Seed and seedling predation by vertebrates mediates the effects of adult trees in two temperate tree species.

Specialised natural enemies can locally suppress seeds and seedlings near conspecific adults more than far from them. Whilst this is thought to facilitate species coexistence, the relative contribution of multiple enemies to whether heterospecific seeds and seedlings rather than conspecifics perform better beneath a particular adult species remains less clear, especially in regions with spatially extensive monodominant stands. We designed a field exclusion experiment to separate the effects of fungi, insects and vertebrates on the seedling establishment and early survival of two temperate tree species, Fagus sylvatica and Picea abies, in the adult tree monocultures of these species.

Distribution of biomass dynamics in relation to tree size in forests across the world.

Tree size shapes forest carbon dynamics and determines how trees interact with their environment, including a changing climate. Here, we conduct the first global analysis of among-site differences in how aboveground biomass stocks and fluxes are distributed with tree size. We analyzed repeat tree censuses from 25 large-scale (4-52 ha) forest plots spanning a broad climatic range over five continents to characterize how aboveground biomass, woody productivity, and woody mortality vary with tree diameter.

Beyond direct neighbourhood effects: higher-order interactions improve modelling and predicting tree survival and growth.

It is known that biotic interactions are the key to species coexistence and maintenance of species diversity. Traditional studies focus overwhelmingly on pairwise interactions between organisms, ignoring complex higher-order interactions (HOIs). In this study, we present a novel method of calculating individual-level HOIs for trees, and use this method to test the importance of size- and distance-dependent individual-level HOIs to tree performance in a 25-ha temperate forest dynamic plot.

A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouse.

Pathogenic variants in the WDR45 (OMIM: 300,526) gene on chromosome Xp11 are the genetic cause of a rare neurological disorder characterized by increased iron deposition in the basal ganglia. As WDR45 encodes a beta-propeller scaffold protein with a putative role in autophagy, the disease has been named Beta-Propeller Protein-Associated Neurodegeneration (BPAN). BPAN represents one of the four most common forms of Neurodegeneration with Brain Iron Accumulation (NBIA).