Relevant bibliographies by topics / Plant cytotaxonomy ; Plant morphology

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Plant cytotaxonomy ; Plant morphology'

Author: Grafiati
Published: 4 June 2021
Last updated: 4 February 2022

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Journal articles on the topic "Plant cytotaxonomy ; Plant morphology"

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Brañas, Marian Oliva, and Joan Vallès Xirau. "Karyological studies in some taxa of the genus Artemisia (Asteraceae)." Canadian Journal of Botany 72, no. 8 (August 1, 1994): 1126–35. http://dx.doi.org/10.1139/b94-138.

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A karyological study of six taxa (eight populations) of the genus Artemisia L. from different geographic origins is presented. The work deals with chromosome number and morphometry. We found the two usual basic numbers in the genus: x = 9, the most common one (in two diploid, two hypotetraploid, one tetraploid and one hexaploid populations) and x = 8 (in two diploid populations). Detailed karyotype analysis allows us to group the different populations and to postulate relationships among them. Key words: Asteraceae, Anthemideae, Artemisia, cytotaxonomy, chromosome morphology, evolution.
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Xirau, Joan Vallès, and Sonja Siljak-Yakovlev. "Cytogenetic studies in the genus Artemisia L. (Asteraceae): fluorochrome-banded karyotypes of five taxa, including the Iberian endemic species Artemisia barrelieri Besser." Canadian Journal of Botany 75, no. 4 (April 1, 1997): 595–606. http://dx.doi.org/10.1139/b97-066.

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Fluorochrome-banded karyotypes of eight populations belonging to five taxa of the genus Artemisia from different European origins are presented. The most common basic number x = 9 is found in six populations of two diploid and two tetraploid species, whereas two populations of one diploid species have the less frequent basic number x = 8. The data on chromosome morphology and fluorochrome banding lead to some karyosystematic and evolutionary considerations, among others the postulation of descendent dysploidy to explain the occurrence of the two basic numbers in the genus. Key words: Asteraceae, Anthemideae, Artemisia, karyotypes, fluorochrome banding, cytotaxonomy, evolution.
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Aiken, Susan G., and George Fedak. "Cytotaxonomic observations on North American Festuca (Poaceae)." Canadian Journal of Botany 70, no. 10 (October 1, 1992): 1940–44. http://dx.doi.org/10.1139/b92-241.

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The presence of B chromosomes is reported in Festuca altaica Trin., where a plant with relatively wide and often flat leaves had a chromosome number of 2n = 4x = 28; an adjacent plant, with conspicuously narrow and tightly rolled leaves, had 2n = 4x = 28 + 2B chromosomes. A first chromosome count of 2n = 42 is reported for Festuca rubra L. ssp. densiuscula (Hackel) Piper, along with observations on the nomenclature and morphology of this west coast subspecies. A first chromosome count for a North American plant of Festuca brevissima Jurtzev is 2n = 14. Collections made in northern Yukon were compared with the type borrowed from Leningrad and with the distribution of this species relative to the other North American diploid Festuca, Festuca aggr. auriculata Drob. A collection of Festuca brachyphylla Schultes from northern Yukon had a chromosome number of 2n = 42, and unusual morphology and phenology were interpreted as the result of a snow patch habitat. A second record for Festuca dasyclada Hackel ex. Beal of a chromosome number of 2n = 28 and justifications for keeping this species in Festuca are presented. Key words: Poaceae, North American, Festuca, chromosomes, morphology, nomenclature.
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Guerra, M. "Chromosome numbers in plant cytotaxonomy: concepts and implications." Cytogenetic and Genome Research 120, no. 3-4 (2008): 339–50. http://dx.doi.org/10.1159/000121083.

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Kalu, Emmanuel Jonah, and Anulika Mercy Kanu. "Cytotaxonomic Studies of Three Ornamental Aroids." International Letters of Natural Sciences 18 (July 2014): 105–13. http://dx.doi.org/10.18052/www.scipress.com/ilns.18.105.

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Cytotaxanomical analysis carried out on three ornamental aroids (Anchomanes difformis, Anchomanes hookeri and Arum maculatum) proved that cytological studies is none negligible tool in phylogeny and scientific classificationns of plants. Aceto-orcein stain squash technique was used in this study. Anchomanes difformis and Anchomanes. hookeri showed more relatedness in chromosome number and chromosome morphology, sharing the same chromosome number 2n=13, while Arum maculatum has 2n=8. The following karyotypes formular were revealed: 2n=8=3M+3SM+2ST in Arum maculatum; 2n=13=5M+1SM+7ST in A. difformis; and 2n=13=3M+6SM+4 A. hookeri. Other karyotype parameters investigated like CI%, AsI and degree of asymmetry of the genomes supported current taxonomic ranking
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Sen, Sumitra. "Cytotaxonomy of Liliales." Feddes Repertorium 86, no. 5 (April 18, 2008): 255–305. http://dx.doi.org/10.1002/fedr.19750860502.

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Brammall, Ronald A., and John C. Semple. "The cytotaxonomy of Solidago nemoralis (Compositae: Astereae)." Canadian Journal of Botany 68, no. 10 (October 1, 1990): 2065–69. http://dx.doi.org/10.1139/b90-271.

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Chromosome number determinations were made from 218 populations of Solidago nemoralis collected throughout the range of the species in Canada and the United States. All individuals of ssp. decemflora were tetraploid (2n = 36; 28 populations); these came from the prairies and adjacent eastern deciduous forest states and provinces. The majority of the collections of ssp. nemoralis were diploid (2n = 18; 161 populations) and came from throughout the eastern deciduous forest region of eastern North America. Tetraploids (2n = 36; 29 populations) of ssp. nemoralis were less frequent and occurred scattered across the eastern and northern portions of the range of the subspecies. The cytotype distribution pattern of the two subspecies of Solidago nemoralis is representative of what appears to be a frequent evolutionary strategy in the goldenrods.
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Dubcovsky, Jorge, and Arturo J. Martínez. "Cytotaxonomy of the Festuca spp. from Patagonia." Canadian Journal of Botany 70, no. 6 (June 1, 1992): 1134–40. http://dx.doi.org/10.1139/b92-140.

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Chromosome number and karyotypes of Festuca argentina (2n = 28), Festuca magellanica (2n = 42 and 2n = 56), and Festuca purpurascens (2n = 42) are described here for the first time, as well as new data on the karyotype of Festuca contracta (2n = 42). Multivariate analysis based on chromosome size and shape showed significant (p < 0.05) differences among these species but not among the populations of F. magellanica analyzed. The correlation between a distance matrix among all the Patagonian species based on nine karyotype parameters and one based on morphoreproductive characters was significant (r = 0.60, p < 0.01) but it was not significant when compared with vegetative characters (r = 0.25, p > 0.05). The morphoreproductive and cytological data supported the classification of the Patagonian species in four different subgenera reflecting that the Patagonian Festuca spp. had different phylogenetic origins. Key words: Festuca, karyotype, cytotaxonomy.
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Mastrogiuseppe, Joy D., Steven J. Gill, Karen S. Simmons, and Gregory K. Brown. "Morphologic and Cytotaxonomic Evaluation of Lomatium tuberosum (Apiaceae)." Brittonia 37, no. 3 (July 1985): 252. http://dx.doi.org/10.2307/2806072.

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Franklin de Melo, Natoniel, Marcelo Guerra, Ana Maria Benko-Iseppon, and Nanuza Luiza de Menezes. "Cytogenetics and cytotaxonomy ofVelloziaceae." Plant Systematics and Evolution 204, no. 3-4 (1997): 257–73. http://dx.doi.org/10.1007/bf00989209.

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Dissertations / Theses on the topic "Plant cytotaxonomy ; Plant morphology"

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Brown, Brian Wayne. "Interactive versus non-interactive platforms for teaching plant morphology." Auburn, Ala., 2005. http://repo.lib.auburn.edu/2005%20Fall/Thesis/BROWN_BRIAN_48.pdf.

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Parmar, C. T. "The morphology of plant names in the Celtic languages." Thesis, Queen's University Belfast, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.419516.

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van, Blerk Justin. "Sexual dimorphism in the genus Leucadendron : Morphology and plant hydraulics." Bachelor's thesis, University of Cape Town, 2013. http://hdl.handle.net/11427/14014.

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The genus, Leucadendron, of the Cape Proteaceae family, is made up of over 70 dioecious species that vary in their degree of sexual dimorphism. Males are generally more highly ramified (branched) with smaller leaves compared to corresponding females. It has been hypothesised that sexual dimorphism in Leucadendrons is linked to serotiny (a fire-adapted reproductive strategy), where highly serotinous females may incur extra resource costs in order to keep their transpiring cones alive between fires. This hypothesis predicts that the female morphology might be associated with more efficient resource acquisition compared to males in order to support their greater resource requirements. Another hypothesis suggests that selection for greater floral display in males has lead to a higher degree of ramification as male cones are borne terminally on branches. This highly branched morphology may be associated with subsequent physiological costs. The idea that different male and female morphologies might be associated with different physiological costs or benefits was tested in this experiment with a focus on plant hydraulics. Hydraulic supply is known to affect photosynthetic capacity and maximum assimilation rate. Using a specially designed vacuum chamber, leaf-specific and xylem-specific hydraulic conductance was measured in males and females of the highly dimorphic Leucadendron rubrum and non/marginally dimorphic Leucadendron daphnoides. Using microscopic imagery, xylem anatomy was analysed in an attempt to explain the hydraulic conductance results.
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Li, Zhuo. "Bio-based composites that mimic the plant cell wall." Thesis, Virginia Tech, 2009. http://hdl.handle.net/10919/32088.

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Nature creates high performance materials under modest conditions, i.e., neutral pH and ambient temperature and pressure. One of the most significant materials is the plant cell wall. The plant cell wall is a composite of oriented cellulose microfibrils reinforcing a lignin/hemicellulose matrix. In principle, the plant cell wall composite is designed much like a synthetic fiber-reinforced polymer composite. Unlike synthetic composites, the plant cell wall has an excellent combination of high modulus, strength, toughness and low density that originates in the optimal interactions between the biopolymers. Therefore, to produce high performance composites, a unique route may be to mimic a biological system like the plant cell wall. The present work focuses on understanding the thermodynamics of biopolymer assembly to exploit the process in vitro. In our system, we use an already polymerized nanocellulose template and polymerize phenolic monomers on the template using a peroxidase enzyme. In the first part, we have polymerized phenol using horseradish peroxidase (HRP) in the presence of TEMPO-oxidized nanocellulose. Similar to native plant cell wall structures, the polyphenol-nanocellulose composite had intimate mixing of polyphenol and cellulose at the nanoscale with the presence of cellulose promoting a uniquely organized structure. The obtained composite material showed synergy that enhanced the thermal stability, hydrophobicity, and possibly mechanical properties. In the second part, monolignol coniferyl alcohol was polymerized in the presence of nanocellulose by the same procedure. A comparison between the polyphenol composite and poly(coniferyl alcohol) (PCA) composite revealed that the propanyl substitution imparted flexibility to the PCA molecules so that they could bend and form a hollow globule structure to envelope nanocellulose inside. Polyphenol could not do this because of its rigidity.
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Levy, Foster, and James T. Donaldson. "Morphology, Geographic Distribution, and Conservation of the Southern Appalachian Endemic." Digital Commons @ East Tennessee State University, 2018. https://dc.etsu.edu/etsu-works/5450.

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Taxonomic recognition of Solidago lancifolia (Torrey & A. Gray) Chapman and diagnostic characters used for identification have vacillated among floras and treatments. Fieldwork greatly expanded the specimen base in US herbaria, extended the known range in Tennessee, and identified new occurrences in North Carolina and Virginia. A morphometric analysis of herbarium specimens identified qualitative and quantitative characters unambiguously diagnostic for S. lancifolia. These included the presence of glands on the phyllaries; long, wide-diameter rhizomes; thick stems; and a long pappus on disk florets. Using these characters, an analysis of herbarium specimens corrected widespread misidentifications and showed that S. lancifolia is strictly endemic to a 12-county region encompassing the high elevations (> 1,400 m) in the mountains of southwestern Virginia, northwestern North Carolina, and northeastern Tennessee. Based on the narrow geographic range and small population sizes, prior uncertainty of the taxonomic validity and geographic range of S. lancifolia has been resolved. Consequently, for North Carolina and Virginia, the recommendation is for an upgrade in the conservation status to “Endangered” with a state rank of “S1.” Moreover, the narrow geographic range and small number of populations are consistent with a global rank of “G2” and consideration as a federal Species of Concern.
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Costa, Julia Yamagishi. "Citotaxonia e aspectos evolutivos de especies de Hoffmannsegella H.G.Jones (Orchidaceae)." [s.n.], 2006. http://repositorio.unicamp.br/jspui/handle/REPOSIP/314944.

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Orientador : Eliana Regina Forni-Martins
Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Biologia
Made available in DSpace on 2018-08-06T21:09:05Z (GMT). No. of bitstreams: 1 Costa_JuliaYamagishi_D.pdf: 4268702 bytes, checksum: 5ceb4f75d53e52eb1a73e6e26179508e (MD5) Previous issue date: 2006
Resumo: Dentro da família Orchidaceae, composta por cerca de 25.000 espécies, o gênero Hoffmannseggella (antiga seção Parviflorae do gênero Laelia Lindl.) é composto por espécies rupícolas, endêmicas da Cadeia do Espinhaço/MG. Estudos sugerem uma evolução rápida para o gênero, com a transição do hábito epifítico para o rupícola, mudança de polinizadores e eventos de hibridização e poliploidia como os principais mecanismos evolutivos envolvidos na origem das espécies de Hoffmannseggella. Estudos cromossômicos prévios haviam sugerido o número básico de x=20 para o gênero, com alta incidência de poliplóides. No presente trabalho, foram obtidas contagens cromossômicas para dez espécies: H. angereri n=20/2n=40, H. bradei n=20-21/2n=40, H. briegeri 2n=80, H. caulescens 2n=80, H. cinnabarina 2n=40, H. crispata n=20, H. fournieri n=20/2n=40, H. liliputana 2n=40/60, H. rupestris n=40/2n=80 e 2n=40 e H. viridiflora 2n=44. Foi observada aneussomatia em células de meristema radicular em H. briegeri (2n=80) e H. rupestris (2n=80), ocorrência de citótipos em H. rupestris (2n=40/80) e anormalidades meióticas em várias espécies, com presença de monovalentes, disjunção adiantada de bivalentes e possíveis tetravalentes nas espécies poliplóides. Por ocorrerem em sincronopatria, apresentarem alta similaridade morfológica e pelas características cromossômicas, é provável que H. viridiflora tenha se originado por aneuploidia a partir de H. bradei. Através dos procedimentos de bandamentos C, CMA/DA/DAPI e DAPI/AMD, foi possível observar grandes diferenças entre os cariótipos das espécies H. angereri, H. bradei, H. briegeri, H. caulescens, H. fournieri, H. liliputana e H. rupestris. Em geral, as espécies apresentaram grande número de bandas C (predominantemente centroméricas e subteloméricas), poucas bandas CMA/DA+ (subteloméricas), e grande variação no número de bandas DAPI/AMD+ (predominantemente teloméricas). Apenas H. bradei apresentou somente duas bandas heterocromáticas, uma CMA/DA+ DA/DAPI- e uma DAPI/AMD+ e H. briegeri apresentou polimorfismo para bandas CMA/DA/DAPI. Com relação aos sítios 45S de DNAr, os resultados foram uniformes, sendo que as espécies diplóides, com 2n=40, apresentaram dois sítios, enquanto as espécies poliplóides, com 2n=80, apresentaram 4 sítios
Abstract: Inside Orchidaceae, composed of almost 25,000 species, Hoffmannseggella H.G.Jones (previous genus Laelia Lindl., section Parviflorae) is characterized by rupiculous species, endemic to the Espinhaço Range/ MG. Previous studies suggested an explosive evolution of the genus, with transition from epiphytic to rupiculous habitat, changes on pollinator specificity and events of hibridization and polyploidy as the main evolutionary mechanisms that originated Hoffmannseggella species. Chromosome data from literature suggested the base number of x=20 for the genus, with high incidence of polyploids. The present work presents chromosome counts for ten species: H. Angereri n=20/2n=40, H. bradei n=20-21/2n=40, H. briegeri 2n=80, H. caulescens 2n=80, H. cinnabarina 2n=40, H. crispata n=20, H. fournieri n=20/2n=40, H. liliputana 2n=40/60, H. rupestris n=40/2n=80 and 2n=40 and H. viridiflora 2n=44. We observed aneussomaty on root meristematic cells of H. briegeri (2n=80) and H. rupestris (2n=80), two distinct cytotypes of H. rupestris (2n=40 and 2n=80) and meiotic abnormalities in several species, like monovalents, early disjunction of bivalents and putative tetravalents on polyploid species. Because they are found sinchronopatric, with high morphological and chromosomal similarity, we suggest that H. viridiflora (2n=44) is an aneuploid derived from H. bradei (2n=40). With C, CMA/DA/DAPI and DAPI/AMD banding techniques, we observed great differences among H. angereri, H. bradei, H. briegeri, H. caulescens, H. fournieri, H. liliputana e H. rupestris. With exception of H. bradei, that presented only two heterochromatic, one CMA/DA+ DA/DAPI- and one DAPI/AMD+ bands, all species presented a high number of C-bands (mainly centromeric and subtelomeric), few CMA/DA+ bands (subtelomeric), and great numeric differences of DAPI/AMD+ bands (mainly telomeric). We also observed, in H. briegeri, a polymorphism of CMA/DA/DAPI bands. The hybridization sites of 45S rDNA were uniform among species, with diploid species (2n=40) presenting two hybridization signals and polyploid species (2n=80) presenting four signals
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Doutor em Biologia Vegetal
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Sampson, Dennis Archie. "An assessment of the evolutionary stability of distyly in Hedyotis caerulea (Rubiaceae)." Cleveland State University / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=csu1296756691.

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Ahmad, Nariman Salih. "Genetic analysis of plant morphology in bambara groundnut (Vigna subterranea (L.) Verdc.)." Thesis, University of Nottingham, 2013. http://eprints.nottingham.ac.uk/13150/.

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Bambara groundnut (Vigna subterranea (L.) Verdc.) is an important underutilised legume crop, grown mainly by female subsistence farmers in Africa under traditional low input agricultural systems. Bambara groundnut is known as being of high nutritional value, as an atmospheric nitrogen fixer and to possess high levels of drought, pest and disease tolerance. Bambara groundnut is a predominantly self-pollinated crop and is grown as locally adapted landraces. These are expected to exist as non-identical inbred lines and are generally low yielding. Strategies involving genetic analysis of this species could provide important data for breeding programmes that could enhance food security in Africa. A set of 124 SSR primers designed from different library sources were tested to screen a ‘narrow’ genetic cross (F3) and a ‘wide’ genetic cross (F2) . The former is a cross between domesticated landraces (DipC and Tiga necaru) while the latter is a cross between a domesticated landrace and a wild ancestor (DipC and VSSP11). Residual heterozygosity in the F3 ‘narrow’ cross was confirmed to be around 25% based on 33 polymorphic SSR primers, consistent with an F3 population. A ‘narrow’ cross linkage map was constructed for the first time in bambara groundnut using 269 polymorphic markers (236 DArT and 33 SSR). The map consisted of 238 markers in 21 linkage groups of two or more linked markers, totalling 608.1cM and covering a predicted 54% of the bambara groundnut genome, although the high marker-marker linkage (at 89%) suggests a more comprehensive coverage. QTL analysis was carried out for 73 bulked lines of an F3 population and plants were evaluated for traits in a controlled glasshouse suite and a field trial in Indonesia. Data from single plant analysis of the F2 generation of this cross grown in a controlled environment glasshouse was also used. Most of the QTLs detected were clustered on linkage groups 1, 4 and 12. Major QTLs for internode length and biomass dry weight were detected on LG4 and LG1, respectively, for the FutureCrop glasshouse and field datasets. The highest LOD score of 9.7 was detected for peduncle length and was located within the confidence interval for a QTL for internode length locus. Marker locus bgPabg-596774 was detected to be associated with QTL for six traits; node no./plant, pod no/plant, pod weight, seed no./plant, seed yield and biomass dry weight, on LG1 within one LOD score of confidential interval, potentially suggesting pleiotropic effects of a more limited number (or even one) gene(s). One hundred and fifty-nine additional markers (136 DArT and 23 SSR) were used to improve the existing partial ‘wide’ map (141 AFLP, 1 SSR) constructed in an F2 population of 98 plants. A total of 194 markers were assigned to 20 linkage groups spanning a total of 901 cM. The linkage map derived from the ‘wide’ cross (DipC x VSSP11) had an expected genome coverage of 79.6%. An attempt to combine both maps through 32 common markers allowed a common QTL for days to emergence to be detected in both populations in close association with the common DArT markers 601384 and 601748. The main segregating traits were found to be plant spread, internode length, growth habit, peduncle length, pod weight, seed yield and biomass dry weight. Detecting the same QTL positions for a number of traits, suggested that common underlying genes might be responsible. The QTL-DNA marker associations developed in this study could be used practically for MAS in a future breeding program of this crop.
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Taylor, J. B. "Aspects of the dynamic morphology and branching patterns of rhizomatous plants with special reference to Iris pseudacorus L. and Polygonatum x hybridum Bruegger." Thesis, Bangor University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233696.

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Sherman, JoAnn Davis 1955. "Chromosome morphology, number and behavior of some Arizona Plantago species." Thesis, The University of Arizona, 1987. http://hdl.handle.net/10150/276649.

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Mitosis and meiosis of five Plantago species were analyzed. Plantago argyrea, P. patagonica and P. wrightiana contain 2n = 20 chromosomes and P. rhodosperma and P. virginica 2n = 24 chromosomes. Similar modes of evolution of the karyotypes of the 2n = 20 species are suggested. All species are presumed to be tetraploid, arising from 2n = 10 and 2n = 12 ancestors. Structural changes in the karyotype of 2n = 12 species could produce one or more large chromosomes resulting in a decrease in chromosomes from 6 to 5. Consequently, chromosome lengths in 2n = 10 and derived 2n = 20 species could be increased by addition of repetitive DNA along the length of each chromosome to maintain chromosome field. Chromosomes of 2n = 24 species are more symmetrical and presumably more primitive than the 2n = 20 species. Chiasma frequencies in meiotic cells of all five species are similar. This suggests that the majority of changes DNA content are in repetitive DNA.
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Books on the topic "Plant cytotaxonomy ; Plant morphology"

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Gyulai, Gábor. Plant archaeogenetics. Hauppauge, N.Y: Nova Science Publishers, 2011.

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Lövkvist, Börje. Chromosome numbers in south Swedish vascular plants. Copenhagen: Council for Nordic Publications in Botany, 1999.

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A cytotaxonomical atlas of the Balkan flora. Berlin: J. Cramer, 1987.

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Alan, Bryan, ed. Plant form: An illustrated guide to flowering plant morphology. Oxford: Oxford University Press, 1990.

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Alan, Bryan, ed. Plant form: An illustrated guide to flowering plant morphology. Portland, Or: Timber Press, 2008.

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Alan, Bryan, ed. Plant form: An illustrated guide to flowering plant morphology. Oxford: Oxford University Press, 1993.

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Eames, Arthur J. An introduction to plant anatomy. India: Tata McGraw, 1990.

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V, Kruklis M., and Mili͡u︡tin L. I, eds. Khromosomnye chisla golosemennykh rasteniĭ. Novosibirsk: "Nauka," Sibirskoe otd-nie, 1988.

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Baranec, Tibor. Biosystematické štúdium rodu Crataegus L. na Slovensku. Bratislava: VEDA, 1986.

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Kaussmann, Bernhard. Funktionelle Morphologie und Anatomie der Pflanzen. Stuttgart: G. Fischer, 1989.

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Book chapters on the topic "Plant cytotaxonomy ; Plant morphology"

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Shaffer, Gary P., and Demetra Kandalepas. "Wetland Plant Morphology." In The Wetland Book, 1–7. Dordrecht: Springer Netherlands, 2016. http://dx.doi.org/10.1007/978-94-007-6172-8_73-1.

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Shaffer, Gary P., and Demetra Kandalepas. "Wetland Plant Morphology." In The Wetland Book, 375–82. Dordrecht: Springer Netherlands, 2018. http://dx.doi.org/10.1007/978-90-481-9659-3_73.

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Decraemer, W. "General Morphology." In Developments in Plant Pathology, 4–25. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-015-8482-1_2.

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Eisenback, Jon D. "Morphology and Systematics." In Plant and Nematode Interactions, 37–63. Madison, WI, USA: American Society of Agronomy, Crop Science Society of America, Soil Science Society of America, 2015. http://dx.doi.org/10.2134/agronmonogr36.c3.

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Lupini, Antonio, Fabrizio Araniti, Antonio Mauceri, Maria Princi, Antonino Di Iorio, Agostino Sorgonà, and Maria Rosa Abenavoli. "Root Morphology." In Advances in Plant Ecophysiology Techniques, 15–28. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-93233-0_2.

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Naumann, A., U. Kunz, H. Lehmann, R. Stelzer, and W. J. Horst. "Effect of aluminium on root morphology of Hydrangea macrophylla." In Plant Nutrition, 516–17. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/0-306-47624-x_250.

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Neuhaus, Gunther. "Morphology and Anatomy of Vascular Plants." In Strasburger's Plant Sciences, 161–235. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-15518-5_4.

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Quader, Hartmut, and Michael Zachariadis. "The Morphology and Dynamics of the ER." In Plant Cell Monographs, 1–23. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/7089_063.

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Welander, Margareta, and Li-Hua Zhu. "RolGenes: Molecular Biology, Physiology, Morphology, Breeding Uses." In Plant Breeding Reviews, 79–103. Oxford, UK: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470650325.ch3.

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Sybenga, Jacob. "Chromosome Composition, Structure and Morphology." In Cytogenetics in Plant Breeding, 7–22. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-84083-8_2.

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Conference papers on the topic "Plant cytotaxonomy ; Plant morphology"

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Wahby, Mostafa, Julian Petzold, and Heiko Hamann. "A Concept of Full Plant Morphology Modeling for Robot-Plant Bio-Hybrids." In The 2021 Conference on Artificial Life. Cambridge, MA: MIT Press, 2021. http://dx.doi.org/10.1162/isal_a_00445.

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Earley, Ashley. "Genetic control of stomatal morphology and vein architecture in a diversity panel of cultivated sunflower." In ASPB PLANT BIOLOGY 2020. USA: ASPB, 2020. http://dx.doi.org/10.46678/pb.20.1052950.

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Radin, Ivan. "Moss (Physcomitrella patens) Piezo mechasensitive ion channel homologs positively regulate cell growth and vacuolar morphology." In ASPB PLANT BIOLOGY 2020. USA: ASPB, 2020. http://dx.doi.org/10.46678/pb.20.1372312.

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He, Zhiyong, and Xiaopeng Dai. "Research on the 3D construction of plant morphology." In 5th International Conference on Advanced Design and Manufacturing Engineering. Paris, France: Atlantis Press, 2015. http://dx.doi.org/10.2991/icadme-15.2015.253.

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"Pollen Grain Morphology of Citrus (Rutaceae) in Iraq." In International Conference on Plant, Marine and Environmental Sciences. International Institute of Chemical, Biological & Environmental Engineering, 2015. http://dx.doi.org/10.15242/iicbe.c0115048.

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"Identification of DNA markers associated with starch granules morphology of Solanum tuberosum L." In Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, 2019. http://dx.doi.org/10.18699/plantgen2019-054.

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Tong, Tingting, and Lili Shao. "Analysis of Garden Plant Morphology on Human's Physiology and Psychology." In 2017 4th International Conference on Education, Management and Computing Technology (ICEMCT 2017). Paris, France: Atlantis Press, 2017. http://dx.doi.org/10.2991/icemct-17.2017.159.

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Robaiah, M., M. Rusop, S. Abdullah, Z. Khusaimi, H. Azhan, M. O. Laila, M. J. Salifairus, and N. A. Asli. "Morphology and topography study of graphene synthesized from plant oil." In 8TH INTERNATIONAL CONFERENCE ON NANOSCIENCE AND NANOTECHNOLOGY 2017 (NANO-SciTech 2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5036891.

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Hoehn, Alexander, Marvin W. Luttges, and Louis S. Stodieck. "SEED GERMINATION AND EARLY PLANT MORPHOLOGY - RESULTS FROM THREE MICROGRAVITY MISSIONS." In International Conference On Environmental Systems. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1994. http://dx.doi.org/10.4271/941546.

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BARI, A., A. MARTIN, D. BARRANCO, J. L. GONZALEZ-ANDUJAR, G. AYAD, and S. PADULOSI. "USE OF FRACTALS TO CAPTURE AND ANALYSE BIODIVERSITY IN PLANT MORPHOLOGY." In Conference on Fractals 2002. WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812777720_0046.

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