Three parameters are related to leaf-level physiology: Following the enzyme-kinetic model of @farquhar_1980_biochemical, the rate of photosynthesis is the minimum of light-limited and enzyme-limited reactions. The former are controlled by the quantum efficiency parameter---maximum efficiency with which absorbed photosynthetically active radiation is converted to CO~2~. The latter are controlled by V~cmax~, the maximum rate of carbon fixation by Rubisco. The water demand of photosynthesis is controlled by the stomatal slope, the sensitivity of stomatal conductance of CO~2~ as a function of CO~2~ concentration and humidity at the leaf surface [@leuning_1995_critical; @ball_1987_model]. Three more parameters correspond to the respiration rates of leaves, roots, and "growth maintenance".
Two more parameters control carbon allocation:
One is the ratio of fine root to leaf biomass (fineroot2leaf
, or q
), and another is the ratio of "storage" carbon allocated to reproduction (r_fract
).
Three parameters control various aspects of adult tree mortality. The overall adult mortality rate in ED-2.2 ($M$) is the sum of density-independent mortality from aging ($M_I$, plants year^-1^), density-dependent mortality from C starvation ($M_D$), and mortality from cold/frost ($M_F$) (ED-2.2 technically also includes additional term for fire mortality, but we did not include fire in our simulations):
$$ M = M_I + M_D + M_F $$
Density-independent mortality from aging ($M_I$) is a prescribed, PFT-specific parameter (mort3
).
Density-dependent mortality from C starvation is calculated as a function of a cohort's C balance limitation:
$$ M_D = \frac{y_1}{1 + \exp\left[y_2 \left( \frac{C_k}{C_k^*} \right)\right]} $$
where $C_k$ is the 12 month running mean C balance of the cohort, $C_k^*$ is the running mean ideal C balance if there was no light or water limitation, and $y_1$ (mort1
; plants year^-1^) and $y_2$ (mort2
; unitless) are PFT-specific parameters.
Seedling mortality rate is prescribed as its own PFT-specific parameter.
Several parameters are related to canopy structure and radiative transfer.
Specific leaf area (SLA
) is used to convert leaf biomass to leaf area index, which in turn is used in a variety of calculations related to canopy radiative transfer and micrometeorology.
Canopy clumping factor describes how evenly leaf area is distributed in horizontal space (1 being perfectly evenly; 0 being a "black hole" where all leaves are concentrated in a single point); and
leaf orientation factor describes the average distribution of leaf angles (-1 being perfectly vertical, 1 being perfectly horizontal, and 0 being random).
Four parameters control leaf optical properties, namely the fractions of light reflected or transmitted in visible and near-infrared wavelengths (leaf_(reflect|trans)_(vis|nir)
).
Details of how these parameters influence canopy radiative transfer are described in the Supplementary Information.
Other parameters (TODO, briefly):
f_labile
)repro_min_h
)water_conductance
)c2n_fineroot
) and leaves (c2n_leaf
)leaf_turnover_rate
)nonlocal_dispersal
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