Monitoring of Irgarol 1051 concentrations with concurrent phytoplankton evaluations in East Coast areas of the United States     

Hall LW  Killen WD  Anderson RD  Gardinali PR  Balcomb R 《Marine pollution bulletin》2005,50(6):668-681

The objectives of this study were to measure: (1) Irgarol and GS26575 (major metabolite) during the peak 2004 boating season at selected marinas and reference areas in the Carolinian Zoogeographic Province of the Eastern United States; (2) Irgarol and GS26575 at selected stations during the summer months in the Back Creek/Severn River area in Maryland in 2003 and 2004; and (3) structural and functional characteristics of resident phytoplankton communities concurrently with Irgarol and GS26575 monitoring in Back Creek/Severn River area. Irgarol concentrations from 14 marinas in the Carolinian Province ranged from non-detectable (<1 ng/L) to 85 ng/L; concentrations were less than 16 ng/L at all reference sites. The probability of exceeding the plant 10th centile for Irgarol (251 ng/L) was less than 0.6% for all marinas and 0.01% for all reference areas. These data suggest low ecological risk from Irgarol exposure for both marina and reference areas in the Carolinian Province. Irgarol concentrations ranged from 5 ng/L at the Severn River reference site to 1,816 ng/L in Port Annapolis marina during the two year study. Ecological risk from Irgarol exposure was high for the Port Annapolis marina sites based on a probability of exceeding the plant 10th centile. However, risk was low for Severn River and Severn River reference sites. Functional and structural measures of resident phytoplankton communities in the Back Creek and Severn River did not suggest that these target species are impaired in the Port Annapolis marina area where probabilistic analysis predicted adverse effects from Irgarol exposure.  相似文献   

A Laser-induced Fluorescence Instrument for Detecting Tropospheric OH and HO2: Characteristics and Calibration   总被引：1，自引：0，他引：1  

Ian C. Faloona  David Tan  Robert L. Lesher  Nathan L. Hazen  Christopher L. Frame  James B. Simpas  Hartwig Harder  Monica Martinez  Piero Di Carlo  Xinrong Ren  William H. Brune 《Journal of Atmospheric Chemistry》2004,47(2):139-167

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Occurrence and transport of Irgarol 1051 and its major metabolite in coastal waters from South Florida   总被引：1，自引：0，他引：1  

Gardinali PR  Plasencia MD  Maxey C 《Marine pollution bulletin》2004,49(11-12):1072-1083

Irgarol 1051, a boosting antifouling agent often used to supplement copper based paints was found in surface waters from South Florida at stations collected from the Miami River, Biscayne Bay and selected areas of the Florida Keys. Concentrations of the herbicide ranged from below the method detection limit (1 ng/L) to as high as 182 ng/L in a canal system in Key Largo. The herbicide was present at 93% of the stations and often found in conjunction with its descyclopropyl metabolite (M1) previously reported to be the major degradation product of Irgarol under natural environmental conditions. The 90th percentile concentration calculated for all South Florida samples was 57.6 ng/L. Based on available data on the toxicity of Irgarol to algae and coral, only two stations (approximately 3%) ranked above the LC50 of 136 ng/L reported for the marine algae Naviculla pelliculosa and above the 100 ng/L level reported to reversibly inhibit photosynthesis of intact corals. However, a basic dissipation model for Irgarol using the Key Largo Harbor station as a point source indicated that concentrations of the herbicide decreased rapidly and concentrations below the MDL are observed within 2000 m of the source. No major coral based benthic habitats are documented for all the stations surveyed at distances that Irgarol may pose a substantial risk. However, other types of submerged vegetation like seagrasses are common around the marinas and the effects of Irgarol to such endpoints should be investigated further.  相似文献   

Pressure dependence of viscosity of rhyolitic melts     

Hejiu Hui  Youxue Zhang  Piero Del Gaudio  Harald Behrens 《Geochimica et cosmochimica acta》2009,73(12):3680-3693

Viscosity of silicate melts is a critical property for understanding volcanic and igneous processes in the Earth. We investigate the pressure effect on the viscosity of rhyolitic melts using two methods: indirect viscosity inference from hydrous species reaction in melts using a piston cylinder at pressures up to 2.8 GPa and direct viscosity measurement by parallel-plate creep viscometer in an internally-heated pressure vessel at pressures up to 0.4 GPa. Comparison of viscosities of a rhyolitic melt with 0.8 wt% water at 0.4 GPa shows that both methods give consistent results. In the indirect method, viscosities of hydrous rhyolitic melts were inferred based on the kinetics of hydrous species reaction in the melt upon cooling (i.e., the equivalence of rheologically defined glass transition temperature and chemically defined apparent equilibrium temperature). The cooling experiments were carried out in a piston-cylinder apparatus using hydrous rhyolitic samples with 0.8-4 wt% water. Cooling rates of the kinetic experiments varied from 0.1 K/s to 100 K/s; hence the range of viscosity inferred from this method covers 3 orders of magnitude. The data from this method show that viscosity increases with increasing pressure from 1 GPa to 3 GPa for hydrous rhyolitic melts with water content ?0.8 wt% in the high viscosity range. We also measured viscosity of rhyolitic melt with 0.13 wt% water using the parallel-plate viscometer at pressures 0.2 and 0.4 GPa in an internally-heated pressure vessel. The data show that viscosity of rhyolitic melt with 0.13 wt% water decreases with increasing pressure. Combining our new data with literature data, we develop a viscosity model of rhyolitic melts as a function of temperature, pressure and water content.  相似文献   

Ab initio quantum mechanical study of γ-AlOOH boehmite: structure and vibrational spectrum     

Yves Noel  Raffaella Demichelis  Fabien Pascale  Piero Ugliengo  Roberto Orlando  Roberto Dovesi 《Physics and Chemistry of Minerals》2009,36(1):47-59

The structure and vibrational spectrum of boehmite have been investigated at the quantum-mechanical level with the CRYSTAL code, using a Gaussian-type basis set and the B3LYP Hamiltonian. Three space groups are considered in this study: Cmcm, Cmc2₁, P2₁/c. Cmcm turns out to correspond to a transition state, whereas Cmc2₁ and P2₁/c are minimum energy structures. The difference among them is the position of H atoms only, the Al-O frame being essentially the same. Harmonic frequencies at the Γ point have been computed. The comparison between calculated and experimental frequencies shows a good agreement for the Al-O part of the spectrum (under 790 cm⁻¹). For the Al-OH bending modes (800–1,300 cm⁻¹) an absolute differences of 50–100 cm⁻¹ is observed; for the OH stretching modes (3,200–3,500 cm⁻¹) it increases to 120–200 cm⁻¹: anharmonicity is large because OH groups are involved in strong hydrogen bonds.  相似文献   

The Huygens scientific data archive: Technical overview     

Olivier Witasse  Lyle Huber  Jean-Pierre Lebreton  David Heather  John Zarnecki  Roland Trautner  Piero Leon Stoppato  Chuck See  Cyril Pennanech  Lisa McFarlane  Bobby Kazeminejad  Brijen Hathi  John Haberman  Francesca Ferri  Lyn Doose  Giacomo Colombatti  Michael Bird  Alessio Aboudan 《Planetary and Space Science》2008,56(5):770-777

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A brief sketch of my scientific career     

Piero Guilizzoni 《Journal of Paleolimnology》2017,57(2):165-179

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Assessment of water vapor retrievals from a GPS receiver network     

Stefania Bonafoni  Augusto Mazzoni  Domenico Cimini  Mario Montopoli  Nazzareno Pierdicca  Patrizia Basili  Piero Ciotti  Giovanni Carlesimo 《GPS Solutions》2013,17(4):475-484

We present an assessment of a GPS receiver operational network to produce accurate integrated precipitable water vapour (IPWV) during a two-week field experiment carried out in Central Italy around the city of Rome, where different instruments were operative. This experimental activity provided an excellent opportunity to compare the GPS products with independent measurements provided by ground-based and space-based sensors and to evaluate their quality in terms of absolute accuracy of IPWV, analyzing also the spatial scale of GPS estimates. For instance, the assimilation into Numerical Weather Prediction models of IPWV provided by a GPS network or its exploitation in space geodesy applications to correct tropospheric effects requires an accuracy in the order of 0.1 cm to be ascribed to IPWV observations. In this work, we assessed that the accuracy for GPS IPWV estimates is 0.07 cm. Moreover, this experiment has pointed out strengths and limitations of an operational network for the water vapor estimation, such as a proper receiver distribution to achieve the desired spatial resolution and a coverage of GPS stations in both flat and mountains regions.  相似文献   

The Banhad?o Alkaline Complex, Southeastern Brazil: source and evolution of potassic SiO2-undersaturated high-Ca and low-Ca magmatic series     

Excelso Ruberti  Gaston E. R. Enrich  Rogério G. Azzone  Piero Comin-Chiaramonti  Angelo De Min  Celso B. Gomes 《Mineralogy and Petrology》2012,104(1-2):63-80

The Cretaceous Banhad?o alkaline complex in southeastern Brazil presents two potassic SiO₂-undersaturated series. The high-Ca magmatic series consist of initially fractionated olivine (Fo_92-91) + diopside (Wo_48-43En_49-35Ae_0-7), as evidenced by the presence of xenocrysts and xenoliths. In that sequence, diopside (Wo_47-38En_46-37Ae_0-8) + phlogopite + apatite + perovskite (Prv_>92) crystallized to form the phlogopite melteigite and led to the Ca enrichment of the magma. Diopside (Wo_47-41En_32-24 Ae_3-14) continued to crystallize as an early mafic mineral, followed by nepheline (Ne_74.8-70.1Ks_26.3-21.2Qz_7.6-0.9) and leucite (Lc_65-56) and subsequently by melanite and potassic feldspar (Or_85-99Ab_1-7) to form melanite ijolites, wollastonite-melanite urtites and melanite-nepheline syenites. Melanite-pseudoleucite-nepheline syenites are interpreted to be a leucite accumulation. Melanite nephelinite dykes are believed to represent some of the magmatic differentiation steps. The low-Ca magmatic series is representative of a typical fractionation of aegirine-augite (Wo_36-29En_25-4Ae_39-18) + alkali feldspar (Or_57-96Ab_3-43) + nepheline (Ne_76.5-69.0Ks_19.9-14.4Qz_15.1-7.7) + titanite from phonolite magma. The evolution of this series from potassic nepheline syenites to sodic sodalite syenites and sodalitolites is attributed to an extensive fractionation of potassic feldspar, which led to an increase of the NaCl activity in the melt during the final stages forming sodalite-rich rocks. Phonolite dykes followed a similar evolutionary process and also registered some crustal assimilation. The mesocratic nepheline syenites showed interactions with phlogopite melteigites, such as compatible trace element enrichments and the presence of diopside xenocrysts, which were interpreted to be due to a mixing/mingling process of phonolite and nephelinite magmas. The geochemical data show higher TiO₂ and P₂O₅ contents and lower SiO₂ contents for the high-Ca series and different LILE evolution trends and REE chondrite-normalized patterns as compared to the low-Ca series. The ⁸⁷Sr/⁸⁶Sr, ¹⁴³Nd/¹⁴⁴Nd, ²⁰⁶Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb initial ratios for the high-Ca series (0.70407–0.70526, 0.51242–0.51251, 17.782–19.266 and 38.051–39.521, respectively) were slightly different from those of the low-Ca series (0.70542–0.70583, 0.51232–0.51240, 17.758–17.772 and 38.021–38.061, respectively). For both series, a CO₂-rich potassic metasomatized lithospheric mantle enriched the source with rutile-bearing phlogopite clinopyroxenite veins. Kamafugite-like parental magma is attributed to the high-Ca series with major contributions from the melting of the veins. Potassic nephelinite-like parental magma is assigned to the low-Ca series, where the metasomatized wall-rock played a more significant role in the melting process.  相似文献   

Contrasting surface active faults and deep seismogenic sources unveiled by the 2009 L’Aquila earthquake sequence (Italy)     

Sabina Bigi  Piero Casero  Claudio Chiarabba  Daniela Di Bucci 《地学学报》2013,25(1):21-29

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