ALBERT

Description: Author Posting. © John Wiley & Sons, 2009. This is the author's version of the work. It is posted here by permission of John Wiley & Sons for personal use, not for redistribution. The definitive version was published in Marine Ecology 30 (2009): 133-150, doi:10.1111/j.1439-0485.2009.00288.x.

Description: Climate change will alter turbulence intensity, motivating greater attention to mechanisms of turbulence effects on organisms. Many analytic and analog models used to simulate and assess effects of turbulence on plankton rely on a one-dimensional simplification of the dissipative scales of turbulence, i.e., simple, steady, uniaxial shears, as produced in Couette vessels. There shear rates are constant and spatially uniform, and hence so is vorticity. Studies in such Couette flows have greatly informed, spotlighting stable orientations of nonspherical particles and predictable, periodic, rotational motions of steadily sheared particles in Jeffery orbits that steepen concentration gradients around nutrient-absorbing phytoplankton and other chemically (re)active particles. Over the last decade, however, turbulence research within fluid dynamics has focused on the structure of dissipative vortices in space and time and on spatially and temporally varying 2 vorticity fields in particular. Because steadily and spatially uniformly sheared flows are exceptional, so therefore are stable orientations for particles in turbulent flows. Vorticity gradients, finite net diffusion of vorticity and small radii of curvature of streamlines are ubiquitous features of turbulent vortices at dissipation scales that are explicitly excluded from simple, steady Couette flows. All of these flow components contribute instabilities that cause rotational motions of particles and so are important to simulate in future laboratory devices designed to assess effects of turbulence on nutrient uptake, particle coagulation and predatorprey encounter in the plankton. The Burgers vortex retains these signature features of turbulence and provides a simplified “cartoon” of vortex structure and dynamics that nevertheless obeys the Navier-Stokes equations. Moreover, this idealization closely resembles many dissipative vortices observed in both the laboratory and the field as well as in direct numerical simulations of turbulence. It is simple enough to allow both simulation in numerical models and fabrication of analog devices that selectively reproduce its features. Exercise of such numerical and analog models promises additional insights into mechanisms of turbulence effects on passive trajectories and local accumulations of both living and nonliving particles, into solute exchange with living and nonliving particles and into more subtle influences on sensory processes and swimming trajectories of plankton, including demersal organisms and settling larvae in turbulent bottom boundary layers. The literature on biological consequences of vortical turbulence has focused primarily on the smallest, Kolmogorov-scale vortices of length scale η. Theoretical dissipation spectra and direct numerical simulation, however, indicate that typical dissipative vortices with radii of 7η to 8η, peak azimuthal speeds of order 1 cm s-1 and lifetimes of order 10 s as a minimum (and much longer for moderate pelagic turbulence intensities) deserve new attention in studies of biological effects of turbulence.

Description: This research was supported by collaborative U.S. National Science Foundation grant (OCE- 0724744) to Jumars and Karp-Boss.

Description: © The Author(s), 2021. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Siegel, D. A., Cetinic, I., Graff, J. R., Lee, C. M., Nelson, N., Perry, M. J., Ramos, I. S., Steinberg, D. K., Buesseler, K., Hamme, R., Fassbender, A. J., Nicholson, D., Omand, M. M., Robert, M., Thompson, A., Amaral, V., Behrenfeld, M., Benitez-Nelson, C., Bisson, K., Boss, E., Boyd, P. W., Brzezinski, M., Buck, K., Burd, A., Burns, S., Caprara, S., Carlson, C., Cassar, N., Close, H. H., D’Asaro, E., Durkin, C., Erickson, Z., Estapa, M. L., Fields, E., Fox, J., Freeman, S., Gifford, S., Gong, W., Gray, D., Guidi, L., Haëntjens, N., Halsey, K., Huot, Y., Hansell, D., Jenkins, B., Karp-Boss, L., Kramer, S., Lam, P., Lee, J-M., Maas, A., Marchal, O., Marchetti, A., McDonnell, A., McNair, H., Menden-Deuer, S., Morison, F., Niebergall, A. K., Passow, U., Popp, B., Potvin, G., Resplandy, L., Roca-Martí, M., Roesler, C., Rynearson, T., Traylor, S., Santoro, A., Seraphin, K. D., Sosik, H. M., Stamieszkin, K., Stephens, B., Tang, W., Van Mooy, B., Xiong, Y., Zhang, X. An operational overview of the EXport Processes in the Ocean from RemoTe Sensing (EXPORTS) Northeast Pacific field deployment. Elementa: Science of the Anthropocene, 9(1), (2021): 1, https://doi.org/10.1525/elementa.2020.00107.

Description: The goal of the EXport Processes in the Ocean from RemoTe Sensing (EXPORTS) field campaign is to develop a predictive understanding of the export, fate, and carbon cycle impacts of global ocean net primary production. To accomplish this goal, observations of export flux pathways, plankton community composition, food web processes, and optical, physical, and biogeochemical (BGC) properties are needed over a range of ecosystem states. Here we introduce the first EXPORTS field deployment to Ocean Station Papa in the Northeast Pacific Ocean during summer of 2018, providing context for other papers in this special collection. The experiment was conducted with two ships: a Process Ship, focused on ecological rates, BGC fluxes, temporal changes in food web, and BGC and optical properties, that followed an instrumented Lagrangian float; and a Survey Ship that sampled BGC and optical properties in spatial patterns around the Process Ship. An array of autonomous underwater assets provided measurements over a range of spatial and temporal scales, and partnering programs and remote sensing observations provided additional observational context. The oceanographic setting was typical of late-summer conditions at Ocean Station Papa: a shallow mixed layer, strong vertical and weak horizontal gradients in hydrographic properties, sluggish sub-inertial currents, elevated macronutrient concentrations and low phytoplankton abundances. Although nutrient concentrations were consistent with previous observations, mixed layer chlorophyll was lower than typically observed, resulting in a deeper euphotic zone. Analyses of surface layer temperature and salinity found three distinct surface water types, allowing for diagnosis of whether observed changes were spatial or temporal. The 2018 EXPORTS field deployment is among the most comprehensive biological pump studies ever conducted. A second deployment to the North Atlantic Ocean occurred in spring 2021, which will be followed by focused work on data synthesis and modeling using the entire EXPORTS data set.

Description: DAS, NN, KB, EF, SK, AB, AM, UP: NASA 80NSSC17K0692. MJB, EB, JG, LG, KH, LKB, JF, NH: NASA 80NSSC17K0568. KB, CBN, LR, MRM: NASA 80NSSC17K0555. CC, DH, BS: NASA 80NSSC18K0437. HC: NSF 1830016. BP, KDS: NSF 1829425. ME, KB, CD, MO: NASA 80NSSC17K0662. AF: NSF 1756932. BJ, KB, MB, SB, SC: NSF 1756442. PH, OM, JML: NSF 1829614. CL, ED, DN, MO, MJP, AT, ZN, ST: NASA 80NSSC17K0663. AM, NC, SG, WT, AN, WG: NASA 80NSSC17K0552. SMD, TR, HM, FM: NASA 80NSSC17K0716. CR, HS: NASA 80NSSC17K0700. AS, PB: NASA 80NSSC18K1431. DS, AM, KS NASA 80NSSC17K0654. BVM: NSF 1756254. XZ, DG, LG, YH: NASA 80NSSC17K0656 and 80NSSC20K0350.