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Habitat heterogeneity is a key driver of biodiversity of macroorganisms, yet how heterogeneity structures belowground microbial communities is not well understood. Importantly, belowground microbial communities may respond to any number of abiotic, biotic, and spatial drivers found in heterogeneous environments. Here, we examine potential drivers of prokaryotic and fungal communities in soils across the heterogenous landscape of the imperiled Florida scrub, a pyrogenic ecosystem where slight differences in elevation lead to large changes in water and nutrient availability and vegetation composition. We employ a comprehensive, large-scale sampling design to characterize the communities of prokaryotes and fungi associated with three habitat types and two soil depths (crust and subterranean) to evaluate (i) differences in microbial communities across these heterogeneous habitats, (ii) the relative roles of abiotic, biotic, and spatial drivers in shaping community structure, and (iii) the distribution of fungal guilds across these habitats. We sequenced soils from 40 complete replicates of habitat × soil depth combinations and sequenced the prokaryotic 16S and fungal internal transcribed spacer (ITS) regions using Illumina MiSeq. Habitat heterogeneity generated distinct communities of soil prokaryotes and fungi. Spatial distance played a role in structuring crust communities, whereas subterranean microbial communities were primarily structured by the shrub community, whose roots they presumably interacted with. This result helps to explain the unexpected transition we observed between arbuscular mycorrhiza–dominated soils at low-elevation habitats to ectomycorrhiza-dominated soils at high-elevation habitats. Our results challenge previous notions of environmental determinism of microbial communities and generate new hypotheses regarding symbiotic relationships across heterogeneous environments. 

Introductions are a critical tool in the recovery of many imperiled species, yet adequate evaluation and development of best practices has lagged. Importantly, long‐term post‐introduction data are typically lacking, as well as suitable comparisons to wild populations to provide a baseline against which to assess performance. Here, we report on three experimental introductions ofCrotalaria avonensis(Fabaceae), a federally endangered perennial herb that is narrowly endemic to scrub of the Lake Wales Ridge in peninsular Florida, U.S.A. We synthesize 10 years of post‐introduction monitoring at both the introduced and a nearby, protected wild population to (1) develop best practices for conservation, and (2) evaluate the success of the introduction. First, our study identified best practices that included using transplants propagated from stem cuttings, as well as several factors that may increase seed germination such as habitat choice, seed burial, and litter addition. Second, during the 10 years following the introduction, population density in the introduced population was higher than in a nearby protected, wild population, and a comparison of vital rates revealed that this result was due to relatively high clonal and seedling recruitment rates in the introduced population. Furthermore, the source population, which occurred on unprotected lands, precipitously declined during this time period, further highlighting the importance of safeguarding plants from that population. We report that a new, growing population ofC. avonensishas been established to date, with important implications for the species' conservation as well as how introductions are evaluated.

 

Translocated populations often show vigorous initial dynamics but eventually collapse. Modeling tools that incorporate basic ecological knowledge and allow for propagation of uncertainty can help identify potential risks. Here, we use Bayesian Integral Projection Models to estimate population growth rates (λs), associated elasticities, and extinction risks for the endangeredDicerandra christmanii. Our study compared natural populations in gaps (open areas) within the shrub matrix and roadsides, unoccupied gaps augmented with transplants, and introduced populations. These populations experienced different management, including prescribed fires, and had different initial conditions. Augmented gaps showed lower means but similar variation in λs as natural gaps. Yet, simulations indicate that augmentations can delay quasi‐extinction (40% of simulations) by 4 years at the population level. Introduced populations showed higher means and variation in λs as wild gaps. While vital rate estimates suggested initial translocation success, time to quasi‐extinction was projected to be 7 years shorter for introductions in gaps than for natural gap populations. These contradictory results are partially explained by the lack of established seed banks in introduced populations, which affected the response of early life stage transitions to a prescribed fire. This study highlights the need to account for site‐specific information in models of population dynamics, including initial conditions and management history, and especially cryptic life stages such as dormant seeds.

 

Species translocations are increasingly common in rare plant conservation. Wild populations can provide basic ecological knowledge to improve their chance of success. In the heavily fragmented Florida scrub, USA, many listed species require translocations to persist, includingDicerandra christmanii. In 1994, we began monitoring the only protected population ofD. christmaniigrowing both in gaps (open areas) within the shrub matrix and on roadsides. In 2010, we augmented this population by adding plants and seeds to unoccupied gaps. In 2012, we introduced plants to a separate protected site to create a new population. We evaluated early translocation success using generalized linear mixed‐effect models of vital rate variation among habitat types. Survival probability increased with size, peaking at 0.6–0.8, and was lowest in augmentations and highest in introductions. Growth increased with plant size across all habitat types, except for the largest adults which experienced senescence. Naturally recruited plants in gaps showed the highest reproduction probability and fecundity at smaller sizes, but larger plants in translocations had the highest fecundity. Yearling recruitment was higher in translocated plants relative to naturally recruited plants in gaps during the initial years following outplanting. Experimental components of translocations also affected outplanting performance with positive effects of fire. These analyses suggest a high potential for translocations to become established and contribute to species recovery.

 

Environmental stress is increasing worldwide, yet we lack a clear picture of how stress disrupts the stability of microbial communities and the ecosystem services they provide. Here, we present the first evidence that naturally-occurring microbiomes display network properties characteristic of unstable communities when under persistent stress. By assessing changes in diversity and structure of soil microbiomes along 40 replicate stress gradients (elevation/water availability gradients) in the Florida scrub ecosystem, we show that: (1) prokaryotic and fungal diversity decline in high stress, and (2) two network properties of stable microbial communities—modularity and negative:positive cohesion—have a clear negative relationship with environmental stress, explaining 51–78% of their variation. Interestingly, pathogenic taxa/functional guilds decreased in relative abundance along the stress gradient, while oligotrophs and mutualists increased, suggesting that the shift in negative:positive cohesion could result from decreasing negative:positive biotic interactions consistent with the predictions of the Stress Gradient Hypothesis. Given the crucial role microbiomes play in ecosystem functions, our results suggest that, by limiting the compartmentalization of microbial associations and creating communities dominated by positive associations, increasing stress in the Anthropocene could destabilize microbiomes and undermine their ecosystem services.

 

Advances in remote sensing technologies offer new means to monitor habitats of importance on large scales. Florida rosemary scrub is one such threatened habitat, found in patches across the landscape in relatively elevated areas, and is often characterized by shrub‐less areas (gaps) among the dominant shrubs, which provide favorable microhabitats for many endemic and endangered plants and animals. However, gaps are difficult and time‐consuming to characterize, especially across large areas, using traditional ground‐based field methods. We developed and tested a method for rapidly classifying gaps using an unmanned aerial vehicle (UAV or drone). Aerial data were collected by a UAV‐mounted camera in April 2018, and stratified, random ground surveys to verify UAV data were conducted March through April 2018 at Archbold Biological Station in south‐central Florida, USA. We used mosaicked and georeferenced digital surface and terrain models to calculate vegetation height across 33 rosemary scrub sites (~230,000 m²at 0.064 m²pixel resolution). Gaps were defined as >1 m²areas where vegetation height was <10 cm. We found that gap areas from UAV models and field surveys were significantly correlated across varying gap sizes, times‐since‐fire, and relative elevations. We also observed a significant decrease in mean gap area and percent gap space with increasing time‐since‐fire, a pattern consistent with smaller‐scale, ground‐based sampling, and a marginally significant increase in gap area with relative elevation. This remote sensing method lends itself to better exploration of how gap areas, their spatiotemporal patterns, and associated fire history, elevation, soil, and other geographic data affect structural vegetation dynamics across the landscape. This study illustrates the success of UAV modeling of gap space in Florida rosemary scrub, a result of regional consequence for the southeastern United States, but more broadly, it encourages the use of UAV technology as a tool to enhance traditional field‐based methods in systems globally. As habitat fragmentation and loss become increasingly problematic for the conservation of threatened habitats, understanding these complex spatial dynamics is crucial to the conservation and management of vegetation communities and their biodiversity.

 

Fire plays a major role in structuring plant communities across the globe. Interactions with soil microbes impact plant fitness, scaling up to influence plant populations and distributions. Here we present the first factorial manipulation of both fire and soil microbiome presence to investigate their interactive effects on plant performance across a suite of plant species with varying life history traits.

We conducted fully factorial experiments on 11 species from the Florida scrub ecosystem to test plant performance responses to soils with varying fire histories (36 soil sources), the presence/absence of a microbiome, and exposure to an experimental burn.

Results revealed interactive ‘pulse’ effects between fire and the soil microbiome on plant performance. On average, post‐fire soil microbiomes strongly reduced plant productivity compared to unburned or sterilized soils. Interestingly, longer‐term fire ‘legacy’ effects had minor impacts on plant performance and were unrelated to soil microbiomes.

While pulse fire effects on plant–microbiome interactions are short‐term, they could have long‐term consequences for plant communities by establishing differential microbiome‐mediated priority effects during post‐disturbance succession. The prominence of pulse fire effects on plant–microbe interactions has even greater import due to expected increases in fire disturbances resulting from anthropogenic climate change.

 

Seed bank, seed dispersal and historical disturbance are critical factors affecting plant population persistence. However, because of difficulties collecting data on these factors they are often ignored.

We evaluated the roles of seed bank, seed dispersal and historical disturbance on metapopulation persistence ofHypericum cumulicola, a Florida endemic. We took advantage of long‐term demographic data of multiple populations (22 years; ~11 K individuals; 15 populations) and a wealth of information on burn history (1962–present), and habitat attributes (patch specific location, elevation, area and aggregation) of a system of 92 patches of Florida rosemary scrub. We used previously developed integral projection models to assess the relative ability of simulations with different levels of seed dormancy for recently produced and older seeds and different dispersal kernels (including no dispersal) to predict regional observed occupancy and plant abundance in patches in 2016–2018. We compared a simulation with this model using historical burn history to 500 model simulations with the same average fire regime (using a Weibull distribution to determine the probability of ignition) but with random ignition years.

The most likely model had limited dispersal (mean = 0.5 m) and the highest dormancy (field estimates × 1.2 %) and its predictions were associated with observed occurrences (67% correct) and densities (20% of variance explained). Historical burn synchrony among neighbouring patches (skewness in the number of patches burned by year = 1.79) probably explains the higher densities predicted by the simulation with the historical fire regime compared with predicted abundances after simulations using random ignition years (skewness = 0.20 +SE= 0.01).

Synthesis.Our findings demonstrate the pivotal role of seed dormancy, dispersal and fire history on population dynamics, distribution and abundance. Because of the prevalence of metapopulation dynamics, we should be aware of the significance of changes in the availability and configuration of suitable habitat associated with human or non‐human landscape changes. Decisions on prescribed fires (or other disturbances) will benefit from our knowledge of consequences of fire frequency, but also of location of ignition and the probability of fire spread.

 

Vegetative dormancy, that is the temporary absence of aboveground growth for ≥ 1 year, is paradoxical, because plants cannot photosynthesise or flower during dormant periods. We test ecological and evolutionary hypotheses for its widespread persistence. We show that dormancy has evolved numerous times. Most species displaying dormancy exhibit life‐history costs of sprouting, and of dormancy. Short‐lived and mycoheterotrophic species have higher proportions of dormant plants than long‐lived species and species with other nutritional modes. Foliage loss is associated with higher future dormancy levels, suggesting that carbon limitation promotes dormancy. Maximum dormancy duration is shorter under higher precipitation and at higher latitudes, the latter suggesting an important role for competition or herbivory. Study length affects estimates of some demographic parameters. Our results identify life historical and environmental drivers of dormancy. We also highlight the evolutionary importance of the little understood costs of sprouting and growth, latitudinal stress gradients and mixed nutritional modes.