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21 results for “1970s”

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edi52/100

Summary of tundra pond zooplankton and associated environmental data from the Barrow, AK IBP tundra ponds (1970s & 2010s)

A comparison of historic (1970s) and more recent (2010s) zooplankton and environmental data from Arctic tundra ponds near Utqiaġvik, AK has given us valuable insight into changes in zooplankton communities that have occurred in recent times.

openCC0Jan 2026View details →
zenodo44/100

Building locations in Poland in 1970s and 1980s

<p>Dataset contains building locations in Poland in 1970-80s. The source information were polish archival 1:10 000 topographical maps. Buildings were extracted from maps using Mask R-CNN model implemented in Esri ArcGIS Pro software. In post processing we have removed most of the false possitives. The dataset of building locations covers the entire country and contains approximately 11 million buildings. The accuracy of the dataset was assessed manually on randomly selected map sheets. The overall accuracy is 95% (F1 0.98).</p>

opencc-by-4.0Sep 2023View details →
zenodo44/100

A new inventory of High Mountain Asia surging glaciers derived from multiple elevation datasets since the 1970s

<p>Glacier surging is an unusual undulation instability of ice flow and complete surging glacier inventories are important for regional mass balance studies and assessing glacier-related hazards. Glacier surge events in High Mountain Asia (HMA) are widely reported. Through the estimated elevation changes from multiple DEMs sources that acquired from 1970s to 2020, and morphologic changes from 1986 to 2021, here we present a new surging glacier inventory across HMA. The inventory has incorporated 890 surging and 336 surge-like glaciers, each glacier is assigned with indicators of surging feature and surge possibility. Compared to previous surging glacier inventory in HMA, our inventory is theoretically more complete because of the much longer observation period. This data repository contains the surging glacier inventory and glacier elevation change maps. The inventory is stored in the format of GeoPackage (.gpkg) and ESRI Shapefile format (.shp), which is represented by glacier polygon (from GAMDAM2) or surface point with geometric attributes. The multi-temporal elevation change maps of identified surging glaciers were divided into 1&times;1&deg; tiles, storing in the format of GeoTiff(*.tif). Detailed description of the dataset including the file contents and attributes information can be found in the metadata file (README.txt).</p>

opencc-by-4.0Dec 2022View details →
zenodo40/100

Wildland-Urban Interface maps for the Polish Carpathians for 1860s, 1970s and 2013

<p>The dataset contains three (1860s, 1970s, 2013) detailed&nbsp;Wildland-Urban Interface (WUI)&nbsp;maps of the Polish Carpathians, including information on building density. The maps, available in the form of 10m raster GeoTIFF files,&nbsp;are based on&nbsp;the WUI definition of US Federal Register&nbsp;(USDA and USDI, 2001) as operationalized by&nbsp;(Radeloff et al., 2005), which distinguishes two kinds of WUI: intermix, where housing intermingle with wildland vegetation, and interface, where settlement abuts the wildland areas. Either WUI type requires a housing density higher than 6.17 houses/km2 (1 house/40 acres in the US context). In intermix WUI, there has to be also &gt; 50% wildland vegetation, while the interface WUI, has &lt; 50% wildland vegetation but is within 2.4 km of a wildland vegetation patch larger &gt; 5 km2. Given the ecological context of the Polish Carpathians, we defined wildland vegetation as forests, because forests are the climax vegetation type below the treeline. To assess settlements, we analysed all buildings locations (residential and non-residential), because all buildings reflect human activities. The building density and forest cover share were calculated by using a 500m circular moving window algorithm.</p><p>Acknowledgements<br>The study was supported by the National Science Centre, Poland, contract no. UMO-2019/35/D/HS4/00117 and by the NASA Land Use and Land Cover Change Program.</p>

opencc-by-4.0Nov 2023View details →
edi40/100

Microbial biomass and soil properties data, global scale,1970s-2010s

The data for Microbial Data System. We will collect data for soil and microbial characteristics in terrestrial ecosystems and update regularly. The date of publications used spans from the late 1970s to 2012. The data were aggregated into 11 major biome types. These data points were collected exclusively for surface soils, primarily 0–15 cm depth with some 0–30 cm. We obtained 3259 data points with geographical information.

openCC (other)Mar 2023View details →
zenodo36/100

Cataloguing the Landscape: Photography in 1970s America

<p>4<sup>th</sup> Presentation</p>

opencc-by-4.0Jul 2017View details →
dryad36/100

Data from: 1970s and 'Patient 0' HIV-1 genomes illuminate early HIV/AIDS history in North America

The emergence of HIV-1 group M subtype B in North American men who have sex with men was a key turning point in the HIV/AIDS pandemic. Phylogenetic studies have suggested cryptic subtype B circulation in the United States (US) throughout the 1970s1, 2 and an even older presence in the Caribbean2. However, these temporal and geographical inferences, based upon partial HIV-1 genomes that postdate the recognition of AIDS in 1981, remain contentious3, 4 and the earliest movements of the virus within the US are unknown. We serologically screened &gt;2,000 1970s serum samples and developed a highly sensitive approach for recovering viral RNA from degraded archival samples. Here, we report eight coding-complete genomes from US serum samples from 1978–1979—eight of the nine oldest HIV-1 group M genomes to date. This early, full-genome 'snapshot' reveals that the US HIV-1 epidemic exhibited extensive genetic diversity in the 1970s but also provides strong evidence for its emergence from a pre-existing Caribbean epidemic. Bayesian phylogenetic analyses estimate the jump to the US at around 1970 and place the ancestral US virus in New York City with 0.99 posterior probability support, strongly suggesting this was the crucial hub of early US HIV/AIDS diversification. Logistic growth coalescent models reveal epidemic doubling times of 0.86 and 1.12 years for the US and Caribbean, respectively, suggesting rapid early expansion in each location3. Comparisons with more recent data reveal many of these insights to be unattainable without archival, full-genome sequences. We also recovered the HIV-1 genome from the individual known as 'Patient 0' (ref. 5) and found neither biological nor historical evidence that he was the primary case in the US or for subtype B as a whole. We discuss the genesis and persistence of this belief in the light of these evolutionary insights.

opencc-zeroDec 2015View details →
zenodo36/100

Abandoned 1970s Postal Truck (Free Raw Scan)

At one point in time, this was used for delivering mail. I suppose it was retired, but just sat around because it's not that useful as anything but a mail carrier. Processed from 310 photos taken with my Canon EOS Rebel XSI Source: Objaverse 1.0 / Sketchfab

opencc-byApr 2019View details →
dryad36/100

Data from: 1970s and ‘Patient 0’ HIV-1 genomes illuminate early HIV/AIDS history in North America

Open the record for dataset details and reuse information.

publicAug 2017View details →
edi36/100

McMurdo Sound, Antarctica: Benthic macrofaunal abundances in Explorers Cove in 1970s and 2010 and in Salmon Bay in 1988-89 and 2010

In 2010 we had the opportunity to revisit historical transects and experiments set up by Dayton et al. in the 1960s, 70s, and 80s. Using the SCINI ROV we were able to revisit sites we had dived previously, including some deeper sites that are no longer diveable by current United States Antarctic Program policies. Revisitng these sites enabled us to study and document long-term changes in benthic biota at McMurdo Sound, Antarctica. These are data on benthic macrofaunal abundance collected in the 1970s, late 1980s, and 2010. We are making these data available to researchers for future observations of community change in the nearly pristine environment of the Ross Sea, Antarctica.

openCC0Oct 2018View details →
dryad32/100

Data from: Shells of the bivalve Astarte moerchi give new evidence of a strong pelagic-benthic coupling shift occurring since the late 1970s in the NOW Polynya

<p>Climate changes in the Arctic may weaken the currently tight pelagic-benthic coupling. In response to decreasing sea ice cover, arctic marine systems are expected to shift from a 'sea-ice algae-benthos' to a 'phytoplankton-zooplankton' dominance. We used mollusk shells as bioarchives and fatty acid trophic markers to estimate the effects of the reduction of sea ice cover on the exported food to the seafloor. Bathyal bivalve <i>Astarte moerchi</i> that lives at 600 m depth in northern Baffin Bay reveals a clear shift in growth variations and Ba/Ca ratios since the late 1970s that we relate to a change in food availability. Fatty acid compositions of tissues show that this species feeds mainly on microalgae exported from the euphotic zone to the seabed. We thus suggest that changes in pelagic-benthic coupling are likely due to either local changes in sea ice dynamics, mediated through bottom-up regulation exerted by sea ice on phytoplankton production or to a mismatch between phytoplankton bloom and zooplankton grazing due to change in their phenology. Both possibilities allow a more regular and increased transfer of food to the seabed.</p>

opencc-zeroJul 2020View details →
dryad32/100

Data from: Deforestation and forest fragmentation in South Ecuador since the 1970s - losing a hotspot of biodiversity

Deforestation and fragmentation are major components of global change; both are contributing to the rapid loss of tropical forest area with important implications for ecosystem functioning and biodiversity conservation. The forests of South Ecuador are a biological 'hotspot' due to their high diversity and endemism levels. We examined the deforestation and fragmentation patterns in this area of high conservation value using aerial photographs and Aster satellite scenes. The registered annual deforestation rates of 0.75% (1976–1989) and 2.86% (1989–2008) for two consecutive survey periods, the decreasing mean patch size and the increasing isolation of the forest fragments show that the area is under severe threat. Approximately 46% of South Ecuador's original forest cover had been converted by 2008 into pastures and other anthropogenic land cover types. We found that deforestation is more intense at lower elevations (premontane evergreen forest and shrubland) and that the deforestation front currently moves in upslope direction. Improved awareness of the spatial extent, dynamics and patterns of deforestation and forest fragmentation is urgently needed in biologically diverse areas like South Ecuador.

opencc-zeroDec 2014View details →
zenodo32/100

Curious George vintage 1970s stuffed animal

Created with Polycam using photomode. Reasonably decent lighting and clean table (for a change). Fur surface looks polygonalized when very close, not bad from a distance. Toy was sitting up on it's own so no supports to deal with. Source: Objaverse 1.0 / Sketchfab

opencc-by-nc-1.0Sep 2021View details →
dryad32/100

Flowering time advances since the 1970s in a sagebrush steppe community: implications for management and restoration

<p>Climate change is widely known to affect plant phenology, but little is known about how these impacts manifest in the widespread sagebrush ecosystem of the Western US which supports a number of wildlife species of concern. Shifts in plant phenology can trigger consequences for the plants themselves as well as the communities of consumers that depend upon them. We assembled historical observations of first flowering dates for 51 species collected in the 1970 and 80s in a montane sagebrush community in the Greater Yellowstone Ecosystem and compared these to contemporary phenological observations targeting the same species and locations (2016-2019). We also assembled regional climate data (average spring temperature, day of spring snowmelt, and growing degree days) and tested the relationship between first flowering time and these variables for each species. We observed the largest change in phenology in early spring flowers, which as a group bloomed on average 17 days earlier, and as much as 36 days earlier, in the contemporary data set. Mid-summer flowers bloomed on average 10 days earlier, nonnative species 15 days earlier, and berry-producing shrubs 5 days earlier, while late summer flowering plants did not shift. The greatest correlates of early spring and mid-summer flowering were average spring temperature and day of snowmelt, which was 21 days earlier, on average, in 2016-2019 relative to the 1973-1978. The shifts in flowering phenology that we observed could indicate developing asynchronies or novel synchronies of these plant resources and wildlife species of conservation concern including: Greater sage-grouse, whose nesting success is tied to availability of spring forbs; grizzly bears -- which rely heavily on berries for their fall diet; and pollinators. This underscores the importance of maintaining a diverse portfolio of native plants in terms of species composition, genetics, phenological responsiveness to climatic cues, and ecological importance to key wildlife and pollinator species. Redundancy within ecological niches may also be important considering that species roles in the community may shift as climate change affects them differently. These considerations are particularly relevant to restoration and habitat-enhancement projects in sagebrush communities across western North America.</p>

opencc-zeroDec 2021View details →
zenodo32/100

Distribution. SE Kenya and NE Tanzania. The Fringe-eared Oryx is geographically separated from the Galla Oryx by the Tana River and Aberdare Mts in S Kenya. Its range began to spread into the Serengeti in the 1970s. in Bovidae

Distribution. SE Kenya and NE Tanzania. The Fringe-eared Oryx is geographically separated from the Galla Oryx by the Tana River and Aberdare Mts in S Kenya. Its range began to spread into the Serengeti in the 1970s.

opennotspecifiedAug 2011View details →
zenodo32/100

Replication Package for: "Stalled Racial Progress and Japanese Trade in the 1970s and 1980s"

<p>Batistich, Mary Kate and Timothy N. Bond. forthcoming. &quot;Stalled Racial Progress and Japanese Trade in the 1970s and 1980s.&quot; <em>Review of Economic Studies</em></p> <p>These files contain the data and code to replicate the main results and online appendix for<br> &quot;Stalled Racial Progress and Japanese Trade in the 1970s and 1980s&quot; by Mary Kate Batistich and Timothy N.&nbsp;Bond.&nbsp;</p>

opencc-by-4.0Nov 2022View details →
dryad32/100

Data from: Deforestation and forest fragmentation in South Ecuador since the 1970s - losing a hotspot of biodiversity

Open the record for dataset details and reuse information.

publicJul 2016View details →
dryad32/100

Data from: Shells of the bivalve Astarte moerchi give new evidence of a strong pelagic-benthic coupling shift occurring since the late 1970s in the NOW Polynya

Open the record for dataset details and reuse information.

publicJul 2020View details →
dryad32/100

Flowering time advances since the 1970s in a sagebrush steppe community: implications for management and restoration

Open the record for dataset details and reuse information.

publicDec 2021View details →
edi32/100

Maine Department of Environment Protection lake monitoring and assessment, 1970s-2011, compiled all ME DEP programs for metadata unpublished data

Much of the lake monitoring in the state is done to assess "trophic state" or the productivity of the water. Our 30 year record includes data on over 1000 of our 5785 lakes, including parameters such as transparency, conductivity, alkalinity, total phosphorus and chlorophyll-a. These, along with extensive data sets from the University of Maine and clarity readings from volunteers, have produced one of the most comprehensive lake data sets in the country. DEP regular monitoring includes annual Baseline Sampling Program and special projects of one or more years’ duration. Each year between August 10 and September 10, we visit over 100 lakes and take a number of types of data. The timing coincides with the period when lakes usually show their worst water quality: lowest dissolved oxygen, lowest transparency and highest algae and phosphorus levels. Besides these measures, we sample for conductivity, alkalinity and acid neutralizing capacity (ANC), true and apparent color, and a variety of cations and anions. Lakes sampled generally include TMDL lakes, 33-50 lakes in the VLMP, lakes of special concern (e.g., anecdotal report of algal bloom), long-term monitoring lakes in ecoreserves and special project lakes.

openCC (other)Jan 2020View details →

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allen-brain-atlas
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Last verified 2026-04-30Open record

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abode-home-cage
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dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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Last verified 2026-04-29Open record

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