Smap Revised Final
Smap Revised Final
Smap Revised Final
of carbon-water-climate interactions
TABLE OF CONTENTS
Scientific Narrative. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
1.0 Project Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
2.0 Relevance to NASA and SMAP Priorities. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
3.0 Background. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
4.0 Methodology. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
5.0 Work Plan. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
5.1 Task 1: Evaluation of modeled soil moisture state. . . . . . . . . . . . . . . . . 9
5.2 Task 2: Process level water-energy-carbon metrics . . . . . . . . . . . . . . . 10
5.3 Task 3: Parameter testing.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
5.4 Task 4: Understanding long-term impacts. . . . . . . . . . . . . . . . . . . . . . 14
6.0 Project Team, Management and Timeline. . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
6.1 Project team and qualifications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
6.2 Project management. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
6.3 Timeline. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
References. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Biographical Sketches. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
A.L. Steiner. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
G. Keppel-Aleks. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
R. De Roo .................................................... 24
Summary of Work Effort. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Current and Pending Support. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
A.L. Steiner. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
G. Keppel-Aleks. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
R. De Roo. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Budget Justification. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
Facilities and Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
Detailed Budget. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
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deal with the intersections of these cycles.” Our collaborative research will use SMAP
radiometer data to improve our understanding of the coupled water-carbon-climate system.
SMAP data will facilitate process-based studies with the CLM, a land surface model used in
weather and climate models as well as data assimilation systems. Specifically, this work will
address SMAP specific goals to “understand processes that link the terrestrial water, energy and
carbon cycles” and “quantify net carbon flux in boreal landscapes.” (SMAP Handbook Project
Goals 1 and 3).
3.0 Background
3.1 Soil moisture-water-carbon relationships
Soil moisture acts as a key driver in the climate system by controlling water and carbon
exchange between the surface and the atmosphere [Seneviratne et al., 2010]. In vegetated
regions, this relationship becomes more complex because vegetation relies on water from its
rooting system. As a result, the amount of soil moisture present controls the photosynthetic and
evaporative demand of vegetated regions. While other environmental drivers such as
temperature and precipitation are often used to explain the exchange of water and carbon, the
role of soil moisture and its limiting effects on ecosystem functioning is possibly more
fundamental but still very poorly constrained. Therefore, understanding the soil moisture-water-
carbon interactions is key to understanding regional hydroclimatology and precipitation
[Dirmeyer et al., 2009; Seneviratne et al., 2010], as well as understanding the regional and global
projections of the terrestrial carbon [Suyker et al., 2003].
Terrestrial vegetation mobilizes moisture from the subsurface to the non-woody parts of
the plant (e.g., stems and leaves) through its rooting system. Green biomass converts radiant
energy to chemical energy through photosynthesis, the process that converts CO2 into
carbohydrates and new biomass. To draw CO2 from the atmosphere into the leaf for fixation,
leaves have openings on their surface known as stomates. When the stomates open to allow CO2
into the leaf, water vapor inexorably escapes due to the strong gradient from the nearly saturated
environment inside the leaf to the relatively dry atmosphere. This biological process of stomatal
control inherently couples the water and carbon cycle when vegetation is present. In this regard,
it is impossible to examine carbon exchange without understanding the relative role of
evapotranspiration and the limitations of soil moisture.
In vegetated regions, evapotranspiration (ET) is the sum of evaporation from the ground,
evaporation from water stored within the canopy, and transpiration or the release of water from
the internal plant tissues during stomatal opening. Ground-based observations from flux towers
[Baldocchi et al., 2001] and satellite-derived ET [Mu et al., 2011] both estimate total
evapotranspiration from ecosystems. However, models still show difficulty in accurately
simulating ET in vegetated regions over a range of time scales from daily [Matheny et al., 2014]
to interannual [Jung et al., 2010]. To understand the role of soil moisture on modeled ET,
observationally based metrics indicate that ET is still underestimated by models, particularly
during the summer months when soil moisture may not be properly represented. For example,
NLDAS experiments show that even with data assimilation techniques, models still
underestimate summer ET [Xia et al., 2015]. At the climate time scale, [Bryan et al., 2015]
shows that the Community Land Model (CLM) under predicts the observed temperature-
evapotranspiration relationship in mid-latitude deciduous forests, which may be related to
erroneous soil water content or poorly parameterized transpiration processes.
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Because of the tight coupling of transpiration with carbon, soil moisture also has the
potential to influence global gross primary productivity (GPP, or the net carbon assimilated
during photosynthesis after accounting for autotrophic respiration) on a range of time scales (e.g.
[Lei et al., 2014] ). Global scale simulations suggest that moisture stress in temperate Northern
Hemisphere ecosystems is an important driver of interannual variability of carbon sinks [Keppel-
Aleks et al., 2014], and the precipitation-productivity relationship is largely derived through
vegetation uptake of soil water. Until recently, the terrestrial carbon sink has been thought to
respond mainly to tropical temperature variability [Wang et al., 2013]. However, when
variations in the
atmospheric CO2
growth rate are
analyzed as a
function of latitude,
variations in the
growth rate can be
traced to several
environmental
drivers, including
drought (Figure 2).
Most relevant for
the proposed
research,
temperature and
drought anomalies
(measured by
Palmer Drought
Severity Index) in the Northern Hemisphere mid- to high-latitudes contribute 0.23 Pg C y-1
variability to the global carbon sink (or about 10% of the average annual sink). We note that
temperature and drought stress co-vary, and that means soil moisture may affect the temperature
anomaly over land via the key role of latent heat in determining the surface energy balance. The
process-based research proposed here will strengthen our understanding of the mechanisms that
link water-carbon cycling, regional differences and temporal trends.
While most studies suggest that soil moisture is a strong driver in water and carbon
exchange, the lack of broad scale soil moisture observations has precluded clear observable
metrics to quantify soil moisture’s role. Frequently, the role of soil moisture as a driver has been
recently explained in the energy-limited vs. moisture-limited framework (e.g., as reviewed in
[Seneviratne et al., 2010]), yet clearly defining the soil moisture limitations is still needed to
understand the role of soil moisture limitations on water and carbon fluxes (Science Question 2).
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subsequent soil moisture. Despite these challenges, quantifying the role of soil moisture on
forest ecosystem functioning is greatly needed.
In this proposal, we will focus on the temperate to boreal transition region over North
America (Figure 3). Boreal forests represent the regions across Eurasia and Northern America
just south of the tundra line, and they can be either evergreen needleleaf forest (ENF) or in some
cases, deciduous broadleaf forest (DBF). In the temperate forests of North America, trees are
dominantly DBF allowing several months of the year without foliage (~November-March).
Modeled soil moisture in the region shows a strong seasonal cycle, with a 50% variation in
boreal regions and 30% variability in temperature regions, with substantial spatial heterogeneity
(Figure 3). Overall, we select the transition from temperate to boreal forests to capture a range
of the northern hemisphere carbon sink and understand the role of soil moisture across this
transect.
4.0 Methodology
As we investigate the role of soil moisture on evapotranspiration and carbon fluxes, we will
use a single land model (Section 4.1) coupled a global climate model (Section 4.2). These
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simulations will be evaluated and tested with Level 2 radiometer and Level 4 model SMAP data
(Section 4.3) and other ground-based observational sets (Section 4.4).
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limitation among the Rubisco-, light-, and export-limited rates [Bonan et al., 2011]. CLM4.5 has
been revised to better parameterize light use for sunlit and shaded leaves [Bonan et al., 2012],
and the maximum rate of carboxylation, VCmax, is calculated separately for sunlit and shaded
leaves since nitrogen allocation decreases with depth in the canopy. Leaf area index (LAI) in
CLM4.5 is derived from a monthly climatology of multi-year satellite records. Stomatal
conductance of the leaves, and thus carbon assimilation, is multiplied by a soil water stress
factor, βt, which ranges from 1 when soil is wet to nearly zero when soils are dry, depending on
the simulated soil water potential, PFT-dependent root distribution, and PFT-dependent wilting
factor.
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Level 2 9 km active/passive combined soil moisture) and therefore we will still be able to
develop a unique application of the Level 2 radiometer products. We propose to use the Level 2
radiometer soil moisture product (L2_SM_P) on the 36 km grid for CESM-CLM model
evaluation and process-level analysis. This product, estimated for the top 5cm of the soil
column, will be compared with the equivalent depth from the CESM-CLM (approximately the
first three soil layers). Additionally, we will use the Level 4 surface and root zone soil moisture
(L4_SM) net ecosystem exchange product (L4_C) that uses the land surface model to compare
Level 4 NEE (assumed to be 36 km resolution due to revised data sources) and root zone soil
moisture with those from the CESM-CLM.
Due to the differences in scale of the SMAP L2 and L4 products and the global climate
model, we will aggregate the finer-resolution SMAP data (36 km) to the CESM-CLM climate
model grid cell resolution (100 km). Within each CESM-CLM grid cell, we will compare the
PFT and land cover type variability in conjunction with the spatial soil moisture variability to
understand the role of the SMAP spatial resolution upscaling.
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(1) For surface soil moisture, how does CESM-CLM modeled surface soil moisture compare
with observed SMAP surface (5cm) Level 2 radiometer-derived soil water at sites that meet
the VWC criteria?
(2) For root zone soil moisture and sites with vegetation, how does CLM modeled soil moisture
compare to SMAP Level 4 derived data?
(3) Can we define different soil moisture states by region to evaluate the ability of this specific
land model to capture SMAP Level 2 radiometer and Level 4 data products?
For example, Figure 3 shows the interannual variability produced by the CESM-CLM for
temperate and boreal regions. The boreal region shows a late-summer drying with relatively low
interannual variability, yet the temperate forests do not exhibit as much variability in the summer
drying. We will examine the potential for the CLM to be “locked in” to a soil moisture state for
different regions and components of the seasonal cycle.
Task 1c: Evaluation with ground-based observations The third evaluation task will focus on
understanding observed relationships between soil moisture from SMAP (including both L2 and
L4 products), ground-based observations from the SCAN network, and the modeled CLM soil
moisture. While we will be limited to one full seasonal cycle in Year 1 of the project, we can
evaluate past relationships for the other datasets (SCAN, FLUXNET) versus that simulated to
understand soil moisture transition states (e.g., dry to wet) in other regions. We will focus on the
temperate-boreal transition region shown in Figure 3, and use the ground-based data available
from SCAN and FLUXNET towers (Table 1).
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limited systems in
the models. This
will allow us to use
SMAP observations
to quantify the role
of soil moisture in
the climate system
and improve global
and seasonal
estimates of ET.
Task 2b: Carbon
cycle metrics We
will similarly
analyze the
relationships
between carbon fluxes and environmental drivers at FLUXNET sites. We will use gross primary
production (GPP), which represents the gross carbon uptake via photosynthesis in an ecosystem
and net ecosystem exchange (NEE), which represents the residual carbon uptake between GPP
and respiration. Like GPP, heterotrophic respiration in the soil depends both on temperature and
soil moisture [Saleska et al., 2003; Davidson and Janssens, 2006].
As described above for evapotranspiration, we will regress SMAP observations in the
vicinity of FLUXNET sites against carbon fluxes measured on FLUXNET towers. Although
NEE is the raw quantity measured using the eddy covariance technique, GPP and thus total
respiration can be inferred by considering daytime and nighttime measurements separately. One
limitation of this approach is that for sites within high VWC canopies, we will not be able to
infer a mid-summer soil moisture level from SMAP observations.
We hypothesize that the soil moisture-GPP relationship will be stronger than the soil-
moisture NEE relationship. We will investigate multivariate linear and nonlinear regressions to
account for the combined role of temperature and soil moisture on controlling ecosystem carbon
fluxes. The slopes calculated for each metric (Temperature-GPP, soil moisture-GPP,
temperature-NEE, and soil moisture-NEE) will be an important metric for considering parameter
adjustments within the CLM model, but the scatter between carbon flux data and environmental
driving data will also provide information because we expect that both drivers affect carbon
fluxes in nature.
After establishing metrics at FLUXNET sites, we will leverage solar-induced fluorescence
(SIF) data from the OCO-2 satellite [Frankenberg et al., 2014]. SIF scales with instantaneous
canopy photosynthesis or GPP. Thus, SIF can infer how much carbon ecosystems
photosynthesize while XCO2 can be used to infer how much of the carbon remains in terrestrial
ecosystems at seasonal or longer timescales. SIF is well-suited for the proposed research, since
the SIF signal captures the response of carbon uptake to water stress even in situations where
conventional remote sensing vegetation indices, which essentially measure greenness, remain
stable [Lee et al., 2013]. We anticipate that by coupling these two satellite data products, we can
more clearly illuminate the effect of mean state on seasonal soil moisture impacts on GPP.
Task 2c: Precipitation recycling An additional metric for quantifying the role of soil moisture on
terrestrial feedbacks through ET is with the precipitation recycling term:
!! !
!
= !!!"
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where PE/P is the fraction of precipitation derived from evaporation and IF is the advective
moisture inflow into a specified region [Schar et al., 1999]. This metric can identify the impact
of soil moisture via ET on regional precipitation and climate. For the specified temperate and
boreal regions in Figure 3, we will calculate the modeled recycling ratios. Because the models
have sufficient information to calculate E over broad spatial regions and IF from the atmospheric
output (not possible for observations due to the dependence on atmospheric reanalysis products,
which are known to have biases), we can assess the potential atmospheric feedback errors that
derive from soil moisture. In this manner, we can use the SMAP data to understand the strength
of the soil moisture response in the atmosphere. While there are other more complex metrics to
determine land-atmosphere coupling, this is one that requires no additional, fixed-seasonality soil
moisture as used in other methods (e.g., GLACE [Koster et al., 2004]).
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NLDAS suggest that the participating models (including CLM in NLDAS-1) generally
underestimate ET, particularly in the summer months [Xia et al., 2012; Xia et al., 2015].
NLDAS-2 yielded greater inter-model agreement that has been attributed to improvements in
forcing data and some model parameterizations for potential ET [Xia et al., 2012]. [Xia et al.,
2015] evaluation of NLDAS-2 shows both seasonal and PFT based deficiencies, e.g., where the
summer and winter show greater deficiencies in modeled ET versus observations, and that DBF
evaluates better than ENF.
These cross-model differences from the ILAMB and NLDAS experiments suggest that
different land model components simulates the coupling between the water and carbon cycles
differently, which is not a surprising fact but one that is not well tested. In all cases, we will
conduct short-term (e.g., 1 year) CESM-CLM simulations that modify individual parameters and
re-evaluate metrics from Task 2. We propose testing three canopy-based factors that can affect
the simulation of soil moisture in global climate models, including:
Task 3a: Rooting profile One vegetation-dependent driver of inter-model differences is the
parameterization of root zone soil moisture. Many of these differences are due to the prescribed
distribution of roots in the CLM, which is static in time and varies in space based on PFT. [Hou
et al., 2012] showed that sensitivity depends on the depth of the rooting system, where shallow
root zones tend to be more sensitive to hydrologic variables. In CLM, the water removed from
each soil layer is a function of the effective root fraction within that layer, where the effective
root fraction is weighted by the root contribution from individual PFTs that share the single soil
column. For each PFT, two rooting parameters (ra, rb) are described by [Zeng, 2001]. As part of
our parameter testing, we will examine literature values to determine site-specific rooting depths
for the selected FLUXNET sites and compare these site-based values to those estimated by the
CLM ra/rb scaling. Specifically, we are looking to determine how these rooting profiles change
along the temperate-to-boreal transect in Figure 3, and determine any intra-PFT and climatic
zone dependence to these parameters. As part of this parameter testing, we will design a series
of short-term simulations (restarted from soil moisture equilibrated runs) that test several
different root distributions and evaluate these with SMAP soil moisture and surface fluxes.
Again, we note that different models use very different parameterizations than the one employed
in this single model, but our findings on the role of root zone distribution from this study will
likely cross-over to other models to highlight key spatial (e.g., temperate versus boreal) and
seasonal factors across all model types.
Task 3b: Photosynthesis-stomatal conductance model The use of the Ball-Berry photosynthesis
stomatal conductance model [Collatz et al., 1991] has become the standard method to link ET
and carbon assimilation in most Earth System models. This purely empirical relationship is
described as:
1 𝑚 𝐴 𝑅𝐻
= + 𝑏𝛽!
𝑟! 𝐶!
where rs is the stomatal resistance, m is a dimensionless slope, A is the carbon assimilation rate
(equivalent to GPP when aggregated to the ecosystem scale), RH is the relative humidity at the
leaf surface, Cs is the CO2 concentration at the leaf surface, b is the minimal stomatal
conductance, and βt is the soil water stress function. While several of the parameters (A, RH, Cs)
are calculated online within the model, the slope and intercept (m and b, respectively) are
determined based on values for C3 and C4 plants (m = 9 or 4, and b = 10,000 or 40,000 for C3 and
C4, respectively). The soil water stress, βt, is determined by:
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𝛽! = 𝑤! 𝑟!
!
where for each soil layer i, w is the plant wilting factor and r is the root fraction. In this manner,
βt controls the stomatal conductance and also plays a role in the assimilation rate (A). Its value
ranges from 1 when the soil is wet (e.g., no stress) to 0 when the soil is dry (e.g., high stress),
effectively shutting down transpiration when vegetation is under soil water stress. In this manner,
changes to the root zone structure in Task 2 can also then influence stomatal conductance.
However, here we will focus predominantly on the stomatal resistance empirical parameters of m
and b, and use FLUXNET-based observations of rs (typically calculated at all FLUXNET sites)
to evaluate the modeled calculation of this term. Because of the coupled nature of the
transpiration with soil moisture, we can evaluate the role of the stomatal conductance
parameterization and soil moisture limitations (as constrained by SMAP) on the ET and C fluxes.
Task 3c: Temperature stress Another important driver for understanding water and carbon
fluxes is temperature stress and its effects on vegetation. Sunlit leaves are often a few degrees
Celsius warmer than ambient air temperature, and increased high temperature stress under
climate change may reduce GPP and stomatal closure [Doughty and Goulden, 2008].
The photosynthetic parameters in CLM4.5, including Vcmax and the maximum electron
transport rate (Jmax), leaf nitrogen content, are calculated for an optimum leaf temperature (Tv) of
25°C. To calculate photosynthesis rates at other temperatures, photosynthetic parameters are
scaled by the product of two leaf temperature-dependent function, f(Tv) and fH(Tv):
!"#.!"∆!! ∆!!
!!!"#
∆!! !"#.!" !"#.!"!!"#
𝑓 𝑇! = 𝑒𝑥𝑝 !"#.!"!!"#
1− !!
𝑓! 𝑇! = ∆!!! !∆!!
!!!"#
!!
which increases and decreases with Tv, respectively, such that the product declines about some
optimum temperature. In these equations, Ha is the activation energy, Hd is the deactivation
energy, S is an entropy term, and Rgas is the universal gas constant [8.314 J/molK]. This
optimum is slightly different for each process because the parameters ΔHa, ΔHd, and ΔS vary for
each photosynthetic parameter (Vcmax, Jmax, etc.) [Bonan et al., 2011]. CLM4.5 has the ability for
Vcmax and Jmax to acclimate to temperature changes by modifying the ΔS term, although this
process occurs at timescales longer than the duration of our study [Kattge and Knorr, 2007].
We will investigate whether modifications to ΔHa, ΔHd, and ΔS permit better
parameterization of the temperature dependence of photosynthesis rates (linked to ET rates via
the Ball-Berry formulation). [Bonan et al., 2011] credits the improvement to GPP rates in
CLM4.5 compared to CLM4 in part to the improved temperature dependence of this
parameterization, but we will extend this analysis to test not just gross rates of carbon uptake, but
also against the metrics from Task 3 (e.g., GPP vs soil moisture and ET vs temperature). We
hypothesize that many ESMs simulate high ET rates that prevents carbon uptake in late summer
and that may contribute to a persistent low soil moisture bias.
For Tasks 3a-c, we will identify the most promising configurations based on our parameter
sensitivity tests and identify an optimal configuration for Task 4.
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change and associated changes in terrestrial ecosystems, will affect regional temperature
extremes [Hirschi et al., 2011]. The impact of water stress is likely to be a primary control on
carbon uptake by terrestrial ecosystems, and thus the amount of anthropogenic CO2 that remains
in the atmosphere to alter Earth’s radiative forcing [Friedlingstein et al., 2013]. This final
synthesis task will extend the temporal scale of Science Question 2 by incorporating new
findings from Tasks 2 and 3 to understand the implications of soil moisture state on long-term
water and carbon fluxes.
We will run three 50-year CESM simulations with CLM4.5-BGC coupled to CAM to
quantify the evolution of soil moisture, carbon uptake, and temperature variability. Each
simulation will use a modified model configuration, including a control run with the standard
CLM4.5-BGC and two simulations where CLM4.5 has been changed according to the parameter
sensitivity tests described in Task 3. We will identify two configurations from Task 3 that best
match both the spatial distribution of SMAP soil moisture and the metrics developed under Task
2 that relate carbon and water fluxes to their environmental drivers. We will use these
simulations to quantify the impact of our parameterizations on the long-term evolution of soil
moisture, as well as the cumulative change to the terrestrial carbon sink owing to more realistic
soil moisture – carbon cycle interactions. Because the seasonal soil moisture and canopy fluxes
govern long-term feedbacks to climate change, we expect that improving the representation at
seasonal timescales will likewise improve our ability to make long-term predictions.
For long-term climate runs, prediction of carbon fluxes enables explicit prediction of the
radiative feedbacks from changing land carbon sinks. We will leverage this capability to assess
how altering the parameterizations that affect soil moisture patterns affect future climate
trajectories. This task will also synthesize our findings on the short time scales (Tasks 1-3) to
understand their implications for the Earth System.
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located within the same department at UM, this will enable convenient meeting times with
minimal travel costs. One postdoctoral fellow will be hired to work on the project, and will work
closely with Steiner, Keppel-Aleks, and De Roo (see Table 2). Results will be disseminated
through participation in annual SMAP Science Team meetings, attendance at national
conferences such as the American Geophysical Union (AGU), and peer-reviewed publications.
6.3 Timeline
Table 2 shows the proposed timeline of the project as well as individual team member’s
responsibilities. With a start date of 1 April 2016, we anticipate that the first full year of SMAP
data (including one full growing season plus portions of the second year) will be available in
year 1 of the project. Task 1 will take place in year 1, including understanding the data
constraints of the vegetation water content (VWC) criteria and developing novel techniques to
use SMAP data in off-seasons for deciduous forested regions (Task 1a), as well as evaluation of
the modeled soil moisture state (Task 1b) and evaluation of modeled soil moisture and SMAP
versus ground-based observations (Task 1c). At the end of Year 1, we will begin Task 2,
including developing an understanding of observed and modeled soil moisture-water-carbon
feedbacks. In years 2 and 3, we will conduct the parameter testing of Task 3. In the final year of
the project (year 3), we will extend our results to longer-term simulations and identify key
features that may affect the regional hydroclimate as well as long-term carbon storage (Task 4).
We have built in overlap in the timeline to account for changes in the work plan schedule, to
allow for lags in data availability. We have also developed a contingency plan with regard to the
VWC criteria of Task 1a, and plan to focus on deciduous broadleaf forests in the event that we
are unable to determine off-season data for boreal regions. Due to the experience of the project
team, we will be able to quickly adapt to these data limitations and still meet the objectives of the
proposal.
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REFERENCES
Baldocchi, D. D., et al. (2001), FLUXNET: A New Tool to Study the Temporal and Spatial
Variability of Ecosystem-Scale Carbon Dioxide, Water Vapor and Energy Flux Densities,
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CMIP5 models, paper presented at American Geophysical Union Fall Meeting, San
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CVs
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BUDGET JUSTIFICATION
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The scientific research will be conducted on the campus of the University of Michigan (UM) in
Ann Arbor, MI. All investigators on the project (Steiner, Keppel-Aleks, De Roo) and the
postdoctoral fellow will be located in the Climate and Space Sciences and Engineering (CLaSP)
building on the North Campus location of the University of Michigan.
Office: Existing office and library resources will be utilized for the investigators and the
postdoctoral fellows at no cost to the project.
Computer modeling: High performance computing will be conducted using the Flux cluster at the
University of Michigan Advanced Research Computing. Flux is an HPC Linux-based cluster
intended to support parallel and other applications that are not suitable for departmental or
individual computers. Each Flux compute node comprises multiple CPU cores with at least 4 GB
of RAM per core; Flux has more than 19,000 cores. All compute nodes are interconnected with
InfiniBand networking. Computing jobs on Flux are managed through a combination of the
Moab Scheduler, the Terascale Open-Source Resource and QUEue Manager (Torque) and the
GOLD Allocation Manager from Adaptive Computing. The system also includes high-speed
scratch storage using the Lustre parallel network file system. The storage is connected with
InfiniBand. This file system allows researchers to store data on a short-term basis to perform
calculations; it is not for long-term data storage or archival purposes. All Flux nodes are
interconnected with quad-data rate InfiniBand, delivering up to 40 Gbps of bandwidth and less
than 5µs latency. Flux is connected to the University of Michigan’s campus backbone to provide
access to student and researcher desktops as well as other campus computing and storage
systems. The campus backbone provides 100 Gbps connectivity to the commodity Internet and
the research networks Internet2 and MiLR. Flux is housed in the Modular Data Center (MDC).
The MDC uses ambient air for cooling approximately 75% of the year, thus significantly
reducing the amount of energy needed for cooling, and contributing to U-M’s sustainability
efforts. Flux computing services are provided through a collaboration of University of Michigan
units: Advanced Research Computing (in the Office of the VP of Research and the Provost’s
Office), and computing groups in schools and colleges at the university. For this project,
dedicated nodes and storage space will be purchased on the cluster (see “Other Direct costs,”
above) to ensure constant availability for project simulations.
The PI Steiner has an additional Linux server available for the research group at no cost for data
transfer, post-processing and analysis. Students will use existing laptops for individual
workstations, and use the Flux computing cluster and value-added data storage for simulations
and storage of model and SMAP data.
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Budget Detail
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