Institution
Colorado State University
Education•Fort Collins, Colorado, United States•
About: Colorado State University is a education organization based out in Fort Collins, Colorado, United States. It is known for research contribution in the topics: Population & Laser. The organization has 31430 authors who have published 69040 publications receiving 2724463 citations. The organization is also known as: CSU & Colorado Agricultural College.
Topics: Population, Laser, Radar, Poison control, Soil water
Papers published on a yearly basis
Papers
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California Institute of Technology1, Goddard Space Flight Center2, University of Bremen3, National Institute of Water and Atmospheric Research4, Woods Hole Oceanographic Institution5, University of California, Berkeley6, Harvard University7, Haverford College8, Commonwealth Scientific and Industrial Research Organisation9, Colorado State University10, Climate Monitoring and Diagnostics Laboratory11, Goodrich Corporation12
TL;DR: The Orbiting Carbon Observatory (OCO) as mentioned in this paper is the first global, space-based measurements of atmospheric carbon dioxide (CO 2 ) with the precision, resolution and coverage needed to characterize CO 2 sources and sinks on regional scales.
539 citations
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TL;DR: It is shown that the proposed methods also possess the sure screening property with vanishing false selection rate, which justifies the applicability of such a simple method in a wide spectrum.
Abstract: Ultrahigh-dimensional variable selection plays an increasingly important role in contemporary scientific discoveries and statistical research. Among others, Fan and Lv [J. R. Stat. Soc. Ser. B Stat. Methodol. 70 (2008) 849-911] propose an independent screening framework by ranking the marginal correlations. They showed that the correlation ranking procedure possesses a sure independence screening property within the context of the linear model with Gaussian covariates and responses. In this paper, we propose a more general version of the independent learning with ranking the maximum marginal likelihood estimates or the maximum marginal likelihood itself in generalized linear models. We show that the proposed methods, with Fan and Lv [J. R. Stat. Soc. Ser. B Stat. Methodol. 70 (2008) 849-911] as a very special case, also possess the sure screening property with vanishing false selection rate. The conditions under which the independence learning possesses a sure screening is surprisingly simple. This justifies the applicability of such a simple method in a wide spectrum. We quantify explicitly the extent to which the dimensionality can be reduced by independence screening, which depends on the interactions of the covariance matrix of covariates and true parameters. Simulation studies are used to illustrate the utility of the proposed approaches. In addition, we establish an exponential inequality for the quasi-maximum likelihood estimator which is useful for high-dimensional statistical learning.
538 citations
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Cornell University1, University of Virginia2, University of Texas Health Science Center at San Antonio3, University of Illinois at Chicago4, University of Pennsylvania5, Stanford University6, Colorado State University7, Providence Portland Medical Center8, Johns Hopkins University9, Brown University10, University of California, San Diego11, Northwestern University12, University of California, Davis13, Harvard University14, International University, Cambodia15, University of Bonn16, University of Washington17, Mayo Clinic18, Rush University Medical Center19, Keio University20, University of Texas Medical Branch21, Baylor College of Medicine22
TL;DR: Given that the majority of the biological and human health variables remained stable, or returned to baseline, after a 340-day space mission, these data suggest that human health can be mostly sustained over this duration of spaceflight.
Abstract: INTRODUCTION To date, 559 humans have been flown into space, but long-duration (>300 days) missions are rare (n = 8 total). Long-duration missions that will take humans to Mars and beyond are planned by public and private entities for the 2020s and 2030s; therefore, comprehensive studies are needed now to assess the impact of long-duration spaceflight on the human body, brain, and overall physiology. The space environment is made harsh and challenging by multiple factors, including confinement, isolation, and exposure to environmental stressors such as microgravity, radiation, and noise. The selection of one of a pair of monozygotic (identical) twin astronauts for NASA’s first 1-year mission enabled us to compare the impact of the spaceflight environment on one twin to the simultaneous impact of the Earth environment on a genetically matched subject. RATIONALE The known impacts of the spaceflight environment on human health and performance, physiology, and cellular and molecular processes are numerous and include bone density loss, effects on cognitive performance, microbial shifts, and alterations in gene regulation. However, previous studies collected very limited data, did not integrate simultaneous effects on multiple systems and data types in the same subject, or were restricted to 6-month missions. Measurement of the same variables in an astronaut on a year-long mission and in his Earth-bound twin indicated the biological measures that might be used to determine the effects of spaceflight. Presented here is an integrated longitudinal, multidimensional description of the effects of a 340-day mission onboard the International Space Station. RESULTS Physiological, telomeric, transcriptomic, epigenetic, proteomic, metabolomic, immune, microbiomic, cardiovascular, vision-related, and cognitive data were collected over 25 months. Some biological functions were not significantly affected by spaceflight, including the immune response (T cell receptor repertoire) to the first test of a vaccination in flight. However, significant changes in multiple data types were observed in association with the spaceflight period; the majority of these eventually returned to a preflight state within the time period of the study. These included changes in telomere length, gene regulation measured in both epigenetic and transcriptional data, gut microbiome composition, body weight, carotid artery dimensions, subfoveal choroidal thickness and peripapillary total retinal thickness, and serum metabolites. In addition, some factors were significantly affected by the stress of returning to Earth, including inflammation cytokines and immune response gene networks, as well as cognitive performance. For a few measures, persistent changes were observed even after 6 months on Earth, including some genes’ expression levels, increased DNA damage from chromosomal inversions, increased numbers of short telomeres, and attenuated cognitive function. CONCLUSION Given that the majority of the biological and human health variables remained stable, or returned to baseline, after a 340-day space mission, these data suggest that human health can be mostly sustained over this duration of spaceflight. The persistence of the molecular changes (e.g., gene expression) and the extrapolation of the identified risk factors for longer missions (>1 year) remain estimates and should be demonstrated with these measures in future astronauts. Finally, changes described in this study highlight pathways and mechanisms that may be vulnerable to spaceflight and may require safeguards for longer space missions; thus, they serve as a guide for targeted countermeasures or monitoring during future missions.
538 citations
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University of California, San Diego1, University of Montana2, San Diego State University3, North Carolina State University4, University of Oregon5, University of Queensland6, Broad Institute7, Harvard University8, King's College London9, University of Minnesota10, University of California, San Francisco11, Saint Petersburg State University12, Colorado State University13, Carnegie Mellon University14, University of Nantes15, University of Pittsburgh16, University of Colorado Boulder17, Argonne National Laboratory18, University of Southern Mississippi19, Atlantic Oceanographic and Meteorological Laboratory20, Duke University21
TL;DR: The utility of the living data resource and cross-cohort comparison is demonstrated to confirm existing associations between the microbiome and psychiatric illness and to reveal the extent of microbiome change within one individual during surgery, providing a paradigm for open microbiome research and education.
Abstract: Although much work has linked the human microbiome to specific phenotypes and lifestyle variables, data from different projects have been challenging to integrate and the extent of microbial and molecular diversity in human stool remains unknown. Using standardized protocols from the Earth Microbiome Project and sample contributions from over 10,000 citizen-scientists, together with an open research network, we compare human microbiome specimens primarily from the United States, United Kingdom, and Australia to one another and to environmental samples. Our results show an unexpected range of beta-diversity in human stool microbiomes compared to environmental samples; demonstrate the utility of procedures for removing the effects of overgrowth during room-temperature shipping for revealing phenotype correlations; uncover new molecules and kinds of molecular communities in the human stool metabolome; and examine emergent associations among the microbiome, metabolome, and the diversity of plants that are consumed (rather than relying on reductive categorical variables such as veganism, which have little or no explanatory power). We also demonstrate the utility of the living data resource and cross-cohort comparison to confirm existing associations between the microbiome and psychiatric illness and to reveal the extent of microbiome change within one individual during surgery, providing a paradigm for open microbiome research and education. IMPORTANCE We show that a citizen science, self-selected cohort shipping samples through the mail at room temperature recaptures many known microbiome results from clinically collected cohorts and reveals new ones. Of particular interest is integrating n = 1 study data with the population data, showing that the extent of microbiome change after events such as surgery can exceed differences between distinct environmental biomes, and the effect of diverse plants in the diet, which we confirm with untargeted metabolomics on hundreds of samples.
538 citations
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TL;DR: It is shown that the fine submicrometer particles accounting for most cloud condensation nuclei are predominantly composed of secondary organic material formed by oxidation of gaseous biogenic precursors, which is relevant as ice nuclei.
Abstract: The Amazon is one of the few continental regions where atmospheric aerosol particles and their effects on climate are not dominated by anthropogenic sources. During the wet season, the ambient conditions approach those of the pristine pre-industrial era. We show that the fine submicrometer particles accounting for most cloud condensation nuclei are predominantly composed of secondary organic material formed by oxidation of gaseous biogenic precursors. Supermicrometer particles, which are relevant as ice nuclei, consist mostly of primary biological material directly released from rainforest biota. The Amazon Basin appears to be a biogeochemical reactor, in which the biosphere and atmospheric photochemistry produce nuclei for clouds and precipitation sustaining the hydrological cycle. The prevailing regime of aerosol-cloud interactions in this natural environment is distinctly different from polluted regions.
536 citations
Authors
Showing all 31766 results
Name | H-index | Papers | Citations |
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Mark P. Mattson | 200 | 980 | 138033 |
Stephen J. O'Brien | 153 | 1062 | 93025 |
Ad Bax | 138 | 486 | 97112 |
David Price | 138 | 1687 | 93535 |
Georgios B. Giannakis | 137 | 1321 | 73517 |
James Mueller | 134 | 1194 | 87738 |
Christopher B. Field | 133 | 408 | 88930 |
Steven W. Running | 126 | 355 | 76265 |
Simon Lin | 126 | 754 | 69084 |
Jitender P. Dubey | 124 | 1344 | 77275 |
Gregory P. Asner | 123 | 613 | 60547 |
Steven P. DenBaars | 118 | 1366 | 60343 |
Peter Molnar | 118 | 446 | 53480 |
William R. Jacobs | 118 | 490 | 48638 |
C. Patrignani | 117 | 1754 | 110008 |