Archive for upper water column

Shipboard LiDAR: A powerful tool for measuring the distribution and composition of particles in the ocean

Posted by mmaheigan 
· Tuesday, October 23rd, 2018 

Despite major advances in ocean observing capabilities, characterizing the vertical distribution of materials in the ocean with high spatial resolution remains challenging. Light Detection and Ranging (LiDAR), a technique that relies on measurement of the “time-of-flight” of a backscattered laser pulse to determine the range to a scattering object, could potentially fill this critical gap in our sampling capabilities by providing remote estimates of the vertical distribution of optical properties and suspended particles in the ocean.

A recent article in Remote Sensing of Environment details the development of a portable shipboard LiDAR and its capabilities for extending high-frequency measurements of scattering particles into the vertical dimension. The authors deployed the experimental system (shown in Figure 1a) during research cruises off the coast of Virginia and during a passenger ferry crossing of the Gulf of Maine (associated with the Gulf of Maine North Atlantic Time Series program-GNATS). Remote measurements of LiDAR signal attenuation corresponded well with simultaneous in situ measurements of water column optical properties and proxies for the concentration of suspended particles. Interestingly, the researchers also observed that the extent to which the return signal was depolarized (also known as the LiDAR depolarization ratio) may provide information regarding the composition of particles within the scattering volume. This is evidenced by the strong relationship between the depolarization ratio and the backscattering ratio, an indicator of the bulk composition (mineral vs. organic) of the particles within a scattering medium (Figure 1b).

Figure 1. a) LiDAR system deployed to look through a chock at the bow of the M/V Nova Star. b) Relationship between the LiDAR linear depolarization ratio (ρ) and coincident measurements of the particulate backscattering ratio (bbp/bp). The black line represents a least-squares exponential fit to the data.

As LiDAR technology becomes increasingly rugged, compact, and inexpensive, the regular deployment of oceanographic LiDAR on a variety of sampling platforms will become an increasingly practical method for characterizing the vertical and horizontal distribution of particles in the ocean. This has the potential to greatly improve our ability to investigate the role of particles in physical and biogeochemical oceanographic processes, especially when sampling constraints limit observations to the surface ocean.

 

Authors:
Brian L. Collister (Old Dominion University)
Richard C. Zimmerman (Old Dominion University)
Charles I. Sukenik (Old Dominion University
Victoria J. Hill (Old Dominion University)
William M. Balch (Bigelow Laboratory for Ocean Sciences)

Lasers shed light on giant larvacean filtration impact on the ocean’s biological pump

Posted by mmaheigan 
· Thursday, January 4th, 2018 

To accurately assess the impacts of climate change, we need to understand how atmospheric carbon is transported from surface waters to the deep sea. Grazers and filter feeders drive the ocean’s biological pump as they remove and sequester carbon at various rates. This pump extends down into the midwater realm, the largest habitat on earth. Giant larvaceans are fascinating and enigmatic occupants of the upper 400 m of the water column, where they build complex filtering structures out of mucus that can reach diameters greater than 1 m in longest dimension (Figure 1A). Because of the fragility of these structures, direct measurements of filtration rates require us to study them in situ. We developed DeepPIV, an ROV-deployable instrument (Figure 1B) to directly measure fluid motion and filtration rates in situ (Figure 1C).

Figure 1. (A) Traditional view of a giant larvacean illuminated by white ROV lights. (B) DeepPIV instrument is seen attached to Monterey Bay Aquarium Research Institute’s (MBARI) MiniROV. (C) DeepPIV-illuminated interior view of a giant larvacean house, where particle motion in ambient seawater serves as a proxy for fluid motion. White arrows in (A) and (C) indicate larvacean head/trunk; white arrow in (B) indicates DeepPIV.

The filtration rates we measured for giant larvaceans are far greater than for any other zooplankton filter feeder. When combined with abundance data from a 22-year time series, the grazing impact of giant larvaceans indicates that within 13 days, they can filter the total volume of water within their habitable depth range (~100-300 m; based on maximum abundance and measured filtration rates). Our results reveal that the contribution of giant larvaceans to vertical carbon flux is much greater than previously thought. Small larvaceans, which are present in the water column in even larger quantities than giant larvaceans, may also have a measurable impact on carbon fluxes. New technologies such as DeepPIV are yielding more quantitative observations of midwater filter feeders, which is improving our understanding of the roles that deep-water biota play in the long-term removal of carbon from the atmosphere.

Read the full journal article: http://advances.sciencemag.org/content/3/5/e1602374.full

Authors: (All at MBARI)
Kakani Katija
Rob E. Sherlock
Alana D. Sherman
Bruce H. Robison

International team of researchers reports ocean acidification is spreading rapidly in the western Arctic Ocean

Posted by mmaheigan 
· Thursday, March 30th, 2017 

The Arctic Ocean is particularly sensitive to climate change and ocean acidification such that aragonite saturation state is expected to become undersaturated (Ωarag <1) there sooner than in other oceans. However, the extent and expansion rate of ocean acidification (OA) in this region are still unknown.

In the March 2017 issue of Nature Climate Change, Qi et al. show that, between 1994 and 2010, low Ωarag waters have expanded northwards at least 5º, to 85ºN, and deepened from 100 m to 250 m depth. Data from multiple trans-western Arctic Ocean cruises show that Ωarag<1 water has increased in the upper 250 m from 5 to 31% of the total area north of 70ºN. Tracer data and model simulations suggest that increased transport of Pacific Winter Water (which is already acidified due to both natural and anthropogenic sources), driven by sea-ice retreat and the circulation changes, are primarily responsible for the expansion, while local carbon recycling and anthropogenic CO2 uptake have also contributed. These results indicate more rapid acidification is occurring in the Arctic Ocean, two to four times faster than the Pacific and Atlantic Oceans, with the western Arctic Ocean the first open-ocean region with large-scale expansion of “acidified” water directly observed in the upper water column.

The rapid spread of ocean acidification in the western Arctic has implications for marine life, particularly clams, mussels and pteropods that may have difficulty building or maintaining their shells in increasingly acidified waters. The pteropods are part of the Arctic food web and important to the diet of salmon and herring. Their decline could affect the larger marine ecosystem.

Authors:
Richard A. Feely (NOAA Pacific Marine Environmental Laboratory)
Leif G. Anderson (Univ. of Gothenburg)
Heng Sun (SOA Third Institute of Oceanography)
Jianfang Chen (SOA Second Institute of Oceanography
Min Chen (Univ. of Delaware)
Liyang Zhan (SOA Third Institute of Oceanography)
Yuanhui Zhang (SOA Third Institute of Oceanography)
Wei-Jun Cai (Univ. of Delaware, Univ. of Georgia)

Filter by Keyword

abundance acidification additionality advection africa air-sea air-sea interactions algae alkalinity allometry ammonium AMO AMOC anoxic Antarctic Antarctica anthro impacts anthropogenic carbon anthropogenic impacts appendicularia aquaculture aquatic continuum aragonite saturation arctic Argo argon arsenic artificial seawater Atlantic atmospheric CO2 atmospheric nitrogen deposition authigenic carbonates autonomous platforms bacteria bathypelagic BATS BCG Argo benthic bgc argo bio-go-ship bio-optical bioavailability biogeochemical cycles biogeochemical models biogeochemistry Biological Essential Ocean Variables biological pump biophysics bloom blue carbon bottom water boundary layer buffer capacity C14 CaCO3 calcification calcite carbon carbon-climate feedback carbon-sulfur coupling carbonate carbonate system carbon budget carbon cycle carbon dioxide carbon export carbon fluxes carbon sequestration carbon storage Caribbean CCA CCS changing marine chemistry changing marine ecosystems changing marine environments changing ocean chemistry chemical oceanographic data chemical speciation chemoautotroph chesapeake bay chl a chlorophyll circulation CO2 coastal and estuarine coastal darkening coastal ocean cobalt Coccolithophores commercial community composition competition conservation cooling effect copepod copepods coral reefs CTD currents cyclone daily cycles data data access data assimilation database data management data product Data standards DCM dead zone decadal trends decomposers decomposition deep convection deep ocean deep sea coral denitrification deoxygenation depth diatoms DIC diel migration diffusion dimethylsulfide dinoflagellate dinoflagellates discrete measurements distribution DOC DOM domoic acid DOP dust DVM ecology economics ecosystem management ecosystems eddy Education EEZ Ekman transport emissions ENSO enzyme equatorial current equatorial regions ESM estuarine and coastal carbon fluxes estuary euphotic zone eutrophication evolution export export fluxes export production extreme events faecal pellets fecal pellets filter feeders filtration rates fire fish Fish carbon fisheries fishing floats fluid dynamics fluorescence food webs forage fish forams freshening freshwater frontal zone functional role future oceans gelatinous zooplankton geochemistry geoengineering geologic time GEOTRACES glaciers gliders global carbon budget global ocean global warming go-ship grazing greenhouse gas greenhouse gases Greenland ground truthing groundwater Gulf of Maine Gulf of Mexico Gulf Stream gyre harmful algal bloom high latitude human food human impact human well-being hurricane hydrogen hydrothermal hypoxia ice age ice cores ice cover industrial onset inland waters in situ inverse circulation ions iron iron fertilization iron limitation isotopes jellies katabatic winds kelvin waves krill kuroshio lab vs field land-ocean continuum larvaceans lateral transport LGM lidar ligands light light attenuation lipids low nutrient machine learning mangroves marine carbon cycle marine heatwave marine particles marine snowfall marshes mCDR mechanisms Mediterranean meltwater mesopelagic mesoscale mesoscale processes metagenome metals methane methods microbes microlayer microorganisms microplankton microscale microzooplankton midwater mitigation mixed layer mixed layers mixing mixotrophs mixotrophy model modeling model validation mode water molecular diffusion MPT MRV multi-decade n2o NAAMES NCP nearshore net community production net primary productivity new ocean state new technology Niskin bottle nitrate nitrogen nitrogen cycle nitrogen fixation nitrous oxide north atlantic north pacific North Sea nuclear war nutricline nutrient budget nutrient cycles nutrient cycling nutrient limitation nutrients OA observations ocean-atmosphere ocean acidification ocean acidification data ocean alkalinity enhancement ocean carbon storage and uptake ocean carbon uptake and storage ocean color ocean modeling ocean observatories ocean warming ODZ oligotrophic omics OMZ open ocean optics organic particles oscillation outwelling overturning circulation oxygen pacific paleoceanography PAR parameter optimization parasite particle flux particles partnerships pCO2 PDO peat pelagic PETM pH phenology phosphate phosphorus photosynthesis physical processes physiology phytoplankton PIC piezophilic piezotolerant plankton POC polar polar regions policy pollutants precipitation predation predator-prey prediction pressure primary productivity Prochlorococcus productivity prokaryotes proteins pteropods pycnocline radioisotopes remineralization remote sensing repeat hydrography residence time resource management respiration resuspension rivers rocky shore Rossby waves Ross Sea ROV salinity salt marsh satellite scale seafloor seagrass sea ice sea level rise seasonal seasonality seasonal patterns seasonal trends sea spray seawater collection seaweed secchi sediments sensors sequestration shelf ocean shelf system shells ship-based observations shorelines siderophore silica silicate silicon cycle sinking sinking particles size SOCCOM soil carbon southern ocean south pacific spatial covariations speciation SST state estimation stoichiometry subduction submesoscale subpolar subtropical sulfate surf surface surface ocean Synechococcus technology teleconnections temperate temperature temporal covariations thermocline thermodynamics thermohaline thorium tidal time-series time of emergence titration top predators total alkalinity trace elements trace metals trait-based transfer efficiency transient features trawling Tris trophic transfer tropical turbulence twilight zone upper ocean upper water column upwelling US CLIVAR validation velocity gradient ventilation vertical flux vertical migration vertical transport warming water clarity water mass water quality waves weathering western boundary currents wetlands winter mixing zooplankton

Copyright © 2025 - OCB Project Office, Woods Hole Oceanographic Institution, 266 Woods Hole Rd, MS #25, Woods Hole, MA 02543 USA Phone: 508-289-2838  •  Fax: 508-457-2193  •  Email: ocb_news@us-ocb.org

link to nsflink to noaalink to WHOI

Funding for the Ocean Carbon & Biogeochemistry Project Office is provided by the National Science Foundation (NSF) and the National Aeronautics and Space Administration (NASA). The OCB Project Office is housed at the Woods Hole Oceanographic Institution.