36 research outputs found

    Fire Effects on Three Trophic Levels in a Central Arkansas Grassland

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    We studied the effect of a late growing-season fire on the plant and foliar arthropod communities in a naturally occurring grassland. In central Arkansas, these grasslands are common on south-facing slopes where shallow soils and hot/dry weather conditions during the summer cannot support the growth of a forest community. Patches of grassland were burned in the autumn (4 November, late growing season), often the time of natural fires in Arkansas, and compared to unburned areas. Fire increased the biomass of forbs and decreased the biomass of grasses, although overall biomass was not different between treatments. Among the foliar arthropods, herbivores were significantly reduced by burning, especially the Homoptera. Carnivorous arthropods as a whole were not affected by burning, although spiders showed a small but significant reduction. The response of arthropods to fire occurred almost one year after the burn, showing that fire effects can be delayed for a substantial period of time. This experiment shows that fire occurring during the natural burning period in Arkansas can have substantial effects on grasslands communities. The response of plants in Arkansas is similar to that of plants in nearby grasslands on the Great Plains and southeastern United States which also show a great increase in forbs under late growing season burning regimes. The changes seen in this experiment demonstrate that the suppression of fire by humans has probably modified the structure of Arkansas grasslands. With the increasing use of fire as a management tool in Arkansas, changes to grassland systems are likely to be profound

    Researching COVID to enhance recovery (RECOVER) pregnancy study: Rationale, objectives and design.

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    ImportancePregnancy induces unique physiologic changes to the immune response and hormonal changes leading to plausible differences in the risk of developing post-acute sequelae of SARS-CoV-2 (PASC), or Long COVID. Exposure to SARS-CoV-2 during pregnancy may also have long-term ramifications for exposed offspring, and it is critical to evaluate the health outcomes of exposed children. The National Institutes of Health (NIH) Researching COVID to Enhance Recovery (RECOVER) Multi-site Observational Study of PASC aims to evaluate the long-term sequelae of SARS-CoV-2 infection in various populations. RECOVER-Pregnancy was designed specifically to address long-term outcomes in maternal-child dyads.MethodsRECOVER-Pregnancy cohort is a combined prospective and retrospective cohort that proposes to enroll 2,300 individuals with a pregnancy during the COVID-19 pandemic and their offspring exposed and unexposed in utero, including single and multiple gestations. Enrollment will occur both in person at 27 sites through the Eunice Kennedy Shriver National Institutes of Health Maternal-Fetal Medicine Units Network and remotely through national recruitment by the study team at the University of California San Francisco (UCSF). Adults with and without SARS-CoV-2 infection during pregnancy are eligible for enrollment in the pregnancy cohort and will follow the protocol for RECOVER-Adult including validated screening tools, laboratory analyses and symptom questionnaires followed by more in-depth phenotyping of PASC on a subset of the overall cohort. Offspring exposed and unexposed in utero to SARS-CoV-2 maternal infection will undergo screening tests for neurodevelopment and other health outcomes at 12, 18, 24, 36 and 48 months of age. Blood specimens will be collected at 24 months of age for SARS-CoV-2 antibody testing, storage and anticipated later analyses proposed by RECOVER and other investigators.DiscussionRECOVER-Pregnancy will address whether having SARS-CoV-2 during pregnancy modifies the risk factors, prevalence, and phenotype of PASC. The pregnancy cohort will also establish whether there are increased risks of adverse long-term outcomes among children exposed in utero.Clinical trials.gov identifierClinical Trial Registration: http://www.clinicaltrials.gov. Unique identifier: NCT05172011
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