Organic Geochemistry 92 (2016) e34–e76
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Geochemistry Articles - December 2015 Analytical Chemistry
Imaging mass spectrometry: Instrumentation, applications, and combination with other visualization techniques Bodzon-Kulakowska, A., Suder, P., 2016. Mass Spectrometry Reviews 35, 147–169. http://dx.doi.org/10.1002/mas.21468 A simple and easy approach to the derivatization of alcohols for study by soft ionization mass spectrometry methods Borisov, R.S., Polovkov, N.Y., Zhilyaev, D.I., Zaikin, V.G., 2015. Journal of Analytical Chemistry 70, 1542–1545. http://dx.doi.org/10.1134/S106193481513002X Polymer-coated micro-optofluidic ring resonator detector for a comprehensive two-dimensional gas chromatographic microsystem: lGC lGC-lOFRR Collin, W.R., Scholten, K.W., Fan, X., Paul, D., Kurabayashi, K., Zellers, E.T., 2016. Analyst 141, 261–269. http://dx.doi.org/10.1039/C5AN01570G Electrospray ionization tandem mass spectrometry analysis of isopimarane diterpenes from Velloziaceae da Cunha Pinto, A., Vessecchi, R., da Silva, C.G., Amorim, A.C.L., dos Santos Júnior, H.M., Rezende, M.J.C., Gates, P.J., Rezende, C.M., Lopes, N.P., 2016. Rapid Communications in Mass Spectrometry 30, 61–68. http://dx.doi.org/10.1002/rcm.7411 Identification of double-bond positions in isomeric alkenones from a lacustrine haptophyte Dillon, J.T., Longo, W.M., Zhang, Y., Torozo, R., Huang, Y., 2016. Rapid Communications in Mass Spectrometry 30, 112–118. http://dx.doi.org/10.1002/rcm.7414 Advances in comprehensive two-dimensional gas chromatography (GCGC) Eiserbeck, C., Nelson, R.K., Reddy, C.M., Grice, K., 2015. In: Grice, K. (Ed.), Principles and Practice of Analytical Techniques in Geosciences. The Royal Society of Chemistry, pp. 324–365. http://dx.doi.org/10.1039/9781782625025-00324 Evaluation of scale-up from analytical to preparative supercritical fluid chromatography Enmark, M., Åsberg, D., Leek, H., Öhlén, K., Klarqvist, M., Samuelsson, J., Fornstedt, T., 2015. Journal of Chromatography A 1425, 280–286. http://www.sciencedirect.com/science/article/pii/S0021967315015903 Microscale sealed vessel pyrolysis Horsfield, B., Leistner, F., Hall, K., 2015. In: Grice, K. (Ed.), Principles and Practice of Analytical Techniques in Geosciences. The Royal Society of Chemistry, pp. 209–250. http://dx.doi.org/10.1039/9781782625025-00209 Electron-induced dissociation (EID) for structure characterization of glycerophosphatidylcholine: Determination of double-bond positions and localization of acyl chains Jones, J.W., Thompson, C.J., Carter, C.L., Kane, M.A., 2015. Journal of Mass Spectrometry 50, 1327–1339. http://dx.doi.org/10.1002/jms.3698 Nanoscale secondary ion mass spectrometry (nanoSIMS) as an analytical tool in the geosciences Kilburn, M.R., Wacey, D., 2015. In: Grice, K. (Ed.), Principles and Practice of Analytical Techniques in Geosciences. The Royal Society of Chemistry, pp. 1–34. http://dx.doi.org/10.1039/9781782625025-00001
http://dx.doi.org/10.1016/j.orggeochem.2015.12.012
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From mass to structure: An aromaticity index for high-resolution mass data of natural organic matter Koch, B.P., Dittmar, T., 2016. Rapid Communications in Mass Spectrometry 30, 250–250. http://dx.doi.org/10.1002/rcm.7433 Advances in fluorescence spectroscopy for petroleum geosciences Liu, K., Sherwood, N., Zhao, M., 2015. In: Grice, K. (Ed.), Principles and Practice of Analytical Techniques in Geosciences. The Royal Society of Chemistry, pp. 94–121. http://dx.doi.org/10.1039/9781782625025-00094 Exploitation of a microporous organic polymer as a stationary phase for capillary gas chromatography Lu, C., Liu, S., Xu, J., Ding, Y., Ouyang, G., 2016. Analytica Chimica Acta 902, 205–211. http://www.sciencedirect.com/science/article/pii/S0003267015013136 Quantification of nitrogen compounds in diesel fuel samples by comprehensive two-dimensional gas chromatography coupled with quadrupole mass spectrometry Maciel, G.P.S., Machado, M.E., da Cunha, M.E., Lazzari, E., da Silva, J.M., Jacques, R.A., Krause, L.C., Barros, J.A.S., Caramão, E.B., 2015. Journal of Separation Science 38, 4071–4077. http://dx.doi.org/10.1002/jssc.201500011 Gas chromatography-quadrupole time-of-flight mass spectrometry-based determination of isotopologue and tandem mass isotopomer fractions of primary metabolites for 13C-metabolic flux analysis Mairinger, T., Steiger, M., Nocon, J., Mattanovich, D., Koellensperger, G., Hann, S., 2015. Analytical Chemistry 87, 11792–11802. http://dx.doi.org/10.1021/acs.analchem.5b03173 Development and use of catalytic hydropyrolysis (HyPy) as an analytical tool for organic geochemical applications Meredith, W., Snape, C.E., Love, G.D., 2015 In: Grice, K. (Ed.), Principles and Practice of Analytical Techniques in Geosciences. The Royal Society of Chemistry, pp. 171–208. http://dx.doi.org/10.1039/9781782625025-00171 Determination of oxygen and nitrogen derivatives of polycyclic aromatic hydrocarbons in fractions of asphalt mixtures using liquid chromatography coupled to mass spectrometry with atmospheric pressure chemical ionization Nascimento, P.C., Gobo, L.A., Bohrer, D., Carvalho, L.M., Cravo, M.C., Leite, L.F.M., 2015. Journal of Separation Science 38, 4055–4062. http://dx.doi.org/10.1002/jssc.201500893 Development and validation of a generic nontarget method based on liquid chromatography – high resolution mass spectrometry analysis for the evaluation of different wastewater treatment options Nürenberg, G., Schulz, M., Kunkel, U., Ternes, T.A., 2015. Journal of Chromatography A 1426, 77–90. http://www.sciencedirect.com/science/article/pii/S0021967315016222 The use of high-speed multicapillary column in comprehensive two-dimensional gas chromatography with flow modulation Patrushev, Y.V., Sidelnikov, V.N., 2015. Journal of Chromatography A 1426, 183–190. http://www.sciencedirect.com/science/article/pii/S0021967315016921 Opportunities and challenges in liquid cell electron microscopy Ross, F.M., 2015. Science (6267). http://www.sciencemag.org/content/350/6267/aaa9886.abstract Prioritizing unknown transformation products from biologically-treated wastewater using high-resolution mass spectrometry, multivariate statistics, and metabolic logic Schollée, J.E., Schymanski, E.L., Avak, S.E., Loos, M., Hollender, J., 2015. Analytical Chemistry 87, 12121–12129. http://dx.doi.org/10.1021/acs.analchem.5b02905 Gas chromatography coupled to atmospheric pressure chemical ionization FT-ICR mass spectrometry for improvement of data reliability Schwemer, T., Rüger, C.P., Sklorz, M., Zimmermann, R., 2015. Analytical Chemistry 87, 11957–11961. http://dx.doi.org/10.1021/acs.analchem.5b02114 Laser desorption sample transfer for gas chromatography/mass spectrometry Seneviratne, C.A., Ghorai, S., Murray, K.K., 2016. Rapid Communications in Mass Spectrometry 30, 89–94. http://dx.doi.org/10.1002/rcm.7419 Turnover rates in microorganisms by laser ablation electrospray ionization mass spectrometry and pulse-chase analysis Stopka, S.A., Mansour, T.R., Shrestha, B., Maréchal, É., Falconet, D., Vertes, A., 2016. Analytica Chimica Acta 902, 1–7. http://www.sciencedirect.com/science/article/pii/S0003267015010594
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Time-of-flight secondary ion mass spectrometry (TOF-SIMS): Principles and practice in the biogeosciences Thiel, V., Sjövall, P., 2015. In: Grice, K. (Ed.), Principles and Practice of Analytical Techniques in Geosciences. The Royal Society of Chemistry, pp. 122–170. http://dx.doi.org/10.1039/9781782625025-00122 Real time online correction of mass shifts and intensity fluctuations in extractive electrospray ionization mass spectrometry Tian, Y., Yu, M., Chen, J., Liu, C., Shi, J., Chen, H., Jiang, G., 2015. Analytical Chemistry 87, 11962–11966. http://dx.doi.org/10.1021/acs.analchem.5b04372 Application of acetone acetals as water scavengers and derivatization agents prior to the gas chromatographic analysis of polar residual solvents in aqueous samples van Boxtel, N., Wolfs, K., Van Schepdael, A., Adams, E., 2015. Journal of Chromatography A 1425, 62–72. http://www.sciencedirect.com/science/article/pii/S0021967315016313 A soft ionization method for semivolatile compounds Verenchikov, A.N., Kolosov, A.P., 2015. Journal of Analytical Chemistry 70, 1527–1532. http://dx.doi.org/10.1134/S1061934815130092 Molecular-shape selectivity by naphthalimido-modified silica stationary phases: Insight into the substituents effect of naphthalene on shape recognition and p–p interactions via electrostatic potential Yamada, Y., Ohyama, K., Onodera, G., Kuriyama, M., Kishikawa, N., Kuroda, N., 2015. Journal of Chromatography A 1425, 173–179. http://www.sciencedirect.com/science/article/pii/S0021967315016416 Combined urea-thin layer chromatography and silver nitrate-thin layer chromatography for micro separation and determination of hard-to-detect branched chain fatty acids in natural lipids Yan, Y., Wang, X., Liu, Y., Xiang, J., Wang, X., Zhang, H., Yao, Y., Liu, R., Zou, X., Huang, J., Jin, Q., 2015. Journal of Chromatography A 1425, 293–301. http://www.sciencedirect.com/science/article/pii/S0021967315016192 Single-particle time-of-flight mass spectrometry utilizing a femtosecond desorption and ionization laser Zawadowicz, M.A., Abdelmonem, A., Mohr, C., Saathoff, H., Froyd, K.D., Murphy, D.M., Leisner, T., Cziczo, D.J., 2015. Analytical Chemistry 87, 12221–12229. http://dx.doi.org/10.1021/acs.analchem.5b03158 Computer simulation and optimization for reversed-phase HPLC separation: A novel algorithm simulating and optimizing the non-linear and non-ideal separation process in analytical chromatography Zhang, Y., 2015. Chemometrics and Intelligent Laboratory Systems 149, Part B, 73–80. http://www.sciencedirect.com/science/article/pii/S016974391500266X Ambient mass spectrometry imaging with picosecond infrared laser ablation electrospray ionization (PIR-LAESI) Zou, J., Talbot, F., Tata, A., Ermini, L., Franjic, K., Ventura, M., Zheng, J., Ginsberg, H., Post, M., Ifa, D.R., Jaffray, D., Miller, R.J.D., Zarrine-Afsar, A., 2015. Analytical Chemistry 87, 12071–12079. http://dx.doi.org/10.1021/acs.analchem.5b02756 Development, optimization, validation and application of faster gas chromatography – flame ionization detector method for the analysis of total petroleum hydrocarbons in contaminated soils Zubair, A., Pappoe, M., James, L.A., Hawboldt, K., 2015. Journal of Chromatography A 1425, 240–248. http://www.sciencedirect.com/science/article/pii/S0021967315014466 Archaeological/Art Organic Chemistry
Identification and mode of formation of hopanoid nitriles in archaeological soils Adam, P., Schaeffer, P., Schmitt, G., Bailly, L., Courel, B., Fresnais, M., Fossurier, C., Rohmer, M., 2016. Organic Geochemistry 91, 100–108. http://www.sciencedirect.com/science/article/pii/S0146638015002156 Feeding Stonehenge: Cuisine and consumption at the Late Neolithic site of Durrington Walls Craig, O.E., Shillito, L.-M., Albarella, U., Viner-Daniels, S., Chan, B., Cleal, R., Ixer, R., Jay, M., Marshall, P., Simmons, E., Wright, E., Pearson, M.P., 2015. Antiquity 89, 1096–1109. http://dx.doi.org/10.15184/aqy.2015.110
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Animal origin of 13th-century uterine vellum revealed using noninvasive peptide fingerprinting Fiddyment, S., Holsinger, B., Ruzzier, C., Devine, A., Binois, A., Albarella, U., Fischer, R., Nichols, E., Curtis, A., Cheese, E., Teasdale, M.D., Checkley-Scott, C., Milner, S.J., Rudy, K.M., Johnson, E.J., Vnoucˇek, J., Garrison, M., McGrory, S., Bradley, D.G., Collins, M.J., 2015. Proceedings of the National Academy of Sciences 112, 15066–15071. http://www.pnas.org/content/early/2015/11/18/1512264112.abstract The origins of inebriation: Archaeological evidence of the consumption of fermented beverages and drugs in prehistoric Eurasia Guerra-Doce, E., 2015. Journal of Archaeological Method and Theory 22, 751–782. http://dx.doi.org/10.1007/s10816-014-9205-z Retroviral DNA sequences as a means for determining ancient diets Rivera-Perez, J.I., Cano, R.J., Narganes-Storde, Y., Chanlatte-Baik, L., Toranzos, G.A., 2015. PLoS ONE 10, Article number e0144951. http://dx.doi.org/10.1371%2Fjournal.pone.0144951 Analysis and quantitation of volatile organic compounds emitted from plastics used in museum construction by evolved gas analysis–gas chromatography–mass spectrometry Samide, M.J., Smith, G.D., 2015. Journal of Chromatography A 1426, 201–208. http://www.sciencedirect.com/science/article/pii/S0021967315017100 Characterisation of oriental lacquers from Rhus succedanea and Melanorrhoea usitata using in situ pyrolysis/silylation-gas chromatography mass spectrometry Tamburini, D., Bonaduce, I., Colombini, M.P., 2015. Journal of Analytical and Applied Pyrolysis 116, 129–141. http://www.sciencedirect.com/science/article/pii/S0165237015302217 Characterization of Tang Dynasty lamp oil remains by using pyrolysis gas chromatography and mass spectrometry Wei, S., Li, Y., Ma, Q., Lou, S., Schreiner, M., 2015. Journal of Analytical and Applied Pyrolysis 116, 237–242. http://www.sciencedirect.com/science/article/pii/S0165237015301819 Astrobiology
Remote sensing of life: Polarimetric signatures of photosynthetic pigments as sensitive biomarkers Berdyugina, S.V., Kuhn, J.R., Harrington, D.M., Šantl-Temkiv, T., Messersmith, E.J., 2016. International Journal of Astrobiology 15, 45–56. http://dx.doi.org/10.1017/S1473550415000129 Simulating super earth atmospheres in the laboratory Claudi, R., Erculiani, M.S., Galletta, G., Billi, D., Pace, E., Schierano, D., Giro, E., D’Alessandro, M., 2016. International Journal of Astrobiology 15, 35–44. http://dx.doi.org/10.1017/S1473550415000117 Pressurized Martian-like pure CO2 atmosphere supports strong growth of cyanobacteria, and causes significant changes in their metabolism Murukesan, G., Leino, H., Mäenpää, P., Ståhle, K., Raksajit, W., Lehto, H., Allahverdiyeva-Rinne, Y., Lehto, K., 2016. Origins of Life and Evolution of Biospheres 46, 119–131. http://dx.doi.org/10.1007/s11084-015-9458-x Isolation of radiation-resistant bacteria from Mars analog Antarctic Dry Valleys by preselection, and the correlation between radiation and desiccation resistance Musilova, M., Wright, G., Ward, J.M., Dartnell, L.R., 2015. Astrobiology 15, 1076–1090. http://dx.doi.org/10.1089/ast.2014.1278 Survival of Antarctic cryptoendolithic fungi in simulated Martian conditions on board the International Space Station Onofri, S., de Vera, J.-P., Zucconi, L., Selbmann, L., Scalzi, G., Venkateswaran, K.J., Rabbow, E., de la Torre, R., Horneck, G., 2015. Astrobiology 15, 1052–1059. http://dx.doi.org/10.1089/ast.2015.1324 Sustainable life support on Mars – the potential roles of cyanobacteria Verseux, C., Baqué, M., Lehto, K., de Vera, J.-P.P., Rothschild, L.J., Billi, D., 2016. International Journal of Astrobiology 15, 65–92. http://dx.doi.org/10.1017/S147355041500021X On the detection of carbon monoxide as an anti-biosignature in exoplanetary atmospheres Wang, Y., Tian, F., Li, T., Hu, Y., 2016. Icarus 266, 15–23. http://www.sciencedirect.com/science/article/pii/S0019103515005205
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Biosignatures for astrobiology Westall, F., Cockell, C.S., 2016. Origins of Life and Evolution of Biospheres 46, 105–106. http://dx.doi.org/10.1007/s11084-015-9459-9 Biochemistry
The siderophore metabolome of Azotobacter vinelandii Baars, O., Zhang, X., Morel, F.M.M., Seyedsayamdost, M.R., 2016. Applied and Environmental Microbiology 82, 27–39. http://aem.asm.org/content/82/1/27.abstract Novel tri- and tetra-unsaturated highly branched isoprenoid (HBI) alkenes from the marine diatom Pleurosigma intermedium Brown, T.A., Belt, S.T., 2016. Organic Geochemistry 91, 120–122. http://www.sciencedirect.com/science/article/pii/S0146638015002120 Complete nitrification by Nitrospira bacteria Daims, H., Lebedeva, E.V., Pjevac, P., Han, P., Herbold, C., Albertsen, M., Jehmlich, N., Palatinszky, M., Vierheilig, J., Bulaev, A., Kirkegaard, R.H., von Bergen, M., Rattei, T., Bendinger, B., Nielsen, P.H., Wagner, M., 2015. Nature 528, 504–509. http://dx.doi.org/10.1038/nature16461 Sulfate to go Fritz, G., Kroneck, P.M.H., 2015. Science 350, 1476–1477. http://www.sciencemag.org/content/350/6267/1476.short Mono-, di- and trimethylated homologues of isoprenoid tetraether lipid cores in archaea and environmental samples: Mass spectrometric identification and significance Knappy, C., Barillà, D., Chong, J., Hodgson, D., Morgan, H., Suleman, M., Tan, C., Yao, P., Keely, B., 2015. Journal of Mass Spectrometry 50, 1420–1432. http://dx.doi.org/10.1002/jms.3709 The bioenergetic costs of a gene Lynch, M., Marinov, G.K., 2015. Proceedings of the National Academy of Sciences 112, 15690–15695. http://www.pnas.org/content/112/51/15690.abstract How bacteria use Type IV pili machinery on surfaces Maier, B., Wong, G.C.L., 2015. Trends in Microbiology 23, 775–788. http://www.sciencedirect.com/science/article/pii/S0966842X15002048 Isolation and characterization of bacterium producing lipid from short-chain fatty acids Okamura, Y., Nakai, S., Ohkawachi, M., Suemitsu, M., Takahashi, H., Aki, T., Matsumura, Y., Tajima, T., Nakashimada, Y., Matsumoto, M., 2016. Bioresource Technology 201, 215–221. http://www.sciencedirect.com/science/article/pii/S0960852415015667 A protein trisulfide couples dissimilatory sulfate reduction to energy conservation Santos, A.A., Venceslau, S.S., Grein, F., Leavitt, W.D., Dahl, C., Johnston, D.T., Pereira, I.A.C., 2015. Science 350, 1541–1545. http://www.sciencemag.org/content/350/6267/1541.abstract Horizontal DNA transfer from bacteria to eukaryotes and a lesson from experimental transfers Suzuki, K., Moriguchi, K., Yamamoto, S., 2015. Research in Microbiology 166, 753–763. http://www.sciencedirect.com/science/article/pii/S0923250815001308 Complete nitrification by a single microorganism van Kessel, M.A.H.J., Speth, D.R., Albertsen, M., Nielsen, P.H., Op den Camp, H.J.M., Kartal, B., Jetten, M.S.M., Lücker, S., 2015. Nature 528, 555–559. http://dx.doi.org/10.1038/nature16459 Insights into the life of an oxygenic phototroph Whitman, W.B., 2015. Proceedings of the National Academy of Sciences 112, 14747–14748. http://www.pnas.org/content/112/48/14747.short
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Biodegradation
Phenol biodegradation by halophilic archaea Acikgoz, E., Ozcan, B., 2016. International Biodeterioration & Biodegradation 107, 140–146. http://www.sciencedirect.com/science/article/pii/S0964830515301384 Bioaccessible porosity in soil aggregates and implications for biodegradation of high molecular weight petroleum compounds Akbari, A., Ghoshal, S., 2015. Environmental Science & Technology 49, 14368–14375. http://dx.doi.org/10.1021/acs.est.5b03618 Promising approaches towards biotransformation of polycyclic aromatic hydrocarbons with Ascomycota fungi Aranda, E., 2016. Current Opinion in Biotechnology 38, 1–8. http://www.sciencedirect.com/science/article/pii/S0958166915001652 Biotransformation of cyclohexane and related alicyclic hydrocarbons by Candida maltosa and Trichosporon species Dallinger, A., Duldhardt, I., Kabisch, J., Schlüter, R., Schauer, F., 2016. International Biodeterioration & Biodegradation 107, 132–139. http://www.sciencedirect.com/science/article/pii/S0964830515301372 Commentary: Oil degradation and biosurfactant production by the deep sea bacterium Dietzia maris As-13-3 Rahman, P.K.S.M., Sekhon Randhawa, K.K., 2015. Frontiers in Microbiology 6, 1557. doi: 10.3389/fmicb.2015.01557. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01557/full Biodegradation of different petroleum hydrocarbons by free and immobilized microbial consortia Shen, T., Pi, Y., Bao, M., Xu, N., Li, Y., Lu, J., 2015. Environmental Science: Processes & Impacts 17, 2022–2033. http://dx.doi.org/10.1039/C5EM00318K Degradation of oil by fungi isolated from Gulf of Mexico beaches Simister, R.L., Poutasse, C.M., Thurston, A.M., Reeve, J.L., Baker, M.C., White, H.K., 2015. Marine Pollution Bulletin 100, 327–333. http://www.sciencedirect.com/science/article/pii/S0025326X15005330 Anaerobic degradation of alcohol ethoxylates and polyethylene glycols in marine sediments Traverso-Soto, J.M., Rojas-Ojeda, P., Sanz, J.L., González-Mazo, E., Lara-Martín, P.A., 2016. Science of The Total Environment 544, 118–124. http://www.sciencedirect.com/science/article/pii/S0048969715311219 Biodegradability of dissolved organic carbon in permafrost soils and aquatic systems: A meta-analysis Vonk, J.E., Tank, S.E., Mann, P.J., Spencer, R.G.M., Treat, C.C., Striegl, R.G., Abbott, B.W., Wickland, K.P., 2015. Biogeosciences 12, 6915–6930. http://www.biogeosciences.net/12/6915/2015/ Bioaugmentation and biostimulation of hydrocarbon degradation and the microbial community in a petroleum-contaminated soil Wu, M., Dick, W.A., Li, W., Wang, X., Yang, Q., Wang, T., Xu, L., Zhang, M., Chen, L., 2016. International Biodeterioration & Biodegradation 107, 158–164. http://www.sciencedirect.com/science/article/pii/S0964830515301414 Marine oil-degrading microorganisms and biodegradation process of petroleum hydrocarbon in marine environments: A review Xue, J., Yu, Y., Bai, Y., Wang, L., Wu, Y., 2015. Current Microbiology 71, 220–228. http://dx.doi.org/10.1007/s00284-015-0825-7 Biodegradation pathways/genomics
Degradation of benzene by Pseudomonas veronii 1YdBTEX2 and 1YB2 is catalyzed by enzymes encoded in distinct catabolism gene clusters de Lima-Morales, D., Chaves-Moreno, D., Wos-Oxley, M.L., Jáuregui, R., Vilchez-Vargas, R., Pieper, D.H., 2016. Applied and Environmental Microbiology 82, 167–173. http://aem.asm.org/content/82/1/167.abstract Isolation and characterization of two novel halotolerant catechol 2,3-dioxygenases from a halophilic bacterial consortium Guo, G., Fang, T., Wang, C., Huang, Y., Tian, F., Cui, Q., Wang, H., 2015. Scientific Reports 5, Article number 17603. http://dx.doi.org/10.1038/srep17603
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Complete genome sequence of Chelatococcus sp. CO-6, a crude-oil-degrading bacterium Wang, Y., Cui, D., Li, A., Yang, J., Ma, F., 2016. Journal of Biotechnology 219, 20–21. http://www.sciencedirect.com/science/article/pii/S0168165615302182 Use of mass spectrometry for characterizing the growth of Pseudomonas bacteria bearing naphthalene degradation plasmids Zyakun, A.M., Kochetkov, V.V., Zakharchenko, V.N., Baskunov, B.P., Laurinavichius, K.S., Peshenko, V.P., Siunova, T.V., Anokhina, T.O., Boronin, A.M., 2015. Journal of Analytical Chemistry 70, 1569–1575. http://dx.doi.org/10.1134/S1061934815130122 Biogeochemistry
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Ecophysiology of Zetaproteobacteria associated with shallow hydrothermal iron-oxyhydroxide deposits in Nagahama Bay of Satsuma Iwo-Jima, Japan Hoshino, T., Kuratomi, T., Morono, Y., Hori, T., Oiwane, H., Kiyokawa, S., Inagaki, F., 2015. Frontiers in Microbiology 6, 1554. doi: 10.3389/fmicb.2015.01554. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01554/abstract Impact of anaerobic oxidation of methane on geochemical cycle of redox-sensitive elements at cold seep sites of the northern South China Sea Hu, Y., Feng, D., Liang, Q., Zhen, X., Chen, L., Chen, D., 2015. Deep Sea Research Part II: Topical Studies in Oceanography 122, 84–94. http://www.sciencedirect.com/science/article/pii/S0967064515002143 Toxic metal resistance in biofilms: Diversity of microbial responses and their evolution Koechler, S., Farasin, J., Cleiss-Arnold, J., Arsène-Ploetze, F., 2015. Research in Microbiology 166, 764–773. http://www.sciencedirect.com/science/article/pii/S0923250815000601 Evidence for methane production by marine algae (Emiliana huxleyi) and its implication for the methane paradox in oxic waters Lenhart, K., Klintzsch, T., Langer, G., Nehrke, G., Bunge, M., Schnell, S., Keppler, F., 2015. Biogeosciences Discussions 12, 20323–20360. http://www.biogeosciences-discuss.net/12/20323/2015/ Microbial methane production associated with carbon steel corrosion in a Nigerian oil field Mand, J., Park, H.S., Okoro, C., Lomans, B.P., Smith, S., Chiejina, L., Voordouw, G., 2015. Frontiers in Microbiology 6, 1538. doi: 10.3389/fmicb.2015.01538. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01538/abstract Discovery of symbiotic nitrogen fixation and chemoautotrophy in cold-water corals Middelburg, J.J., Mueller, C.E., Veuger, B., Larsson, A.I., Form, A., van Oevelen, D., 2015. Scientific Reports 5, Article number 17962. http://dx.doi.org/10.1038/srep17962 Ordinary stoichiometry of extraordinary microorganisms Neveu, M., Poret-Peterson, A.T., Anbar, A.D., Elser, J.J., 2016. Geobiology 14, 33–53. http://dx.doi.org/10.1111/gbi.12153 Metalliferous biosignatures for deep subsurface microbial activity Parnell, J., Brolly, C., Spinks, S., Bowden, S., 2016. Origins of Life and Evolution of Biospheres 46, 107–118. http://dx.doi.org/10.1007/s11084-015-9466-x Phytoplankton versus macrophyte contribution to primary production and biogeochemical cycles of a coastal mesotidal system. A modelling approach Plus, M., Auby, I., Maurer, D., Trut, G., Del Amo, Y., Dumas, F., Thouvenin, B., 2015. Estuarine, Coastal and Shelf Science 165, 52–60. http://www.sciencedirect.com/science/article/pii/S0272771415300810 Bacterially-mediated weathering of crystalline and amorphous Cu-slags Potysz, A., Grybos, M., Kierczak, J., Guibaud, G., Lens, P.N.L., van Hullebusch, E.D., 2016. Applied Geochemistry 64, 92–106. http://www.sciencedirect.com/science/article/pii/S0883292715300160 Principles of geobiochemistry Shock, E.L., Boyd, E.S., 2015. Elements 11, 395–401. http://elements.geoscienceworld.org/content/11/6/395.abstract Emerging frontiers in geomicrobiology Templeton, A., Benzerara, K., 2015. Elements 11, 423–429. http://elements.geoscienceworld.org/content/11/6/423.abstract The mineralosphere concept: Mineralogical control of the distribution and function of mineral-associated bacterial communities Uroz, S., Kelly, L.C., Turpault, M.-P., Lepleux, C., Frey-Klett, P., 2015. Trends in Microbiology 23, 751-762. http://www.sciencedirect.com/science/article/pii/S0966842X15002309 Nitrogen cycling in the deep sedimentary biosphere: Nitrate isotopes in porewaters underlying the oligotrophic North Atlantic Wankel, S.D., Buchwald, C., Ziebis, W., Wenk, C.B., Lehmann, M.F., 2015. Biogeosciences 12, 7483–7502. http://www.biogeosciences.net/12/7483/2015/
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Environmental Geochemistry
The effect of oil sands process-affected water and model naphthenic acids on photosynthesis and growth in Emiliania huxleyi and Chlorella vulgaris Beddow, J., Johnson, R.J., Lawson, T., Breckels, M.N., Webster, R.J., Smith, B.E., Rowland, S.J., Whitby, C., 2016. Chemosphere 145, 416–423. http://www.sciencedirect.com/science/article/pii/S0045653515303787 Bioremediation of oil polluted marine sediments: A bio-engineering treatment Cappello, S., Calogero, R., Santisi, S., Genovese, M., Denaro, R., Genovese, L., Giuliano, L., Mancini, G., Yakimov, M.M., 2015. International Microbiology 18, 127–134. http://dx.doi.org/10.2436/20.1501.01.242 Impact of temperature, pH, and salinity changes on the physico-chemical properties of model naphthenic acids Celsie, A., Parnis, J.M., Mackay, D., 2016. Chemosphere 146, 40–50. http://www.sciencedirect.com/science/article/pii/S0045653515304537 Advances in Biodegradation and Bioremediation of Industrial Waste Chandra, R., 2015. CRC Press 479 pp. https://www.crcpress.com/Advances-in-Biodegradation-and-Bioremediation-of-Industrial-Waste/Chandra/9781498700542 A semi-quantitative approach for the rapid screening and mass profiling of naphthenic acids directly in contaminated aqueous samples Duncan, K.D., Letourneau, D.R., Vandergrift, G.W., Jobst, K., Reiner, E., Gill, C.G., Krogh, E.T., 2016. Journal of Mass Spectrometry 51, 44–52. http://onlinelibrary.wiley.com/doi/10.1002/jms.3721/abstract Disposal in the unconventional oil and gas sector: Challenges and solutions Fennell, J., 2015. Environmental Geosciences 22, 127–138. http://eg.geoscienceworld.org/content/22/4/127.abstract Assessment of anthropogenic contamination with sterol markers in surface sediments of a tropical estuary (Itajaí-Açu, Brazil) Frena, M., Bataglion, G.A., Tonietto, A.E., Eberlin, M.N., Alexandre, M.R., Madureira, L.A.S., 2016. Science of The Total Environment 544, 432–438. http://www.sciencedirect.com/science/article/pii/S0048969715310901 Chemical dispersants can suppress the activity of natural oil-degrading microorganisms Kleindienst, S., Seidel, M., Ziervogel, K., Grim, S., Loftis, K., Harrison, S., Malkin, S.Y., Perkins, M.J., Field, J., Sogin, M.L., Dittmar, T., Passow, U., Medeiros, P.M., Joye, S.B., 2015. Proceedings of the National Academy of Sciences 112, 14900–14905. http://www.pnas.org/content/112/48/14900.abstract Equilibrium passive sampling as a tool to study polycyclic aromatic hydrocarbons in Baltic Sea sediment pore-water systems Lang, S.-C., Hursthouse, A., Mayer, P., Kötke, D., Hand, I., Schulz-Bull, D., Witt, G., 2015. Marine Pollution Bulletin 101, 296–303. http://www.sciencedirect.com/science/article/pii/S0025326X15301429 Effect of rhamnolipid biosurfactant on solubilization of polycyclic aromatic hydrocarbons Li, S., Pi, Y., Bao, M., Zhang, C., Zhao, D., Li, Y., Sun, P., Lu, J., 2015. Marine Pollution Bulletin 101, 219–225. http://www.sciencedirect.com/science/article/pii/S0025326X15300746 Presence of aliphatic and polycyclic aromatic hydrocarbons in near-surface sediments of an oil spill area in Bohai Sea Li, S., Zhang, S., Dong, H., Zhao, Q., Cao, C., 2015. Marine Pollution Bulletin 100, 169–175. http://www.sciencedirect.com/science/article/pii/S0025326X15300266 Sources and distribution of polycyclic aromatic hydrocarbons in a an urbanized tropical estuary and adjacent shelf, northeast of Brazil Maciel, D.C., de Souza, J.R.B., Taniguchi, S., Bícego, M.C., Zanardi-Lamardo, E., 2015. Marine Pollution Bulletin 101, 429–433. http://www.sciencedirect.com/science/article/pii/S0025326X15300667 From spill to sequestration: The molecular journey of contamination via comprehensive multiphase NMR Masoom, H., Courtier-Murias, D., Soong, R., Maas, W.E., Fey, M., Kumar, R., Monette, M., Stronks, H.J., Simpson, M.J., Simpson, A.J., 2015. Environmental Science & Technology 49, 13983–13991. http://dx.doi.org/10.1021/acs.est.5b03251
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Assessment of the toxic potential of polycyclic aromatic hydrocarbons (PAHs) affecting Gulf menhaden (Brevoortia patronus) harvested from waters impacted by the BP Deepwater Horizon Spill Olson, G.M., Meyer, B.M., Portier, R.J., 2016. Chemosphere 145, 322–328. http://www.sciencedirect.com/science/article/pii/S0045653515304185 A case study on effects of oil spills and tar-ball pollution on beaches of Goa (India) Rekadwad, B.N., Khobragade, C.N., 2015. Marine Pollution Bulletin 100, 567–570. http://www.sciencedirect.com/science/article/pii/S0025326X15005238 Efficient dispersion of crude oil by blends of food-grade surfactants: Toward greener oil-spill treatments Riehm, D.A., Neilsen, J.E., Bothun, G.D., John, V.T., Raghavan, S.R., McCormick, A.V., 2015. Marine Pollution Bulletin 101, 92–97. http://www.sciencedirect.com/science/article/pii/S0025326X15301624 Spatial and temporal patterns in black carbon deposition to dated Fennoscandian Arctic lake sediments from 1830 to 2010 Ruppel, M.M., Gustafsson, Ö., Rose, N.L., Pesonen, A., Yang, H., Weckström, J., Palonen, V., Oinonen, M.J., Korhola, A., 2015. Environmental Science & Technology 49, 13954–13963. http://dx.doi.org/10.1021/acs.est.5b01779 Impact of oil spills on coral reefs can be reduced by bioremediation using probiotic microbiota Santos, H.F., Duarte, G.A.S., Rachid, C.T.d.C., Chaloub, R.M., Calderon, E.N., Marangoni, L.F.d.B., Bianchini, A., Nudi, A.H., Carmo, F.L.d, van Elsas, J.D., Rosado, A.S., Castro, C.B.e., Peixoto, R.S., 2015. Scientific Reports 5, Article number 18268. http://dx.doi.org/10.1038/srep18268 Wastewater recycling and reuse trends in Pennsylvania shale gas wells Schmid, K., Yoxtheimer, D., 2015. Environmental Geosciences 22, 115–125. http://eg.geoscienceworld.org/content/22/4/115.abstract Long-term incubation reveals methanogenic biodegradation of C5 and C6 iso-alkanes in oil sands tailings Siddique, T., Mohamad Shahimin, M.F., Zamir, S., Semple, K., Li, C., Foght, J.M., 2015. Environmental Science & Technology 49, 14732–14739. http://dx.doi.org/10.1021/acs.est.5b04370 Studies on polycyclic aromatic hydrocarbons in surface sediments of Mithi River near Mumbai, India: Assessment of sources, toxicity risk and biological impact Singare, P.U., 2015. Marine Pollution Bulletin 101, 232–242. http://www.sciencedirect.com/science/article/pii/S0025326X15300722 Adventures in groundwater monitoring: Why has it been so difficult to obtain groundwater data near shale gas wells? Soeder, D.J., 2015. Environmental Geosciences 22, 139–148. http://eg.geoscienceworld.org/content/22/4/139.abstract The assessment of the spatial and seasonal variability of chromophoric dissolved organic matter in the southern Yellow Sea and the East China Sea Su, R., Bai, Y., Zhang, C., Shi, X., 2015. Marine Pollution Bulletin 100, 523–533. http://www.sciencedirect.com/science/article/pii/S0025326X15300217 Lessons learned while building the Deepwater Horizon Database: Toward improved data sharing in coastal science Thessen, A.E., McGinnis, S., North, E.W., 2016. Computers & Geosciences 87, 84–90. http://www.sciencedirect.com/science/article/pii/S009830041530090X Forensic investigation of aliphatic hydrocarbons in the sediments from selected mangrove ecosystems in the west coast of Peninsular Malaysia Vaezzadeh, V., Zakaria, M.P., Shau-Hwai, A.T., Ibrahim, Z.Z., Mustafa, S., Abootalebi-Jahromi, F., Masood, N., Magam, S.M., Alkhadher, S.A.A., 2015. Marine Pollution Bulletin 100, 311–320. http://www.sciencedirect.com/science/article/pii/S0025326X1500538X Impacts of Deepwater Horizon oil and associated dispersant on early development of the Eastern oyster Crassostrea virginica Vignier, J., Donaghy, L., Soudant, P., Chu, F.L.E., Morris, J.M., Carney, M.W., Lay, C., Krasnec, M., Robert, R., Volety, A.K., 2015. Marine Pollution Bulletin 100, 426–437. http://www.sciencedirect.com/science/article/pii/S0025326X15005159 Was the extreme and wide-spread marine oil-snow sedimentation and flocculent accumulation (MOSSFA) event during the Deepwater Horizon blow-out unique? Vonk, S.M., Hollander, D.J., Murk, A.J., 2015. Marine Pollution Bulletin 100, 5–12. http://www.sciencedirect.com/science/article/pii/S0025326X15005275
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Non-target screening of organic pollutants in sediments and sludges using gas chromatography-mass spectrometry and automated mass spectral deconvolution Wang, G., Ma, H., Wang, L., Chen, J., Hou, X., 2015. Chinese Journal of Chromatography 33, 1294–1300. http://www.chrom-china.com/EN/abstract/abstract13997.shtml Determination of oxygen, nitrogen, and sulfur-containing polycyclic aromatic hydrocarbons (PAHs) in urban stream sediments Witter, A.E., Nguyen, M.H., 2016. Environmental Pollution 209, 186–196. http://www.sciencedirect.com/science/article/pii/S026974911530138X Reconciling divergent estimates of oil and gas methane emissions Zavala-Araiza, D., Lyon, D.R., Alvarez, R.A., Davis, K.J., Harriss, R., Herndon, S.C., Karion, A., Kort, E.A., Lamb, B.K., Lan, X., Marchese, A.J., Pacala, S.W., Robinson, A.L., Shepson, P.B., Sweeney, C., Talbot, R., Townsend-Small, A., Yacovitch, T.I., Zimmerle, D.J., Hamburg, S.P., 2015. Proceedings of the National Academy of Sciences 112, 15597–15602. http://www.pnas.org/content/112/51/15597.abstract The NET effect of dispersants — a critical review of testing and modelling of surface oil dispersion Zeinstra-Helfrich, M., Koops, W., Murk, A.J., 2015. Marine Pollution Bulletin 100, 102–111. http://www.sciencedirect.com/science/article/pii/S0025326X15300394 Simulation of scenarios of oil droplet formation from the Deepwater Horizon blowout Zhao, L., Boufadel, M.C., Adams, E., Socolofsky, S.A., King, T., Lee, K., Nedwed, T., 2015. Marine Pollution Bulletin 101, 304–319. http://www.sciencedirect.com/science/article/pii/S0025326X15301417 Evolution/Paleontology/Palynology
A new time tree reveals Earth history’s imprint on the evolution of modern birds Claramunt, S., Cracraft, J., 2015. Science Advances 1. Article number e1501005 http://advances.sciencemag.org/content/1/11/e1501005.abstract 3D chemical map and a theoretical life model for Neuropteris ovata var. simonii (index fossil, Asturian, Late Pennsylvanian, Canada) D’Angelo, J.A., Zodrow, E.L., 2016. International Journal of Coal Geology 153, 12–27. http://www.sciencedirect.com/science/article/pii/S0166516215300768 Nematophytes from the Lower Devonian of Podolia, Ukraine Filipiak, P., Szaniawski, H., 2016. Review of Palaeobotany and Palynology 224, Part 2, 109–120. http://www.sciencedirect.com/science/article/pii/S0034666715001748 Exceptional preservation of tiny embryos documents seed dormancy in early angiosperms Friis, E.M., Crane, P.R., Raunsgaard Pedersen, K., Stampanoni, M., Marone, F., 2015. Nature 528, 551–554. http://dx.doi.org/10.1038/nature16441 New data about anatomy, branching, and inferred growth patterns in the Early Devonian plant Armoricaphyton chateaupannense, Montjean-sur-Loire, France Gerrienne, P., Gensel, P.G., 2016. Review of Palaeobotany and Palynology 224, Part 1, 38–53. http://www.sciencedirect.com/science/article/pii/S0034666715001438 Ediacaran marine redox heterogeneity and early animal ecosystems Li, C., Planavsky, N.J., Shi, W., Zhang, Z., Zhou, C., Cheng, M., Tarhan, L.G., Luo, G., Xie, S., 2015. Scientific Reports 5, Article number 17097. http://dx.doi.org/10.1038/srep17097 Mandibular and dental characteristics of Late Triassic mammaliaform Haramiyavia and their ramifications for basal mammal evolution Luo, Z.-X., Gatesy, S.M., Jenkins, F.A., Amaral, W.W., Shubin, N.H., 2015. Proceedings of the National Academy of Sciences 112, E7101–E7109. http://www.pnas.org/content/early/2015/11/11/1519387112.abstract Growth architecture and microsporangiate strobilus of Sublepidodendron grabaui (Lycopsida) from the Late Devonian of south China Meng, M.-C., Liu, L., Wang, D.-M., Yao, J.-X., 2016. Review of Palaeobotany and Palynology 224, Part 1, 83–93. http://www.sciencedirect.com/science/article/pii/S0034666715001177 The terrestrialization process: A palaeobotanical and palynological perspective Meyer-Berthaud, B., Servais, T., Vecoli, M., Gerrienne, P., 2016. Review of Palaeobotany and Palynology 224, Part 1, 1–3. http://www.sciencedirect.com/science/article/pii/S0034666715001980
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Evolution of habitat depth in the Jurassic–Cretaceous ammonoids Moriya, K., 2015. Proceedings of the National Academy of Sciences 112, 15540–15541. http://www.pnas.org/content/112/51/15540.short How complexity originates: The evolution of animal eyes Oakley, T.H., Speiser, D.I., 2015. Annual Review of Ecology, Evolution, and Systematics 46, 237–260. http://dx.doi.org/10.1146/annurev-ecolsys-110512-135907 Late Devonian plant communities of north Russia Orlova, O.A., Jurina, A.L., Snigirevsky, S.M., 2016. Review of Palaeobotany and Palynology 224, Part 1, 94–107. http://www.sciencedirect.com/science/article/pii/S0034666715001621 Genomic data do not support comb jellies as the sister group to all other animals Pisani, D., Pett, W., Dohrmann, M., Feuda, R., Rota-Stabelli, O., Philippe, H., Lartillot, N., Wörheide, G., 2015. Proceedings of the National Academy of Sciences 112, 15402–15407. http://www.pnas.org/content/early/2015/11/24/1518127112.abstract Cryptospores from the Katian (Upper Ordovician) of the Tungus Basin: The first evidence for early land plants from the Siberian paleocontinent Raevskaya, E., Dronov, A., Servais, T., Wellman, C.H., 2016. Review of Palaeobotany and Palynology 224, Part 1, 4–13. http://www.sciencedirect.com/science/article/pii/S0034666715001979 The palynological record across the Ordovician/Silurian boundary in the Cordillera Oriental, Central Andean Basin, northwestern Argentina Rubinstein, C.V., de la Puente, G.S., Delabroye, A., Astini, R.A., 2016. Review of Palaeobotany and Palynology 224, Part 1, 14–25. http://www.sciencedirect.com/science/article/pii/S0034666715001268 The impact of the ‘Terrestrialisation Process’ in the Late Palaeozoic: pCO2, pO2, and the ‘Phytoplankton Blackout’ Servais, T., Martin, R.E., Nützel, A., 2016. Review of Palaeobotany and Palynology 224, Part 1, 26–37. http://www.sciencedirect.com/science/article/pii/S0034666715001633 Anatomy of the Middle Devonian cladoxylopsid Panxia gabata Y. Wang et Berry from Yunnan Province, southwestern China Xue, J., Huang, P., Wang, D., Wang, Q., Hao, S., 2016. Review of Palaeobotany and Palynology 224, Part 1, 66–82. http://www.sciencedirect.com/science/article/pii/S0034666715000950 Evolution: Origins of Life/Microbial Genomics
The gene repertoire of animal stem cells Alié, A., Hayashi, T., Sugimura, I., Manuel, M., Sugano, W., Mano, A., Satoh, N., Agata, K., Funayama, N., 2015. Proceedings of the National Academy of Sciences 112, E7093–E7100. http://www.pnas.org/content/112/51/E7093.abstract The life story of hydrogen peroxide III: Chirality and physical effects at the dawn of life Ball, R., Brindley, J., 2016. Origins of Life and Evolution of Biospheres 46, 81–93. http://dx.doi.org/10.1007/s11084-015-9465-y Thiosulfate-hydrogen peroxide redox oscillator as pH driver for ribozyme activity in the RNA world Ball, R., Brindley, J., 2016. Origins of Life and Evolution of Biospheres 46, 133–147. http://dx.doi.org/10.1007/s11084-015-9448-z The activation of free dipeptides promoted by strong activating agents in water does not yield diketopiperazines Beaufils, D., Jepaul, S., Liu, Z., Boiteau, L., Pascal, R., 2016. Origins of Life and Evolution of Biospheres 46, 19–30. http://dx.doi.org/10.1007/s11084-015-9455-0 The role of autocatalysis on the chemical diversity of the prebiotic ocean of early Earth Canepa, C., 2016. International Journal of Astrobiology 15, 57–64. http://dx.doi.org/10.1017/S1473550415000099 A proposal of the proteome before the last universal common ancestor (LUCA) de Farias, S.T., Rêgo, T.G., José, M.V., 2016. International Journal of Astrobiology 15, 27–31. http://dx.doi.org/10.1017/S1473550415000464
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Hydrothermal conditions and the origin of cellular life Deamer, D.W., Georgiou, C.D., 2015. Astrobiology 15, 1091–1095. http://dx.doi.org/10.1089/ast.2015.1338 Origin of life: LUCA and extracellular membrane vesicles (EMVs) Gill, S., Forterre, P., 2016. International Journal of Astrobiology 15, 7–15. http://dx.doi.org/10.1017/S1473550415000282 Nucleoside phosphorylation by the mineral schreibersite Gull, M., Mojica, M.A., Fernández, F.M., Gaul, D.A., Orlando, T.M., Liotta, C.L., Pasek, M.A., 2015. Scientific Reports 5, Article number 17198. http://dx.doi.org/10.1038/srep17198 Evolvability is an evolved ability: The coding concept as the arch-unit of natural selection Jankovic´, S., C´irkovic´, M.M., 2016. Origins of Life and Evolution of Biospheres 46, 67–79. http://dx.doi.org/10.1007/s11084-015-9464-z The routes of emergence of life from LUCA during the RNA and viral world Jheeta, S., 2016. International Journal of Astrobiology 15, 1–1. http://dx.doi.org/10.1017/S1473550415000361 Predicting thermodynamic behaviors of non-protein amino acids as a function of temperature and pH Kitadai, N., 2016. Origins of Life and Evolution of Biospheres 46, 3–18. http://dx.doi.org/10.1007/s11084-015-9457-y Re-criticizing RNA-mediated cell evolution: A radical perspective Kotakis, C., 2016. International Journal of Astrobiology 15, 3–5. http://dx.doi.org/10.1017/S1473550415000191 A model of isotope separation in cells at the early stages of evolution Melkikh, A.V., Bokunyaeva, A.O., 2016. Origins of Life and Evolution of Biospheres 46, 95–104. http://dx.doi.org/10.1007/s11084-015-9463-0 History of the ribosome and the origin of translation Petrov, A.S., Gulen, B., Norris, A.M., Kovacs, N.A., Bernier, C.R., Lanier, K.A., Fox, G.E., Harvey, S.C., Wartell, R.M., Hud, N.V., Williams, L.D., 2015. Proceedings of the National Academy of Sciences 112, 15396–15401. http://www.pnas.org/content/112/50/15396.abstract Formamide reaction network in gas phase and solution via a unified theoretical approach: Toward a reconciliation of different prebiotic scenarios Pietrucci, F., Saitta, A.M., 2015. Proceedings of the National Academy of Sciences 112, 15030–15035. http://www.pnas.org/content/112/49/15030.abstract Origin of marine planktonic cyanobacteria Sánchez-Baracaldo, P., 2015. Scientific Reports 5, Article number 17418. http://dx.doi.org/10.1038/srep17418 A strategy for origins of life research Scharf, C., Virgo, N., Cleaves, H.J., Aono, M., Aubert-Kato, N., Aydinoglu, A., Barahona, A., Barge, L.M., Benner, S.A., Biehl, M., Brasser, R., Butch, C.J., Chandru, K., Cronin, L., Danielache, S., Fischer, J., Hernlund, J., Hut, P., Ikegami, T., Kimura, J., Kobayashi, K., Mariscal, C., McGlynn, S., Menard, B., Packard, N., Pascal, R., Pereto, J., Rajamani, S., Sinapayen, L., Smith, E., Switzer, C., Takai, K., Tian, F., Ueno, Y., Voytek, M., Witkowski, O., Yabuta, H., 2015. Astrobiology 15, 1031–1042. http://dx.doi.org/10.1089/ast.2015.1113 Possible role of Prussian blue nanoparticles in chemical evolution: Interaction with ribose nucleotides Sharma, R., Iqubal, M.A., Kamaluddin, 2016. International Journal of Astrobiology 15, 17–25. http://dx.doi.org/10.1017/S1473550415000348 Alpha-oxo acids assisted transformation of FeS to Fe3S4 at low temperature: Implications for abiotic, biotic, and prebiotic mineralization Wang, W., Song, Y., Wang, X., Yang, Y., Liu, X., 2015. Astrobiology 15, 1043–1051. http://dx.doi.org/10.1089/ast.2015.1373
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Fluid Inclusions
Threshold size for fluid inclusion decrepitation Campione, M., Malaspina, N., Frezzotti, M.L., 2015. Journal of Geophysical Research: Solid Earth 120, 7396–7402. http://dx.doi.org/10.1002/2015JB012086 Thermodynamic modeling of binary CH4–CO2 fluid inclusions Mao, S., Shi, L., Peng, Q., Lü, M., 2016. Applied Geochemistry 66, 65–72. http://www.sciencedirect.com/science/article/pii/S0883292715300810 Geology
The effect of a thiol-containing organic molecule on molybdenum adsorption onto pyrite Freund, C., Wishard, A., Brenner, R., Sobel, M., Mizelle, J., Kim, A., Meyer, D.A., Morford, J.L., 2016. Geochimica et Cosmochimica Acta 174, 222–235. http://www.sciencedirect.com/science/article/pii/S0016703715006481 Talc-dominated seafloor deposits reveal a new class of hydrothermal system Hodgkinson, M.R.S., Webber, A.P., Roberts, S., Mills, R.A., Connelly, D.P., Murton, B.J., 2015. Nature Communications 6, Article number 10150. http://dx.doi.org/10.1038/ncomms10150 Olivine versus peridotite during serpentinization: Gas formation Huang, R.F., Sun, W.D., Ding, X., Liu, J.Z., Peng, S.B., 2015. Science China Earth Sciences 58, 2165–2174. http://dx.doi.org/10.1007/s11430-015-5222-3 Basin deconstruction–construction: Seeking thermal–tectonic consistency through the integration of geochemical thermal indicators and seismic fault mechanical stratigraphy – Example from Faras Field, North Western Desert, Egypt Pigott, J.D., Abouelresh, M.O., 2016. Journal of African Earth Sciences 114, 110–124. http://www.sciencedirect.com/science/article/pii/S1464343X1530100X Enigmatic spheres from the Upper Triassic Lockatong Formation, Newark Basin of eastern Pennsylvania: Evidence for microbial activity in marginal-lacustrine strandline deposits Simpson, E.L., Fillmore, D.L., Szajna, M.J., Bogner, E., Malenda, M.G., Livingston, K.M., Hartline, B., 2015. Palaeobiodiversity and Palaeoenvironments 95, 521–529. http://dx.doi.org/10.1007/s12549-015-0207-y Hydrates
Gas hydrate dissociation prolongs acidification of the Anthropocene oceans Boudreau, B.P., Luo, Y., Meysman, F.J.R., Middelburg, J.J., Dickens, G.R., 2015. Geophysical Research Letters 42, 9337–9344. http://dx.doi.org/10.1002/2015GL065779 Effect of NaCl on methane hydrate formation and dissociation in porous media Chong, Z.R., Chan, A.H.M., Babu, P., Yang, M., Linga, P., 2015. Journal of Natural Gas Science and Engineering 27, Part 1, 178–189. http://www.sciencedirect.com/science/article/pii/S1875510015301207 Permeability and porosity of hydrate-bearing sediments in the northern Gulf of Mexico Daigle, H., Cook, A., Malinverno, A., 2015. Marine and Petroleum Geology 68, Part A, 551–564. http://www.sciencedirect.com/science/article/pii/S0264817215301069 Influence of hydrate saturation on methane hydrate dissociation by depressurization in conjunction with warm water stimulation in the silica sand reservoir Feng, J.-C., Wang, Y., Li, X.-S., Zhang, Y., 2015. Energy & Fuels 29, 7875–7884. http://dx.doi.org/10.1021/acs.energyfuels.5b01970 Analysis of bubble plume distributions to evaluate methane hydrate decomposition on the continental slope Johnson, H.P., Miller, U.K., Salmi, M.S., Solomon, E.A., 2015. Geochemistry, Geophysics, Geosystems 16, 3825–3839. http://dx.doi.org/10.1002/2015GC005955
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Methane hydrate formation and dissociation in the presence of silica sand and bentonite clay Kumar Saw, V., Udayabhanu, G., Mandal, A., Laik, S., 2015. Oil & Gas Science and Technology – Revue d’IFP Energies nouvelles 70, 1087–1099. http://dx.doi.org/10.2516/ogst/2013200 Study of the effect of the degree of overcooling during the formation of hydrates of a methane-propane gas mixture on the equilibrium conditions of their decomposition Medvedev, V.I., Gushchin, P.A., Yakushev, V.S., Semenov, A.P., 2015. Chemistry and Technology of Fuels and Oils 51, 470–479. http://dx.doi.org/10.1007/s10553-015-0627-4 Initiation of gas-hydrate pockmark in deep-water Nigeria: Geo-mechanical analysis and modelling Riboulot, V., Sultan, N., Imbert, P., Ker, S., 2016. Earth and Planetary Science Letters 434, 252–263. http://www.sciencedirect.com/science/article/pii/S0012821X15007517 Isotope Geochemistry
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Formation and stability of 14C-containing organic compounds in alkaline iron-water systems: Preliminary assessment based on a literature survey and thermodynamic modelling Wieland, E., Hummel, W., 2015. Mineralogical Magazine 79, 1275–1286. http://minmag.geoscienceworld.org/content/79/6/1275.abstract Vanadium isotope measurement by MC-ICP-MS Wu, F., Qi, Y., Yu, H., Tian, S., Hou, Z., Huang, F., 2016. Chemical Geology 421, 17–25. http://www.sciencedirect.com/science/article/pii/S0009254115301182 Investigation of the controlled factors influencing carbon isotope composition of foxtail and common millet on the Chinese Loess Plateau Yang, Q., Li, X.Q., 2015. Science China Earth Sciences 58, 2296–2308. http://dx.doi.org/10.1007/s11430-015-5181-8 Microbiology/Extremophiles – Microbial Ecology
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Ubiquitous presence and novel diversity of anaerobic alkane degraders in cold marine sediments Gittel, A., Donhauser, J., Røy, H., Girguis, P.R., Jørgensen, B.B., Kjeldsen, K.U., 2015. Frontiers in Microbiology 6, 1414. doi: 10.3389/ fmicb.2015.01414. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01414/abstract Diverse bacterial groups contribute to the alkane degradation potential of chronically polluted subantarctic coastal sediments Guibert, L.M., Loviso, C.L., Borglin, S., Jansson, J.K., Dionisi, H.M., Lozada, M., 2016. Microbial Ecology 71, 100–112. http://dx.doi.org/10.1007/s00248-015-0698-0 Confluentimicrobium naphthalenivorans sp. nov., a naphthalene-degrading bacterium isolated from sea-tidal-flat sediment, and emended description of the genus Confluentimicrobium Park et al. 2015 Jeong, H.I., Jin, H.M., Jeon, C.O., 2015. International Journal of Systematic and Evolutionary Microbiology 65, 4191–4195. http://ijs.microbiologyresearch.org/content/journal/ijsem/10.1099/ijsem.0.000561 Alteromonas naphthalenivorans sp. nov., a polycyclic aromatic hydrocarbon-degrading bacterium isolated from tidal-flat sediment Jin, H.M., Kim, K.H., Jeon, C.O., 2015. International Journal of Systematic and Evolutionary Microbiology 65, 4208–4214. http://ijs.microbiologyresearch.org/content/journal/ijsem/10.1099/ijsem.0.000563 Archaeal and bacterial communities across a chronosequence of drained lake basins in Arctic Alaska Kao-Kniffin, J., Woodcroft, B.J., Carver, S.M., Bockheim, J.G., Handelsman, J., Tyson, G.W., Hinkel, K.M., Mueller, C.W., 2015. Scientific Reports 5, Article number 18165. http://dx.doi.org/10.1038/srep18165 Diversity and habitat preferences of cultivated and uncultivated aerobic methanotrophic bacteria evaluated based on pmoA as molecular marker Knief, C., 2015. Frontiers in Microbiology 6, 1346. doi: 10.3389/fmicb.2015.01346. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01346/abstract Microbiology: A division of labour combined Kuypers, M.M.M., 2015. Nature 528, 487–488. http://dx.doi.org/10.1038/528487a Shifts in bacterial community composition associated with increased carbon cycling in a mosaic of phytoplankton blooms Landa, M., Blain, S., Christaki, U., Monchy, S., Obernosterer, I., 2016. ISME Journal 10, 39–50. http://dx.doi.org/10.1038/ismej.2015.105 Ecological speciation in bacteria: Reverse ecology approaches reveal the adaptive part of bacterial cladogenesis Lassalle, F., Muller, D., Nesme, X., 2015. Research in Microbiology 166, 729–741. http://www.sciencedirect.com/science/article/pii/S0923250815001187 Microbial communities on seafloor basalts at Dorado Outcrop reflect level of alteration and highlight global lithic clades Lee, M.D., Walworth, N.G., Sylvan, J.B., Edwards, K.J., Orcutt, B.N., 2015. Frontiers in Microbiology 6, 1470. doi: 10.3389/fmicb.2015.01470. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01470/abstract The impact of temperature on microbial diversity and AOA activity in the Tengchong Geothermal Field, China Li, H., Yang, Q., Li, J., Gao, H., Li, P., Zhou, H., 2015. Scientific Reports 5, Article number 17056. http://dx.doi.org/10.1038/srep17056 Micro- and mesozooplankton community response to increasing CO2 levels in the Baltic Sea: Insights from a large-scale mesocosm experiment Lischka, S., Bach, L.T., Schulz, K.G., Riebesell, U., 2015. Biogeosciences Discussions 12, 20025–20070. http://www.biogeosciences-discuss.net/12/20025/2015/ Rarity in aquatic microbes: Placing protists on the map Logares, R., Mangot, J.-F., Massana, R., 2015. Research in Microbiology 166, 831–841. http://www.sciencedirect.com/science/article/pii/S0923250815001655 Hidden biosphere in an oxygen-deficient Atlantic open-ocean eddy: Future implications of ocean deoxygenation on primary production in the eastern tropical North Atlantic Löscher, C.R., Fischer, M.A., Neulinger, S.C., Fiedler, B., Philippi, M., Schütte, F., Singh, A., Hauss, H., Karstensen, J., Körtzinger, A., Künzel, S., Schmitz, R.A., 2015. Biogeosciences 12, 7467–7482. http://www.biogeosciences.net/12/7467/2015/
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An abyssal mobilome: Viruses, plasmids and vesicles from deep-sea hydrothermal vents Lossouarn, J., Dupont, S., Gorlas, A., Mercier, C., Bienvenu, N., Marguet, E., Forterre, P., Geslin, C., 2015. Research in Microbiology 166, 742–752. http://www.sciencedirect.com/science/article/pii/S0923250815000637 Snow and ice ecosystems: Not so extreme Maccario, L., Sanguino, L., Vogel, T.M., Larose, C., 2015. Research in Microbiology 166, 782–795. http://www.sciencedirect.com/science/article/pii/S0923250815001576 Carbon-fixation rates and associated microbial communities residing in arid and ephemerally wet Antarctic Dry Valley soils Niederberger, T., Sohm, J.A., Gunderson, T., Tirindelli, J., Capone, D.G., Carpenter, E.J., Cary, C.S., 2015. Frontiers in Microbiology 6, 1347. doi: 10.3389/fmicb.2015.01347. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01347/abstract Mycobiota of underground habitats: Case study of Harmanecká Cave in Slovakia ˇ ovská, Z., Tancˇinová, D., 2016. Microbial Ecology 71, 87–99. Ogórek, R., Višn http://dx.doi.org/10.1007/s00248-015-0686-4 Cellular maintenance processes that potentially underpin the survival of subseafloor fungi over geological timescales Orsi, W.D., Richards, T.A., Santoro, A.E., 2015. Estuarine, Coastal and Shelf Science 164, A1–A9. http://www.sciencedirect.com/science/article/pii/S0272771415001390 Phylogenetic congruence and ecological coherence in terrestrial Thaumarchaeota Oton, E.V., Quince, C., Nicol, G.W., Prosser, J.I., Gubry-Rangin, C., 2016. ISME Journal 10, 85–96. http://dx.doi.org/10.1038/ismej.2015.101 Exploration of microbial diversity and community structure of Lonar Lake: The only hypersaline meteorite crater lake within basalt rock Paul, D., Kumbhare, S., Mhatre, S.M., Chowdhury, S.P., Shetty, S.A., Marrthe, N.P., Bhute, S., Shouche, Y.S., 2015. Frontiers in Microbiology 6, 1553. doi: 10.3389/fmicb.2015.01553. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01553/abstract Succession within the prokaryotic communities during the VAHINE mesocosms experiment in the New Caledonia lagoon Pfreundt, U., Van Wambeke, F., Bonnet, S., Hess, W.R., 2015. Biogeosciences Discussions 12, 20179–20222. http://www.biogeosciences-discuss.net/12/20179/2015/ Bacterial diversity in microbial mats and sediments from the Atacama Desert Rasuk, M.C., Fernández, A.B., Kurth, D., Contreras, M., Novoa, F., Poiré, D., Farías, M.E., 2016. Microbial Ecology 71, 44–56. http://dx.doi.org/10.1007/s00248-015-0649-9 Actinobacterial diversity in volcanic caves and associated geomicrobiological interactions Riquelme, C., Marshall Hathaway, J.J., Enes Dapkevicius, M.D.L., Miller, A.Z., Kooser, A., Northup, D.E., Jurdo, V., Fernandaz, O., Saiz-Jimenez, C., Cheeptham, N., 2015. Frontiers in Microbiology 6, 1342. doi: 10.3389/fmicb.2015.01342. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01342/abstract Bacterioplankton of the Kara Sea shelf Romanova, N.D., Sazhin, A.F., 2015. Oceanology 55, 858–862. http://dx.doi.org/10.1134/S000143701506017X Unravelling core microbial metabolisms in the hypersaline microbial mats of Shark Bay using high-throughput metagenomics Ruvindy, R., White III, R.A., Neilan, B.A., Burns, B.P., 2016. ISME Journal 10, 183–196. http://dx.doi.org/10.1038/ismej.2015.87 The activated sludge ecosystem contains a core community of abundant organisms Saunders, A.M., Albertsen, M., Vollertsen, J., Nielsen, P.H., 2016. ISME Journal 10, 11–20. http://dx.doi.org/10.1038/ismej.2015.117 Stone-dwelling actinobacteria Blastococcus saxobsidens, Modestobacter marinus and Geodermatophilus obscurus proteogenomes Sghaier, H., Hezbri, K., Ghodhbane-Gtari, F., Pujic, P., Sen, A., Daffonchio, D., Boudabous, A., Tisa, L.S., Klenk, H.-P., Armengaud, J., Normand, P., Gtari, M., 2016. ISME Journal 10, 21–29. http://dx.doi.org/10.1038/ismej.2015.108
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Similar microbial communities found on two distant seafloor basalts Singer, E., Chong, L., Heidelberg, J., Edwards, K., 2015. Frontiers in Microbiology 6, 1409. doi: 10.3389/fmicb.2015.01409. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01409/abstract Genomic reconstruction of an uncultured hydrothermal vent gammaproteobacterial methanotroph (family Methylothermaceae) indicates multiple adaptations to oxygen limitation Skennerton, C.T., Ward, L.M., Michel, A., Metcalfe, K., Valiente, C., Mullin, S., Chan, K.Y., Gradinaru, V., Orphan, V.J., 2015. Frontiers in Microbiology 6, 1425. doi: 10.3389/fmicb.2015.01425. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01425/abstract Elemental sulfur and acetate can support life of a novel strictly anaerobic haloarchaeon Sorokin, D.Y., Kublanov, I.V., Gavrilov, S.N., Rojo, D., Roman, P., Golyshin, P.N., Slepak, V.Z., Smedile, F., Ferrer, M., Messina, E., La Cono, V., Yakimov, M.M., 2016. ISME Journal 10, 240–252. http://dx.doi.org/10.1038/ismej.2015.79 High diversity of anaerobic alkane-degrading microbial communities in marine seep sediments based on (1-methylalkyl)succinate synthase genes Stagars, M.H., Ruff, S.E., Amann, R., Knittel, K., 2015. Frontiers in Microbiology 6, 1511. doi: 10.3389/fmicb.2015.01511. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01511/abstract Novel barite chimneys at the Lokis Castle Vent Field shed light on key factors shaping microbial communities and functions in hydrothermal systems Steen, I.H., Dahle, H., Stokke, R., Roalkvam, I., Daae, F.-L., Rapp, H.-T., Pedersen, R.-B., Thorseth, I.H., 2015. Frontiers in Microbiology 6, 1510. doi: 10.3389/fmicb.2015.01510. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01510/abstract Microbes are trophic analogs of animals Steffan, S.A., Chikaraishi, Y., Currie, C.R., Horn, H., Gaines-Day, H.R., Pauli, J.N., Zalapa, J.E., Ohkouchi, N., 2015. Proceedings of the National Academy of Sciences 112, 15119–15124. http://www.pnas.org/content/112/49/15119.abstract Hydroxy fatty acids in fresh snow samples from northern Japan: Long-range atmospheric transport of Gram-negative bacteria by Asian winter monsoon Tyagi, P., Yamamoto, S., Kawamura, K., 2015. Biogeosciences 12, 7071–7080. http://www.biogeosciences.net/12/7071/2015/ Microbiome analysis across a natural copper gradient at a proposed northern Canadian mine site Van Rossum, T., Pylatuk, M., Osachoff, H., Griffiths, E., Lo, R., Quach, M., Lower, N., Palmer, R., Brinkman, F.S.L., Kennedy, C.J., 2015. Frontiers in Environmental Science 3, 84. doi: 10.3389/fenvs.2015.00084. http://journal.frontiersin.org/article/10.3389/fenvs.2015.00084/abstract Expansion of cultured bacterial diversity by large-scale dilution-to-extinction culturing from a single seawater sample Yang, S.-J., Kang, I., Cho, J.-C., 2016. Microbial Ecology 71, 29–43. http://dx.doi.org/10.1007/s00248-015-0695-3 Spatio-temporal variation of sediment methanotrophic microorganisms in a large eutrophic lake Yang, Y., Zhao, Q., Cui, Y., Wang, Y., Xie, S., Liu, Y., 2016. Microbial Ecology 71, 9–17. http://dx.doi.org/10.1007/s00248-015-0667-7 Bacterial diversity in submarine groundwater along the coasts of the Yellow Sea Ye, Q., Liu, J., Du, J., Zhang, J., 2015. Frontiers in Microbiology 6, 1519. doi: 10.3389/fmicb.2015.01519. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01519/abstract
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Paleoclimatology/Palaeoceanography
Stable (d13C and d15N) isotopes and magnetic susceptibility record of late Holocene climate change from a lake profile of the northeast Himalaya Agrawal, S., Srivastava, P., Sonam, Meena, N.K., Rai, S., Bhushan, R., Misra, D.K., Gupta, A.K., 2015. Journal of the Geological Society of India 86, 696–705. http://dx.doi.org/10.1007/s12594-015-0362-9 Early Cenomanian ‘‘hot greenhouse” revealed by oxygen isotope record of exceptionally well-preserved foraminifera from Tanzania Ando, A., Huber, B.T., MacLeod, K.G., Watkins, D.K., 2015. Paleoceanography 30, 1556–1572. http://dx.doi.org/10.1002/2015PA002854 Glacier response to North Atlantic climate variability during the Holocene Balascio, N.L., D’Andrea, W.J., Bradley, R.S., 2015. Climate of the Past 11, 1587–1598. http://www.clim-past.net/11/1587/2015/ Was millennial scale climate change during the Last Glacial triggered by explosive volcanism? Baldini, J.U.L., Brown, R.J., McElwaine, J.N., 2015. Scientific Reports 5, Article number 17442. http://dx.doi.org/10.1038/srep17442 Atlantic multi-decadal oscillation covaries with Agulhas leakage Biastoch, A., Durgadoo, J.V., Morrison, A.K., van Sebille, E., Weijer, W., Griffies, S.M., 2015. Nature Communications 6, Article number 10082. http://dx.doi.org/10.1038/ncomms10082 Holocene North Atlantic Overturning in an atmosphere-ocean-sea ice model compared to proxy-based reconstructions Blaschek, M., Renssen, H., Kissel, C., Thornalley, D., 2015. Paleoceanography 30, 1503–1524. http://dx.doi.org/10.1002/2015PA002828 Mg/Ca in fossil oyster shells as palaeotemperature proxy, an example from the Palaeogene of Central Asia Bougeois, L., de Rafélis, M., Reichart, G.-J., de Nooijer, L.J., Dupont-Nivet, G., 2016. Palaeogeography, Palaeoclimatology, Palaeoecology 441, Part 4, 611–626. http://www.sciencedirect.com/science/article/pii/S0031018215005623 Links between eastern equatorial Pacific stratification and atmospheric CO2 rise during the last deglaciation Bova, S.C., Herbert, T., Rosenthal, Y., Kalansky, J., Altabet, M., Chazen, C., Mojarro, A., Zech, J., 2015. Paleoceanography 30, 1407–1424. http://dx.doi.org/10.1002/2015PA002816 Central Mediterranean Mid-Pleistocene paleoclimatic variability and its association with global climate Capotondi, L., Girone, A., Lirer, F., Bergami, C., Verducci, M., Vallefuoco, M., Afferri, A., Ferraro, L., Pelosi, N., De Lange, G.J., 2016. Palaeogeography, Palaeoclimatology, Palaeoecology 442, 72–83. http://www.sciencedirect.com/science/article/pii/S0031018215006653 Characterization of micropyrite populations in low-grade metamorphic slate: A study using high-resolution X-ray tomography Cárdenes, V., Merinero, R., De Boever, W., Rubio-Ordóñez, Á., Dewanckele, J., Cnudde, J.-P., Boone, M., Van Hoorebeke, L., Cnudde, V., 2016. Palaeogeography, Palaeoclimatology, Palaeoecology 441, Part 4, 924–935. http://www.sciencedirect.com/science/article/pii/S0031018215006069 Mo marine geochemistry and reconstruction of ancient ocean redox states Cheng, M., Li, C., Zhou, L., Xie, S., 2015. Science China Earth Sciences 58, 2123–2133. http://dx.doi.org/10.1007/s11430-015-5177-4 Anomalous SST warming during MIS 13 in the Gulf of Lions (northwestern Mediterranean Sea) Cortina, A., Grimalt, J.O., Martrat, B., Rigual-Hernández, A., Sierro, F.J., Flores, J.A., 2016. Organic Geochemistry 92, 16–23. http://www.sciencedirect.com/science/article/pii/S0146638015002351 Constraining early to middle Eocene climate evolution of the southwest Pacific and Southern Ocean Dallanave, E., Bachtadse, V., Crouch, E.M., Tauxe, L., Shepherd, C.L., Morgans, H.E.G., Hollis, C.J., Hines, B.R., Sugisaki, S., 2016. Earth and Planetary Science Letters 433, 380–392. http://www.sciencedirect.com/science/article/pii/S0012821X15007086
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Eocene benthic foraminiferal assemblages from central Anatolia (Turkey): Biostratigraphy, stable isotope data, paleoenvironmental and paleontological interpretations Dinçer, F., 2016. Journal of African Earth Sciences 114, 143–157. http://www.sciencedirect.com/science/article/pii/S1464343X15301187 Climate-vegetation modelling and fossil plant data suggest low atmospheric CO2 in the late Miocene Forrest, M., Eronen, J.T., Utescher, T., Knorr, G., Stepanek, C., Lohmann, G., Hickler, T., 2015. Climate of the Past 11, 1701–1732. http://www.clim-past.net/11/1701/2015/ Development of a regional glycerol dialkyl glycerol tetraether (GDGT)–temperature calibration for Antarctic and sub-Antarctic lakes Foster, L.C., Pearson, E.J., Juggins, S., Hodgson, D.A., Saunders, K.M., Verleyen, E., Roberts, S.J., 2016. Earth and Planetary Science Letters 433, 370–379. http://www.sciencedirect.com/science/article/pii/S0012821X15007220 Ocean warming, not acidification, controlled coccolithophore response during past greenhouse climate change Gibbs, S.J., Bown, P.R., Ridgwell, A., Young, J.R., Poulton, A.J., O’Dea, S.A., 2016. Geology 44, 59–62. http://geology.gsapubs.org/content/44/1/59.abstract The relative contribution of orbital forcing and greenhouse gases to the North American deglaciation Gregoire, L.J., Valdes, P.J., Payne, A.J., 2015. Geophysical Research Letters 42, 9970–9979. http://dx.doi.org/10.1002/2015GL066005 Comparison of eastern tropical Pacific TEX86 and Globigerinoides ruber Mg/Ca derived sea surface temperatures: Insights from the Holocene and Last Glacial Maximum Hertzberg, J.E., Schmidt, M.W., Bianchi, T.S., Smith, R.K., Shields, M.R., Marcantonio, F., 2016. Earth and Planetary Science Letters 434, 320–332. http://www.sciencedirect.com/science/article/pii/S0012821X15007542 Did high Neo-Tethys subduction rates contribute to early Cenozoic warming? Hoareau, G., Bomou, B., van Hinsbergen, D.J.J., Carry, N., Marquer, D., Donnadieu, Y., Le Hir, G., Vrielynck, B., Walter-Simonnet, A.V., 2015. Climate of the Past 11, 1751–1767. http://www.clim-past.net/11/1751/2015/ Fluctuations of the oxygen minimum zone at the end of Oceanic Anoxic Event 2 in the Gulf of Mexico and the response of ammonites Ifrim, C., 2015. Swiss Journal of Palaeontology 134, 217–225. http://dx.doi.org/10.1007/s13358-015-0089-7 Water isotope systematics: Improving our palaeoclimate interpretations Jones, M.D., Dee, S., Anderson, L., Baker, A., Bowen, G., Noone, D.C., 2016. Quaternary Science Reviews 131, Part B, 243–249. http://www.sciencedirect.com/science/article/pii/S0277379115003406 Development of a novel empirical framework for interpreting geological carbon isotope excursions, with implications for the rate of carbon injection across the PETM Kirtland Turner, S., Ridgwell, A., 2016. Earth and Planetary Science Letters 435, 1–13. http://www.sciencedirect.com/science/article/pii/S0012821X15007311 On the state dependency of the equilibrium climate sensitivity during the last 5 million years Köhler, P., de Boer, B., von der Heydt, A.S., Stap, L.B., van de Wal, R.S.W., 2015. Climate of the Past 11, 1801–1823. http://www.clim-past.net/11/1801/2015/ Jurassic climate mode governed by ocean gateway Korte, C., Hesselbo, S.P., Ullmann, C.V., Dietl, G., Ruhl, M., Schweigert, G., Thibault, N., 2015. Nature Communications 6, Article number 10015. http://dx.doi.org/10.1038/ncomms10015 Neogene ice volume and ocean temperatures: Insights from infaunal foraminiferal Mg/Ca paleothermometry Lear, C.H., Coxall, H.K., Foster, G.L., Lunt, D.J., Mawbey, E.M., Rosenthal, Y., Sosdian, S.M., Thomas, E., Wilson, P.A., 2015. Paleoceanography 30, 1437–1454. http://dx.doi.org/10.1002/2015PA002833 Late Jurassic biogeochemical microenvironments associated with microbialite-coated unionids (Bivalvia), Asturias (N Spain) Lozano, R.P., Delvene, G., Piñuela, L., García-Ramos, J.C., 2016. Palaeogeography, Palaeoclimatology, Palaeoecology 443, 80–97. http://www.sciencedirect.com/science/article/pii/S0031018215006872
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Palaeogeographic controls on climate and proxy interpretation Lunt, D.J., Farnsworth, A., Loptson, C., Foster, G.L., Markwick, P., O’Brien, C.L., Pancost, R.D., Robinson, S.A., Wrobel, N., 2015. Climate of the Past Discussions 11, 5683–5725. http://www.clim-past-discuss.net/11/5683/2015/ Palaeoclimatic and site-specific conditions in the early Permian fossil forest of Chemnitz—Sedimentological, geochemical and palaeobotanical evidence Luthardt, L., Rößler, R., Schneider, J.W., 2016. Palaeogeography, Palaeoclimatology, Palaeoecology 441, Part 4, 627–652. http://www.sciencedirect.com/science/article/pii/S0031018215005775 Continuous 1.3-million-year record of East African hydroclimate, and implications for patterns of evolution and biodiversity Lyons, R.P., Scholz, C.A., Cohen, A.S., King, J.W., Brown, E.T., Ivory, S.J., Johnson, T.C., Deino, A.L., Reinthal, P.N., McGlue, M.M., Blome, M.W., 2015. Proceedings of the National Academy of Sciences 112, 15568–15573. http://www.pnas.org/content/112/51/15568.abstract Was atmospheric CO2 capped at 1000 ppm over the past 300 million years? McElwain, J.C., Montañez, I., White, J.D., Wilson, J.P., Yiotis, C., 2016. Palaeogeography, Palaeoclimatology, Palaeoecology 441, Part 4, 653–658. http://www.sciencedirect.com/science/article/pii/S0031018215005799 Palaeoenvironmental changes in the northwestern Tethys during the Late Campanian Radotruncana calcarata Zone: Implications from stable isotopes and geochemistry Neuhuber, S., Gier, S., Hohenegger, J., Wolfgring, E., Spötl, C., Strauss, P., Wagreich, M., 2016. Chemical Geology 420, 280–296. http://www.sciencedirect.com/science/article/pii/S0009254115301145 Climate variability and long-term expansion of peat lands in Arctic Norway during the late Pliocene (ODP Site 642, Norwegian Sea) Panitz, S., Salzmann, U., Risebrobakken, B., De Schepper, S., Pound, M.J., 2015. Climate of the Past Discussions 11, 5755–5798. http://www.clim-past-discuss.net/11/5755/2015/ Tropical North Atlantic subsurface warming events as a fingerprint for AMOC variability during Marine Isotope Stage 3 Parker, A.O., Schmidt, M.W., Chang, P., 2015. Paleoceanography 30, 1425–1436. http://dx.doi.org/10.1002/2015PA002832 Expansion and diversification of high-latitude radiolarian assemblages in the late Eocene linked to a cooling event in the southwest Pacific Pascher, K.M., Hollis, C.J., Bohaty, S.M., Cortese, G., McKay, R.M., Seebeck, H., Suzuki, N., Chiba, K., 2015. Climate of the Past 11, 1599–1620. http://www.clim-past.net/11/1599/2015/ The biotic crisis across the Oceanic Anoxic Event 2: Palaeoenvironmental inferences based on foraminifera and geochemical proxies from the South Iberian Palaeomargin Reolid, M., Sánchez-Quiñónez, C.A., Alegret, L., Molina, E., 2016. Cretaceous Research 60, 1–27. http://www.sciencedirect.com/science/article/pii/S0195667115300902 Cretaceous oceanic anoxic events (OAEs) recorded in the northern margin of Africa as possible oil and gas shale potential in Tunisia: An overview Soua, M., 2016. International Geology Review 58, 277–320. http://dx.doi.org/10.1080/00206814.2015.1065516 Carbon isotope ratios suggest no additional methane from boreal wetlands during the rapid Greenland Interstadial 21.2 Sperlich, P., Schaefer, H., Mikaloff Fletcher, S.E., Guillevic, M., Lassey, K., Sapart, C.J., Röckmann, T., Blunier, T., 2015. Global Biogeochemical Cycles 29, 1962–1976. http://dx.doi.org/10.1002/2014GB005007 New conodont d18O records of Silurian climate change: Implications for environmental and biological events Trotter, J.A., Williams, I.S., Barnes, C.R., Männik, P., Simpson, A., 2016. Palaeogeography, Palaeoclimatology, Palaeoecology 443, 34–48. http://www.sciencedirect.com/science/article/pii/S0031018215006677 Carbon isotope analyses reveal relatively high abundance of C4 grasses during early–middle Miocene in southwestern Europe Urban, M.A., Nelson, D.M., Jiménez-Moreno, G., Hu, F.S., 2016. Palaeogeography, Palaeoclimatology, Palaeoecology 443, 10–17. http://www.sciencedirect.com/science/article/pii/S0031018215006689 Deep circulation changes in the South Atlantic since the Last Glacial Maximum from Nd isotope and multi-proxy records Wei, R., Abouchami, W., Zahn, R., Masque, P., 2016. Earth and Planetary Science Letters 434, 18–29. http://www.sciencedirect.com/science/article/pii/S0012821X15006913
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Warming-induced northwestward migration of the East Asian monsoon rain belt from the Last Glacial Maximum to the mid-Holocene Yang, S., Ding, Z., Li, Y., Wang, X., Jiang, W., Huang, X., 2015. Proceedings of the National Academy of Sciences 112, 13178–13183. http://www.pnas.org/content/early/2015/10/06/1504688112.abstract Calcareous nannofossils and paleoenvironments of the Paleocene–Eocene thermal maximum (PETM) interval in central Egypt Youssef, M., 2016. Journal of African Earth Sciences 114, 203–219. http://www.sciencedirect.com/science/article/pii/S1464343X15301151 A new paleoclimate classification for deep time Zhang, L., Wang, C., Li, X., Cao, K., Song, Y., Hu, B., Lu, D., Wang, Q., Du, X., Cao, S., 2016. Palaeogeography, Palaeoclimatology, Palaeoecology 443, 98–106. http://www.sciencedirect.com/science/article/pii/S0031018215007117 Excluding the di-unsaturated alkenone in the UK 37 index strengthens temperature correlation for the common lacustrine and brackishwater haptophytes Zheng, Y., Huang, Y., Andersen, R.A., Amaral-Zettler, L.A., 2016. Geochimica et Cosmochimica Acta 175, 36–46. http://www.sciencedirect.com/science/article/pii/S0016703715006638 Paleoecology of Extinction Events
Incomplete Bayesian model rejects contradictory radiocarbon data for being contradictory Boslough, M., Nicoll, K., Daulton, T.L., Scott, A.C., Claeys, P., Gill, J.L., Marlon, J.R., Bartlein, P.J., 2015. Proceedings of the National Academy of Sciences 112, E6722. http://www.pnas.org/content/112/49/E6722.short Geochemical characterization of the Permian–Triassic transition at outcrop, central Saudi Arabia Eltom, H.A., Abdullatif, O.M., Babalola, L.O., Bashari, M.A., Yassin, M., Osman, M.S., Abdulraziq, A.M., 2016. Journal of Petroleum Geology 39, 95–113. http://dx.doi.org/10.1111/jpg.12630 Problematic dating of claimed Younger Dryas boundary impact proxies Holliday, V.T., 2015. Proceedings of the National Academy of Sciences 112, E6721. http://www.pnas.org/content/112/49/E6721.short Rarity in mass extinctions and the future of ecosystems Hull, P.M., Darroch, S.A.F., Erwin, D.H., 2015. Nature 528, 345–351. http://dx.doi.org/10.1038/nature16160 Reply to Holliday and Boslough et al.: Synchroneity of widespread Bayesian-modeled ages supports Younger Dryas impact hypothesis Kennett, J.P., Kennett, D.J., Culleton, B.J., Aura Tortosa, J.E., Bunch, T.E., Erlandson, J.M., Johnson, J.R., Jordá Pardo, J.F., LeCompte, M.A., Mahaney, W.C., Tankersley, K.B., Wittke, J.H., Wolbach, W.S., West, A., 2015. Proceedings of the National Academy of Sciences 112, E6723–E6724. http://www.pnas.org/content/112/49/E6723.short Gourds and squashes (Cucurbita spp.) adapted to megafaunal extinction and ecological anachronism through domestication Kistler, L., Newsom, L.A., Ryan, T.M., Clarke, A.C., Smith, B.D., Perry, G.H., 2015. Proceedings of the National Academy of Sciences 112, 15107–15112. http://www.pnas.org/content/112/49/15107.abstract Phylogenetic clustering of origination and extinction across the Late Ordovician mass extinction Krug, A.Z., Patzkowsky, M.E., 2015. PLoS ONE 10, Article number e0144354. http://dx.doi.org/10.1371%2Fjournal.pone.0144354 Madagascar’s climate at the K/P boundary and its impact on the island’s biotic suite Ohba, M., Samonds, K.E., LaFleur, M., Ali, J.R., Godfrey, L.R., 2016. Palaeogeography, Palaeoclimatology, Palaeoecology 441, Part 4, 688–695. http://www.sciencedirect.com/science/article/pii/S0031018215005908 Physils and organic matter-base palaeoenvironmental records of the K/Pg boundary transition from the late Cretaceous-early Palaeogene succession of the Um-Sohryngkew River section of Meghalaya, India Pal, S., Shrivastava, J.P., Mukhopadhyay, S.K., 2015. Chemie der Erde – Geochemistry 75, 445–463. http://www.sciencedirect.com/science/article/pii/S000928191530009X
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Microbialites in the shallow-water marine environments of the Holy Cross Mountains (Poland) in the aftermath of the Frasnian–Famennian biotic crisis Rakocin´ski, M., Racki, G., 2016. Global and Planetary Change 136, 30–40. http://www.sciencedirect.com/science/article/pii/S0921818115301387 Late Ordovician glaciation initiated by early land plant evolution and punctuated by greenhouse mass extinctions Retallack, G.J., 2015. The Journal of Geology 123, 509–538. http://www.jstor.org/stable/10.1086/683663 Sedimentary PGE signatures in the Late Triassic ejecta deposits from Japan: Implications for the identification of impactor Sato, H., Shirai, N., Ebihara, M., Onoue, T., Kiyokawa, S., 2016. Palaeogeography, Palaeoclimatology, Palaeoecology 442, 36–47. http://www.sciencedirect.com/science/article/pii/S0031018215006719 Selective environmental stress from sulphur emitted by continental flood basalt eruptions Schmidt, A., Skeffington, R.A., Thordarson, T., Self, S., Forster, P.M., Rap, A., Ridgwell, A., Fowler, D., Wilson, M., Mann, G.W., Wignall, P.B., Carslaw, K.S., 2016. Nature Geoscience 9, 77–82. http://dx.doi.org/10.1038/ngeo2588 Petroleum Geochemistry
Formation of magnetic minerals at hydrocarbon-generation conditions Abubakar, R., Muxworthy, A.R., Sephton, M.A., Southern, P., Watson, J.S., Fraser, A.J., Almeida, T.P., 2015. Marine and Petroleum Geology 68, Part A, 509–519. http://www.sciencedirect.com/science/article/pii/S0264817215301045 Geochemical investigation, oil–oil and oil–source rock correlation in the Dezful Embayment, Marun oilfield, Zagros, Iran Asadi Mehmandosti, E., Adabi, M.H., Bowden, S.A., Alizadeh, B., 2015. Marine and Petroleum Geology 68, Part A, 648–663. http://www.sciencedirect.com/science/article/pii/S0264817215000422 Synthesis of heavy hydrocarbons at the core-mantle boundary Belonoshko, A.B., Lukinov, T., Rosengren, A., Bryk, T., Litasov, K.D., 2015. Scientific Reports 5, Article number: 18382. http://dx.doi.org/10.1038/srep18382 Changes in concentration and distribution of biomarkers in biodegraded oils from Dongying Depression, China Chen, Z., Wang, T.G., Yan, D., 2015. Applied Biochemistry and Biotechnology 177, 713–731. http://dx.doi.org/10.1007/s12010-015-1775-z Integration of biodegradation and migration of hydrocarbons in a 2D petroleum systems model: Application to the Potiguar Basin, NE Brazil Ducros, M., Carpentier, B., Wolf, S., Cacas, M.C., 2016. Journal of Petroleum Geology 39, 61–78. http://dx.doi.org/10.1111/jpg.12628 Dibenzothiophenes and benzo[b]naphthothiophenes: Molecular markers for tracing oil filling pathways in the carbonate reservoir of the Tarim Basin, NW China Fang, R., Wang, T.G., Li, M., Xiao, Z., Zhang, B., Huang, S., Shi, S., Wang, D., Deng, W., 2016. Organic Geochemistry 91, 68–80. http://www.sciencedirect.com/science/article/pii/S0146638015002004 Three-dimensional hydrocarbon migration and accumulation modeling based on finite volume method Guo, Q., Chen, N., Xie, H., Wu, X., Liu, J., Zhao, X., Gao, R., Hu, J., 2015. Petroleum Exploration and Development 42, 893–903. http://www.sciencedirect.com/science/article/pii/S1876380415300884 Characteristics and origin of tuff-type tight oil in Jimusaer sag, Junggar Basin, NW China Jiang, Y., Liu, Y., Yang, Z., Nan, Y., Wang, R., Zhou, P., Yang, Y., Kou, J., Zhou, N., 2015. Petroleum Exploration and Development 42, 810–818. http://www.sciencedirect.com/science/article/pii/S187638041530077X Marine oil source of the Yingmaili oilfield in the Tarim Basin Li, S., Pang, X., Zhang, B., Sun, H., Sun, A., 2015. Marine and Petroleum Geology 68, Part A, 18–39. http://www.sciencedirect.com/science/article/pii/S0264817215300374
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Petroleum source, maturity, alteration and mixing in the southwestern Barents Sea: New insights from geochemical and isotope data Murillo, W.A., Vieth-Hillebrand, A., Horsfield, B., Wilkes, H., 2016. Marine and Petroleum Geology 70, 119–143. http://www.sciencedirect.com/science/article/pii/S0264817215301331 Temporal changes of fault seal and early charge of the Maui Gas-condensate field, Taranaki Basin, New Zealand Reilly, C., Nicol, A., Walsh, J.J., Kroeger, K.F., 2016. Marine and Petroleum Geology 70, 237–250. http://www.sciencedirect.com/science/article/pii/S0264817215301410 The organic geochemistry of asphaltenes and occluded biomarkers Snowdon, L.R., Volkman, J.K., Zhang, Z., Tao, G., Liu, P., 2016. Organic Geochemistry 91, 3–15. http://www.sciencedirect.com/science/article/pii/S0146638015002016 Geochemistry and origin of heavy oil in Lower Cretaceous of Chagan Depression Wang, P., Liu, G.D., Cao, Z., Su, H., Niu, Z.C., Zhang, J.Y., Luo, W.B., 2015. Acta Sedimentologica Sinica 33, 1265–1274. http://www.cjxb.ac.cn/EN/abstract/abstract3609.shtml The genesis and prospecting significance of high-sulfur gas condensates in the deep dolomite reservoirs beneath gypsum rocks: A case study of the Cambrian reservoir in Tarim Basin Xiao, Z., Su, J., Yang, H., Wang, Y., Huang, S., Huang, L., Zhang, B., Weng, N., Lu, Y., Zhang, K., 2015. Petroleum Science and Technology 33, 1643–1652. http://dx.doi.org/10.1080/10916466.2015.1079537 Formation of low permeability reservoirs and gas accumulation process in the Daniudi Gas Field, northeast Ordos Basin, China Yang, Z., He, S., Guo, X., Li, Q., Chen, Z., Zhao, Y., 2016. Marine and Petroleum Geology 70, 222–236. http://www.sciencedirect.com/science/article/pii/S0264817215301227 Unmixing of mixed oil using chemometrics Zhan, Z.-W., Zou, Y.-R., Shi, J.-T., Sun, J.-N., Peng, P.a., 2016. Organic Geochemistry 92, 1–15. http://www.sciencedirect.com/science/article/pii/S0146638015002028 Genetic origin of sour gas condensates in the Paleozoic dolomite reservoirs of the Tazhong Uplift, Tarim Basin Zhang, S., Su, J., Huang, H., He, K., Wang, Y., Wang, H., Zhang, B., Wang, X., Hu, J., 2015. Marine and Petroleum Geology 68, Part A, 107–119. http://www.sciencedirect.com/science/article/pii/S0264817215300684 Re-exploration program for petroleum-rich sags and its significance in Bohai Bay Basin, East China Zhao, X., Wang, Q., Jin, F., Luo, N., Fan, B., Li, X., Qin, F., Zhang, H., 2015. Petroleum Exploration and Development 42, 790–801. http://www.sciencedirect.com/science/article/pii/S1876380415300756 Precambrian Geochemistry
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Estimates of atmospheric O2 in the Paleoproterozoic from paleosols Kanzaki, Y., Murakami, T., 2016. Geochimica et Cosmochimica Acta 174, 263–290. http://www.sciencedirect.com/science/article/pii/S0016703715006572 Tracing Earth’s O2 evolution using Zn/Fe ratios in marine carbonates Liu, X.M., Kah, L.C., Knoll, A.H., Cui, H., Kaufman, A.J., Shahar, A., Hazen, R.M., 2016. Geochemical Perspectives Letters 2, 24–34. http://www.geochemicalperspectivesletters.org/article1603 Emerging biogeochemical views of Earth’s ancient microbial worlds Lyons, T.W., Fike, D.A., Zerkle, A., 2015. Elements 11, 415–421. http://elements.geoscienceworld.org/content/11/6/415.abstract Commentary ‘‘Is the Neoproterozoic oxygen burst a supercontinent legacy?” Nedelec, A., Borisova, A.Y., 2015. Frontiers in Earth Science 3, 80. doi: 10.3389/feart.2015.00080. http://journal.frontiersin.org/article/10.3389/feart.2015.00080/full Nanoscale petrographic and geochemical insights on the origin of the Palaeoproterozoic stromatolitic phosphorites from Aravalli Supergroup, India Papineau, D., De Gregorio, B., Fearn, S., Kilcoyne, D., McMahon, G., Purohit, R., Fogel, M., 2016. Geobiology 14, 3–32. http://dx.doi.org/10.1111/gbi.12164 Selenium isotope evidence for progressive oxidation of the Neoproterozoic biosphere Pogge von Strandmann, P.A.E., Stueken, E.E., Elliott, T., Poulton, S.W., Dehler, C.M., Canfield, D.E., Catling, D.C., 2015. Nature Communications 6, Article number 10157. http://dx.doi.org/10.1038/ncomms10157 Composition and genesis of the oldest (4.28 Ga) sediments on Earth Rosen, O.M., Abbyasov, A.A., Zlobin, V.L., 2015. Doklady Earth Sciences 465, 1117–1120. http://dx.doi.org/10.1134/S1028334X15110136 Free energy distribution and hydrothermal mineral precipitation in Hadean submarine alkaline vent systems: Importance of iron redox reactions under anoxic conditions Shibuya, T., Russell, M.J., Takai, K., 2016. Geochimica et Cosmochimica Acta 175, 1–19. http://www.sciencedirect.com/science/article/pii/S0016703715006560 A mineralogical, chemical and isotopic investigation of shales from the Barberton Greenstone Belt, South Africa, to constrain source materials and post-deposition evolution Toulkeridis, T., Clauer, N., Kröner, A., Todt, W., 2015. South African Journal of Geology 118, 389–410. http://sajg.geoscienceworld.org/content/118/4/389.abstract Recognition of a novel Precambrian petroleum system based on isotopic and biomarker evidence in Yangtze platform, south China Wang, G., Wang, T.G., Han, K., Wang, L., Shi, S., 2015. Marine and Petroleum Geology 68, Part A, 414–426. http://www.sciencedirect.com/science/article/pii/S026481721530091X Spurious thermoluminescence characteristics of the Ediacaran Doushantuo Formation (ca. 635–551 Ma) and its implications for marine dissolved organic carbon reservoir Wang, H., Li, C., Hu, C., Xie, S., 2015. Journal of Earth Science 26, 883–892. http://dx.doi.org/10.1007/s12583-015-0650-3 Timescales of oxygenation following the evolution of oxygenic photosynthesis Ward, L.M., Kirschvink, J.L., Fischer, W.W., 2016. Origins of Life and Evolution of Biospheres 46, 51–65. http://dx.doi.org/10.1007/s11084-015-9460-3 Features and origin of natural gas in the Sinian–Cambrian of central Sichuan paleo-uplift, Sichuan Basin, SW China Wei, G., Xie, Z., Song, J., Yang, W., Wang, Z., Li, J., Wang, D., Li, Z., Xie, W., 2015. Petroleum Exploration and Development 42, 768–777. http://www.sciencedirect.com/science/article/pii/S1876380415300732
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Deriving the molecular composition of vacuum distillates by integrating statistical modeling and detailed hydrocarbon characterization Alvarez-Majmutov, A., Gieleciak, R., Chen, J., 2015. Energy & Fuels 29, 7931–7940. http://dx.doi.org/10.1021/acs.energyfuels.5b02082 Prediction of the gas injection effect on the asphaltene phase envelope Bahrami, P., Kharrat, R., Mahdavi, S., Firoozinia, H., 2015. Oil & Gas Science and Technology – Revue d’IFP Energies nouvelles 70, 1075–1086. http://dx.doi.org/10.2516/ogst/2014037 A comparative study of the chemical structure of asphaltenes from Algerian petroleum collected at different stages of extraction and processing Daaou, M., Larbi, A., Martínez-Haya, B., Rogalski, M., 2016. Journal of Petroleum Science and Engineering 138, 50–56. http://www.sciencedirect.com/science/article/pii/S0920410515302047 Structural study of asphaltenes from Iranian heavy crude oil Davarpanah, L., Vahabzadeh, F., Dermanaki, A., 2015. Oil & Gas Science and Technology – Revue d’IFP Energies nouvelles 70, 1035–1049. http://dx.doi.org/10.2516/ogst/2012066 Formation of resins in used oils as a result of conformation-structure change of their hydrocarbons Dmitrieva, Z.T., 2015. Chemistry and Technology of Fuels and Oils 51, 464–469. http://dx.doi.org/10.1007/s10553-015-0626-5 Towards the development of bitumen carbonates: An integrated analysis of Grosmont steam pilots Ezeuko, C.C., Wang, J., Kallos, M.S., Gates, I.D., 2015. Oil & Gas Science and Technology – Revue d’IFP Energies nouvelles 70, 983–1005. http://dx.doi.org/10.2516/ogst/2013111 Non-isothermal conversion of the Kashpir sulfur-rich oil shale in a supercritical water flow Fedyaeva, O.N., Antipenko, V.R., Dubov, D.Y., Kruglyakova, T.V., Vostrikov, A.A., 2016. The Journal of Supercritical Fluids 109, 157–165. http://www.sciencedirect.com/science/article/pii/S0896844615301935 Quantification of trace O-containing compounds in GTL process samples via Fischer–Tropsch reaction by comprehensive two-dimensional gas chromatography/mass spectrometry Fernandes, D.R., Pereira, V.B., Stelzer, K.T., Gomes, A.O., Aquino Neto, F.R., Azevedo, D.A., 2015. Talanta 144, 627–635. http://www.sciencedirect.com/science/article/pii/S003991401530062X Analysis and identification of oxygen compounds in Longkou shale oil and Shenmu coal tar Geng, C., Li, S., Ma, Y., Yue, C., He, J., Shang, W., 2015. Oil Shale 32, 322–333. http://www.kirj.ee/21477/?tpl=1061&c_tpl=1064 Estimation of the normal boiling point of organic compounds via a new group contribution method Ghasemitabar, H., Movagharnejad, K., 2016. Fluid Phase Equilibria 411, 13–23. http://www.sciencedirect.com/science/article/pii/S037838121530234X A study of crude oil fouling propensity Ho, T.C., 2016. International Journal of Heat and Mass Transfer 95, 62–68. http://www.sciencedirect.com/science/article/pii/S0017931015304853 Surface charge at the bitumen/water interface investigated by phase-sensitive sum frequency generation vibrational spectroscopy: Effects of pH, ions, and surfactants Hu, D., Chou, K.C., 2015. Energy & Fuels 29, 7885–7888. http://dx.doi.org/10.1021/acs.energyfuels.5b02011 Investigation of wax precipitation in crude oil: Experimental and modeling Jafari Behbahani, T., Beigi, A.A.M., Taheri, Z., Ghanbari, B., 2015. Petroleum 1, 223–230. http://www.sciencedirect.com/science/article/pii/S2405656115000371 Experimental study and mathematical modeling of asphaltene deposition mechanism in core samples Jafari Behbahani, T., Ghotbi, C., Taghikhani, V., Shahrabadi, A., 2015. Oil & Gas Science and Technology – Revue d’IFP Energies nouvelles 70, 1051–1074. http://dx.doi.org/10.2516/ogst/2013128
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Effect of the temperature on the characteristics of retorting products obtained by Yaojie oil shale pyrolysis Lan, X., Luo, W., Song, Y., Zhou, J., Zhang, Q., 2015. Energy & Fuels 29, 7800–7806. http://dx.doi.org/10.1021/acs.energyfuels.5b01645 Effect of transition metal polymers with varying side alkyl chain on viscosity reduction of crude oil and aggregation behavior of asphaltene Li, J.-j., Wang, X., Tang, X.-d., Wang, F., Qing, D.-y., 2015. Energy & Fuels 29, 7771–7780. http://dx.doi.org/10.1021/acs.energyfuels.5b01013 Role of ethyl cellulose in bitumen extraction from oil sands ores using an aqueous–nonaqueous hybrid process Lin, F., He, L., Hou, J., Masliyah, J., Xu, Z., 2015. Energy & Fuels. http://dx.doi.org/10.1021/acs.energyfuels.5b01960 Influence of pyrite on hydrocarbon generation during pyrolysis of type-III kerogen Ma, X., Zheng, J., Zheng, G., Xu, W., Qian, Y., Xia, Y., Wang, Z., Wang, X., Ye, X., 2016. Fuel 167, 329–336. http://www.sciencedirect.com/science/article/pii/S0016236115012193 Experimental study of water-based nanofluid alternating gas injection as a novel enhanced oil-recovery method in oil-wet carbonate reservoirs Moradi, B., Pourafshary, P., Jalali, F., Mohammadi, M., Emadi, M.A., 2015. Journal of Natural Gas Science and Engineering 27, Part 1, 64–73. http://www.sciencedirect.com/science/article/pii/S1875510015300342 Conversion of acidic heavy resid to surfactant for separating water-oil emulsions and increasing oil production Movsum-zade, E.M., Nikitina, A.A., Belyaeva, A.S., Kunakova, R.V., 2015. Chemistry and Technology of Fuels and Oils 51, 493–500. http://dx.doi.org/10.1007/s10553-015-0630-9 Asphaltenes explained for the nonchemist Mullins, O.C., Pomerantz, A.E., Andrews, A.B., Zuo, J.Y., 2015. Petrophysics 56, 266–275. https://www.onepetro.org/download/journal-paper/SPWLA-2015-v56n3a3?id=journal-paper%2FSPWLA-2015-v56n3a3 Application of magnetic treatment to changing the composition and physicochemical properties of crude oil and petroleum products Musina, N.S., Maryutina, T.A., 2016. Journal of Analytical Chemistry 71, 27–34. http://dx.doi.org/10.1134/S1061934816010081 Molecular analysis of microbial community structures in Nigerian oil production and processing facilities in order to access souring corrosion and methanogenesis Okoro, C., Ekun, O.A., Nwume, M.I., Lin, J., 2016. Corrosion Science 103, 242–254. http://www.sciencedirect.com/science/article/pii/S0010938X15301669 An investigation into the electrical behavior of oil/water/reservoir rock interfaces: The implication for improvement in wettability prediction Sadeqi-Moqadam, M., Riahi, S., Bahramian, A., 2016. Colloids and Surfaces A: Physicochemical and Engineering Aspects 490, 268–282. http://www.sciencedirect.com/science/article/pii/S0927775715303642 Investigation of oil recovery and CO2 storage during secondary and tertiary injection of carbonated water in an Iranian carbonate oil reservoir Shakiba, M., Ayatollahi, S., Riazi, M., 2016. Journal of Petroleum Science and Engineering 137, 134–143. http://www.sciencedirect.com/science/article/pii/S0920410515301923 Potential to increase condensate oil production by huff-n-puff gas injection in a shale condensate reservoir Sheng, J.J., Mody, F., Griffith, P.J., Barnes, W.N., 2016. Journal of Natural Gas Science and Engineering 28, 46–51. http://www.sciencedirect.com/science/article/pii/S1875510015302717 Pyrolysis of Yaojie oil shale in a Sanjiang-type pilot-scale retort Shi, Y., Li, S., Ma, Y., Yue, C., Shang, W., Hu, H., He, J., 2015. Oil Shale 32, 368–375. http://www.kirj.ee/21446/?tpl=1061&c_tpl=1064 Oil/water nanoemulsions: Activity at the water–oil interface and evaluation on asphaltene aggregates Souza, V.B., Mansur, C.R.E., 2015. Energy & Fuels 29, 7855–7865. http://dx.doi.org/10.1021/acs.energyfuels.5b01996
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Investigation of relationships between petroleum properties and their impact on crude oil compatibility Stratiev, D., Shishkova, I., Nedelchev, A., Kirilov, K., Nikolaychuk, E., Ivanov, A., Sharafutdinov, I., Veli, A., Mitkova, M., Tsaneva, T., Petkova, N., Sharpe, R., Yordanov, D., Belchev, Z., Nenov, S., Rudnev, N., Atanassova, V., Sotirova, E., Sotirov, S., Atanassov, K., 2015. Energy & Fuels 29, 7836–7854. http://dx.doi.org/10.1021/acs.energyfuels.5b01822 Control of microbial sulfide production with biocides and nitrate in oil reservoir simulating bioreactors Xue, Y., Voordouw, G., 2015. Frontiers in Microbiology 6, 1387. doi: 10.3389/fmicb.2015.01387. http://journal.frontiersin.org/article/10.3389/fmicb.2015.01387/abstract A micro-CT study of changes in the internal structure of Daqing and Yan’an oil shales at high temperatures Zhao, J., Yang, D., Kang, Z., Feng, Z., 2015. Oil Shale 32, 357–367. http://www.kirj.ee/21456/?tpl=1061&c_tpl=1064 Structural characteristics of asphaltenes derived from condensation of maltenes in supercritical water Zhu, D.-Q., Liu, Q.-K., Tan, X.-C., Yang, J.-Y., Yuan, P.-Q., Cheng, Z.-M., Yuan, W.-K., 2015. Energy & Fuels 29, 7807–7815. http://dx.doi.org/10.1021/acs.energyfuels.5b01664 The numerical simulation of thermal recovery based on hydraulic fracture heating technology in shale gas reservoir Zhu, G.-p., Yao, J., Sun, H., Zhang, M., Xie, M.-j., Sun, Z.-x., Lu, T., 2016. Journal of Natural Gas Science and Engineering 28, 305–316. http://www.sciencedirect.com/science/article/pii/S1875510015302912 High-pressure microscopic investigation on the oil recovery mechanism by in situ biogases in petroleum reservoirs Zhu, W.Y., Zhao, J.X., Han, H.Y., Sun, G.Z., Song, Z.Y., 2015. Energy & Fuels 29, 7866–7874. http://dx.doi.org/10.1021/acs.energyfuels.5b01906 Recent Sediments/Hydrosphere
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Geochemistry Articles / Organic Geochemistry 92 (2016) e34–e76
Soil Geochemistry
Ecological interpretations of nitrogen isotope ratios of terrestrial plants and soils Craine, J.M., Brookshire, E.N.J., Cramer, M.D., Hasselquist, N., Koba, K., Marin-Spiotta, E., Wang, L., 2015. Plant and Soil 396, 1–26. http://dx.doi.org/10.1007/s11104-015-2542-1 Direct incorporation of fatty acids into microbial phospholipids in soils: Position-specific labeling tells the story Dippold, M.A., Kuzyakov, Y., 2016. Geochimica et Cosmochimica Acta 174, 211–221. http://www.sciencedirect.com/science/article/pii/S0016703715006547 European scale analysis of phospholipid fatty acid composition of soils to establish operating ranges Francisco, R., Stone, D., Creamer, R.E., Sousa, J.P., Morais, P.V., 2016. Applied Soil Ecology 97, 49–60. http://www.sciencedirect.com/science/article/pii/S0929139315300809 Pathways of anaerobic organic matter decomposition in tundra soils from Barrow, Alaska Herndon, E.M., Mann, B.F., Roy Chowdhury, T., Yang, Z., Wullschleger, S.D., Graham, D., Liang, L., Gu, B., 2015. Journal of Geophysical Research: Biogeosciences 120, 2345–2359. http://dx.doi.org/10.1002/2015JG003147 Geochemical drivers of organic matter decomposition in arctic tundra soils Herndon, E.M., Yang, Z., Bargar, J., Janot, N., Regier, T.Z., Graham, D.E., Wullschleger, S.D., Gu, B., Liang, L., 2015. Biogeochemistry 126, 397–414. http://dx.doi.org/10.1007/s10533-015-0165-5 The contentious nature of soil organic matter Lehmann, J., Kleber, M., 2015. Nature 528, 60–68. http://www.nature.com/nature/journal/v528/n7580/full/nature16069.html Black carbon aerosol dynamics and isotopic composition in Alaska linked with boreal fire emissions and depth of burn in organic soils Mouteva, G.O., Czimczik, C.I., Fahrni, S.M., Wiggins, E.B., Rogers, B.M., Veraverbeke, S., Xu, X., Santos, G.M., Henderson, J., Miller, C.E., Randerson, J.T., 2015. Global Biogeochemical Cycles 29, 1977–2000. http://dx.doi.org/10.1002/2015GB005247 Autotrophic fixation of geogenic CO2 by microorganisms contributes to soil organic matter formation and alters isotope signatures in a wetland mofette Nowak, M.E., Beulig, F., von Fischer, J., Muhr, J., Küsel, K., Trumbore, S.E., 2015. Biogeosciences 12, 7169–7183. http://www.biogeosciences.net/12/7169/2015/ Lipid, sterol and saccharide sources and dynamics in surface soils during an annual cycle in a temperate climate region Rushdi, A.I., Oros, D.R., Al-Mutlaq, K.F., He, D., Medeiros, P.M., Simoneit, B.R.T., 2016. Applied Geochemistry 66, 1–13. http://www.sciencedirect.com/science/article/pii/S0883292715300731 Sample storage-induced changes in the quantity and quality of soil labile organic carbon Sun, S.-Q., Cai, H.-Y., Chang, S.X., Bhatti, J.S., 2015. Scientific Reports 5, Article number 17496. http://dx.doi.org/10.1038/srep17496 Expanded compilations of references with abstracts in Microsoft Word and ISI EndNote formats are available at: http://eaog.org/?cat=16 Compiled by Clifford C. Walters