Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.11.07.687215

The phylogenetic Janzen-Connell effect can explain multiple macroecological and macroevolutionary patterns

Abstract

The classical Janzen-Connell (J-C) hypothesis states that species-specific natural enemies induce local-density dependence which explains high diversity observed in tropical tree communities. Recent studies have extended the hypothesis to include the fact that these natural enemies often attack phylogenetically related species as well, which reduces diversity and hence the explanatory power of the hypothesis. However, these studies consider ecological time scales at which the phylogenetic relatedness between species is constant, and thus ignore that at evolutionary time scales the population dynamics change the phylogeny. We use a spatially explicit eco-evolutionary model of the interplay between the dynamics of the phylogeny and the species abundances to study the predictions for common macroevolutionary and macroecological patterns. We confirm that hyperdiversity can be maintained by the J-C effect but the phylogenetic relatedness effect weakens the rarity advantage, reducing diversity. Incorporating protracted speciation further improves the result. Our model predicts a triphasic species-area relationship at much shorter time scales than in neutral scenarios. The species-abundance distribution can have one or two modes depending on the dispersal distance. Phylogenetic trees show diversification slowdowns and imbalance, consistent with empirical patterns. We study a new pattern of phylogenetic relatedness through space and find that small dispersal distance causes clusters of species with large phylogenetic distance to the community while large dispersal distance makes species distribute uniformly. As an illustration of how our models predictions can be compared to empirical data we study macroecological and phylogenetic patterns of the Barro Colorado Island (BCI) tree community. We conclude that the spatially explicit eco-evolutionary phylogenetic J-C effect can explain commonly observed macroevolutionary and macroecological patterns, providing an alternative way, while the traditional methods are prone, to demonstrate the role of J-C effect on species community assembly.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Xu, L., Hildenbrandt, H., Etienne, R.. 2025-11-10. The phylogenetic Janzen-Connell effect can explain multiple macroecological and macroevolutionary patterns. https://doi.org/10.1101/2025.11.07.687215

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Measuring the strength of selection and pollen limitation on flower colour along an urban rural cline in Hesperis matronalis

Closely located urban and rural environments can differ in temperature, water availability, species diversity, and more. As a result, organisms in urban environments may experience different selection than those in rural environments. We investigated whether differences in selection might explain a previously identified urban-rural cline in the flower colour of Hesperis matronalis (dame's rocket). To explore whether plants in urban and rural environments are impacted by possible differences in pollinator availability or behavior, we performed a pollen supplementation experiment. We did not detect an effect of pollen supplementation on seed production in either setting (urban or rural), indicating that there is limited opportunity for any differences in pollinator availability or visitation to explain the cline in flower colour. We also measured the strength of selection acting on flower colour to investigate if it differed between urban and rural populations. In all but one population, we failed to detect significant linear or non-linear selection on flower colour, suggesting that selection on flower colour does not differ between urban and rural populations. Our results suggest that the urban-rural flower colour cline is likely not caused by differences in selection or pollen-limitation and may be due to stochastic forces.

evolutionary biology↗

An elongated lifespan is associated with higher oxidative protection of flight tissue in Heliconiini butterflies

Evolutionary theories of ageing often invoke trade-offs in resource allocation between somatic maintenance and other important physiological functions. One proposed mechanistic mediator of these trade-offs is oxidative stress, which arises from an imbalance between an organism's production of reactive oxygen species and its ability to detoxify them. Accordingly, many long-lived species across the animal kingdom show evidence for resistance to oxidative stress. However, it can be difficult to associate lifespan differences with oxidative phenotypes when comparing species across wide taxonomic distances, which may also show large differences in physiology. Butterflies in the long-lived Heliconius genus show a 3-fold lifespan extension and slowed ageing in comparison with their close relatives in the Heliconiini tribe, to whom they are phylogenetically, ecologically, and physiologically similar. However, proximate explanations for this extended longevity are currently lacking. Here, we leverage the neat comparative framework between Heliconius hecale and Dryas iulia, a shorter-lived Heliconiini outgroup, to test whether the observed lifespan differences between the two species are associated with differences in oxidative physiology. Our findings suggest superior oxidative protection of thoracic tissue in the longer-lived H. hecale compared to D. iulia, as evidenced by increased superoxide dismutase activity, increased total antioxidant capacity, and a corresponding reduction in lipid peroxidation in this tissue. Considering the metabolic demands of insect flight, we suggest that this oxidative phenotype may contribute to the extended longevity of Heliconius by enhancing protection of thoracic tissues against oxidative damage, representing a plausible proximate pro-longevity mechanism in this genus.

evolutionary biology↗

Both genetic and social inheritance influence female aggressive and submissive behavior in a wild primate

Agonistic interactions are important determinants of resource access in wild animals, but their genetic basis remains poorly understood. Here we use a quantitative genetics approach to estimate the heritability of aggressive and submissive behavior of wild female baboons, considering relative rates of both individual and dyadic aggression and submission. To control for the social inheritance that creates kin-based dominance hierarchies, we implemented a multi-matrix model that included a social status similarity matrix alongside the additive genetic matrix. Despite a substantial contribution of social inheritance, especially for submissive behavior, we found heritable components for both aggressive and submissive behavior (h2=0.21 and h2=0.09-0.11, respectively). In dyadic models, aggressive behavior was primarily influenced by the aggressor's genotype (a direct genetic effect), while submissive behavior was primarily affected by the social partner's genotype (an indirect genetic effect). Finally, we found evidence for a negative genetic (but not phenotypic) correlation between aggressive and submissive behavior within dyads, and a negative genetic correlation between submissive behavior and eliciting submissive behavior. Together, our results highlight how direct genetic, indirect genetic, and social inheritance effects combine to influence primate social behavior.

evolutionary biology↗