Skip to main content
Powered by ShareScore

Find research datasets worth reusing

Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.

427

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

427 results for “Ducks”

Learn how ShareScore rates datasets ↗
zenodo36/100

Ocotea argyrophylla Ducke from Colombia collected by F. Moreno y C. Carvajal #1271

<p><strong>File Name</strong>: <span>TOLI-25217-PER-01-P5-5.jpg</span></p> <p><strong>CÓDIGO FOTO</strong>: <span>TOLI-25217-PER-01-P5-5-</span></p> <p><strong>Fotografía</strong>: <span>SI</span></p> <p><strong>Nº TOLI</strong>: <span>TOLI-25217</span></p> <p><strong>PARCELA</strong>: <span>PER-01</span></p> <p><strong>CÓDIGO</strong>: <span>P5-5</span></p> <p><strong>Nº COLECTA</strong>: <span>1271</span></p> <p><strong>NUEVOS COLECTORES</strong>: <span>Esteban Álvarez Dávila</span></p> <p><strong>COLECTORES</strong>: <span>F. Moreno y C. Carvajal</span></p> <p><strong>Nº MUESTRAS MONTADAS</strong>: <span>1</span></p> <p><strong>Homologación</strong>: <span>Homologado</span></p> <p><strong>Nueva fecha del evento </strong>: <span>20/12/2018.</span></p> <p><strong>Fecha del evento</strong>: <span>01/09/2012.</span></p> <p><strong>Proyecto </strong>: <span>Recursos Botánicos Disponibles en Línea (BRAVO) para la flora Colombiana</span></p> <p><strong>Hábitat</strong>: <span>Bosque húmedo tropical (bh-T)</span></p> <p><strong>Comentario del evento</strong>: <span>Bosque de tierra firme, dosel abierto, de 25-30 m, emergentes de 35 m, estrato medio de 15 m, sotobosque denso con alta regeneración natural, presencia de palmas como Lepidocaryum tenue, Oenocarpus bataua, Geonoma sp., capa de hojarazca de 15 cm, abundante materia orgánica. Pendientes pronunciadas. Poca intervención antrópica.</span></p> <p><strong>Continente</strong>: <span>SA</span></p> <p><strong>Pais</strong>: <span>Colombia</span></p> <p><strong>Estado/Provincia</strong>: <span>Amazonas</span></p> <p><strong>Municipio</strong>: <span>Puerto Santander</span></p> <p><strong>Localidad</strong>: <span>Resguardo indígena Nonuya de Villazul.</span></p> <p><strong>Elevación minima en metros</strong>: <span>250</span></p> <p><strong>Elevación maxima en metros</strong>: <span>400</span></p> <p><strong>Latitud</strong>: <span>-0.654</span></p> <p><strong>Longitud original</strong>: <span>-72.072</span></p> <p><strong>datum geodésico</strong>: <span>WGS 84</span></p> <p><strong>Latitud decimal</strong>: <span>-0.654</span></p> <p><strong>Longitud decimal</strong>: <span>-72.072</span></p> <p><strong>Identificado por</strong>: <span>Diego Suescún </span></p> <p><strong>Fecha de identificación</strong>: <span>25/01/2019.</span></p> <p><strong>Nombre cientifico</strong>: <span>Ocotea argyrophylla Ducke</span></p> <p><strong>Reino</strong>: <span>Plantae</span></p> <p><strong>Filo</strong>: <span>Magnoliophyta</span></p> <p><strong>Clase</strong>: <span>Equisetopsida</span></p> <p><strong>Orden</strong>: <span>Laurales</span></p> <p><strong>Familia nueva</strong>: <span>Lauraceae</span></p> <p><strong>Género nuevo</strong>: <span>Ocotea </span></p> <p><strong>especie nueva</strong>: <span>argyrophylla</span></p> <p><strong>Autoría del nombre científico</strong>: <span>Ducke</span></p> <p><strong></strong>: <span>Lauraceae</span></p> <p><strong>genero herbario</strong>: <span>Ocotea</span></p> <p><strong>especie herbario</strong>: <span>argyrophylla</span></p> <p><strong>Especie de herbario para TNRS</strong>: <span>Ocotea argyrophylla</span></p> <p><strong>Especie corregida herbario y desde TNRS</strong>: <span>Ocotea argyrophylla</span></p> <p><strong>Familia corregida desde TNRS</strong>: <span>Lauraceae</span></p> <p><strong></strong>: <span>4232</span></p>

opencc-by-4.0Aug 2012View details →
zenodo36/100

Ocotea argyrophylla Ducke from Colombia collected by F. Moreno y C. Carvajal #2390

<p><strong>File Name</strong>: <span>TOLI-25215-PER-01-V4&lt;10-25.jpg</span></p> <p><strong>CÓDIGO FOTO</strong>: <span>TOLI-25215-PER-01-V4&lt;10-25-</span></p> <p><strong>Fotografía</strong>: <span>SI</span></p> <p><strong>Nº TOLI</strong>: <span>TOLI-25215</span></p> <p><strong>PARCELA</strong>: <span>PER-01</span></p> <p><strong>CÓDIGO</strong>: <span>V4&lt;10-25</span></p> <p><strong>Nº COLECTA</strong>: <span>2390</span></p> <p><strong>NUEVOS COLECTORES</strong>: <span>Esteban Álvarez Dávila</span></p> <p><strong>COLECTORES</strong>: <span>F. Moreno y C. Carvajal</span></p> <p><strong>Nº MUESTRAS MONTADAS</strong>: <span>1</span></p> <p><strong>Homologación</strong>: <span>No homologado</span></p> <p><strong>Nueva fecha del evento </strong>: <span>20/12/2018.</span></p> <p><strong>Fecha del evento</strong>: <span>01/09/2012.</span></p> <p><strong>Proyecto </strong>: <span>Recursos Botánicos Disponibles en Línea (BRAVO) para la flora Colombiana</span></p> <p><strong>Hábitat</strong>: <span>Bosque húmedo tropical (bh-T)</span></p> <p><strong>Comentario del evento</strong>: <span>Bosque de tierra firme, dosel abierto, de 25-30 m, emergentes de 35 m, estrato medio de 15 m, sotobosque denso con alta regeneración natural, presencia de palmas como Lepidocaryum tenue, Oenocarpus bataua, Geonoma sp., capa de hojarazca de 15 cm, abundante materia orgánica. Pendientes pronunciadas. Poca intervención antrópica.</span></p> <p><strong>Continente</strong>: <span>SA</span></p> <p><strong>Pais</strong>: <span>Colombia</span></p> <p><strong>Estado/Provincia</strong>: <span>Amazonas</span></p> <p><strong>Municipio</strong>: <span>Puerto Santander</span></p> <p><strong>Localidad</strong>: <span>Resguardo indígena Nonuya de Villazul.</span></p> <p><strong>Elevación minima en metros</strong>: <span>250</span></p> <p><strong>Elevación maxima en metros</strong>: <span>400</span></p> <p><strong>Latitud</strong>: <span>-0.654</span></p> <p><strong>Longitud original</strong>: <span>-72.072</span></p> <p><strong>datum geodésico</strong>: <span>WGS 84</span></p> <p><strong>Latitud decimal</strong>: <span>-0.654</span></p> <p><strong>Longitud decimal</strong>: <span>-72.072</span></p> <p><strong>Nombre cientifico</strong>: <span>Ocotea argyrophylla Ducke</span></p> <p><strong>Reino</strong>: <span>Plantae</span></p> <p><strong>Filo</strong>: <span>Magnoliophyta</span></p> <p><strong>Clase</strong>: <span>Equisetopsida</span></p> <p><strong>Orden</strong>: <span>Laurales</span></p> <p><strong>Familia nueva</strong>: <span>Lauraceae</span></p> <p><strong>Género nuevo</strong>: <span>Ocotea </span></p> <p><strong>especie nueva</strong>: <span>argyrophylla</span></p> <p><strong>Autoría del nombre científico</strong>: <span>Ducke</span></p> <p><strong></strong>: <span>Lauraceae</span></p> <p><strong>genero herbario</strong>: <span>Ocotea</span></p> <p><strong>especie herbario</strong>: <span>argyrophylla</span></p> <p><strong>Especie de herbario para TNRS</strong>: <span>Ocotea argyrophylla</span></p> <p><strong>Especie corregida herbario y desde TNRS</strong>: <span>Ocotea argyrophylla</span></p> <p><strong>Familia corregida desde TNRS</strong>: <span>Lauraceae</span></p> <p><strong></strong>: <span>4230</span></p>

opencc-by-4.0Aug 2012View details →
zenodo36/100

Vatairea cf. erythrocarpa (Ducke) Ducke. from Colombia collected by W. López #1992

<p><strong>File Name</strong>: <span>TOLI-24938-CAU-01-A9-99.jpg</span></p> <p><strong>CÓDIGO FOTO</strong>: <span>TOLI-24938-CAU-01-A9-99-</span></p> <p><strong>Fotografía</strong>: <span>SI</span></p> <p><strong>Nº TOLI</strong>: <span>TOLI-24938</span></p> <p><strong>PARCELA</strong>: <span>CAU-01</span></p> <p><strong>CÓDIGO</strong>: <span>A9-99</span></p> <p><strong>Nº COLECTA</strong>: <span>1992</span></p> <p><strong>NUEVOS COLECTORES</strong>: <span>Wilmar López Oviedo</span></p> <p><strong>COLECTORES</strong>: <span>W. López</span></p> <p><strong>Nº MUESTRAS MONTADAS</strong>: <span>1</span></p> <p><strong>Homologación</strong>: <span>Homologado</span></p> <p><strong>Nueva fecha del evento </strong>: <span>15/12/2018.</span></p> <p><strong>Fecha del evento</strong>: <span>30/10/2018.</span></p> <p><strong>Proyecto </strong>: <span>Recursos Botánicos Disponibles en Línea (BRAVO) para la flora Colombiana</span></p> <p><strong>Hábitat</strong>: <span>Bosque muy húmedo tropical (bmh-T)</span></p> <p><strong>Continente</strong>: <span>SA</span></p> <p><strong>Pais</strong>: <span>Colombia</span></p> <p><strong>Estado/Provincia</strong>: <span>Chocó</span></p> <p><strong>Municipio</strong>: <span>Acandí</span></p> <p><strong>Localidad</strong>: <span>Capurganá. A-Bosque </span></p> <p><strong>Elevación minima en metros</strong>: <span>200</span></p> <p><strong>Elevación maxima en metros</strong>: <span>400</span></p> <p><strong>Latitud</strong>: <span>8.627</span></p> <p><strong>Longitud original</strong>: <span>-77.366</span></p> <p><strong>datum geodésico</strong>: <span>WGS 84</span></p> <p><strong>Latitud decimal</strong>: <span>8.627</span></p> <p><strong>Longitud decimal</strong>: <span>-77.366</span></p> <p><strong>Identificado por</strong>: <span>William Ariza</span></p> <p><strong>Fecha de identificación</strong>: <span>25/01/2019.</span></p> <p><strong>Familia antigua</strong>: <span>NN</span></p> <p><strong>Especie antigua</strong>: <span>NN</span></p> <p><strong>Nombre cientifico</strong>: <span>Vatairea cf. erythrocarpa (Ducke) Ducke.</span></p> <p><strong>Reino</strong>: <span>Plantae</span></p> <p><strong>Filo</strong>: <span>Magnoliophyta</span></p> <p><strong>Clase</strong>: <span>Equisetopsida</span></p> <p><strong>Orden</strong>: <span>Fabales</span></p> <p><strong>Familia nueva</strong>: <span>Fabaceae</span></p> <p><strong>Género nuevo</strong>: <span>Vatairea </span></p> <p><strong>especie nueva</strong>: <span>erythrocarpa </span></p> <p><strong>Autoría del nombre científico</strong>: <span>(Ducke) Ducke.</span></p> <p><strong>genero herbario</strong>: <span>Vatairea</span></p> <p><strong>especie herbario</strong>: <span>erythrocarpa</span></p> <p><strong>Especie de herbario para TNRS</strong>: <span>Vatairea erythrocarpa</span></p> <p><strong>Especie corregida herbario y desde TNRS</strong>: <span>Vatairea erythrocarpa</span></p> <p><strong>Familia corregida desde TNRS</strong>: <span>Fabaceae</span></p> <p><strong></strong>: <span>3971</span></p>

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

Scleronema praecox (Ducke) Ducke. from Colombia collected by F. Moreno y C. Carvajal #3392

<p><strong>File Name</strong>: <span>TOLI-24710-PER-01-T4-15.jpg</span></p> <p><strong>CÓDIGO FOTO</strong>: <span>TOLI-24710-PER-01-T4-15-</span></p> <p><strong>Fotografía</strong>: <span>SI</span></p> <p><strong>Nº TOLI</strong>: <span>TOLI-24710</span></p> <p><strong>PARCELA</strong>: <span>PER-01</span></p> <p><strong>CÓDIGO</strong>: <span>T4-15</span></p> <p><strong>Nº COLECTA</strong>: <span>3392</span></p> <p><strong>NUEVOS COLECTORES</strong>: <span>Esteban Álvarez Dávila</span></p> <p><strong>COLECTORES</strong>: <span>F. Moreno y C. Carvajal</span></p> <p><strong>Nº MUESTRAS MONTADAS</strong>: <span>1</span></p> <p><strong>Homologación</strong>: <span>Homologado</span></p> <p><strong>Nueva fecha del evento </strong>: <span>20/12/2018.</span></p> <p><strong>Fecha del evento</strong>: <span>01/09/2012.</span></p> <p><strong>Proyecto </strong>: <span>Recursos Botánicos Disponibles en Línea (BRAVO) para la flora Colombiana</span></p> <p><strong>Hábitat</strong>: <span>Bosque húmedo tropical (bh-T)</span></p> <p><strong>Comentario del evento</strong>: <span>Bosque de tierra firme, dosel abierto, de 25-30 m, emergentes de 35 m, estrato medio de 15 m, sotobosque denso con alta regeneración natural, presencia de palmas como Lepidocaryum tenue, Oenocarpus bataua, Geonoma sp., capa de hojarazca de 15 cm, abundante materia orgánica. Pendientes pronunciadas. Poca intervención antrópica.</span></p> <p><strong>Continente</strong>: <span>SA</span></p> <p><strong>Pais</strong>: <span>Colombia</span></p> <p><strong>Estado/Provincia</strong>: <span>Amazonas</span></p> <p><strong>Municipio</strong>: <span>Puerto Santander</span></p> <p><strong>Localidad</strong>: <span>Resguardo indígena Nonuya de Villazul.</span></p> <p><strong>Elevación minima en metros</strong>: <span>250</span></p> <p><strong>Elevación maxima en metros</strong>: <span>400</span></p> <p><strong>Latitud</strong>: <span>-0.654</span></p> <p><strong>Longitud original</strong>: <span>-72.072</span></p> <p><strong>datum geodésico</strong>: <span>WGS 84</span></p> <p><strong>Latitud decimal</strong>: <span>-0.654</span></p> <p><strong>Longitud decimal</strong>: <span>-72.072</span></p> <p><strong>Identificado por</strong>: <span>James Richardson</span></p> <p><strong>Fecha de identificación</strong>: <span>23/01/2019.</span></p> <p><strong>Familia antigua</strong>: <span>Malvaceae</span></p> <p><strong>Especie antigua</strong>: <span>NN</span></p> <p><strong>Nombre cientifico</strong>: <span>Scleronema praecox (Ducke) Ducke.</span></p> <p><strong>Reino</strong>: <span>Plantae</span></p> <p><strong>Filo</strong>: <span>Magnoliophyta</span></p> <p><strong>Clase</strong>: <span>Equisetopsida</span></p> <p><strong>Orden</strong>: <span>Malvales</span></p> <p><strong>Familia nueva</strong>: <span>Malvaceae</span></p> <p><strong>Género nuevo</strong>: <span>Scleronema</span></p> <p><strong>especie nueva</strong>: <span>praecox </span></p> <p><strong>Autoría del nombre científico</strong>: <span>(Ducke) Ducke </span></p> <p><strong></strong>: <span>Malvaceae</span></p> <p><strong>genero herbario</strong>: <span>Scleronema</span></p> <p><strong>especie herbario</strong>: <span>praecox</span></p> <p><strong>Especie de herbario para TNRS</strong>: <span>Scleronema praecox</span></p> <p><strong>Especie corregida herbario y desde TNRS</strong>: <span>Scleronema praecox</span></p> <p><strong>Familia corregida desde TNRS</strong>: <span>Malvaceae</span></p> <p><strong></strong>: <span>3761</span></p>

opencc-by-4.0Aug 2012View details →
zenodo36/100

Zygia racemosa (Ducke) Barneby & J.W. Grimes from Colombia collected by F. Moreno y C. Carvajal #3544

<p><strong>File Name</strong>: <span>TOLI-24726-PER-01-G4-2.jpg</span></p> <p><strong>CÓDIGO FOTO</strong>: <span>TOLI-24726-PER-01-G4-2-</span></p> <p><strong>Fotografía</strong>: <span>SI</span></p> <p><strong>Nº TOLI</strong>: <span>TOLI-24726</span></p> <p><strong>PARCELA</strong>: <span>PER-01</span></p> <p><strong>CÓDIGO</strong>: <span>G4-2</span></p> <p><strong>Nº COLECTA</strong>: <span>3544</span></p> <p><strong>NUEVOS COLECTORES</strong>: <span>Esteban Álvarez Dávila</span></p> <p><strong>COLECTORES</strong>: <span>F. Moreno y C. Carvajal</span></p> <p><strong>Nº MUESTRAS MONTADAS</strong>: <span>1</span></p> <p><strong>Homologación</strong>: <span>Homologado</span></p> <p><strong>Nueva fecha del evento </strong>: <span>20/12/2018.</span></p> <p><strong>Fecha del evento</strong>: <span>01/09/2012.</span></p> <p><strong>Proyecto </strong>: <span>Recursos Botánicos Disponibles en Línea (BRAVO) para la flora Colombiana</span></p> <p><strong>Hábitat</strong>: <span>Bosque húmedo tropical (bh-T)</span></p> <p><strong>Comentario del evento</strong>: <span>Bosque de tierra firme, dosel abierto, de 25-30 m, emergentes de 35 m, estrato medio de 15 m, sotobosque denso con alta regeneración natural, presencia de palmas como Lepidocaryum tenue, Oenocarpus bataua, Geonoma sp., capa de hojarazca de 15 cm, abundante materia orgánica. Pendientes pronunciadas. Poca intervención antrópica.</span></p> <p><strong>Continente</strong>: <span>SA</span></p> <p><strong>Pais</strong>: <span>Colombia</span></p> <p><strong>Estado/Provincia</strong>: <span>Amazonas</span></p> <p><strong>Municipio</strong>: <span>Puerto Santander</span></p> <p><strong>Localidad</strong>: <span>Resguardo indígena Nonuya de Villazul.</span></p> <p><strong>Elevación minima en metros</strong>: <span>250</span></p> <p><strong>Elevación maxima en metros</strong>: <span>400</span></p> <p><strong>Latitud</strong>: <span>-0.654</span></p> <p><strong>Longitud original</strong>: <span>-72.072</span></p> <p><strong>datum geodésico</strong>: <span>WGS 84</span></p> <p><strong>Latitud decimal</strong>: <span>-0.654</span></p> <p><strong>Longitud decimal</strong>: <span>-72.072</span></p> <p><strong>Identificado por</strong>: <span>Wilson Rodríguez</span></p> <p><strong>Fecha de identificación</strong>: <span>25/01/2019.</span></p> <p><strong>Familia antigua</strong>: <span>Fabaceae</span></p> <p><strong>Especie antigua</strong>: <span>NN</span></p> <p><strong>Nombre cientifico</strong>: <span>Zygia racemosa (Ducke) Barneby &amp; J.W. Grimes</span></p> <p><strong>Reino</strong>: <span>Plantae</span></p> <p><strong>Filo</strong>: <span>Magnoliophyta</span></p> <p><strong>Clase</strong>: <span>Equisetopsida</span></p> <p><strong>Orden</strong>: <span>Fabales</span></p> <p><strong>Familia nueva</strong>: <span>Fabaceae</span></p> <p><strong>Género nuevo</strong>: <span>Zygia</span></p> <p><strong>especie nueva</strong>: <span>racemosa</span></p> <p><strong>Autoría del nombre científico</strong>: <span>(Ducke) Barneby &amp; J.W. Grimes</span></p> <p><strong></strong>: <span>Fabaceae</span></p> <p><strong>genero herbario</strong>: <span>Zygia</span></p> <p><strong>especie herbario</strong>: <span>racemosa</span></p> <p><strong>Especie de herbario para TNRS</strong>: <span>Zygia racemosa</span></p> <p><strong>Especie corregida herbario y desde TNRS</strong>: <span>Zygia racemosa</span></p> <p><strong>Familia corregida desde TNRS</strong>: <span>Fabaceae</span></p> <p><strong></strong>: <span>3777</span></p>

opencc-by-4.0Aug 2012View details →
zenodo36/100

Data: Assessing year-round habitat use by migratory sea ducks in a multi-species context reveals seasonal variation in habitat selection and partitioning

<p>This data file consists of state-space model-derived locations and individual data used to analyze transmitter effects&nbsp;for sea ducks in Eastern North America and is associated with the manuscript &quot;Assessing year-round habitat use by migratory sea ducks in a multi-species context reveals seasonal variation in habitat selection and partitioning&quot; published in Ecography. Columns are organized as follows:</p> <p>id - unique identifier</p> <p>species - species from which the centroid was obtained (BLSC = black scoter, COEI = common eider, LTDU = long-tailed duck, SUSC = surf scoter, WWSC = white-winged scoter)</p> <p>date&nbsp;- date of location (mm/dd/yy)</p> <p>jday - Julian date of location</p> <p>year - calendar year of location</p> <p>lon - longitude of location</p> <p>lat - latitude of location</p> <p>b - average assignment of location to either migrant (1) or resident (2) across all runs of the state-space model</p> <p>b.5 - most probable behavioral category based on average state assignment&nbsp;(1 = b &le;&nbsp;1.5 ; 2 = b &gt; 1.5)</p> <p>sex - sex of individual (M = male, F = female)</p> <p>age - age of individual (HY = hatch year, SY = second year, TY = third year, ASY = after second year, ATY = after third year, AHY = after hatch year</p> <p>capture_reg - general area where individual was captured</p> <p>capture_subreg - specific region within capture region where individual was captured</p> <p>stage - period of the annual cycle to which the centroid belongs (W = winter, B = breeding, S = spring staging, M = fall staging and molt, WM = winter migration, BM = breeding migration, MM = molt migration, SM = spring migration)</p> <p>site - position of centroid within season (i.e., W1 = first site occupied during winter, W2 = second site occupied, etc.)</p> <p>cycle - number of annual cycles following transmitter attachment (1 = first cycle after attachment, 2 = second cycle after attachment, etc.)</p> <p>season - season of annual cycle in which centroid occurred (W = winter, F = fall, B = breeding, S = spring)</p>

opencc-by-4.0Aug 2020View details →
dryad36/100

Assessing changes in genomic divergence following a century of human mediated secondary contact among wild and captive-bred ducks

<p>Along with manipulating habitat, the direct release of domesticated individuals into the wild is a practice used world-wide to augment wildlife populations. We test between possible outcomes of human-mediated secondary contact using genomic techniques at both historical and contemporary time scales for two iconic duck species. First, we sequence several thousand ddRAD-seq loci for contemporary mallards (<i>Anas platyrhynchos</i>) throughout North America, and two domestic mallard-types (i.e., known game-farm mallards and feral Khaki Campbell's). We show that North American mallards may well be becoming a hybrid swarm due to interbreeding with domesticated game-farm mallards released for hunting. Next, to attain a historical perspective, we applied a bait-capture array targeting thousands of loci in century-old (1842-1915) and contemporary (2009-2010) mallard and American black duck (<i>A. rubripes</i>) specimens. We conclude that American black ducks and mallards have always been closely related, with a divergence time of ~600,000 years before present, and likely evolved through prolonged isolation followed by limited bouts of gene flow (i.e., secondary contact). They continue to maintain genetic separation, a finding that overturns decades of prior research and speculation suggesting the genetic extinction of the American black duck due to contemporary interbreeding with mallards. Thus, despite having high rates of hybridization, actual gene flow is limited between mallards and American black ducks. Conversely, our historical and contemporary data confirm that the intensive stocking of game-farm mallards during the last ~100 years has fundamentally changed the genetic integrity of North America's wild mallard population, especially in the east. It thus becomes of great interest to ask whether the iconic North American mallard is declining in the wild due to introgression of maladaptive traits from domesticated forms. Moreover, we hypothesize that differential gene flow from domestic game-farm mallards into the wild mallard population may explain the overall temporal increase in differentiation between wild black ducks and mallards, as well as the uncoupling of genetic diversity and effective population size estimates across time in our results. Finally, our findings highlight how genomic methods can recover complex population histories by capturing DNA preserved in traditional museum specimens.</p>

opencc-zeroJan 2020View details →
dryad36/100

Blood and muscle O2 storage capacity in North American diving ducks

<p>Breath-hold diving presents air-breathing vertebrates with the challenge of maintaining aerobic respiration while exercising underwater. Adaptive increases in the oxygen (O<sub>2</sub>) storage capacity in the lungs, blood, or muscle tissues can enhance these reserves and greatly extend aerobic foraging time underwater. Here, we report blood- and muscle-O<sub>2</sub> storage parameters (blood hemoglobin concentration ([Hb]), hematocrit, and myoglobin concentration ([Mb]) in the pectoralis and gastrocnemius) for 16 species of diving and dabbling ducks found in North America, and investigate which parameters are correlated with the diving behaviors reported in both the sea ducks (<em>Mergini</em>) and the pochards (<em>Aythini</em>). Both [Hb] in the blood and [Mb] in the gastrocnemius, a major leg muscle used in propulsion for these predominantly leg-propelled divers, were significantly higher in the sea ducks compared to the dabblers (<em>Anatini</em>). The pochards also showed a significant increase in [Hb] and were intermediate between the sea ducks and the dabblers in hematocrit and [Mb] in the gastrocnemius. Among these four variables and total body mass, [Mb] in the gastrocnemius was the most significant predictor of mean species dive time, and these two variables were correlated across the phylogeny. Our results indicate that the observed changes in O<sub>2</sub> storage capacity in the blood and muscles are positively correlated with diving behavior in two clades of ducks, such that larger increases are correlated with longer dive times.</p>

opencc-zeroNov 2023View details →
zenodo36/100

Data and code from Lamb et al., "Evaluating conservation units using network analysis: a sea duck case study"

<p>This file consists of data and code used to construct network models for scoters in North America and is associated with the manuscript "<strong>Evaluating conservation units using network analysis: a sea duck case study</strong>" published in Frontiers in Ecology and the Environment.&nbsp;</p><p>&nbsp;</p><p><strong>Continental scoter network mapping </strong>is the R script used to run analyses.</p><p>&nbsp;</p><p><strong>duck_nodes</strong> is the main datafile. Columns are organized as follows:</p><p>id - unique identifier</p><p>species - species from which the centroid was obtained (BLSC = black scoter, SUSC = surf scoter, WWSC = white-winged scoter)</p><p>stage - period of the annual cycle to which the centroid belongs (W = winter, B = breeding, S = spring staging, M = fall staging and molt, WM = winter migration, BM = breeding migration, MM = molt migration, SM = spring migration)</p><p>site - position of centroid within season (i.e., W1 = first site occupied during winter, W2 = second site occupied, etc.)</p><p>cycle - number of annual cycles following transmitter attachment (1 = first cycle after attachment, 2 = second cycle after attachment, etc.)</p><p>sex - sex of individual (M = male, F = female)</p><p>age - age of individual (HY = hatch year, SY = second year, TY = third year, ASY = after second year, ATY = after third year, AHY = after hatch year</p><p>capture_reg - general area where individual was captured</p><p>capture_subreg - specific region within capture region where individual was captured</p><p>lon - longitude of centroid</p><p>lat - latitude of centroid</p><p>duration - number of days spent at centroid</p><p>start - date of arrival at centroid</p><p>end - date of departure from centroid</p><p>jstart - Julian date of arrival at centroid</p><p>jend - Julian date of departure from centroid</p><p>season - season of annual cycle in which centroid occurred (W = winter, F = fall, B = breeding, S = spring)</p><p>year - calendar year in which centroid began</p><p>to - node in which centroid is grouped</p><p>from - node in which previous centroid is grouped (i.e., node in which indiviual was located before moving to present node)</p><p>to_sea - season of annual cycle in which&nbsp;centroid occurred</p><p>from_sea - season of annual cycle in which previous centroid occurred</p><p>type - movement type to centroid; the first letter represents the season (coded as in "season" column), and the second represents the nature of the movement&nbsp;(WD = dispersal within a season, M = migration among seasons)</p><p>type2 - same as "type", but with dispersal movements coded by the stage in which they occur (W = winter, B = breeding, SM = spring migration, WM = winter migration)</p><p>ew - capture location in eastern (east; Atlantic and Great Lakes) or western (west; Pacific) North America</p><p>count_ind_sp - total number of tracked individuals of the species represented by centroid</p><p>wt - base centroid weight&nbsp;(all centroids equal, deployments excluded)</p><p>wt_sp - species-adjusted centroid weight:&nbsp;for centroid <i>x</i> in species <i>s</i>, weight<i>x</i> = (<i>N </i>centroids) × (1 / (<i>n </i>centroids in <i>s</i>))</p><p>wt_dur -&nbsp;duration-adjusted centroid weight:&nbsp;for centroid <i>x</i>, weight<i>x</i> = (days at centroid location) × 365-1</p><p>wt_ind -&nbsp; individual-adjusted centroid weight:&nbsp;for centroid <i>x</i> in individual<i> j</i>, weight<i>x</i> = 1 / (<i>n </i>centroids in <i>j</i>)</p><p>wt_ind_sp - individual and species adjusted centroid weight:&nbsp;for centroid <i>x</i>, individual <i>j</i>, and species <i>s</i>, weight<i>x</i> = (<i>N </i>centroids / (<i>N </i>species * <i>n</i> individuals in <i>s</i>)) × (1 / (<i>n </i>centroids in <i>j</i>))</p><p>wt_cap - capture location adjusted centroid weight: for centroid <i>x</i> and capture location <i>c, </i>weight<i>x </i>= (<i>N </i>centroids / <i>N</i> capture locations) / <i>n</i> centroids in <i>c</i></p><p>wt_ew - east-west adjusted centroid weight: for for centroid <i>x</i> and region <i>r, </i>weight<i>x </i>= (<i>N </i>centroids / <i>N</i> regions) / <i>n</i> centroids in <i>r</i></p><p>wt_spew - species and east-west adjusted centroid weight: for centroid <i>x</i> species <i>s</i>, and region <i>r, </i>weight<i>x </i>= (<i>N </i>centroids / (<i>N</i> species × <i>N</i> regions)) / <i>n </i>centroids for species <i>s</i> in region <i>r</i></p><p>wt_indspew - individual, species, and east-west adjusted centroid weight: for centroid <i>x,</i> individual<i> j, </i>species <i>s</i>, and region <i>r, </i>weight<i>x </i>= <i>N </i>centroids / (<i>N</i> species × <i>N</i> regions × <i>n</i> centroids for individual <i>j </i>× <i>n</i> individuals for species <i>s</i> in region <i>r</i>)</p><p>wt_spewcap - species, east-west, and capture location adjusted centroid weight: for centroid <i>x,</i> species <i>s</i>, capture location <i>c,&nbsp;</i>and region <i>r, </i>weight<i>x </i>= <i>N </i>centroids / (<i>N</i> species × <i>N</i> regions × <i>n</i> centroids for species <i>s</i> in capture location <i>c </i>× <i>n</i> capture locations for species <i>s</i> in region <i>r</i>)</p>

opencc-by-4.0Nov 2023View details →
dryad36/100

Above and belowground plant traits of dominant dune grasses from Duck, Outer Banks, USA

<p>We examined above and belowground traits among four prominent dune grasses of the Atlantic and Gulf Coasts of North America: <i>Ammophila breviligulata</i>, <i>Panicum amarum</i>, <i>Spartina patens</i>, and <i>Uniola paniculata</i>. Whole plant samples of each species were collected from the foredune at the US Army Engineer Research and Development Center's Field Research Facility in Duck, North Carolina, USA and quantified for several above and belowground traits (e.g., stem height, rhizome number and length, root surface area by diameter class, root tensile strength, mycorrhizal percent infection).</p>

opencc-zeroJan 2022View details →
zenodo36/100

Aeolian Saltation Data at Duck, NC - 8 Nov 2021

<p>Aeolian saltation data collected on the north property of the Field Research Facility (FRF) in Duck, NC associated with the passing of a Nor&#39;Easter system. Time series data includes 1Hz measurements from a Sensit H14-LIN sensor, 1 Hz wind measurements from a horizontally mounted ZX TM doppler wind lidar sensor, and tidal measurements made from the end of the FRF pier. These time series data are provided as CSV files individually for each sensor, with headers of the CSV files indicating the variables of interest. Addititionally, a Sequoia LISST-Holo2 sensor was deployed to measure properties of the aeolian saltation layer at 10Hz. Particle grain size&nbsp;information exported from the HoloBatch program is additionally provided, with the raw reconstructed particle height relative to the sensor lens provided. More details regarding these measurements can be found in the following manuscript:</p> <p>Cohn, Dickhudt, and Marshall (2022). In-situ measurement of grain size characteristics within the aeolian saltation layer on a coastal beach. Earth Surface Processes and Landforms</p>

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

Stable-isotopes (δ2H, δ13C) within feathers from harvested American black ducks (2017-2020)

<p>Stable isotope data from American Black Duck feathers (n = 665) and associated harvest data. The first primary feather (P1) was collected from wings submitted to the Species Composition Survey in Canada and Parts Collection Survey in the United States. From available feathers, we selected individuals for stable-isotope analysis stratified by black duck conservation region, sex, age, and date of harvest, where possible. These data are those that were selected for stable-hydrogen isotope analysis. See Kusack et al. (in press) - 'Origins of harvested American black ducks: stable isotopes support the flyover hypothesis' for additional information on our use of this data.</p>

opencc-zeroJul 2022View details →
dryad36/100

Duck harvest and crippling in Illinois in 2018-19

<p>Crippling loss (waterfowl downed, but not retrieved) is a recognized component of waterfowl harvest, but there are few contemporary estimates. We used a zero-inflated negative binomial model to account for false reporting of zeros and estimated true waterfowl crippling losses from harvest data reported in a 2018–19 survey of waterfowl hunters in Illinois, USA. We found that crippling rates declined rapidly with increasing harvest and moderately with increasing days afield. For the most active hunters (days afield), the probability of falsely reporting zero crippling loss increased with the number of ducks they reported harvesting, whereas for the least active hunters we found the reverse. We suggest that modest improvements in hunter skill could produce significant reductions in crippling loss.</p>

opencc-zeroAug 2022View details →
zenodo36/100

Ancestral Hopi Duck Effigy (Replica)

This model represents technology in my work coming full circle. This was my first try at replicating ancient Southwesern ceramics. I made this vessel with clay from the Homol'ovi region, based upon a design published from the excavation of Awat'ovi, in 1988. For giggles, I used reality capture to model the object, and today I went on to print the vessel in PLA. Good fun on a Saturday afternoon. Source: Objaverse 1.0 / Sketchfab

opencc-byDec 2021View details →
dryad36/100

Data from: Colorado aquatic macroinvertebrate samples and duck counts

<p>Food availability varies considerably over space and time in wetland systems, and consumers must be able to track those changes during nutrient demanding points in the life cycle like breeding. Resource tracking has been studied frequently among herbivores, but receives less attention among consumers of macroinvertebrates. We evaluated the change in resource availability across habitat types and time, and the simultaneous density of waterfowl consumers throughout their breeding season in a high-elevation, flood-irrigated system. We also assessed whether the macroinvertebrate resource density better predicted waterfowl density across habitats, compared to consistency (i.e., temporal evenness) of the invertebrate resource or taxonomic richness. Resource density varied marginally across wetland types but was highest in basin wetlands (i.e., ponds) and peaked early in the breeding season, whereas it remained relatively low and stable in other wetland habitats. Breeding duck density was positively related to resource density, more so than temporal resource stability, for all species. Resource density was negatively related to duckling density, however. These results have the potential to not only elucidate mechanisms of habitat selection among breeding ducks in flood-irrigated landscapes, but also suggest there is not a consequential trade-off to selecting wetland sites based on energy density versus temporal resource stability and that good-quality wetland sites provide both.</p>

opencc-zeroJun 2024View details →
zenodo36/100

Fig. 15 in Notes on social wasps of the group of Mischocyttarus (Omega) punctatus (Ducke), with description of six new species (Hymenoptera, Vespidae, Polistinae)

Fig. 15. Map with distribution of the studied species of the M. punctatus group.

opencc-by-4.0Jul 2015View details →
dryad36/100

Data from: Gradual evolution towards flightlessness in Steamer-Ducks

Flightlessness in birds is the product of changes in suites of characters--including increased body size and reduced anterior limbs--that have evolved repeatedly and independently under similar ecological conditions (generally insularity). It remains unknown whether this phenotypic convergence extends to the genomic level, partially because many losses of flight occurred long ago (such as in penguins or ratites), thus complicating the study of the genetic pathways to flightlessness. Here we use genome sequencing to study the evolution of flightlessness in a group of ducks that are current and dynamic exemplars of this major functional transition. These recently diverged Tachyeres steamer-ducks differ in their ability to fly: one species is predominantly flighted and three are mainly flightless. Through a genome-wide association analysis we identify two narrow candidate genomic regions implicated in the morphological changes that led to flightlessness, and reconstruct the number of times flightnesses has evolved in Tachyeres. The strongest association is with DYRK1A, a gene that when knocked-out in mice leads to alterations in growth and bone morphogenesis. These findings, together with phylogenetic and demographic analyses, imply that the genomic changes leading to flightlessness in Tachyeres may have evolved once, and that this trait remains functionally polymorphic in two species.

opencc-zeroMay 2019View details →
dryad36/100

Louisiana mottled duck telemetry summer survival data 2018-2020 and water level data from Hurricane Laura surge

<p>Tropical cyclones are the most powerful storms on earth, causing catastrophic damage to human lives and infrastructure. Hurricanes also cause wildlife mortality when they make landfall, but the severity of these effects is difficult to quantify because data collection is either logistically impossible or deprioritized in the wake of human tragedy. On 27 August 2020, Hurricane Laura made landfall in southwestern Louisiana with maximum sustained winds of 241 kph (150 mph), making it one of the most powerful storms to strike the mainland United States. Hurricane Laura passed directly over the core breeding range of the Western Gulf Coast population of Mottled Duck (<i>Anas fulvigula</i>), during a time when many adult birds were undergoing a simultaneous wing feather molt and were flightless. We used GPS-GSM telemetry data to evaluate survival rates of adult female Mottled Ducks in late summer 2020 (bracketing 27 August by one month on either side) relative to the same period in 2018 and 2019. Mortality was lower in 2018 (12 out of 29; 41%) and 2019 (8 out of 28; 29%) than in 2020 (12 out of 18; 67%), and 7 out of 12 mortalities documented in 2020 occurred when Hurricane Laura made landfall. Survival analyses in Program MARK confirmed lower survival probability in 2020, but there was overlap in 85% confidence intervals in all years. This single storm resulted in the death of ~40% of all marked birds in our sample, suggesting that hurricanes have the potential to influence population demographics. In addition, Hurricane Laura resulted in widespread habitat loss and degradation that has reduced available nesting habitat in 2021, and possibly for years to come. The acute and chronic effects of hurricanes may exacerbate Mottled Duck population declines, which may worsen in the face of increasingly frequent and more severe tropical storms.</p>

opencc-zeroOct 2022View details →
dryad36/100

Louisiana black-bellied whistling-duck clutch characteristics in the presence of conspecific and interspecific brood parasitism

<p>Black-bellied Whistling-Ducks (Dendrocygna autumnalis; hereafter Whistling-Duck) are undergoing a rapid range expansion northward and now breed throughout the southeastern United States. As a facultative cavity-nesting species, they have the potential to compete with Wood Ducks (Aix sponsa) and Hooded Mergansers (Lophodytes cucullatus) for nest sites. Little is known about Whistling-Duck breeding biology, and estimates of clutch characteristics and rates of conspecific and interspecific brood parasitism (hereafter, CBP and IBP respectively) are lacking. We monitored Whistling-Duck nests in Louisiana to describe nesting chronology, clutch size of parasitized and unparasitized (hereafter, normal) nests, and hatchability (i.e., the portion of eggs that hatched) for clutches of different sizes and types. We monitored a total of 558 nest boxes 2020–2021 and determined the presence of brood parasitism for 231 Whistling-Duck nests. CBP was detected in 73 (31.6%) nests, and IBP was observed in 51 (22.1%) nests parasitized by Wood Ducks, 2 (0.9%) nests parasitized by Hooded Mergansers, and 1 nest contained eggs from all three species. Normal clutches were smaller (15.4 ± 4.4 eggs) than CBP clutches (26.1 ± 8.8 eggs) and mixed clutches (22.2 ± 5.3 eggs; clutches containing Wood Duck or Hooded Merganser eggs; all pairwise P &lt; 0.0001). However, within-clutch repeatability estimates for egg morphology data (i.e., length, width, and mass) were low (&lt; 0.40) for normal clutches, suggesting CBP went undetected. Of 180 fated nests used to determine hatchability, 66 (36.7%) were successful, 49 (27.2%) were abandoned, 64 (35.6%) were depredated, and 1 (0.6%) was nonviable. Considering successful nests, hatchability was high for all clutch size bins ranging from 67.4% (41-45 eggs) to 81.6% (11-15 eggs). This study is the first to document Whistling-Ducks successfully hatching mixed-species broods, and such high productivity could be contributing to whistling-duck range expansion.</p>

opencc-zeroNov 2022View details →
dryad36/100

Evidence that long-distance dispersal of aquatic invertebrates by ducks increases with propagule size

<ol> <li> <span>Migratory ducks are key dispersal agents for aquatic organisms, yet </span><span>differences in their potential for short- and long-distance dispersal are still poorly understood, particularly differences among </span><span>aquatic invertebrate taxa</span><span>. </span> </li> <li> <span>Using seven species of </span><span>aquatic invertebrates and </span><span>a duck species known to feed on them in the wild (the northern shoveler) </span><span>as a model system, we evaluated whether their potential for endozoochorous dispersal varies among 5 of the species and scales with propagule size for the 7 species. We also tested the expectation of a lower dispersal potential for invertebrate propagules, as compared to plant seeds; and evaluated whether intra-specific variation (in particular, sexual dimorphism) influences the potential of waterbirds as dispersal vectors. </span> </li> <li><span>An experiment with 5 invertebrate species demonstrated that most resting eggs (68–95%) were retrieved by 4 h after ingestion, with maximum gut passage times ranging from 16 h for <em>Daphnia</em> <em>magna</em> to 36 h for <em>Artemia</em> <em>salina</em> and <em>Thamnocephalus</em> <em>platyurus</em>. Using models that combine migratory duck movements with gut passage times, we show that aquatic invertebrates may disperse frequently over distances of 15–16 km (median dispersal distance) and regularly over distances up to 110–166 km (Q99 distance). </span></li> <li> <span>I</span><span>ncreasing propagule size resulted in increasing gut passage times, decreasing survival of gut passage and decreasing hatching success. While propagule size had no effects on 'regular' dispersal distances (mean, median, Q95 and Q99), the frequency of long-distance dispersal (LDD) increased with it. </span> </li> <li><span>Increasing propagule size therefore had two contrasting effects on invertebrate dispersal potential, decreasing the frequency of dispersal (less seeds dispersed) but increasing the potential for long-distance dispersal. </span></li> <li><span><em>Conclusions</em>: We provide evidence that endozoochory of invertebrate propagules by waterbirds results in frequent dispersal among wetlands (tens of km) and regular dispersal at regional scale (over a hundred km).</span></li> </ol>

opencc-zeroJul 2023View details →

ScienceDex guides

Understand access before you commit

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