Biological ocean data collected from ships find reuse in aggregations of historical data. These data are heavily relied upon to document long term change, validate satellite algorithms for ocean biology and are useful in assessing the performance of autonomous platforms and biogeochemical models. Existing aggregate products have largely been restricted to the surface ocean, omit physical data or have limited biological data. We present the first version of a BIOlogical ocean data reforMATting Effort (BIO-MATE) to begin to fill a gap in subsurface bio-physical data aggregates in a reproducible way. BIO-MATE uses open-source R software that reformats openly sourced published datasets from oceanographic voyages. These reformatted biological and physical data from underway sensors, profiling sensors, pigments analysis and particulate organic carbon analysis are stored in an interoperable BIO-MATE data product for easy access and use. Specific QA/QC protocols can now be easily applied to the BIO-MATE data product to support a variety of surface and subsurface applications.

The equatorial Pacific is the largest oceanic source of carbon dioxide to the atmosphere. This outgassing varies depending on the El Niño‐Southern Oscillation (ENSO) and decadal climate variability. New production, the amount of phytoplankton net primary production driven by upwelled nitrate, plays a significant role in modulating air‐sea CO2 fluxes as the biological carbon pump removes carbon from the surface ocean. We aim to understand how the physical drivers of sea surface temperature and wind speed influence interannual and decadal variability of the equatorial Pacific carbon cycle. In the equatorial Pacific, there are three biogeochemical regimes: the upwelling cold tongue east of 140°W and south of the equator (3°N–15°S); the eastern Pacific warm pool north of the equator (3°–15°N); and the 28.5°C western Pacific warm pool, west of 140°W. We find that between 2000 and 2020, air‐sea CO2 flux and ΔpCO2 increased in the cold tongue (45 mmolC m−2 yr−2, 1.5 μatm yr−1, respectively) but decreased elsewhere, while new production decreased everywhere. The western Pacific occasionally became a weak carbon sink, depending on ENSO and this sink was strongest at 165°E during central Pacific “Modoki” El Niño events. We find that changes in wind speed, temperature and ENSO frequency have altered the surface carbon budget. The mean basin‐wide (150°E−90°W and 15°N–15°S) new production for 2000–2020 was 1.2 ± 0.1 PgC yr−1 and air‐sea CO2 flux was 0.5 ± 0.1 PgC yr−1. New production decreased at −7.7 ± 1.6 TgC yr−2, compared to the CO2 flux trend of −1.7 ± 1.4 TgC yr−2.

During the Last interglacial period of constant sea level, large coral reefs formed on the tectonically rising island of Barbados, and a broad lagoon with a small barrier reef formed at the Cane Vale site. The constant sea level was ended by a rapid glaciation, causing a fall of world sea level of 2.4 m, as measured by surveys of features associated with breaking waves on Barbados. The fall began about 120 ka BP, and lasted roughly 400 years, according to a lake pollen record from western Europe. That rapid fall was terminated at a wave-cut step on Barbados and with a quite small reversal in falling sea level. The rise was caused by rapid melting of the marine-based Barents Sea ice dome and other ice masses, due to a restored strong Atlantic Meridional Overturning Circulation (AMOC) flow. The sea level fall then resumed until it was halted at a wave-cut step at a world sea level 12.3 m below the last interglacial level, as recorded at the University of the West Indies site on Barbados. Following the erosion of that second step, a zonal northern North Atlantic circulation prevailed, causing a glacial ice-volume decrease and rise in sea level of 3.8 m. These two sea level fall reversals were caused respectively by the formation and destruction of a Hudson Strait ice dam and the resulting increase and much later decrease in the rate of AMOC flow.

Antarctic krill ( Euphausia superba ) are a key component of the Antarctic food web with considerable lipid reserves that are vital for their health and higher predator survival. Krill lipids are primarily derived from their diet of plankton, in particular diatoms and flagellates. Few attempts have been made to link the spatial and temporal variations in krill lipids to those in their food supply. Remotely-sensed environmental parameters provide large-scale information on the potential availability of krill food, although relating this to physiological and biochemical differences has only been performed on small scales and with limited samples. Our study utilised remotely-sensed data (chlorophyll a and sea surface temperature) coupled with krill lipid data obtained from 3 years of fishery-derived samples. We examined within and between year variation of trends in both the environment and krill biochemistry data. Chlorophyll a levels were positively related to krill lipid levels, particularly triacylglycerol. Plankton fatty acid biomarkers analysed in krill (such as n-3 polyunsaturated fatty acids) increased with decreasing sea surface temperature and increasing chlorophyll a levels. Our study demonstrates the utility of combining remote-sensing and biochemical data in examining biological and physiological relationships between Antarctic krill and the Southern Ocean environment.

The tropical Pacific Ocean is a globally significant region of climate‐driven biogeochemical variability. Satellite ocean color algorithms have been used for over 20 years, providing a substantial historical record of global ocean chlorophyll‐a variability. Current chlorophyll algorithms perform better in the tropical Pacific than for the globe. Nevertheless, improvements can be made to produce a robust historical record of chlorophyll variability, which is essential to accurately identify ocean‐atmosphere carbon fluxes and long‐term trends in ocean productivity. We use a large in situ chlorophyll database to tune empirical ocean color algorithms to reduce bias in the equatorial Pacific. Traditional band ratio chlorophyll algorithms (OCx) perform adequately but exhibit errors at low chlorophyll concentrations. A new algorithm, the Ocean Color Index (OCI; Hu et al., 2012, https://doi.org/10.1029/2011JC007395), is more effective at calculating low chlorophyll concentrations in the mesotrophic tropical Pacific Ocean. Existing ocean color algorithms underestimate tropical Pacific chlorophyll by 5.8%, 14%, and 2% for three satellite ocean color sensors: SeaWiFS, MODIS‐Aqua, and MERIS. In this paper, we develop regionally tuned sensor‐specific coefficients and blending windows between the OCI to OCx algorithms to reduce systematic biases in the tropical Pacific. We assess cross‐sensor consistency to produce robust 21‐year time series trends. These updated estimates increase chlorophyll concentrations in open water and decrease around island and warm‐pool regions, with implications for our understanding of El Nino‐Southern Oscillation driven carbon fluxes and net primary productivity.

This review represents the Southern Ocean community's satellite data needs for the coming decade. Developed through widespread engagement and incorporating perspectives from a range of stakeholders (both research and operational), it is designed as an important community-driven strategy paper that provides the rationale and information required for future planning and investment. The Southern Ocean is vast but globally connected, and the communities that require satellite-derived data in the region are diverse. This review includes many observable variables, including sea ice properties, sea surface temperature, sea surface height, atmospheric parameters, marine biology (both micro and macro) and related activities, terrestrial cryospheric connections, sea surface salinity, and a discussion of coincident and in situ data collection. Recommendations include commitment to data continuity, increases in particular capabilities (sensor types, spatial, temporal), improvements in dissemination of data/products/uncertainties, and innovation in calibration/validation capabilities. Full recommendations are detailed by variable as well as summarized. This review provides a starting point for scientists to understand more about Southern Ocean processes and their global roles, for funders to understand the desires of the community, for commercial operators to safely conduct their activities in the Southern Ocean, and for space agencies to gain greater impact from Southern Ocean-related acquisitions and missions.

The impacts of anthropogenic enhancement of the partial pressure of carbon dioxide (pCO(2)) on marine organisms remain unclear, especially in Antarctic waters, which are predicted to be amongst the earliest and most severely affected by the consequent changes in ocean chemistry. Marine microbes are the base of the Antarctic food chain, and the nature of their response to elevated pCO(2) is important as they are key determinants of the biogeochemical cycles that affect global climate. We studied the response of a natural community of Antarctic marine microbes from near-shore waters off Davis Station, Antarctica, to pCO(2) ranging from the concentration in the water column at the time the experiment began (ambient, 84 mu atm) to that predicted by the year 2300 (2423 mu atm) using 6 gas-tight, environmentally controlled tanks (minicosms; 650 l) to which CO2-saturated seawater was added. The microbial community showed little difference between 84 and 643 mu atm CO2 (0.2 to 1.7 times present), indicating that they can tolerate the large seasonal range in pCO(2) in Antarctic coastal waters. Concentrations >= 1281 mu atm reduced the accumulation rate of chlorophyll and particulate carbon, changed the microbial community, and enhanced the relative abundance of small phytoplankton. If our results are indicative of the future responses of Antarctic marine microbes, elevated CO2 could profoundly affect the structure and function of the Antarctic food web by reducing the availability of food for higher trophic levels and decreasing the efficiency of the biological pump.

Sea ice is an influential feature in Southern Ocean-Antarctic marine environments creating a 2-phase vertical ecosystem. The lack of information on how this system influences community structure during the winter-spring transition, however, is largely lacking. Zooplankton form the link that bridges these environments, with the meiofaunal and algal communities within sea ice directly influencing the epipelagic zooplankton community at the ice-water interface. A combination of methods including sea-ice coring, umbrella net sampling and Laser Optical Plankton Counter were used to describe the vertical structure of zooplankton and meiofaunal communities. The distribution of meiofauna and chlorophyll a both played important roles in structuring the zooplankton community within this dynamic region. Many dominant taxa, including Calanus propinquus and Oithona similis, directly responded to the high availability of algae present within the bottom strata of sea ice. The sea-ice associated species Stephos longipes represented a strong link between this 2-phase ecosystem. Observations of the vertical distribution of biomass obtained from the LOPC suggests that the responses of these species to the sea ice directly influences the vertical structure of zooplankton during the winter-spring transition.

Remote sensing of Southern Ocean chlorophyll concentrations is the most effective way to detect large-scale changes in phytoplankton biomass driven by seasonality and climate change. However, the current algorithms for the Sea-viewing Wide Field-of-view Sensor (SeaWiFS, algorithm OC4v6), the Moderate Resolution Imaging Spectroradiometer (MODIS-Aqua, algorithm OC3M), and GlobColour significantly underestimate chlorophyll concentrations at high latitudes. Here, we use a long-term data set from the Southern Ocean (20 degrees-160 degrees E) to develop more accurate algorithms for all three of these products in southern high-latitude regions. These new algorithms improve in situ versus satellite chlorophyll coefficients of determination (r(2)) from 0.27 to 0.46, 0.26 to 0.51, and 0.25 to 0.27, for OC4v6, OC3M, and GlobColour, respectively, while addressing the underestimation problem. This study also revealed that pigment composition, which reflects species composition and physiology, is key to understanding the reasons for satellite chlorophyll underestimation in this region. These significantly improved algorithms will permit more accurate estimates of standing stocks and more sensitive detection of spatial and temporal changes in those stocks, with consequences for derived products such as primary production and carbon cycling.

All photosynthetic organisms endeavor to balance energy supply with demand. For sea‐ice diatoms, as with all marine photoautotrophs, light is the most important factor for determining growth and carbon‐fixation rates. Light varies from extremely low to often relatively high irradiances within the sea‐ice environment, meaning that sea‐ice algae require moderate physiological plasticity that is necessary for rapid light acclimation and photoprotection. This study investigated photoprotective mechanisms employed by bottom Antarctic sea‐ice algae in response to relatively high irradiances to understand how they acclimate to the environmental conditions presented during early spring, as the light climate begins to intensify and snow and sea‐ice thinning commences. The sea‐ice microalgae displayed high photosynthetic plasticity to increased irradiance, with a rapid decline in photochemical efficiency that was completely reversible when placed under low light. Similarly, the photoprotective xanthophyll pigment diatoxanthin (Dt) was immediately activated but reversed during recovery under low light. The xanthophyll inhibitor dithiothreitol (DTT) and state transition inhibitor sodium fluoride (NaF) were used in under‐ice in situ incubations and revealed that nonphotochemical quenching (NPQ) via xanthophyll‐cycle activation was the preferred method for light acclimation and photoprotection by bottom sea‐ice algae. This study showed that bottom sea‐ice algae from the east Antarctic possess a high level of plasticity in their light‐acclimation capabilities and identified the xanthophyll cycle as a critical mechanism in photoprotection and the preferred means by which sea‐ice diatoms regulate energy flow to PSII.

WIKLIAMS'S subdivision of calderas into ‘Krakatoan’ and ‘Glen Coe’ types1 has been the subject of recent discussion2–4. Williams's concept of the ‘Krakatoan’ mechanism is that explosive eruption of pumiceous volcanic products from the vents of a central-type volcano produces a void in the underlying magma chamber; the unsupported chamber roof then collapses, producing a caldera at surface level bounded by a ring-fault escarpment. The ‘Glen Coe’ type, on the other hand, is said to involve the stoping of magma up ring fractures and the coeval descent of the enclosed cylindrical block.