Sinking of Gelatinous Zooplankton Biomass Increases Deep Carbon Transfer Efficiency Globally

Gelatinous zooplankton (Cnidaria, Ctenophora, and Urochordata, namely, Thaliacea) are ubiquitous members of plankton communities linking primary production to higher trophic levels and the deep ocean by serving as food and transferring “jelly‐carbon” (jelly‐C) upon bloom collapse. Global biomass within the upper 200 m reaches 0.038 Pg C, which, with a 2–12 months life span, serves as the lower limit for annual jelly‐C production. Using over 90,000 data points from 1934 to 2011 from the Jellyfish Database Initiative as an indication of global biomass (JeDI: http://jedi.nceas.ucsb.edu, http://www.bco‐dmo.org/dataset/526852), upper ocean jelly‐C biomass and production estimates, organism vertical migration, jelly‐C sinking rates, and water column temperature profiles from GLODAPv2, we quantitatively estimate jelly‐C transfer efficiency based on Longhurst Provinces. From the upper 200 m production estimate of 0.038 Pg C year−1, 59–72% reaches 500 m, 46–54% reaches 1,000 m, 43–48% reaches 2,000 m, 32–40% reaches 3,000 m, and 25–33% reaches 4,500 m. This translates into ~0.03, 0.02, 0.01, and 0.01 Pg C year−1, transferred down to 500, 1,000, 2,000, and 4,500 m, respectively. Jelly‐C fluxes and transfer efficiencies can occasionally exceed phytodetrital‐based sediment trap estimates in localized open ocean and continental shelves areas under large gelatinous blooms or jelly‐C mass deposition events, but this remains ephemeral and transient in nature. This transfer of fast and permanently exported carbon reaching the ocean interior via jelly‐C constitutes an important component of the global biological soft‐tissue pump, and should be addressed in ocean biogeochemical models, in particular, at the local and regional scale

RV POSEIDON Cruise Report POS473 LORELEI II: LOphelia REef Lander Expedition and Investigation II, Tromsø – Bergen – Esbjerg, 15.08. – 31.08. – 04.09.2014

As a result of the raising CO2-emissions and the resultant ocean acidification (decreasing pH and carbonate ion concentration), the impact on marine organism that build their skeletons and protective shells with calcium carbonate (e.g., mollusks, sea urchins, coccolithophorids, and stony corals) becomes more and more detrimental. In the last few years, many experiments with tropical reef building corals have shown, that a lowering of the carbonate ion concentration significantly reduces calcification rates and therefore growth (e.g., Gattuso et al. 1999; Langdon et al. 2000, 2003; Marubini et al. 2001, 2002). In the middle of this century, many tropical coral reefs may well erode faster than they can rebuild. Cold-water corals are living in an environment (high geographical latitude, cold and deep waters) already close to a critical carbonate ion concentration below calcium carbonate dissolves. Actual projections indicate that about 70% of the currently known Lophelia reef structures will be in serious danger until the end of the century (Guinotte et al. 2006). Therefore L. pertusa was cultured at GEOMAR to determine its long-term response to ocean acidification. Our work has revealed that – unexpectedly and controversially to the majority of warm-water corals – this species is potentially able to cope with elevated concentrations of CO2. Whereas short-term (1 week) high CO2 exposure resulted in a decline of calcification by 26-29 % for a pH decrease of 0.1 units and net dissolution of calcium carbonate, L. pertusa was capable to acclimate to acidified conditions in long-term (6 months) incubations, leading to slightly enhanced rates of calcification (Form & Riebesell, 2012). But all these studies were carried out in the laboratory under controlled conditions without considering natural variability and ecosystem interactions with the associated fauna. Moreover, only very little is known about the nutrition (food sources and quantity) of cold-water corals in their natural habitat. In a multifactorial laboratory study during BIOACID phase II we could show that food availability is one of the key drivers that promote the capability of these organisms to withstand environmental pressures such as alterations in the carbonate chemistry and temperature (Büscher, Form & Riebesell, in prep.). To take into account the influences of natural fluctuations and interactions (e.g. bioerosion), we aim to merge in-situ results from the two research cruises POS455 and POS473 with laboratory experimental studies for a comprehensive understanding of likely ecosystem responses under past, present and future environmental conditions

Global variability in seawater Mg:Ca and Sr:Ca ratios in the modern ocean

Seawater Mg:Ca and Sr:Ca ratios are biogeochemical parameters reflecting the Earth–ocean–atmosphere dynamic exchange of elements. The ratios’ dependence on the environment and organisms' biology facilitates their application in marine sciences. Here, we present a measured single-laboratory dataset, combined with previous data, to test the assumption of limited seawater Mg:Ca and Sr:Ca variability across marine environments globally. High variability was found in open-ocean upwelling and polar regions, shelves/neritic and river-influenced areas, where seawater Mg:Ca and Sr:Ca ratios range from ∼4.40 to 6.40 mmol:mol and ∼6.95 to 9.80 mmol:mol, respectively. Open-ocean seawater Mg:Ca is semiconservative (∼4.90 to 5.30 mol:mol), while Sr:Ca is more variable and nonconservative (∼7.70 to 8.80 mmol:mol); both ratios are nonconservative in coastal seas. Further, the Ca, Mg, and Sr elemental fluxes are connected to large total alkalinity deviations from International Association for the Physical Sciences of the Oceans (IAPSO) standard values. Because there is significant modern seawater Mg:Ca and Sr:Ca ratios variability across marine environments we cannot absolutely assume that fossil archives using taxa-specific proxies reflect true global seawater chemistry but rather taxa- and process-specific ecosystem variations, reflecting regional conditions. This variability could reconcile secular seawater Mg:Ca and Sr:Ca ratio reconstructions using different taxa and techniques by assuming an error of 1 to 1.50 mol:mol, and 1 to 1.90 mmol:mol, respectively. The modern ratios’ variability is similar to the reconstructed rise over 20 Ma (Neogene Period), nurturing the question of seminonconservative behavior of Ca, Mg, and Sr over modern Earth geological history with an overlooked environmental effect

Correction for Lebrato et al., Global variability in seawater Mg:Ca and Sr:Ca ratios in the modern ocean

4 pages, 5 figures.-- Correction Global variability in seawater Mg:Ca and Sr:Ca ratios in the modern ocean; Proceedings of the National Academy of Sciences of the USA 117(36): 22281-22292 (2020); doi: 10.1073/pnas.1918943117; http://hdl.handle.net/10261/221953The authors wish to note the following: “This study’s seawater Sr:Ca values were systematically low as a consequence of normalization to another published low value for the International Association for the Physical Sciences of the Oceans (IAPSO) (1). IAPSO has been used at the Ocean Drilling Program, Texas A&M University (ODP-TAMU) (http://www-odp.tamu.edu/), and is still being used as the primary standard for elemental composition of seawater/interstitial water. Consequently, our seawater value of Sr:Ca = 8.28 mmol:mol was systematically low by approx. 3.70%, if we accept seawater Sr:Ca 8.60 mmol:mol as the recommended value for IAPSO North Atlantic surface water salinity standard. The uncertainty budget should be expanded including the uncertainty of IAPSO composition. The largest contribution to expanded uncertainty of our data comes from the uncertainty of the IAPSO reference composition, which is 3.29% using all published values. This will result in 3.30% (1 SD) expanded uncertainty for seawater Sr:Ca (and 0.5%, for seawater Mg:Ca) of the entire data set with respect to accuracy. We have corrected all seawater Sr:Ca values with a factor of 1.0243 in all our tables (e.g., SI Appendix, Table S1 averages) and in the figures (Fig. 4, Fig. 5), where a ratio was used. Note that the seawater Sr:Ca % changes are small, thus changes are hardly noticeable on large displays (e.g., Figures), but they can be seen in the tables and averages/SD calculations. Seawater Sr:Ca ratios are also corrected in the main text where relevantPeer reviewe

Oxygen consumption and polyp extension rates of the scleractinian cold-water coral Lophelia pertusa under different CO2 end-of-the-century scenarios

The scleractinian coral Lophelia pertusa forms large reefs and provides habitat for a huge number of associated species. These ecosystems are often described as biomass and biodiversity hotspots. Thus, the ecological relevance of this species is very high. Due to destruction by bottom trawling and hydrocarbon mining, these reefs are in danger. Additionally, they are endangered by climate change. The rise of temperature and the decrease in seawater pH are known to especially affect calcifying organisms. Since the industrial time, the ocean pH decreased from values around 8.2 to circa 8.1 and for the end of the century another 0.3 to 0.4 pH units of decrease is expected. The performed study dealed with mid-term physiological responses of the cold-water coral Lophelia pertusa in terms of shifts in oxygen consumption and behavior towards elevated carbon dioxide concentrations. The behavior of the corals was documented via 24 hours video observation and the polyp extension rates of single polyps were analyzed. Five replicates were kept under control conditions (8°C; 390 μatm pC02 ), while another five replicates ran through three successive elevated C02 scenarios (800 μatm/1000 μatm/1200 μatm). Each phase lasted 5 weeks, including one week of acclimatization and four following weeks of measurements. Each replicate was equipped with one coral fragment of a white color morph of L. pertusa and one coral fragment of a red color morph of L. pertusa, in order to estimate if the two color morphs occurring in Norwegian waters differ in physiological responses towards elevated pC02 conditions. Slight elevations of respiration rates in the red color morph were recognized, but were not approved to be significant. Respiration rates recorded for the control treatment ranged from 0.112 to 0.191 μmol 02 g -1 dry weight h-1 for the white color morph and from 0.114 to 0.238 μmol 02 g-1 dry weight h-1 for the red color morph. Respiration rates of the elevated treatment did not differ significantly from control values ( on average 0.185 μmol 02 g-1 dry weight h-1 for the white color morph and 0.204 μmol 02 g-1 dry weight h-1 for the red color morph). Corals might have acclimatized to changing conditions. Polyp extension rates of white corals in turn changed with increasing pC02 conditions. Mean polyp extension rates of the control were 24 ± 3 % throughout the entire experiment, while extension rates of the elevated treatment increased by 75 % during the first elevated pC02 phase and decreased down to 50 % of control values during the following phases of the experiment. This study shows that elevated pC02 conditions influence the behavior in terms of polyp extension rates of L. pertusa, but that respiration rates can be maintained during a mid-term period exposure to elevated pC02 conditions

Global variability in seawater Mg:Ca and Sr:Ca ratios in the modern ocean

Seawater Mg:Ca and Sr:Ca ratios are biogeochemical parameters reflecting the Earth–ocean–atmosphere dynamic exchange of elements. The ratios’ dependence on the environment and organisms' biology facilitates their application in marine sciences. Here, we present a measured single-laboratory dataset, combined with previous data, to test the assumption of limited seawater Mg:Ca and Sr:Ca variability across marine environments globally. High variability was found in open-ocean upwelling and polar regions, shelves/neritic and river-influenced areas, where seawater Mg:Ca and Sr:Ca ratios range from ∼4.40 to 6.40 mmol:mol and ∼6.95 to 9.80 mmol:mol, respectively. Open-ocean seawater Mg:Ca is semiconservative (∼4.90 to 5.30 mol:mol), while Sr:Ca is more variable and nonconservative (∼7.70 to 8.80 mmol:mol); both ratios are nonconservative in coastal seas. Further, the Ca, Mg, and Sr elemental fluxes are connected to large total alkalinity deviations from International Association for the Physical Sciences of the Oceans (IAPSO) standard values. Because there is significant modern seawater Mg:Ca and Sr:Ca ratios variability across marine environments we cannot absolutely assume that fossil archives using taxa-specific proxies reflect true global seawater chemistry but rather taxa- and process-specific ecosystem variations, reflecting regional conditions. This variability could reconcile secular seawater Mg:Ca and Sr:Ca ratio reconstructions using different taxa and techniques by assuming an error of 1 to 1.50 mol:mol, and 1 to 1.90 mmol:mol, respectively. The modern ratios’ variability is similar to the reconstructed rise over 20 Ma (Neogene Period), nurturing the question of seminonconservative behavior of Ca, Mg, and Sr over modern Earth geological history with an overlooked environmental effect