Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
Add more filters











Database
Language
Publication year range
1.
Sci Total Environ ; 794: 148715, 2021 Nov 10.
Article in English | MEDLINE | ID: mdl-34217086

ABSTRACT

Agriculture disturbs the biogeochemical cycles of major elements, which alters the elemental stoichiometry of surface stream waters, with potential impacts on their ecosystems. However, models of catchment hydrology and water quality remain relatively disconnected, even though the observation that dissolved organic carbon (DOC) and nitrate (NO3-) have opposite spatial and temporal patterns seems relevant for improving our representation of hydrological transport pathways within catchments. We tested the ability of a parsimonious model to simultaneously reproduce intra-annual dynamics of stream flow, DOC and NO3- concentrations using 15 years of daily data from a small headwater agricultural catchment (AgrHyS observatory). The model consists of an unsaturated reservoir, a slow reservoir representing the groundwater and a fast reservoir representing the riparian zone and preferential flow paths. The sources of DOC and NO3- are assumed to behave as infinite pools with a fixed concentration in each reservoir that contributes to the stream. Stream concentrations thus result from simple mixing of slow and fast reservoir contributions. The model simultaneously reproduced annual and storm-event dynamics of discharge, DOC and NO3- concentrations in the stream, with calibration KGE scores of 0.77, 0.64 and 0.58 respectively, and validation KGE scores of 0.72, 0.58 and 0.43 respectively. These results suggest that the dynamics of these concentrations can be explained by hydrological transport processes and thus by temporally variable contributions from slow (NO3- rich and DOC poor) and fast reservoirs (DOC rich and NO3- poor), with a poor representation of the biogeochemical transformations. Unexpectedly, using the concentration time series to calibrate the model increased uncertainty in the parameters that control hydrological fluxes of the model. The legacy storage of NO3- resulting from agricultural history in the studied catchment supports the assumption that the main DOC and NO3- sources behave as infinite pools at the scale of several years. Nevertheless, reproducing the long-term trends in solute concentration would require additional information about DOC and NO3- trends within the reservoirs.


Subject(s)
Carbon , Rivers , Agriculture , Carbon/analysis , Ecosystem , Environmental Monitoring
2.
Sci Total Environ ; 468-469: 1255-66, 2014 Jan 15.
Article in English | MEDLINE | ID: mdl-24060142

ABSTRACT

The EU Water Framework Directive (WFD) obliges Member States to improve the quality of surface water and groundwater. The measures implemented to date have reduced the contribution of point sources of pollution, and hence diffuse pollution from agriculture has become more important. In many catchments the water quality remains poor. COST Action 869 was an EU initiative to improve surface water quality that ran from 2006 to 2011, in which 30 countries participated. Its main aim was a scientific evaluation of the suitability and cost-effectiveness of options for reducing nutrient loss from rural areas to surface waters at catchment scale, including the feasibility of the options under different climatic and geographical conditions. This paper gives an overview of various categories of mitigation options in relation to phosphorus (P). The individual measures are described in terms of their mode of action, applicability, effectiveness, time frame, environmental side-effects (N cycling) and cost. In total, 83 measures were evaluated in COST Action 869.


Subject(s)
Agriculture/methods , Agrochemicals/analysis , Conservation of Natural Resources/methods , Phosphorus/analysis , Water Movements , Water Pollution, Chemical/prevention & control , Water Quality/standards
3.
Sci Total Environ ; 437: 276-84, 2012 Oct 15.
Article in English | MEDLINE | ID: mdl-22944220

ABSTRACT

Among possible mitigation options to reduce agricultural-borne nitrate fluxes to water bodies, introduction of catch crop before spring crops is acknowledged as a cost-efficient solution at the plot scale, but it was rarely assessed at the catchment level. This study aims to evaluate a set of catch crop implantation scenarios and their consequences in a coastal catchment prone to eutrophication. The objectives are (i) to discuss the potential benefits of catch crop introduction taking into account the limitations due to the physiographic and agricultural context of the area (ii) to propose a multicriteria classification of these scenarios as a basis for discussion with stakeholders. We used the distributed agro-hydrological model TNT2 to simulate 25 scenarios of catch crop management, differing in length of catch crop growing period, place in the crop rotation and residue management. The scenarios were classified considering the variations in main crop yields and either nitrogen fluxes in stream or the global nitrogen mass balance at the catchment level. The simulations showed that in the catchment studied, little improvement can be expected from increasing the catch crop surface. Catch crop cultivation was always beneficial to reduce nitrogen losses, but led to adverse effects on main crop yields in some cases. Among the scenarios involving additional catch crop surface, introducing catch crop between two winter cereals appeared as the most promising. The classification of scenarios depended on the chosen criteria: when considering only the reduction of nitrogen fluxes in streams, exporting catch crop residues was the most efficient while when considering the global nitrogen mass balance, soil incorporation of catch crop residues was the most beneficial. This work highlights the interest, while using integrated models, of assessing simulated scenarios with multicriteria approach to provide stakeholder with a picture as complete as possible of the consequences of prospective policies.


Subject(s)
Agriculture , Crops, Agricultural , Water Pollutants, Chemical/analysis , Computer Simulation , Edible Grain , Europe , Humans , Models, Biological , Nitrogen Cycle , Rivers/chemistry
4.
J Thorac Cardiovasc Surg ; 119(4 Pt 1): 795-803, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10733772

ABSTRACT

OBJECTIVE: Our objective was to determine whether paclitaxel-induced apoptosis in human lung cancer cells is Fas dependent. METHODS: Human lung cancer cell lines were evaluated for morphologic evidence of apoptosis, DNA fragmentation (TUNEL positivity), and caspase-3 activation after paclitaxel treatment. Human lung adenocarcinoma, squamous cell carcinoma, undifferentiated lung carcinoma, and bronchoalveolar carcinoma cell lines were each cultured in 10 micromol/L paclitaxel. RESULTS: After 24 hours of culture in paclitaxel, a 22% to 69% increase in the number of apoptotic cells was evident by means of methylene blue-azure A-eosin staining with characteristic blebbing and nuclear condensation. TUNEL assay also confirmed an increase of 19.9% to 73.0% of cells with nuclear fragmentation. Caspase-3 activity, assayed by Z-DEVD cleavage, increased from 20% to 215% (P <.05). ZB4, an antagonistic anti-Fas antibody, did not block paclitaxel induction of caspase-3 activity (155.8 vs 165.8 U, not significant). Apoptotic morphologic changes were inhibited in cells cultured in the presence of paclitaxel and Ac-DEVD-CHO, a caspase-3 inhibitor. CONCLUSIONS: Paclitaxel induces apoptosis in lung cancer cell lines, as assessed by a consistent increase in caspase-3 activity, DNA laddering, and characteristic morphologic changes. Paclitaxel-induced apoptosis in human lung cancer cells is associated with caspase-3 activation but is not Fas dependent.


Subject(s)
Antineoplastic Agents, Phytogenic/pharmacology , Apoptosis/drug effects , Carcinoma, Non-Small-Cell Lung/pathology , Caspases/metabolism , Lung Neoplasms/pathology , Paclitaxel/pharmacology , Carcinoma, Non-Small-Cell Lung/chemistry , Carcinoma, Non-Small-Cell Lung/enzymology , Caspase 3 , Caspase Inhibitors , DNA Fragmentation , Humans , In Situ Nick-End Labeling , Lung Neoplasms/chemistry , Lung Neoplasms/enzymology , Oligopeptides/pharmacology , Tumor Cells, Cultured , fas Receptor/analysis
5.
Eur Respir J ; 11(2): 392-9, 1998 Feb.
Article in English | MEDLINE | ID: mdl-9551744

ABSTRACT

The purpose of the study was to describe endothelin (ET) production and to characterize the effect of hypoxia on preproendothelin-1 (preproET-1) messenger ribonucleic acid (mRNA) expression and ET secretion by rat type II pneumocytes in vitro. Rat type II pneumocytes were incubated in a sealed chamber containing a normoxic (21% O2) or hypoxic (1% O2) atmosphere for increasing durations. Immunoreactive ET (irET) was measured in cell supernatants using a radioimmunoassay. Rat preproET-1 mRNA was detected by Northern blot. Rat type II pneumocytes expressed preproET-1 mRNA, contained irET and secreted irET in a time-dependent manner. ET secretion was dependent on de novo ribonucleic acid (RNA) and protein synthesis. Hypoxia decreased irET secretion by 27% and reduced the steady-state level of preproET-1 mRNA by 60% whereas intracellular irET concentration was unchanged. Inhibition was partially reversible with the return to a normoxic atmosphere. Inhibition of nitric oxide synthesis did not prevent the inhibitory effect of hypoxia. In conclusion, rat type II pneumocytes in primary culture secreted immunoreactive endothelin and expressed preproendothelin-1 messenger ribonucleic acid. Hypoxia reversibly reduced endothelin-1 production through a reduction of the steady-state preproendothelin-1 messenger ribonucleic acid level. Nitric oxide synthesis did not mediate the inhibitory effect of hypoxia.


Subject(s)
Endothelins/metabolism , Hypoxia/metabolism , Pulmonary Alveoli/metabolism , Animals , Cell Survival/physiology , Cells, Cultured , Endothelin-1 , Endothelins/genetics , Hypoxia/pathology , Hypoxia/physiopathology , Male , Nitric Oxide/pharmacology , Protein Precursors/genetics , Pulmonary Alveoli/pathology , RNA, Messenger/metabolism , Radioimmunoassay , Rats , Rats, Sprague-Dawley , Reference Values , Time Factors
6.
Am J Respir Crit Care Med ; 156(5): 1429-35, 1997 Nov.
Article in English | MEDLINE | ID: mdl-9372656

ABSTRACT

Endothelin-1 (ET-1), a potent fibroblast/smooth muscle cells mitogen, has been implicated in the pathogenesis of systemic sclerosis lung disease (SSc). Since monocytes and macrophages are thought to be activated in SSc, we hypothesized that alveolar macrophages (AM) and their precursors blood monocytes from patients with SSc produced more ET-1 than cells from healthy subjects. ET-1 and big ET-1 concentrations were measured in plasma, in bronchoalveolar lavage (BAL) fluids and in cell culture supernatants from monocytes and alveolar macrophages derived from 13 patients with definite SSc with lung involvement and from 10 control subjects. Plasma and BAL fluid ET-1 and big ET-1 levels were similar in both controls and patients with SSc. ET-1 and big ET-1 concentrations in unstimulated alveolar macrophage supernatants were similar in both groups. In contrast, LPS-stimulated alveolar macrophages from patients with SSc secreted higher amounts of ET-1 and big ET-1 than control subjects. ET-1 and big ET-1 concentrations in monocyte supernatants (either LPS-stimulated or not) were not different in patients and controls. These results show that AM from patients with SSc are hyperresponsive to LPS in vitro in terms of ET-1 and big ET-1 production and suggest that AM could participate in vivo in the overproduction of this potentially profibrotic mediator in patients with SSc.


Subject(s)
Endothelin-1/metabolism , Macrophages, Alveolar/metabolism , Scleroderma, Systemic/physiopathology , Adolescent , Adult , Aged , Bronchoalveolar Lavage Fluid/chemistry , Bronchoalveolar Lavage Fluid/cytology , Cells, Cultured , Endothelins/metabolism , Female , Humans , Lipopolysaccharides/pharmacology , Lung Diseases, Interstitial/physiopathology , Macrophages, Alveolar/drug effects , Male , Middle Aged , Monocytes/drug effects , Monocytes/metabolism , Prospective Studies , Protein Precursors/metabolism
7.
Am J Physiol ; 273(1 Pt 1): L193-200, 1997 Jul.
Article in English | MEDLINE | ID: mdl-9252556

ABSTRACT

The aim of this study was to characterize the effect of alveolar macrophage (AM) secretory products on endothelin (ET)-1 production by rat alveolar type II (ATII) cells in primary culture. We quantified preproendothelin (ppET)-1 mRNA by Northern blot and ET-1 concentrations in cell supernatants by enzyme-linked immunosorbent assay. Conditioned medium (CM) from rat adherent AM decreased the ppET-1 mRNA levels in ATII cells and reduced ET-1 concentrations in cell culture supernatants. This effect was mediated by interleukin (IL)-1 beta as shown by pretreatment of CM with an anti-IL-1 beta neutralizing antiserum. IL-1 beta effect was dependent on protein synthesis, was partially prevented with indomethacin, and was totally prevented with dexamethasone. Specific inhibition of cyclooxygenase 2 activity completely reversed the effect of IL-1 beta. We conclude that rat AM inhibit ET-1 production by rat ATII cells in vitro through IL-1 beta secretion. The IL-1 beta-mediated inhibition is dependent on the cyclooxygenase 2 pathway. Downregulation of ET-1 production by activated AM could limit the intra-alveolar burden of this profibrogenic peptide and thus could prevent fibrosis development.


Subject(s)
Endothelin-1/biosynthesis , Endothelins/biosynthesis , Interleukin-1/pharmacology , Isoenzymes/metabolism , Macrophages, Alveolar/physiology , Prostaglandin-Endoperoxide Synthases/metabolism , Protein Precursors/biosynthesis , Pulmonary Alveoli/metabolism , Animals , Bronchoalveolar Lavage Fluid , Cells, Cultured , Culture Media, Conditioned , Cyclooxygenase 2 , Dactinomycin/pharmacology , Endothelin-1/antagonists & inhibitors , Humans , Interleukin-6/pharmacology , Male , Membrane Proteins , Pulmonary Alveoli/cytology , Pulmonary Alveoli/drug effects , RNA, Messenger/biosynthesis , Rats , Rats, Sprague-Dawley , Recombinant Proteins/pharmacology , Transcription, Genetic/drug effects , Tumor Necrosis Factor-alpha/pharmacology
SELECTION OF CITATIONS
SEARCH DETAIL