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395 results for “floristics”

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Fig. 2 in Floristic traits and biogeographic characterization of the Gennargentu massif (Sardinia)

Fig. 2. – Life forms percentages, referred to the whole flora. H = hemicryptophytes; C = chamaephytes; G = geophytes; NP = nanophanerophytes; P = phanerophytes; T = therophytes; Hy = hydrophytes.

opencc-by-4.0Nov 2013View details →
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Fig. 4 in Floristic traits and biogeographic characterization of the Gennargentu massif (Sardinia)

Fig. 4. – Life forms percentages of the endemic flora of Gennargentu. H = hemicryptophytes; C = chamaephytes; G = geophytes; NP = nanophanerophytes; P = phanerophytes; T = therophytes.

opencc-by-4.0Nov 2013View details →
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Text-fig. 1. Locality map with the approximate extent of Clarkia Lake during Miocene times in what is today northern Idaho, USA. Black dots mark three of the localities yielding the Miocene Clarkia flora; the fossil leaf of Nymphaea sp. described here comes from locality P-33. Other symbols: Dashed lines for county boundaries; a thin dotted line for Idaho State Hwy 3; a triangle for the local peak of Bechtel Butte; and a star for the town of Clarkia. Inset: Location of the map in northern Idaho. Abbreviations: WA – Washington state, OR – Oregon, ID – Idaho, MT – Montana. Map redrawn from Ladderud et al. (2015). in First Water Lily, A Leaf Of Nymphaea Sp., From The Miocene Clarkia Flora, Northern Idaho, Usa: Occurrence, Taphonomic Observations, Floristic Implications

Text-fig. 1. Locality map with the approximate extent of Clarkia Lake during Miocene times in what is today northern Idaho, USA. Black dots mark three of the localities yielding the Miocene Clarkia flora; the fossil leaf of Nymphaea sp. described here comes from locality P-33. Other symbols: Dashed lines for county boundaries; a thin dotted line for Idaho State Hwy 3; a triangle for the local peak of Bechtel Butte; and a star for the town of Clarkia. Inset: Location of the map in northern Idaho. Abbreviations: WA – Washington state, OR – Oregon, ID – Idaho, MT – Montana. Map redrawn from Ladderud et al. (2015).

opencc-by-4.0Aug 2022View details →
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Text-fig. 2. Nymphaea sp. from the Miocene Clarkia Lake flora, Locality P-33. a: Photograph of the fossil leaf. b: Sketch of leaf showing the salient features of shape, basal lobes and margin, eccentric insertion point of the abaxial petiole, and primary actinodromous venation. Dashed lines represent torn edge of lamina; dotted line is outline of right basal lobe. Line drawing by P. Martin Sander. Scale bar applies to both photo and drawing. in First Water Lily, A Leaf Of Nymphaea Sp., From The Miocene Clarkia Flora, Northern Idaho, Usa: Occurrence, Taphonomic Observations, Floristic Implications

Text-fig. 2. Nymphaea sp. from the Miocene Clarkia Lake flora, Locality P-33. a: Photograph of the fossil leaf. b: Sketch of leaf showing the salient features of shape, basal lobes and margin, eccentric insertion point of the abaxial petiole, and primary actinodromous venation. Dashed lines represent torn edge of lamina; dotted line is outline of right basal lobe. Line drawing by P. Martin Sander. Scale bar applies to both photo and drawing.

opencc-by-4.0Aug 2022View details →
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Text-fig. 1. Modern vegetation proxies as delivered by the Drudge 1 and 2 tools for Parschlug. Left column results from KovarEder et al. (2021) based on the floristic spectrum published by Kovar-Eder et al. (2004). The other three columns result from three variants using the enlarged floristic spectrum herein. Differences between variants 1–3 from this study are caused by differences in assignment of some taxa and morphotypes (see Appendix 1). European vegetation formations: Formation C – Subarctic, boreal and nemoral-montane open woodlands as well as subalpine and oro-Mediterranean vegetation; Formation D – Mesophytic and hygromesophytic coniferous and mixed broad-leaved-coniferous forests; Formation F – Mesophytic broadleaved deciduous and mixed broadleaved/conifer forests; Formation G – Thermophilous mixed deciduous broadleaved forests; Formation J – Mediterranean sclerophyllous forests and scrub; Formation K – Xerophytic coniferous forests, coniferous woodland and scrub. East Asian vegetation types: MCF China, Japan – Montane Coniferous Forests China, Honshu, Yakushima; BLDF N and NE Provinces, China – Broad-leaved Deciduous Forests of the Northern and Northeastern Provinces (China); BLDF Upper Yangtze, Honshu – Broad-leaved Deciduous Forest, Upper Yangtze Provinces, Mt. Emei, and Honshu; MMF China – Mixed Mesophytic Forest, Lower Yangtze Provinces; BLEF China, Japan – Broad-leaved Evergreen Forests, China, Japan; Meili Snow Mt. high altitude SCL and BLF, China – Meili Snow Mt., Sclerophyllous and broad-leaved forest zone (2,580-3,650 m alt.). (Designations of European vegetation formations follow Bohn et al. (2004) and Asian ones follow Kovar-Eder et al. (2021). in Floristic, Vegetation And Climate Assessment Of The Early/Middle Miocene Parschlug Flora Indicates A Distinctly Seasonal Climate

Text-fig. 1. Modern vegetation proxies as delivered by the Drudge 1 and 2 tools for Parschlug. Left column results from KovarEder et al. (2021) based on the floristic spectrum published by Kovar-Eder et al. (2004). The other three columns result from three variants using the enlarged floristic spectrum herein. Differences between variants 1–3 from this study are caused by differences in assignment of some taxa and morphotypes (see Appendix 1). European vegetation formations: Formation C – Subarctic, boreal and nemoral-montane open woodlands as well as subalpine and oro-Mediterranean vegetation; Formation D – Mesophytic and hygromesophytic coniferous and mixed broad-leaved-coniferous forests; Formation F – Mesophytic broadleaved deciduous and mixed broadleaved/conifer forests; Formation G – Thermophilous mixed deciduous broadleaved forests; Formation J – Mediterranean sclerophyllous forests and scrub; Formation K – Xerophytic coniferous forests, coniferous woodland and scrub. East Asian vegetation types: MCF China, Japan – Montane Coniferous Forests China, Honshu, Yakushima; BLDF N and NE Provinces, China – Broad-leaved Deciduous Forests of the Northern and Northeastern Provinces (China); BLDF Upper Yangtze, Honshu – Broad-leaved Deciduous Forest, Upper Yangtze Provinces, Mt. Emei, and Honshu; MMF China – Mixed Mesophytic Forest, Lower Yangtze Provinces; BLEF China, Japan – Broad-leaved Evergreen Forests, China, Japan; Meili Snow Mt. high altitude SCL and BLF, China – Meili Snow Mt., Sclerophyllous and broad-leaved forest zone (2,580-3,650 m alt.). (Designations of European vegetation formations follow Bohn et al. (2004) and Asian ones follow Kovar-Eder et al. (2021).

opencc-by-4.0Aug 2022View details →
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Text-fig. 5. Vegetation zones in P. R. China (Editorial Committee of Vegetation Map of China, The Chinese Academy of Sciences 2007), and assumed location of extant reference vegetation type of Wiesa fossil assemblage (rectangle), as revealed from qualitative floristic analysis. Extant reference vegetation type present in southern belt of zone of subtropical evergreen broadleaved forest, with minor overlap into zone of tropical forest. in Assessment Of Phytogeographic Reference Regions For Cenozoic Vegetation: A Case Study On The Miocene Flora Of Wiesa (Germany)

Text-fig. 5. Vegetation zones in P. R. China (Editorial Committee of Vegetation Map of China, The Chinese Academy of Sciences 2007), and assumed location of extant reference vegetation type of Wiesa fossil assemblage (rectangle), as revealed from qualitative floristic analysis. Extant reference vegetation type present in southern belt of zone of subtropical evergreen broadleaved forest, with minor overlap into zone of tropical forest.

opencc-by-4.0Aug 2022View details →
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Text-fig. 3. Litho- and biostratigraphic position of fossil floras treated herein, based on lithostratigraphic standard section of upper Oligocene and Miocene in central and eastern Germany (Standke et al. 2010, Escher et al. 2020); only exception from standard section: ** – Thierbach Member restricted to central Germany, replaces Branitz Member in eastern Germany; correlated to global scale of International Chronostratigraphic Chart 2022/02 (Cohen et al. 2013); maximum age ranges of sites/floras indicated by black bars; floristic complexes according to definitions by Mai and Walther 1991 for upper Oligocene, Mai 2000b, 2001b for Miocene; age range of MCO from Steinthorsdottir et al. 2021. in Assessment Of Phytogeographic Reference Regions For Cenozoic Vegetation: A Case Study On The Miocene Flora Of Wiesa (Germany)

Text-fig. 3. Litho- and biostratigraphic position of fossil floras treated herein, based on lithostratigraphic standard section of upper Oligocene and Miocene in central and eastern Germany (Standke et al. 2010, Escher et al. 2020); only exception from standard section: ** – Thierbach Member restricted to central Germany, replaces Branitz Member in eastern Germany; correlated to global scale of International Chronostratigraphic Chart 2022/02 (Cohen et al. 2013); maximum age ranges of sites/floras indicated by black bars; floristic complexes according to definitions by Mai and Walther 1991 for upper Oligocene, Mai 2000b, 2001b for Miocene; age range of MCO from Steinthorsdottir et al. 2021.

opencc-by-4.0Aug 2022View details →
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Floristic survey of vascular plants of the Parque Estadual da Pedra Selada, Rio de Janeiro, Brazil

<p>The Atlantic Forest is one of the most diverse and threatened phytogeographical domains of the world. Despite that, it includes regions of poor floristic knowledge, even in protected areas. Although the importance of protected areas in conserving the Atlantic Forest hotspot is undisputed, it is necessary to recognize the floristic richness of these areas to propose effective conservation actions. In this sense, online databases have proved to be a promising tool for compiling species lists with relevant biodiversity information. This study is based on the list of vascular plants of the &ldquo;Parque Estadual da Pedra Selada&rdquo;, published in the &ldquo;Cat&aacute;logo de Plantas das Unidades de Conserva&ccedil;&atilde;o do Brasil&rsquo;. It summarizes species richness, endemism, and conservation status of this protected area.</p>

opencc-zeroFeb 2024View details →
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Figure 2 in Floristic Status And Distribution Trends Of Rosa Rubiginosa L. In Latvia

Figure 2. Oldest known herbarium of Rosa rubiginosa L. in Latvia stored in Museum of Botany, University of Latvia, collected by K. Kupffer. Specimen (left hand-side) collected in 1894 near Koknese castle ruins (right hand-side). Photo: P. Evarts–Bunders.

opencc-by-4.0Dec 2023View details →
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Figure 3 in Floristic Status And Distribution Trends Of Rosa Rubiginosa L. In Latvia

Figure 3. Distribution dynamics of Rosa rubiginosa L. in three stages: historical in Latvia localities by 1940 (A), localities from 1940 till 1991 (B), 1991 – till nowadays, according to all available herbarium collections and our studies (C). ©Māris Nitcis.

opencc-by-4.0Dec 2023View details →
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Figure 1. All historical localities from the 19 in Floristic Status And Distribution Trends Of Rosa Rubiginosa L. In Latvia

Figure 1. All historical localities from the 19th century to the 1980s (white circle) of Rosa rubiginosa L. in Latvia and inventoried localities (2021–2023) (black circle), marked in grid cells. ©Māris Nitcis.

opencc-by-4.0Dec 2023View details →
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Fig. 1 in Landscape-B Asin Approach To The Study Of Floristic Diversity (Heterogeneous Catchments Of Steppe And Forest-Steppe Zones Of Altai Krai, Russia, As A Case Study)

Fig. 1. Landscape and floristic regionalization of neighboring the Kasmalinsky basin and the Barnaulka river basin.

opencc-by-4.0Dec 2015View details →
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Figure 2 in A floristic assessment of grassland diversity loss in South Africa

Figure 2: Non-Metric Multidimensional Scaling (NMDS) ordination for: A, transformed and untransformed grasslands; B, within land-use type transformation. Squares, transformed grasslands; circles, untransformed grasslands; Empty symbols, urban sites; filled symbols, agricultural sites.

opencc-by-4.0Feb 2021View details →
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Figure 1 in Comparative floristic diversity of Southwest Primorye and neighboring areas of the Russian Far East

Figure 1. Geographical location of Southwest Primorye, structured in administrative units, and floristic regionalization of the southern part of the Russian Far East (RFE). 1 - national boundary of the Russian Federation; 2 - boundaries of administrative units; 3 ­ boundaries of floristic districts; 4 ­ boundaries of floristic subdistricts; 5 - boundary of Amur River basin (watershed line); 6 - boundaries of Southwest Primorye. Floristic districts: Okh. - Okhotsk (with subdistricts: C - central, S - southern), Ald. - Aldan, Nyuk. - Nyukzha, Daur. - Dauria, N. Sakh. - North-Sakhalin, U.Z. - Upper-Zeya, L.Z. - Low-Zeya, Bur. - Bureya, Amg. - Amgun, Uss. - Ussuri (with subdistricts: N - northern, C - central, S - southern), S. Sakh. - South Sakhalin. Floristic regionalization is given according to edition "Vascular plants of Soviet Far East" (Kharkevich, 1985-1996; Kharkevich and Tzvelev, 2003).

opencc-by-4.0Dec 2017View details →
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Fig. 3 in Floristic study of Jang-do (Isl.) in Korea

Fig. 3. National distribution of some Jang-do (Isl.) plants. Type (1). Arachniodes aristata. Type (2). Ilex integra. Type (3). Dendropanax morbiferus. Type (4). Saussurea ussuriensis, ● Literature, ○ Specimen.

opencc-by-4.0Aug 2013View details →
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Fig. 2 in Floristic study of Jang-do (Isl.) in Korea

Fig. 2. Two remarkable plants in Jang-do (Isl.). A. Impatiens furcillata. B. Flowers of Hosta yingeri. B2. Fruits of Hosta yingeri.

opencc-by-4.0Aug 2013View details →
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Linked collectors and determiners for: SANBI: Rare and Threatened Plants (Cape Floristic Region, 1864-2008).

Natural history specimen data linked to collectors and determiners held within, "SANBI: Rare and Threatened Plants (Cape Floristic Region, 1864-2008)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/b2cf1219-3804-451d-ad69-95f099569847">https://bionomia.net/dataset/b2cf1219-3804-451d-ad69-95f099569847</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/b2cf1219-3804-451d-ad69-95f099569847">https://gbif.org/dataset/b2cf1219-3804-451d-ad69-95f099569847</a>. Formatted as a Frictionless Data package.

opencc-zeroJan 2024View details →
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Linked collectors and determiners for: FloVegSI - Floristical and fitocenological database of ZRC SAZU.

Natural history specimen data linked to collectors and determiners held within, "FloVegSI - Floristical and fitocenological database of ZRC SAZU". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/89579e3e-f762-11e1-a439-00145eb45e9a">https://bionomia.net/dataset/89579e3e-f762-11e1-a439-00145eb45e9a</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/89579e3e-f762-11e1-a439-00145eb45e9a">https://gbif.org/dataset/89579e3e-f762-11e1-a439-00145eb45e9a</a>. Formatted as a Frictionless Data package.

opencc-zeroJan 2024View details →
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Linked collectors and determiners for: Three new species in the genus Ficinia (Cyperaceae, tribe Cypereae) from the Greater Cape Floristic Region of South Africa.

Natural history specimen data linked to collectors and determiners held within, "Three new species in the genus Ficinia (Cyperaceae, tribe Cypereae) from the Greater Cape Floristic Region of South Africa". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/0be3f6b9-593a-4740-813f-be89e24ef2fd">https://bionomia.net/dataset/0be3f6b9-593a-4740-813f-be89e24ef2fd</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/0be3f6b9-593a-4740-813f-be89e24ef2fd">https://gbif.org/dataset/0be3f6b9-593a-4740-813f-be89e24ef2fd</a>. Formatted as a Frictionless Data package.

opencc-zeroJan 2024View details →
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Linked collectors and determiners for: Floristic records from survey studies of the Bayerisches Landesamt für Umwelt.

Natural history specimen data linked to collectors and determiners held within, "Floristic records from survey studies of the Bayerisches Landesamt für Umwelt". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/8ea4250e-0ff0-44f8-812e-bffc3b9ba2a4">https://bionomia.net/dataset/8ea4250e-0ff0-44f8-812e-bffc3b9ba2a4</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/8ea4250e-0ff0-44f8-812e-bffc3b9ba2a4">https://gbif.org/dataset/8ea4250e-0ff0-44f8-812e-bffc3b9ba2a4</a>. Formatted as a Frictionless Data package.

opencc-zeroJan 2024View details →

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Allen Brain Atlas

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allen-brain-atlas
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Last verified 2026-04-30Open record

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Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

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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