Inducible defense is a common form of phenotypic plasticity, and inducibility (change in defense after herbivore attack) has long been predicted to trade off with constitutive (or baseline) defense to manage resource allocation. Although such trade-offs likely constrain evolution within species, the extent to which they influence divergence among species is unresolved. We studied cardenolide toxins among genetic families in eight North American Asclepias species, spanning the full range of defense in the genus. Using common environment experiments and chemical assays, we report a consistent trade-off (negative genetic correlation) between concentrations of constitutive cardenolides and their inducibility within each species. However, no trade-off was found in a phylogenetic analysis across species. To investigate factors driving differences in defense allocation among species we used latitude as a proxy for growing season and herbivore pressure and found that divergence into lower latitudes resulted in evolution of higher cardenolides overall. Next we used an enzymatic assay of the cellular target of cardenolides (sodium-potassium ATPase) and confirm that higher cardenolides resulted in stronger toxicity to a sensitive species, but not to specialized monarch butterflies. Thus, plant speciation into biogeographic regions with alternative resources or pest pressure resulted in the macroevolution of cardenolide defense, especially against unspecialized herbivores. Nonetheless, trade-offs persist in the extent to which this defense is allocated constitutively or is inducible among genotypes within each species.
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Univ Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
BGI Shenzhen, Shenzhen, Peoples R ChinaUniv Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
Hu, Dingxue
Li, Yan
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BGI Shenzhen, Shenzhen, Peoples R ChinaUniv Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
Li, Yan
Zhang, Detao
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BGI Shenzhen, Shenzhen, Peoples R ChinaUniv Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
Zhang, Detao
Ding, Jiahong
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BGI Shenzhen, Shenzhen, Peoples R ChinaUniv Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
Ding, Jiahong
Song, Zijun
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Zhejiang Univ, Affiliated Hosp 1, Sch Med, Inst Translat Med, Hangzhou, Peoples R ChinaUniv Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
Song, Zijun
Min, Junxia
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Zhejiang Univ, Affiliated Hosp 1, Sch Med, Inst Translat Med, Hangzhou, Peoples R ChinaUniv Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
Min, Junxia
Zeng, Yi
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Peking Univ, Ctr Hlth Aging & Dev Studies, Natl Sch Dev, Beijing, Peoples R China
Duke Univ, Med Sch, Ctr Study Aging & Human Dev, Durham, NC USA
Duke Univ, Med Sch, Geriatr Div, Durham, NC USAUniv Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
Zeng, Yi
Nie, Chao
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BGI Shenzhen, Shenzhen, Peoples R ChinaUniv Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China