Description: A late Pleistocene to Holocene submerged and encrusted speleothem exhibits a complex history including a meteoric phase and two marine phases. A combined study using petrography, mineralogy, and inorganic and organic geochemistry, as well as geochronology has shown that phototrophic and heterotrophic biological activity impacted carbonate precipitation during all phases of carbonate accretion. The stalactite formed ca. 30 m below modern sea level at a marginal overhang in the Blue Hole of Lighthouse Reef Atoll. Unlike purely meteoric speleothems, the Belize example consists of a meteoric core, a marine aragonite crust, and a serpulid-micrite-rich outer crust as a result of postglacial flooding of the karst cave. The core of the stalactite has a tufaceous texture, containing algal or microbial remains, and consists entirely of low-magnesium calcite, formed 19.55-10.68 kyr BP. The texture suggests that the stalactite formed at the cave entrance, and, hence, the former cave ceiling had apparently collapsed earlier during the Pleistocene. Oxygen (δ18O) and carbon (δ13C) isotopes across the core suggest a trend towards drier conditions and reduced soil and plant cover after the last glacial maximum. The marine aragonite crust consists of stacked botryoids in which individual crystals up to 700 lm have dark terminations enriched in high-magnesium calcite. This crust accreted from 10.82 to 9.95 kyr BP in warm shallow water during the early Holocene thermal optimum. Carbonate accretion rates were considerable and averaged 125 μm/yr. The crust has a dense, laminated texture on one side and a porous, shrubby texture on the other. The presence of n-C16:1ω5, n-C17:1ω6, and 10Me-C16 fatty acids in the laminated crust suggests that sulfate-reducing bacteria contributed to aragonite formation in an environment that was less open than the formation environment of the porous crust, where these biomarkers are lacking (n-C16:1ω5,n-C17:1ω6) or are less abundant (10Me-C16). Enrichment of 34S and 18O in carbonate-associated sulfate (CAS) relative to seawater sulfate also suggests sulfate reduction during carbonate formation. The greater contribution of heterotrophic processes to aragonite precipitation in the laminated crust is also reflected in δ13C values as low as -1.3%, whereas no such depletion is observed in the aragonite of the porous crust (δ13C values as low as 0.0%). A pronounced isotopic variability and excursions to positive δ13C values as high as +3.5%0 in the inner half of the laminated crust indicate an episodic, local impact of photosynthesis on aragonite precipitation, whereas the lack of such excursions in the porous crust (δ13C values as high as +1.5%0) is again best explained by a more open environment of formation. After a ca. 5 kyr hiatus, from 4.39 kyr BP, a biogenic crust of abundant serpulids and finely crystalline, microbial and detrital carbonate, consisting of high-magnesium calcite and aragonite, accreted on the outer surface of the stalactite. Outermost crust accretion was probably influenced by the inundation of the Lighthouse Reef lagoon that started to shed abundant fine-grained carbonate sediment into the Blue Hole. The stalactite broke off the cave ceiling either before or after the formation of the outermost crust, likely due to seismic movements along the nearby plate boundary. The study demonstrates that like speleothems from the terrestrial realm, submerged stalactites may have had complex histories with great potential as paleoenvironmental archives.

Description: Highlights • First systematic description of Pleistocene facies of the Maldives reveals shallow-water deposits • Only U-series ages from Pleistocene deposits of the Maldives (MIS 5e) • Geochronology and paleo-bathymetric analyses allow estimation of late Quaternary subsidence of this major carbonate platform location to 0.09 - 0.16 m/kyr To date, there is hardly any knowledge of facies and age of Pleistocene reef limestone in the Maldives. Likewise, there are no robust estimates of Quaternary subsidence in this major shallow-water carbonate platform and reef area. In a core recovered on the windward margin of Rasdhoo Atoll in the central part of the archipelago, Pleistocene coralgal grainstone facies belonging to marine isotope stage (MIS) 5e were recovered underlying a Holocene reef succession, 14.5 m below modern sea level. Based on the occurrence of shallow-water stony corals such as Isopora palifera and possibly Acropora gr. robusta, high-energy coralline algae including Porolithon onkodes, in part associated with vermetids, and grain-supported limestone texture, the paleoenvironment is interpreted as a shallow back reef area with a paleo-waterdepth of 〈10 m. Based on a reliable U-series age from a Pleistocene acroporid coral of 136.9 kyr BP and assuming a + 7.5 m higher-than-present peak sea level during MIS 5e, late Quaternary subsidence is estimated to 0.09 m/kyr (minimum)–0.16 m/kyr (maximum value). A sea level of +2.5 m during the early MIS 5e would reduce the rates to 0.05 m/kyr (minimum)–0.12 m/kyr (maximum). These numbers are significant for reconstructions of depositional environments of this major carbonate platform area in the Quaternary. The subsidence estimates are not as crucial for historical reconstruction of relative sea level and for predictions of the near future in this low-lying archipelago, because they will add only a minor portion to the predicted rates of 21st century sea-level rise.

Description: Tropical coral reefs are among the most diverse marine ecosystems. In order to better understand temporal and spatial variation in late Quaternary biodiversity, foraminiferal faunas of two fossil, raised reef terraces at the southern Sinai Peninsula were studied and compared to modern coral reef faunas. Eleven U-series dates of shell fragments of the giant clam Tridacna sp. indicates deposition largely during marine isotope stage 5 (MIS 5), 77–129 kyr BP, for the two raised terraces. In these terraces, Amphistegina (A. lessonii and A. lobifera) dominates the five fossil foraminiferal associations. The fossil reef-flat association 1 has common Gypsina plana, Homotrema rubra and Acervulina spp., and fossil reef-flat association 2 consists of Amphistegina spp. Of the three fossil fore-reef associations, one has abundant porcelaneous taxa including Sorites, Amphisorus, Peneroplis and Borelis, one has a mix of porcelaneous taxa and attached-arborescent taxa (Homotrema and Placopsilina) and one has abundant attached and arborescent taxa (Miniacina, Gypsina, Acervulina and Planogypsina). The modern fringing reef is dominated by porcelaneous foraminifera, and three modern associations are identified. These include a lagoonal association with abundant Peneroplis pertusus, a reef-flat association dominated by Sorites orbiculus and a fore-reef association with porcelaneous taxa plus common H. rubra, Amphistegina lessonii and A. lobifera. Based on our data and including additional published information on regional biodiversity it appears that during MIS 5 foraminiferal biodiversity was higher and community structure was different than within the modern reefs. These data and regional paleo-climate patterns indicate that oceanographic conditions in the Red Sea were probably closer to normal marine conditions during the last interglacial than they are today.

Description: Major changes in community structure and depositional relief of high-latitude coral communities in the southern Persian Gulf between marine isotope stage (MIS) 7 and the present day suggest that the area has become increasingly restricted. Corals and bivalves from outcrops on Kish Island, Iran, were identified in order to interpret the Late Pleistocene palaeoenvironmental setting. U/Th disequilibrium dating was used to constrain the ages of the stratigraphic units. During MIS 7, two coral-bearing sequences were deposited on what is now Kish Island. The lower sequence is dated as MIS 7.5 and changes laterally from an assemblage dominated by Cyphastrea sp. and Platygyra daedalea in the west to one characterized by branching Montipora in the east. By contrast, the upper sequence, dated as MIS 7.1, transitions from an assemblage dominated by platy Montipora in the west to a diverse assemblage of Platygyra and other faviids in the east. The assemblages of both sequences are within a marl matrix and bounded by thin lithified mollusc-rich layers. Corals and bivalves indicate that the sequences were deposited on gentle slopes in sheltered environments less than 20 m deep. The MIS 7 deposits may be classified as coral carpets or biostromes that developed a low-relief framework. During MIS 5, coral communities were no longer framework building and are now limited to an Acropora-rich layer of coral rubble that covers large parts of the island, and two small incipient reefs with sparse faviids. Similarities between the MIS 5 and modern nearshore coral communities suggest that the environmental conditions during MIS 5 were comparable to those of today. The late Pleistocene coral carpets and non-framework coral communities of the southern Persian Gulf may serve as models for coral biostromes in the fossil record, which formed under restricted environmental conditions such as elevated terrigenous input, high turbidity, and strong seasonal changes in temperature and/or salinity.

Description: The universally known subsidence theory of Darwin, based on Bora Bora as a model, was developed without information from the subsurface. To evaluate the influence of environmental factors on reef development, two traverses with three cores, each on the barrier and the fringing reefs of Bora Bora, were drilled and 34 uranium-series dates obtained and subsequently analysed. Sea-level rise and, to a lesser degree, subsidence were crucial for Holocene reef development in that they have created accommodation space and controlled reef architecture. Antecedent topography played a role as well, because the Holocene barrier reef is located on a Pleistocene barrier reef forming a topographic high. The pedestal of the fringing reef was Pleistocene soil and basalt. Barrier and fringing reefs developed contemporaneously during the Holocene. The occurrence of five coralgal assemblages indicates an upcore increase in wave energy. Age–depth plots suggest that barrier and fringing reefs have prograded during the Holocene. The Holocene fringing reef is up to 20 m thick and comprises coralgal and microbial reef sections and abundant unconsolidated sediment. Fringing reef growth started 8780 ± 50 yr bp; accretion rates average 5·65 m kyr−1. The barrier reef consists of 〉30 m thick Holocene coralgal and microbial successions. Holocene barrier-reef growth began 10 030 ± 50 yr bp and accretion rates average 6·15 m kyr−1. The underlying Pleistocene reef formed 116 900 ± 1100 yr bp, i.e. during marine isotope stage 5e. Based on Pleistocene age, depth and coralgal palaeobathymetry, the subsidence rate of Bora Bora was estimated to be 0·05 to 0·14 m kyr−1. In addition to subsidence, reef development on shorter timescales like in the late Pleistocene and Holocene has been driven by glacioeustatic sea-level changes causing alternations of periods of flooding and subaerial exposure. Comparisons with other oceanic barrier-reef systems in Tahiti and Mayotte exhibit more differences than similarities.

Description: Holocene fringing reef development around Bora Bora is controlled by variations in accommodation space (as a function of sea-level and antecedent topography) and exposure to waves and currents. Subsidence ranged from 0 to 0·11 m kyr−1, and did not create significant accommodation space. A windward fringing reef started to grow 8·7 kyr bp, retrograded towards the coast over a Pleistocene fringing reef until ca 6·0 kyr bp, and then prograded towards the lagoon after sea-level had reached its present level. The retrograding portion of the reef is dominated by corals, calcareous algae and microbialite frameworks; the prograding portion is largely detrital. The reef is up to 13·5 m thick and accreted vertically with an average rate of 3·12 m kyr−1. Lateral growth amounts to 13·3 m kyr−1. Reef corals are dominated by an inner Pocillopora assemblage and an outer Acropora assemblage. Both assemblages comprise thick crusts of coralline algae. Palaeobathymetry suggests deposition in 0 to 10 m depth. An underlying Pleistocene fringing reef formed during the sea-level highstand of Marine Isotope Stage 5e, and is also characterized by the occurrence of corals, coralline algal crusts and microbialites. A previously investigated, leeward fringing reef started to form contemporaneously (8·78 kyr bp), but is thicker (up to 20 m) and solely prograded throughout the Holocene. A shallow Pocillopora assemblage and a deeper water Montipora assemblage were identified, but detrital facies dominate. At the Holocene reef base, only basalt was recovered. The Holocene windward–leeward differences are a consequence of less accommodation space on the eastern island side that eventually led to a more complex reef architecture. As a result of higher rates of exposure and flushing, the reef framework on the windward island side is more abundant and experienced stronger cementation. In the Pleistocene, the environmental conditions on the leeward island side were presumably unfavourable for fringing reef growth.

Description: New sedimentological data of facies and diagenesis as well as chronological data including strontium (87Sr/86Sr)-isotope ratios and uranium (U)-series dating, radiocarbon (14C) accelerator mass spectrometry (AMS) dating and biostratigraphy from elevated reef terraces (makatea) in the southern Cook Islands of Mangaia, Rarotonga and Aitutaki contribute to controversial discussions regarding age and sea-level relationships of these occurrences during the Neogene and Quaternary. The oldest limestones of the uplifted makatea island of Mangaia include reef-related facies which are mid-Miocene in age, based on new Sr-isotope and biostratigraphical data. In between these older deposits and the lowest coastal reef terrace of marine isotope stage (MIS) 5e, various older Pleistocene reef-related facies were identified. Based on Sr-isotope ratios, these were deposited during earlier Pleistocene highstands (as old as 2.28 Ma). Rare reef terraces on Rarotonga belong to the Plio-Pleistocene and the late Miocene, according to 87Sr/86Sr ratios. The late Miocene age is enigmatic as it exceeds the age of subaerially exposed volcanic rocks of Rarotonga island. The fossil reef could have formed on an older submarine volcanic high that was later displaced by younger volcanism to its present position, or the Sr-age could be too old due to diagenetic resetting. The Plio-Pleistocene Rarotonga reef terraces are overlain irregularly by Holocene reef deposits that are interpreted as storm rubble. Reef terraces on Aitutaki represent evidence of a higher-than-present (up to 1 m) sea-level during the late Holocene, based on 14C AMS age data. They are very similar to elevated late Holocene reefs of adjacent French Polynesia with regard to composition, elevation and age.

Description: Microbial carbonates are common components of Quaternary tropical coral reefs. Previous studies revealed that sulfate-reducing bacteria trigger microbial carbonate precipitation in supposedly cryptic reef environments. Here, using petrography, lipid biomarker analysis, and stable isotope data, we aim to understand the formation mechanism of microbial carbonate enclosed in deep fore reef limestones from Mayotte and Mohéli, Comoro Islands, which differ from other reefal microbial carbonates in that they contain less microbial carbonate and are dominated by numerous sponges. To discern sponge-derived lipids from lipids enclosed in microbial carbonate, lipid biomarker inventories of diverse sponges from the Mayotte and Mohéli reef systems were examined. Abundant peloidal, laminated, and clotted textures point to a microbial origin of the authigenic carbonates, which is supported by ample amounts of mono- O -alkyl glycerol monoethers (MAGEs) and terminally branched fatty acids; both groups of compounds are attributed to sulfate-reducing bacteria. Sponges revealed a greater variety of alkyl chains in MAGEs, including new, previously unknown, mid-chain monomethyl- and dimethyl-branched MAGEs, suggesting a diverse community of sulfate reducers different from the sulfate-reducers favoring microbialite formation. Aside from biomarkers specific for sulfate-reducing bacteria, lipids attributed to demosponges (i.e., demospongic acids) are also present in some of the sponges and the reefal carbonates. Fatty acids attributed to demosponges show a higher diversity and a higher proportion in microbial carbonate compared to sponge tissue. Such pattern reflects significant taphonomic bias associated with the preservation of demospongic acids, with preservation apparently favored by carbonate authigenesis.

Description: Tropical coral reefs, as prominent marine diversity hotspots, are in decline, and long-term studies help to improve understanding of the effects of global warming, sea-level rise, ocean acidification, deterioration of water quality, and disease. Here, we evaluated relative coral abundance and reef accretion rates over the past 9000 years in Belize barrier and atoll reefs, the largest reef system in the Atlantic Ocean. Acropora palmata and Orbicella spp. have been the most common corals. The abundance of competitive, fast-growing acroporids was constant over multi-millennial timescales. A decline in A. cervicornis abundance, however, and three centennial-scale gaps in A. palmata occurrence, suggest that the modern decline in acroporids was not unprecedented. Stress-tolerant corals predominate at the beginning of Holocene successions. Following the improvement of environmental conditions after inundation of the reef pedestal, their abundance has decreased. The abundance of weedy corals has increased during the Holocene underlining the importance of fecundity for the coral community. Reef-accretion rate, as calculated based on 76 new U-series age dates, has decreased over the Holocene and the mean value of 3.36 m kyr −1 is at the lower end of global reef growth compilations and predicted future rates of rise in sea level.