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  1. Society is confronted by interconnected threats to ecological sustainability. Among these is the devastation of forests by destructive non-native pathogens and insects introduced through global trade, leading to the loss of critical ecosystem services and a global forest health crisis. We argue that the forest health crisis is a public-good social dilemma and propose a response framework that incorporates principles of collective action. This framework enables scientists to better engage policymakers and empowers the public to advocate for proactive biosecurity and forest health management. Collective action in forest health features broadly inclusive stakeholder engagement to build trust and set goals; accountability for destructive pest introductions; pooled support for weakest-link partners; and inclusion of intrinsic and nonmarket values of forest ecosystems in risk assessment. We provide short-term and longer-term measures that incorporate the above principles to shift the societal and ecological forest health paradigm to a more resilient state. Expected final online publication date for the Annual Review of Phytopathology, Volume 61 is September 2023. Please see for revised estimates. 
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    Free, publicly-accessible full text available September 3, 2024
  2. Abstract

    Pesticides and parasites have each been linked to increased mortality in western honey bees (Apis mellifera). Currently, it is uncertain if one makes the other worse; several studies have tested for potential synergistic stressor effects, but results have been mixed.

    Here, we use a hierarchical meta‐analysis of 63 experiments from 26 studies to gain a clearer view of the combined effects of parasites and pesticides on honey bee health.

    We found that combined pesticide–parasite treatments do tend to be deadlier than uncombined treatments but are significantly less deadly than predicted additive or multiplicative effects. In other words, combined treatment effects are not synergistic, but antagonistic.

    Much of the previous uncertainty about the combined effects of pesticides and parasites on honey bee health can be attributed to a bias in the previous research against stressor antagonism; many researchers have excluded the possibility of antagonism a priori.

    Synthesis and applications. Meta‐analysis shows that when honey bees are stressed by a combination of pesticides and parasites, the combined stress effect is antagonistic, that is, less than the sum of its parts. A better understanding of the mechanisms underlying this antagonism could prove critical for effective management of honey bee health.

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  3. Abstract

    Dysregulation of extracellular matrix (ECM) synthesis, organization, and mechanics are hallmark features of diseases like fibrosis and cancer. However, most in vitro models fail to recapitulate the three‐dimensional (3D) multi‐scale hierarchical architecture of collagen‐rich tissues and as a result, are unable to mirror native or disease phenotypes. Herein, using primary human fibroblasts seeded into custom fabricated 3D non‐adhesive agarose molds, a novel strategy is proposed to direct the morphogenesis of engineered 3D ring‐shaped tissue constructs with tensile and histological properties that recapitulate key features of fibrous connective tissue. To characterize the shift from monodispersed cells to a highly‐aligned, collagen‐rich matrix, a multi‐modal approach integrating histology, multiphoton second‐harmonic generation, and electron microscopy is employed. Structural changes in collagen synthesis and alignment are then mapped to functional differences in tissue mechanics and total collagen content. Due to the absence of an exogenously added scaffolding material, this model enables the direct quantification of cell‐derived changes in 3D matrix synthesis, alignment, and mechanics in response to the addition or removal of relevant biomolecular perturbations. To illustrate this, the effects of nutrient composition, fetal bovine serum, rho‐kinase inhibitor, and pro‐ and anti‐fibrotic compounds on ECM synthesis, 3D collagen architecture, and mechanophenotype are quantified.

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