75 research outputs found
Defining the Realized Niche of the Two Major Clades of \u3ci\u3eTrichodesmium\u3c/i\u3e: A Study on the West Florida Shelf
The cyanobacterium Trichodesmium plays an essential role supporting ocean productivity by relieving nitrogen limitation via dinitrogen (N-2) fixation. The two common Trichodesmium clades, T. erythraeum and T. thiebautii, are both observed in waters along the West Florida Shelf (WFS). We hypothesized that these taxa occupy distinct realized niches, where T. thiebautii is the more oceanic clade. Samples for DNA and water chemistry analyses were collected on three separate WFS expeditions (2015, 2018, and 2019) spanning multiple seasons; abundances of the single copy housekeeping gene rnpB from both clades were enumerated via quantitative PCR. We conducted a suite of statistical analyses to assess Trichodesmium clade abundances in the context of the physicochemical data. We observed a consistent coastal vs. open ocean separation of the two clades: T. erythraeum was found in shallow waters where the concentrations of dissolved iron (dFe) and the groundwater tracer Ba were significantly higher, while T. thiebautii abundance was positively correlated with water column depth. The Loop Current intrusion in 2015 with entrained Missisippi River water brought higher dFe and elevated abundance of both clades offshore of the 50 m isobath, suggesting that both clades are subject to Fe limitation on the outer shelf. Whereas, previous work has observed that T. thiebautii is more abundant than T. erythraeum in open ocean surface waters, this is the first study to examine Trichodesmium niche differentiation in a coastal environment. Understanding the environmental niches of these two key taxa bears important implications for their contributions to global nitrogen and carbon cycling and their response to global climate change
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Understanding biodiversity-ecosystem service relationships in urban areas: a comprehensive literature review
Positive relationships between biodiversity and urban ecosystem services (UES) are widely implied within both the scientific and policy literatures, along with the tacit suggestion that enhancing urban green infrastructure will automatically improve both biodiversity and UES. However, it is unclear how much published empirical evidence exists to support these assumptions. We conducted a review of studies published between 1990 and May 2017 that examined urban biodiversity ecosystem service (BES) relationships. In total, we reviewed 317 publications and found biodiversity and UES metrics mentioned 944 times. Only 228 (24%) of the 944 mentions were empirically tested. Among these, 119 (52%) demonstrated a positive BES relationship. Our review showed that taxonomic metrics were used most often as proxies for biodiversity, with very little attention given to functional biodiversity metrics. Similarly, the role of particular species, including non-natives, and specific functional traits are understudied. Finally, we found a paucity of empirical evidence underpinning urban BES relationships. As urban planners increasingly incorporate UES delivery consideration to their decision-making, researchers need to address these substantial knowledge gaps to allow potential trade-offs and synergies between biodiversity conservation and the promotion of UES to be adequately accounted for
Exploring the feasibility of utilizing limited gene panel circulating tumor DNA clearance as a biomarker in patients with locally advanced non-small cell lung cancer
INTRODUCTION: Circulating tumor DNA (ctDNA) testing may identify patients at high risk for recurrence following chemoradiation (CRT) for locally advanced non-small cell lung cancer (LA-NSCLC). We evaluated the feasibility of ctDNA testing on a readily available commercial fixed-gene panel to predict outcomes in patients with LA-NSCLC.
METHODS: Plasma of 43 patients was collected at CRT initiation (pre-CRT), completion (post-CRT1), quarterly follow up for 12 months (post-CRT2, 3, 4, 5 respectively) after CRT, and at disease progression. ctDNA analysis was performed using InVisionFirst
RESULTS: Twenty eight of 43 patients (65%) had detectable variants pre-CRT. Nineteen of 43 patients (44%) had detectable pre-CRT variants and post-CRT1 samples and were included in analysis. Median age at diagnosis was 65 years (43-82), and most patients had stage IIIB disease (10/19, 53%). Two patients died from non-cancer related causes before post-CRT2 and were excluded from further analysis. All three patients who did not clear ctDNA had tumor relapse with a median time to relapse of 74 days (30-238), while 50% (7/14) of those who cleared ctDNA have remained disease free. Progression free survival was longer in patients who cleared ctDNA compared to those who did not (median 567 vs 74 d, p = 0.01).
CONCLUSIONS: Although it is feasible to use ctDNA testing on a limited gene panel to identify patients with LA-NSCLC who are at high risk for disease recurrence following CRT, further studies will be necessary to optimize these assays before they can be used to inform clinical care in patients with lung cancer
A Critical Review of the \u3csup\u3e15\u3c/sup\u3eN\u3csub\u3e2\u3c/sub\u3e Tracer Method to Measure Diazotrophic Production in Pelagic Ecosystems
Dinitrogen (N2) fixation is an important source of biologically reactive nitrogen (N) to the global ocean. The magnitude of this flux, however, remains uncertain, in part because N2 fixation rates have been estimated following divergent protocols and because associated levels of uncertainty are seldom reported—confounding comparison and extrapolation of rate measurements. A growing number of reports of relatively low but potentially significant rates of N2 fixation in regions such as oxygen minimum zones, the mesopelagic water column of the tropical and subtropical oceans, and polar waters further highlights the need for standardized methodological protocols for measurements of N2 fixation rates and for calculations of detection limits and propagated error terms. To this end, we examine current protocols of the 15N2 tracer method used for estimating diazotrophic rates, present results of experiments testing the validity of specific practices, and describe established metrics for reporting detection limits. We put forth a set of recommendations for best practices to estimate N2 fixation rates using 15N2 tracer, with the goal of fostering transparency in reporting sources of uncertainty in estimates, and to render N2 fixation rate estimates intercomparable among studies
Functional analysis of frequently expressed Chinese rhesus macaque MHC class I molecules Mamu-A1*02601 and Mamu-B*08301 reveals HLA-A2 and HLA-A3 supertypic specificities
The Simian immunodeficiency virus (SIV)-infected Indian rhesus macaque (Macaca mulatta) is the most established model of HIV infection and AIDS-related research, despite the potential that macaques of Chinese origin is a more relevant model. Ongoing efforts to further characterize the Chinese rhesus macaques’ major histocompatibility complex (MHC) for composition and function should facilitate greater utilization of the species. Previous studies have demonstrated that Chinese-origin M. mulatta (Mamu) class I alleles are more polymorphic than their Indian counterparts, perhaps inferring a model more representative of human MHC, human leukocyte antigen (HLA). Furthermore, the Chinese rhesus macaque class I allele Mamu-A1*02201, the most frequent allele thus far identified, has recently been characterized and shown to be an HLA-B7 supertype analog, the most frequent supertype in human populations. In this study, we have characterized two additional alleles expressed with high frequency in Chinese rhesus macaques, Mamu-A1*02601 and Mamu-B*08301. Upon the development of MHC–peptide-binding assays and definition of their associated motifs, we reveal that these Mamu alleles share peptide-binding characteristics with the HLA-A2 and HLA-A3 supertypes, respectively, the next most frequent human supertypes after HLA-B7. These data suggest that Chinese rhesus macaques may indeed be a more representative model of HLA gene diversity and function as compared to the species of Indian origin and therefore a better model for investigating human immune responses
The 2.5 m Telescope of the Sloan Digital Sky Survey
We describe the design, construction, and performance of the Sloan Digital
Sky Survey Telescope located at Apache Point Observatory. The telescope is a
modified two-corrector Ritchey-Chretien design which has a 2.5-m, f/2.25
primary, a 1.08-m secondary, a Gascoigne astigmatism corrector, and one of a
pair of interchangeable highly aspheric correctors near the focal focal plane,
one for imaging and the other for spectroscopy. The final focal ratio is f/5.
The telescope is instrumented by a wide-area, multiband CCD camera and a pair
of fiber-fed double spectrographs. Novel features of the telescope include: (1)
A 3 degree diameter (0.65 m) focal plane that has excellent image quality and
small geometrical distortions over a wide wavelength range (3000 to 10,600
Angstroms) in the imaging mode, and good image quality combined with very small
lateral and longitudinal color errors in the spectroscopic mode. The unusual
requirement of very low distortion is set by the demands of
time-delay-and-integrate (TDI) imaging; (2) Very high precision motion to
support open loop TDI observations; and (3) A unique wind baffle/enclosure
construction to maximize image quality and minimize construction costs. The
telescope had first light in May 1998 and began regular survey operations in
2000.Comment: 87 pages, 27 figures. AJ (in press, April 2006
The Sloan Digital Sky Survey: Technical Summary
The Sloan Digital Sky Survey (SDSS) will provide the data to support detailed
investigations of the distribution of luminous and non- luminous matter in the
Universe: a photometrically and astrometrically calibrated digital imaging
survey of pi steradians above about Galactic latitude 30 degrees in five broad
optical bands to a depth of g' about 23 magnitudes, and a spectroscopic survey
of the approximately one million brightest galaxies and 10^5 brightest quasars
found in the photometric object catalog produced by the imaging survey. This
paper summarizes the observational parameters and data products of the SDSS,
and serves as an introduction to extensive technical on-line documentation.Comment: 9 pages, 7 figures, AAS Latex. To appear in AJ, Sept 200
Astrophysical Origins of Ultrahigh Energy Cosmic Rays
In the first part of this review we discuss the basic observational features
at the end of the cosmic ray energy spectrum. We also present there the main
characteristics of each of the experiments involved in the detection of these
particles. We then briefly discuss the status of the chemical composition and
the distribution of arrival directions of cosmic rays. After that, we examine
the energy losses during propagation, introducing the Greisen-Zaptsepin-Kuzmin
(GZK) cutoff, and discuss the level of confidence with which each experiment
have detected particles beyond the GZK energy limit. In the second part of the
review, we discuss astrophysical environments able to accelerate particles up
to such high energies, including active galactic nuclei, large scale galactic
wind termination shocks, relativistic jets and hot-spots of Fanaroff-Riley
radiogalaxies, pulsars, magnetars, quasar remnants, starbursts, colliding
galaxies, and gamma ray burst fireballs. In the third part of the review we
provide a brief summary of scenarios which try to explain the super-GZK events
with the help of new physics beyond the standard model. In the last section, we
give an overview on neutrino telescopes and existing limits on the energy
spectrum and discuss some of the prospects for a new (multi-particle)
astronomy. Finally, we outline how extraterrestrial neutrino fluxes can be used
to probe new physics beyond the electroweak scale.Comment: Higher resolution version of Fig. 7 is available at
http://www.angelfire.com/id/dtorres/down3.html. Solicited review article
prepared for Reports on Progress in Physics, final versio
The Eleventh and Twelfth Data Releases of the Sloan Digital Sky Survey: Final Data from SDSS-III
The third generation of the Sloan Digital Sky Survey (SDSS-III) took data from 2008 to 2014 using the original SDSS wide-field imager, the original and an upgraded multi-object fiber-fed optical spectrograph, a new near-infrared high-resolution spectrograph, and a novel optical interferometer. All of the data from SDSS-III are now made public. In particular, this paper describes Data Release 11 (DR11) including all data acquired through 2013 July, and Data Release 12 (DR12) adding data acquired through 2014 July (including all data included in previous data releases), marking the end of SDSS-III observing. Relative to our previous public release (DR10), DR12 adds one million new spectra of galaxies and quasars from the Baryon Oscillation Spectroscopic Survey (BOSS) over an additional 3000 deg2 of sky, more than triples the number of H-band spectra of stars as part of the Apache Point Observatory (APO) Galactic Evolution Experiment (APOGEE), and includes repeated accurate radial velocity measurements of 5500 stars from the Multi-object APO Radial Velocity Exoplanet Large-area Survey (MARVELS). The APOGEE outputs now include the measured abundances of 15 different elements for each star. In total, SDSS-III added 5200 deg2 of ugriz imaging; 155,520 spectra of 138,099 stars as part of the Sloan Exploration of Galactic Understanding and Evolution 2 (SEGUE-2) survey; 2,497,484 BOSS spectra of 1,372,737 galaxies, 294,512 quasars, and 247,216 stars over 9376 deg2; 618,080 APOGEE spectra of 156,593 stars; and 197,040 MARVELS spectra of 5513 stars. Since its first light in 1998, SDSS has imaged over 1/3 of the Celestial sphere in five bands and obtained over five million astronomical spectra. \ua9 2015. The American Astronomical Society
The genetic architecture of the human cerebral cortex
The cerebral cortex underlies our complex cognitive capabilities, yet little is known about the specific genetic loci that influence human cortical structure. To identify genetic variants that affect cortical structure, we conducted a genome-wide association meta-analysis of brain magnetic resonance imaging data from 51,665 individuals. We analyzed the surface area and average thickness of the whole cortex and 34 regions with known functional specializations. We identified 199 significant loci and found significant enrichment for loci influencing total surface area within regulatory elements that are active during prenatal cortical development, supporting the radial unit hypothesis. Loci that affect regional surface area cluster near genes in Wnt signaling pathways, which influence progenitor expansion and areal identity. Variation in cortical structure is genetically correlated with cognitive function, Parkinson's disease, insomnia, depression, neuroticism, and attention deficit hyperactivity disorder
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