Reproductive compensatory photosynthesis in a semi-arid rangeland bunchgrass.

While increased foliar photosynthesis is well documented across many plant species in response to diverse modes of herbivory, the compensatory ability of photosynthetically active reproductive structures is unknown. To address this, we partially defoliated basal florets in seed heads of crested wheatgrass (Agropyron cristatum (L.) Gaertn.), an exotic Eurasian perennial bunchgrass widely distributed across North American sagebrush steppe. We followed direct and indirect responses by tracking post-clipping photosynthesis in clipped basal and unclipped distal florets, respectively, and comparing these to similar florets on unclipped seed heads. Compensatory photosynthesis was apparent 24 h after clipping; over the pre-anthesis period, clipped basal floret photosynthesis was + 62%, stomatal conductance was + 82%, and PSII photochemical yield was - 39% of unclipped controls. After anthesis, intact florets distal to clipped florets had modestly higher photosynthetic rates compared to controls, while basal floret rates did not differ between treatments. Compensatory photosynthesis reduced intrinsic water use efficiency (iWUE; photosynthesis/stomatal conductance) 68-40% below controls over pre- and post-anthesis periods, respectively. Specific mass (dry mass/area) of clipped florets was - 15% of controls, while florets distal to these had specific mass 11% greater than distal or basal florets on unclipped seed heads. These results suggest damaged basal florets provided carbon to unaffected distal florets. This could explain crested wheatgrass's ability to produce viable seeds under conditions limiting to native bunchgrasses, and presents a novel mechanism germane to the development of convergent drought- and grazing-tolerance traits important to arid and semi-arid rangeland plant community resilience to climate variability.

Plant community data from a statewide survey of paired serpentine and non-serpentine soils in California, USA.

Soils derived from ultramafic parent materials (hereafter serpentine) provide habitat for unique plant communities containing species with adaptations to the low nutrient levels, high magnesium : calcium ratios, and high metal content (Ni, Zn) that characterize serpentine. Plants on serpentine have long been studied in evolution and ecology, and plants adapted to serpentine contribute disproportionately to plant diversity in many parts of the world. In 2000-2003, serpentine plant communities were sampled at 107 locations representing the full range of occurrence of serpentine in California, USA, spanning large gradients in climate. In 2009-2010, plant communities were similarly sampled at 97 locations on nonserpentine soil, near to and paired with 97 of the serpentine sampling locations. (Some serpentine locations were revisited in 2009-2010 to assess the degree of change since 2000-2003, which was minimal.) At each serpentine or nonserpentine location, a north- and a south-facing 50 × 10 m plot were sampled. This design produced 97 "sites" each consisting of four "plots" (north-south exposure, serpentine-nonserpentine soil). All plots were initially visited three or more times over two years to record plant diversity and cover, and a subset were revisited in 2014 to examine community change after a drought. The original question guiding the study was how plant diversity is shaped by the spatially patchy nature of the serpentine habitat. Subsequently, we investigated how climate drives plant diversity at multiple scales (within locations, between locations on the same and different soil types, and across entire regions) and at different levels of organization (taxonomic, functional, and phylogenetic). There are no copyright restrictions and users should cite this data paper in publications that result from use of the data.

The biggest bang for the buck: cost-effective vegetation treatment outcomes across drylands of the western United States.

Restoration and rehabilitation are globally implemented to improve ecosystem condition but often without tracking treatment expenditures relative to ecological outcomes. We evaluated the cost-effectiveness of widely conducted woody plant and herbaceous invasive plant removals and seeding treatments in drylands of the western United States from 2004 to 2018 to determine how land managers can optimize efforts. Woody plant cover decreased at a similar rate per dollar spent regardless of vegetation removal type, and the dominant invasive species was reduced by herbicide application. Relatively inexpensive herbicide application also had a large positive effect on seeded perennial grass cover that was enhanced by additional cost; while expensive woody mastication treatments had little effect regardless of additional cost. High seed cost was driven by including a large proportion of native species in seed mixes, and combined with high seeding cost, promoted a short-term (2-3 yr) gain in perennial forb cover and species richness. In contrast, seeding and seed mix cost had no bearing on seeded perennial grass cover, in part, because relatively cheap nonnative seeded species rapidly increased in cover. Our results suggest the differential benefits of commonly implemented treatments aimed at reducing wildfire risk, improving wildlife habitat and forage, and reducing erosion. Given the growing need and cost of restoration and rehabilitation, we raise the importance of specifying treatment budgets and objectives, coupled with effectiveness monitoring, to improve future outcomes.

Shading and litter mediate the effects of soil fertility on the performance of an understorey herb.

BACKGROUND AND AIMS: Soil fertility and topographic microclimate are common determinants of plant species distributions. However, biotic conditions also vary along these abiotic gradients, and may mediate their effects on plants. In this study, we investigated whether soils and topographic microclimate acted directly on the performance of a focal understorey plant, or indirectly via changing biotic conditions. METHODS: We examined direct and indirect relationships between abiotic variables (soil fertility and topographic microclimate) and biotic factors (overstorey and understorey cover, litter depth and mycorrhizal colonization) and the occurrence, density and flowering of a common understorey herb, Trientalis latifolia, in the Klamath-Siskiyou Mountains, Oregon, USA. RESULTS: We found that the positive effects of soil fertility on Trientalis occurrence were mediated by greater overstorey shading and deeper litter. However, we did not find any effects of topographic microclimate on Trientalis distribution that were mediated by the biotic variables we measured. The predictive success of Trientalis species distribution models with soils and topographic microclimate increased by 12 % with the addition of the biotic variables. CONCLUSIONS: Our results reinforce the idea that species distributions are the outcome of interrelated abiotic gradients and biotic interactions, and suggest that biotic conditions, such as overstorey density, should be included in species distribution models if data are available.

Climate-driven diversity loss in a grassland community.

Local ecological communities represent the scale at which species coexist and share resources, and at which diversity has been experimentally shown to underlie stability, productivity, invasion resistance, and other desirable community properties. Globally, community diversity shows a mixture of increases and decreases over recent decades, and these changes have relatively seldom been linked to climatic trends. In a heterogeneous California grassland, we documented declining plant diversity from 2000 to 2014 at both the local community (5 m(2)) and landscape (27 km(2)) scales, across multiple functional groups and soil environments. Communities became particularly poorer in native annual forbs, which are present as small seedlings in midwinter; within native annual forbs, community composition changed toward lower representation of species with a trait indicating drought intolerance (high specific leaf area). Time series models linked diversity decline to the significant decrease in midwinter precipitation. Livestock grazing history, fire, succession, N deposition, and increases in exotic species could be ruled out as contributing causes. This finding is among the first demonstrations to our knowledge of climate-driven directional loss of species diversity in ecological communities in a natural (nonexperimental) setting. Such diversity losses, which may also foreshadow larger-scale extinctions, may be especially likely in semiarid regions that are undergoing climatic trends toward higher aridity and lower productivity.

Plant communities on infertile soils are less sensitive to climate change.

BACKGROUND AND AIMS: Much evidence suggests that plant communities on infertile soils are relatively insensitive to increased water deficit caused by increasing temperature and/or decreasing precipitation. However, a multi-decadal study of community change in the western USA does not support this conclusion. This paper tests explanations related to macroclimatic differences, overstorey effects on microclimate, variation in soil texture and plant functional traits. METHODS: A re-analysis was undertaken of the changes in the multi-decadal study, which concerned forest understorey communities on infertile (serpentine) and fertile soils in an aridifying climate (southern Oregan) from 1949-1951 to 2007-2008. Macroclimatic variables, overstorey cover and soil texture were used as new covariates. As an alternative measure of climate-related change, the community mean value of specific leaf area was used, a functional trait measuring drought tolerance. We investigated whether these revised analyses supported the prediction of lesser sensitivity to climate change in understorey communities on infertile serpentine soils. KEY RESULTS: Overstorey cover, but not macroclimate or soil texture, was a significant covariate of community change over time. It strongly buffered understorey temperatures, was correlated with less change and averaged >50 % lower on serpentine soils, thereby counteracting the lower climate sensitivity of understorey herbs on these soils. Community mean specific leaf area showed the predicted pattern of less change over time in serpentine than non-serpentine communities. CONCLUSIONS: Based on the current balance of evidence, plant communities on infertile serpentine soils are less sensitive to changes in the climatic water balance than communities on more fertile soils. However, this advantage may in some cases be lessened by their sparser overstorey cover.