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Foundation species such as corals, trees, and bivalves enhance ecosystem function and biodiversity by creating habitat for associated organisms, ameliorating stress, and modifying energy flow. However, theory generally ignores their ecological functions after death. Here we review the traits and functions of dead foundation species relative to their living counterparts, and the processes that control their persistence. We also conduct a meta-analysis to quantify where the effect of dead foundation species on community functions is unique or redundant to their living counterparts. We focus on marine ecosystems due to the greater diversity of foundation species they support and the increasing prevalence of mass-mortality events in these systems. Our study reveals how foundation species continue to provide important functions after death and exhibit new functions that are distinct from when they are alive. We develop a framework using broad, trait-based functional differences among types of dead foundation species to predict whether they will promote stability by enhancing ecosystem resilience or promote shifts to alternate states. Our synthesis establishes how an understanding of the ecological importance of dead foundation species can assist in predicting system trajectories, enhance restoration and conservation efforts, and contribute to ecological theory on habitat heterogeneity and ecosystem function.

Insect phenological lability is key for determining which species will adapt under environmental change. However, little is known about when adult insect activity terminates, and overall activity duration. We used community-science and museum specimen data to investigate the effects of climate and urbanization on timing of adult insect activity for 101 species varying in life history traits. We found detritivores and species with aquatic larval stages extend activity periods most rapidly in response to increasing regional temperature. Conversely, species with subterranean larval stages have relatively constant durations regardless of regional temperature. Multivoltine and univoltine species both extended their period of adult activity similarly in warmer conditions. Longer adult durations may represent a general response to warming, but voltinism data in subtropical environments is likely underreported. This effort provides a framework to address drivers of adult insect phenology at continental scales, and a basis for predicting species response to environmental change.

A wave of green leaves and multi-colored flowers advances from low to high latitudes each spring. However, little is known about how flowering offset (i.e., ending of flowering) and duration of populations of the same species vary along environmental gradients. Understanding these patterns is critical for predicting the effects of future climate and land-use change on plants, pollinators, and herbivores. Here, we investigated potential climatic and landscape drivers of flowering onset, offset, and duration of 52 plant species with varying key traits. We generated phenology estimates using >270,000 community-science photographs and a novel presence-only phenometric estimation method. We found longer flowering durations in warmer areas, which is more obvious for summer-blooming species compared to spring-bloomers driven by their strongly differing offset dynamics. We also found that higher human population density and higher annual precipitation are associated with delayed flowering offset and extended flowering duration. Finally, offset of woody perennials was more sensitive than herbaceous species to both climate and urbanization drivers. Empirical forecast models suggested that flowering durations will be longer in 2030 and 2050 under representative concentration pathway (RCP) 8.5, especially for summer-blooming species. Our study provides critical insight into drivers of key flowering phenophases and confirms that Hopkins' Bioclimatic Law also applies to flowering durations for summer-blooming species and herbaceous spring-blooming species.

Throughout the world DNA banks are used as storage repositories for genetic diversity of organisms ranging from plants to insects to mammals. Designed to preserve the genetic information for organisms of interest, these banks also indirectly preserve organisms’ associated microbiomes, including fungi associated with plant tissues. Studies of fungal biodiversity lag far behind those of macroorganisms, such as plants, and estimates of global fungal richness are still widely debated. Utilizing previously collected specimens to study patterns of fungal diversity could significantly increase our understanding of overall patterns of biodiversity from snapshots in time. Here, we investigated the fungi inhabiting the phylloplane among species of the endemic Hawaiian plant genus, Clermontia (Campanulaceae). Utilizing next generation DNA amplicon sequencing, we uncovered approximately 1,780 fungal operational taxonomic units from just 20 DNA bank samples collected throughout the main Hawaiian Islands. Using these historical samples, we tested the macroecological pattern of decreasing community similarity with decreasing geographic proximity. We found a significant distance decay pattern among Clermontia associated fungal communities. This study provides the first insights into elucidating patterns of microbial diversity through the use of DNA bank repository samples.