A Four-Scale Bidirectional Reflectance Model Based on Canopy Architecture
Jing M. Chen
Sylvain G. Leblanc
Canada Centre for Remote Sensing
588 Booth Street, 4th floor
Ottawa, Ontario
Canada K1A 0Y7
Published in IEEE TGARS, 1997, vol. 35, pp.1316-1337
Modiffications, corrections, comments are in red
(May, 2000)
|
Abstract
Open boreal forests present a challenge in understanding remote sensing
signals acquired with various solar and view geometries. Much research
is needed to improve our ability to model the bidirectional reflectance
distribution (BRD) for retrieving the surface information using measurements
at a few angles. The geometric-optical bidirectional reflectance model
presented in this paper considers four scales of canopy architecture: tree
groups, tree crowns, branches and shoots. It differs from the Li-Strahler's
model in the following respects:
1) the assumption of random spatial distribution of trees is replaced
by the Neyman distribution which is able to model the patchiness or clumpiness
of a forest stand;
2) the multiple mutual shadowing effect between tree crowns is considered
using a negative binomial and the Neyman distribution theory;
3) the effect of the sunlit background is modelled using a canopy gap
size distribution function that affects the magnitude and width of the
hotspot;
4) the branch architecture affecting the directional reflectance is
simulated using a simple angular radiation penetration function;
5) the tree crown surface is treated as a complex surface with micro-scale
structures which themselves generate mutual shadows and a hotspot. All
these scales of canopy architecture are shown to have effects on the directional
distribution of the reflected radiance from conifer forests. The model
results compare well with a data set from a boreal spruce forest. |
1 Introduction
Solar radiance reflected from the earth's surface is strongly anisotropic
and depends on both the sun and observation directions. Such bidirectional
reflection behaviour has been extensively investigated over various surfaces
with remote sensing data (Cihlar et al. [8]
and Wu et al. [37]), ground-based
measurements (Deering et al. [10])
and numerical models (see Myneni and Ross [26]).
In bidirectional reflectance distribution (BRD) models, vegetated surfaces
are often described as turbid media (Gao [12],
Jupp and Strahler [17], Otterman
and Brakke [30] Verhoef [34],
Verstraete [35]) that represent
well agricultural crops and grassland. For forests, geometric-optical models
(Li and Strahler [21] [22],
Strahler and Jupp [33]) and hybrid-models (Li
et al. [23],
Nilson and Peterson [29]) combining
geometrical and turbid media have been used. One common challenge for canopy
models of all types is the difficulty in simulating the multiple scattering
processes within the canopy. Much attention has been given to this problem.
The other major challenge is the effect of plant canopy architecture on
radiative transfer processes. This challenge has not yet been rigorously
tackled in the literature although there have also been quite a few publications
on this problem (Borel et al. [1],
Goel et al. [15], Myneni and Ross
[26])
in addition to geometric-optical models. The meaning of architecture here
goes beyond the usual angle distribution of leaves. It also includes the
spatial distribution patterns of leaves and higher-level structures such
as shoots, branches and trees. Architecture at all levels in a plant canopy
affects not only the transmission of the solar beam through the canopy,
but also the multiple scattering processes contributing to the observed
radiances. In forest stands, for example, the number of multiple scattering
events between tree crowns is undoubtedly much smaller than between leaves,
and the modelling methodology would be exceedingly complex and depend on
the treatment of the canopy architecture. In the modelling effort presented
here, the attention is first given to a detailed mathematical descriptions
of the canopy architecture at various levels.
In Li and Strahler's BRD models [22],
a forest stand is assumed to consist of randomly-distributed objects containing
leaves as turbid media. These two-scale models mark a major advancement
in simulating radiation regimes in forest stands as compared with the one-scale
turbid-media models, but also dramatically increase the complexity of the
models. However, two-scale models may be regarded as much simplified mathematical
descriptions of the physical reality. First, trees are generally not randomly
distributed in space but are usually clustered at large scales due to variations
in the soil and topographic conditions, creating patchiness of forest stands.
They are also not randomly positioned when close to each other because
of the natural repulsion effect in competition for resources (Franklin
et al. [11]). Second, leaves are
not randomly distributed within tree crowns. In conifer stands, for example,
needles are grouped into shoots, branches and whirls, and all these sub-canopy
structures are important in determining the radiation regime, especially
the directional reflectance. In the present paper, these two additional
scales of plant canopy architecture are considered.
Figure
1 shows the concept of the different radiation transfer models based
on canopy architecture at several scales. The objective of this paper is
to present the first four-scale BRD model for the purpose of investigating
the effect of the different architectural scales on the directional reflection
behaviour of plant canopies.
|
2 Model description
A BRD model computes the percentage of incident radiation that is reflected
by a forest in various directions. It is the proportions of the sunlit
and shadowed areas of foliage and ground that are used to determine the
BRD. Our model contains several ``modules'', each with specific tasks.
The first module constructs the forest. It includes the spatial distribution
of trees within a modelling domain and the macro-scale geometry of the
trees. By considering the tree crown geometry, the shadowed and illuminated
areas of an isolated tree are calculated, and by combining the geometry
and tree distribution, the gap fraction and gap size distribution of the
canopy are computed as functions of solar or view zenith angle. The gap
size distribution is then used to model the hotspot effect. The hotspot
occurs on both the tree crowns and the ground. The mathematical treatments
on the canopy architecture are presented below. |
2.1 Tree distribution
BRD models based on discrete canopy structures usually assume that trees
are randomly distributed within a spatial domain. This distribution is
described using the Poisson theory:
where m is the average value of the number of objects (in our case, trees)
in a sub-domain called quadrat, and P(x) is the probability of finding
x
objects in the sub-domain. However, in reality, trees are generally not
randomly distributed but rather grouped together in various ways. Measurements
from a boreal jack pine stand (Fig. 2) show
an obvious deviation of the tree distribution from Poisson's random case,
i.e. the number of quadrats having a certain number of trees is distributed
narrowly around the mean number of trees per quadrat while the measured
distribution is much broader. The Poisson tree distribution is in fact
an averaging process: as the quadrat size (or the mean number of trees
per quadrat) increases trees become more evenly distributed among the various
quadrats. The application of this process to represent reality requires
a forest stand to be uniform at both small and large scales. However, variations
in environmental conditions such as topography, soil and sucessional processes
often make trees irregularly distributed, forming patches at various scales.
The simple Poisson theory is incapable of describing such patchiness. Nilson
and Peterson [29] made a correction
to the Poisson theory to model non-randomness of tree distribution. Neyman
[27]
(with application to geography by Getis and Boot [13])
developed a method for describing the contagious distribution of larvae.
This method called Neyman type A has been used by Franklin et al.[11]
for the investigation of tree distributions. It assumes that trees are
first combined in groups and the spatial distribution of the centre of
a group follows the Poisson process. The mean size of the groups is a required
model input depending on the degree of clumping of trees. Centred around
a given mean group size, there are also probabilities for other group sizes
determined again by the Poisson theory. Hence, the Neyman type A distribution
can also be called the double-Poisson distribution. For the convenience
of mathematical description, a group must fall completely into a quadrat
with the centre of the group. The size of the quadrat denoted by A, used
in the model, should represent the extent of radiation interaction between
trees, i.e., the horizontally-projected path length of a solar beam through
the canopy. The modelling domain is equivalent to the size of a pixel in
remote sensing. In selecting the quadrat size there is also a computational
constraint: the larger the group, the larger should be the quadrat. For
a 100 × 100 m2 domain with 3000 trees, for example, it
is preferable to divide the domain into at least 10 quadrats to avoid overly
populated quadrats that could be difficult to handle numerically.
According to the conditional probability theory, the probability of
having i trees given j groups in a quadrat, P(i|j),
times the probability of having j groups in the quadrat, P(j), gives
the probability of having i trees in the quadrat given j groups. The probability
of having i trees in the quadrat, P(i), is the summation
of all the conditional probabilities for j:
When both P(j) and P(i|j) are
determined by the Poisson process, we obtain
PN(i;m1;m2)
= e-m1 |
mi2
i! |
|
¥
å
j = 1 |
|
[ m1 e-m2
]j
j! |
·ji for i
= 0, 1, 2, ... , |
|
(3) |
where
is the mean number of groups per quadrat and
is the cluster mean size. m = m1 m2 is the mean and
n
= m1 m2[1+m2] is the variance of the distribution
of the number of trees per quadrat and can be measured in a real forest
stand. In creating this distribution, the following implicit assumptions
are used [13]: Within the modelling
domain each quadrat is equally likely to receive a cluster and the placement
of a cluster is independent of the placement of any other clusters.
1) The parameter m1 corresponds to a priori value
of the density of a cluster and m2 corresponds to a priori
value of the mean size of clusters (optional).
2) In conformity with a Poisson model the variance about the mean size
of cluster is equal to the mean size of cluster.
3) The assignment of a cluster size to one location is independent
of the assignment of any other cluster size or cluster location (optional).
4) The points in a cluster are propagated by a `progenitor' who is
located at the site of each cluster (pseudo-contagious assumption).
If the real distribution is not known, m2 will be
fixed at a low value ( m2 = 1 implies a tree distribution
close to the random case). Comparison with field data will later determine
the values for those parameters.
Figure 3 shows a random tree distribution
(Poisson) in comparison with Neyman distributions with the mean grouping
m2
of 1, 5, and 20 trees per group. In the calculation, the average density
was 75 trees per quadrat (1500 trees/ha with 20 quadrats of 500 m2
each). Groupings of 1 and 5 produce distributions centred at 75 and increase
the standard deviation from the random case.
m2 = 1 means
that the grouping is mostly random (group of one) but it contains probabilities
of having groups of two trees or more and therefore has a broader distribution
than the random case. If the group size is too large compared to the overall
mean (m), the Neyman distribution becomes variable with peaks at
multiples of that size. As a result, the curve for m2
= 20 in Fig. 3 shows maxima at 20, 40, and 60
trees per quadrat. At i = 0, the number of quadrats (having no trees) increases
with group size, suggesting that for larger group sizes, the probability
of having empty quadrats is greater. In Fig. 2,
measurements from a jack pine forest are compared with the Poisson and
Neyman distributions. The domain studied was one hectare with 1793 trees
divided into 100 quadrats. A Neyman distribution with grouping of 3 simulates
the measurements more closely than the Poisson theory. Processes other
than Neyman could be used in this kind of analysis. For its simplicity
and for the first analysis of tree clumping in forest canopies, only the
Neyman, i.e., the double-Poisson process is used in this paper. |
2.2 Tree crown projection
Conifer tree crowns have been modelled with a cone shape by Li and Strahler
[19].
Nilson and Peterson [29] added
a cylinder below the cone in their simulations. A photograph taken in a
mature black spruce stand near Candle Lake, Saskatchewan, Canada (Figure
4), shows that the trees essentially have a cylindrical shape with
a conical top. In our model, a tree crown is then assumed to consist of
a cone and a cylinder. In common with Li and Strahler's [19] model, the
conical part is described with two factors: its radius (r) and its
half apex angle (a). In this paper, all trees
have the same half apex angle (a = 13°)
. Figure 5 shows how a tree crown is modelled.
Hb
is the height of the cylinder. The height of the cone is defined by its
apex angle and the radius of the tree: Hc = r/tan(a).
The total height of the tree crown is Ht = Hb
+ Hc.
A cone casts a shadow on the ground in addition to the cylinder beneath
it only if the solar zenith angle is larger than one-half of the apex angle.
This shadow area is expressed as [19]:
Sgc = |
é
ê
ë |
1
tan(gs) |
- |
p
2 |
+gs |
ù
ú
û |
r2 , |
|
(6) |
where gs (see Fig.
5 ) is defined as
gs = sin-1 |
æ
ç
è |
tan(a)
tan(qs) |
ö
÷
ø |
, |
|
(7) |
where qs is the solar zenith angle.
The shadow cast by the cylinder on the ground has an area given by
To obtain the total area of a tree projected on the ground surface, the
base of the tree, a disc, should also be included:
In this model, the cylinders can either rest on the ground surface or have
their bases elevated to the same height (Ha). Since the
lower part of a forest is generally a trunk space without much foliage,
it is more realistic to elevate the bases, i.e. to have the crown ``on
a stick''. In our model, the height of tree crown base affects the contribution
of the ground surface to the hotspot. The summation of (6),
(8) and (9) gives the
total area within the outline of a tree crown projected on the ground surface
:
Sg = |
ì
ï
ï
í
ï
ï
î |
|
|
|
|
é
ê
ë |
1
tan(gs) |
+ |
p
2 |
+gs |
ù
ú
û |
r2 + 2tan(qs)Hb
r |
|
|
|
|
|
(10) |
This projected area can be used to find the ground area not seen by a viewer,
if the viewer is far enough so that the parallax won't change the view.
For this reason, we only need to replace qs
in (10) with qv.
This quantity is denoted by VG, which is the area on the ground
covered by opaque crowns in the viewer's direction:
Vg = |
ì
ï
ï
í
ï
ï
î |
|
|
|
|
é
ê
ë |
1
tan(gv) |
+ |
p
2 |
+gv |
ù
ú
û |
r2 + 2tan(qv)Hb
r |
|
|
|
|
|
(11) |
After calculating the shadow area that a single tree casts on the ground,
the sunlit crown proportion seen by the viewer is computed from the total
surface area of the tree visible to the viewer projected to a plane perpendicular
to the view line. For the cylinder we have
The total tree surface area projected on a plane perpendicular to the view
line is
tact of (13) is described in Appendix
A.
For cylinders, the self-shadowing and illumination geometry are very
simple: half the surface is illuminated and half in shadow. The illumination
part seen by the viewer is then
tib = 2rsin(qv)Hb· |
é
ê
ë |
1- |
f
p |
ù
ú
û |
, |
|
(14) |
where f is the azimuth angle difference between
the sun and the viewer. The sunlit part of a cone seen by a viewer, denoted
tic,
cannot be easily expressed in a simple equation, but is described in Appendix
A. This quantity depends on the apex angle of the trees and the positions
of the sun and the viewer. If qs
is smaller than a, no self-shadow occurs
on the cone, but as qs gets larger
than
a, a portion of the cone is shaded. The
proportion of the tree that is illuminated and seen by the viewer (Pti)
can be found by adding the areas illuminated and dividing by the total
surface area of the tree presented to the viewer. However, the contributions
from both the cone and the cylinder part of a tree must be included. Thus
Pti = |
tic + tib
tac+tab |
. |
|
(15) |
2.3 Canopy gap fraction
The canopy gap fraction determines the contribution of the underlying surface
to the reflectance measured above the canopy. It is based on the method
described above for calculating the shadow area. If the trees are distributed
randomly within the domain and the tree crowns are opaque, the probability
of seeing the ground is
Pvg-r= |
é
ê
ë |
1- |
Vg
A |
ù
ú
û |
D/n |
, |
|
(16) |
where D is the number of trees in the domain B and A = B/n is a quadrat.
By definition there are n quadrats in the domain. If the trees are clustered,
the probability PN(i), found in (3),
is used to compute this effect. We have
Pvg-c = |
k
å
i = 0 |
PN(i) |
é
ê
ë |
1- |
Vg
A |
ù
ú
û |
i |
, |
|
(17) |
where i is the number of trees in A, and PN(i) is the probability
of having i trees in A. In this equation, gaps within tree crown are not
considered. Pvg-c represents the
ground that can be seen between tree crowns. If we allow gaps in crowns
and overlapping of crowns to occur, (17) becomes
Pvg = |
k
å
j = 1 |
Ptj(Vg)Pgapj(qv)+Pt0, |
|
(18) |
where
Pgapj(qv)
= |
j
Õ
1 |
Pgap(qv) |
|
(19) |
is the gap probability (depending on qv)
inside the trees, and Ptj(Vg), the probability of
having j trees intercepting the view line is calculated with a negative
binomial:
Ptj(Vg) = |
k
å
i = j |
PN(i) |
é
ê
ë |
(i+j-1)!
(i-1)! j! |
ù
ú
û |
|
é
ê
ë |
1- |
Vg
A |
ù
ú
û |
i |
|
é
ê
ë |
Vg
A |
ù
ú
û |
j |
, |
|
(20) |
where PN(i) is the Neyman distribution (3)
and k is an integer which should be large enough
to consider all overlapping of the trees in a quadrat. It must correspond
to PN(k) = 0 or Pt(j
= k)(Vg) = 0. In this
paper, k = 350. In the case of j = 0, Pt0
is equal to (17). Likewise the probability
of the ground surface being illuminated, Pig, can be found by
replacing Vg by Sg and qv
by qs. In real forests, trees found
in clusters are usually smaller than the average tree size. In one quadrat,
we have m = m1m2 = D/n trees on average. The model
assumes that for the probability of having more than m trees in a quadrat,
the size of the trees will decrease inversely with the number of trees
per quadrat:
With the setting used in the first section, m = 75, the probability of
having 100 trees in a quadrat, the individual tree shadow area is reduced
by 75%. For i less than or equal to 75 all trees have the same size.
The gap probability, Pgap(q),
is well known for a continuous medium [28].
For a discontinuous canopy, we use an equation similar to Li and Strahler
[21]
but modified to consider the foliage clumping effect [4]:
Pgap(qs)
= e-G(qs)Lo
·WE/gE
, |
|
(22) |
where
and
is the foliage density, and
|
_
s |
(qs)
= |
V
Sg(qs) cos(qs) |
, |
|
(25) |
is the mean path length of the solar beam through a tree. V is the
volume contained within the tree crown outline, D/B is the number
of trees per m2, WEis
a clumping index of the shoots within tree crowns [4],
L
is the leaf area index (LAI) defined as half the total needle area per
unit ground surface area [4].
(22) gives the probability of the solar beam
passing through a single tree. Using qv
instead of qs gives the probability
of seeing the background through a single tree. For a canopy with a random
foliage angle distribution, G(q) = 0.5.
For canopies with branch architecture [3],
G(q)
= a-bq, where
a and b are positive constants. Adding a gap probability to tree crowns
gives less shadow on the ground and more ground area seen by the viewer. |
3 Mutual shadowing effect
At large qv values, a viewer
sees mostly the upper part of the trees. Without considering the height-dependent
mutual shadowing effect, the model will underestimate the proportion of
sunlit canopy Pti in view because the illuminated top
part is less likely in shadow. In this version of our model, we only separate
a tree crown into two parts: cone and cylinder, and calculate the mutual
shadow effects for these two parts in two steps. In step one, the mutual
shadowing effects among the cones can be found by allowing the projected
conical areas to overlap. The probability of cone overlapping is obtained
by summing (20) from j = 2 to k,
based on the shadow area of a cone cast on the ground in the sun's direction
(Sgc) and in the viewer's direction (Vgc).
Psc = |
k
å
j = 2 |
Ptj(Sgc) [ 1-Pgap(qs)j] |
|
(26) |
is the overlapping probability for Sgc and
Pvc = |
k
å
j = 2 |
Ptj(Vgc) [ 1-Pgap(qv)j] |
|
(27) |
is the overlapping probability for Vgc. In 26
and (27), 1-Pgap(qv)j
is multiplied to discount the gaps within the crowns. In step two, the
mutual shadowing effects on the cylindrical part are calculated as the
difference between the total overlapping and the cone overlapping. The
total overlapping effects, denoted by Ps and Pv,
are calculated by replacing Sgc and Vgc with Sg
and Vg in (26) and (27),
where Sg and Vg are the ground shadow areas of a
single tree crown in the sun's and viewer's directions, respectively. After
weighting the overlapping probabilities of the crown and cylinder parts
by their respective areas, the mutual shadowing effects for the cylindrical
(base) part are then:
Psb = |
Ps·Sg -
Psc·Sgc
Sgb |
|
|
(28) |
and
Pvb = |
Pv·Vg -
Pvc·Vgc
Vgb |
, |
|
(29) |
where Sgb and Vgb are the projected areas on the
ground in the sun and view directions, respectively. For the calculation
of the probability of viewing the sunlit portion of tree crowns, the quantities
needed are the proportions of the tree crowns that are not overlapped under
the various scenarios, i.e.
If the illumination and viewing directions are far apart, Qsc
and Qvs, as well as Qsb and Qvb, are considered
to be independent. The products of the pairs, i.e. Qvc ·Qsc
and Qvb ·Qsb, are the probabilities of actually
seeing the illuminated part of the cones and cylinders, respectively. We
must multiply tib, the illuminated area of one tree, by Qvb
·Qsb in (15), and tic
by Qvc ·Qsc, and tac and tab
in the same equation are multiplied by Qvc and Qvb,
respectively, to obtain the actual areas of the conical and cylindrical
parts of one tree seen by a viewer.
Near the principal plane on the backscatter side, the illumination and
observation of a sunlit area can occur in the same gap in the canopy. In
such a case, the processes of illumination and viewing are correlated.
The angle range over which the correlation occurs depends on the tree size
and the average tree spacing. A function f(f),
depending on the difference in the azimuth angle between the sun and the
viewer, is used to consider this correlation effect. Using the mean distance
between tree centres [] calculated by:
we can determine the azimuthal angle range within which overlapping of
one tree with the other occurs in both the illumination and view directions:
A linear equation is used between f = 0 and
f
= qE:
where f(f) is a kernel with non zero values
only when 0 < f < qE.
The overall mutual shadowing effects, Qc and Qb,
for the conical and cylindrical parts, respectively, are then given by
Qc = Qvc ·Qsc
+ f(f)·[Qsvc-Qvc
·Qsc] |
|
(37) |
and
Qb = Qvb ·Qsb
+f(f) ·[Qsvb-Qvb
·Qsb], |
|
(38) |
where Qsvc is the minimum of Qsc and Qvc,
and Qsvb is the minimum of Qsb and Qsb.
With considerations of these mutual shadowing effects, the probability
of seeing illuminated tree crowns becomes
Pti = |
Qc ·tic + Qb
·tib
Qvc ·tac + Qvb
·tab |
. |
|
(39) |
Much of the complexity of the mutual shadow calculations arises from the
fact that the conical and the cylindrical parts have different geometry
and have to be separately modelled. Since conifer trees are better represented
using the combination of these two parts than the single cone shape, we
believe that the formulation presented above is an improvement over previous
models based on cone geometry when used for conifer forests. |
4 Canopy gap size and hotspot
The hotspot is a phenomenon that occurs when the observation and the illumination
directions coincide within the same canopy gap [16].
At the hotspot, the viewer sees either sunlit foliage or the sunlit background,
resulting in large observed reflectance factors. In this case, the probability
of seeing the ground, Pvg, is equal to the probability of having
the ground illuminated, Pig, and the probability of seeing tree
crowns, Pst = 1-Pvg, is
equal to 1-Pig. As the viewer moves
away from the hotspot, the view line and the solar beam are less likely
to fall in the same canopy gap and Pig and Pvg gradually
become independent of each other. The product of the pair (Pig
and Pvg ) then determines the probability of seeing the sunlit
ground. However, around the hotspot, such simple calculations are invalid
because of the correlation of these two processes. The importance of the
correlation in determining the hotspot has been investigated by many modellers
including Kuusk [18], who devised
a correlation function based on the leaf size. We found that leaf size
is irrelevant for the correlation in conifer canopies. Nilson and Peterson
[29] used a correlation based on
a characteristic gap size. In the present paper, we introduce a canopy
gap size distribution function for the calculation of the correlation.
The function closely relates the hotspot to the canopy attributes.
The theory of gap size distribution in plant canopies was first derived
by Miller and Norman [25] and further
investigated by Chen and Black [5]
and Chen and Cihlar [6]. The accumulated
gap size distribution can be calculated from:
Fat(l) = |
é
ê
ë |
1+Lt |
l
Wt |
ù
ú
û |
e- Lt[1+[(l)/(Wt)]]
, |
|
(40) |
for gaps ³ l,
where Wt is the characteristic width of a tree crown projected
on the ground; and Lt is the clumping-adjusted projected tree
crown area index. This formulation is made according to the finding of
Chen and Cihlar [7] that a large
part of the gap size distribution curve measured in boreal forests is determined
by tree crowns as discrete objects. Wt and Lt are
computed as follows:
and
where Sg is the area of a tree crown projected on the ground
in the sun's direction and Wt is
a tree clumping index, determined by the Neyman distribution as
Wt
= log(Pig(Neyman))/log(Pig(Poisson)) |
|
(43) |
It is 0.95 obtained from simulation with a Neyman grouping of 4 for a forest
with 4000 stems per hectare divided into 25 quadrats.
Similar to (40), a distribution for gaps inside
crowns can be computed where the shoots are taken as the foliage elements:
Fas(l)
= |
é
ê
ë |
1+Ls |
l
Ws |
ù
ú
û |
e- Ls[1+[(l)/(Ws)]]
. |
|
(44) |
where
Ls = |
G(qs)WE
L
gE cos(qs) |
|
|
(45) |
is the clumping-adjusted foliage area index and the characteristic width
of the foliage elements is
WE is a clumping index
for the effect of confining shoots within tree crowns; gE
is the needle-to-shoot area ratio quantifying the effect of needle grouping
in shoots on the radiation interception; and As is the average
shoot projected area. According to Chen [2],
for the black spruce stand investigated in this paper, L = 4.5,
G(q)
= 0.5, WE= 0.70, gE
= 1.41 and
Ws = 35 mm. Only very small gaps are computed
inside trees, but they contribute significantly to the total canopy gap
fraction because of their large numbers. In the calculation of the hotspot,
these small gaps are of critical importance in determining the shape of
the hotspot.
[small
modifications: equation (45) is use with LAI=1; WEis
modified in the code since TRAC measurements include clumping between crowns.
The clumping is reduced by half, e.g. 0.70 becomes 0.85]
Table 1:
Ha |
0.5 m |
Hb |
6.5 m |
Radius of crown |
0.45 m |
G(q) |
0.5 |
LAI |
4.5 |
Domain |
1 ha |
Density |
4000 tress/ha |
Quadrat size |
400 m2 |
Neyman grouping |
4 |
a |
13o |
gE |
1.41 |
WE |
0.70 |
Ws |
0.035 |
RG (red) |
0.06 |
RT (red) |
0.13 |
RZG(red) |
0.006 |
RZT(red) |
0.01 |
RG (nir) |
0.20 |
RT (nir) |
0.53 |
RZG(nir) |
0.05 |
RZT(nir) |
0.08 |
Figure 6 shows accumulated gap size
distributions measured along a 300 m transect in the black spruce forest
[2].
The measured gap size distribution can be separated into two parts: between
and within the tree crowns. (40) and (44)
are used to simulate these two parts respectively. The parameters used
in (40) and (44) are those
found in Table 1 except Wt that
was fixed at 1.4 m to reflect the typical width of tree crowns encountered
on the transect at about 45°
to the sun. The characteristic width Ws for black spruce shoots
was measured to be three cm. Same Wt and Ws
values were used for both gap size distributions, i.e., Figs.
6(a) and (b). In both cases, the contributions of gaps between and
within tree crowns to the measured gap size distributions are distinct,
but there is a portion of the distribution curve in the range of 10-50
cm which can not be fitted using the crown and shoot attributes. This out-lying
portion is a result of the branch architecture because the gaps between
branches are larger than those between shoots but smaller than those between
tree crowns. |
4.1 Hotspot between crowns
Fat(l) and Fas(l)
are quantities that can be measured directly in a forest canopy. From the
measurements of Fat(l) and
Fas(l)
the following gap size distribution can be derived:
Pt(l)
= e- Lt[1+[l/Wt]]
. |
|
(47) |
Pt(l) is defined as the probability
of a horizontal probe of length l falling completely
within a gap between tree crowns. This gap size distribution between tree
crowns is important in determining the contribution of the ground surface
to the hotspot. Figure 7(a) shows how Pt(l)
varies with l at different solar zenith
angles. For the calculation of the hotspot kernel for the ground, a gap
number density function is used, which is defines as
Nt(l)
=
- |
dPt(l)
dl |
= |
Lt
Wt |
e-Lt[1+[l/Wt]]. |
|
(48) |
The probability PG of observing the sunlit ground under the
tree crowns can then be written in the general form:
PG = PigPvg+
[Pig-Pig Pvg]Ft(x), |
|
(49) |
where Ft(x) is a hotspot kernel,
which is unity at the hotspot and zero when the illumination and view angles
are far apart, and x is the angle between
the sun and the viewer determined by cos(x)
= cos(qs) cos(qv)
+ sin(qs)sin(qv)cos(f).
The first term on the right hand side of (49) is
the probability of observing the sunlit ground when Pig
and Pvg are not correlated, i.e., the viewer sees the
sunlit ground through a gap different from that of illumination. The second
term gives the additional probability resulting from the correlation. Figure
8 shows how a gap of certain size contributes to the hotspot kernel.
The angle range in which the viewer can see the sunlit ground through the
same gap as the illumination is determined by the gap size and the effective
height of the gap column that depends on the view zenith angle. For one
gap of size l, we have the hotspot function:
Ft(x)
= 1- |
x
tan-1(l/H) |
. |
|
(50) |
where H = [Ha+Hb+Hc/3]/cos(qs).
For the whole canopy containing multiple gaps of different sizes with a
number density of N(l), the hotspot function
is obtained through the following integration:
Ft(x) = |
|
ó
õ |
¥
lmin |
|
é
ê
ë |
1- |
x
tan-1(l/H) |
ù
ú
û |
N(l) dl |
|
. |
|
(51) |
For a given angle difference between the sun and the viewer, there is a
minimum gap size lmin in which the
view line penetrates through the same gap as the solar beam. It is determined
by
The ground reflectance is assumed to be isotropic in this paper. |
4.2 Hotspot within tree crowns
In the estimation of the hotspot within the tree crown, a gap size distribution
within individual tree crowns is used. In previous geometric-optical models,
the imaginary tree crown surface has been treated as a smooth surface in
the calculation of the hotspot [22].
Some more elaborate models have dealt with the crowns as object containing
turbid media with multiscattering [29][23].
Since shadows can be observed on the sunlit side of real tree crowns, the
micro-scale structures within tree crowns have important contributions
to the hotspot, modifying the hotspot shape and magnitude. An important
structure within conifer trees is the shoots, which are the basic collections
of needles. Needles are grouped tightly in shoots, which allow little radiation
penetration and can be treated as the basic foliage units for radiation
modelling [7]. Similar to the distribution
between crowns, a gap size distribution within the crown is used to calculate
the gap number density function:
Ns(l) = - |
dPs(l)
dl |
= |
Ls
Ws |
e-Ls[1+[(l)/(Ws)]]. |
|
(53) |
The formulation presented above has implications on the inversion of
the model for leaf area index because the micro-scale structures within
the tree crowns affect the BRD and cannot be ignored.
In computing the hotspot within the tree crowns, the self-shadowing
and the vertical tree crown structure must be considered. Discontinuities
in mathematical expressions are found at nadir or the boundary between
sunlit and shaded sides of a crown. Therefore, we treat the two sides separately.
On the sunlit side, the probability of seeing the illuminated foliage PT
at the hotspot is simply 1 - Pig,
i.e. the viewer sees either the sunlit ground or the sunlit foliage. Considerable
complication arises when we treat the tree crown surface as a complex surface
with micro-scale structures. In this case, a view line can penetrate into
the depth of the crown and reach to the shaded foliage behind the sunlit
part even though the imaginary tree crown surface is theoretically sunlit.
The problem may be understood in the extreme cases: 1) a tree crown is
very dense - the imaginary surface can reasonably represent the tree crown,
and 2) a tree crown is very sparse - the imaginary surface ceases to have
meaning. The reality is in between these two extremes, i.e. the imaginary
surface exists but is unsmooth or complex. In this case, the effect of
mutual shadowing among foliage elements within a tree crown cannot be ignored.
Figure 10 shows the physics involved in
the determination of the hotspot within a tree crown, where a tree is considered
as a vertical structure with spherical foliage elements (shoots) dispersed
within it. Using L(x) as the accumulated LAI from the imaginary surface
to a given location x within the crown, the accumulated sunlit leaf area
from 0 to L(x) is 1-e-Cs
L(x), where Cs = G(qs)
WE/gE
sin(qs + a)
to take into account the cone inclination and the vertical structure. At
position x, the increment of sunlit leaf area with increasing L(x) is
|
d
dL(x) |
[1-e-Cs
L(x)] = Cs e-Cs
L(x) |
|
(54) |
Similarly, the increment of leaf area seen after dL(x) is
|
d
dL(x) |
[1-e-Cv
L(x)] = Cv e-Cv
L(x). |
|
(55) |
If we denote LH as the leaf area index accumulated horizontally
from the sunlit side to the shaded side, the total probability of viewing
sunlit leaf area from 0 to LH is then
|
|
= G(x) |
ó
õ |
LH
0 |
Cv Cse-CvL(x)
e-CsL(x) dL(x) |
|
|
= G(x)[1-
e-LH(Cs +Cv)] |
é
ê
ë |
CsCv
Cs +Cv |
ù
ú
û |
|
|
|
|
|
(56) |
where G(x) is the
first-order scattering (geometric shadow) phase function of the foliage
elements. It is defined as
G(x)
= |
é
ê
ë |
1- |
Cp x
p |
ù
ú
û |
|
|
(57) |
where Cp is a coefficient determined by the optical properties
of foliage elements. If the elements are solid spheres with a Lambertian
surface, Cp is unity, resulting in the phase function being
1.0 at x = 0, 0.5 at x
= p/2 and 0 at x
= p. The phase function in this case gives the
proportion of the sunlit sphere surface seen by the viewer. Although a
conifer shoot can be approximated by a sphere to describe the projected
area [2], it can not be treated
as a solid because of the gaps within it. The value of Cp for
porous elements is smaller than unity. Because of lack of data, we assume
that Cp = 0.75 in this paper. This constant is found to affect
the sharpness of the hotspot. Q1 must be calculated for all
trees, it gives:
Q1 tot = |
k
å
j = 1 |
Q1(j ·LH)·Ptj(Vg) |
|
(58) |
where Ptj(Vg) is the probability of a view line going
through j tree crowns calculated by (20).
[Q1tot is no longer computed with
(58). It uses the same reasonning as Q2tot] On the shaded
side, the probability of observing sunlit leaves also exists, especially
in canopies with sparse tree crowns. The increment of sunlit leaf area
along the sun's direction is calculated using (54),
but the increment of leaf area viewed from the opposite side is calculated
differently as follows:
|
d
dL(x) |
[1-e-Cv(LH-L(x))]
= -Cv e-Cv(LH-L(x)). |
|
(59) |
At a given depth x, the probability of observing sunlit foliage is
G(x)Cs
e-Cs L(x)(-Cv
e-Cv(LH-
L(x))). |
|
(60) |
After integration from LH to 0 across the tree crown, the overall
probability becomes
Q2(LH) = |
é
ê
ë |
1- |
Cp x
p |
ù
ú
û |
[e-CsLH-
e-CvLH] |
é
ê
ë |
CsCv
Cv - Cs |
ù
ú
û |
. |
|
(61) |
This phenomenon must be considered on each tree along the path of view.
On the first tree, it is simply Q2(LH). For i trees
along the path it is:
Q2 tot = Q2(LH) |
k
å
i = 1 |
·Ptt(i) ·K(i) |
|
(62) |
where
Ptt (i) = Pat(i) Pat(i-1)
Pgapi-1(qv). |
|
(63) |
in which
Pat(i) = |
k
å
j = i |
Ptj(Vg). |
|
(64) |
Pat(i) represents the probability of having i trees within one
path. The probability of seeing the ith tree behind i-1
trees is found by the probability of having i-1
tree overlapping, Pat(i-1), times
the probability of passing through i-1 trees,
Pgapi-1(qv).
As the view line penetrates through the forest, it reaches the lower portion
of the canopy where shaded foliage is more likely to be observed. For the
ith tree on the path, this height attenuation is considered by
K(i) = e-i GE(qv)
·cos(qv)/cos(qs). |
|
(65) |
With the proportion of sunlit and shaded tree crown as Pti and
(1-Pti) respectively, we can then
calculate the probability of seeing the illuminated foliage as follows:
PTf = Pti ·Q1
tot + [1-Pti]·Q2
tot. |
|
(66) |
This equation is only valid far from the hotspot. A hotspot function, similar
to (51), can also be defined. Fs(x)
follows the same principles as Ft(x)
but it involves foliage elements (shoots) instead of tree crowns.
Fs(x) = |
|
ó
õ |
¥
lmins |
|
é
ê
ë |
1- |
x
tan-1(l/Hs) |
ù
ú
û |
Ns(l) dl |
|
, |
|
(67) |
where Hs is the effective distance between two layers of leaves
inside a tree crown. In our model, it is inversely proportional to the
leaf area density in the tree crown or Lo, i.e.
where r is the tree crown radius. This definition produces sharper hotspots
in canopies with sparser tree crowns. After considering the hotspot on
tree crowns, the overall probability of observing sunlit foliage is
PT = PTf + [(1-Pig)-PTf]Fs(x)
. |
|
(69) |
This gives PTf outside of the hotspot where Fs(x)
= 0 and (1-Pig) at the centre
of the hotspot where Fs(x)
= 1. Figure 9 shows examples of the hotspot
kernel calculated using (51) and (67)
along the principal solar plane at a solar zenith angle of 45°.
As the first approximation, the shape of the kernel is the same in all
directions, i.e., the hotspot has a circular shape. |
4.3 Canopy reflectance
For estimating the first order scattering, the model computes the various
components: sunlit foliage (PT), sunlit ground (PG),
shaded foliage (1-Pvg-PT)
and the shaded ground (Pvg - PG).
If direct solar beams are the sole source of illumination and no multiple
scattering occurs, only the first two components are responsible for the
reflectance of the canopy. However, since the diffuse radiation from the
sky is considerable compared with the direct radiation and the multiple
scattering is also inevitable, the shaded components cannot be ignored.
These components are considered in our model by assigning the appropriate
reflectivities to them as follows:
and
where RZT and RZG are the reflectivities
for shaded foliage and ground, respectively; RT and RZ
are the reflectivities for sunlit foliage and ground, respectively; Fdt
and Fdg are the fractions of diffuse irradiance in the
total incoming solar irradiance above and below the stand, respectively;
and Cm is a multiple-scattering factor. RZT
and RZG can also be measured directly from a forest stand.
The total canopy reflectance is
r = RT
·PT + RG ·PG + RZT
·ZT + RZG ·ZG, |
|
(72) |
where ZT = 1-Pvg-PT
and ZG = Pvg -PG.
All these reflectivities are wavelength dependent. In modelling canopy
reflectance in red and near-infrared bands, (72)
is used with a different value for each reflectivity. |
5 Model results
5.1 Effect of Neyman grouping
The model first computes the canopy gap fraction Pvg
(18). Measurements from a boreal black spruce
forest were used to validate the computation. According to Chen [2],
the following values are used: 4000 for the tree density (stems per hectare),
6.5 m for the average tree height, 4.5 for LAI, and 0.45 m for the crown
radius. The quadrat size is fixed at 400 m2, having an average
of 200 trees per quadrat. Figure 11 shows Pvg
distributions calculated using the Poisson model and the Neyman model with
groupings of 4, 12, and 24. Near the vertical view direction, the different
sizes of Neyman grouping do not have much effect because the forest is
very open. The effect of the grouping is more pronounced for qv
between 15° and 60°.
The best fits are found with small Neyman groups. An analysis of 24 quadrats
of 10×10 m2 each measured in black spruce stands gives
m2
= 2 calculated with (5), but when grouped into
six 400 m2 quadrats, m2 = 4. A grouping of
4 is used in all simulations unless noted otherwise.
The measured gap fraction data at large zenith angles are positively
biased because of the effect of multiple scattering on the measurements
using an optical instrument [2]. The modelled curves all show a sharp increase
near the vertical direction because of the simple geometry to represent
the tree crown and overlapping of the crowns without considering the repulsion
effect. This creates unsmoothness of the model results at the nadir as
shown later. In reality, the tree crown geometry is more variable and the
reflectance distribution are usually smoother around nadir.
To understand the effect of the Neyman grouping, Fig.
12 shows different components of the model for a range of m2
values from 1 to 50 at qv
= 30°,
qs
= 55° and f
= 0. The grouping of trees produces a larger gap fraction because it increases
the probability of having quadrats with few trees. With the increasing
grouping size, the proportion of canopy illuminated (Pti)
decreases, and so does the probability of seeing a tree illuminated (PT).
This is mainly because of the increase in the gap fraction. In accordance
with Pvg, the probability of seeing the illuminated ground
surface (PG) increases. Red and near infra-red reflectances
decrease with the Neyman grouping because ground reflectivity is low compared
to the crown reflectivity. |
5.2 BRD and hotspot
The plots in Fig. 13 were computed using the
same inputs as in Fig. 12 and the
reflectivities summarised in table 1. Based on measured spectra (White
et al. [36], Middleton et al. [24],
Soffer [32]) , RG
= 0.06 and RT = 0.13 for the red band and RG
= 0.20 and RT = 0.53 for the near-infrared band. The ground
reflectivity in the red band is smaller than that of leaves even though
the overall reflectivity of the stand is lower than the ground reflectivity
because of the shadow components in the stand. Using (70)
and (71) we can attribute the appropriate reflectivities
to the shaded tree crown and ground surfaces. Because of the small contributions
from shaded ground and crowns, we use constant multiscatterring factors,
leading to Cm ·Fdt = 0.08 and Cm
·Fdg = 0.10 for the red band and Cm
·Fdt = 0.15 and Cm ·Fdg
= 0.25 for the near infra-red band. The six plots in Fig.
13 show the same components as those in Fig.
12 but as distributions against qv
on the principal solar plane at qs
= 35°. For the view angle qv,
we use the following sign convention: negative for backscatter and positive
for forwardscatter. Figure 13a shows the gap
fraction versus the view zenith angle for a Neyman grouping of 4. Figure
13b is the proportion of the imaginary tree crown surface seen by the
viewer that is illuminated. From qv
= -90°
to -35°
it equals unity, meaning that all tree crowns imaginary surface in view
are illuminated in the principal solar plane. At nadir (qv
= 0), there is a discontinuity because the viewer can only see the cone
part of the tree crown which is mostly illuminated. On the backscattering
side, Pti decreases near the vertical direction because the
viewer can see the lower part of the cylinder that is shaded by other cylinders.
On the fowardscattering side, the cylinder is completely shaded, and as
qv
increases, more of the shaded cylinder occupies the view. At very large
qv
values, the conical part dominates the view, and the proportion of the
tree in view that is illuminated increases because more than half of the
cone surface is usually sunlit. Figure 13c
represents the probability of seeing illuminated foliage within tree crowns.
It includes the probability of observing sunlit foliage from the shaded
side and the hotspot effect on the illuminated side. A pronounced hotspot
peak is computed at qv = 35°.
Figure
13d is the probability of seeing the ground illuminated by the sun.
The bi-module distribution pattern results from the peaks at the hotspot
and at nadir. The peak at the nadir is due to the largest gap probability
at that angle. The other peak at the hotspot is obtained after the introduction
of the hotspot function (51), otherwise the
PG
curve would be symmetric about the centre. At the hotspot, all the ground
areas in view are illuminated, and the value of
PG is
simply
Pvg at the same angle (0.35 at qv
= 35°).
Figs.
13e and 13f describe the BRD in the red and near-infrared bands. Both
distributions resemble the probability of seeing illuminated foliage (PT)
because of the large
PT values and the large reflectivity
values for the foliage. Although the magnitudes of the red and near-infrared
reflectances are very different, the shapes of the distributions are remarkably
similar because only the first-order scattering is considered in the calculation
and the multiple scattering effects are included as invariant offsets.
However, there are subtle differences in the shapes due to the different
foliage and ground reflectivity combinations with PT
and PG. These small differences have implications on
the angular distribution of vegetation indices calculated from the two
bands and deserve further investigation.
Comparisons of the model results were made with measurements of a boreal
black spruce forest [9]. Figures
14a and 14b show the calculated and measured reflectance in the red
band for two different qs values,
40° and 55°,
in the principal plane. At qs
= 40°, the model is overestimating
the reflectance on the forwardscattering side. This is mainly due to the
constant reflectivities used for the shaded foliage and ground. The model
uses constant values for Fdt and
Fdg
in (70) and (71) for the fraction
of diffuse radiation in the total incident solar irradiance. As the fraction
changes during the course of the day, these constant values better represent
the average daily conditions. Near solar noon when the sun is high, the
diffuse fraction is smaller than the daily average and the reflectivities
for the shaded components are also correspondingly smaller than the daily
average, resulting in the discrepancies between the modelled and observed
values at qs = 40°.
The comparisons suggest that the model will benefit from accurate separation
of the diffuse and direct solar radiation. The model shows sharp spikes
at the hotspot in comparison with the measurements. The gentle variation
in the measurements may be a result of the low angular resolution (15°)
which effectively produced window-averaged results. The effect of the averaging
is to dampen and broaden the peak at the hotspot. For qs
= 40° and other small qs
values not shown here, the width of the hotspot is well modelled. The model
does not perform as well at the larger solar zenith angles like Fig.
14(b) for qs = 55°.
This model deficiency may have resulted from the simplified geometry used
to represent the tree crowns. The model geometry is such that, all foliage
is confined within the cone or cylinder, while in reality branches extend
much further than the mean radius and intercept more radiation than the
model prediction. One way to handle the problem is to increase the mean
radius of the tree crowns, but in that case the branch structure needs
to be more vigorously described to allow more gaps within the tree crown.
This suggests that geometric-optical models are still approximations to
reality and accurate simulation of BRD requires accurate descriptions of
the canopy architecture at all scales. Figure 14c
shows a comparison between the model and measurements for the reflectance
in the near-infrared band at qs
= 40°. The model is able to simulate
the measurements closely. In Fig. 14d where
qs
= 60°, the model performs well
except for the largest qv,
especially on the backscattering side, indicating the effect of non-uniform
distribution of multiple scattering on BRD which is not considered in the
present study.
Figure 15 shows hemispheric distributions
of reflectance in the red band at four solar zenith angles. The hotspot
varies in size, being generally larger when the sun is higher in the sky.
The model does not show much of the usual bowl-shape because of the high
LAI and the fixed diffuse fractions used in the model. Some of the bowl-shape
can be seen in Fig. 15c and 15d.
Figure
16 shows the corresponding distributions in the NIR band. The distributions
are similar to those in Fig. but the bowl-shape is more pronounced
for qs = 60°
and 75°. The increase in reflectance
at large qv values, where
the ground is hidden under the tree crowns is due in part to the larger
reflectivity of the shaded foliage as compared to the shaded ground A singularity
is seen at nadir for the large solar zenith angles, i.e. Fig.
16(d) because of the large shaded ground components viewed vertically. |
6 Discussion
The 4-Scale model presented here was developed to investigate the effect
of canopy architecture at different scales on the bidirectional distribution.
Since we have incorporated mathematics descriptions of canopy architecture
at scales larger and smaller than the tree crown, it becomes a fuzzy geometric-optical
model in the sense that the clearly defined canopy geometry, such as that
of Li and Strahler's models, is disintegrated and defined probalistically.
The inclusion of canopy architecture at the various scales in a geometric-optical
model may be considered as an influx of negative entropy which increases
the orderliness of the system under investigation and is expected to approximate
more closely natural living organisms. We believe that such a model contains
more flexibility to adapt to different plant canopies than previous models.
Much mathematical complexity arises, though still tractable, when we
treat the tree crown surface as a complex surface within which mutual shadows
and the hotspot also occur. Through our numerical simulation, we believe
that the sub-canopy structures have profound effects on the directional
reflection behaviour of the canopy and deserve such attention. Figure
17 shows the sensitivity of the model to the foliage density within
tree crowns. With the fixed stand density and tree crown shape and dimensions
(Table 1), the foliage density increases proportionally
with LAI. For these simulations, we kept the multiscattering factors constant,
and realised that some inaccuracies occurred in the model results because
larger LAI should induce more multiscattering in the canopy. Both the red
and NIR reflectances increase with decreasing LAI in the forward scattering
direction due to the increased probabilities of observing sunlit foliage
from the shaded side through sparse tree crowns. The hotspot is smaller
for a sparser canopy (lower LAI) because of the increased probability of
observing the ground, which has a lower reflectivity than the foliage.
These model results support the findings of Soffer [32]
that the measured reflectance on the shaded side of jack pine crowns is
considerably larger than the predictions of a Li and Strahler model. Black
spruce crowns are generally denser and the shaded side appears darker than
the jack pine. Our model is able to simulate such differences.
The assumption of random tree distribution is removed at the expense
of lengthy mathematical descriptions using the combined Neyman and binomial
distributions. Apparently, such effort has not been very rewarding with
regard to its impact on the final BRD results for the stand investigated.
Figure
18a shows that the Neyman grouping increases the reflectance in the
red band only on the forward scattering side near the vertical direction.
The increased openness of the forest due to the Neyman grouping is the
main cause of the increase in the modelled reflectance. The Neyman grouping
decreases the width of the hotspot because a larger
m2
gives a smaller
Wt which affects
the hotspot kernel for the ground. At large view angles, a larger Neyman
grouping gives a smaller reflectance because the contribution of the ground
to the reflectance becomes very small and the tree crown properties dominate
at these angles. The change of the hotspot width is more important in the
NIR than the red band because the Neyman grouping affects the proportion
of the ground illuminated (PG). Our present simulation
is limited to small quadrats with small Neyman groupings. More research
is needed to determine the grouping effect at larger scales (large quadrats
with large groupings).
Sub-canopy architecture is not only important in investigating the BRD
of vegetated surfaces but also critical in the inversion of the model to
obtain biophysical parameters such as leaf area index. Clumping of needles
within shoots, for example, affects the radiation interception in the plant
canopy and hence vegetation indices derived from the reflectances in red
and near-infrared bands. Grouping of shoots in branches also has similar
effects. Accurate estimation of LAI from the model requires appropriate
descriptions of architecture at these sub-canopy levels.
In this paper, the effect of multiple scattering on BRD is not investigated.
Our attention is first given to canopy architecture because the first order
scattering is usually much larger than the sum of multiple scattering and
the angular distribution of the multiply scattered radiances is usually
considered to be isotropic [31].
However, at NIR wavelengths, the multiple scattering effect is larger than
that at visible wavelengths and the isotropic assumption may lead to some
inaccuracies in the BRD results. Such subtle differences may have significant
effects on the simulated vegetation indices using reflectance factors for
these two bands. We hold the believe that in modelling the multiple scattering,
the canopy architecture is foremost important because it dictates the direction
of first order scattering and the probability of observing the reflecting
surfaces at different steps of the scattering sequence. The approaches
of Goel et al. [14] and
Strahler and Jupp [33] in the description
of plant canopy architecture have such merits, but forest canopies are
much more complex than what have been described. The model presented here
provides a framework in which the effect of canopy architecture at various
scales on BRD can be systematically investigated.
|
7 Conclusion
In contrast to the turbid-medium type of models suitable for short
vegetation canopies without distinct foliage structures, geometric-optical
models are more appropriate for forest canopies which are usually well
organised at various scales. Compared with previous 2-scale geometric-optical
models, which describe trees as randomly-distributed discrete objects containing
turbid media, the 4-scale model presented in this paper includes the effects
of two additional scales of canopy architecture: tree distribution pattern
and foliage distribution pattern within trees. The 4-scale model simulates
closely the measurements of tree distribution, canopy gap fraction and
the bidirectional reflectance. It is shown in model simulation that the
architecture within tree crowns has profound effects on the bidirectional
reflectance distribution (BRD). Tree distribution patterns have small but
significant effects on BRD for the stand investigated and may have larger
effects for more patchy stands.
In our model, a tree crown consists of conical and cylindrical parts.
An effective mathematical scheme is devised to estimate the mutual shadowing
effect between tree crowns and among foliage elements within tree crowns.
The canopy gap size distributions between and within tree crowns are used
to describe the hotspot size and shape. The description, for the first
time, closely relates the bidirectional reflection behaviour to canopy
attributes.
8 Acknowledgements
We are indebted to Drs. Don Deering and Tom Eck for the permission to use
a sample of PARABOLA data. We thank Dr. Josef Cihlar for his support and
stimulating discussions in the development of the model. The paper was
internally reviewed by Drs. Robert Gauthier and Phil Teillet before submission.
We also thank Louis Moreau for technical discussions. The model in C code
is available on request. |
|
List of symbols
A |
Quadrat size |
B |
Domain size (pixel size) |
C(q) |
G(q)/sin(q) |
D |
Number of trees in the domain B |
Fas(l) |
Accumulated gap size distribution inside tree crowns |
Fat(l) |
Accumulated gap size distribution between tree crowns |
G(q) |
Projection of unit leaf area |
H |
Effective height ( Ha + Hb + 1/3 Hc
)/cos(qs) |
Ha |
Height of the lower part of the tree (trunk space) |
Hb |
Height of cylinders |
Hc |
Height of cones |
Ht |
Total height of the tree crown (Hc + Hb) |
L |
Leaf area index (LAI) |
LH |
LAI accumulated horizontally (L·`s(q
= 90°) ) |
Lo |
Mean LAI accumulated over the view or sun path within one tree crown |
Ls |
Clumping-adjusted projected tree crown element area index |
Lt |
Clumping-adjusted projected tree crown area index |
m |
Mean number of trees in a quadrat |
m1 |
Mean number of cluster per quadrat |
m2 |
Cluster mean size |
n |
Number of quadrats in the domain B |
PG |
Probability of seeing illuminated ground area |
Pgap (q) |
Gap Probability within a tree at the angle q |
Pig |
Probability of having sunlit ground area |
Ps |
Total shadowing effect |
Pvg |
Probability of seeing the ground (including clusters and overlap) |
Pvg-r |
Probability of seeing the ground (random tree distribution) |
Pvg-c |
Probability of seeing the ground (clustered tree, without overlap) |
Pst |
Probability of seeing tree crown area (1-Pvg) |
PT |
Probability of seeing sunlit trees |
Pti |
Proportion of tree crown surface viewed that is illuminated |
Ptj |
Probability that j trees overlap |
Pv |
Total view overlapping effect |
P(x) |
Poisson distribution |
PN(i) |
Neyman distribution |
Ps(l) |
Probability of having a gap of size l in
a crown |
Pt(l) |
Probability of having a tree gap of size l
between trees |
Q1tot, Q2tot |
Probability of seeing sunlit shoots inside the tree crowns (no hotspot
consideration) |
r |
Radius of the crowns |
`s(q) |
Mean path length within a crown |
RG |
Ground reflectivity |
RT |
Foliage reflectivity |
RZG |
Shaded ground reflectivity |
RZT |
Shaded foliage reflectivity |
R |
Total reflectance (pixel) |
Sg |
Shaded area on the ground produced by one tree |
Sgc |
Shadowed area on the ground produced by the cone part of the tree |
Sgb |
Shadowed area on the ground produced by the cylinder (base) part of
the tree |
tic tib |
Tree illuminated surface visible to the viewer |
tac tab |
Tree crown surface visible to the viewer |
V |
Volume of a tree |
Vg |
Ground surface not seen by viewer because of one tree |
Vgc |
Ground surface not seen by viewer because of the cone part of one tree |
Ws |
Mean width of element shadows cast inside tree crowns |
Wt |
Characteristic mean width of tree crowns projected to the ground |
a |
Half apex angle |
gs , gv |
Angle related to the self-shadowing of the cone |
gE |
Needle-to-shoot area ratio |
G(x) |
First-order scattering (geometric shadow) phase function of the foliage |
m |
Crown foliage density |
WE |
Clumping index for shoots |
Wt |
Clumping index for trees |
l |
Gap size |
lmin |
Minimum gap size for having an illuminated surface |
f |
Relative azimuth angle between the sun and the viewer |
qs |
Solar zenith angle |
qv |
View zenith angle |
x |
Angle difference between the sun and the viewer (phase angle) |
|
A Cone geometry
The computation of the proportion of illuminated area on a cone is done
using simple geometry. The area of the cone projected to a viewer can be
separated into two parts: an ellipse and a triangle. The nine schematic
representations in Fig. show the typical shaded areas viewed on the cone.
The origin of the coordinates is always the centre of the ellipse and the
x-coordinate of each point stays the same. The ellipse is expressed by
where xA = r cos(qv);
(xA,yA) is point A; and yA = 0. r is the
base radius of the cone. For qv £a
the cone area seen is
tac = p·r
·xA = pr2 cos(qv). |
|
(74) |
When qv > a,
the point B is outside the ellipse. This new area (called tact
in the paper) can be easily computed by integrating twice from the ellipse
to the segment [`BD] from 0 to yD:
tac = pr2
cos(qv) + 2 |
ó
õ |
yD
0 |
|
é
ê
ë |
|
xA
r |
|
|
______
Ör2-
y2 |
- |
y-bBD
mBD |
ù
ú
û |
dy , |
|
(75) |
where bBD and mBD are the intercept and the slope
of the [`BD] segment. (xB,yB)
denotes point B, which is the projected tip of the cone (yB
= 0). (xD,yD) is the intercept between the triangle
and the ellipse. The integral in (75) has an
analytical solution.
When the solar zenith angle qs
is less than the apex angle a, self-shadowing
on the cone occurs. At nadir, the illuminated area is expressed by
tic = |
é
ê
ë |
p
2 |
+ g |
ù
ú
û |
r2 ,, |
|
(76) |
where g = sin-1
[[(tan(a))/(tan(qs))]]
[19].
This is valid for all azimuth angles f. On the
backscattering side of the principal plane (Fig.
19a), the shadow can be seen while qv
< qs. For qv
£a we have
tic = yE ·(xE-xB)
+ rxA ·[ sin(g)cos(g)
-g+p/2
] |
|
(77) |
where (xE,yE) denotes point E. xE = xA
·sin(g+f)
and yE = r·cos(g+f)
As qv increases, the triangular part
appears to the viewer. Two shadowed areas can be seen on the triangle part.
Outside the principal plane, the symmetry does not exist, but the same
equations can still be used. The third plate of Fig.
19b shows such a case. The computation of the shaded area is an integration
of areas inside the ellipse which is separated into four parts to facilitate
the selection of integral limits. Figure 19b
for a > qv
> 0 we have the shadowed area in three parts of the ellipse, it is calculated
as follow:
|
|
ó
õ |
yE
0 |
|
é
ê
ë |
y-bBE
mBE |
- |
xa
r |
|
|
______
Ör2-
y2 |
ù
ú
û |
dy |
|
+ |
p
4 |
·r2 cos(qv)
- |
|xB·bBF|
2 |
|
|
+ |
ó
õ |
xF
0 |
|
é
ê
ë |
mBFx+bBF- |
r
xa |
|
|
_______
ÖxA2-
x2 |
ù
ú
û |
dy. |
|
|
|
|
(78) |
The first term is for the area formed by the points E, B, and A, denoted
EBA, the second and third are for the area ABGC and GFC, respectively.
The point G is the intercept of [`BF] on y.
The area illuminated (tic) is found by substracting ( 78)
from (75).
In (78) mBE and bBE are
the slope and intercept of [`BE] on y defined
by the equation of the curve that has the 2 points B and E. mBF
and bBF have similar definitions. yE and yF
do not depend on qv. Once they are
found at nadir, their values can be apply to other view angle at any given
f.
When qv > a,
the amount of shadowed surface in the triangle is calculated as follows:
the integration is like the one in (75). We divide
the triangle into two parts separated by the x-axis. The areas of the two
triangles are:
|
ó
õ |
yI
0 |
|
é
ê
ë |
xA
r |
|
|
______
Ör2-
y2 |
- |
y-bBE
mBE |
ù
ú
û |
dy |
|
(79) |
and
|
ó
õ |
yJ
0 |
|
é
ê
ë |
xA
r |
|
|
______
Ör2-
y2 |
- |
y-bBF
mBF |
ù
ú
û |
dy. |
|
(80) |
The shadow on the ellipse is, as above, calculated by separating the ellipse
into four parts: HOAJ, GOAI, FGOK, and EHOK. |
|
Figure 3: Comparison between Poisson and Neyman distribution of
various group sizes (m2)
Figure 4: Old black spruce forest, a BOREAS site, near Candle Lake,
Saskatchewan, investigated in this paper.
Figure 5: Tree crown geometry and the definition of variables
Figure 6: Two gap size accumulation curves measured.
Figure 7: Calculated gap size distributions between (a) and within
(b) tree crowns at three solar zenith angles.
Figure 8: Geometry determining the hotspot on the ground: the solar
beam and the view line coincide within the same canopy gap.
Figure 9: Hotspot kernel
Figure 10: Gap probability used in the hotspot modelling
Figure 11: Measured and modelled gap fraction for a black spruce
forest
Figure 12: Different components of the model versus m2
Figure 13: Different components of the reflectance in the principal
plane
Figure 14: Comparisons of BRDF measurements and the model in the
principal plane for a black spruce in the red band
more text
Figure 15: Plots of BRDF with different qs
for all visual angle (red)
Figure 16: Plots of BRDF with different qs
for all visual angles (near-infrared)
this is more text
Figure 17: Effects of different LAI on the BRD curves in the principal
plane, a) in the red band, b) in the infrared band. qs
= 45°
Figure 18: Effects of different Neyman grouping on the BRD curves
in the principal plane, a) in the red band, b) in the infrared band. qs
= 45°
|