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Ecology Letters · 2025 · Vol. 28 · Issue 12 · Wiley
Proximity to natural habitat is known to enhance pollination services in large‐scale agriculture, but it remains unclear whether this holds in tropical smallholder farms. These systems are embedded in ecologically complex landscapes, central to global food security, and depend heavily on biodiversity‐derived ecosystem services. We conducted a systematic review and meta‐analysis of 35 studies assessing the relationship between...
Ecology Letters · 2025 · Vol. 28 · Issue 6 · Wiley
Global change will create new species interactions and alter or eliminate existing ones, a process known as interaction rewiring. This rewiring can significantly affect how ecosystems function. To better predict the future structure of ecological networks, assessing their ability to adapt to changes is crucial. Here, we introduce two concepts: ‘rewiring capacity’ of a single species (the multidimensional trait space of all its...
Ecology Letters · 2025 · Vol. 28 · Issue 1 · Wiley
Biotic interactions play an important role in species diversification and maintenance and, thus, are regarded as the architecture of biodiversity. Since Darwin and Wallace, biologists have debated whether biotic interactions are stronger towards the tropics and on continents, when compared to temperate regions and islands. Here, based on 354 avian frugivory networks accounting for 22,199 interactions between 1247 bird species...
Trends in Ecology & Evolution · 2024 · Vol. 39 · Issue 7 · Elsevier Current Trends
Aoife Leonard; Javier Abalos; Titus Adhola; Windsor Aguirre; Ostaizka Aizpurua; Shahzad Ali; Franco Andreone; Fabien Aubret; Hefer D. Ávila-Palma; Lizbeth Fabiola Bautista Alcantara; Juan F. Beltrán; Rachel Berg; Thomas Bjørneboe Berg; Sandro Bertolino; Daniel T. Blumstein; Bazartseren Boldgiv; Zbigniew Borowski; Jean Philippe Boubli; Sven Büchner; Carlos Cabido; Carlos Camacho; Juan C. Chaparro; Anne Charmantier; Guillermo D'Elía; Luis P. da Silva; Bo Dalsgaard; Christophe de Franceschi; Ferran de la Cruz; Noé U. de la Sancha; Mathieu Denoël; Raphael Eisenhofer; Nathalie Feiner; Joana M. Fernandes; Jordi Figuerola; Leonida Fusani; Laura Gangoso; Roberto García-Roa; Stefania Gasperini; Nanna Gaun; M. Thomas; P. Gilbert; Ivan Gomez-Mestre; Gary R. Graves; Jim Groombridge; Emilie A. Hardouin; Mauricio Hernández; L. Gerardo Herrera M.; Kathy Hodder; Peter A. Hosner; Natali Hurtado; Javier Juste; Sarah C.L. Knowles; Kevin D. Kohl; Carmi Korine; Yurii V. Kornilev; Stephanie Kramer-Schadt; Xavier Lambin; Ella Z. Lattenkamp; Jonas Lauritsen; Guoliang Li; Celeste María López; Adrià López Baucells; Tali Magory Cohen; Emiliano Manzo; Mélanie Marteau; Lynn B. Martin; Garazi Martin Bideguren; Maria Vittoria Mazzamuto; Ara Monadjem; Pirmin Nietlisbach; Daniel Bilyeli Øksnebjerg; Jasmin G. Packer; Michael L. Pepke; Juan M. Peralta-Sánchez; Adrián Perdomo; Guillem Pérez i de Lanuza; Carlotta Pietroni; Mathilde Poyet; Carsten Rahbek; Thiruvarangan Ramaraj; Yuliaxis Ramayo Caldas; Orly Razgour; Hugo Rebelo; Jiří Reif; Rebecca Rimbach; Ricardo Rocha; Rita G. Rocha; Carlos Rodríguez Fernandes; Claudia Romeo; Suvi Ruuskanen; Scott K. Sakaluk; Francesca Santicchia; Tom Sarraude; Rune Sørås; Martina Spada; Michael A. Steele; Mason R. Stothart; Emina Sunje; Alex O. Sutton; Marta Szulkin; Yu Takahata; Charles F. Thompson; Kasper Thorup; Geizecler Tomazetto; Laura Torrent; Nia Toshkova; Claudia Tranquillo; Manfredo Alejandro Turcios-Casco; Tobias Uller; Isolde van Riemsdijk; Guillermo Velo-Antón; Goedele Verbeylen; Elin Videvall; Christian C. Voigt; Lucas A. Wauters; Maren Wellenreuther; Alexey Yanchukov; Antton Alberdi
Ecology · 2024 · Vol. 105 · Issue 2 · Wiley
Seed dispersal by frugivorous birds facilitates plant invasions, but it is poorly known how invasive plants integrate into native communities in fragmented landscapes. We surveyed plant–frugivore interactions, including an invasive plant ( Phytolacca americana ), on 22 artificial land‐bridge islands (fragmented forests) in the Thousand Island Lake, China. Focusing on frugivory interactions that may lead to seed dispersal, we b...
Ecology · 2022 · Vol. 103 · Issue 3 · Wiley
Alfonso Allen‐Perkins; Ainhoa Magrach; Matteo Dainese; Lucas A. Garibaldi; David Kleijn; Romina Rader; James R. Reilly; Rachael Winfree; Ola Lundin; Carley M. McGrady; Claire Brittain; David J. Biddinger; Derek R. Artz; Elizabeth Elle; George Hoffman; James D. Ellis; Jaret Daniels; Jason Gibbs; Joshua W. Campbell; Julia Brokaw; Julianna K. Wilson; Keith Mason; Kimiora L. Ward; Knute B. Gundersen; Kyle Bobiwash; Larry Gut; Logan M. Rowe; Natalie K. Boyle; Neal M. Williams; Neelendra K. Joshi; Nikki Rothwell; Robert L. Gillespie; Rufus Isaacs; Shelby J. Fleischer; Stephen S. Peterson; Sujaya Rao; Theresa L. Pitts‐Singer; Thijs Fijen; Virginie Boreux; Maj Rundlöf; Blandina Felipe Viana; Alexandra‐Maria Klein; Henrik G. Smith; Riccardo Bommarco; Luísa G. Carvalheiro; Taylor H. Ricketts; Jaboury Ghazoul; Smitha Krishnan; Faye E. Benjamin; João Loureiro; Sílvia Castro; Nigel E. Raine; Gerard Arjen de Groot; Finbarr G. Horgan; Juliana Hipólito; Guy Smagghe; Ivan Meeus; Maxime Eeraerts; Simon G. Potts; Claire Kremen; Daniel García; Marcos Miñarro; David W. Crowder; Gideon Pisanty; Yael Mandelik; Nicolas J. Vereecken; Nicolas Leclercq; Timothy Weekers; Sandra A. M. Lindstrom; Dara A. Stanley; Carlos Zaragoza‐Trello; Charlie C. Nicholson; Jeroen Scheper; Carlos Rad; Evan A. N. Marks; Lucie Mota; Bryan Danforth; Mia Park; Antônio Diego M. Bezerra; Breno M. Freitas; Rachel E. Mallinger; Fabiana Oliveira da Silva; Bryony Willcox; Davi L. Ramos; Felipe D. da Silva e Silva; Amparo Lázaro; David Alomar; Miguel A. González‐Estévez; Hisatomo Taki; Daniel P. Cariveau; Michael P. D. Garratt; Diego N. Nabaes Jodar; Rebecca I. A. Stewart; Daniel Ariza; Matti Pisman; Elinor M. Lichtenberg; Christof Schüepp; Felix Herzog; Martin H. Entling; Yoko L. Dupont; Charles D. Michener; Gretchen C. Daily; Paul R. Ehrlich; Katherine L. W. Burns; Montserrat Vilà; Andrew Robson; Brad Howlett; Leah Blechschmidt; Frank Jauker; Franziska Schwarzbach; Maike Nesper; Tim Diekötter; Volkmar Wolters; Helena Castro; Hugo Gaspar; Brian A. Nault; Isabelle Badenhausser; Jessica D. Petersen; Teja Tscharntke; Vincent Bretagnolle; D. Susan Willis Chan; Natacha Chacoff; Georg K. S. Andersson; Shalene Jha; Jonathan F. Colville; Ruan Veldtman; Jeferson Coutinho; Felix J. J. A. Bianchi; Louis Sutter; Matthias Albrecht; Philippe Jeanneret; Yi Zou; Anne L. Averill; Agustin Saez; Amber R. Sciligo; Carlos H. Vergara; Elias H. Bloom; Elisabeth Oeller; Ernesto I. Badano; Gregory M. Loeb; Heather Grab; Johan Ekroos; Vesna Gagic; Saul A. Cunningham; Jens Åström; Pablo Cavigliasso; Alejandro Trillo; Alice Classen; Alice L. Mauchline; Ana Montero‐Castaño; Andrew Wilby; Ben A. Woodcock; C. Sheena Sidhu; Ingolf Steffan‐Dewenter; Ioannis N. Vogiatzakis; José M. Herrera; Mark Otieno; Mary W. Gikungu; Sarah J. Cusser; Thomas Nauss; Lovisa Nilsson; Jessica Knapp; Jorge J. Ortega‐Marcos; José A. González; Juliet L. Osborne; Rosalind Blanche; Rosalind F. Shaw; Violeta Hevia; Jane Stout; Anthony D. Arthur; Betina Blochtein; Hajnalka Szentgyorgyi; Jin Li; Margaret M. Mayfield; Michał Woyciechowski; Patrícia Nunes‐Silva; Rosana Halinski de Oliveira; Steve Henry; Benno I. Simmons; Bo Dalsgaard; Katrine Hansen; Tuanjit Sritongchuay; Alison D. O'Reilly; Fermín José Chamorro García; Guiomar Nates Parra; Camila Magalhães Pigozo; Ignasi Bartomeus
Seventy five percent of the world's food crops benefit from insect pollination. Hence, there has been increased interest in how global change drivers impact this critical ecosystem service. Because standardized data on crop pollination are rarely available, we are limited in our capacity to understand the variation in pollination benefits to crop yield, as well as to anticipate changes in this service, develop predictions, and...
Ecology · 2020 · Vol. 101 · Issue 11 · Wiley
Species phenology plays a key role in determining mutualistic interactions, such as those between plants and pollinators. Notably, temporal synchrony shapes the patterns of interactions by influencing the probability of encounters between interacting partners; thus, species phenology greatly contributes to structuring ecological communities. In these communities, specialized species are expected to show a high level of synchro...
Journal of Biogeography · 2018 · Vol. 45 · Issue 8 · Wiley
Aim We examined the effects of space, climate, phylogeny and species traits on module composition in a cross‐biomes plant–hummingbird network. Location Brazil, except Amazonian region. Methods We compiled 31 local binary plant–hummingbird networks, combining them into one cross‐biomes metanetwork. We conducted a modularity analysis and tested the relationship between species’ module membership with traits, geographical locatio...
Journal of Biogeography · 2017 · Vol. 44 · Issue 8 · Wiley
Aim Among the world's three major nectar‐feeding bird taxa, hummingbirds are the most phenotypically specialized for nectarivory, followed by sunbirds, while the honeyeaters are the least phenotypically specialized taxa. We tested whether this phenotypic specialization gradient is also found in the interaction patterns with their floral resources. Location Americas, Africa, Asia and Oceania/Australia. Methods We compiled inter...
Global Ecology and Biogeography · 2015 · Vol. 24 · Issue 11 · Wiley
Aim To investigate the association between hummingbird–plant network structure and species richness, phylogenetic signal on species' interaction pattern, insularity and historical and current climate. Location Fifty‐four communities along a c . 10,000 km latitudinal gradient across the A mericas (39° N –32° S ), ranging from sea level to c . 3700 m a.s.l., located on the mainland and on islands and covering a wide range of cli...
Global Ecology and Biogeography · 2015 · Vol. 24 · Issue 3 · Wiley
Aim We aim to characterize the macroecological patterns in the structure of mutualistic seed‐dispersal networks. Tropical areas hold more species than temperate ones. This difference in species number may favour ecological processes that minimize interspecific competition in species‐rich areas. There is theoretical evidence that both modularity (i.e. the presence of semi‐independent groups of highly interacting species) and ne...
Environmental Microbiology · 2014 · Vol. 16 · Issue 10 · Wiley
Summary We investigated anammox, denitrification and dissimilatory reduction of nitrite to ammonium ( DNRA ) activity in the E astern T ropical S outh P acific oxygen minimum zone ( OMZ ) off northern C hile, at high‐depth resolution through the oxycline into the anoxic OMZ core. This was accompanied by high‐resolution nutrient and oxygen profiles to link changes in nitrogen transformation rates to physicochemical characterist...
Ecology Letters · 2014 · Vol. 17 · Issue 4 · Wiley
Modularity is a recurrent and important property of bipartite ecological networks. Although well‐resolved ecological networks describe interaction frequencies between species pairs, modularity of bipartite networks has been analysed only on the basis of binary presence–absence data. We employ a new algorithm to detect modularity in weighted bipartite networks in a global analysis of avian seed‐dispersal networks. We define rol...
Ecology Letters · 2013 · Vol. 16 · Issue 5 · Wiley
How many dimensions (trait‐axes) are required to predict whether two species interact? This unanswered question originated with the idea of ecological niches, and yet bears relevance today for understanding what determines network structure. Here, we analyse a set of 200 ecological networks, including food webs, antagonistic and mutualistic networks, and find that the number of dimensions needed to completely explain all inter...
Limnology and Oceanography · 2012 · Vol. 57 · Issue 5 · Wiley
We quantified the removal of fixed nitrogen as N 2 production by anammox and N 2 and N 2 O production by denitrification over a distance of 1900 km along the coasts of Chile and Peru, using short‐term incubations with 15 N‐labeled substrates. The eastern South Pacific contains an oxygen minimum zone (OMZ) characterized by an anoxic, nitrate‐ and nitrite‐rich layer of ∼ 200‐m thickness below 30–90 m of oxic water. Anammox and d...