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1.
Ecology ; 89(12): 3515-27, 2008 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19137956

RESUMO

Allochthonous inputs act as resource subsidies to many ecosystems, where they exert strong influences on metabolism and material cycling. At the same time, metabolic theory proposes endogenous thermal control independent of resource supply. To address the relative importance of exogenous and endogenous influences, we quantified spatial and temporal variation in ecosystem metabolism and nitrogen (N) uptake using seasonal releases of 15N as nitrate in six streams differing in riparian-stream interaction and metabolic character. Nitrate removal was quantified using a nutrient spiraling approach based on measurements of downstream decline in 15N flux. Respiration (R) and gross primary production (GPP) were measured with whole-stream diel oxygen budgets. Uptake and metabolism metrics were addressed as z scores relative to site means to assess temporal variation. In open-canopied streams, areal uptake (U; microg N x m(-2) x s(-1)) was closely related to GPP, metabolic rates increased with temperature, and R was accurately predicted by metabolic scaling relationships. In forested streams, N spiraling was not related to GPP; instead, uptake velocity (v(f); mm/s) was closely related to R. In contrast to open-canopied streams, N uptake and metabolic activity were negatively correlated to temperature and poorly described by scaling laws. We contend that streams differ along a gradient of exogenous and endogenous control that relates to the relative influences of resource subsidies and in-stream energetics as determinants of seasonal patterns of metabolism and N cycling. Our research suggests that temporal variation in the propagation of ecological influence between adjacent systems generates phases when ecosystems are alternatively characterized as endogenously and exogenously controlled.


Assuntos
Ecossistema , Monitoramento Ambiental/métodos , Água Doce/química , Nitrogênio/análise , Nitrogênio/metabolismo , Carbono/análise , Carbono/metabolismo , Isótopos de Nitrogênio , Rios , Estações do Ano
2.
ScientificWorldJournal ; 1 Suppl 2: 623-31, 2001 Nov 09.
Artigo em Inglês | MEDLINE | ID: mdl-12805817

RESUMO

Groundwater-surface water (GW-SW) interaction lengthens hydraulic residence times, increases contact between solutes and biologically active surfaces, and often creates a gradient of redox conditions conducive to an array of biogeochemical processes. As such, the interaction of hydraulic patterns and biogeochemical activity is suspected to be an important determinant of elemental spiraling in streams. Hydrologic interactions may be particularly important in headwater streams, where the extent of the GW-SW mixing environment (i.e., hyporheic zone) is proportionately greater than in larger streams. From our current understanding of stream ecosystem function, we discuss nitrogen (N) spiraling, present a conceptual model of N retention in streams, and use both of these issues to generate specific research questions and testable hypotheses regarding N dynamics in streams.


Assuntos
Ecossistema , Água Doce/química , Nitrogênio/análise , Modelos Teóricos , Nitrogênio/metabolismo , Fixação de Nitrogênio , América do Norte , Oxirredução , Rios/química , Solventes/química , Árvores
3.
J Biol Chem ; 269(22): 15481-7, 1994 Jun 03.
Artigo em Inglês | MEDLINE | ID: mdl-8195191

RESUMO

It was previously shown that the reductive debromination of BrCCl3 to trichloromethyl radical by human hemoglobin leads to formation of dissociable altered heme products, two of which are identical to those formed from myoglobin and one which is novel. In this study, we have elucidated the structure of this novel adduct with the use of mass spectrometry, as well as 1H and 13C NMR as a substitution product of a -C(Cl) = CCl2 moiety for a beta-hydrogen atom on the prosthetic heme's ring I vinyl group. From studies with the use of 13C-enriched BrCCl3, it was determined that the added carbon atoms were derived from 2 eq of BrCCl3. A mechanism that involves multiple reductive events and a radical cation heme intermediate is proposed. Consistent with this mechanism, cellular reductants were found to selectively enhance the amount of this novel dissociable heme adduct. These studies reveal fine differences between myoglobin and hemoglobin in the accessibility of reactive intermediates to the ring I vinyl group, as well as the potential importance of cellular reductants on the course of heme alteration.


Assuntos
Bromotriclorometano/sangue , Eritrócitos/metabolismo , Heme/metabolismo , Hemoglobinas/metabolismo , Ácido Ascórbico/farmacologia , Sítios de Ligação , Bromotriclorometano/metabolismo , Isótopos de Carbono , Glutationa/farmacologia , Heme/química , Hemoglobinas/química , Hemoglobinas/efeitos dos fármacos , Hemólise , Humanos , Cinética , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Mioglobina/metabolismo
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