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Molecular Ecology · 2026 · Vol. 35 · Issue 3 · Wiley
Urbanisation has led to increasing homogenization of plant communities across cities. However, it is unclear whether these patterns extend to cosmopolitan plant species at the genetic level. We examined genome‐wide genetic patterns in six widespread plant species (three Poaceae and three Asteraceae) across five cities in the USA (Boston, Baltimore, Minneapolis‐St. Paul, Phoenix, and Los Angeles) using reduced‐representation se...
Global Change Biology · 2025 · Vol. 31 · Issue 5 · Wiley
The timescales over which soil carbon responds to global change are a major uncertainty in the terrestrial carbon cycle. Radiocarbon measurements on archived soil samples are an important tool for addressing this uncertainty. We present time series (1969–2023) of radiocarbon measurements for litter (Oi/Oe and Oa/A) and mineral (0–10 cm) soils from the Hubbard Brook Experimental Forest, a predominantly hardwood forest in the no...
Oecologia · 2023 · Vol. 202 · Issue 2 · Springer
Land-use change is highly dynamic globally and there is great uncertainty about the effects of land-use legacies on contemporary environmental performance. We used a chronosequence of urban grasslands (lawns) that were converted from agricultural and forested lands from 10 to over 130 years prior to determine if land-use legacy influences components of soil biodiversity and composition over time. We used historical aerial imag...
Global Change Biology · 2023 · Vol. 29 · Issue 12 · Wiley
Urban land‐use change has the potential to affect local to global biogeochemical carbon (C) and nitrogen (N) cycles and associated greenhouse gas (GHG) fluxes. We conducted a meta‐analysis to (1) assess the effects of urbanization‐induced land‐use conversion on soil nitrous oxide (N 2 O) and methane (CH 4 ) fluxes, (2) quantify direct N 2 O emission factors (EF d ) of fertilized urban soils used, for example, as lawns or fores...
Limnology and Oceanography · 2019 · Vol. 64 · Issue S1 · Wiley
The steadily rising global urban population has placed substantial strain on urban water quality, and this strain is projected to increase for the foreseeable future. Considerable attention has been given to the hydrological and physico‐chemical effects of urbanization on stream ecosystems. However, due to the relative infancy of the field of urban ecology, long‐term water quality analyses in urban streams are sparse. Using a...
Global Change Biology · 2017 · Vol. 23 · Issue 8 · Wiley
Crop yields in sub‐Saharan Africa remain stagnant at 1 ton ha −1 , and 260 million people lack access to adequate food resources. Order‐of‐magnitude increases in fertilizer use are seen as a critical step in attaining food security. This increase represents an unprecedented input of nitrogen (N) to African ecosystems and will likely be accompanied by increased soil emissions of nitric oxide ( NO ). NO is a precursor to troposp...
Ecology · 2016 · Vol. 97 · Issue 12 · Wiley
Snow cover is projected to decline during the next century in many ecosystems that currently experience a seasonal snowpack. Because snow insulates soils from frigid winter air temperatures, soils are expected to become colder and experience more winter soil freeze‐thaw cycles as snow cover continues to decline. Tree roots are adversely affected by snowpack reduction, but whether loss of snow will affect root‐microbe interacti...
Global Change Biology · 2015 · Vol. 21 · Issue 10 · Wiley
Climate change and atmospheric nitrogen (N) deposition are two of the most important global change drivers. However, the interactions of these drivers have not been well studied. We aimed to assess how the combined effect of soil N additions and more frequent soil drying–rewetting events affects carbon (C) and N cycling, soil:atmosphere greenhouse gas ( GHG ) exchange, and functional microbial diversity. We manipulated the fre...