Flow cytometry on >2000 plants from 141 populations (93 European, 48 North American; ~14β15 plants/population) revealed a near-complete replacement of cytotypes during invasion: Europe has 56% diploid, 40% tetraploid, and 4% mixed populations; North America is 98% tetraploid and 2% mixed, with only two diploid plants among 731 sampled .
Outlying mean index (OMI) analyses showed significant niche-optima shifts: native tetraploids differ from diploids along a temperature-energy axis, and native vs. invasive tetraploids differ along climatic, vegetation, and local-abiotic gradients, with invasive tetraploids occupying drier, more continental climates . Logistic regression identified PET and GDD as variables showing sequential shifts among geo-cytotypes, consistent with preadaptation . Field traits support an enemy-release/EICA-like pathway: North American plants had more stems (median 5.47 vs 1.88), higher polycarpy, and larger covered areas .
The study is correlative: niche analyses reflect the realized niche, and the authors explicitly note founder effects and environmental (vs. genetic) causes of trait differences cannot be excluded pending common-garden work . Taxonomic ambiguity of C. maculosa s.l. and ambiguous 4x ploidy in southern France are known blind spots (addressed via sensitivity analyses in Appendix C). The cytotype-shift finding aligns with later theory showing polyploid establishment depends on mating-system context , and with broader literature showing biocontrol herbivory can even increase competitive ability of this invader . Confidence is moderate-to-high for the cytotype frequency and niche-shift observations; low-to-moderate for causal attribution.
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