Academic literature on the topic 'Vascular plants'
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Journal articles on the topic "Vascular plants"
Ascaso Martorel, Joaquín, and Joan Pcdrol Solanes. "De plantis vascularibus praesertim ibericis. III." Acta Botanica Malacitana 26 (December 1, 2001): 213–16. http://dx.doi.org/10.24310/abm.v26i0.7421.
Full textDel Egido Mazuelas, Fermín, Emilio Puente García, Francisco Gómiz García, and Elena De Paz Canuria. "De plantis legionensibus. Notula XVIII." Acta Botanica Malacitana 30 (December 1, 2005): 166–69. http://dx.doi.org/10.24310/abm.v30i0.7191.
Full textFuentes-Carretero, Julián Manuel. "Aportaciones corológicas a la flora vascular de las Alpujarras (Granada y Almeria, España). Chorological contributions for the vascular flora of the Alpujarras (Granada & Almeria, Spain)." Acta Botanica Malacitana 39 (December 1, 2014): 254–59. http://dx.doi.org/10.24310/abm.v39i1.2580.
Full textSánchez Gómez, Pedro, Miguel Ángel Carrión Vilches, Antonio Hernández González, Juan Bautista Vera Pérez, and Antonio Félix Carrillo López. "Aportaciones a la flora del sureste ibérico." Acta Botanica Malacitana 26 (December 1, 2001): 217–18. http://dx.doi.org/10.24310/abm.v26i0.7422.
Full textAru, Mª Bárbara, Elena De Paz, Ruth Martínez, Raquel Alonso, and Marta Eva García. "Nuevos táxones para la Flora de la Montaña Palentina (España)." Acta Botanica Malacitana 33 (December 1, 2008): 325–29. http://dx.doi.org/10.24310/abm.v33i0.6994.
Full textFerrer, Pedro Pablo, and Miguel Guara Requena. "Nuevos datos florísticos para el este peninsular ibérico." Acta Botanica Malacitana 31 (December 1, 2006): 149–52. http://dx.doi.org/10.24310/abm.v31i31.7134.
Full textSHCHEGLOVA, I. P., and V. M. VAN. "“Oldzhikansky” sanctuary vascular plants." Вестник ДВО РАН, no. 6 (2021): 77–93. http://dx.doi.org/10.37102/0869-7698_2021_220_06_08.
Full textDing, Yiliang, and Chun Kit Kwok. "Emergence of vascular plants." Nature Plants 4, no. 6 (May 28, 2018): 325–26. http://dx.doi.org/10.1038/s41477-018-0159-0.
Full textDoyle, James A. "PHYLOGENY OF VASCULAR PLANTS." Annual Review of Ecology and Systematics 29, no. 1 (November 1998): 567–99. http://dx.doi.org/10.1146/annurev.ecolsys.29.1.567.
Full textLepp, Nicholas W. "Vascular Transport in Plants." Journal of Environmental Quality 35, no. 2 (March 2006): 688. http://dx.doi.org/10.2134/jeq2005.0019br.
Full textDissertations / Theses on the topic "Vascular plants"
Rai, Hardeep Singh. "Molecular phylogenetic studies of the vascular plants." Thesis, University of British Columbia, 2008. http://hdl.handle.net/2429/3889.
Full textSutherland, Margery Louise. "Recognition of host plants by vascular pathogens." Thesis, University of Reading, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.303155.
Full textHaig, David. "Applications of allocation and kinship models to the interpretation of vascular plant life cycles." Phd thesis, Australia : Macquarie University, 1990. http://hdl.handle.net/1959.14/23227.
Full textThesis (PhD) -- Macquarie University, School of Biological Sciences, 1990.
Bibliography: leaves 269-324.
Introduction -- Models of parental allocation -- Sex expression in homosporous pteridophytes -- The origin of heterospory -- Pollination and the origin of the seed habit -- Brood reduction in gymnosperms -- Pollination: costs and consequences -- Adaptive explanations for the rise of the angiosperms -- Parent-specific gene expression and the triploid endosperm -- New perspectives on the angiosperm female gametophyte -- Overview -- Glossary -- Kinship terms in plants -- Literature Cited.
Among vascular plants/ different life cycles are associated with characteristic ranges of propagule size. In the modern flora, isospores of homosporous pteridophytes are almost all smaller than 150 urn diameter, megaspores of heterosporous pteridophytes fall in the range 100-1000 urn diameter, gymnosperm seeds are possibly all larger than the largest megaspores, but the smallest angiosperm seeds are of comparable size to large isospores. -- Propagule size is one of the most important features of a sporophyte's reproductive strategy. Roughly speaking, larger propagules have larger food reserves, and a greater probability of successful establishment, than smaller propagules, but a sporophyte can produce more smaller propagules from the same quantity of resources. Different species have adopted very different size-versus-number compromises. The characteristic ranges of propagule size, in each of the major groups of vascular plants, suggest that some life cycles are incompatible with particular size-versus-number compromises. -- Sex expression in homosporous plants is a property of gametophytes (homosporous sporophytes are essentially asexual). Gametophytes should produce either eggs or sperm depending on which course of action gives the greatest chance of reproductive success. A maternal gametophyte must contribute much greater resources to a young sporophyte than the paternal gametophyte. Therefore, smaller gametophytes should tend to reproduce as males, and gametophytes with abundant resources should tend to reproduce as females. Consistent with these predictions, large female gametophytes release substances (antheridiogens) which induce smaller neighbouring ametophytes to produce sperm. -- The mechanism of sex determination in heterosporous species appears to be fundamentally different. Large megaspores develop into female gametophytes, and small icrospores develop into male gametophytes. Sex expression appears to be determined by the sporophyte generation. This is misleading. As argued above, the optimal sex expression of a homosporous gametophyte is influenced by its access to resources. This is determined by (1) the quantity of food reserves in its spore and (2) the quantity of resources accumulated by the gametophyte's own activities. If a sporophyte produced spores of two sizes, gametophytes developing from the larger spores' would be more likely to reproduce as females than gametophytes developing from the smaller spores, because the pre-existing mechanisms of sex determination would favor production of archegonia by larger gametophytes. Thus, the predicted mechanisms of sex determination in homosporous species could also explain the differences in sex expression of gametophytes developing from large and small spores in heterosporous species.
Megaspores of living heterosporous pteridophytes contain sufficient resources for female reproduction without photosynthesis by the gametophyte (Platyzoma excepted), whereas microspores only contain sufficient resources for male reproduction. Furthermore, many more microspores are produced than megaspores. A gametophyte's optimal sex expression is overwhelmingly determined by the amount of resources supplied in its spore by the sporophyte, and is little influenced by the particular environmental conditions where the spore lands. Gametophytes determine sex expression in heterosporous species, as well as homosporous species. A satisfactory model for the evolution of heterospory needs to explain under what circumstances sporophytes will benefit from producing spores of two distinct sizes. -- In Chapter 4, I present a model for the origin of heterospory that predicts the existence of a "heterospory threshold". For propagule sizes below the threshold, homosporous reproduction is evolutionarily stable because gametophytes must rely on their own activities to accumulate sufficient resources for successful female reproduction. Whether a gametophyte can accumulate sufficient resources before its competitors is strongly influenced by environmental conditions. Gametophytes benefit from being able to adjust their sex expression in response to these conditions. For propagule sizes above the threshold, homosporous reproduction is evolutionarily unstable, because the propagule's food reserves are more than sufficient for a "male" gametophyte to fertilize all eggs within its neighbourhood. A population of homosporous sporophytes can be invaded by sporophytes that produce a greater number of smaller spores which could land in additional locations and fertilize additional eggs. Such'spores would be male-specialists on account of their size. Therefore, both spore types would be maintained in the population because of frequency-dependent selection. -- The earliest vascular plants were homosporous. Several homosporous groups gave rise to heterosporous lineages, at least one of which was the progeniture of the seed plants. The first heterosporous species appear in the Devonian. During the Devonian, there was a gradual increase in maximum spore size, possibly associated with the evolution of trees and the appearance of the first forests. As the heterospory threshold was approached, the optimal spore size for female reproduction diverged from the optimal spore size for male reproduction. Below the threshold, a compromise spore size gave the highest fitness returns to sporophytes, but above the threshold, sporophytes could attain higher fitness by producing two types of spores. -- The evolution of heterospory had profound consequences. Once a sporophyte produced two types of spores, microspores and megaspores could become specialized for male and female function respectively. The most successful heterosporous lineage (or lineages) is that of the seed plants. The feature that distinguishes seed plants from other heterosporous lineages is pollination, the capture of microspores before, rather than after, propagule dispersal. Traditionally, pollination has been considered to be a major adaptive advance because it frees sexual reproduction from dependence on external fertilization by freeswimming sperm, but pollination has a more important advantage. In heterosporous pteridophytes, a megaspore is provisioned whether or not it will be fertilized whereas seeds are only provisioned if they are pollinated.
The total cost per seed cannot be assessed solely from the seed's energy and nutrient content. Rather, each seed also has an associated supplementary cost of adaptations for pollen capture and of resources committed to ovules that remain unpollinated. The supplementary cost per seed has important consequences for understanding reproductive strategies. First, supplementary costs are expected to be proportionally greater for smaller seeds. Thus, the benefits of decreasing seed size (in order to produce more seeds) are reduced for species with small seeds. This effect may explain minimum seed sizes. Second, supplementary costs are greater for populations at lower density. Thus, there is a minimum density below which a species cannot maintain its numbers. -- By far the most successful group of seed plants in the modern flora are the angiosperms. Two types of evidence suggest that early angiosperms had a lower supplementary cost per seed than contemporary gymnosperms. First, the minimum size of angiosperm seeds was much smaller than the minimum size of gymnosperm seeds. This suggests that angiosperms could produce small seeds more cheaply than could gymnosperms. Second, angiosperm-dominated floras were more speciose than the gymnosperm-dominated floras they replaced. This suggests that the supplementary cost per seed of angiosperms does not increase as rapidly as that of gymnosperms, as population density decreases. In consequence, angiosperms were able to displace gymnosperms from many habitats, because the angiosperms had a lower cost of rarity. -- Angiosperm embryology has a number of distinctive features that may be related to the group's success. In gymnosperms, the nutrient storage tissue of the seed is the female gametophyte. In most angiosperms, this role is taken by the endosperm. Endosperm is initiated by the fertilization of two female gametophyte nuclei by a second sperm that is genetically identical to the sperm which fertilizes the egg. Endosperm has identical genes to its associated embryo, except that there are two copies of maternal genes for every copy of a paternal gene. -- Chapter 9 presents a hypothesis to explain the unusual genetic constitution of endosperm. Paternal genes benefit from their endosperm receiving more resources than the amount which maximizes the fitness of maternal genes, and this conflict is expressed as parent-specific gene expression in endosperm. The effect of the second maternal genome is to increase maternal control of nutrient acquisition. -- Female gametophytes of angiosperms are traditionally classified as monosporic, bisporic or tetrasporic. Bisporic and tetrasporic embryo sacs contain the derivatives of more than one megaspore nucleus. Therefore, there is potential for conflict between the different nuclear types within an embryo sac, but this possibility has not been recognized by plant embryologists. In Chapter 10, I show that many previously inexplicable observations can be understood in terms of genetic conflicts within the embryo sac.
Mode of access: World Wide Web.
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Kücükoglu, Melis. "CLE/RLK regulated vascular signalling pathways in plants." Thesis, Umeå University, Plant Physiology, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-26276.
Full textEntire postembryonic production of plant tissues are maintained by meristems. These specialized structures provide a pool of undifferentiated stem cells and a limited population of proliferating cells which are destined for differentiation in order to generate a variety of tissues in the plant body. For the forest trees, a large part of the biomass is produced by a secondary meristem called vascular cambium. Vascular cambium forms a continuous cylinder of meristematic cells in the stem, producing both secondary phloem and secondary xylem or wood. Maintenance and differentiation of meristems are much conserved and strictly regulated for the production of correct tissues and organs. Receptor-like kinases (RLKs) are characterized by the presence of a signal sequence, a putative amino-terminal extracellular domain connected to a carboxyl-terminal intracellular kinase domain with a trans-membrane domain. They control a wide-range of physiological processes, including development, disease resistance, hormone perception, and self-incompatibility. Leucine-rich repeat receptor-like kinases (LRR-RLKs) represent the largest group of RLKs in the Arabidopsis thaliana genome, with more than 200 members.Several LRR-RLKs and their putative ligands CLAVATA3 (CLV3)/ Endosperm Surrounding Region (ESR)-related (CLE) peptides have been found to be involved in the regulation of vascular development. In the current study, the main aim was to study the tissue-specific expression patterns of LRR-RLK genes in A. thaliana by generating promoter::GUS transcriptional fusions. The results confirmed that these genes are expressed in the vasculature of the plants. Moreover, Populus orthologs of the CLE genes were detected by bioinformatic tools as putative ligands of LRR-RLKs and an extensive quantitative Real-Time Reverse Transcriptase PCR (qRT-PCR) analysis was performed to test for significant changes in transcript levels across different tissue types. As a result, a collection of potential candidate genes for vascular development were identified.
Gersbach, Paul Vincent, University of Western Sydney, and of Science Technology and Environment College. "Aspects of essential oil secretion in vascular plants." THESIS_CSTE_XXX_Gersbach_P.xml, 2001. http://handle.uws.edu.au:8081/1959.7/775.
Full textDoctor of Philosophy (PhD) (Science)
Gersbach, Paul V. "Aspects of essential oil secretion in vascular plants /." View thesis, 2001. http://library.uws.edu.au/adt-NUWS/public/adt-NUWS20031223.143208/index.html.
Full text"This thesis is presented in fulfilment of the degree of Doctor of Philosophy in Science at the University of Western Sydney, Richmond, New South Wales, Australia" Bibliography : p. 145-163.
Balogh, Zsuzsanna. "Chemical hydrology of vascular plant growth : role of root-fungus associations." Online access for everyone, 2006. http://www.dissertations.wsu.edu/Dissertations/Summer2006/z%5Fbalogh%5F071806.pdf.
Full textBruchmann, Ines [Verfasser]. "Plant endemism in Europe : spatial distribution and habitat affinities of endemic vascular plants / Ines Bruchmann." Flensburg : Zentrale Hochschulbibliothek Flensburg, 2011. http://d-nb.info/1019372133/34.
Full textChowdhury, Anurag. "Studies on the diversity and ethnic uses of wetland vascular plants in Terai and Duars of West Bengal, India." Thesis, University of North Bengal, 2015. http://ir.nbu.ac.in/hdl.handle.net/123456789/1871.
Full textHarrelson, Sarah M. "A floristic survey of the terrestrial vascular plants of Strouds Run State Park, Athens County, Ohio." Ohio : Ohio University, 2005. http://www.ohiolink.edu/etd/view.cgi?ohiou1113581854.
Full textBooks on the topic "Vascular plants"
Vascular plants and paleobotany. Toronto: Apple Academic Press, 2012.
Find full text1952-, Iqbal M., ed. Growth patterns in vascular plants. Portland, Or: Dioscorides Press, 1994.
Find full textLüttge, Ulrich, ed. Vascular Plants as Epiphytes. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74465-5.
Full textHobohm, Carsten, ed. Endemism in Vascular Plants. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-6913-7.
Full textDorn, Robert D. Vascular plants of Wyoming. Cheyenne, Wyo: Mountain West Pub., 1988.
Find full textDorn, Robert D. Vascular plants of Wyoming. 2nd ed. Cheyenne, Wyoming: Mountain West Publishing, 1992.
Find full textDorn, Robert D. Vascular plants of Wyoming. 3rd ed. Cheyenne, Wyo: Mountain West Pub., 2001.
Find full textA, Zwieniecki Maciej, ed. Vascular transport in plants. Burlington, MA: Elsevier Academic Press, 2005.
Find full textIUCN Regional Office for Europe and IUCN Species Survival Commission, eds. European red list of vascular plants. Luxembourg: Publications Office of the European Union, 2011.
Find full text1951-, Kershaw Linda, and Alberta Native Plant Council, eds. Rare vascular plants of Alberta. Edmonton, Alta: University of Alberta Press, 2001.
Find full textBook chapters on the topic "Vascular plants"
Kelcey, John G. "Plants (Non-vascular)." In Provisional Bibliography of Atlases, Floras and Faunas of European Cities: 1600–2014, 85–87. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31120-3_7.
Full textEvert, Ray F. "Seedless Vascular Plants." In Sieve Elements, 35–62. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-74445-7_3.
Full textEvert, Ray F., and Susan E. Eichhorn. "Seedless Vascular Plants." In Raven Biology of Plants, 391–429. New York: Macmillan Learning, 2013. http://dx.doi.org/10.1007/978-1-319-15626-8_18.
Full textKelcey, John G. "Plants (Vascular including Pteridophytes)." In Provisional Bibliography of Atlases, Floras and Faunas of European Cities: 1600–2014, 89–111. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31120-3_8.
Full textOwfi, Reza E. "Cryptogamaes—Non-Vascular Plants." In Natural Products and Botanical Medicines of Iran, 219–26. First edition. | Boca Raton : CRC Press, 2020. | Series: Natural products chemistry of global plants: CRC Press, 2020. http://dx.doi.org/10.1201/9781003008996-8.
Full textReitz, Elizabeth J., and Myra Shackley. "Bryophytes and Vascular Plants." In Manuals in Archaeological Method, Theory and Technique, 191–230. Boston, MA: Springer US, 2012. http://dx.doi.org/10.1007/978-1-4614-3339-2_7.
Full textSperry, John S. "Hydraulics of Vascular Water Transport." In Mechanical Integration of Plant Cells and Plants, 303–27. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-19091-9_12.
Full textHobohm, Carsten, and Caroline M. Tucker. "The Increasing Importance of Endemism: Responsibility, the Media and Education." In Endemism in Vascular Plants, 3–9. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6913-7_1.
Full textHobohm, Carsten, and Caroline M. Tucker. "How to Quantify Endemism." In Endemism in Vascular Plants, 11–48. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6913-7_2.
Full textBruchmann, Ines, and Carsten Hobohm. "Factors That Create and Increase Endemism." In Endemism in Vascular Plants, 51–68. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6913-7_3.
Full textConference papers on the topic "Vascular plants"
Leslie, Andrew. "GENOME DUPLICATION AND REPRODUCTIVE COMPLEXITY IN VASCULAR PLANTS." In GSA Connects 2023 Meeting in Pittsburgh, Pennsylvania. Geological Society of America, 2023. http://dx.doi.org/10.1130/abs/2023am-390684.
Full textEvkaykina, A. I., E. A. Klimova, E. V. Tyutereva, K. S. Dobryakova, A. N. Ivanova, C. Rydin, L. Berke, et al. "Evolution of the mechanisms of regulation of the apical meristem and laying of leaves in vascular plants." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-160.
Full textSheremetova, S. A., and I. A. Khrustaleva. "VASCULAR PLANTS OF KUZBASS — THE CURRENT STATE OF RESEARCH." In VI Международная конференция "Проблемы промышленной ботаники индустриально развитых регионов". Кемерово: Федеральный исследовательский центр угля и углехимии Сибирского отделения Российской академии наук, 2021. http://dx.doi.org/10.53650/9785902305606_25.
Full textTrofimova, I. G., and N. V. Nikolaeva. "Protected species of vascular plants in Yakutsk and its environs." In Botanical Gardens as Centers for Study and Conservation of Phyto-Diversity. TSU Press, 2020. http://dx.doi.org/10.17223/978-5-94621-956-3-2020-62.
Full textDegtyareva, S. I., and V. D. Dorofeeva. "METHODS FOR ASSESSING THE STATE OF FOREST ECOSYSTEMS USING A TEST OBJECT." In Modern machines, equipment and IT solutions for industrial complex: theory and practice. Voronezh State University of Forestry and Technologies named after G.F. Morozov, Voronezh, Russia, 2021. http://dx.doi.org/10.34220/mmeitsic2021_49-55.
Full textMaute, K., M. L. Dunn, R. Bischel, M. Howard, and J. M. Pajot. "Multiscale Design of Vascular Plates." In ASME 2005 International Mechanical Engineering Congress and Exposition. ASMEDC, 2005. http://dx.doi.org/10.1115/imece2005-82203.
Full textHuang, Tianzheng, Yuanlin Sun, Zhouqiao Zhao, Chao Li, Hong Zhao, Ting Nie, Jinzhuang Xue, and Bing Shen. "RECONSTRUCTION THE WEATHERING INTENSITY DURING THE EARLY EVOLUTION OF VASCULAR LAND PLANTS." In GSA Annual Meeting in Seattle, Washington, USA - 2017. Geological Society of America, 2017. http://dx.doi.org/10.1130/abs/2017am-299870.
Full textVaraldo, Lucia, Maria Guerrina, Davide Dagnino, Luigi Minuto, and Gabriele Casazza. "Assessing the Effect of Climate Change in Vascular Plants with Disjunct Populations." In IECD 2022. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/iecd2022-12419.
Full textSukhikh, Stanislav, Natalia Chupakhina, Sofia Voronova, Alina Bakhtiyarova, and Victoria Larina. "Obtaining total extracts of some vascular plants of the Kaliningrad region flora." In INTERNATIONAL SCIENTIFIC AND PRACTICAL CONFERENCE “CURRENT ISSUES OF BIOLOGY, BREEDING, TECHNOLOGY AND PROCESSING OF AGRICULTURAL CROPS” (CIBTA2022) (To the 110th anniversary of V.S. Pustovoit All-Russian Research Institute of Oil Crops). AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0140394.
Full textSellier, Damien, and Jonathan J. Harrington. "Phloem sap flow and carbohydrate transport in vascular plants: A generic surface model." In 2012 IEEE 4th International Symposium on Plant Growth Modeling, Simulation, Visualization and Applications (PMA). IEEE, 2012. http://dx.doi.org/10.1109/pma.2012.6524854.
Full textReports on the topic "Vascular plants"
Sackschewsky, Michael R., and Janelle L. Downs. Vascular Plants of the Hanford Site. Office of Scientific and Technical Information (OSTI), September 2001. http://dx.doi.org/10.2172/789922.
Full textSackschewsky, Michael R., and Janelle L. Downs. Vascular Plants of the Hanford Site. Office of Scientific and Technical Information (OSTI), September 2001. http://dx.doi.org/10.2172/965728.
Full textBrown, Richard M, Jr, and Inder Mohan Saxena. Cellulose synthesizing Complexes in Vascular Plants andProcaryotes. Office of Scientific and Technical Information (OSTI), July 2009. http://dx.doi.org/10.2172/958293.
Full textLarson, Gary E. Aquatic and wetland vascular plants of the northern Great Plains. Ft. Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky Mountain Forest and Range Experiment Station, 1993. http://dx.doi.org/10.2737/rm-gtr-238.
Full textLackschewitz, Klaus. Vascular plants of west-central Montana-identification guidebook. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Research Station, 1991. http://dx.doi.org/10.2737/int-gtr-277.
Full textGranot, David, and Noel Michelle Holbrook. Role of Fructokinases in the Development and Function of the Vascular System. United States Department of Agriculture, January 2011. http://dx.doi.org/10.32747/2011.7592125.bard.
Full textFoxx, T., L. Pierce, G. Tierney, and L. Hansen. Annotated checklist and database for vascular plants of the Jemez Mountains. Office of Scientific and Technical Information (OSTI), March 1998. http://dx.doi.org/10.2172/589248.
Full textBrace, Sarah, David L. Peterson, and Darci Bowers. A guide to ozone injury in vascular plants of the Pacific Northwest. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Research Station, 1999. http://dx.doi.org/10.2737/pnw-gtr-446.
Full textAwl, D. J., L. R. Pounds, B. A. Rosensteel, A. L. King, and P. A. Hamlett. Survey of protected vascular plants on the Oak Ridge Reservation, Oak Ridge, Tennessee. Office of Scientific and Technical Information (OSTI), June 1996. http://dx.doi.org/10.2172/262979.
Full textHazlett, Donald L., Michael H. Schiebout, and Paulette L. Ford. Vascular plants and a brief history of the Kiowa and Rita Blanca National Grasslands. Ft. Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, 2009. http://dx.doi.org/10.2737/rmrs-gtr-233.
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