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Volume 14, issue 22
Biogeosciences, 14, 5253–5269, 2017
https://doi.org/10.5194/bg-14-5253-2017
© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/bg-14-5253-2017
© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.
Biogeosciences, 14, 5253–5269, 2017
https://doi.org/10.5194/bg-14-5253-2017
© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/bg-14-5253-2017
© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.
Research article 24 Nov 2017
Research article | 24 Nov 2017
Coral calcifying fluid aragonite saturation states derived from Raman spectroscopy
Thomas M. DeCarlo et al.Related authors
Thomas M. DeCarlo, Michael Holcomb, and Malcolm T. McCulloch
Biogeosciences, 15, 2819–2834, https://doi.org/10.5194/bg-15-2819-2018, https://doi.org/10.5194/bg-15-2819-2018, 2018
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Understanding the mechanisms of coral calcification is limited by the isolation of the calcifying environment. The boron systematics (B / Ca and δ11B) of aragonite have recently been developed as a proxy for the carbonate chemistry of the calcifying fluid, but a variety of approaches have been utilized. We assess the available experimental B / Ca partitioning data and present a computer code for deriving calcifying fluid carbonate chemistry from the boron systematics of coral skeletons.
Jens Zinke, Juan P. D'Olivo, Christoph J. Gey, Malcolm T. McCulloch, J. Henrich Bruggemann, Janice M. Lough, and Mireille M. M. Guillaume
Biogeosciences, 16, 695–712, https://doi.org/10.5194/bg-16-695-2019, https://doi.org/10.5194/bg-16-695-2019, 2019
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Here we report seasonally resolved sea surface temperature (SST) reconstructions for the southern Mozambique Channel in the SW Indian Ocean, a region located along the thermohaline ocean surface circulation route, based on multi-trace-element temperature proxy records preserved in two Porites sp. coral cores for the past 42 years. Particularly, we show the suitability of both separate and combined Sr / Ca and Li / Mg proxies for improved multielement SST reconstructions.
Julie A. Trotter, Charitha Pattiaratchi, Paolo Montagna, Marco Taviani, James Falter, Ron Thresher, Andrew Hosie, David Haig, Federica Foglini, Quan Hua, and Malcolm T. McCulloch
Biogeosciences Discuss., https://doi.org/10.5194/bg-2018-319, https://doi.org/10.5194/bg-2018-319, 2018
Manuscript not accepted for further review
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The first ROV exploration of the Perth Canyon offshore southwest Australia discovered diverse
hot spotsof deep-sea biota to depths of ~ 2000 m. Some corals were living below the carbonate saturation horizon. Extensive coral graveyards found at ~ 700 and ~ 1700 m are between ~ 18 000 and ~ 30 000 years old, indicating these corals flourished during the last ice age. Anthropogenic carbon detected within the upper ~ 800 m highlights the increasing threat of climate change to deep-sea ecosystems.
Thomas M. DeCarlo, Michael Holcomb, and Malcolm T. McCulloch
Biogeosciences, 15, 2819–2834, https://doi.org/10.5194/bg-15-2819-2018, https://doi.org/10.5194/bg-15-2819-2018, 2018
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Understanding the mechanisms of coral calcification is limited by the isolation of the calcifying environment. The boron systematics (B / Ca and δ11B) of aragonite have recently been developed as a proxy for the carbonate chemistry of the calcifying fluid, but a variety of approaches have been utilized. We assess the available experimental B / Ca partitioning data and present a computer code for deriving calcifying fluid carbonate chemistry from the boron systematics of coral skeletons.
J. P. D'Olivo, M. T. McCulloch, S. M. Eggins, and J. Trotter
Biogeosciences, 12, 1223–1236, https://doi.org/10.5194/bg-12-1223-2015, https://doi.org/10.5194/bg-12-1223-2015, 2015
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The boron isotope composition in the skeleton of massive Porites corals from the central Great Barrier Reef is used to reconstruct the seawater pH over the 1940-2009 period. The long-term decline in the coral-reconstructed seawater pH is in close agreement with estimates based on the CO2 uptake by surface waters due to rising atmospheric levels. We also observed a significant relationship between terrestrial runoff data and the inshore coral boron isotopes records.
Related subject area
Biogeochemistry: Biomineralization
Subaqueous speleothems (Hells Bells) formed by the interplay of pelagic redoxcline biogeochemistry and specific hydraulic conditions in the El Zapote sinkhole, Yucatán Peninsula, Mexico
Kinetics of calcite precipitation by ureolytic bacteria under aerobic and anaerobic conditions
Coupled calcium and inorganic carbon uptake suggested by magnesium and sulfur incorporation in foraminiferal calcite
Planktonic foraminiferal spine versus shell carbonate Na incorporation in relation to salinity
Precipitation of calcium carbonate mineral induced by viral lysis of cyanobacteria: evidence from laboratory experiments
Mineral formation induced by cable bacteria performing long-distance electron transport in marine sediments
Variation in brachiopod microstructure and isotope geochemistry under low-pH–ocean acidification conditions
Weaving of biomineralization framework in rotaliid foraminifera: implications for paleoceanographic proxies
Architecture, Growth Dynamics and Biomineralization of Pulsed Sr-Labelled Katelysia rhytiphora (Mollusca, Bivalvia)
Marine and freshwater micropearls: biomineralization producing strontium-rich amorphous calcium carbonate inclusions is widespread in the genus Tetraselmis (Chlorophyta)
Carbon and nitrogen turnover in the Arctic deep sea: in situ benthic community response to diatom and coccolithophorid phytodetritus
Technical note: A refinement of coccolith separation methods: measuring the sinking characteristics of coccoliths
Improving the strength of sandy soils via ureolytic CaCO3 solidification by Sporosarcina ureae
Impact of salinity on element incorporation in two benthic foraminiferal species with contrasting magnesium contents
Calcification in a marginal sea – influence of seawater [Ca2+] and carbonate chemistry on bivalve shell formation
Effect of temperature rise and ocean acidification on growth of calcifying tubeworm shells (Spirorbis spirorbis): an in situ benthocosm approach
Phosphorus limitation and heat stress decrease calcification in Emiliania huxleyi
Anatomical structure overrides temperature controls on magnesium uptake – calcification in the Arctic/subarctic coralline algae Leptophytum laeve and Kvaleya epilaeve (Rhodophyta; Corallinales)
Impact of trace metal concentrations on coccolithophore growth and morphology: laboratory simulations of Cretaceous stress
Ba incorporation in benthic foraminifera
Size-dependent response of foraminiferal calcification to seawater carbonate chemistry
Technical note: an economical apparatus for the observation and harvest of mineral precipitation experiments with light microscopy
Physiology regulates the relationship between coccosphere geometry and growth phase in coccolithophores
Trends in element incorporation in hyaline and porcelaneous foraminifera as a function of pCO2
Decoupled carbonate chemistry controls on the incorporation of boron into Orbulina universa
Mineralogical response of the Mediterranean crustose coralline alga Lithophyllum cabiochae to near-future ocean acidification and warming
Temperature affects the morphology and calcification of Emiliania huxleyi strains
Skeletal mineralogy of coral recruits under high temperature and pCO2
Direct uptake of organically derived carbon by grass roots and allocation in leaves and phytoliths: 13C labeling evidence
pH up-regulation as a potential mechanism for the cold-water coral Lophelia pertusa to sustain growth in aragonite undersaturated conditions
Iron encrustations on filamentous algae colonized by Gallionella-related bacteria in a metal-polluted freshwater stream
Ocean acidification does not affect magnesium composition or dolomite formation in living crustose coralline algae, Porolithon onkodes in an experimental system
Reconsidering the role of carbonate ion concentration in calcification by marine organisms
Impact of seawater carbonate chemistry on the calcification of marine bivalves
Impact of seawater [Ca2+] on the calcification and calciteMg / Ca of Amphistegina lessonii
Evaluation of coral reef carbonate production models at a global scale
New highlights of phytolith structure and occluded carbon location: 3-D X-ray microscopy and NanoSIMS results
Limpets counteract ocean acidification induced shell corrosion by thickening of aragonitic shell layers
Identifying vital effects in Halimeda algae with Ca isotopes
Experimental evidence for foraminiferal calcification under anoxia
Fluctuations of sulfate, S-bearing amino acids and magnesium in a giant clam shell
Unravelling the enigmatic origin of calcitic nanofibres in soils and caves: purely physicochemical or biogenic processes?
Polar coralline algal CaCO3-production rates correspond to intensity and duration of the solar radiation
Downward fluxes of sinking particulate matter in the deep Ionian Sea (NESTOR site), eastern Mediterranean: seasonal and interannual variability
A new model for biomineralization and trace-element signatures of Foraminifera tests
Calcification intensity in planktonic Foraminifera reflects ambient conditions irrespective of environmental stress
Effect of ocean acidification on the benthic foraminifera Ammonia sp. is caused by a decrease in carbonate ion concentration
The role of microorganisms in the formation of a stalactite in Botovskaya Cave, Siberia – paleoenvironmental implications
Cyanobacterial calcification in modern microbialites at the submicrometer scale
Growth increment periodicity in the shell of the razor clam Ensis directus using stable isotopes as a method to validate age
Simon Michael Ritter, Margot Isenbeck-Schröter, Christian Scholz, Frank Keppler, Johannes Gescher, Lukas Klose, Nils Schorndorf, Jerónimo Avilés Olguín, Arturo González-González, and Wolfgang Stinnesbeck
Biogeosciences, 16, 2285–2305, https://doi.org/10.5194/bg-16-2285-2019, https://doi.org/10.5194/bg-16-2285-2019, 2019
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Unique and spectacular under water speleothems termed as Hells Bells were recently reported from sinkholes (cenotes) of the Yucatán Peninsula, Mexico. However, the mystery of their formation remained unresolved. Here, we present detailed geochemical analyses and delineate that the growth of Hells Bells results from a combination of biogeochemical processes and variable hydraulic conditions within the cenote.
Andrew C. Mitchell, Erika J. Espinosa-Ortiz, Stacy L. Parks, Adrienne J. Phillips, Alfred B. Cunningham, and Robin Gerlach
Biogeosciences, 16, 2147–2161, https://doi.org/10.5194/bg-16-2147-2019, https://doi.org/10.5194/bg-16-2147-2019, 2019
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Microbially induced carbonate mineral precipitation (MICP) is a natural process that is also being investigated for subsurface engineering applications including radionuclide immobilization and microfracture plugging. We demonstrate that rates of MICP from microbial urea hydrolysis (ureolysis) vary with different bacterial strains, but rates are similar in both oxygenated and oxygen-free conditions. Ureolysis MICP is therefore a viable biotechnology in the predominately oxygen-free subsurface.
Inge van Dijk, Christine Barras, Lennart Jan de Nooijer, Aurélia Mouret, Esmee Geerken, Shai Oron, and Gert-Jan Reichart
Biogeosciences, 16, 2115–2130, https://doi.org/10.5194/bg-16-2115-2019, https://doi.org/10.5194/bg-16-2115-2019, 2019
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Systematics in the incorporation of different elements in shells of marine organisms can be used to test calcification models and thus processes involved in precipitation of calcium carbonates. On different scales, we observe a covariation of sulfur and magnesium incorporation in shells of foraminifera, which provides insights into the mechanics behind shell formation. The observed patterns imply that all species of foraminifera actively take up calcium and carbon in a coupled process.
Eveline M. Mezger, Lennart J. de Nooijer, Jacqueline Bertlich, Jelle Bijma, Dirk Nürnberg, and Gert-Jan Reichart
Biogeosciences, 16, 1147–1165, https://doi.org/10.5194/bg-16-1147-2019, https://doi.org/10.5194/bg-16-1147-2019, 2019
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Seawater salinity is an important factor when trying to reconstruct past ocean conditions. Foraminifera, small organisms living in the sea, produce shells that incorporate more Na at higher salinities. The accuracy of reconstructions depends on the fundamental understanding involved in the incorporation and preservation of the original Na of the shell. In this study, we unravel the Na composition of different components of the shell and describe the relative contribution of these components.
Hengchao Xu, Xiaotong Peng, Shijie Bai, Kaiwen Ta, Shouye Yang, Shuangquan Liu, Ho Bin Jang, and Zixiao Guo
Biogeosciences, 16, 949–960, https://doi.org/10.5194/bg-16-949-2019, https://doi.org/10.5194/bg-16-949-2019, 2019
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Viruses have been acknowledged as important components of the marine system for the past 2 decades, but understanding of their role in the functioning of the geochemical cycle remains poor. Results show viral lysis of cyanobacteria can influence the carbonate equilibrium system remarkably and promotes the formation and precipitation of carbonate minerals. Amorphous calcium carbonate (ACC) and aragonite are evident in the lysate, implying that different precipitation processes have occurred.
Nicole M. J. Geerlings, Eva-Maria Zetsche, Silvia Hidalgo-Martinez, Jack J. Middelburg, and Filip J. R. Meysman
Biogeosciences, 16, 811–829, https://doi.org/10.5194/bg-16-811-2019, https://doi.org/10.5194/bg-16-811-2019, 2019
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Multicellular cable bacteria form long filaments that can reach lengths of several centimeters. They affect the chemistry and mineralogy of their surroundings and vice versa. How the surroundings affect the cable bacteria is investigated. They show three different types of biomineral formation: (1) a polymer containing phosphorus in their cells, (2) a sheath of clay surrounding the surface of the filament and (3) the encrustation of a filament via a solid phase containing iron and phosphorus.
Facheng Ye, Hana Jurikova, Lucia Angiolini, Uwe Brand, Gaia Crippa, Daniela Henkel, Jürgen Laudien, Claas Hiebenthal, and Danijela Šmajgl
Biogeosciences, 16, 617–642, https://doi.org/10.5194/bg-16-617-2019, https://doi.org/10.5194/bg-16-617-2019, 2019
Yukiko Nagai, Katsuyuki Uematsu, Chong Chen, Ryoji Wani, Jarosław Tyszka, and Takashi Toyofuku
Biogeosciences, 15, 6773–6789, https://doi.org/10.5194/bg-15-6773-2018, https://doi.org/10.5194/bg-15-6773-2018, 2018
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We interpret detailed SEM and time-lapse observations of the calcification process in living foraminifera, which we reveal to be directly linked to the construction mechanism of organic membranes where the calcium carbonate precipitation takes place. We show that these membranes are a highly perforated outline is first woven by skeletal pseudopodia and then later overlaid by a layer of membranous pseudopodia to close the gaps. The chemical composition is related to these structures.
Laura M. Otter, Oluwatoosin B. A. Agbaje, Matt R. Kilburn, Christoph Lenz, Hadrien Henry, Patrick Trimby, Peter Hoppe, and Dorrit E. Jacob
Biogeosciences Discuss., https://doi.org/10.5194/bg-2018-469, https://doi.org/10.5194/bg-2018-469, 2018
Revised manuscript accepted for BG
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This study uses a trace elemental marker and high resolution nano-analytical techniques to label the growth fronts of bivalves in controlled aquaculture conditions. The growing shells incorporate the labels and are used as
snapshotsvisualizing the growth processes across different shell microstructures and architectures.
Agathe Martignier, Montserrat Filella, Kilian Pollok, Michael Melkonian, Michael Bensimon, François Barja, Falko Langenhorst, Jean-Michel Jaquet, and Daniel Ariztegui
Biogeosciences, 15, 6591–6605, https://doi.org/10.5194/bg-15-6591-2018, https://doi.org/10.5194/bg-15-6591-2018, 2018
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The unicellular microalga Tetraselmis cordiformis (Chlorophyta) was recently discovered to form intracellular mineral inclusions, called micropearls, which had been previously overlooked. The present study shows that 10 Tetraselmis species out of the 12 tested share this biomineralization capacity, producing amorphous calcium carbonate inclusions often enriched in Sr. This novel biomineralization process can take place in marine, brackish or freshwater and is therefore a widespread phenomenon.
Ulrike Braeckman, Felix Janssen, Gaute Lavik, Marcus Elvert, Hannah Marchant, Caroline Buckner, Christina Bienhold, and Frank Wenzhöfer
Biogeosciences, 15, 6537–6557, https://doi.org/10.5194/bg-15-6537-2018, https://doi.org/10.5194/bg-15-6537-2018, 2018
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Global warming has altered Arctic phytoplankton communities, with unknown effects on deep-sea communities that depend strongly on food produced at the surface. We compared the responses of Arctic deep-sea benthos to input of phytodetritus from diatoms and coccolithophorids. Coccolithophorid carbon was 5× less recycled than diatom carbon. The utilization of the coccolithophorid carbon may be less efficient, so a shift from diatom to coccolithophorid blooms could entail a delay in carbon cycling.
Hongrui Zhang, Heather Stoll, Clara Bolton, Xiaobo Jin, and Chuanlian Liu
Biogeosciences, 15, 4759–4775, https://doi.org/10.5194/bg-15-4759-2018, https://doi.org/10.5194/bg-15-4759-2018, 2018
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The sinking speeds of coccoliths are relevant for laboratory methods to separate coccoliths for geochemical analysis. However, in the absence of estimates of coccolith settling velocity, previous implementations have depended mainly on time-consuming method development by trial and error. In this study, the sinking velocities of cocooliths were carefully measured for the first time. We also provide an estimation of coccolith sinking velocity by shape, which will make coccolith separation easier.
Justin Michael Whitaker, Sai Vanapalli, and Danielle Fortin
Biogeosciences, 15, 4367–4380, https://doi.org/10.5194/bg-15-4367-2018, https://doi.org/10.5194/bg-15-4367-2018, 2018
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Materials, like soils or cements, can require repair. This study used a new bacterium (Sporosarcina ureae) in a repair method called "microbially induced carbonate precipitation" (MICP). In three trials, benefits were shown: S. ureae could make a model sandy soil much stronger by MICP, in fact better than a lot of other bacteria. However, MICP-treated samples got weaker in three trials of acid rain. In conclusion, S. ureae in MICP repair shows promise when used in appropriate climates.
Esmee Geerken, Lennart Jan de Nooijer, Inge van Dijk, and Gert-Jan Reichart
Biogeosciences, 15, 2205–2218, https://doi.org/10.5194/bg-15-2205-2018, https://doi.org/10.5194/bg-15-2205-2018, 2018
Jörn Thomsen, Kirti Ramesh, Trystan Sanders, Markus Bleich, and Frank Melzner
Biogeosciences, 15, 1469–1482, https://doi.org/10.5194/bg-15-1469-2018, https://doi.org/10.5194/bg-15-1469-2018, 2018
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The distribution of mussel in estuaries is limited but the mechanisms are not well understood. We document for the first time that reduced Ca2+ concentration in the low saline, brackish Baltic Sea affects the ability of mussel larvae to calcify the first larval shell. As complete formation of the shell is a prerequisite for successful development, impaired calcification during this sensitive life stage can have detrimental effects on the species' ability to colonize habitats.
Sha Ni, Isabelle Taubner, Florian Böhm, Vera Winde, and Michael E. Böttcher
Biogeosciences, 15, 1425–1445, https://doi.org/10.5194/bg-15-1425-2018, https://doi.org/10.5194/bg-15-1425-2018, 2018
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Spirorbis tube worms are common epibionts on brown algae in the Baltic Sea. We made experiments with Spirorbis in the
Kiel Outdoor Benthocosmsat CO2 and temperature conditions predicted for the year 2100. The worms were able to grow tubes even at CO2 levels favouring shell dissolution but did not survive at mean temperatures over 24° C. This indicates that Spirorbis worms will suffer from future excessive ocean warming and from ocean acidification fostering corrosion of their protective tubes.
Andrea C. Gerecht, Luka Šupraha, Gerald Langer, and Jorijntje Henderiks
Biogeosciences, 15, 833–845, https://doi.org/10.5194/bg-15-833-2018, https://doi.org/10.5194/bg-15-833-2018, 2018
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Calcifying phytoplankton play an import role in long-term CO2 removal from the atmosphere. We therefore studied the ability of a representative species to continue sequestrating CO2 under future climate conditions. We show that CO2 sequestration is negatively affected by both an increase in temperature and the resulting decrease in nutrient availability. This will impact the biogeochemical cycle of carbon and may have a positive feedback on rising CO2 levels.
Merinda C. Nash and Walter Adey
Biogeosciences, 15, 781–795, https://doi.org/10.5194/bg-15-781-2018, https://doi.org/10.5194/bg-15-781-2018, 2018
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Past seawater temperatures can be reconstructed using magnesium / calcium ratios of biogenic carbonates. As temperature increases, so does magnesium. Here we show that for these Arctic/subarctic coralline algae, anatomy is the first control on Mg / Ca, not temperature. When using coralline algae for temperature reconstruction, it is first necessary to check for anatomical influences on Mg / Ca.
Giulia Faucher, Linn Hoffmann, Lennart T. Bach, Cinzia Bottini, Elisabetta Erba, and Ulf Riebesell
Biogeosciences, 14, 3603–3613, https://doi.org/10.5194/bg-14-3603-2017, https://doi.org/10.5194/bg-14-3603-2017, 2017
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The main goal of this study was to understand if, similarly to the fossil record, high quantities of toxic metals induce coccolith dwarfism in coccolithophore species. We investigated, for the first time, the effects of trace metals on coccolithophore species other than E. huxleyi and on coccolith morphology and size. Our data show a species-specific sensitivity to trace metal concentration, allowing the recognition of the most-, intermediate- and least-tolerant taxa to trace metal enrichments.
Lennart J. de Nooijer, Anieke Brombacher, Antje Mewes, Gerald Langer, Gernot Nehrke, Jelle Bijma, and Gert-Jan Reichart
Biogeosciences, 14, 3387–3400, https://doi.org/10.5194/bg-14-3387-2017, https://doi.org/10.5194/bg-14-3387-2017, 2017
Michael J. Henehan, David Evans, Madison Shankle, Janet E. Burke, Gavin L. Foster, Eleni Anagnostou, Thomas B. Chalk, Joseph A. Stewart, Claudia H. S. Alt, Joseph Durrant, and Pincelli M. Hull
Biogeosciences, 14, 3287–3308, https://doi.org/10.5194/bg-14-3287-2017, https://doi.org/10.5194/bg-14-3287-2017, 2017
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It is still unclear whether foraminifera (calcifying plankton that play an important role in cycling carbon) will have difficulty in making their shells in more acidic oceans, with different studies often reporting apparently conflicting results. We used live lab cultures, mathematical models, and fossil measurements to test this question, and found low pH does reduce calcification. However, we find this response is likely size-dependent, which may have obscured this response in other studies.
Chris H. Crosby and Jake V. Bailey
Biogeosciences, 14, 2151–2154, https://doi.org/10.5194/bg-14-2151-2017, https://doi.org/10.5194/bg-14-2151-2017, 2017
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In the course of experiments exploring the formation of calcium phosphate minerals in a polymeric matrix, we developed a small-scale, reusable, and low-cost setup that allows microscopic observation over time for use in mineral precipitation experiments that use organic polymers as a matrix. The setup uniquely accommodates changes in solution chemistry during the course of an experiment and facilitates easy harvesting of the precipitates for subsequent analysis.
Rosie M. Sheward, Alex J. Poulton, Samantha J. Gibbs, Chris J. Daniels, and Paul R. Bown
Biogeosciences, 14, 1493–1509, https://doi.org/10.5194/bg-14-1493-2017, https://doi.org/10.5194/bg-14-1493-2017, 2017
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Our culture experiments on modern Coccolithophores find that physiology regulates shifts in the geometry of their carbonate shells (coccospheres) between growth phases. This provides a tool to access growth information in modern and past populations. Directly comparing modern species with fossil coccospheres derives a new proxy for investigating the physiology that underpins phytoplankton responses to environmental change through geological time.
Inge van Dijk, Lennart J. de Nooijer, and Gert-Jan Reichart
Biogeosciences, 14, 497–510, https://doi.org/10.5194/bg-14-497-2017, https://doi.org/10.5194/bg-14-497-2017, 2017
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Culturing foraminifera under controlled pCO2 conditions shows that incorporation of certain elements (Zn, Ba) into foraminiferal shells is impacted by the inorganic carbonate system. Modeling the chemical speciation of these elements suggests that incorporation is determined by the availability of free ions. Furthermore, analyzing and comparing trends in element incorporation in hyaline and porcelaneous species may provide constrains on the differences between their calcification strategies.
Ella L. Howes, Karina Kaczmarek, Markus Raitzsch, Antje Mewes, Nienke Bijma, Ingo Horn, Sambuddha Misra, Jean-Pierre Gattuso, and Jelle Bijma
Biogeosciences, 14, 415–430, https://doi.org/10.5194/bg-14-415-2017, https://doi.org/10.5194/bg-14-415-2017, 2017
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To calculate the seawater carbonate system, proxies for 2 out of 7 parameters are required. The boron isotopic composition of foraminifera shells can be used as a proxy for pH and it has been suggested that B / Ca ratios may act as a proxy for carbonate ion concentration. However, differentiating between the effects of pH and [CO32−] is problematic, as they co-vary in natural systems. To deconvolve the effects, we conducted culture experiments with the planktonic foraminifer Orbulina universa.
Merinda C. Nash, Sophie Martin, and Jean-Pierre Gattuso
Biogeosciences, 13, 5937–5945, https://doi.org/10.5194/bg-13-5937-2016, https://doi.org/10.5194/bg-13-5937-2016, 2016
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We carried out a 1-year experiment on coralline algae to test how higher CO2 and temperature might change the mineral composition of the algal skeleton. We expected there to be a decline in magnesium with CO2 and an increase with temperature. We found that CO2 did not change the mineral composition, but higher temperature increased the amount of magnesium.
Anaid Rosas-Navarro, Gerald Langer, and Patrizia Ziveri
Biogeosciences, 13, 2913–2926, https://doi.org/10.5194/bg-13-2913-2016, https://doi.org/10.5194/bg-13-2913-2016, 2016
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The global warming debate has sparked an unprecedented interest in temperature effects on coccolithophores. We show that sub-optimal growth temperatures lead to an increase in malformed coccoliths in a strain-specific fashion and the inorganic / organic carbon has a minimum at optimum growth temperature. Global warming might cause a decline in coccoliths' inorganic carbon contribution to the "rain ratio", as well as improved fitness in some genotypes by reducing coccolith malformation.
T. Foster and P. L. Clode
Biogeosciences, 13, 1717–1722, https://doi.org/10.5194/bg-13-1717-2016, https://doi.org/10.5194/bg-13-1717-2016, 2016
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In recent years much research has focussed on whether corals will be able to build their skeletons under predicted ocean acidification. One strategy corals may employ is changing the mineralogy of their skeletons from aragonite to the less soluble polymorph of calcium carbonate; calcite. Here we show that newly settled coral recruits are unable to produce calcite in their skeletons under near-future elevations in pCO2, which may leave them more vulnerable to ocean acidification.
Anne Alexandre, Jérôme Balesdent, Patrick Cazevieille, Claire Chevassus-Rosset, Patrick Signoret, Jean-Charles Mazur, Araks Harutyunyan, Emmanuel Doelsch, Isabelle Basile-Doelsch, Hélène Miche, and Guaciara M. Santos
Biogeosciences, 13, 1693–1703, https://doi.org/10.5194/bg-13-1693-2016, https://doi.org/10.5194/bg-13-1693-2016, 2016
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This 13C labeling experiment demonstrates that carbon can be absorbed by the roots, translocated in the plant, and ultimately fixed in organic compounds subject to occlusion in silica particles that form inside plant cells (phytoliths). Plausible forms of carbon absorbed, translocated, and fixed in phytoliths are assessed. Implications for our understanding of the C cycle at the plant-soil-atmosphere interface are discussed.
M. Wall, F. Ragazzola, L. C. Foster, A. Form, and D. N. Schmidt
Biogeosciences, 12, 6869–6880, https://doi.org/10.5194/bg-12-6869-2015, https://doi.org/10.5194/bg-12-6869-2015, 2015
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We investigated the ability of cold-water corals to deal with changes in ocean pH. We uniquely combined morphological assessment with boron isotope analysis to determine if changes in growth are related to changes in control of calcification pH. We found that the cold-water coral Lophelia pertusa can maintain the skeletal morphology, growth patterns as well as internal calcification pH. This has important implications for their future occurrence and explains their cosmopolitan distribution.
J. F. Mori, T. R. Neu, S. Lu, M. Händel, K. U. Totsche, and K. Küsel
Biogeosciences, 12, 5277–5289, https://doi.org/10.5194/bg-12-5277-2015, https://doi.org/10.5194/bg-12-5277-2015, 2015
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We studied filamentous macroscopic algae growing in metal-rich stream water that leaked from a former uranium-mining district. These algae were encrusted with Fe-deposits that were associated with microbes, mainly Gallionella-related Fe-oxidizing bacteria, and extracellular polymeric substances. Algae with a lower number of chloroplasts often exhibited discontinuous series of precipitates, likely due to the intercalary growth of algae which allowed them to avoid detrimental encrustation.
M. C. Nash, S. Uthicke, A. P. Negri, and N. E. Cantin
Biogeosciences, 12, 5247–5260, https://doi.org/10.5194/bg-12-5247-2015, https://doi.org/10.5194/bg-12-5247-2015, 2015
L. T. Bach
Biogeosciences, 12, 4939–4951, https://doi.org/10.5194/bg-12-4939-2015, https://doi.org/10.5194/bg-12-4939-2015, 2015
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Calcification by marine organisms reacts to changing seawater carbonate chemistry, but it is unclear which components of the carbonate system drive the observed response. This study uncovers proportionalities between different carbonate chemistry parameters. These enable us to understand why calcification often correlates well with carbonate ion concentration, and they imply that net CaCO3 formation in high latitudes is not more vulnerable to ocean acidification than formation in low latitudes.
J. Thomsen, K. Haynert, K. M. Wegner, and F. Melzner
Biogeosciences, 12, 4209–4220, https://doi.org/10.5194/bg-12-4209-2015, https://doi.org/10.5194/bg-12-4209-2015, 2015
A. Mewes, G. Langer, S. Thoms, G. Nehrke, G.-J. Reichart, L. J. de Nooijer, and J. Bijma
Biogeosciences, 12, 2153–2162, https://doi.org/10.5194/bg-12-2153-2015, https://doi.org/10.5194/bg-12-2153-2015, 2015
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A culture study with the benthic foraminifer Amphistegina lessonii was conducted at varying seawater [Ca2+] and constant [Mg2+]. Results showed optimum growth rates and test thickness at ambient seawater Mg/Ca and a calcite Mg/Ca which is controlled by the relative seawater ratio. Results support the conceptual biomineralization model by Nehrke et al. (2013); however, our refined flux-based model suggests transmembrane transport fractionation that is slightly weaker than expected.
N. S. Jones, A. Ridgwell, and E. J. Hendy
Biogeosciences, 12, 1339–1356, https://doi.org/10.5194/bg-12-1339-2015, https://doi.org/10.5194/bg-12-1339-2015, 2015
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Production of calcium carbonate by coral reefs is important in the global carbon cycle. Using a global framework we evaluate four models of reef calcification against observed values. The temperature-only model showed significant skill in reproducing coral calcification rates. The absence of any predictive power for whole reef systems highlights the importance of coral cover and the need for an ecosystem modelling approach accounting for population dynamics in terms of mortality and recruitment.
A. Alexandre, I. Basile-Doelsch, T. Delhaye, D. Borshneck, J. C. Mazur, P. Reyerson, and G. M. Santos
Biogeosciences, 12, 863–873, https://doi.org/10.5194/bg-12-863-2015, https://doi.org/10.5194/bg-12-863-2015, 2015
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Phytoliths contain occluded organic compounds called phytC. The nature and location of phytC in biogenic silica structures is poorly understood. Here, we reconstructed the 3-D structure of phytoliths using 3-D Xray microscopy. We further evidenced a pool of phytC, continuously distributed in the silica structure, using nanoscale secondary ion mass spectrometry (NanoSIMS). Our findings allowed the re-evaluation of previous suggestions regarding phytC quantification and environmental meaning.
G. Langer, G. Nehrke, C. Baggini, R. Rodolfo-Metalpa, J. M. Hall-Spencer, and J. Bijma
Biogeosciences, 11, 7363–7368, https://doi.org/10.5194/bg-11-7363-2014, https://doi.org/10.5194/bg-11-7363-2014, 2014
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Specimens of the patellogastropod limpet Patella caerulea were collected within and outside a CO2 vent site at Ischia, Italy. The distribution of different crystal structures across shell sections was analysed. Patella caerulea counteracts shell dissolution in corrosive waters by enhanced production of aragonitic parts of the shell. We conclude that it is not possible to predict the dissolution behaviour of a composite biomineral on the basis of the properties of its constituent mineral.
C. L. Blättler, S. M. Stanley, G. M. Henderson, and H. C. Jenkyns
Biogeosciences, 11, 7207–7217, https://doi.org/10.5194/bg-11-7207-2014, https://doi.org/10.5194/bg-11-7207-2014, 2014
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Halimeda algae were used as a test organism to untangle some of the specific factors that influence skeletal composition, in particular Ca-isotope composition. Algae were stimulated to precipitate both calcite and aragonite by growth in artificial Cretaceous seawater. Comparison of the skeletal Ca-isotope ratios with inorganic carbonate forms indicates the effects of mineralogy and Rayleigh distillation of Ca on the geochemistry of their carbonate skeletons.
M. P. Nardelli, C. Barras, E. Metzger, A. Mouret, H. L. Filipsson, F. Jorissen, and E. Geslin
Biogeosciences, 11, 4029–4038, https://doi.org/10.5194/bg-11-4029-2014, https://doi.org/10.5194/bg-11-4029-2014, 2014
T. Yoshimura, Y. Tamenori, H. Kawahata, and A. Suzuki
Biogeosciences, 11, 3881–3886, https://doi.org/10.5194/bg-11-3881-2014, https://doi.org/10.5194/bg-11-3881-2014, 2014
S. Bindschedler, G. Cailleau, O. Braissant, L. Millière, D. Job, and E. P. Verrecchia
Biogeosciences, 11, 2809–2825, https://doi.org/10.5194/bg-11-2809-2014, https://doi.org/10.5194/bg-11-2809-2014, 2014
S. Teichert and A. Freiwald
Biogeosciences, 11, 833–842, https://doi.org/10.5194/bg-11-833-2014, https://doi.org/10.5194/bg-11-833-2014, 2014
S. Stavrakakis, A. Gogou, E. Krasakopoulou, A. P. Karageorgis, H. Kontoyiannis, G. Rousakis, D. Velaoras, L. Perivoliotis, G. Kambouri, I. Stavrakaki, and V. Lykousis
Biogeosciences, 10, 7235–7254, https://doi.org/10.5194/bg-10-7235-2013, https://doi.org/10.5194/bg-10-7235-2013, 2013
G. Nehrke, N. Keul, G. Langer, L. J. de Nooijer, J. Bijma, and A. Meibom
Biogeosciences, 10, 6759–6767, https://doi.org/10.5194/bg-10-6759-2013, https://doi.org/10.5194/bg-10-6759-2013, 2013
M. F. G. Weinkauf, T. Moller, M. C. Koch, and M. Kučera
Biogeosciences, 10, 6639–6655, https://doi.org/10.5194/bg-10-6639-2013, https://doi.org/10.5194/bg-10-6639-2013, 2013
N. Keul, G. Langer, L. J. de Nooijer, and J. Bijma
Biogeosciences, 10, 6185–6198, https://doi.org/10.5194/bg-10-6185-2013, https://doi.org/10.5194/bg-10-6185-2013, 2013
M. Pacton, S. F. M. Breitenbach, F. A. Lechleitner, A. Vaks, C. Rollion-Bard, O. S. Gutareva, A. V. Osintcev, and C. Vasconcelos
Biogeosciences, 10, 6115–6130, https://doi.org/10.5194/bg-10-6115-2013, https://doi.org/10.5194/bg-10-6115-2013, 2013
E. Couradeau, K. Benzerara, E. Gérard, I. Estève, D. Moreira, R. Tavera, and P. López-García
Biogeosciences, 10, 5255–5266, https://doi.org/10.5194/bg-10-5255-2013, https://doi.org/10.5194/bg-10-5255-2013, 2013
J. F. M. F. Cardoso, G. Nieuwland, R. Witbaard, H. W. van der Veer, and J. P. Machado
Biogeosciences, 10, 4741–4750, https://doi.org/10.5194/bg-10-4741-2013, https://doi.org/10.5194/bg-10-4741-2013, 2013
Cited articles
Addadi, L., Raz, S., and Weiner, S.: Taking advantage of disorder: amorphous calcium carbonate and its roles in biomineralization, Adv. Mater., 15, 959–970, 2003.
Al-Horani, F. A., Al-Moghrabi, S. M., and De Beer, D.: The mechanism of calcification and its relation to photosynthesis and respiration in the scleractinian coral Galaxea fascicularis, Mar. Biol., 142, 419–426, https://doi.org/10.1007/s00227-002-0981-8, 2003.
AlKhatib, M. and Eisenhauer, A.: Calcium and Strontium Isotope Fractionation during Precipitation from Aqueous Solutions as a Function of Temperature and Reaction Rate; II. Aragonite, Geochim. Cosmochim. Ac., 209, 320–342, https://doi.org/10.1016/j.gca.2017.04.012, 2017.
Allison, N., Cohen, I., Finch, A. A., Erez, J., and Tudhope, A. W.: Corals concentrate dissolved inorganic carbon to facilitate calcification, Nature Commun., 5, 5741, https://doi.org/10.1038/ncomms6741, 2014.
Barkley, H. C., Cohen, A. L., Golbuu, Y., Starczak, V. R., DeCarlo, T. M., and Shamberger, K. E.: Changes in coral reef communities across a natural gradient in seawater pH, Sci. Adv., 1, e1500328, https://doi.org/10.1126/sciadv.1500328, 2015.
Barkley, H. C., Cohen, A. L., McCorkle, D. C., and Golbuu, Y.: Mechanisms and thresholds for pH tolerance in Palau corals, J. Exp. Mar. Biol. Ecol., 489, 7–14, https://doi.org/10.1016/j.jembe.2017.01.003, 2017.
Barnes, D. J.: Coral skeletons: an explanation of their growth and structure, Science, 170, 1305–1308, https://doi.org/10.1126/science.170.3964.1305, 1970.
Bischoff, W. D., Sharma, S. K., and MacKenzie, F. T.: Carbonate ion disorder in synthetic and biogenic magnesian calcites; a Raman spectral study, Am. Mineral., 70, 581–589, 1985.
Borromeo, L., Zimmermann, U., Andò, S., Coletti, G., Bersani, D., Basso, D., Gentile, P., Schulz, B., and Garzanti, E.: Raman spectroscopy as a tool for magnesium estimation in Mg-calcite, J. Raman Spectrosc., 48, 983–992, https://doi.org/10.1002/jrs.5156, 2017.
Brahmi, C., Meibom, A., Smith, D. C., Stolarski, J., Auzoux-Bordenave, S., Nouet, J., Doumenc, D., Djediat, C., and Domart-Coulon, I.: Skeletal growth, ultrastructure and composition of the azooxanthellate scleractinian coral Balanophyllia regia, Coral Reefs, 29, 175–189, 2010.
Burton, E. A. and Walter, L. M.: Relative precipitation rates of aragonite and Mg calcite from seawater: Temperature or carbonate ion control?, Geology, 15, 111–114, 1987.
Cai, W.-J., Ma, Y., Hopkinson, B. M., Grottoli, A. G., Warner, M. E., Ding, Q., Hu, X., Yuan, X., Schoepf, V., Xu, H., Han, C., Melman, T. F., Hoadley, K. D., Pettay, D. T., Matsui, Y., Baumann, J. H., Levas, S., Ying, Y., and Wang, Y.: Microelectrode characterization of coral daytime interior pH and carbonate chemistry, Nature Commun., 7, 11144, https://doi.org/10.1038/ncomms11144, 2016.
Caldeira, K. and Wickett, M. E.: Anthropogenic carbon and ocean pH, Nature, 425, 365, 2003.
Chan, N. C. S. and Connolly, S. R.: Sensitivity of coral calcification to ocean acidification: a meta-analysis, Glob. Change Biol., 19, 282–290, https://doi.org/10.1111/gcb.12011, 2013.
Chen, X., Deng, W., Zhu, H., Zhang, Z., Wei, G., and McCulloch, M. T.: Assessment of coral δ44∕40Ca as a paleoclimate proxy in the Great Barrier Reef of Australia, Chem. Geol., 435, 71–78, https://doi.org/10.1016/j.chemgeo.2016.04.024, 2016.
Clarke, H., D'Olivo, J. P., Falter, J., Zinke, J., Lowe, R., and McCulloch, M.: Differential response of corals to regional mass-warming events as evident from skeletal Sr/Ca and Mg/Ca ratios, Geochem. Geophy. Geosy., 18, 1794–1809, https://doi.org/10.1002/2016GC006788, 2017.
Clode, P. and Marshall, A.: Low temperature FESEM of the calcifying interface of a scleractinian coral, Tissue and Cell, 34, 187–198, https://doi.org/10.1016/S0040-8166(02)00031-9, 2002.
Clode, P. L., Lema, K., Saunders, M., and Weiner, S.: Skeletal mineralogy of newly settling Acropora millepora (Scleractinia) coral recruits, Coral Reefs, 30, 1–8, https://doi.org/10.1007/s00338-010-0673-7, 2011.
Cohen, A. L. and Holcomb, M.: Why corals care about ocean acidification: uncovering the mechanism, Oceanography, 22, 118–127, https://doi.org/10.5670/oceanog.2009.102, 2009.
Cohen, A. L. and McConnaughey, T. A.: Geochemical Perspectives on Coral Mineralization, Rev. Mineral. Geochem., 54, 151–187, https://doi.org/10.2113/0540151, 2003.
Comeau, S., Tambutté, E., Carpenter, R. C., Edmunds, P. J., Evensen, N. R., Allemand, D., Ferrier-Pagès, C., Tambutté, S., and Venn, A. A.: Coral calcifying fluid pH is modulated by seawater carbonate chemistry not solely seawater pH, Proceedings of the Royal Society of London B: Biological Sciences, 284, 2017.
Costanza, R., de Groot, R., Sutton, P., van der Ploeg, S., Anderson, S. J., Kubiszewski, I., Farber, S., and Turner, R. K.: Changes in the global value of ecosystem services, Glob. Environ. Chang., 26, 152–158, https://doi.org/10.1016/j.gloenvcha.2014.04.002, 2014.
Dandeu, A., Humbert, B., Carteret, C., Muhr, H., Plasari, E., and Bossoutrot, J. M.: Raman Spectroscopy – A Powerful Tool for the Quantitative Determination of the Composition of Polymorph Mixtures: Application to CaCO3 Polymorph Mixtures, Chem. Eng. Technol., 29, 221–225, https://doi.org/10.1002/ceat.200500354, 2006.
DeCarlo, T. M.: Data and code for “Coral calcifying fluid aragonite saturation states derived from Raman spectroscopy”, available at: https://doi.org/10.5281/zenodo.1035493 (last access: November 2017), 2017.
DeCarlo, T. M.: Code for “Coral calcifying fluid aragonite saturation states derived from Raman spectroscopy”, available at: https://doi.org/10.24433/CO.ff54fd98-a010-43f5-ad6a-c10c675387fc (last access: November 2017), 2017.
DeCarlo, T. M. and Cohen, A. L.: coralCT: software tool to analyze computerized tomography (CT) scans of coral skeletal cores for calcification and bioerosion rates, available at: https://doi.org/10.5281/zenodo.57855 (last access: November 2017), 2016.
DeCarlo, T. M., Gaetani, G. A., Holcomb, M., and Cohen, A. L.: Experimental determination of factors controlling U/Ca of aragonite precipitated from seawater: implications for interpreting coral skeleton, Geochim. Cosmochim. Ac., 162, 151–165, https://doi.org/10.1016/j.gca.2015.04.016, 2015.
Dickson, A. G.: Standard potential of the reaction: AgCl (s)+ 1/2H2 (g)= Ag (s)+ HCl (aq), and the standard acidity constant of the ion HSO4− in synthetic sea water from 273.15 to 318.15 K, J. Chem. Thermodynam., 22, 113–127, 1990.
D'Olivo, J. P. and McCulloch, M. T.: Response of coral calcification and calcifying fluid composition to thermally induced bleaching stress, Scientific Reports, 7, 2207, 2017.
Doney, S. C., Fabry, V. J., Feely, R. A., and Kleypas, J. A.: Ocean acidification: the other CO2 problem, Mar. Sci., 1, 169–192, https://doi.org/10.1146/annurev.marine.010908.163834, 2009.
Fabricius, K. E., Langdon, C., Uthicke, S., Humphrey, C., Noonan, S., De'ath, G., Okazaki, R., Muehllehner, N., Glas, M. S., and Lough, J. M.: Losers and winners in coral reefs acclimatized to elevated carbon dioxide concentrations, Nature Clim. Change, 1, 165–169, 2011.
Foster, G. L., Pogge von Strandmann, P. A. E., and Rae, J. W. B.: Boron and magnesium isotopic composition of seawater, Geochem. Geophy. Geosy. 11, Q08015, https://doi.org/10.1029/2010GC003201, 2010.
Foster, T. and Clode, P. L.: Skeletal mineralogy of coral recruits under high temperature and pCO2, Biogeosciences, 13, 1717–1722, https://doi.org/10.5194/bg-13-1717-2016, 2016.
Foster, T., Gilmour, J. P., Chua, C. M., Falter, J. L., and McCulloch, M. T.: Effect of ocean warming and acidification on the early life stages of subtropical Acropora spicifera, Coral Reefs, 34, 1217–1226, https://doi.org/10.1007/s00338-015-1342-7, 2015.
Foster, T., Falter, J. L., McCulloch, M. T., and Clode, P. L.: Ocean acidification causes structural deformities in juvenile coral skeletons, Science Advances, 2, e1501130, https://doi.org/10.1126/sciadv.1501130, 2016.
Gaetani, G. A. and Cohen, A. L.: Element partitioning during precipitation of aragonite from seawater: A framework for understanding paleoproxies, Geochim. Cosmochim. Ac., 70, 4617–4634, https://doi.org/10.1016/j.gca.2006.07.008, 2006.
Gaetani, G. A., Cohen, A. L., Wang, Z., and Crusius, J.: Rayleigh-Based, Multi-Element Coral Thermometry: a Biomineralization Approach to Developing Climate Proxies, Geochim. Cosmochim. Ac., 75, 1920–1932, https://doi.org/10.1016/j.gca.2011.01.010, 2011.
Gagnon, A. C., Adkins, J. F., and Erez, J.: Seawater transport during coral biomineralization, Earth Planet. Sc. Lett., 329, 150–161, 2012.
Gattuso, J.-P., Frankignoulle, M., Bourge, I., Romaine, S., and Buddemeier, R.: Effect of calcium carbonate saturation of seawater on coral calcification, Global Planet. Change, 18, 37–46, https://doi.org/10.1016/S0921-8181(98)00035-6, 1998.
Gattuso, J. P., Allemand, D., and Frankignoulle, M.: Photosynthesis and calcification at cellular, organismal and community levels in coral reefs: a review on interactions and control by carbonate chemistry, Am. Zool., 39, 160–183, https://doi.org/10.1093/icb/39.1.160, 1999.
Georgiou, L., Falter, J., Trotter, J., Kline, D. I., Holcomb, M., Dove, S. G., Hoegh-Guldberg, O., and McCulloch, M.: pH homeostasis during coral calcification in a free ocean CO2 enrichment (FOCE) experiment, Heron Island reef flat, Great Barrier Reef, P. Natl. Acad. Sci., 112, 13219–13224, https://doi.org/10.1073/pnas.1505586112, 2015.
Gothmann, A. M., Bender, M. L., Blättler, C. L., Swart, P. K., Giri, S. J., Adkins, J. F., Stolarski, J., and Higgins, J. A.: Calcium isotopes in scleractinian fossil corals since the Mesozoic: Implications for vital effects and biomineralization through time, Earth Planet. Sc. Lett., 444, 205–214, https://doi.org/10.1016/j.epsl.2016.03.012, 2016.
Gussone, N., Eisenhauer, A., Heuser, A., Dietzel, M., Bock, B., Böhm, F., Spero, H. J., Lea, D. W., Bijma, J., and Nägler, T. F.: Model for kinetic effects on calcium isotope fractionation (δ44Ca) in inorganic aragonite and cultured planktonic foraminifera, Geochim. Cosmochim. Ac., 67, 1375–1382, https://doi.org/10.1016/S0016-7037(02)01296-6, 2003.
Gussone, N., Böhm, F., Eisenhauer, A., Dietzel, M., Heuser, A., Teichert, B. M., Reitner, J., Wörheide, G., and Dullo, W.-C.: Calcium isotope fractionation in calcite and aragonite, Geochim. Cosmochim. Ac., 69, 4485–4494, https://doi.org/10.1016/j.gca.2005.06.003, 2005.
Hathorne, E. C., Gagnon, A., Felis, T., Adkins, J., Asami, R., Boer, W., Caillon, N., Case, D., Cobb, K. M., Douville, E., DeMenocal, P., Eisenhauer, A., Garbe-Schönberg, D., Geibert, W., Goldstein, S., Hughen, K., Inoue, M., Kawahata, H., Kölling, M., Cornec, F. L., Linsley, B. K., McGregor, H. V., Montagna, P., Nurhati, I. S., Quinn, T. M., Raddatz, J., Rebaubier, H., Robinson, L., Sadekov, A., Sherrell, R., Sinclair, D., Tudhope, A. W., Wei, G., Wong, H., Wu, H. C., and You, C.-F.: Interlaboratory study for coral Sr/Ca and other element/Ca ratio measurements, Geochem. Geophy. Geosy., 14, 3730–3750, https://doi.org/10.1002/ggge.20230, 2013.
Hennige, S. J., Morrison, C. L., Form, A. U., Büscher, J., Kamenos, N. A., and Roberts, J. M.: Self-recognition in corals facilitates deep-sea habitat engineering, Scientific Reports, 4, 6782, https://doi.org/10.1038/srep06782, 2014.
Hennige, S. J., Wicks, L. C., Kamenos, N. A., Perna, G., Findlay, H. S., and Roberts, J. M.: Hidden impacts of ocean acidification to live and dead coral framework., Proceedings Biological sciences / The Royal Society, 282, 20150 990, https://doi.org/10.1098/rspb.2015.0990, 2015.
Hippler, D., Schmitt, A.-D., Gussone, N., Heuser, A., Stille, P., Eisenhauer, A., and Nägler, T. F.: Calcium Isotopic Composition of Various Reference Materials and Seawater, Geostand. Geoanal. Res., 27, 13–19, https://doi.org/10.1111/j.1751-908X.2003.tb00709.x, 2003.
Hoegh-Guldberg, O., Mumby, P. J., Hooten, A. J., Steneck, R. S., Greenfield, P., Gomez, E., Harvell, C. D., Sale, P. F., Edwards, A. J., and Caldeira, K.: Coral reefs under rapid climate change and ocean acidification, Science, 318, 1737–1742, https://doi.org/10.1126/science.1152509, 2007.
Hoegh-Guldberg, O., Cai, R., Poloczanska, E., Brewer, P., Sundby, S., Helmi, K., Fabry, V., and Jung, S.: The Ocean, in: Climate Change 2014: Impacts, Adaptation, and Vulnerability. Contribution of Working Group 2 to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change, edited by Barros, V., Field, C., Dokken, D., Mastrandrea, M., Mach, K., Bilir, T., Chatterjee, M., Ebi, K., Estrada, Y., Genova, R., Girma, B., Kissel, E., Levy, A., MacCracken, S., Mastrandrea, P., and White, L., Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA, 2014.
Holcomb, M., Venn, A. A., Tambutté, E., Tambutté, S., Allemand, D., Trotter, J., and McCulloch, M.: Coral calcifying fluid pH dictates response to ocean acidification, Scientific Reports, 4, 2014.
Holcomb, M., DeCarlo, T., Gaetani, G., and McCulloch, M.: Factors affecting B/Ca ratios in synthetic aragonite, Chem. Geol., 437, 67–76, https://doi.org/10.1016/j.chemgeo.2016.05.007, 2016.
Hönisch, B., Ridgwell, A., Schmidt, D. N., Thomas, E., Gibbs, S. J., Sluijs, A., Zeebe, R., Kump, L., Martindale, R. C., and Greene, S. E.: The geological record of ocean acidification, Science, 335, 1058–1063, https://doi.org/10.1126/science.1208277, 2012.
Inoue, M., Gussone, N., Koga, Y., Iwase, A., Suzuki, A., Sakai, K., and Kawahata, H.: Controlling factors of Ca isotope fractionation in scleractinian corals evaluated by temperature, pH and light controlled culture experiments, Geochim. Cosmochim. Ac., 167, 80–92, https://doi.org/10.1016/j.gca.2015.06.009, 2015.
Kamenos, N. A., Burdett, H. L., Aloisio, E., Findlay, H. S., Martin, S., Longbone, C., Dunn, J., Widdicombe, S., and Calosi, P.: Coralline algal structure is more sensitive to rate, rather than the magnitude, of ocean acidification, Glob. Change Biol., 19, 3621–3628, 2013.
Kamenos, N. A., Perna, G., Gambi, M. C., Micheli, F., and Kroeker, K. J.: Coralline algae in a naturally acidified ecosystem persist by maintaining control of skeletal mineralogy and size, Proceedings of the Royal Society of London B: Biological Sciences, 283, 2016.
Kinsman, D. J. J. and Holland, H. D.: The co-precipitation of cations with CaCO3-IV. The co-precipitation of Sr2+ with aragonite between 16 and 96 C, Geochim. Cosmochim. Ac., 33, 1–17, https://doi.org/10.1016/0016-7037(69)90089-1, 1969.
Knowlton, N., Brainard, R. E., Fisher, R., Moews, M., Plaisance, L., and Caley, M.: Coral Reef Biodiversity, in: Life in the World's Oceans: Diversity, Distribution, and Abundance, 2010.
Kubota, K., Yokoyama, Y., Ishikawa, T., and Suzuki, A.: A new method for calibrating a boron isotope paleo-pH proxy using massive Porites corals, Geochem. Geophy. Geosy., 16, 3333–3342, https://doi.org/10.1002/2015GC005975, 2015.
Levitus, S.: NOAA Atlas NESDIS 68-71, US Government Printing Office, Washington, D.C., 2010.
Lin, F., Sum, A. K., and Bodnar, R. J.: Correlation of methane Raman ν1 band position with fluid density and interactions at the molecular level, J. Raman Spectrosc., 38, 1510–1515, https://doi.org/10.1002/jrs.1804, 2007.
Lough, J.: Coral calcification from skeletal records revisited, Mar. Ecol. Prog. Ser., 373, 257–264, https://doi.org/10.3354/meps07398, 2008.
McConnaughey, T.: 13C and 18O isotopic disequilibrium in biological carbonates: I. Patterns, Geochim. Cosmochim. Ac., 53, 151–162, https://doi.org/10.1016/0016-7037(89)90282-2, 1989.
McCulloch, M. T., Falter, J., Trotter, J., and Montagna, P.: Coral resilience to ocean acidification and global warming through pH up-regulation, Nature Climate Change, 2, 623–627, 2012.
McCulloch, M. T., Holcomb, M., Rankenburg, K., and Trotter, J. A.: Rapid, high-precision measurements of boron isotopic compositions in marine carbonates, Rap. Commun. Mass Spectrom., 28, 2704–2712, https://doi.org/10.1002/rcm.7065, 2014.
McCulloch, M. T., D'Olivo Cordero, J. P., Falter, J., Holcomb, M., and Trotter, J. A.: Coral calcification in a changing World: the interactive dynamics of pH and DIC up-regulation, Nature Commun., 8, 15686, https://doi.org/10.1038/ncomms15686, 2017.
McElderry, J.-D. P., Zhu, P., Mroue, K. H., Xu, J., Pavan, B., Fang, M., Zhao, G., McNerny, E., Kohn, D. H., Franceschi, R. T., Holl, M. M., Tecklenburg, M. M., Ramamoorthy, A., and Morris, M. D.: Crystallinity and compositional changes in carbonated apatites: Evidence from 31P solid-state NMR, Raman, and AFM analysis, J. Solid State Chem., 206, 192–198, https://doi.org/10.1016/j.jssc.2013.08.011, 2013.
Montagna, P., McCulloch, M., Douville, E., López Correa, M., Trotter, J., Rodolfo-Metalpa, R., Dissard, D., Ferrier-Pagès, C., Frank, N., Freiwald, A., Goldstein, S., Mazzoli, C., Reynaud, S., Rüggeberg, A., Russo, S., and Taviani, M.: Li/Mg systematics in scleractinian corals: Calibration of the thermometer, Geochim. Cosmochim. Ac., 132, 288–310, https://doi.org/10.1016/j.gca.2014.02.005, 2014.
Nasdala, L., Wenzel, M., Vavra, G., Irmer, G., Wenzel, T., and Kober, B.: Metamictisation of natural zircon: accumulation versus thermal annealing of radioactivity-induced damage, Contributions to Mineralogy and Petrology, 141, 125–144, https://doi.org/10.1007/s004100000235, 2001.
Nehrke, G., Reichart, G., Van Cappellen, P., Meile, C., and Bijma, J.: Dependence of calcite growth rate and Sr partitioning on solution stoichiometry: Non-Kossel crystal growth, Geochim. Cosmochim. Ac., 71, 2240–2249, https://doi.org/10.1016/J.GCA.2007.02.002, 2007.
Nehrke, G. and Nouet, J.: Confocal Raman microscope mapping as a tool to describe different mineral and organic phases at high spatial resolution within marine biogenic carbonates: case study on Nerita undata (Gastropoda, Neritopsina), Biogeosciences, 8, 3761–3769, https://doi.org/10.5194/bg-8-3761-2011, 2011.
Okai, T., Suzuki, A., Kawahata, H., Terashima, S., and Imai, N.: Preparation of a New Geological Survey of Japan Geochemical Reference Material: Coral JCp-1, Geostandards Newsletter, 26, 95–99, https://doi.org/10.1111/j.1751-908X.2002.tb00627.x, 2002.
Pandolfi, J. M., Connolly, S. R., Marshall, D. J., and Cohen, A. L.: Projecting coral reef futures under global warming and ocean acidification, Science, 333, 418–422, 2011.
Pauly, M., Kamenos, N. A., Donohue, P., and LeDrew, E.: Coralline algal Mg-O bond strength as a marine pCO2 proxy, Geology, 43, 267–270, https://doi.org/10.1130/G36386.1, 2015.
Perrin, J., Vielzeuf, D., Laporte, D., Ricolleau, A., Rossman, G. R., and Floquet, N.: Raman characterization of synthetic magnesian calcites, American Mineralogist, 101, 2525–2538, 2016.
Raybaud, V., Tambutté, S., Ferrier-Pagès, C., Reynaud, S., Venn, A. A., Tambutté, É., Nival, P., and Allemand, D.: Computing the carbonate chemistry of the coral calcifying medium and its response to ocean acidification, J. Theor. Biol., 424, 26–36, https://doi.org/10.1016/j.jtbi.2017.04.028, 2017.
R Core Team: R: A language and environment for statistical computing, 2016.
Ries, J. B.: A physicochemical framework for interpreting the biological calcification response to CO2-induced ocean acidification, Geochim. Cosmochim. Ac., 75, 4053–4064, 2011.
Riley, J. P. and Tongudai, M.: The major cation/chlorinity ratios in sea water, Chem. Geol., 2, 263–269, 1967.
Roger, L. M., George, A. D., Shaw, J., Hart, R. D., Roberts, M., Becker, T., McDonald, B. J., and Evans, N. J.: Geochemical and microstructural characterisation of two species of cool-water bivalves (Fulvia tenuicostata and Soletellina biradiata) from Western Australia, Biogeosciences, 14, 1721–1737, https://doi.org/10.5194/bg-14-1721-2017, 2017.
Shamberger, K. E., Cohen, A. L., Golbuu, Y., McCorkle, D. C., Lentz, S. J., and Barkley, H. C.: Diverse coral communities in naturally acidified waters of a Western Pacific reef, Geophys. Res. Lett., 41, 499–504, https://doi.org/10.1002/2013GL058489, 2014.
Smith, E. and Dent, G.: Modern Raman spectroscopy: a practical approach, John Wiley & Sons, West Sussex, England, 2005.
Stock, S. R., Veis, A., Xiao, X., Almer, J. D., and Dorvee, J. R.: Sea urchin tooth mineralization: Calcite present early in the aboral plumula, J. Struct. Biol., 180, 280–289, https://doi.org/10.1016/j.jsb.2012.08.004, 2012.
Stolarski, J., Bosellini, F. R., Wallace, C. C., Gothmann, A. M., Mazur, M., Domart-Coulon, I., Gutner-Hoch, E., Neuser, R. D., Levy, O., Shemesh, A., and Meibom, A.: A unique coral biomineralization pattern has resisted 40 million years of major ocean chemistry change., Scientific Reports, 6, 27579, https://doi.org/10.1038/srep27579, 2016.
Tambutté, E., Tambutté, S., Segonds, N., Zoccola, D., Venn, A., Erez, J., and Allemand, D.: Calcein labelling and electrophysiology: insights on coral tissue permeability and calcification, Proceedings of the Royal Society B: Biological Sciences, 279, 19–27, https://doi.org/10.1098/rspb.2011.0733, 2012.
Tambutté, E., Venn, A. A., Holcomb, M., Segonds, N., Techer, N., Zoccola, D., Allemand, D., and Tambutté, S.: Morphological plasticity of the coral skeleton under CO2-driven seawater acidification, Nature Communications, 6, 7368, https://doi.org/10.1038/ncomms8368, 2015.
Trotter, J., Montagna, P., McCulloch, M., Silenzi, S., Reynaud, S., Mortimer, G., Martin, S., Ferrier-Pagès, C., Gattuso, J. P., and Rodolfo-Metalpa, R.: Quantifying the pH 'vital effect' in the temperate zooxanthellate coral Cladocora caespitosa: Validation of the boron seawater pH proxy, Earth Planet. Sc. Lett., 303, 163–173, 2011.
Urmos, J., Sharma, S. K., and Mackenzie, F. T.: Characterization of some biogenic carbonates with Raman spectroscopy, American Mineralogist, 76, 641–646, 1991.
Váczi, T.: A New, Simple Approximation for the Deconvolution of Instrumental Broadening in Spectroscopic Band Profiles, Appl. Spectrosc., 68, 1274–1278, https://doi.org/10.1366/13-07275, 2014.
Venn, A., Tambutte, E., Holcomb, M., Allemand, D., and Tambutte, S.: Live tissue imaging shows reef corals elevate pH under their calcifying tissue relative to seawater, PLoS One, 6, e20013, https://doi.org/10.1371/journal.pone.0020013, 2011.
Wall, M. and Nehrke, G.: Reconstructing skeletal fiber arrangement and growth mode in the coral Porites lutea (Cnidaria, Scleractinia): a confocal Raman microscopy study, Biogeosciences, 9, 4885–4895, https://doi.org/10.5194/bg-9-4885-2012, 2012.
Wang, D., Hamm, L. M., Bodnar, R. J., and Dove, P. M.: Raman spectroscopic characterization of the magnesium content in amorphous calcium carbonates, J. Raman Spectrosc., 43, 543–548, 2012.
Watson, E. B.: A conceptual model for near-surface kinetic controls on the trace-element and stable isotope composition of abiogenic calcite crystals, Geochim. Cosmochim. Ac., 68, 1473–1488, 2004.
Wehrmeister, U., Soldati, A. L., Jacob, D. E., Häger, T., and Hofmeister, W.: Raman spectroscopy of synthetic, geological and biological vaterite: a Raman spectroscopic study, J. Raman Spectrosc., 41, 193–201, https://doi.org/10.1002/jrs.2438, 2009.
Weisstein, E.: Gaussian Function, available at: http://mathworld.wolfram.com/GaussianFunction.html (last access: November 2017), 2017.
White, W.: The carbonate minerals, in: The Infra-red Spectra of minerals, edited by: Farmer, V., 227–284, Mineralogical Society, London, 1974.
Wu, H. C., Dissard, D., Le Cornec, F., Thil, F., Tribollet, A., Moya, A., and Douville, E.: Primary Life Stage Boron Isotope and Trace Elements Incorporation in Aposymbiotic Acropora millepora Coral under Ocean Acidification and Warming, Front. Mar. Sci., 4, 129, https://doi.org/10.3389/fmars.2017.00129, 2017.
Zakaria, F. Z., Mihály, J., Sajó, I., Katona, R., Hajba, L., Aziz, F. A., and Mink, J.: FT-Raman and FTIR spectroscopic characterization of biogenic carbonates from Philippine venus seashell and Porites sp. coral, J. Raman Spectrosc., 39, 1204–1209, https://doi.org/10.1002/jrs.1964, 2008.
Zeebe, R. E., Ridgwell, A., and Zachos, J. C.: Anthropogenic carbon release rate unprecedented during the past 66 million years, Nature Geoscience, 9, 325–329, https://doi.org/10.1038/ngeo2681, 2016.
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We present a new technique to quantify the chemical conditions under which corals build their skeletons by analysing them with lasers at a very fine resolution, down to 1/100th the width of a human hair. Our first applications to laboratory-cultured and wild corals demonstrates the complex interplay among seawater conditions (temperature and acidity), calcifying fluid chemistry, and bulk skeleton accretion, which will define the sensitivity of coral calcification to 21st century climate change.
We present a new technique to quantify the chemical conditions under which corals build their...
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