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Article history: High-resolution (ca. 1 m) synthetic aperture radar (SAR) sensors have great potential for all-weather monitoring
Received 22 June 2013 of crop biophysical variables in small and mosaic crop fields in Asia. Rice is the most important staple crop in
Received in revised form 30 August 2013 monsoon Asia, and the timely monitoring of rice growth is critical for precision farming and the assessment of
Accepted 1 September 2013
productivity. The objective of this study was to determine the potential capability of backscattering coefficients
Available online 28 September 2013
(σ0) from satellite C-band SAR sensors for the assessment of biophysical variables in rice. SAR images were ac-
Keywords:
quired by a Radarsat-2 sensor in spotlight mode during the critical growth stages over 4 years in one of the
C-band major rice-producing areas of Japan. Detailed plant biophysical measurements were made concurrently with
fAPAR the SAR observations. The seasonal consistency of C-band σ0 was clearly demonstrated. The baseline σ0 values
LAI (minimum σ0 for zero-biomass paddy fields) were determined to be −28.5 dB in VH and −21.1 dB in HH
Microwave and VV, respectively. The dynamic change in σ0 during the full range of rice growth was similar (ca. 12 dB) in
Paddy rice all polarizations. A comprehensive analysis revealed the response of C-band σ0 to biophysical canopy variables.
Radarsat-2 High or moderate sensitivity of σ0 to canopy height, water content, or chlorophyll content was superficial and
SAR
was attributable to the change in leaf biomass and structure. Both the leaf area index (LAI) and leaf biomass
Spotlight mode
were significantly and consistently correlated with σ0 throughout all growth stages. These relationships were
expressed by exponential curves with high coefficients of determination, although σ0 saturates at around a LAI
of 3 and a leaf biomass of 180 gDW m−2. The response of σ0 to total biomass was expressed by an exponential
function with a high coefficient of determination, but the sensitivity was clear only within the lower 20% range
of the seasonal maximum biomass. The C-band σ0 had the highest correlation with fAPAR, and the σ0–fAPAR re-
lationship was linear throughout the growth stages. The results suggest the suitability of C-band σ0 for the assess-
ment of LAI or fAPAR and show promise for the timely monitoring of rice growth by C-band SAR and/or through
its constellation with optical sensors.
© 2013 Elsevier Inc. All rights reserved.
1. Introduction Rice (Oryza sativa L.) is an important stable crop in monsoon Asia, but
rice productivity is strongly affected by water, temperature, and solar
A wide range of satellite sensors are available in the optical, thermal, radiation. Therefore, timely and high-resolution observation is essential
and microwave spectral domains for the observation of terrestrial eco- for monitoring rice crops in Asia. Accordingly, SAR sensors have great
systems. However, agricultural applications are highly demanding for potential for the timely assessment of biophysical and ecophysiological
advanced specifications in spatial, spectral, and temporal resolutions variables of rice in Asia (e.g., Le Toan et al., 1997; Ribbes & Le Toan,
(Inoue, 2003; Moran, Inoue, & Barnes, 1997). In crop monitoring for 1999). The extraction of rice fields is relatively robust due to the specular
precision farming and yield forecasting, the timely observation of features under flooded surface conditions (e.g., Choudhury, Chakraborty,
plant biophysical and ecophysiological status (e.g., leaf area, biomass, Santra, & Parihar, 2012; Kurosu, Fujita, & Chiba, 1997; Ribbes & Le Toan,
and chlorophyll content) is critical (Doraiswamy et al., 2004; Inoue, 1999). The combined use of multiple polarizations can effectively classify
2003; Moran, Inoue, et al., 1997). High spatial resolution is required agricultural fields (e.g., Bouvet, Le Toan, & Lam-Dao, 2009; McNairn,
when observing regions with small and mosaic crop fields, as in many Champagne, Shang, Holmstrom, & Reichert, 2009). Cropping systems or
countries in Asia. agricultural management practices in rice-growing regions can be identi-
fied successfully from SAR observations (e.g., Bouvet & Le Toan 2011;
Lopez-Sanchez, Ballester-Berman, & Hajnsek, 2011). However, quantita-
⁎ Corresponding author. Tel.: +81 29 838 8220; fax: +81 29 838 8199. tive assessments of biophysical and ecophysiological plant variables
E-mail address: yinoue@affrc.go.jp (Y. Inoue). using SAR signatures remain challenging.
0034-4257/$ – see front matter © 2013 Elsevier Inc. All rights reserved.
http://dx.doi.org/10.1016/j.rse.2013.09.001
258 Y. Inoue et al. / Remote Sensing of Environment 140 (2014) 257–266
Fig. 1. Examples of rice canopies in the study area; nadir and side view of typical rice canopies at (1) transplanting, (2) early-vegetative, (3) late-vegetative, and (4) mid-maturing stages,
respectively.
speckle noise. The high spatial resolution of the spotlight mode allowed These structural, morphological, and physiological variables were used
the extraction of signatures for the exact area of interest in each paddy to investigate the sensitivity of σ0 to rice canopies. They can be used as in-
field. We compared the average σ0 values for the area of interest puts to physically based scattering models or for the interpretation of var-
(around 300 pixels for uniform surfaces) using the raw σ0 data and ious responses of σ0 to rice-canopy conditions in a range of studies.
the processed data by enhanced Lee filters (with 3 × 3 and 5 × 5), but
their differences were negligible (b 0.02 dB). From these results, we 2.4. Physically-based backscattering models for a rice canopy
assumed that the speckle reduction filters may not have significant
impacts on the spatial average values in case the surfaces are uniform In support of the analysis of the dataset obtained by the satellite SAR
and sufficient numbers of pixels are averaged. The σ0 values were sensor and ground-based measurements, we used two types of canopy
extracted from the individual areas of interest in paddy fields, and backscattering models; i.e., 1) a simple process-based model (the water
plant samples were taken as well as from nearby water surfaces (rivers cloud model; Attema & Ulaby, 1978; Prévot et al., 1993), and 2) a structur-
and ponds). Such nearby water surfaces were assumed to be usable as a al canopy backscattering model (Karam et al., 1995; Wang et al., 2009).
reference throughout a growing season because there was no difference
between the calm water surfaces and flooded paddy fields just before 2.4.1. Water cloud model
transplanting. In the water cloud (WC) model, a crop canopy is represented by two
layers, i.e., vegetation layer and soil layer. The backscattering coefficient
2.3. Biophysical measurements of rice canopies σ0 for the whole canopy is expressed by the following equations.
0 0 2 0
Detailed biophysical and ecophysiological measurements were σ ¼σ veg þτ σ soil ð1Þ
made concurrently with the SAR observations at 41, 52, 12, and 24
paddy fields in 2009, 2010, 2011, and 2012, respectively. Fig. 1 shows σ
0
¼ AV1 cosθ 1−τ
2
ð2Þ
veg
the nadir and side view of typical rice canopies at the transplanting,
early-vegetative, late-vegetative, and mid-maturing stages. Hill density, 2
plant height, and water depth were recorded for each field. τ ¼ exp½−2BV2 = cosθ ð3Þ
Rice plants in each field were very uniform (e.g., the maximum coef-
ficient of variance was 10%). Therefore, five representative hills (a bun- where, σ0veg and σ0soil are the backscattering coefficients in power units
dle of plants) were sampled from each paddy field to characterize the (m2 m−2) for vegetation and soil, respectively; τ2 is the two-way atten-
biophysical structure of the canopy. The wet biomass and dry biomass uation through the canopy; θ is the incident angle; V1 and V2 are the de-
of leaves, stems, panicles, and whole plants were determined by de- scriptors of the canopy; and A and B are coefficients that depend on
structive measurements of the sampled plants based on normal gravi- canopy type. σ0soil is usually expressed as a function of soil moisture.
metric processes. Canopy structural variables such as stem density, However, in paddy rice, the σ0soil can be simplified to be constant
LAI, number of leaves per stem, and the vertical position of panicles (σ0BG) due to the flooded surface conditions (Inoue et al., 2002). By as-
and leaves, and major morphological variables such as panicle size, suming the V1 = V2 = V = LAI or TFW (Inoue et al., 2002; Prévot et al.,
leaf size (length, width, and thickness), and stem diameter were mea- 1993), the backscatter for the rice paddy can be expressed (in dB) as
sured for each sample. The chlorophyll content of three fully expanded follows:
leaves in the upper canopy layer was measured using a SPAD 502 chloro- n o
0 0
phyll meter (Minolta) and then averaged for each canopy. The fAPAR was σ ¼ 10 log AV cosθð1− exp½−2BV= cosθÞ þ exp½−2BV= cosθÞσ BG : ð4Þ
derived from the ascending and descending values of photosynthetic
photon flux density (PPFD) measured at the top and bottom of a canopy In this study, we applied iterative parameterization to determine the
using a line PPFD sensor (LI-191, Li-Cor). coefficients A and B of the WC model using LAI as a key vegetation
260 Y. Inoue et al. / Remote Sensing of Environment 140 (2014) 257–266
variable (V = LAI). The σ0BG was derived from the image data. In general, polarizations, irrespective of the rice growing stage. The average σ0
the degree of fitness of measured data (LAI and σ0 in this case) to theoret- value was −28.5 dB in VH, whereas it was −21.1 dB in HH and VV;
ical models can be a useful indicator to infer the physical backscattering each value indicates the baseline for zero biomass (i.e., no scattering
processes in a canopy. elements in paddy fields). Accordingly, the σ0 value for rice canopies
changes along the arrow lines in Fig. 2 in response to the scattering
2.4.2. Structural canopy scattering model characteristics of the rice canopy. Note that the scattering characteris-
This model is based on a radiative transfer model for forests (Karam tics are determined by the structural, morphological, and dielectric
et al., 1995), so modified to express the scattering processes in a paddy conditions of the canopy, i.e., they are not always related to the growth
rice canopy with several assumptions; 1) the ground surface is a smooth stage of rice. Even in a specific growth stage, rice canopies in a region
surface with dielectric constant of water since paddy fields are flooded display large variability in biophysical variables, and this variability
during the growing season, 2) a rice canopy consists of three layers between fields has to be assessed for crop diagnosis.
(i.e., panicle-, leaf-, and stem-layers), 3) panicles and stems are expressed Overall, the range of seasonal change in σ0 (i.e., between the seed-
as short cylinders, 4) leaves are expressed as narrow and long ellipses, ling and hull growth stages) was 12 dB in all polarizations. The dotted
and 5) the leaf angle distribution is expressed by a specific probability line connecting the VH (20110716) and HH (20110715) points was
distribution function with a few parameters. Accordingly, the total back- nearly parallel to 1:1. Because these two images of the same canopy
scattering coefficient from a canopy (σtotal) is expressed as a linear com- were taken only 1 day apart, the response of σ0 in VH and HH to the
bination of volume scattering from each component, its double bounce rice canopy at the vegetative stage was considered almost equivalent, al-
with ground, and ground surface scattering (in power unit); though HH appeared to be slightly more sensitive than VH. The seasonal
consistency of the C-band σ0 from the Radarsat-2 spotlight mode was
σ total ¼ σ leaf þ σ leaf–ground þ σ stem þ σ stem–ground þ σ panicle clearly confirmed by the results over 4 years. The seasonal baseline
þ σ panicle–ground þ σ ground ð5Þ values (minimum σ0 for zero-biomass paddy fields) were determined
for cross and like polarizations. The results provide much more definitive
where the σleaf, σstem, and σpanicle are volume scattering of leaves, stems, information for the monitoring of rice growth compared with preceding
and panicles, respectively. The σleaf–ground, σstem–ground, and σpanicle–ground studies (e.g., Chakraborty et al., 2005; Choudhury & Chakraborty, 2006;
are double bounce between each component and ground. The σground Ribbes & Le Toan, 1999; Shao et al., 2001).
is ground surface scattering. Details of the model structure are given
in Wang et al. (2009) and Karam et al. (1995).
3.2. A comprehensive analysis of the relationship between C-band σ0 and
Consequently, the model enables us to simulate the σtotal in all polar-
biophysical variables
izations at any incidence angles for given frequency bands. The neces-
sary inputs and parameters were derived from the ground-based
Because the response of the C-band σ0 in VH was similar to that in HH
biophysical and morphological measurements (Section 2.3) and default
and VV, we assumed that an intensive analysis of the relationship be-
values in Wang et al. (2009).
tween the C-band σ0 in VH would provide useful insights on the overall
capability of C-band SAR sensors in other configurations. Accordingly,
3. Results and discussion
we focused on the VH images because the multi-polarization measure-
ment was not yet possible in the spotlight model. Fig. 3 summarizes the
3.1. Characteristics of C-band σ0 over paddy fields in VH, HH, and
correlation coefficients between C-band σ0 in VH and canopy biophysical
VV polarizations
and ecophysiological variables. Figs. 4–8 show scatter plots for the major
canopy variables.
Fig. 2 shows the average σ0 values extracted for rice canopies and
Overall, the whole-canopy structural variables such as canopy height,
water surfaces in VH, HH, and VV images. The σ0 values for water
biomass, and LAI were strongly correlated with σ0, although stem densi-
surfaces were very consistent in cross (VH) and like (HH & VV)
ty, leaf density, and hill density were only moderately correlated. These
results agreed well with the results of a ground-based study by Inoue
0
et al. (2002). Results included some weak or negligible relationships as
1)
well as strong ones. However, both negative and positive results are
:
(1
C-VH σ0 (dB)
LAI((m2 m-22 )
fAPAR
SPAD (digital number) -20
C-VH σ0 (dB)
Leaf density (m-2)
Leaf length (m)
Leaf width (m) -20
Leaf thickness (m)
3-D Leafdensity(m-3)
-25
Layer-1 thickness (m)
Layer-2 thickness (m) 20090906VH
Layer-3 thickness (m) -30 20100716VH
Stem radius (m) 20120627VH
P=0.01 P=0.01
-35
0
0 10 20 30 40 50
Fig. 3. Correlation of C-band σ with biophysical variables in rice canopies over a wide
range of growth stages. SPAD: chlorophyll index by SPAD 502; FW: fresh biomass; DW: SPAD (DN)
dry biomass; W: water content; Layer-1, -2, and -3: thickness of layers for panicles (1),
0
leaves (2), and stems (3), respectively. The correlation coefficient (r) at significance levels Fig. 4. Relationship of C-band σ with a) canopy height and b) SPAD.
of P = 0.01 and P = 0.05 is 0.33 and 0.25, respectively.
respectively), but their relationships were not consistent for individual the amount of leaves; i.e., leaf area increase is associated with a decrease
growth stages (r b 0.58 and r b 0.76). in chlorophyll. In fact, SPAD was negatively correlated with increasing
biomass and LAI (r = −0.65 and −0.61, respectively). There is a weak
3.2.2. Water content and chlorophyll content relationship between σ0 and the SPAD values for the data in each growth
Interestingly, ecophysiological variables such as water content and stage (Fig. 4b). The apparent high correlation for the canopy structural
SPAD (chlorophyll content) were negatively correlated with σ0 (Fig. 3). variables such as canopy layer thickness (Layers 2, 3) or morphological
These correlations were also indirect or superficial because these variables (e.g., leaf length and leaf width) can also be explained by
variables are strongly affected by both phenology and canopy synchronous changes in the amount of leaves with elongation of
structure. Fig. 5a clearly shows that stem water content is very stable internodes or an enlargement of leaf size, respectively (Fig. 3). For exam-
throughout the growth stage, suggesting that σ0 could change signif- ple, the thickness of Layer 2 (leaf layer) and the thickness of Layer 3 (stem
icantly without any substantial change in stem water content. Fig. 5b layer) were best correlated with leaf biomass (r = 0.88) and stem bio-
also indicates no sensitivity of σ0 to leaf water content during the mass (r = 0.96), respectively. Leaf length was also best correlated to can-
vegetative stage. Additionally, σ0 displays little variation despite the opy leaf biomass (r = 0.89).
large variability of leaf water content, i.e., a clear decreasing trend with
senescence. Water area index (LAI × leaf water content; Dabrowska- 3.2.3. Leaf area and leaf biomass
Zielinska, Inoue, Kowalik, & Gruszczynska, 2007) is much more closely re- Both LAI and leaf biomass produce significantly high correlations
lated to σ0 (Fig. 5c), but the relationship is mainly determined by LAI; the with σ0 (Fig. 3). The scatter plots between σ0 and LAI (Fig. 6a) and
leaf water content has only a minor effect. Therefore, plant water status leaf biomass (Fig. 6b) indicate consistent relationships throughout
may not be directly detected by C-band σ0 under the normal conditions all growth stages. Overall, even within a single stage (i.e., single
of paddy rice under flood irrigation. The difference in water content image), data points are plotted along the similar fitted lines. The C-band
would be detected only though significant changes in leaf biomass and σ0 increases exponentially with increasing LAI or leaf biomass. These
structure. relationships produce exponential curves with high coefficients of deter-
The highest negative correlation was found between SPAD and σ0 mination (r2 = 0.84–0.85).
(Fig. 3) despite the absence of any direct mechanistic influence of chloro-
phyll content on the microwave scattering processes. This is also attribut-
0 2
able to the physiological relationship between chlorophyll content and σ ¼ −15:17ð1 þ 0:879 exp½−0:637 LAIÞ r ¼ 0:844 ð6Þ
262 Y. Inoue et al. / Remote Sensing of Environment 140 (2014) 257–266
-5 -5
a) a)
-10 -10
σ0 = -15.17 (1 + 0.879 exp [-0.637 LAI])
r2 = 0.844*
-15
C-VH σ0 (dB)
-15
C-VH σ0 (dB)
-20
-20
-25
20090906VH -25
-30 20100716VH
20090906VH
20120627VH -30 20100716VH
-35 20120627VH
0 20 40 60 80 100
-35
Stem W (%) 0 1 2 3 4 5 6
LAI (m2m2)
-5 -5
b) b)
-10 σ0 = -15.15 (1+0.886 exp [-0.0117 LDW])
-10
r2 = 0.850*
-15
C-VH σ0 (dB)
-15
-25
20090906VH -25
-30 20100716VH 20090906VH
20120627VH -30 20100716VH
-35 20120627VH
0 20 40 60 80 100
Leaf W (%) -35
0 100 200 300
Leaf DW (g m-2)
-5
Fig. 6. Relationship of C-band σ0 with a) leaf area index (LAI) and b) leaf biomass (leaf
c) DW). * indicates the statistical significance at P = 0.001.
-10
(e.g., Asrar, Myneni, & Kanemasu, 1989; Huete, 1988). The normal-
ized difference vegetation index (NDVI) using reflectance values in
-20 the red and near-infrared has been used extensively in various applica-
tions. Both σ0 and NDVI are saturated at an LAI of around 3, and they
-25
20090906VH
20100716VH -5
-30
20120627VH σ0 = -16.51(1 + 0.737 exp[-0.00588 TDW] )
-10 r2 = 0.869*
-35
0 1 2 3 4
C-VH σ0 (dB)
Fig. 5. Relationship of C-band σ0 with a) stem water content, b) leaf water content, and -20
c) water area index (water content × LAI).
-25 20090906VH
20100716VH
0
σ ¼ −15:15ð1 þ 0:886 exp½−0:0117 LDWÞ
2
r ¼ 0:850 ð7Þ -30 20120627VH
20110930VH
-35
The σ0 value saturates at a LAI of around 3 and a leaf biomass of 0 500 1000 1500 2000 2500
180 gDW m−2. The asymptotic values for the equations, i.e., −15.17 dB Total DW (g m-2)
for LAI and −15.15 dB, suggest that the maximum σ0 for rice canopies
is approximately −15.2 dB in VH polarization of the Radarsat-2 spotlight Fig. 7. Relationship between C-band σ0 and total biomass (total DW). * indicates the sta-
mode. tistical significance at P = 0.001.
Y. Inoue et al. / Remote Sensing of Environment 140 (2014) 257–266 263
0 -10
σ 0 = 13.81 fAPAR -27.85
-15
-20
-20
-25 -25
-30
20090906VH
0090906V -30
-35 20100716VH
20120627VH
-40 -35
0.0 0.2 0.4 0.6 0.8 1.0 -35 -30 -25 -20 -15 -10
fAPAR Measured C-VH σ0 (dB)
Fig. 8. Relationship between C-band σ0 and fAPAR. * indicates the statistical significance at Fig. 9. Comparison of measured C-VH σ0 values with those estimated by a parameterized
P = 0.001. water cloud (WC) model. LAI was used as a key canopy variable for parameterization of
the model. *indicates the statistical significance at P = 0.001.
Ribbes & Le Toan, 1999). When full-polarimetric images are available in a that of NDVI, implying a similar scattering process in vegetation cano-
high-resolution mode in the near future, more sensitive components of pies for optical and microwave signatures. The response of σ0 to total
the signatures may be extracted, allowing greater accuracy in the assess- biomass was expressed by an exponential equation with a high coeffi-
ment of biophysical variables. cient of determination, but the sensitivity was clear only within the
The accuracy of assessment may be further improved by taking lower 20% of the full biomass. This sensitivity was attributable to the
account of some supplemental information related to field conditions structural changes due to leaf growth, and C-band σ0 proved to have a
such as row orientation and soil roughness, which affect the backscatter- relatively poor predictive ability for estimating total biomass.
ing processes. For example, the shape, orientation, and fractional vegeta- Of all the biophysical and ecophysiological variables, the C-band σ0
tion cover of a field can be derived from the segmentation of high- had the highest correlation with fAPAR. A scatter plot suggested that
resolution multispectral images (e.g., Inoue et al., 2010; Liu & Xia, the σ0–fAPAR relationship is linear throughout the growth stages.
2010). Such supplemental information regarding the confounding factors These results suggest the capability of C-band σ0 for the assessment of
from other types of sensors is useful to reduce the variability or uncer- LAI or fAPAR. This is a promising basis for the timely monitoring of
tainty in the relationships between C-band σ0 and biophysical variables. fAPAR by C-band SAR and/or through a constellation of SAR and optical
Several studies have demonstrated the potential of the synergistic use sensors.
of SAR and optical sensors (e.g., McNairn et al., 2009; Moran, Vidal, Not only the positive results but also some of the negative results
et al., 1997; Qi, Wang, Inoue, & Zhang, 2003). would be useful for basic studies on backscattering processes and for
Mechanistic models may be useful to improve the accuracy of assess- operational applications of SAR sensors in the future.
ment. Backscattering signatures from land surfaces are affected by many
factors, including plant biomass, canopy structure (e.g., LAI), soil mois- Acknowledgments
ture, and roughness. Interactions with sensor configurations, such as fre-
quency, polarization, and incidence angle, strongly affect backscattering This work was supported financially by the JSPS and MEXT, Japan. The
coefficients (Inoue et al., 2002; Lopez-Sanchez & Ballester-Berman, authors are grateful for the efficient help from the technical staff of the
2009; Qi et al., 2003). Therefore, a simple water-cloud model or more National Institute for Agro-Environmental Sciences. We would like to
detailed models are useful for the interpretation or rough prediction of thank Dr. Thuy Le Toan (CESBIO, France) and Prof. Juan M. Lopez-
microwave backscattering processes in plant canopies (e.g., Karam Sanchez (University of Alicante, Spain) for their helpful comments.
et al., 1995; Prévot et al., 1993; Ulaby, Allen, Eger, & Kanemasu, 1984;
Wang et al., 2009). However, the retrieval of biophysical variables by References
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