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      Is body size important? Seasonal changes in morphology in two grass-feeding Abacarus mites

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          Abstract

          Overwintering strategies in herbivorous mites (Acariformes: Eriophyoidea) are poorly understood. A study of two Abacarus spp. was conducted to compare body size parameters of adult females in different seasons. Mites of Abacarus n. sp. (under description) and A. lolli were sampled from Bromopsis inermis and Lolium perenne, respectively, in April, September and December of 2001 in Poznań, Poland; 21 morphological traits were measured for each specimen. A principal component analysis revealed significant differences in body size parameters between collection dates, with larger females collected in December in both species. Larger body size in winter is consistent with the hypothesis that mites of these species, for which deutogyny has not been observed, undergo physiological changes such as accumulation of nutritional reserves, that enable them to withstand adverse environmental conditions. Larger body size has also been shown in other invertebrates to reduce heat loss in cold conditions. Filling gaps in the current knowledge of eriophyoid overwintering strategies, whether in the presence or absence of deutogyny, will contribute to both basic and applied future studies of this important arthropod group.

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          The online version of this article (doi:10.1007/s10493-017-0159-1) contains supplementary material, which is available to authorized users.

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            Body size variation in insects: a macroecological perspective.

            Body size is a key feature of organisms and varies continuously because of the effects of natural selection on the size-dependency of resource acquisition and mortality rates. This review provides a critical and synthetic overview of body size variation in insects from a predominantly macroecological (large-scale temporal and spatial) perspective. Because of the importance of understanding the proximate determinants of adult size, it commences with a brief summary of the physiological mechanisms underlying adult body size and its variation, based mostly on findings for the model species Drosophila melanogaster and Manduca sexta. Variation in nutrition and temperature have variable effects on critical weight, the interval to cessation of growth (or terminal growth period) and growth rates, so influencing final adult size. Ontogenetic and phylogenetic variation in size, compensatory growth, scaling at the intra- and interspecific levels, sexual size dimorphism, and body size optimisation are then reviewed in light of their influences on individual and species body size frequency distributions. Explicit attention is given to evolutionary trends, including gigantism, Cope's rule and the rates at which size change has taken place, and to temporal ecological trends such as variation in size with succession and size-selectivity during the invasion process. Large-scale spatial variation in size at the intraspecific, interspecific and assemblage levels is considered, with special attention being given to the mechanisms proposed to underlie clinal variation in adult body size. Finally, areas particularly in need of additional research are identified.
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              The evolution of body size under environmental gradients in ectotherms: why should Bergmann's rule apply to lizards?

              Background The impact of environmental gradients on the evolution of life history traits is a central issue in macroecology and evolutionary biology. A number of hypotheses have been formulated to explain factors shaping patterns of variation in animal mass. One such example is Bergmann's rule, which predicts that body size will be positively correlated with latitude and elevation, and hence, with decreasing environmental temperatures. A generally accepted explanation for this phenotypic response is that as body mass increases, body surface area gets proportionally smaller, which contributes to reduced rates of heat-loss. Phylogenetic and non-phylogenetic evidence reveals that endotherms follow Bergmann's rule. In contrast, while previous non-phylogenetic studies supported this prediction in up to 75% of ectotherms, recent phylogenetic comparative analyses suggest that its validity for these organisms is controversial and less understood. Moreover, little attention has been paid to why some ectotherms conform to this rule, while others do not. Here, we investigate Bergmann's rule in the six main clades forming the Liolaemus genus, one of the largest and most environmentally diverse genera of terrestrial vertebrates. A recent study conducted on some species belonging to four of these six clades concluded that Liolaemus species follow Bergmann's rule, representing the only known phylogenetic support for this model in lizards. However, a later reassessment of this evidence, performed on one of the four analysed clades, produced contrasting conclusions. Results Our results fail to support Bergmann's rule in Liolaemus lizards. Non-phylogenetic and phylogenetic analyses showed that none of the studied clades experience increasing body size with increasing latitude and elevation. Conclusion Most physiological and behavioural processes in ectotherms depend directly upon their body temperature. In cold environments, adaptations to gain heat rapidly are under strong positive selection to allow optimal feeding, mating and predator avoidance. Therefore, evolution of larger body size in colder environments appears to be a disadvantageous thermoregulatory strategy. The repeated lack of support for Bergmann's rule in ectotherms suggests that this model should be recognized as a valid rule exclusively for endotherms.
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                Author and article information

                Contributors
                0048 618295749 , alicja.laska@amu.edu.pl
                Journal
                Exp Appl Acarol
                Exp. Appl. Acarol
                Experimental & Applied Acarology
                Springer International Publishing (Cham )
                0168-8162
                1572-9702
                27 July 2017
                27 July 2017
                2017
                : 72
                : 4
                : 317-328
                Affiliations
                [1 ]ISNI 0000 0001 2097 3545, GRID grid.5633.3, Population Ecology Lab, Institute of Environmental Biology, Faculty of Biology, , Adam Mickiewicz University, Poznań, ; Umultowska 89, 61–614 Poznań, Poland
                [2 ]ISNI 0000 0004 0478 6311, GRID grid.417548.b, Great Basin Rangelands Research Unit, ; 920 Valley Road, Reno, NV 89512 USA
                Author information
                http://orcid.org/0000-0002-6743-6015
                http://orcid.org/0000-0003-3498-5445
                http://orcid.org/0000-0002-9485-532X
                Article
                159
                10.1007/s10493-017-0159-1
                5583266
                28752482
                26b9ad28-87d8-4dd4-bdc5-45e5da969ecc
                © The Author(s) 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 30 May 2017
                : 21 July 2017
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100006047, Polish Scientific Research Committee;
                Award ID: No. 6 P04 C0 5418
                Award Recipient :
                Categories
                Article
                Custom metadata
                © Springer International Publishing AG 2017

                Entomology
                eriophyoidea,herbivores,invertebrates,phenotype
                Entomology
                eriophyoidea, herbivores, invertebrates, phenotype

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