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1

Doyle, James A. « PHYLOGENY OF VASCULAR PLANTS ». Annual Review of Ecology and Systematics 29, no 1 (novembre 1998) : 567–99. http://dx.doi.org/10.1146/annurev.ecolsys.29.1.567.

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2

Chawla, Amit, Om Parkash, Varun Sharma, S. Rajkumar, Brij Lal, Gopichand, R. D. Singh et A. K. Thukral. « Vascular plants, Kinnaur, Himachal Pradesh, India ». Check List 8, no 3 (1 juin 2012) : 321. http://dx.doi.org/10.15560/8.3.321.

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In the present study, we provide a checklist of the vascular plants of Kinnaur district situated in the Himachal Pradesh state of India in the western Himalaya. This checklist includes 893 taxa (viz., species, subspecies and varieties) belonging to 881 species of angiosperms and gymnosperms distributed among 102 families and 433 genera, and 30 species of pteridophytes. Information about the growth habit, threat and endemicity status is also provided. Our results show that family Compositae is by far the most species rich family with 122 species, followed by Poaceae (69), Rosaceae (58), Leguminosae (49) and Lamiaceae (38). Among the genera, Artemisia is the most diverse genus with 19 species, followed by Potentilla (14), Saussurea (13), Polygonum (11), Astragalus (10), Lonicera (10) and Nepeta (10). Similar to other regions in the western Himalayan range, family-to-genera ratio was 1:4.25 and the genera-to-species ratio was 1:2.04. Out of 893 taxa, our checklist includes 606 herb species, 63 trees, 108 shrubs, 28 climbers, 67 graminoids and 21 sedges and rushes. Of all the species recorded, 108 (12.2%) are endemic to western Himalaya and 27 (3%) are placed under IUCN threatened categories. The present checklist on the flora of Kinnaur provides an important baseline data for further quantitative studies on the characteristics of plant communities in this region and will help in the identification of priority conservation areas.
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3

Bowles, David E. « Vascular plants of Mammoth Spring, Arkansas1 ». Journal of the Torrey Botanical Society 147, no 1 (17 février 2020) : 87. http://dx.doi.org/10.3159/torrey-d-19-00019.1.

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Crandall-Stotler, Barbara, et Mohammad Iqbal. « Growth Patterns of Vascular Plants ». Bryologist 101, no 2 (1998) : 353. http://dx.doi.org/10.2307/3244215.

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Walles, Björn. « Growth patterns in vascular plants ». Nordic Journal of Botany 15, no 6 (décembre 1995) : 582. http://dx.doi.org/10.1111/j.1756-1051.1995.tb02125.x.

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König, Christian, Patrick Weigelt et Holger Kreft. « Dissecting global turnover in vascular plants ». Global Ecology and Biogeography 26, no 2 (13 novembre 2016) : 228–42. http://dx.doi.org/10.1111/geb.12536.

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7

Major, Jack. « Distribution of Vascular Plants in Utah ». Ecology 71, no 2 (avril 1990) : 830–31. http://dx.doi.org/10.2307/1940338.

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8

Atsatt, Peter R. « Are Vascular Plants "Inside-Out" Lichens ? » Ecology 69, no 1 (février 1988) : 17–23. http://dx.doi.org/10.2307/1943156.

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Einarsson, Eythór, et Eythor Einarsson. « Vascular Plants of the Thingvallavatn Area ». Oikos 64, no 1/2 (mai 1992) : 117. http://dx.doi.org/10.2307/3545047.

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Večeřa, Martin, Jan Divíšek, Jonathan Lenoir, Borja Jiménez‐Alfaro, Idoia Biurrun, Ilona Knollová, Emiliano Agrillo et al. « Alpha diversity of vascular plants in European forests ». Journal of Biogeography 46, no 9 (7 juin 2019) : 1919–35. http://dx.doi.org/10.1111/jbi.13624.

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11

Frahm, Jan-Peter, Anja Specht, Kerstin Reifenrath et Yelitza León Vargas. « Allelopathic effect of crustaceous lichens on epiphytic bryophytes and vascular plants ». Nova Hedwigia 70, no 1-2 (1 février 2000) : 245–54. http://dx.doi.org/10.1127/nova.hedwigia/70/2000/245.

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Luu-dam, Ngoc A., Ngan T. Lu, Thai H. Pham et Truong V. Do. « Classification of Vascular Plants in Vietnam According to Modern Classification Systems ». Plants 12, no 4 (20 février 2023) : 967. http://dx.doi.org/10.3390/plants12040967.

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Vietnam is extremely rich in biodiversity, with a remarkable range of habitats and more than 13,500 species of vascular plants recorded for the flora of Vietnam. This number represents about 3 to 5% of the world’s diversity of vascular plants. Over the past 30 years, there were two important documents on the vascular plants of Vietnam published, An Illustrated Flora of Vietnam (IFV) and Checklist of Plant Species of Vietnam (CPSV). During the past half century, the advent of molecular phylogenetics has witnessed dramatic changes in the classifications of vascular plants, and some modern classification systems of vascular plants have been established, e.g., PPG I, GPG, and APG. However, the vascular plants of Vietnam have not yet been classified according to these modern classification systems. In this paper, we present the history of the classification of vascular plants in Vietnam, compare the circumscription of all families of vascular plants occurring within Vietnam in IFV, CPSV, and the modern classification systems when applicable, and summarize familial assignments of all controversial genera in the different classifications. Furthermore, we also arrange the 37 families of lycophytes and ferns occurring within Vietnam according to the latest classification system (PPG I) and the 8 families of gymnosperms according to the latest Christenhusz’s system (GPG). The 246 families of angiosperms are arranged according to the fourth edition of the latest Angiosperm Phylogeny Group (APG IV). These results are the foundation stones and would be helpful for future research on the flora of Vietnam and the arrangement of plant collections in Vietnamese herbaria based on the updated classifications.
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13

Schmid, Rudolf, et Ernest M. Gifford. « Morphology and Evolution of Vascular Plants ». Taxon 38, no 4 (novembre 1989) : 613. http://dx.doi.org/10.2307/1222641.

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Ferguson, David K., et Wentsai Wang. « Vascular Plants of the Hengduan Mountains ». Taxon 46, no 2 (mai 1997) : 386. http://dx.doi.org/10.2307/1224129.

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15

BARINA, ZOLTÁN, GABRIELLA SOMOGYI, DÁNIEL PIFKÓ et MARASH RAKAJ. « Checklist of vascular plants of Albania ». Phytotaxa 378, no 1 (26 novembre 2018) : 1. http://dx.doi.org/10.11646/phytotaxa.378.1.1.

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This work includes all names of higher plants reported or collected in the present territory of Albania. The records are critically evaluated; the origin of them was tracked down and possible vouchers were searched for, revised and evaluated. Altogether, 6,419 basionyms were identified with 5,480 recently accepted taxa and their nativity status were examined.
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16

Aedo, C., L. Medina, P. Barberá et M. Fernández-Albert. « Extinctions of vascular plants in Spain ». Nordic Journal of Botany 33, no 1 (5 septembre 2014) : 83–100. http://dx.doi.org/10.1111/njb.00575.

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17

Larsen, Kai. « Vascular plants synopsis of Vietnamese flora ». Nordic Journal of Botany 16, no 5 (décembre 1996) : 504. http://dx.doi.org/10.1111/j.1756-1051.1996.tb00264.x.

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18

Dentant, Cédric. « The highest vascular plants on Earth ». Alpine Botany 128, no 2 (30 juillet 2018) : 97–106. http://dx.doi.org/10.1007/s00035-018-0208-3.

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19

Zotz, Gerhard, Peter Hietz et Gerold Schmidt. « Small plants, large plants : the importance of plant size for the physiological ecology of vascular epiphytes ». Journal of Experimental Botany 52, no 363 (1 octobre 2001) : 2051–56. http://dx.doi.org/10.1093/jexbot/52.363.2051.

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Smirnov, Sergey V., Aleksey A. Kechaykin, Vladislav S. Tenigin, Ilja A. Shestakov et Alexander I. Shmakov. « New records of vascular plants in the West Altai ». Turczaninowia 24, no 4 (20 décembre 2021) : 131–39. http://dx.doi.org/10.14258/turczaninowia.24.4.13.

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The article presents new data on the distribution in the territory of Western Altai of 20 species of vascular plants from the families Asteraceae, Betulaceae, Boraginaceae, Crassulaceae, Huperziaceae, Grossulariaceae, Lamiaceae, Onagraceae, Orchidaceae, Papaveraceae, Polygonaceae, Ranunculaceae, Rosaceae, Saxifragaceae и Violaceae. All of them were collected in the highlands of the Korgon Range within the Altai Territory. Of these, Potentilla crebridens is reported for the first time for the Altai Territory and Western Altai; for other species, new localities are indicated. For the first time for the Korgon Range within the Altai Territory, Saxifraga terektensis, Viola tigirekica are presented, and the exact location of Potentilla nivea is noted. New localities of rare and protected species were discovered: Callianthemum sajanense, Huperzia appressa, Pyrethrum alatavicum, Saussurea baicalensis, Scutellaria altaica. For each species, the general distribution, ecology data are given, for some species, notes on the difference and differentiation of them from the closest taxa are indicated. If necessary, the locations of the species previously registered in the Western Altai are indicated. For the species included in the “Red Data Book of the Altai Territory”, we provide an information on the approximate number of individuals in the found populations. Based on the analysis of herbarium material, we exclude Potentilla nervosa from the list of flora of the Altai Territory.
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21

Keener, Carl S., Ernest M. Gifford et Adriance S. Foster. « Morphology and Evolution of Vascular Plants. » Systematic Botany 15, no 2 (avril 1990) : 348. http://dx.doi.org/10.2307/2419189.

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22

Scarnecchia, David L., et N. N. Tzvelev. « Vascular Plants of the Russian Far East ». Journal of Range Management 57, no 3 (mai 2004) : 325. http://dx.doi.org/10.2307/4003803.

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23

Brunton, Daniel F. « The Rare Vascular Plants of British Columbia ». Canadian field-naturalist 100, no 4 (1986) : 588–89. http://dx.doi.org/10.5962/p.355729.

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24

Kaplan, Zdeněk, Jiří Danihelka, Jindřich Chrtek, Jiří Zázvorka, Petr Koutecký, Libor Ekrt, Radomír Řepka et al. « Distributions of vascular plants in the Czech Republic ». Preslia 91, no 4 (décembre 2019) : 257–368. http://dx.doi.org/10.23855/preslia.2019.257.

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25

Kaplan, Zdeněk, Jiří Danihelka, Libor Ekrt, Milan Štech, Radomír Řepka, Jindřich Chrtek, Vít Grulich et al. « Distributions of vascular plants in the Czech Republic ». Preslia 92, no 3 (2020) : 255–340. http://dx.doi.org/10.23855/preslia.2020.255.

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Kaplan, Zdeněk, Jiří Danihelka, Pavel Dřevojan, Radomír Řepka, Petr Koutecký, Vít Grulich et Jan Wild. « Distributions of vascular plants in the Czech Republic ». Preslia 93, no 3 (2021) : 255–304. http://dx.doi.org/10.23855/preslia.2021.255.

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Kaplan, Zdeněk, Jiří Danihelka, Jindřich Chrtek, Jan Prančl, Vít Grulich, Boleslav Jelínek, Luboš Úradníček et al. « Distributions of vascular plants in the Czech Republic ». Preslia 94, no 3 (2022) : 335–427. http://dx.doi.org/10.23855/preslia.2022.335.

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28

Ingerpuu, Nele, Jaan Liira et Meelis Pärtel. « Vascular Plants Facilitated Bryophytes in a Grassland Experiment ». Plant Ecology 180, no 1 (septembre 2005) : 69–75. http://dx.doi.org/10.1007/s11258-005-2508-0.

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Kaplan, Zdeněk, Jiří Danihelka, Kateřina Šumberová, Jan Prančl, Jiří Velebil, Pavel Dřevojan, Michal Ducháček et al. « Distributions of vascular plants in the Czech Republic ». Preslia 95, no 1 (2023) : 1–118. http://dx.doi.org/10.23855/preslia.2023.001.

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Kaplan, Zdeněk, Jiří Danihelka, Jan Prančl, Jindřich Chrtek, Michal Ducháček, Kateřina Šumberová, Klára Nunvářová Kabátová, Vojtěch Taraška et Jan Wild. « Distributions of vascular plants in the Czech Republic ». Preslia 96, no 1 (2024) : 1–96. http://dx.doi.org/10.23855/preslia.2024.001.

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Sokoloff, Paul C. « The flora of Cunningham Inlet, Somerset Island, Nunavut : history, analysis, and new collections of vascular plants, mosses, lichens, and algae ». Canadian Field-Naturalist 129, no 1 (31 mai 2015) : 24. http://dx.doi.org/10.22621/cfn.v129i1.1664.

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New collections of vascular plants, bryophytes, lichen, and algae are reported for Cunningham Inlet on the north coast of Somerset Island, Nunavut. This list of 48 species of vascular plants, 13 bryophytes, 10 lichens, and five algae includes 136 specimens collected in 2013 and 39 previously unreported specimens from the National Herbarium of Canada at the Canadian Museum of Nature (CAN), Agriculture and Agri-Food Canada’s Vascular Plant Herbarium (DAO), and University of Alberta (ALTA). Ten vascular plants from previous collecting in 1958 are re-reported here to give a comprehensive account of the vascular plant flora of the region. Two vascular plants are recorded for the first time for Somerset Island: Smooth Draba (Draba glabella Pursh) and Edlund’s Fescue (Festuca edlundiae S. G. Aiken, Consaul & Lefkovitch).
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McKown, Athena D., et Nancy G. Dengler. « Vein patterning and evolution in C4 plants ». Botany 88, no 9 (septembre 2010) : 775–86. http://dx.doi.org/10.1139/b10-055.

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The C4 photosynthetic pathway provides a platform to gain insight into the formation, regulation, and biological consequences of leaf vein pattern modification. This review examines the functional role of the vascular system in C4 photosynthesis and the development of veins in C3 and C4 plants, highlighting the contribution of vasculature in the evolution of the C4 pathway. With interest in developing C3 plant crops into C4 systems, it is essential to understand vascular patterning as a necessary element for C4 functioning. Leaf venation in C4 plants generally shows a higher vein density through a greater network complexity (more veins) compared with the ancestral C3 condition. Thus, C4 plants can provide a model that links the development of vein patterning with evolutionary selection pressures and molecular mechanisms (i.e., modifications of different components of vascular development). Numerous studies, including a comparative C3 and C4 Flaveria case study, highlight that the overall process of vein formation and patterning is complex, involving interactions between procambium and ground meristem during leaf ontogeny, and points to potential roles of changes in auxin production, transport, and perception.
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Lin, Qinwen, Chaoran Wu, Xia Cui et Jinshuang Ma. « Thirty-year changes of vascular plants in Beijing ». Biodiversity Science 30, no 6 (2022) : 22107. http://dx.doi.org/10.17520/biods.2022107.

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Ma, Jinshuang, et Chong-wook Park. « The Genera of Vascular Plants of Korea ». Taxon 57, no 2 (1 mai 2008) : 681. http://dx.doi.org/10.2307/25066061.

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Odorico, Délcio, Enrico Nicosia, Castigo Datizua, Clayton Langa, Raquel Raiva, Joelma Souane, Sofia Nhalungo et al. « An updated checklist of Mozambique’s vascular plants ». PhytoKeys 189 (28 janvier 2022) : 61–80. http://dx.doi.org/10.3897/phytokeys.189.75321.

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An updated checklist of Mozambique’s vascular plants is presented. It was compiled referring to several information sources such as existing literature, relevant online databases and herbaria collections. The checklist includes 7,099 taxa (5,957 species, 605 subspecies, 537 varieties), belonging to 226 families and 1,746 genera. There are 6,804 angiosperms, 257 pteridophytes, and 38 gymnosperms. A total of 6,171 taxa are native to Mozambique, while 602 are introduced and the remaining 326 taxa were considered as uncertain status. The endemism level for Mozambique’s flora was assessed at 9.59%, including 278 strict-endemic taxa and 403 near-endemic. 58.2% of taxa are herbaceous, while shrubs and trees account respectively for 26.5% and 9.2% of the taxa. The checklist also includes ferns (3.6%), lianas (1.7%), subshrubs (0.5%) and cycads (0.3%). Fabaceae, Poaceae and Asteraceae are the three most represented families, with 891, 543 and 428 taxa, respectively. The extinction risk of 1,667 taxa is included, with 158 taxa listed as Vulnerable, 119 as Endangered and as 24 Critically Endangered. The geographical distribution, known vernacular names and plants traditional uses are also recorded.
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Schmid, Rudolf. « Three Electronic Databases for Californian Vascular Plants ». Taxon 45, no 1 (février 1996) : 161. http://dx.doi.org/10.2307/1222623.

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Schmid, Rudolf, K. (Klaus) Kubitzki, K. (Klaus) Kubitzki et J. (Joachim) W. Kadereit. « The Families and Genera of Vascular Plants ». Taxon 54, no 2 (1 mai 2005) : 574. http://dx.doi.org/10.2307/25065407.

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Korrensalo, Aino, Tomáš Hájek, Timo Vesala, Lauri Mehtätalo et Eeva-Stiina Tuittila. « Variation in photosynthetic properties among bog plants ». Botany 94, no 12 (décembre 2016) : 1127–39. http://dx.doi.org/10.1139/cjb-2016-0117.

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Plant functional types (PFTs) are used to make generalizations in modeling how plants impact ecosystem functioning. In boreal bogs the number of plant species is small, but several PFTs are represented, namely sedges, deciduous and evergreen dwarf-shrubs, as well as hummock, lawn, and hollow Sphagna. Despite the use of PFTs in modeling, the value of PFTs to describe the photosynthetic properties of bog plants has not been systematically studied. We aim to quantify the photosynthetic properties of typical bog plant species and assess how well PFT divisions reflect differences among species. We measured photosynthetic light response and physiological state of photosystem II of 19 species, monthly, over a growing season. Differences were assessed using principal component analysis and mixed models. Photosynthetic properties separated Sphagna into traditional PFTs, of which hollow species had the highest gross photosynthesis. Sphagnum photosynthesis had large seasonal variation, as monthly differences exceeded those among PFTs or species. The photosynthetic properties of vascular plants differed widely among species but did not follow traditional PFTs. Vascular plant seasonal changes were of less importance than interspecific differences. The results justify using PFTs to describe the ability of bog Sphagna to bind carbon, but do not justify the same approach for vascular plants.
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Falkengren-Grerup, U., et M. Schöttelndreier. « Vascular plants as indicators of nitrogen enrichment in soils ». Plant Ecology (formerly Vegetatio) 172, no 1 (mai 2004) : 51–62. http://dx.doi.org/10.1023/b:vege.0000026033.43070.e9.

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Jiménez-Alfaro, Borja, Luis Carlón, Eduardo Fernández-Pascual, Carmen Acedo, Estrella Alfaro-Saiz, Raquel Alonso Redondo, Eduardo Cires et al. « Checklist of the vascular plants of the Cantabrian Mountains ». Mediterranean Botany 42 (27 octobre 2021) : e74570. http://dx.doi.org/10.5209/mbot.74570.

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We present the first standardized list of the vascular flora of the Cantabrian Mountains, a transitional zone between the Eurosiberian and Mediterranean biogeographic regions in northwestern Spain. The study area comprises 15000 km2 divided in UTM grid cells of 10 km x 10 km, for which we revised occurrence data reported in the Spanish Plant Information System (Anthos) and the online database of Iberian and Macaronesian Vegetation (SIVIM). We used a semi-automatic procedure to standardize taxonomic concepts into a single list of names, which was further updated by expert-based revision with the support of national and regional literature. In the current version, the checklist of the Cantabrian Mountains contains 2338 native species and subspecies, from which 56 are endemic to the study area. The nomenclature of the checklist follows Euro+Med in 97% of taxa, including annotations when other criteria has been used and for taxa with uncertain status. We also provide a list of 492 non-native taxa that were erroneously reported in the study area, a list of local apomictic taxa, a phylogenetic tree linked to The Plant List, a standardized calculation of Ellenberg Ecological Indicator Values for 80% of the flora, and information about life forms, IUCN threat categories and legal protection status. Our review demonstrates how the Cantabrian mountains represent a key floristic region in southern Europe and a relevant phytogeographical hub in south-western Europe. The checklist and all related information are freely accessible in a digital repository for further uses in basic and applied research
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Dorr, Laurence J., et Marshall C. Johnston. « The Vascular Plants of Texas. A List, Up-Dating the Manual of the Vascular Plants of Texas. Second Edition. » Brittonia 42, no 4 (octobre 1990) : 293. http://dx.doi.org/10.2307/2806822.

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Tyler, Torbjörn, Lina Herbertsson, Johan Olofsson et Pål Axel Olsson. « Ecological indicator and traits values for Swedish vascular plants ». Ecological Indicators 120 (janvier 2021) : 106923. http://dx.doi.org/10.1016/j.ecolind.2020.106923.

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Eliáš Jr., Pavol, Jana Májeková, Katarína Hegedüšová, Matej Dudáš, Dominik Letz, Pavol Mereďa Jr., Ladislav Bakay et al. « New alien vascular plants of Slovakia : records from 2008–2021 ». BioInvasions Records 12, no 1 (2023) : 1–30. http://dx.doi.org/10.3391/bir.2023.12.1.01.

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Lambinon, J. « Morphology and Evolution of Vascular Plants (Third Edition) ». Biochemical Systematics and Ecology 18, no 4 (juillet 1990) : 295–96. http://dx.doi.org/10.1016/0305-1978(90)90075-q.

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Yang, Bo, Qinwen Lin, Qiang Zhu, Long Ma et Xiaowei Li. « Species cataloging of vascular plants in Ningxia, northwestern China ». Biodiversity Science 30, no 6 (2022) : 22039. http://dx.doi.org/10.17520/biods.2022039.

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Wan, Xia, et Libing Zhang. « Global new species of vascular plants published in 2020 ». Biodiversity Science 29, no 8 (2021) : 1003–10. http://dx.doi.org/10.17520/biods.2021156.

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Wan, Xia, et Li-Bing Zhang. « Global new taxa of vascular plants published in 2021 ». Biodiversity Science 30, no 8 (2022) : 22116. http://dx.doi.org/10.17520/biods.2022116.

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Kull, Tiiu, Marek Sammul, Kalevi Kull, Kaire Lanno, Kadri Tali, Bernd Gruber, Dirk Schmeller et Klaus Henle. « Necessity and reality of monitoring threatened European vascular plants ». Biodiversity and Conservation 17, no 14 (16 juillet 2008) : 3383–402. http://dx.doi.org/10.1007/s10531-008-9432-2.

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An, Chang, Yixue Zhuang, Ping Zheng, Yanxiang Lin, Chengzi Yang et Yuan Qin. « A checklist of vascular plants in Fujian Province, China ». Biodiversity Science 31, no 6 (2023) : 22537. http://dx.doi.org/10.17520/biods.2022537.

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Wei, Yigang, Fang Wen, Zibing Xin et Longfei Fu. « A checklist of wild vascular plants in Guangxi, China ». Biodiversity Science 31, no 6 (2023) : 23078. http://dx.doi.org/10.17520/biods.2023078.

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