1. Introduction
In the central and southeastern United States, deciduous forested wetlands located in broad floodplain areas bordering large river systems such as within the Lower Mississippi Alluvial Valley (LMAV) are referred to as Bottomland Hardwood Forests (BHFs) [
1]. Many ecosystem services provided by BHFs, including water quality regulation, flood control, wildlife habitat, timber production, waste treatment and disturbance regulation, and climate moderation through carbon balance are of global importance [
2,
3]. Like other wetland types, a hydrological regime of alternating wet and dry cycles driven by fluctuating water levels of the associated rivers and groundwater level changes is characteristic of BHFs [
4,
5]. The sustainability of BHFs depends primarily on the longitudinal (upstream to downstream), lateral (river to floodplain to uplands and vice-versa), vertical (surface water to groundwater and vice versa), and temporal (seasonal and annual flooding) variability of water availability [
6]. The primary force controlling the biota in BHFs is the flooding pulse from adjacent water sources which deposits dissolved nutrients, organic matter, and sediment, also contributing to the formation of young floodplains with each flooding pulse [
7]. Even small changes in the duration and frequency of water levels can result in a distinct shift in the plant community as many species are adapted to a certain range of flood tolerance [
8]. Therefore, a deeper understanding of the water use pattern and surface energy balance in these BHFs is crucial to preserving this dwindling ecosystem along the LMAV.
The study of BHF ecology remains incomplete without the assessment of factors that are integral to the proper functioning of these systems – evapotranspiration (ET), flood regimes, and precipitation. ET has been reported as a major component of BHF’s water balance in a number of studies along with LE (heat energy equivalent to ET) dominating the surface heat balance [
9,
10]. Several previous studies have identified biological and climatic drivers of bottomland hardwood ET using chrono sequence analysis [
9], sap-flux measurements [
11], and statistical modeling approaches [
12] in the southeastern US. These studies report a strong correlation between net radiation (R
n), temperature, and other climatic conditions consistent with the site-specificities and variations in ET during different seasonal cycles. Vapor Pressure Deficit (VPD) has been established as one of the primary drivers of ET and is used increasingly in global simulation studies [
13]. For example, [
14] used maximum likelihood estimation methods to show a complex chain of correlations among ET, VPD, radiations, and temperature in northern high-latitude woodland ecosystems. The complex interrelationships among these atmospheric variables, which are essential for an assessment of the ultimate drivers of variations of ET can be explored using structural equation modeling (SEM). The use of SEM approach to diagnose the independent contributions of atmospheric drivers in determining the ET variability from the BHFs largely remains unexplored.
The complexity of interrelationships among multiple variables and their dependencies makes it challenging to quantify the actual contributions of the drivers of ET. SEM, a multivariate statistical modelling technique with factor analysis and path analysis, provides a framework to quantitatively evaluate these interrelationships that need to be untangled to characterize the role and independent contribution of each driver of the variations observed in ET. SEM analysis carried out with the data measured at multi-site high latitude regions showed that radiation, temperature, windspeed and relative humidity (RH) loaded heavily on the first factor during the warm season (May-September) [
15,
16]. Previous studies have applied path analysis to diagnose the drivers of ET in temperate [
17], Arctic, and subarctic [
15] regions, however, to our knowledge there is not a study reported on the water fluxes in the BHFs - where altered hydrologic cycle under global change scenarios, are critical and complex.
This paper is a comprehensive assessment of the drivers of variations in bottomland hardwood ET over hourly, daily, and weekly timescales across seasons. The main objectives were: (i) to characterize the interrelationships among variables driving ET over these timescales, and (ii) to characterize ET dependencies on various factors across different seasons. This study is unique to those mentioned above in various important ways. First, it utilizes SEM factor analysis and path analysis to provide a framework for quantitively evaluating the relative importance of drivers of ET variability in this system. Second, this is the first study of the drivers of ET in the BHF of Russel Sage Wildlife Management Area (RSWMA), a representative of floodplain forests in the entire LMAV. This study will fill the knowledge-gap in trying to understand the water flux dynamics from this region.
4. Discussion
The SEM approach has been used to diagnose drivers of ET using high-frequency data collected using the EC method for forested systems. The results of this study in a BHF at RSWMA revealed that the variability in ET is directly influenced by Rn during spring, summer, and autumn, primarily vegetatively active seasons. However, during times of vegetative dormancy (i.e., in winter) the variability in ET is largely influenced by VPD and temperature, indirect controls of Rn. These results are consistent with the strong seasonal cycle for the variables that gradually increase from winter to summer and gradually diminish from summer to winter. This typical seasonal cycle also suggests that the influence of temperature and VPD on ET is indirectly driven by Rn. The greater control of temperature and VPD as drivers of ET during winter is suggestive of the temperature-dependent ET, especially when the Rn-dependent direct control on ET is minimal. Hence, the direct as well as indirect (through strong control of Rn on temperature and VPD) control of Rn on ET across all seasons reinforces the role of Rn as a primary driver of ET in this forest.
The results from the best-fit model in AIC modeling support the inference from SEM that there’s an interaction between R
n and temperature. Furthermore, VPD showed independent influence as a predictor of ET than in interaction with R
n. This corroborates the increased influence of temperature on ET during vegetatively-dormant seasons as opposed to the higher impact of R
n on ET during vegetatively-active seasons. Although the independent, the positive impact of WS on ET has been previously established in many other studies [
15,
24], the interaction of WS with other variables like temperature and precipitation is likely to attenuate dryness (latent construct) and augment wetness, subsequently, regulating the rate of ET in this system. The best model from AIC suggested that these interactions are highly plausible and significant in determining the dynamics of ET in this BHF.
Consistent with the findings from the data collected in a BHF at RSWMA from 2014-2021, which showed R
n as the major direct and indirect driver of ET variability across different times of the year, the research at most other forest types have characterized R
n as a primary driver of ET. For example, [
15] carried out SEM analysis in various boreal, tundra and permafrost ecosystems of high-latitude regions to demonstrate that R
n is the major driver of ET variability, albeit smaller independent contribution due to its control on other variables. On the contrary, a similar path analysis conducted in a mid-latitude agricultural site in northern China reported that R
n had the largest direct independent contribution on ET [
17]. Brown [
10] suggested that the increase in the amount of R
n received by the BHF in Missouri resulted in higher ET. Its vegetation composition, however, was silver maple (
Acer saccharinum), Eastern cottonwood (
Populus deltoides), Boxelder (
Acer negundo), Sycamore (
Platanus occidentalis) and are mostly different from those found around the US-ULM tower at RSWMA. Mackay [
30] reported R
n as a major driver in upland hardwood growth forests whereas VPD as a major driver in wetland ecosystem during vegetatively active time of the year in Northern Wisconsin. The dominant hardwood vegetation composition at this site was sugar maple (
Acer saccharum), basswood (
Tilia americana L.), and green ash (
Fraxinus pennsylvanica Marsh), mostly different from hardwood community found at RSWMA. However, a much higher effect of precipitation was reported in water-limited ecosystems as BHFs and seasonal cycles of canopy greenness in energy-limited ecosystems in higher latitudes using path analysis [
31]. Similarly, in humid boreal regions, VPD and R
n were characterized as major drivers of sap-flow and thus transpiration during growing season as well as during drought [
32].
In closed-canopy deciduous BHFs like the one in this study, R
n controls the variability of ET through two different pathways: first the direct pathway in which throughout the growing period (spring to summer) and early autumn, the R
n directly promotes the transpiration, which contributes about 80-90% of total ET as shown by [
24]; second the indirect pathway in which when there are no leaves in vegetatively dormant period, the direct impact of R
n is somehow attenuated and the R
n influences ET variability indirectly via temperature and VPD. This is also supported by the consistent variability pattern shown by R
n and ET at diurnal and seasonal plots in
Figure 5a b, and as reported by others [
33,
34].
Seasonally, albeit small, WS and precipitation play a critical role during summer when the atmospheric humidity is higher compared to other seasons. The increase in WS and precipitation positively influences wetness (one of the latent constructs), subsequently, affecting ET negatively in the process (path coefficients = 0.70 and -0.26 for dryness-ET and wetness-ET respectively). However, the negative effect of WS on ET as seen in
Figure 5a could be due to its significant negative impact on temperature, which in turn has a strong influence on ET through VPD. As observed in the structural model in
Figure 5b, WS contributes significantly as a major driver of atmospheric wetness, a latent construct with a significant negative effect on ET. In a study by Lobos-Roco [
35] in the Atacama Desert ecosystem of Chile, it was shown that strong winds in the afternoon enhance mechanical turbulence and increase evaporation. A similar path analysis conducted in a mid-latitude agricultural site in China found similar results with WS having the least direct and indirect effects on ET [
17]. On the other hand, precipitation has a minor positive impact as a driver of ET as seen in correlograms (
Figure 2). However, the increasing negative impact of precipitation as seen in
Figure 3 and its significant negative contribution to latent construct wetness, hence, ET over larger timescales is suggestive of reduction on ET as precipitation is observed for longer periods. From a similar research carried out at high latitude regions, Thunberg [
15] reported similar control of precipitation as a driver of ET and suggested it as a potentially relevant driver of ET in mid-latitude regions such as these BHFs. These findings of seasonal relations of ET with meteorological variables are consistent with those from similar studies in Canadian forest ecosystems [
36]. This also strengthens the conclusion that precipitation contributes positively to short-term enhancement in ET and negatively in the long run. These conclusions can be further strengthened by the simultaneous measurement of soil water content and heat flux on the site, one of the limitations of this study.
Since temperature and VPD are largely controlled by R
n, the importance of these variables as a driver of ET is more complex to understand, multifaceted, and largely dependent on the direct and indirect influence of the timing, duration, and intensity of solar energy in association with the seasonal phenological characteristics. The results from factor analysis suggested that their importance as a driver of ET becomes more prominent only during vegetatively dormant seasons when the direct control of R
n on ET remains lower. Rather these thermal variables share communality in their variability patterns and have a greater impact on ET by increasing the dryness (one of the latent constructs in the structural model) of the atmosphere as observed in
Figure 5b. The ambient temperature not only positively influences VPD but also negatively impacts R
n. This could be due to lower retention of incoming radiation as the canopy gets heat saturated and higher loss of longwave radiation from the canopy as the temperature of the canopy increases. For example, with the increase in R
n before noon, all variables ET, temperature, and VPD increase consistently until the canopy gets saturated with heat, thus, leading to a decrease in R
n and ET after noon while the temperature and VPD increase further. This has implications for stomatal regulation of water loss, GPP, and canopy temperature regulation in this forested system as also suggested by [
18]. The independent contributions of several other phenological and hydro-meteorological variables including temperature and VPD need to be further investigated to better understand the key role played by these variables as drivers of ET in this forested system.
Figure 1.
(a) Location map showing the study area Russel Sage Wildlife Management Area in Northeast Louisiana with the position of the US-ULM tower location indicated by the arrow tip, and (b) The study site shown flooded, as is typical during the late-winter and early-spring (Photo: JB).
Figure 1.
(a) Location map showing the study area Russel Sage Wildlife Management Area in Northeast Louisiana with the position of the US-ULM tower location indicated by the arrow tip, and (b) The study site shown flooded, as is typical during the late-winter and early-spring (Photo: JB).
Figure 2.
Correlation matrices among all variables for all seasons at the (a) hourly, (b) daily, and (c) weekly timescales.
Figure 2.
Correlation matrices among all variables for all seasons at the (a) hourly, (b) daily, and (c) weekly timescales.
Figure 3.
Factor loadings for Evapotranspiration (ET), Net radiation (Rn), Sensible heat flux (H), Temperature of air (Ta), Vapor Pressure Deficit (VPD), Windspeed (WS), Rain, and Pressure (Pa) on the first pattern of factor analysis for Spring, Summer, Autumn, and Winter seasons.
Figure 3.
Factor loadings for Evapotranspiration (ET), Net radiation (Rn), Sensible heat flux (H), Temperature of air (Ta), Vapor Pressure Deficit (VPD), Windspeed (WS), Rain, and Pressure (Pa) on the first pattern of factor analysis for Spring, Summer, Autumn, and Winter seasons.
Figure 4.
Score plots of the first and second factor loadings by various timescales across different seasons. Variables include Evapotranspiration (ET), Net radiation (Rn), Sensible heat flux (H), Vapor Pressure Deficit (VPD), Temperature of air (Ta), Pressure (Pa), Windspeed (WS), and Precipitation (rain).
Figure 4.
Score plots of the first and second factor loadings by various timescales across different seasons. Variables include Evapotranspiration (ET), Net radiation (Rn), Sensible heat flux (H), Vapor Pressure Deficit (VPD), Temperature of air (Ta), Pressure (Pa), Windspeed (WS), and Precipitation (rain).
Figure 5.
The (a) path diagram and (b) SEM of all the observed variables (ET, Rn, Ta, VPD, WS and P) and latent constructs (Dryness and Wetness) within the path analysis with positive (black) and negative (red) path coefficients for hourly timescale across all seasons. Dashed line indicates direct contribution.
Figure 5.
The (a) path diagram and (b) SEM of all the observed variables (ET, Rn, Ta, VPD, WS and P) and latent constructs (Dryness and Wetness) within the path analysis with positive (black) and negative (red) path coefficients for hourly timescale across all seasons. Dashed line indicates direct contribution.
Figure 6.
Distributions of regression coefficients from all significant results of path analysis SEM at hourly, daily, and weekly timescales with sample size (n=12) for each variable. Black solid lines represent median values and boxes represent interquartile range.
Figure 6.
Distributions of regression coefficients from all significant results of path analysis SEM at hourly, daily, and weekly timescales with sample size (n=12) for each variable. Black solid lines represent median values and boxes represent interquartile range.
Figure 7.
Distributions of regression coefficients from all significant results of path analysis SEM across different seasons with sample size (n=12) for each variable. Black solid lines represent median values and boxes represent interquartile range.
Figure 7.
Distributions of regression coefficients from all significant results of path analysis SEM across different seasons with sample size (n=12) for each variable. Black solid lines represent median values and boxes represent interquartile range.
Table 1.
Results of AIC model selection with shortlisted candidate models with the number of parameters (K), Akaike’s Information Criteria (AIC), delta AIC, AIC weights, and log-likelihood (LL) values.
Table 1.
Results of AIC model selection with shortlisted candidate models with the number of parameters (K), Akaike’s Information Criteria (AIC), delta AIC, AIC weights, and log-likelihood (LL) values.
Model |
K |
AIC |
ΔAIC |
AIC weight |
LL |
|
|
|
|
|
|
ET ~ Rn*Ta + VPD + WS*P |
9 |
-104579 |
0 |
0.98 |
52298.53 |
ET ~ Rn*Ta + VPD + WS + P |
8 |
-104570 |
8.25 |
0.02 |
52293.40 |
ET ~ Rn*Ta + VPD + WS |
7 |
-104383 |
195.37 |
0 |
52198.84 |
ET ~ Rn*Ta + VPD ET ~ Rn*VPD + Ta + WS*P |
6 9 |
-104344 -99185 |
234.54 5393.08 |
0 0 |
52178.26 49601.99 |