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      High association strengths are linked to phenotypic similarity, including plumage color and patterns, of participants in mixed-species bird flocks of southwestern China

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          Abstract

          Participants in mixed-species bird flocks (MSFs) have been shown to associate with species that are similar in body size, diet, and evolutionary history, suggesting that facilitation structures these assemblages. In addition, several studies have suggested that species in MSFs resemble each other in their plumage, but this question has not been systematically investigated for any MSF system. During the nonbreeding season of 2020 and 2021, we sampled 585 MSFs on 14 transects in 2 habitats of Tongbiguang Nature Reserve in western Yunnan Province, China. We performed social network analysis and the Multiple Regression Quadratic Assignment Procedure to evaluate the effect of 4 species traits (body size, overall plumage color, distinctive plumage patterns, and diet) and evolutionary history on species association strength at the whole-MSF and within-MSF levels. All 41 significant relationships showed that species with stronger associations were more similar in their various traits. Body size had the strongest effect on association strength, followed by phylogeny, plumage patterns, and plumage color; diet had the weakest effect. Our results are consistent with the hypotheses that the benefits of associating with phenotypically similar species outweigh the potential costs of interspecific competition, and that trait matching can occur in plumage characteristics, albeit more weakly than in other traits. Several explanations exist as to why similarities in plumage may occur in MSFs, including that they could reduce predators’ ability to target phenotypically “odd” individuals. Whether trait matching in plumage occurs through assortative processes in ecological time or is influenced by co-evolution requires further study.

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          The global diversity of birds in space and time.

          Current global patterns of biodiversity result from processes that operate over both space and time and thus require an integrated macroecological and macroevolutionary perspective. Molecular time trees have advanced our understanding of the tempo and mode of diversification and have identified remarkable adaptive radiations across the tree of life. However, incomplete joint phylogenetic and geographic sampling has limited broad-scale inference. Thus, the relative prevalence of rapid radiations and the importance of their geographic settings in shaping global biodiversity patterns remain unclear. Here we present, analyse and map the first complete dated phylogeny of all 9,993 extant species of birds, a widely studied group showing many unique adaptations. We find that birds have undergone a strong increase in diversification rate from about 50 million years ago to the near present. This acceleration is due to a number of significant rate increases, both within songbirds and within other young and mostly temperate radiations including the waterfowl, gulls and woodpeckers. Importantly, species characterized with very high past diversification rates are interspersed throughout the avian tree and across geographic space. Geographically, the major differences in diversification rates are hemispheric rather than latitudinal, with bird assemblages in Asia, North America and southern South America containing a disproportionate number of species from recent rapid radiations. The contribution of rapidly radiating lineages to both temporal diversification dynamics and spatial distributions of species diversity illustrates the benefits of an inclusive geographical and taxonomical perspective. Overall, whereas constituent clades may exhibit slowdowns, the adaptive zone into which modern birds have diversified since the Cretaceous may still offer opportunities for diversification.
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            Phylogenetic niche conservatism, phylogenetic signal and the relationship between phylogenetic relatedness and ecological similarity among species.

            Ecologists are increasingly adopting an evolutionary perspective, and in recent years, the idea that closely related species are ecologically similar has become widespread. In this regard, phylogenetic signal must be distinguished from phylogenetic niche conservatism. Phylogenetic niche conservatism results when closely related species are more ecologically similar that would be expected based on their phylogenetic relationships; its occurrence suggests that some process is constraining divergence among closely related species. In contrast, phylogenetic signal refers to the situation in which ecological similarity between species is related to phylogenetic relatedness; this is the expected outcome of Brownian motion divergence and thus is necessary, but not sufficient, evidence for the existence of phylogenetic niche conservatism. Although many workers consider phylogenetic niche conservatism to be common, a review of case studies indicates that ecological and phylogenetic similarities often are not related. Consequently, ecologists should not assume that phylogenetic niche conservatism exists, but rather should empirically examine the extent to which it occurs.
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              Phylogenies and Community Ecology

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                Author and article information

                Contributors
                Role: Handling Editor
                Journal
                Curr Zool
                Curr Zool
                czoolo
                Current Zoology
                Oxford University Press (UK )
                1674-5507
                2396-9814
                February 2024
                03 December 2022
                03 December 2022
                : 70
                : 1
                : 34-44
                Affiliations
                Guangxi Key Laboratory of Forest Ecology and Conservation, College of Forestry, Guangxi University , Nanning 530004, China
                Kunming Natural History Museum of Zoology, Kunming Institute of Zoology, Chinese Academy of Sciences , Kunming 650223, China
                Nature Conservation Unit, Frederick University , 7, Yianni Frederickou Street, Pallouriotissa, Nicosia 1036, Cyprus
                State Key Laboratory of Vegetation and Environmental Change, Institute of Botany, Chinese Academy of Sciences , Beijing 100093, China
                Florida Museum of Natural History, University of Florida , Gainesville, FL 34201, USA
                Department of Biology, University of Florida , Gainesville, FL 34201, USA
                School of Life Science and Institute of Wetland Ecology, Nanjing University , Nanjing 210000, China
                Department of Biology, University of Florida , Gainesville, FL 34201, USA
                Department of Biology, University of Florida , Gainesville, FL 34201, USA
                State Key Laboratory of Biocontrol, School of Ecology, Sun-Yatsen University , Guangzhou 510275, China
                Florida Museum of Natural History, University of Florida , Gainesville, FL 34201, USA
                Guangxi Key Laboratory of Forest Ecology and Conservation, College of Forestry, Guangxi University , Nanning 530004, China
                Department of Health and Environmental Science, Xi’an Jiaotong Liverpool University , Suzhou 215123, China
                Author notes
                Address correspondence to Liping Zhou and Eben Goodale. E-mail: zhou.lp@ 123456outlook.com , zhouliping@ 123456mail.kiz.ac.cn (L.Z.)
                Author information
                https://orcid.org/0000-0001-7750-7262
                https://orcid.org/0000-0003-1747-175X
                https://orcid.org/0000-0002-7655-5761
                https://orcid.org/0000-0002-2669-3285
                https://orcid.org/0000-0002-8292-5263
                https://orcid.org/0000-0003-1643-5212
                https://orcid.org/0000-0001-5449-5481
                https://orcid.org/0000-0003-4580-5518
                https://orcid.org/0000-0003-1321-4924
                https://orcid.org/0000-0003-3403-2847
                Article
                zoac096
                10.1093/cz/zoac096
                10926261
                38476134
                e11a0905-4f54-4f7e-9531-dc5df6b3f60d
                © The Author(s) 2022. Published by Oxford University Press on behalf of Editorial Office, Current Zoology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License ( https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 20 May 2022
                : 24 November 2022
                : 16 February 2023
                Page count
                Pages: 11
                Funding
                Funded by: Guangxi University, DOI 10.13039/501100012253;
                Award ID: A3360051014
                Award ID: A3360051010
                Funded by: Guangxi Key Laboratory of Forest Ecology and Conservation;
                Award ID: AE33600102
                Categories
                Original Articles
                AcademicSubjects/SCI01080
                AcademicSubjects/SCI01130
                AcademicSubjects/SCI01130

                co-evolution,interaction networks,mixed-species animal groups,phenotypic similarity,trait convergence

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