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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Analyse de la croissance et morphogenèse de l'igname Dioscorea complexe D. cayenensis-D. rotundata

Trouslot, Marie Francine. January 1985 (has links)
Thesis (doctoral)--Université de Clermont-Ferrand II, 1983. / Errata slip inserted. Includes bibliographical references (p. 241-263).
2

Analyse de la croissance et morphogenèse de l'igname Dioscorea complexe D. cayenensis-D. rotundata

Trouslot, Marie Francine. January 1985 (has links)
Thesis (doctoral)--Université de Clermont-Ferrand II, 1983. / Errata slip inserted. Includes bibliographical references (p. 241-263).
3

Micropropagation "in vitro" et effets des polyamines sur la microtubérisation de l'igname du complexe "Dioscorea cayenensis - D. rotundata"

Ondo Ovono, Paul 22 October 2009 (has links)
Les Dioscorea cultivées, dont la reproduction sexuée est aléatoire, sont multipliées essentiellement par voie végétative, ce qui entraîne la dissémination dagents pathogènes dans les plantations, provoquant une baisse de rendement et de qualité des récoltes. Dans ces conditions, les besoins en semences sont rarement comblés et les possibilités dextension de la culture restent limitées. En effet, devant une demande quantitative toujours croissante et qualitative de plus en plus restrictive, les techniques classiques encore employées aussi bien pour la multiplication que pour lamélioration de la production des végétaux sont relativement lentes. En revanche, les opportunités offertes par les cultures de tissus peuvent remédier efficacement aux insuffisances et offrir des améliorations irréalisables par les autres méthodes. La multiplication en alternance par bourgeonnement axillaire à partir de nuds pendant 28 semaines et par mise en germination des microtubercules découpés pendant 16 semaines peut remédier à cette situation. Plusieurs facteurs peuvent avoir un impact sur lefficacité de cette approche: la présence ou labsence de régulateurs de croissance, la teneur en saccharose ou en éléments minéraux du milieu de culture. Dans le cadre de cette étude, les tests réalisés ont montré une formation plus précoce du tubercule en présence de polyamines et dacide jasmonique. Si les teneurs en polyamines endogènes et leur métabolisme sont significativement affectés par les polyamines exogènes, les modifications des teneurs en polyamines endogènes, quant à elles, ne peuvent être directement corrélées avec la formation du tubercule. Un retard dans la formation des tubercules lors dune réduction de la teneur en sucre du milieu de culture a aussi été constaté. Ce retard dans nest pas lié à une réduction de losmolarité du milieu de culture, comme nous avons pu le montrer en remplaçant partiellement le saccharose par du sorbitol. La putrescine et ses précurseurs larginine et lornithine favorisent aussi le développement des tubercules, ceux- ci sont plus longs et plus lourds lorsque ces composés sont ajoutés au milieu de culture à faible concentration. Une augmentation de la teneur endogène en putrescine et en auxine a été observée dans ces conditions. Laddition dacide jasmonique a un effet similaire. Une réduction du développement des tubercules est, par contre, observée en présence dune teneur en saccharose réduite. La réduction de la teneur en sucre dans le milieu de tubérisation a aussi un effet négatif sur la germination ultérieure des microtubercules. Pour pouvoir utiliser les microtubercules comme semences, il faut être assuré dun taux de germination élevé et dun stockage possible. Les microtubercules récoltés après 9 mois de culture et transférés sur un nouveau milieu sans régulateur de croissance germent très rapidement. Aucune dormance nest observée. Les microtubercules peuvent aussi être stockés pendant au moins 18 semaines. Les meilleures conditions pour une germination élevée sont une conservation à lobscurité, sous ± 50% dhumidité relative et à 25°C. Une période de dormance secondaire sinstalle une fois le stockage en cours qui varie entre 20 et 28 semaines respectivement pour les microtubercules les plus rapides et les plus lents. Seuls les tubercules de taille supérieure à 350 mm devront être utilisés pour la germination in vitro ou ex vitro.
4

Botanický průzkum nivy regulovaného úseku potoka Hučiny (Černý Kříž, Šumava) / Botanical survey of the disturbed part of the Hučina stream (Černý Kříž, Šumava Mts.)

LAZÁRKOVÁ, Kateřina January 2012 (has links)
The thesis is part of the project ?Bohemian Revitalization of wetlands and peatlands?. The aim is to capture the current state of vegetation and flora, with an emphasis on the existence of rare or endangered species in Hučina plains in the southeastern part of the Bohemian Forest. A generic list of sites added phytosociological images taken during the field survey. The area was defined by the 26 permanent plots. The grasslands of the plains area had dimensions 4 × 4 m, in the original channel and channel Hučina main drainage trench 8 × 2 m and forested floodplain of the 10 × 10 m in these areas. I made a complete inventory of all species found and I identified the vegetation cover. Species were recorded after the floors ? floor starting tree. Overall, it was found 106 plant species and 7 species of lichens. Most plant species occurring in individual areas belonged to bryophytes.
5

Vodní režim blatkových borů na Třeboňsku a vodní provoz jejich dominant / Vodní režim blatkových borů na Třeboňsku a vodní provoz jejich dominant

Kučerová, Andrea January 2011 (has links)
The thesis was intended to fill the information gap in the ecohydrology of the Pinus rotundata dominated peatbogs in the Třeboň Basin Biosphere Reserve, Czech Republic by studying various aspects of their water régime (i.e., transpiration of the dominant tree species, soil water chemistry, retention ability). The study is based on regular monitoring of the water table, water discharge, soil water chemistry and precipitation (during 1995-2000, study sites Červené blato and Žofinka peatbogs). Additionally, the transpiration of adult Pinus rotundata trees was measured in the field during 1999-2000 at the experimental plot in the Červené blato peatbog (330 ha, 465-475 m a.s.l.). Nowadays, the Pinus rotundata-dominated peatbogs represent almost natural (peaty) forests inside of otherwise human-made forest plantations. Long-term vegetation changes after natural disturbances such as windstorms, insect infestation and fire are only occasionally reported for the central European natural forests. Therefore the evaluation of vegetation changes after disturbances, typical of boreal forests, and their impact on peatbog hydrology has also been included in this thesis (study site Žofinka peatbog, 130 ha, 470-475 m a.s.l.). Transpiration of the central European endemic tree species, Pinus rotundata Link, was...
6

Understanding the multiple resource needs of leaf-cutter bees to inform pollinator conservation and the restoration of reclaimed mines

Ballas, John Peter, II 24 September 2020 (has links)
No description available.
7

Pollination biology of <i>Echinacea angustifolia</i> and <i>E. purpurea</i> (<i>Asteraceae</i>) in Saskatchewan

Wist, Tyler Jonathan 28 October 2005
The goals of this research project were to identify the various insects observed to visit inflorescences of Echinacea angustifolia DC, and to rank these visitors according to their importance as pollinators of E. angustifolia in Saskatchewan. Studying nectar and the nectary is essential to understanding the interaction of disc florets with pollinators. Nectar-sugar production by disc florets of E. angustifolia and E. purpurea (L. Moench) was quantified from anthesis to cessation with production per disc floret peaking in the afternoon of the staminate phase (191.7 µg) and at midday of the first day of the pistillate phase (156.6 µg), respectively. Morphology of the disc-like floral nectaries of both Echinacea species was studied, as well as the ultrastructure of the nectary of E. purpurea. Modified stomata on the nectary rim are the most likely exits for nectar, but creases in the epidermis may also participate. The nectary of E. purpurea is vascularized by phloem alone, which occurred adjacent to the epidermis. Companion cells possessed wall ingrowths, and these cells may unload arriving sugar destined for either an apoplastic or symplastic pathway. Lobed nuclei were a key feature of secretory parenchyma cells, as was a predominance of mitochondria, suggesting that energy-requiring eccrine secretion predominates in E. purpurea. E. angustifolia exhibited a generalist pollination system, with pollinating insects belonging to the orders Coleoptera, Diptera, Hymenoptera, and Lepidoptera. The pollination efficiency of visitors was determined by single insect visits to bagged, virgin inflorescences followed by quantifying pollen tubes at the bases of receptive styles and/or calculating the percentage of shrivelled styles. It was determined that bumble bees (Bombus spp.) were efficient pollinators, indicating that they would likely contribute much to the pollination of E. angustifolia. Grasshopper bee flies (Systoechus vulgaris Loew) were plentiful but individually were not efficient pollinators, but taken together, they provided much pollination. Golden blister beetles (Epicauta ferruginea Say) were efficient pollinators but where yellow-petalled flowers occurred, their numbers on E. angustifolia decreased. Honey bees (Apis mellifera L.) were efficient pollinators and were present in low numbers without managed introduction. Pierid (2003) butterflies were regular visitors and efficient pollinators, and likely contributed significantly to E. angustifolia pollination. When introduced, the alfalfa leafcutter bee (Megachile rotundata Fabr.) preferred not to forage on E. angustifolia and as such, these solitary bees were not suitable as managed pollinators. In large agricultural plantings of E. angustifolia, however, native insects may not be capable of providing sufficient pollination for seed production when floral competition occurs.
8

Pollination biology of <i>Echinacea angustifolia</i> and <i>E. purpurea</i> (<i>Asteraceae</i>) in Saskatchewan

Wist, Tyler Jonathan 28 October 2005 (has links)
The goals of this research project were to identify the various insects observed to visit inflorescences of Echinacea angustifolia DC, and to rank these visitors according to their importance as pollinators of E. angustifolia in Saskatchewan. Studying nectar and the nectary is essential to understanding the interaction of disc florets with pollinators. Nectar-sugar production by disc florets of E. angustifolia and E. purpurea (L. Moench) was quantified from anthesis to cessation with production per disc floret peaking in the afternoon of the staminate phase (191.7 µg) and at midday of the first day of the pistillate phase (156.6 µg), respectively. Morphology of the disc-like floral nectaries of both Echinacea species was studied, as well as the ultrastructure of the nectary of E. purpurea. Modified stomata on the nectary rim are the most likely exits for nectar, but creases in the epidermis may also participate. The nectary of E. purpurea is vascularized by phloem alone, which occurred adjacent to the epidermis. Companion cells possessed wall ingrowths, and these cells may unload arriving sugar destined for either an apoplastic or symplastic pathway. Lobed nuclei were a key feature of secretory parenchyma cells, as was a predominance of mitochondria, suggesting that energy-requiring eccrine secretion predominates in E. purpurea. E. angustifolia exhibited a generalist pollination system, with pollinating insects belonging to the orders Coleoptera, Diptera, Hymenoptera, and Lepidoptera. The pollination efficiency of visitors was determined by single insect visits to bagged, virgin inflorescences followed by quantifying pollen tubes at the bases of receptive styles and/or calculating the percentage of shrivelled styles. It was determined that bumble bees (Bombus spp.) were efficient pollinators, indicating that they would likely contribute much to the pollination of E. angustifolia. Grasshopper bee flies (Systoechus vulgaris Loew) were plentiful but individually were not efficient pollinators, but taken together, they provided much pollination. Golden blister beetles (Epicauta ferruginea Say) were efficient pollinators but where yellow-petalled flowers occurred, their numbers on E. angustifolia decreased. Honey bees (Apis mellifera L.) were efficient pollinators and were present in low numbers without managed introduction. Pierid (2003) butterflies were regular visitors and efficient pollinators, and likely contributed significantly to E. angustifolia pollination. When introduced, the alfalfa leafcutter bee (Megachile rotundata Fabr.) preferred not to forage on E. angustifolia and as such, these solitary bees were not suitable as managed pollinators. In large agricultural plantings of E. angustifolia, however, native insects may not be capable of providing sufficient pollination for seed production when floral competition occurs.

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