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Text-fig. 12. Lectotype specimen of Potentilla×hybrida WALLROTH. in Wallroth´S Collection Of Vascular Plants In The Herbarium Of The National Museum, Prague
Text-fig. 12. Lectotype specimen of Potentilla×hybrida WALLROTH.
Text-fig. 13. Lectotype specimen of Senecio germanicus WALLROTH. in Wallroth´S Collection Of Vascular Plants In The Herbarium Of The National Museum, Prague
Text-fig. 13. Lectotype specimen of Senecio germanicus WALLROTH.
Text-fig. 11. Lectotype specimen Orobanche rubens WALLROTH. in Wallroth´S Collection Of Vascular Plants In The Herbarium Of The National Museum, Prague
Text-fig. 11. Lectotype specimen Orobanche rubens WALLROTH.
Text-fig. 8. Lectotype specimen of Malva neglecta WALLROTH. in Wallroth´S Collection Of Vascular Plants In The Herbarium Of The National Museum, Prague
Text-fig. 8. Lectotype specimen of Malva neglecta WALLROTH.
Text-fig. 4. Lectotype specimen of Camelina sylvestris WALLROTH. in Wallroth´S Collection Of Vascular Plants In The Herbarium Of The National Museum, Prague
Text-fig. 4. Lectotype specimen of Camelina sylvestris WALLROTH.
Text-fig. 1. Wallroth´s original handwriten page dealing with Valeriana collina WALLROTH. in Wallroth´S Collection Of Vascular Plants In The Herbarium Of The National Museum, Prague
Text-fig. 1. Wallroth´s original handwriten page dealing with Valeriana collina WALLROTH.
Arctic Biodiversity: Arctic Vascular Plants
Biogeography and other attributes for Arctic organisms, various sources.<p></p>Meltofte, H. (ed.) 2013. Arctic Biodiversity Assessment. Status and trends in Arctic biodiversity. Conservation of Arctic Flora and Fauna, Akureyri. <p></p>https://arcticbiodiversity.is/index.php/the-report/chapters/plants
Vascular Damage and Repair - Are Small-diameter Vascular Grafts Still the "Holy Grail" of Tissue Engineering?
Open the record for dataset details and reuse information.
Vascular KATP channel structural dynamics reveal regulatory mechanism by Mg-nucleotides
<p>MD simulation data for vascular KATP channel focusing on Kir6.1-pore and SUR2B in the presence and absence of MgADP. </p>
Dataset on vascular plants, Rhopalocera and Orthoptera of 35 industrial water-abstraction sites in France, including landscape and local variables
<p>Site : Site name</p> <p>X : X coordinate</p> <p>Y : Y coordinate</p> <p>Richness : Species richness taking into account individuals identified to the genus and species levels (based on data from the Vigie-Flore protocol for Flora (www.vigie-flore.fr), the STERF protocol for Rhopalocera (Manil and Henry, 2007) and the protocol of Lacoeuilhe et al. (2020) for Orthoptera)</p> <p>Richness2 : Species richness taking into account only the individuals identified to the species level</p> <p>Shannon_Diversity : Shannon index</p> <p>Abondance : For Flora, abundance is the total number of quadrats in which each species is present, and for Rhopalocera and Orthoptera, abundance is the total number of individuals</p> <p>CWM_dispersal : Community weighted mean (Garnier et al., 2004) for dispersal :</p> <ul> <li>For Flora, maximum seed-releasing height as a proxy for dispersal</li> <li>For Rhopalocera and Orthoptera, 3 classes of dispersal (1-Low dispersal, 2-Medium dispersal, 3-High dispersal)</li> </ul> <p>CWM_specialisation : Community weighted mean (Garnier et al., 2004) for specialisation :</p> <ul> <li>For Flora, Index θwb calculated using species co-occurrence data (Mobaied et al., 2015)</li> <li>For Rhopalocera, 4 classes of specialisation based on the optimal habitat of the caterpillar (1-Generalist species whose caterpillars grow in many types of habitat ; 2-Moderately generalist species whose caterpillars grow mainly in the associated habitat ; 3-Specialist species whose caterpillars grow mainly in the associated habitat ; 4-Specialist species with a very localised distribution)</li> <li>For Orthoptera, 2 classes of specialisation based on moisture preferences (0-Generalist species (mesophilic), 1-Specialist species (xerothermic and hygrophilic))</li> </ul> <p>CWM_dep_pol : Percentage of times “insects” appears as a pollen vector for a given species across various databases (Martin, 2018)</p> <p>dPC_Flora_150m : Delta Probability of Connectivty (Saura & Pascual-Hortal, 2007) calculated for Flora with dispersal distances of 150m</p> <p>dPC_Flora_500m : Delta Probability of Connectivty (Saura & Pascual-Hortal, 2007) calculated for Flora with dispersal distances of 500m</p> <p>dPC_Rhopalocera_100m : Delta Probability of Connectivty (Saura & Pascual-Hortal, 2007) calculated for Rhopalocera with dispersal distances of 100m</p> <p>dPC_Rhopalocera_300m : Delta Probability of Connectivty (Saura & Pascual-Hortal, 2007) calculated for Rhopalocera with dispersal distances of 300m</p> <p>dPC_Orthoptera_100m : Delta Probability of Connectivty (Saura & Pascual-Hortal, 2007) calculated for Orthoptera with dispersal distances of 100m</p> <p>dPC_ Orthoptera _300m : Delta Probability of Connectivty (Saura & Pascual-Hortal, 2007) calculated for Orthoptera with dispersal distances of 300m</p> <p>IFT_Herbicides_100m : Average Treatment Frequency Indice for herbicides within a radius of 100m</p> <p>IFT_Herbicides_300m : Average Treatment Frequency Indice for herbicides within a radius of 300m</p> <p>Soil : Qualitative variable, divided into 2 categories: clay vs. sandy soil</p> <p>Humidity : Semi-quantitative variable based on site habitat vegetation, divided into 3 categories: 1 (xerophilous), 2 (mesoxerophilous), 3 (meso-hygrophylous)</p> <p>Floral_dispo : Average cover of flowering plants over the 4 visits on the site (%)</p> <p>Low_herbaceous_cover : Low herbaceous cover (<20 cm) on the site (%)</p> <p>Hight_herbaceous_cover : High herbaceous cover (>40 cm) on the site (%)</p>
Data from: High vascular plant species richness in the Usumacinta River Basin: a comprehensive floristic checklist for a natural region in the Mesoamerican biodiversity hotspot
<p><span>Background: </span><span>Mesoamerica is one of the most important biodiversity hotspots on the planet. Despite significant efforts made over two centuries to contribute to the floristic knowledge of this region, our understanding of its flora is still scattered and uneven.</span></p> <p><span>Questions:</span> <span>What is the magnitude of the vascular plant species richness in the Usumacinta River Basin?</span></p> <p><span>Study site and dates: </span><span>Usumacinta River Basin (Guatemala and Mexico), 1838–2018.</span></p> <p><span>Methods: </span><span>We compiled the checklist by systematizing the floristic information acquired from various sources derived from numerous floristic and ecological studies.</span></p> <p><span>Results:</span><span> W</span><span>e recorded 6,977 species, 1,892 genera, and 274 families. The largest numbers of species (5,746) and records (58,859) correspond to the Mexican portion of the Usumacinta River Basin, compared to its Guatemalan counterpart (4,445 species and 19,952 records). The most species-rich families were Orchidaceae (598 species), Fabaceae (512), and Asteraceae (476). The prevalence of these and all other families with significant contributions to the flora varied among three elevation-defined sectors into which the Usumacinta River Basin was subdivided (lower, middle, and upper basin).</span></p> <p><span>Conclusions: </span><span>The Usumacinta River Basin is a strategic region for plant biodiversity conservation as it hosts almost one-third of all vascular plant species known for Mesoamerica and ca. 6 % of the entire flora in the Americas. Further botanical exploration should focus on those areas of the basin for which little or no information is available in order to gain a better appreciation of its flora.</span></p>
A dataset on alien vascular plant species in Japan
<p>This dataset contains a list of 1,753 alien vascular plant taxa (i.e., species, infraspecific taxa and hybrids; hereafter species for simplicity) found in Japan and data on the year of first record and pathways of introduction for many, if not all, of these species. The dataset was created during the study documented in the following article:</p> <p><strong>Egawa C. & Koyama A. (2023) Temporal trends in the accumulation of alien vascular plant species through intentional and unintentional introductions in Japan. NeoBiota 83: 179-196. https://doi.org/</strong><strong>10.3897/neobiota.83.101416</strong></p> <p>Procedures for creating the dataset are detailed in the article. Concise explanation of the dataset can be found in the README sheet in the file.</p>
Vascular variants in seed plants – a developmental perspective
<p>Over centuries of plant morphological research, biologists have enthusiastically explored how distinct vascular arrangements have diversified. These investigations have focused on the evolution of steles and secondary growth and examined the diversity of vascular tissues (xylem and phloem), including atypical developmental pathways generated through modifications to the typical development of ancestral ontogenies. A shared vernacular has evolved for communicating on the diversity of alternative ontogenies in seed plants. Botanists have traditionally used the term “anomalous secondary growth” which was later renamed to “cambial variants” by late Dr. Sherwin Carlquist (1988). However, the term “cambial variants” can be vague in meaning since it is applied for developmental pathways that do not necessarily originate from cambial activity. Here, we review the “cambial variants” concept and propose the term “vascular variants” as a more inclusive overarching framework to interpret alternative vascular ontogenies in plants. In this framework, vascular variants are defined by their developmental origin (instead of anatomical patterns), allowing the classification of alternative vascular ontogenies into three categories: (1) <strong>procambial variants</strong>, (2) <strong>cambial variants</strong> and (3) <strong>ectopic cambia</strong>. Each category includes several anatomical patterns. Vascular variants, which represent broader developmental-based groups, can be applied to both extant and fossil plants, and thereby offer a more adequate term from an evolutionary perspective. An overview of the developmental diversity and phylogenetic distribution of vascular variants across selected seed plants is provided. Finally, the evolutionary implications of vascular variants are discussed.</p>
Spatial patterns of phylogenetic and species diversity of Fennoscandian vascular plants in protected areas
<p>Protected areas are one of the main strategic means for conserving biodiversity. Yet, the design of protected areas usually neglects phylogenetic diversity, an important diversity measure. In this paper, we assess the phylogenetic diversity and species richness of vascular plants in Fennoscandian protected areas. We evaluate how much species richness and phylogenetic diversity is found within and outside protected areas, and the differences in diversity between different categories of protected areas. We also assess the differences in the diversity-area relationship of the different protected area categories in terms of both species richness and phylogenetic diversity. We build a multi-locus phylogeny of 1,519 native vascular plants of Norway, Sweden, and Finland. We estimate the phylogenetic diversity and species richness by combining the phylogeny with publicly available occurrence data and the currently protected area system of Fennoscandia. Our results indicate that protected areas in Fennoscandia hold more diversity when larger, and that phylogenetic diversity increases faster with area than species richness. We found evidence for more diversity outside of protected areas of the different countries of Fennoscandia than inside of protected areas, but no evidence for diversity differences between areas with different protection status. Hence, our results indicate that the current protected area system in Fennoscandia is no more effective in conserving phylogenetic diversity and species richness of vascular plants than a random selection of localities. Our results also indicate that planning conservation strategies around phylogenetic diversity, rather than species richness, might be more effective in protecting vascular plant diversity.</p>
A RELEVÂNCIA DA CIRURGIA VASCULAR NO PERÍODO DA PANDEMIA DA COVID-19
<p><strong>Objetivo: </strong>O presente estudo tem como objetivo analisar os principais aspectos relacionados a relevância da assistência da enfermagem relacionada a cirurgia vascular adotados na Pandemia da Covid-19 no paciente em tratamento. <strong>Métodos: </strong>Nesse ínterim, uso do método afirmativo com revisão bibliográfica, pesquisa de natureza qualitativa, com busca ativa realizada nas bases de dados dos periódicos virtuais, tais como: Google Acadêmico, Scielo, Bireme, Lilacs, Pubmed usando os descritores: Cirurgia Vascular, Pandemia da Covid-19, Procedimentos Cirurgicos, Tratamento. Os critérios de inclusão aplicados foram: artigos publicados entre os anos 2020 a 2022, com exceção de obras anteriores que fazem referência a temática. Foram encontrados 60 artigos, 40 na Língua Portuguesa e 20 na Língua Inglesa, sendo selecionados dez para o entendimento final do trabalho. <strong>Resultados: </strong>O estudo obteve a contemplação do objetivo a partir da revisão bibliográfica, pois trouxe um alerta sobre a importância de conhecimentos na área da cirurgia vascular no período da Pandemia da Covid-19 com ênfase no tratamento e recuperação dos pacientes. <strong>Conclusão:</strong>Conhecimentos sobre a relevãncia da cirurgia vascular no período da Pandemia da Covid-19 foi fator determinante para compreender diante do exposto a necessidade que está direcionada a uma rotina dos pacientes na busca pela recuperação, essa preocupação que se torna constante por parte dos profissionais e de todos os envolvidos.</p>
MANTA Registry for Vascular Large-bore Closure
ClinicalTrials.gov study NCT03330002. IPD Sharing: UNDECIDED. Countries: 5. Publications: 2.
Hemodialysis Reliable Outflow (HeRO) Vascular Access Patency Study
ClinicalTrials.gov study NCT00890045. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Vascular Dysfunction in Black Individuals: Roles of Nitric Oxide and Endothelin-1
ClinicalTrials.gov study NCT04770155. IPD Sharing: YES. Countries: 1. Publications: 5.
Study Effect of VIA-2291 on Vascular Inflammation
ClinicalTrials.gov study NCT00358826. IPD Sharing: Not stated. Countries: 2. Publications: 2.
Cross-Seal Closure Device IDE Trial - Study of the Cross-SealTM Suture-Mediated Vascular Closure Device System
ClinicalTrials.gov study NCT03756558. IPD Sharing: NO. Countries: 1. Publications: 1.
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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)
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.