Hutchinson, G. E. Cold Spring Harbor Symposia on Quantitative Biology. Concluding Remarks 22 415–427 (1957).
Smith, E. P. Niche breadth, resource availability, and inference. Ecology 63, 1675–1681. https://doi.org/10.2307/1940109 (1982).
Google Scholar
Leibold, M. A. The niche concept revisited: Mechanistic models and community context. Ecology 76, 1371–1382. https://doi.org/10.2307/1938141 (1995).
Google Scholar
Sexton, J. P., Montiel, J., Shay, J. E., Stephens, M. R. & Slatyer, R. A. Evolution of ecological niche breadth. Annu. Rev. Ecol. Evol. Syst. 48, 183–206. https://doi.org/10.1146/annurev-ecolsys-110316-023003 (2017).
Google Scholar
Jaenike, J. Host specialization in phytophagous insects. Annu. Rev. Ecol. Syst. 21, 243–273. https://doi.org/10.1146/annurev.es.21.110190.001331 (1990).
Google Scholar
Thompson, J. N. The Coevolutionary Process (University of Chicago Press, 1994).
Google Scholar
Krasnov, B. R., Mouillot, D., Shenbrot, G. I., Khokhlova, I. S. & Poulin, R. Geographical variation in host specificity of fleas (Siphonaptera) parasitic on small mammals: The influence of phylogeny and local environmental conditions. Ecography 27, 787–797. https://doi.org/10.1111/j.0906-7590.2004.04015.x (2004).
Google Scholar
Poullain, V., Gandon, S., Brockhurst, M. A., Buckling, A. & Hochberg, M. E. The evolution of specificity in evolving and coevolving antagonistic interactions between bacteria and its phage. Evolution 62, 1–11. https://doi.org/10.1111/j.1558-5646.2007.00260.x (2008).
Google Scholar
Whitlock, M. C. The Red Queen beats the Jack-Of-All-Trades: The limitations on the evolution of phenotypic plasticity and niche breadth. Am. Nat. 148, S65–S77. https://doi.org/10.1086/285902 (1996).
Google Scholar
Gandon, S. Local adaptation and the geometry of host–parasite coevolution. Ecol. Lett. 5, 246–256. https://doi.org/10.1046/j.1461-0248.2002.00305.x (2002).
Google Scholar
Alizon, S. & Michalakis, Y. Adaptive virulence evolution: The good old fitness-based approach. Trends Ecol. Evol. 30, 248–254. https://doi.org/10.1016/j.tree.2015.02.009 (2015).
Google Scholar
Frank, S. A. & Schmid-Hempel, P. Mechanisms of pathogenesis and the evolution of parasite virulence. J. Evol. Biol. 21, 396–404. https://doi.org/10.1111/j.1420-9101.2007.01480.x (2008).
Google Scholar
Beadell, J. S. et al. Global phylogeographic limits of Hawaii’s avian malaria. Proc. R. Soc. B: Biol. Sci. 273, 2935–2944. https://doi.org/10.1098/rspb.2006.3671 (2006).
Google Scholar
Krasnov, B. R. Functional and Evolutionary Ecology of Fleas: A Model for Ecological Parasitology (Cambridge University Press, 2008).
Google Scholar
Poulin, R. Evolutionary Ecology of Parasites (Princeton University Press, 2011).
Google Scholar
Välimäki, P. et al. Geographical variation in host use of a blood-feeding ectoparasitic fly: Implications for population invasiveness. Oecologia 166, 985–995. https://doi.org/10.1007/s00442-011-1951-y (2011).
Google Scholar
Theodosopoulos, A. N., Hund, A. K. & Taylor, S. A. Parasites and host species barriers in animal hybrid zones. Trends Ecol. Evol. 34, 19–30. https://doi.org/10.1016/j.tree.2018.09.011 (2019).
Google Scholar
Mackenzie, A. A trade-off for host plant utilization in the black bean aphid, Aphis fabae. Evolution 50, 155–162. https://doi.org/10.1111/j.1558-5646.1996.tb04482.x (1996).
Google Scholar
Harrington, L. C., Edman, J. D. & Scott, T. W. Why do female Aedes aegypti (Diptera: Culicidae) feed preferentially and frequently on human blood?. J. Med. Entomol. 38, 411–422. https://doi.org/10.1603/0022-2585-38.3.411 (2001).
Google Scholar
Dick, C. W. & Patterson, B. D. Against all odds: Explaining high host specificity in dispersal-prone parasites. Int. J. Parasitol. 37, 871–876. https://doi.org/10.1016/j.ijpara.2007.02.004 (2007).
Google Scholar
Torchin, M. E. & Mitchell, C. E. Parasites, pathogens, and invasions by plants and animals. Front. Ecol. Environ. 2, 183–190. https://doi.org/10.1890/1540-9295(2004)002[0183:PPAIBP]2.0.CO;2 (2004).
Google Scholar
Clark, N. J. & Clegg, S. M. The influence of vagrant hosts and weather patterns on the colonization and persistence of blood parasites in an island bird. J. Biogeogr. 42, 641–651. https://doi.org/10.1111/jbi.12454 (2015).
Google Scholar
Kawecki, T. J. Red Queen meets Santa Rosalia: Arms races and the evolution of host specialization in organisms with parasitic lifestyles. Am. Nat. 152, 635–651. https://doi.org/10.1086/286195 (1998).
Google Scholar
Egas, M., Dieckmann, U. & Sabelis, M. W. Evolution restricts the coexistence of specialists and generalists: The role of trade-off structure. Am. Nat. 163, 518–531. https://doi.org/10.1086/382599 (2004).
Google Scholar
Poulin, R. & Keeney, D. B. Host specificity under molecular and experimental scrutiny. Trends Parasitol. 24, 24–28. https://doi.org/10.1016/j.pt.2007.10.002 (2008).
Google Scholar
Lyimo, I. N. & Ferguson, H. M. Ecological and evolutionary determinants of host species choice in mosquito vectors. Trends Parasitol. 25, 189–196. https://doi.org/10.1016/j.pt.2009.01.005 (2009).
Google Scholar
Visher, E. & Boots, M. The problem of mediocre generalists: Population genetics and eco-evolutionary perspectives on host breadth evolution in pathogens. Proc. R. Soc. B: Biol. Sci. 287, 20201230. https://doi.org/10.1098/rspb.2020.1230 (2020).
Google Scholar
Sarfati, M. et al. Energy costs of blood digestion in a host-specific haematophagous parasite. J. Exp. Biol. 208, 2489. https://doi.org/10.1242/jeb.01676 (2005).
Google Scholar
Fry, J. D. The evolution of host specialization: Are trade-offs overrated?. Am. Nat. 148, S84–S107. https://doi.org/10.1086/285904 (1996).
Google Scholar
Fessl, B. et al. Galápagos landbirds (passerines, cuckoos, and doves): Status, threats, and knowledge gaps. Galápagos Rep. 2016, 149 (2015).
Fessl, B., Heimpel, G. E. & Causton, C. E. Invasion of an avian nest parasite, Philornis downsi, to the Galapagos Islands: colonization history, adaptations to novel ecosystems, and conservation challenges. In Disease Ecology: Galapagos Birds and their Parasites (ed Patricia G. Parker) 213–266 (Springer International Publishing, 2018).
Frankham, R. Do island populations have less genetic variation than mainland populations?. Heredity 78, 311–327. https://doi.org/10.1038/hdy.1997.46 (1997).
Google Scholar
Reichard, M. et al. The bitterling–mussel coevolutionary relationship in areas of recent and ancient sympatry. Evolution 64, 3047–3056. https://doi.org/10.1111/j.1558-5646.2010.01032.x (2010).
Google Scholar
Wiedenfeld, D. A., Jiménez, G. U., Fessl, B., Kleindorfer, S. & Carlos Valarezo, J. Distribution of the introduced parasitic fly Philornis downsi (Diptera, Muscidae) in the Galápagos Islands. Pacific Conserv. Biol. 13, 14–19. https://doi.org/10.1071/PC070014 (2007).
Google Scholar
Fessl, B., Sinclair, B. J. & Kleindorfer, S. The life-cycle of Philornis downsi (Diptera: Muscidae) parasitizing Darwin’s finches and its impacts on nestling survival. Parasitology 133, 739–747. https://doi.org/10.1017/S0031182006001089 (2006).
Google Scholar
Kleindorfer, S. & Dudaniec, R. Y. Host-parasite ecology, behavior and genetics: A review of the introduced fly parasite Philornis downsi and its Darwin’s finch hosts. BMC Zool. 1, 1. https://doi.org/10.1186/s40850-016-0003-9 (2016).
Google Scholar
Galligan, T. H. & Kleindorfer, S. Naris and beak malformation caused by the parasitic fly, Philornis downsi (Diptera: Muscidae), in Darwin’s small ground finch, Geospiza fuliginosa (Passeriformes: Emberizidae). Biol. J. Lin. Soc. 98, 577–585. https://doi.org/10.1111/j.1095-8312.2009.01309.x (2009).
Google Scholar
Kleindorfer, S., Custance, G., Peters Katharina, J. & Sulloway Frank, J. Introduced parasite changes host phenotype, mating signal and hybridization risk: Philornis downsi effects on Darwin’s finch song. Proc. R. Soc. B: Biol. Sci. 286, 20190461. https://doi.org/10.1098/rspb.2019.0461 (2019).
Google Scholar
Kleindorfer, S., Peters, K. J., Custance, G., Dudaniec, R. Y. & O’Connor, J. A. Changes in Philornis infestation behavior threaten Darwin’s finch survival. Curr. Zool. 60, 542–550. https://doi.org/10.1093/czoolo/60.4.542 (2014).
Google Scholar
O’Connor, J. A., Sulloway, F. J., Robertson, J. & Kleindorfer, S. Philornis downsi parasitism is the primary cause of nestling mortality in the critically endangered Darwin’s medium tree finch (Camarhynchus pauper). Biodivers. Conserv. 19, 853–866. https://doi.org/10.1007/s10531-009-9740-1 (2010).
Google Scholar
Knutie, S. A. et al. Galápagos mockingbirds tolerate introduced parasites that affect Darwin’s finches. Ecology https://doi.org/10.1890/15-0119 (2016).
Google Scholar
Peters, K. J., Evans, C., Aguirre, J. D. & Kleindorfer, S. Genetic admixture predicts parasite intensity: Evidence for increased hybrid performance in Darwin’s tree finches. R. Soc. Open Sci. 6, 181616. https://doi.org/10.1098/rsos.181616 (2019).
Google Scholar
Kleindorfer, S. The ecology of clutch size variation in Darwin’s Small Ground Finch Geospiza fuliginosa: Comparison between lowland and highland habitats. Ibis 149, 730–741. https://doi.org/10.1111/j.1474-919X.2007.00694.x (2007).
Google Scholar
Fessl, B. & Tebbich, S. Philornis downsi– a recently discovered parasite on the Galápagos archipelago: A threat for Darwin’s finches?. Ibis 144, 445–451. https://doi.org/10.1046/j.1474-919X.2002.00076.x (2002).
Google Scholar
Dudaniec, R. Y., Fessl, B. & Kleindorfer, S. Interannual and interspecific variation in intensity of the parasitic fly, Philornis downsi, Darwin’s finches. Biol. Cons. 139, 325–332. https://doi.org/10.1016/j.biocon.2007.07.006 (2007).
Google Scholar
Cimadom, A. et al. Invasive parasites, habitat change and heavy rainfall reduce breeding success in Darwin’s Finches. PLoS ONE 9, e107518. https://doi.org/10.1371/journal.pone.0107518 (2014).
Google Scholar
Cimadom, A. et al. Weed management increases the detrimental effect of an invasive parasite on arboreal Darwin’s finches. Biol. Cons. 233, 93–101. https://doi.org/10.1016/j.biocon.2019.02.025 (2019).
Google Scholar
Kleindorfer, S. & Dudaniec, R. Y. Love thy neighbour? Social nesting pattern, host mass and nest size affect ectoparasite intensity in Darwin’s tree finches. Behav. Ecol. Sociobiol. 63, 731–739. https://doi.org/10.1007/s00265-008-0706-1 (2009).
Google Scholar
Common, L. K., Dudaniec, R. Y., Colombelli-Négrel, D. & Kleindorfer, S. Taxonomic shifts in Philornis larval behaviour and rapid changes in Philornis downsi Dodge & Aitken (Diptera: Muscidae): An invasive avian parasite on the Galápagos Islands. in Life Cycle and Development of Diptera (ed Muhammad Sarwar) (IntechOpen, 2019).
McNew, S. M. et al. Annual environmental variation influences host tolerance to parasites. Proc. R. Soc. B: Biol. Sci. 286, 20190049. https://doi.org/10.1098/rspb.2019.0049 (2019).
Google Scholar
McNew, S. M. & Clayton, D. H. Alien invasion: Biology of Philornis flies highlighting Philornis downsi, an introduced parasite of Galápagos birds. Annu. Rev. Entomol. 63, 369–387. https://doi.org/10.1146/annurev-ento-020117-043103 (2018).
Google Scholar
Kleindorfer, S. & Dudaniec, R. Y. Hybridization fluctuates with rainfall in Darwin’s tree finches. Biol. J. Lin. Soc. 130, 79–88. https://doi.org/10.1093/biolinnean/blaa029 (2020).
Google Scholar
Peters, K. J., Myers, S. A., Dudaniec, R. Y., O’Connor, J. A. & Kleindorfer, S. Females drive asymmetrical introgression from rare to common species in Darwin’s tree finches. J. Evol. Biol. 30, 1940–1952. https://doi.org/10.1111/jeb.13167 (2017).
Google Scholar
Kleindorfer, S. et al. Species collapse via hybridization in Darwin’s Tree Finches. Am. Nat. 183, 325–341. https://doi.org/10.1086/674899 (2014).
Google Scholar
Loo, W. T., Dudaniec, R. Y., Kleindorfer, S. & Cavanaugh, C. M. An inter-island comparison of Darwin’s finches reveals the impact of habitat, host phylogeny, and island on the gut microbiome. PLoS ONE 14, e0226432. https://doi.org/10.1371/journal.pone.0226432 (2019).
Google Scholar
Galapagos Conservancy. Galapagos Vital Signs: A satellite-based environmental monitoring system for the Galapagos Archipelago, https://galapagosvitalsigns.org (2021).
Couri, M. Considerações sobre as relações ecológicas das larvas de Philornis Meinert, 1890 (Diptera, Muscidae) com aves. Revista Brasileira de Entomologia 29, 17–20. https://doi.org/10.1017/S0031182006001089 (1985).
Google Scholar
Skidmore, P. The Biology of the Muscidae of the World Vol. 29 (Springer, 1985).
O’Connor, J. A., Robertson, J. & Kleindorfer, S. Video analysis of host–parasite interactions in nests of Darwin’s finches. Oryx 44, 588–594. https://doi.org/10.1017/S0030605310000086 (2010).
Google Scholar
O’Connor, J. A., Robertson, J. & Kleindorfer, S. Darwin’s finch begging intensity does not honestly signal need in parasitised nests. Ethology 120, 228–237. https://doi.org/10.1111/eth.12196 (2014).
Google Scholar
Kleindorfer, S. & Sulloway, F. J. Naris deformation in Darwin’s finches: Experimental and historical evidence for a post-1960s arrival of the parasite Philornis downsi. Glob. Ecol. Conserv. 7, 122–131. https://doi.org/10.1016/j.gecco.2016.05.006 (2016).
Google Scholar
Lahuatte, P. F., Lincango, M. P., Heimpel, G. E. & Causton, C. E. Rearing larvae of the avian nest parasite, Philornis downsi (Diptera: Muscidae), on chicken blood-based diets. J. Insect Sci. https://doi.org/10.1093/jisesa/iew064 (2016).
Google Scholar
Kleindorfer, S. Nesting success in Darwin’s small tree finch, Camarhynchus parvulus: Evidence of female preference for older males and more concealed nests. Anim. Behav. 74, 795–804. https://doi.org/10.1016/j.anbehav.2007.01.020 (2007).
Google Scholar
Nijhout, H. F. & Callier, V. Developmental mechanisms of body size and wing-body scaling in insects. Annu. Rev. Entomol. 60, 141–156. https://doi.org/10.1146/annurev-ento-010814-020841 (2015).
Google Scholar
Singh, D. & Bala, M. The effect of starvation on the larval behavior of two forensically important species of blow flies (Diptera: Calliphoridae). For. Sci. Int. 193, 118–121. https://doi.org/10.1016/j.forsciint.2009.09.022 (2009).
Google Scholar
Coulson, S. J. & Bale, J. S. Characterisation and limitations of the rapid cold-hardening response in the housefly Musca domestica (Diptera: Muscidae). J. Insect Physiol. 36, 207–211. https://doi.org/10.1016/0022-1910(90)90124-X (1990).
Google Scholar
R Core Team. R: A language and environment for statistical computing. R version 4.0.3 (R Foundation for Statistical Computing, Vienna, Austria, 2020).
Bates, D., Mächler, M., Bolker, B. & Walker, S. Fitting linear mixed-effects models using lme4. J. Stat. Softw. https://doi.org/10.18637/jss.v067.i01 (2015).
Google Scholar
Venables, B. & Ripley, B. Modern Applied Statistics with S-PLUS (Springer Science & Business Media, 2002).
Fox, J. & Weisberg, S. An R Companion to Applied Regression (Sage publications, 2011).
Sarkar, D. Lattice: Multivariate Data Visualization with R (Springer, 2008).
Google Scholar
Wickham, H. ggplot2: Elegant Graphics for Data Analysis (Springer, 2009).
Google Scholar
Fox, J. Effect displays in R for generalised linear models. J. Stat. Softw. https://doi.org/10.18637/jss.v008.i15 (2003).
Google Scholar
Burnham, K. P. & Anderson, D. R. Model Selection and Multimodal Inference: A Practical Information-Theoretic Approach (eds Kenneth P. Burnham & David R. Anderson) 75–117 (Springer New York, 1998).
Grueber, C. E., Nakagawa, S., Laws, R. J. & Jamieson, I. G. Multimodel inference in ecology and evolution: Challenges and solutions. J. Evol. Biol. 24, 699–711. https://doi.org/10.1111/j.1420-9101.2010.02210.x (2011).
Google Scholar
Haaland, T. R., Wright, J. & Ratikainen, I. I. Generalists versus specialists in fluctuating environments: A bet-hedging perspective. Oikos 129, 879–890. https://doi.org/10.1111/oik.07109 (2020).
Google Scholar
Davies, N. Cuckoos, Cowbirds and Other Cheats (Bloomsbury Publishing, 2010).
Dudaniec, R. Y., Gardner, M. G. & Kleindorfer, S. Offspring genetic structure reveals mating and nest infestation behaviour of an invasive parasitic fly (Philornis downsi) of Galápagos birds. Biol. Invas. 12, 581–592. https://doi.org/10.1007/s10530-009-9464-x (2010).
Google Scholar
Fredensborg, B. L. & Poulin, R. Larval helminths in intermediate hosts: Does competition early in life determine the fitness of adult parasites?. Int. J. Parasitol. 35, 1061–1070. https://doi.org/10.1016/j.ijpara.2005.05.005 (2005).
Google Scholar
Begon, M., Harper, J. L. & Townsend, C. R. Ecology: Individuals, Populations and Communities (Blackwell Scientific Publications, 1986).
Fraik, A. K. et al. Disease swamps molecular signatures of genetic-environmental associations to abiotic factors in Tasmanian devil (Sarcophilus harrisii) populations. Evolution 74, 1392–1408. https://doi.org/10.1111/evo.14023 (2020).
Google Scholar
Dvorak, M. et al. Conservation status of landbirds on Floreana: The smallest inhabited Galápagos Island. J. Field Ornithol. 88, 132–145. https://doi.org/10.1111/jofo.12197 (2017).
Google Scholar
Hedrick, P. W., Kim, T. J. & Parker, K. M. Parasite resistance and genetic variation in the endangered Gila topminnow. Anim. Conserv. 4, 103–109. https://doi.org/10.1017/S1367943001001135 (2001).
Google Scholar
Lewontin, R. C. & Birch, L. C. Hybridization as a source of variation for adaptation to new environments. Evolution 20, 315–336. https://doi.org/10.2307/2406633 (1966).
Google Scholar
Wolinska, J., Lively, C. M. & Spaak, P. Parasites in hybridizing communities: The Red Queen again?. Trends Parasitol. 24, 121–126. https://doi.org/10.1016/j.pt.2007.11.010 (2008).
Google Scholar
Floate, K. D. & Whitham, T. G. The, “Hybrid Bridge” Hypothesis: Host shifting via plant hybrid swarms. Am. Nat. 141, 651–662. https://doi.org/10.1086/285497 (1993).
Google Scholar
Le Brun, N., Renaud, F., Berrebi, P. & Lambert, A. Hybrid zones and host-parasite relationships: Effect on the evolution of parasitic specificity. Evolution 46, 56–61. https://doi.org/10.1111/j.1558-5646.1992.tb01984.x (1992).
Google Scholar
Fritz, R. S., Moulia, C. & Newcombe, G. Resistance of hybrid plants and animals to herbivores, pathogens, and parasites. Annu. Rev. Ecol. Syst. 30, 565–591. https://doi.org/10.1146/annurev.ecolsys.30.1.565 (1999).
Google Scholar
Moulia, C., Brun, N. L., Loubes, C., Marin, R. & Renaud, F. Hybrid vigour against parasites in interspecific crosses between two mice species. Heredity 74, 48–52. https://doi.org/10.1038/hdy.1995.6 (1995).
Google Scholar
Gibson, A. K., Refrégier, G., Hood, M. E. & Giraud, T. Performance of a hybrid fungal pathogen on pure-species and hybrid host plants. Int. J. Plant Sci. 175, 724–730. https://doi.org/10.1086/676621 (2014).
Google Scholar
Arnold, M. L. & Martin, N. H. Hybrid fitness across time and habitats. Trends Ecol. Evol. 25, 530–536. https://doi.org/10.1016/j.tree.2010.06.005 (2010).
Google Scholar
Ben-Yosef, M. et al. Host-specific associations affect the microbiome of Philornis downsi, an introduced parasite to the Galápagos Islands. Mol. Ecol. 26, 4644–4656. https://doi.org/10.1111/mec.14219 (2017).
Google Scholar
Loo, W. T., García-Loor, J., Dudaniec, R. Y., Kleindorfer, S. & Cavanaugh, C. M. Host phylogeny, diet, and habitat differentiate the gut microbiomes of Darwin’s finches on Santa Cruz Island. Sci. Rep. 9, 18781. https://doi.org/10.1038/s41598-019-54869-6 (2019).
Google Scholar
Knutie, S. A. Relationships among introduced parasites, host defenses, and gut microbiota of Galapagos birds. Ecosphere 9, e02286. https://doi.org/10.1002/ecs2.2286 (2018).
Google Scholar
Knutie, S. A., Chaves, J. A. & Gotanda, K. M. Human activity can influence the gut microbiota of Darwin’s finches in the Galapagos Islands. Mol. Ecol. 28, 2441–2450. https://doi.org/10.1111/mec.15088 (2019).
Google Scholar
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