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As sea‐level rise converts coastal forest to salt marsh, marsh arthropods may migrate inland; however, the resulting changes in arthropod communities, including the stage of forest retreat that first supports saltmarsh species, remain unknown. Furthermore, the ghost forest that forms in the wake of rapid forest retreat offers an unknown quality of habitat to marsh arthropods. In a migrating marsh in Virginia, USA, ground‐dwelling arthropod communities were assessed across the forest‐to‐marsh gradient, and functional use of ghost forest and high marsh habitats was evaluated to determine whether marsh arthropods utilized expanded marsh in the same way as existing marsh. Diet and body condition were compared for two marsh species found in both high marsh and ghost forest (the detritivore amphipod,Orchestia grillus, and the hunting spider,Pardosa littoralis). Community composition differed among zones along the gradient, driven largely by retreating forest taxa (e.g., Collembola), marsh taxa migrating into the forest (e.g.,O. grillus), and unique taxa (e.g., Hydrophilinae beetles) at the ecotone. The low forest was the most inland zone to accommodate the saltmarsh speciesO. grillus, suggesting that inland migration of certain saltmarsh arthropods may co‐occur with early saltmarsh plant migration and precede complete tree canopy die‐off. Functionally,O. grillusoccupied a larger trophic niche in the ghost forest than the high marsh, likely by consuming both marsh and terrestrial material. Despite this, both observed marsh species primarily consumed from the marsh grass food web in both habitats, and no lasting differences in body condition were observed. For the species and functional traits assessed, the ghost forest and high marsh did not show major differences at this site. Forest retreat and marsh migration may thus provide an important opportunity for generalist saltmarsh arthropods to maintain their habitat extent in the face of marsh loss due to sea‐level rise.

 

The resource‐availability hypothesis (RAH) and the intraspecific RAH (RAH intra ), posit that resources, (i.e. nutrients) control plant antiherbivore defenses. Both hypotheses predict that in low‐resource environments, plant growth is slow, and constitutive defense is high. In high‐resource environments, however, the RAH predicts that plant growth is fast, and constitutive defense is low, whereas the RAH intra predicts that increased resources attract more herbivores, and this intensified grazing pressure leads to high constitutive defense. Salt marshes are nutrient‐limited ecosystems threatened by eutrophication and chronic herbivory, yet we know little about how these stressors shape saltmarsh plant antiherbivore defenses, which influence trophic interactions and ecosystem resilience. We manipulated resource availability via nutrient addition and herbivory via the marsh periwinkle Littoraria irrorata , on the saltmarsh foundation species Spartina alterniflora , in mesocosms. Because plant age can also influence trait variation, we measured traits in both original and clonally‐grown new stems. Feeding assays then evaluated how treatments and plant age affected subsequent Littoraria consumption of Spartina . Nutrient addition stimulated growth, while decreasing defensive traits (e.g. fiber and silica content), following the RAH. Herbivory enhanced belowground production and increased stem diameter, yet did not induce defensive traits, contrary to our expectations. Herbivory plus nutrients increased Spartina biomass and reduced phenolics, a defensive trait, further supporting the RAH. Regardless of treatment, clonally‐grown new stems had greater variation in measured traits. Despite altered traits, however, treatments and plant age did not affect Littoraria consumption. Our results support the RAH and part of the RAH intra and suggest: 1) nutrient availability is a primary driver of plant trait change and 2) plant age controls the magnitude of trait variation in Spartina . Further, our findings indicate that eutrophic conditions may not always increase top‒down control by herbivores, and in some instances can enhance saltmarsh resilience against sea‐level rise via stimulated Spartina biomass production. 

We utilize a coupled economy–agroecology–hydrology modeling framework to capture the cascading impacts of climate change mitigation policy on agriculture and the resulting water quality cobenefits. We analyze a policy that assigns a range of United States government’s social cost of carbon estimates ($51, $76, and $152/ton of CO₂-equivalents) to fossil fuel–based CO₂emissions. This policy raises energy costs and, importantly for agriculture, boosts the price of nitrogen fertilizer production. At the highest carbon price, US carbon emissions are reduced by about 50%, and nitrogen fertilizer prices rise by about 90%, leading to an approximate 15% reduction in fertilizer applications for corn production across the Mississippi River Basin. Corn and soybean production declines by about 7%, increasing crop prices by 6%, while nitrate leaching declines by about 10%. Simulated nitrate export to the Gulf of Mexico decreases by 8%, ultimately shrinking the average midsummer area of the Gulf of Mexico hypoxic area by 3% and hypoxic volume by 4%. We also consider the additional benefits of restored wetlands to mitigate nitrogen loading to reduce hypoxia in the Gulf of Mexico and find a targeted wetland restoration scenario approximately doubles the effect of a low to moderate social cost of carbon. Wetland restoration alone exhibited spillover effects that increased nitrate leaching in other parts of the basin which were mitigated with the inclusion of the carbon policy. We conclude that a national climate policy aimed at reducing greenhouse gas emissions in the United States would have important water quality cobenefits.

 

Species across the planet are shifting or expanding their ranges because of climate change. These are climate migrants. Although climate migrants are well documented, their impacts on recipient ecosystems are not. Climate migrants that are also ecosystem engineers (species that modify or create habitats) will likely have profound effects on ecosystems. The Atlantic marsh fiddler crab,Minuca pugnax, is a burrowing crab that recently expanded its range into the northeastern United States. In its historical range,M. pugnaxenhances the aboveground growth of the cordgrassSpartina alterniflora, a plant critical to marsh persistence. In a control‐impact study, however, we found thatSpartinaaboveground biomass was 40% lower whenM. pugnaxwas present. Thus, the positive effect ofM. pugnaxonSpartinaaboveground biomass flipped to a negative one in its expanded range.Spartinabelowground biomass was also 30% lower on average when crabs were present, a finding consistent with what is seen in the historical range. These impacts onSpartinaare likely due to burrowing byM. pugnax.Benthic microalgae was, on average, 45% lower when crabs were present. Fiddler crabs eat benthic microalgae, and these results suggest that fiddler crabs can control algal biomass via grazing. Because fiddler crabs reduced the biomass of foundational primary producers in its expanded range, our results imply thatM. pugnaxcan influence other saltmarsh functions such as carbon storage and accretion as they expand north. Most strikingly, our results suggest that as species expand or shift their range with climate change, not only can they have profound impacts in their new ranges but those impacts can be the inverse of what is seen in their historical ranges.

 

The exploitation of ecosystem services, through processes like agricultural production, is associated with myriad negative environmental impacts, which are felt by stakeholders on local, regional, and global scales. The varying type and scale of impacts leads naturally to fragmented and siloed approaches to mitigating externalities by diverse governmental and non-governmental institutions. However, policies designed to address a single impact may worsen other negative impacts. As a result, even when groups have the expertise to design policy solutions in one dimension, policies addressing single issues may conflict and result in less than ideal outcomes in combination. In this paper, we present a conceptual framework and examples of this kind of ‘policy collision,’ where policies produce mutual negative interference so that policies designed independently may fail to achieve their goals. We argue that an integrated systems perspective is needed to overcome this problem and present several positive examples where this has been put into practice. Policy collision provides a useful framework for determining how each colliding policy should be modified in improve outcomes.

 

The interplay between charge transfer and electronic disorder in transition-metal dichalcogenide multilayers gives rise to superconductive coupling driven by proximity enhancement, tunneling and superconducting fluctuations, of a yet unwieldy variety. Artificial spacer layers introduced with atomic precision change the density of states by charge transfer. Here, we tune the superconductive coupling between$\text{NbS}{\text{e}}_{\text{2}}$monolayers from proximity-enhanced to tunneling-dominated. We correlate normal and superconducting properties in${\left[{\left(\text{SnSe}\right)}_{1+\delta }\right]}_m{\left[\text{NbS}{\text{e}}_{\text{2}}\right]}_1$tailored multilayers with varying SnSe layer thickness ($m=1-15$). From high-field magnetotransport the critical fields yield Ginzburg–Landau coherence lengths with an increase of$140\mathrm{\%}$cross-plane ($m=1-9$), trending towards two-dimensional superconductivity for$m>9$. We show cross-overs between three regimes: metallic with proximity-enhanced coupling ($m=1-4$), disordered-metallic with intermediate coupling ($m=5-9$) and insulating with Josephson tunneling ($m>9$). Our results demonstrate that stacking metal mono- and dichalcogenides allows to convert a metal/superconductor into an insulator/superconductor system, prospecting the control of two-dimensional superconductivity in embedded layers.

 

Abstract A parasite can change its host’s behavior in spectacular ways. When the saltmarsh amphipod Orchestia grillus (Bosc, 1802) is infected with the trematode Levinseniella byrdi (Heard, 1968) it is bright orange and is found in the open unlike uninfected individuals. I tested the hypothesis that infected amphipods are found in the open because L. byrdi reverses their innate photophobia. During daytime treatments and when placed in a dark chamber, 0% of the uninfected and 20% of the infected amphipods, on average, moved to the light chamber after 30 minutes. When placed in a light chamber, 91% of the uninfected and 53% of the infected amphipods, on average, went to the dark side after 30 minutes. These results clearly indicate that O. grillus is normally photophobic, but not drawn to light when infected with L. byrdi. Instead, L. byrdi appears to neutralize the amphipod’s photophobia. Uninfected O. grillus are typically found under vegetation. I hypothesize that O. grillus with L. byrdi infections wander into open, unvegetated habitats randomly. In addition, 94% of infected amphipods could be touched by a finger in the field suggesting they can be easily caught by predators. Levinseniella byrdi infects at least three other amphipod hosts, Chelorchestia forceps (Smith & Heard, 2001), Uhlorchestia spartinophila (Bousfield & Heard, 1986), and U. uhleri (Shoemaker, 1930). The parasite-manipulation hypothesis suggests that the parasite-induced changes (conspicuous body color and neutralized light response) are adaptive for L. byrdi to make amphipod hosts more susceptible to bird predators, the definitive hosts. This hypothesis remains to be tested.