Full text: Technical Commission VIII (B8)

  
   
    
IX-B8, 2012 
nced from their 
e) files. Polygons 
1 both dates (May 
lantations' stands: 
rage behaviour of 
and processing 
trometer detects 
interval from 350 
hannels), of which 
Onm with a 1.4nm 
ver the range from 
erval. 
active leaves, one 
ine and, randomly, 
> collected. At the 
aves/tree, of which 
cess was done one 
18 and June 17% 
th were resampled 
orne sensor. 
y and leaf level for 
tral data generated 
ackburn (2007). In 
seen the clones and 
:terogeneity, ratios 
SION 
show that, between 
e greatest losses of 
ures 2 and 3). The 
nly in this region, 
is moment the GTI 
ldish leaves with 
1se of the carotenes 
af scale and in this 
ilarity between the 
-SE (Figure 3). 
      
   
  
  
e GILMAY 
"mn GI JUNE 
-0 ue PRIÉSEMAY | 
meee PP 135.SE JUNE | 
PRIIENW MAY | 
PRIN JUNE | 
     
    
  
   
2 Vr 94, ug 
ale from 600 to 
ees stands: GT1, 
/ 
  
  
   
International Archives of the Photogrammetry, Remote Sensing and Spatial Information Sciences, Volume XXXIX-B8, 2012 
XXII ISPRS Congress, 25 August — 01 September 2012, Melbourne, Australia 
  
  
mue GEL MAY 
9 GT1 JUNE 
© vH PRIM-SE MAY 
: gor TTR UE 
se ; ce PRIMCNW MAY 
oie PRIS. NW JUNE 
  
  
  
pr emt 
  
"T Figy 5195 5M, 5204 G31, Wy, Nas Gp, Ag An, be 1p. € Gy Myo 
Wavelength (om) 
  
  
— GTEMAY 
7o --GTLJUNE 
cu PBIM.SE MAY 
—PB255.SE JUNE 
cese PBISS-NWE MAY 
sepes PBIMCNN JUNE 
Reflectance (%) 
  
Sag Ses so 5574 ras a 
Wavelength (am) 
  
  
Figure 3. Spectral behaviour in leaf scale from 600 to 700nm, 
for May and June, of the Rubber trees stands: GT1, PB235-SE 
and PB235-NW 
The carotenes, which have not been spoiled during the period, 
are very present on the leaves of the GT1 clone. That fact 
explains the maintenance of the spectral behaviour all over the 
blue region, from 450 to 480nm (Figures 4 and 5). This spectral 
region coincides with the b chlorophyll absorption peak, which 
suffered degradation, as well as it covers wide and important 
absorption by carotenes, mainly the photo-protectors ones. 
  
  
weer GTI MAY 
me CTI JUNE 
vov PB338-SE MAY 
o PB1N.SE JUNE 
vov PB33ENVE MAY 
is PRIMENW JUNE 
  
  
Reflectance (96) 
m 
  
  
  
  
  
iy 39, M Yong ?u, 
Wavelength (nm) 
  
  
  
Figure 4. Spectral behaviour in canopy scale from 450 to 
480nm, for May and June, of the Rubber trees stands: GT1, 
PB235-SE and PB235-NW 
  
  
  
t 
ev GTI MAY 
m GT1 JUNE 
cos FRIESE MAY 
  
non PB235_SE JUNE 
ur A e FHIMCNW MAY 
& d = 
à © dp YBIM-NW JUNE 
Reflectance (94) 
E 
  
© 
  
  
  
  
  
“iy we; fang ors ny 
Wavelength (om) 
Figure 5. Spectral behaviour in leaf scale from 450 to 480nm, 
for May and June, of the Rubber trees stands: GT1, PB235-SE 
and PB235-NW 
  
  
  
Around 550nm, when the anthocyanin absorption peak 
happens, the increase of reflectance was observed for all the 
three stands, exceeding for the PB235-NW stand in canopy 
scale (Figures 6 and 7). It is interesting to observe that this fact 
happened for both anthocyanin and chlorophylls and only for 
this stand, and in this specific scale. This spectral behaviour 
indicates a close relation between these compounds, what is 
also observed by Blackburn (2007) and Amaral et al. (2009). 
  
  
ws GTI MAY 
— GTI JUNE 
cse PBIM-SE MAY 
c B235-SE JUNE 
M. ae PB235-NW MAY 
vete PRIMCNW JUNE 
  
  
  
  
s Se, su A Sarg 52, 
Wavelength (am) 
  
  
Figure 6. Spectral behaviour in canopy scale, for May and June, 
in the region of 550nm of the Rubber trees stands: GT1, PB235- 
SE and PB235-NW 
Figure 7. Spectral behaviour in leaf scale, for May and June, in 
the region of 550nm of the Rubber trees stands: GT1, PB235- 
SE and PB235-NW 
As it is observed in the spectral regions already presented, for 
the stands of the same clone, it is visible a pattern in the spectral 
behaviour that is different from that for GT1 clone. 
The ratios among the spectra of the three stands indicated in the 
region VIS (400-700nm) a pattern for the stands of the PB235 
clone, which differs from that for the GT1 clone (Figure 8 and 
9). That demonstrates that, regardless of the environmental 
conditions and the period of data collection, in this spectral 
region, the genetic is highlighted as the origin of spectral 
differences. Clearly, there is a behaviour pattern among the 
ratios GTI/PB235-SE and GTI/PB235-NW that differs from 
that found among clones PB235. This behaviour is close to 
opposite around 550 nm, in the May data, in leaf and canopy 
scales. This also happens in leaf scale around 650 nm and is 
particularly significant in June data. 
  
c GIHPBIM.SE MAY 
— GTIPBINCNW MAY 
o FB23-SEOBISS-NW MAY 
Ratio value 
  
75 
May 416 726, 32,7356 Dp Kay Wry Sty Ry Ny Sy Sup, Sw Sas 61,024,418, 68) 072 814 
Wavelengtb (n) 
  
e GELPRISS-SE JUNE 
am GTUPBT3S NW JUNE 
ann PRIIE-SE/PRIIS-NW JUNE 
  
  
  
me M AE MR ARE 
Wavelength (am) 
Figure 8. Ratios among spectra of the Rubber trees stands (GT1, 
PB235-SE and PB235-NW) from 400-700nm for May and 
June, in canopy scale 
  
  
  
  
cr GTUFBAISSE MAY 
mec GTLFBIS-NW MAY 
mn PBIS-SEPBIISNW MAY 
  
Tag Ie V20 4 V2 386,2 ai 439 $925 Ty Msp Nu NG ayy Seg gy np Soy Win, NG Mig Beg 
Wavelength (nm) 
ere GEMPBIIT-SE JUNE 
c—GIDPB213-NW JUNE 
cose PRIMSEPBIS-NW JUNE 
Ratío value 
  
28 r 
Yong fn 19 H8, 904,381, 25 Slr g Rs, Ne Ta Sup; Suu 595,9 M0 4 EI R3 any Bg 
  
  
Wavelength (nm) 
  
Figura 9. Ratios among spectra of the Rubber trees stands (GT1, 
PB235-SE and PB235-NW) from 400-700nm for May and 
June, in leaf scale 
   
  
  
  
   
   
   
    
       
     
    
   
    
    
    
    
   
    
    
   
   
    
    
   
    
    
   
   
     
   
    
   
     
     
   
    
  
   
    
 
	        
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