The sea surface microlayer ( SML) is the boundary interface between the atmosphere and ocean, covering about 70% of Earth's surface. With an operationally defined thickness between 1 and , the SML has physicochemical and biological properties that are measurably distinct from underlying waters. Recent studies now indicate that the SML covers the ocean to a significant extent, and evidence shows that it is an aggregate-enriched biofilm environment with distinct microbial communities. Because of its unique position at the air-sea interface, the SML is central to a range of global marine biogeochemical and climate-related processes.
The sea surface microlayer is the boundary layer where all Gas exchange occurs between the atmosphere and the ocean. The chemical, physical, and biological properties of the SML differ greatly from the sub-surface water just a few centimeters beneath.Zhang, Zhengbin et al. (2003). Studies on the sea surface microlayer II. The layer of sudden change of physical and chemical properties. Journal of Colloid and Interface Science. 264, 148-159.
Despite the huge extent of the ocean's surface, until now relatively little attention has been paid to the sea surface microlayer (SML) as the ultimate interface where Heat transfer, momentum and Mass transfer between the ocean and the atmosphere takes place. Via the SML, large-scale environmental changes in the ocean such as warming, acidification, deoxygenation, and eutrophication potentially influence cloud formation, precipitation, and the global radiation balance. Due to the deep connectivity between biological, chemical, and physical processes, studies of the SML may reveal multiple sensitivities to global and regional changes.
Understanding the processes at the ocean's surface, in particular involving the SML as an important and determinant interface, could provide an essential contribution to the reduction of uncertainties regarding ocean-climate feedbacks. As of 2017, processes occurring within the SML, as well as the associated rates of material exchange through the SML, remained poorly understood and were rarely represented in marine and atmospheric numerical models.
In 1983, Sieburth hypothesised that the SML was a Gel layer formed by a complex mixture of , , and .
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Historically, the SML has been summarized as being a microhabitat composed of several layers distinguished by their ecological, chemical and physical properties with an operational total thickness of between 1 and 1000 μm. In 2005 Hunter defined the SML as a "microscopic portion of the surface ocean which is in contact with the atmosphere and which may have physical, chemical or biological properties that are measurably different from those of adjacent sub-surface waters".Hunter, K. A. (1977) Chemistry of the sea-surface microlayer University of East Anglia. School of Environmental Sciences. He avoids a definite range of thickness as it depends strongly on the feature of interest. A thickness of 60 μm has been measured based on sudden changes of the pH, and could be meaningfully used for studying the physicochemical properties of the SML. At such thickness, the SML represents a laminar layer, free of turbulence, and greatly affecting the exchange of gases between the ocean and atmosphere. As a habitat for neuston (surface-dwelling organisms ranging from bacteria to larger siphonophores), the thickness of the SML in some ways depends on the organism or ecological feature of interest. In 2005, Zaitsev described the SML and associated near-surface layer (down to 5 cm) as an incubator or nursery for eggs and larvae for a wide range of aquatic organisms.
Hunter's definition includes all interlinked layers from the laminar layer to the nursery without explicit reference to defined depths. In 2017, Wurl et al. proposed Hunter's definition be validated with a redeveloped SML paradigm that includes its global presence, biofilm-like properties and role as a nursery. The new paradigm pushes the SML into a new and wider context relevant to many ocean and climate sciences.
According to Wurl et al., the SML can never be devoid of organics due to the abundance of surface-active substances (e.g., surfactants) in the upper ocean and the phenomenon of surface tension at air-liquid interfaces.Levich VG (1962) Physicochemical hydrodynamics, Prentice Hall International. The SML is analogous to the thermal boundary layer, and remote sensing of the sea surface temperature shows ubiquitous anomalies between the sea surface skin and bulk temperature. Even so, the differences in both are driven by different processes. Enrichment, defined as concentration ratios of an analyte in the SML to the underlying bulk water, has been used for decades as evidence for the existence of the SML. Consequently, depletions of organics in the SML are debatable; however, the question of enrichment or depletion is likely to be a function of the thickness of the SML (which varies with sea state; including losses via sea spray, the concentrations of organics in the bulk water, and the limitations of sampling techniques to collect thin layers .Cunliffe M, Wurl O.(2014) Guide to best practices to study the ocean's surface, Plymouth Occasional Publications of the Marine Biological Association of the United Kingdom. Enrichment of surfactants, and changes in the sea surface temperature and salinity, serve as universal indicators for the presence of the SML. Organisms are perhaps less suitable as indicators of the SML because they can actively avoid the SML and/or the harsh conditions in the SML may reduce their populations. However, the thickness of the SML remains "operational" in field experiments because the thickness of the collected layer is governed by the sampling method. Advances in SML sampling technology are needed to improve our understanding of how the SML influences air-sea interactions.
Marine surface habitats sit at the interface between the atmosphere and the ocean. The biofilm habitat at the surface of the ocean harbours surface-dwelling microorganisms, commonly referred to as neuston. The sea surface microlayer (SML) constitutes the uppermost layer of the ocean, only 1–1000 μm thick, with unique chemical and biological properties that distinguish it from the underlying water (ULW). Due to the location at the air-sea interface, the SML can influence exchange processes across this boundary layer, such as air-sea gas exchange and the formation of sea spray aerosols. Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
Due to its exclusive position between the atmosphere and the hydrosphere and by spanning about 70% of the Earth's surface, the sea-surface microlayer (sea-SML) is regarded as a fundamental component in air–sea exchange processes and in biogeochemical cycling. Although having a minor thickness of <1000 μm, the elusive SML is long known for its distinct physicochemical characteristics compared to the underlying water, e.g., by featuring the accumulation of dissolved and particulate organic matter, transparent exopolymer particles (TEP), and surface-active molecules. Therefore, the SML is a gelatinous biofilm, maintaining physical stability through surface tension forces. It also forms a vast habitat for different organisms, collectively termed as neuston with a recent global estimate of 2 × 1023 microbial cells for the sea-SML.
Life at air–water interfaces has never been considered easy, mainly because of the harsh environmental conditions that influence the SML. However, high abundances of microorganisms, especially of bacteria and picophytoplankton, accumulating in the SML compared to the underlying water were frequently reported, accompanied by a predominant heterotrophic activity. This is because primary production at the immediate air–water interface is often hindered by photoinhibition. However, some exceptions of photosynthetic organisms, e.g., Trichodesmium, Synechococcus, or Sargassum, show more tolerance towards high light intensities and, hence, can become enriched in the SML. Previous research has provided evidence that neustonic organisms can cope with wind and wave energy, solar and ultraviolet (UV) radiation, fluctuations in temperature and salinity,
An improved understanding of the biological, chemical, and physical processes at the ocean's upper surface could provide an essential contribution to the reduction of uncertainties regarding ocean-climate feedbacks. Due to its positioning between atmosphere and ocean, the SML is the first to be exposed to climate changes including temperature, climate relevant trace gases, wind speed, and precipitation as well as to pollution by human waste, including nutrients, toxins, nanomaterials, and plastic debris.
Even less is known about the community control mechanisms in the SML and how the bacterial community assembles at the air-sea interface. The bacterioneuston community could be altered by differing wind conditions and radiation levels, with high wind speeds inhibiting the formation of a distinct bacterioneuston community. Wind speed and radiation levels refer to external controls, however, bacterioneuston community composition might also be influenced by internal factors such as nutrient availability and organic matter (OM) produced either in the SML or in the ULW.
One of the principal OM components consistently enriched in the SML are transparent exopolymer particles (TEP), which are rich in carbohydrates and form by the aggregation of dissolved precursors excreted by phytoplankton in the euphotic zone. Higher TEP formation rates in the SML, facilitated through wind shear and dilation of the surface water, have been proposed as one explanation for the observed enrichment in TEP. Also, due to their natural positive buoyancy, when not ballasted by other particles sticking to them, TEP ascend through the water column and ultimately end up at the SML . A second possible pathway of TEP from the water column to the SML is by bubble scavenging.
Next to rising bubbles, another potential transport mechanism for bacteria from the ULW to the SML could be ascending particles or more specifically TEP. Bacteria readily attach to TEP in the water column. TEP can serve as microbial hotspots and can be used directly as a substrate for bacterial degradation, and as grazing protection for attached bacteria, e.g., by acting as an alternate food source for zooplankton. TEP have also been suggested to serve as light protection for microorganisms in environments with high irradiation.
Viruses are the most abundant biological entities in the water column of the world's oceans. In the free water column, the virioplankton typically outnumbers the bacterioplankton by one order of magnitude reaching typical bulk water concentrations of 107 viruses mL−1. Moreover, they are known as integral parts of global biogeochemical cycles to shape and drive microbial diversity and to structure trophic networks. Like other neuston members, the virioneuston likely originates from the bulk seawater. For instance, in 1977 Baylor et al. postulated adsorption of viruses onto air bubbles as they rise to the surface, or viruses can stick to organic particles also being transported to the SML via bubble scavenging.
Within the SML, viruses interacting with the bacterioneuston will probably induce the viral shunt, a phenomenon that is well known for marine pelagic systems. The term viral shunt describes the release of organic carbon and other nutritious compounds from the virus-mediated lysis of host cells, and its addition to the local dissolved organic matter (DOM) pool. The enriched and densely packed bacterioneuston forms an excellent target for viruses compared to the bacterioplankton populating the subsurface. This is because high host-cell numbers will increase the probability of host–virus encounters. The viral shunt might effectively contribute to the SML's already high DOM content enhancing bacterial production as previously suggested for pelagic ecosystems and in turn replenishing host cells for viral infections. By affecting the DOM pool, viruses in the SML might directly interfere with the microbial loop being initiated when DOM is microbially recycled, converted into biomass, and passed along the food web. In addition, the release of DOM from lysed host cells by viruses contributes to organic particle generation. However, the role of the virioneuston for the microbial loop has never been investigated.
The glass plate sampler is commonly used. Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License. It was first described in 1972 by Harvey and Burzell as a simple but effective method of collecting small sea surface microlayer samples. A clean glass plate is immersed vertically into the water and then withdrawn in a controlled manner. Harvey and Burzell used a plate which was 20 cm square and 4 mm thick. They withdrew it from the sea at the rate of 20 cm per second. Typically the uppermost 20–150 μm of the surface microlayer adheres to the plate as it is withdrawn. The sample is then wiped from both sides of the plate into a sampling vial.Cunliffe, M. and Wurl, O. (2014) Guide to best practices to study the ocean's surface. Occasional publication of the Marine Biological Association of the United Kingdom.
For a plate of the size used by Harvey and Burzel, the resulting sample volumes are between about 3 and 12 cubic centimetres. The sampled SML thickness h in micrometres is given by:
where V is the sample volume in cm3, A is the total immersed plate area of both sides in cm2, and N is the number of times the sample was dipped.
Unlike coloured algal blooms, surfactant-associated bacteria may not be visible in ocean colour imagery. Having the ability to detect these "invisible" surfactant-associated bacteria using synthetic aperture radar has immense benefits in all-weather conditions, regardless of cloud, fog, or daylight. This is particularly important in very high winds, because these are the conditions when the most intense air-sea gas exchanges and marine aerosol production take place. Therefore, in addition to colour satellite imagery, SAR satellite imagery may provide additional insights into a global picture of biophysical processes at the boundary between the ocean and atmosphere, air-sea greenhouse gas exchanges and production of climate-active marine aerosols.
Compared to the sub-surface waters, the sea surface microlayer contains elevated concentration of bacteria and viruses, as well as toxic metals and organic pollutants.Blanchard, D.C., 1983. The production, distribution and bacterial enrichment of the sea-salt aerosol. In: Liss, P.S., Slinn, W.G.N. ŽEds.., Air–Sea Exchange of Gases and Particles. D. Reidel Publishing Co., Dordrecht, Netherlands, pp. 407-444.Hoffmann, G.L., Duce, R.A., Walsh, P.R., Hoffmann, E.J., Ray, B.J., 1974. Residence time of some particulate trace metals in the oceanic surface microlayer: significance of atmospheric deposition. J. Rech. Atmos. 8, 745–759.Hunter, K.A., 1980. Process affecting particulate trace metals in the sea surface microlayer. Mar. Chem. 9, 49–70.Hardy, J.T., Word, J., 1986. Contamination of the water surface of Puget Sound. Puget Sound Notes, U.S. EPA. Region 10 Seattle, WA, pp. 3–6. These materials can be transferred from the sea-surface to the atmosphere in the form of wind-generated aqueous aerosols due to their high vapor tension and a process known as volatilisation. When airborne, these microbes can be transported long distances to coastal regions. If they hit land they can have detrimental effects on animals, vegetation and human health.WHO, 1998. Draft guidelines for safe recreational water environments: coastal and fresh waters, draft for consultation. World Health Organization, Geneva, EOSrDRAFTr98 14, pp. 207–299. Marine aerosols that contain viruses can travel hundreds of kilometers from their source and remain in liquid form as long as the humidity is high enough (over 70%).Klassen, R. D., & Roberge, P. R. (1999). Aerosol transport modeling as an aid to understanding atmospheric corrosivity patterns. Materials & Design, 20, 159–168.Moorthy, K. K., Satheesh, S. K., & Krishna Murthy, B.V. (1998). Characteristics ofspectral optical depths and size distributions of aerosols over tropical oceanic regions. Journal of Atmospheric and Solar–Terrestrial Physics, 60, 981–992.
Chow, J. C., Watson, J. G., Green, M. C., Lowenthal, D. H., Bates, B., Oslund, W., & Torre, G. (2000). Cross-border transport and spatial variability of suspended particles in Mexicali and California's Imperial Valley. Atmospheric Environment, 34, 1833–1843. These aerosols are able to remain suspended in the atmosphere for about 31 days. Evidence suggests that bacteria can remain viable after being transported inland through aerosols. Some reached as far as 200 meters at 30 meters above sea level. It was also noted that the process which transfers this material to the atmosphere causes further enrichment in both bacteria and viruses in comparison to either the SML or sub-surface waters (up to three orders of magnitude in some locations).Cincinelli A.; Stortini A.M.; Perugini M.; Checchini L.; Lepri L., 2001. Organic Pollutants in sea-surface microlayer and aerosol in the coastal environment Of Leghorn- (Tyrrhenian Sea). Marine Chemistry, Volume 76, Number 1, pp. 77-98(22)Marks, R., Kruczalak, K., Jankowska, K., & Michalska, M. (2001). Bacteria and fungi in air over the GulfofGdansk and Baltic sea. Journal of Aerosol Science, 32, 237–250.
Virioneuston
Measurement
Remote sensing
Aeroplankton
Mathematical modeling
See also
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