Ocean Acidification Refugia in Variable Environments

Climate change refugia in the terrestrial biosphere are areas where species are protected from global environmental change and arise from natural heterogeneity in landscapes and climate. Within the marine realm, ocean acidification, or the global decline in seawater pH, remains a pervasive threat to organisms and ecosystems. Natural variability in seawater carbon dioxide (CO2) chemistry, however, presents an opportunity to identify ocean acidification refugia (OAR) for marine species. Here, we review the literature to examine the impacts of variable CO2 chemistry on biological responses to ocean acidification and develop a framework of definitions and criteria that connects current OAR research to management goals. Under the concept of managing vulnerability, the most likely mechanisms by which OAR can mitigate ocean acidification impacts are by reducing exposure to harmful conditions or enhancing adaptive capacity. While local management options such as OAR show some promise, they present unique challenges and reducing global anthropogenic CO2 emissions must remain a priority

Ocean Acidification Refugia in Variable Environments

Climate change refugia in the terrestrial biosphere are areas where species are protected from global environmental change and arise from natural heterogeneity in landscapes and climate. Within the marine realm, ocean acidification, or the global decline in seawater pH, remains a pervasive threat to organisms and ecosystems. Natural variability in seawater carbon dioxide (CO2) chemistry, however, presents an opportunity to identify ocean acidification refugia (OAR) for marine species. Here, we review the literature to examine the impacts of variable CO2 chemistry on biological responses to ocean acidification and develop a framework of definitions and criteria that connects current OAR research to management goals. Under the concept of managing vulnerability, the most likely mechanisms by which OAR can mitigate ocean acidification impacts are by reducing exposure to harmful conditions or enhancing adaptive capacity. While local management options such as OAR show some promise, they present unique challenges and reducing global anthropogenic CO2 emissions must remain a priority

Morphological and Phylogenetic Description of an Unusual Amphidinium (Dinophyceae) Species

Amphidinium carterae, an important harmful algal species that produces powerful antifungal and hemolytic compounds (amphidinols) and cytotoxic macrolides (amphidinolides) is ubiquitous in coastal waters. Samples from coral rubble contained an unusual and previously unreported Amphidinium (D2) with a circular outline. Genetic analysis of clone D2 of this species, involving the sequencing of large subunit (LSU) rDNA, revealed a relationship between Amphidinium sp. D2 and both A. carterae and A. massartii. However, morphological and genetic differences suggest that Amphidinium sp. D2 is not conspecific with A. carterae or A. massartii. Further studies to describe this species are presently underway

Temperature-induced viral resistance in Emiliania huxleyi (Prymnesiophyceae)

© The Author(s), 2014. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in PLoS One 9 (2014): e112134, doi:10.1371/journal.pone.0112134.Annual Emiliania huxleyi blooms (along with other coccolithophorid species) play important roles in the global carbon and sulfur cycles. E. huxleyi blooms are routinely terminated by large, host-specific dsDNA viruses, (Emiliania huxleyi Viruses; EhVs), making these host-virus interactions a driving force behind their potential impact on global biogeochemical cycles. Given projected increases in sea surface temperature due to climate change, it is imperative to understand the effects of temperature on E. huxleyi’s susceptibility to viral infection and its production of climatically active dimethylated sulfur species (DSS). Here we demonstrate that a 3°C increase in temperature induces EhV-resistant phenotypes in three E. huxleyi strains and that successful virus infection impacts DSS pool sizes. We also examined cellular polar lipids, given their documented roles in regulating host-virus interactions in this system, and propose that alterations to membrane-bound surface receptors are responsible for the observed temperature-induced resistance. Our findings have potential implications for global biogeochemical cycles in a warming climate and for deciphering the particular mechanism(s) by which some E. huxleyi strains exhibit viral resistance.This study was supported by funding from the National Science Foundation (OCE-1061883 to KDB, BVM, and OCE-1061876 to GRD) and in part by grants from The Gordon and Betty Moore Foundation (to BVM and KDB)

Hysteresis Between Coral Reef Calcification and the Seawater Aragonite Saturation State

Some predictions of how ocean acidification (OA) will affect coral reefs assume a linear functional relationship between the ambient seawater aragonite saturation state (Ωa) and net ecosystem calcification (NEC). We quantified NEC in a healthy coral reef lagoon in the Great Barrier Reef during different times of the day. Our observations revealed a diel hysteresis pattern in the NEC versus Ωa relationship, with peak NEC rates occurring before the Ωa peak and relatively steady nighttime NEC in spite of variable Ωa. Net ecosystem production had stronger correlations with NEC than light, temperature, nutrients, pH, and Ωa. The observed hysteresis may represent an overlooked challenge for predicting the effects of OA on coral reefs. If widespread, the hysteresis could prevent the use of a linear extrapolation to determine critical Ωa threshold levels required to shift coral reefs from a net calcifying to a net dissolving state

Seasonal Variability of Calcium Carbonate Precipitation and Dissolution in Shallow Coral Reef Sediments

Shallow, permeable calcium carbonate (CaCO3) sediments make up a large proportion of the benthic cover on coral reefs and account for a large fraction of the standing stock of CaCO3. There have been a number of laboratory, mesocosm, and in situ studies examining shallow sediment metabolism and dissolution, but none of these have considered seasonal variability. Advective benthic chambers were used to measure in situ net community calcification (NCC) rates of CaCO3 sediments on Heron Island, Australia (Great Barrier Reef) over an annual cycle. Sediments were, on average, net precipitating during the day and net dissolving at night throughout the year. Night dissolution rates (−NCCNIGHT) were highest in the austral autumn and lowest in the austral winter driven by changes in respiration (R) and to a lesser extent temperature and Ωarag/pH. Similarly, precipitation during the day (+NCCDAY) was highest in March and lowest in winter, driven primarily by benthic net primary production (NPP) and temperature. On average, sediments were net precipitating over a diel cycle (NCC24h) but shifted to net dissolving in July and December. This shift was largely caused by the differential effects of seasonal cycles in organic metabolism and carbonate chemistry on NCCDAY and NCCNIGHT. The results from this study highlight the large variability in sediment CaCO3 dynamics and the need to include repeated measurements over different months and seasons, particularly in shallow reef systems that can experience large swings in light, temperature, and carbonate chemistry

Groundwater and Porewater as Major Sources of Alkalinity to a Fringing Coral Reef Lagoon (Muri Lagoon, Cook Islands)

To better predict how ocean acidification will affect coral reefs, it is important to understand how biogeochemical cycles on reefs alter carbonate chemistry over various temporal and spatial scales. This study quantifies the contribution of shallow porewater exchange (as quantified from advective chamber incubations) and fresh groundwater discharge (as traced by 222Rn) to total alkalinity (TA) dynamics on a fringing coral reef lagoon along the southern Pacific island of Rarotonga over a tidal and diel cycle. Benthic alkalinity fluxes were affected by the advective circulation of water through permeable sediments, with net daily flux rates of carbonate alkalinity ranging from −1.55 to 7.76 mmol m−2 d−1, depending on the advection rate. Submarine groundwater discharge (SGD) was a source of TA to the lagoon, with the highest flux rates measured at low tide, and an average daily TA flux of 1080 mmol m−2 d−1 at the sampling site. Both sources of TA were important on a reef-wide basis, although SGD acted solely as a delivery mechanism of TA to the lagoon, while porewater advection was either a sink or source of TA dependent on the time of day. This study describes overlooked sources of TA to coral reef ecosystems that can potentially alter water column carbonate chemistry. We suggest that porewater and groundwater fluxes of TA should be taken into account in ocean acidification models in order to properly address changing carbonate chemistry within coral reef ecosystems