405 research outputs found

    PENENTUAN AKUIFER BERDASARKAN ANALISIS HIDROKIMIA AIRTANAH DAN PENGARUH KONDISI GEOLOGI PADA AREA TAMBANG BAWAH TANAH (UNDER GROUND) BIG GOSSAN, PAPUA

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    Area Tambang Bawah Tanah Big Gossan, PT Freeport Indonesia (PTFI) dengan posisi kordinat 733250–734250 Easthing; 951250–952250 Northing Zona UTM 53 S. Terletak di Pegunungan Jayawijaya, Kecamatan Mimika Timur, Kabupaten Mimika, Propinsi Papua. Tambang Big Gossan terdiri dari beberapa formasi batuan yang batuan penyusun setiap formasi berbeda. Selain itu pada tambang Big Gossan terdiri dari beberapa tipe alterasi dan mineralisasi. Dari faktor tersebut, maka akan memungkinkan terjadinya perubahan kimia air pada daerah tangkapan (recharge area) dan conto airtanah yang berada pada level 2540 m , karena pada saat air bergerak melalui pori-pori atau rekahan dalam batuan maka akan terjadi proses pelarutan mineral- mineral yang ada pada batuan yang dilewatinya. Geologi area Tambang Bawah Tanah Big Gossan terdiri dari Formasi Ekmai yang berumur kapur akhir, Formasi Waripi berumur Paleosen – Eosen Awal, dan intrusi diorite Ertsberg yang berumur paleosen dengan litologi batuan dari tua ke muda adalah batupasir, batugamping, hornfels, dolomit dan intrusi diorit. Berdasarkan analisa struktur kekar didapati arah umum kekar tertutup (shear fracture) N 271 ˚E – N 270 ˚E dan arah umum kekar terbuka (gash fracture) N 173 ˚ - N 179 ˚E E, tegasan utamanya berarah Tenggara – Barat Laut dengan jenis sesar adalah sesar kiri turun (Normal left slip fault). Jenis alterasi pada area penelitian termasuk dalam jenis alterasi Skarn. Zonasi skarn diendapan Big Gossan secara berturut-turut dari batas hornfels (Kkeh) sampai kearah marmer/dolomit menjadi zona garnet + piroksen skarn dan piroksen + garnet skarn. Penentuan akuifer pada area penelitian dilakukan dengan metode diagram stiff dan trilinear piper, water intersect, dan diagram schoeller didapati 2 tipe akuifer, yaitu akuifer kontak Kkel-exoskarn Waripi dengan tipe Ca-SO4 dan Ca-Mg-SO4 dan dolomi Waripi dengan tipe Ca- Mg-SO4-HCO3, kedua akuifer tersebut masuk kedalam jenis akuifer rekahan. Jenis airtanah area Big Gossan berdasarkan asal dan proses terjadinya adalah air meteorik berupa air hujan dan berdasarkan tempat terdapatnya airtanah yaitu air rekahan. Air yang keluar berasal dari air hujan dapat dibuktikan dengan perbandingan nilai kimia antara air hujan dan airtanah (Ph dan EC), selain itu dari hasil tracer test menunjukkan bahwa perjalan dye dari permukaan sampai pada 2540/L hanya membutuhkan waktu 74 jam, dari sini kemungkinan besar airtanah pada tambang Big Gossan merupakan air hujan. Analisa geokimia batuan terhadap perubahan kimia airtanah terdapat dua (2) litologi batuan yang mempunyai peranan penting, yaitu litologi batuan karbonat dan alterasi Waripi skarn. Litologi batuan kerbonat berpengaruh terhadap jumlah kation – anion terlarut (Ca, Mg dan HCO3) sedangkan untuk Waripi skarn berpengaruh terhadap nilai kandungan SO4 dan Ca yang berasal dari mineral anhidrit dan piroksen, serta nilai kandungan mineral logam berupa Fe dan Cu yang berasal dari mineral pirit dan kalkopiri

    Jarosite: A silver bearing mineral of the gossan of Rio Tinto (Huelva) and La Union (Cartagena, Spain)

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    The mineralogy of the gossans of Rio Tinto and La Unión is studied. Special emphasis has been paid to the occurrence of jarosite group minerals because they constitute silver bearing material of technical importance. After granulometric separation of the fractions, magnetic separation was used to concentrate the jarosite-group minerals. Plumbojarosite, natrojarosite and argentojarosite were identified by X-ray diffraction techniques. The spatial deposition of jarosite, goethite and hematites has been studied in different samples and the sequence interpreted on the basis of the known literature. The silver content, as determined by SEM, indicates abundant silver deposition in an early phase of gossanization. The recovery in the industrial plant has been analyzed comparing the mineralogy of the whole one and the residues of flotation. This study reveals that the industrial process used today leaves unaltered the proportion of the jarosite minerals entering and leaving the plant.En este trabajo se estudia la mineralogía del gossan de Rio Tinto y La Unión. Se hace enfasis especial en los minerales del grupo de la jarosita, por ser los principales portadores de plata y de importancia técnica. Para concentrar los minerales de la jarosita se realizó una separación magnética previa. Plumbojarosita, natrojarosita y argentojarosita se identificaron mediante difracción de rayos X. Se ha estudiado la deposición espacial de jarosita, goethita y hematites y se ha interpratado sus secuencias en base a la bibliografía que se conoce. La distribución del contenido en plata, realizada mediante S. E. M. a puesto de manifiesto que la deposición de plata es más abundante en la primera fase de gossanización. La recuperación de la plata en la planta industrial ha sido analizada comparando la mineralogía del todo uno y del residuo del proceso de flotación. En general el proceso de flotación no concentra la plata quedando practicamente inalterada la proporción de minerales de la jarosita que entran y salen de la planta de tratamiento.Depto. de Mineralogía y PetrologíaFac. de Ciencias GeológicasTRUEpu

    Salt glands enable salt but not metal(loid)s excretion in Limonium daveaui under amended saline and contaminated soils

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    Soil–plant interactions are essential for understanding adaptive responses to abiotic stressors such as salinity and metal(loid)s contamination. This study analyzed plant behavior of the recretohalophyte Limonium daveaui Erben when cultivated in saline and in gossan mine soils, both with and without organic–inorganic amendments. Analysis included soil physicochemical and biological parameters, multielemental composition of plant tissues, and the cationic profile of salts excreted by foliar salt glands. All plants grown in unamended gossan soil died, whereas amendment addition substantially improved both gossan and saline Fluvisol properties, raising pH in gossan soil, reducing salinity, increasing nutrient availability, generally stimulating microbial enzymatic activity, thereby allowing normal plant development. In amended gossan soil, plants accumulated high concentrations of As and Pb and moderate levels of other potentially hazardous elements (PHE) in roots and shoots without visible toxicity symptoms. Transfer coefficients revealed low PHE translocation but high biological absorption, indicating efficient uptake. Microscopic analyses showed the presence of the typical Limonium salt glands on both leaf surfaces through which plants excreted salts with macroelements but not As and Pb. The findings indicate that plant's primary tolerance strategy is based on accumulation of metal(loi)s in roots, rather than exclusion or excretion through foliar salt glands.Open access funding provided by FCT|FCCN (b-on). This work was supported by FCT—Fundação para a Ciência e Tecnologia, I.P. through project reference UID/04129/2025. Antonio Aguilar-Garrido (AA-G) thanks the SPANISH MINISTRY OF SCIENCE, INNOVATION AND UNIVERSITIES for its predoctoral fellowship and the mobility grant under application references FPU-18/02901 and EST21/00734, respectively

    Bullion production in imperial China and its significance for sulphide ore smelting world-wide

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    Gold and silver production was of major importance for almost all ancient societies but has been rarely studied archaeologically. Here we present a reconstruction of a previously undocumented technology used to recover gold, silver and lead at the site of Baojia in Jiangxi province, China dated between the 7th and 13th centuries AD. Smelting a mixture of sulphidic and gossan ores in a relatively low temperature furnace under mildly reducing conditions, the process involved the use of metallic iron to reduce lead sulphide to lead metal, which acted as the collector of the precious metals. An experimental reconstruction provides essential information, demonstrating both the significant influence of sulphur on the silicate slag system, and that iron reduction smelting of lead can be carried out at a relatively low temperature. These new findings are relevant for further studies of lead and precious metal smelting slags world-wide. The technological choices of ancient smelters at this site are then discussed in their specific geographical and social-economic settings

    Mapping hydrothermal and supergene alteration zones associated with carbonate-hosted Zn-Pb deposits by using PRISMA satellite imagery supported by field-based hyperspectral data, mineralogical and geochemical analysis

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    Delineating hydrothermal alteration and supergene caps is fundamental for mineral exploration of sulfide ores. The aim of this study is to apply a multi-scale workflow based on hyperspectral remote and proximal sensing data in order to delineate hydrothermal dolomitization and supergene alteration associated with the Mississippi Valley-Type Zn-Pb(-Ag) deposit of Jabali (Western Yemen). The area was investigated through hyperspectral images derived from the new launched Italian Space Agency’s PRISMA satellite, which has a higher spectral resolution compared to multispectral sensors and covers the mineral-diagnostic wavelength regions (such as the 2100 nm to 2300 nm range) with a Signal to Noise Ratio (SNR) ≥ 100. Spectral mineral maps were produced through the band ratios method using specific feature extraction indices applied to the hyperspectral satellite data. The results were validated by using Visible Near InfraRed (VNIR) to Short Wave InfraRed (SWIR) reflectance spectra, mineralogical (XRPD) and geochemical (ICP-ES/MS) analyses on rock samples collected in the Jabali area. The dolomites footprint was mapped using a PRISMA Level 2C image, by enhancing the spectral differences between limestones and dolomites in the SWIR-2 region (major features centered at 2340 nm and 2320 nm, respectively). Gossans were detected due to the Fe3+ absorption band in the VNIR region at 900 nm. The Zn-Pb mineralized area, extended for approximately 25 km2, was thus identified by recognizing gossan occurrences in dolomites. The study demonstrates that the PRISMA satellite is effective in identifying Zn-Pb mineralized outcrops in sedimentary basins

    Synthesis, characterization and thermochemistry of synthetic Pb–As, Pb–Cu and Pb–Zn jarosites

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    The enthalpy of formation from the elements of well characterized Pb-As, Pb-Cu, and Pb-Zn synthetic jarosites, corresponding to chemical formulas (H3O)0.68±0.03Pb0.32±0.002Fe2.86±0.14(SO4)1.69±0.08(AsO4)0.31±0.02(OH)5.59±0.28(H2O)0.41±0.02, (H3O)0.67±0.03Pb0.33±0.02Fe2.71±0.14Cu0.25±0.01(SO4)2±0.00(OH)5.96±0.30(H2O)0.04±0.002 and (H3O)0.57±0.03Pb0.43±0.02Fe2.70±0.14Zn0.21±0.01(SO4)2±0.00(OH)5.95±0.30(H2O)0.05±0.002, was measured by high temperature oxide melt solution calorimetry and gave ΔH°f = -3691.2 ± 8.6 kJ/mol, ΔH°f = -3653.6 ± 8.2 kJ/mol, and ΔH°f = -3669.4 ± 8.4 kJ/mol, respectively. Using estimated entropies, the standard Gibbs free energy of formation from elements at 298 K ΔG°f of the three compounds were calculated to be -3164.8 ± 9.1 kJ/mol, -3131.4 ± 8.7 kJ/mol, and -3153.6 ± 8.9 kJ/mol, respectively. Based on these free energies, their logKsp values are -13.94 ± 1.89, -4.38 ± 1.81 and -3.75 ± 1.80, respectively. For this compounds, a log10{Pb2+} - pH diagram is presented. The diagram shows that the formation of Pb-As jarosite may decrease aqueous arsenic and lead concentrations to meet drinking water standards. The new thermodynamic data confirm that transformation of Pb-As jarosite to plumbojarosite is thermodynamically possible

    Observing gravitational waves from core-collapse supernovae in the advanced detector era

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    The next galactic core-collapse supernova (CCSN) has already exploded, and its electromagnetic (EM) waves, neutrinos, and gravitational waves (GWs) may arrive at any moment. We present an extensive study on the potential sensitivity of prospective detection scenarios for GWs from CCSNe within 5 Mpc, using realistic noise at the predicted sensitivity of the Advanced LIGO and Advanced Virgo detectors for 2015, 2017, and 2019. We quantify the detectability of GWs from CCSNe within the Milky Way and Large Magellanic Cloud, for which there will be an observed neutrino burst. We also consider extreme GW emission scenarios for more distant CCSNe with an associated EM signature. We find that a three-detector network at design sensitivity will be able to detect neutrino-driven CCSN explosions out to ∼5.5  kpc, while rapidly rotating core collapse will be detectable out to the Large Magellanic Cloud at 50 kpc. Of the phenomenological models for extreme GW emission scenarios considered in this study, such as long-lived bar-mode instabilities and disk fragmentation instabilities, all models considered will be detectable out to M31 at 0.77 Mpc, while the most extreme models will be detectable out to M82 at 3.52 Mpc and beyond

    AVALIAÇÃO GEOQUÍMICA DE AMBIENTES CONTAMINADOS PELA EXTRACÇÃO MINEIRA EM DUAS DISTINTAS REGIÕES GEOLÓGICAS E CLIMÁTICAS

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    A nível mundial a indústria mineira é responsável pela adição de 1,16 milhões de toneladas de metais por ano, em ecossistemas terrestres e aquáticos. A poluição do solo e de sistemas aquáticos por metais pesados é um dos factores que mais contribui para a degradação da qualidade do meio, constituindo um risco eminente de intoxicação para o Homem. Foram selecionadas, no Brasil e em Portugal, duas regiões com forte impacto mineiro, para avaliar a influência da geologia e do clima, na geoquímica de ambientes sujeitos à contaminação pela exploração mineira. Bacia do Paraopeba: situada na região do Quadrilátero Ferrífero, Minas Gerais, sob clima tropical seco, foi selecionada pela sua geodiversidade, importância socioeconómica, associada a graves problemas ambientais devido à intensa actividade mineira que se exerce há mais de 300 anos. Geologicamente é constituída por gnaisses, granitoides, rochas metavulcânicas e vulcânicas intercaladas por rochas sedimentares, quartzitos, metaconglomerados-metarenitos, metapelitos, itabiritos e mármores. Mina de S. Domingos: explorada desde o período calcolítico foi encerrada em 1966 após esgotamento do minério. Situa-se no Sul de Portugal, sob clima Mediterrânico e integra-se na Faixa Piritosa Ibérica, que constitui uma das mais importantes Províncias Metalogénicas de sulfuretos maciços polimetálicos à escala mundial. Possui resíduos mineiros muito heterogéneos, encontrando-se escórias romanas e modernas, cinzas de fundição, resíduos ricos em pirite e outros resíduos provenientes da extracção de minério, como resíduos de gossan e de rochas-mãe (quartzitos e filitos, rochas vulcânicas ácidas com intercalações sedimentares, depósitos do tipo “flisch”). Realizou-se um estudo geoquímico de várias componentes geológicas (solos, sedimentos de lagoas de decantação e de linhas de água, água intersticial e coluna de água) em áreas sujeitas a diversas influências dos processos de extracção mineira. Devido à ocorrência sob distintas formas minerais, óxidos de ferro na Bacia do Paraopeba e sulfuretos maciços em S. Domingos, as características geoquímicas do meio e a solubilidade e biodisponibilidade dos elementos metálicos apresentam diferenças acentuadas, tendo como consequência distintos impactos ambientais. Os valores das fracções potencialmente mais poluentes, extraíveis com aqua regia, são significativamente superiores para As, Pb, Zn e Cu em S. Domingos, possuindo a Bacia do Paraopeba valores mais elevados de Mn e Cr. O Fe tem valores idênticos nas duas regiões. Em S. Domingos, os baixos valores de pH (2,47-4,10), aumentam a solubilidade dos metais, representando uma situação de maior risco ambiental. Apenas o Mn, nas fracções biodisponíveis, (fases dissolvidas na água intersticial, fracções de troca e ligadas a carbonatos) tem teores mais elevados na Bacia do Paraopeba, onde as concentrações sob a forma de óxidos são muito elevadas (>2000 ppm). A especiação dos elementos metálicos constitui importante ferramenta para a monitorização da poluição ambiental em regiões mineiras. A sua mobilidade, biodisponibilidade e ecotoxicidade depende da sua proporção nas diferentes fases minerais ou orgânicas às quais está associado, variando em função das condições químicas do meio, clima e natureza das rochas parentais. A análise das formas químicas dos metais, distintas nas duas regiões mineiras, forneceu uma ferramenta imprescindível para o conhecimento das medidas de recuperação e reabilitação a adoptar

    Core-Collapse Supernovae, Neutrinos, and Gravitational Waves

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    Core-collapse supernovae are among the most energetic cosmic cataclysms. They are prodigious emitters of neutrinos and quite likely strong galactic sources of gravitational waves. Observation of both neutrinos and gravitational waves from the next galactic or near extragalactic core-collapse supernova will yield a wealth of information on the explosion mechanism, but also on the structure and angular momentum of the progenitor star, and on aspects of fundamental physics such as the equation of state of nuclear matter at high densities and low entropies. In this contribution to the proceedings of the Neutrino 2012 conference, we summarize recent progress made in the theoretical understanding and modeling of core-collapse supernovae. In this, our emphasis is on multi-dimensional processes involved in the explosion mechanism such as neutrino-driven convection and the standing accretion shock instability. As an example of how supernova neutrinos can be used to probe fundamental physics, we discuss how the rise time of the electron antineutrino flux observed in detectors can be used to probe the neutrino mass hierarchy. Finally, we lay out aspects of the neutrino and gravitational-wave signature of core-collapse supernovae and discuss the power of combined analysis of neutrino and gravitational wave data from the next galactic core-collapse supernova

    Multi-messenger observations of a binary neutron star merger

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    open3614siOn 2017 August 17 a binary neutron star coalescence candidate (later designated GW170817) with merger time 12:41:04 UTC was observed through gravitational waves by the Advanced LIGO and Advanced Virgo detectors. The Fermi Gamma-ray Burst Monitor independently detected a gamma-ray burst (GRB 170817A) with a time delay of ~1.7 s with respect to the merger time. From the gravitational-wave signal, the source was initially localized to a sky region of 31 deg2 at a luminosity distance of 40 8 8-+ Mpc and with component masses consistent with neutron stars. The component masses were later measured to be in the range 0.86 to 2.26 M. An extensive observing campaign was launched across the electromagnetic spectrum leading to the discovery of a bright optical transient (SSS17a, now with the IAU identification of AT 2017gfo) in NGC 4993 (at ~40 Mpc) less than 11 hours after the merger by the One-Meter, Two Hemisphere (1M2H) team using the 1 m Swope Telescope. The optical transient was independently detected by multiple teams within an hour. Subsequent observations targeted the object and its environment. Early ultraviolet observations revealed a blue transient that faded within 48 hours. Optical and infrared observations showed a redward evolution over ~10 days. Following early non-detections, X-ray and radio emission were discovered at the transient's position ~9 and ~16 days, respectively, after the merger. Both the X-ray and radio emission likely arise from a physical process that is distinct from the one that generates the UV/optical/near-infrared emission. No ultra-high-energy gamma-rays and no neutrino candidates consistent with the source were found in follow-up searches. These observations support the hypothesis that GW170817 was produced by the merger of two neutron stars in NGC4993 followed by a short gamma-ray burst (GRB 170817A) and a kilonova/macronova powered by the radioactive decay of r-process nuclei synthesized in the ejecta.openAbbott, B. P.; Abbott, R.; Abbott, T. D.; Acernese, F.; Ackley, K.; Adams, C.; Adams, T.; Addesso, P.; Adhikari, R. X.; Adya, V. B.; Affeldt, C.; Afrough, M.; Agarwal, B.; Agathos, M.; Agatsuma, K.; Aggarwal, N.; Aguiar, O. D.; Aiello, L.; Ain, A.; Ajith, P.; Allen, B.; Allen, G.; Allocca, A.; Altin, P. A.; Amato, A.; Ananyeva, A.; Anderson, S. B.; Anderson, W. G.; Angelova, S. V.; Antier, S.; Appert, S.; Arai, K.; Araya, M. C.; Areeda, J. S.; Arnaud, N.; Arun, K. G.; Ascenzi, S.; Ashton, G.; Ast, M.; Aston, S. M.; Astone, P.; Atallah, D. V.; Aufmuth, P.; Aulbert, C.; Aultoneal, K.; Austin, C.; Avila-Alvarez, A.; Babak, S.; Bacon, P.; Bader, M. K. M.; Bae, S.; Baker, P. T.; Baldaccini, F.; Ballardin, G.; Ballmer, S. W.; Banagiri, S.; Barayoga, J. C.; Barclay, S. E.; Barish, B. C.; Barker, D.; Barkett, K.; Barone, F.; Barr, B.; Barsotti, L.; Barsuglia, M.; Barta, D.; Barthelmy, S. D.; Bartlett, J.; Bartos, I.; Bassiri, R.; Basti, A.; Batch, J. C.; Bawaj, M.; Bayley, J. C.; Bazzan, M.; Bã©csy, B.; Beer, C.; Bejger, M.; Belahcene, I.; Bell, A. S.; Berger, B. K.; Bergmann, G.; Bero, J. J.; Berry, C. P. L.; Bersanetti, D.; Bertolini, A.; Betzwieser, J.; Bhagwat, S.; Bhandare, R.; Bilenko, I. A.; Billingsley, G.; Billman, C. R.; Birch, J.; Birney, R.; Birnholtz, O.; Biscans, S.; Biscoveanu, S.; Bisht, A.; Bitossi, M.; Biwer, C.; Bizouard, M. A.; Blackburn, J. K.; Blackman, J.; Blair, C. D.; Blair, D. G.; Blair, R. M.; Bloemen, S.; Bock, O.; Bode, N.; Boer, M.; Bogaert, G.; Bohe, A.; Bondu, F.; Bonilla, E.; Bonnand, R.; Boom, B. A.; Bork, R.; Boschi, V.; Bose, S.; Bossie, K.; Bouffanais, Y.; Bozzi, A.; Bradaschia, C.; Brady, P. R.; Branchesi, M.; Brau, J. E.; Briant, T.; Brillet, A.; Brinkmann, M.; Brisson, V.; Brockill, P.; Broida, J. E.; Brooks, A. F.; Brown, D. A.; Brown, D. D.; Brunett, S.; Buchanan, C. C.; Buikema, A.; Bulik, T.; Bulten, H. J.; Buonanno, A.; Buskulic, D.; Buy, C.; Byer, R. L.; Cabero, M.; Cadonati, L.; Cagnoli, G.; Cahillane, C.; Calderón Bustillo, J.; Callister, T. A.; Calloni, E.; Camp, J. B.; Canepa, M.; Canizares, P.; Cannon, K. C.; Cao, H.; Cao, J.; Capano, C. D.; Capocasa, E.; Carbognani, F.; Caride, S.; Carney, M. F.; Casanueva Diaz, J.; Casentini, C.; Caudill, S.; Cavagliã , M.; Cavalier, F.; Cavalieri, R.; Cella, G.; Cepeda, C. B.; Cerdá-Durán, P.; Cerretani, G.; Cesarini, E.; Chamberlin, S. J.; Chan, M.; Chao, S.; Charlton, P.; Chase, E.; Chassande-Mottin, E.; Chatterjee, D.; Chatziioannou, K.; Cheeseboro, B. D.; Chen, H. Y.; Chen, X.; Chen, Y.; Cheng, H. -. P.; Chia, H.; Chincarini, A.; Chiummo, A.; Chmiel, T.; Cho, H. S.; Cho, M.; Chow, J. H.; Christensen, N.; Chu, Q.; Chua, A. J. K.; Chua, S.; Chung, A. K. W.; Chung, S.; Ciani, G.; Ciolfi, R.; Cirelli, C. E.; Cirone, A.; Clara, F.; Clark, J. A.; Clearwater, P.; Cleva, F.; Cocchieri, C.; Coccia, E.; Cohadon, P. -. F.; Cohen, D.; Colla, A.; Collette, C. G.; Cominsky, L. R.; Constancio, M.; Conti, L.; Cooper, S. J.; Corban, P.; Corbitt, T. R.; Cordero-Carrión, I.; Corley, K. R.; Cornish, N.; Corsi, A.; Cortese, S.; Costa, C. A.; Coughlin, M. W.; Coughlin, S. B.; Coulon, J. -. P.; Countryman, S. T.; Couvares, P.; Covas, P. B.; Cowan, E. E.; Coward, D. M.; Cowart, M. J.; Coyne, D. C.; Coyne, R.; Creighton, J. D. E.; Creighton, T. D.; Cripe, J.; Crowder, S. G.; Cullen, T. J.; Cumming, A.; Cunningham, L.; Cuoco, E.; Dal Canton, T.; Dã¡lya, G.; Danilishin, S. L.; D'Antonio, S.; Danzmann, K.; Dasgupta, A.; Da Silva Costa, C. F.; Dattilo, V.; Dave, I.; Davier, M.; Davis, D.; Daw, E. J.; Day, B.; S., De; Debra, D.; Degallaix, J.; De Laurentis, M.; Delã©glise, S.; Del Pozzo, W.; Demos, N.; Denker, T.; Dent, T.; De Pietri, R.; Dergachev, V.; De Rosa, R.; Derosa, R. T.; De Rossi, C.; Desalvo, R.; De Varona, O.; Devenson, J.; Dhurandhar, S.; Dã­az, M. C.; Di Fiore, L.; Di Giovanni, M.; Di Girolamo, T.; Di Lieto, A.; Di Pace, S.; Di Palma, I.; Di Renzo, F.; Doctor, Z.; Dolique, V.; Donovan, F.; Dooley, K. L.; Doravari, S.; Dorrington, I.; Douglas, R.; Dovale Ãlvarez, M.; Downes, T. P.; Drago, M.; Dreissigacker, C.; Driggers, J. C.; Du, Z.; Ducrot, M.; Dupej, P.; Dwyer, S. E.; Edo, T. B.; Edwards, M. C.; Effler, A.; Eggenstein, H. -. B.; Ehrens, P.; Eichholz, J.; Eikenberry, S. S.; Eisenstein, R. A.; Essick, R. C.; Estevez, D.; Etienne, Z. B.; Etzel, T.; Evans, M.; Evans, T. M.; Factourovich, M.; Fafone, V.; Fair, H.; Fairhurst, S.; Fan, X.; Farinon, S.; Farr, B.; Farr, W. M.; Fauchon-Jones, E. J.; Favata, M.; Fays, M.; Fee, C.; Fehrmann, H.; Feicht, J.; Fejer, M. M.; Fernandez-Galiana, A.; Ferrante, I.; Ferreira, E. C.; Ferrini, F.; Fidecaro, F.; Finstad, D.; Fiori, I.; Fiorucci, D.; Fishbach, M.; Fisher, R. P.; Fitz-Axen, M.; Flaminio, R.; Fletcher, M.; Fong, H.; Font, J. A.; Forsyth, P. W. F.; Forsyth, S. S.; Fournier, J. -. D.; Frasca, S.; Frasconi, F.; Frei, Z.; Freise, A.; Frey, R.; Frey, V.; Fries, E. M.; Fritschel, P.; Frolov, V. V.; Fulda, P.; Fyffe, M.; Gabbard, H.; Gadre, B. U.; Gaebel, S. M.; Gair, J. R.; Gammaitoni, L.; Ganija, M. R.; Gaonkar, S. G.; Garcia-Quiros, C.; Garufi, F.; Gateley, B.; Gaudio, S.; Gaur, G.; Gayathri, V.; Gehrels, N.; Gemme, G.; Genin, E.; Gennai, A.; George, D.; George, J.; Gergely, L.; Germain, V.; Ghonge, S.; Ghosh, Abhirup; Ghosh, Archisman; Ghosh, S.; Giaime, J. A.; Giardina, K. D.; Giazotto, A.; Gill, K.; Glover, L.; Goetz, E.; Goetz, R.; Gomes, S.; Goncharov, B.; Gonzã¡lez, G.; Gonzalez Castro, J. M.; Gopakumar, A.; Gorodetsky, M. L.; Gossan, S. 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J.; Tacca, M.; Tait, S. C.; Talbot, C.; Talukder, D.; Tanner, D. B.; Tã¡pai, M.; Taracchini, A.; Tasson, J. D.; Taylor, J. A.; Taylor, R.; Tewari, S. V.; Theeg, T.; Thies, F.; Thomas, E. G.; Thomas, M.; Thomas, P.; Thorne, K. A.; Thorne, K. S.; Thrane, E.; Tiwari, S.; Tiwari, V.; Tokmakov, K. V.; Toland, K.; Tonelli, M.; Tornasi, Z.; Torres-Forné, A.; Torrie, C. I.; Tã¶yrã¤, D.; Travasso, F.; Traylor, G.; Trinastic, J.; Tringali, M. C.; Trozzo, L.; Tsang, K. W.; Tse, M.; Tso, R.; Tsukada, L.; Tsuna, D.; Tuyenbayev, D.; Ueno, K.; Ugolini, D.; Unnikrishnan, C. S.; Urban, A. L.; Usman, S. A.; Vahlbruch, H.; Vajente, G.; Valdes, G.; Van Bakel, N.; Van Beuzekom, M.; Van Den Brand, J. F. J.; Van Den Broeck, C.; Vander-Hyde, D. C.; Van Der Schaaf, L.; Van Heijningen, J. V.; Van Veggel, A. A.; Vardaro, M.; Varma, V.; Vass, S.; Vasãºth, M.; Vecchio, A.; Vedovato, G.; Veitch, J.; Veitch, P. J.; Venkateswara, K.; Venugopalan, G.; Verkindt, D.; Vetrano, F.; Vicerã©, A.; Viets, A. 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P.; Koskinen, D. J.; Kowalski, M.; Krings, K.; Kroll, M.; Krã¼ckl, G.; Kunnen, J.; Kunwar, S.; Kurahashi, N.; Kuwabara, T.; Kyriacou, A.; Labare, M.; Lanfranchi, J. L.; Larson, M. J.; Lauber, F.; Lesiak-Bzdak, M.; Leuermann, M.; Liu, Q. R.; Lu, L.; Lã¼nemann, J.; Luszczak, W.; Madsen, J.; Maggi, G.; Mahn, K. B. M.; Mancina, S.; Maruyama, R.; Mase, K.; Maunu, R.; Mcnally, F.; Meagher, K.; Medici, M.; Meier, M.; Menne, T.; Merino, G.; Meures, T.; Miarecki, S.; Micallef, J.; Momentã©, G.; Montaruli, T.; Moore, R. W.; Moulai, M.; Nahnhauer, R.; Nakarmi, P.; Naumann, U.; Neer, G.; Niederhausen, H.; Nowicki, S. C.; Nygren, D. R.; Obertacke Pollmann, A.; Olivas, A.; O'Murchadha, A.; Palczewski, T.; Pandya, H.; Pankova, D. V.; Peiffer, P.; Pepper, J. A.; Pérez De Los Heros, C.; Pieloth, D.; Pinat, E.; Price, P. B.; Przybylski, G. T.; Raab, C.; Rã¤del, L.; Rameez, M.; Rawlins, K.; Rea, I. C.; Reimann, R.; Relethford, B.; Relich, M.; Resconi, E.; Rhode, W.; Richman, M.; Robertson, S.; Rongen, M.; Rott, C.; Ruhe, T.; Ryckbosch, D.; Rysewyk, D.; Sã¤lzer, T.; Sanchez Herrera, S. E.; Sandrock, A.; Sandroos, J.; Santander, M.; Sarkar, S.; Sarkar, S.; Satalecka, K.; Schlunder, P.; Schmidt, T.; Schneider, A.; Schoenen, S.; Schã¶neberg, S.; Schumacher, L.; Seckel, D.; Seunarine, S.; Soedingrekso, J.; Soldin, D.; Song, M.; Spiczak, G. M.; Spiering, C.; Stachurska, J.; Stamatikos, M.; Stanev, T.; Stasik, A.; Stettner, J.; Steuer, A.; Stezelberger, T.; Stokstad, R. G.; Stã¶ssl, A.; Strotjohann, N. L.; Stuttard, T.; Sullivan, G. W.; Sutherland, M.; Taboada, I.; Tatar, J.; Tenholt, F.; Ter-Antonyan, S.; Terliuk, A.; Teå¡ic, G.; Tilav, S.; Toale, P. A.; Tobin, M. N.; Toscano, S.; Tosi, D.; Tselengidou, M.; Tung, C. F.; Turcati, A.; Turley, C. F.; Ty, B.; Unger, E.; Usner, M.; Vandenbroucke, J.; Van Driessche, W.; Van Eijndhoven, N.; Vanheule, S.; Van Santen, J.; Vehring, M.; Vogel, E.; Vraeghe, M.; Walck, C.; Wallace, A.; Wallraff, M.; Wandler, F. D.; Wa
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