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At least 55 records · Page 3

A season of heat, water vapor, total hydrocarbon, and ozone fluxes at a subarctic fen

High-latitude environments are thought to play several critical roles in the global balance of radiatively active trace gases. Adequate documentation of the source and sink strengths for trace gases requires long time series of detailed measurements, including heat and moisture budgets. A fen near Schefferville, Quebec, was instrumented during the summer of 1990 for the measurement of the surface energy, radiation, and moisture balances as well as for eddy correlation estimates of ozone and methane flux. Despite the limited fetch at this site, analysis of the tower flux 'footprint' indicates that at least 80% of the flux observed originates from sources within the fen. Sensible heat fluxes averaged 25% of the daytime net radiation at the site, while the latent heat flux, determined from the energy balance, was 63%; the Bowen ratio varied from 0.2 to 0.8 from day to day, without a seasonal trend to the variation. The competing effects of rooted macrophyte development (with concomitant effects on roughness and transpiration) and the normal shift in synoptic pattern around day 200 to warm, dry conditions results in a lack of net seasonal effect on the energy partitioning. Over the period from days 170 to 230, the evaporation (167 mm) was double the rainfall, while the decline in water level was 107 mm, leaving a net runoff of 0.44 mm/d. The total hydrocarbon flux was 75-120 mg m(exp -2)/d, following a diurnal pattern similar to heat or moisture flux, while the daytime ozone flux was about -1.11 x 10(exp 11) molecules cm(exp -2)/s. A period near the end of the experiment, during week 30, produced the strongest total hydrocarbon flux, associated with warmer deep (1 m) soil temperatures, lower fen water levels, and the late summer shift in wind direction at that time. An early summer 'flush' of total hydrocarbon was not observed.

Moore, Kathleen E.↗

Bio-optical and physical variability in the subarctic North Atlantic Ocean during the spring of 1989

A unique set of physical, bio-optical, and meteorological observations were made from a mooring located in the open ocean south of Iceland (59 deg 29.5 min N, 20 deg 49.8 min W) from April 13 to June 12 1989. The present measurements are apparently the first to resolve the rapid transition to springtime physical and biological conditions at such a high latitude site. Our data were collected with bio-optical and physical moored systems every few minutes. The abrupt onset of springtime stratification was observed with the mixed layer shoaling from approximately 550 m to approximately 50 m in approximately 5 days. During this period a major phytoplankton bloom occurred with a tenfold increase in near-surface chlorophyll concentration in less than 3 weeks. Our statistical analysis indicates that the velocity shear in the upper layer is driven primarily by local wind stress. Mesoscale variability is also apparent from these and concurrent airborne oceangraphic lidar observations. Our complementary modeling results suggest that the near-surface layer may be reasonably well described by a one-dimensional model and that the spring bloom was initiated during incipient near-surface restratification.

Dickey, T.↗

Satellite Observations to Monitor Subarctic Rain-On-Snow Events

Rain-on-snow (ROS) events have been the focus of numerous studies in the past five years. Their characteristics(frequency, extent, and duration) represent a new and relevant climate indicator. However, monitoring ROS occurrences remotely using satellite observations is deemed challenging. The ROS events can be sporadic, of very different intensities, and the outcome of the rain water uncertain (either it freezes in the snow cover or runs off). Using passive and active microwave remote sensing observations, our study proposes new approaches to monitor the occurrence of ROS events.Specifically, we utilize observations from Advanced Microwave Scanning Radiometer 2 (AMSR2), and Global Precipitation Measurements (GPM) Microwave Imager (GMI), and GPM Dual-frequency Precipitation Radar (DPR). We compare our ROS detection against weather stations and recently published algorithms using a different set of microwave frequencies.

Brucker, Ludovic↗

Role of the Hudson Bay lowland as a source of atmospheric methane

Based on point measurements of methane flux from wetlands in the boreal and subarctic regions, northern wetlands are a major source of atmospheric methane. However, measurements have not been carried out in large continuous peatlands such as the Hudson Bay Lowland (HBL) (320,000 sq km) and the Western Siberian lowland (540,000 sq km), which together account for over 30% of the wetlands north of 40 deg N. To determine the role the Hudson Bay Lowland as a source of atmospheric methane, fluxes were measured by enclosures throughout the 1990 snow-free period in all the major wetland types and also by an aircraft in July. Two detailed survey areas were investigated: one (approximately 900 sq km) was in the high subarctic region of the northern lowland and the second area (approximately 4,800 sq km) straddled the Low Subarctic and High Boreal regions of the southern lowland. The fluxes were integrated over the study period to produce annual methane emissions for each wetland type. The fluxes were then weighted by the area of 16 different habitats for the southern area and 5 habitats for the northern area, as determined from Landsat thematic mapper to yield an annual habitat-weighted emission. On a per unit area basis, 1.31 +/- 0.11 and 2.79 +/- 0.39 g CH4 m(exp -2)/yr were emitted from the southern and northern survey areas, respectively. The extrapolated enclosure estimates for a 3-week period in July were compared to within 10% of the flux derived by airborne eddy correlation measurements made during the same period. The aircraft mean flux of 10 +/- 9 mg CH4 m(exp -2)/d was not statistically different from the extrapolated mean flux of 20 +/- 16 mg CH4 m(exp -2)/d. The annual habitat-weighted emission for the entire HBL using six wetland classes is estimated as 0.538 +/- 0.187 Tg CH4/yr (range of extreme cases is 0.057 to 2.112 Tg CH4/yr). This value is much lower than expected, based on previous emission estimates from northern wetlands.

Roulet, Nigel T.↗

Carbon monoxide and methane over Canada: July - August 1990

Carbon monoxide (CO) and methane (CH4) were measured in the 0.15- to 6-km portion of the troposphere over subarctic and boreal landscapes of midcontinent and eastern Canada during July - August 1990. In the mid-continent region, Arctic air entering the region was characterized by relatively uniform CO concentrations (86-108 parts per billion by volume (ppbv)) and CH4 concentrations (1729-1764 ppbv). Local biomass burning and long-range transport of CO into the area from industrial/urban sources and distant fires did frequently produce enhanced and variable concentrations. Emissions of CH4 from the Hudson Bay lowlands was the primary source for enhanced and variable concentrations, especially at altitudes of 0.15-1 km. In eastern Canada, most of the observed variability in CO and CH4 was similar in origin to the phenomena described for the midcontinent region. However, unexpectedly low concentrations of CO (51 ppbv) and CH4 (1688 ppbv) were measured in the midtroposphere on several flights. Combined meteorological and chemical data indicated that the low CO-CH4 events were the result of long-range transport of tropical Pacific marine air to subarctic latitudes.

Harriss, R. C.↗

Chemical composition of the atmospheric aerosol in the troposphere over the Hudson Bay lowlands and Quebec-Labrador regions of Canada

Atmospheric aerosols were collected in the boundary layer and free troposphere over continental and coastal subarctic regions of Canada during the July - August 1990 joint U.S.-Canadian Arctic Boundary Layer Expedition (ABLE) 3B/Northern Wetlands Study (NOWES). The samples were analyzed for the following water soluble species: sulfate, nitrate, ammonium, potassium, sodium, chloride, oxalate, methylsulfonate, and total amine nitrogen. Ammonium and sulfate were the major water soluble components of these aerosols. The nearly neutral (overall) chemical composition of summertime aerosol particles contrasts their strongly acidic wintertime composition. Aerosol samples were separated into several air mass categories and characterized in terms of chemical composition, associated mixing ratios of gaseous compounds, and meteorological parameters. The fundamental category represented particles associated with 'background' air masses. The summertime atmospheric aerosols in background air over the North American subarctic and Arctic regions were characterized by relatively small and spatially uniform mixing ratios of the measured species. These aerosol particles were aged to the extent that they had lost their primary source signature. The chemical profile of the background air aerosols was frequently modified by additions from biomass fire plumes, aged tropical marine air, and intrusions of upper tropospheric/lower stratospheric air. Aerosols in boundary layer background air over the boreal forest region of Quebec-Labrador had significantly larger mixing ratios of ammonium and sulfate relative to the Hudson Bay region. This may reflect infiltration of anthropogenic pollution or be due to natural emissions from this region.

Gorzelska, K.↗

One-Dimensional Coupled Ecosystem-Carbon Flux Model for the Simulation of Biogeochemical Parameters at Ocean Weather Station P

In this Technical Publication, we describe the model functionality and analyze its application to the seasonal and interannual variations of phytoplankton, nutrients, pCO2 and CO2 concentrations in the eastern subarctic Pacific at Ocean Weather Station P (OWSP, 50 deg. N 145 deg. W). We use a verified one-dimensional ecosystem model, coupled with newly incorporated carbon flux and carbon chemistry components, to simulate 22 years (1958-1980) of pCO2 and CO2 variability at Ocean Weather Station P (OWS P). This relatively long period of simulation verifies and extends the findings of previous studies using an explicit approach for the biological component and realistic coupling with the carbon flux dynamics. The slow currents and the horizontally homogeneous ocean in the subarctic Pacific make OWS P one of the best available candidates for modeling the chemistry of the upper ocean in one dimension. The chlorophyll and ocean currents composite for 1998 illustrates this premise. The chlorophyll concentration map was derived from SeaWiFS data and the currents are from an OGCM simulation (from R. Murtugudde).

Signorini, S.↗

Radar and ice surveys

High resolution radar from high altitudes for accurate ice cover surveys in arctic and subarctic areas

HIGH ALTITUDE↗

On vegetation mapping in Alaska using LANDSAT imagery with primary concerns for method and purpose in satellite image-based vegetation and land-use mapping and the visual interpretation of imagery in photographic format

The author has identified the following significant results. A simulated color infrared LANDSAT image covering the western Seward Peninsula was used for identifying and mapping vegetation by direct visual examination. The 1:1,083,400 scale print used was prepared by a color additive process using positive transparencies from MSS bands 4, 5, and 7. Seven color classes were recognized. A vegetation map of 3200 sq km area just west of Fairbanks, Alaska was made. Five colors were recognized on the image and identified to vegetation types roughly equivalent to formations in the UNESCO classification: orange - broadleaf deciduous forest; gray - needleleaf evergreen forest; light violet - subarctic alpine tundra vegetation; violet - broadleaf deciduous shrub thicket; and dull violet - bog vegetation.

Anderson, J. H.↗

Computations of transmittance and radiance in infrared water vapor sounding channels

The wing-scaling approximation/k-distribution method, previously developed for computing solar heating rates (Chou and Arking, 1981) was applied to the computation of the transmittance and outgoing radiance in infrared water vapor sounding channels. Functions necessary for the transmittance and radiance computations were computed from molecular line parameters using line-by-line methods. The method was applied to the three HIRS/2 water vapor sounding channels on the TIROS-N satellite, and its accuracy was tested using 11 widely separated atmospheres which ranged from hot-wet tropical atmospheres to cold-dry subarctic atmospheres. Compared to line-by-line calculations, maximum errors were shown to be less than 0.017 in transmittance and 0.4 K in brightness temperature for all cases. The rms errors are less than 0.009 in transmittance and 0.2 K in brightness temperature, the brightness temperature rms error being much smaller than the instrument noise.

Chou, M.-D.↗

Evaluation of photographic enhancements of Landsat imagery

The photographic processing of color Landsat imagery was evaluated to determine the optimal enhancement techniques. Twenty-six images were examined to explore the effects of gamma values upon image interpretation in a subarctic environment. Gamma values were varied on the images of bands 4 through 7 prior to the creation of the color composites. This yielded color-composited images with various color balances. These images were evaluated in terms of visible geological features (drainage, lineaments, landforms, etc.) and landcover features (exposed rock and ground, coniferous forest, etc.). The results indicate that the most informative images are created by using gamma values of 2.0 for band 4, 1.0 for band 5, and 2.0 for band 6 or 7. Other photographic enhancements tend to enhance some features at the expense of others.

Dean, K. G.↗

Broadband water vapor transmission functions for atmospheric IR flux computations

Transmission functions associated with water vapor molecular line and e-type absorption in the IR spectra regions are presented in the form of simple analytical functions and small tables, from which atmospheric IR fluxes and cooling rates can be easily computed. For typical clear atmospheres ranging from the tropics to the subarctic region, the difference with respect to line-by-line calculations is less than 0.15 C/day in the cooling rate and approximately equal to or less than 1 percent in fluxes.

Chou, M.-D.↗

Primary production control of methane emission from wetlands

Based on simultaneous measurements of CO2 and CH4 exchange in wetlands extending from subarctic peatlands to subtropical marshes, a positive correlation between CH4 emission and net ecosystem production is reported. It is suggested that net ecosystem production is a master variable integrating many factors which control CH4 emission in vegetated wetlands. It is found that about 3 percent of the daily net ecosystem production is emitted back to the atmosphere as CH4. With projected stimulation of primary production and soil microbial activity in wetlands associated with elevated atmospheric CO2 concentration, the potential for increasing CH4 emission from inundated wetlands, further enhancing the greenhouse effect, is examined.

Whiting, G. J.↗

The Arctic Boundary Layer Expedition (ABLE-3B): July - August 1990

The Arctic Boundary Layer Expedition (ABLE) 3B used data from ground-based, aircraft, and satellite platforms to characterize the chemistry and dynamics of the troposphere in subarctic and Arctic regions of midcontinent and eastern Canada during July - August 1990. This paper reports the experimental design for ABLE 3B and a brief overview of results. The detailed results are presented in a series of papers in this issue. The chemical composition of the atmospheric mixed layer over remote tundra, boreal wetland, and forested environments was influenced by emissions of CH4 and nonmethane hydrocarbons from biogenic sources, emissions of gases and aerosols from local biomass burning, and transport of pollutants into the study areas from urban/industrial sources. Minimum concentrations of both trace gas and aerosol species in boundary layer air were associated with Arctic source areas. In the free troposphere the biospheric influence was undetectable, and major sources of chemical variability were related to long-range transport of pollutants into the study areas from biomass burning and industrial sources in Alaska and the Great Lakes regions, respectively. Minimum concentrations of both trace gas and aerosol species in the free troposphere were associated with a persistent, widespread air mass which both chemistry and air mass trajectory analyses suggested had originated in the tropical Pacific. Subsidence of air from the upper troposphere and lower stratosphere frequently enhanced ozone and influenced other trace gas and aerosol species at midtropospheric altitudes. The North American Arctic is a complex dynamical and chemical environment with considerable spatial and temporal variability in aerosol and trace gas concentrations. The use of atmospheric chemical indicators for climate change detection will require a much more comprehensive Arctic monitoring program than currently exists.

Harriss, R. C.↗

Enhancement of acidic gases in biomass burning impacted air masses over Canada

Biomass-burning impacted air masses sampled over central and eastern Canada during the summer of 1990 as part of ABLE 3B contained enhanced mixing ratios of gaseous HNO3, HCOOH, CH3COOH, and what appears to be (COOH)2. These aircraft-based samples were collected from a variety of fresh burning plumes and more aged haze layers from different source regions. Values of the enhancement factor, delta X/delta CO, where X represents an acidic gas, for combustion-impacted air masses sampled both near and farther away from the fires, were relatively uniform. However, comparison of carboxylic acid emission ratios measured in laboratory fires to field plume enhancement factors indicates significant in-plume production of HCOOH. Biomass-burning appears to be an important source of HNO3, HCOOH, and CH3COOH to the troposphere over subarctic Canada.

Lefer, B. L.↗

Summertime distribution and relations of reactive odd nitrogen species and NO(y) in the troposphere over Canada

We report here large-scale features of the distribution of NO(x), HNO3, PAN, particle NO3, and NO(y) in the troposphere from 0.15 to 6 km altitude over central Canada. These measurements were conducted in July - August 1990 from the NASA Wallops Electra aircraft as part of the joint United States-Canadian Arctic Boundary Layer Expedition (ABLE) 3B-Northern Wetlands Study. Our findings show that this region is generally NO(x) limited, with NO(x) mixing ratios typically 20-30 parts per trillion by volume (pptv). We found little direct evidence for anthropogenic enhancement of mixing ratios of reactive odd nitrogen species and NO(y) above those in 'background' air. Instead, it appears that enhancements in the mixing ratios of these species were primarily due to emissions from several day old or CO-rich-NO(x)-poor smoldering local biomass-burning fires. NO(x) mixing ratios in biomass-burning impacted air masses were usually less than 50 pptv, but those of HNO3 and PAN were typically 100-300 pptv representing a twofold-threefold enhancement over 'background' air. During our study period, inputs of what appeared to be aged tropical air were a major factor influencing the distribution of reactive odd nitrogen in the midtroposphere over northeastern North America. These air masses were quite depleted in NO(y) (generally less than 150 pptv), and a frequent summertime occurrence of such air masses over this region would imply a significant influence on the reactive odd nitrogen budget. Our findings show that the chemical composition of aged air masses over subarctic Canada and those documented in the Arctic during ABLE 3A have strikingly similar chemistries, suggesting large-scale connection between the air masses influencing these regions.

Talbot, R. W.↗