Articles | Volume 7, issue 8
https://doi.org/10.5194/bg-7-2509-2010
© Author(s) 2010. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/bg-7-2509-2010
© Author(s) 2010. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Feedbacks and responses of coral calcification on the Bermuda reef system to seasonal changes in biological processes and ocean acidification
N. R. Bates
Bermuda Institute of Ocean Sciences, Ferry Reach, Bermuda
A. Amat
Bermuda Institute of Ocean Sciences, Ferry Reach, Bermuda
A. J. Andersson
Bermuda Institute of Ocean Sciences, Ferry Reach, Bermuda
Related subject area
Biogeochemistry: Biomineralization
The calcitic test growth rate of Spirillina vivipara (Foraminifera)
Impact of seawater sulfate concentration on sulfur concentration and isotopic composition in calcite of two cultured benthic foraminifera
Marked recent declines in boron in Baltic Sea cod otoliths – a bellwether of incipient acidification in a vast hypoxic system?
Ocean acidification enhances primary productivity and nocturnal carbonate dissolution in intertidal rock pools
Biomineralization of amorphous Fe-, Mn- and Si-rich mineral phases by cyanobacteria under oxic and alkaline conditions
Biogenic calcium carbonate as evidence for life
Element ∕ Ca ratios in Nodosariida (Foraminifera) and their potential application for paleoenvironmental reconstructions
Deciphering the origin of dubiofossils from the Pennsylvanian of the Paraná Basin, Brazil
Properties of exopolymeric substances (EPSs) produced during cyanobacterial growth: potential role in whiting events
Inorganic component in oak waterlogged archaeological wood and volcanic lake compartments
Ultradian rhythms in shell composition of photosymbiotic and non-photosymbiotic mollusks
Extracellular enzyme activity in the coastal upwelling system off Peru: a mesocosm experiment
Multi-proxy assessment of brachiopod shell calcite as a potential archive of seawater temperature and oxygen isotope composition
Upper-ocean flux of biogenic calcite produced by the Arctic planktonic foraminifera Neogloboquadrina pachyderma
Do bacterial viruses affect framboid-like mineral formation?
Calcification response of reef corals to seasonal upwelling in the northern Arabian Sea (Masirah Island, Oman)
Growth rate rather than temperature affects the B∕Ca ratio in the calcareous red alga Lithothamnion corallioides
Heavy metal uptake of nearshore benthic foraminifera during multi-metal culturing experiments
A stable ultrastructural pattern despite variable cell size in Lithothamnion corallioides
Decoupling salinity and carbonate chemistry: low calcium ion concentration rather than salinity limits calcification in Baltic Sea mussels
Technical note: A universal method for measuring the thickness of microscopic calcite crystals, based on bidirectional circular polarization
The patterns of elemental concentration (Ca, Na, Sr, Mg, Mn, Ba, Cu, Pb, V, Y, U and Cd) in shells of invertebrates representing different CaCO3 polymorphs: a case study from the brackish Gulf of Gdańsk (the Baltic Sea)
Carbonic anhydrase is involved in calcification by the benthic foraminifer Amphistegina lessonii
Distribution of chlorine and fluorine in benthic foraminifera
Rare earth elements in oyster shells: provenance discrimination and potential vital effects
Determining how biotic and abiotic variables affect the shell condition and parameters of Heliconoides inflatus pteropods from a sediment trap in the Cariaco Basin
Intercomparison of four methods to estimate coral calcification under various environmental conditions
Technical note: The silicon isotopic composition of choanoflagellates: implications for a mechanistic understanding of isotopic fractionation during biosilicification
Insights into architecture, growth dynamics, and biomineralization from pulsed Sr-labelled Katelysia rhytiphora shells (Mollusca, Bivalvia)
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
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)
Coral calcifying fluid aragonite saturation states derived from Raman spectroscopy
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
Yukiko Nagai, Katsuyuki Uematsu, Briony Mamo, and Takashi Toyofuku
Biogeosciences, 21, 1675–1684, https://doi.org/10.5194/bg-21-1675-2024, https://doi.org/10.5194/bg-21-1675-2024, 2024
Short summary
Short summary
This research highlights Spirillina vivipara's calcification strategy, highlighting variability in foraminiferal test formation. By examining its rapid growth and high calcification rate, we explain ecological strategies correlating with its broad coastal distribution. These insights amplify our understanding of foraminiferal ecology and underscore their impact on marine carbon cycling and paleoclimate studies, advocating for a species-specific approach in future research.
Caroline Thaler, Guillaume Paris, Marc Dellinger, Delphine Dissard, Sophie Berland, Arul Marie, Amandine Labat, and Annachiara Bartolini
Biogeosciences, 20, 5177–5198, https://doi.org/10.5194/bg-20-5177-2023, https://doi.org/10.5194/bg-20-5177-2023, 2023
Short summary
Short summary
Our study focuses on one of the most used microfossils in paleoenvironmental reconstructions: foraminifera. We set up a novel approach of long-term cultures under variable and controlled conditions. Our results highlight that foraminiferal tests can be used as a unique record of both SO42−/CaCO3 and δ34S seawater variation. This establishes geological formations composed of biogenic carbonates as a potential repository of paleoenvironmental seawater sulfate chemical and geochemical variation.
Karin E. Limburg, Yvette Heimbrand, and Karol Kuliński
Biogeosciences, 20, 4751–4760, https://doi.org/10.5194/bg-20-4751-2023, https://doi.org/10.5194/bg-20-4751-2023, 2023
Short summary
Short summary
We found a 3-to-5-fold decline in boron in Baltic cod otoliths between the late 1990s and 2021. The trend correlates with declines in oxygen and pH but not with increased salinity. Otolith B : Ca correlated with phosphorus in a healthy out-group (Icelandic cod) but not in Baltic cod. The otolith biomarkers Mn : Mg (hypoxia proxy) and B : Ca in cod otoliths suggest a general increase in both hypoxia and acidification within Baltic intermediate and deep waters in the last decade.
Narimane Dorey, Sophie Martin, and Lester Kwiatkowski
Biogeosciences, 20, 4289–4306, https://doi.org/10.5194/bg-20-4289-2023, https://doi.org/10.5194/bg-20-4289-2023, 2023
Short summary
Short summary
Human CO2 emissions are modifying ocean carbonate chemistry, causing ocean acidification and likely already impacting marine ecosystems. Here, we added CO2 to intertidal pools at the start of emersion to investigate the influence of future ocean acidification on net community production (NCP) and calcification (NCC). By day, adding CO2 fertilized the pools (+20 % NCP). By night, pools experienced net community dissolution, a dissolution that was further increased (+40 %) by the CO2 addition.
Karim Benzerara, Agnès Elmaleh, Maria Ciobanu, Alexis De Wever, Paola Bertolino, Miguel Iniesto, Didier Jézéquel, Purificación López-García, Nicolas Menguy, Elodie Muller, Fériel Skouri-Panet, Sufal Swaraj, Rosaluz Tavera, Christophe Thomazo, and David Moreira
Biogeosciences, 20, 4183–4195, https://doi.org/10.5194/bg-20-4183-2023, https://doi.org/10.5194/bg-20-4183-2023, 2023
Short summary
Short summary
Iron and manganese are poorly soluble in oxic and alkaline solutions but much more soluble under anoxic conditions. As a result, authigenic minerals rich in Fe and/or Mn have been viewed as diagnostic of anoxic conditions. However, here we reveal a new case of biomineralization by specific cyanobacteria, forming abundant Fe(III)- and Mn(IV)-rich amorphous phases under oxic conditions in an alkaline lake. This might be an overlooked biotic contribution to the scavenging of Fe from water columns.
Sara Ronca, Francesco Mura, Marco Brandano, Angela Cirigliano, Francesca Benedetti, Alessandro Grottoli, Massimo Reverberi, Daniele Federico Maras, Rodolfo Negri, Ernesto Di Mauro, and Teresa Rinaldi
Biogeosciences, 20, 4135–4145, https://doi.org/10.5194/bg-20-4135-2023, https://doi.org/10.5194/bg-20-4135-2023, 2023
Short summary
Short summary
The history of Earth is a story of the co-evolution of minerals and microbes. We present the evidence that moonmilk precipitation is driven by microorganisms within the rocks and not only on the rock surfaces. Moreover, the moonmilk produced within the rocks contributes to rock formation. The calcite speleothem moonmilk is the only known carbonate speleothem on Earth with undoubted biogenic origin, thus representing a biosignature of life.
Laura Pacho, Lennart de Nooijer, and Gert-Jan Reichart
Biogeosciences, 20, 4043–4056, https://doi.org/10.5194/bg-20-4043-2023, https://doi.org/10.5194/bg-20-4043-2023, 2023
Short summary
Short summary
We analyzed Mg / Ca and other El / Ca (Na / Ca, B / Ca, Sr / Ca and Ba / Ca) in Nodosariata. Their calcite chemistry is markedly different to that of the other calcifying orders of foraminifera. We show a relation between the species average Mg / Ca and its sensitivity to changes in temperature. Differences were reflected in both the Mg incorporation and the sensitivities of Mg / Ca to temperature.
João Pedro Saldanha, Joice Cagliari, Rodrigo Scalise Horodyski, Lucas Del Mouro, and Mírian Liza Alves Forancelli Pacheco
Biogeosciences, 20, 3943–3979, https://doi.org/10.5194/bg-20-3943-2023, https://doi.org/10.5194/bg-20-3943-2023, 2023
Short summary
Short summary
We analyze a complex and branched mineral structure with an obscure origin, considering form, matrix, composition, and context. Comparisons eliminate controlled biominerals. The structure's intricate history suggests microbial influence and alterations, followed by a thermal event. Complex interactions shaped its forms, making origin classification tougher. This study highlights the elaborated nature of dubiofossils, identifying challenges in distinguishing biominerals from abiotic minerals.
Marlisa Martinho de Brito, Irina Bundeleva, Frédéric Marin, Emmanuelle Vennin, Annick Wilmotte, Laurent Plasseraud, and Pieter T. Visscher
Biogeosciences, 20, 3165–3183, https://doi.org/10.5194/bg-20-3165-2023, https://doi.org/10.5194/bg-20-3165-2023, 2023
Short summary
Short summary
Cyanobacterial blooms are associated with whiting events – natural occurrences of fine-grained carbonate precipitation in the water column. The role of organic matter (OM) produced by cyanobacteria in these events has been overlooked in previous research. Our laboratory experiments showed that OM affects the size and quantity of CaCO3 minerals. We propose a model of OM-associated CaCO3 precipitation during picoplankton blooms, which may have been neglected in modern and ancient events.
Giancarlo Sidoti, Federica Antonelli, Giulia Galotta, Maria Cristina Moscatelli, Davor Kržišnik, Vittorio Vinciguerra, Swati Tamantini, Rosita Marabottini, Natalia Macro, and Manuela Romagnoli
Biogeosciences, 20, 3137–3149, https://doi.org/10.5194/bg-20-3137-2023, https://doi.org/10.5194/bg-20-3137-2023, 2023
Short summary
Short summary
The mineral content in archaeological wood pile dwellings and in the surrounding sediments in a volcanic lake was investigated. Calcium was the most abundant element; the second most abundant element was arsenic in sapwood. Sulfur, iron and potassium were also present. The mineral compounds are linked to the volcanic origin of the lake, to bioaccumulation processes induced by bacteria (i.e. sulfate-reducing bacteria) and to biochemical processes.
Niels J. de Winter, Daniel Killam, Lukas Fröhlich, Lennart de Nooijer, Wim Boer, Bernd R. Schöne, Julien Thébault, and Gert-Jan Reichart
Biogeosciences, 20, 3027–3052, https://doi.org/10.5194/bg-20-3027-2023, https://doi.org/10.5194/bg-20-3027-2023, 2023
Short summary
Short summary
Mollusk shells are valuable recorders of climate and environmental changes of the past down to a daily resolution. To explore this potential, we measured changes in the composition of shells of two types of bivalves recorded at the hourly scale: the king scallop Pecten maximus and giant clams (Tridacna) that engaged in photosymbiosis. We find that photosymbiosis produces more day–night fluctuation in shell chemistry but that most of the variation is not periodic, perhaps recording weather.
Kristian Spilling, Jonna Piiparinen, Eric P. Achterberg, Javier Arístegui, Lennart T. Bach, Maria T. Camarena-Gómez, Elisabeth von der Esch, Martin A. Fischer, Markel Gómez-Letona, Nauzet Hernández-Hernández, Judith Meyer, Ruth A. Schmitz, and Ulf Riebesell
Biogeosciences, 20, 1605–1619, https://doi.org/10.5194/bg-20-1605-2023, https://doi.org/10.5194/bg-20-1605-2023, 2023
Short summary
Short summary
We carried out an enclosure experiment using surface water off Peru with different additions of oxygen minimum zone water. In this paper, we report on enzyme activity and provide data on the decomposition of organic matter. We found very high activity with respect to an enzyme breaking down protein, suggesting that this is important for nutrient recycling both at present and in the future ocean.
Thomas Letulle, Danièle Gaspard, Mathieu Daëron, Florent Arnaud-Godet, Arnauld Vinçon-Laugier, Guillaume Suan, and Christophe Lécuyer
Biogeosciences, 20, 1381–1403, https://doi.org/10.5194/bg-20-1381-2023, https://doi.org/10.5194/bg-20-1381-2023, 2023
Short summary
Short summary
This paper studies the chemistry of modern marine shells called brachiopods. We investigate the relationship of the chemistry of these shells with sea temperatures to test and develop tools for estimating sea temperatures in the distant past. Our results confirm that two of the investigated chemical markers could be useful thermometers despite some second-order variability independent of temperature. The other chemical markers investigated, however, should not be used as a thermometer.
Franziska Tell, Lukas Jonkers, Julie Meilland, and Michal Kucera
Biogeosciences, 19, 4903–4927, https://doi.org/10.5194/bg-19-4903-2022, https://doi.org/10.5194/bg-19-4903-2022, 2022
Short summary
Short summary
This study analyses the production of calcite shells formed by one of the main Arctic pelagic calcifiers, the foraminifera N. pachyderma. Using vertically resolved profiles of shell concentration, size and weight, we show that calcification occurs throughout the upper 300 m with an average production flux below the calcification zone of 8 mg CaCO3 m−2 d−1 representing 23 % of the total pelagic biogenic carbonate production. The production flux is attenuated in the twilight zone by dissolution.
Paweł Działak, Marcin D. Syczewski, Kamil Kornaus, Mirosław Słowakiewicz, Łukasz Zych, and Andrzej Borkowski
Biogeosciences, 19, 4533–4550, https://doi.org/10.5194/bg-19-4533-2022, https://doi.org/10.5194/bg-19-4533-2022, 2022
Short summary
Short summary
Bacteriophages comprise one of the factors that may influence mineralization processes. The number of bacteriophages in the environment usually exceeds the number of bacteria by an order of magnitude. One of the more interesting processes is the formation of framboidal pyrite, and it is not entirely clear what processes determine its formation. Our studies indicate that some bacterial viruses may influence the formation of framboid-like or spherical structures.
Philipp M. Spreter, Markus Reuter, Regina Mertz-Kraus, Oliver Taylor, and Thomas C. Brachert
Biogeosciences, 19, 3559–3573, https://doi.org/10.5194/bg-19-3559-2022, https://doi.org/10.5194/bg-19-3559-2022, 2022
Short summary
Short summary
We investigate the calcification rate of reef corals from an upwelling zone, where low seawater pH and high nutrient concentrations represent a recent analogue for the future ocean. Calcification rate of the corals largely relies on extension growth. Variable responses of extension growth to nutrients either compensate or exacerbate negative effects of weak skeletal thickening associated with low seawater pH – a mechanism that is critical for the persistence of coral reefs under global change.
Giulia Piazza, Valentina A. Bracchi, Antonio Langone, Agostino N. Meroni, and Daniela Basso
Biogeosciences, 19, 1047–1065, https://doi.org/10.5194/bg-19-1047-2022, https://doi.org/10.5194/bg-19-1047-2022, 2022
Short summary
Short summary
The coralline alga Lithothamnion corallioides is widely distributed in the Mediterranean Sea and NE Atlantic Ocean, where it constitutes rhodolith beds, which are diversity-rich ecosystems on the seabed. The boron incorporated in the calcified thallus of coralline algae (B/Ca) can be used to trace past changes in seawater carbonate and pH. This paper suggests a non-negligible effect of algal growth rate on B/Ca, recommending caution in adopting this proxy for paleoenvironmental reconstructions.
Sarina Schmidt, Ed C. Hathorne, Joachim Schönfeld, and Dieter Garbe-Schönberg
Biogeosciences, 19, 629–664, https://doi.org/10.5194/bg-19-629-2022, https://doi.org/10.5194/bg-19-629-2022, 2022
Short summary
Short summary
The study addresses the potential of marine shell-forming organisms as proxy carriers for heavy metal contamination in the environment. The aim is to investigate if the incorporation of heavy metals is a direct function of their concentration in seawater. Culturing experiments with a metal mixture were carried out over a wide concentration range. Our results show shell-forming organisms to be natural archives that enable the determination of metals in polluted and pristine environments.
Valentina Alice Bracchi, Giulia Piazza, and Daniela Basso
Biogeosciences, 18, 6061–6076, https://doi.org/10.5194/bg-18-6061-2021, https://doi.org/10.5194/bg-18-6061-2021, 2021
Short summary
Short summary
Ultrastructures of Lithothamnion corallioides, a crustose coralline alga collected from the Atlantic and Mediterranean Sea at different depths, show high-Mg-calcite cell walls formed by crystals with a specific shape and orientation that are unaffected by different environmental conditions of the living sites. This suggests that the biomineralization process is biologically controlled in coralline algae and can have interesting applications in paleontology.
Trystan Sanders, Jörn Thomsen, Jens Daniel Müller, Gregor Rehder, and Frank Melzner
Biogeosciences, 18, 2573–2590, https://doi.org/10.5194/bg-18-2573-2021, https://doi.org/10.5194/bg-18-2573-2021, 2021
Short summary
Short summary
The Baltic Sea is expected to experience a rapid drop in salinity and increases in acidity and warming in the next century. Calcifying mussels dominate Baltic Sea seafloor ecosystems yet are sensitive to changes in seawater chemistry. We combine laboratory experiments and a field study and show that a lack of calcium causes extremely slow growth rates in mussels at low salinities. Subsequently, climate change in the Baltic may have drastic ramifications for Baltic seafloor ecosystems.
Luc Beaufort, Yves Gally, Baptiste Suchéras-Marx, Patrick Ferrand, and Julien Duboisset
Biogeosciences, 18, 775–785, https://doi.org/10.5194/bg-18-775-2021, https://doi.org/10.5194/bg-18-775-2021, 2021
Short summary
Short summary
The coccoliths are major contributors to the particulate inorganic carbon in the ocean. They are extremely difficult to weigh because they are too small to be manipulated. We propose a universal method to measure thickness and weight of fine calcite using polarizing microscopy that does not require fine-tuning of the light or a calibration process. This method named "bidirectional circular polarization" uses two images taken with two directions of a circular polarizer.
Anna Piwoni-Piórewicz, Stanislav Strekopytov, Emma Humphreys-Williams, and Piotr Kukliński
Biogeosciences, 18, 707–728, https://doi.org/10.5194/bg-18-707-2021, https://doi.org/10.5194/bg-18-707-2021, 2021
Short summary
Short summary
Calcifying organisms occur globally in almost every environment, and the process of biomineralization is of great importance in the global carbon cycle and use of skeletons as environmental data archives. The composition of skeletons is very complex. It is determined by the mechanisms of biological control on biomineralization and the response of calcifying organisms to varying environmental drivers. Yet for trace elements, such as Cu, Pb and Cd, an impact of environmental factors is pronounced.
Siham de Goeyse, Alice E. Webb, Gert-Jan Reichart, and Lennart J. de Nooijer
Biogeosciences, 18, 393–401, https://doi.org/10.5194/bg-18-393-2021, https://doi.org/10.5194/bg-18-393-2021, 2021
Short summary
Short summary
Foraminifera are calcifying organisms that play a role in the marine inorganic-carbon cycle and are widely used to reconstruct paleoclimates. However, the fundamental process by which they calcify remains essentially unknown. Here we use inhibitors to show that an enzyme is speeding up the conversion between bicarbonate and CO2. This helps the foraminifera acquire sufficient carbon for calcification and might aid their tolerance to elevated CO2 level.
Anne Roepert, Lubos Polerecky, Esmee Geerken, Gert-Jan Reichart, and Jack J. Middelburg
Biogeosciences, 17, 4727–4743, https://doi.org/10.5194/bg-17-4727-2020, https://doi.org/10.5194/bg-17-4727-2020, 2020
Short summary
Short summary
We investigated, for the first time, the spatial distribution of chlorine and fluorine in the shell walls of four benthic foraminifera species: Ammonia tepida, Amphistegina lessonii, Archaias angulatus, and Sorites marginalis. Cross sections of specimens were imaged using nanoSIMS. The distribution of Cl and F was co-located with organics in the rotaliids and rather homogeneously distributed in miliolids. We suggest that the incorporation is governed by the biomineralization pathway.
Vincent Mouchi, Camille Godbillot, Vianney Forest, Alexey Ulianov, Franck Lartaud, Marc de Rafélis, Laurent Emmanuel, and Eric P. Verrecchia
Biogeosciences, 17, 2205–2217, https://doi.org/10.5194/bg-17-2205-2020, https://doi.org/10.5194/bg-17-2205-2020, 2020
Short summary
Short summary
Rare earth elements (REEs) in coastal seawater are included in bivalve shells during growth, and a regional fingerprint can be defined for provenance and environmental monitoring studies. We present a large dataset of REE abundances from oysters from six locations in France. The cupped oyster can be discriminated from one locality to another, but this is not the case for the flat oyster. Therefore, provenance studies using bivalve shells based on REEs are not adapted for the flat oyster.
Rosie L. Oakes and Jocelyn A. Sessa
Biogeosciences, 17, 1975–1990, https://doi.org/10.5194/bg-17-1975-2020, https://doi.org/10.5194/bg-17-1975-2020, 2020
Short summary
Short summary
Pteropods are a group of tiny swimming snails whose fragile shells put them at risk from ocean acidification. We investigated the factors influencing the thickness of pteropods shells in the Cariaco Basin, off Venezuela, which is unaffected by ocean acidification. We found that pteropods formed thicker shells when nutrient concentrations, an indicator of food availability, were highest, indicating that food may be an important factor in mitigating the effects of ocean acidification on pteropods.
Miguel Gómez Batista, Marc Metian, François Oberhänsli, Simon Pouil, Peter W. Swarzenski, Eric Tambutté, Jean-Pierre Gattuso, Carlos M. Alonso Hernández, and Frédéric Gazeau
Biogeosciences, 17, 887–899, https://doi.org/10.5194/bg-17-887-2020, https://doi.org/10.5194/bg-17-887-2020, 2020
Short summary
Short summary
In this paper, we assessed four methods (total alkalinity anomaly, calcium anomaly, 45Ca incorporation, and 13C incorporation) to determine coral calcification of a reef-building coral. Under all conditions (light vs. dark incubations and ambient vs. lowered pH levels), calcification rates estimated using the alkalinity and calcium anomaly techniques as well as 45Ca incorporation were highly correlated, while significantly different results were obtained with the 13C incorporation technique.
Alan Marron, Lucie Cassarino, Jade Hatton, Paul Curnow, and Katharine R. Hendry
Biogeosciences, 16, 4805–4813, https://doi.org/10.5194/bg-16-4805-2019, https://doi.org/10.5194/bg-16-4805-2019, 2019
Short summary
Short summary
Isotopic signatures of silica fossils can be used as archives of past oceanic silicon cycling, which is linked to marine carbon uptake. However, the biochemistry that lies behind such chemical fingerprints remains poorly understood. We present the first measurements of silicon isotopes in a group of protists closely related to animals, choanoflagellates. Our results highlight a taxonomic basis to silica isotope signatures, possibly via a shared transport pathway in choanoflagellates and animals.
Laura M. Otter, Oluwatoosin B. A. Agbaje, Matt R. Kilburn, Christoph Lenz, Hadrien Henry, Patrick Trimby, Peter Hoppe, and Dorrit E. Jacob
Biogeosciences, 16, 3439–3455, https://doi.org/10.5194/bg-16-3439-2019, https://doi.org/10.5194/bg-16-3439-2019, 2019
Short summary
Short summary
This study uses strontium as a trace elemental marker in combination with 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 architectures. These observations are combined with structural investigations across length scales and altogether allow for a detailed understanding of this shell.
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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.
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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
Short summary
Short summary
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.
Thomas M. DeCarlo, Juan P. D'Olivo, Taryn Foster, Michael Holcomb, Thomas Becker, and Malcolm T. McCulloch
Biogeosciences, 14, 5253–5269, https://doi.org/10.5194/bg-14-5253-2017, https://doi.org/10.5194/bg-14-5253-2017, 2017
Short summary
Short summary
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.
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
Short summary
Short summary
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
Short summary
Short summary
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.
Cited articles
Abramovitch-Gottlib, L., Katoshevski, D., and Vago, R.: Responses of Stylophora pistillata and Millepora dichotoma to seawater temperature elevation, B. Mar. Sci., 73(3), 745–755, 2003.
Allemand, D., Furla, P., and Benazet-Tambutte, S.: Mechanisms of carbon acquisition for endosymbiont photosynthesis in Anthozoa, Can. J. Botany, 76, 925–941, 1998.
Al-Horani, F. A., Al-Moghrabi, S. M., and de Beer, D.: Microsensor study of photosynthesis and calcification in the scleractinian coral, Galaxea fascicularis: active internal carbon cycle, J. Exp. Mar. Biol. Ecol., 288, 1–15, 2003a.
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, 2003b.
Al-Moghrabi, S., Goiran, C., Allemand, D, Speziale, N., and Jaubert, J.: Inorganic carbon uptake for photosynthesis by the symbiotic coral-dinoflagellate association II. Mechanisms for bicarbonate uptake, J. Exper. Mar. Biol. Ecol., 199, 227–248, 1996.
Amat, A.: Croissance corallienne et variations du CO2 atmopshérique: implications Biologiques et Climatiques. Ph. D. thesis. Université Pierre et Marie Curie, Paris, France, 322 pp., 2002.
Amat, A. and Bates, N. R.: High latitude reefs: A potential refuge for reef builders, European Geophysical Society (EGS) Meeting, Nice, April 2003, EAE03-A-01385, 2003.
Amat, A. and Bates, N. R.: Concomitant impact of carbon dioxide and temperature on coral metabolism: from the seasonal to the global change scales. Case study of the high latitude reef of Bermuda, 10th International Coral Reefs Symposium, Okinawa, June 2004, 2004.
Andersson, A. J., Mackenzie, F. T., and Ver, L. M.: Solution of shallow-water carbonates: An insignificant buffer against rising atmospheric CO2, Geology, 31, 513–516, 2003.
Andersson, A. J., Mackenzie, F. T., and Lerman, A.: Coastal ocean and carbonate systems in the high CO2 world of the Anthropocene, A. J. Sci., 305, 875–918, 2005.
Andersson, A. J., Mackenzie, F. T., and Lerman, A.: Coastal ocean CO2-carbonic acid-carbonate sediment system of the Anthropocene. Global Biogeochem. Cy., 20, GB4S09, https://doi.org/10.1029/2005GB002506, 13 pp., 2006.
Andersson, A. J., Bates, N. R., and Mackenzie, F. T.: Dissolution of carbonate sediments under rising pCO2 and ocean acidification: Observations from Devil's Hole, Bermuda, Aquat. Geochem, 13(3), 237–264, https://doi.org/10.1007/s10498-007-9018-8, 2007.
Andersson, A. J., Mackenzie, F. T., and Bates, N. R.: Life on the margin: implications of ocean acidification on Mg-calcite, high latitude and cold-water marine calcifiers, Mar. Ecol. Prog. Ser., 373, 265–273, 2008.
Andersson, A. J., Kuffner, I. B., Mackenzie, F. T., Jokiel, P. L., Rodgers, K. S., and Tan, A.: Net Loss of CaCO3 from a subtropical calcifying community due to seawater acidification: mesocosm-scale experimental evidence, Biogeosciences, 6, 1811–1823, https://doi.org/10.5194/bg-6-1811-2009, 2009.
Atkinson, M. J. and Cuet, P.: Possible effects of ocean acidification on coral reef biogeochemistry: topics for research, Mar. Ecol. Prog. Ser., 373, 249–256, 2008.
Bacastow, R. D. and Keeling, C. D.: Atmospheric carbon dioxide and radiocarbon in the natural carbon cycle. II. Changes from AD1700 to 2070 as deduced from a geochemical model, in: Carbon and tthe Biosphere, edited by: Woodwell, G. M. and Pecan, E. V., US Atomic Energy Commision, Washington DC, 86–135, 1973.
Baker, K. S. and Frouin, R.: Relationship between photosynthetically available radiation and total insolation at the surface of the ocean under clear skies, Limnol. Oceanogr., 32, 1370–1377, 1987.
Barnes, D. J. and Lazar, B.: Metabolic performance of a shallow reef patch near Eilat on the Red Sea, J. Exp. Mar. Biol. Ecol., 174(1), 1–13, 1987.
Bates, N. R.: Seasonal variability of the impact of coral reefs on ocean CO2 and air-sea CO2 exchange, Limnol. Oceanogr., 47(1), 43–52, 2002.
Bates, N. R.: Interannual variability of the oceanic CO2 sink in the subtropical gyre of the North Atlantic Ocean over the last two decades. J. Geophys. Res., Oceans, 112(C9), C09013, https://doi.org/2006JC003759, 2007.
Bates, N. R. and Peters, A. J.: The contribution of acid deposition to ocean acidification in the subtropical North Atlantic Ocean, Mar. Chem., 107, 547–558, https://doi.org/10.1016/j.marchem.2007.08.002, 2007.
Bates, N. R., Michaels, A. F., and Knap A. H.: Seasonal and interannual variability of the oceanic carbon dioxide system at the US JGOFS Bermuda Atlantic Time-series Site, Deep-Sea Res. II, 43, 347–383, https://doi.org/10.1016/0967-0645(95)00093-3, 1996a.
Bates, N. R., Michaels, A. F., and Knap, A. H.: Alkalinity changes in the Sargasso Sea: geochemical evidence of calcification?, Mar. Chem., 51, 347–358, https://doi.org/10.1016/0304-4203(95)00068-2, 1996b.
Bates, N. R., Takahashi, T., Chipman, D. W., and Knap, A. H.: Variability of pCO2 on diel to seasonal time scales in the Sargasso Sea. J. Geophys. Res., 103, 15567–15585, 1998a.
Bates, N. R., Merlivat, L., Beaumont, L., and Pequignet, A. C.: Intercomparison of shipboard and moored CARIOCA buoy seawater fCO2 measurements in the Sargasso Sea, Mar. Chem., 72(2–4), 239–255, https://doi.org/10.1016/S0304-4203(00)00084-0, 2000.
Bates, N. R., Samuels, L., and Merlivat, L.: Biogeochemical and physical factors influencing seawater fCO2 and air-sea CO2 exchange on the Bermuda coral reef, Limnol. Oceanogr., 46(4), 833–846, 2001.
Bates, N. R., Pequignet, A. C., and Johnson, R. J.: Changes in the oceanic sink of CO2 in Subtropical Mode Water of the North Atlantic Ocean, Nature, 420, 489–493, https://doi.org/10.1038/nature01253, 2002.
Bates, N. R., Mathis, J. T., and Cooper, L.: The effect of ocean acidification on biologically induced seasonality of carbonate mineral saturation states in the Western Arctic Ocean, J. Geophys. Res.-Oceans, 114, C11009, https://doi.org/10.1029/2008JC004862., 2009.
Beriland, T. G.: Methods of climatological computation of total incoming solar radiation, Meteorol. Gidrol, 6, 9–12, 1960.
Bindoff, N. L., Willebrand, J., Artale, V., Cazenave, A., Gregory, J., Gulev, S., Hanawa, K., Le Quéré, C., Levitus, S., Nojiri, Y., Shum, C. K., Talley, L. D., and Unnikrishnan, A.: Observations: Oceanic Climate Change and Sea Level, in: Climate Change 2007: The Physical Science Basis. Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change, edited by: Solomon, S., Qin, D., Manning, M., Chen, Z., Marquis, M., Averyt, K. B., Tignor, M., and Miller, H. L., Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA, 2007.
Broecker, W. S. and Takahashi, T.: calcium carbonate precipitation on the Bahama Banks, J. Geophys. Res., 71, 1575–1602., 1966.
Broecker, W. S., Li, Y. H., and Peng, T.-H.: Carbon dioxide – man's unseen artifact, in: Impingement of Man on the Oceans, edited by: Hood, D. W., John Wiley & Sons, New York, 287–324, 1971.
Buddemeier, R. W., Kleypas, J. A., and Aronson, R. B.: Coral Reefs and Global Climate Change: Potential Contributions of Climate Change to Stresses on Coral Reef Ecosystems. Pew Center on Climate Change, 44 pp., 2004.
Caldeira, K. and Wickett, M. E.: Anthropogenic carbon and ocean pH, Nature, 425, 365–368, 2003.
Caldeira, K. and Wickett, M. E.: Ocean model predictions of chemistry changes from carbon dioxide emissions to the atmosphere and ocean, J. Geophy. Res. Oceans, 110(C9), C09S04, https://doi.org/10.1029/2004JC002671., 2005.
CARICOMP: CARICOMP monitoring of coral reefs, Procedings of the 8th International Coral Reef Symposium, Panama, 1, 651–656, 1997a.
CARICOMP: Meteorological and oceanographic characterization of coral reef, seagrass and mangorve habitats in the wider Caribbean, Procedings of the 8th International Coral Reef Symposium, Panama, 1, 657–662, 1997b.
CARICOMP: Status and Trends at CARICOMP coral reef sites, Procedings of the 9th International Coral Reef Symposium, Bali, 1, 325–330, 2000.
Chisholm, J. R. M., and Gattuso, J.-P.: Validation of the alkalinity anomaly technique for investigating calcification and photosynthesis in coral reef communities, Limnol. Oceanogr., 36, 1232–1239, 1991.
Chisholm, J. R. M. and Barnes, D. J.: Anomalies in coral reef community metabolism and their potential importance in the reef CO2 source-sink debate, P. Natl. Acad. Sci. USA, 95, 6566–6569, 1998.
Clarke, L., Edmonds, J., Jacoby, H., Pitcher, H., Reilly, J., and Richels, R.: Scenarios of Greenhouse Gas Emissions and Atmospheric Concentrations. Sub-report 2.1A of Synthesis and Assessment Product 2.1 by the US Climate Change Science Program and the Subcommittee on Global Change Research, Department of Energy, Office of Biological & Environmental Research, Washington, DC, USA, 154 pp., 2007.
Cohen, A. L. and McConnaughey, T. A.: Geochemical perspectives on coral mineralization in Biomineralization, Rev. Mineral. Geochem., 54, 151–187, 2003.
Cohen, A. L., Smith, S. R., McCartney, M. S., and van Etten, J.: How brain corals record climate: an integration of skeletal structure, growth and chemistry of Diploria labyrinthiformis from Bermuda, Mar. Ecol. Prog. Ser., 271, 147–158, 2004.
Cohen, A. L. and Hlcomb, M.: Why corals care about ocean acidification, Oceanography, 22(4), 118–127, 2009.
Cooper, T. F., De'ath, G., Fabricius, K. E., and Lough, J. M.: Declining coral calcification in massive Porites in two nearshore regions of the northern Great Barrier Reef, Glob. Change Biol., 14, 529–538, 2008.
Crossland, C. J., Hatcher, B. G., and Smith, S. V.: Role of coral reefs in global ocean production, Coral Reefs, 10, 55–64, 1991.
Davies, P. S.: Short-term measurements of corals using an accurate buoyant weighing technique, Mar. Biol., 101, 389–395, 1989.
Davies, P. S.: A rapid method for assessing growth rates of corals in relation to water pollution, Mar. Pollut. Bull., 21, 346–348., 1990.
De'ath, G., Lough, J. M., and Fabricius, K. E.: Declining coral calcification on the Great Barrier Reef, Science, 323, 116–119, 2009.
de Beer, D., Kuhl, M., Stambler, N., and Vaki, L.: A microsensor study of light enhanced Ca2+ uptake and photosynthesis in the reef-building hermatypic coral Favia sp., Mar. Ecol. Prog. Ser., 194, 75–85, 2000.
Dickson, A. G.: Thermodynamics of the dissociation of boric acid in potassium chloride solutions from 273.15 K to 318.15 K, J. Chem. Eng. Data., 35(3), 253–257, 1990.
Dickson, A. G. and Millero, F. J.: A comparison of the equilibrium constants for the dissociation of carbonic acid in seawater media, Deep-Sea Res., 34, 1733–1743, 1987.
Dickson, A. G., Sabine, C. L., and Christian, J. R.: Guide to best practices for ocean CO2 measurements. Sidney, British Columbia, North Pacific Marine Science Organization, PICES Special Publication 3, 2007.
Dobson, F. W. and Smith, S. D.: Estimation of solar radiation at sea, in: the Ocean Surface, edited by: Toba, Y. and Mitsuyasa, H., Reidel, Dordrecht, 525–533, 1980.
Dodge, R. E. and Vaisnys, J. R.: Coral populations and growth patterns: responses to sedimentation and turbidity associated with dredging, J. Mar. Res., 35, 715–730, 1977.
Dodge, R. E., Wyers, S. C., Frith, H. R., Knap, A. H., Smith, S. R., Cook, C. B., and Sleeter, T. D.: Coral calcification rates by the buoyant weight technique. Effects of alizarin staining, J. Exp. Mar. Biol. Ecol., 75, 217–232, 1984.
DOE: Handbook of Methods for the Analysis of the Various Parameters of the Carbon Dioxide System in Seawater; version 2.0, edited by: Dickson, A. G. and Goyet, C., US Department of Energy CO2 Science Team Report, 1994.
Doney, S. C.: The dangers of ocean acidification, Scientific American, March 2006, 58–65, 2006.
Doney, S. C., Fabry, V. J., Feely, R. A., and Kleypas, J. A.: Ocean acidification: the other CO2 problem, Ann. Rev. Mar. Sci., 1, 169–192, 2009.
Dore, J. E., Lukas, R., Sadler, D. W., Church, M. J., and Karl, D. M.: Physical and biogeochemical modulation of ocean acidification in the central North Pacific, P. Natl. Acad. Sci., 106, 12235–12240, 2009.
Ducklow, H. W. and McAllister, S. L.: Biogeochemistry of carbon dioxide in the coastal oceans, in: The Sea, Volume 13, The Global Coastal Ocean-Multiscale Interdisciplinary Processes, edited by: Robinson, A. R. and Brink, K., J. Wiley and Sons, NY, 2005.
Duffie, J. A. and Beckman, W. A.: Solar Engineering of Thermal Processes, J. Wiley and Sons, New York, 2nd edition, 1991.
Dutton, E. G.: Basic measurements of radiation at station Bermuda (2002–2003), Climate Monitoring & Diagnostics Laboratory, Boulder, https://doi.org/10.1594/PANGAEA.667769, 2007.
Edmunds, P. J.: Evidence for a decade-scale decline in the growth rates of juvenile scleractinian corals, Mar. Ecol. Prog. Ser., 341, 1–13, 2007.
Edmunds, P. J. and Elahi, R.: The demographics of a 15-year decline in cover of the Caribbean reef coral Montastraea annularis, Ecol. Monogr., 77(1), 3–18, 2007.
Feely, R. A., Byrne, R. H., Acker, J. G., Betzer, P. R., Chen, C. T.-A., Gendron, J. R., and Lamb, M. F.: Winter summer variations of calcite and aragonite saturation in the northeast Pacific, Mar. Chem., 25(3), 227–241., 1988.
Fine, M. and Tchenov, D.: Scleractinian coral species survive and recover from decalcification, Science, 315, 1811–1813, 2007.
Frankignoulle, M., Canon, D., and Gattuso, J. P.: Marine calcification as a source of carbon dioxide – Positive feedback of increasing atmospheric CO2, Limnol. Oceanogr., 39(2), 458–462, 1994.
Frankignoulle, M., Gattuso, J. P., Biondo, R., Bourge, I., Copin-Montegut, G., and Pichon, M.: Carbon fluxes in coral reefs 2. Eulerian study of inorganic carbon dynamics and measurement of air- sea CO2 exchanges, Mar. Ecol. Prog. Ser., 145(1–3), 123–132, 1996.
Furla, P., Galgani, I., Durand, I., and Allemand, D.: Sources and mechanisms of inorganic carbon transport for coral calcification and photosynthesis, J. Exp. Biol., 203, 3445–3457, 2000.
Gattuso, J.-P.: Photosynthesis and calcification at cellular, organismal and community levels in coral reefs: a review on interactions and control by carbonate chemistry, American Zoologist, 39, 160–183, 1999.
Gattuso, J.-P. and Jaubert, J.: Effect of light on oxygen and carbon-dioxide fluxes and on metabolic quotients measured in situ in a zooxanthellate coral, Limnol. Oceanogr., 35(8), 1796–1804, 1990.
Gattuso, J.-P., Pichon, M., Delesalle, B., and Frankignoulle, M.: Community metabolism and air–sea CO2 fluxes in a coral reef ecosystem (Moorea, French Polynesia), Mar. Ecol. Prog. Ser., 96, 259–267, 1993.
Gattuso, J.-P., Pichon, M., and Frankignoulle, M.: Biological control of air-sea fluxes: effects of photosynthetic and calcifyingg marine organisms and ecosystems, Mar. Ecol. Prog. Ser., 129, 307–312, 1995.
Gattuso, J.-P., Pichon, M., Delesalle, B., Canon, C., and Frankignoulle, M.: Carbon fluxes in coral reefs. I. Lagrangian measurement of community metabolism and resulting air-sea CO2 disequilibrium, Mar. Ecol. Prog. Ser., 145, 109–121, 1996.
Gattuso, J.-P., Payri, C. E., Pichon, M., Delesalle, B., and Frankignoulle, M.: Primary production, calcification, and air-sea CO2 fluxes of a macroalgal-dominated coral reef community (Moorea, French Polynesia), J. Phycology, 33, 729–738, 1997.
Gattuso, J.-P., Frankignoulle, M., Bourge, I., Romaine, S., and R. W. Buddemeier, R. W.: Effect of calcium carbonate saturation of seawater on coral calcification, Global Planetary Change, 18, 37–46, 1998.
Gattuso, J.-P., Allemand, P. D., and Frankignoulle, M. Interactions between the carbon and carbonate cycles at organism and community levels on coral reefs: a review of processes and control by carbonate chemistry. American Zoologist, 39, 160–188, 1999.
Gattuso, J.-P., Reynaud-Vaganay, S., Furla, P., Romaine-Lioud, S., Jaubert, J., Bourge, I., and Frankignoulle, M.: Calcification does not stimulate photosynthesis in the zooxanthellate scleractinian coral Stylophora pistillata, Limnol. Oceanogr., 45, 246–250, 2000.
Glud, R. N., Eyre, B. D., and Patten, N. Biogeochemical responses to mass coral spawning at the Great Barrier Reef: effects on respiration and primary production, Limnol. Oceanogr., 53(3), 1014–1024, 2008.
Goiran, C., Al-Moghrabi, S., Allemand, D., and Jaubert, J.: Inorganic carbon uptake for photosynthesis by the symbiotic coral/dinoflagellate association I. Photosynthetic performances of symbionts and dependence on sea water bicarbonate, J. Exp. Mar. Biol. Ecol., 199(2), 207–225, 1996.
Goreau, T. F.: The physiology of skeleton formation in corals I. A method for measuring the rate of calcium deposition by corals under different conditions, Biol. Bull., 116, 59–75, 1959.
Grottoli, A. G.: Effect of light and brine shrimp in skeletal d13C in the Hawaiian coral Porites compresa: a tank experiment, Geochimica Cosmochimica Acta, 66, 1955–1967, 2002.
Grottoli A. G. and Wellington, G. M.: Effect of light and zooplankton on skeletal d13C values in the eastern Pacific corals Pavona clavus and Pavona gigantean, Coral Reefs, 18, 29–41, 1999.
Guinotte, J. M., and Fabry, V. J.: Ocean acidification and its potential effects on marine ecosystems, Year in Ecology and Conservation Biology, 2008; Annals of the New York Academy of Sciences, 1134, 320–342, 2008.
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., Caldeira, K., Knowlton, N., Eakin, C. M., Iglesias-Prieto, R., Muthiga, N., Bradbury, R. H., Dubi, A., and Hatziolos, M. E.: Coral reefs under rapid climate change and ocean acidification, Science, 318, 1737–1742, 2007.
Hood, E. M., Merlivat, L., and Johannessen, T.: Variations of fCO2 and air-sea flux of CO2 in the Greenland Sea using high-frequency time-series data from CARIOCA drift-buoys, J. Geophys. Res., 104, 20571–20583, 1999.
Hughes, T. P.: Catastrophes, phase shifts, and large-scale degradation of a Caribbean coral reef, Science, 271, 1298–1299, 1994.
IPCC, Climate Change 1995: The science of climate change, Contribution of working group I to the Second Assessment Report of the intergovernmental Panel on Climate Change, edited by: Houghton, J. T., Meiro Filho, L. G., Callander, B. A., Harris, N., Kattenberg, A., and Maskell, K., Cambridge University Press, Cambridge, 572 pp., 1996.
IPCC, Climate change 2001: The scientific basis, Contribution of Working Group I to the Third Assessment Report of the Intergovernmental Panel on Climate Change, edited by: Houghton, J. T., Ding, Y., Griggs, D. J., Noguer, M., van der Linden, P. J., Dai, X., Maskell, K., and Johnson, C. A., Cambridge University Press, Cambridge, 881 pp., 2001.
IPCC, Climate Change 2007: The Physical Science Basis. Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change. Solomon, S., D. Qin, M. Manning, Z. Chen, M. Marquis, K. B. Averyt, M. Tignor and H. L. Miller (eds.), Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA, 996 p., 2007.
Johnson, R. J.: Climatic and Mesoscale Eddy Modulation of the Upper Ocean at the Bermuda Time-series Site, Ph.D. dissertation, University of Southampton, UK, 247 pp., 2003.
Jokiel, P. L., Maragos, J. E., and Franzisket, L.: Coral growth: buoyant weight technique, in: Coral Reef Research Methods, edited by: Stoddart, D. R., and Johannes, R. E., UNESCO Monograph Oceanographic Methods, 529–542, 1978.
Jokiel, P., Rodgers, K. S., Kuffner, I. B., Andersson, A. J., Mackenzie, F. T., and Cox, E. F.: Ocean acidification and calcifying reef organisms: a mesocosm investigation, Coral Reefs, 27, 473–483, 2008.
Kawahata, H., Suzuki, A., and Goto, K.: Coral reef ecosystems as a source of atmospheric CO2: evidence from pCO2 measurements of surface waters, Coral Reefs, 16, 261–266, 1997.
Kawahata, H., Suzuki, A., Ayukai, T., and Goto, K.: Distibution of the fugacity of carbon dioxide in the surface seawater of the Great Barrier Reef, Mar. Chem., 72, 257–272, 2000.
Kayanne, H., Suzuki, A., and Saito, H.: Diurnal changes in the partial pressure of carbon dioxide in coral reef water, Science, 269, 214–216, 1995.
Kayanne, H., Suzuki, A., and Saito, H.: Coral reefs and carbon dioxide, Science, 271, 1299–1300, 1996.
Kayanne, H., Hata, H., Kudo, S., Yamano, H., Watanabe, A., Ikeda, Y., Nozaki, K., Kato, K., Negishi A., and Saito, H.: Seasonal and bleaching-induced changes in coral reef metabolism and CO2 flux. Global Biogeochem. Cy., 19(3), https://doi.org/10.1029/2004GB002400, 27 Aug 2005, 2005.
Kinsey, D. W.: Alkalinity changes and coral reef calcification. Limnol. Oceanogr., 23, 989–991, 1978.
Kinsey, D. W.: Metabolism, calcification and carbon production. I. System Level Studies. Proceedings of the 5th International Coral Reef Congress, Tahiti, pp. 22, 1985.
Kleypas, J. A. and Yates, K. K.: Coral reefs and ocean acidification, Oceanography, 22(4), 108–117, 2009.
Kleypas, J. A., Buddemeier, R. W., Archer, D., Gattuso, J.-P., Langdon, C., and Opdyke, B. N.: Geochemical consequences of increased atmospheric carbon dioxide on coral reefs, Science, 284, 118–120, 1999a.
Kleypas, J. A., McManus, J., and Menez, L.: Using environmental data to define reef habitat: where do we draw the line?, Am. Zool., 39, 146–159, 1999b.
Kleypas, J. A., Buddemeier, R. W., and Gattuso, J.-P.: The future of coal reefs in an age of global change, International Journal of Earth Sciences (Geologische Rundschau), 90, 426–437, 2001.
Kleypas, J. A., Feely, R. A ., Fabry, V. J., Langdon, C., Sabine, C .L., and Robbins, L. L.: Impacts of Ocean Acid- ification on Coral Reefs and Other Marine Calcifiers: a Guide for Future Research, report of a workshop held 18–20 April 2005, St. Petersburg, FL, sponsored by NSF, NOAA, and the US Geological Survey, 88 pp., 2006.
Langdon C.: Review of experimental evidence for effects of CO2 on calcification of reef builders, Proceedings of the 9th International Coral Reefs Symposium, Bali, Indonesia, October 2000, 2001.
Langdon, C. and Atkinson, M. J.: Effect of elevated pCO2 on photosynthesis and calcification of corals and interactions with seasonal change in temperature/irradiance and nutrient enrichment, J. Geophys. Res., Oceans, 110, C09S07, https://doi.org/10.1029/2004JC002576, 2005.
Langdon, C., Takahashi, T., Sweeney, C., Chipman, D., Goddard, J., Marubini, F., Aveces, H., Barnett, H., and Atkinson, M. J.: Effect of calcium carbonate saturation state on the calcification rate of an experimental coral reef, Global Biogeochem. Cy., 14(2), 639–654, 2000.
Langdon, C., Broecker, W. S., Hammond, D. E., Glenn, E., Fitzsimmons, K., Nelson, S. G., Peng, T.H., Hajdas, I., and Bonani, G.: Effect of elevated CO2 on the community metabolism of an experimental coral reef. Global Biogeochem. Cy., 17(1), 1011, https://doi.org/10.1029/2002GB001941, 2003.
Langdon C., Gattuso, J.-P., and Andersson, A. J.: Measurements of calcification and dissolution of benthic organisms and communities. In: guide to Beast Practices in Ocean Acidification Reseach and Data Reporting, edited by: Riebesell, U., Fabry, V. J., Hansson, L., and Gattuso, J.-P., Luxembourg, Office for Official Publications of the European Communities, 155–174, 2010.
Leclercq, N., Gattuso, J. P., and Jaubert, J.: CO2 partial pressure controls the calcification rate of a coral community, Glob. Change Biol., 6(3), 329–334, 2000.
Leclercq, N., Gattuso, J. P., and Jaubert, J.: Primary production, respiration and calcification of a coral reef mesocosm under increased CO2 partial pressure, Limnol. Oceanogr., 47(2), 558–564, 2002.
Lerman, A. and Mackenzie, F. T.: CO2 air-sea exchange due to calcium carbonate and organic matter storage, and its implications for the global carbon cycle, Aquat. Geochem., 11(4), 345–390, https://doi.org/10.1007/s10498-005-8620-x, 2005.
Logan, A. and Tomascik, T.: Extension growth rates in two coral species from high latitude reefs of Bermuda, Coral Reefs, 10, 155–160, 1991.
Logan, A., Yang, L., and Tomascik, T.: Linear skeletal extension rates in two species of Diploria form high-latitude reefs in Bermuda, Coral Reefs, 13, 225–230, 1994.
Manzello, D. P.: Ocean acidification hot spots: Spatiotemporal dynamics of the seawater CO2 system of eastern Pacific coral reefs, Limnol. Oceanogr., 55(1), 239–248, 2010.
Manzello, D. P., Kleypas, J. A., Budd, D. A., Eakin, C. M., Glynn, P. W., and Langdon, C.: Poorly cemented coral reefs of the eastern tropical Pacific: Possible insights into reef development in a high-CO2 world, P. Natl. Acad. Sci., 105(30), 10450–10455, 2008.
Marshall A. T.: Calcification in hermatypic and ahermatypic corals. Science, 271, 637–639, 1996.
Marshall A. T. and Clode, P. L.: Calcification rate and the effect of temperature in a zooxanthellatre and azooxanthelllate scleractinian reef coral, Coral Reefs, 23(2), 216–224, 2004.
Marubini, F. and Atkinson, M. J.: Effects of lowered pH and elevated nitrate on coral calcification, Mar. Ecol. Prog. Ser., 188, 117–121, 1999.
Marubini, F. and Thake, B.: Bicarbonate addition promotes coral growth, Limnol. Oceanogr., 44(3), 716–720, 1999.
Marubini, F., Barnett, H., Langdon, C., and Atkinson, M. J.: Dependence of calcification on light and carbonate ion concentration for the hermatypic coral Porites compressa, Mar. Ecol. Prog. Ser., 228, 153–162, 2001.
Marubini, F., Ferrier-Pages, C., and Cuif, J. P.: Suppression of skeletal growth in scleractinian corals by decreasing ambient carbonate-ion concentration: a cross-family comparison, Proceedings of the Royal Society London B, 270, 179–184, 2003.
Marubini, F., Ferrier-Pages, C., Fulra, P., and Allemand, D.: Coral calcification responds to seawater acidification: a working hypothesis towards a physiological mechanism, Coral Reefs, 27, 491–499, 2008.
McConnaughey, T. A.: 13C and 18O isotope disequilibria in biological carbonates. 1. Patterns, Geochimica Cosmochimica Acta, 53, 151–162, 1989a.
McConnaughey, T. A.: 13C and 18O isotope disequilibria in biological carbonates. 2. In vitro simulation of kinetic isotope effects, Geochim. Cosmochim. Ac., 53, 163–171, 1989b.
McConnaughey, T. A.: Calcification generates protons for nutrient and bicarbonate uptake, Earth-Sci. Rev., 42, 95–117, 1997.
McConnaughey, T. A.: Sub-equilibrium oxygen-18 and carbon-13 levels in biological carbonates: carbonate and kinetic models, Coral Reefs, 22, 316–327, 2004.
McConnaughey, T. A. and Whelan, J. F.: Calcification generates protons for nutrient and bicarbonate uptake, Earth-Sci. Rev., 42, 95–117, 1997.
Mehrbach, C., Culberson, C. H., Hawley, J. E., and Pytkowicz, R. M.: Measurement of the apparent dissociation constants of carbonic acid in seawater at atmospheric pressure, Limnol. Oceanogr., 18, 897–907, 1973.
MEP: BIOS Marine Environmental Program (MEP) Annual Report 2005/06. Report to the Government of Bermuda, 128 pp., (http://www.bios-mep.info/), 2006.
Merlivat, L, and Brault, P.: CARIOCA buoy-Carbon dioxide monitor, Sea Technol., 36(10), 23, 1995.
Morris, B., Barnes, J., Brown, F., and Markham, J.: The Bermuda Marine Environment, Bermuda Biological Station Special Publication, 15, 72 pp., 1977.
Morse, J. W., Andersson, A. J., and Mackenzie, F. T.: Initial responses of carbonate-rich shelf sediments to rising atmospheric pCO2 and ocean acidification: Role of high Mg-calcites, Geochim. Cosmochim. Ac., 70, 5814–5830, 2006.
Mucci, A.: The solubility of calcite and aragonite in seawater at various salinities, temperatures, and one atmosphere total pressure, Am. J. Sci., 283, 780–799, 1983.
Ohde, S. and van Woesik, R.: Carbon dioxide flux and metabolic processes of a coral reef, Okinawa, B. Mar. Sci., 65, 559–576, 1999.
Orr, J. C., Fabry, V. J., Aumont, O., Bopp, L., Doney, S .C., Feely, R. A., Gnanadesikan, A., Gruber, N., Ishida, A., Joos, F., Key, R. M., Lindsay, K., Maier-Reimer, E., Matear, R., Monfray, P., Mouchet, A., Najjar, R. G., Plattner, G. K., Rodgers, K. B., Sabine, C. L., Sarmiento, J. L., Schlitzer, R., Slater, R. D., Totterdell, I. J., Weirig, M. F., Yamanaka, Y., and Yool, A.: Anthropogenic ocean acidification over the twenty-first century and its impacts on calcifying organisms, Nature, 437, 681–686, 2005.
Partridge, G. W.: Radiative Processes in Meteorology and Climatology, Elsevier Scientific Pub. Co, 1976.
Payne, R. E.: Albedo of the surface of the sea, J. Atmos. Sci., 29, 77–88, 1972.
Pichon, M.: Coral reef metabolism in the IndoPacific: the broader picture, Proceedings of the 8th International Coral Reef Symposium, Panama, 1, 977–980, 1997.
Reynaud, S., Leclercq, N., Romaine-Lioud, S., Ferrier-Pages, C., Jaubert, J., and Gattuso, J. P.: Interacting effects of CO2 partial pressure and temperature on photosynthesis and calcification in a scleractinian coral, Glob. Change Biol., 9(11), 1660–1668, 2003.
Royal Society: Ocean acidification due to increasing atmospheric carbon dioxide, the Clyvedon Press, Ltd, Cardiff, UK, 2005.
Santana-Casiano, J. M., Gonzalez-Davila, M., Rueda, M. J., Llinas, O., and Gonzalez-Davila, E. F.: The interannual variability of oceanic CO2 parameters in the northeast Atlantic subtropical gyre at the ESTOC site. Global Biogeochem. Cy., 21(1), GB1015, https://doi.org/10.1029/2006GB002788, 8 March 2007, 2007.
Schneider, K. and Erez, J.: The effect of carbonate chemistry on calcification and photosynthesis in the hermatypic coral Acropora eurystoma, Limnol. Oceanogr., 51, 1284–1293, 2006.
Silverman, J., Lazar, B., and Erez, J.: Effect of aragonite saturation, temperature, and nutrients on the community calcification rate of a coral reef, J. Geophys. Res. Oceans, 112(C5), C05004, https://doi.org/10.1029/2006JC003770, 2007.
Silverman, J., Lazar, B., Cao, L., Caldeira, K., and Erez, J.: Coral may start dissolving when atmospheric CO2 doubles, Geophys. Res. Lett., 36, L05606, https://doi.org/10.1029/2008GL036282, 2009.
Smith, S. D.: Coefficients for sea-surface wind stress, heat-flux, and wind profiles as a function of wind-speed and temperature, J. Geophys. Res., 93(C12), 15467–15472, 1988.
Smith, S. V.: Carbon dioxide dynamics: a record of organic carbon production, respiration, and calcification in the Eniwetok reef flat community, Limnol. Oceanogr., 18, 106–120, 1973.
Smith S. V. and Key, G. S.: Carbon dioxide and metabolism in marine environments, Limnol. Oceanogr., 20, 493–495, 1975.
Smith, S. V. and Buddemeier, R. W.: Global change and coral reef ecosystems, Annu. Rev. Ecol. Syst., 23, 89–118, 1992.
Steinberg, D. K, Carlson, C. A., Bates, N. R., Johnson, R. J., Michaels, A. F., and A. H. Knap, A. H.: The US JGOFS Bermuda Atlantic Time-series Study: a decade-scale look at ocean biology and biogeochemistry, Deep-Sea Res. II, 48(8–9), 1405–1447, https://doi.org/10.1016/S0967-0637(99)00052-7, 2001.
Suzuki, A., Nakamori, T., and Kayanne, H.: The mechanism of production enhancement in coral reef carbonate systems: model and empirical results, Sediment. Geol., 99, 259–280, 1995.
Suzuki, A. and Kawahata, H.: Carbon budget of coral reef systems: an overview of observations in fringing reefs, barrier reefs and atolls in the Indo-Pacific regions, Tellus, 55B, 428–444, 2003.
Watt Engineering Ltd.: On the Nature and Distribution of Solar Radiation. US Printing Office Stock No. 016-000-00044-5, March 1978, 1978.
Weis, V. M.: The induction of carbonic anhydrase in the symbiotic sea anemone Aiptasia pulchella, Biol. Bull., 180, 496–504, 1991
Weis, V. M.: Effect of dissolved inorganic carbon concentration on the photosynthesis of the symbiotic sea anemone Aiptasia pulchella Carlgren: role of carbonic anhydrase, J. Exp. Mar. Biol. Ecol., 174, 209–225, 1993.
Weis, V. M. and Reynolds, W. S.: Carbonic anhydrase expression and synthesis in the sea anemone Anthopleura elegantissima are enhanced by the presence of dinoflagellate symbionts, Physiol. Biochem. Zool., 72(3), 307–316, 1999.
Weiss, R. F.: Carbon dioxide in water and seawater; the solubility of a non-ideal gas, Mar. Chem., 2, 203–215, 1974.
Wilkinson, C.: Status of coral reefs of the world: Queensland, Australian Institute of Marine Science, 2000.
Winn, C. D., Li, Y.-H., Mackenzie, F. T., and Karl, D. M.: Rising surface ocean dissolved inorganic carbon at the Hawaii Ocean Time-series site, Mar. Chem., 60, 33–47, 1998.
Wollast, R., Garrels, R. M., and Mackenzie F. T.: Calcite-seawater reactions in ocean surface waters, Am. J. Sci., 280(9), 831–848, 1980.
Yates, K. K. and Halley, R. B.: Measuring coral reef community metabolism using new benthic chamber technology, Coral Reefs, 22, 247–255, 2003.
Yates, K. K. and Halley, R. B.: CO$_{3}^{2-}$ concentration and pCO2 thresholds for calcification and dissolution on the Molokai reef flat, Hawaii, Biogeosciences, 3, 357–369, https://doi.org/10.5194/bg-3-357-2006, 2006.
Zeebe, R. and Wolf-Gladrow, D.: CO2 in Seawater: equilibrium, Kinetics, Isotopes, Elsevier Oceanography Series, 65, 2001.
Download
The requested paper has a corresponding corrigendum published. Please read the corrigendum first before downloading the article.
- Article
(1818 KB) - Metadata XML
Altmetrics
Final-revised paper
Preprint