Dispersing individuals are expected to encounter costs during transfer and in the novel environment, and may also have experienced stress in their natal patch. Given this, a non-random subset of the population should engage in dispersal and show divergent stress-related responses. This includes physiological shifts as expressed in the metabolome, which form a major part of responses to stress. We analyzed how metabolic profiles and life-history traits varied between dispersers and residents of the model two-spotted spider mite , and whether and how these syndromes varied with exposure to a stressful new host plant (tomato). Regardless of the effect of host plant, we found a physiological dispersal syndrome where, relative to residents, dispersers were characterized by lower leaf consumption and a lower concentration of several amino acids, indicating a potential dispersal-foraging trade-off. As a possible consequence of this lower food intake, dispersers also laid smaller eggs. Responses to tomato were consistent with this plant being a stressor for , including reduced fecundity and reduced feeding. Tomato-exposed mites laid larger eggs, which we interpret as a plastic response to food stress, increasing survival to maturity. Contrary to what was expected from the costs of dispersal and from previous meta-population level studies, there was no interaction between dispersal status and host plant for any of the examined traits, meaning stress impacts were equally incurred by residents and dispersers. We thus provide novel insights into the processes shaping dispersal and the feedbacks on ecological dynamics in spatially structured populations.
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http://dx.doi.org/10.1242/jeb.203596 | DOI Listing |
Ann Entomol Soc Am
January 2025
Department of Entomology, Michigan State University, East Lansing, MI, USA.
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Department of General Surgery, Medical Centre of West Kazakhstan Marat Ospanov Medical University, Aktobe, Kazakhstan.
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Pest Manag Sci
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Key Laboratory of Integrated Pest Management on Crops in Central China, Ministry of Agriculture and Rural Affairs, Hubei Key Laboratory of Crop Disease, Insect Pests and Weeds Control, Institute of Plant Protection and Soil Science, Hubei Academy of Agricultural Sciences, Wuhan, China.
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National Engineering Research Center of Sugarcane, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
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View Article and Find Full Text PDFSci Rep
January 2025
Institute of Ecology and Evolutionary Biology, National Taiwan University, Taipei, Taiwan.
How does the fig tree Ficus benguetensis protect its investment in the production of figs and pollinating fig wasps against parasitism from non-pollinating fig wasps? This study documents a previously overlooked defense mechanism: fig abscission-the natural shedding of the fig fruit as a defense mechanism. Our bagging experiments showed that both the absence of pollination and high parasitism levels lead to the abortion of F. benguetensis figs, with positive correlations between parasitism levels, increased abscission rates, and decreased pollinator production.
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