Quantifying land surface temperature variability for two Sahelian mesoscale regions during the wet season

Land-atmosphere feedbacks play an important role in the weather and climate of many semi-arid regions. These feedbacks are strongly controlled by how the surface responds to precipitation events, which regulate the return of heat and moisture to the atmosphere. Characteristics of the surface can result in both differing amplitudes and rates of warming following rain. We used spectral analysis to quantify these surface responses to rainfall events using land surface temperature (LST) derived from Earth Observations (EO). We analysed two mesoscale regions in the Sahel and identified distinct differences in the strength of the short-term (< 5–day) spectral variance, notably a shift towards lower frequency variability in forest pixels relative to non-forest areas, and an increase in amplitude with decreasing vegetation cover. Consistent with these spectral signatures, we found that areas of forest, and to a lesser extent grassland regions, warm up more slowly than sparsely vegetated or barren pixels. We applied the same spectral analysis method to simulated LST data from the the Joint UK Land Environment Simulator (JULES) land surface model. We found a reasonable level of agreement with the EO spectral analysis, for two contrasting land surface regions. However JULES shows a significant underestimate in the magnitude of the observed response to rain compared to EO. A sensitivity analysis of the JULES model highlights an unrealistically high level of soil water availability as a key deficiency, which dampens the models response to rainfall events

Does predictability of fluxes vary between FLUXNET sites?

The FLUXNET dataset contains eddy covariance measurements from across the globe and represents an invaluable estimate of the fluxes of energy, water, and carbon between the land surface and the atmosphere. While there is an expectation that the broad range of site characteristics in FLUXNET result in a diversity of flux behaviour, there has been little exploration of how predictable site behaviour is across the network. Here, 155 datasets with 30&thinsp;min temporal resolution from the Tier 1 of FLUXNET 2015 were analysed in a first attempt to assess individual site predictability. We defined site uniqueness as the disparity in performance between multiple empirical models trained globally and locally for each site and used this along with the mean performance as measures of predictability. We then tested how strongly uniqueness was determined by various site characteristics, including climatology, vegetation type, and data quality. The strongest determinant of predictability appeared to be that drier sites tended to be more unique. We found very few other clear predictors of uniqueness across different sites, in particular little evidence that flux behaviour was well discretised by vegetation type. Data length and quality also appeared to have little impact on uniqueness. While this result might relate to our definition of uniqueness, we argue that our approach provides a useful basis for site selection in LSM evaluation, and we invite critique and development of the methodology.</p

Thirty-eight years of CO&lt;sub&gt;2&lt;/sub&gt; fertilization has outpaced growing aridity to drive greening of Australian woody ecosystems

Climate change is projected to increase the imbalance between the supply (precipitation) and atmospheric demand for water (i.e., increased potential evapotranspiration), stressing plants in water-limited environments. Plants may be able to offset increasing aridity because rising CO2 increases water use efficiency. CO2 fertilization has also been cited as one of the drivers of the widespread "greening" phenomenon. However, attributing the size of this CO2 fertilization effect is complicated, due in part to a lack of long-term vegetation monitoring and interannual- to decadalscale climate variability. In this study we asked the question of how much CO2 has contributed towards greening. We focused our analysis on a broad aridity gradient spanning eastern Australia's woody ecosystems. Next we analyzed 38 years of satellite remote sensing estimates of vegetation greenness (normalized difference vegetation index, NDVI) to examine the role of CO2 in ameliorating climate change impacts. Multiple statistical techniques were applied to separate the CO2-attributable effects on greening from the changes in water supply and atmospheric aridity. Widespread vegetation greening occurred despite a warming climate, increases in vapor pressure deficit, and repeated record-breaking droughts and heat waves. Between 1982-2019 we found that NDVI increased (median 11.3 %) across 90.5 % of the woody regions. After masking disturbance effects (e.g., fire), we statistically estimated an 11.7 % increase in NDVI attributable to CO2, broadly consistent with a hypothesized theoretical expectation of an 8.6 % increase in water use efficiency due to rising CO2. In contrast to reports of a weakening CO2 fertilization effect, we found no consistent temporal change in the CO2 effect. We conclude rising CO2 has mitigated the effects of increasing aridity, repeated record-breaking droughts, and record-breaking heat waves in eastern Australia. However, we were unable to determine whether trees or grasses were the primary beneficiary of the CO2-induced change in water use efficiency, which has implications for projecting future ecosystem resilience. A more complete understanding of how CO2-induced changes in water use efficiency affect trees and non-tree vegetation is needed

Examining the evidence for decoupling between photosynthesis and transpiration during heat extremes

Recent experimental evidence suggests that during heat extremes, wooded ecosystems may decouple photosynthesis and transpiration, reducing photosynthesis to near zero but increasing transpiration into the boundary layer. This feedback may act to dampen, rather than amplify, heat extremes in wooded ecosystems. We examined eddy covariance databases (OzFlux and FLUXNET2015) to identify whether there was field-based evidence to support these experimental findings. We focused on two types of heat extremes: (i) the 3 days leading up to a temperature extreme, defined as including a daily maximum temperature &gt;37&thinsp;∘C (similar to the widely used TXx metric), and (ii) heatwaves, defined as 3 or more consecutive days above 35&thinsp;∘C. When focusing on (i), we found some evidence of reduced photosynthesis and sustained or increased latent heat fluxes at seven Australian evergreen wooded flux sites. However, when considering the role of vapour pressure deficit and focusing on (ii), we were unable to conclusively disentangle the decoupling between photosynthesis and latent heat flux from the effect of increasing the vapour pressure deficit. Outside of Australia, the Tier-1 FLUXNET2015 database provided limited scope to tackle this issue as it does not sample sufficient high temperature events with which to probe the physiological response of trees to extreme heat. Thus, further work is required to determine whether this photosynthetic decoupling occurs widely, ideally by matching experimental species with those found at eddy covariance tower sites. Such measurements would allow this decoupling mechanism to be probed experimentally and at the ecosystem scale. Transpiration during heatwaves remains a key issue to resolve, as no land surface model includes a decoupling mechanism, and any potential dampening of the land–atmosphere amplification is thus not included in climate model projections.</p

Towards species-level forecasts of drought-induced tree mortality risk

Predicting species-level responses to drought at the landscape scale is critical to reducing uncertainty in future terrestrial carbon and water cycle projections. We embedded a stomatal optimisation model in the Community Atmosphere Biosphere Land Exchange (CABLE) land surface model and parameterised the model for 15 canopy dominant eucalypt tree species across South-Eastern Australia (mean annual precipitation range: 344–1424 mm yr−1). We conducted three experiments: applying CABLE to the 2017–2019 drought; a 20% drier drought; and a 20% drier drought with a doubling of atmospheric carbon dioxide (CO2). The severity of the drought was highlighted as for at least 25% of their distribution ranges, 60% of species experienced leaf water potentials beyond the water potential at which 50% of hydraulic conductivity is lost due to embolism. We identified areas of severe hydraulic stress within-species’ ranges, but we also pinpointed resilience in species found in predominantly semiarid areas. The importance of the role of CO2 in ameliorating drought stress was consistent across species. Our results represent an important advance in our capacity to forecast the resilience of individual tree species, providing an evidence base for decision-making around the resilience of restoration plantings or net-zero emission strategies

How representative are FLUXNET measurements of surface fluxes during temperature extremes?

In response to a warming climate, temperature extremes are changing in many regions of the world. Therefore, understanding how the fluxes of sensible heat, latent heat and net ecosystem exchange respond and contribute to these changes is important. We examined 216 sites from the open access Tier 1 FLUXNET2015 and free fair-use La Thuile data sets, focussing only on observed (non-gap-filled) data periods. We examined the availability of sensible heat, latent heat and net ecosystem exchange observations coincident in time with measured temperature for all temperatures, and separately for the upper and lower tail of the temperature distribution, and expressed this availability as a measurement ratio. We showed that the measurement ratios for both sensible and latent heat fluxes are generally lower (0.79 and 0.73 respectively) than for temperature measurements, and the measurement ratio of net ecosystem exchange measurements are appreciably lower (0.42). However, sites do exist with a high proportion of measured sensible and latent heat fluxes, mostly over the United States, Europe and Australia. Few sites have a high proportion of measured fluxes at the lower tail of the temperature distribution over very cold regions (e.g. Alaska, Russia) or at the upper tail in many warm regions (e.g. Central America and the majority of the Mediterranean region), and many of the world's coldest and hottest regions are not represented in the freely available FLUXNET data at all (e.g. India, the Gulf States, Greenland and Antarctica). However, some sites do provide measured fluxes at extreme temperatures, suggesting an opportunity for the FLUXNET community to share strategies to increase measurement availability at the tails of the temperature distribution. We also highlight a wide discrepancy between the measurement ratios across FLUXNET sites that is not related to the actual temperature or rainfall regimes at the site, which we cannot explain. Our analysis provides guidance to help select eddy covariance sites for researchers interested in understanding and/or modelling responses to temperature extremes.</p

Inferring the effects of sink strength on plant carbon balance processes from experimental measurements

The lack of correlation between photosynthesis and plant growth under sink-limited conditions is a long-standing puzzle in plant ecophysiology that currently severely compromises our models of vegetation responses to global change. To address this puzzle, we applied data assimilation to an experiment in which the sink strength of Eucalyptus tereticornis seedlings was manipulated by restricting root volume. Our goals were to infer which processes were affected by sink limitation and to attribute the overall reduction in growth observed in the experiment to the effects on various carbon (C) component processes. Our analysis was able to infer that, in addition to a reduction in photosynthetic rates, sink limitation reduced the rate of utilization of nonstructural carbohydrate (NSC), enhanced respiratory losses, modified C allocation and increased foliage turnover. Each of these effects was found to have a significant impact on final plant biomass accumulation. We also found that inclusion of an NSC storage pool was necessary to capture seedling growth over time, particularly for sink-limited seedlings. Our approach of applying data assimilation to infer C balance processes in a manipulative experiment enabled us to extract new information on the timing, magnitude and direction of the internal C fluxes from an existing dataset. We suggest that this approach could, if used more widely, be an invaluable tool to develop appropriate representations of sink-limited growth in terrestrial biosphere models.</p

Towards species‐level forecasts of drought‐induced tree mortality risk

Predicting species-level responses to drought at the landscape scale is critical to reducing uncertainty in future terrestrial carbon and water cycle projections. We embedded a stomatal optimisation model in the Community Atmosphere Biosphere Land Exchange (CABLE) land surface model and parameterised the model for 15 canopy dominant eucalypt tree species across South-Eastern Australia (mean annual precipitation range: 344–1424 mm yr−1). We conducted three experiments: applying CABLE to the 2017–2019 drought; a 20% drier drought; and a 20% drier drought with a doubling of atmospheric carbon dioxide (CO2). The severity of the drought was highlighted as for at least 25% of their distribution ranges, 60% of species experienced leaf water potentials beyond the water potential at which 50% of hydraulic conductivity is lost due to embolism. We identified areas of severe hydraulic stress within-species’ ranges, but we also pinpointed resilience in species found in predominantly semiarid areas. The importance of the role of CO2 in ameliorating drought stress was consistent across species. Our results represent an important advance in our capacity to forecast the resilience of individual tree species, providing an evidence base for decision-making around the resilience of restoration plantings or net-zero emission strategies