Seawater carbonate chemistry, productivity and calcification of Marginopora vertebralis in a laboratory experiment

Changes in the seawater carbonate chemistry (ocean acidification) from increasing atmospheric carbon dioxide (CO2 ) concentrations negatively affect many marine calcifying organisms, but may benefit primary producers under dissolved inorganic carbon (DIC) limitation. To improve predictions of the ecological effects of ocean acidification, the net gains and losses between the processes of photosynthesis and calcification need to be studied jointly on physiological and population levels. We studied productivity, respiration, and abundances of the symbiont-bearing foraminifer species Marginopora vertebralis on natural CO2 seeps in Papua New Guinea and conducted additional studies on production and calcification on the Great Barrier Reef (GBR) using artificially enhanced pCO2 . Net oxygen production increased up to 90% with increasing pCO2 ; temperature, light, and pH together explaining 61% of the variance in production. Production increased with increasing light and increasing pCO2 and declined at higher temperatures. Respiration was also significantly elevated (~25%), whereas calcification was reduced (16-39%) at low pH/high pCO2 compared to present-day conditions. In the field, M. vertebralis was absent at three CO2 seep sites at pHTotal levels below ~7.9 (pCO2 ~700 µatm), but it was found in densities of over 1000 m(-2) at all three control sites. The study showed that endosymbiotic algae in foraminifera benefit from increased DIC availability and may be naturally carbon limited. The observed reduction in calcification may have been caused either by increased energy demands for proton pumping (measured as elevated rates of respiration) or by stronger competition for DIC from the more productive symbionts. The net outcome of these two competing processes is that M. vertebralis cannot maintain populations under pCO2 exceeding 700 µatm, thus are likely to be extinct in the next century.

Geochemistry and stable isotope record of carbonate oozes and chalks of ODP Hole 130-807B

Light greenish gray and pale purple color bands are common in the ooze and chalk of the Ontong Java Plateau. Analyses of Pleistocene and Pliocene ooze samples that contain abundant bands indicate that the purple bands are colored by finely disseminated iron sulfide, whereas the green bands are colored by finely disseminated Fe- and Al-bearing silicates (probably clays). No local contrasts in the total organic carbon contents, carbon and oxygen isotopic compositions, and grain sizes were found. Band abundances, counted from core photographs of all Leg 130 holes, can be correlated from hole to hole on the basis of age rather than depth. The temporal distribution of these color bands is also comparable with that of the green bands described from the Lord Howe Rise, which were previously interpreted as products of altered volcanic glass. This may indicate that the green and purple bands on the Ontong Java Plateau originate from the early alteration of volcanic ash. The crosscutting relationships between the green and purple bands and original structures in the host sediment indicate that the bands have been locally altered by redox conditions in the sediments after the bands were formed.

Calcium carbonate stratigraphy of ODP Site 177-1090

A total of 776 sediment samples were measured for percent CaCO3 using a coulometer. These data are compared with percent blue reflectance (450-550 nm) measured with the Oregon State University split-core analysis track. In previous studies percent blue reflectance has been an excellent proxy for percent CaCO3 and in this study shows many of the main depositional trends (i.e., a 100-k.y. cycle, with a 55% reflectance range is evident in the upper 900 k.y., underlain by sediments exhibiting a 40-k.y. cycle with only a 30% reflectance range). Between ~21 and 5 Ma the average percent reflectance decreases from ~35% to ~8%. A similar decrease is also recorded between ~24 and 22 Ma. Percent CaCO3 trends closely match those of the percent blue spectral reflectance. This is especially well shown in the 100-k.y. cyclicity and in the interval between 24.5 and 21.5 Ma. In both intervals CaCO3 analyses are abundant. An exception occurs in the interval between 2 and 5 meters composite depth (~193 and 240 k.y.). There, percent CaCO3 and percent reflectance are out of phase. The lack of agreement is not likely to be due to a very wet core, in which water would dominate the spectral reflectance instead of sediment, or to problems with the composite depth slice. The discrepancy remains unexplained and provides clear evidence that when noninvasive measurements are used as proxies for chemical measurements they must be substantiated by the actual chemical or physical measurements.

Orbital control on carbonate-lignite cycles on sediment core KAP-107 in the Ptolemais Basin, northern Greece

Time control is essential for the reconstruction of geological processes. We use a combination of relative and absolute methods to establish the chronology and related paleoclimatic processes for Late Neogene lacustrine sediment from the Ptolemais Basin, northern Greece. We determined changes in magnetic polarity and correlated them to the global magnetic polarity time scale, which again is calibrated by radiometric methods, to provide a low-resolution age model for the Upper Miocene to Lower Pliocene (7 - 3 Ma). Sedimentary successions show rhythmic alterations of lignites, clays, and marls. Using photospetrometry we measured this variability at 1-cm resolution, and correlated the pattern to known changes in earth's orbital parameters, namely to eccentricity and precession. For 230-m long borehole KAP-107 from the Amynteon Sub-Basin we obtained a high-resolution age model that spans 2 myr from 5.1 to 3.1 Ma, with age control points at insolation maxima (20-kyr resolution). We recommend using photospectrometry as reliable tool to establish orbital-based chronologies and to reconstruct paleoclimate variability at high resolution.