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22 results for “Piedmont forests”
Aquatic Insect Adult Metals Dataset: Urban and Forested Watersheds in the Piedmont of NC - 2021-2022
This dataset reports concentrations of 6 target trace metals (copper, zinc, nickel, lead, chromium, and selenium) in unfiltered water, emergent aquatic adult insects (by family), biofilm mats (predominately algae), and tree roots submerged under stream water. Biological and water samples were collected from three streams in the Piedmont region of North Carolina, USA: a wastewater dominated site (Ellerbe Creek, near the USGS gage at Glen Road ), a stormwater dominated site (Ellerbe Creek, near the USGS gage on Club Blvd), and a stream draining a predominately forested watershed (New Hope Creek, near a StreamPULSE site at Hollow Rock Preserve). This data was submitted for publication in a manuscript that explores how metals are transported by aquatic emergent insects from stream ecosystems into terrestrial food webs.
Text-fig. 1. Context and location of the Govone outcrop. a: Location of the Piedmont Basin at the northern margin of the Mediterranean Basin and distribution of Messinian evaporites. b: Simplified geological map of the Piedmont Basin showing the location of the Govone outcrop close to the town of Alba. in Remains Of A Subtropical Humid Forest In A Messinian Evaporitebearing Succession At Govone, Northwestern Italy - Preliminary Results
Text-fig. 1. Context and location of the Govone outcrop. a: Location of the Piedmont Basin at the northern margin of the Mediterranean Basin and distribution of Messinian evaporites. b: Simplified geological map of the Piedmont Basin showing the location of the Govone outcrop close to the town of Alba.
Fig. 2 in Saproxylic weevils and edaphic beetles as indicators of environmental quality of relict forests in Piedmont lowlands (Coleoptera)
Fig. 2 – Map of Parco della Partecipanza, completely surrounded by agroecosystems. Map data: Google Earth, Maxar Technologies, used according to Google Earth Terms of Service.
Fig. 1 in Saproxylic weevils and edaphic beetles as indicators of environmental quality of relict forests in Piedmont lowlands (Coleoptera)
Fig. 1 – The collecting sites. Map data: Google Earth, Maxar Technologies, used according to Google Earth Terms of Service.
Fig. 5 in Saproxylic weevils and edaphic beetles as indicators of environmental quality of relict forests in Piedmont lowlands (Coleoptera)
Fig. 5 – Some of the weevils collected in the research. a, Kyklioacalles navieresi (Boheman, 1837); b, Kyklioacalles aubei (Boheman, 1837); c, Acalles echinatus (Germar, 1824); d, Echinodera hypocrita (Boheman, 1837). From Stüben (2014-2020), used with permission.
FIGURE 9 in Riparian and valley-margin hardwood species of pre-colonial Piedmont forests: A preliminary study of subfossil leaves from White Clay Creek, southeastern Pennsylvania, USA
FIGURE 9. Acer negundo (Box Elder). 1, Leaflet, showing shallow lobes and rounded sinuses, EMS 425016; 2, Trichomes along veins, EMS 425016; 3, Trichomes along tooth margin, EMS 425016, with increased density on basal side of tooth; 4, Tooth of modern A. negundo from York County, Pennsylvania (collection Y2.2 of Wilf, 1997), showing the same general trichome pattern.
FIGURE 7 in Riparian and valley-margin hardwood species of pre-colonial Piedmont forests: A preliminary study of subfossil leaves from White Clay Creek, southeastern Pennsylvania, USA
FIGURE 7. Liriodendron tulipifera (Tulip Tree). 1, Subfossil samara, EMS 425015; 2, Thickened ridge at basal attachment site of EMS 425015; 3, Mucronate samara tip from EMS 425014.
FIGURE 4 in Riparian and valley-margin hardwood species of pre-colonial Piedmont forests: A preliminary study of subfossil leaves from White Clay Creek, southeastern Pennsylvania, USA
FIGURE 4. Fagus grandifolia (American Beech). 1, Leaf fragment, showing regularly spaced secondary veins, EMS 425004; 2, Detail of venation on EMS 425004; 3, Trichomes at vein junction, EMS 425004; 4, Trichomes at the vein junction of a modern F. grandifolia leaf from York County, Pennsylvania (collection Y1.2 of Wilf, 1997); 5, Rounded tooth on subfossil, EMS 425005; 6, Tooth and rounded sinus on modern F. grandifolia leaf from York County, Pennsylvania (collection Y1.2 of Wilf, 1997); 7, Trichome, EMS 425004.
FIGURE 6 in Riparian and valley-margin hardwood species of pre-colonial Piedmont forests: A preliminary study of subfossil leaves from White Clay Creek, southeastern Pennsylvania, USA
FIGURE 6. Quercus Section Quercus (White Oak group). 1, Lobe of modern Q. alba from York County Pennsylvania (collection of Wilf, 1997); 2, Subfossil, EMS 425008, showing entire margin with fimbrial vein and retuse, asymmetrical apex.
FIGURE 8 in Riparian and valley-margin hardwood species of pre-colonial Piedmont forests: A preliminary study of subfossil leaves from White Clay Creek, southeastern Pennsylvania, USA
FIGURE 8. Three Salix spp. (Willow) subfossils. 1, EMS 425022; 2, EMS 425021; 3, EMS 425023; 4, Salicoid tooth, EMS 425021.
FIGURE 3 in Riparian and valley-margin hardwood species of pre-colonial Piedmont forests: A preliminary study of subfossil leaves from White Clay Creek, southeastern Pennsylvania, USA
FIGURE 3. Alnus serrulata (Hazel Alder), EMS 425002. 1, Whole specimen; 2, Peltate scale and simple trichomes; 3, Stipitate gland trichome; 4, Detail of teeth; 5, Trichomes at vein junction; 6, Areolation with simple and branching freely ending veinlets.
FIGURE 5 in Riparian and valley-margin hardwood species of pre-colonial Piedmont forests: A preliminary study of subfossil leaves from White Clay Creek, southeastern Pennsylvania, USA
FIGURE 5. Quercus Section Lobatae (Red Oak group). 1, Leaf fragment showing asymmetrical lobe with acute apex, EMS 425011; 2, Abaxial leaf surface of EMS 425011, with randomly oriented stomata; 3, Simple trichome on leaf surface near secondary vein, EMS 425011. 4, Trichomes along a tertiary vein, EMS 425011; 5, Individual stoma of modern Q. rubra from York County, Pennsylvania (collection Y2.3 of Wilf, 1997) showing T-shape junction; 6, Individual stoma of EMS 425011.
FIGURE 2 in Riparian and valley-margin hardwood species of pre-colonial Piedmont forests: A preliminary study of subfossil leaves from White Clay Creek, southeastern Pennsylvania, USA
FIGURE 2. White Clay Creek leaf mat site, illustrating the contact (at trowel) between the darker hydric soil layer containing subfossil leaves and the overlying, lighter-colored legacy sediments. Stadia rod for scale.
Fig. 3 in New records of Osmoderma eremita in protected relict forests of Piedmont lowlands (NW Italy) (Coleoptera: Scarabaeidae, Cetoniinae)
Fig. 3 – Phenology of the target species close RP in the 2021 season.
Fig. 2 in New records of Osmoderma eremita in protected relict forests of Piedmont lowlands (NW Italy) (Coleoptera: Scarabaeidae, Cetoniinae)
Fig. 2 – Phenology of the target species at MW in the 2023 season.
Fig. 1 in New records of Osmoderma eremita in protected relict forests of Piedmont lowlands (NW Italy) (Coleoptera: Scarabaeidae, Cetoniinae)
Fig. 1 – Geographical location of the study areas.
FIGURE 1 in Riparian and valley-margin hardwood species of pre-colonial Piedmont forests: A preliminary study of subfossil leaves from White Clay Creek, southeastern Pennsylvania, USA
FIGURE 1. Location of the White Clay Creek leaf mat site, Chester County, Pennsylvania.
Subspecies and Distribution. L. lL. lagothricha Humboldt, 1812 — SE Colombia, NE Ecuador, NW Brazil, and N Peru, from the Cordillera Oriental, N of the rios Napo and Amazonas, to the Rio Uva, a N bank affluent of the Rio Guaviare (Vichada Department, Colombia), E to the Rio Orinoco and upper Rio Negro to the Venezuelan border and NW Brazil; it is not known if it occurs in Venezuela. L. [. lugens Elliot, 1907 — Colombia, E of the Rio Atrato, throughout the Cordillera Oriental, W of the Rio Ariari (Meta Department), and parts of the Cordillera Central to the northernmost parts of the Serrania de San Lucas (SE Bolivar & N Antioquia departments), in some places up to elevations of 3000 m, and northward in the piedmont forest (now mostly destroyed) to the Rio Arauca (Arauca Department); there is no evidence thatits occurs in neighboring SW Venezuela. in Atelidae
Subspecies and Distribution. L. lL. lagothricha Humboldt, 1812 — SE Colombia, NE Ecuador, NW Brazil, and N Peru, from the Cordillera Oriental, N of the rios Napo and Amazonas, to the Rio Uva, a N bank affluent of the Rio Guaviare (Vichada Department, Colombia), E to the Rio Orinoco and upper Rio Negro to the Venezuelan border and NW Brazil; it is not known if it occurs in Venezuela. L. [. lugens Elliot, 1907 — Colombia, E of the Rio Atrato, throughout the Cordillera Oriental, W of the Rio Ariari (Meta Department), and parts of the Cordillera Central to the northernmost parts of the Serrania de San Lucas (SE Bolivar & N Antioquia departments), in some places up to elevations of 3000 m, and northward in the piedmont forest (now mostly destroyed) to the Rio Arauca (Arauca Department); there is no evidence thatits occurs in neighboring SW Venezuela.
Subspecies and Distribution. A. h. hybridus 1. Geoffroy Saint-Hilaire, 1829 — N Colombia (from the right bank of the Rio Magdalena, N to the S slopes of the Sierra Nevada de Santa Marta and the N of the Serrania de Perija, and in the middle Rio Magdalena Valley at least to the departments of Caldas and Cundinamarca; two populations on the slopes of the Cordillera Oriental on the Venezuelan border (one in the Rio Catatumbo watershed in the Norte de Santander Department and the other in the NE piedmont forest in Arauca Department) and N & NW Venezuela (along the SE part of the Cordillera de la Costa in the states of Miranda and probably Vargas, and on both sides of the Venezuelan Andesin the states of Zulia, Tachira, Mérida, Trujillo, Portuguesa, Apure, and Barinas, in the E in the piedmont and lowland forests of San Camilo and Ticoporo, and in the Win the piedmont forest around S Lake Maracaibo to the Sierra de Perija). A. h. brunneus Gray, 1871 — N Colombia in the departments of Antioquia, Bolivar, and Caldas, between the lower rios Cauca and Magdalena. in Atelidae
Subspecies and Distribution. A. h. hybridus 1. Geoffroy Saint-Hilaire, 1829 — N Colombia (from the right bank of the Rio Magdalena, N to the S slopes of the Sierra Nevada de Santa Marta and the N of the Serrania de Perija, and in the middle Rio Magdalena Valley at least to the departments of Caldas and Cundinamarca; two populations on the slopes of the Cordillera Oriental on the Venezuelan border (one in the Rio Catatumbo watershed in the Norte de Santander Department and the other in the NE piedmont forest in Arauca Department) and N & NW Venezuela (along the SE part of the Cordillera de la Costa in the states of Miranda and probably Vargas, and on both sides of the Venezuelan Andesin the states of Zulia, Tachira, Mérida, Trujillo, Portuguesa, Apure, and Barinas, in the E in the piedmont and lowland forests of San Camilo and Ticoporo, and in the Win the piedmont forest around S Lake Maracaibo to the Sierra de Perija). A. h. brunneus Gray, 1871 — N Colombia in the departments of Antioquia, Bolivar, and Caldas, between the lower rios Cauca and Magdalena.
Fig. 3 in Saproxylic weevils and edaphic beetles as indicators of environmental quality of relict forests in Piedmont lowlands (Coleoptera)
Fig. 3 – Scatter graph of study areas, relative to abundance data; × = sampling plots of Vaj (v), △ = sampling plots of Partecipanza (p), ○ = sampling plots of Merlino (m), + = sampling plots of Stupinigi (s).
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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.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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.
OpenNeuro
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