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• W3216960309 endingPage "22" @default.
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• W3216960309 abstract "Abstract Parasite populations associated with different host species can encounter a variety of isolating reproductive barriers, leading to each population independently accumulating genome‐wide genetic differences due to their host associations. This phenomenon is called host‐associated differentiation (HAD) and has been proposed as an indicator of early diversification among parasitic arthropods. Although many parasite–host case study systems have been tested for the genetic signature of HAD (e.g., F ST ≥0.15 between sympatric, host‐associated populations in the absence of allopatry), it is unknown which isolating reproductive barriers best predict the general occurrence of HAD. HAD development has been attributed to biological and ecological factors that either directly generate reproductive isolation between parasites living on different hosts, such as ‘immigrant inviability’ (i.e., lower fitness of immigrants in non‐native environments), or that promote the accumulation of host‐specific genetic adaptations, such as the gallmaking feeding mode. In fact, some of these factors are shared across multiple case studies, suggesting that the occurrence of HAD is generalizable and can be predicted based on the incidence of significant biological and ecological factors. By means of a discriminant function analysis (DFA), this research assessed 108 arthropod parasite–host case studies for ecological and biological factors significantly correlated with the occurrence of HAD and whether these factors could be used to distinguish the presence of HAD from its absence. The DFA demonstrated that case studies that developed HAD could be distinguished from case studies that did not develop HAD. The results of the DFA were corroborated by a ‘non‐iterative partial least squares’ (NIPALS) discriminant model and a nominal logistic regression. Case studies with HAD could be robustly separated from case studies without HAD based on the incidence of these predictive factors: immigrant inviability, gallmaking, endophagy, recent range invasions of either hosts or parasites, differential host phenology, and differential parasite morphology. These results were used in an infinite random forest analysis to generate a hierarchy of conditional probabilities that separated HAD presence from absence. The results provide researchers with a tool for reliably predicting which untested parasite–host system would likely develop HAD. Immigrant inviability, gallmaking, and their combination were strongly correlated with the presence of HAD, which indicated parasite–host systems with these traits were highly likely to develop HAD. Contrary to expectation, endophagous feeding was negatively correlated with HAD presence, which indicated phytophagous endophagous feeders (excepting gallmakers) were highly unlikely to develop HAD. Furthermore, parasitoids were shown to be just as likely to develop HAD as not. Unfortunately, potentially significant predictive factors (e.g., allochrony) were excluded from analysis because too few case studies have been specifically tested for these factors. Furthermore, this analysis was biased by the lack of ‘negative’ publication results and the overrepresentation of research laboratories that primarily study HAD. Future research should accumulate novel HAD case studies that specifically test for allochrony, differential microbial associations, and morphological differentiation." @default.
• W3216960309 created "2021-12-06" @default.
• W3216960309 creator A5010978125 @default.
• W3216960309 creator A5039599341 @default.
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• W3216960309 creator A5048819235 @default.
• W3216960309 date "2021-11-24" @default.
• W3216960309 modified "2023-10-17" @default.
• W3216960309 title "Predicting the occurrence of host‐associated differentiation in parasitic arthropods: a quantitative literature review" @default.
• W3216960309 cites W1497190308 @default.
• W3216960309 cites W1518546884 @default.
• W3216960309 cites W1528995999 @default.
• W3216960309 cites W1550765943 @default.
• W3216960309 cites W1577166592 @default.
• W3216960309 cites W1601391681 @default.
• W3216960309 cites W1608757365 @default.
• W3216960309 cites W1619623942 @default.
• W3216960309 cites W1775655276 @default.
• W3216960309 cites W1870129114 @default.
• W3216960309 cites W1891857422 @default.
• W3216960309 cites W1896206265 @default.
• W3216960309 cites W1937223277 @default.
• W3216960309 cites W1969699984 @default.
• W3216960309 cites W1969910634 @default.
• W3216960309 cites W1970611097 @default.
• W3216960309 cites W1972136915 @default.
• W3216960309 cites W1974076666 @default.
• W3216960309 cites W1976223073 @default.
• W3216960309 cites W1979721747 @default.
• W3216960309 cites W1980122972 @default.
• W3216960309 cites W1980303461 @default.
• W3216960309 cites W1982557102 @default.
• W3216960309 cites W1984730955 @default.
• W3216960309 cites W1988201492 @default.
• W3216960309 cites W1988406367 @default.
• W3216960309 cites W1988987622 @default.
• W3216960309 cites W1992089046 @default.
• W3216960309 cites W1992774532 @default.
• W3216960309 cites W1992909022 @default.
• W3216960309 cites W1997389295 @default.
• W3216960309 cites W1998437216 @default.
• W3216960309 cites W1999163726 @default.
• W3216960309 cites W2000537771 @default.
• W3216960309 cites W2002926417 @default.
• W3216960309 cites W2003699052 @default.
• W3216960309 cites W2005811719 @default.
• W3216960309 cites W2006113436 @default.
• W3216960309 cites W2010765102 @default.
• W3216960309 cites W2011371164 @default.
• W3216960309 cites W2014688262 @default.
• W3216960309 cites W2016298186 @default.
• W3216960309 cites W2022157748 @default.
• W3216960309 cites W2022751627 @default.
• W3216960309 cites W2023405098 @default.
• W3216960309 cites W2032271189 @default.
• W3216960309 cites W2036451130 @default.
• W3216960309 cites W2036903077 @default.
• W3216960309 cites W2037101020 @default.
• W3216960309 cites W2038792294 @default.
• W3216960309 cites W2039034652 @default.
• W3216960309 cites W2042260095 @default.
• W3216960309 cites W2047230721 @default.
• W3216960309 cites W2047727977 @default.
• W3216960309 cites W2048498997 @default.
• W3216960309 cites W2050442456 @default.
• W3216960309 cites W2051079048 @default.
• W3216960309 cites W2053736189 @default.
• W3216960309 cites W2057376327 @default.
• W3216960309 cites W2060115931 @default.
• W3216960309 cites W2060150214 @default.
• W3216960309 cites W2063223203 @default.
• W3216960309 cites W2063282250 @default.
• W3216960309 cites W2067174381 @default.
• W3216960309 cites W2068579576 @default.
• W3216960309 cites W2068589866 @default.
• W3216960309 cites W2068919087 @default.
• W3216960309 cites W2069259487 @default.
• W3216960309 cites W2074097929 @default.
• W3216960309 cites W2074454785 @default.
• W3216960309 cites W2076395872 @default.
• W3216960309 cites W2090678672 @default.
• W3216960309 cites W2093278089 @default.
• W3216960309 cites W2094532447 @default.
• W3216960309 cites W2095953655 @default.
• W3216960309 cites W2097522701 @default.
• W3216960309 cites W2098994219 @default.
• W3216960309 cites W2099549461 @default.
• W3216960309 cites W2100076656 @default.
• W3216960309 cites W2101083023 @default.
• W3216960309 cites W2101157993 @default.
• W3216960309 cites W2101944780 @default.
• W3216960309 cites W2102159748 @default.
• W3216960309 cites W2105925291 @default.
• W3216960309 cites W2106165750 @default.
• W3216960309 cites W2106436109 @default.
• W3216960309 cites W2107984417 @default.
• W3216960309 cites W2112388438 @default.
• W3216960309 cites W2120032653 @default.

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