Juergen Burkhardt

Hygroscopic particles on leaves: nutrients or desiccants?

Aerosols have always been part of the atmosphere, and plant surfaces are a major aerosol sink. Given the nutrient content of aerosols and the natural stability of aerosol concentrations over evolutionary time, plants may have developed adaptations to aerosol input. Although little is known about such adaptations, leaf surface micro-roughness appears to play a key role. This review focuses on the deposition and fate of fine aerosols that are less than 2.5 μm in diameter. Most of these aerosols are hygroscopic, and they are often deliquescent (liquid) on transpiring leaves. Such concentrated solutions may be taken up by both the cuticle and stomata, contradicting previous concepts. The establishment of a continuous liquid water connection along stomatal walls affects individual stomata and is a new concept called “hydraulic activation of stomata” (HAS). HAS enables the efficient bidirectional transport of water and solutes between the leaf interior and leaf surface and makes stomatal transpiration partly in...

Stomatal penetration by aqueous solutions – an update involving leaf surface particles

The recent visualization of stomatal nanoparticle uptake ended a 40-yr-old paradigm. Assuming clean, hydrophobic leaf surfaces, the paradigm considered stomatal liquid water transport to be impossible as a result of water surface tension. However, real leaves are not clean, and deposited aerosols may change hydrophobicity and water surface tension. Droplets containing NaCl, NaClO(3), (NH(4))(2) SO(4), glyphosate, an organosilicone surfactant or various combinations thereof were evaporated on stomatous abaxial and astomatous adaxial surfaces of apple (Malus domestica) leaves. The effects on photosynthesis, necrosis and biomass were determined. Observed using an environmental scanning electron microscope, NaCl and NaClO(3) crystals on hydrophobic tomato (Solanum lycopersicum) cuticles underwent several humidity cycles, causing repeated deliquescence and efflorescence of the salts. All physiological parameters were more strongly affected by abaxial than adaxial treatments. Spatial expansion and dendritic crystallization of the salts occurred and cuticular hydrophobicity was decreased more rapidly by NaClO(3) than NaCl. The results confirmed the stomatal uptake of aqueous solutions. Humidity fluctuations promote the spatial expansion of salts into the stomata. The ion-specific effects point to the Hofmeister series: chaotropic ions reduce surface tension, probably contributing to the defoliant action of NaClO(3), whereas the salt spray tolerance of coastal plants is probably linked to the kosmotropic nature of chloride ions.

Multiplication of microbes below 0.690 water activity : implications for terrestrial and extraterrestrial life

Since a key requirement of known life forms is available water (water activity; aw ), recent searches for signatures of past life in terrestrial and extraterrestrial environments have targeted places known to have contained significant quantities of biologically available water. However, early life on Earth inhabited high-salt environments, suggesting an ability to withstand low water-activity. The lower limit of water activity that enables cell division appears to be ∼ 0.605 which, until now, was only known to be exhibited by a single eukaryote, the sugar-tolerant, fungal xerophile Xeromyces bisporus. The first forms of life on Earth were, though, prokaryotic. Recent evidence now indicates that some halophilic Archaea and Bacteria have water-activity limits more or less equal to those of X. bisporus. We discuss water activity in relation to the limits of Earths present-day biosphere; the possibility of microbial multiplication by utilizing water from thin, aqueous films or non-liquid sources; whether prokaryotes were the first organisms able to multiply close to the 0.605-aw limit; and whether extraterrestrial aqueous milieux of ≥ 0.605 aw can resemble fertile microbial habitats found on Earth.

“Breath figures” on leaf surfaces—formation and effects of microscopic leaf wetness

“Microscopic leaf wetness” means minute amounts of persistent liquid water on leaf surfaces which are invisible to the naked eye. The water is mainly maintained by transpired water vapor condensing onto the leaf surface and to attached leaf surface particles. With an estimated average thickness of less than 1 μm, microscopic leaf wetness is about two orders of magnitude thinner than morning dewfall. The most important physical processes which reduce the saturation vapor pressure and promote condensation are cuticular absorption and the deliquescence of hygroscopic leaf surface particles. Deliquescent salts form highly concentrated solutions. Depending on the type and concentration of the dissolved ions, the physicochemical properties of microscopic leaf wetness can be considerably different from those of pure water. Microscopic leaf wetness can form continuous thin layers on hydrophobic leaf surfaces and in specific cases can act similar to surfactants, enabling a strong potential influence on the foliar exchange of ions. Microscopic leaf wetness can also enhance the dissolution, the emission, and the reaction of specific atmospheric trace gases e.g., ammonia, SO2, or ozone, leading to a strong potential role for microscopic leaf wetness in plant/atmosphere interaction. Due to its difficult detection, there is little knowledge about the occurrence and the properties of microscopic leaf wetness. However, based on the existing evidence and on physicochemical reasoning it can be hypothesized that microscopic leaf wetness occurs on almost any plant worldwide and often permanently, and that it significantly influences the exchange processes of the leaf surface with its neighboring compartments, i.e., the plant interior and the atmosphere. The omission of microscopic water in general leaf wetness concepts has caused far-reaching, misleading conclusions in the past.

Atmospheric composition change

Publisher Summary The coupling between climate change and atmospheric composition results from the basic structure of the Earth atmosphere climate system, and the fundamental processes within it. The composition of the atmosphere is determined by natural and human-related emissions, and the energy that flows into, out of, and within the atmosphere. Atmospheric composition influences climate by regulating the radiation budget. Potentially significant contributions to the climate impact are provided by compounds such as CO2, CH4, O3, particles, and cirrus clouds. For the chemically active gases, processes in the atmosphere are important, with large spatial and temporal variations. The climate–chemistry interactions are therefore characterized by significant regional differences with regions such as South East Asia being a future key region due to significant increases in energy use and pollution emission. Likewise, ship and air traffic represent important sectors because of significant increases in emissions in recent years. The relative contributions to the emissions from various sectors are expected to change significantly over the next few decades due to differences in mitigation options and costs.Chemically active climate compounds are either primary compounds like methane (CH4), removed by oxidation in the atmosphere, or secondary compounds like ozone (O-3), sulfate and organic aerosols, both formed and removed in the atmosphere. Man-induced climate-chemistry interaction is a two-way process: Emissions of pollutants change the atmospheric composition contributing to climate change through the aforementioned climate components, and climate change, through changes in temperature, dynamics, the hydrological cycle, atmospheric stability, and biosphere-atmosphere interactions, affects the atmospheric composition and oxidation processes in the troposphere. Here we present progress in our understanding of processes of importance for climate-chemistry interactions, and their contributions to changes in atmospheric composition and climate forcing. A key factor is the oxidation potential involving compounds like O-3 and the hydroxyl radical (OH). Reported studies represent both current and future changes. Reported results include new estimates of radiative forcing based on extensive model studies of chemically active climate compounds like O-3, and of particles inducing both direct and indirect effects. Through EU projects like ACCENT, QUANTIFY, and the AeroCom project, extensive studies on regional and sector-wise differences in the impact on atmospheric distribution are performed. Studies have shown that land-based emissions have a different effect on climate than ship and aircraft emissions, and different measures are needed to reduce the climate impact. Several areas where climate change can affect the tropospheric oxidation process and the chemical composition are identified. This can take place through enhanced stratospheric-tropospheric exchange of ozone, more frequent periods with stable conditions favoring pollution build up over industrial areas, enhanced temperature induced biogenic emissions, methane releases from permafrost thawing, and enhanced concentration through reduced biospheric uptake. During the last 5-10 years, new observational data have been made available and used for model validation and the study of atmospheric processes. Although there are significant uncertainties in the modeling of composition changes, access to new observational data has improved modeling capability. Emission scenarios for the coming decades have a large uncertainty range, in particular with respect to regional trends, leading to a significant uncertainty range in estimated regional composition changes and climate impact.

Ambient aerosol increases minimum leaf conductance and alters the aperture–flux relationship as stomata respond to vapor pressure deficit (VPD)

Aerosols are important components of the global plant environment, with beneficial and deleterious impacts. The direct effects of aerosol deposition on plant-water relationships remain poorly characterized but potentially important. Vicia faba was grown in ambient urban air and in the same air with aerosol excluded, in a moderately polluted environment using two exposure protocols. Simultaneous measurement of gas exchange and stomatal pore aperture was combined with leaf dehydration kinetics and microscopic evaluation of leaf wetness formation and aerosol deposition patterns. The ambient aerosol was shown to be hygroscopic. Aerosol exposure increased minimum leaf conductance, shown by dehydration kinetics, and nocturnal water vapor flux, shown by dark-adapted gas exchange. Aerosol exposure decreased stomatal apertures at each level of vapor pressure deficit (VPD) and increased stomatal conductance at comparable levels of aperture. Overall, these effects were modest, and largest when stomata were wide open. The uncoupling of conductance (flux-based) from aperture (directly measured microscopically) implies that aerosol-induced water loss is not fully under stomatal control. This reduces drought tolerance and may provide a mechanism by which deposited aerosol plays a direct role in stomatal response to VPD.

Aerosol and acid gases

The background for this discussion was the background document in this book entitled: “Surface/atmosphere exchange of atmospheric acids and aerosols, including the effect and model treatment of chemical interactions”.

Impact of Leaf Surface and In-canopy Air Chemistry on the Ecosystem/Atmosphere Exchange of Atmospheric Pollutants

Chemical processes occurring on leaf surface and in air inside vegetation canopies play significant and sometimes dominant roles on pollutant dry deposition budgets. Yet, these processes are seldom explicitly treated in dry deposition parameterizations/models. This report briefly summarizes the current knowledge, outstanding issues, and recommendations for pollutant leaf surface exchange including ammonia (NH3), ozone (O3) and nitrogen oxides (NOx = NO + NO2), acidifying pollutants, volatile organic compounds (VOCs), and atmospheric aerosols.