Populations and Evolution (q-bio.PE)
Tue, 30 May 2023
1.Wind turbine power and land cover effects on cumulative bat deaths
Authors:Aristides Moustakas, Panagiotis Georgiakakis, Elzbieta Kret, Eleftherios Kapsalis
Abstract: Wind turbines (WT) cause bird and bat mortalities which depend on the WT and landscape features. The effects of WT features and environmental variables at different spatial scales associated to bat deaths in a mountainous and forested area in Thrace, NE Greece were investigated. Initially, we sought to quantify the most lethal WT characteristic between tower height, rotor diameter and power. The scale of interaction distance between bat deaths and the land cover characteristics surrounding the WTs was quantified. A statistical model was trained and validated against bat deaths and WT, land cover and topography features. Variance partitioning between bat deaths and the explanatory covariates was conducted. The trained model was used to predict bat deaths attributed to existing and future wind farm development in the region. Results indicated that the optimal interaction distance between WT and surrounding land cover was 5 km, the larger distance than the ones examined. WT power, natural land cover type and distance from water explained 40 %, 15 % and 11 % respectively of the total variance in bat deaths by WTs. The model predicted that operating but not surveyed WTs comprise of 377.8% and licensed but not operating yet will contribute to 210.2% additional deaths than the ones recorded. Results indicate that among all WT features and land cover characteristics, wind turbine power is the most significant factor associated to bat deaths. Results indicated that WTs located within 5 km buffer comprised of natural land cover types have substantial higher deaths. More WT power will result in more deaths. Wind turbines should not be licensed in areas where natural land cover at a radius of 5km exceeds 50%. These results are discussed in the climate-land use-biodiversity-energy nexus.
2.Steady-state analysis of networked epidemic models
Authors:Sei Zhen Khong, Lanlan Su
Abstract: Compartmental epidemic models with dynamics that evolve over a graph network have gained considerable importance in recent years but analysis of these models is in general difficult due to their complexity. In this paper, we develop two positive feedback frameworks that are applicable to the study of steady-state values in a wide range of compartmental epidemic models, including both group and networked processes. In the case of a group (resp. networked) model, we show that the convergence limit of the susceptible proportion of the population (resp. the susceptible proportion in at least one of the subgroups) is upper bounded by the reciprocal of the basic reproduction number (BRN) of the model. The BRN, when it is greater than unity, thus demonstrates the level of penetration into a subpopulation by the disease. Both non-strict and strict bounds on the convergence limits are derived and shown to correspond to substantially distinct scenarios in the epidemic processes, one in the presence of the endemic state and another without. Formulae for calculating the limits are provided in the latter case. We apply the developed framework to examining various group and networked epidemic models commonly seen in the literature to verify the validity of our conclusions.
3.Closed ecosystems extract energy through self-organized nutrient cycles
Authors:Akshit Goyal, Avi I. Flamholz, Alexander P. Petroff, Arvind Murugan
Abstract: Our planet is roughly closed to matter, but open to energy input from the sun. However, to harness this energy, organisms must transform matter from one chemical (redox) state to another. For example, photosynthetic organisms can capture light energy by carrying out a pair of electron donor and acceptor transformations (e.g., water to oxygen, CO$_2$ to organic carbon). Closure of ecosystems to matter requires that all such transformations are ultimately balanced, i.e., other organisms must carry out corresponding reverse transformations, resulting in cycles that are coupled to each other. A sustainable closed ecosystem thus requires self-organized cycles of matter, in which every transformation has sufficient thermodynamic favorability to maintain an adequate number of organisms carrying out that process. Here, we propose a new conceptual model that explains the self-organization and emergent features of closed ecosystems. We study this model with varying levels of metabolic diversity and energy input, finding that several thermodynamic features converge across ecosystems. Specifically, irrespective of their species composition, large and metabolically diverse communities self-organize to extract roughly 10% of the maximum extractable energy, or 100 fold more than randomized communities. Moreover, distinct communities implement energy extraction in convergent ways, as indicated by strongly correlated fluxes through nutrient cycles. As the driving force from light increases, however, these features -- fluxes and total energy extraction -- become more variable across communities, indicating that energy limitation imposes tight thermodynamic constraints on collective metabolism.
4.Species interactions reproduce abundance correlations patterns in microbial communities
Authors:José Camacho-Mateu, Aniello Lampo, Matteo Sireci, Miguel Ángel Muñoz, José A. Cuesta
Abstract: During the last decades macroecology has identified broad-scale patterns of abundances and diversity of microbial communities and put forward some potential explanations for them. However, these advances are not paralleled by a full understanding of the dynamical processes behind them. In particular, abundance fluctuations over metagenomic samples are found to be correlated, but reproducing populations through appropriate population models remains still an open task. The present paper tackles this problem and points to species interactions as a necessary mechanism to account for them. Specifically, we discuss several possibilities to include interactions in population models and recognize Lotka-Volterra constants as successful ansatz. We design a Bayesian inference algorithm to obtain sets of interaction constants able to reproduce the experimental correlation distributions much better than the state-of-the-art attempts. Importantly, the model still reproduces single-species, experimental, macroecological patterns previously detected in the literature, concerning the abundance fluctuations across both species and communities. Endorsed by the agreement with the observed phenomenology, our analysis provides insights on the properties of microbial interactions, and suggests their sparsity as a necessary feature to balance the emergence of different patterns.