles, circulate in the peripheral blood and can stimulate cellular signaling. In this study, we hypothesized that under normal healthy conditions, microvesicles contain miRNAs, contributing to biological homeostasis.Microvesicles were isolated from the plasma of normal healthy individuals. RNA was isolated from both the microvesicles and matched mononuclear cells and profiled for 420 known mature miRNAs by real-time PCR. Hierarchical clustering of the data sets indicated significant differences in miRNA expression between peripheral blood mononuclear cells (PBMC) and plasma microvesicles. We observed 71 miRNAs co-expressed between microvesicles and PBMC. Notably, we found 33 and 4 significantly differentially expressed miRNAs in the plasma microvesicles and mononuclear cells, respectively. Prediction of the gene targets and associated biological pathways regulated by the detected miRNAs was performed. The majority of the miRNAs expressed in the microvesicles from the blood were predicted to regulate cellular differentiation of blood cells and metabolic pathways. Interestingly, a select few miRNAs were also predicted to be important modulators of immune function.This study is the first to identify and define miRNA expression in circulating plasma microvesicles of normal subjects. The data generated from this study provides a basis for future studies to determine the predictive role of peripheral blood miRNA signatures in human disease and will enable the definition of the biological processes regulated by these miRNA

The Magnitude of Global Marine Species Diversity

Background: The question of how many marine species exist is important because it provides a metric for how much we do and do not know about life in the oceans. We have compiled the first register of the marine species of the world and used this baseline to estimate how many more species, partitioned among all major eukaryotic groups, may be discovered. Results: There are ∼226,000 eukaryotic marine species described. More species were described in the past decade (∼20,000) than in any previous one. The number of authors describing new species has been increasing at a faster rate than the number of new species described in the past six decades. We report that there are ∼170,000 synonyms, that 58,000–72,000 species are collected but not yet described, and that 482,000–741,000 more species have yet to be sampled. Molecular methods may add tens of thousands of cryptic species. Thus, there may be 0.7–1.0 million marine species. Past rates of description of new species indicate there may be 0.5 ± 0.2 million marine species. On average 37% (median 31%) of species in over 100 recent field studies around the world might be new to science. Conclusions: Currently, between one-third and two-thirds of marine species may be undescribed, and previous estimates of there being well over one million marine species appear highly unlikely. More species than ever before are being described annually by an increasing number of authors. If the current trend continues, most species will be discovered this century

Observation of the Decay Λ0b→Λ+cτ−¯ν

The first observation of the semileptonic b-baryon decay Λb0→Λc+τ-ν¯τ, with a significance of 6.1σ, is reported using a data sample corresponding to 3 fb-1 of integrated luminosity, collected by the LHCb experiment at center-of-mass energies of 7 and 8 TeV at the LHC. The τ- lepton is reconstructed in the hadronic decay to three charged pions. The ratio K=B(Λb0→Λc+τ-ν¯τ)/B(Λb0→Λc+π-π+π-) is measured to be 2.46±0.27±0.40, where the first uncertainty is statistical and the second systematic. The branching fraction B(Λb0→Λc+τ-ν¯τ)=(1.50±0.16±0.25±0.23)% is obtained, where the third uncertainty is from the external branching fraction of the normalization channel Λb0→Λc+π-π+π-. The ratio of semileptonic branching fractions R(Λc+)B(Λb0→Λc+τ-ν¯τ)/B(Λb0→Λc+μ-ν¯μ) is derived to be 0.242±0.026±0.040±0.059, where the external branching fraction uncertainty from the channel Λb0→Λc+μ-ν¯μ contributes to the last term. This result is in agreement with the standard model prediction