Dennis D. Baldocchi’s research while affiliated with National Oceanic and Atmospheric Administration and other places

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Publications (5)


Turbulent transfer in a deciduous forest
  • Article

October 1989

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14 Reads

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37 Citations

Tree Physiology

Dennis D. Baldocchi

Carbon dioxide, water vapor and other passive scalars are physically transferred between a plant canopy and the atmosphere by turbulence. Intense and intermittent sweep and ejection events transfer most of the mass. Although the capacity for turbulence to transfer material is high, mass transfer is coupled to the diffusive source or sink strength of the foliage and soil and is ultimately limited to a minimum level set by the supply of material, or the demand for it. The diffusive source/sink strength of material leaving or entering leaves and the soil is a function of many physical, biological and chemical attributes and processes. These attributes and processes include the amount and distribution of foliage, the leaf boundary layer and surface resistances, the turbulence and radiative regimes in the canopy, biochemical and photochemical reactions and the scalar concentration field within and above the canopy and inside leaves and the soil. Here we discuss how these factors contribute to turbulent transfer in a deciduous forest.



Pollutant Deposition to Individual Leaves and Plant Canopies: Sites of Regulation and Relationship to Injury

January 1987

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3 Reads

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52 Citations

The objective was twofold: (1) to characterize the processes governing the deposition of pollutants to individual leaves and plant canopies and (2) to relate deposition to the pollutant's effects on a plant's physiology and growth. The focus is principally dry deposited, regionally distributed gases of importance because of either their phytotoxicity (e.g., ozone, O/sub 3/; sulfur dioxide, SO/sub 2/; nitrogen dioxide, NO/sub 2/; peroxyacetyl nitrate, PAN; hydrogen sulfide, H/sub 2/S; hydrogen peroxide, H/sub 2/O/sub 2/) or influence on biogeochemical cycling in terrestrial ecosystems (e.g., carbonyl sulfide; COS; ammonia, NH/sub 3/; nitric acid vapor, HNO/sub 3/). Where appropriate, the sedimentation of particles and the interception of cloud water by plant canopies and individual leaves are discussed.



A canopy stomatal resistance model for gaseous deposition to vegetated surfaces

January 1987

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61 Reads

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469 Citations

Atmospheric Environment (1967)

A gaseous deposition model, based on a realistic canopy stomatal resistance submodel, is described, analyzed and tested. This model is designed as one of a hierarchy of simulations, leading up to a “big-leaf” model of the processes contributing to the exchange of trace gases between the atmosphere and vegetated surfaces. Computations show that differences in plant species and environmental and physiological conditions can affect the canopy stomatal resistance by a factor of four. Canopy stomatal resistances to water vapor transfer computed with the present model are compared against values measured with a porometer and computed with the Penman-Monteith equation. Computed stomatal resistances from a soybean canopy in both well-watered and water-stressed conditions yield good agreement with test data. The stomatal resistance submodel responds well to changing environmental and physiological conditions. Model predictions of deposition velocities are evaluated for the case of ozone, transferred to maize. Calculated deposition velocities of O3 overestimate measured values on the average by about 30%, probably largely as a consequence of uncertainties in leaf area index, soil and cuticle resistances, and other modeling parameters, but also partially due to imperfect measurement of O3 deposition velocities.

Citations (5)


... The mesophyll and cuticular resistance values are set based on those reported in the literature: for NO2, rm = 100 s m −1 (Hosker and Lindberg 1982) and rt = 20,000 s m −1 (Wesley 1989); for O3, rm = 10 s m −1 (Hosker and Lindberg 1982) and rt = 10,000 s m −1 (Taylor et al. 1988;Lovett 1994); and for SO2, rm = 0 (Wesley 1989) and rt = 8000 s m −1 . As CO reduction is assumed to be independent of photosynthesis and transpiration, the resistance value for CO is set to 50,000 s m −1 in the in-leaf season and 1,000,000 s m −1 in the out-leaf season for all trees (Bidwell and Fraser 1972). ...

Reference:

Modeling ecosystem services of urban trees to improve air quality and microclimate
Pollutant Deposition to Individual Leaves and Plant Canopies: Sites of Regulation and Relationship to Injury
  • Citing Conference Paper
  • January 1987

... Hourly removals of CO, NO 2 , O 3 , SO 2 , PM 10 , and PM 2.5 throughout the year were estimated using the dry deposition model, which is an integral part of Ecov6.0 (Nowak et al., 2008). The pollutant flux (F in μg m − 2 h − 1 ), which represents the density of gaseous pollutants at the vegetation surface, is calculated according to Baldocchi et al. (1987): ...

A canopy stomatal resistance model for gaseous deposition to vegetated surfaces
  • Citing Article
  • January 1987

Atmospheric Environment (1967)

... As extensive reviews of NH 3 surface exchange models are available (Flechard et al., 2015;Massad et al., 2010), only a brief overview is provided here. Models of bidirectional NH 3 surface exchange consider the control of fluxes to be analogous to electrical resistances (Baldocchi, 1988;Monteith and Unsworth, 2013). Whether emission occurs from the atmosphere to the canopy or vice versa is dependent upon the relative magnitude of ambient and canopy concentrations, with resistances acting in series or in parallel impeding the exchange. ...

A multi-layer model for estimating sulphur dioxide deposition to a deciduous oak forest canopy
  • Citing Article
  • January 1988

... Both olfactory and magnetic cues have been proposed to provide map information in other vertebrates (Gould 1982(Gould , 1998Wallraff 2005;Lohmann and Lohmann 2008;Lohmann et al. 2008). In newts, however, although odors emanating from the home pond could provide local cues that play a role when newts are in the final stages of the return migration (McGregor and Teska 1989;Joly and Miaud 1993;Sinsch 2007), turbulence in the understory of the forested habitat (Baldocchi 1989) makes it unlikely that wind-borne odors from more widely distributed odor sources could be used to provide a source of geographic position ('map') information (Phillips 1996). Furthermore, I. alpestris do not require olfactory cues to determine the home direction, since homeward orientation is not affected by whether or not newts had access to natural wind-borne odors (Diego-Rasilla and Phillips 2021). ...

Turbulent transfer in a deciduous forest
  • Citing Article
  • October 1989

Tree Physiology