The sea surface microlayer (SML) is the boundary interface between the atmosphere and ocean, covering about 70% of the Earth's surface. The SML has physicochemical and biological properties that are measurably distinct from underlying waters. Because of its unique position at the air-sea interface, the SML is central to a range of global biogeochemical and climate-related processes. Although known for the last six decades, the SML often has remained in a distinct research niche, primarily as it was not thought to exist under typical oceanic conditions. Recent studies now indicate that the SML covers the ocean to a significant extent, highlighting its global relevance as the boundary layer linking two major components of the Earth system – the ocean and the atmosphere. In recent years, his hypothesis has been confirmed, and scientific evidence indicates that the SML is an aggregate-enriched biofilm environment with distinct microbial communities. In 1999 Ellison et al. estimated that 200
Tg C yr−1 (200 million tonnes of carbon per year) accumulates in the SML, similar to
sedimentation rates of carbon to the ocean's seabed, though the accumulated carbon in the SML probably has a very short
residence time. Although the total volume of the microlayer is very small compared to the ocean's volume, Carlson suggested in his seminal 1993 paper that unique interfacial reactions may occur in the SML that may not occur in the underlying water or at a much slower rate there. He therefore hypothesised that the SML plays an important role in the
diagenesis of carbon in the upper ocean. 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". 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. 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. 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, 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. 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. 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. e.g., by featuring the accumulation of dissolved and particulate organic matter, transparent exopolymer particles (TEP), and surface-active molecules. maintaining physical stability through surface tension forces. It also forms a vast habitat for different organisms, collectively termed as neuston 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, fluctuations in temperature and salinity, and a higher potential predation risk by the zooneuston. Furthermore, wind action promoting sea spray formation and bubbles rising from deeper water and bursting at the surface release SML-associated microbes into the atmosphere. In addition to being more concentrated compared to planktonic counterparts, the bacterioneuston, algae, and protists display distinctive community compositions compared to the underlying water, in both marine and freshwater habitats. Furthermore, the bacterial community composition was often dependent on the SML sampling device being used. While being well defined with respect to bacterial community composition, little is known about viruses in the SML, i.e., the virioneuston. This review has its focus on virus–bacterium dynamics at air–water interfaces, even if viruses likely interact with other SML microbes, including archaea and the phytoneuston, as can be deduced from viral interference with their planktonic counterparts. Although viruses were briefly mentioned as pivotal SML components in a recent review on this unique habitat, a synopsis of the emerging knowledge and the major research gaps regarding bacteriophages at air–water interfaces is still missing in the literature. == Properties ==