For questions about GMD seminars, contact
Irina Petropavlovskikh, Phone: (303) 497-6279 or
Ann Thorne, Phone: (303) 497-4600.
Visitors from outside the NOAA campus need to contact Irina or Ann at least one day before
the seminar date to be added to the visitor's list at the security gate.
*NEW Additional Requirement for Visitors:* Names of all off-site
visitors without a U.S. government issued ID badge must be collected and
submitted to security in advance of every seminar. Please call Ann
Thorne at 303-497-4600 (leave a message including your name) or send an
e-mail to Irina Petropavlovskikh
by the day before the seminar if you plan to attend.
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Speaker: |
Dr. Christopher Barnet, Integrated Observing System Science and Product Development Team (IOSSPDT) NOAA/NESDIS/STAR, Camp Springs, MD
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Date/Time: |
Thursday, September 11, 2008 03:30PM
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Location: |
Multi-purpose Room (GC-402) David Skaggs Research Center (DSRC) NOAA Building - DOC Boulder Campus
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Title: |
Deriving atmospheric trace gas products from hyperspectral sounders.
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ABSTRACT
Operational hyperspectral thermal sounders, designed for retrieving high accuracy global atmospheric temperature, moisture, and cloud products for weather and climate applications, are also capable of retrieval of trace gases. At NOAA/NESDIS we have been exploring the use of these instruments for the retrieval of ozone, carbon monoxide, methane, carbon dioxide, nitric acid, and nitrous oxide. The Atmospheric Infrared Sounder (AIRS), launched on the NASA Aqua platform in 2002, has been used to characterize these products and an assessment of the current capabilities will be discussed in the context of AIRS and other existing and planned satellite assets. This presentation will focus on the advantages and limitations of thermal sounders and will encourage discussion on the potential utility of these long-term, global, multi-gas datasets in climate and carbon-cycle applications.
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Speaker: |
Charles Miller, Climate, Oceans and Solid Earth Science, Jet Propulsion Laboratory, Pasadena, CA
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Date/Time: |
Wednesday, September 17, 2008 10:00AM
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Location: |
Multi-purpose Room (GC-402) David Skaggs Research Center (DSRC), NOAA Building - DOC Boulder Campus
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Title: |
The Orbiting Carbon Observatory (OCO)
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ABSTRACT
The Orbiting Carbon
Observatory
(OCO) is scheduled for launch into the Earth Observing System Afternoon
Constellation (A-Train) in January 2009. This NASA Earth System Science
Pathfinder (ESSP) mission will make spatially resolved measurements of
the
column averaged CO
2 dry air mole fraction, X
CO2, over the sunlit hemisphere of
the Earth. These measurements
will be analyzed with chemical tracer transport models to infer CO
2 sources and sinks on regional
scales and quantify
their variability over the seasonal cycle. The observatory consists of
a 3-axis
stabilized spacecraft bus that carries and points a single instrument.
The
instrument incorporates 3 bore sighted, high resolution grating
spectrometers
that will make coincident measurements of reflected sunlight in
near-infrared CO
2
and molecular oxygen (O
2) bands.
High
spectral resolution (λ/Δλ > 20,000) measurements within the CO
2 absorption bands near 1.61 and
2.06 μm yield
column abundance estimates that are most sensitive to the CO
2 mixing ratios near the surface,
where most
sources and sinks are located. High resolution (λ/Δλ > 17,000)
measurements
within the 0.765-μm O
2 A-band
spectra
yield clear sky surface pressure estimates with accuracies near 1 mbar
over
most of the sunlit hemisphere and constrain cloud and aerosol profiles
to
reduce uncertainties associated with multiple scattering. The
instrument integration and
test was completed at the NASA Jet Propulsion Laboratory in March 2008.
Analysis
of the test data indicate that all 3 spectrometers meet the stringent
spectroscopic performance requirements needed to yield regional-scale
XCO2 estimates with errors
and systematic biases no larger than 0.3% (1 ppm).
Recently
instrument-spacecraft integration
was completed at Orbital Sciences in
Dulles, VA.
Operational tests of the
science data processing system are under way.
The launch will take place from Vandenberg Air Force Base.
The first space-based data is anticipated in
early 2009.
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Speaker: |
John Lupton, NOAA Pacific Marine Environmental Laboratory, Newport, Oregon
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Date/Time: |
Friday, October 3, 2008 10:00AM
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Location: |
Multi-purpose Room (GC-402)
David Skaggs Research Center (DSRC)
NOAA Building, DOC Boulder Campus
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Title: |
Natural CO2 from Submarine Hydrothermal Systems
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ABSTRACT
Although dozens of mid-ocean ridge (MOR) hydrothermal systems have been
studied over the past few decades, a significant discharge of a pure gas
phase has been found at only one site on the Explorer Ridge, northeast
Pacific. In contrast to MOR systems, recent studies of submarine
volcanoes on volcanic arcs have found several sites that, in addition to
discharging hot vent fluid, are also venting a separate CO2 -rich phase
either in the form of gas bubbles or liquid CO2 droplets. Submersible
dives on 22 active submarine volcanoes on the Mariana and Tonga-Kermadec
Arcs have discovered systems on 6 of these volcanoes that are venting a
free gas phase in addition to hot vent fluids.
This talk will focus on the Champagne vent field on NW Eifuku volcano
in the northern Mariana Arc, which is discharging cold droplets of
liquid CO2 as well as hot gas-rich vent fluid. The other 5 volcanoes
in this study are shallower and therefore the free gas discharge takes
the form of gas bubbles rather than liquid CO2 droplets. At NW Eifuku,
collecting samples of the liquid CO2 droplets required the development
of special sampling technology that could be deployed from a robotic
submersible. The carbon flux from this small vent field is quite large,
estimated at 23 moles/s, about 0.1% of the global mid-ocean ridge carbon
flux. Detailed analysis of the helium and carbon discharging at the
Champagne site has provided clues to the origin of this high carbon
flux. One follow-up biological study at NW Eifuku has shown that the
mussels at the Champagne site are drastically affected by the low pH
environment. Thus these CO2 -rich systems may be important natural
laboratories for studying the effects of high CO2 concentrations on
marine ecosystems, with relevance to ocean acidification and seabed
sequestration of anthropogenic carbon.