Dissertations / Theses on the topic 'Herbivores Multitrophic interactions (Ecology)'
Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles
Consult the top 33 dissertations / theses for your research on the topic 'Herbivores Multitrophic interactions (Ecology).'
Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.
You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.
Browse dissertations / theses on a wide variety of disciplines and organise your bibliography correctly.
Reidinger, Stefan. "Multitrophic interactions between insect herbivores and soil microbial communities." Thesis, Royal Holloway, University of London, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.487317.
Full textVicari, Mark. "Interactions between grasses, their fungal invaders, and herbivores." Thesis, Lancaster University, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.264680.
Full textBennett, Alison. "Mechanisms underlying complex interactions between plants, herbivores, and arbuscular mycorrhizal fungi." [Bloomington, Ind.] : Indiana University, 2006. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&res_dat=xri:pqdiss&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:3204279.
Full textSource: Dissertation Abstracts International, Volume: 67-01, Section: B, page: 0048. Adviser: James D. Bever. "Title from dissertation home page (viewed Feb. 9, 2007)."
Barber, Nicholas A. "Tritrophic interactions in forests direct and indirect interactions between birds, insect herbivores, and oaks /." Diss., St. Louis, Mo. : University of Missouri--St. Louis, 2009. http://etd.umsl.edu/r3561.
Full textLiess, Antonia. "Nutrient Stoichiometry in Benthic Food Webs – Interactions Between Algae, Herbivores and Fish." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Universitetsbiblioteket [distributör], 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-6933.
Full textParker, John. "Plant-herbivore interactions consequences for the structure of freshwater communities and exotic plant invasions /." Available online, Georgia Institute of Technology, 2005, 2005. http://etd.gatech.edu/theses/available/etd-11182005-131013/.
Full textMark E. Hay, Committee Chair ; Julia Kubanek, Committee Member ; Joseph Montoya, Committee Member ; J. Todd Streelman, Committee Member ; David M. Lodge, Committee Member. Includes bibliographical references.
Sieg, Robert Drew. "Chemically-mediated interactions in salt marshes: mechanisms that plant communities use to deter closely associated herbivores and pathogens." Diss., Georgia Institute of Technology, 2013. http://hdl.handle.net/1853/47590.
Full textParker, John D. "Plant-herbivore interactions : consequences for the structure of freshwater communities and exotic plant invasions." Diss., Georgia Institute of Technology, 2005. http://hdl.handle.net/1853/9460.
Full textShewhart, Lauren Elizabeth. "How specialist and generalist herbivores are responding to invasive plant threats." Wright State University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=wright1462797971.
Full textHumphrey, Parris Taylor. "The Ecology Of Co-Infection In The Phyllosphere: Unraveling The Interactions Between Microbes, Insect Herbivores, And The Host Plants They Share." Diss., The University of Arizona, 2015. http://hdl.handle.net/10150/565900.
Full textGillett, David James. "Effects of habitat quality on secondary production in shallow estuarine waters and the consequences for the benthic-pelagic food web." W&M ScholarWorks, 2010. http://www.vims.edu/library/Theses/Gillett10.pdf.
Full textBarthelemy, Hélène. "Herbivores influence nutrient cycling and plant nutrient uptake : insights from tundra ecosystems." Doctoral thesis, Umeå universitet, Institutionen för ekologi, miljö och geovetenskap, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-120191.
Full textKenworthy, Nigel. "The influence of bottom-up effects on trophic cascades : a case study of Orchestia (Amphipoda) affecting redshank (Tringa totanus) predation risk in a saltmarsh ecosystem." Thesis, University of St Andrews, 2018. http://hdl.handle.net/10023/12775.
Full textKay, M. K. (Nod). "An experimental evaluation of resource allocation in island plants with respect to their invertebrate herbivores." Lincoln University, 2008. http://hdl.handle.net/10182/1442.
Full textIitembu, Johannes Angala. "Trophic relationships of hake (Merluccius capensis Castelnau, 1851 and M. paradoxus Franca 1960) from the Northern Benguela current ecosystem (Namibia) : inferences from stable isotopes and fatty acids." Thesis, Rhodes University, 2014. http://hdl.handle.net/10962/d1020296.
Full textHazelwood, Kirsten. "The role of trophic interactions in shaping tropical tree communities." Thesis, University of Stirling, 2018. http://hdl.handle.net/1893/28637.
Full textLøe, Geir. "Ecology and Evolution of Resistance to Herbivory : Trichome Production in Arabidopsis lyrata." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-6359.
Full textVidal, Mayra Cadorin 1989. "A predação de formigas por Rhinoleucophenga sp. nov. (Diptera, Drosophilidae) e seus efeitos no mutualismo entre formigas e Qualea grandiflora (Vochysiaceae)." [s.n.], 2013. http://repositorio.unicamp.br/jspui/handle/REPOSIP/316186.
Full textDissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia
Made available in DSpace on 2018-08-23T06:11:49Z (GMT). No. of bitstreams: 1 Vidal_MayraCadorin_M.pdf: 1986442 bytes, checksum: da9ed52c0a73527b0590731f5ee8d10b (MD5) Previous issue date: 2013
Resumo: Exploradores do mutualismo - indivíduos que utilizam recursos/serviços produzidos pelos mutualistas sem recompensá-lo - podem trazer sérios danos aos mutualistas explorados, principalmente quando acaba matando um dos parceiros mutualistas. Plantas portadoras de NEFs podem manter mutualismos com formigas visitantes, que defendem a planta contra insetos herbívoros. No cerrado de Itirapina (SP), encontramos larvas de uma nova espécie de díptero do gênero Rhinoleucophenga (Drosophilidae) que constroem abrigos de consistência pegajosa em cima dos NEFs de Q. grandiflora. Assim, larvas de Rhinoleucophenga podem interferir no mutualismo formiga-planta, agindo potencialmente como exploradora dessa interação. O presente estudo teve como objetivos principais investigar a história natural dessas larvas, principalmente aspectos do comportamento e interação com Qualea e formigas, e analisar seu possível efeito sobre o mutualismo formiga-Q.grandiflora. Durante observações de campo comprovamos que formigas e outros insetos visitantes dos NEFs podem ficar presos ao abrigo larval e servir de alimento para o díptero. Larvas de Rhinoleucophenga sp. nov. ocorrem em 85% dos indivíduos de Q. grandiflora, principalmente na época chuvosa ocupando preferencialmente nectários ativos, perto do ápice e na face abaxial dos ramos. No levantamento da mirmecofauna visitante de Q. grandiflora encontramos 27 morfoespécies de formigas, sendo as duas mais frequentes Camponotus crassus, e uma espécie do gênero Brachymyrmex, as mesmas que foram mais comumente encontradas presas aos abrigos das larvas mirmecófagas. Vimos que as larvas expõem uma substância líquida na abertura de seu abrigo, que comprovamos possuir composição química muito similar a do néctar extrafloral de Q. grandiflora, o que sugere que as larvas utilizam o néctar da própria planta para atrair suas presas. Na presença de larvas de Rhinoleucophenga, menos formigas visitam as plantas e também por menos tempo. Esse forrageamento diferenciado resultou em menor ataque de formigas a cupins vivos (herbívoros simulados). Além disso, na presença das larvas mirmecófagas houve maior abundância de herbívoros mastigadores e maior área foliar removida por herbívoros. Podemos afirmar que as larvas de Rhinoleucophenga sp. nov. utilizam o recurso da planta sem beneficiá-la. Além disso, as larvas do díptero também prejudicam a planta e suas formigas mutualísticas, uma vez que alimentando-se delas, aumentam a incidência de herbívoros e a herbivoria foliar na planta. Dessa forma, as larvas de Rhinoleucophenga sp. nov. estão agindo como exploradoras e do mutualismo formiga-Qualea grandiflora e predadoras de topo, causando efeito cascata nesse sistema
Abstract: Exploiters of mutualism - individuals that use resources/services offered by mutualists giving nothing in return - can cause serious damages to mutualists, especially when it involves the death of one of the partners. Plants bearing EFNs usually maintain mutualism with aggressive ants, which defend the plant against herbivores. In a cerrado area at Itirapina (SP), we found a new dipteran species of the genus Rhinoleucophenga (Drosophilidae) whose larvae construct sticky shelters on top of active EFNs of Q. grandiflora. Field observations revealed those ants and others insects that visit the EFNs can get trapped at the sticky larval shelters, and are consumed by the larvae. We hypothesized that Rhinoleucophenga larvae could be interfering with the ant-Qualea mutualism, and thus be acting as an exploiter of this interaction. Here, we investigate the natural history of Rhinoleucophenga larvae, mainly its behavior and association with ants and Qualea, and their possible effect on the ant-Qualea mutualism. Larvae of Rhinoleucophenga sp. nov. occur in 85% of the individuals of Qualea grandiflora inspected at Itirapina. Rhinoleucophenga larvae occur mostly during the rainy season, mainly at the apex and abaxial surface of the branches. We found 27 ant species visiting Qualea. The two most frequent visiting species, Brachymyrmex sp. 1 and Camponotus crassus, were most common insects trapped at larval shelters. Chemical analyses revealed that Rhinoleucophenga larvae use Qualea's extrafloral nectar to attract insect prey to their shelters. Qualea branches infested by ant-preying Rhinoleucophenga larvae had ant visitors for less time and in lower numbers than dipteran-free branches. This negative effect on ant foraging activity resulted in decreased levels of ant aggression to live termite-baits (i.e., simulated herbivores) on leaves of dipteran-infested compared to dipteran-free branches. Controlled field experiments demonstrated that branches hosting Rhinoleucophenga larvae had higher numbers of chewing herbivores and higher levels of foliar herbivory than dipteran-free branches. By using Qualea's EFNs as larval shelters and as attractants to ant prey, larvae of Rhinoleucophenga sp. nov. negatively affect both the plant and ant visitors, with cascading effects ultimately resulting in increased herbivore damage to leaves. Thus we can conclude that ant-eating Rhinoleucophenga larvae are acting as exploiters of the mutualism between ants and Q. grandiflora and also as top predator, causing cascade effect on this system
Mestrado
Ecologia
Mestra em Ecologia
Rossignol, Nicolas. "Hétérogénéité de la végétation et du pâturage : conséquences fonctionnelles en praireis naturelle." Phd thesis, Université Rennes 1, 2006. http://tel.archives-ouvertes.fr/tel-00520859.
Full textLawrence, Janet L. "Conservation of insect natural enemies in heterogeneous vegetable landscapes." Connect to this title online, 2004. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1092761676.
Full textTitle from first page of PDF file. Document formatted into pages; contains xvi, 166 p.; also includes graphics (some col.). Includes bibliographical references. Available online via OhioLINK's ETD Center.
Wemheuer, Franziska. "Influence of Grassland Management and Herbivory on Diversity and Ecology of plant-associated Bacterial Communities." Doctoral thesis, 2013. http://hdl.handle.net/11858/00-1735-0000-0022-5FFE-F.
Full textSentis, Arnaud. "Effet de la température sur les interactions trophiques et intraguildes au sein d’un système plante-herbivore-ennemis naturels : modélisation et approches expérimentales." Thèse, 2012. http://hdl.handle.net/1866/8487.
Full textThere are several pieces of evidence that climate change significantly impact plants, herbivores, and predators. For ectotherms, temperature is the most important factor associated with these changes as it regulates their metabolism. Although the effects of temperature on individual organisms or populations have been well documented, our understanding about their consequences on trophic and guild interactions remains limited. In this context, we investigated the effects of temperature on complex interactions between a plant, the pepper Capsicum annuum L.; an herbivore, the aphid Myzus persicae Sulzer (extraguild prey); and two of its natural enemies, the ladybeetle Coleomegilla maculata lengi Timberlake (intraguild predator) and the predatory midge Aphidoletes aphidimyza Rondani (intraguild prey). We combined two approaches: (1) modeling predator–prey and intraguild (predation between two species that compete for the same resource) interactions, and (2) testing model predictions and characterizing the effects of temperature on components of our biological system through laboratory experiments. As predicted by the first model, we found that when temperature rises, C. maculata is more efficient at finding and handling prey, which increases predation rate. However, search rate decreases at high temperatures, leading to a reduction in predation. The predatory activity is therefore limited to a temperature window outside of which predation is reduced or absent. The next objective was to compare two models, one linear and one nonlinear, to determine which one best describes the functional response (the relationship between the number of prey consumed and prey density) of an intraguild predator. Results indicated that predictions of the nonlinear model (i.e., saturating at high prey densities) fit empirical observations well while the linear model greatly overestimates the number of prey consumed and the incidence of intraguild predation. Subsequently, we derived the nonlinear model to include the effect of temperature. As predicted by this model, we found that the incidence of intraguild predation increases with temperature but decreases when extraguild prey are more abundant. In a last experiment, we investigated the effects of temperature peaks on each component of our biological system. Results showed that temperature peaks reduce aphid fecundity and thereby population growth, decrease the weight of ladybeetle larvae, and decrease aphid control by ladybeetles, but have no effect on plants or plant–insect relationships. We also observed that the food chain is more resistant to temperature peaks when ladybeetles are included in the system than when they are absent. This suggests that ecosystems with predators exerting strong biotic control on prey population should be more resistant to climate change than ecosystem lacking them. In conclusion, our study highlights the importance of considering temperature in trophic and guild interactions since it influences the behavior of organisms as well as the frequency of interactions that affect population and community dynamics.
Doctorat réalisé en cotutelle entre l'Université de Montréal et l'Université Paul Sabatier-Toulouse III
Krumins, Jennifer Adams. "The causes and consequences of biodiversity in multitrophic communities." 2007. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.16526.
Full textSchlinkert, Hella. "Multitrophic interactions along a plant size gradient in Brassicaceae." Doctoral thesis, 2014. http://hdl.handle.net/11858/00-1735-0000-0022-5DC4-E.
Full textDean, Jennifer M. "Chemical ecology of plant-microbe interactions and effects on insect herbivores." 2008. http://etda.libraries.psu.edu/theses/approved/WorldWideIndex/ETD-2563/index.html.
Full text"Algal-herbivore interactions in coastal communities in Tung Ping Chau, Hong Kong." 2005. http://library.cuhk.edu.hk/record=b5892538.
Full textThesis (M.Phil.)--Chinese University of Hong Kong, 2005.
Includes bibliographical references (leaves 243-255).
Abstracts in English and Chinese.
Acknowledgements --- p.i
Abstract --- p.iii
Contents --- p.ix
List of Tables --- p.xii
List of Figures --- p.xix
Chapter Chapter 1 --- General Introduction
Chapter 1.1 --- Introduction --- p.1
Chapter 1.2 --- General Objectives --- p.11
Chapter 1.3 --- Study Site --- p.12
Chapter 1.4 --- Organization of the Thesis --- p.13
Chapter Chapter 2 --- "General Surveys on the Abundance of Algae and Herbivores in A Ma Wan, A Ye Wan and Lung Lok Shui, Tung Ping Chau, Hong Kong"
Chapter 2.1 --- Introduction --- p.16
Chapter 2.2 --- Materials and Methods --- p.20
Chapter 2.2.1 --- Study site --- p.20
Chapter 2.2.2 --- Measurement of water temperature --- p.21
Chapter 2.2.3 --- Measurement of algal percentage cover --- p.22
Chapter 2.2.4 --- Measurement of herbivore density --- p.22
Chapter 2.2.5 --- Investigation on the species richness and diversity of algae and herbivores --- p.23
Chapter 2.2.6 --- Statistical analysis --- p.24
Chapter 2.3 --- Results --- p.27
Chapter 2.3.1 --- Measurement of algal abundance and diversity --- p.27
Chapter 2.3.1.1 --- Percentage cover and morphology --- p.28
Chapter 2.3.1.2 --- Species richness --- p.29
Chapter 2.3.1.3 --- Species diversity --- p.29
Chapter 2.3.1.4 --- Dominance and composition --- p.30
Chapter 2.3.2 --- Measurement of herbivore abundance and diversity --- p.32
Chapter 2.3.2.1 --- Density of herbivores --- p.32
Chapter 2.3.2.2 --- Species richness --- p.33
Chapter 2.3.2.3 --- Species diversity --- p.34
Chapter 2.3.2.4 --- Dominance and composition --- p.34
Chapter 2.3.3 --- Relationships between algae and herbivores --- p.37
Chapter 2.3.3.1 --- Pairwise Pearson Correlation between algae and herbivores in different sites --- p.37
Chapter 2.3.3.2 --- Canonical correlations between algal and herbivorous species --- p.38
Chapter 2.3.4 --- "Water temperature and its relationships with the abundance, richness and diversity of algae and herbivores" --- p.39
Chapter 2.4 --- Discussion --- p.40
Chapter 2.4.1 --- Spatial distribution of algae and herbivores --- p.40
Chapter 2.4.2 --- Seasonal distributions of algae and herbivores --- p.46
Chapter 2.4.3 --- Interactions between algae and herbivores --- p.50
Chapter Chapter 3 --- Growth of Algae in Herbivore-exclusion Manipulative Experiment
Chapter 3.1 --- Introduction --- p.106
Chapter 3.2 --- Materials and Methods --- p.111
Chapter 3.2.1 --- Study site --- p.111
Chapter 3.2.2 --- Manipulative experiment --- p.111
Chapter 3.2.3 --- Investigation on the manipulative experiment --- p.112
Chapter 3.2.3.1 --- Species composition of algae and herbivores --- p.113
Chapter 3.2.3.2 --- Percentage cover of algae and density of herbivores --- p.113
Chapter 3.2.3.3 --- Sizes of herbivores --- p.113
Chapter 3.2.4 --- Detecting the cage effect --- p.114
Chapter 3.2.5 --- Statistical analyses --- p.114
Chapter 3.3 --- Results --- p.117
Chapter 3.3.1 --- Algae --- p.117
Chapter 3.3.1.1 --- Percentage cover --- p.117
Chapter 3.3.1.2 --- Species richness --- p.120
Chapter 3.3.1.3 --- Composition between treatments --- p.121
Chapter 3.3.1.4 --- Compositions between set-ups --- p.121
Chapter 3.3.1.5 --- Effects from caging and clearing --- p.122
Chapter 3.3.2 --- Herbivores --- p.123
Chapter 3.3.2.1 --- Density --- p.123
Chapter 3.3.2.2 --- Species richness --- p.124
Chapter 3.3.2.3 --- Compositions between treatments --- p.124
Chapter 3.3.2.4 --- Compositions between set-ups --- p.125
Chapter 3.3.3 --- Relationships between algae and herbivores --- p.125
Chapter 3.3.3.1 --- Abundance --- p.125
Chapter 3.3.3.2 --- Composition --- p.126
Chapter 3.3.4 --- Sizes of herbivores --- p.128
Chapter 3.3.5 --- Irradiance between treatments --- p.128
Chapter 3.4 --- Discussion --- p.129
Chapter 3.4.1 --- Effects of clearing on algal and herbivore dynamics --- p.130
Chapter 3.4.2 --- Effects of caging on algal and herbivore dynamics --- p.135
Chapter 3.4.3 --- Effects of seasonality of clearing on algal and herbivore dynamics --- p.139
Chapter 3.4.4 --- Interactions of algae and herbivores --- p.142
Chapter Chapter 4 --- Feeding Behavior of Common Herbivores in the Artificial Food Experiment
Chapter 4.1 --- Introduction --- p.216
Chapter 4.2 --- Materials and Methods --- p.218
Chapter 4.2.1 --- Sample collections --- p.218
Chapter 4.2.2 --- Production of artificial foods --- p.219
Chapter 4.2.3 --- Feeding experiments --- p.219
Chapter 4.2.4 --- Statistical analysis --- p.220
Chapter 4.3 --- Results --- p.221
Chapter 4.4 --- Discussion --- p.222
Chapter Chapter 5 --- Summary and Conclusion --- p.233
References --- p.243
Ranganathan, Yuvaraj. "Ants, Figs, Fig Wasps : The Chemical Ecology Of A Multitrophic System." Thesis, 2011. http://etd.iisc.ernet.in/handle/2005/1959.
Full textBartlett, Ryan Paul. "Ecological And Evolutionary Interactions Among Plant Resistance, Herbivores, And Predators." Diss., 2006. http://hdl.handle.net/10161/51.
Full textDissertation
Juenger, Thomas E. "The ecology and evolution of species interactions in the scarlet gilia, Ipomopsis aggregata, system /." 1999. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&res_dat=xri:pqdiss&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:9943081.
Full textTiede, Julia. "Plant diversity and landscape-scale effects on multitrophic interactions involving invertebrates." Thesis, 2017. http://hdl.handle.net/11858/00-1735-0000-002E-E4F6-C.
Full textBörschig, Carmen. "Effects of land-use intensity in grasslands on diversity, life-history traits and multitrophic interactions." Doctoral thesis, 2012. http://hdl.handle.net/11858/00-1735-0000-000D-F0CE-0.
Full textLaurin-Lemay, Simon. "Phylogéographie comparée d’un système multitrophique : les parasitoïdes du genre Horismenus spp. ont-ils échappé au processus de domestication du haricot au Mexique?" Thèse, 2010. http://hdl.handle.net/1866/4762.
Full textThis study aims to compare the evolutionary history of Horismenus parasitoids (Hymenoptera: Eulophidae) to that of their bruchid beetle hosts (Coleoptera: Bruchidae) and their domesticated host plant (Phaseolus vulgaris L.) in the context of traditional agriculture within their Mesoamerican center of domestication. We analyzed the genetic structure of 23 populations of four Horismenus species in Mexico using COI mitochondrial gene fragments and compared the structures to previously published data on bean plant and beetle hosts. We predicted that because parasitoids complete their development within their beetle hosts, within the bean, the genetic structure of both the host and the parasitoid would be similar and equally influenced by human-mediated migration (HMM). Furthermore, because of reproductive manipulation strategies often used by the alpha-proteobacteria endosymbionte Wolbachia spp. to ensure its transmission, the genetic structure of parasitoid populations inferred from mitochondrial genome would be bias consequently to the conjoint transmission of mitochondria and the bacteria according to propagation of the infection within parasitoids populations. The populations of H. missouriensis parasitoids are infected by Wolbachia spp. As predicted, these populations are not differentiated (FST = 0.06) which prevents us to infer on a parallel evolutionary history. Unlike their bruchids hosts, Acanthoscelides obtectus and A. ovelatus, the HMM is not a contemporary process influencing H. depressus population genetic structure according to the strong populations differentiation (FST = 0.34). The genetic structure observed within H. depressus populations is similar to that of its host plant (i.e. historical random dispersal from a highly diversified ancestral gene pool) and is probably the result of extensive gene flow from parasitoids associated with wild beans populations adjacent to crop fields. The study of evolutionary history integrating multitrophic levels has proved to be fruitful in detecting different evolutionary responses among members of the trophic module face to human and parasite interactions, but also points out the pertinence of analyzing ecological systems as a whole.
(11186766), Geoffrey M. Williams. "Thousand Cankers Disease of Eastern Black Walnut: Ecological Interactions in the Holobiont of a Bark Beetle-Fungal Disease." Thesis, 2021.
Find full textEastern black walnut (Juglans nigra 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 Juglans spp. (Juglandaceae), J. nigra is threatened by thousand cankers disease (TCD), an insect-vectored disease first described in 2009. TCD is caused by the bark beetle Pityophthorus juglandis Blackman (Corthylini) and the phytopathogenic fungus Geosmithia morbida Kol. Free. Ut. & Tiss. (Bionectriaceae). Together, the P. juglandis-G. morbida 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 J. nigra and J. regia planted outside their native distributions.
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 J. nigra 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 G. morbida in J. nigra 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 holobiont is defined as the whole multitrophic community of organisms—including J. nigra, microinvertebrates, fungi and bacteria—that interact with one another and with the host.
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 G. morbida 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 G. morbida was also associated with a distinct community of microbes in stems compared to G. morbida-negative trees. The soil microbiome from intensively-managed plantations facilitated positive feedback between G. morbida and a disease-promomting endophytic Fusarium solani species complex sp. in roots of J. nigra seedlings. Finally, the nematode species Bursaphelenchus juglandis associated with P. juglandis synergizes with G. morbida to cause foliar symptoms in seedlings in a shadehouse; conversely, experiments and observations indicated that the nematode species Panagrolaimus sp. and cf. Ektaphelenchus sp. could suppress WTB populations and/or TCD outbreaks.
In conclusion, the composition, function, and interactions within the P. juglandis and J. nigra 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.e., J. nigra) growing in environments that are favorable to novel pests or pest complexes (i.e., the western U.S.) may provide connectivity between emergent forest health threats (i.e., TCD) and native host populations (i.e., J. nigra in its native range).