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Evolution of phytophagy in trombidiform mites
This paper reviews the evolutionary aspects of obligate phytophagy (excluding mycophagy and phycophagy) in the mite suborder Trombidiformes. Phytophagy in the other acariform suborder, Sarcoptiformes, is limited to just a few species, amidst otherwise saprophagous or fungivorous taxa, that attack th...
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Published in: | Experimental & applied acarology 1998-02, Vol.22 (2), p.81-100 |
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description | This paper reviews the evolutionary aspects of obligate phytophagy (excluding mycophagy and phycophagy) in the mite suborder Trombidiformes. Phytophagy in the other acariform suborder, Sarcoptiformes, is limited to just a few species, amidst otherwise saprophagous or fungivorous taxa, that attack the living tissues of higher plants. The phylogenetic relationships of lineages that contain taxa of plant-feeding mites are reviewed briefly, to facilitate hypotheses about the number of times that phytophagy has arisen within the Trombidiformes. The relationship between the two most important plant-feeding taxa, the Tetranychoidea and Eriophyoidea, is so distant that their obligate phytophagy represents independent events. Outgroup comparisons allow an estimate of the relative ages when phytophagy arose. This background facilitates analyses of the evolutionary patterns of attributes relevant to phytophagy as a way of life. Styliform modifications of chelate chelicerae for predation or fungivory were fundamental pre-adaptations for effective phytophagy. Dispersal among the major lineages of phytophagous mites seems generally passive, with little evidence of phoretic behaviour. Continued individual mobility seems to be needed during ontogeny and adulthood, such that no scale-like or sac-like instars have arisen. Trends towards physogastric reproduction and ovoviviparity are not evident. Arrhenotokous sex determination predominates among lineages of phytophagous mites. The primary sex ratios are not usually highly female biased. Direct sperm transfer does not seem to have been advantageous or disadvantageous to adaptive radiations of plant-feeding lineages. Adaptive trends towards thelytoky are scattered and do not seem to have played major roles in speciation, diversification or trends towards increasing host specificity in lineages. Alternate asexual and sexual generations and life cycles on different species of hosts, as occur among families of aphid and scale insects, are not known. Among unrelated lineages of trombidiform mites, there appears to have been convergent evolution of attributes, such as those noted above, in response to similar selective pressures for a phytophagous way of life. The patterns of attributes discussed need experimental analysis and detailed documentation to test their accuracy and generality and to understand the selective pressures that have formed them. |
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This background facilitates analyses of the evolutionary patterns of attributes relevant to phytophagy as a way of life. Styliform modifications of chelate chelicerae for predation or fungivory were fundamental pre-adaptations for effective phytophagy. Dispersal among the major lineages of phytophagous mites seems generally passive, with little evidence of phoretic behaviour. Continued individual mobility seems to be needed during ontogeny and adulthood, such that no scale-like or sac-like instars have arisen. Trends towards physogastric reproduction and ovoviviparity are not evident. Arrhenotokous sex determination predominates among lineages of phytophagous mites. The primary sex ratios are not usually highly female biased. Direct sperm transfer does not seem to have been advantageous or disadvantageous to adaptive radiations of plant-feeding lineages. Adaptive trends towards thelytoky are scattered and do not seem to have played major roles in speciation, diversification or trends towards increasing host specificity in lineages. Alternate asexual and sexual generations and life cycles on different species of hosts, as occur among families of aphid and scale insects, are not known. Among unrelated lineages of trombidiform mites, there appears to have been convergent evolution of attributes, such as those noted above, in response to similar selective pressures for a phytophagous way of life. 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This background facilitates analyses of the evolutionary patterns of attributes relevant to phytophagy as a way of life. Styliform modifications of chelate chelicerae for predation or fungivory were fundamental pre-adaptations for effective phytophagy. Dispersal among the major lineages of phytophagous mites seems generally passive, with little evidence of phoretic behaviour. Continued individual mobility seems to be needed during ontogeny and adulthood, such that no scale-like or sac-like instars have arisen. Trends towards physogastric reproduction and ovoviviparity are not evident. Arrhenotokous sex determination predominates among lineages of phytophagous mites. The primary sex ratios are not usually highly female biased. Direct sperm transfer does not seem to have been advantageous or disadvantageous to adaptive radiations of plant-feeding lineages. Adaptive trends towards thelytoky are scattered and do not seem to have played major roles in speciation, diversification or trends towards increasing host specificity in lineages. Alternate asexual and sexual generations and life cycles on different species of hosts, as occur among families of aphid and scale insects, are not known. Among unrelated lineages of trombidiform mites, there appears to have been convergent evolution of attributes, such as those noted above, in response to similar selective pressures for a phytophagous way of life. The patterns of attributes discussed need experimental analysis and detailed documentation to test their accuracy and generality and to understand the selective pressures that have formed them.</description><subject>Animal and plant ecology</subject><subject>Animal, plant and microbial ecology</subject><subject>Animals</subject><subject>Autoecology</subject><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Protozoa. 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E</creatorcontrib><collection>Pascal-Francis</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Experimental & applied acarology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LINDQUIST, E. E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evolution of phytophagy in trombidiform mites</atitle><jtitle>Experimental & applied acarology</jtitle><date>1998-02-01</date><risdate>1998</risdate><volume>22</volume><issue>2</issue><spage>81</spage><epage>100</epage><pages>81-100</pages><issn>0168-8162</issn><eissn>1572-9702</eissn><coden>EAACEM</coden><abstract>This paper reviews the evolutionary aspects of obligate phytophagy (excluding mycophagy and phycophagy) in the mite suborder Trombidiformes. Phytophagy in the other acariform suborder, Sarcoptiformes, is limited to just a few species, amidst otherwise saprophagous or fungivorous taxa, that attack the living tissues of higher plants. The phylogenetic relationships of lineages that contain taxa of plant-feeding mites are reviewed briefly, to facilitate hypotheses about the number of times that phytophagy has arisen within the Trombidiformes. The relationship between the two most important plant-feeding taxa, the Tetranychoidea and Eriophyoidea, is so distant that their obligate phytophagy represents independent events. Outgroup comparisons allow an estimate of the relative ages when phytophagy arose. This background facilitates analyses of the evolutionary patterns of attributes relevant to phytophagy as a way of life. Styliform modifications of chelate chelicerae for predation or fungivory were fundamental pre-adaptations for effective phytophagy. Dispersal among the major lineages of phytophagous mites seems generally passive, with little evidence of phoretic behaviour. Continued individual mobility seems to be needed during ontogeny and adulthood, such that no scale-like or sac-like instars have arisen. Trends towards physogastric reproduction and ovoviviparity are not evident. Arrhenotokous sex determination predominates among lineages of phytophagous mites. The primary sex ratios are not usually highly female biased. Direct sperm transfer does not seem to have been advantageous or disadvantageous to adaptive radiations of plant-feeding lineages. Adaptive trends towards thelytoky are scattered and do not seem to have played major roles in speciation, diversification or trends towards increasing host specificity in lineages. Alternate asexual and sexual generations and life cycles on different species of hosts, as occur among families of aphid and scale insects, are not known. Among unrelated lineages of trombidiform mites, there appears to have been convergent evolution of attributes, such as those noted above, in response to similar selective pressures for a phytophagous way of life. The patterns of attributes discussed need experimental analysis and detailed documentation to test their accuracy and generality and to understand the selective pressures that have formed them.</abstract><cop>Dordrecht</cop><pub>Springer</pub><doi>10.1023/A:1006041609774</doi><tpages>20</tpages></addata></record> |
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subjects | Animal and plant ecology Animal, plant and microbial ecology Animals Autoecology Biological and medical sciences Fundamental and applied biological sciences. Psychology Protozoa. Invertebrata |
title | Evolution of phytophagy in trombidiform mites |
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