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Chemical ecology of rhizophagus grandis (Coleoptera: Monotomidae) and its application to the biological control of dendroctonus micans (Coleoptera: Scolytinae) / Etudes des médiateurs chimiques chez rhizophagus grandis (Coleoptera: Monotomidae) et application à la lutte biologique contre dendroctonus micans (Coleoptera: Scolytinae)Meurisse, Nicolas 15 February 2008 (has links)
The Eurasian spruce bark beetle Dendroctonus micans is a major pest of spruce which is expanding its range in France, Turkey, England and Wales. Its monospecific predator Rhizophagus grandis has followed naturally the bark beetle into most areas and, since the 1960s, has also been mass-produced and successfully released within newly infested locations. <p>In this scope, the development of an effective trapping method would be very useful to assess the bark-beetle presence at previously uninfested sites, or predator establishment after release or natural spread. We demonstrated the efficiency of oxygenated monoterpenes-baited kairomone traps to monitor R. grandis in various epidemiological conditions, including areas localized behind or at the limit of the pest’s distribution, or in areas where artificial releases were performed. Because the predator is strictly species-specific, another exciting possibility offered by the kairomone trapping is the indirect monitoring of the pest itself in areas of unknown status (e.g. areas under colonization, or considered as at risk at medium- term).<p>R. grandis is also considered as one of the most valuable natural enemies to strike aggressive North-American Dendroctonus species. In this respect, R. grandis has been recently applied in a neo-classical biological program against the red turpentine beetle D. valens, which invaded China from North America in the late 1990’s. In laboratory tests conducted on pine logs in the laboratory, or on living pine trees in the field, we demonstrated that R. grandis adults can successfully enter and reproduce into D. valens galleries. <p>In Europe, R. grandis is the only species regularly found in the brood systems of D. micans, where adults and larvae attack the gregarious larvae of their prey. In such enclosed systems, R. grandis’ functional response is therefore influenced by various interrelated components, such as the prey density, the predator density, or the prey distribution. Measuring the predator’s success in terms of larval survival and growth rates, we demonstrated the time spent by R. grandis larvae to wound and kill their prey to be the main factor limiting their development. This factor may be considerably influenced by the proportions of diseased, wounded or molting prey rise in the brood system, for instance as a result of an increase in prey density, or due to the presence of conspecific adults (which wound their prey but do not consume them entirely). Furthermore, our tests suggest that no cannibalism or noticeable intraspecific competition occurred between R. grandis larvae, whereas some lighter mode of competition probably took place. <p>R. grandis also exhibits a reproductive numerical response to prey density, which mainly relies on the perception of chemical stimuli and inhibitors released in the bark beetle brood system. In the current study, we developed a non-destructive approach to follow the dynamics of volatile compound production, using sequential sample collection on SPME fibers. Our tests demonstrated that the larval activity of D. micans or D. valens strongly influences the release of some oxygenated monoterpenes. However, our attempts to correlate the relative quantities of some identified chemicals to offspring production were less successful as it concerns the identification of potential oviposition stimuli and inhibitors. <p>The problematic rose by the progression of D. micans, as well as detailed results of each of the described above studies are discussed in the two published papers and the three manuscripts forming this thesis. Bringing all these studies together, several perspectives are also presented in the general discussion. <p>/<p>Ravageur des épicéas, Dendroctonus micans est toujours en voie d’extension en France, en Turquie, en Angleterre et au Pays de Galles. Dans la plupart de ces zones, le dendroctone est accompagné de manière naturelle par son prédateur monospécifique, Rhizophagus grandis. Depuis les années 1960, le prédateur a également fait l’objet d’une production de masse et de programmes de lâchers dans les zones d’arrivée récente du scolyte.<p>Dans le cadre de la lutte biologique contre D. micans, les gestionnaires forestiers doivent donc estimer au plus tôt la présence du ravageur dans des zones jusque là indemnes, mais également vérifier l’établissement du prédateur par progression naturelle ou résultant d’introductions délibérées. Dans la présente étude, nous avons démontré l’efficacité de pièges d’interception appatés à l’aide de monoterpènes oxygénés pour la capture de R. grandis. Celle-ci s’est faite dans différentes conditions épidémiologiques, incluant notamment des zones situées en arrière du front de progression du scolyte et des zones où des lâchers artificiels ont été réalisés. Comme R. grandis est strictement inféodé au dendroctone, un autre avantage de la technique est la possibilité de réaliser un dépistage indirect du ravageur dans les zones où son statut est incertain (zones en cours de colonisation, ou considérées comme à risque à moyen terme).<p>Par ailleurs, R. grandis est également considéré comme un des meilleurs ennemis naturels potentiels pour lutter contre d’autres espèces de Dendroctonus aggressifs. Dans cette optique, R. grandis a été récemment utilisé dans un programme de lute biologique contre D. valens, ravageur invasif arrivé en Chine dans la fin des années 1990 en provenance d’Amérique du Nord. Nous avons démontré la capacité de R. grandis à s’introduire et à se reproduire dans les galeries de D. valens lors de tests de laboratoire, mais aussi sur des arbres vivants en pinèdes. <p>En Europe, R. grandis est strictement inféodé aux galeries de D. micans, où larves et adultes du prédateur s’attaquent aux larves grégaires du scolyte. Dans ce système clos, la réponse fonctionelle de R. grandis est influencée par plusieurs facteurs étroitement corrélés, la densité de proies, la densité de prédateurs, et la distribution des proies. En mesurant l’efficacité de prédation de R. grandis en termes de survie des larves et de taux de croissance, nous avons démontré l’influence sur leur développement du temps passé par les larves à blesser et à tuer leurs proies. Ce facteur est par ailleurs fortement dépendant de la proportion de larves malades, blessées ou en cours de mue au sein du système ;une proportion qui peut augmenter en réponse à une augmentation de la densité de proies, ou lorsque des adultes sont présents (ceux-ci blessent les proies mais ne les consomment pas entièrement). Enfin, nos tests suggèrent qu’il n’existe que peu de cannibalisme ou de compétition intraspécifique entre larves de R. grandis, tandis que des modes de compétition moins importants prennent vraisemblablement place.<p>R. grandis présente également une réponse numérique reproductive à la densité de proies disponibles, principalement basée sur la perception de stimuli et d’inhibiteurs présents dans les galeries du scolyte. Par la collecte de composés volatils présents dans ces systèmes à l’aide de fibres SPME, nous avons développé une méthode non-destructive pour suivre la dynamique de production des médiateurs chimiques. Nos tests ont démontré que l’activité des larves de D. micans ou D. valens influence fortement la dynamique de production de certains monoterpènes oxygénés. En revanche, il n’a pas été été possible de corréler les différents composés identifiés au nombre de larves de R. grandis présentes dans le système. <p>La problématique soulevée par la progression de D. micans, de même que les résultats détaillés de chacune des études décrites ci-dessus sont discutés dans les deux papiers publiés et les trois manuscrits formant cette thèse. Les différentes perspectives apportées par ce travail sont également présentées dans la discussion générale.<p> / Doctorat en Sciences agronomiques et ingénierie biologique / info:eu-repo/semantics/nonPublished
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Thousand Cankers Disease of Eastern Black Walnut: Ecological Interactions in the Holobiont of a Bark Beetle-Fungal DiseaseGeoffrey M Williams (11186766) 27 July 2021 (has links)
<p>Eastern black walnut (<i>Juglans
nigra</i> L.) ranks among the most highly valued timber species in the central
hardwood forest and across the world. This valuable tree fills a critical role
in native ecosystems as a mast bearing pioneer on mesic sites. Along with other
<i>Juglans</i> spp. (Juglandaceae), <i>J. nigra</i> is threatened by thousand
cankers disease (TCD), an insect-vectored disease first described in 2009. TCD
is caused by the bark beetle <i>Pityophthorus
juglandis</i> Blackman (Corthylini) and the phytopathogenic fungus <i>Geosmithia morbida</i> Kol. Free. Ut. &
Tiss. (Bionectriaceae). Together, the <i>P.
juglandis</i>-<i>G. morbida</i> complex has
expanded from its historical range in southwest North America throughout the
western United States (U.S.) and Europe. This range expansion has led to
widespread mortality among naïve hosts <i>J.
nigra</i> and <i>J. regia</i> planted
outside their native distributions.</p>
<p> The severity
of TCD was previously observed to be highest in urban and plantation
environments and outside of the host native range. Therefore, the objective of
this work was to provide information on biotic and abiotic environmental
factors that influence the severity and impact of TCD across the native and
non-native range of <i>J. nigra</i> and
across different climatic and management regimes. This knowledge would enable a
better assessment of the risk posed by TCD and a basis for developing
management activities that impart resilience to natural systems. Through a
series of greenhouse-, laboratory- and field-based experiments, environmental
factors that affect the pathogenicity and/or survival of <i>G. morbida</i> in <i>J. nigra</i>
were identified, with a focus on the microbiome, climate, and opportunistic
pathogens. A number of potentially important interactions among host, vector,
pathogen and the rest of the holobiont of TCD were characterized. The <i>holobiont</i> is defined as the whole
multitrophic community of organisms—including <i>J. nigra</i>, microinvertebrates, fungi and bacteria—that interact with
one another and with the host.</p>
<p>Our findings indicate that
interactions among host, vector, pathogen, secondary pathogens, novel microbial
communities, and novel abiotic environments modulate the severity of TCD in
native, non-native, and managed and unmanaged contexts. Prevailing climatic
conditions favor reproduction and spread of <i>G.
morbida</i> in the western United States due to the effect of wood moisture
content on fungal competition. The microbiome of soils, roots, and stems of
trees and seedlings grown outside the host native range harbor distinct,
lower-diversity communities of bacteria and fungi compared to the native range,
including different communities of beneficial or pathogenic functional groups
of fungi. The pathogen <i>G. morbida</i> was
also associated with a distinct community of microbes in stems compared to <i>G. morbida</i>-negative trees. The soil
microbiome from intensively-managed plantations facilitated positive feedback
between <i>G. morbida</i> and a
disease-promomting endophytic <i>Fusarium
solani</i> species complex sp. in roots of <i>J.
nigra</i> seedlings. Finally, the nematode species <i>Bursaphelenchus juglandis</i> associated with <i>P. juglandis</i> synergizes with <i>G.
morbida</i> to cause foliar symptoms in seedlings in a shadehouse; conversely,
experiments and observations indicated that the nematode species <i>Panagrolaimus</i> sp. and cf. <i>Ektaphelenchus</i> sp. could suppress WTB
populations and/or TCD outbreaks.</p>
<p>In conclusion, the composition,
function, and interactions within the <i>P.
juglandis</i> and <i>J. nigra</i> holobiont play
important roles in the TCD pathosystem. Managers and conservationists should be
aware that novel associations outside the host native range, or in monocultures,
intensive nursery production, and urban and low-humidity environments may favor
progression of the disease through the effects of associated phytobiomes,
nematodes, and climatic conditions on disease etiology. Trees in higher
diversity, less intensively managed growing environments within their native
range may be more resilient to disease. Moreover, expatriated, susceptible host
species (<i>i.e.</i>, <i>J. nigra</i>) growing in environments that are favorable to novel pests
or pest complexes (<i>i.e.</i>, the western
U.S.) may provide connectivity between emergent forest health threats (<i>i.e.</i>, TCD) and native host populations (<i>i.e.</i>, <i>J. nigra</i> in its native range).</p>
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