[6] | 1 | !$Header: /home/ssipsl/CVSREP/ORCHIDEE/src_stomate/stomate_constants.f90,v 1.21 2010/05/17 14:25:41 ssipsl Exp $ |
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| 2 | !IPSL (2006) |
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| 3 | ! This software is governed by the CeCILL licence see ORCHIDEE/ORCHIDEE_CeCILL.LIC |
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| 4 | !- |
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| 5 | MODULE stomate_constants |
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| 6 | !--------------------------------------------------------------------- |
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| 7 | USE defprec |
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| 8 | USE constantes_veg |
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| 9 | USE ioipsl |
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| 10 | USE parallel |
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| 11 | ! bare soil in Sechiba |
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| 12 | INTEGER(i_std),PARAMETER :: ibare_sechiba = 1 |
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| 13 | !- |
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| 14 | ! 0 = no, 4 = full online diagnostics |
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| 15 | INTEGER(i_std),SAVE :: bavard=1 |
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| 16 | ! write forcing file for carbon spinup? |
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| 17 | LOGICAL,SAVE :: write_carbonforce |
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| 18 | ! Horizontal indices |
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| 19 | INTEGER(i_std),ALLOCATABLE,SAVE,DIMENSION(:) :: hori_index |
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| 20 | ! Horizonatal + PFT indices |
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| 21 | INTEGER(i_std),ALLOCATABLE,SAVE,DIMENSION(:) :: horipft_index |
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| 22 | !- |
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| 23 | ! Land cover change |
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| 24 | ! Horizontal + P10 indices |
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| 25 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: horip10_index |
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| 26 | ! Horizontal + P100 indices |
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| 27 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: horip100_index |
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| 28 | ! Horizontal + P11 indices |
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| 29 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: horip11_index |
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| 30 | ! Horizontal + P101 indices |
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| 31 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: horip101_index |
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| 32 | !- |
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| 33 | ! time step |
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| 34 | INTEGER(i_std),SAVE :: itime |
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| 35 | ! STOMATE history file ID |
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| 36 | INTEGER(i_std),SAVE :: hist_id_stomate |
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| 37 | ! STOMATE history file ID for IPCC output |
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| 38 | INTEGER(i_std),SAVE :: hist_id_stomate_IPCC |
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| 39 | ! STOMATE restart file ID |
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| 40 | INTEGER(i_std),SAVE :: rest_id_stomate |
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| 41 | !- |
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| 42 | ! Freezing point |
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| 43 | REAL(r_std),PARAMETER :: ZeroCelsius = 273.15 |
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| 44 | ! e |
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| 45 | REAL(r_std),PARAMETER :: euler = 2.71828182846 |
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| 46 | ! Epsilon to detect a near zero floating point |
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| 47 | REAL(r_std),PARAMETER :: min_stomate = 1.E-8_r_std |
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| 48 | ! some large value |
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| 49 | REAL(r_std),PARAMETER :: large_value = 1.E33_r_std |
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| 50 | ! Special value |
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| 51 | REAL(r_std),PARAMETER :: undef = -9999. |
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| 52 | !- |
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| 53 | ! maximum reference long term temperature (K) |
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| 54 | REAL(r_std),PARAMETER :: tlong_ref_max=303.1 |
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| 55 | ! minimum reference long term temperature (K) |
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| 56 | REAL(r_std),PARAMETER :: tlong_ref_min=253.1 |
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| 57 | !- |
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| 58 | ! trees and litter: indices for the parts of heart- and sapwood above |
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| 59 | ! and below the ground |
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| 60 | INTEGER(i_std),PARAMETER :: iabove = 1 |
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| 61 | INTEGER(i_std),PARAMETER :: ibelow = 2 |
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| 62 | INTEGER(i_std),PARAMETER :: nlevs = 2 |
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| 63 | !- |
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| 64 | ! litter: indices for metabolic and structural part |
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| 65 | INTEGER(i_std),PARAMETER :: imetabolic = 1 |
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| 66 | INTEGER(i_std),PARAMETER :: istructural = 2 |
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| 67 | INTEGER(i_std),PARAMETER :: nlitt = 2 |
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| 68 | !- |
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| 69 | ! carbon pools: indices |
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| 70 | INTEGER(i_std),PARAMETER :: iactive = 1 |
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| 71 | INTEGER(i_std),PARAMETER :: islow = 2 |
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| 72 | INTEGER(i_std),PARAMETER :: ipassive = 3 |
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| 73 | INTEGER(i_std),PARAMETER :: ncarb = 3 |
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| 74 | !- |
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| 75 | ! litter fractions: indices |
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| 76 | INTEGER(i_std),PARAMETER :: ileaf = 1 |
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| 77 | INTEGER(i_std),PARAMETER :: isapabove = 2 |
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| 78 | INTEGER(i_std),PARAMETER :: isapbelow = 3 |
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| 79 | INTEGER(i_std),PARAMETER :: iheartabove = 4 |
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| 80 | INTEGER(i_std),PARAMETER :: iheartbelow = 5 |
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| 81 | INTEGER(i_std),PARAMETER :: iroot = 6 |
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| 82 | INTEGER(i_std),PARAMETER :: ifruit = 7 |
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| 83 | INTEGER(i_std),PARAMETER :: icarbres = 8 |
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| 84 | INTEGER(i_std),PARAMETER :: nparts = 8 |
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| 85 | !- |
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| 86 | ! transformation between types of surface |
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| 87 | INTEGER(i_std),PARAMETER :: ito_natagri = 1 |
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| 88 | INTEGER(i_std),PARAMETER :: ito_total = 2 |
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| 89 | !- |
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| 90 | ! leaf age discretisation ( 1 = no discretisation ) |
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| 91 | INTEGER(i_std),PARAMETER :: nleafages = 4 |
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| 92 | !- |
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| 93 | ! alpha's : ? |
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| 94 | REAL(r_std),PARAMETER :: alpha_grass = .5 |
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| 95 | REAL(r_std),PARAMETER :: alpha_tree = 1. |
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| 96 | !- |
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| 97 | ! type declaration for photosynthesis |
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| 98 | TYPE t_photo_type |
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| 99 | REAL(r_std), DIMENSION(nvm) :: t_max_a |
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| 100 | REAL(r_std), DIMENSION(nvm) :: t_max_b |
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| 101 | REAL(r_std), DIMENSION(nvm) :: t_max_c |
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| 102 | REAL(r_std), DIMENSION(nvm) :: t_opt_a |
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| 103 | REAL(r_std), DIMENSION(nvm) :: t_opt_b |
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| 104 | REAL(r_std), DIMENSION(nvm) :: t_opt_c |
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| 105 | REAL(r_std), DIMENSION(nvm) :: t_min_a |
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| 106 | REAL(r_std), DIMENSION(nvm) :: t_min_b |
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| 107 | REAL(r_std), DIMENSION(nvm) :: t_min_c |
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| 108 | END TYPE t_photo_type |
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| 109 | !- |
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| 110 | ! type declaration for phenology |
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| 111 | TYPE pheno_type |
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| 112 | REAL(r_std), DIMENSION(nvm,3) :: gdd |
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| 113 | REAL(r_std), DIMENSION(nvm) :: ngd |
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| 114 | REAL(r_std), DIMENSION(nvm) :: ncdgdd_temp |
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| 115 | REAL(r_std), DIMENSION(nvm) :: hum_frac |
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| 116 | REAL(r_std), DIMENSION(nvm) :: lowgpp_time |
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| 117 | REAL(r_std), DIMENSION(nvm) :: leaffall |
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| 118 | REAL(r_std), DIMENSION(nvm) :: leafagecrit |
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| 119 | REAL(r_std) :: tau_hum_month |
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| 120 | REAL(r_std) :: tau_hum_week |
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| 121 | REAL(r_std) :: tau_t2m_month |
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| 122 | REAL(r_std) :: tau_t2m_week |
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| 123 | REAL(r_std) :: tau_tsoil_month |
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| 124 | REAL(r_std) :: tau_soilhum_month |
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| 125 | REAL(r_std) :: tau_gpp_week |
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| 126 | REAL(r_std) :: tau_gdd |
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| 127 | REAL(r_std) :: tau_ngd |
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| 128 | REAL(r_std) :: tau_longterm |
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| 129 | REAL(r_std), DIMENSION(nvm) :: lai_initmin |
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| 130 | CHARACTER(len=6), DIMENSION(nvm) :: pheno_model |
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| 131 | CHARACTER(len=6), DIMENSION(nvm) :: senescence_type |
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| 132 | REAL(r_std), DIMENSION(nvm,3) :: senescence_temp |
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| 133 | REAL(r_std), DIMENSION(nvm) :: senescence_hum |
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| 134 | REAL(r_std), DIMENSION(nvm) :: nosenescence_hum |
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| 135 | REAL(r_std), DIMENSION(nvm) :: max_turnover_time |
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| 136 | REAL(r_std), DIMENSION(nvm) :: min_leaf_age_for_senescence |
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| 137 | REAL(r_std), DIMENSION(nvm) :: min_turnover_time |
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| 138 | !- |
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| 139 | REAL(r_std), DIMENSION(nvm) :: hum_min_time |
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| 140 | END TYPE pheno_type |
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| 141 | !- |
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| 142 | ! parameters for the pipe model |
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| 143 | !- |
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| 144 | ! crown area = pipe_tune1. stem diameter**(1.6) (Reinicke's theory) |
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| 145 | REAL(r_std),PARAMETER :: pipe_tune1 = 100.0 |
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| 146 | ! height=pipe_tune2 * diameter**pipe_tune3 |
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| 147 | REAL(r_std),PARAMETER :: pipe_tune2 = 40.0 |
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| 148 | REAL(r_std),PARAMETER :: pipe_tune3 = 0.5 |
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| 149 | ! needed for stem diameter |
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| 150 | REAL(r_std),PARAMETER :: pipe_tune4 = 0.3 |
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| 151 | ! Density |
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| 152 | REAL(r_std),PARAMETER :: pipe_density = 2.e5 |
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| 153 | ! one more parameter |
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| 154 | REAL(r_std),PARAMETER :: pipe_k1 = 8.e3 |
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| 155 | !- |
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| 156 | ! Maximum tree establishment rate |
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| 157 | REAL(r_std),PARAMETER :: estab_max_tree = 0.12 |
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| 158 | ! Maximum grass establishment rate |
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| 159 | REAL(r_std),PARAMETER :: estab_max_grass = 0.12 |
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| 160 | ! initial density of individuals |
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| 161 | REAL(r_std),PARAMETER :: ind_0 = 0.02 |
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| 162 | !- |
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| 163 | ! Do we treat PFT expansion across a grid point after introduction? |
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| 164 | ! default = .FALSE. |
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| 165 | LOGICAL,SAVE :: treat_expansion = .FALSE. |
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| 166 | !- |
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| 167 | ! herbivores? |
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| 168 | LOGICAL,SAVE :: ok_herbivores = .FALSE. |
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| 169 | !- |
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| 170 | ! harvesting ? |
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| 171 | LOGICAL,SAVE :: harvest_agri = .TRUE. |
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| 172 | !- |
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| 173 | ! For trees, minimum fraction of crown area occupied |
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| 174 | ! (due to its branches etc.) |
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| 175 | ! This means that only a small fraction of its crown area |
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| 176 | ! can be invaded by other trees. |
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| 177 | REAL(r_std),PARAMETER :: min_cover = 0.05 |
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| 178 | !- |
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| 179 | ! climatic parameters |
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| 180 | !- |
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| 181 | ! minimum precip, in mm/year |
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| 182 | REAL(r_std),PARAMETER :: precip_crit = 100. |
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| 183 | ! minimum gdd for establishment of saplings |
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| 184 | REAL(r_std),PARAMETER :: gdd_crit = 150. |
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| 185 | ! critical fpc, needed for light competition and establishment |
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| 186 | REAL(r_std),PARAMETER :: fpc_crit = 0.95 |
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| 187 | !- |
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| 188 | ! critical value for being adapted (1-1/e) |
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| 189 | REAL(r_std),PARAMETER :: adapted_crit = 1. - ( 1. / euler ) |
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| 190 | ! critical value for being regenerative (1/e) |
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| 191 | REAL(r_std),PARAMETER :: regenerate_crit = 1. / euler |
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| 192 | !- |
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| 193 | ! fraction of GPP which is lost as growth respiration |
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| 194 | REAL(r_std),PARAMETER :: frac_growthresp = 0.28 |
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| 195 | !- |
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| 196 | ! radius of the Earth (m) |
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| 197 | REAL(r_std),PARAMETER :: R_Earth = 6378000. |
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| 198 | !- |
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| 199 | ! description of the PFT |
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| 200 | CHARACTER(len=34), SAVE, DIMENSION(nvm) :: PFT_name = & |
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| 201 | & (/ 'bared ground ', & ! 1 |
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| 202 | & 'tropical broad-leaved evergreen ', & ! 2 |
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| 203 | & 'tropical broad-leaved raingreen ', & ! 3 |
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| 204 | & 'temperate needleleaf evergreen ', & ! 4 |
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| 205 | & 'temperate broad-leaved evergreen ', & ! 5 |
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| 206 | & 'temperate broad-leaved summergreen', & ! 6 |
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| 207 | & 'boreal needleleaf evergreen ', & ! 7 |
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| 208 | & 'boreal broad-leaved summergreen', & ! 8 |
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| 209 | & 'boreal needleleaf summergreen', & ! 9 |
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| 210 | & ' C3 grass ', & ! 10 |
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| 211 | & ' C4 grass ', & ! 11 |
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| 212 | & ' C3 agriculture', & ! 12 |
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| 213 | & ' C4 agriculture' /) ! 13 |
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| 214 | ! extinction coefficient of the Monsi&Seaki (53) relationship |
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| 215 | REAL(r_std), SAVE, DIMENSION(nvm) :: ext_coeff |
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| 216 | ! is pft a tree |
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| 217 | LOGICAL, SAVE, DIMENSION(nvm) :: tree |
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| 218 | ! leaf type |
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| 219 | ! 1=broad leaved tree, 2=needle leaved tree, 3=grass 4=bared ground |
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| 220 | INTEGER(i_std), SAVE, DIMENSION(nvm) :: leaf_tab = & |
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| 221 | & (/ 4, 1, 1, 2, 1, 1, 2, & |
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| 222 | & 1, 2, 3, 3, 3, 3 /) |
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| 223 | ! natural? |
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| 224 | LOGICAL, SAVE, DIMENSION(nvm) :: natural = & |
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| 225 | & (/ .TRUE., .TRUE., .TRUE., .TRUE., .TRUE., .TRUE., .TRUE., & |
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| 226 | & .TRUE., .TRUE., .TRUE., .TRUE., .FALSE., .FALSE. /) |
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| 227 | ! flamability: critical fraction of water holding capacity |
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| 228 | REAL(r_std), SAVE, DIMENSION(nvm) :: flam |
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| 229 | ! fire resistance |
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| 230 | REAL(r_std), SAVE, DIMENSION(nvm) :: resist |
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| 231 | ! specific leaf area (m**2/gC) |
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| 232 | REAL(r_std), SAVE, DIMENSION(nvm) :: sla |
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| 233 | ! sapling biomass (gC/ind) |
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| 234 | REAL(r_std), SAVE, DIMENSION(nvm,nparts) :: bm_sapl |
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| 235 | ! migration speed (m/year) |
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| 236 | REAL(r_std), SAVE, DIMENSION(nvm) :: migrate |
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| 237 | ! maximum stem diameter from which on crown area no longer increases (m) |
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| 238 | REAL(r_std), SAVE, DIMENSION(nvm) :: maxdia |
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| 239 | ! crown of tree when sapling (m**2) |
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| 240 | REAL(r_std), SAVE, DIMENSION(nvm) :: cn_sapl |
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| 241 | ! critical minimum temperature (K) |
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| 242 | REAL(r_std), SAVE, DIMENSION(nvm) :: tmin_crit |
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| 243 | ! critical temperature of the coldest month (K) |
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| 244 | REAL(r_std), SAVE, DIMENSION(nvm) :: tcm_crit |
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| 245 | ! critical values for phenology |
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| 246 | TYPE(pheno_type),SAVE :: pheno_crit |
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| 247 | ! time constant for leaf age discretisation (d) |
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| 248 | REAL(r_std), SAVE, DIMENSION(nvm) :: leaf_timecst |
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| 249 | ! maximum LAI, PFT-specific |
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| 250 | REAL(r_std), SAVE, DIMENSION (nvm) :: lai_max |
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| 251 | |
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| 252 | ! maintenance respiration coefficient (g/g/day) at 0 deg C |
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| 253 | REAL(r_std), SAVE, DIMENSION(nvm,nparts) :: coeff_maint_zero |
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| 254 | ! slope of maintenance respiration coefficient (1/K, 1/K^2, 1/K^3) |
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| 255 | REAL(r_std), SAVE, DIMENSION(nvm,3) :: maint_resp_slope |
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| 256 | |
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| 257 | ! residence time (y) of trees |
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| 258 | REAL(r_std), SAVE, DIMENSION(nvm) :: residence_time |
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| 259 | |
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| 260 | ! leaf lifetime, tabulated |
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| 261 | REAL(r_std), SAVE, DIMENSION(nvm) :: leaflife_tab |
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| 262 | |
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| 263 | ! type of phenology |
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| 264 | ! 0=bared ground 1=evergreen, 2=summergreen, 3=raingreen, 4=perennial |
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| 265 | ! Pour l'instant, le phénotype de sol nu n'est pas géré aussi on traitera les sols nu comme "evergreen" |
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| 266 | INTEGER(i_std), SAVE, DIMENSION(nvm) :: pheno_type_tab |
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| 267 | |
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| 268 | ! critical tmin, tabulated (C) |
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| 269 | REAL(r_std), SAVE, DIMENSION(nvm) :: tmin_crit_tab |
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| 270 | |
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| 271 | ! critical tcm, tabulated (C) |
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| 272 | REAL(r_std), SAVE, DIMENSION(nvm) :: tcm_crit_tab |
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| 273 | |
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| 274 | ! critical gdd, tabulated (C), constant c of aT^2+bT+c |
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| 275 | REAL(r_std), SAVE, DIMENSION(nvm) :: gdd_crit1_tab |
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| 276 | |
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| 277 | ! critical gdd, tabulated (C), constant b of aT^2+bT+c |
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| 278 | REAL(r_std), SAVE, DIMENSION(nvm) :: gdd_crit2_tab |
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| 279 | |
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| 280 | ! critical gdd, tabulated (C), constant a of aT^2+bT+c |
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| 281 | REAL(r_std), SAVE, DIMENSION(nvm) :: gdd_crit3_tab |
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| 282 | |
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| 283 | ! critical ngd, tabulated. Threshold -5 degrees |
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| 284 | REAL(r_std), SAVE, DIMENSION(nvm) :: ngd_crit_tab |
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| 285 | |
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| 286 | ! critical temperature for the ncd vs. gdd function in phenology |
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| 287 | REAL(r_std), SAVE, DIMENSION(nvm) :: ncdgdd_temp_tab |
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| 288 | |
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| 289 | ! critical humidity (relative to min/max) for phenology |
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| 290 | REAL(r_std), SAVE, DIMENSION(nvm) :: hum_frac_tab |
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| 291 | |
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| 292 | ! minimum duration of dormance (d) for phenology |
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| 293 | REAL(r_std), SAVE, DIMENSION(nvm) :: lowgpp_time_tab |
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| 294 | |
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| 295 | ! minimum time elapsed since moisture minimum (d) |
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| 296 | REAL(r_std), SAVE, DIMENSION(nvm) :: hum_min_time_tab |
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| 297 | |
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| 298 | ! sapwood -> heartwood conversion time (d) |
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| 299 | REAL(r_std), SAVE, DIMENSION(nvm) :: tau_sap |
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| 300 | |
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| 301 | ! fruit lifetime (d) |
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| 302 | REAL(r_std), SAVE, DIMENSION(nvm) :: tau_fruit |
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| 303 | |
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| 304 | ! fraction of primary leaf and root allocation put into reserve |
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| 305 | REAL(r_std), SAVE, DIMENSION(nvm) :: ecureuil |
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| 306 | |
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| 307 | ! Maximum rate of carboxylation |
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| 308 | REAL(r_std), SAVE, DIMENSION(nvm) :: vcmax_opt |
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| 309 | |
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| 310 | ! Maximum rate of RUbp regeneration |
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| 311 | REAL(r_std), SAVE, DIMENSION(nvm) :: vjmax_opt |
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| 312 | |
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| 313 | !- |
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| 314 | ! constants needed for photosynthesis temperatures |
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| 315 | TYPE(t_photo_type), SAVE :: t_photo |
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| 316 | ! lenth of death of leaves, tabulated (d) |
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| 317 | REAL(r_std), SAVE, DIMENSION(nvm) :: leaffall_tab |
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| 318 | |
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| 319 | ! critical leaf age, tabulated (d) |
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| 320 | REAL(r_std), SAVE, DIMENSION(nvm) :: leafagecrit_tab |
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| 321 | |
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| 322 | ! which phenology model is used? (tabulated) |
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| 323 | CHARACTER(len=6), SAVE, DIMENSION(nvm) :: pheno_model_tab |
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| 324 | ! List of avaible phenology models : |
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| 325 | ! 'hum ', 'moi ', 'ncdgdd', 'ngd ', 'humgdd', 'moigdd', 'none ' |
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| 326 | |
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| 327 | ! type of senescence, tabulated |
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| 328 | CHARACTER(len=6), SAVE, DIMENSION(nvm) :: senescence_type_tab |
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| 329 | !- |
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| 330 | ! List of avaible types of senescence : |
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| 331 | ! 'cold ', 'dry ', 'mixed ', 'none ' |
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| 332 | |
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| 333 | ! critical temperature for senescence (C), |
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| 334 | ! constant c of aT^2+bT+c , tabulated |
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| 335 | REAL(r_std), SAVE, DIMENSION(nvm) :: senescence_temp1_tab |
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| 336 | |
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| 337 | ! critical temperature for senescence (C), |
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| 338 | ! constant b of aT^2+bT+c , tabulated |
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| 339 | REAL(r_std), SAVE, DIMENSION(nvm) :: senescence_temp2_tab |
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| 340 | |
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| 341 | ! critical temperature for senescence (C), |
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| 342 | ! constant a of aT^2+bT+c , tabulated |
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| 343 | REAL(r_std), SAVE, DIMENSION(nvm) :: senescence_temp3_tab |
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| 344 | |
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| 345 | ! critical relative moisture availability for senescence |
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| 346 | REAL(r_std), SAVE, DIMENSION(nvm) :: senescence_hum_tab |
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| 347 | |
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| 348 | ! relative moisture availability above which |
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| 349 | ! there is no humidity-related senescence |
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| 350 | REAL(r_std), SAVE, DIMENSION(nvm) :: nosenescence_hum_tab |
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| 351 | |
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| 352 | ! maximum turnover time for grasse |
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| 353 | REAL(r_std), SAVE, DIMENSION(nvm) :: max_turnover_time_tab |
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| 354 | |
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| 355 | ! minimum turnover time for grasse |
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| 356 | REAL(r_std), SAVE, DIMENSION(nvm) :: min_turnover_time_tab |
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| 357 | |
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| 358 | ! minimum leaf age to allow senescence g |
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| 359 | REAL(r_std), SAVE, DIMENSION(nvm) :: min_leaf_age_for_senescence_tab |
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| 360 | |
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| 361 | !- |
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| 362 | ! slope of maintenance respiration coefficient (1/K), |
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| 363 | ! constant c of aT^2+bT+c , tabulated |
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| 364 | REAL(r_std), SAVE, DIMENSION(nvm) :: maint_resp_slope1_tab |
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| 365 | |
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| 366 | ! slope of maintenance respiration coefficient (1/K), |
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| 367 | ! constant b of aT^2+bT+c , tabulated |
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| 368 | REAL(r_std), SAVE, DIMENSION(nvm) :: maint_resp_slope2_tab |
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| 369 | |
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| 370 | ! slope of maintenance respiration coefficient (1/K), |
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| 371 | ! constant a of aT^2+bT+c , tabulated |
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| 372 | REAL(r_std), SAVE, DIMENSION(nvm) :: maint_resp_slope3_tab |
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| 373 | |
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| 374 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
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| 375 | ! for leaves, tabulated |
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| 376 | REAL(r_std), SAVE, DIMENSION(nvm) :: cm_zero_leaf_tab |
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| 377 | |
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| 378 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
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| 379 | ! for sapwood above, tabulated |
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| 380 | REAL(r_std), SAVE, DIMENSION(nvm) :: cm_zero_sapabove_tab |
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| 381 | |
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| 382 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
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| 383 | ! for sapwood below, tabulated |
---|
| 384 | REAL(r_std), SAVE, DIMENSION(nvm) :: cm_zero_sapbelow_tab |
---|
| 385 | |
---|
| 386 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
---|
| 387 | ! for heartwood above, tabulated |
---|
| 388 | REAL(r_std), SAVE, DIMENSION(nvm) :: cm_zero_heartabove_tab |
---|
| 389 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
---|
| 390 | ! for heartwood below, tabulated |
---|
| 391 | REAL(r_std), SAVE, DIMENSION(nvm) :: cm_zero_heartbelow_tab |
---|
| 392 | |
---|
| 393 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
---|
| 394 | ! for roots, tabulated |
---|
| 395 | REAL(r_std), SAVE, DIMENSION(nvm) :: cm_zero_root_tab |
---|
| 396 | |
---|
| 397 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
---|
| 398 | ! for fruits, tabulated |
---|
| 399 | REAL(r_std), SAVE, DIMENSION(nvm) :: cm_zero_fruit_tab |
---|
| 400 | |
---|
| 401 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
---|
| 402 | ! for carbohydrate reserve, tabulated |
---|
| 403 | REAL(r_std), SAVE, DIMENSION(nvm) :: cm_zero_carbres_tab |
---|
| 404 | |
---|
| 405 | !- |
---|
| 406 | ! minimum photosynthesis temperature, |
---|
| 407 | ! constant a of ax^2+bx+c (deg C), tabulated |
---|
| 408 | REAL(r_std), SAVE, DIMENSION(nvm) :: tphoto_min_a_tab |
---|
| 409 | |
---|
| 410 | ! minimum photosynthesis temperature, |
---|
| 411 | ! constant b of ax^2+bx+c (deg C), tabulated |
---|
| 412 | REAL(r_std), SAVE, DIMENSION(nvm) :: tphoto_min_b_tab |
---|
| 413 | |
---|
| 414 | ! minimum photosynthesis temperature, |
---|
| 415 | ! constant c of ax^2+bx+c (deg C), tabulated |
---|
| 416 | REAL(r_std), SAVE, DIMENSION(nvm) :: tphoto_min_c_tab |
---|
| 417 | |
---|
| 418 | !- |
---|
| 419 | ! optimum photosynthesis temperature, |
---|
| 420 | ! constant a of ax^2+bx+c (deg C), tabulated |
---|
| 421 | |
---|
| 422 | REAL(r_std), SAVE, DIMENSION(nvm) :: tphoto_opt_a_tab |
---|
| 423 | |
---|
| 424 | ! optimum photosynthesis temperature, |
---|
| 425 | ! constant b of ax^2+bx+c (deg C), tabulated |
---|
| 426 | REAL(r_std), SAVE, DIMENSION(nvm) :: tphoto_opt_b_tab |
---|
| 427 | |
---|
| 428 | ! optimum photosynthesis temperature, |
---|
| 429 | ! constant c of ax^2+bx+c (deg C), tabulated |
---|
| 430 | REAL(r_std), SAVE, DIMENSION(nvm) :: tphoto_opt_c_tab |
---|
| 431 | |
---|
| 432 | !- |
---|
| 433 | ! maximum photosynthesis temperature, |
---|
| 434 | ! constant a of ax^2+bx+c (deg C), tabulated |
---|
| 435 | REAL(r_std), SAVE, DIMENSION(nvm) :: tphoto_max_a_tab |
---|
| 436 | |
---|
| 437 | ! maximum photosynthesis temperature, |
---|
| 438 | ! constant b of ax^2+bx+c (deg C), tabulated |
---|
| 439 | REAL(r_std), SAVE, DIMENSION(nvm) :: tphoto_max_b_tab |
---|
| 440 | |
---|
| 441 | ! maximum photosynthesis temperature, |
---|
| 442 | ! constant c of ax^2+bx+c (deg C), tabulated |
---|
| 443 | REAL(r_std), SAVE, DIMENSION(nvm) :: tphoto_max_c_tab |
---|
| 444 | |
---|
| 445 | ! NEW - allocation above/below = f(age) - 30/01/04 NV/JO/PF |
---|
| 446 | REAL(r_std), SAVE, DIMENSION(nvm) :: alloc_min |
---|
| 447 | REAL(r_std), SAVE, DIMENSION(nvm) :: alloc_max |
---|
| 448 | REAL(r_std), SAVE, DIMENSION(nvm) :: demi_alloc |
---|
| 449 | |
---|
| 450 | ! Coeff of biomass export for the year |
---|
| 451 | REAL(r_std), SAVE, DIMENSION(nvm) :: coeff_lcchange_1 |
---|
| 452 | |
---|
| 453 | ! Coeff of biomass export for the decade |
---|
| 454 | REAL(r_std), SAVE, DIMENSION(nvm) :: coeff_lcchange_10 |
---|
| 455 | |
---|
| 456 | ! Coeff of biomass export for the century |
---|
| 457 | REAL(r_std), SAVE, DIMENSION(nvm) :: coeff_lcchange_100 |
---|
| 458 | |
---|
| 459 | CONTAINS |
---|
| 460 | SUBROUTINE stomate_constants_init () |
---|
| 461 | ! flamability: critical fraction of water holding capacity |
---|
| 462 | flam(2:nvm) = & |
---|
| 463 | & (/ .15, .25, .25, .25, .25, .25, & |
---|
| 464 | .25, .25, .25, .25, .35, .35 /) |
---|
| 465 | !!$ flam(2:nvm) = & |
---|
| 466 | !!$ & (/ .25, .25, .25, .25, .25, .25, & |
---|
| 467 | !!$ .25, .25, .30, .30, .35, .35 /) |
---|
| 468 | ! flam = & |
---|
| 469 | ! & (/ .15, .15, .15, .15, .15, .15, & |
---|
| 470 | ! & .15, .15, .15, .15, .15, .15 /) |
---|
| 471 | ! fire resistance |
---|
| 472 | resist(2:nvm) = & |
---|
| 473 | & (/ .95, .90, .12, .50, .12, .12, & |
---|
| 474 | & .12, .12, .0, .0, .0, .0 /) |
---|
| 475 | !!$ resist(2:nvm) = & |
---|
| 476 | !!$ & (/ .12, .50, .12, .50, .12, .12, & |
---|
| 477 | !!$ & .12, .12, .0, .0, .0, .0 /) |
---|
| 478 | ! maximum LAI, PFT-specific |
---|
| 479 | lai_max(2:nvm) = & |
---|
| 480 | & (/ 7., 7., 5., 5., 5., 4.5, & |
---|
| 481 | & 4.5, 3.0, 2.5, 2.5, 5., 5. /) |
---|
| 482 | ! residence time (y) of trees |
---|
| 483 | residence_time(2:nvm) = & |
---|
| 484 | & (/ 30.0, 30.0, 40.0, 40.0, 40.0, 80.0, & |
---|
| 485 | & 80.0, 80.0, 0.0, 0.0, 0.0, 0.0 /) |
---|
| 486 | ! leaf lifetime, tabulated |
---|
| 487 | !SZ modif to LPJ values |
---|
| 488 | leaflife_tab(2:nvm) = & |
---|
| 489 | & (/ .5, 2., .33, 1., 2., .33, & |
---|
| 490 | & 2., 2., 2., 2., 2., 2. /) |
---|
| 491 | !!$ leaflife_tab(2:nvm) = & |
---|
| 492 | !!$ & (/ .5, 1., .5, .5, 1., .5, & |
---|
| 493 | !!$ & 1., 1., 1., 1., 1., 1. /) |
---|
| 494 | ! type of phenology |
---|
| 495 | ! 0=bared ground 1=evergreen, 2=summergreen, 3=raingreen, 4=perennial |
---|
| 496 | ! Pour l'instant, le phénotype de sol nu n'est pas géré aussi on traitera les sols nu comme "evergreen" |
---|
| 497 | pheno_type_tab(2:nvm) = & |
---|
| 498 | & (/ 1, 3, 1, 1, 2, 1, & |
---|
| 499 | & 2, 2, 4, 4, 2, 3 /) |
---|
| 500 | ! critical tmin, tabulated (C) |
---|
| 501 | tmin_crit_tab(2:nvm) = & |
---|
| 502 | & (/ 0.0, 0.0, -45.0, -10.0, -45.0, -60.0, & |
---|
| 503 | & -60.0, undef, undef, undef, undef, undef /) |
---|
| 504 | ! critical tcm, tabulated (C) |
---|
| 505 | tcm_crit_tab(2:nvm) = & |
---|
| 506 | & (/ undef, undef, 5.0, 15.5, 15.5, -2.0, & |
---|
| 507 | & 5.0, -2.0, undef, undef, undef, undef /) |
---|
| 508 | ! critical gdd, tabulated (C), constant c of aT^2+bT+c |
---|
| 509 | gdd_crit1_tab(2:nvm) = & |
---|
| 510 | & (/ undef, undef, undef, undef, undef, undef, & |
---|
| 511 | & undef, undef, 270., 400., 125., 400. /) |
---|
| 512 | !!$ gdd_crit1_tab(2:nvm) = & |
---|
| 513 | !!$ & (/ undef, undef, undef, undef, undef, undef, & |
---|
| 514 | !!$ & undef, undef, 184.375, 400., 125., 400. /) |
---|
| 515 | ! critical gdd, tabulated (C), constant b of aT^2+bT+c |
---|
| 516 | gdd_crit2_tab(2:nvm) = & |
---|
| 517 | & (/ undef, undef, undef, undef, undef, undef, & |
---|
| 518 | & undef, undef, 6.25, 0., 0., 0. /) |
---|
| 519 | ! critical gdd, tabulated (C), constant a of aT^2+bT+c |
---|
| 520 | gdd_crit3_tab(2:nvm) = & |
---|
| 521 | & (/ undef, undef, undef, undef, undef, undef, & |
---|
| 522 | & undef, undef, 0.03125, 0., 0., 0. /) |
---|
| 523 | ! critical ngd, tabulated. Threshold -5 degrees |
---|
| 524 | ngd_crit_tab(2:nvm) = & |
---|
| 525 | & (/ undef, undef, undef, undef, undef, undef, & |
---|
| 526 | & undef, 17., undef, undef, undef, undef /) |
---|
| 527 | ! critical temperature for the ncd vs. gdd function in phenology |
---|
| 528 | ncdgdd_temp_tab(2:nvm) = & |
---|
| 529 | & (/ undef, undef, undef, undef, 5., undef, & |
---|
| 530 | & 0., undef, undef, undef, undef, undef /) |
---|
| 531 | ! critical humidity (relative to min/max) for phenology |
---|
| 532 | hum_frac_tab(2:nvm) = & |
---|
| 533 | & (/ undef, .5, undef, undef, undef, undef, & |
---|
| 534 | & undef, undef, .5, .5, .5, .5 /) |
---|
| 535 | ! minimum duration of dormance (d) for phenology |
---|
| 536 | lowgpp_time_tab(2:nvm) = & |
---|
| 537 | & (/ undef, 30., undef, undef, 30., undef, & |
---|
| 538 | & 30., 30., 30., 30., 30., 30. /) |
---|
| 539 | ! minimum time elapsed since moisture minimum (d) |
---|
| 540 | hum_min_time_tab(2:nvm) = & |
---|
| 541 | & (/ undef, 50., undef, undef, undef, undef, & |
---|
| 542 | & undef, undef, 35., 35., 75., 75. /) |
---|
| 543 | ! sapwood -> heartwood conversion time (d) |
---|
| 544 | tau_sap(2:nvm) = & |
---|
| 545 | & (/ 730., 730., 730., 730., 730., 730., & |
---|
| 546 | & 730., 730., undef, undef, undef, undef /) |
---|
| 547 | ! fruit lifetime (d) |
---|
| 548 | tau_fruit(2:nvm) = & |
---|
| 549 | & (/ 90., 90., 90., 90., 90., 90., & |
---|
| 550 | & 90., 90., undef, undef, undef, undef /) |
---|
| 551 | ! fraction of primary leaf and root allocation put into reserve |
---|
| 552 | ecureuil(2:nvm) = & |
---|
| 553 | & (/ .0, 1., .0, .0, 1., .0, & |
---|
| 554 | & 1., 1., 1., 1., 1., 1. /) |
---|
| 555 | ! Maximum rate of carboxylation |
---|
| 556 | !Shilong |
---|
| 557 | vcmax_opt(2:nvm) = & |
---|
| 558 | & (/ 65., 65., 35., 45., 55., 35., & |
---|
| 559 | & 45., 35., 70., 70., 70., 70. /) |
---|
| 560 | CALL getin_p("vcmax_opt", vcmax_opt) |
---|
| 561 | ! 1.9.3 |
---|
| 562 | !!$ vcmax_opt(2:nvm) = & |
---|
| 563 | !!$ & (/ 65., 65., 35., 40., 55., 35., & |
---|
| 564 | !!$ & 45., 35., 70., 70., 70., 70. / |
---|
| 565 | ! OLD HEAD before 1.9.3 |
---|
| 566 | !!$ vcmax_opt(2:nvm) = & |
---|
| 567 | !!$ & (/ 65., 65., 35., 40., 55., 35., & |
---|
| 568 | !!$ & 45., 35., 80., 80., 100., 100. /) |
---|
| 569 | !modif jerome carbofor |
---|
| 570 | ! vcmax_opt = & |
---|
| 571 | ! & (/ 65., 65., 50., 40., 75., 35., & |
---|
| 572 | ! & 45., 35., 80., 80., 100., 100. /) |
---|
| 573 | !DATA vcmax_opt_tab / 0., 65., 65., 37.5, 45., 60., 37.5, & |
---|
| 574 | ! 50., 40., 100., 100., 100., 100. / |
---|
| 575 | !- |
---|
| 576 | ! Maximum rate of RUbp regeneration |
---|
| 577 | vjmax_opt(2:nvm) = & |
---|
| 578 | & (/ 130., 130., 70., 80., 110., 70., & |
---|
| 579 | & 90., 70., 160., 160., 200., 200. /) |
---|
| 580 | !- |
---|
| 581 | !DATA vjmax_opt_tab / 0., 130., 130., 75., 90., 120., 75., & |
---|
| 582 | ! 100., 80., 200., 200., 200., 200. / |
---|
| 583 | !- |
---|
| 584 | ! length of death of leaves, tabulated (d) |
---|
| 585 | leaffall_tab(2:nvm) = & |
---|
| 586 | & (/ undef, 10., undef, undef, 10., undef, & |
---|
| 587 | & 10., 10., 10., 10., 10., 10. /) |
---|
| 588 | ! critical leaf age, tabulated (d) |
---|
| 589 | ! Shilong modification |
---|
| 590 | leafagecrit_tab(2:nvm) = & |
---|
| 591 | & (/ 730., 180., 910., 730., 180., 910., & |
---|
| 592 | & 180., 180., 120., 120., 90., 90. /) |
---|
| 593 | ! OLD HEAD |
---|
| 594 | !!$ DATA leafagecrit_tab / 730., 180., 910., 730., 180., 910., & |
---|
| 595 | !!$ 180., 180., 120., 120., 120., 120. / |
---|
| 596 | !NEW SHILONG |
---|
| 597 | ! & (/ 730., 180., 910., 730., 180., 910., & |
---|
| 598 | ! & 180., 180., 120., 120., 70., 70. /) |
---|
| 599 | !- |
---|
| 600 | ! which phenology model is used? (tabulated) |
---|
| 601 | pheno_model_tab(1:nvm) = & |
---|
| 602 | & (/ 'none ', 'none ', 'moi ', 'none ', 'none ', & |
---|
| 603 | & 'ncdgdd', 'none ', 'ncdgdd', 'ngd ', 'moigdd', & |
---|
| 604 | & 'moigdd', 'moigdd', 'moigdd' /) |
---|
| 605 | ! List of avaible phenology models : |
---|
| 606 | ! 'hum ', 'moi ', 'ncdgdd', 'ngd ', 'humgdd', 'moigdd', 'none ' |
---|
| 607 | !- |
---|
| 608 | ! type of senescence, tabulated |
---|
| 609 | senescence_type_tab(1:nvm) = & |
---|
| 610 | & (/ 'none ', 'none ', 'dry ', 'none ', 'none ', & |
---|
| 611 | & 'cold ', 'none ', 'cold ', 'cold ', 'mixed ', & |
---|
| 612 | & 'mixed ', 'mixed ', 'mixed ' /) |
---|
| 613 | !- |
---|
| 614 | ! List of avaible types of senescence : |
---|
| 615 | ! 'cold ', 'dry ', 'mixed ', 'none ' |
---|
| 616 | !- |
---|
| 617 | ! critical temperature for senescence (C), |
---|
| 618 | ! constant c of aT^2+bT+c , tabulated |
---|
| 619 | senescence_temp1_tab(2:nvm) = & |
---|
| 620 | & (/ undef, undef, undef, undef, 12., undef, & |
---|
| 621 | & 7., 2., -1.375, 5., 5., 10. /) |
---|
| 622 | ! critical temperature for senescence (C), |
---|
| 623 | ! constant b of aT^2+bT+c , tabulated |
---|
| 624 | senescence_temp2_tab(2:nvm) = & |
---|
| 625 | & (/ undef, undef, undef, undef, 0., undef, & |
---|
| 626 | & 0., 0., .1, 0., 0., 0. /) |
---|
| 627 | ! critical temperature for senescence (C), |
---|
| 628 | ! constant a of aT^2+bT+c , tabulated |
---|
| 629 | senescence_temp3_tab(2:nvm) = & |
---|
| 630 | & (/ undef, undef, undef, undef, 0., undef, & |
---|
| 631 | & 0., 0., .00375, 0., 0., 0. /) |
---|
| 632 | ! critical relative moisture availability for senescence |
---|
| 633 | !SZ 080806, reparameterisation of TrBR: reduce criticial moisture from .6 to .3 |
---|
| 634 | ! to mimic a leaf dropping at -1.49 MPa, buffered to account for sechiba |
---|
| 635 | senescence_hum_tab(2:nvm) = & |
---|
| 636 | & (/ undef, .3, undef, undef, undef, undef, & |
---|
| 637 | & undef, undef, .2, .2, .3, .2 /) |
---|
| 638 | ! 1.9.3 |
---|
| 639 | !!$ senescence_hum_tab(2:nvm) = & |
---|
| 640 | !!$ & (/ undef, .6, undef, undef, undef, undef, & |
---|
| 641 | !!$ & undef, undef, .2, .2, .3, .2 /) |
---|
| 642 | ! relative moisture availability above which |
---|
| 643 | ! there is no humidity-related senescence |
---|
| 644 | !SZ 080806, reparameterisation of TrBR: reduce nosenencemoisture to avoid leaf dropping |
---|
| 645 | ! when phenology routine would give new flushing of leaves: 1.0 to 0.8 |
---|
| 646 | nosenescence_hum_tab(2:nvm) = & |
---|
| 647 | & (/ undef, .8, undef, undef, undef, undef, & |
---|
| 648 | & undef, undef, .3, .3, .3, .3 /) |
---|
| 649 | ! 1.9.3 |
---|
| 650 | !!$ nosenescence_hum_tab(2:nvm) = & |
---|
| 651 | !!$ & (/ undef, 1., undef, undef, undef, undef, & |
---|
| 652 | !!$ & undef, undef, .3, .3, .3, .3 /) |
---|
| 653 | |
---|
| 654 | ! maximum turnover time for grasse |
---|
| 655 | max_turnover_time_tab(2:nvm) = & |
---|
| 656 | & (/ undef, undef, undef, undef, undef, undef, & |
---|
| 657 | & undef, undef, 80., 80., 80., 80. /) |
---|
| 658 | ! minimum turnover time for grasse |
---|
| 659 | min_turnover_time_tab(2:nvm) = & |
---|
| 660 | & (/ undef, undef, undef, undef, undef, undef, & |
---|
| 661 | & undef, undef, 10., 10., 10., 10. /) |
---|
| 662 | ! minimum leaf age to allow senescence g |
---|
| 663 | min_leaf_age_for_senescence_tab(2:nvm) = & |
---|
| 664 | & (/ undef, 90., undef, undef, 90., undef, & |
---|
| 665 | & 60., 60., 30., 30., 30., 30. /) |
---|
| 666 | !- |
---|
| 667 | ! slope of maintenance respiration coefficient (1/K), |
---|
| 668 | ! constant c of aT^2+bT+c , tabulated |
---|
| 669 | !SZ - 1.9.3 |
---|
| 670 | maint_resp_slope1_tab(2:nvm) = & |
---|
| 671 | & (/ .12, .12, .16, .16, .16, .16, & |
---|
| 672 | & .16, .16, .16, .12, .16, .12 /) |
---|
| 673 | !OLD MERGE |
---|
| 674 | !!$ maint_resp_slope1_tab(2:nvm) = & |
---|
| 675 | !!$ & (/ .16, .16, .16, .16, .16, .16, & |
---|
| 676 | !!$ & .16, .16, .16, .12, .16, .16 /) |
---|
| 677 | !Shilong |
---|
| 678 | !!$ maint_resp_slope1_tab(2:nvm) = & |
---|
| 679 | !!$ & (/ .12, .12, .16, .16, .16, .16, & |
---|
| 680 | !!$ & .16, .16, .16, .16, .16, .16 /) |
---|
| 681 | !- |
---|
| 682 | ! slope of maintenance respiration coefficient (1/K), |
---|
| 683 | ! constant b of aT^2+bT+c , tabulated |
---|
| 684 | maint_resp_slope2_tab(2:nvm) = & |
---|
| 685 | & (/ .0, .0, .0, .0, .0, .0, & |
---|
| 686 | & .0, .0, -.00133, .0, -.00133, .0 /) |
---|
| 687 | ! DATA maint_resp_slope2_tab / .0, .0, .0, .0, .0, .0, .0, & |
---|
| 688 | ! .0, .0, .0, .0, .0, .0 / |
---|
| 689 | ! slope of maintenance respiration coefficient (1/K), |
---|
| 690 | ! constant a of aT^2+bT+c , tabulated |
---|
| 691 | maint_resp_slope3_tab(2:nvm) = & |
---|
| 692 | & (/ .0, .0, .0, .0, .0, .0, & |
---|
| 693 | & .0, .0, .0, .0, .0, .0 /) |
---|
| 694 | !- |
---|
| 695 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
---|
| 696 | ! for leaves, tabulated |
---|
| 697 | cm_zero_leaf_tab(2:nvm) = & |
---|
| 698 | & (/ 2.35E-3, 2.62E-3, 1.01E-3, 2.35E-3, 2.62E-3, 1.01E-3, & |
---|
| 699 | & 2.62E-3, 2.05E-3, 2.62E-3, 2.62E-3, 2.62E-3, 2.62E-3 /) |
---|
| 700 | !- |
---|
| 701 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
---|
| 702 | ! for sapwood above, tabulated |
---|
| 703 | cm_zero_sapabove_tab(2:nvm) = & |
---|
| 704 | & (/ 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, & |
---|
| 705 | & 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4 /) |
---|
| 706 | !- |
---|
| 707 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
---|
| 708 | ! for sapwood below, tabulated |
---|
| 709 | cm_zero_sapbelow_tab(2:nvm) = & |
---|
| 710 | & (/ 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, & |
---|
| 711 | & 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4 /) |
---|
| 712 | !- |
---|
| 713 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
---|
| 714 | ! for heartwood above, tabulated |
---|
| 715 | cm_zero_heartabove_tab(2:nvm) = & |
---|
| 716 | & (/ 0., 0., 0., 0., 0., 0., & |
---|
| 717 | & 0., 0., 0., 0., 0., 0. /) |
---|
| 718 | !- |
---|
| 719 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
---|
| 720 | ! for heartwood below, tabulated |
---|
| 721 | cm_zero_heartbelow_tab(2:nvm) = & |
---|
| 722 | & (/ 0., 0., 0., 0., 0., 0., & |
---|
| 723 | & 0., 0., 0., 0., 0., 0. /) |
---|
| 724 | !- |
---|
| 725 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
---|
| 726 | ! for roots, tabulated |
---|
| 727 | cm_zero_root_tab(2:nvm) = & |
---|
| 728 | & (/ 1.67E-3, 1.67E-3, 1.67E-3, 1.67E-3, 1.67E-3, 1.67E-3, & |
---|
| 729 | & 1.67E-3, 1.67E-3, 1.67E-3, 1.67E-3, 1.67E-3, 1.67E-3 /) |
---|
| 730 | !- |
---|
| 731 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
---|
| 732 | ! for fruits, tabulated |
---|
| 733 | cm_zero_fruit_tab(2:nvm) = & |
---|
| 734 | & (/ 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, & |
---|
| 735 | & 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4 /) |
---|
| 736 | !- |
---|
| 737 | ! maintenance respiration coefficient (g/g/day) at 0 deg C, |
---|
| 738 | ! for carbohydrate reserve, tabulated |
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| 739 | cm_zero_carbres_tab(2:nvm) = & |
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| 740 | & (/ 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, & |
---|
| 741 | & 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4, 1.19E-4 /) |
---|
| 742 | !- |
---|
| 743 | ! minimum photosynthesis temperature, |
---|
| 744 | ! constant a of ax^2+bx+c (deg C), tabulated |
---|
| 745 | tphoto_min_a_tab(2:nvm) = & |
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| 746 | & (/ 0., 0., 0., 0., 0., 0., & |
---|
| 747 | & 0., 0., 0.0025, 0., 0., 0. /) |
---|
| 748 | !- |
---|
| 749 | ! minimum photosynthesis temperature, |
---|
| 750 | ! constant b of ax^2+bx+c (deg C), tabulated |
---|
| 751 | tphoto_min_b_tab(2:nvm) = & |
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| 752 | & (/ 0., 0., 0., 0., 0., 0., & |
---|
| 753 | & 0., 0., 0.1, 0., 0., 0. /) |
---|
| 754 | !- |
---|
| 755 | ! minimum photosynthesis temperature, |
---|
| 756 | ! constant c of ax^2+bx+c (deg C), tabulated |
---|
| 757 | tphoto_min_c_tab(2:nvm) = & |
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| 758 | & (/ 2., 2., -4., -3., -2., -4., & |
---|
| 759 | & -4., -4., -3.25, 13., -5., 13. /) |
---|
| 760 | !- |
---|
| 761 | ! optimum photosynthesis temperature, |
---|
| 762 | ! constant a of ax^2+bx+c (deg C), tabulated |
---|
| 763 | tphoto_opt_a_tab(2:nvm) = & |
---|
| 764 | & (/ 0., 0., 0., 0., 0., 0., & |
---|
| 765 | 0., 0., 0.0025, 0., 0., 0. /) |
---|
| 766 | ! optimum photosynthesis temperature, |
---|
| 767 | ! constant b of ax^2+bx+c (deg C), tabulated |
---|
| 768 | tphoto_opt_b_tab(2:nvm) = & |
---|
| 769 | & (/ 0., 0., 0., 0., 0., 0., & |
---|
| 770 | & 0., 0., 0.25, 0., 0., 0. /) |
---|
| 771 | !- |
---|
| 772 | ! optimum photosynthesis temperature, |
---|
| 773 | ! constant c of ax^2+bx+c (deg C), tabulated |
---|
| 774 | tphoto_opt_c_tab(2:nvm) = & |
---|
| 775 | & (/ 37., 37., 25., 32., 26., 25., & |
---|
| 776 | & 25., 25., 27.25, 36., 30., 36. /) |
---|
| 777 | !- |
---|
| 778 | ! maximum photosynthesis temperature, |
---|
| 779 | ! constant a of ax^2+bx+c (deg C), tabulated |
---|
| 780 | tphoto_max_a_tab(2:nvm) = & |
---|
| 781 | & (/ 0., 0., 0., 0., 0., 0., & |
---|
| 782 | & 0., 0., 0.00375, 0., 0., 0. /) |
---|
| 783 | !- |
---|
| 784 | ! maximum photosynthesis temperature, |
---|
| 785 | ! constant b of ax^2+bx+c (deg C), tabulated |
---|
| 786 | tphoto_max_b_tab(2:nvm) = & |
---|
| 787 | & (/ 0., 0., 0., 0., 0., 0., & |
---|
| 788 | & 0., 0., 0.35, 0., 0., 0. /) |
---|
| 789 | !- |
---|
| 790 | ! maximum photosynthesis temperature, |
---|
| 791 | ! constant c of ax^2+bx+c (deg C), tabulated |
---|
| 792 | tphoto_max_c_tab(2:nvm) = & |
---|
| 793 | & (/ 55., 55., 38., 48., 38., 38., & |
---|
| 794 | & 38., 38., 41.125, 55., 45., 55. /) |
---|
| 795 | !- |
---|
| 796 | ! NEW - allocation above/below = f(age) - 30/01/04 NV/JO/PF |
---|
| 797 | alloc_min(2:nvm) = & |
---|
| 798 | & (/ 0.2, 0.2, 0.2, 0.2, 0.2, 0.2, & |
---|
| 799 | & 0.2, 0.2, undef, undef, undef, undef /) |
---|
| 800 | alloc_max(2:nvm) = & |
---|
| 801 | & (/ 0.8, 0.8, 0.8, 0.8, 0.8, 0.8, & |
---|
| 802 | & 0.8, 0.8, undef, undef, undef, undef /) |
---|
| 803 | demi_alloc(2:nvm) = & |
---|
| 804 | & (/ 5., 5., 5., 5., 5., 5., & |
---|
| 805 | & 5., 5., undef, undef, undef, undef /) |
---|
| 806 | |
---|
| 807 | ! Coeff of biomass export for the year |
---|
| 808 | coeff_lcchange_1(2:nvm) = & |
---|
| 809 | & (/ 0.597, 0.597, 0.597, 0.597, 0.597, 0.597, & |
---|
| 810 | & 0.597, 0.597, 0.597, 0.597, 0.597, 0.597 /) |
---|
| 811 | ! Coeff of biomass export for the decade |
---|
| 812 | coeff_lcchange_10(2:nvm) = & |
---|
| 813 | & (/ 0.403, 0.403, 0.299, 0.299, 0.299, 0.299, & |
---|
| 814 | & 0.299, 0.299, 0.299, 0.403, 0.299, 0.403 /) |
---|
| 815 | ! Coeff of biomass export for the century |
---|
| 816 | coeff_lcchange_100(2:nvm) = & |
---|
| 817 | & (/ 0., 0., 0.104, 0.104, 0.104, 0.104, & |
---|
| 818 | & 0.104, 0.104, 0.104, 0., 0.104, 0. /) |
---|
| 819 | |
---|
| 820 | END SUBROUTINE stomate_constants_init |
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| 821 | |
---|
| 822 | !--------------------------- |
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| 823 | END MODULE stomate_constants |
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