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      Large- and Small-Scale Environmental Factors Drive Distributions of Ant Mound Size Across a Latitudinal Gradient

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          Abstract

          Red wood ants are keystone species of forest ecosystems in Europe. Environmental factors and habitat characteristics affect the size of their nest mounds, an important trait being in concordance with a colony’s well-being and impact on its surroundings. In this study, we investigated the effect of large-scale (latitude and altitude) and small-scale environmental factors (e.g., characteristics of the forest) on the size of nest mounds of Formica polyctena in Central Europe. We predicted that the change in nest size is in accordance with Bergmann’s rule that states that the body size of endotherm animals increases with the higher latitude and/or altitude. We found that the size of nests increased along the latitudinal gradient in accordance with Bergmann’s rule. The irradiation was the most important factor responsible for the changes in nest size, but temperature and local factors, like the perimeter of the trees and their distance from the nest, were also involved. Considering our results, we can better understand the long-term effects and consequences of the fast-changing environmental factors on this ecologically important group. This knowledge can contribute to the planning of forest management tactics in concordance with the assurance of the long-term survival of red wood ants.

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          Geographic gradients in body size: a clarification of Bergmann's rule. BIODIVERSITY RESEARCH

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            Bergmann and converse bergmann latitudinal clines in arthropods: two ends of a continuum?

            Two seemingly opposite evolutionary patterns of clinal variation in body size and associated life history traits exist in nature. According to Bergmann's rule, body size increases with latitude, a temperature effect. According to the converse Bergmann rule, body size decreases with latitude, a season length effect. A third pattern causally related to the latter is countergradient variation, whereby populations of a given species compensate seasonal limitations at higher latitudes by evolving faster growth and larger body sizes compared to their low latitude conspecifics. We discuss these patterns and argue that they are not mutually exclusive because they are driven by different environmental causes and proximate mechanisms; they therefore can act in conjunction, resulting in any intermediate pattern. Alternatively, Bergmann and converse Bergmann clines can be interpreted as over- and undercompensating countergradient variation, respectively. We illustrate this with data for the wide-spread yellow dung fly, Scathophaga stercoraria (Diptera: Scathophagidae), which in Europe shows a Bergmann cline for size and a converse Bergmann cline (i.e., countergradient variation) for development time. A literature review of the available evidence on arthropod latitudinal clines further shows a patterned continuum of responses. Converse Bergmann clines due to end-of-season time limitations are more common in larger species with longer development times. Our study thus provides a synthesis to the controversy about the importance of Bergmann's rule and the converse Bergmann rule in nature.
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              Ant biodiversity and its relationship to ecosystem functioning: a review

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                Author and article information

                Journal
                Insects
                Insects
                insects
                Insects
                MDPI
                2075-4450
                04 June 2020
                June 2020
                : 11
                : 6
                : 350
                Affiliations
                [1 ]Department of Ecology, University of Szeged, Közép fasor 52, H-6726 Szeged, Hungary; zbatory@ 123456gmail.com (Z.B.); lorinczig@ 123456gmail.com (G.L.); modragabi@ 123456gmail.com (G.M.); imolaboni@ 123456gmail.com (I.B.); kisspeterjanos003@ 123456gmail.com (P.J.K.); ddaguilon@ 123456up.edu.ph (D.J.A.); bikmakk@ 123456gmail.com (I.M.)
                [2 ]Doctoral School in Biology, Faculty of Science and Informatics, University of Szeged, Közép fasor 52, H-6726 Szeged, Hungary
                [3 ]Museum and Institute of Zoology, Polish Academy of Sciences, Wilcza Street 64, 00-679 Warsaw, Poland; getriral@ 123456googlemail.com
                [4 ]Doctoral School of Environmental Sciences, University of Szeged, Rerrich Béla Square 1, H-6720 Szeged, Hungary
                [5 ]Department of Forest Biological Sciences, College of Forestry and Natural Resources, University of the Philippines Los Baños, Laguna 4031, Philippines
                [6 ]Department of Physical Geography and Geoinformatics, University of Szeged, Egyetem Street 2-6, H-6722 Szeged, Hungary; a2na9211@ 123456gmail.com
                Author notes
                Author information
                https://orcid.org/0000-0002-0456-444X
                https://orcid.org/0000-0002-4995-9090
                Article
                insects-11-00350
                10.3390/insects11060350
                7348728
                32512838
                963eb8ff-5c50-4ee2-a8a9-fc8e29b685cb
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 11 May 2020
                : 01 June 2020
                Categories
                Article

                altitudinal gradient,bergmann’s rule,formica polyctena,latitudinal gradient,nest mound

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