Search bioRxiv⌕ Search

Biology subjects

Vesk, P.

Publications and source records attributed to Vesk, P..

4 recordsLinked to original sources

A general framework explaining variation in plant economics traits with environment and through ontogeny

Plant economics traits, such as leaf mass per unit leaf area (LMA) and stem specific density (SSD), capture diversity among plant species in how common tissues (leaf, wood, root) are constructed. These traits are key descriptors of plant strategy, yet it has proven difficult to explain this variation with theory and process-based models. Here we reveal a general explanation on why these economics traits vary with environment, through ontogeny, and with other plant traits. This explanation relies on three core assumptions: 1) plants seek to maximise growth rate, 2) growth rate can be decomposed into a product, and 3) there is a tradeoff between the efficiency of tissue construction and tissue turnover rate. Formulation of growth as a product is essential, as it causes the optimal value of an economics trait to vary with the plants biomass production rate, which means economics traits will naturally covary with the abiotic environment, the competitive context, and other strategical features of the plant. Finally, we show how a modification of the trait into plastic and non-plastic components alters the magnitude of intra-specific responses, aligning model responses with empirical trends. Broadly, our results help explain how plant form and function for a wide diversity of species is shaped to suit their environment and, moreover, they reveal insight into a general fast-slow spectrum (Reich 2014) with coordinated shifts among organs (leaf & stem) through tradeoffs between efficient tissue construction and turnover.

ecology↗

Neighbor density-dependent facilitation promotescoexistence and internal oscillation

The ability of species to form diverse communities is not fully understood. Species are known to interact in various ways with their neighborhood. Despite this, common models of species coexistence assume that per capita interactions are constant and competitive, even as the environment changes. In this study, we investigate how neighbor density-dependent variation in the strength and sign of species interactions changes species and community dynamics. We show that by including these sources of variation, predictions of ecological dynamics are significantly improved compared to outcomes of typical models that hold interaction strengths constant. We compared how well models based on different functions of neighbor density and identity did in describing population trajectories (i.e., persistence over time) and community dynamics (i.e., temporal stability, synchrony and degree of oscillation) in simulated two-species communities and a real diverse annual plant system. In our simulated communities, we found the highest level of coexistence between species pairs when species interactions varied from competitive to facilitative according to neighbor density (i.e., following a sigmoid function). Introducing within-guild facilitation through a nonlinear bounded function allowed populations, both simulated and empirical, to avoid extinction or runaway growth. In fact, nonlinear bounded functions (i.e., exponential and sigmoid functions) predicted population trends over time within the range of abundances observed over the last 10 years. With the sigmoid function, the simulated communities of two species displayed a higher probability of synchrony and oscillation than other functional forms. These simulated communities did not always show temporal stability but were predicted to coexist. Overall, varying species interactions lead to realistic ecological trajectories and community dynamics when bounded by asymptotes based on neighbor density. These findings are important for advancing our understanding of how diverse communities are sustained and for operationalizing ecological theory in the study of the real world.

ecology↗

The AusTraits Plant Dictionary

Traits with intuitive names, a clear scope and explicit description are essential for all trait databases. Reanalysis of data from a single database, or analyses that integrate data across multiple databases, can only occur if researchers are confident the trait concepts are consistent within and across sources. The lack of a unified, comprehensive resource for plant trait definitions has previously limited the utility of trait databases. Here we describe the AusTraits Plant Dictionary (APD), which extends the trait definitions included in the new trait database AusTraits. The development process of the APD included three steps: review and formalisation of the scope of each trait and the accompanying trait description; addition of trait meta-data; and publication in both human and machine-readable forms. Trait definitions include keywords, references and links to related trait concepts in other databases, and the traits are grouped into a hierarchy for easy searching. As well as improving the usability of AusTraits, the Dictionary will foster the integration of trait data across global and regional plant trait databases.

ecology↗

Introduction bias: Imbalance in species introductions may obscure the identification of traits associated with invasiveness

1The introduction stage is usually overlooked in trait-based studies of invasiveness, implicitly assuming that species introductions are random. However, human activities promote the movement of specific types of species. Thus, species deliberately introduced for distinct purposes (e.g. gardening, forestry) or as contaminants of human commodities (e.g. stowaway) will likely show particular traits. If species with certain traits have been preferentially introduced (i.e. introduction bias), some traits may have been mistakenly linked to species invasion abilities due to their influence on introduction probability. In this work, we propose a theoretical framework with different scenarios of introduction bias. The introduction scenarios are: (1) Random introduction, independent from traits; (2) Biologically biased introduction, following the worldwide distribution of the trait; and (3) Human biased introduction, following a theoretical introduction pathway that favours the introduction of species with high values of the trait. We evaluate how the introduced trait distributions in these scenarios may affect trait distributions in naturalized and invasive species pools under different hypothesized associations between traits and the probabilities of naturalization and invasion. The aim of this work is to identify situations where ignoring introduction bias may lead to spurious correlations being found between species traits and species ability to become naturalized or invasive. Our framework strongly points to the need to evaluate the traits of species that have become naturalized or invasive along with the traits of species that have failed to do so in order to unravel any existing introduction bias that may confound the correlation between species traits and invasion success. Overlooking a possible introduction bias may lead to the overestimation of the correlation between the trait and the species invasion ability, especially in cases when the pool of introduced species shows extreme values of the trait distribution (as compared to a random introduction). Trait-based studies that deserve special attention to avoid undesired effects of introduction bias on their findings are: those that investigate naturalization using only the pool of naturalized species, and those studies that examine invasiveness by comparing invasive species with native species.

ecology↗