Modelling Photosynthesis in Monocultures and Mixtures

1989 ◽  
Vol 16 (6) ◽  
pp. 501 ◽  
Author(s):  
IR Johnson ◽  
AJ Parsons ◽  
MM Ludlow

A comparison is made between two models of canopy photosynthesis for monocultures that differ in their treatment of the variation of the rate of single-leaf photosynthesis in response to the irradiance in which the leaves have grown. Both are shown to be deficient, and a simple modification to one that results in a much improved performance is presented. The theory uses the non-rectangular hyperbola for the rate of single-leaf photosynthesis and incorporates the Monsi-Saeki approach for the light-intercepting characteristics of the canopy. The model is then extended to describe the photosynthesis of mixed canopies, which requires knowledge of the relative position of each leaf-area component within the sward. Analytical expressions can be derived for the case where the leaf-area components are homogeneously distributed relative to each other through the depth of the canopy. This is shown to be a good representation of leaf-area distributions in continuously grazed temperate grass-clover swards as well as frequently cut tropical grass-legume swards, and so is an important special case.

1995 ◽  
Vol 22 (4) ◽  
pp. 603 ◽  
Author(s):  
PJ Sands

This paper presents a simple algorithm for calculating daily canopy photosynthesis given parameters of the single-leaf light response, the canopy extinction coefficient, canopy leaf area index, daylength, daily solar irradiance and daily maximum and minimum temperatures. Analytical expressions are derived for total daily production by a canopy of leaves whose light response is either a rectangular hyperbola or a Blackman response. An expression which gives an excellent approximation to canopy photosynthesis for an arbitrary hyperbolic light response is then derived. These expressions assume photosynthetically active radiation (PAR) within the canopy follows Beer's law, light-saturated photosynthetic rate at any point in the canopy is proportional to the ratio of local PAR to full-sun PAR, diurnal variation of PAR is sinusoidal, and parameters of the single-leaf photosynthetic light response do not vary diurnally. It is shown how these expressions can be used to accommodate diurnal temperature variation of photosynthesis in a simple manner. The accuracy of the approximation to the basic integral of leaf photosynthesis over the canopy and over time is illustrated by applying the algorithm to compute the seasonal variation of daily canopy photosynthesis and comparing these data with corresponding values obtained by numerical integration.


1997 ◽  
Vol 62 ◽  
Author(s):  
R. Samson ◽  
S. Follens ◽  
R. Lemeur

A  multi-layer model (FORUG) was developed, to simulate the canopy  photosynthesis of a mixed deciduous forest during the growing season.  Measured photosynthesis parameters, for beech (Fagus  sylvatica), oak (Quercus  robur) and ash (Fraxinus  excelsior), were used as input to the model. This  information at the leaf level is then scaled up to the level of the canopy,  taking into account the radiation profiles (diffuse and direct PAR) in the  canopy, the vertical LAI distribution, the evolution of the LAI and the  photosynthesis parameters during the growing season, and the temperature  dependence of the latter parameters.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Keisuke Sasaki ◽  
Yuuki Ida ◽  
Sakihito Kitajima ◽  
Tetsu Kawazu ◽  
Takashi Hibino ◽  
...  

Abstract Alteration in the leaf mesophyll anatomy by genetic modification is potentially a promising tool for improving the physiological functions of trees by improving leaf photosynthesis. Homeodomain leucine zipper (HD-Zip) transcription factors are candidates for anatomical alterations of leaves through modification of cell multiplication, differentiation, and expansion. Full-length cDNA encoding a Eucalyptus camaldulensis HD-Zip class II transcription factor (EcHB1) was over-expressed in vivo in the hybrid Eucalyptus GUT5 generated from Eucalyptus grandis and Eucalyptus urophylla. Overexpression of EcHB1 induced significant modification in the mesophyll anatomy of Eucalyptus with enhancements in the number of cells and chloroplasts on a leaf-area basis. The leaf-area-based photosynthesis of Eucalyptus was improved in the EcHB1-overexpression lines, which was due to both enhanced CO2 diffusion into chloroplasts and increased photosynthetic biochemical functions through increased number of chloroplasts per unit leaf area. Additionally, overexpression of EcHB1 suppressed defoliation and thus improved the growth of Eucalyptus trees under drought stress, which was a result of reduced water loss from trees due to the reduction in leaf area with no changes in stomatal morphology. These results gave us new insights into the role of the HD-Zip II gene.


2004 ◽  
Vol 04 (01) ◽  
pp. 63-76 ◽  
Author(s):  
OLIVER JENKINSON

Given a non-empty finite subset A of the natural numbers, let EA denote the set of irrationals x∈[0,1] whose continued fraction digits lie in A. In general, EA is a Cantor set whose Hausdorff dimension dim (EA) is between 0 and 1. It is shown that the set [Formula: see text] intersects [0,1/2] densely. We then describe a method for accurately computing dimensions dim (EA), and employ it to investigate numerically the way in which [Formula: see text] intersects [1/2,1]. These computations tend to support the conjecture, first formulated independently by Hensley, and by Mauldin & Urbański, that [Formula: see text] is dense in [0,1]. In the important special case A={1,2}, we use our computational method to give an accurate approximation of dim (E{1,2}), improving on the one given in [18].


2010 ◽  
Vol 21 (1) ◽  
pp. 73-76 ◽  
Author(s):  
Jun Diao ◽  
Xiang-dong Lei ◽  
Ling-xia Hong ◽  
Jian-tao Rong ◽  
Qiang Shi

2005 ◽  
Vol 48 (2) ◽  
pp. 221-236 ◽  
Author(s):  
Matt Kerr

AbstractWe state and prove an important special case of Suslin reciprocity that has found significant use in the study of algebraic cycles. An introductory account is provided of the regulator and norm maps on Milnor K2-groups (for function fields) employed in the proof.


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