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187 results for “mixing effects”

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zenodo36/100

Dataset: Testing for effects of growth rate on isotope trophic discrimination factors and evaluating the performance of Bayesian stable isotope mixing models experimentally: a moment of truth?

<p><span>Discerning assimilated diets of wild animals using stable isotopes is well established where potential dietary items in food webs are isotopically distinct. With the advent of mixing models, and Bayesian extensions of such models (Bayesian Stable Isotope Mixing Models, BSIMMs), statistical techniques available for these efforts have been rapidly increasing. The accuracy with which BSIMMs quantify diet, however, depends on several factors including uncertainty in tissue discrimination factors (TDFs; <em>&Delta;</em>) and identification of appropriate error structures. Whereas performance of BSIMMs has mostly been evaluated with simulations, here we test the efficacy of BSIMMs by raising domestic broiler chicks (<em>Gallus gallus domesticus</em>) on four isotopically distinct diets under controlled environmental conditions, ideal for evaluating factors that affect TDFs and testing how BSIMMs allocate individual birds to diets that vary in isotopic similarity. For both liver and feather tissues,<em> &delta;</em><sup>13</sup>C and <em>&delta; </em><sup>15</sup>N values differed among dietary groups. <em>&Delta;</em><sup>13</sup>C of liver, but not feather, was negatively related to the rate at which individuals gained body mass. For <em>&Delta;</em><sup>15</sup>N, we identified effects of dietary group, sex, and tissue type, as well as an interaction between sex and tissue type</span><span><span>, </span></span><span><span>with f</span></span><span>emales having higher liver <em>&Delta;</em><sup>15</sup>N relative to males. For both tissues, BSIMMs allocated most chicks to correct dietary groups, especially for models using combined TDFs rather than diet specific TDFs, and those applying a multiplicative error structure. These findings provide new information on how biological processes affect TDFs and confirm that adequately accounting for variability in consumer isotopes is necessary to optimize performance of BSIMMs. Moreover, they demonstrate experimentally that these types of models reliably characterize consumed diets when appropriately parameterized.<span>&nbsp; </span></span></p>

opencc-by-4.0Apr 2024View details →
dryad36/100

Flight training and dietary antioxidants have mixed effects on the oxidative status of multiple tissues in a female migratory songbird

<p>Birds, like other vertebrates, rely on a robust antioxidant system to protect themselves against oxidative imbalance caused by energy-intensive activities such as flying. Such oxidative challenges may be especially acute for females during spring migration, since they must pay the oxidative costs of flight while preparing for reproduction; however, little previous work has examined how the antioxidant system of female spring migrants responds to dietary antioxidants and the oxidative challenges of regular flying. We fed two diets to female European starlings, one supplemented with a dietary antioxidant and one without, and then flew them daily in a windtunnel for two weeks during the fall and spring migration periods. We measured the activity of enzymatic antioxidants (GPx, SOD, CAT), non-enzymatic antioxidant capacity (ORAC), and markers of oxidative damage (protein carbonyls and lipid hydroperoxides) in four tissues: pectoralis, leg, liver, and heart. Dietary antioxidants affected enzymatic antioxidant activity and lipid damage in the heart, and non-enzymatic antioxidant capacity in the pectoralis and protein damage in leg muscle. In general, birds fed less antioxidants appear to incur increased oxidative damage while upregulating non-enzymatic and enzymatic antioxidant activity, though these effects were strongly tissue-specific. We also found a significant diet x training interaction for enzymatic antioxidant activity in the leg, and strong trends for diet x training interactions for enzymatic antioxidant activity in the heart and liver. Flight-training may condition the antioxidant system of females to dynamically respond to oxidative challenges, and females during spring migration may shift antioxidant allocation to reduce oxidative damage.</p>

opencc-zeroDec 2020View details →
dryad36/100

Season, anthocyanin supplementation, and flight training have mixed effects on the antioxidant system of migratory European starlings (Sturnus vulgaris)

<p>Migratory birds engage in two periods of endurance flight annually as they travel between summer breeding and overwintering grounds, and such endurance flights likely incur oxidative costs. These costs may differ between fall and spring migration, especially for females who must prepare for breeding and egg laying in spring. The objective of this study of a migratory bird was to test proposed hypotheses about how key components of the female's antioxidant system differ in response to flight training in the fall and spring and to dietary antioxidant supplementation. We hand-raised female European starlings (<i>Sturnus vulgaris</i>) and then fed them either a diet supplemented with dietary anthocyanins or a diet without added anthocyanins. <a name="_Hlk53656115">We then flew females in a windtunnel for 15 days during fall and spring migration seasons and measured over time oxidative damage (d-ROMs) and three components of the antioxidant system</a>—non-enzymatic antioxidant capacity (OXY), uric acid, and glutathione peroxidase (GPx) activity. Prior to flight training, non-enzymatic antioxidant capacity and oxidative damage were lower in females during spring compared to fall, and females fed a low-antioxidant diet had consistently higher circulating uric acid. GPx activity decreased more in spring immediately after a long-duration flight. Females fed a high-antioxidant diet had a greater decrease in non-enzymatic antioxidant capacity after the 15-day flight training. <a name="_Hlk53656268">Flight-trained females had higher circulating uric acid than untrained females immediately after the longest-duration flight</a>, and decreased GPx activity after the 15-day flight training. In sum, females upregulated enzymatic and non-enzymatic endogenous antioxidants in spring, and females fed a diet with less antioxidants appear to compensate by increasing circulating uric acid. Our findings emphasize the important role of dietary antioxidants for birds during migration, <a name="_Hlk53656372">and that similar flights in fall and spring likely represent distinct oxidative challenges in the life history of female birds.</a></p>

opencc-zeroFeb 2022View details →
zenodo36/100

Effectiveness of Softening Agents for Enhancing Properties of Asphalt Mixes with High RAP Contents

<p>A high percentage of reclaimed asphalt pavement (RAP) in new asphalt concrete can lead to developing premature failure of asphalt pavements due to fatigue or low-temperature cracking. The use of softening agents in asphalt binders can resolve these problems. The aim of this study is to evaluate the effectiveness of softening agents for enhancing the properties of asphalt mixes with high RAP contents. Two waste products, namely, waste cooking oil (WCO), and engine bottom oil (EBO) along with a commercially produced rejuvenator were investigated in this study. The following three types of Performance Grade (PG) binders, each collected from two different sources, were considered in this study: PG 64-22, PG 70-22, and PG 76-22. These PG binders blended with different amounts (0, 15, 25, 40, and 60%) of RAP binders were rejuvenated with different dosages (0, 10, 15, and 20%) of the selected softening agents. Empirical tests (e.g., penetration and pH), Superpave tests, Atomic Force Microscope (AFM), Scanning Electron Microscope (SEM), Fourier Transform Infrared Spectroscopy (FTIR), and limited laboratory and field performance of asphalt mixture samples were also evaluated. It was found that the rejuvenators reduced the viscosity of the binder samples. The results showed that the rejuvenated binders reduce the production temperatures as well as the brittleness of the hard binders. The AFM results showed that modulus and deformation values of rejuvenated binders were significantly less than those of their unrejuvenated counterparts. Similarly, distinct peaks were observed in the FTIR peaks due to the rejuvenation. The findings of this study will help pavement professionals in selecting suitable rejuvenators in the construction of pavements with high RAP contents.</p>

opencc-by-4.0Jul 2021View details →
zenodo36/100

Supporting Data for Figures in "Wind Effects on Near and Midfield Mixing in Tidally Pulsed River Plumes"

<p>Supporting data for figures in &quot;Wind Effects on Near and Midfield Mixing in Tidally Pulsed River Plumes&quot; by Preston S. Spicer, Kelly L. Cole, Kimberly D. Huguenard, Daniel G. MacDonald, and Michael M. Whitney. The scientific journal article is published in the Journal of Geophysical Research: Oceans&nbsp;(2022). The main objectives of this study on the tidal Merrimack River plume are (1) quantify the net influence of straining, advection, and mixing on tidal plume stratification under realistic winds and (2) evaluate the mechanisms responsible for variability in mixing within the near and midfield plume regions over multiple tidal pulses under differing winds. A&nbsp;numerical modeling approach is taken. Data are from the Regional Ocean Modeling System (ROMS) results for the study area. Files are in MATLAB data format and are named FigXX_data. mat. Variable names and units correspond to graphed data of each figure in the journal article.</p>

opencc-by-4.0May 2022View details →
zenodo36/100

Short-term effect of thinning on red maple transpiration in a temperate mixed forest

<p>Under climate change, forests are expected to experience drier conditions that may increase tree mortality. Silvicultural treatments, such as thinning, have been proposed to reduce moisture competition and to improve forest resistance to drought events. Most studies have investigated the effectiveness of thinning under semi-arid conditions, while little information is available regarding temperate forest responses, together with the residual basal area (BA) that is required to reap the benefits of these treatments. This research aims to understand how the residual BA influences transpiration in mixed temperate forest stands that are dominated by red maple (<em>Acer rubrum</em>) in southeastern Canada. We monitored the sap flux density (Fd) with thermal dissipation-type sensors for 18 red maples spread across nine experimental plots that were thinned to obtain a gradient of residual BA (20, 12.5, 6 m<sup>2</sup> ha<sup>-1</sup>). The study was conducted during the first growing season following treatment. Low residual BA plots (6 m<sup>2</sup> ha<sup>-1</sup>) incurred drier atmospheric conditions as shown by a greater vapor pressure deficit (VPD) compared to high residual BA plots (20 m<sup>2</sup> ha<sup>-1</sup>). At the tree scale, Fd increased with residual BA, with the most pronounced differences under dry atmospheric conditions: when daily VPD exceeded 1.1 kPa, mean Fd in high residual BA plots was respectively 20% and 75% greater than in medium (12.5 m<sup>2</sup> ha<sup>-1</sup>) and low residual BA plots. At the stand level, we simulated total transpiration considering the stand as only made of red maples. The transpiration in medium and low residual BA plots amounted to 41% and 79% of transpiration simulated in the high residual BA plot. Overall, this work highlighted broad variation in response to residual BA treatments, emphasizing the need to better model forest water budgets, and partitioning overstory and understory evapotranspiration to make more adequate residual BA prescriptions in temperate forests.</p>

opencc-by-4.0Jul 2022View details →
dryad36/100

Emerging stability of forest productivity by mixing two species buffers temperature destabilizing effect

<p><span>The increasing disturbances in monocultures around the world </span><span>are</span><span> testimony to their instability under global change. Many studies have claimed that temporal stability of productivity increase with species richness, although the ecological fundaments have mainly been investigated through diversity experiments. To adequately manage forest ecosystems, it is necessary to have a comprehensive understanding of the effect of mixing species on the temporal stability of productivity and the way in which this it is influenced by climate conditions across large geographical areas. </span></p> <p><span>Here, we </span><span>used a unique dataset of 261 stands combining pure and two-species mixtures of four relevant tree species over a wide range of climate conditions in Europe to examine the effect of species mixing on the level and temporal stability of productivity. </span><span>Structural equation modelling was employed to further explore the direct and</span> <span>indirect influence of</span><span> climate</span><span>, overyielding, species asynchrony and additive effect (i.e. temporal stability expected from the species growth in monospecific stands) on temporal stability in mixed forests. </span></p> <p><span>We showed that by adding only one tree species to monocultures</span><span>,</span><span> the level (overyielding: +6%) </span><span>and </span><span>stability (temporal stability: +12%) of stand growth increased significantly. We </span><span>identified </span><span>the key effect of temperature on destabilizing stand growth, which may be mitigated by mixing species. We further </span><span>confirmed</span><span> asynchrony as </span><span>the </span><span>main driver of temporal stability in mixed stands, through both the additive effect and species interactions, which modify between-species asynchrony in mixtures in comparison to monocultures. </span></p> <p><span>Synthesis and applications</span><span>.</span> <span>This study highlights the emergent properties associated with mixing two-species, which result in resource efficient and temporally stable production systems. We reveal the negative impact of mean temperature on temporal stability of forest productivity and how the stabilizing effect of mixing two species can counterbalance this impact. </span><span>The overyielding and temporal stability of growth addressed in this paper are essential for ecosystem services closely linked with the level and rhythm of forest growth. </span><span>Our results underline that mixing two species can be a realistic and effective nature-based climate solution, which could contribute towards meeting EU climate target policies. </span></p>

opencc-zeroDec 2021View details →
zenodo36/100

Mixed higher-order topology: boundary non-Hermitian skin effect induced by a Floquet bulk

<p>Code and data used to&nbsp;produce&nbsp;the numerical results of &quot;Mixed higher-order topology: boundary non-Hermitian skin effect induced by a Floquet bulk&quot;</p>

opencc-by-4.0Oct 2022View details →
zenodo36/100

Glacial ice sheet extent effects on tidal mixing and the global overturning circulation - Model Output

<p>This dataset contains the output from the tide model and climate model simulations from the publication Wilmes et al. (2018)&nbsp;&quot;Glacial ice sheet extent effects on tidal mixing and the global overturning circulation&quot; submitted to Paleoceanography.&nbsp;The user is referred to the paper for details on the methodology.</p> <p>Dissipation files:</p> <p>Files beginning with &quot;diss&quot; contain tidal dissipation files calculated from the OTIS tide model output at 1/8th deg using the direct method. Files with the M2 constituent only are in .mat format and extend from 86deg S to 89deg N&nbsp;whereas the files containing all constituents (M2, S2, K1 and O1)&nbsp;are in netcdf format and extend from 90deg S to 90deg N. These files regridded and are used as the climate model tidal forcing.</p> <p>Dissipation file list:</p> <p>diss_dir_ze_1_8_rtp_21kyrBP_i6g_-I1.5_-t_8299008.nc Dissipation for&nbsp;LGM ICE-6G ZE ITdrag&nbsp;1/8th deg<br> diss_dir_ze_1_8_rtp_21kyrBP_i5g_-I1.5_-t_8299031.nc&nbsp;Dissipation for&nbsp;LGM ICE-5G ZE ITdrag&nbsp;1/8th deg<br> diss_dir_ze_1_8_rtp_00kyrBP_-I1.5_pdsal_8299034.nc&nbsp;Dissipation for&nbsp;PD ZE ITdrag&nbsp;1/8th deg</p> <p>diss_dir_js_1_8_rtop_21kyrBP_i6g_-t_-I6.0_7673000.nc&nbsp;Dissipation for&nbsp;LGM ICE-6G JS&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_js_1_8_rtop_21kyrBP_i5g_-t_-I6.0_7672999.nc&nbsp;Dissipation for&nbsp;LGM ICE-5G JS&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_js_1_8_rtop_00kyrBP_-I6.0_7672998.nc&nbsp;&nbsp;Dissipation for&nbsp;PD JS ITdrag&nbsp;1/8th deg</p> <p>diss_dir_ze_m2_1_8_rtp_21kyrBP_i5g_blk5_NH_lmsk_-I1.5_8299652.mat&nbsp;&nbsp;M2 dissipation for&nbsp;LGM ICE-5G blk1 + NH ICE-6G land mask&nbsp;ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_i5g_blk5_-I1.5_8299534.mat&nbsp;&nbsp;M2 dissipation for&nbsp;LGM ICE-5G blk5&nbsp;ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_i5g_blk4_-I1.5_8299533.mat&nbsp;&nbsp;M2 dissipation for&nbsp;LGM ICE-5G blk4&nbsp;ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_i5g_blk3_-I1.5_8299531.mat&nbsp;&nbsp;M2 dissipation for&nbsp;LGM ICE-5G blk3&nbsp;ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_i5g_blk2_-I1.5_8299530.mat&nbsp;M2 dissipation for&nbsp;LGM ICE-5G blk2&nbsp;ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_i5g_blk1_-I1.5_8299529.mat&nbsp;&nbsp;M2 dissipation for&nbsp;LGM ICE-5G blk1&nbsp;ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_140mSLD_i6g_lmsk_-I1.5_8299543.mat&nbsp;M2 dissipation for&nbsp;PD 140mSLD&nbsp;ICE-6G land mask ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_140mSLD_i5g_lmsk_-I1.5_8299542.mat&nbsp;M2 dissipation for&nbsp;PD 140mSLD&nbsp;ICE-5G land mask ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_130mSLD_i6g_lmsk_-I1.5_8299544.mat&nbsp;M2 dissipation for&nbsp;PD 130mSLD&nbsp;ICE-6G land mask ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_130mSLD_i5g_lmsk_-I1.5_8299541.mat&nbsp;M2 dissipation for&nbsp;PD 130mSLD&nbsp;ICE-5G land mask ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_120mSLD_i6g_lmsk_-I1.5_8299545.mat&nbsp;M2 dissipation for&nbsp;PD 120mSLD&nbsp;ICE-6G land mask ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_120mSLD_i5g_lmsk_-I1.5_8299540.mat&nbsp;M2 dissipation for&nbsp;PD 120mSLD&nbsp;ICE-5G land mask ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_110mSLD_i6g_lmsk_-I1.5_8299546.mat&nbsp;M2 dissipation for&nbsp;PD 110mSLD&nbsp;ICE-6G land mask ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_110mSLD_i5g_lmsk_-I1.5_8299539.mat&nbsp;M2 dissipation for&nbsp;PD 110mSLD&nbsp;ICE-5G land mask ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_100mSLD_i6g_lmsk_-I1.5_8299547.mat&nbsp;M2 dissipation for&nbsp;PD 100mSLD&nbsp;ICE-6G land mask ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_100mSLD_i5g_lmsk_-I1.5_8299538.mat&nbsp;M2 dissipation for&nbsp;PD 100mSLD&nbsp;ICE-5G land mask ZE&nbsp;ITdrag&nbsp;1/8th deg<br> diss_dir_ze_m2_1_8_rtp_21kyrBP_120mSLD_-I1.5_8299537.mat M2 dissipation for&nbsp;PD 120mSLD&nbsp;JS ITdrag&nbsp;1/8th deg</p> <p>&nbsp;</p> <p>Climate model output:</p> <p>UVic climate model output for all simulations in the paper has been compressed using tar and zip. Each folder contains the output yearly averages (tavg.xxx.nc) which have been used in the results section of the paper. The model input&nbsp;files&nbsp;are located in /data. The tidal input file is in /data/O_tideenrg_green.nc. Furthermore included are restart files (rest.xxx.nc), model code in /code, and the model exectuables.</p> <p>Climate mode output list:</p> <p>preind_tidal_ze_00kyr_rtop_-1.5_8299034_dir.tgz&nbsp;&nbsp;Output from PIC<br> lgm_tidal_ze_21kyr_i6g_rtop_-1.5_8299008_dir_tau_lgm.tgz Output from LGM_i6gT_lgmW<br> lgm_tidal_ze_21kyr_i6g_rtop_-1.5_8299008_dir.tgz Output from LGM_i6gT_pdW<br> lgm_tidal_ze_21kyr_i5g_rtop_-1.5_8299031_dir_tau_lgm.tgz Output from LGM_i5gT_lgmW<br> lgm_tidal_ze_21kyr_i5g_rtop_-1.5_8299031_dir.tgz Output from LGM_i5gT_pdW<br> lgm_tidal_ze_00kyr_rtop_-1.5_8299034_dir_tau_lgm.tgz Output from LGM_pdT_lgmW<br> lgm_tidal_ze_00kyr_rtop_-1.5_8299034_dir.tgz Output from LGM_pdT_pdW</p> <p>preind_tidal_js_1_2_rtp_00kyrBP_-I1.0_7881173.tgz Output from PIC_1_2_rtp82<br> preind_js_1_2_SandS8.2_00kyrBP_82SNcb_-I1.0_8317333_dir.tgz&nbsp;Output from PIC_1_2_SS82<br> lgm_tidal_js_1_2_SandS8.2_00kyrBP_120mSLD_82SNcb_-t_-I1.0_8317331_dir.tgz&nbsp;Output from LGM_1_2_SS82_sldT<br> lgm_tidal_js_1_2_SandS8.2_00kyrBP_82SNcb_-I1.0_8317333_dir.tgz&nbsp;Output from LGM_1_2_SS82_pdT<br> lgm_tidal_js_1_2_rtop_00kyrBP_120mSLD_82SN_-t_-I1.0_8315693.tgz&nbsp;Output from LGM_1_2_rtp82_sldT<br> lgm_tidal_js_1_2_rtop_00kyrBP_82SN_pdsal_-I1.0_8315702.tgz&nbsp;Output from LGM_1_2_rtp82_pdT<br> <br> &nbsp;</p> <p>&nbsp;</p> <p>&nbsp;</p>

opencc-by-4.0Jan 2018View details →
zenodo36/100

Data and Script used in "Effects of canopy gaps on microclimate, soil biological activity and their relationship in a European mixed floodplain forest"

<p>The R code and data provided in this repository allow to reproduce the data carpentry, analysis and visualization of &ldquo;Effects of canopy gaps on microclimate, soil biological activity and their relationship in a European mixed floodplain forest&rdquo; (https://doi.org/10.1016/j.scitotenv.2024.173572).</p> <p>&nbsp;</p> <p>Folder structure</p> <p>&nbsp;</p> <p>Data abstracts:</p> <p>Data_abstract_climate.pdf</p> <p>Data_abstract_soil_biotics.pdf</p> <p>Data_abstract_soil_abiotics_openness.pdf</p> <p>&nbsp;</p> <p>Data:</p> <p>Climate_data.xlsx</p> <p>Soil_biotics.xlsx</p> <p>Soil_abiotics_openness.xlsx</p> <p>&nbsp;</p> <p>R Scripts:</p> <p>00-preamble.R loads all required packages</p> <p>01-data-carpentry.R loads all datasets and prepares the analysis of all experimental periods.</p> <p>02-data-analyses-microclimate.R compares understorey air and soil microclimate between forest types and treatments, presents diurnal and seasonal variations and tests the relationship of under- and overstorey openness on microclimate.</p> <p>03-data-analyses-decomposition.R compares decomposition rates and feeding activity between forest types and treatments and models the dependencies of soil biological activity on microclimate and soil abiotic factors.</p> <p>&nbsp;</p> <p>Information of related software and package versions used in the script:<br>R version 4.3.2 (2023-10-31 ucrt)<br>Platform: x86_64-w64-mingw32/x64 (64-bit)<br>Running under: Windows 10 x64 (build 19045)<br>Matrix products: default</p> <p>&nbsp;</p> <p>Contact</p> <p>Please contact me at annalena.lenk@uni-leipzig.de if you have further questions.</p>

opencc-by-4.0Jun 2024View details →
zenodo36/100

Underlying data for "Development of a framework of potential adverse effects of interventions to improve critical thinking about health choices: A mixed methods study."

Open the record for dataset details and reuse information.

opencc-by-4.0Oct 2024View details →
dryad36/100

Data from: Developmental lead exposure has mixed effects on butterfly cognitive processes

While the effects of lead pollution have been well studied in vertebrates, it is unclear to what extent lead may negatively affect insect cognition. Lead pollution in soils can elevate lead in plant tissues, suggesting it could negatively affect neural development of insect herbivores. We used the cabbage white butterfly (Pieris rapae) as a model system to study the effect of lead pollution on insect cognitive processes, which play an important role in how insects locate and handle resources. Cabbage white butterfly larvae were reared on a 4-ppm lead diet, a concentration representative of vegetation in polluted sites; we measured eye size and performance on a foraging assay in adults. Relative to controls, lead-reared butterflies did not differ in time or ability to search for a food reward associated with a less preferred color. Indeed, lead-treated butterflies were more likely to participate in the behavioral assay itself. Lead exposure did not negatively affect survival or body size, and it actually sped up development time. The effects of lead on relative eye size varied with sex: lead tended to reduce eye size in males, but increase eye size in females. These results suggest that low levels of lead pollution may have mixed effects on butterfly vision, but only minimal impacts on performance in foraging tasks, although follow-up work is needed to test whether this result is specific to cabbage whites, which are often associated with disturbed areas.

opencc-zeroDec 2015View details →
dryad36/100

Data from: Demographic effects of a megafire on a declining prairie grouse in the mixed-grass prairie

<p>Recent studies have documented benefits of small, prescribed fire and wildfire for grassland-dependent wildlife, such as lesser prairie-chickens (<em>Tympanuchus</em> <em>pallidicintus</em>), but wildlife demographic response to the scale and intensity of megafire (wildfire &gt; 40,000 ha) in modern fragmented grasslands remains unknown. Limited available grassland habitat makes it imperative to understand if increasing frequency of megafires could further reduce already declining lesser prairie-chicken populations, or if historical evolutionary interactions with fire make lesser prairie-chickens resilient. To evaluate lesser prairie-chicken demographic response to megafires, we compared lek counts, nest density, and survival rates of adults, nests, and chicks before (2014–2016) and after (2018–2020) a 2017 megafire in the mixed-grass prairie of Kansas, USA (Starbuck fire ~254,000 ha). There was a 67% decline in attending males on leks post-fire and a 46% decline in occupied leks post-fire. Despite population declines as indicated by lek counts, adult female breeding season survival (Ŝ) was similar pre- (Ŝ <span>= </span>0.65 ± 0.08 [SE]) and post-fire (0.61 ± 0.08), as was chick survival (pre-fire: 0.23 ± 0.07; post-fire: 0.27 ± 0.11). Nest survival appeared lower post-fire (pre-fire: 0.38 ± 0.06; post-fire: 0.20 ± 0.06), <span>but did not differ at the 95% confidence interval.</span> Nest density of marked females declined 73% in areas burned by megafire. Although lesser prairie-chickens persisted in the study area and we documented minimal effects on most demographic rates, reduced lesser prairie-chicken abundance and reproductive output suggests full recovery may take &gt;3 years. Increased propensity for megafire resulting from suppression of smaller fires, compounded by climate change and woody encroachment, may impose a short-term (3-5 year) threat to already declining lesser prairie-chicken populations.</p>

opencc-zeroNov 2022View details →
dryad36/100

The effects of N-addition on litter mixture effects depend on decomposition time: a case from mixed-litter decomposition in the Gurbantunggut Desert

<p>Changes in nitrogen (N) deposition and litter mixtures have been shown to influence ecosystem processes such as litter decomposition. However, the interactive effects of litter mixing and N-deposition on decomposition process in desert regions remain poorly identified. We assessed the simultaneous effects of both N addition and litter mixture on mass loss in a litterbag decomposition experiment using six native plants in single-species samples with diverse quality and 14 species-combinations in the Gurbantunggut Desert under two N addition treatments (control and N addition). The N addition had no significant effect on decomposition rate of single-species litter (except <em>Haloxylon ammodendron</em>), whereas litter mass loss and decomposition rate differed significantly among species, with variations positively correlated with initial phosphorus concentration and negatively correlated with initial lignin concentration. After 18 months, the average mass loss across litter mixtures did not overall differ from those predicted from single-species either in control or N addition treatments, that is, mixing of different species had no non-additive effects on decomposition. The N addition, however, did modify the direction of mixture effects, and interacted with incubation time. Added N transformed synergistic effects of litter mixtures to antagonistic effects on mass loss after 1 month of decomposition, while transforming neutral effects of litter mixture to synergistic effects after 6 months of decomposition. Our results demonstrated that initial chemical properties played an important role in litter decomposition, while no effects of litter mixture on decomposition process in this desert region. The N addition altered the litter mixture effects on mass loss with incubation time, implying that increased N deposition in the future may have profound effects on carbon turnover to a greater extent than previously thought in desert ecosystems.</p>

opencc-zeroJul 2023View details →
zenodo36/100

Data Set Accompanying "Free Energy Decompositions Illuminate Synergistic Effects in Interfacial Binding Thermodynamics of Mixed Surfactant Systems"

<p>This data set accompanies &quot;Free Energy Decompositions Illuminate Synergistic Effects in Interfacial Binding<br> Thermodynamics of Mixed Surfactant Systems&quot; by Colin K. Egan and Ali Hassanali.&nbsp; It includes example GROMACS<br> input files for all simulations analyzed in the paper, as well as example data sets and analysis scripts.&nbsp; See<br> https://doi.org/10.26434/chemrxiv-2023-h11k5 for the preprint manuscript.</p>

opencc-by-4.0Aug 2023View details →
ClinicalTrials.gov36/100

A Study to Examine the Clinical Effectiveness of Tafamidis in Patients With Mixed Phenotype Hereditary Transthyretin Amyloidosis

ClinicalTrials.gov study NCT05139680. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov36/100

Effect of Electroacupuncture Versus PFMT Plus Solifenacin for Mixed Urinary Incontinence

ClinicalTrials.gov study NCT02047032. IPD Sharing: NO. Countries: 1. Publications: 4.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov36/100

A Study to Investigate the Effectiveness and Safety of Bempedoic Acid in Patients With Primary Hypercholesterolemia or Mixed Dyslipidemia in Taiwan

ClinicalTrials.gov study NCT06925100. IPD Sharing: YES. Countries: 1. Publications: 0.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov36/100

Safety and Maintenance of Effect of Ziprasidone Plus a Mood Stabilizer in Bipolar I Disorder (Manic or Mixed)

ClinicalTrials.gov study NCT00280566. IPD Sharing: Not stated. Countries: 13. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov36/100

The Effects of Mixed Working Memory Training on Subsequent Training Gains Among Older Adults

ClinicalTrials.gov study NCT05672771. IPD Sharing: YES. Countries: 1. Publications: 8.

controlledIPD-YESFeb 2026View details →

ScienceDex guides

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

Compare curated datasets

Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

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

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record