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.
38
datasets available to search
ShareScore release 0.7.1
Dataset results
38 results for “lowland rivers”
Distribution. CE Madagascar, known only from its type locality, the Sahafina Forest (29-230 m above sea level), a lowland rainforest fragment of 15-6 km2, and its surrounding "savoka" (fallow farmland with cultivated trees), about 58 km E of Andasibe-Mantadia National Park and 18 km W of the Indian Ocean. The geographic range is presumably limited to the lowland areas (below 700 m) between the Mangoro River to the S and the Rianila River to the N, an area of about 7600 km?2. in Cheirogaleidae
Distribution. CE Madagascar, known only from its type locality, the Sahafina Forest (29-230 m above sea level), a lowland rainforest fragment of 15-6 km2, and its surrounding "savoka" (fallow farmland with cultivated trees), about 58 km E of Andasibe-Mantadia National Park and 18 km W of the Indian Ocean. The geographic range is presumably limited to the lowland areas (below 700 m) between the Mangoro River to the S and the Rianila River to the N, an area of about 7600 km?2.
On following pages: 4. Southern Greater Glider (Petauroides volans); 5. Lowland Ring-tailed Possum (Pseudochirulus (Pseudochirulus cinereus); 8. Painted Ring-tailed Possum (Pseudochirulus forbesi); 9. Herbert River Ring-tailed Possum tailed Possum (Pseudochirulus mayeri); 12. Arfak Ring-tailed Possum (Pseudochirulus schlegel)). canescens); 6. Weyland Ring-tailed Possum (Pseudochirulus carol); 7. Daintree River Ring-tailed Possum (Pseudochirulus herbertensis); 10. Masked Ring-tailed Possum (Pseudochirulus larvatus); 11. Pygmy Ring- in Pseudocheiridae
On following pages: 4. Southern Greater Glider (Petauroides volans); 5. Lowland Ring-tailed Possum (Pseudochirulus (Pseudochirulus cinereus); 8. Painted Ring-tailed Possum (Pseudochirulus forbesi); 9. Herbert River Ring-tailed Possum tailed Possum (Pseudochirulus mayeri); 12. Arfak Ring-tailed Possum (Pseudochirulus schlegel)). canescens); 6. Weyland Ring-tailed Possum (Pseudochirulus carol); 7. Daintree River Ring-tailed Possum (Pseudochirulus herbertensis); 10. Masked Ring-tailed Possum (Pseudochirulus larvatus); 11. Pygmy Ring-
Distribution. EC DR Congo, lowlands E of the Lualaba River from the Lowa and Oso rivers in the N to the Elila River in the S, and Mts between the Lowa and Oso rivers in the N to ¢.6° Sin the S, along the W side of Lake Tanganyika. in Cercopithecidae
Distribution. EC DR Congo, lowlands E of the Lualaba River from the Lowa and Oso rivers in the N to the Elila River in the S, and Mts between the Lowa and Oso rivers in the N to ¢.6° Sin the S, along the W side of Lake Tanganyika.
Distribution. NW DR Congo and NE Republic of the Congo, in lowland forests of the Congo Basin on both sides of the lower and middle Congo (c.16" E to 26°-27° E); S of the Congo Riverits distribution extends E to the Lomami River system (c.3° N to 6° 30° S); it has also been recorded on twoislands in the Sangha River. Its presence in NE Angola requires confirmation. in Cercopithecidae
Distribution. NW DR Congo and NE Republic of the Congo, in lowland forests of the Congo Basin on both sides of the lower and middle Congo (c.16" E to 26°-27° E); S of the Congo Riverits distribution extends E to the Lomami River system (c.3° N to 6° 30° S); it has also been recorded on twoislands in the Sangha River. Its presence in NE Angola requires confirmation.
On following pages: 218. Kalinga Shrew Mouse (Soricomys kalinga); 219. Leonardo Shrew Mouse (Soricomys leonardocoi); 220. Mountain Shrew Mouse (Soricomys montanus); 221. Sierra Madre Shrew Mouse (Soricomys musseri); 222. Sundaic Ranee Mouse (Haeromys pusillus); 223. Margaret's Ranee Mouse (Haeromys margarettae); 224. Lowland Sulawesi Ranee Mouse (Haeromys minahassae); 225. Papuan Highland Brush Mouse (Abeomelomys sevia); 226. Uneven-toothed Rat (Anisomys imitator); 227. Mountain Water Rat (Baiyankamys habbema); 228. Shaw Mayer's Water Rat (Baiyankamys shawmayeri); 229. \White-toothedMouse (Brassomys albidens); 230. Forbes's Tree Mouse (Chiruromys forbesi); 231. Broad-headed Tree Mouse (Chiruromys lamia); 232. Lesser Tree Mouse (Chiruromys vates); 233. Tawny Brush Mouse (Coccymys kirrhos); 234. Rimmler's Brush Mouse (Coccymys ruemmleri); 235. Central Cordillera Brush Mouse (Coccymys shawmayeri), 236. Earless New Guinea Water Rat (Crossomys moncktoni); 237. Common Water Rat (Hydromys chrysogasten; 238. Husson's Water Rat (Hydromys hussoni); 239. New Britain Water Rat (Hydromys neobritannicus); 240. Ziegler's Water Rat (Hydromys ziegleri); 241. Western White-eared Giant Rat (Hyomys dammermani); 242. Eastern White-eared Giant Rat (Hyomys goliath); 243. Arfak Water Rat (Leptomys arfakensis), 244. Elegant Water Rat (Leptomys elegans); 245. Ernst Mayr's Water Rat (Leptomys ernstmayri); 246. Small Water Rat (Leptomys paulus); 247. Fly River Water Rat (Leptomys signatus). in Muridae
On following pages: 218. Kalinga Shrew Mouse (Soricomys kalinga); 219. Leonardo Shrew Mouse (Soricomys leonardocoi); 220. Mountain Shrew Mouse (Soricomys montanus); 221. Sierra Madre Shrew Mouse (Soricomys musseri); 222. Sundaic Ranee Mouse (Haeromys pusillus); 223. Margaret's Ranee Mouse (Haeromys margarettae); 224. Lowland Sulawesi Ranee Mouse (Haeromys minahassae); 225. Papuan Highland Brush Mouse (Abeomelomys sevia); 226. Uneven-toothed Rat (Anisomys imitator); 227. Mountain Water Rat (Baiyankamys habbema); 228. Shaw Mayer's Water Rat (Baiyankamys shawmayeri); 229. \White-toothedMouse (Brassomys albidens); 230. Forbes's Tree Mouse (Chiruromys forbesi); 231. Broad-headed Tree Mouse (Chiruromys lamia); 232. Lesser Tree Mouse (Chiruromys vates); 233. Tawny Brush Mouse (Coccymys kirrhos); 234. Rimmler's Brush Mouse (Coccymys ruemmleri); 235. Central Cordillera Brush Mouse (Coccymys shawmayeri), 236. Earless New Guinea Water Rat (Crossomys moncktoni); 237. Common Water Rat (Hydromys chrysogasten; 238. Husson's Water Rat (Hydromys hussoni); 239. New Britain Water Rat (Hydromys neobritannicus); 240. Ziegler's Water Rat (Hydromys ziegleri); 241. Western White-eared Giant Rat (Hyomys dammermani); 242. Eastern White-eared Giant Rat (Hyomys goliath); 243. Arfak Water Rat (Leptomys arfakensis), 244. Elegant Water Rat (Leptomys elegans); 245. Ernst Mayr's Water Rat (Leptomys ernstmayri); 246. Small Water Rat (Leptomys paulus); 247. Fly River Water Rat (Leptomys signatus).
Distribution. Recorded from montane localities isolated by intervening areas of lowland habitat in New Guinea, including Foja Mts, Adelbert Range, Huon Peninsula (Finisterre and Saruwaged ranges), and E Central Cordillera, including both N (Jimi and Ramu rivers) and S catchments (Purari and Aroa rivers). in Muridae
Distribution. Recorded from montane localities isolated by intervening areas of lowland habitat in New Guinea, including Foja Mts, Adelbert Range, Huon Peninsula (Finisterre and Saruwaged ranges), and E Central Cordillera, including both N (Jimi and Ramu rivers) and S catchments (Purari and Aroa rivers).
FIGURE 1. Genlisea multiflora. A. habit. B in A new species of corkscrew plant (Genlisea, Lentibulariaceae) from the Amazon lowlands of Brazil, including a key to all species occurring north of the Amazon River
FIGURE 1. Genlisea multiflora. A. habit. B. indumentum of peduncle upper part. C. bract (left) and one bracteole (right) attached to peduncle and pedicel. D. indumentum of pedicel. E. calyx. F. corolla. G. capsule. H. seed. A, B from S.M. Costa 1299, C–H from S. R. Chavez 70. Drawing by A. Fleischmann.
FIGURE 2. Genlisea multiflora. A. habitat. B in A new species of corkscrew plant (Genlisea, Lentibulariaceae) from the Amazon lowlands of Brazil, including a key to all species occurring north of the Amazon River
FIGURE 2. Genlisea multiflora. A. habitat. B. habit of a plant with prostrate scape. C, D. corollae, face view (tinged pale lilac and white specimens). E. highly branched infructescence. F. corolla, lateral view. G. scape indumentum of a flowering specimen. H. fruits. J. SEM image of seed, base view (micropylar end). K. SEM image of seed, top (chalazal) view. Photos B–E, G, H by Volker Bittrich, rest by Suzana Costa.
Data from: Spatial scaling of environmental variables improves species-habitat models of fishes in a small, sand-bed lowland river
Open the record for dataset details and reuse information.
Figure 4 from: Vilenica M, Kerovec M, Pozojević I, Mihaljević Z (2020) Mayfly response to different stress types in small and mid-sized lowland rivers. ZooKeys 980: 57-77. https://doi.org/10.3897/zookeys.980.54805
Figure 4 Scatterplot of mayfly species richness (S), abundance (N) and local diversity (Shannon index) against ratios of areas with intensive agriculture (CLC_I.A.) present in the catchment area of each study site.
Figure 3 from: Vilenica M, Kerovec M, Pozojević I, Mihaljević Z (2020) Mayfly response to different stress types in small and mid-sized lowland rivers. ZooKeys 980: 57-77. https://doi.org/10.3897/zookeys.980.54805
Figure 3 F1×F2 plane of the Canonical correspondence analysis (CCA) based on 21 mayfly taxa and 14 environmental variables. For the abbreviations of the taxa codes (blue triangle symbols) see Table 2. Legend: Environmental variables (red arrow symbols): Tw – water temperature (°C), Oxy – dissolved oxygen content (mg/L), Con – conductivity (μS/cm), pH – pH, NH4+ – ammonium (mgN/L), NO3- – nitrates (mgN/L), TN – total nitrogen (mgN/L), PO43− – orthophosphates (mgP/L), TOC – total organic carbon (mg/L), BOD5 – biological oxygen demand (mgO2/L), CODMn – chemical oxygen demand (mgO2/L), vegetation – aquatic vegetation/phytal, fine sediment – silt, mud and sand, lithal – stones and gravel.
Figure 2 from: Vilenica M, Kerovec M, Pozojević I, Mihaljević Z (2020) Mayfly response to different stress types in small and mid-sized lowland rivers. ZooKeys 980: 57-77. https://doi.org/10.3897/zookeys.980.54805
Figure 2 a Longitudinal zonal associations and b trophic structure of mayfly assemblages at the 46 degraded lowland streams and rivers investigated in Croatia. Study site codes are presented in Fig. 1.
Figure 1 from: Vilenica M, Kerovec M, Pozojević I, Mihaljević Z (2020) Mayfly response to different stress types in small and mid-sized lowland rivers. ZooKeys 980: 57-77. https://doi.org/10.3897/zookeys.980.54805
Figure 1 Map of the 46 study sites located in the Pannonian lowland ecoregion in Croatia. *Legend: Study sites: 1 Bednja, Stažnjevec village 2 Ždalica, Ždala village 3 Krapina, Bedekovčina village 4 Krapina, Zaprešić town 5 Krapina, Kupljenovo village 6 Krapinica, Zabok town 7 Krapinica, Krapina town 8 Rajna, between Vrbovec town and Lonjica village 9 Zlenin, Vrbovec village 10 Vukšinac, Stubice village 11 Deanovac lateral canal, near Ivanić Grad town 12 Reka, Lovrečan village 13 Brodec, Peklenica village 14 Lateral canal Mihovljan, Čakovec town 15 Poloj, between Legrad and Đelekovec villages 16 Zdelja, Molve village 17 Lonja, near Ivanić Grad town 18 Jalšovnica, Ferketinec village 19 Bošćak, Domašinec village 20 Bistrec, Rakovnica I 21 Bistrec, Rakovnica II 22 Zelina, Božjakovina village 23 Connecting canal Zelina-Lonja-Glogovnica-Česma, Poljanski lug village 24 Glogovnica, before mouth to Česma 25 Česma, Obedišće village 26 Česma, Pavlovac village 27 Česma, Sišćani village 28 Česma, Narta village 29 Sutla, Luke Poljanske village 30 Rogostrug, Podravske Sesvete village 31 Kosteljina, Jalšje village 32 Horvatska, Veliko Trgovišće village 33 Bistra Koprivnička, Molve village 34 Toplica, Sokolovac village 35 Toplica, downstream from Daruvar town 36 Toplica, upstream from Daruvar town 37 Luka, Vrbovec town 38 Sewage collector, Prelog town 39 Gornji potok, between Selnica and Praporčan villages 40 Kotoribski kanal, Kotoriba village 41 Črnec, Gornji Dubovec vilage 42 Gostiraj, Ježdovec village 43 Tomašica, Tomašica village 44 Jalšovec, between Bukovje and Štrigova villages 45 Murščak, between Domašinec and Stara Straža villages 46 Glogovnica, Koritna village.
River network rearrangements promote speciation in lowland Amazonian birds
<p>Large Amazonian rivers impede dispersal for many species, but lowland river networks frequently rearrange, thereby altering the location and effectiveness of river-barriers through time. These rearrangements may promote biotic diversification by facilitating episodic allopatry and secondary contact among populations. We sequenced genome-wide markers to evaluate histories of divergence and introgression in six Amazonian avian species-complexes. We first tested the assumption that rivers are barriers for these taxa and found that even relatively small rivers facilitate divergence. We then tested whether species diverged with gene flow and recovered reticulate histories for all species, including one potential case of hybrid speciation. Our results support the hypothesis that river dynamics promote speciation and reveal that many rainforest taxa are micro-endemic, unrecognized and thus threatened with imminent extinction. We propose that Amazonian hyper-diversity originates in part from fine-scale barrier displacement processes –including river dynamics– which allow small populations to differentiate and disperse into secondary contact.</p>
Distribution. Scattered Amazonian lowland localities in NC Brazil S of Amazon River. in Cricetidae
Distribution. Scattered Amazonian lowland localities in NC Brazil S of Amazon River.
River network rearrangements promote speciation in lowland Amazonian birds
Open the record for dataset details and reuse information.
Data from: Increased population size of fish in a lowland river following restoration of structural habitat
Open the record for dataset details and reuse information.
Distribution. Scattered Amazonian lowland localities in French Guiana, S Surinam, and neighboring Brazilian territories N of Amazon River. in Cricetidae
Distribution. Scattered Amazonian lowland localities in French Guiana, S Surinam, and neighboring Brazilian territories N of Amazon River.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research 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.
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.
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.
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
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.