An approach for particle sinking velocity measurements in the 3–400 μm size range and considerations on the effect of temperature on sinking rates
The flux of organic particles below the mixed layer is one major pathway of carbon from the surface into the deep ocean. The magnitude of this export flux depends on two major processes—remineralization rates and sinking velocities. Here, we present an efficient method to measure sinking velocities of particles in the size range from approximately 3–400 μm by means of video microscopy (FlowCAM®). The method allows rapid measurement and automated analysis of mixed samples and was tested with polystyrene beads, different phytoplankton species, and sediment trap material. Sinking velocities of polystyrene beads were close to theoretical values calculated from Stokes’ Law. Sinking velocities of the investigated phytoplankton species were in reasonable agreement with published literature values and sinking velocities of material collected in sediment trap increased with particle size. Temperature had a strong effect on sinking velocities due to its influence on seawater viscosity and density. An increase in 9 °C led to a measured increase in sinking velocities of ~40 %. According to this temperature effect, an average temperature increase in 2 °C as projected for the sea surface by the end of this century could increase sinking velocities by about 6 % which might have feedbacks on carbon export into the deep ocean.
Equivalent spherical diameter
Temperature-dependent term in Stokes’ Law
Earth’s gravitational acceleration
Coefficient of drag
Measured sinking velocity
Dynamic viscosity of seawater
Density of spherical particles
Density of seawater
Distance between particle and wall
Radius of a sphere
Coefficient of determination
Sinking velocity of a particle corrected for wall effects
Sinking velocities of marine particles are generally determined by two major properties—size and excess density over seawater. Most organic particles within the oceans are relatively small (<100 μm) and their individual contribution to the downward flux of organic matter is therefore minor (Clegg and Whitfield 1990). However, in case small particles aggregate to form larger ones, they might eventually sink fast enough to end up below winter mixed layer depths without severe remineralization. Aggregation is mediated either by zooplankton that graze on small particles and enclose them in larger fecal pellets, or by highly adhesive organic materials (e.g., Pilskaln and Honjo 1987; Passow et al. 1994). The excess density of particles is primarily determined by the amount of inorganic ballast material incorporated in them. Ballast materials can be either lithogenic (e.g., dust) or biogenic (opal and calcium carbonate).
It has been hypothesized that organic carbon export into the deep ocean is tightly coupled to these ballasting materials (Armstrong et al. 2002; Francois et al. 2002; Klaas and Archer 2002; but see also Passow 2004), since particles associated with them sink considerably faster than those consisting of organic matter alone (e.g., Honjo 1976; Engel et al. 2009; Iversen and Ploug 2010). Hence, a change in the ballast loading of particles may feedback on organic carbon export and consequently on atmospheric carbon dioxide levels (Riebesell et al. 2009). In this respect, sinking velocity measurements are a key parameter in estimating organic carbon export (e.g., Feinberg and Dam 1998; Ploug et al. 2008; Fischer and Karakas 2009).
Here, we introduce an efficient method to determine sinking velocities by means of video microscopy. This approach is easy to set up, can be applied to a wide particle size range, and allows precise measurement and analysis of high numbers of samples per day. Furthermore, particles within a mixed sample can be distinguished automatically during analysis so that only sinking velocities of particles fulfilling defined criteria are evaluated. It, therefore, offers new possibilities to determine sinking velocities of individual particle classes with high temporal resolution and without much effort over the course of long-lasting laboratory and field experiments.
Materials and methods
Four different kinds of particles were prepared for sinking velocity measurements. These are small polystyrene beads, large polystyrene beads, monospecific phytoplankton cultures, and sediment trap material.
Small polystyrene beads (10 μm in diameter, Beckman) were delivered in an aqueous solution containing surfactants and preservatives. To remove this solution, they were rinsed on a polycarbonate filter (0.8-μm pore size) with 100 mL of filtered seawater. The beads that remained on the filter were resuspended in ~2 mL of filtered seawater (salinity = 35) and transferred using a pipette into the glass cuvette where sinking velocities were determined in. The larger beads (75–400 μm in diameter, Polysciences) were delivered as dry powder so that it was not necessary to rinse them. They were added directly to ~10 mL of filtered seawater (salinity = 33.5). In order to load the glass cuvette with the large beads, a 30-cm-long plastic pipe (inner diameter 6 mm) was connected to the top of the glass cuvette with a silicon tube. A pipetting ball was attached to the other side of the plastic pipe to suck the filtered seawater containing the large beads into the glass cuvette. Plastic pipe and pipetting ball remained on top of the glass cuvette during measurements and were stabilized with cable ties.
Measured sinking velocities (corrected for wall effects with Eq. 3) of various phytoplankton species at individual culture conditions (temperature T (°C), salinity S, light (μmol m−2 s−1))
Sinking velocity (m day−1)
ρparticle (kg m−3)
Crocosphaera watsonii (WH8501)
Nutrient replete; T = 28; S = 35; light = 150
Dictyocha spec. (isolated at N54° 19′ 48″ E10° 7′ 48″ in March 2011)
Nutrient replete; T = 15; S = 13.8; light = 150
Without visible silicate skeleton
Rhodomonas spec. (unknown)
Nutrient replete; T = 15; S = 15; light = 150
Only non-motile cells were investigated
Emiliania huxleyi (B92/11)
Nutrient replete; T = 15 °C; S = 35; light = 180
aEmiliania huxleyi (B92/11)
3 days of phosphorus limitation; T = 15; S = 35; light = 150
Emiliania huxleyi without CaCO3 covering (B92/11)
Nutrient replete but grown at low dissolved inorganic carbon(~500 μmol kg−1) and low pH (~7.2) so that cells were not able to produce CaCO3. T = 15; S = 35; light = 150
aGephyrocapsa oceanica (RCC1303)
Nutrient replete; T = 20; S = 35; light = 150
Gephyrocapsa oceanica without CaCO3 covering (RCC1303)
Nutrient replete but grown at low dissolved inorganic carbon(~500 μmol kg−1) and low pH (~7.2) so that cells were not able to produce CaCO3. T = 15; S = 35; light = 150
Calcidiscus leptoporus (isolated at N38° 39′ 22″ W27° 14′ 08″ in April 2010)
Nutrient replete; T = 16; S = 35; light = 160
Calcidiscus leptoporus coccoliths (see above)
Nutrient replete; T = 16; S = 35; light = 160
Thalassiosira oceanica (CCMP1005)
Nutrient replete; T = 24.6; S = 35; light = 65
Thalassiosira pseudonana (CCMP1012)
Nutrient replete; T = 17; S = 35; light = 50
Thalassiosira weissflogii (CCMP1052)
Nutrient replete; T = 17; S = 35; light = 50
Phaeodactylum tricornutum (unknown)
Nutrient replete; T = 17; S = 35; light = 50
Sediment trap material was obtained in spring 2011 during the SOPRAN mesocosm CO2 enrichment study off the coast of Bergen (Norway; 60° 15′ 36″ N 5° 12′ 0″ E). The material was collected for 24 h in the sediment trap and consisted to a large proportion of complete or fragmented fecal pellets produced by copepods (Calanus finmarchicus, Calanus helgolandicus, and Temora spec.) and appendicularians (probably Oikopleura dioica). The material was partitioned using a 300-μm sieve to remove large aggregates and gelatinous material which would have otherwise clogged the glass cuvette in which particle sinking velocity was determined. The particles passing through the sieve were collected in a petri dish and diluted with filtered seawater of known salinity (33.5). This sample was transferred into the glass cuvette in the same way as described for large polystyrene beads.
Measurement of sinking velocities
Dimensions of glass cuvettes used for sinking velocity measurements
Convection during measurements
Convection can result from temperature gradients within the glass cuvette and influence sinking velocities of particles. Temperature control is, therefore, essential and was closely monitored during all measurements. Furthermore, glass cuvettes were constantly ventilated with air to avoid the formation of local temperature gradients in the vicinity of heat sources. Measurements in glass cuvettes (larger polystyrene beads and sediment trap material; Table 2) were performed in either temperature-controlled rooms (variation ±0.3 °C) or light chambers for phytoplankton culturing (Rubarth Apparate GmbH, variation ±0.04 °C). Measurements in glass cuvettes <300 μm (small beads and phytoplankton cells; Table 2) were performed in temperature-controlled rooms (variation ±1 °C).
Evaporation at the air–water interface at the top of the glass cuvette is another potential source of convection as the water cools and becomes more saline, thereby inducing downwelling and upwelling. This can be minimized by sealing the top of the sedimentation column with a lid (Ploug et al. 2010). The 3,000-μm large glass cuvettes used for the measurements of large polystyrene beads and sediment trap material (Table 2) were sealed airtight by the pipetting ball used to transfer the sample into the sedimentation column (see section on “Sample preparation”). Glass cuvettes <3,000 μm (Table 2) were not entirely closed but a thin and ~5-cm-long silicon tube connected to the top of the cuvettes reduced evaporation since it minimized the gas exchange between the atmosphere and the air above the air–water interface.
The presence of convection cells was investigated by testing whether polystyrene beads of similar size and density sink constantly downward at every position inside the cuvette. We tested 100-, 300-, 600-, 1,000-, and 3,000-μm glass cuvettes (Table 2). Convection was usually present in glass cuvettes larger 300 μm at non-temperature-controlled conditions but was absent in all cuvettes when temperature was controlled. Convection was not detected in 100- and 300-μm glass cuvettes even in rooms with relatively large temperature variations of approximately ±1 °C. This might be due to adhesion effects in these comparatively thin and capillary-like glass cuvettes which prevent the formation of convection cells.
Evaluation of sinking velocities
Each particle photographed by the FlowCAM® was automatically characterized by 45 properties with the software “visual spreadsheet” (Fluid Imaging). The most important properties for the evaluation of sinking velocities were as follows: First, the horizontal and vertical position of the particles on the display window (X- and Y-coordinates) and the corresponding time the particle was photographed at that position. Second, several shape properties of the particle such as for example length, width, edge gradient, and equivalent spherical diameter (ESD). We developed a script using MATLAB (MathWorks®) which made use of these properties to automatically calculate sinking velocities together with mean particle length, width, and ESD of each particle. Furthermore, the script allowed definition of certain criteria so that only particles fulfilling these criteria were considered in the automatic evaluation. This ability was important (i) to discard particles that were not focused (by defining a minimum edge gradient of 0.8), and (ii) to distinguish, for example, fecal pellets and fecal pellet fragments within the sediment trap material from all other particles (by defining a minimum length of 150 μm and a maximum width to length ratio of 0.38). Note that these length values were determined visually before the evaluation with the MATLAB script. The basic functioning of the script shall be outlined in the following.
During measurement, particles are always sinking vertically through the area photographed by the camera (Fig. 1a) so that they change their position on the Y-coordinate in consecutive pictures but (if at all) only marginally on the X-coordinate. Since a sinking particle is photographed and characterized several times when sinking through the area monitored by the camera, its X- and Y-coordinates appear as vertical lines of dots when all coordinates are plotted into the same figure (Fig. 1b). Plotting the Y-position of every particle to the corresponding point in time instead of the corresponding X-position shows that sinking particles appear as separate lines of dots with certain slopes (Fig. 1c). The slopes of these lines depict the change of the vertical position of the particle per unit time and therefore their sinking velocity. The MATLAB script checks that all the dots within such line belong to the same particle by comparing several of their properties to each other (e.g., length, width, and ESD). Dots with inconsistent properties are removed from the line, while those with consistent properties are defined as one sinking particle. In the following step, the script fits a linear regression including only the dots with consistent properties. This regression is rejected from further evaluation by the script if the fit is based on less then 8 data points or if the coefficient of determination (R2) is below 0.995. This second procedure erases irregular lines which accidentally pass the first sorting. In case a line of dots pass the two sorting procedures, the script stores the slopes of the regression lines as sinking velocity of the particles and calculates their average lengths, widths, and ESDs from the mean of all regression points. Furthermore, we implemented equations to calculate the Reynolds number of a sinking particle and its density.
The evaluation script can be supplied by the corresponding author.
Quantification of wall effects
Next to particle interactions with walls, particle interactions among each other can affect sinking velocities too. Particle–particle interactions depend (among other factors) on the distance between them, their shapes and sizes, and their orientations to each other (Happel and Brenner 1991). For example, two equally large spheres sinking directly next too each other sink roughly 30 % faster than each one would sink individually (Happel and Brenner 1991). Particle–particle interactions occur more frequently at high particle densities. It was not possible to quantify these interactions reliably within a measurement. Hence, they were avoided by keeping track of the density inside the sample and diluting the sample if necessary.
Sinking velocities of polystyrene beads
The reliability of the method was assessed by repeated measurements of spherical polystyrene beads of known density and size and comparing the results with theoretical sinking velocities calculated from Stokes’ Law (Eq. 1). The mean sinking velocity of polystyrene beads with a certified diameter of 10 μm showed a maximum difference of 10 % based on eight repeated measurements. The difference between the mean of all eight measurements (corrected for wall effects) and the theoretical sinking velocity calculated from Stokes’ law (Eq. 1) was less then 1 % (Fig. 2a). Measured sinking velocities of beads ranging from 75 to 400 μm were increasing exponentially with increasing size as predicted by Stokes’ Law but were systematically lower than the theoretical ones due to wall effects (Fig. 2b). Correcting for wall effects with Eq. 3 improved the consistency between theoretical and measured values (Fig. 2c). The decelerating effect of the cuvette walls was growing with increasing bead diameter as predicted by Eq. 3.
Sinking velocities of phytoplankton cells
Sinking velocities of phytoplankton cells varied with size and ballasting material such as calcium carbonate. The fastest sinking species investigated here was the calcified coccolithophore Calcidiscus leptoporus with about 4.3 m day−1, while the slowest sinking one was the un-calcified coccolithophore Emiliania huxleyi (0.03 m day−1). The presence of ballasting calcium carbonate in the coccolithophores E. huxleyi and Gephyrocapsa oceanica increased sinking velocities by about a factor of ten. Individual coccoliths of C. leptoporus were sinking with about 0.74 m day−1 which is faster than complete cells of E. huxleyi and G. oceanica. Phosphorus-limited E. huxleyi cells sank on average slightly slower than the exponentially growing ones (~0.3 and ~0.38 m day−1, respectively, Table 1).
The small and uncalcified cyanobacterium Croccosphaera watsonii with a diameter of ~3 μm had an average sinking velocity of ~0.06 m day−1 which is faster than the uncalcified coccolithophores E. huxleyi and G. oceanica. The cryptophyte Rhodomonas spec. and the silicoflagellate Dictyocha spec. were sinking with ~0.25 and ~0.48 m day−1, respectively. Note that we could not detect any signs of a silicified skeleton for Dictyocha spec. (Table 1).
Highest sinking velocities among the investigated diatoms were found in Thalassiosira oceanica (~0.2 m day−1), while the slowest sinking species were Phaedactylum tricornutum (0.065 m day−1). Thalassiosira weissflogii was by far the largest investigated diatom (ESD = 14 μm) but its sinking velocity of ~0.07 m day−1 was smaller than that of the other Thalassiosira species (Table 1).
Particle densities of spherical phytoplankton species ranged from 1,080 kg m−3 in Dictyocha spec. to 1,282 kg m−3 in C. leptoporus. Densities were higher in calcifying compared with non-calcifying species (Table 1).
Sinking velocities of sediment trap material ranging from 80–400 μm in ESD
Average size properties and sinking velocities of all investigated fecal pellets
Sinking velocity (m day−1)
Volume × 106 (μm3)
Influence of water temperature on sinking velocities
Further theoretical considerations with Stokes’ Law showed that the influence of temperature on sinking velocities is more pronounced when the density of the sinking particle gets closer to the density of the seawater medium. A particle with a density of 1,038 kg m−3 sank ~90 % faster at 25 °C compared with 10 °C. The sinking velocity of particles with a density of 1,200 kg m−3, however, increased only about 50 % over the same temperature range (Fig. 4b). The effect of temperature increased exponentially the closer the density of the sinking particle approached the density of the seawater medium (Fig. 4c).
Applicability of the method
The method for sinking velocity determinations of particles between ~3–400 μm in ESD presented here is easy to set up and permits the processing of a comparatively high number of samples per day. The very good agreement of measured (FlowCAM®) and calculated (Stokes’ Law) sinking velocities of polystyrene beads with a representative size range indicates that our method is useful to determine sinking rates of marine (and limnic) particles and results are not biased by convection or wall effects. Nevertheless, there are some aspects of the method, which have to be discussed in more detail.
Due to the relatively short distance over which particles are tracked in the display window of the camera, it becomes difficult to measure particles sinking faster than ~200 m day−1. Such fast sinking particles would pass the area monitored by the camera too quick to get a reasonable amount of pictures even at the highest frame rate. The method is, therefore, inadequate to determine sinking velocities of large and heavily ballasted fecal pellets which can sink several hundreds or even thousands of meters per day (e.g. Bruland and Silver 1981; Ploug et al. 2008). Furthermore, the short distance the particles are tracked for can lead to higher variability in measured average sinking velocities in case particles are non-spherical. For example, relatively long cylindrical particles such as fecal pellets will sink faster if they are oriented vertically in the water column compared with a horizontal orientation (Holland 2010). It must, therefore, be assured to measure a relatively high number of these particles so that the number of vertically to horizontally oriented particles is balanced.
Comparison with other methods: Phytoplankton
There is a variety of other methods available which have been successfully applied to quantify phytoplankton sinking velocities in earlier studies. Phytoplankton sinking velocities were usually measured with non-optical methods (Eppley et al. 1967; Bienfang 1981), although direct measurements using a video camera and laser scanning techniques have been established more recently (O’Brien et al. 2006; Walsby and Holland 2006). The most commonly applied method to determine sinking velocities of phytoplankton cells is the SETCOL method (Bienfang 1981). Here, sinking velocities are measured as change in bulk biomass per unit time. The difference between the SETCOL method and optical measurements with a camera is that the former monitors changes in bulk biomass distributions while individual cells are targeted in the latter. Advantages and disadvantages of the SETCOL method and direct optical measurements using a video camera are discussed in detail by O’Brien et al. (2006). They argue that video methods permit comparisons of sinking velocities with cell size, which is not possible with the SETCOL method. On the other hand, the SETCOL method could be advantageous if particles are sinking homogenously because in this case sinking velocities of a whole population and not only of a small number of particles can be investigated.
A direct comparison between sinking velocities of the coccolithophore E. huxleyi measured with the SETCOL method (Lecourt et al. 1996) and the FlowCAM® method presented here shows that results are slightly different. Coccolith bearing and naked cells were sinking with up to ~0.5 and 0.3 m day−1, respectively, when measured with the SETCOL method (Lecourt et al. 1996), while they were sinking with ~0.4 and ~0.03 m day−1 when measured with the FlowCAM® (Table 2). These differences, however, do not necessarily have to be attributed to the different measuring techniques but could rather result from different culture conditions. Bienfang et al. (1982) and Waite et al. (1997) measured sinking velocities of different diatom species with the SETCOL method. Nutrient replete cells of Chaetoceros graciale (length of 8.2 μm) were sinking with ~0.15 m day−1 (Bienfang et al. 1982), comparable with sinking velocities of similar sized cells reported here (Table 2). Furthermore, Waite et al. (1997) reported sinking velocities of ~0.07 m day−1 for Thalassiosira pseudonana and ~0.06 m day−1 for Thalassiosira weissflogii which is also in reasonable agreement with 0.13 and 0.07 m day−1 determined here (Table 2).
Comparison with other methods: Sediment trap material
Sediment trap material was carefully partitioned with a 300-μm sieve prior to the measurements (see section on “Sample preparation”). During this procedure, large and robust aggregates remained on the sieve, while large and more fragile aggregates disintegrated and passed the sieve as smaller particles. The exclusive measurement of small aggregates and fragments of larger ones can lead to a systematic underestimation of the particle flux in the water column because it does not take the aggregation potential and the in situ size of the investigated material into account. Nevertheless, the method has the potential to provide valuable information on the ballasting effect of various biogenic or lithogenic materials because ballasting material influences particles of every size class.
Compared with aggregates, fecal pellets are much more resistant to mechanical stress due to the peritrophic membrane that surrounds them. Fecal pellets seemed unaffected by the sieving procedure and breakup or disintegration could not be observed during handling of the sample. Good knowledge of fecal pellet sinking velocities is important since they are, at least in some marine regions, the most important transport vehicle for organic carbon into the deep ocean (Turner 2002). In the following, we will focus on the comparison of sinking velocities of fecal pellets, since there are more data available which can be used for comparisons.
Sinking velocities of zooplankton fecal pellets range from ~5 (Paffenhöfer and Knowles 1979) up to more than 2,000 m day−1 (Bruland and Silver 1981) and are generally higher than the mean sinking velocity of 12.5 m day−1 reported here. This discrepancy is unlikely resulting from the applied method since measured sinking velocities of polystyrene beads in the same size range as fecal pellets were in good agreement with theoretical values calculated from Stokes’ Law (Fig. 2a, b).
Fecal pellet sinking velocities were shown to increase with particle size and density (reviewed in Turner 2002). Fecal pellet size cannot explain the relatively slow sinking velocities reported in our study because size and volume of the pellets (Table 3) are not fundamentally different compared to other studies where higher sinking velocities were reported (Turner 1977; Yoon et al. 2001; Ploug et al. 2008). Relatively slow sinking velocities should, therefore, rather be caused by smaller excess densities. Fecal pellet density was shown to depend on the amount of ballast material such as calcium carbonate or silicate incorporated by the pellet producers (e.g., Honjo 1976; Small et al. 1979; Harris 1994; Ploug et al. 2008). The phytoplankton biomass in the mesocosm on the days before sampling was dominated by species not forming ballasting material, with only a comparatively small fraction contributed by the small diatom Arcocellulus spec. This suggests low ballast loading of fecal pellets. Furthermore, the phytoplankton community was in a post-bloom phase during the time of sampling and the total biomass was low. Small et al. (1979) reported a decreased density and compactness of fecal pellets and sometimes almost empty peritrophic membranes when copepods were incubated in seawater with very low food source. The same phenomenon was also described by Yoon et al. (2001) and Bruland and Silver (1981) when zooplankton was kept for a long time in the same container which was probably depleted in food. Low ballast loading and low food availability for pellet producers could therefore explain the relatively slow sinking velocities of fecal pellets reported in this study (Table 3).
Next to fecal pellets properties, water temperature of the media at which sinking velocities are determined can make a significant difference (Figs. 2a, b, 4b, c, see the following section). Water temperature was 10 °C during measurements, which is lower than in most other studies. The same fecal pellets would sink ~70 % faster at 25 °C, assuming a fecal pellet density of 1,050 kg m−3.
Effect of seawater temperature on sinking velocities
Density and viscosity of seawater are a function of temperature and salinity (Sharqawy et al. 2010). A particle with a Reynolds number smaller than ~0.5 will sink faster in less viscous and dense seawater (Fig. 4b). Hence, temperature and salinity indirectly influence sinking velocities. In the following, we will focus on the temperature component, since it strongly influences sinking velocities of particles with high and low densities, while salinity only influences sinking velocities considerably if the particle density is very close to that of the surrounding seawater.
The term in the numerator is the excess density of the particle. It is very influential on f(T), and therefore, on sinking velocities, if the difference between ρparticle and ρseawater is less than ~1 % (Fig. 4c). The temperature effect should therefore be most pronounced on marine aggregates that have excess densities lower than 1 % (Iversen and Ploug 2010). However, this straightforward estimate of the influence of changing ρseawater neglects that ρparticle itself could possibly also change when it is transferred into warmer water. This change could result from the particular structure of aggregates. Aggregates are usually very fluffy (Iversen and Ploug 2010) and consist to a large extent of water. The density of the water inside the aggregate, and therefore, ρparticle will also decrease when it is transferred to warmer water. Hence, the excess density of the aggregate would change differently in such a case when not only changes in ρseawater are accounted for. The influence of seawater temperature on excess density is, therefore, particularly hard to quantify.
In contrast, the influence of changing viscosity is easier to quantify since particle properties do not come into play. The influence of viscosity on f(T) in Eq. 4 becomes more pronounced with increasing particle excess density. Passive sinking of more compact organic matter such as bacteria (Logan and Hunt 1987) or fecal pellets (Komar et al. 1981) that do not control their buoyancy would therefore be mostly influenced by temperature driven viscosity changes. For example, a sinking particle (Re < 0.5; ρparticle = 1,140 kg m−3; no buoyancy control) would sink ~30 % faster in the surface water of temperate regions (19 °C) than in higher latitude surface waters (10 °C). Furthermore, (assuming particle properties do not change during settling) sinking velocities would decrease when entering cooler deep water masses and retain at thermoclines where sharp temperature gradients cause an abrupt slowdown.
It is also interesting to consider the temperature effect on sinking velocities in the context of projected climate change (IPCC 2007). A marine biogeochemical model based on the rather moderate CO2 emission scenario SRES A2 (IPCC 2007) projects a mean surface ocean temperature increase in approximately 2 °C until 2100 AD (Schmittner et al. 2008). According to this projection, particles with sinking velocities following Stokes’ Law and an excess density between 30–180 kg m−3 would sink approximately 6 % faster in the surface ocean in 2100 compared with 2000 AD. Of course, it would be an extreme oversimplification to conclude that this translates in an enhanced future carbon export of the same percentage since climate change does probably affect many other parameters with strong feedback on carbon export such as nutrient distribution, primary production or bacterial remineralization (reviewed in Riebesell et al. 2009). Nevertheless, this “viscosity effect” might have the potential to slightly modify expected changes of carbon export into the deep.
According to the data provided in this study, we come to the following conclusions: (1) The proposed method of measuring sinking velocities with a FlowCAM® is easy to set up and provides reliable data for particles within a size range of approximately 3–400 μm and sinking velocities of up to ~200 m day−1. (2) Sinking velocities of phytoplankton cells were in reasonable agreement with reported literature values and were highest when the cells were ballasted with calcium carbonate. (3) The comparatively slow sinking velocities of fecal pellets stemming from sediment trap material of a mesocosm experiment are probably the result of low ballast loading and low compactness of the fecal pellets, as well as comparatively low measurement temperatures. (4) Temperature can have a large influence on sinking velocities due to the temperature-dependent change in seawater density and viscosity. This might be worth considering with respect to future carbon export.
We thank Tim Boxhammer and Rafael Bermúdez Monsalve for their support with the sediment trap material as well as Tania Klüver, Tobias Grosskopf, Cordula Meyer, Lena Eggers, Jörn Thomsen, Luisa Federwisch, and Julia Saphörster for providing various phytoplankton species. This research was funded by the Federal Ministry of Education and Research (Bundesministerium für Bildung und Forschung; 03F0608A) in the framework of the Biological Impacts of Ocean Acidification (BIOACID) project (subproject 3.1.1). The experiments comply with the current laws of the country in which they were performed.
This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
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