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1 ry, with a unit of measure of millimeters of mercury.
2 eilites formed in bodies as large as Mars or Mercury.
3 ated with real samples inherently containing mercury.
4 queuine/queuosine, and excretion of dietary mercury.
5 the upstream use problematic, especially for mercury.
6 , and less noble metals, such as cadmium and mercury.
7 aluminium, cobalt, copper, zinc, cadmium and mercury.
8 temporal concentrations of gaseous elemental mercury.
9 and the environment from adverse effects of mercury.
10 to probe pore spaces inaccessible to N2 and mercury.
11 rtant tool for future studies of atmospheric mercury.
12 on of threatened species and species high in mercury.
13 -day variability and diel cycles in oxidized mercury (0 to 200 pg m(-3)) and will be an important too
14 Urinary antimony (2.69%, 0.45, 4.99) and mercury (1.91%, 0.42, 3.43) exposure were positively ass
17 and the University of Nevada, Reno-Reactive Mercury Active System (UNR-RMAS) at a rural/suburban fie
18 lood levels of lead, cadmium, manganese, and mercury after supplementation with vitamin D during preg
22 nel system to measure elemental and oxidized mercury and deployed it with an automated calibration sy
23 e tendency of these proteins to be linked to mercury and elucity the possibles existing physiological
26 ectrometry (GFAAS) for the quantification of mercury and Mass Spectrometry (ESI-MS/MS) were used for
30 oposed for the simultaneous determination of mercury and selenium in fish samples using Atomic Fluore
32 phases suggests their potential existence on Mercury and their magnetism may contribute to its presen
34 ing the source processes of the exosphere at Mercury, and the use of plasma spectrometers will be cru
36 ocyanide products were increased markedly by mercury arc UV photolysis, which covers the zinc atomic
38 ot declining environmental concentrations of mercury, are driving short-term declines in THg concentr
39 rom 0.23+/-0.03 mul/minute per millimeter of mercury at baseline to 0.38+/-0.03 mul/minute per millim
40 taining DOM from a Carex peat with complexed mercury at initial concentrations of 14 nM to 724 nM.
44 ubella vaccine and autism; (2) thimerosal, a mercury-based vaccine preservative and the risk of neuro
45 (aq))) and toxic methylmercury (MeHg) govern mercury bioavailability and fate in northern ecosystems.
47 he aim of this study is to identify possible mercury biomarkers in muscle samples of Plagioscion squa
49 oped, to date, the most sensitive whole-cell mercury biosensor using NanoLuc as reporter, with an LOD
50 us clones of Daphnia magna, screened for the mercury-biotransforming merA gene, and determined their
51 e fractionation, identification and study of mercury - bound proteins present in samples of muscular
53 er light source, a thermoelectrically cooled mercury cadmium telluride balanced detection module was
54 the present study are to evaluate levels of mercury, cadmium, lead, and arsenic in dried mushrooms,
57 ne (0.10+/-0.04 mul/minute per millimeter of mercury) compared with the sham procedure (-0.08+/-0.05
59 les that laid eggs with the highest observed mercury concentration (0.53 mug/g fww) spent an average
62 e suitable and easy-to-use method to monitor mercury concentration in tunas, since they allowed accur
63 identified based on the availability of the mercury concentration of cord tissue as a measure of pre
65 ESI-MS/MS and showing the highest values of mercury concentration, may be considered possible mercur
67 onal dynamics and interannual variability in mercury concentrations (inorganic divalent mercury (IHg)
68 ings are suitable proxies for historical air mercury concentrations and that mercury concentrations h
70 rbonate clumped isotope paleothermometry and mercury concentrations as measured from a broad geograph
71 increases in coastal marine temperatures and mercury concentrations at a global scale, which appear a
73 storical air mercury concentrations and that mercury concentrations have increased since the Industri
77 gel electrophoresis (2D-PAGE), and the total mercury concentrations in protein spots were determined
78 the Mediterranean Sea, detects variations on mercury concentrations in relation to biological paramet
81 esults suggest that environmentally relevant mercury concentrations may negatively influence reproduc
85 belled samples also had significantly higher mercury concentrations than correctly labelled samples.
92 were much higher than those in roots and the mercury content of vegetable leaves decreased significan
95 of Hg(II) has recently been shown to change mercury cycling significantly in the atmosphere and its
96 chemical cycling of Hg (through 'atmospheric mercury depletion events', or AMDEs) and wet deposition
100 id depletions in ozone and gaseous elemental mercury due to reactions with halogen atoms, influencing
103 zing radiation (IR), heavy metals (chromium, mercury), elevated temperature (up to 50 degrees C), and
108 exhibited higher survival and fecundity than mercury-exposed daphnids supplemented with parental micr
109 bers that are eco-responsive and tolerant to mercury exposure and can aid in host survival and mainta
114 ling feathers as indicators of site-specific mercury exposure, we discuss both advantages and possibl
117 res were chlorpyrifos ([Formula: see text]), mercury ([Formula: see text]), and lead ([Formula: see t
118 re particulate matter ([Formula: see text]), mercury ([Formula: see text]), nonspecific air pollution
120 terol into a 9,11-secoenol ether employing a mercury-free desaturation of the Treibs type, an oxidati
121 n the Tibetan Plateau; release of carbon and mercury from melting polar ice and thawing permafrost; n
123 is currently the primary method at NIST for mercury gas standards traceability to the International
124 nitoring networks quantify gaseous elemental mercury (GEM) concentrations, but not isotopic compositi
125 ods for the measurement of gaseous elemental mercury (GEM) mass concentration: isotope dilution cold-
126 osition during sampling of gaseous elemental mercury (GEM) with a passive air sampler (PAS) that uses
129 orted throughout the atmosphere as elemental mercury Hg(0) and its oxidized forms Hg(I) and Hg(II) .
130 nts, thermodynamics and kinetics of divalent mercury Hg(II) chemical speciation need to be understood
131 ry (Hg(II)(i)) to volatile dissolved gaseous mercury (Hg(0)((aq))) and toxic methylmercury (MeHg) gov
134 ransformations of aqueous inorganic divalent mercury (Hg(II)(i)) to volatile dissolved gaseous mercur
135 ed to assess the bioavailability of divalent mercury (Hg(II)) complexed in dissolved organic matter (
137 as environments in which inorganic divalent mercury (Hg(II)) is transformed to methylmercury (MeHg)
139 ement and speciation procedure for inorganic mercury (Hg(IN)) and methylmercury (CH(3)Hg) was develop
140 atio = 1.42; 95% CI: 1.20, 1.68), 89% higher mercury (Hg) (GM ratio = 1.89; 95% CI: 1.47, 2.41) and a
142 sphere is a significant global reservoir for mercury (Hg) and its isotopic characterization is import
144 We conducted a national-scale assessment of mercury (Hg) bioaccumulation in aquatic ecosystems, usin
145 ining (ASGM) is a significant contributor of mercury (Hg) contamination and deforestation across the
152 ropogenic emissions of the toxic heavy metal mercury (Hg) have substantially increased atmospheric Hg
153 y- and perfluoroalkyl substances (PFASs) and mercury (Hg) in eggs of herbivorous barnacle geese ( Bra
154 es -70 degrees N) extensive records of total mercury (Hg) in freshwater fish showed consistent declin
155 of persistent organic pollutants (POPs) and mercury (Hg) in springtails from the field, and to study
156 Streams in the northeastern U.S. receive mercury (Hg) in varying proportions from atmospheric dep
157 yet crucial in the context of anthropogenic mercury (Hg) inputs and potential threats to human healt
158 Despite the limited direct anthropogenic mercury (Hg) inputs in the circumpolar Arctic, elevated
166 tural dissolved organic matter (DOM) affects mercury (Hg) redox reactions and anaerobic microbial met
167 though more research is required to evaluate mercury (Hg) speciation in DBS and to validate the agree
173 n that the anaerobic microbial conversion of mercury (Hg) to MeHg requires the Hg-methylation genes h
174 scientific understanding of bacteria-driven mercury (Hg) transformation processes in natural environ
176 CVD, environmental and dietary exposures to mercury (Hg), a highly toxic metal traditionally regarde
185 ctant was tested for speciation of inorganic mercury, Hg(II) and methylmercury, MeHg(I) in water and
186 n mercury concentrations (inorganic divalent mercury (IHg) and MeHg) and loads at four reservoir infl
188 electrochemical sensor for determination of mercury(II) using deoxyribonucleic acid/poly-L-methionin
191 1.48 per mille (+/-0.34, n = 10) for methyl-mercury in fish that feed at ~500-m depth in the central
192 copy to characterize the structural order of mercury in Hg(II)-DOM-sulfide systems for a range of sul
193 This study determines the levels of total mercury in muscle tissue from 268 reared Atlantic bluefi
200 The applicability to the determination of mercury in tuna of square wave anodic stripping voltamme
204 BS-based method to assess MeHg and inorganic mercury (InHg) exposure in human population studies.
205 dy highlights the potential for increases in mercury inputs to arctic ecosystems downstream of glacie
210 In addition to highlighting the potential of mercury isotopes to decipher the complex ecological cycl
213 high temperature or extreme radiation (e.g. Mercury, Jupiter's moon Europa, near-Sun comets), as wel
214 The source of radiation was a mid-pressure mercury lamp (460 W), emitting between 250 and 740 nm.
217 rs for the detection of heavy metals (mainly mercury, lead, cadmium, and arsenic) are summarized.
218 d and that over a quarter of all samples had mercury levels above the upper limit recommended by the
220 the photolysis of HgBr increases atmospheric mercury lifetime, contributing to its global distributio
222 od matched the permeation rates observed via mercury measurement devices to within 25% when the mercu
225 ion is also linked to the composition of non-mercury methylating bacterial communities, likely provid
227 es some first insights into the diversity of mercury methylating microorganisms in boreal forest soil
228 trophic status, and geochemical data suggest mercury methylation pathways vary between wetlands.
230 gh-throughput sequencing of 16S rRNA and the mercury methyltransferase, hgcA, combined with geochemic
231 er metals-arsenic, cobalt, chromium, copper, mercury, molybdenum, lead, tin, and vanadium--in relatio
238 rcury, thereby enhancing deposition of toxic mercury, particularly in the Arctic near-surface troposp
240 y measurement devices to within 25% when the mercury permeation rate was relatively high (up to 30 pg
241 asons, were contaminated with high levels of mercury, phosphate and cyanobacteria known to produce de
242 c, barium, beryllium, cadmium, cesium, lead, mercury, platinum, thallium, tin, and uranium), and thei
244 y in an amalgam adds to global environmental mercury pollution and can contribute to adverse health e
245 vel of microbial demethylation of the methyl-mercury pool before incorporation into the base of the f
246 Herein, we show that all oxidized forms of mercury rapidly revert directly and indirectly to Hg(0)
249 gna and quantified its merA gene expression, mercury reduction capability, and measured its impact on
251 at dissolved organic matter (DOM) influences mercury retention in wetland pore waters by complexing H
252 ragonfly larvae for estimating the potential mercury risk to fish and wildlife in aquatic ecosystems
254 his method eliminates the need for the toxic mercury salts and pungent thiophenol historically used i
255 Arsenic, cadmium, copper, lead, manganese, mercury, selenium, and zinc concentrations were measured
256 the addition of other reaction media such as mercury, silica gel, or inert salts as for previous proc
257 NOPD) as a chelating agent was developed for mercury speciation in water and fish samples by ETAAS.
259 s on geochemical factors influencing aqueous mercury speciation should be considered in context of th
260 s study quantified concentrations of aqueous mercury species (Hg(II)(i), Hg(0)((aq)), MeHg) and relev
265 ility of 1 week of HBP, 3 office visits with mercury sphygmomanometry, and 24-h ABP were 0.938, 0.894
269 ased on higher spatial resolution MESSENGER (MErcury Surface Space ENvironment GEochemistry and Rangi
272 anisms differ in their capacity to methylate mercury, the abundance and distribution of methylating p
273 gen chemistry, depleting ozone and elemental mercury, thereby enhancing deposition of toxic mercury,
276 ximately 2-fold) and the percentage of total mercury (THg) as MeHg (>=4-fold) coincident with reservo
279 ants and analysed the concentration of total mercury (THg) in a sub-sample (271 samples) of these.
280 we calculated methylmercury (MeHg) and total mercury (THg) mass balances for Lake Hazen, the world's
282 inorganic Hg(II) bound to DOM is a source of mercury to biota with dithiolate Hg(SR)(2) complexes as
286 the understanding of seasonal variability in mercury transport through and transformation within a re
292 nt (0.38+/-0.07 mul/minute per millimeter of mercury) was greater than baseline (0.28+/-0.03 mul/minu
297 analyze the effect of precipitation type on mercury wet deposition using a new database of individua
298 n sources and transformations of atmospheric mercury with Hg stable isotopes depends on the ability t
299 g POP is able to remove aqueous and airborne mercury with uptake capacities of 1216 and 630 mg g(-1)
300 n below a MAP of 65 mm Hg (in millimeters of mercury) x time spent below a MAP of 65 mm Hg (in minute