The Large Area Collectors are flown on the ER-2 in support of the NASA-Johnson Space Flight Center Cosmic Dust Program. The LACs are used to collect comparatively unaltered cosmic dust from the stratosphere at ER-2 flight altitudes of 65,000 feet and above. Sufficient quantities of extraterrestrial materials are collected to allow chemical and mineralogical compositions of individual particles to be determined. Study of these materials whose sources may be comets, asteroid collisions, planetary impacts, and meteorite ablation provide valuable information about the origin and the history of the solar system.
ER-2 - AFRC
The JPL Laser Hygrometer (JLH) is an autonomous spectrometer to measure atmospheric water vapor from airborne platforms. It is designed for high-altitude scientific flights of the NASA ER-2 aircraft to monitor upper tropospheric (UT) and lower stratospheric (LS) water vapor for climate studies, atmospheric chemistry, and satellite validation. JLH will participate in the NASA SEAC4RS field mission this year. The light source for JLH is a near-infrared distributed feedback (DFB) tunable diode laser that scans across a strong water vapor vibrational-rotational combination band absorption line in the 1.37 micrometer band. Both laser and detector are temperature‐stabilized on a thermoelectrically-cooled aluminum mount inside an evacuated metal housing. A long optical path is folded within a Herriott Cell for sensitivity to water vapor in the UT and LS. A Herriott cell is an off-axis multipass cell using two spherical mirrors [Altmann et al., 1981; Herriott et al., 1964]. The laser beam enters the Herriott cell through a hole in the mirror that is closest to the laser. The laser beam traverses many passes of the Herriott cell and then returns through the same mirror hole to impinge on a detector.
The Harvard CRDS/ICOS instrument is an absorption spectrometer that uses the relatively new and highly sensitive techniques of integrated cavity output spectroscopy (ICOS) and cavity ringdown spectroscopy (CRDS) with a high-finesse optical cavity and a cw quantum cascade laser (QCL) source. The primary spectroscopic technique employed is ICOS, in which intra-cavity absorption is measured from the steady-state output of the cavity. Light from a high power, tunable, single mode, solid-state laser source is coupled into a cavity consisting of two concave, highly reflective mirrors (R ≈ 0.9999), through which air continuously flows. The laser is scanned over a spectral region of 1–2 cm-1 containing an absorption feature, and the cavity output is detected by an LN2-cooled HgCdTe detector. The resultant output approximates an absorption spectrum with an effective pathlength of > 5 km, far greater than that of standard multipass Herriott or White cells.
The Harvard CRDS/ICOS instrument is an absorption spectrometer that uses the relatively new and highly sensitive techniques of integrated cavity output spectroscopy (ICOS) and cavity ringdown spectroscopy (CRDS) with a high-finesse optical cavity and a cw quantum cascade laser (QCL) source. The primary spectroscopic technique employed is ICOS, in which intra-cavity absorption is measured from the steady-state output of the cavity. Light from a high power, tunable, single mode, solid-state laser source is coupled into a cavity consisting of two concave, highly reflective mirrors (R ≈ 0.9999), through which air continuously flows. The laser is scanned over a spectral region of 1–2 cm-1 containing an absorption feature, and the cavity output is detected by an LN2-cooled HgCdTe detector. The resultant output approximates an absorption spectrum with an effective pathlength of > 5 km, far greater than that of standard multipass Herriott or White cells.
The design of the newly developed total water instrument is based on the same principles as the water vapor instrument, and is intended to fly in conjunction with it. Conceptually, the total water instrument can be thought of as containing four subsystems:
1. An inlet through which liquid and/or solid water particles can be brought into an instrument duct without perturbing the ambient particle density.
2. A heater that efficiently evaporates the liquid/solid water before it reaches the detection axis.
3. Ducting through which the air flows to the detection axis without perturbing the (total) water vapor mixing ratio.
4. A water vapor detection axis that accurately and precisely measures the total water content of the ambient air.
The Harvard Water Vapor (HWV) instrument combines two independent measurement methods for the simultaneous in situ detection of ambient water vapor mixing ratios in a single duct. This dual axis instrument combines the heritage of the Harvard Lyman-α photo-fragment fluorescence instrument (LyA) with the newly designed tunable diode laser direct absorption instrument (HHH). The Lyman-α detection axis functions as a benchmark measurement, and provides a requisite link to the long measurement history of Harvard Lyman-α aboard NASA’s WB-57 and ER-2 aircraft [Weinstock et al., 1994; Hintsa et al., 1999; Weinstock et al., 2009]. The inclusion of HHH provides a second high precision measurement that is more robust than LyA to changes in its measurement sensitivity [Smith et al., in preparation]. The simultaneous utilization of radically different measurement techniques facilitates the identification, diagnosis, and constraint of systematic errors both in the laboratory and in flight. As such, it constitutes a significant step toward resolving the controversy surrounding water vapor measurements in the upper troposphere and lower stratosphere.
The high-sensitivity fast response CO2 instrument measures CO2 concentrations in situ using the light source, gas cells, and solid-state detector from a modified nondispersive infrared CO2 analyzer (Li-Cor, Inc., Lincoln, NE). These components are stabilized along the detection axis, vibrationally isolated, and housed in a temperature-controlled pressure vessel. Sample air enters a rear-facing inlet, is preconditioned using a Nafion drier (to remove water vapor), then is compressed by a Teflon diaphragm pump. A second water trap, using dry ice, reduces the sample air dewpoint to less than 70C prior to detection. The CO2 mixing ratio of air flowing through the sample gas cell is determined by measuring absorption at 4.26 microns relative to a reference gas of known concentration. In-flight calibrations are performed by replacing the air sample with reference gas every 10 minutes, with a low-span and a high-span gas every 20 minutes, and with a long-term primary standard every 2 hours. The long-term standard is used sparingly and serves as a check of the flight-to-flight accuracy and precision of the measurements, augmented by ground-based calibrations before and after flights.
<p>OH is detected by direct laser induced fluorescence in the (0-1) band of the 2?-2? electronic transition. A pulsed dye-laser system produces frequency tunable laser light at 282 nm. An on-board frequency reference cell is used by a computer to lock the laser to the appropriate wavelength. Measurement of the signal is then made by tuning the laser on and off resonance with the OH transition.</p>
<p>Stratospheric air is channeled into the instrument using a double-ducted system that both maintains laminar flow through the detection region and slows the flow from free stream velocity (200 m/s) to 40 m/s. The laser light is beam-split and directed to two detection axes where it passes through the stratospheric air in multipass White cells.</p>
<p>Fluorescence from OH (centered at 309 nm) is detected orthogonal to both the flow and the laser propagation using a filtered PMT assembly. Optical stability is checked periodically by exchanging the 309 nm interference filter with a filter centered at 302 nm, where Raman scattering of N2 is observed.</p>
<p>HO2 is measured as OH after chemical titration with nitric oxide: HO2 + NO → OH + NO2. Variation of added NO density and flow velocity as well as the use of two detection axes aid in diagnosis of the kinetics of this titration. Measurements of ozone (by uv absorption) and water vapor (by photofragment fluorescence) are made as diagnostics of potential photochemical interference from the mechanism: O3 + hv (282 nm) → O(1D) + O2, followed by: O(1D) + H2O → OH + OH</p>
The High Altitude Monolithic Microwave integrated Circuit (MMIC) Sounding Radiometer (HAMSR) is a microwave atmospheric sounder developed by JPL under the NASA Instrument Incubator Program. Operating with 25 spectral channels in 3 bands (50-60 Ghz, 118 Ghz, 183 Ghz), it provides measurements that can be used to infer the 3-D distribution of temperature, water vapor, and cloud liquid water in the atmosphere, even in the presence of clouds. The new UAV-HAMSR with 183GHz LNA receiver reduces noise to less than a 0.1K level improving observations of small-scale water vapor. HAMSR is mounted in payload zone 3 near the nose of the Global Hawk.
HAMSR was designed and built at the Jet Propulsion Laboratory under the NASA Instrument Incubator Program and uses advanced technology to achieve excellent performance in a small package. It was first deployed in the field in the 2001 Fourth Convection and Moisture Experiment (CAMEX-4) - a hurricane field campaign organized jointly by NASA and the Hurricane Research Division (HRD) of NOAA in Florida. HAMSR also participated in the Tropical Cloud Systems and Processes (TCSP) hurricane field campaign in Costa Rica in 2005. In both campaigns HAMSR flew as a payload on the NASA high-altitude ER-2 aircraft. It was also one of the payloads in the 2006 NASA African Monsoon Multidisciplinary Activities (NAMMA) field campaign in Cape Verde - this time using the NASA DC-8. HAMSR provides observations similar to those obtained with microwave sounders currently operating on NASA, NOAA and ESA spacecraft, and this offers an opportunity for valuable comparative analyses.
The FCAS II sizes particles in the approximate diameter range from 0.07 mm to 1 mm. Particles are sampled from the free stream with a near isokinetic sampler and are transported to the instrument. They are then passed through a laser beam and the light scattered by individual particles is measured. Particle size is related to the scattered light. The data reduction for the FCAS II takes into account the water which is evaporated from the particle in sampling and the effects of anisokinetic sampling (Jonsson et al., 1995).
The FCAS II and its predecessors have provided accurate aerosol size distribution measurements throughout the evolution of the volcanic cloud produced by the eruption of Mt. Pinatubo. (Wilson et al., 1993). Near co-incidences between FCAS II and SAGE II measurements show good agreement between optical extinctions calculated from FCAS size distributions and extinctions measured by SAGE II.
Accuracy: The instrument has been calibrated with monodisperse aerosol carrying a single charge. The FCAS III and the electrometer agree to within 10%. Sampling errors may increase the uncertainty but a variety of comparisons suggests that total uncertainties in aerosol surface are near 30% (Jonsson, et al., 1995).
Precision: The precision equals 1/ÖN where N is the number of particles counted. In many instances the precision on concentration measurements may reach 7% for 0.1 Hz data. If better precision is desired, it is necessary only to accumulate over longer time intervals.
Response Time: Data are processed at 0.1 Hz. However, the response time depends upon the precision required to detect the change in question. Small changes may require longer times to detect. Plume measurements may be processed with 1 s resolution.
Weight: Approximately 50 lbs.