Controls on zooplankton methane production in the central Baltic Sea
- 1Leibniz Institute for Baltic Sea Research Warnemünde, Seestrasse 15, 18119 Rostock, Germany
- 2Geoscience Center, Georg-August University of Göttingen, Goldschmidtstr. 3, 37077 Göttingen, Germany
- 3Federal Institute for Geosciences and Natural Resources, Stilleweg 2, 30655 Hannover, Germany
Correspondence: Oliver Schmale (firstname.lastname@example.org)
Several methanogenic pathways in oxic surface waters were recently discovered, but their relevance in the natural environment is still unknown. Our study examines distinct methane (CH4) enrichments that repeatedly occur below the thermocline during the summer months in the central Baltic Sea. In agreement with previous studies in this region, we discovered differences in the methane distributions between the western and eastern Gotland Basin, pointing to in situ methane production below the thermocline in the latter (concentration of CH4 14.1±6.1 nM, δ13C CH4 −62.9 ‰). Through the use of a high-resolution hydrographic model of the Baltic Sea, we showed that methane below the thermocline can be transported by upwelling events towards the sea surface, thus contributing to the methane flux at the sea–air interface. To quantify zooplankton-associated methane production rates, we developed a sea-going methane stripping-oxidation line to determine methane release rates from copepods grazing on 14C-labelled phytoplankton. We found that (1) methane production increased with the number of copepods, (2) higher methane production rates were measured in incubations with Temora longicornis (125±49 fmol methane copepod−1 d−1) than in incubations with Acartia spp. (84±19 fmol CH4 copepod−1 d−1) dominated zooplankton communities, and (3) methane was only produced on a Rhodomonas sp. diet, and not on a cyanobacteria diet. Furthermore, copepod-specific methane production rates increased with incubation time. The latter finding suggests that methanogenic substrates for water-dwelling microbes are released by cell disruption during feeding, defecation, or diffusion from fecal pellets. In the field, particularly high methane concentrations coincided with stations showing a high abundance of DMSP/DMSO-rich Dinophyceae. Lipid biomarkers extracted from phytoplankton- and copepod-rich samples revealed that Dinophyceae are a major food source of the T. longicornis dominated zooplankton community, supporting the proposed link between copepod grazing, DMSP/DMSO release, and the build-up of subthermocline methane enrichments in the central Baltic Sea.
Climate change, caused by increased greenhouse gas concentrations in the atmosphere, has an indisputable influence on societal and economical evolution on local, regional and global scales. In order to better predict future climate development, a more precise quantitative and mechanistic understanding of individual sources and sinks of relevant greenhouse gases, such as methane, is crucial. Methane as an atmospheric component has a relevant impact on the earth's climate (Etminan et al., 2016; IPCC, 2013). In general, biogenic sources of methane are associated with microorganisms (Archaea) in anoxic habitats, for example, in the ocean and lake sediments, wetlands, landfills, rice fields or the gastrointestinal tracts of termites and ruminants (IPCC, 2013). However, recent studies demonstrated that methanogenesis also occurs in oxic environments. These unconventional methanogenic pathways are mediated by aerobic prokaryotes (Yao et al., 2016) as well as eukaryotes, including plants (Keppler et al., 2006; Lenhart et al., 2016), animals (Tuboly et al., 2013), lichens (Lenhart et al., 2015), and fungi (Lenhart et al., 2012).
Methane concentrations in the oxygenated surface ocean and lake waters show strong regional and seasonal fluctuations (e.g. Jakobs et al., 2014; Donis et al., 2017). Large areas are supersaturated with methane and act as a net source to the atmosphere (e.g. Bange et al., 1994; Lamontagne et al., 1973; Tang et al., 2014). It is assumed that climate-driven modifications in aquatic systems such as increasing water temperatures, enhanced stratification, and nutrient limitation could further reinforce aquatic methane production (Karl et al., 2008). Such modifications are particularly important for shallow oxic methane production that largely bypasses microbial methane consumption as it places the methane source close to the water surface, intensifying fluxes to the atmosphere. However, the origin of methane in the oxic upper water column is still unclear and hence also referred to as the “methane paradox” (Scranton and Brewer, 1977).
Recently, a growing number of studies have identified several pathways that could explain methane enrichments in shallow oxic waters. The postulated CH4 production pathways include (i) direct CH4 production by algae from methyl sulfides such as methionine (Lenhart et al., 2016); (ii) bacterial break-down of methylphosphonate (MPn) under phosphate-stressed conditions (Repeta et al., 2016; Karl et al., 2008; Wang et al., 2017; Teikari et al., 2018); (iii) transfer of diazotroph-derived hydrogen among methanogens attached to algae (Grossart et al., 2011); (iv) CH4 production through microbial degradation of dimethylsulfide (DMS), dimethylsulfoniopropionate (DMSP) and dimethylsulfoxide (DMSO; Damm et al., 2010; Zindler et al., 2013); (v) photochemical production of methane from coloured dissolved organic matter (chromophoric dissolved organic matter, Zhang and Xie, 2015); and (vi) the microbial formation of methane in anoxic microniches within decaying organic aggregates or zooplankton fecal pellets (Holmes et al., 2000; Karl and Tilbrook, 1994; Oremland, 1979). The latter hypothesis is supported by oxygen microsensor studies that showed that anoxic conditions can exist in carbon- and nutrient-rich aggregates (Ploug, 2001; Ploug et al., 1997, 2008; Ploug and Jørgensen, 1999). Furthermore, molecular biological studies identified methanogenic archaea within fecal pellets produced by Temora longicornis and Acartia clausi (Ditchfield et al., 2012). These results are in agreement with the studies conducted by de Angelis and Lee (1994), who observed methane production during experimental zooplankton grazing on unialgal cultures. The authors used selected growth stages (adult and C5 stages) from pure cultures of T. longicornis, Acartia tonsa, and Calanus pacificus, which had been isolated from the coastal waters from the North Atlantic. In these laboratory experiments, methane production was only detected in incubations containing T. longicornis.
The Baltic Sea is characterized by pronounced lateral gradients including e.g. temperature, salinity, oxygen and methane concentrations, which altogether strongly influence the biology of the ecosystem (Feistel et al., 2008, and references therein). It consists of several sub-basins, of which the eastern Gotland Basin is the largest. The eastern Gotland Basin has a maximum depth of 248 m and establishes a seasonal thermocline at 10–30 m water depth in the summer months, and a permanent halocline at 70–90 m (Omstedt et al., 2004). In general, bottom waters in this basin are anoxic, unless episodic inflow events of more saline and oxygen-rich North Sea water into the deep basins lead to temporary oxic conditions (Franck et al., 1987; Mohrholz et al., 2015).
Methane concentrations in the Baltic Sea tend to increase with depth due to its release from the anoxic sediments (Schmale et al., 2010). However, recent studies revealed a recurring methane accumulation in oxic waters right below the thermocline during the summer months (Jakobs et al., 2014; Schmale et al., 2018). Stable carbon isotopes indicated an in situ biogenic methane origin, whereas clonal sequences pointed towards methanogenic Archaea as potential producers (Schmale et al., 2018). It was further shown that zooplankton-associated methane production contributed to the subthermocline methane enrichment (Schmale et al., 2018). The authors found that methane increased with increasing amounts of zooplankton and they suggested that changes in the copepod community and food web structure may influence the spatial heterogeneity of methane accumulation in the upper part of the water column. However, zooplankton-associated methane production rates alone were not sufficient to fully explain the observed methane enrichment. They concluded that this was most likely a consequence of using incubations with very dense and probably food-limited zooplankton communities (1000 times the natural density), leading to results that are difficult to transfer into the natural environment (Schmale et al., 2018). To overcome these experimental deficits, we developed a methane stripping-oxidation line to study zooplankton-associated methane production rates in the field. Our ship-based incubation experiments were performed with different zooplankton communities obtained from either the surface or from below the thermocline. We used almost natural copepod densities (1.5–8.5 times the natural density), and different diets of 14C-labelled phytoplankton. In conjunction with field investigations of methane concentrations and plankton distributions, the present study gives important insights into the controls of zooplankton-associated methane production in the central Baltic Sea.
2.1 Hydrographical and chemical characteristics of the water column
During cruise AL483 on R/V Alkor in August 2016 in the central Baltic Sea, seven stations in the western (TF0283, TF0284) and eastern (from south to north: TF0250, TF0260, TF0271, TF0286, TF0285) Gotland Basin (Fig. 1) were investigated. At each station, the hydrographical variables, including temperature, salinity and oxygen concentrations, of the water column were examined along vertical profiles using a SBE 911 plus CTD system (Seabird Electronics, USA; see Sect. S1 in the Supplement). In addition, the vertical methane distribution pattern and the stable carbon isotope ratio of methane (δ13C CH4) were measured to differentiate between regions affected and regions unaffected by subthermocline methane production. For these studies, subsamples were taken from the rosette water sampler and analysed in the home laboratory using a purge and trap system for methane concentration measurements and a continuous-flow isotope ratio mass spectrometer (IRMS) for stable carbon isotope analyses (see Sect. S1). In order to investigate whether station TF0284 was affected by coastal upwelling during the time of sampling, we analysed the output of a numerical ocean model, covering the North Sea/Baltic Sea. This hydrodynamical model computed a reconstruction of the state of the Baltic Sea with a spatial resolution of 1 nautical mile and 50 vertical levels. Further details of the model are given in Gräwe et al. (2015).
Surface water methane saturation is calculated following Eq. (1), where SV is the saturation value, Cw the measured concentration of methane in seawater and Cequi the concentration in equilibrium with the atmosphere using the solubility coefficient given by Wiesenburg et al. (1979).
2.2 Plankton community and lipid biomarker analyses
Phytoplankton samples for water column community analysis were taken from the 10 L free-flow bottles at stations TF0271, TF0284 and TF0286 (Fig. 1). Equal amounts of water from the mixed layer (depths: 0–1, 2.5, 5, 7.5 and 10 m) were pooled in accordance with the guidelines of the Helsinki Commission (HELCOM, 2017). At stations characterized by a distinct subthermocline methane enrichment (TF0271, TF0260, TF0285 and TF0286), additional samples were taken from the subthermocline chlorophyll a maximum at about 20 m water depth. At station TF0271, three samples were taken on 12 and 18 August to investigate the temporal variability in the community composition at this location. All phytoplankton samples were transferred into 250 mL brown glass bottles and preserved with 1 mL of acetic Lugol solution (2 % final concentration). For later community analyses, 25 mL sub-samples were concentrated in settling chambers (Utermöhl, 1958). They were counted using an inverted microscope and the counts were converted into carbon biomass using the cell volumes (Olenina et al., 2006; HELCOM, 2017).
Zooplankton samples for water column community analyses were collected with a WP2 net (towed at 0.5 m s−1, mouth opening, 25 m2, mesh size 100 µm, according to HELCOM, 2017) independent of daytime. Vertically integrated hauls from two depth intervals were taken to obtain zooplankton samples: (i) thermocline to surface (e.g. 20–0 m, depending on the physical structure of the water column), and (ii) halocline to thermocline (e.g. 60–20 m). The concentrated samples (500 mL) were preserved in borax-buffered formalin (4 % final concentration). For later copepod-specific community analyses, sub-samples were counted using a compound microscope until at least 500 individual copepods were taxonomically classified. Nauplii were pooled together for all copepod species, while C1–C5 copepodite stages and adults were pooled for individual species. Finally, to exclude potential daytime effects through vertical migration of the zooplankton communities above the halocline, counts from both integrated hauls were averaged according to the filtered volume. Similar to the phytoplankton sampling strategy, three samples at TF0271 were taken in a period of 10 days to investigate the temporal variability in the community composition at this station.
Lipid biomarkers were analysed to obtain information on the trophic relationships of copepods in the field at station TF0271 that showed a distinct methane enrichment below the thermocline. For this purpose, their putative food source, phytoplankton in the mixed layer, was sampled with an Apstein net. The phytoplankton were separated from co-sampled zooplankton using a simple self-built trap consisting of a 1.5 L transparent plastic bottle with a closable outlet at the bottom. The zooplankton were attracted towards the trap using a light source attached close to the outlet, and drained off. Then the phytoplankton, which remained in the bottle, were sampled. The target copepod T. longicornis has been known to migrate diurnally from the light-penetrated surface layer towards greater depths to escape predation (Hansen et al., 2006; Schmale et al., 2018). For lipid biomarker studies, a concentrated sample of zooplankton rich in T. longicornis was retrieved, avoiding major co-sampling of phytoplankton. This sampling was performed at station TF0271 by hauling a WP-2 net (see above) in the subthermocline layer (25–60 m) during the daytime. For comparison, a zooplankton sample was taken at station TF0250 without a distinct methane enrichment below the thermocline. Here, the community composition was low in T. longicornis and instead was dominated by Acartia spp. and Pseudocalanus spp. All samples were concentrated by sieving (20 µm) and kept frozen until further workup in the home laboratory. The samples were lyophilized and extracted (3×, ultrasound, 15 min, 20 ∘C) with dichloromethane (DCM) ∕ methanol (MeOH) (2:1, v:v), DCM ∕ MeOH (3:1, v:v) and DCM ∕ n-hexane (2:1, v:v). From the resulting total organic extract, neutral lipids (NL, largely containing storage lipids such as triglycerides, wax esters, and sterols) were separated using silica gel column chromatography by elution with DCM ∕ acetone (9:1, v:v). After drying, fatty acids (FA) in the NL fraction were transesterified by reaction with trimethylchlorosilane (TMCS) ∕ MeOH (1:9, v:v; 90 min, 80 ∘C). After partitioning into n-hexane (3×, 1 mL) and drying, alcohols contained in the NL were converted to their trimethylsilyl (TMS-) derivatives by reacting with 200 µl of a n-hexane/BSTFA/pyridine mixture (, ; 40 ∘C, 60 min). The derivatized NL fractions were analysed by coupled gas chromatography–mass spectrometry (GC–MS), as described elsewhere (Thiel and Hoppert 2018).
2.3 Sampling for ship-based laboratory experiments
Three ship-based grazing experiments were conducted at station TF0271, where a persistent and distinct methane enrichment below the thermocline was detected during the cruise. These experiments were designed to examine how (i) the abundance of copepods and (ii) their food source impact zooplankton-associated methane production, and how (iii) the methane production rates vary between different copepod communities. To measure copepod species-specific methane production rates, zooplankton communities were sampled from the surface (e.g. 20–0 m) and from the subthermocline waters (e.g. 60–20 m). In the central Baltic Sea, these layers are commonly dominated by Acartia spp. and T. longicornis, respectively (Hansen et al., 2006), and will be referred to as the surface and subthermocline communities. For the sampling hauls the cod end of the WP2 net was sealed from outside and towed 0.1 m s−1 to reduce damage to the zooplankton, and the content was transferred immediately into a 25 L bucket filled with seawater from the depth where the zooplankton was sampled (i.e. surface or subthermocline water). The zooplankton mainly comprised copepods and was left in the cold room at 10 ∘C for an hour to allow damaged individuals to settle to the bottom of the bucket. A subsample of living copepods was removed gently with a 500 mL beaker from the upper layer of the bucket to avoid injured animals, and checked for species composition under the dissecting microscope before subsamples were used for the grazing experiments. The sampling took place at 14:00 UTC, before vertical migration of one of the target copepods, T. longicornis, started (Hansen et al., 2006). This time was chosen because it was more likely that T. longicornis in the deeper water column would be starved and, thus, would start grazing within the experiments.
Two phytoplankton compositions were used to test for the influence of the diet on zooplankton-associated methane production: (i) a Rhodomonas sp. (Cryptophyceae) laboratory culture, and (ii) a Nodularia spumigena (Cyanophyceae) dominated culture from the surface mixed layer in the field, which is typically found in these waters of the central Baltic Sea in summer (Wasmund, 1997). The laboratory culture of Rhodomonas sp. was grown in f/2 medium (Guillard, 1962), prepared in autoclaved bottles from 0.2 µm filtered seawater from 10 m depth. A new sub-culture was established every 3–5 days and the inoculum was chosen to be sufficient to keep the culture in exponential growth (cf. Knuckey et al., 2005). The second phytoplankton culture was established from the top chlorophyll a fluorescence maximum (0–10 m) sampled with an Apstein net (55 µm mesh size, Hydro-Bios). The culture was re-suspended in 500 mL of seawater and left for an hour to allow the N. spumigena cells to float on top. The cells were carefully collected with a pipette and transferred into an autoclaved 1 L glass bottle, which was filled up with surface seawater. Then, 36.2 µM of NaH2PO4 as for the f/2 medium was added. Both the Rhodomonas sp. and the N. spumigena culture bottles were incubated in 90 L tubs, which were placed in a shaded location on deck and continuously flushed with sea surface water at a temperature of ∼18.5 ∘C. A third phytoplankton culture was collected from a subthermocline chlorophyll a peak closely below the thermocline (∼20 m depth), where mixotrophic Dinophyceae were expected to be dominant (Carpenter et al., 1995; Hällfors et al., 2011). For this, up to 150 L of seawater was obtained from a CTD rosette and concentrated on a 20 µm mesh. However, this culture did not grow sufficiently under similar temperature and light conditions as in situ, and could not be used within the grazing experiments.
2.4 Phytoplankton 14C-labelling
Once a phytoplankton culture was selected for grazing experiments, three aliquots were split between three autoclaved 1 L incubation bottles (DURAN®, borosilicate glass 3.3, clear, GL45) and filled up with the corresponding medium. One of these bottles was spiked with 18.5 MBq of 14C-labelled sodium bicarbonate (NaHCO3, 2.18 GBq mmol−1, Moravek Biochemicals, USA) for 14CH4 production measurements (Sect. 2.5.1 Methane production and consumption rates). The other two bottles received equal amounts of unlabelled NaHCO3 for measuring the particulate organic carbon concentration (Sect. 2.5.2 Analysis of particulate organic carbon) and microbial methane consumption (Sect. 2.5.1 Methane production and consumption rates). All bottles were incubated for 3–5 days to allow cells to grow and to take up the 14C label (Welschmeyer and Lorenzen, 1984). The specific activity of the labelled phytoplankton (SAphy) was measured daily by filtering 1–5 mL of the culture through a 0.45 µm cellulose nitrate filter (Millipore) and rinsing it thoroughly with Milli-Q water. The filter was then dissolved in Filter Count scintillation cocktail (Perkin Elmer) by vortexing and the amount of 14C label that was incorporated into particles was measured on a liquid scintillation counter (Perkin Elmer, Tri-Carb 2800TR). Blanks for the specific activity of the cultures were collected and analysed immediately after the label had been added to the incubation bottle.
SAphy was calculated using Eq. (2) and used for calculating methane production rates (de Angelis and Lee, 1994), where SAphy is the specific activity of the phytoplankton, Disintegrationsfilter are the disintegrations mL−1 on the filter, Volumeculture is the total volume of the incubated culture, 6×107 dpm MBq−1 is the constant for converting dpm into units of MBq, activityadded is the total activity of the tracer, which was added to the incubation, and SAtracer is the specific activity of the tracer.
2.5 Zooplankton grazing experiments
Three experiments with zooplankton grazing on phytoplankton (Table 1) were conducted. In experiment 1 we tested whether there was (i) a linear relationship between methane produced and the number of copepods incubated, and (ii) a difference in methane production between the surface and subthermocline zooplankton communities. In experiment 2 only the subthermocline zooplankton community was used and the incubation time was varied from 1 to 3 days to test whether the increase in methane was stable over time and the production rate per copepod stayed constant. In experiments 1 and 2 a laboratory strain of Rhodomonas sp. (Cryptophyceae), a standard food for copepod culturing (Dutz et al., 2008), was fed to the zooplankton communities. Rhodomonas sp. may be considered a model representative of the Cryptophyceae, which account for 5.5 % of the total phytoplankton biomass in the Baltic Sea in summer 2016 (IOW monitoring database: https://www.io-warnemuende.de/datenportal.html, last access: February 2018). In experiment 3 the subthermocline zooplankton community was fed the cyanobacterium N. spumigena and the incubation time was varied the same way as in experiment 2. Here we selected N. spumigena as a food source, because this species was the dominant phytoplankton in the surface waters during our field campaign and accounted for 23 % of the phytoplankton biomass. The different phytoplankton communities fed in these experiments allow one to assess the impact of the food source on zooplankton-associated methane production rates.
Each of the three grazing experiments consisted of three sets of incubations. The first set of incubations was conducted with zooplankton grazing on 14C-labelled phytoplankton for methane production measurements (Sect. 2.5.1 Methane production and consumption). The second set of incubations was conducted with zooplankton grazing on unlabelled phytoplankton to determine the food availability over the course of the grazing experiments (Sect. 2.5.2 Analysis of particulate organic carbon). Also, the third set of incubations was conducted with zooplankton grazing on unlabelled phytoplankton to measure the loss of methane by microbial oxidation under the experimental conditions (Sect. 2.5.1 Methane production and consumption).
In selective incubations the oxygen saturation was monitored over time using oxygen spots (5 mm, PreSens Precision Sensing) and an optode (Single Channel Oxygen Meter, Fibox 3 LCD, PreSens Precision Sensing). The average oxygen saturation was 75.2±2.9 % throughout the experiments.
2.5.1 Methane production and consumption rates
For the methane production incubations, 250 mL gastight bottles (DURAN®, borosilicate glass 3.3, clear, GL45) were used. The bottle lids were modified with one inlet and one outlet tube (Fig. 2), each sealed with autoclaved silicone stoppers. The inlet tube was long enough to reach into the lower third of the medium and had a glass frit attached at the end. The outlet tube was short enough to remain in the headspace of the bottle. Each bottle was filled with 50 mL of 14C-labelled phytoplankton and 3–15 mL of zooplankton stock culture and topped up to a total volume of 200 mL with 0.2 µm filtered seawater (Millipore GVWP filter) from either 10 or 20 m depth, according to the depth from which the zooplankton community was obtained. All bottles were kept in the dark at in situ temperature for 1 to 3 days in temperature-controlled incubators. The methane, which was produced within the time of incubation, was finally measured with a methane stripping-oxidation line (modified following de Angelis and Lee, 1994; Fig. 2; details on the work principle in Sect. S2). In brief, the bottles were connected to the line, the water samples were purged with helium carrier gas and the methane (and other hydrocarbons) was concentrated on a cold trap. After heating the trap the methane was released and separated from other hydrocarbons by gas chromatography (GC) and transferred to a furnace, where it was converted to 14C-labelled carbon dioxide (CO2). The 14CO2 was trapped in scintillation vials and the activity was measured by liquid scintillation counting. Finally, the activities were used for calculating methane production rates with Eq. (3), where activityzoo + phy is the activity measured in incubations containing zooplankton and phytoplankton, and activityphy is the activity measured in blank incubations.
Blank incubations were conducted with phytoplankton and seawater only and the volume of zooplankton was replaced with the corresponding amount of GF/F (Whatman) filtered seawater in which the zooplankton was kept before incubations. The CH4 concentrations of all blank incubations were not different from the blank of the methane stripping-oxidation line (Mann–Whitney U test, p=0.9, df=1).
Microbial methane oxidation rates were measured and the production rates corrected accordingly. For these measurements, 14C-labelled methane was injected into 600 mL incubation bottles, which were filled with the corresponding volumes of plankton and water as in the incubations for methane production measurements. The amount of produced 14CO2 was measured according to the method of Jakobs et al. (2013). The rates were similar in all incubations and in the range of 0.13–0.44 pM d−1. Neither the presence of copepods nor the composition of their community or their food had a significant influence on the methane consumption rates. In incubations with Rhodomonas sp., methane oxidation rates were 0.13–0.39 pM d−1 and accounted for a loss of 0.2–2.3 % of the produced methane. In incubations with cyanobacteria, the oxidation rates were slightly higher (0.3–0.44 pM d−1).
All sets of incubations included two to three replicates. To estimate the linear or exponential trends in methane concentration or production in relationship with the number of copepods or time, the Gauss–Newton method was used for minimizing the sum of squares between the fits and the measurements (Mystat 12, Systat software).
2.5.2 Analysis of particulate organic carbon
The particulate organic carbon (POC) content in the incubations was quantified at the beginning and end of our incubation experiments to determine the food availability over the course of the grazing experiments. For this, a larger volume of sample was required for later POC analysis using a Carlo Erba Elemental Analyser (Typ EA 1110; Carlo Erba; Nieuwenhuize et al., 1994), and 1 L bottles (DURAN®, borosilicate glass 3.3, clear, GL45) were used for incubations. To achieve similar concentrations of zooplankton and phytoplankton (mL−1) as in the first set of incubations, stock culture volumes were increased accordingly. For ambient POC analysis, one 50 mL sample was taken from each bottle at the beginning and at the end of the experiment on pre-combusted GF/F filters. The initial sample was removed from the experimental bottle before the copepods were added to it, and the final sample was taken after copepods had been removed with a 50 µm sieve. All POC measurements (Table 1) at the beginning and at the end of the incubations exceeded the threshold for food limitation of 1–0.5 mg C L−1 (Berggreen et al., 1988). As the food was diluted with 0.2 µm filtered seawater, all POC at the beginning of the experiments can be assigned to the diet that was added. However, at the end of the grazing experiments, excreted fecal pellets of the zooplankton may have added up to the organic carbon pool. Further, it was difficult to separate the copepods from N. spumigena by the 50 µm sieve, as N. spumigena typically exceeds 50 µm in size. In consequence, no grazing rates based on the decrease in POC were calculated for the individual incubations.
3.1 Subthermocline methane distribution
Surface waters were oversaturated with methane with respect to the atmosphere at all stations (saturation values between 118 % and 198 %) using the mean atmospheric methane concentrations for August 2016 obtained from atmospheric tower measurements at Utö (1919 ppb; position 59∘46′50 N, 21∘22′23 E; Juha Hatakka, Finnish Meterological Institute, personal communication, 2018). However, the eastern Gotland Basin had much higher maximum subthermocline methane concentrations than the western Gotland Basin (14.1±6.1 nM vs. 8.7±0.3 nM; Fig. 3). Such regional differences have previously been documented in the central Baltic Sea (Schmale et al., 2010, 2018; Jakobs et al., 2014).
Concentration profiles and stable carbon isotopes obtained in these earlier studies indicated that the subthermocline methane enrichments resulted from in situ production within the oxic water body. A transport from the deep anoxic waters was excluded because the methane from this pool is efficiently oxidized by aerobic methanotrophic bacteria situated in the oxic–anoxic transition zone at about 100 m water depth (Jakobs et al., 2013; Schmale et al., 2012, 2016). As their metabolism favours the turnover of 12CH4, the remaining 13CH4 becomes enriched and δ13C CH4 values in the respective water layer are comparably high (e.g. −40 ‰ in 80 m water depth; Jakobs et al., 2013). In the present study, subthermocline methane enrichments in the eastern Gotland Basin were characterized by strikingly depleted δ13C CH4 values (−62.9 ‰ at 27 m at TF0271, Fig. 3), supporting the idea that the pronounced methane anomaly in this area originated from in situ biogenic production. In contrast, stable isotope ratios of methane in the upper water column of the western Gotland Basin showed δ13C CH4 values of −47.7 ‰ at 20 m water depth (TF0284, Fig. 3) that are close to atmospheric equilibrium (−47 ‰).
Seasonal observations in the Baltic Sea revealed that the development of a thermocline, which functions as a barrier and limits fluxes to the atmosphere, was essential for the build-up of subthermocline methane enrichments (Jakobs et al., 2014; Schmale et al., 2018). Upwelling events can offset water column stratification through a replacement of warm, mostly nutrient-depleted surface water by cooler and usually nutrient-enriched subthermocline waters (Gidhagen, 1987; Lehmann and Myrberg, 2008; Reissmann et al., 2009). Such events may also cause a rapid decline in phytoplankton biomass in the surface water and affect the plankton composition (Vahtera et al., 2005; Nausch et al., 2009; Wasmund et al., 2012). Upwelling significantly increase surface water methane concentrations in the area around Gotland during the summer (Gülzow et al., 2013; Schneider et al., 2014). During our field campaign the sea surface temperature at station TF0284 in the western Gotland Basin dropped from 18 to 12 ∘C, as indicated by our oceanographic model output (Fig. 4; see also the temperature profile of station TF0284 in Fig. 3). Assuming the thermocline was located at 18–20 m depth we estimated that the upwelled water masses must have had originated from a depth of 25–35 m. Upwelling of cold, methane-rich subthermocline water can plausibly explain the strong surface water methane oversaturation observed at TF0284 (saturation value of 198 %). The other stations were not affected by upwelling events during the time of sampling. Even though our oceanographic model output indicated that the water mass at station TF0283 (sampled on 11 August) was located at the upwelling front (Fig. 4), our field measurements showed that the station was not affected by the event, as there is no drop in the surface water temperature visible (Fig. 3). However, our study indicates that in contrast to the deep water methane pool, which is efficiently separated from the surface water through the halocline at about 60 m depth (Schmale et al., 2010; Jakobs et al., 2014), upwelling of subthermocline waters has to be considered an important mechanism that contributes to the sea–air methane fluxes in the Baltic Sea.
3.2 Controls on zooplankton associated methane production
We obtained species- and food-specific methane production rates in incubations, which contained field copepods (surface and subthermocline communities, Fig. 5) in nearly natural abundances (1.5–8.5 times the natural density) by using the methane stripping-oxidation line. We found a substantial increase in methane production with the number of copepods in the incubations, but no production in controls containing phytoplankton only (Fig. 6). This implies that the production of methane is associated with the active grazing of zooplankton.
The incubations with a high proportion of T. longicornis had higher production rates than the Acartia spp. dominated setups (125±49 vs. 84±19 fmol CH4 copepod−1 d−1). This indicates that methane production may depend on the composition of the zooplankton community (Fig. 6a). However, the differences were not significant (Kruskall–Wallis test; p=0.150, df=1), which may be a consequence of the limited number of incubations. Similar observations were made in laboratory experiments using cultured species from the North Atlantic (de Angelis and Lee, 1994). These authors observed methane production in all experiments for T. longicornis grazing on phytoplankton, but not for Acartia tonsa. These differences may be due to species-specific differences in grazing rates, food preferences and gut floras. Furthermore, the methane production rates per copepod reported by de Angelis and Lee (1994) were 2 orders of magnitude higher (4–20 pmol CH4 copepod−1 d−1) than the rates measured in our experiments. Still, our results are in agreement with those of previous zooplankton incubation experiments conducted in the central Baltic Sea (0.3 pmol CH4 copepod−1 d−1, Schmale et al., 2018). This similarity is notable as the previous experiments used zooplankton abundances that were about 1000 times higher than the natural density in the field. The obvious discrepancy from the methane production rates reported by de Angelis and Lee (1994) might be related to the physiological differences (e.g. animal size) between the copepods used (length T. longicornis North Atlantic: 1300 µm vs. Baltic Sea: 700 µm). The methane production rates may also be lower for younger development stages of copepods, which contributed to the natural surface community used in our incubations (Fig. 5). Animal size affects the oxygen gradient in the guts of these copepods and affects the dimension of produced fecal pellets and, thus, the penetration depth of oxygen into the pellet (Ploug and Jörgensen, 1999; Tang et al., 2011). Alternatively, lower methane production rates observed in our experiments may have reflected a response of the animals to stress of being removed from their natural environment. In contrast to the study of de Angelis and Lee (1994), who used cultured animals in their experiments, we immediately transferred the field copepods into incubation bottles and fed phytoplankton that were not representative of the phytoplankton biomass of the Baltic Sea (i.e. the cryptophyte Rhodomonas sp.) and thus did not belong to their natural food source. To lower the capture stress, we selected a rather gentle method for sampling, and we avoided food shortage, which was shown to be more influential on the decrease in physiological rates (Ikeda and Skjoldal, 1980). Also, we used a food source which was previously shown to be of good quality (e.g. Knuckey et al., 2005; Koski and Breteler, 2003). Another factor which may have led to lower methane production rates than measured by de Angelis and Lee (1994) is the quality of the filtered seawater used in the incubations. In our experiments we used filters with a pore size of 0.2 µm, while de Angelis and Lee (1994) used filters with a pore size of 1.2 µm to prepare the incubation water. Our intention was to exclusively investigate the methane production by zooplankton while minimizing the influence of particulate material (e.g. fecal pellets) in the seawater. However, we are aware that the smaller pore size used in our studies reduced the number of bacteria in the incubation water, which may have been important for the methane production outside the body of the copepods.
Measurable methane production occurred when the T. longicornis-dominated community was fed on Rhodomonas sp., while no production occurred when it was fed on the cyanobacterium N. spumigena (Fig. 6b). In fact it appears that these cyanobacteria are a rather negligible food source for planktonic herbivores due to their toxic properties, large size, and low lipide concentrations (Sellner et al., 1994; Eglite et al., 2018). Our experiments therefore reveal that the availability of a suitable phytoplankton diet is an important control on the zooplankton-associated methane production.
The observed exponential increase in methane with increasing incubation time implies that zooplankton-associated methane production is a continuous process (Fig. 6b). In addition, we measured a linear increase in the methane production rates per individual with increasing incubation time (Fig. 7). Potential explanations include (1) a delay in grazing by stress through experimental conditions, (2) the accumulation of fecal pellets within the incubation bottles followed by methane production in anoxic microenvironments, and (3) enhanced methane production through release of methane precursor substances from fecal pellets or from disrupted phytoplankton cells into the incubation water. In the first case we would expect the production rates to stabilize within the 3 days of the experiment; instead, we observed a linear increase and a rather low variability among the replicates. In the second case, the fecal pellets could temporarily act as anoxic microenvironments for methanogenic archaea (Oremland et al., 1979; Bianchi et al., 1992; Marty et al., 1993; Karl and Tilbrook, 1994; Ditchfield et al., 2012). However, it is debatable whether anoxic conditions can persist within fecal pellets outside of the anoxic digestive tracts of the copepods (Ditchfield et al., 2012; Ploug et al., 2008). For T. longicornis fed on Rhodomonas sp., the diffusive boundary layer of the fecal pellets through which the exchange of gases occurs was shown to be very thin, and no indications of anoxic conditions were detected (Ploug et al., 2008). Studies investigating the anoxic potential within particle aggregates were only able to confirm anoxic conditions in the interior of nutrient- and carbon-rich particles >600 µm and suggest that anoxia in marine aggregates is more likely to occur in an oxygen-depleted water column (Ploug et al., 1997; Ploug et al., 2001). On our cruise, a fecal pellet size of only <150 µm was measured for the surface and subthermocline zooplankton communities. We therefore suggest that anaerobic methanogenesis by archaea thriving within fecal pellets played only a minor role. Instead, continuous release of methanogenic substrates (like organic sulfur compounds) by cell disruption during feeding, defecation, or diffusion from fecal pellets may have resulted in an enrichment of these substances in the incubation water, and fostered a subsequent microbial turnover of these precursors outside the body of the copepod.
3.3 Organic sulfur compounds as possible substrates for methane production in oxic waters
The phytoplankton community composition in the surface (Fig. 8) and subthermocline waters (Fig. 9) was similar at all investigated stations during our field campaign. However, the phytoplankton biomass was lower at station TF0284, which was recently influenced by an upwelling event. Hence, it needs to be considered that also the phytoplankton composition at this station could have been altered by the event. Dinophyceae, in particular the mixotrophic Dinophysis norvegica, were more abundant at stations with a distinct subthermocline methane enrichment. They produce relatively high amounts of DMSP and DMSO compared to the other phytoplankton species observed within our study (Keller et al., 1989; Hatton and Wilson, 2007; Caruana and Malin, 2014). Also, positive correlations have previously been observed between DMSP and CH4 and DMSO and CH4 in the surface ocean (Zindler et al., 2013). Damm et al. (2010) suggested that the microbial metabolization of DMSP and its degradation products dimethylsulfide (DMS) and methanethiol to methane is favoured under nitrogen-stressed conditions in oligotrophic waters. In the central Baltic Sea the dissolved inorganic nitrogen pool that builds up over the winter months is already exhausted after the first spring bloom in the photic zone and leaves behind nitrogen-stressed conditions for phytoplankton taxa, which are unable to fix molecular nitrogen (Schneider et al., 2009). These nitrogen-stressed conditions can lead to an accumulation of DMSP in phytoplankton cells (Sunda et al., 2007) that exceeds 10 % of the cell carbon (Matrai, 1994). In the central Baltic Sea a pronounced DMS maximum was detected during summer months in the surface waters (Leck et al., 1990). No correlation was identified between high DMS concentrations and any particular phytoplankton species. Instead, DMS production in the surface water was accelerated through phytoplankton growth under nitrogen-limited conditions, and correlated significantly with copepod and total zooplankton biomass. Hence, the release of DMSP, DMSO and DMS from phytoplankton was suggested to be controlled by zooplankton and heterotrophic bacteria (Leck et al., 1990; Kwint et al., 1996; Wolfe et al., 1997; Simo et al., 2002; Lee et al., 2003).
Similar to phytoplankton, zooplankton, in particular copepods, may use DMSP for osmoregulation and were shown to increasingly assimilate DMSP at higher salinities (Tang et al., 1999). Likewise, DMSP ingestion by copepods increased with increasing DMSP content of the food (Tang et al., 1999). De Angelis and Lee (1994) showed that T. longicornis feeding on Dinophyceae (Prorocentrum minimum) resulted in the highest methane production rates per copepod, which suggests a link between the DMSP/DMSO content of the diet and zooplankton-associated methane production. Based on the observed zooplankton and phytoplankton distributions (Figs. 8, 9 and 10), we speculate that the development of distinct subthermocline methane enrichments in the central Baltic Sea is influenced by the combination of T. longicornis and relatively high abundances of Dinophyceae.
To retrieve further information about potential trophic relationships between T. longicornis and Dinophyceae, lipid biomarkers of concentrated plankton samples from two depths, the surface layer and subthermocline waters were analysed. Also, samples from stations with (TF0271) and without (TF0250) distinct subthermocline methane enrichment were compared. Although individual fatty acids have to be assigned cautiously to specific taxonomic groups, the distribution of these compounds in copepod neutral lipids has been shown to largely reflect the lipid composition of the prey (Peters et al., 2013). Figure 11a shows the neutral lipids extracted from the surface-layer phytoplankton obtained at station TF0271. The fatty acids contained in samples from this depth revealed major contributions from cyanobacteria (typically high in 16:0 and C18 fatty acids), diatoms (high in 20:5), and Dinophyceae (22:6; cf. Peters et al., 2013), which corresponds to the phytoplankton community composition observed at this station by microscopy (Fig. 8a). The relatively high abundance of Dinophyceae in the surface layer was further reflected in the presence of 24-norcholesta-5,22-dien-3β-ol (265,22), an unusual sterol that is regarded as a specific marker for these algae in temperate waters (Rampen et al., 2007).
Compounds extracted from the subthermocline zooplankton community at station TF0271, dominated by T. longicornis (52 %), revealed a broad similarity to the phytoplankton-derived lipids, and reflected the diurnal feeding behaviour of these copepods in the surface mixed layer (Fig. 11b). Notably though, lipids of putative dinophyte origin were considerably enriched, supporting the idea of a preferential uptake of these algae by T. longicornis. In contrast, mixed zooplankton obtained at reference station TF0250 contained few T. longicornis (10 %) but relatively more Acartia spp. (37 %) and Pseudocalanus spp. (32 %). This sample showed much lower relative amounts of the Dinophyceae-derived biomarkers 22:6ω3 and 265,22, indicating only a minor importance of this food source at the reference station (Fig. 11c). Altogether, our biomarker data further corroborate our suggestion that the feeding of T. longicornis on (DMSP/DMSO-rich) Dinophyceae may be an essential factor in the development of subthermocline methane enrichments in the central Baltic Sea.
We further assume that zooplankton-associated production of fecal pellets and the transit of these pellets through the water column play a critical role in the build-up of the pool of organic sulfur compounds in the central Baltic Sea. Sinking velocities are low for pellets produced from Dinophyceae (Hansen and Bech, 1996; Thor et al., 2003). Hence, we propose that high degradation rates of those fecal pellets and an efficient microbial turnover of the contained organic sulfur compounds (e.g. DMSP; Tang, 2001) contribute to the subthermocline methane enrichment. The gradual loss of organic sulfur compounds from fecal pellets could plausibly explain the increase in copepod-specific methane production over time, as measured in our incubation study (Figs. 6b and 7). Unfortunately, no Dinophyceae culture was available for our field experiments, because of their relatively low growth rates (Carpenter et al., 1995) and mixotrophic feeding requirements (Tong et al., 2010) that did not allow an adequate radio labelling of the culture with sodium bicarbonate. Likewise, the relatively low production rates observed in our experiments could be explained by the lack of appropriate substrates for methane production, as Cryptophyceae (i.e. Rhodomonas sp.) contain only low amounts of DMSP as compared to other phytoplankton groups (Dong et al., 2013). Furthermore, we used 0.2 µm filtered seawater in our incubations, which was depleted in microorganisms. However, these microorganisms might be relevant for the turnover of DMSP to methane outside of the copepod bodies.
Several processes that produce methane in oxic waters have been recently identified and it is assumed that climate change will impact their source strength, with far-reaching consequences for methane flux and climate feedback. However, mechanisms and magnitudes of these sources remain vague. Based on our findings, we conclude that zooplankton contributes to subthermocline methane enrichments in the central Baltic Sea by (1) direct methane production within the digestive track of copepods and/or (2) indirect contribution to methane production through release of methane precursor substances into the surrounding water, followed by microbial degradation to methane outside the copepod's body. Further, our field observations combined with lipid biomarker studies indicate that a distinct food web segment consisting of DMSP-rich Dinophyceae and the copepod T. longicornis may foster the build-up of methane anomalies in oxic waters of the central Baltic Sea. For future studies, we recommend using unfiltered in situ water for the incubations. We further suggest cultivating Dinophyceae under controlled laboratory conditions before the field campaign and feeding these radio-labelled organisms to in situ copepods directly after sampling in the field. These incubations should be accompanied by a quantification of the DMSP and DMS content in phytoplankton and zooplankton as well as in the water column.
The data presented here are included in the Supplement.
The supplement related to this article is available online at: https://doi.org/10.5194/bg-16-1-2019-supplement.
BS, OS, and SO designed and built the methane stripping-oxidation line and performed the incubation experiments. JW and NLW supported the plankton sampling and the grazing experiments. VT and AKW conducted the lipid biomaker analysis. UG performed the oceanographic modelling of the upwelling event. SS performed the stable carbon isotope analyses. GR, ML, and NW helped with the data analyses and interpretation. All the authors co-wrote the manuscript.
The authors declare that they have no conflict of interest.
We thank Nicole C. Power Guerra for her help at sea and in the laboratory. We
would also like to thank Michael Glockzin for producing the map and Juha
Hatakka (Finnish Meteorological Institute) for providing the atmospheric
methane concentration data from station Utö. Further, we appreciate the
critical comments by Jörg Dutz. We thank the captain and crew of R/V
Alkor for technical support. This work was supported by the German
Research Foundation (DFG) through grant SCHM 2530/5-1 to Oliver Schmale, DFG
grant LA 1466/10-1 to Matthias Labrenz, and DFG grant LO 1820/4-1 to Natalie Loick-Wilde.
The publication of this article was funded by the
Open Access Fund of the Leibniz Association.
Edited by: Helge Niemann
Reviewed by: Susan Mau and one anonymous referee
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