Stable Water Isotopes Reveal Effects of Intermediate Disturbance and Canopy Structure on Forest Water Cycling

Forests play an integral role in the terrestrial water cycle and link exchanges of water between the land surface and the atmosphere. To examine the effects of an intermediate disturbance on forest water cycling, we compared vertical profiles of stable water vapor isotopes in two closely located forest sites in northern lower Michigan. At one site, all canopy‐dominant early successional species were stem girdled to induce mortality and accelerate senescence. At both sites, we measured the isotopic composition of atmospheric water vapor at six heights during three seasons (spring, summer, and fall) and paired vertical isotope profiles with local meteorology and sap flux. Disturbance had a substantial impact on local water cycling. The undisturbed canopy was moister, retained more transpired vapor, and at times was poorly mixed with the free atmosphere above the canopy. Differences between the disturbed and undisturbed sites were most pronounced in the summer when transpiration was high. Differences in forest structure at the two sites also led to more isotopically stratified vapor within the undisturbed canopy. Our findings suggest that intermediate disturbance may increase mixing between the surface layer and above‐canopy atmosphere and alter ecosystem‐atmosphere gas exchange.Plain Language SummaryForests play an important role in the climate system and link water fluxes between the land surface and the atmosphere. Here we compare water vapor isotopes in two adjacent forest sites in the northern lower peninsula of Michigan to understand the effects of intermediate disturbance and canopy structure on forest water cycling. One site is dominated by aspen and birch and has a thick, closed canopy. All of the aspen and birch were killed at the second site. As a result, the disturbed site has a more open‐canopy structure. From our comparison, we found that both the species of tree and the spacing around trees are important controls on forest water cycling. With more space between trees, air mixes more freely into the canopy, which dries the forest air. Alternatively, air may be poorly mixed within and above thick, closed canopies.Key PointsIntermediate disturbance can change the contribution of entrained, evaporated, and transpired water vapor to forest canopiesCanopy gaps increase hydrologic mixing between the surface layer and the free atmosphereThe assumption of a well‐mixed canopy atmosphere may be violated in the case of thick, homogeneous forest canopiesPeer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/152563/1/jgrg21482_am.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/152563/2/jgrg21482.pd

An isotopic approach to partition evapotranspiration in a mixed deciduous forest

Transpiration (T) is perhaps the largest fluxes of water from the land surface to the atmosphere and is susceptible to changes in climate, land use and vegetation structure. However, predictions of future transpiration fluxes vary widely and are poorly constrained. Stable water isotopes can help expand our understanding of land–atmosphere water fluxes but are limited by a lack of observations and a poor understanding of how the isotopic composition of transpired vapour (δT) varies. Here, we present isotopic data of water vapour, terrestrial water and plant water from a deciduous forest to understand how vegetation affects water budgets and land–atmosphere water fluxes. We measured subdiurnal variations of δ18OT from three tree species and used water isotopes to partition T from evapotranspiration (ET) to quantify the role of vegetation in the local water cycle. We find that δ18OT deviated from isotopic steady‐state during the day but find no species‐specific patterns. The ratio of T to ET varied from 53% to 61% and was generally invariant during the day, indicating that diurnal evaporation and transpiration fluxes respond to similar atmospheric and micrometeorological conditions at this site. Finally, we compared the isotope‐inferred ratio of T to ET with results from another ET partitioning approach that uses eddy covariance and sap flux data. We find broad midday agreement between these two partitioning techniques, in particular, the absence of a diurnal cycle, which should encourage future ecohydrological isotope studies. Isotope‐inferred estimates of transpiration can inform land surface models and improve our understanding of land–atmosphere water fluxes.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/162787/2/eco2229.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/162787/1/eco2229_am.pd

Variability and Controls on δ18O, d‐excess, and ∆′17O in Southern Peruvian Precipitation

The isotopic composition of precipitation is used to trace water cycling and climate change, but interpretations of the environmental information recorded in central Andean precipitation isotope ratios are hindered by a lack of multi‐year records, poor spatial distribution of observations, and a predominant focus on Rayleigh distillation. To better understand isotopic variability in central Andean precipitation, we present a three‐year record of semimonthly δ18Op and δ2Hp values from 15 stations in southern Peru and triple oxygen isotope data, expressed as ∆′17Op, from 32 precipitation samples. Consistent with previous work, we find that elevation correlates negatively with δ18Op and that seasonal δ18Op variations are related to upstream rainout and local convection. Spatial δ18Op variations and atmospheric back trajectories show that both eastern‐ and western‐derived air masses bring precipitation to southern Peru. Seasonal d‐excessp cycles record moisture recycling and relative humidity at remote moisture sources, and both d‐excessp and ∆′17Op clearly differentiate evaporated and non‐evaporated samples. These results begin to establish the natural range of unevaporated ∆′17Op values in the central Andes and set the foundation for future paleoclimate and paleoaltimetry studies in the region. This study highlights the hydrologic understanding that comes from a combination of δ18Op, d‐excessp, and ∆′17Op data and helps identify the evaporation, recycling, and rainout processes that drive water cycling in the central Andes.Key PointsThe isotopic composition of central Andean precipitation records upstream precipitation, local convection, and remote moisture sourcesPrecipitation on the flank of the western central Andes is sourced from the Pacific Ocean∆’17O can separate evaporated and non‐evaporated samples and provides key baseline information for Andean paleoclimate and paleoaltimetryPeer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/171158/1/2020JD034009-sup-0001-Supporting_Information_SI-S01.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/171158/2/jgrd57452.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/171158/3/jgrd57452_am.pd

An international laboratory comparison of dissolved organic matter composition by high resolution mass spectrometry : Are we getting the same answer?

High-resolution mass spectrometry (HRMS) has become a vital tool for dissolved organic matter (DOM) characterization. The upward trend in HRMS analysis of DOM presents challenges in data comparison and interpretation among laboratories operating instruments with differing performance and user operating conditions. It is therefore essential that the community establishes metric ranges and compositional trends for data comparison with reference samples so that data can be robustly compared among research groups. To this end, four identically prepared DOM samples were each measured by 16 laboratories, using 17 commercially purchased instruments, using positive-ion and negative-ion mode electrospray ionization (ESI) HRMS analyses. The instruments identified similar to 1000 common ions in both negative- and positive-ion modes over a wide range of m/z values and chemical space, as determined by van Krevelen diagrams. Calculated metrics of abundance-weighted average indices (H/C, O/C, aromaticity and m/z) of the commonly detected ions showed that hydrogen saturation and aromaticity were consistent for each reference sample across the instruments, while average mass and oxygenation were more affected by differences in instrument type and settings. In this paper we present 32 metric values for future benchmarking. The metric values were obtained for the four different parameters from four samples in two ionization modes and can be used in future work to evaluate the performance of HRMS instruments