Neil D. Bettez
Marine Biological Laboratory
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Featured researches published by Neil D. Bettez.
Biogeochemistry | 2013
Robert W. Pinder; Neil D. Bettez; Gordon B. Bonan; Tara L. Greaver; William R. Wieder; William H. Schlesinger; Eric A. Davidson
Nitrogen cycling processes affect radiative forcing directly through emissions of nitrous oxide (N2O) and indirectly because emissions of nitrogen oxide
Hydrobiologia | 2005
Philip W. Lienesch; Michael E. McDonald; Anne E. Hershey; W. John O’Brien; Neil D. Bettez
Hydrobiologia | 1995
Parke A. Rublee; Neil D. Bettez
(hbox{NO}_{x})
Hydrobiologia | 2001
Parke A. Rublee; Neil D. Bettez
Oecologia | 2016
Laura Gough; Neil D. Bettez; Karie A. Slavik; William B. Bowden; Anne E. Giblin; George W. Kling; James A. Laundre; Gaius R. Shaver
and ammonia (NH3) affect atmospheric concentrations of methane (CH4), carbon dioxide (CO2), water vapor (H2O), ozone (O3) and aerosols. The emissions of N2O are mostly from agriculture and they contribute to warming on both short and long time scales. The effects of
Climatic Change | 2005
Larry D. Hinzman; Neil D. Bettez; W. Robert Bolton; F. Stuart Chapin; Mark B. Dyurgerov; Chris L. Fastie; Brad Griffith; Robert D. Hollister; Allen Hope; Henry P. Huntington; Anne M. Jensen; Gensuo Jia; T. M. Jorgenson; Douglas L. Kane; David R. Klein; Gary P. Kofinas; Amanda H. Lynch; Andrea H. Lloyd; A. David McGuire; Frederick E. Nelson; Walter C. Oechel; T. E. Osterkamp; Charles H. Racine; Vladimir E. Romanovsky; Robert S. Stone; Douglas A. Stow; Matthew Sturm; Craig E. Tweedie; George L. Vourlitis; Marilyn D. Walker
Polar Research | 1999
John E. Hobbie; Bruce J. Peterson; Neil D. Bettez; Linda A. Deegan; W. John O'Brien; George W. Kling; George W. Kipphut; William B. Bowden; Anne E. Hershey
hbox{NO}_{{x}}
Limnology and Oceanography | 2009
Sally MacIntyre; Jonathan P. Fram; Paul J. Kushner; Neil D. Bettez; W. J. O'Brien; John E. Hobbie; George W. Kling
Limnology and Oceanography | 2004
W. John O'Brien; Michael Barfield; Neil D. Bettez; Gretchen M. Gettel; Anne E. Hershey; Michael E. McDonald; Michael C. Miller; Howard D. Mooers; John Pastor; Carl Richards; Jeff A. Schuldt
and NH3 on CH4, O3, and aerosols are complex, and quantification of these effects is difficult. However, the net result on time scales of decades is likely one of cooling, which becomes less significant on longer time scales. Deposition of N onto ecosystems also affects sources and sinks of N2O, CH4, and CO2, but the dominant effect is changes in carbon (C) stocks. Primary productivity in most temperate ecosystems is limited by N, so inputs from atmospheric deposition tend to stimulate plant growth and plant litter production, leading in some cases to significant C sequestration in biomass and soils. The literature reviewed here indicates a range of estimates spanning 20–70xa0kg C sequestered per kg N deposited in forests, which are the dominant C sinks. Most of the sequestration occurs in aboveground forest biomass, with less consistency and lower rates reported for C sequestration in soils. The permanency of the forest biomass sink is uncertain, but data for the fate of forest products in the US indicate that only a small fraction of enhanced forest biomass C is sequestered in long-term harvest products or in unmanaged forests. The net effect of all of these N cycle processes on radiative forcing in the US is probably a modest cooling effect for a 20-year time frame, although the uncertainty of this estimate includes zero net effect, and a modest warming for a 100-year time frame. We know that N-cycling processes are important and that biotic feedbacks to climate change are unlikely to be properly modeled or assessed without including C–N interactions. However, due to the complexity of biological processes involving C–N–climate interactions, biogeochemical models are still poorly constrained with respect to ecosystem responses to impacts of N deposition and climate change. Only recently have N-cycling processes been incorporated into Earth system models for C–N interactions. The robustness of these models remains to be demonstrated. Much work remains for improving their representation in models used to simulate climate forcing scenarios.
Archive | 2005
Larry D. Hinzman; Neil D. Bettez; F. Stuart Chapin; Mark B. Dyurgerov; Chris L. Fastie; Brad Griffith; Robert D. Hollister; Allen Hope; Henry P. Huntington; Anne M. Jensen
We tested whether increased phosphorus and nitrogen concentrations would affect a lake trout (Salvelinus namaycush) population in a small oligotrophic lake with a benthically dominated food web. From 1990 to 1994, nitrogen and phosphorus were added to Lake N1 (4.4xa0ha) at the arctic Long-Term Ecological Research site in Alaska. We used mark/recapture methods to determine the lake trout population size, size structure, recruitment, and individual growth from 1987 to 1999. Data were also collected on water chemistry and food availability. Fertilization resulted in increased pelagic primary productivity, chlorophyll a, turbidity, snail density, and hypoxia in summer and winter. Lake trout density was not affected by the manipulation however growth and average size increased. Recruitment was high initially, but declined throughout the fertilization. These results suggest that lake trout were affected through increased food availability and changes to the physical characteristics of the lake. During fertilization, hypoxia near the sediments may have killed over-wintering embryos and decreased habitat availability. Although lake trout responded strongly to increased nutrients, loss of recruitment might jeopardize lake trout persistence if arctic lakes undergo eutrophication.