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India Annual Winter Cropped Area, 2001-2016
data.nasa.gov | Last Updated 2022-01-17T05:29:43.000ZThe India Annual Winter Cropped Area, 2001 - 2016 consists of annual winter cropped areas for most of India (except the Northeastern states) from 2000-2001 to 2015-2016. This data set utilizes the NASA Moderate Resolution Imaging Spectroradiometer (MODIS) Enhanced Vegetation Index (EVI; spatial resolution: 250m) for the winter growing season (October-March). The methodology uses an automated algorithm identifying the EVI peak in each pixel for each year and linearly scales the EVI value between 0% and 100% cropped area within that particular pixel. Maps were then resampled to 1 km and were validated using high-resolution QuickBird, RapidEye, SkySat, and WorldView-2 images spanning 2008 to 2016 across 11 different agricultural regions of India. The spatial resolution of the data set is 1 km, resampled from 250m. The data are distributed as GeoTIFF and NetCDF files and are in WGS 84 projection.
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GPM Ground Validation SEA FLUX ICE POP V1
data.nasa.gov | Last Updated 2022-06-07T06:12:15.000ZThe GPM Ground Validation SEA FLUX ICE POP dataset includes estimates of ocean surface latent and sensible heat fluxes, 10m wind speed, 10m air temperature, 10m air humidity, and skin sea surface temperature in support of the International Collaborative Experiments for Pyeongchang 2018 Olympic and Paralympic Winter Games (ICE-POP) field campaign in South Korea. The two major objectives of ICE-POP were to study severe winter weather events in regions of complex terrain and improve the short-term forecasting of such events. These data contributed to the Global Precipitation Measurement mission Ground Validation (GPM GV) campaign efforts to improve satellite estimates of orographic winter precipitation. This data file is available in netCDF-4 format from September 1, 2017 through April 30, 2018.
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2008 Environmental Performance Index (EPI)
data.nasa.gov | Last Updated 2022-01-17T05:02:20.000ZThe 2008 Environmental Performance Index (EPI) centers on two broad environmental protection objectives: (1) reducing environmental stresses on human health, and (2) promoting ecosystem vitality and sound natural resource management. Derived from a careful review of the environmental literature, these twin goals mirror the priorities expressed by policymakers. Environmental health and ecosystem vitality are gauged using 25 indicators tracked in six well-established policy categories: Environmental Health (Environmental Burden of Disease, Water, and Air Pollution), Air Pollution (effects on ecosystems), Water (effects on ecosystems), Biodiversity and Habitat, Productive Natural Resources (Forestry, Fisheries, and Agriculture), and Climate Change. The 2008 EPI utilizes a proximity-to-target methodology in which performance on each indicator is rated on a 0 to 100 scale (100 represents �at target�). By identifying specific targets and measuring how close each country comes to them, the EPI provides a foundation for policy analysis and a context for evaluating performance. Issue-by-issue and aggregate rankings facilitate cross-country comparisons both globally and within relevant peer groups. The 2008 EPI is the result of collaboration among the Yale Center for Environmental Law and Policy (YCELP), Columbia University Center for International Earth Science Information Network (CIESIN), World Economic Forum (WEF), and the Joint Research Centre (JRC), European Commission.
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Experimental and Analytical Development of a Health Management System for Electro-Mechanical Actuators
data.nasa.gov | Last Updated 2020-01-29T01:49:29.000ZExpanded deployment of Electro-Mechanical Actuators (EMAs) in critical applications has created much interest in EMA Prognostic Health Management (PHM), a key enabling technology of Condition Based Maintenance (CBM). As such, Impact Technologies, LLC is collaborating with the NASA Ames Research Center to perform a number of research efforts in support of NASA’s Integrated Vehicle Health Management (IVHM) initiatives. These efforts have combined experimental test stand development, laboratory seeded fault testing, and physical model-based health monitoring in a comprehensive PHM system development strategy. This paper discusses two closely related EMA research programs being conducted by Impact and NASA Ames. The first of these efforts resulted in the creation of an electro-mechanical actuator test stand for the Prognostics Center of Excellence at the NASA Ames Research Center. The second effort is ongoing and is utilizing physics-based modeling techniques to develop an algorithm and software package toolset for PHM of aircraft EMA systems using a hybrid (virtual sensor) approach.
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OWLETS-1 Ozonesonde Data
data.nasa.gov | Last Updated 2022-07-18T13:04:47.000ZOWLETS1_Sondes_Data_1 is the Ozone Water-Land Environmental Transition Study (OWLETS-1) ozone data collected via synchronous ozonesonde launches at the NASA Langley Research Center ground site and Chesapeake Bay Bridge Tunnel site during the OWLETS field campaign. OWLETS was supported by the NASA Science Innovation Fund (SIF). Data collection is complete. Coastal regions have typically posed a challenge for air quality researchers due to a lack of measurements available over water and water-land boundary transitions. Supported by NASA’s Science Innovation Fund (SIF), the Ozone Water-Land Environmental Transition Study (OWLETS) field campaign examined ozone concentrations and gradients over the Chesapeake Bay from July 5, 2017 – August 3, 2017, with twelve intensive measurement days occurring during this time period. OWLETS utilized a unique combination of instrumentation, including aircraft, TOLNet ozone lidars (NASA Goddard Space Flight Center Tropospheric Ozone Differential Absorption Lidar and NASA Langley Research Center Mobile Ozone Lidar), UAV/drones, ozonesondes, AERONET sun photometers, and mobile and ship-based measurements, to characterize the land-water differences in ozone and other pollutants. Two main research sites were established as part of the campaign: an over-land site at NASA LaRC, and an over-water site at the Chesapeake Bay Bridge Tunnel. These two research sites were established to provide synchronous vertical measurements of meteorology and pollutants over water and over land. In combination with mobile observations between the two sites, pollutant gradients were able to be observed and used to better understand the fundamental processes occurring at the land-water interface. OWLETS-2 was completed from June 6, 2018 – July 6, 2018 in the upper Chesapeake Bay region. Research sites were established at the University of Maryland, Baltimore County (UMBC), Hart Miller Island (HMI), and Howard University Beltsville (HUBV), with HMI representing the over-water location and UMBC and HUBV representing the over-land sites. Similar measurements were carried out to further characterize water-land gradients in the upper Chesapeake Bay. The measurements completed during OWLETS are of importance in enhancing air quality models, and improving future satellite retrievals, particularly, NASA’s Tropospheric Emissions: Monitoring of Pollution, which is scheduled to launch in 2022.
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Global gene expression analysis highlights microgravity sensitive key genes in soleus and EDL of 30 days space flown mice
data.nasa.gov | Last Updated 2023-01-26T18:49:58.000ZMicrogravity exposure as well as chronic muscle disuse are two of the main causes of physiological adaptive skeletal muscle atrophy in humans and murine animals in physiological condition. The aim of this study was to investigate at both morphological and global gene expression level skeletal muscle adaptation to microgravity in mouse soleus and extensor digitorum longus (EDL). Adult male mice C57BL/N6 were flown aboard the BION-M1 biosatellite for 30 days on orbit (BF) or housed in a replicate flight habitat on Earth (BG) as reference flight control. In this study we investigated for the first time gene expression adaptation to 30 days of microgravity exposure in mouse soleus and EDL highlighting potential new targets for improvement of countermeasures able to ameliorate or even prevent microgravity-induced atrophy in future spaceflights. Overall Design: C57BL/N6 mice were randomly divided in 3 groups: Bion Flown (BF) mice flown aboard the Bion M1 biosatellite in microgravity environment for 30 days; Bion Ground (BG) mice housed in the same habitat of flown animals but exposed to earth gravity; and Flight Control (FC) mice housed in a standard animal facility.
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Rapid Electrochemical Detection and Identification of Microbiological and Chemical Contaminants for Manned Spaceflight Project
data.nasa.gov | Last Updated 2020-01-29T03:33:53.000Z<p>A great deal of effort has gone into the development of point-of-use methods to meet the challenge of rapid bacterial identification for both environmental monitoring and clinical applications.&nbsp; Unfortunately, most of the methods developed rely on Preliminary Chain Reaction (PCR) and face inherent limitations because of the requirement for enzymatic components and thermal control.&nbsp; Other methods based on surface plasmon resonance, quartz crystal microbalance, and fluorescence has been reported with good detection limits, but, these methods are immunological and cannot provide genetic-level information.&nbsp; Further, they require labeled markers, complicated fluid handling systems, and sensitive optics that drive up cost and complexity and preclude them from outside the laboratory.&nbsp; Recent work by a group at the University of Toronto has focused on developing an electrochemical platform that combines ultrasensitive detection, straightforward sample processing, and inexpensive components to create a cost-effective, user-friendly device for detection and identification of microorganisms.&nbsp; The platform combines an electrical cell lysis chamber, and electrochemical reporter system, and nanostructured microelectrodes (NMEs) to detect specific nucleic acid sequences.&nbsp; The nucleic acid sequences are unique to a given type of microorganism and can be used to identify the microorganisms present in a sample.</p><p>From the perspective of the anticipated prototype device &nbsp;(Lam, et al. 2012. <em>Polymerase Chain Reaction-Free, Sample-to-Answer Bacterial Detection in 30 Minutes with Integrated Cell Lysis</em>. Anal. Chem. <strong>84(1)</strong>: 21-5), detection of microbial contaminants will begin with a lysis chamber designed to release DNA and RNA from microorganisms present in the sample using ultrasonic or electrochemical technology.&nbsp; The DNA and RNA mixture is then passed into an analysis chamber containing an array of nanostructured microelectrodes (NMEs).&nbsp; The surface of the NMEs will be functionalized with probe molecules for DNA or RNA sequences specific to the bacteria being targeted.&nbsp; Binding of the DNA or RNA to the appropriate detection probe on the NME surface in the presence of an electrochemical reporter system will change the electrochemical properties of the NMEs.&nbsp; A potentiostat is used to measure the current at each individual electrode before and after addition of the DNA and RNA mixture.&nbsp; The difference in current before and after addition of the mixture to the NMEs is compared against a pre-determined threshold to check for the presence of target bacteria in the sample.&nbsp; The process for detection of chemical contaminants is very similar.&nbsp; The lysis chamber would be bypassed and the sample would flow directly into the analysis chamber.&nbsp; The NMEs will be functionalized with molecules to selectively bind the desired targets (analytes) and the change in the electrochemical response of each NME can again be used to detect and quantify the contaminants.&nbsp; Depending on the analyte of interest, it may be possible to directly measure analyte binding on the surface of the NMEs without the use of an electrochemical reporter system. The overall project will focus on optimization of the individual aspects of the detection platform in preparation for construction of a prototype for a flight experiment.&nbsp; The scope of the work in this proposal is limited to characterization and optimization of the lysis step/sample preparation, probe selection, and NME structure.&nbsp; Lysis conditions will be optimized by evaluating parameters associated with the oscillation frequency and lysis time for ultrasonic techniques and applied voltage for the electrochemical techniques.&nbsp; Cell viability, as determined by fluorescent detection of DNA or R
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Transcriptional analysis of dorsal skin from mice flown on the RR-6 mission
data.nasa.gov | Last Updated 2023-01-26T18:45:51.000ZThe objective of the Rodent Research-6 (RR-6) study was to evaluate muscle atrophy in mice during spaceflight and to test the efficacy of a novel therapeutic to mitigate muscle wasting. The experiment involved an implantable subcutaneous nanochannel delivery system (nDS; between scapula) which delivered the drug formoterol (FMT; a selective Beta-2 adrenoceptor agonist) over the course of time. To this end a cohort of forty 32-weeks-old female C57BL/6NTac mice were either sham operated. or implanted with vehicle or treatment-filled nDS and launched in two Transporters (20 mice per Transporter) on SpaceX-13 on December 15 2017. They were transferred to Rodent Habitats onboard the International Space Station (ISS) and maintained in microgravity for 29 days (N=20 Live Animal Return [LAR]) or >50 days (N=20 ISS Terminal). After 29 days the 20 LAR animals were returned live to back to Earth on January 13 2018. After splashdown the animals were ambulatory on-ground for ~4 days until all subjects were processed during one day of dissections. There were two Baseline groups of animals sacrificed (LAR Baseline & FLT Baseline; N=20; 40 animals; ~36 weeks old) at Kennedy Space Center (KSC; 12/9/17). A Ground Control group mimicked the Flight LAR group which was housed at KSC then shipped alive to Novartis facilities where both the LAR and LAR Ground Control groups were processed (~41 weeks old; 1/16/18). All were anesthetized with isoflurane blood samples were obtained by closed-chest cardiac puncture and the animals were euthanized by exsanguination and thoracotomy. The 20 ISS Terminal mice were anesthetized via intraperitoneal injection of ketamine/xylazine/acepromazine over the course of a four days of dissections (2/6/18 until 2/9/18; 53-56 days after launch; 44 weeks old at time of on-orbit dissections). Blood samples and euthanasia were conducted the same as LAR and Baseline. Following blood draw and hind limb dissection the ISS-terminal animal carcasses were wrapped in aluminum foil placed in a ziploc bag and placed in storage at -80C or colder until return. The ISS-terminal Ground Controls (at KSC) followed the same euthanasia timeline methods and preservation. The final processing of frozen ISS-terminal frozen ISS-terminal Ground Controls and frozen 0-day FLT baseline animals were completed at Houston Methodist Research Institute in Houston TX (5/21/18 until 5/24/18). GeneLab received samples of dorsal skin from only sham treated animals (no drug treated animals) from the following groups Flight: LAR (n=9) ISS Terminal (n=9); Ground Controls: LAR GC (N=9) ISS Terminal GC (N=10) LAR Baseline (n=10) ISS Terminal Baseline (n=6). Total RNA was extracted and sequenced at a target depth of 60 M clusters per sample (ribodepleted paired end 150).
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Metagenomic analysis of feces from mice flown on the RR-6 mission
data.nasa.gov | Last Updated 2023-01-26T18:46:14.000ZThe objective of the Rodent Research-6 (RR-6) study was to evaluate muscle atrophy in mice during spaceflight and to test the efficacy of a novel therapeutic to mitigate muscle wasting. The experiment involved an implantable subcutaneous nanochannel delivery system (nDS; between scapula) which delivered the drug formoterol (FMT; a selective xce xb22 adrenoceptor agonist) over the course of time. To this end a cohort of forty 32-weeks-old female C57BL/6NTac mice were either sham operated or implanted with vehicle or treatment-filled nDS launched in two Transporters (20 mice per Transporter) on SpaceX-13 on December 15 2017. They were transferred to Rodent Habitats onboard the International Space Station (ISS) and maintained in microgravity for 29 days (N=20 Live Animal Return Spaceflight [LAR FLT]) or >50 days (N=20 ISS Terminal Spaceflight [ISS-T FLT]). After 29 days the 20 LAR FLT animals were returned live to back to Earth on January 13 2018. After splashdown the animals were ambulatory on-ground for ~4 days until all subjects were processed during one day of dissections. There were two Basal (BSL) groups of animals sacrificed (LAR BSL & ISS-T BSL; N=20; 40 animals; ~36 weeks old) at Kennedy Space Center (KSC; 12/9/17). LAR BSL animals were dissected and samples were collected upon euthanasia. A Ground Control (GC) group LAR GC mimicked the LAR FLT group which was housed at KSC then shipped alive to Novartis xe2 x80 x99s Facilities where both the LAR FLT and LAR GC groups were processed (~41 weeks old; 1/16/18). All were anesthetized with isoflurane blood samples were obtained by closed-chest cardiac puncture and the animals were euthanized by exsanguination and thoracotomy. The 20 ISS-T FLT mice were anesthetized via intraperitoneal injection of ketamine/xylazine/acepromazine over the course of a four days of dissections (2/6/18 until 2/9/18; 53-56 days after launch; 44 weeks old at time of on-orbit dissections). Blood samples and euthanasia were conducted the same as LAR groups. Following blood draw and hind limb dissection the ISS-T FLT animal carcasses were wrapped in aluminum foil placed in a ziploc bag and placed in storage at -80 xcb x9aC or colder until return. The ISS-T Ground Control (ISS-T GC) (at KSC) followed the same euthanasia timeline methods and preservation. The final processing of frozen ISS-T FLT frozen ISS-T GC and frozen 0-day ISS-T BSL animals were completed at Houston Methodist Research Institute in Houston TX (5/21/18 until 5/24/18). GeneLab received feces from only sham treated animals (no drug treated animals) from the following groups. FLT: LAR (n=9) ISS-T (n=7); GC: LAR (N=7) ISS-T (N=9); BSL: LAR (n=7) ISS-T (n=9). DNA was extracted and analyzed by sequencing using a variety of different targeted and un-targeted metagenome profiling assays.
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2002 Environmental Sustainability Index (ESI)
data.nasa.gov | Last Updated 2022-01-17T05:02:16.000ZThe 2002 Environmental Sustainability Index (ESI) measures overall progress toward environmental sustainability for 142 countries based on environmental systems, stresses, human vulnerability, social and institutional capacity and global stewardship. The addition of a climate change indicator, reduction in number of capacity indicators, and an improved imputation methodology contributed to an improvement from the 2001 ESI. The index was unveiled at the World Economic Forum's annual meeting, January 2002, New York. The 2002 ESI is the result of collaboration among the World Economic Forum (WEF), Yale Center for Environmental Law and Policy (YCELP), and the Columbia University Center for International Earth Science Information Network (CIESIN).