Solar energy capture and transformation in the sea

is based on energy. Energy is the source and control of all things, all value, and all the actions of human beings and nature . measure all possible pathways of energy capture, transformation, and dissipation and needs to integrate over both space and time. Two possible experimental approaches have been employed to estimate total energy flow through marine planktonic assemblages: (1) heat flow via microcalorimetry, and (2) total ATP pool turnover rate, but additional methods need to be devised, calibrated, and field-tested. Future developments in the emergent field of metabolomics, especially energy transduction and energy storage molecules, will likely provide new opportunities for field application.

complexity, with a trend for a decreasing flow of energy per unit biomass as succession occurs. He suggested that climax ecosystems with complex structures and high information content could be maintained with a relatively low expenditure of energy (Margalef 1963). Despite great scientific progress in the intervening half-century, we are still unable to examine this unifying principle in ocean ecosystems due, in large part, to inadequate methodology for energy flux estimation and an incomplete understanding of the pathways of solar energy capture and transformation in marine microbial assemblages. Ironically, two pioneering methods developed to analyze key aspects of planktonic microbial communities, the adenosine triphosphate (ATP) assay (Holm-Hansen and Booth 1966) and the electron transport system (ETS) assay (Packard 1971), were laboratory calibrated to yield estimates of living carbon and oxygen consumption, respectively, rather than the equally appropriate parameters of total energy content and flux.

Phototrophy in the deep blue sea
In marine planktonic systems, green plant-like photosynthesis, termed oxygenic phototrophy (OP; Table 1 and Figure 1), is generally assumed to be the primary, if not exclusive, process of solar energy capture. Light-driven oxidation of water provides electrons and hydrogen ions that partially conserve the solar energy absorbed by chlorophyll a to catalyze the production of a variety of reduced inorganic and organic molecules. Estimates of the magnitude of chlorophyll a -based solar energy capture can be made by measuring the fundamental biophysical properties of photosynthetic energy conversion (e.g., by fast repetition rate fluorescence; Kolber et al. 1998) or gross oxygen production during in situ incubations using 18 O-labeled H 2 O (Grande et al. 1989), and applying assumptions regarding energy-to-oxygen stoichiometry. Based upon the energy requirements for OP and cell maintenance, it has been estimated that approximately 5 × 10 14 W of solar energy are captured per year to support oceanic primary production (Kolber 2007). This power expenditure of marine phytoplankton is nearly two orders of magnitude greater than that expended by the human-based global economies, but as Kolber (2007) laments it is still less than 1% of the full potential of solar radiation incident on the ocean's surface. Consequently, marine systems appear to be relatively inefficient at using the solar energy that is available to them. Ultimately, solar energy capture in the sea by OP is controlled by chlorophyll a concentration (e.g., phytoplankton biomass) and phytoplankton growth rate, which in turn are controlled primarily by nutrient availability. Global distributions of OP and, hence, patterns of solar energy capture coincide with maximum nutrient rather than maximum solar fluxes (e.g., coastal upwelling regions; Kolber 2007). However, even in nutrient-poor environments like the oligotrophic North Pacific Subtropical Gyre (NPSG), the solar energy that is absorbed appears to be very efficiently utilized in photosynthesis . During the past decade, there has been a "quiet revolution" in our conceptualization of energy flow in marine systems. This change has resulted in large part from two independent discoveries of unexpected pathways of phototrophy that supplement the better understood OP pathway (Karl 2002; Figure 1 and Table 1). These two novel pathways differ significantly in the mechanism of solar energy capture and in the quantitative and mechanistic role that light energy plays in cellular metabolism. For example, both aerobic anoxygenic phototrophy (AAP) and proteorhodopsin (PR) phototrophy appear to be facultative solar energy capture processes that supplement an otherwise chemoorganoheterotrophic metabolism ( Figure 1). Quantitative analysis of energy flow through these alternate pathways will require the development of new instrumentation and methodology, and will likely lead to a new paradigm of energy flow in the sea.
Bacteriochlorophyll a-containing marine bacteria were first reported by Shiba et al. (1979) from coastal marine habitats. They were later rediscovered in the oligotrophic waters of the North Pacific Ocean using a Elementa: Science of the Anthropocene • 2: 000021 • doi: 10.12952/journal.elementa.000021 purpose-built infrared fast repetition rate (IRFRR) fluorometer that detected variable fluorescence transients as evidence of bacterial photosynthetic electron transport (Kolber et al. 2000). AAPs differ from oxygenic phototrophs in that their photosynthetic activity neither reduces carbon dioxide nor evolves oxygen (Koblížek et al. 2010). Subsequent laboratory and field investigations of AAP bacteria determined that they are facultative photoheterotrophs, using light energy when organic matter is limiting for growth (Kolber et al. 2001;Koblížek et al. 2003). Laboratory study of an isolated member of the Roseobacter clade (strain COL2P) determined that respiration decreased by ∼ 30% in the light for an equivalent production rate (Koblížek et al. 2010), suggesting a much more efficient metabolism when the microorganism was living as a mixotroph (e.g., part phototroph, part chemotroph). AAPs are numerically abundant, globally distributed, and metabolically active with respect to solar energy capture where they appear to coexist with OPs (Kolber et al. 2001). However, measurement of total energy flow through these bacteriochlorophyll-containing microbial assemblages (solar plus organic matter) will require a novel experimental approach.
The second novel pathway of solar energy capture in the sea is via PR-containing microorganisms (Béjà et al. 2000;. These novel microbes contain transmembrane light-driven proton pumps that produce ATP. During PR phototrophy, photon capture leads to a conformational change in the retinal molecule resulting in proton export from the cell. This process generates a proton motive force across the cell membrane, setting up the possibility for ATP production. Gómez-Consarnau et al. (2007) were the first to demonstrate enhanced growth efficiency in the light for a PR-containing marine bacterium. Martinez et al. (2007) documented PR-based photophosphorylation (ATP production) in a genetically transformed heterologous host, and PR-dependent proton pumping activity sufficient to generate ATP has also been demonstrated in laboratoryreared marine bacteria (Wang et al. 2012;Yoshizawa et al. 2012). PR-phototrophy has since been shown to increase the long-term survival of diverse bacteria that favor either carbon-rich (e.g., Vibrio; Gómez-Consarnau et al. 2010) or carbon-poor (e.g., Pelagibacter; Steindler et al. 2011) marine habitats. PR genes have also been found in archaea (Frigaard et al. 2006) and eukaryotes, including both photosynthetic (Marchetti et al. 2012) and predatory (Slamovits et al. 2011) protists. Recently, Kimura et al. (2011) surveyed the transcriptional and growth responses of a PR-containing marine flavobacterium during carbon-limited growth under light and dark conditions. Their results demonstrated a direct role for retinal-based, PR-phototrophy and the previously observed light-enhanced growth response. Our current, but still evolving, understanding is that the light-driven, PR-based proton pumps enhance survival, and therefore may be a significant pathway for the flow of energy in oligotrophic habitats (DeLong and Béjà 2010). This phototrophic process, which is now believed to be ubiquitous in the well-lit portions of the euphotic zone, enhances solar energy capture in the ecosystem without direct impacts on either carbon dioxide or oxygen reservoirs. The indirect effects, however, will scale on the total energy budgets of these unique phototrophic microbes, specifically on the role of PRs in the efficiency of heterotrophic metabolism of dissolved organic matter.
Recently, Kirchman and Hanson (2013) have reviewed the current state-of-knowledge concerning the bioenergetics of photoheterotrophic bacteria in the sea, including both bacteriochlorophyll-(AAP) and PR-based pathways. In the absence of any in situ experimental data, they provided a theoretical cost vs. benefit analysis of phototrophy. This scholarly assessment included estimates of the number of photosynthetic units per cell, the absorption cross-sectional area and wavelength dependent absorption of light, the quantum efficiency, and the number of protons pumped per photon of absorbed light. Most of the data used in these calculations were derived from laboratory studies of model organisms, and in some cases were "best

Figure 1 Schematic view of the flow of energy (red arrows), carbon (blue arrows), or energy plus carbon (purple arrows) through a hypothetical marine system.
Solar energy capture processes of OP (oxygenic phototrophy), AAP (aerobic anoxygenic phototrophy), and PR (proteorhodopsin-based phototrophy) convert solar energy into chemical bond energy as ATP plus heat, and in the case of OP a portion of the energy gain is used to reduce carbon dioxide (CO 2 ) to organic carbon (Org-C). The light-independent heterotrophic (HETERO) flow of carbon and energy ultimately dissipates the potential energy in Org-C to heat. guesses" -but it is a great start. The theoretical gross energy yield via these two types of photoheterotrophy was compared to a model marine cyanobacterium, Synechococcus elongatus (MacKenzie et al. 2004), grown as an obligate photolithoautotroph (i.e., OP; Table 1). By their analysis, a "typical" PR-containing phototrophic bacterium would gain ∼ 10% of energy captured by a "typical" AAP bacterium, and ∼ 0.2-0.3% of the cyanobacterium (Kirchman and Hanson 2013). These estimates may be a bit misleading because they are expressed on a per cell basis. Given the fact that many PR-containing marine bacteria have biovolumes that are only a few percent of the model cyanobacterium used for comparison, the potential solar energy gain relative to their total energy demand for the PR-containing microbes may be greater than reported.

Quantitative assessments of energy flow
This brief commentary has focused on new pathways for solar energy capture and transformation in the deep blue sea. However, there are also other important aspects to marine system energy flow that need to be considered. These include the cycling of: (1) dissolved organic matter (DOM), especially labile products of photosynthesis; (2) reduced biogenic gases, especially methane and hydrogen; and (3) reduced inorganic derivatives of nitrogen, phosphorus, and sulfur. These reservoirs store and shunt potential energy, and enhance the overall magnitude and efficiency of solar energy capture and transformation in the sea. In the case of DOM, the energy content of the fairly large reservoir (∼ 75-100 mmol C per cubic meter in the euphotic zone) greatly exceeds the daily capture of solar energy and may regulate energy flow in stable oceanic communities. Even the more refractory portion (∼ 30-40%) of the total surface DOM pool, with a mean age of a few thousand years, may represent a longer term potential energy reservoir for the growth of "low-energy" specialists. Any quantitative assessment of ocean system energy flow must be able to measure all possible pathways of energy capture, transformation, and dissipation and needs to integrate over both space and time. Two possible experimental approaches have been employed to estimate total energy flow through marine planktonic assemblages: (1) heat flow via microcalorimetry, and (2) total ATP pool turnover rate, but additional methods need to be devised, calibrated, and field-tested. Future developments in the emergent field of metabolomics, especially energy transduction and energy storage molecules, will likely provide new opportunities for field application.
Microcalorimetry has only rarely been used to estimate heat flow in marine ecosystems (Pamatmat et al. 1981;Pamatmat 1982), primarily in coastal benthic habitats where metabolic activities are relatively high. Comparison of heat flow estimated from dark rates of oxygen uptake using assumptions regarding organic substrate composition and utilization efficiencies can lead to large discrepancies with direct heat flow estimation (Pamatmat 2003). In one of the few published studies of heat flow in marine plankton (Friday Harbor, Washington), the direct calorimetric-based value of 200-300 µW per liter was 4-6 times larger than that derived from extrapolation based on oxygen utilization (Pamatmat 2003). However, calorimetry currently suffers from several limitations. First, the nature of the differential microcalorimeters used for ecological studies cannot be used to assess solar energy for capture directly or to resolve biotic versus abiotic reactions. Second, the specialized nature of differential microcalorimeters limits sample throughput and replication. Finally, the relatively insensitive limits of heat detection preclude measurements in most open ocean planktonic ecosystems and, even for those systems that can be measured, calorimetry requires fairly long incubation periods which may bias estimates of in situ energy flow.
Recently, Djamali et al. (2012) have employed a purpose-built, differential microcalorimeter to measure the heat output of the marine microbial food web with an emphasis on the role of viral lysis. They experimented with aquarium-reared, size-fractionated model systems that were diluted to provide treatments with or without viruses. Their results indicated that approximately 25% of the total heat flow in their artificial planktonic communities could be attributed to viral activities. While the claim is made that their novel instrument is capable of measuring the heat produced from open ocean assemblages of ∼ 10 5 bacterial cells ml -1 without pre-concentration (Djamali et al. 2012), no such data are presented, or to my knowledge published elsewhere. Nevertheless, recent improvements in technology are very encouraging for possible use in future field studies (see review by Braissant et al. 2010). The three major limitations of calorimetry, however, remain: (1) inability to resolve biotic from abiotic processes, (2) difficulty measuring light versus dark energy heat fluxes, and (3) low sample throughput and lack of sample and reference replication for most commercial microcalorimeters.
An alternative to direct estimation of heat flow is the measurement of the turnover rate of the ATP pool in the microbial community (Karl and Bossard 1985). The central role of ATP in the stoichiometric coupling of all energy transforming metabolic reactions (phototrophic as well as chemotrophic) has been known since the pioneering work of Lipmann (1941). While intracellular ATP concentrations (i.e., the so-called "ATP pool") are fairly well buffered at 1-3 mM, the turnover rate of the pool tracks metabolic energy flow. ATP pool turnover results from the hydrolysis of one or both "high energy" phosphate bonds, followed by regeneration of ATP via substrate level, oxidative, or photophosphorylation. Because ATP is the common energy currency in all organisms and because the free energy of ATP hydrolysis is well constrained (46 ± 4 kJ per mol; Bridger and Henderson 1983), direct measurements of ATP pool turnover coupled with ATP Elementa: Science of the Anthropocene • 2: 000021 • doi: 10.12952/journal.elementa.000021 concentration should provide a quantitative estimation of biological energy flux (Karl 1993). Both heat flow and ATP pool turnover might be viewed as the epitome of reductionism because neither approach provides explicit information on which organisms or which pathways are most important in natural systems. Clearly in order to be useful, energy flow measurements need to be part of the holistic study of ecosystems and used as a tool in experimental perturbation studies to learn more about the controls on energy capture, transformation, and dissipation in marine systems.

Future research prospectus
As we move further into the anthropocene and continue to alter the sea around us, we need to have the capacity to monitor changes in the most fundamental property of the system, namely energy flow. The future ocean will be warmer, more stratified and nutrient starved, more acidic, and less oxygenated as a consequence of anthropogenic forcing by greenhouse gas emissions (Gruber 2011). These habitat changes will impact solar energy capture and transformation by microbial assemblages, so there is an urgent need to improve our conceptual understanding and quantitative assessments of energy flow in the open sea. I consider this to be one of the greatest contemporary challenges in microbial oceanography and marine ecology. The Center for Microbial Oceanography: Research and Education (C-MORE) is poised to begin a systematic two-year study (2014)(2015) of planktonic community energy flow in the NPSG with an emphasis on pathways and controls. Once a comprehensive energy budget is available for the NPSG microbial assemblage, other fundamental properties including the maximum empower selection principle (Odum 1983b;Sciubba 2011), net metabolic balance (Ducklow and Doney 2013), the concept of energy equivalents and transformity (Odum 1983a), and the enigma of microbial production of recalcitrant organic matter ( Jiao et al. 2010) can be systematically investigated. The development of a new theoretical framework for solar energy capture and energy flow via microorganisms in the sea may also be of practical value for policy makers and society as a whole (Prosser et al. 2007). As our demands for renewable energy continue to increase, a better understanding of the unique evolutionary adaptations of our magnificent marine microbes might improve our standard of living and extend our survival as a species.