Abstract
Worldwide, with the decline of natural habitats, species with reduced niche breadth (specialists) are at greater risk of extinction as they cannot colonise or persist in disturbed habitat types. However, the role of thermal tolerance as a critical trait in understanding changes in species diversity in disturbed habitats, e.g., due to forest replacement by tree plantations, is still understudied. To examine the role of thermal tolerance on the responses of specialist and generalist species to habitat disturbances, we measured and compared local temperature throughout the year and thermotolerance traits [upper (CTmax) and lower (CTmin) thermal limits] of the most abundant species of spiders from different guilds inhabiting pine tree plantations and native Atlantic Forests in South America. Following the thermal adaptation hypothesis, we predicted that generalist species would show a wider thermal tolerance range (i.e., lower CTmin and higher CTmax) than forest specialist species. As expected, generalist species showed significantly higher CTmax and lower CTmin values than specialist species with wider thermal tolerance ranges than forest specialist species. These differences are more marked in orb weavers than in aerial hunter spiders. Our study supports the specialisation disturbance and thermal hypotheses. It highlights that habitat-specialist species are more vulnerable to environmental changes associated with vegetation structure and microclimatic conditions. Moreover, thermal tolerance is a key response trait to explain the Atlantic Forest spider's ability (or inability) to colonise and persist in human-productive land uses.
Similar content being viewed by others
Availability of data and materials
The data was deposited in figshare under the reference number https://figshare.com/s/9418a4b359e9122a5594.
Code availability
Not applicable.
References
Abram PK, Boivin G, Moiroux J, Brodeur J (2017) Behavioural effects of temperature on ectothermic animals: unifying thermal physiology and behavioural plasticity. Biol Rev 92(4):1859–1876. https://doi.org/10.1111/brv.12312
Angilletta MJ Jr (2009) Thermal adaptation: a theoretical and empirical synthesis. Oxford University Press, Oxford. https://doi.org/10.1093/acprof:oso/9780198570875.001.1
Angilletta MJ, Niewiarowski PH, Navas CA (2002) The evolution of thermal physiology in ectotherms. J Therm Biol 27(4):249–268. https://doi.org/10.1016/S0306-4565(01)00094-8
Anthony SE, Buddle CM, Høye TT, Hein N, Sinclair BJ (2021) Thermal acclimation has limited effect on the thermal tolerances of summer-collected Arctic and sub-Arctic wolf spiders. Comp Biochem Physiol A Mol Integr Physiol 257:110974. https://doi.org/10.1016/j.cbpa.2021.110974
Aratrakorn S, Thunhikorn S, Donald PF (2006) Changes in bird communities following conversion of lowland forest to oil palm and rubber plantations in southern Thailand. Bird Conserv Int 16(1):71–82. https://doi.org/10.1017/S0959270906000062
Araújo MB, Ferri-Yáñez F, Bozinovic F, Marquet PA, Valladares F, Chown SL (2013) Heat freezes niche evolution. Ecol Lett 16(9):1206–1219. https://doi.org/10.1111/ele.12155
Barahona-Segovia RM, Crespin SJ, Grez AA, Veloso C (2019) Anthropogenic thermal gradient in managed landscapes determines physiological performance and explains the edge-biased distribution of ectothermic arthropods. For Ecol Manage 440:147–157. https://doi.org/10.1016/j.foreco.2019.03.018
Barahona-Segovia RM, Grez AA, Veloso C (2022) Forestry clear-cuts increase environmental temperatures, affecting the ecophysiological responses of specialised beetles in fragmented landscapes. J Appl Entomol 146(5):557–569. https://doi.org/10.1111/jen.12980
Bates D, Mächler M, Bolker B, Walker S (2015) Fitting linear mixed-effects models using lme4. J Stat Softw 67:1–48. https://doi.org/10.18637/jss.v067.i01
Belliard SA, De la Vega GJ, Schilman PE (2019) Thermal tolerance plasticity in chagas disease vectors Rhodnius prolixus (Hemiptera: Reduviidae) and Triatoma infestans. J Med Entomol 56(4):997–1003. https://doi.org/10.1093/jme/tjz022
Benamú MA, Lacava M, García LF, Santana M, Viera C (2017) Spiders associated with agroecosystems: roles and perspectives. In: Viera C, Gonzaga MO (eds) Behaviour and ecology of spiders: contributions from the neotropical region. Springer, Berlin, pp 275–302. https://doi.org/10.1007/978-3-319-65717-2_11
Bogert CM (1949) Thermoregulation in reptiles, a factor in evolution. Evolution 3(3):195–211. https://doi.org/10.2307/2405558
Bota-Sierra CA, García-Robledo C, Escobar F, Novelo-Gutiérrez R, Londoño GA (2022) Environment, taxonomy and morphology constrain insect thermal physiology along tropical mountains. Funct Ecol 36:1924–1935. https://doi.org/10.1111/1365-2435.14083
Brescovit AD (1996) Revisão de Anyphaeninae Bertkau a nível de gêneros na Região Neotropical (Araneae, Anyphaenidae). Rev Brasil Zool 13:1–187. https://doi.org/10.1590/S0101-81751996000500001
Brown JH. On the relationship between abundance and distribution of species. Am Natl. 1984;124(2):255–279. http://www.jstor.org/stable/2461494
Bujan J, Roeder KA, de Beurs K, Weiser MD, Kaspari M (2020) Thermal diversity of North American ant communities: cold tolerance but not heat tolerance tracks ecosystem temperature. Glob Ecol Biogeogr 29:1486–1494. https://doi.org/10.1111/geb.13121
Chichorro F, Urbano F, Teixeira D, Väre H, Pinto T, Brummitt N, He X, Hochkirch A, Hyvönen J, Kaila L, Juslén A, Cardoso P (2022) Trait-based prediction of extinction risk across terrestrial taxa. Biol Cons 274:109738. https://doi.org/10.1016/j.biocon.2022.109738
Chown SL, Jumbam KR, Sørensen JG, Terblanche JS (2009) Phenotypic variance, plasticity and heritability estimates of critical thermal limits depend on methodological context. Funct Ecol 23(1):133–140. https://doi.org/10.1111/j.1365-2435.2008.01481.x
Cifuentes-Croquevielle C, Stanton DE, Armesto JJ (2020) Soil invertebrate diversity loss and functional changes in temperate forest soils replaced by exotic pine plantations. Sci Rep 10(1):1. https://doi.org/10.1038/s41598-020-64453-y
Cloudsley-Thompson JL (1983) Desert adaptations in spiders. J Arid Environ 6(4):307–317. https://doi.org/10.1016/S0140-1963(18)31410-1
Costa HCM, Benchimol M, Peres CA (2021) Wild ungulate responses to anthropogenic land use: a comparative pantropical analysis. Mamm Rev 51(4):528–539. https://doi.org/10.1111/mam.12252
de Bello F, Lavorel S, Hallett LM, Valencia E, Garnier E, Roscher C, Conti L, Galland T, Goberna M, Májeková M, Montesinos-Navarro A, Pausas JG, Verdú M, E-Vojtkó A, Götzenberger L, Lepš J (2021) Functional trait effects on ecosystem stability: assembling the jigsaw puzzle. Trends Ecol Evol 36(9):822–836. https://doi.org/10.1016/j.tree.2021.05.001
de la Vega GJ, Medone P, Ceccarelli S, Rabinovich J, Schilman PE (2015) Geographical distribution, climatic variability and thermo-tolerance of Chagas disease vectors. Ecography 38(8):851–860. https://doi.org/10.1111/ecog.01028
de la Vega GJ, Schilman PE (2018) Ecological and physiological thermal niches to understand distribution of Chagas disease vectors in Latin America. Med Vet Entomol 32(1):1–13. https://doi.org/10.1111/mve.12262
Devictor V, Clavel J, Julliard R, Lavergne S, Mouillot D, Thuiller W, Venail P, Villéger S, Mouquet N (2010) Defining and measuring ecological specialization. J Appl Ecol 47(1):15–25. https://doi.org/10.1111/j.1365-2664.2009.01744.x
DeVito J, Meik JM, Gerson MM, Formanowicz DR Jr (2004) Physiological tolerances of three sympatric riparian wolf spiders (Araneae: Lycosidae) correspond with microhabitat distributions. Can J Zool 82(7):1119–1125. https://doi.org/10.1139/z04-090
Dharmarathne WDSC, Herberstein ME (2022) Limitations of sperm transfer in the complex reproductive system of spiders. Biol J Lin Soc 135(3):417–428. https://doi.org/10.1093/biolinnean/blab158
Diamond SE, Chick LD (2018) The Janus of macrophysiology: stronger effects of evolutionary history, but weaker effects of climate on upper thermal limits are reversed for lower thermal limits in ants. Curr Zool 64(2):223–230. https://doi.org/10.1093/cz/zox072
Dias SC, Carvalho LS, Bonaldo AB, Brescovit AD (2009) Refining the establishment of guilds in Neotropical spiders (Arachnida: Araneae). J Nat Hist 44(3–4):219–239. https://doi.org/10.1080/00222930903383503
Díaz S, Purvis A, Cornelissen JHC, Mace GM, Donoghue MJ, Ewers RM, Jordano P, Pearse WD (2013) Functional traits, the phylogeny of function, and ecosystem service vulnerability. Ecol Evol 3(9):2958–2975. https://doi.org/10.1002/ece3.601
Dolný A, Ožana S, Burda M, Harabiš F (2021) Effects of landscape patterns and their changes to species richness, species composition, and the conservation value of Odonates (Insecta). InSects 12(6):6. https://doi.org/10.3390/insects12060478
Durak T, Durak R, Węgrzyn E, Leniowski K (2015) The impact of changes in species richness and species replacement on patterns of taxonomic homogenization in the carpathian forest ecosystems. Forests 6(12):12. https://doi.org/10.3390/f6124376
Ernst R, Rödel M-O (2005) Anthropogenically induced changes of predictability in tropical anuran assemblages. Ecology 86(11):3111–3118. https://doi.org/10.1890/04-0800
Filgueiras BKC, Tabarelli M, Leal IR, Vaz-de-Mello FZ, Iannuzzi L (2015) Dung beetle persistence in human-modified landscapes: combining indicator species with anthropogenic land use and fragmentation-related effects. Ecol Ind 55:65–73. https://doi.org/10.1016/j.ecolind.2015.02.032
Foelix RF (2011) Biology of spiders, 3rd edn. Oxford University Press, Oxford
Fonseca CR, Ganade G, Baldissera R, Becker CG, Boelter CR, Brescovit AD, Campos LM, Fleck T, Fonseca VS, Hartz SM, Joner F, Käffer MI, Leal-Zanchet AM, Marcelli MP, Mesquita AS, Mondin CA, Paz CP, Petry MV, Piovensan FN et al (2009) Towards an ecologically-sustainable forestry in the Atlantic Forest. Biol Conserv 142(6):1209–1219. https://doi.org/10.1016/j.biocon.2009.02.017
Galindo-Leal C, Cãmara I, Sayre D (2003) The Atlantic Forest of South America: biodiversity status, threats, and outlook. Electron Green J. https://doi.org/10.5070/G311910541
Garcia-Robledo C, Chuquillanqui H, Kuprewicz EK, Escobar-Sarria F (2018) Lower thermal tolerance in nocturnal than in diurnal ants: a challenge for nocturnal ectotherms facing global warming. Ecol Entomol 43:162–167. https://doi.org/10.1111/een.12481
Giménez Gómez VC, Verdú JR, Zurita GA (2020) Thermal niche helps to explain the ability of dung beetles to exploit disturbed habitats. Sci Rep 10(1):1. https://doi.org/10.1038/s41598-020-70284-8
Gómez-Cifuentes A, Munevar A, Gimenez VC, Gatti MG, Zurita GA (2017) Influence of land use on the taxonomic and functional diversity of dung beetles (Coleoptera: Scarabaeinae) in the southern Atlantic forest of Argentina. J Insect Conserv 21(1):147–156. https://doi.org/10.1007/s10841-017-9964-4
Gotcha N, Machekano H, Cuthbert RN, Nyamukondiwa C (2021) Low-temperature tolerance in coprophagic beetle species (Coleoptera: Scarabaeidae): implications for ecological services. Ecol Entomol 46:1101–1112. https://doi.org/10.1111/een.13054
Halekoh U, Højsgaard S (2014) A Kenward–Roger approximation and parametric bootstrap methods for tests in linear mixed models—the R package pbkrtest. J Stat Softw 59:1–32. https://doi.org/10.18637/jss.v059.i09
Harvey JA, Dong Y (2023) Climate change, extreme temperatures and sex-related responses in spiders. Biology 12(4):4. https://doi.org/10.3390/biology12040615
Harvey CA, González Villalobos JA (2007) Agroforestry systems conserve species-rich but modified assemblages of tropical birds and bats. Biodivers Conserv 16(8):2257–2292. https://doi.org/10.1007/s10531-007-9194-2
Harvey JA, Tougeron K, Gols R, Heinen R, Abarca M, Abram PK, Basset Y, Berg M, Boggs C, Brodeur J, Cardoso P, de Boer JG, De Snoo GR, Deacon C, Dell JE, Desneux N, Dillon ME, Duffy GA, Dyer LA et al (2023) Scientists’ warning on climate change and insects. Ecol Monogr 93(1):e1553. https://doi.org/10.1002/ecm.1553
Hoffmann AA, Sgrò CM (2018) Comparative studies of critical physiological limits and vulnerability to environmental extremes in small ectotherms: how much environmental control is needed? Integr Zool 13(4):355–371. https://doi.org/10.1111/1749-4877.12297
Huey RB, Kingsolver JG (1989) Evolution of thermal sensitivity of ectotherm performance. Trends Ecol Evol 4(5):131–135. https://doi.org/10.1016/0169-5347(89)90211-5
Humphreys WF (1987) Behavioural temperature regulation. In: Nentwig EW (ed) Ecophysiology of spiders. Springer, Berlin, pp 56–65. https://doi.org/10.1007/978-3-642-71552-5_4
Ives A, Dinnage R, Nell LA, Helmus M, Li D (2023) phyr: Model Based Phylogenetic Analysis. https://daijiang.github.io/phyr/, https://github.com/daijiang/phyr/
Jocqué R, Dippenaar-Schoeman AS (2006) Spider families of the world. Musée Royal de l’Afrique Central, Tervuren
Jumbam KR, Terblanche JS, Deere JA, Somers MJ, Chown SL (2008) Critical thermal limits and their responses to acclimation in two sub-Antarctic spiders: Myro kerguelenensis and Prinerigone vagans. Polar Biol 31(2):215–220. https://doi.org/10.1007/s00300-007-0349-0
Kaspari M, Clay NA, Lucas J, Yanoviak SP, Kay A (2015) Thermal adaptation generates a diversity of thermal limits in a rainforest ant community. Glob Change Biol 21(3):1092–1102. https://doi.org/10.1111/gcb.12750
Kaspari M, Clay NA, Lucas J, Revzen S, Kay A, Yanoviak SP (2016) Thermal adaptation and phosphorus shape thermal performance in an assemblage of rainforest ants. Ecology 97:1038–1047. https://doi.org/10.1890/15-1225.1
Kovács B, Tinya F, Ódor P (2017) Stand structural drivers of microclimate in mature temperate mixed forests. Agric for Meteorol 234–235:11–21. https://doi.org/10.1016/j.agrformet.2016.11.268
Krakauer T (1972) Thermal responses of the orb-weaving spider, Nephila clavipes (Araneae: Argiopidae). Am Midl Nat 88(1):245. https://doi.org/10.2307/2424505
Lancaster L (2016) Widespread range expansions shape latitudinal variation in insect thermal limits. Nat Clim Change 6:618–621. https://doi.org/10.1038/nclimate2945
Lebrija-Trejos E, Bongers F, Pérez-García EA, Meave JA (2008) Successional change and resilience of a very dry tropical deciduous forest following shifting agriculture. Biotropica 40(4):422–431. https://doi.org/10.1111/j.1744-7429.2008.00398.x
Lenth R (2023) Emmeans: estimated marginal means, aka least-squares means_. R package version 1.9.0. https://CRAN.Rproject.org/package=emmeans
Levins R (1968) Evolution in changing environments. Princeton University Press, Princeton
Lüdecke D (2018) ggeffects: tidy data frames of marginal effects from regression models. J Open Source Softw 3(26):772. https://doi.org/10.21105/joss.00772
Malmos KG, Lüdeking AH, Vosegaard T, Aagaard A, Bechsgaard J, Sørensen JG, Bilde T (2021) Behavioural and physiological responses to thermal stress in a social spider. Funct Ecol 35(12):2728–2742. https://doi.org/10.1111/1365-2435.13921
Marvier M, Kareiva P, Neubert MG (2004) Habitat destruction, fragmentation, and disturbance promote invasion by habitat generalists in a multispecies metapopulation. Risk Anal 24(4):869–878. https://doi.org/10.1111/j.0272-4332.2004.00485.x
McKechnie AE, Wolf BO (2019) The physiology of heat tolerance in small endotherms. Physiology 34(5):302–313. https://doi.org/10.1152/physiol.00011.2019
Monasterio C, Salvador A, Iraeta P, Díaz JA (2009) The effects of thermal biology and refuge availability on the restricted distribution of an alpine lizard. J Biogeogr 36(9):1673–1684. https://doi.org/10.1111/j.1365-2699.2009.02113.x
Munévar A, Rubio GD, Zurita GA (2018) Changes in spider diversity through the growth cycle of pine plantations in the semi-deciduous Atlantic forest: the role of prey availability and abiotic conditions. For Ecol Manage 424:536–544. https://doi.org/10.1016/j.foreco.2018.03.025
Munévar A, Cardoso P, Zurita GA (2022) From forest to forestry: reassembly of spider communities after native forest replacement by pine monocultures. Ecol Entomol. https://doi.org/10.1111/een.13125
Myers N, Mittermeier RA, Mittermeier CG, da Fonseca GAB, Kent J (2000) Biodiversity hotspots for conservation priorities. Nature 403(6772):6772. https://doi.org/10.1038/35002501
Nowakowski AJ, Watling JI, Whitfield SM, Todd BD, Kurz DJ, Donnelly MA (2017) Tropical amphibians in shifting thermal landscapes under land-use and climate change. Conserv Biol 31(1):96–105. https://doi.org/10.1111/cobi.12769
Nyffeler M, Birkhofer K (2017) An estimated 400–800 million tons of prey are annually killed by the global spider community. Sci Nat 104(3):30. https://doi.org/10.1007/s00114-017-1440-1
Oliveira-Filho AT, Fontes MAL (2000) Patterns of floristic differentiation among Atlantic forests in Southeastern Brazil and the influence of climate. Biotropica 32(4b):793–810. https://doi.org/10.1111/j.1744-7429.2000.tb00619.x
Paaijmans KP, Heinig RL, Seliga RA, Blanford JI, Blanford S, Murdock CC, Thomas MB (2013) Temperature variation makes ectotherms more sensitive to climate change. Glob Change Biol 19(8):2373–2380. https://doi.org/10.1111/gcb.12240
Pacheco R, Vasconcelos HL (2012) Habitat diversity enhances ant diversity in a naturally heterogeneous Brazilian landscape. Biodivers Conserv 21(3):797–809. https://doi.org/10.1007/s10531-011-0221-y
Pandit SN, Kolasa J, Cottenie K (2009) Contrasts between habitat generalists and specialists: an empirical extension to the basic metacommunity framework. Ecology 90(8):2253–2262. https://doi.org/10.1890/08-0851.1
Parratt SR, Walsh BS, Metelmann S et al (2021) Temperatures that sterilize males better match global species distributions than lethal temperatures. Nat Clim Chang 11:481–484. https://doi.org/10.1038/s41558-021-01047-0
Peyras M, Vespa NI, Bellocq MI, Zurita GA (2013) Quantifying edge effects: the role of habitat contrast and species specialization. J Insect Conserv 17(4):807–820. https://doi.org/10.1007/s10841-013-9563-y
Phungula SM, Krüger K, Nofemela RS, Weldon CW (2023) Developmental diet, life stage and thermal acclimation affect thermal tolerance of the fall armyworm, Spodoptera frugiperda. Physiol Entomol 48(4):122–131. https://doi.org/10.1111/phen.12414
Prieto-Benítez S, Méndez M (2011) Effects of land management on the abundance and richness of spiders (Araneae): a meta-analysis. Biol Cons 144(2):683–691. https://doi.org/10.1016/j.biocon.2010.11.024
QGIS.org (2023) QGIS geographic information system. Open Source Geospatial Foundation Project. http://qgis.osgeo.org
R Core Team (2023) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. https://www.R-project.org
Rao D, Mendoza-Cuenca L (2016) The effect of colour polymorphism on thermoregulation in an orb web spider. Sci Nat 103(7):63. https://doi.org/10.1007/s00114-016-1388-6
Ratnasingham S, Hebert PD (2007) bold: the barcode of life data system (http://www.barcodinglife.org). Mol Ecol Notes. 7(3):355–364. https://doi.org/10.1111/j.1471-8286.2007.01678.x
Rezende EL, Tejedo M, Santos M (2011) Estimating the adaptive potential of critical thermal limits: methodological problems and evolutionary implications. Funct Ecol 25(1):111–121. https://doi.org/10.1111/j.1365-2435.2010.01778.x
Riechert SE (1976) Web-site selection in the desert Spider Agelenopsis aperta. Oikos 27(2):311. https://doi.org/10.2307/3543911
Rolandi C, Schilman PE (2018) The costs of living in a thermal fluctuating environment for the tropical haematophagous bug, Rhodnius prolixus. J Therm Biol 74:92–99. https://doi.org/10.1016/j.jtherbio.2018.03.022
Santoandré S, Filloy J, Zurita GA, Bellocq MI (2021) Variations in habitat metrics along plantation chronosequences: contrasting tree plantations in subtropical forest and grassland. For Stud 75(1):55–63. https://doi.org/10.2478/fsmu-2021-0011
Searle SR, Speed FM, Milliken GA (1980) Population marginal means in the linear model: an alternative to least squares means. Am Stat 34(4):216–221. https://doi.org/10.1080/00031305.1980.10483031
Stevenson RD (1985) Body size and limits to the daily range of body temperature in terrestrial ectotherms. Am Nat 125(1):102–117. https://doi.org/10.1086/284330
Terblanche JS, Klok CJ, Krafsur ES, Chown SL (2006) Phenotypic plasticity and geographic variation in thermal tolerance and water loss of the tsetse Glossina pallidipes (Diptera: Glossinidae): implications for distribution modelling. Am J Trop Med Hyg 74(5):786–794. https://doi.org/10.4269/ajtmh.2006.74.786
Tuomainen U, Candolin U (2011) Behavioural responses to human-induced environmental change. Biol Rev 86(3):640–657. https://doi.org/10.1111/j.1469-185X.2010.00164.x
Vázquez DP, Simberloff D (2002) Ecological specialisation and susceptibility to disturbance: conjectures and refutations. Am Nat 159(6):606–623. https://doi.org/10.1086/339991
Wagner DL, Grames EM, Forister ML, Berenbaum MR, Stopak D (2021) Insect decline in the Anthropocene: death by a thousand cuts. Proc Natl Acad Sci 118(2):e2023989118. https://doi.org/10.1073/pnas.2023989118
Walsh BS, Parratt SR, Mannion NLM, Snook RR, Bretman A, Price TAR (2021) Plastic responses of survival and fertility following heat stress in pupal and adult Drosophila virilis. Ecol Evol 11(24):18238–18247. https://doi.org/10.1002/ece3.8418
Weldon CW, Terblanche JS, Chown SL (2011) Time-course for attainment and reversal of acclimation to constant temperature in two Ceratitis species. J Therm Biol 36(8):479–485. https://doi.org/10.1016/j.jtherbio.2011.08.005
Wilson SK, Burgess SC, Cheal AJ, Emslie M, Fisher R, Miller I, Polunin NVC, Sweatman HPA (2008) Habitat utilization by coral reef fish: implications for specialists vs. generalists in a changing environment. J Anim Ecol 77(2):220–228. https://doi.org/10.1111/j.1365-2656.2007.01341.x
Woon JS, Atkinson D, Adu-Bredu S, Eggleton P, Parr CL (2022) Termites have wider thermal limits to cope with environmental conditions in savannas. J Anim Ecol 91(4):766–779. https://doi.org/10.1111/1365-2656.13673
Acknowledgements
We would like to thank the National Scientific and Technical Research Council (CONICET/Argentina). The National Park Administration and the Misiones Ecology Ministry gave the necessary permissions for fieldwork. YMGPE has a doctoral fellowship from CONICET. We thank Jeffrey A. Harvey and an anonymous reviewer whose constructive criticisms improved the paper.
Funding
This work was supported in part by the National Agency for the Promotion of Science and Technology of Argentina (ANPCyT) [PICT 2018-02810 to PES], the University of Buenos Aires (UBA) [UBACyT-20020190200278BA to PES], CONICET (PIP- 11220200102397CO to PES and PUE2016 to M. Di Bitetti).
Author information
Authors and Affiliations
Contributions
YMGPE, PES, and GAZ conceived the ideas and designed the methodology. YMGPE and AM collected the data and performed the analyses. All authors critically contributed to the drafts and gave their final approval for publication.
Corresponding authors
Ethics declarations
Conflict of interest
None of the authors declared a conflict of interest.
Ethical approval
All applicable institutional and/or national guidelines for the care and use of animals were followed. Research authorisation DRNEA-516-Zurita, Gustavo: IF-2021-87003069-APN-DRNEA#APNAC, IF-2022-118456099-APN-DRNEAAPNAC.
Consent to participate
Not applicable.
Consent for publication (include appropriate statements)
Not applicable.
Additional information
Communicated by Stefan Scheu.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Piñanez-Espejo, Y.M.G., Munévar, A., Schilman, P.E. et al. It is hot and cold here: the role of thermotolerance in the ability of spiders to colonize tree plantations in the southern Atlantic Forest. Oecologia (2024). https://doi.org/10.1007/s00442-024-05529-8
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s00442-024-05529-8