Tree-mycorrhiza symbiosis accelerate mineral weathering: Evidences from nanometer-scale elemental fluxes at the hypha-mineral interface

In soils, mycorrhiza (microscopic fungal hypha) living in symbiosis with plant roots are the biological interface by which plants obtain, from rocks and organic matter, the nutrients necessary for their growth and maintenance. Despite their central role in soils, the mechanism and kinetics of mineral alteration by mycorrhiza are poorly constrained quantitatively. Here, we report in situ quantification of weathering rates from a mineral substrate, (0 0 1) basal plane of biotite, by a surface-bound hypha of Paxillus involutus, grown in association with the root system of a Scots pine, Pinus sylvestris. Four thin-sections were extracted by focused ion beam (FIB) milling along a single hypha grown over the biotite surface. Depth-profile of Si, O, K, Mg, Fe and Al concentrations were performed at the hypha-biotite interface by scanning transmission electron microscopy-energy dispersive X-ray spectroscopy (STEM-EDX). Large removals of K (50-65%), Mg (55-75%), Fe (80-85%) and Al (75-85%) were observed in the topmost 40 nm of biotite underneath the hypha while Si and O are preserved throughout the depth-profile. A quantitative model of alteration at the hypha-scale was developed based on solid-state diffusion fluxes of elements into the hypha and the break-down/mineralogical re-arrangement of biotite. A strong acidification was also observed with hypha bound to the biotite surface reaching pH < 4.6. When consistently compared with the abiotic biotite dissolution, we conclude that the surface-bound mycorrhiza accelerate the biotite alteration kinetics between pH 3.5 and 5.8 to ∼0.04 μmol biotite m⁻² h⁻¹. Our current work reaffirms that fungal mineral alteration is a process that combines our previously documented bio-mechanical forcing with the μm-scale acidification mediated by surface-bound hypha and a subsequent chemical element removal due to the fungal action. As such, our study presents a first kinetic framework for mycorrhizal alteration at the hypha-scale under close-to-natural experimental conditions.     

Optimal estimation of catch by the continuous underway fish egg sampler based on a model of the vertical distribution of American plaice (Hippoglossoides platessoides) eggs

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Observations of canopy storage capacity and wet canopy evaporation in a humid boreal forest

Evaporation of intercepted rain by a canopy is an important component of evapotranspiration, particularly in the humid boreal forest, which is subject to frequent precipitation and where conifers have a large surface water storage capacity. Unfortunately, our knowledge of interception processes for this type of environment is limited by the many challenges associated with experimental monitoring of the canopy water balance. The objective of this study is to observe and estimate canopy storage capacity and wet canopy evaporation at the sub-daily and seasonal time scales in a humid boreal forest. This study relies on field-based estimates of rainfall interception and evapotranspiration partitioning at the Montmorency Forest, Québec, Canada (mean annual precipitation: 1600 mm, mean annual evapotranspiration: 550 mm), in two balsam fir-white birch forest stands. Evapotranspiration was monitored using eddy covariance sensors and sap flow systems, whereas rainfall interception was measured using 12 sets of throughfall and six stemflow collectors randomly placed inside six 400-m² plots. Changes in the amount of water stored on the canopy were also directly monitored using the stem compression method. The amount of water intercepted by the forest canopy was 11 ± 5% of the total rainfall during the snow-free (5 July–18 October) measurement periods of 2017 and 2018. The maximum canopy storage estimated from rainfall interception measurements was on average 1.6 ± 0.7 mm, though a higher value was found using the stem compression method (2.2 ± 1.6 mm). Taking the average of the two forest stands studied, evaporation of intercepted water represented 21 ± 8% of evapotranspiration, while the contribution of transpiration and understory evapotranspiration was 36 ± 9% and 18 ± 8%. The observations of each of the evapotranspiration terms underestimated the total evapotranspiration observed, so that 26 ± 12% of it was not attributed. These results highlight the importance to account for the evaporation of rain intercepted by humid boreal forests in hydrological models.     

The case for a martian origin of the shergottites: nitrogen and noble gases in EETA 79001

Nitrogen and noble gases were measured in samples of a glass inclusion and the surrounding basaltic matrix from the antarctic shergottite EETA 79001. A nitrogen component trapped in the glass, but not present in the matrix, has a δ¹⁵N value at least as high as +190‰. Ratios of⁴⁰Ar/¹⁴N and¹⁵N/¹⁴N in the glass are consistent with dilution of a martian atmospheric component (δ¹⁵N = 620 ± 160‰,⁴⁰Ar/¹⁴N= 0.33 ± 0.03) by either terrestrial atmosphere adsorbed on the samples or by indigenous nitrogen from the minerals of the rock. Trapped noble gases in the glass reproduce, within error, the elemental and isotopic compositions measured in Mars' atmosphere by Viking, and are in general agreement with previous measurements except for much lower abundances of neutron-generated krypton and xenon isotopes. The most reasonable explanation at the present time for the noble gas pattern and the isotopically heavy nitrogen is that a sample of martian atmosphere has been trapped in the EETA 79001 glass, and that this meteorite, and thus the shergottites and probably the nakhlites and chassignites as well, originated on Mars.Nitrogen in the non-glassy matrix of EETA 79001 amounts to less than 0.5 ppm and has a spallation-corrected δ¹⁵N value in the range 0 to ?20‰; it may reflect indigenous nitrogen in the basalt or a mixture of indigenous and adsorbed terrestrial nitrogen. Spallogenic noble gases yield single-stage exposure ages between 400,000 and 900,000 years, depending on irradiation geometry. Trapped argon may have an unusually low³⁶Ar/³⁸Ar ratio. Trapped krypton, except for a small excess at⁸⁰Kr, is smoothly mass-fractionated with respect to either terrestrial or chondritic Kr. The trapped xenon composition is consistent with addition of neutron-capture, radiogenic and fissiogenic isotopes to a base composition resembling terrestrial atmospheric Xe. The elemental⁸⁴Kr/¹³²Xe ratio of 25 is close to the terrestrial value and very different from the chondritic ratio.