Hutchinson, G. E. An Introduction to Population Ecology (Yale University Press, 1978).
Google Scholar
Fussman, G. F. & Heber, G. Food web complexity and chaotic population dynamics. Ecol. Lett. 5, 394–401 (1978).
Google Scholar
Maron, J. L. & Crone, E. Herbivory: effects on plant abundance, distribution, and population growth. Proc. R. Soc. B. 272, 2575–2584 (1978).
Johst, K., Berryman, A. & Lima, M. From individual interactions to population dynamics: Individual resource partitioning simulation exposes the causes of nonlinear intra-specific competition. Pop. Ecol. 50, 79–90 (2008).
Google Scholar
McIntire, K. M. & Juliano, S. A. How can mortality increase population size? A test of two hypotheses. Ecology 99, 1660–1670 (2018).
Google Scholar
Mylius, S. D. & Deikmann, O. On evolutionary stable life histories, optimization and the need to be specific about density dependence. Oikos 74, 218–224 (1995).
Google Scholar
Courchamp, F., Clutton-Brock, T. & Grenfell, B. Inverse density dependence and the Allee effect. Trends Ecol. Evol. 14, 405–410 (1999).
Google Scholar
MacLean, R. C. & Gudelj, I. Resource competition and social conflict in experimental populations of yeast. Nature 44, 498–501 (2006).
Google Scholar
Khatchikian, C. E. et al. Recent and rapid population growth and range expansion of the Lyme disease tick vector, Ixodes scapularis North America. Evolution 69, 1678–1689 (2015).
Google Scholar
Lafferty, K. D. & Holt, R. D. How should environmental stress affect the population dynamics of disease?. Ecol. Lett. 6, 654–664 (2003).
Google Scholar
Sibley, R. M., Barker, D., Denham, M. C., Hone, J. & Pagel, M. On the regulation of populations of mammals, birds, fish, and insects. Science 309, 607–610 (2005).
Google Scholar
Bjorndal, K., Bolten, A. B. & Chaloupka, M. Y. Green turtle somatic growth model: evidence for density-dependence. Ecol. App. 10, 269–282 (2000).
Lamb, J. S., Satgé, Y. G. & Jodice, P. G. R. Influence of density-dependent competition on foraging and migratory behavior of a subtropical colonial seabird. Ecol. Evol. 7, 6469–6481 (2017).
Google Scholar
Kobayashi, K. Sexual selection sustains biodiversity via producing negative density-dependent population growth. J. Ecol. 107, 1433–1438 (2018).
Google Scholar
López-Sepulcre, A. & Kokko, H. Territorial defense, territory size, and population regulation. Am. Nat. 166, 317–325 (2005).
Google Scholar
Maag, N., Cozzi, G., Clutton-Brock, T. & Ozgul, A. Density-dependent dispersal strategies in a cooperative breeder. Ecology 99, 1932–1941 (2018).
Google Scholar
Bonenfant, C. et al. Empirical evidence of density- dependence in populations of large herbivores. Adv. Ecol. Res. 41, 313–357 (2009).
Google Scholar
Legros, M., Lloyd, A. L., Huang, Y. & Gould, F. Density-dependent intraspecific competition in the larval stage of Aedes aegypt (Diptera: Culicidae): Revisiting the current paradigm. J. Med. Entomol. 46, 409–419 (2009).
Google Scholar
Hixon, M. A. & Jones, G. P. Competition, predation, and density-dependent mortality in demersal marine fishes. Ecology 86, 2847–2859 (2006).
Google Scholar
Vonesh, J. R. & De La Cruz, O. Complex life cycles and density dependence: Assessing the contribution of egg mortality to amphibian declines. Oecologia 133, 325–333 (2002).
Google Scholar
Southwood, T. R., Murdie, G., Yasuno, M., Tonn, R. J. & Reader, P. M. Studies on the life budget of Ae. aegypti in Wat Samphaya, Bangkok, Thailand. Bull. World Health Organ. 46, 211–226 (1972).
Google Scholar
Dye, C. Intraspecific competition amongst larval Aedes aegypti: food exploitation or chemical interference. Ecol. Entomol. 7, 39–46 (1982).
Google Scholar
Dye, C. Models for the population dynamics of the yellow fever mosquito, Aedes aegypti. J. Anim. Ecol. 53, 247–268 (1984).
Google Scholar
Livdahl, T. P. & Willey, M. S. Prospects for an invasion: competition between Aedes albopictus and native Aedes triseriatus. Science 253, 189–191 (1991).
Google Scholar
Alto, B. W., Lounibos, L. P., Higgs, S. & Juliano, S. A. Larval competition differentially affects arbovirus infection in Aedes mosquito. Ecology 86, 3279–3288 (2005).
Google Scholar
Juliano, S. A. Population dynamics. J. Am. Mosq. Control Assoc. 23, 265–275 (2007).
Google Scholar
Focks, D. A., Haile, D. G., Daniels, E. & Mount, G. A. Dynamics life table model for Aedes aegypti (diptera: Culicidae): simulation results and validation. J. Med. Entomol. 30, 1018–1028 (1993).
Google Scholar
Ellis, A. M., Garcia, A. J., Focks, D. A., Morrison, A. C. & Scott, T. W. Parameterization and sensitivity analysis of a complex simulation model for mosquito population dynamics, dengue transmission, and their control. Am. J. Trop. Med. Hyg. 85, 257–264 (2011).
Google Scholar
Gilpin, M. E. & McClelland, G. A. H. Systems analysis of the yellow fever mosquito Aedes aegypti. Fortschr. Zool. 25, 355–388 (1979).
Google Scholar
Juliano, S. A. Species introduction and replacement among mosquitoes: Interspecific resource competition or apparent competition?. Ecology 79, 255–268 (1998).
Google Scholar
Lord, C. C. Density dependence in larval Aedes albopictus (Diptera: Culicidae). J. Med. Entomol. 35, 825–829 (1998).
Google Scholar
Agnew, P., Hide, M., Sidobre, C. & Michalakis, Y. A minimalist approach to the effects of density-dependent competition on insect life-history traits. Ecol. Entomol. 27, 396–402 (2002).
Google Scholar
Walsh, R. K., Facchinelli, L., Ramsey, J. M., Bond, J. G. & Gould, F. Assessing the impact of density dependence in field populations of Aedes aegypti. J. Vect. Ecol. 36, 300–307 (2011).
Google Scholar
Walsh, R. K., Bradley, C., Apperson, C. S. & Gould, F. An experimental field study of delayed density dependence in natural populations of Aedes albopictus. PLoS ONE 7, e35959 (2012).
Google Scholar
Walsh, R. K. et al. Regulation of Aedes aegypti population dynamics in field systems: Quantifying direct and delayed density dependence. Am. J. Trop. Med. Hyg. 89, 68–77 (2013).
Google Scholar
Livdahl, T. P. & Sugihara, G. Non-linear interactions of populations and the importance of estimating per capita rates of change. J. Anim. Ecol. 53, 573–580 (1984).
Google Scholar
Getz, W. M. A hypothesis regarding the abruptness of density dependence and the growth rate of populations. Ecology 77, 2014–2026 (1996).
Google Scholar
Tenan, S., Tavecchia, G., Oro, D. & Pradel, R. Assessing the effect of density on population growth when modeling individual encounter data. Ecology 100, e02595 (2019).
Google Scholar
Arditi, R., Bersier, L. & Rohr, R. P. The perfect mixing paradox and the logistic equation: Verhulst vs. Lotka. Ecosphere 7, e01599 (2016).
Google Scholar
Cortés, E. Perspectives on the intrinsic rate of population growth. Meth. Ecol. Evol. 7, 1136–1145 (2016).
Google Scholar
Smith, F. E. Population dynamics in Daphnia magna and a new model for population growth. Ecology 4, 651–663 (1963).
Google Scholar
Ayala, F. J., Gilpin, M. E. & Ehrenfeld, J. G. Competition between species: Theoretical models and experimental tests. Theor. Pop. Biol. 4, 331–356 (1973).
Google Scholar
Borlestean, A., Frost, P. C. & Murray, D. L. A mechanistic analysis of density dependence in algal population dynamics. Front. Ecol. Evol. 3, 37 (2015).
Google Scholar
Clark, F., Brook, B. W., Delean, S., Akçakaya, H. R. & Bradshaw, C. J. A. The theta-logistic is unreliable for modelling most census data. Methods Ecol. Evol. 1, 253–262 (2010).
Google Scholar
Chmielewski, M. W., Khatchikian, C. & Livdahl, T. Estimating the per capita rate of population change: How well do life-history surrogates perform?. Ann. Entomol. Soc. Am. 103, 734–741 (2010).
Google Scholar
Neale, J. T. & Juliano, S. A. Finding the sweet spot: What levels of larval mortality lead to compensation or overcompensation in adult production?. Ecosphere. 10, e02855 (2019).
Google Scholar
Armistead, J. S., Arias, J. R., Nishimura, N. & Lounibos, L. P. Interspecific larval competition between Aedes albopictus and Aedes japonicus (Diptera: Culicidae) in northern Virginia. J. Med. Entomol. 45, 629–637 (2008).
Google Scholar
Kaplan, L., Kendell, D., Robertson, D., Livdahl, T. & Khatchikian, C. Aedes aegypti and Aedes albopictus in Bermuda: Extinction, invasion, invasion and extinction. Bio. Invasions. 12, 3277–3288 (2010).
Google Scholar
Juliano, S. A. Coexistence, exclusion, or neutrality? A meta-analysis of competition between Aedes albopictus and resident mosquitoes. Isr. J. Ecol. Evol. 56, 325–351 (2010).
Google Scholar
Murrell, E. G. & Juliano, S. A. Competitive abilities in experimental microcosms are accurately predicted by a demographic index for R*. PLoS ONE 7, e43458 (2012).
Google Scholar
Leisnham, P. T. & Juliano, S. A. Interpopulation differences in competitive effect and response of the mosquito Aedes aegypti and resistance to invasion of a superior competitor. Oecologia 164, 221–230 (2010).
Google Scholar
Leisnham, P. T., Lounibos, L. P., O’Meara, G. F. & Juliano, S. A. Interpopulation divergence in competitive interactions of the mosquito Aedes albopictus. Ecology 90, 2405–2413 (2009).
Google Scholar
Evans, M. V., Drake, J. M., Jones, L. & Murdock, C. C. Assessing temperature-dependent competition between two invasive mosquito species. Ecol. Appl. 31, e02334 (2021).
Google Scholar
Léonard, P. M. & Juliano, S. A. Effects of leaf litter and density on fitness and population performance of the hole mosquito Aedes triseriatus. Ecol. Entomol. 20, 125–136 (1995).
Google Scholar
Chandrasegaran, K. & Juliano, S. A. How do trait-mediated non-lethal effects of predation affect population-level performance of mosquitoes?. Front. Ecol. Evol. 7, 25 (2019).
Google Scholar
Yee, D. A., Kaufman, M. G. & Juliano, S. A. The significance of ratios of detritus types and microorganism productivity to competitive interactions between aquatic insect detritivores. J. Anim. Ecol. 76, 1105–1115 (2007).
Google Scholar
Fader, J. E. & Juliano, S. A. An empirical test of the aggregation model of coexistence and consequences for competing container-dwelling mosquitoes. Ecology 94, 478–488 (2013).
Google Scholar
Murrell, E. G., Damal, K., Lounibos, L. P. & Juliano, S. A. Distributions of competing container mosquitoes depend on detritus types, nutrient ratios, and food availability. Ann. Entomol. Soc. Am. 104, 688–698 (2011).
Google Scholar
Tjørve, K. M. C. & Tjørve, E. The use of Gompertz models in growth analyses, and new Gompertz-model approach: An addition to the Unified-Richards family. PLoS ONE 12, e0178691 (2017).
Google Scholar
Motulsky, H. & Christopoulos, A. Fitting Models to Biological Data using Linear and Nonlinear Regression: A Practical Guide to Curve Fitting (Oxford University Press, 2004).
Google Scholar
Osenberg, C. W. et al. Rethinking ecological inference: density dependence in reef fishes. Ecol. Lett. 5, 715–721 (2002).
Google Scholar
Schmitt, R. J., Holbrook, S. J. & Osenberg, C. W. Quantifying the effects of multiple processes on local abundance: A cohort approach for open populations. Ecol. Lett. 2, 294–303 (1999).
Google Scholar
Fish, D. An analysis of adult size variation within natural mosquito population. In Ecology of Mosquitoes: Proceedings of a Workshop (eds Lounibos, L. P. et al.) 419–429 (Medical Entomology Laboratory, 1985).
Schneider, J. R., Chadee, D. D., Mori, A., Romero-Severson, J. & Severson, D. W. Heritability and adaptive phenotypic plasticity of adult body size in the mosquito Aedes aegypti with implications for dengue vector competence. Infect. Genet. Evol. 11, 11–16 (2011).
Google Scholar
Wormington, J. D. & Juliano, S. A. Sexually dimorphic body size and development time plasticity in Aedes mosquitoes (Diptera: Culicidae). Evol. Ecol. Res. 16, 1–12 (2014).
Steinwascher, K. Competition and growth among Aedes aegypti larvae: Effects of distributing food inputs over time. PLoS ONE 15, e0234676 (2020).
Google Scholar
Barrera, R. Competition and resistance to starvation in larvae of container-inhabiting Aedes mosquitoes. Ecol. Entomol. 21, 117–127 (1996).
Google Scholar
Servanty, S. et al. Assessing whether mortality is additive using marked animals: A Bayesian state-space modeling approach. Ecology 91, 1916–1923 (2010).
Google Scholar
Wolfe, M. L. et al. Is anthropogenic cougar mortality compensated by changes in natural mortality in Utah? Insights from long-term studies. Biol. Conserv. 182, 187–196 (2015).
Google Scholar
Kogan, M. Integrated pest management: Historical perspectives and contemporary developments. Ann. Rev. Entomol. 43, 243–270 (1998).
Google Scholar
Lounibos, L. P. Invasions by insect vectors of human diseases. Ann. Rev. Entomol. 47, 233–266 (2002).
Google Scholar
Juliano, S. A. & Lounibos, L. P. Ecology of invasive mosquitoes: Effects on resident species and on human health. Ecol. Lett. 8, 558–574 (2005).
Google Scholar
Source: Ecology - nature.com