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social networks are descriptions of social structure which, aside from their intrinsic interest for understanding sociality, can have significant bearing across many fields of biology.\u003C\u002Fjats:p>\n\u003C\u002Fjats:list-item>\n\n\u003Cjats:list-item>\n\u003Cjats:p>Network analysis provides a flexible toolbox for testing a broad range of hypotheses, and for describing the social system of species or populations in a quantitative and comparable manner. However, it requires careful consideration of underlying assumptions, in particular differentiating real from observed networks and controlling for inherent biases that are common in social data.\u003C\u002Fjats:p>\n\u003C\u002Fjats:list-item>\n\n\u003Cjats:list-item>\n\u003Cjats:p>We provide a practical guide for using this framework to analyse animal social systems and test hypotheses. First, we discuss key considerations when defining nodes and edges, and when designing methods for collecting data. We discuss different approaches for inferring social networks from these data and displaying them. We then provide an overview of methods for quantifying properties of nodes and networks, as well as for testing hypotheses concerning network structure and network processes. Finally, we provide information about assessing the power and accuracy of an observed network.\u003C\u002Fjats:p>\n\u003C\u002Fjats:list-item>\n\n\u003Cjats:list-item>\n\u003Cjats:p>Alongside this manuscript, we provide appendices containing background information on common programming routines and worked examples of how to perform network analysis using the \u003Cjats:sc>\u003Cjats:italic>r\u003C\u002Fjats:italic>\u003C\u002Fjats:sc> programming language.\u003C\u002Fjats:p>\n\u003C\u002Fjats:list-item>\n\n\u003Cjats:list-item>\n\u003Cjats:p>We conclude by discussing some of the major current challenges in social network analysis and interesting future directions. 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It has been proposed that a similar mechanism could apply to carnivorous predators too, although the evidence is still lacking.\u003C\u002Fjats:p>\u003Cjats:p>\u003Cjats:bold>2.\u003C\u002Fjats:bold> Here, we show that the differentiation of biotypes of specialized ant‐eating spiders of the genus\u003Cjats:italic>Zodarion\u003C\u002Fjats:italic>has probably been induced by prey‐shifting. We focused on two forms of one species\u003Cjats:italic>Z. styliferum\u003C\u002Fjats:italic>from the Iberian Peninsula that presumably represent ecological races. We conducted geographic, ecological, venom‐oriented, reproductive and genetic divergence analysis among multiple populations collected at a number of sites across Portugal and Madeira.\u003C\u002Fjats:p>\u003Cjats:p>\u003Cjats:bold>3.\u003C\u002Fjats:bold> Geographic analysis revealed that the two forms occur in mosaic sympatry. Each form was found to associate in nature with a different ant species in a different habitat. Specifically, the\u003Cjats:italic>styliferum\u003C\u002Fjats:italic>form hunted predominantly\u003Cjats:italic>Messor\u003C\u002Fjats:italic>ants, and the\u003Cjats:italic>extraneum\u003C\u002Fjats:italic>form hunted mainly\u003Cjats:italic>Camponotus\u003C\u002Fjats:italic>ants. Laboratory experiments revealed that the two forms exhibit a significant preference for attacking focal ants, demonstrating higher paralysis efficiency, and also show different venom composition. Cross‐mating of the two forms was significantly less likely than between pairs of the same form, suggesting moderate assortative mating. Phylogenetic analyses indicate low genetic differentiation of the two forms and parallel‐repeated evolution of biotypes.\u003C\u002Fjats:p>\u003Cjats:p>\u003Cjats:bold>4.\u003C\u002Fjats:bold> Adaptive prey‐shifting correlated with habitat preference are at present the most valid explanations for biotype formation in\u003Cjats:italic>Zodarion\u003C\u002Fjats:italic>. The speciation of ant‐eating\u003Cjats:italic>Zodarion\u003C\u002Fjats:italic>spiders thus appears to follow a scenario similar to that of host‐shifting in parasites and herbivores.\u003C\u002Fjats:p>",{"EN":1345},"Prey‐race drives differentiation of biotypes in ant‐eating 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southern forms of Phidippus audax (Hentz) (Araneida, Salticidae), Journal of Arachnology, 2, 89",{},{"id":24,"text":1830,"url":24,"identifiers":1831},"10.1046\u002Fj.1365-294X.2002.01529.x",{"doi":1830},{"id":24,"text":1833,"url":24,"identifiers":1834},"10.1038\u002Fnature05857",{"doi":1833},{"id":24,"text":1836,"url":24,"identifiers":1837},"10.1046\u002Fj.1420-9101.2001.00335.x",{"doi":1836},{"id":24,"text":1839,"url":24,"identifiers":1840},"10.1002\u002Fsim.1650",{"doi":1839},{"id":1842,"createTime":1843,"updateTime":1844,"relativeEntities":1845,"slug":1846,"properties":1847,"entityType":158,"verifyStatus":396,"verifyTime":1843,"verifyNote":397,"languages":1864,"translateLanguages":1865,"viewCount":25,"primaryUrl":1866,"fullTextUrl":24,"authors":1867,"publicationType":205,"publisherRelationship":1885,"citationCount":1939,"citationInfo":1940,"publishDate":1948,"publishYear":1941,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":1949,"openAccess":24,"references":1950,"isForceReanalyzing":374},"5e9c0955-e46b-4d34-abf3-a0d61e673235","2025-01-24T03:17:20.571+00:00","2025-02-09T23:02:13.370+00:00",[],"Linking-movement-behaviour-dispersal-and-population-processes-is-individual-variation-a-key-",{"mag":1848,"keywords":1850,"openalex":1852,"abstract":1854,"title":1857,"pm":1860,"doi":1862},{"VOID":1849},"2159798876",{"VI":1851},"di chuyển, phân tán, quần thể, sự biến đổi cá nhân",{"VOID":1853},"W2159798876",{"EN":1855,"VI":1856},"\u003Cjats:title>Summary\u003C\u002Fjats:title>\u003Cjats:p>\u003Cjats:list list-type=\"explicit-label\">\u003Cjats:list-item>\u003Cjats:p>Movement behaviour has become increasingly important in dispersal ecology and dispersal is central to the development of spatially explicit population ecology. The ways in which the elements have been brought together are reviewed with particular emphasis on dispersal distance distributions and the value of mechanistic models.\u003C\u002Fjats:p>\u003C\u002Fjats:list-item>\u003Cjats:list-item>\u003Cjats:p>There is a continuous range of movement behaviours and in some species, dispersal is a clearly delineated event but not in others. The biological complexities restrict conclusions to high‐level generalizations but there may be principles that are common to dispersal and other movements.\u003C\u002Fjats:p>\u003C\u002Fjats:list-item>\u003Cjats:list-item>\u003Cjats:p>Random walk and diffusion models when appropriately elaborated can provide an understanding of dispersal distance relationships on spatial and temporal scales relevant to dispersal. Leptokurtosis in the relationships may be the result of a combination of factors including population heterogeneity, correlation, landscape features, time integration and density dependence. The inclusion in diffusion models of individual variation appears to be a useful elaboration. The limitations of the negative exponential and other phenomenological models are discussed.\u003C\u002Fjats:p>\u003C\u002Fjats:list-item>\u003Cjats:list-item>\u003Cjats:p>The dynamics of metapopulation models are sensitive to what appears to be small differences in the assumptions about dispersal. In order to represent dispersal realistically in population models, it is suggested that phenomenological models should be replaced by those based on movement behaviour incorporating individual variation.\u003C\u002Fjats:p>\u003C\u002Fjats:list-item>\u003Cjats:list-item>\u003Cjats:p>The conclusions are presented as a set of candidate principles for evaluation. The main features of the principles are that uncorrelated or correlated random walk, not linear movement, is expected where the directions of habitat patches are unpredictable and more complex behaviour when organisms have the ability to orientate or navigate. Individuals within populations vary in their movement behaviour and dispersal; part of this variation is a product of random elements in movement behaviour and some of it is heritable. Local and metapopulation dynamics are influenced by population heterogeneity in dispersal characteristics and heritable changes in dispersal propensity occur on time‐scales short enough to impact population dynamics.\u003C\u002Fjats:p>\u003C\u002Fjats:list-item>\u003C\u002Fjats:list>\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>\u003Cjats:list list-type=\"explicit-label\">\u003Cjats:list-item>\u003Cjats:p>Hành vi di chuyển đã trở thành yếu tố ngày càng quan trọng trong sinh học phân tán và sự phân tán là trung tâm của sự phát triển sinh thái quần thể không gian. Cách thức mà các yếu tố được kết hợp đã được xem xét với trọng tâm đặc biệt vào phân phối khoảng cách phân tán và giá trị của các mô hình cơ chế.\u003C\u002Fjats:p>\u003C\u002Fjats:list-item>\u003Cjats:list-item>\u003Cjats:p>Có một loạt hành vi di chuyển liên tục và ở một số loài, sự phân tán là một sự kiện được phân định rõ ràng nhưng không ở những loài khác. Các phức tạp sinh học hạn chế các kết luận chỉ ở các tổng quát cấp cao nhưng có thể tồn tại những nguyên lý chung cho sự phân tán và các chuyển động khác.\u003C\u002Fjats:p>\u003C\u002Fjats:list-item>\u003Cjats:list-item>\u003Cjats:p>Các mô hình đi bộ ngẫu nhiên và khuếch tán khi được mở rộng một cách thích hợp có thể cung cấp hiểu biết về mối quan hệ khoảng cách phân tán trên các tỷ lệ không gian và tạm thời liên quan đến sự phân tán. Hệ số leptokurtosis trong các mối quan hệ có thể là kết quả của một sự kết hợp các yếu tố bao gồm sự không đồng nhất của quần thể, tương quan, đặc điểm cảnh quan, tích hợp thời gian và sự phụ thuộc vào mật độ. Việc bao gồm sự biến đổi cá nhân trong các mô hình khuếch tán dường như là một sự mở rộng hữu ích. Những hạn chế của mô hình hàm mũ âm và các mô hình hiện tượng khác được thảo luận.",{"EN":1858,"VI":1859},"Linking movement behaviour, dispersal and population processes: is individual variation a key?","Liên kết hành vi di chuyển, sự phân tán và các quá trình quần thể: liệu sự biến đổi cá nhân có phải là yếu tố quyết định?",{"VOID":1861},"19302396",{"VOID":1863},"10.1111\u002Fj.1365-2656.2009.01534.x",[161],[163],"https:\u002F\u002Fbesjournals.onlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.1365-2656.2009.01534.x",[1868],{"id":1869,"sortIndex":25,"researcher":24,"roles":1870,"affiliations":1871,"properties":1880,"displayName":1882,"givenName":24,"familyName":24},"c248954c-23d2-403f-bb12-62933ef5ff6f",[],[1872],{"id":1873,"sortIndex":25,"affiliation":1874,"properties":24},"2e1c8022-8346-498c-b4c2-d7a83784ea16",{"id":1873,"createTime":24,"updateTime":24,"relativeEntities":1875,"slug":24,"properties":1876,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1879,"statistic":24},[],{"title":1877},{"EN":1878},"School of Life Sciences, University of the West of England, Bristol BS16 1QY, UK",[],{"title":1881,"openalex":1883},{"EN":1882},"C. 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\u003Cjats:bold>1.\u003C\u002Fjats:bold> Life history theoreticians have traditionally assumed that juvenile growth rates are maximized and that variation in this trait is due to the quality of the environment. In contrast to this assumption there is a large body of evidence showing that juvenile growth rates may vary adaptively both within and between populations. This adaptive variation implies that high growth rates may be associated with costs.\u003C\u002Fjats:p>\u003Cjats:p> \u003Cjats:bold>2.\u003C\u002Fjats:bold> Here, I explicitly evaluate the often‐proposed trade‐off between growth rate and predation risk, in a study of the temperate butterfly, \u003Cjats:italic>Pararge aegeria\u003C\u002Fjats:italic> (L).\u003C\u002Fjats:p>\u003Cjats:p> \u003Cjats:bold>3.\u003C\u002Fjats:bold> By rearing larvae with a common genetic background in different photoperiods it was possible to experimentally manipulate larval growth rates, which vary in response to photoperiod. Predation risk was assessed by exposing larvae that were freely moving on their host plants to the predatory heteropteran, \u003Cjats:italic>Picromerus bidens\u003C\u002Fjats:italic> (L.).\u003C\u002Fjats:p>\u003Cjats:p> \u003Cjats:bold>4.\u003C\u002Fjats:bold> The rate of predation was significantly higher in the fast‐growing larvae. An approximately four times higher relative growth rate was associated with a 30% higher daily predation risk.\u003C\u002Fjats:p>\u003Cjats:p> \u003Cjats:bold>5.\u003C\u002Fjats:bold> The main result demonstrates a trade‐off between growth rate and predation risk, and there are reasons to believe that this trade‐off is of general significance in free‐living animals. The results also suggest that juvenile development of \u003Cjats:italic>P. aegeria\u003C\u002Fjats:italic> is governed by a strategic decision process within individuals.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p> \u003Cjats:bold>1.\u003C\u002Fjats:bold> Các nhà lý thuyết về lịch sử sinh học truyền thống đã giả định rằng tốc độ tăng trưởng của ấu trùng là tối ưu hóa và rằng sự biến đổi trong đặc điểm này là do chất lượng môi trường. Ngược lại với giả định này, có một lượng lớn bằng chứng cho thấy tốc độ tăng trưởng của ấu trùng có thể thay đổi một cách thích nghi cả trong và giữa các quần thể. Sự biến đổi thích nghi này ngụ ý rằng tốc độ tăng trưởng cao có thể gắn liền với các chi phí.\u003C\u002Fjats:p>\u003Cjats:p> \u003Cjats:bold>2.\u003C\u002Fjats:bold> Tại đây, tôi sẽ đánh giá rõ ràng sự đánh đổi thường được đề xuất giữa tốc độ tăng trưởng và nguy cơ bị thú dữ ăn, trong một nghiên cứu về loài bướm ôn đới, \u003Cjats:italic>Pararge aegeria\u003C\u002Fjats:italic> (L).\u003C\u002Fjats:p>\u003Cjats:p> \u003Cjats:bold>3.\u003C\u002Fjats:bold> Bằng cách nuôi ấu trùng có cùng nền tảng gen trong các chu kỳ ánh sáng khác nhau, tôi đã có thể thao tác một cách thực nghiệm tốc độ tăng trưởng của ấu trùng, điều mà thay đổi theo chu kỳ ánh sáng. Nguy cơ bị thú dữ ăn được đánh giá bằng cách phơi bày ấu trùng đang di chuyển tự do trên cây chủ của chúng với loài chân đầu mối ăn thịt, \u003Cjats:italic>Picromerus bidens\u003C\u002Fjats:italic> (L.).\u003C\u002Fjats:p>\u003Cjats:p> \u003Cjats:bold>4.\u003C\u002Fjats:bold> Tốc độ bị thú dữ ăn cao hơn đáng kể ở những ấu trùng có tốc độ tăng trưởng nhanh. Tốc độ tăng trưởng tương đối cao hơn gấp khoảng bốn lần đi kèm với nguy cơ bị thú dữ ăn hàng ngày cao hơn 30%.\u003C\u002Fjats:p>\u003Cjats:p> \u003Cjats:bold>5.\u003C\u002Fjats:bold> Kết quả chính cho thấy sự đánh đổi giữa tốc độ tăng trưởng và nguy cơ bị thú dữ ăn, và có lý do để tin rằng đánh đổi này có ý nghĩa chung trong các loài động vật sống tự do. Các kết quả cũng gợi ý rằng sự phát triển của ấu trùng \u003Cjats:italic>P. aegeria\u003C\u002Fjats:italic> được điều chỉnh bởi một quá trình quyết định chiến lược trong từng cá thể.\u003C\u002Fjats:p>",{"EN":2374,"VI":2375},"Increased risk of predation as a cost of high growth rate: an experimental test in a butterfly","Tăng nguy cơ bị thú dữ ăn như là chi phí của tốc độ tăng trưởng cao: một thử nghiệm thực nghiệm trên một loài 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list-type=\"explicit-label\">\n\u003Cjats:list-item>\u003Cjats:p>Habitat requirements of solitary bees include nesting sites, food resources and nesting material. We used translocation experiments to establish foraging distances and measured foraging trip duration to analyse how solitary bees cope with the distance between nesting sites and suitable food plants in different habitat types.\u003C\u002Fjats:p>\u003C\u002Fjats:list-item>\n\u003Cjats:list-item>\u003Cjats:p>Maximum foraging distance between nesting site and food patch was 150–600 m for the 16 bee species examined. Foraging distance was correlated positively with body length. Mean foraging trip duration, measured for seven bee species, ranged from 6 to 28 min and was also correlated with body length. In a study of the polylectic species \u003Cjats:italic>Osmia rufa\u003C\u002Fjats:italic>\n              , we found a significant decrease in foraging trip duration with increasing number of plant species. Logistic regressions showed that the oligolectic \n              \u003Cjats:italic>Megachile lapponica\u003C\u002Fjats:italic>\n               nested in trap nests with a probability of 50% if the distance between trap nest and food patch was less than 250 m. The oligolectic \n              \u003Cjats:italic>Chelostoma rapunculi\u003C\u002Fjats:italic> utilized trap nests when the distance to the nearest food patch was less than 300 m.\u003C\u002Fjats:p>\u003C\u002Fjats:list-item>\n\u003Cjats:list-item>\u003Cjats:p>These experiments showed that solitary bees have a rather small foraging range so local habitat structure appears to be of more importance than large‐scale landscape structure. All requirements for sustaining viable populations must be within this range. Therefore, it is necessary to maintain and restore a dense network of habitat patches in landscapes to ensure long‐term sustainability of wild bee diversity and their ecological function as pollinators.\u003C\u002Fjats:p>\u003C\u002Fjats:list-item>\n\u003C\u002Fjats:list>\n\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>\n\u003Cjats:list list-type=\"explicit-label\">\n\u003Cjats:list-item>\u003Cjats:p>Các yêu cầu về môi trường sống của ong đơn độc bao gồm các địa điểm làm tổ, nguồn thực phẩm và vật liệu làm tổ. Chúng tôi đã sử dụng các thí nghiệm chuyển giao để xác định khoảng cách tìm kiếm và đo thời gian chuyến đi tìm kiếm nhằm phân tích cách mà ong đơn độc đối phó với khoảng cách giữa các địa điểm làm tổ và các loại cây thực phẩm phù hợp trong các loại môi trường sống khác nhau.\u003C\u002Fjats:p>\u003C\u002Fjats:list-item>\n\u003Cjats:list-item>\u003Cjats:p>Khoảng cách tìm kiếm tối đa giữa địa điểm làm tổ và khu vực thực phẩm là từ 150–600 m đối với 16 loài ong được nghiên cứu. Khoảng cách tìm kiếm có mối tương quan tích cực với chiều dài cơ thể. Thời gian chuyến đi tìm kiếm trung bình, được đo cho bảy loài ong, dao động từ 6 đến 28 phút và cũng có mối tương quan với chiều dài cơ thể. Trong một nghiên cứu về loài đa thực vật \u003Cjats:italic>Osmia rufa\u003C\u002Fjats:italic>, chúng tôi nhận thấy sự giảm đáng kể thời gian chuyến đi tìm kiếm khi số lượng loài thực vật tăng lên. Các hồi quy logistic cho thấy rằng loài trưởng thành aoligoleptic \u003Cjats:italic>Megachile lapponica\u003C\u002Fjats:italic> làm tổ trong tổ bẫy với xác suất 50% nếu khoảng cách giữa tổ bẫy và khu vực thực phẩm nhỏ hơn 250 m. Loài aoligoleptic \u003Cjats:italic>Chelostoma rapunculi\u003C\u002Fjats:italic> sử dụng tổ bẫy khi khoảng cách đến khu vực thực phẩm gần nhất nhỏ hơn 300 m.\u003C\u002Fjats:p>\u003C\u002Fjats:list-item>\n\u003Cjats:list-item>\u003Cjats:p>Các thí nghiệm này cho thấy rằng ong đơn độc có phạm vi tìm kiếm khá nhỏ, vì vậy cấu trúc môi trường sống địa phương dường như quan trọng hơn cấu trúc cảnh quan quy mô lớn. Tất cả các yêu cầu để duy trì quần thể bền vững phải nằm trong phạm vi này. Do đó, cần thiết phải duy trì và khôi phục một mạng lưới dày đặc các khu vực môi trường sống trong các cảnh quan để đảm bảo tính bền vững lâu dài của sự đa dạng của ong hoang dã và chức năng sinh thái của chúng như những người thụ phấn.\u003C\u002Fjats:p>\u003C\u002Fjats:list-item>\n\u003C\u002Fjats:list>\n\u003C\u002Fjats:p>",{"EN":2850,"VI":2851},"Foraging ranges of solitary bees","Phạm vi tìm kiếm của ong đơn độc",{"VI":2367},{"VOID":2854},"10.1046\u002Fj.1365-2656.2002.00641.x",[161],[163],"https:\u002F\u002Fbesjournals.onlinelibrary.wiley.com\u002Fdoi\u002F10.1046\u002Fj.1365-2656.2002.00641.x",[2859,2876],{"id":2860,"sortIndex":25,"researcher":24,"roles":2861,"affiliations":2862,"properties":2871,"displayName":2873,"givenName":24,"familyName":24},"e4aef331-c81e-4655-aa01-bf6732910ee0",[],[2863],{"id":2864,"sortIndex":25,"affiliation":2865,"properties":24},"8603faa1-febd-44db-b428-027049cba34a",{"id":2864,"createTime":24,"updateTime":24,"relativeEntities":2866,"slug":24,"properties":2867,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":2870,"statistic":24},[],{"title":2868},{"VI":2869},"Agroecology, University of Göttingen, Waldweg 26, D-37073 Göttingen, Germany",[],{"title":2872,"openalex":2874},{"EN":2873},"Achim 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