Abstract
We have recently argued that marine interfacial surface tension must have a distinctive biogeography because it is mediated by fresh surfactant macromolecules released locally through the food web. Here we begin the process of quantification for associated climate flux implications. A low dimensionality (planar) equation of state is invoked at the global scale as our main analysis tool. For the reader’s convenience, fundamental surfactant physical chemistry principles are reviewed first, as they pertain to tangential forces that may alter oceanic eddy, ripple, and bubble fields. A model Prandtl (neutral) wind stress regime is defined for demonstration purposes. It is given the usual dependence on roughness, but then in turn on the tension reduction quantity known as surface pressure. This captures the main net influences of biology and detrital organics on global microlayer physics. Based on well-established surrogate species, tangent pressures are related to distributed ecodynamics as reflected by the current marine systems science knowledge base. Reductions to momentum and related heat-vapor exchange plus gas and salt transfer are estimated and placed on a coarse biogeographic grid. High primary production situations appear to strongly control all types of transfer, whether seasonally or regionally. Classic chemical oceanographic data on boundary state composition and behaviors are well reproduced, and there is a high degree of consistency with conventional micrometeorological wisdom. But although our initial best guesses are quite revealing, coordinated laboratory and field experiments will be required to confirm the broad hypotheses even partially. We note that if the concepts have large scale validity, they are super-Gaian. Biological control over key planetary climate-transfer modes may be accomplished through just a single rapidly renewed organic monolayer.
Highlights
The equation of state (EOS) concept relating force to generic density is central to all of material science, from microscopic to galactic scales [1]
The material we develop is highly interdisciplinary in nature, running the gamut from surface physicochemistry through upper ocean biology to micrometeorology and beyond -as reflected, for instance, in the keyword list just below our abstract
Our preferred source regarding surfactant physical chemistry is the 1960s era textbook, Davies and Rideal [4], which places the interaction of organics with interfacial mixing in an engineering context
Summary
The equation of state (EOS) concept relating force to generic density is central to all of material science, from microscopic to galactic scales [1]. Active macromolecules reside ubiquitously along the atmospheric interface [3], establishing measurable planar densities and exerting tangential forces regulatory of energy-mass transfer across the full planetary surface [4,5,6] Such effects occur primarily via a single monolayer of organic carbon, distributed unevenly yet systematically by the food web. We take the step of linking it to local intermolecular forces operating in a conceptual organic tangent plane [4,5,6,7,8] This allows for a global, systems-level biogeographic distribution to be proposed for surfactant properties and influence [10]. Some readers may find it helpful to scan these end notes before proceeding
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