Microbial Respiration, the Engine of Ocean Deoxygenation
- Centre for Ocean and Atmospheric Sciences, School of Environmental Sciences, University of East Anglia, Norwich, United Kingdom
Microbial plankton respiration is the key determinant in the balance between the storage of organic carbon in the oceans or its conversion to carbon dioxide with accompanying consumption of dissolved oxygen. Over the past 50 years, dissolved oxygen concentrations have decreased in many parts of the world’s oceans, and this trend of ocean deoxygenation is predicted to continue. Yet despite its pivotal role in ocean deoxygenation, microbial respiration remains one of the least constrained microbial metabolic processes. Improved understanding of the magnitude and variability of respiration, including attribution to component plankton groups, and quantification of the respiratory quotient, would enable better predictions, and projections of the intensity and extent of ocean deoxygenation and of the integrative impact of ocean deoxygenation, ocean acidification, warming, and changes in nutrient concentration and stoichiometry on marine carbon storage. This study will synthesize current knowledge of respiration in relation to deoxygenation, including the drivers of its variability, identify key unknowns in our ability to project future scenarios and suggest an approach to move the field forward.
Dissolved oxygen (O2) is fundamental to all aerobic life and thus plays a major role in marine microbial ecology and the biogeochemical cycling of elements such as carbon, nitrogen, phosphorus and sulfur. The measurement of seawater O2 began during the 1873–1876 HMS Challenger expedition, and O2 continues to be the most commonly measured indicator of marine biogeochemistry, with the current global database amounting to millions of measurements (Keeling et al., 2010; Schmidtko et al., 2017). Time series data over the past 50 years show declining O2 in many regions of the world’s oceans, and a significant increase in the aerial extent of oxygen minimum zones (OMZs) in the eastern tropical North Atlantic (ETNA) and equatorial Pacific. Stramma et al. (2008) determined the decrease in O2 for the region of the ETNA between 10–14°N and 20–30°W in the depth range 300–700 m to be 0.09–0.34 μmol kg-1 year-1 between 1960 and 2008, while later studies revealed variations in this long term decline at interannual to multidecadal timescales consistent with natural climate variability (Brandt et al., 2015). The latest collation of global ocean dissolved oxygen data shows a decrease of more than 2% (4.8 ± 2.1 pmol), in the global oceanic oxygen content since 1960 (Schmidtko et al., 2017), however, at regional scales the changes are more complex. Deutsch et al. (2014) showed evidence for a decrease in the extent of oxygen minimum zones in the tropical Pacific Ocean over most of the 20th century. This was related to weakening easterly trade winds in a warming climate which decrease the intensity of upwelling and therefore the magnitude of biological production, export of organic carbon and respiratory oxygen demand. In the coastal zone, low or zero oxygen conditions are induced by anthropogenic nutrient enrichment and eutrophication, with the number of these coastal zone hypoxic sites having increased by an order of magnitude since the 1960s (Diaz and Rosenberg, 2008). This “deoxygenation” of the open and coastal ocean is predicted to continue. Coupled climate – marine biogeochemical models all project a continued long term decrease in the global ocean O2 inventory of between 1 and 7% by 2100 (Bopp et al., 2002; Keeling and Garcia, 2002; Keeling et al., 2010). Henson et al. (2017) investigated the trend in a multi-model mean ensemble of the Coupled Model Inter-comparison Project Phase 5 (CMIP5) output, run under a “business-as-usual” scenario (RCP8.5). This suggested that most of the world’s oceans will experience a 1–2% decrease in the oxygen inventory per decade with respect to the mean of 1986–2005. However, the regions where temperature and O2 changes are likely to have the greatest impact on marine ecosystems and biogeochemistry, the poles and the tropics, including the major eastern boundary upwelling systems where oxygen minimum zones occur (Gruber, 2011), are also the regions where inter-model agreement is low (Henson et al., 2017).
A number of physical, ecological, and biogeochemical mechanisms could contribute to the process of deoxygenation (Figure 1) including:
Figure 1. Potential physical, ecological and biogeochemical mechanisms contributing to ocean deoxygenation in the Anthropocene.
(1) The direct effect of increasing temperature reducing the solubility of oxygen in seawater. This physical chemical process is well constrained, with estimates of a decrease in O2 of ca. 5 mmol m-3 for each 1°C increase in water temperature (Deutsch et al., 2011). Within the upper 1000 m, 50% of the observed O2 loss is attributed to changes in solubility. This percentage decreases to 25% of the O2 loss in the upper 2000 m and 15% of the O2 loss over the full oceanic depth (Schmidtko et al., 2017).
(2) The indirect effect of increasing sea surface temperatures causing increased surface ocean stratification and reduced ventilation of the deep ocean, therefore increasing the length of time that deep water is separated from contact with the atmosphere. This delays the re-equilibration of dissolved oxygen to atmospheric concentrations while microbial degradation of organic matter associated with aerobic respiration consuming oxygen and producing carbon dioxide (CO2) continues.
(3) The direct effect of increasing temperature on the metabolic rates of the plankton, with the expectation that for the same increase in temperature, heterotrophic processes such as microbial respiration which consume oxygen will increase more than autotrophic processes such as photosynthesis which produce oxygen (López-Urrutia et al., 2006; Wohlers et al., 2009), and that bacterioplankton growth efficiencies (the proportion of the carbon assimilated by bacterioplankton that is converted to biomass rather than being respired to CO2) decrease with increasing temperature (Rivkin and Legendre, 2001). A warming ocean is therefore expected to change the depth distribution of oxygen consumption, with an increase in shallower warmer waters and a decrease at depth due to the reduced supply of organic matter. Whether this redistribution of oxygen consumption will lead to a decrease or increase in average oxygen concentrations remains uncertain.
(4) The direct effect of increasing CO2 leading to increased bacterioplankton cell-specific respiration. The anthropogenically derived CO2 in the atmosphere which is causing global warming is also dissolving in seawater, leading to increasing pCO2 and decreasing seawater pH and carbonate ion concentration (ocean acidification). Elevated pCO2 has been shown to increase the activity of bacterioplankton extracellular enzymes such as α and β–glucosidase (Piontek et al., 2010, 2013) and enhance bacterioplankton respiration (James et al., 2017).
(5) The indirect effect of increased photosynthesis caused by increasing concentrations of seawater CO2. Increased CO2 can enhance photosynthesis, producing an increased amount of particulate organic material (Riebesell and Tortell, 2011), a greater proportion of exudation of dissolved organic material (DOM; Engel et al., 2004) and increased carbon:nitrogen and carbon:phosphorus ratios of the DOM (Riebesell et al., 2007), leading to increased microbial respiration.
(6) The indirect effect of reduced calcium carbonate ballast due to decreasing seawater pH and carbonate ion concentration. The reduction in plankton extra-cellular calcium carbonate reduces the sinking rate of the plankton cells allowing respiration to occur at a shallower depth (Barker et al., 2003), and potentially allows a greater proportion of the exposed organic material to be respired in a given time.
(7) The indirect effect of increased coastal discharge of inorganic nutrients leading to increased primary production and thus increased phytoplankton derived particulate and dissolved organic carbon (or eutrophication), which when degraded by heterotrophic bacteria supports increased microbial respiration. The indirect effect of increased discharge of inorganic nutrients and/or increased phytoplankton production of labile dissolved organic carbon “priming” the degradation of previously recalcitrant dissolved organic carbon (Jiao et al., 2011). The indirect effect of increased pollution-derived atmospheric deposition of soluble iron and fixed nitrogen leading to increased primary production and then increased respiration (Ito et al., 2016).
The inter-dependencies and feedbacks between these mechanisms mean that their individual effects on deoxygenation can be counteracted or exacerbated. For example, increased stratification due to increased surface temperature will reduce nutrient supply to the surface ocean, reducing primary production by an estimated 24% by the year 2300 when RCP8.5 predicts a fivefold increase in atmospheric CO2 (Moore et al., 2018) which will offset the 27% increase in primary production due to carbon fertilization, estimated for a doubling of atmospheric CO2 (Riebesell et al., 2007).
Apart from the temperature related decrease in oxygen solubility and ocean ventilation, all of these potential mechanisms causing deoxygenation depend on microbial aerobic respiration, the metabolic process driven by the degradation of dissolved and particulate organic carbon, which consumes oxygen, produces carbon dioxide and generates energy in the form of adenosine triphosphate (ATP). Midwater microbial communities – predominantly bacterioplankton, archaeoplankton and zooplankton – are therefore central to the challenge that is ocean deoxygenation because they both influence and are influenced by decreasing oxygen concentrations. Since the depletion of oxygen caused by microbial respiration is always accompanied by an increase in CO2, ocean deoxygenation is always a dual stressor problem – both oxygen and CO2 change (Brewer and Peltzer, 2009). Due to this complexity of feedbacks and interdependency, ocean deoxygenation is therefore a “wicked” problem contributing to the “super wicked” problem of climate change (Levin et al., 2012).
The aim of this paper is to explore this wicked problem from the perspective of microbial respiration, focusing on the key role that microbial respiration plays in enabling ocean deoxygenation and on how microbial respiration, and therefore the storage of carbon in the ocean, might be affected by ocean deoxygenation. I will build on previous reviews of microbial respiration (e.g., del Giorgio and Duarte, 2002; Robinson and Williams, 2005; Robinson, 2008; Arístegui et al., 2009; Regaudie-de-Gioux and Duarte, 2012, 2013) synthesizing what we know about midwater microbial respiration that could help us predict how microbial respiration might change in waters with reduced oxygen and increased carbon dioxide concentrations, and then identify areas of research that still need to be addressed and some emerging approaches that could be used.
The magnitude and variability of marine microbial aerobic respiration is fundamental to deoxygenation, the formation of oxygen minimum zones and the efficiency of the biological carbon pump. Yet due to methodological limitations, the number of direct measurements and therefore our understanding of respiration, especially below the euphotic zone, is only loosely constrained.
The magnitude of midwater (i.e., between 100 and 1000 m depth range) respiration can be determined either from the oxygen consumption of an incubated water sample (Arístegui et al., 2005; Reinthaler et al., 2006; Baltar et al., 2010; Holtappels et al., 2014), from plankton electron transport system (ETS) activity (e.g., Packard et al., 2015; Osma et al., 2016; Martínez-García, 2017), from 14CO2 production during incubations with 14C labeled compounds (Hill et al., 2013), from measurements of bacterioplankton production and bacterioplankton growth efficiency (BGE = proportion of assimilated carbon used to produce bacterioplankton biomass) or from a time resolved estimate of the amount of oxygen consumed since a given water body left the sea surface where the dissolved oxygen concentration was in equilibrium with that in the atmosphere – the apparent (AOU; Sarmiento and Gruber, 2006), true (TOU) or evaluated (EOU; Duteil et al., 2013) oxygen utilization. Combining the estimate of oxygen utilization with an estimate of ventilation age from the distribution of tritium, radiocarbon or chlorofluorocarbons (CFCs), gives an average oxygen utilization rate (OUR; Jenkins, 1987). The efficiency of mesopelagic remineralization can also be inferred from the vertical profile of particle flux derived from underwater imaging, sediment trap data or thorium isotope disequilibria (Guidi et al., 2015) or reconstructed from large-scale ocean nutrient distributions (Weber et al., 2016).
Midwater respiration rates (60–300 μmol O2 m-3 day-1) have been derived from direct measurements of oxygen consumption during incubations of 2–4 days. To minimize any potential artifacts due to such long incubations, data are only used when linearity in oxygen consumption and cell abundance are confirmed, or when significant relationships between oxygen consumption and bacterioplankton production during the incubations can be used with in situ bacterioplankton production measurements to “back-correct” the respiration to in situ values (Arístegui et al., 2005; Reinthaler et al., 2006; Mazuecos et al., 2015). The ETS method estimates the maximum activity (Vmax) of the enzymes associated with the respiratory electron transport system of both eukaryotes and prokaryotes under substrate (NADH, NADPH) saturation, and is therefore a maximum “potential” respiration rate rather than the actual respiration rate. Vmax is converted into rates of oxygen consumption using either an empirical relationship determined from bacterial cultures or application of an enzyme kinetic model (EKM). It therefore assumes an average relationship between enzyme mass and respiratory activity, and due to this assumption it has an estimated error of 31–38% (Packard et al., 1988). A recent development of the ETS technique uses pyridine nucleotide concentrations and an EKM (Aguiar-González et al., 2012) to derive the actual respiration rate. This method has been used with cultured bacteria and zooplankton (Osma et al., 2016), but has not yet been tested in open waters.
A further modification of the ETS method derives respiration from the relationship between dissolved oxygen consumption and the in vivo reduction of 2-(p-iodophenyl)-3-(p-nitrophenyl)-5-phenyltetrazolium chloride (INT) to INT-formazan (Martínez-García et al., 2009). Martínez-García (2017) presents the first size-fractionated mesopelagic respiration data from station ALOHA in the North Pacific Subtropical Gyre using the INT technique, to show vertical and seasonal variability in respiration ranging from 56 to 107 μmol O2 m-3 day-1 in the 100–1000 m depth horizon. These data are around an order of magnitude higher than earlier ETS estimates (1–7 mol O2 m-2 y-1; 3–25 μmol O2 m-3 day-1; Arístegui et al., 2003), which were calculated using a conversion factor derived from a senescent bacterial culture, suggesting that microbial communities in the mesopelagic ocean are much more active that previously assumed (Arístegui et al., 2009). Respiration can also be derived from the respiration of 14C-leucine by bacterioplankton cells. Hill et al. (2013) determined respiration in the range 0.07–1.9 pmol leu L-1 h-1 between 20 and 160 m in the Atlantic Ocean after additions of 14C-leucine at close to ambient (0.4 nmol L-1) concentrations. Using 3H-leucine bioassay isotope dilution to determine prokaryote production, and published estimates of prokaryote growth efficiencies, Giering et al. (2014) calculated depth integrated (50–1000 m) North Atlantic prokaryote respiration to be 71 mg C m-2 day-1. Oxygen utilization rates including recent ones derived for the Pacific (Sonnerup et al., 2013, 2015) and Atlantic Oceans (Stanley et al., 2012) using transit time distributions, range from 0.3 to 50 μmol O2 m-3 day-1 (0.03–18.2 mol O2 m-2 y-1; Table 1).
Table 1. Recent midwater (100–1000 m) respiration estimates derived from dissolved oxygen consumption during a bottle incubation (ΔO2), activity of the electron transport system (ETS), the reduction of the tetrazolium salt (INT), or the time resolved estimate of the amount of dissolved oxygen consumed since a water parcel was last in contact with the atmosphere, the oxygen utilization rate (OUR).
In the oxygen minimum zones (OMZ) where oxygen concentrations fall below 40 μmol L-1 or, in the most intense OMZs below 20 μmol L-1 (Paulmier and Ruiz-Pino, 2009), it is only relatively recently that techniques to accurately measure extremely low in situ oxygen concentrations and rates of oxygen consumption have become available. While Winkler titrations, electrochemical or optode sensors and oxygen isotope methods have detection limits around 0.1–1 μmol L-1, the switchable trace oxygen (STOX) microsensor has a detection limit in the range 1–10 nmol L-1 (Revsbech et al., 2009, 2011), and in water bodies containing concentrations of O2 less than 1 nmol L-1, the ultra-sensitive Luminescence Measuring Oxygen Sensor (LUMOS) has a sensitivity of 7 pmol L-1 (Lehner et al., 2014, 2015). Good agreement was found between measurements of oxygen concentration and oxygen consumption made by STOX sensors, optode spots and membrane inlet mass spectrometric analysis of 18-18O2 (Holtappels et al., 2014). Using these new nanomolar techniques, in situ oxygen and respiration measurements derived from consumption of oxygen, showed that aerobic respiration occurs efficiently at extremely low oxygen concentrations (Tiano et al., 2014; Kalvelage et al., 2015; Garcia-Robledo et al., 2016). As well as the difficulty in measuring very low oxygen concentrations and rates of oxygen consumption, the imperative to maintain in situ oxygen concentrations during shipboard sample collection, manipulation and analysis remains a significant challenge (Garcia-Robledo et al., 2016).
Apportionment to Microbial Group
In addition to bulk measurements of respiration, an appreciation of the proportion of respiration attributable to bacterioplankton or zooplankton and between particle-attached or free-living bacterioplankton is important for accurate predictions and projections of carbon remineralization and thus deoxygenation and marine carbon storage in a changing environment. Unfortunately, such apportionment of respiration to constituent plankton functional groups is hampered by the lack of a direct method able to differentiate the respiration of any component group from that of the rest of the plankton community. The post-incubation separation by filtration of a size class of the plankton community, coupled with the identification and enumeration of plankton within that size class, has become the pragmatic although imperfect field approach to infer the respiration of a particular group which dominates a particular size class. This is obviously problematic in environments where cells of the same size represent very different functional groups, for example, heterotrophic and autotrophic prokaryotes in the surface waters of oligotrophic gyres, but perhaps is less of a problem in coastal regions or in the mesopelagic.
The relative proportion of mesopelagic bacterioplankton and zooplankton respiration varies with euphotic zone productivity. Bacterioplankton respiration was 2- to 10-fold higher than zooplankton respiration at the oligotrophic ALOHA station in the North Pacific Subtropical Gyre, and up to fivefold higher at the mesotrophic station K2 in the subarctic Pacific (Steinberg et al., 2008). Giering et al. (2014) found bacterioplankton respiration to dominate (70–92%) community respiration in the North Atlantic mesopelagic zone, while McDonnell et al. (2015) showed that the respiration rates of particle-associated microbes contributed 32–98% of the total respiration measured in situ at the Bermuda Atlantic Time-series Study site (BATS). Direct measurements of the oxygen consumption of microbes associated with phytodetrital aggregates collected using marine snow catchers in the northeast Atlantic, showed that the relative importance of particle-associated microbial respiration to the attenuation of particulate organic carbon (POC) increases from ∼8% in the upper mesopelagic (36–128 m) to ∼33% in the mid mesopelagic (129–500 m) as the rate of POC attenuation decreases (Belcher et al., 2016).
Influence of Environmental Conditions
Respiration rates vary in space and time depending on temperature, the quality and quantity of the organic substrate, availability of inorganic nutrients, and microbial community structure. Just like any other chemical reaction or metabolic rate, plankton respiration is related to temperature through an Arrhenius relationship. Mazuecos et al. (2015) derived mesopelagic respiration from oxygen consumption measurements and calculated a Q10 of 3.65 and an activation energy Ea of 0.90 eV for water temperatures between 8.7 and 14.9°C. This compared well with the temperature relationship of previously published mesopelagic respiration data (average Q10 of 4.07 and Ea of 0.98 eV), but is higher than the “optimal” Q10 values of between 1.5 and 2.6 of mesopelagic remineralization of particulate organic carbon derived from data-constrained modeling studies (DeVries and Weber, 2017; Laufkötter et al., 2017; Cram et al., 2018), and of activation energies determined for microbial respiration in surface waters (∼0.58 eV López-Urrutia and Móran, 2007; Yvon-Durocher et al., 2012).
Cell specific mesopelagic bacterioplankton respiration rates (Table 2) tend not to be correlated with temperature due to the ∼50-fold variability in cell specific respiration rates (0.1 to 5 fmol C cell-1 day-1; Baltar et al., 2009a,b) related to the lack of a strong relationship between cell abundance and cell activity (del Giorgio and Gasol, 2008). For example, Reinthaler et al. (2006) found a threefold difference in bacterioplankton cell specific respiration rates in deep water masses of the east and west N Atlantic, with a general increase with depth, and with rates in the oxygen minimum zones intermediate between those in the more oxygenated water masses above and below.
Table 2. Mesopelagic cell specific respiration (fmol C cell-1 day-1) derived from measurements of electron transport system activity (ETS) or dissolved oxygen consumption (ΔO2).
Experiments which mimic the increase in pressure experienced by surface dwelling bacterioplankton as they descend to the mesopelagic zone associated with particles, show that rates of organic matter degradation decrease with increasing pressure (Tamburini et al., 2013). However, bacterioplankton which are endemic to the mesopelagic, adapt to conditions of high pressure, low temperature and low substrate availability, such that measurements of bacterioplankton production made at atmospheric pressure on decompressed samples underestimate in situ mesopelagic activity (Tamburini et al., 2013). As far as I am aware, measurements of mesopelagic bacterioplankton respiration have not yet been made at in situ pressures.
Nutrient addition experiments with oligotrophic and mesotrophic surface water plankton populations show increased plankton community and bacterioplankton respiration after addition of a mixture of glucose and amino acids (Martínez-García et al., 2013), and time series studies and data syntheses show significant correlations between bacterioplankton respiration and concentrations of dissolved organic carbon (Alonso-Sáez et al., 2008; Robinson, 2008). Bioavailability experiments with natural bacterioplankton communities and dissolved organic material harvested from cultures of four coastal diatoms under silicate and/or nitrate stress suggest that DOM remineralization and bacterioplankton growth efficiencies are influenced on time scales of a week by the nutrient stress under which the DOM is produced. However, on seasonal time scales, the diatom source species is more influential (Wear et al., 2015).
The interacting effect of increasing temperature and organic carbon supply on coastal bacterioplankton respiration and growth efficiencies has been studied recently in chemostats and turbidostats. In substrate limited conditions, growth efficiencies showed no trend with temperature, whereas under temperature limited, substrate replete conditions, bacterioplankton growth efficiencies increased with temperature (Maske et al., 2017). This contrasts with the meta-analysis of Rivkin and Legendre (2001) which showed a decrease in bacterioplankton growth efficiencies with increasing temperature.
In addition to the influence of nutrient availability and DOM composition, the bioavailability of DOM (and hence respiration rate) is also controlled by microbial community composition. Mesopelagic microbial communities in the eastern tropical South Pacific were able to utilize surface layer dissolved organic carbon which was recalcitrant to remineralization by surface microbial communities over time scales of 9–14 days (Letscher et al., 2015). Likewise, incubations of ambient seawater amended with DO13C substrates including defined monosaccharides and exudates and lysates from 13C-labeled Synechococcus cultures showed that each DOC substrate stimulated a different community growth response and a different rate of DOC removal (Nelson and Carlson, 2012). While Synechococcus exudates are incorporated by a wide diversity of bacterial taxa, defined monosaccharides and Synechococcus lysates were less bioavailable to ambient bacterioplankton.
The relationship between the production of CO2 and the consumption of O2 during respiration is the respiratory quotient (RQ = ΔCO2/-ΔO2) and this varies depending on the stoichiometry of the organic substrate and the degree of oxidation or metabolic pathway used. Assuming complete oxidation, the RQ could range from 0.13 for lipid (C40H74O5), 0.50 for methane (CH4), 0.67 for saturated fatty acid (-CH2-), 1.00 for glucose (C6H12O6), 1.24 for nucleic acid (C1H1.3O0.7N0.4P0.11), 1.33 for glycolic acid (C2H4O3) and 4.00 for oxalic acid (C2H2O4) (Rodrigues and Williams, 2001; Williams and del Giorgio, 2005; Berggren et al., 2011). Assuming the substrate is similar to the average composition of planktonic material, e.g., 65% protein, 19% lipid, 16% carbohydrate, or the typical composition of a phytoplankton cell, e.g., 40% protein, 40% carbohydrate, 15% lipid, 5% nucleic acid gives an RQ of 0.89 (Williams and del Giorgio, 2005). Quantifying the variability in RQ allows not only the production of CO2 to be calculated from dissolved oxygen consumption, but also reveals shifts in plankton physiology that are not evident from any other measurement. Culture studies with marine bacteria (Vibrio natriegens and Pseudomonas nautica) show that the respiratory quotient varies with physiological state, metabolic pathway and carbon source (acetate or pyruvate) (Berdalet et al., 1995; Roy et al., 1999; Romero-Kutzner et al., 2015).
A systematic field study of the RQs of freshwater bacterioplankton showed large variability (1.2 ±0.45) with a significant negative correlation between RQ and in situ O2 concentration and pH and a significant positive correlation between RQ and in situ pCO2 (Berggren et al., 2011). Bacterioplankton RQs were low (average 0.81) in net autotrophic freshwater systems where reduced substrates derived from phytoplankton excretion are likely to dominate and higher (average 1.35) in net heterotrophic freshwater systems where oxidized substrates such as organic acids formed by photochemical processes could occur (Allesson et al., 2016). However, due to the low rates of oxygen consumption and CO2 production by marine plankton, and the precision of methods to measure changes in dissolved inorganic carbon (DIC; ∼1–2 mmol m-3), there has not been a systematic field study of the magnitude and variability of marine plankton RQs. Most studies of marine plankton respiration rely on measurements of dissolved oxygen consumption and assume a constant RQ of either 0.8 or 1.0 (e.g., Reinthaler et al., 2006; Nguyen et al., 2012; Teira et al., 2013), accepting that this introduces an error into the calculation of CO2 production, since the RQ is likely to vary with environmental conditions and substrate availability.
Field measurements of the concurrent consumption of oxygen (-ΔO2) and production of DIC (ΔCO2) of seawater samples incubated in the dark for 24h, can be used to derive an apparent respiratory quotient (ARQ; Angert et al., 2015). This is the integrative effect of not only the aerobic respiration of bacterio-, archaeo-, phyto-, and microzooplankton in the sample, but also all the other microbial metabolic processes which use or produce O2 or CO2, including nitrification (uptake of O2 without production of CO2), production of methane from acetate or methylamines (production of CO2 without utilization of O2), and production and dissolution of calcium carbonate (production or uptake of CO2 without affecting O2, respectively). The range of ARQs obtained from multiple field studies (Robertson, 1989; Wood, 1992; Robinson et al., 1999, 2002a,b; Sondergaard et al., 2000; Lefèvre et al., 2008 in Figure 2) spans the range of RQs calculated from the stoichiometry of potential substrates for microbial aerobic respiration with a median of 0.88 and an average of 1.11 ±0.76 (n = 149). There is some indication that higher ARQs occur in waters above the oxygen minimum zone in the Arabian Sea (Robinson and Williams, 1999) and lower ARQs occur during blooms of the coccolithophore Emiliania huxleyi (Holligan et al., 1993; Robertson et al., 1994). Until a more sensitive method is developed to measure CO2 or DIC and a systematic study undertaken, derivation of CO2 production from O2 consumption will depend on using a constant ΔCO2/-ΔO2 ratio, accepting the potential 20–40% error (Reinthaler et al., 2006).
Figure 2. Frequency histogram of apparent respiratory quotients (the ratio of oxygen consumption to production of dissolved inorganic carbon).
An apparent respiratory quotient integrated over longer time and larger space scales can also be derived from the relationship between DIC and AOU within a particular water mass. Measurements and models of the DIC:AOU ratio suggest a range between 0.51 and 0.85 depending on the composition of the organic material being degraded – lower ratios are associated with the remineralization of labile and nitrogen-rich organic matter, higher ratios with remineralization of more recalcitrant organic matter (Thomas, 2002; Paulmier et al., 2009) – the combination of biogeochemical processes (e.g., respiration, nitrification, denitrification, anammox) occurring, and the history of the source water in terms of the different sensitivities of O2 and DIC to changes in temperature and the different time scales of O2 and CO2 air-sea exchange (Anderson and Sarmiento, 1994; Thomas, 2002; Loucaides et al., 2012).
The ARQs of waters within oxygen minimum zones (and corresponding carbon maximum zones; Paulmier et al., 2011) vary between 0.6 and 1.5. Paulmier et al. (2011) determined the ARQ of waters in the shallow, very intense oxycline of Chilean coastal waters to be 1.1 ±0.3, potentially due to relatively higher rates of DIC production from more complete degradation of highly carbonated organic matter (Van Mooy et al., 2002; Paulmier et al., 2011).
Sensitivity to Decreasing Oxygen and Increasing Carbon Dioxide
Since the enzymes used during aerobic respiration require oxygen, at some level the rate of respiration will be directly sensitive to the ambient concentration of dissolved oxygen. In addition, dissolved oxygen concentration is a major determinant of microbial abundance and diversity (Wright et al., 2012) and will therefore indirectly affect the rate of respiration and other biogeochemical processes.
Hartnett et al. (1998), originally noted the strong negative relationship between sedimentary organic carbon preservation and length of exposure to oxygen, while Devol and Hartnett (2001) showed the influence of dissolved oxygen on midwater remineralisation. Calculated attenuation rates of particulate organic carbon flux for the oxic water column of the continental margin off Washington State were significantly higher than the attenuation rates calculated for the oxygen-deficient continental margin off northwest Mexico. A synthesis of attenuation length scale estimated from export flux and deep sediment trap data (Henson et al., 2012) shows clearly that mesopelagic remineralization is much reduced at low concentrations of dissolved oxygen (Sanders et al., 2016). Laufkötter et al. (2017) compiled particulate organic carbon flux measurements from 19 globally distributed sites and found that the attenuation of the flux of particulate organic matter depends on oxygen described by a half-saturation constant between 4 and 12 μmol L-1. However, as well as any direct effect of reduced dissolved oxygen on aerobic microbial respiration, these attenuation rates will also include the indirect effect of reduced dissolved oxygen decreasing the depth of zooplankton diel vertical migration and so fragmentation, repackaging and respiration of organic carbon mediated by zooplankton (Cavan et al., 2016).
Due to the technical challenges of both measuring and maintaining extremely low oxygen concentrations, there are relatively few determinations of the oxygen sensitivity of aerobic respiration in low oxygen waters. Garcia-Robledo et al. (2016), using LUMOS optodes, found no apparent change in oxygen consumption rates at oxygen concentrations between ∼1.0 and 10 μmol L-1 in waters collected from the oxygen minimum zones of the eastern tropical Pacific Ocean and derived an apparent half saturation constant of 391 nmol O2 L-1. This agrees with a previous study using STOX microsensors which on average showed little oxygen dependence above oxygen concentrations of 500 nmol L-1 (Tiano et al., 2014). However, Kalvelage et al. (2015) showed an increase in aerobic respiration (from ∼0.1 to 8.0 μmol L-1d-1) with increasing ambient O2 concentrations (from ∼1 to 20 μmol L-1). This change in aerobic respiration is likely associated with changing community structure. Beman and Carolan (2013) sampled across oxygen gradients in the OMZ of the Gulf of California using pyrosequencing of 16S rRNA to show maximum values of bacterial richness on the edge of the OMZ where availability of oxidants and reductants contribute to functional and taxonomic diversity. Predicting the biochemical response of the microbial community to fluctuations in oxygen concentrations is extremely difficult, as both aerobic and anaerobic processes occur simultaneously, even in waters with undetectable oxygen concentrations (Bertagnolli and Stewart, 2018).
Since decreasing O2 due to respiration will always be coupled with increasing CO2, which leads to ocean acidification through decreasing pH and carbonate ion concentration, it is relevant to assess the positive or negative feedbacks associated with the direct and indirect effects of increasing CO2 on plankton respiration. Many bacterial enzymatic processes involved in the utilization of organic compounds increase with increasing CO2, or decreasing pH (e.g., Grossart et al., 2006; Piontek et al., 2010; Mass et al., 2013). Bunse et al. (2016) demonstrated upregulation of respiratory proton pumps at elevated CO2 concentrations, presumably in order to export protons that invade the bacterioplankton cell as a result of low pH. Such proton exporting mechanisms are inherently energy demanding, so that bacterioplankton would need to allocate more energy to cell maintenance instead of growth, implying a decrease in bacterial growth efficiency with increasing CO2 (Bunse et al., 2016). This is consistent with measurements of the direct effect of increased CO2 on bacterioplankton metabolism, revealing systematically greater cell-specific respiration in elevated CO2 (James et al., 2017). This latter study also suggested that high CO2 conditions may increase the ability of bacterioplankton to consume DOC, but with reduced growth efficiencies, leading to decreased storage of DOC.
Indirect effects of increased CO2 on bacterioplankton respiration include increased respiration due to (1) the increased quantity and quality of phytoplankton derived particulate and dissolved organic carbon and/or (2) reduced calcium carbonate ballast enabling greater bacterial access to associated organic material. Mesocosm experiments in a range of nutrient regimes and plankton communities show equivocal results. Some show that bacteria benefitted both directly through enhanced enzymatic hydrolysis of organic matter and indirectly through increased availability of phytoplankton derived organic substrate (Grossart et al., 2006; Piontek et al., 2010), and that copepods increased their respiration rate at elevated CO2 concentrations (Li and Gao, 2012). However, recent mesocosm and microcosm studies in an Arctic fjord, the Mediterranean Sea and the subtropical North Atlantic Ocean found no significant relationship between bacterioplankton or plankton community respiration and CO2 concentrations (Motegi et al., 2013; Tanaka et al., 2013; Mercado et al., 2014; Maugendre et al., 2017; Filella et al., 2018), and Spilling et al. (2016) found a decrease in plankton community respiration at elevated CO2 levels during a mesocosm experiment in the Baltic Sea.
As far as I am aware there have been no CO2 manipulation studies of mesopelagic microbial communities or studies of the cumulative (additive, synergistic or antagonistic) effect of the combination of decreasing dissolved oxygen and increasing CO2 on environmental genomics and plankton respiration, as have been undertaken for metabolic rates of invertebrate and vertebrate marine organisms (Gobler and Baumann, 2016).
Known Unknowns and Recommendations for Future Research
Current models do not reproduce the observed patterns of changes in dissolved oxygen, they underestimate the interannual to decadal variability in dissolved oxygen and they simulate only half of the oceanic oxygen loss inferred from observations (Oschlies et al., 2018). Increased in situ observations and quantitative mechanistic understanding of the influence of both physical and biological processes on dissolved oxygen changes are therefore required to develop and verify these numerical models. In particular, since these models account for the major physical and chemical processes involved in deoxygenation, but do not include some of the microbial processes and feedbacks discussed here, it is relevant to investigate whether including these microbiological processes would account for the additional decrease in oxygen needed to match the model outputs with the observations.
The major biological process influencing a decline in dissolved oxygen concentration is plankton respiration. Hence improved mechanistic understanding of the drivers influencing the variability of respiration, particularly those that are climate sensitive, or currently not represented in numerical models, is required. Examples would include the influence of changing inorganic nutrient concentrations and stoichiometry on plankton community structure including the proportion of respiration attributable to bacterioplankton or vertically migrating zooplankton and the size distribution and composition of exported particles, changes in the respiratory quotient, the interacting effects of increasing CO2 and decreasing O2 on bacterioplankton respiration, and the influence of warming and nutrient stoichiometry on the bacterial utilization of previously recalcitrant dissolved organic carbon (Jiao et al., 2010, 2014; Zhang et al., 2018). On a broader scale, this complex wicked problem also requires an appreciation of the potential feedbacks between primary production, nitrogen cycling, organic matter flux and oxygen consumption (Canfield, 2006; Boyle et al., 2013; Bristow et al., 2016). At the microbial scale, representation of symbiotic metabolic interactions (Wright et al., 2012), including the potential for cryptic oxygen cycling to occur within otherwise anoxic zones (Garcia-Robledo et al., 2017) is required.
A dedicated longtime and large spatial scale observational program is required, linked to a numerical modeling framework (Oschlies et al., 2018), and within which targeted manipulation experiments could take place. The observational program would include a range of methods for determining plankton respiration from the individual organism to the oceanographic region, including those already established (e.g., in vitro O2 consumption, electron transport system activity, 14CO2 production, AOU) and those currently in development (e.g., fluorescence, in situ respirometry, and derivation from optode measurements on moorings, gliders and biogeochemical Argo floats1), measured alongside the plankton community structure and organic/inorganic nutrient regime (e.g., Honjo et al., 2014; Collins et al., 2018). Metagenomic analysis coupled with trace chemical assays and isotope tracer experiments should be incorporated into the observational program to reveal the detail of low oxygen metabolic pathways (Bertagnolli and Stewart, 2018). In addition, established multidisciplinary time series and global surveys (e.g., OceanSITES2 and GO-SHIP3) should begin to place as much emphasis on determining the plankton respiratory processes which utilize dissolved oxygen and convert organic carbon to CO2, as they currently do on the autotrophic processes which produce dissolved oxygen and convert CO2 to particulate and dissolved organic carbon. An implementation plan to specifically quantify the capacity for marine carbon storage through recalcitrant dissolved organic carbon (the microbial carbon pump), and the potential reduction in this capacity due to global change, leading to a positive feedback of increased oxygen consumption and CO2 production, has recently been proposed (Robinson et al., 2018).
Isolation and cultivation of a greater number of microbes from low oxygen waters will help quantify the oxygen thresholds constraining chemical fluxes and identify the enzymes responsible (Bertagnolli and Stewart, 2018). A suite of single species and natural plankton community micro-, meso- and macro-cosm manipulation experiments should be embedded within the observational and modeling framework, specifically to confirm or refute proposed biological mechanisms of increasing ocean deoxygenation and the interacting effects of increasing CO2 and decreasing O2 on plankton metabolism (Figure 1). Since ocean deoxygenation is linked mechanistically to other ocean stressors (or drivers) including warming, acidification and nutrient availability and stoichiometry, these manipulation experiments will need to be multiple stressor experiments and follow appropriate best practice in design, implementation and statistical analysis (Riebesell and Gattuso, 2014; Boyd et al., 2016, 2018). The Scientific Committee on Oceanic Research (SCOR) working group 149 has recently released an open access decision support tool https://scor149-ocean.com/decision-support-tool/ to aid in design and interpretation of multiple stressor experiments, and a Multiple Driver Best Practice Guide will be launched in 2019.
The predictions and projections of the distribution and extent of ocean deoxygenation and the cumulative effects of other drivers of global change afforded by the observational verification of numerical models, need to also extend to predictions of the consequences of ocean deoxygenation on the ecosystem services and human livelihoods and welfare provided by the ocean (Breitburg et al., 2018). This aligns with the scientific objectives of the Integrated Marine Biosphere Research project (IMBeR) to incorporate understanding of the drivers and consequences of global change on marine ecosystems and human societies at multiple scales into models to project and predict future states (Hofmann and The IMBeR Scientific Steering Committee, 2016), and the Intergovernmental Oceanographic Commission (IOC) of UNESCO sponsored expert group, the Global Ocean Oxygen Network GO2NE4 which aims to improve ocean oxygen observation systems, identify and fill knowledge gaps, build capacity, and provide scientific advice to policy makers. GO2NE also maintains the news site www.ocean-oxygen.org for scientists, stakeholders and the interested public.
Only through international co-ordination and collaboration will we be able to quantify the environmental, physiological and ecological drivers of variability in plankton respiration contributing to ocean deoxygenation, and hence predict and project the cumulative effect of ocean deoxygenation and other global change drivers on marine ecosystems and human societies.
CR conceived and wrote the article.
This study was supported by funds from The Leverhulme Trust (Grant RPG-2017-089 awarded to CR) and the Natural Environment Research Council (NERC) of the United Kingdom (Grants NE/R000956/1 and NE/K00168X/1 awarded to CR). I gratefully acknowledge financial support from The Royal Society (United Kingdom), EurOceans and the Integrated Marine Biogeochemistry and Ecosystem Research (IMBER; http://www.imber.info/) project sponsored workshops on “Ocean ventilation and deoxygenation in a warming world” in September 2016 and on “Ocean deoxygenation and implications for marine biogeochemical cycles and ecosystems” in October 2011 which provided financial support for me to attend.
Conflict of Interest Statement
The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
This study arose from invitations to present at the two workshops described above. The manuscript benefits from discussions with Dr. Elena García-Martin (University of East Anglia, United Kingdom), the OCEANic release of Greenhouse gASes under pressure from multiple stressors (OCEAN-GASP) team led by Dr. Andrew Rees (Plymouth Marine Laboratory, United Kingdom), and the editorial and reviewing team at Frontiers.
Aguiar-González, B., Packard, T. T., Berdalet, E., Roy, S., and Gómez, M. (2012). Respiration predicted from an Enzyme Kinetic Model and the Metabolic Theory of Ecology in two species of marine bacteria. J. Exp. Mar. Biol. Ecol. 412, 1–12. doi: 10.1016/j.jembe.2011.09.018
Allesson, L., Ström, L., and Berggren, M. (2016). Impact of photochemical processing of DOC on the bacterioplankton respiratory quotient in aquatic ecosystems. Geophys. Res. Lett. 43, 7538–7545. doi: 10.1002/2016GL069621
Alonso-Sáez, L., Vázquez-Domínguez, E., Cardelús, C., Pinhassi, J., Montserrat Sala, M., Lekunberri, I., et al. (2008). Factors controlling the year-round variability in carbon flux through bacteria in a coastal marine system. Ecosystems 11, 397–409. doi: 10.1007/s10021-008-9129-0
Angert, A., Yakir, D., Rodeghiero, M., Preisler, Y., Davidson, E. A., and Weiner, T. (2015). Using O2 to study the relationships between soil CO2 efflux and soil respiration. Biogeosciences 12, 2089–2099. doi: 10.5194/bg-12-2089-2015
Arístegui, J., Duarte, C. M., Gasol, J. M., and Alonso-Sáez, L. (2005). Active mesopelagic prokaryotes support high respiration in the subtropical northeast Atlantic Ocean. Geophys. Res. Lett. 32:L03608. doi: 10.1029/2004GL021863
Baltar, F., Arístegui, J., Gasol, J. M., and Herndl, G. J. (2010). Prokaryotic carbon utilization in the dark ocean: growth efficiency, leucine-to-carbon conversion factors, and their relation. Aquat. Microb. Ecol. 60, 227–232. doi: 10.3354/ame01422
Baltar, F., Arístegui, J., Gasol, J. M., Sintes, E., and Herndl, G. J. (2009a). Evidence of prokaryotic metabolism on suspended particulate organic matter in the dark waters of the subtropical North Atlantic. Limnol. Oceanogr. 54, 182–193. doi: 10.4319/lo.2009.54.1.0182
Baltar, F., Arístegui, J., Sintes, E., van Aken, H. M., Gasol, J. M., and Herndl, G. J. (2009b). Prokaryotic extracellular enzymatic activity in relation to biomass production and respiration in the meso-and bathypelagic waters of the (sub)tropical Atlantic. Environ. Microbiol. 11, 1998–2014. doi: 10.1111/j.1462-2920.2009.01922.x
Barker, S., Higgins, J. A., and Elderfield, H. (2003). The future of the carbon cycle: review, calcification response, ballast and feedback on atmospheric CO2. Philos. Trans. R. Soc. A Math. Phys. Eng. Sci. 361, 1977–1998; discussion 1998–1999. doi: 10.1098/rsta.2003.1238
Belcher, A., Iversen, M., Giering, S., Riou, V., Henson, S. A., Berline, L., et al. (2016). Depth-resolved particle-associated microbial respiration in the northeast Atlantic. Biogeosciences 13, 4927–4943. doi: 10.5194/bg-13-4927-2016
Berdalet, E., Packard, T., Lagacé, B., Roy, S., St-Amand, L., and Gagné, J.-P. (1995). CO2 production, O2 consumption and isocitrate dehydrogenase in the marine bacterium Vibrio natriegens. Aquat. Microb. Ecol. 9, 211–217. doi: 10.3354/ame009211
Berggren, M., Lapierre, J.-F., and del Giorgio, P. A. (2011). Magnitude and regulation of bacterioplankton respiratory quotient across freshwater environmental gradients. ISME J. 6, 984–993. doi: 10.1038/ismej.2011.157
Blight, S. P., Bentley, T. L., Lefevre, D., Robinson, C., Rodrigues, R., Rowlands, J., et al. (1995). Phasing of autotrophic and heterotrophic plankton metabolism in a temperate coastal ecosystem. Mar. Ecol. Prog. Ser. 128, 61–75. doi: 10.3354/meps128061
Bopp, L., Le Quéré, C., Heimann, M., Manning, A. C., and Monfray, P. (2002). Climate-induced oceanic oxygen fluxes: implications for the contemporary carbon budget. Glob. Biogeochem. Cycles 16, 6-1–6-13. doi: 10.1029/2001GB001445
Boyd, P. W., Collins, S., Dupont, S., Fabricius, K., Gattuso, J.-P., Havenhand, J., et al. (2018). Experimental strategies to assess the biological ramifications of multiple drivers of global ocean change – A review. Glob. Change Biol. 24, 2239–2261. doi: 10.1111/gcb.14102
Boyd, P. W., Dillingham, P. W., McGraw, C. M., Armstrong, E. A., Cornwall, C. E., Feng, Y.-Y., et al. (2016). Physiological responses of a Southern Ocean diatom to complex future ocean conditions. Nat. Clim. Chang. 6, 207–216. doi: 10.1038/nclimate2811
Boyle, R. A., Clark, J. R., Poulton, S. W., Shields-Zhou, G., Canfield, D. E., and Lenton, T. M. (2013). Nitrogen cycle feedbacks as a control on euxinia in the mid-Proterozoic ocean. Nat. Commun. 4:1533. doi: 10.1038/ncomms2511
Brandt, P., Bange, H. W., Banyte, D., Dengler, M., Didwischus, S.-H., Fischer, T., et al. (2015). On the role of circulation and mixing in the ventilation of oxygen minimum zones with a focus on the eastern tropical North Atlantic. Biogeosciences 12, 489–512. doi: 10.5194/bg-12-489-2015
Breitburg, D., Levin, L. A., Oschlies, A., Grégoire, M., Chavez, F. P., Conley, D. J., et al. (2018). Declining oxygen in the global ocean and coastal waters. Science 359:eaam7240. doi: 10.1126/science.aam7240
Bristow, L. A., Callbeck, C. M., Larsen, M., Altabet, M. A., Dekaezemacker, J., Forth, M., et al. (2016). N2 production rates limited by nitrite availability in the Bay of Bengal oxygen minimum zone. Nat. Geosci. 10, 24–29. doi: 10.1038/NGEO2847
Bunse, C., Lundin, D., Karlsson, C. M. G., Akram, N., Vila-Costa, M., Palovaara, J., et al. (2016). Response of marine bacterioplankton pH homeostasis gene expression to elevated CO2. Nat. Clim. Chang. 6, 483–487. doi: 10.1038/NCLIMATE2914
Collins, J. R., Fucile, P. D., McDonald, G., Ossolinski, J. E., Keil, R. G., Valdes, J. R., et al. (2018). An autonomous, in situ light-dark bottle device for determining community respiration and net community production. Limnol. Oceanogr. Methods 16, 323–338. doi: 10.1002/lom3.10247
Cram, J. A., Weber, T., Leung, S. W., McDonnell, A. M. P., Liang, J.-H., and Deutsch, C. (2018). The role of particle size, ballast, temperature, and oxygen in the sinking flux to the deep sea. Glob. Biogeochem. Cycles 32, 858–876. doi: 10.1029/2017GB005710
del Giorgio, P. A., and Gasol, J. M. (2008). “Physiological structure and single-cell activity in marine bacterioplankton,” in Microbial Ecology of the Oceans, 2nd Edn, ed. D. L. Kirchman (Hoboken, NJ: John Wiley & Sons, Inc).
Deutsch, C., Berelson, W., Thunell, R., Weber, T., Tems, C., and McManus, J. (2014). Centennial changes in North Pacific anoxia linked to tropical trade winds. Science 345, 665–668. doi: 10.1126/science.1252332
DeVries, T., and Weber, T. (2017). The export and fate of organic matter in the ocean: new constraints from combining satellite and oceanographic tracer observations. Glob. Biogeochem. Cycles 31, 535–555. doi: 10.1002/2016GB005551
Duteil, O., Koeve, W., Oschlies, A., Bianchi, D., Galbraith, E., Kriest, I., et al. (2013). A novel estimate of ocean oxygen utilization points to a reduced rate of respiration in the ocean interior. Biogeosciences 10, 7723–7738. doi: 10.5194/bg-10-7723-2013
Engel, A., Delille, B., Jacquet, S., Riebesell, U., Rochelle-Newall, E., Terbrüggen, A., et al. (2004). Transparent exopolymer particles and dissolved organic carbon production by Emiliania huxleyi exposed to different CO2 concentrations: a mesocosm experiment. Aquat. Microb. Ecol. 34, 93–104. doi: 10.3354/ame034093
Feely, R. A., Sabine, C. L., Schlitzer, R., Bullister, J. L., Mecking, S., and Greeley, D. (2004). Oxygen utilization and organic carbon remineralization in the upper water column of the Pacific Ocean. J. Oceanogr. 60, 45–52. doi: 10.1023/B:JOCE.0000038317.01279.aa
Fernández-Castro, B., Arístegui, J., Anderson, L., Montero, M. F., Hernández-León, S., Marañón, E., et al. (2016). Mesopelagic respiration near the ESTOC (European Station for Time-Series in the Ocean, 15.5oW, 29.1oN) site inferred from a tracer conservation model. Deep Sea Res. I Oceanogr. Res. Pap. 115, 63–73. doi: 10.1016/j.dsr.2016.05.010
Filella, A., Baños, I., Montero, M. F., Hernández-Hernández, N., Rodriguez-Santos, A., Ludwig, A., et al. (2018). Plankton community respiration and ETS activity under variable CO2 and nutrient fertilization during a mesocosm study in the Subtropical North Atlantic. Front. Mar. Sci. 5:310. doi: 10.3389/fmars.2018.00310
Garcia-Robledo, E., Borisov, S., Klimant, I., and Revsbech, N. P. (2016). Determination of respiration rates in water with sub-micromolar oxygen concentrations. Front. Mar. Sci. 3:244. doi: 10.3389/fmars.2016.00244
Garcia-Robledo, E., Padilla, C. C., Aldunate, M., Stewart, F. J., Ulloa, O., Paulmier, A., et al. (2017). Cryptic oxygen cycling in anoxic marine zones. Proc. Natl. Acad. Sci. U.S.A. 114, 8319–8324. doi: 10.1073/pnas.1619844114
Gasol, J. M., Alonso-Sáez, L., Vaqué, D., Baltar, F., Calleja, M. L., Duarte, C. M., et al. (2009). Mesopelagic prokaryotic bulk and single-cell heterotrophic activity and community composition in the NW Africa-Canary Islands coastal-transition zone. Prog. Oceanogr. 83, 189–196. doi: 10.1016/j.pocean.2009.07.014
Giering, S. L. C., Sanders, R., Lampitt, R. S., Anderson, T. R., Tamburini, C., Boutrif, M., et al. (2014). Reconciliation of the carbon budget in the ocean’s twilight zone. Nature 507, 480–483. doi: 10.1038/nature13123
Grossart, H.-P., Allgaier, M., Passow, U., and Riebesell, U. (2006). Testing the effect of CO2 concentration on the dynamics of marine heterotrophic bacterioplankton. Limnol. Oceanogr. 51, 1–11. doi: 10.4319/lo.2006.51.1.0001
Guidi, L., Legendre, L., Reygondeau, G., Uitz, J., Stemmann, L., and Henson, S. A. (2015). A new look at ocean carbon remineralization for estimating deepwater sequestration. Glob. Biogeochem. Cycles 29, 1044–1059. doi: 10.1002/2014GB005063
Hartnett, H. E., Kell, R. G., Hedges, J. I., and Devol, A. H. (1998). Influence of oxygen exposure time on organic carbon preservation in continental margin sediments. Nature 391, 572–574. doi: 10.1038/35351
Henson, S. A., Beaulieu, C., Ilyina, T., John, J. G., Long, M., Seferian, R., et al. (2017). Rapid emergence of climate change in environmental drivers of marine ecosystems. Nat. Commun. 8:14682. doi: 10.1038/ncomms14682
Henson, S. A., Sanders, R., and Madsen, E. (2012). Global patterns in efficiency of particulate organic carbon export and transfer to the deep ocean. Glob. Biogeochem. Cycles 26:GB1028. doi: 10.1029/2011GB004099
Hill, P. G., Warwick, P. E., and Zubkov, M. V. (2013). Low microbial respiration of leucine at ambient oceanic concentration in the mixed layer of the central Atlantic Ocean. Limnol. Oceanogr. 58, 1597–1604. doi: 10.4319/lo.2013.58.5.1597
Holligan, P. M., Fernández, E., Aiken, J., Balch, W. M., Boyd, P., Burkill, P. H., et al. (1993). A biogeochemical study of the coccolithophore, Emiliania huxleyi, in the North Atlantic. Glob. Biogeochem. Cycles 7, 879–900. doi: 10.1029/93GB01731
Holtappels, M., Tiano, L., Kalvelage, T., Lavik, G., Revsbech, N. P., and Kuypers, M. M. M. (2014). Aquatic respiration rate measurements at low oxygen concentrations. PLoS One 9:e89369. doi: 10.1371/journal.pone.0089369
Honjo, S., Eglinton, T. I., Taylor, C. D., Ulmer, K. M., Sievert, S. M., Bracher, A., et al. (2014). Understanding the role of the biological pump in the global carbon cycle: an imperative for ocean science. Oceanography 27, 10–16. doi: 10.5670/oceanog.2014.78
Ito, T., Nenes, A., Johnson, M. S., Meskhidze, N., and Deutsch, C. (2016). Acceleration of oxygen decline in the tropical Pacific over the past decades by aerosol pollutants. Nat. Geosci. 9, 443–447. doi: 10.1038/NGEO2717
James, A. K., Passow, U., Brzezinski, M. A., Parsons, R. J., Trapani, J. N., and Carlson, C. A. (2017). Elevated pCO2 enhances bacterioplankton removal of organic carbon. PLoS One 12:e0173145. doi: 10.1371/journal.pone.0173145
Jenkins, W. J. (1987). 3H and 3He in the Beta Triangle: observations of gyre ventilation and oxygen utilization rates. J. Phys. Oceanogr. 17, 763–783. doi: 10.1175/1520-0485(1987)017<0763:AITBTO>2.0.CO;2
Jiao, N., Herndl, G. J., Hansell, D. A., Benner, R., Kattner, G., Wilhelm, S. W., et al. (2010). Microbial production of recalcitrant dissolved organic matter: long-term carbon storage in the global ocean. Nat. Rev. Microbiol. 8, 593–599. doi: 10.1038/nrmicro2386
Jiao, N., Robinson, C., Azam, F., Thomas, H., Baltar, F., Dang, H., et al. (2014). Mechanisms of microbial carbon sequestration in the ocean – future research directions. Biogeosciences 11, 5285–5306. doi: 10.5194/bg-11-5285-2014
Jiao, N., Tang, K., Cai, H., and Mao, Y. (2011). Increasing the microbial carbon sink in the sea by reducing chemical fertilization on the land. Nat. Rev. Microbiol. 9, 75–75. doi: 10.1038/nrmicro2386-c2
Jørgensen, N. O. G., Kroer, N., Coffin, R. B., and Hoch, M. P. (1999). Relations between bacterial nitrogen metabolism and growth efficiency in an estuarine and an open-water ecosystem. Aquat. Microb. Ecol. 18, 247–261. doi: 10.3354/ame018247
Kalvelage, T., Lavik, G., Jensen, M. M., Revsbech, N. P., Löscher, C., Schunck, H., et al. (2015). Aerobic microbial respiration in oceanic oxygen minimum zones. PLoS One 10:e0133526. doi: 10.1371/journal.pone.0133526
Laufkötter, C., John, J. G., Stock, C. A., and Dunne, J. P. (2017). Temperature and oxygen dependence of the remineralization of organic matter. Glob. Biogeochem. Cycles 31, 1038–1050. doi: 10.1002/2017GB005643
Lefèvre, D., Guigue, C., and Obernosterer, I. (2008). The metabolic balance at two contrasting sites in the Southern ocean: the iron-fertilised Kerguelen area and HNLC waters. Deep Sea Res. II Top. Stud. Oceanogr. 55, 766–776. doi: 10.1016/j.dsr2.2007.12.006
Lehner, P., Larndorfer, C., Garcia-Robledo, E., Larsen, M., Borisov, S. M., Revsbech, N.-P., et al. (2015). LUMOS – A sensitive and reliable optode system for measuring dissolved oxygen in the nanomolar range. PLoS One 10:e0128125. doi: 10.1371/journal.pone.0128125
Letscher, R. T., Knapp, A. N., James, A. K., Carlson, C. A., Santoro, A. E., and Hansell, D. A. (2015). Microbial community composition and nitrogen availability influence DOC remineralization in the South Pacific Gyre. Mar. Chem. 177, 325–334. doi: 10.1016/j.marchem.2015.06.024
Levin, K., Cashore, B., Bernstein, S., and Auld, G. (2012). Overcoming the tragedy of super wicked problems: constraining our future selves to ameliorate global climate change. Policy Sci. 45, 123–152. doi: 10.1007/s11077-012-9151-0
Loucaides, S., Tyrrell, T., Achterberg, E. P., Torres, R., Nightingale, P. D., Kitidis, V., et al. (2012). Biological and physical forcing of carbonate chemistry in an upwelling filament off northwest Africa: results from a Lagrangian study. Glob. Biogeochem. Cycles 26:GB3008. doi: 10.1029/2011GB004216
Martínez-García, S., Fernández, E., Aranguren-Gassis, M., and Teira, E. (2009). In vivo electron transport system activity: a method to estimate respiration in natural marine microbial planktonic communities. Limnol. Oceanogr. Methods 7, 459–469. doi: 10.4319/lom.2009.7.459
Martínez-García, S., Fernández, E., Calvo-Díaz, A., Cermeño, P., Marañón, E., Morán, X. A. G., et al. (2013). Differential response of microbial plankton to nutrient inputs in oligotrophic versus mesotrophic waters of the North Atlantic. Mar. Biol. Res. 9, 358–370. doi: 10.1080/17451000.2012.745002
Maske, H., Cajal-Medrano, R., and Villegas-Mendoza, J. (2017). Substrate-limited and –unlimited coastal microbial communities show different metabolic responses with regard to temperature. Front. Microbiol. 8:2270. doi: 10.3389/fmicb.2017.02270
Mass, E. W., Law, C. S., Hall, J. A., Pickmere, S., Currie, K. I., Chang, F. H., et al. (2013). Effect of ocean acidification on bacterial abundance, activity and diversity in the Ross Sea, Antarctica. Aquat. Microb. Ecol. 70, 1–15. doi: 10.3354/ame01633
Maugendre, L., Gattuso, J.-P., Poulton, A. J., Dellisanti, W., Gaubert, M., Guieu, C., et al. (2017). No detectable effect of ocean acidification on plankton metabolism in the NW oligotrophic Mediterranean Sea: results from two mesocosm studies. Estuar. Coast. Shelf Sci. 186, 89–99. doi: 10.1016/j.ecss.2015.03.009
Mazuecos, I. P., Arístegui, J., Vázquez-Dominguez, E., Ortega-Retuerta, E., Gasol, J. M., and Reche, I. (2015). Temperature control of microbial respiration and growth efficiency in the mesopelagic zone of the South Atlantic and Indian Oceans. Deep Sea Res. I Oceanogr. Res. Pap. 95, 131–138. doi: 10.1016/j.dsr.2014.10.014
McDonnell, A. M. P., Boyd, P. W., and Buesseler, K. O. (2015). Effects of sinking velocities and microbial respiration rates on the attenuation of particulate carbon fluxes through the mesopelagic zone. Glob. Biogeochem. Cycles 29, 175–193. doi: 10.1002/2014GB004935
Mercado, J. M., Sobrino, C., Neale, P. J., Segovia, M., Reul, A., Amorim, A. L., et al. (2014). Effect of CO2, nutrients and light on coastal plankton. II. Metabolic rates. Aquat. Biol. 22, 43–57. doi: 10.3354/ab00606
Moore, J. K., Fu, W. W., Primeau, F., Britten, G. L., Lindsay, K., and Long, M. (2018). Sustained climate warming drives declining marine biological productivity. Science 359, 1139–1142. doi: 10.1126/science.aao6379
Motegi, C., Tanaka, T., Piontek, J., Brussard, C. P. D., Gattuso, J.-P., and Weinbauer, M. G. (2013). Effect of CO2 enrichment on bacterial metabolism in an Arctic fjord. Biogeosciences 10, 8285–3296. doi: 10.5194/bg-10-3285-2013
Mukhanov, V., Rylkova, O., Lopukhina, O., and Kemp, R. B. (2003). Productivity and thermodynamics of marine bacterioplankton: an inter-ecosystem comparison. Thermochim. Acta 397, 31–35. doi: 10.1016/S0040-6031(02)00313-1
Nelson, C. E., and Carlson, C. A. (2012). Tracking differential incorporation of dissolved organic carbon types among diverse lineages of Sargasso Sea bacterioplankton. Environ. Microbiol. 14, 1500–1516. doi: 10.1111/j.1462-2920.2012.02738.x
Obernoster, I., Christaki, U., Lefèvre, D., Catala, P., van Wambeke, F., and Lebaron, P. (2008). Rapid bacterial mineralization of organic carbon produced during a phytoplankton bloom induced by natural iron fertilization in the Southern Ocean. Deep Sea Res. II Top. Stud. Oceanogr. 55, 777–789. doi: 10.1016/j.dsr2.2007.12.005
Osma, N., Fernández-Urruzola, I., Gómez, M., Montesdeoca-Esponda, S., and Packard, T. T. (2016). Predicting in vivo oxygen consumption rate from ETS activity and bisubstrate enzyme kinetics in cultured marine zooplankton. Mar. Biol. 163:146. doi: 10.1007/s00227-016-2923-x
Packard, T. T., Denis, M., Rodie, M., and Garfield, P. (1988). Deep-ocean metabolic CO2 production: calculations from ETS activity. Deep Sea Res. A Oceanogr. Res. Pap. 35, 371–382. doi: 10.1016/0198-0149(88)90016-7
Packard, T. T., Osma, N., Fernández-Urruzola, I., Codispoti, L. A., Christensen, J. P., and Gómez, M. (2015). Peruvian upwelling plankton respiration: calculations of carbon flux, nutrient retention efficiency, and heterotrophic energy production. Biogeosciences 12, 2641–2654. doi: 10.5194/bg-12-2641-2015
Piontek, J., Borchard, C., Sperling, M., Schulz, K. G., Riebesell, U., and Engel, A. (2013). Response of bacterioplankton activity in an Arctic fjord system to elevated pCO2; results from a mesocosm perturbation study. Biogeosciences 10, 297–314. doi: 10.5194/bg-10-297-2013
Piontek, J., Lunau, M., Handel, N., Borchard, C., Wurst, M., and Engel, A. (2010). Acidification increases microbial polysaccharide degradation in the ocean. Biogeosciences 7, 1615–1624. doi: 10.5194/bg-7-1615-2010
Reinthaler, T., van Aken, H., Veth, C., Arístegui, J., Robinson, C., Williams, P. J., et al. (2006). Prokaryotic respiration and production in the meso- and bathypelagic realm of the eastern and western North Atlantic basin. Limnol. Oceanogr. 51, 1262–1273. doi: 10.4319/lo.2006.51.3.1262
Reinthaler, T., Winter, C., and Herndl, G. J. (2005). Relationship between bacterioplankton richness, respiration, and production in the southern North Sea. Appl. Environ. Microbiol. 71, 2260–2266. doi: 10.1128/AEM.71.5.2260-2266.2005
Revsbech, N. P., Larsen, L. H., Gundersen, J., Dalsgaard, T., Ulloa, O., and Thamdrup, B. (2009). Determination of ultra-low oxygen concentrations in oxygen minimum zones by the STOX sensor. Limnol. Oceanogr. Methods 7, 371–381. doi: 10.4319/lom.2009.7.371
Revsbech, N. P., Thamdrup, B., Dalsgaard, T., and Canfield, D. E. (2011). Construction of STOX oxygen sensors and their application for determination of O2 concentrations in oxygen minimum zones. Methods Enzymol. 486, 325–341. doi: 10.1016/S0076-6879(11)86014-3
Riebesell, U., Schulz, K. G., Bellerby, R. G. J., Botros, M., Fritsche, P., and Meyerhöfer, M. (2007). Enhanced biological carbon consumption in a high CO2 ocean. Nature 450, 545–548. doi: 10.1038/nature06267
Riebesell, U., and Tortell, P. D. (2011). “Effects of ocean acidification on pelagic organisms and ecosystems,” in Ocean Acidification, eds J.-P. Gattuso and L. Hansson (Oxford: Oxford University Press), 99–121.
Robertson, J. E., Robinson, C., Turner, D. R., Holligan, P., Watson, A. J., Boyd, P., et al. (1994). The impact of a coccolithophore bloom on oceanic carbon uptake in the northeast Atlantic during summer 1991. Deep Sea Res. I Oceanogr. Res. Pap. 41, 297–314. doi: 10.1016/0967-0637(94)90005-1
Robertson, J. I. (1989). The Coulometric Determination of Total Inorganic Carbon in Seawater and the Study of the Inter-Relationship Between the Planktonic Metabolism of Carbon Dioxide and Oxygen. Ph.D. Thesis, University College of North Wales, Bangor.
Robinson, C., Archer, S. D., and Williams, P. J. (1999). Microbial dynamics in coastal waters of East Antarctica: plankton production and respiration. Microb. Ecol. Prog. Ser. 180, 23–36. doi: 10.3354/meps180023
Robinson, C., Widdicombe, C. E., Zubkov, M. V., Tarran, G. A., Miller, A. E. J., and Rees, A. P. (2002b). Plankton community respiration during a coccolithophore bloom. Deep Sea Res. II Top. Stud. Oceanogr. 49, 2929–2950. doi: 10.1016/S0967-0645(02)00064-4
Robinson, C., Wallace, D., Hyun, J.-H., Polimene, L., Benner, R., Zhang, Y., et al. (2018). An implementation strategy to quantify the marine microbial carbon pump and its sensitivity to global change. NatL. Sci. Rev. 5, 474–480. doi: 10.1093/nsr/nwy070
Robinson, C., and Williams, P. J. (2005). “Respiration and its measurement in surface marine waters,” in Respiration in Aquatic Ecosystems, eds P. A. del Giorgio and P. J. Williams (Oxford: Oxford University Press).
Robinson, C., and Williams, P. J. L. (1999). Plankton net community production and dark respiration in the Arabian Sea during September 1994. Deep Sea Res. II Top. Stud. Oceanogr. 46, 745–765. doi: 10.1016/S0967-0645(98)00126-X
Rodrigues, R. M. N. V., and Williams, P. J. (2001). Heterotrophic bacterial utilisation of nitrogenous and non-nitrogenous substrates determined from ammonia and oxygen fluxes. Limnol. Oceanogr. 46, 1675–1683. doi: 10.4319/lo.2001.46.7.1675
Romero-Kutzner, V., Packard, T. T., Berdalet, E., Roy, S. O., Gagné, J.-P., and Gómez, M. (2015). Respiration quotient variability: bacterial evidence. Mar. Ecol. Prog. Ser. 519, 47–59. doi: 10.3354/meps11062
Roy, S. O., Packard, T. T., Berdalet, E., and St-Amand, L. (1999). Impact of acetate, pyruvate, and physiological state on respiration and respiratory quotients in Pseudomonas nautica. Aquat. Microb. Ecol. 17, 105–110. doi: 10.3354/ame017105
Sanders, R., Henson, S. A., Martin, A. P., Anderson, T. R., Bernardello, R., and Enderlein, P. (2016). Controls over ocean mesopelagic interior carbon storage (COMICS): fieldwork, synthesis and modelling efforts. Front. Mar. Sci. 3:136. doi: 10.3389/fmars.2016.00136
Sondergaard, M., Williams, P. J., Cauwet, G., Riemann, B., Robinson, C., Terzic, S., et al. (2000). Net accumulation and flux of dissolved organic carbon and dissolved organic nitrogen in marine plankton communities. Limnol. Oceanogr. 45, 1097–1111. doi: 10.4319/lo.2000.45.5.1097
Sonnerup, R. E., Mecking, S., and Bullister, J. L. (2013). Transit time distributions and oxygen utilization rates in the Northeast Pacific Ocean from chlorofluorocarbons and sulfur hexafluoride. Deep Sea Res. I Oceanogr. Res. Pap. 72, 61–71. doi: 10.1016/j.dsr.2012.10.013
Sonnerup, R. E., Mecking, S., Bullister, J. L., and Warner, M. J. (2015). Transit time distributions and oxygen utilization rates from chlorofluorocarbons and sulfur hexafluoride in the Southeast Pacific Ocean. J. Geophys. Res. Oceans 120, 3761–3776. doi: 10.1002/2015JC010781
Spilling, K., Paul, A. J., Virkkala, N., Hastings, T., Lischka, S., Stuhr, A., et al. (2016). Ocean acidification decreases plankton respiration: evidence from a mesocosm experiment. Biogeosciences 13, 4707–4719. doi: 10.5194/bg-13-4707-2016
Stanley, R. H. R., Doney, S. C., Jenkins, W. J., and Lott, D. E. III (2012). Apparent oxygen utilization rates calculated from tritium and helium-3 profiles at the Bermuda Atlantic Time-series Study site. Biogeosciences 9, 1969–1983. doi: 10.5194/bg-9-1969-2012
Steinberg, D. K., Van Mooy, B. A. S., Buesseler, K. O., Boyd, P. W., Kobari, T., and Karl, D. M. (2008). Bacterial vs. zooplankton control of sinking particle flux in the ocean’s twilight zone. Limnol. Oceanogr. 53, 1327–1338. doi: 10.4319/lo.2008.53.4.1327
Tamburini, C., Boutrif, M., Garel, M., Colwell, R. R., and Deming, J. W. (2013). Prokaryotic responses to hydrostatic pressure in the ocean – a review. Environ. Microbiol. 15, 1262–1274. doi: 10.1111/1462-2920.12084
Tanaka, T., Alliouane, S., Bellerby, R. G. B., Czerny, J., de Kluijver, A., Riebesell, U., et al. (2013). Effect of increased pCO2 on the planktonic metabolic balance during a mesocosm experiment in an Arctic fjord. Biogeosciences 10, 315–325. doi: 10.5194/bg-10-315-2013
Teira, E., Hernando-Morales, V., Martínez-García, S., Figueiras, F. G., Arbones, B., and Álvarez-Salgado, X. A. (2013). Response of bacterial community structure and function to experimental rainwater additions in a coastal eutrophic embayment. Estuar. Coast. Shelf Sci. 119, 44–53. doi: 10.1016/j.ecss.2012.12.018
Tiano, L., Garcia-Robledo, E., Dalsgaard, T., Devol, A. H., Ward, B. B., Ulloa, O., et al. (2014). Oxygen distribution and aerobic respiration in the north and south eastern tropical Pacific oxygen minimum zones. Deep Sea Res. I Oceanogr. Res. Pap. 94, 173–183. doi: 10.1016/j.dsr.2014.10.001
Van Mooy, B., Keil, R., and Devol, A. (2002). Impact of suboxia on sinking particulate organic carbon: enhanced carbon flux and preferential degradation of amino acids via denitrification. Geochem. Cosmochim. Acta 66, 457–465. doi: 10.1016/S0016-7037(01)00787-6
Wear, E. K., Carlson, C. A., Windecker, L. A., and Brzezinski, M. A. (2015). Roles of diatom nutrient stress and species identity in determining the short- and long-term bioavailability of diatom exudates to bacterioplankton. Mar. Chem. 177, 335–348. doi: 10.1016/j.marchem.2015.09.001
Weber, T., Cram, J. A., Leung, S. W., DeVries, T., and Deutsch, C. (2016). Deep ocean nutrients imply large latitudinal variation in particle transfer efficiency. Proc. Natl. Acad. Sci. U.S.A. 113, 8606–8611. doi: 10.1073/pnas.1604414113
Weinbauer, M. G., Liu, J., Motegi, C., Maier, C., Pedroti, M. L., Dai, M., et al. (2013). Seasonal variability of microbial respiration and bacterial and archaeal community composition in the upper twilight zone. Aquat. Microb. Ecol. 71, 99–115. doi: 10.3354/ame01666
Williams, P. J. B., and del Giorgio, P. A. (2005). “Respiration in aquatic ecosystems: history and background,” in Respiration in Aquatic Ecosystems, eds P. A. del Giorgio and P. J. Williams (Oxford: Oxford University Press), 315.
Wohlers, J., Engel, A., Zöllner, E., Breithaupt, P., J¨υrgens, K., Hoppe, H.-G., et al. (2009). Changes in biogenic carbon flow in response to sea surface warming. Proc. Natl. Acad. Sci. U.S.A. 106, 7067–7072. doi: 10.1073/pnas.0812743106
Yvon-Durocher, G., Caffrey, J. M., Cescatti, A., Dossena, M., del Giorgio, P., and Gasol, J. M. (2012). Reconciling the temperature dependence of respiration across timescales and ecosystem types. Nature 487, 472–476. doi: 10.1038/nature11205
Keywords: microbial respiration, respiratory quotient, ocean deoxygenation, ocean acidification, multiple stressors
Citation: Robinson C (2019) Microbial Respiration, the Engine of Ocean Deoxygenation. Front. Mar. Sci. 5:533. doi: 10.3389/fmars.2018.00533
Received: 10 August 2018; Accepted: 31 December 2018;
Published: 17 January 2019.
Edited by:Emilio Garcia-Robledo, University of Cádiz, Spain
Reviewed by:Carolin Regina Löscher, University of Southern Denmark, Denmark
Thomas Smith Weber, University of Rochester, United States
Helmut Maske, Ensenada Center for Scientific Research and Higher Education (CICESE), Mexico
Copyright © 2019 Robinson. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Carol Robinson, firstname.lastname@example.org