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356 results for “PIE”

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edi40/100

PIE LTER Year 2014, 15 minute measurements of conductivity, water temperature at the Parker River head of tide, Central St. Dam in Newbury, MA.

Year 2014, continuous measurements, every 15 minutes were made of conductivity, water temperature in the Parker River behind the head of tide Central St. Dam in Newbury, MA.

openCC (other)Apr 2018View details →
edi40/100

PIE LTER Year 2015, 15 minute measurements of conductivity, water temperature at the Parker River head of tide, Central St. Dam in Newbury, MA.

Year 2015, continuous measurements, every 15 minutes were made of conductivity, water temperature in the Parker River behind the head of tide Central St. Dam in Newbury, MA.

openCC (other)Apr 2018View details →
edi40/100

PIE LTER, Hach, OTT RLS measurements of water column depth at 15 minute intervals in the lower Plum Island Sound off the Ipswich Bay Yacht Club pier, Ipswich, MA, year 2018

Measurements of water column depth at 15 minute intervals in Plum Island Sound at the Ipswich Bay Yacht Club, for year 2018. OTT radar level sensor (RLS) installed September 20, 2011 out of the water under the concrete pad on the Ipswich Bay Yacht Club pier, Ipswich, MA. RLS was mounted so that continuous year round measurements can be conducted without the concern of ice flows damaging the sensor.

openCC (other)Feb 2019View details →
edi40/100

Biomass of Spartina alterniflora collected in July 2018 from various marsh edges around Plum Island Sound, MA, PIE LTER.

Biomass of Spartina alterniflora was collected at various locations within the Plum Island Sound estuary. Samples were collected during July 2018. Only Spartina alterniflora was collected. To collect biomass, 25 X 25 cm quadrats were placed over the plants. Aboveground biomass was clipped to soil surface. Biomass was dried in the lab in a drying oven until a constant weight was reached, and then weighed. Biomass values were then convertedto grams of dry weight per square meter (g/m2).

openCC (other)Jan 2020View details →
edi40/100

PIE LTER extensometer measurements of marsh bank sediment deformation, soil creep in West Creek, Rowley, MA.

Muddy banks of marsh channels experience soil creep – a viscous-like slow deformation resulting in a net downslope transport. Here we present the first field evidence of soil creep in a mesotidal salt marsh using high precision measurements of soil deformation taken with a vibrating-wire extensometer over two years.

openCC (other)Jan 2020View details →
edi40/100

PIE LTER location and sample dates for sites used in space for time sea level rise study, Rowley, MA.

This dataset contains the GPS-ed locations of the quadrats used for the 2017-2018 Space for Time substitution experiment in tidal creek marshes off the Rowley River and Plum Island Sound in Rowley Massachusetts. The space for time study uses an intensive and comprehensive approach to compare low elevation, Spartina alterniflora marsh areas to higher elevation Spartina patens marsh areas. Other related data files include: HTL-RO-ST-MAR-Biomass, HTL-RO-ST-MAR-Birds, HTL-RO-ST-MAR-Quads, HTL-RO-ST-MAR-Sediments, HTL-RO-ST-MAR-Bites, HTL-RO-ST-MAR-Sticky, HTL-RO-ST-MAR-Decomp, HTL-RO-ST-MAR-Traps, HTL-RO-ST-MAR-Deep_pitfalls

openCC (other)Jan 2020View details →
edi40/100

PIE LTER bird observations associated with marsh sites used in space for time sea level rise study, Rowley, MA.

This dataset contains observations of birds foraging at high and low tide at space for time substition plots in tidal creek marshes off the Rowley River and Plum Island Sound in Rowley Massachusetts. The space for time study uses an intensive and comprehensive approach to compare low elevation, Spartina alterniflora marsh areas to higher elevation Spartina patens marsh areas. Birds were observed using timed interval observations, with one sampling bout per tide per site. Other related data files include: HTL-RO-ST-MAR-Sites, HTL-RO-ST-MAR-Biomass, HTL-RO-ST-MAR-Quads, HTL-RO-ST-MAR-Sediments, HTL-RO-ST-MAR-Bites, HTL-RO-ST-MAR-Sticky, HTL-RO-ST-MAR-Decomp, HTL-RO-ST-MAR-Traps, HTL-RO-ST-MAR-Deep_pitfalls

openCC (other)Jan 2020View details →
edi40/100

PIE LTER, Year 2013-2018, remote sensing derived sediment concentration maps, movies, transect averaged sediment concentation, water level, dh/dt, wind direction and speed, river discharges at Plum Island Sound, Massachusetts.

PIE LTER, Year 2013-2018, remote sensing (Landsat8 OLI sensors and Sentinel-2A/2B) derived sediment concentration maps, transect averaged sediment concentation, water level, dh/dt, wind direction and speed, river discharges for Plum Island Sound estuary, Massachusetts.

openCC (other)Jan 2020View details →
edi40/100

PIE LTER trapping capacity of suspended cohesive sediments of subdomains at Plum Island Sound, Massachusetts (numerical simulations).

Trapping capacity of suspended cohesive sediments of subdomains at Plum Island Sound, Massachusetts (from numerical simulations) are predicted using 2D Delft3D FLOW/MOR model and vegetation module during different stages of tidal height and direction.

openCC (other)Jan 2020View details →
edi40/100

PIE LTER, Year 2017-2018, locations, date, sediment concentration and spectral reflectance measurement methods of 40 water samples at Plum Island Sound and deep ocean, Massachusetts.

PIE LTER, Year 2017-2018, locations, date, sediment concentration and spectral reflectance measurement methods of 40 water samples at Plum Island Sound and deep ocean, Massachusetts

openCC (other)Jan 2020View details →
edi40/100

PIE LTER predation and herbivory rates associated with marsh sites used in space for time sea level rise study, Rowley, MA.

This dataset contains aggregated observations of predation and herbivory rates on tethered bait in each quadrat of the space for time substitution observations in salt marsh sites in Rowley and Newbury, MA.

openCC (other)Jan 2020View details →
edi40/100

Fiddler crab body size in salt marshes from Florida to Massachusetts, USA at PIE and VCR LTER and NOAA NERR sites during summer 2016.

Bergmann’s rule predicts that organisms at higher latitudes are larger than ones at lower latitudes. Here, we examine the body-size pattern of the Atlantic fiddler crab, Minuca (=Uca) pugnax, from salt marshes on the east coast of the United States across 12 degrees of latitude. We found that M. pugnax followed Bergmann’s rule and that, on average, crab carapace width increased by 0.5 mm per degree of latitude. Minuca pugnax body size also followed the temperature-size rule with body size inversely related to mean water temperature. Because an organism’s size influences its impact on an ecosystem, and Minuca pugnax is an ecosystem engineer that affects marsh functioning, the larger crabs at higher latitudes may have greater per-capita impacts on salt marshes than the smaller crabs at lower latitudes.

openCC (other)Jan 2020View details →
edi40/100

PIE LTER diel surface water chemistry of two high marsh ponds, Rowley, MA, during the summer of 2016.

We measured diel fluctuations in surface water chemistry of two high marsh ponds in July 2016. The ponds are shallow and experience day-night swings in oxygen concentrations, from super-saturation to anoxia. Our goal was to characterize changes in geochemical properties and dissolved organic carbon concentrations that accompany wide swings in oxygen concentrations. These data provide information about the responsiveness of microbial communities and how the dominance of redox-sensitive metabolisms changes over short time scales (e.g., hours) to feed back on pond water chemistry.

openCC (other)Jan 2020View details →
edi40/100

PIE LTER benthic microalgal biomass in fiddler-crab plots in a salt marsh of West Creek, Rowley, MA.

It is well known that species across the world are expanding or shifting their ranges because of climate change. Yet, we know little about their impact on the habitats they colonize. In an observational study, we examined the effect of the fiddler crab Minuca pugnax (Smith, 1870) on benthic microalgal biomass in salt marshes in its expanded range (northeastern Massachusetts, USA). We found that plots with M. pugnax had, on average, 74% lower diatom biomass and 77% lower cyanobacteria biomass than plots without M. pugnax. Our results indicate that this climate migrant can impact saltmarsh functioning by limiting benthic microalgal biomass. See: Johnson, D.S., K.S. Martínez-Soto, S. Wittyngham, M. Pant, and E. Goetz. 2020. The fiddler crab Minuca pugnax (Smith, 1870) (Decapoda: Brachyura: Ocypodidae) reduces saltmarsh algae in its expanded range. Journal of Crustacean Biology 40: 668-672

openCC (other)Jul 2021View details →
edi40/100

PIE LTER, parasites of the fiddler crab, Minuca pugnax, on east coast salt marshes of the USA.

When a species colonizes a new range, it can escape enemies found in its original range. Examples of enemy escape abound for invasive species, but are rare for climate migrants, which are populations of a species that colonize a new range due to climate-driven range shifts or expansions. The fiddler crab Minuca (=Uca) pugnax is found in the intertidal salt marshes of the US east coast. It recently expanded its range north into the Gulf of Maine as a result of ocean warming. We tested the hypothesis that M. pugnax had escaped its parasite enemies. Parasite richness and trematode intensity were lower in populations in the expanded range than in populations in the historical range, but infection prevalence did not differ. Although M. pugnax escaped most of its historical parasites when it migrated northward, it was infected with black-gill lamellae (indicative of Synophrya hypertrophica), which was found in the historical range, and with the trematode Odhneria cf. odhneri, which was not found in the historical range. To our knowledge, this is the first time that O. cf. odhneri has been reported in fiddler crabs. These results demonstrate that although M. pugnax escaped some of its historical parasites when it expanded its range, it appears to have gained a new parasite (O. cf. odhneri) in the expanded range. Overall, our results demonstrate that climate migrants can escape their enemies despite colonizing habitats adjacent to their enemy-filled historical range. See Johnson et al. 2020. A climate migrant escapes its parasites. Marine Ecology Progress Series 641: 111-121 for more details.

openCC (other)Oct 2021View details →
zenodo36/100

Dataset of maternal thyroid hormones transfer in Pied flycatchers

<p>This is the dataset of an experiment conducted on Pied flycatchers (<em>Ficedula hypoleuca</em>) in which we manipulated thyroid hormones in the mother&#39;s circulation. This dataset contains all the responses measured in this experiment.</p>

opencc-by-4.0Apr 2020View details →
zenodo36/100

Pilskalns pie Mārcienas Pilskalniem

Pilskalns pie Mārcienas Pilskalniem. 3D modelis. Koordinātas: 56.768984, 26.028031 https://www.latvijas-pilskalni.lv/pilskalns/ Source: Objaverse 1.0 / Sketchfab

opencc-byOct 2019View details →
zenodo36/100

Barona kapi pie Lielbērzes

Barona kapu 3D modelis. Koordinātas: 56.643323, 23.234573 Informācija saņemta no A.Tomašūna 2020.g. novembrī. Pēc profila līdzinās pilskalnam. Juris Urtāns veica apsekošanu un neatklāja pilskalna apdzīvotības pazīmes. Paugurā ir pamesta jaunāko laiku kapsēta un kādas 19.gs. būves, iespējams kapličas drupas. **Profils:** ![](https://opendata.latvijas-pilskalni.lv/Senvietu_3D_modeli/Latvija/Kurzeme/Barona_kapi_pie_Lielberzes/PlanlaufTerrain/Profils1.jpg) ![](https://opendata.latvijas-pilskalni.lv/Senvietu_3D_modeli/Latvija/Kurzeme/Barona_kapi_pie_Lielberzes/PlanlaufTerrain/Profils2.jpg) Source: Objaverse 1.0 / Sketchfab

opencc-byNov 2020View details →
zenodo36/100

Pied de lit

Pied de lit en argile de datation inconnue issu de pillage archéologique au Mali et saisi en 2004. Dimensions H = 29,5cm DB = 18cm E = 1,2cm Collection Musée National du Mali Source: Objaverse 1.0 / Sketchfab

opencc-byMay 2022View details →
zenodo36/100

Pilenes vieta pie Ķešaniem

Pilenes vieta pie Ķešaniem. 3D modelis. Koordinātas: 57.06382, 24.92707 https://www.latvijas-pilskalni.lv/pilenes-vieta-pie-kesaniem/ Source: Objaverse 1.0 / Sketchfab

opencc-byAug 2020View details →

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