1 | ! ================================================================================================================================= |
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2 | ! MODULE : pft_parameters_var |
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3 | ! |
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4 | ! CONTACT : orchidee-help _at_ ipsl.jussieu.fr |
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5 | ! |
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6 | ! LICENCE : IPSL (2011) |
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7 | ! This software is governed by the CeCILL licence see ORCHIDEE/ORCHIDEE_CeCILL.LIC |
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8 | ! |
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9 | !>\BRIEF This module contains the variables in function of plant funtional type (pft). |
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10 | !! |
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11 | !!\n DESCRIPTION: This module contains the declarations for the externalized variables in function of the |
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12 | !! plant foncional type(pft). \n |
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13 | !! The module is already USE in module pft_parameters. Therefor no need to USE it seperatly except |
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14 | !! if the subroutines in module pft_parameters are not needed.\n |
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15 | !! |
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16 | !! RECENT CHANGE(S): None |
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17 | !! |
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18 | !! REFERENCE(S) : None |
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19 | !! |
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20 | !! SVN : |
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21 | !! $HeadURL: $ |
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22 | !! $Date$ |
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23 | !! $Revision$ |
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24 | !! \n |
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25 | !_ ================================================================================================================================ |
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26 | |
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27 | MODULE pft_parameters_var |
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28 | |
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29 | USE defprec |
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30 | |
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31 | IMPLICIT NONE |
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32 | |
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33 | |
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34 | ! |
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35 | ! PFT GLOBAL |
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36 | ! |
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37 | INTEGER(i_std), SAVE :: nvm = 13 !! Number of vegetation types (2-N, unitless) |
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38 | !$OMP THREADPRIVATE(nvm) |
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39 | |
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40 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: pft_to_mtc !! Table of conversion : we associate one pft to one metaclass |
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41 | !! (1-13, unitless) |
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42 | !$OMP THREADPRIVATE(pft_to_mtc) |
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43 | |
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44 | CHARACTER(LEN=34), ALLOCATABLE, SAVE, DIMENSION(:) :: PFT_name !! Description of the PFT (unitless) |
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45 | !$OMP THREADPRIVATE(PFT_name) |
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46 | |
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47 | LOGICAL, SAVE :: l_first_pft_parameters = .TRUE. !! To keep first call trace of the module (true/false) |
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48 | !$OMP THREADPRIVATE(l_first_pft_parameters) |
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49 | LOGICAL, SAVE :: ok_throughfall_by_pft = .FALSE. !! Flag to use the parameter PERCENT_THROUGHFALL_PFT (true/false) |
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50 | !$OMP THREADPRIVATE(ok_throughfall_by_pft) |
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51 | |
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52 | |
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53 | ! |
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54 | ! VEGETATION STRUCTURE |
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55 | ! |
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56 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: leaf_tab !! leaf type (1-4, unitless) |
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57 | !! 1=broad leaved tree, 2=needle leaved tree, |
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58 | !! 3=grass 4=bare ground |
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59 | !$OMP THREADPRIVATE(leaf_tab) |
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60 | |
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61 | CHARACTER(len=6), ALLOCATABLE, SAVE, DIMENSION(:) :: pheno_model !! which phenology model is used? (tabulated) (unitless) |
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62 | !$OMP THREADPRIVATE(pheno_model) |
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63 | |
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64 | LOGICAL, ALLOCATABLE, SAVE, DIMENSION(:) :: is_tree !! Is the vegetation type a tree ? (true/false) |
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65 | !$OMP THREADPRIVATE(is_tree) |
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66 | |
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67 | LOGICAL, ALLOCATABLE, SAVE, DIMENSION(:) :: is_deciduous !! Is PFT deciduous ? (true/false) |
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68 | !$OMP THREADPRIVATE(is_deciduous) |
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69 | |
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70 | LOGICAL, ALLOCATABLE, SAVE, DIMENSION(:) :: is_tropical !! Is PFT tropical ? (true/false) |
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71 | !$OMP THREADPRIVATE(is_tropical) |
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72 | |
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73 | LOGICAL, ALLOCATABLE, SAVE, DIMENSION(:) :: is_temperate !! Is PFT temperate ? (true/false) |
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74 | !$OMP THREADPRIVATE(is_temperate) |
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75 | |
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76 | LOGICAL, ALLOCATABLE, SAVE, DIMENSION(:) :: is_boreal !! Is PFT boreal ? (true/false) |
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77 | !$OMP THREADPRIVATE(is_boreal) |
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78 | |
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79 | LOGICAL, ALLOCATABLE, SAVE, DIMENSION(:) :: is_evergreen !! Is PFT evegreen ? (true/false) |
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80 | !$OMP THREADPRIVATE(is_evergreen) |
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81 | |
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82 | LOGICAL, ALLOCATABLE, SAVE, DIMENSION(:) :: is_needleleaf !! Is PFT needleleaf ? (true/false) |
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83 | !$OMP THREADPRIVATE(is_needleleaf) |
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84 | |
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85 | LOGICAL, ALLOCATABLE, SAVE, DIMENSION(:) :: natural !! natural? (true/false) |
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86 | !$OMP THREADPRIVATE(natural) |
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87 | |
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88 | CHARACTER(len=5), ALLOCATABLE, SAVE, DIMENSION(:) :: type_of_lai !! Type of behaviour of the LAI evolution algorithm |
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89 | !! for each vegetation type. |
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90 | !! Value of type_of_lai, one for each vegetation type : |
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91 | !! mean or interp |
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92 | !$OMP THREADPRIVATE(type_of_lai) |
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93 | |
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94 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: veget_ori_fixed_test_1 !! Value for veget_ori for tests in 0-dim simulations |
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95 | !! (0-1, unitless) |
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96 | !$OMP THREADPRIVATE(veget_ori_fixed_test_1) |
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97 | |
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98 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: llaimax !! laimax for maximum lai see also type of lai |
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99 | !! interpolation |
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100 | !! @tex $(m^2.m^{-2})$ @endtex |
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101 | !$OMP THREADPRIVATE(llaimax) |
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102 | |
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103 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: llaimin !! laimin for minimum lai see also type of lai |
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104 | !! interpolation |
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105 | !! @tex $(m^2.m^{-2})$ @endtex |
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106 | !$OMP THREADPRIVATE(llaimin) |
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107 | |
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108 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: height_presc !! prescribed height of vegetation.(m) Only used without stomate |
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109 | !! Value for height_presc : one for each vegetation type |
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110 | !$OMP THREADPRIVATE(height_presc) |
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111 | |
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112 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: rveg_pft !! Potentiometer to set vegetation resistance (unitless) |
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113 | !! Nathalie on March 28th, 2006 - from Fred Hourdin, |
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114 | !$OMP THREADPRIVATE(rveg_pft) |
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115 | |
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116 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: sla !! specif leaf area @tex $(m^2.gC^{-1})$ @endtex |
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117 | !$OMP THREADPRIVATE(sla) |
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118 | |
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119 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: lai_happy !! Lai threshold below which carbohydrate |
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120 | !! reserve may be used in functional allocation. |
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121 | !! Also used in phenology to see if mixed classes |
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122 | !! should die. These seem completely arbitrary. |
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123 | !! @tex $(m^2.m^{-2})$ @endtex |
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124 | !$OMP THREADPRIVATE(lai_happy) |
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125 | |
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126 | ! |
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127 | ! EVAPOTRANSPIRATION (sechiba) |
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128 | ! |
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129 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: rstruct_const !! Structural resistance. |
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130 | !! Value for rstruct_const : one for each vegetation type |
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131 | !! @tex $(s.m^{-1})$ @endtex |
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132 | !$OMP THREADPRIVATE(rstruct_const) |
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133 | |
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134 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: kzero !! A vegetation dependent constant used in the calculation |
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135 | !! of the surface resistance. |
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136 | !! Value for kzero one for each vegetation type |
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137 | !! @tex $(kg.m^2.s^{-1})$ @endtex |
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138 | !$OMP THREADPRIVATE(kzero) |
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139 | |
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140 | ! |
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141 | ! WATER (sechiba) |
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142 | ! |
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143 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: wmax_veg !! Volumetric available soil water capacity in each PFT |
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144 | !! @tex $(kg.m^{-3} of soil)$ @endtex |
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145 | !$OMP THREADPRIVATE(wmax_veg) |
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146 | |
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147 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: humcste !! Root profile description for the different vegetation types. |
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148 | !! These are the factor in the exponential which gets |
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149 | !! the root density as a function of depth |
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150 | !! @tex $(m^{-1})$ @endtex |
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151 | !$OMP THREADPRIVATE(humcste) |
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152 | |
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153 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: throughfall_by_pft !! Fraction of rain intercepted by the canopy (0-100, unitless) |
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154 | !$OMP THREADPRIVATE(throughfall_by_pft) |
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155 | |
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156 | ! |
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157 | ! ALBEDO (sechiba) |
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158 | ! |
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159 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: snowa_aged !! Minimum snow albedo value for each vegetation type |
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160 | !! after aging (dirty old snow) (unitless) |
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161 | !! Source : Values are from the Thesis of S. Chalita (1992) |
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162 | !$OMP THREADPRIVATE(snowa_aged) |
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163 | |
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164 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: snowa_dec !! Decay rate of snow albedo value for each vegetation type |
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165 | !! as it will be used in condveg_snow (unitless) |
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166 | !! Source : Values are from the Thesis of S. Chalita (1992) |
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167 | !$OMP THREADPRIVATE(snowa_dec) |
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168 | |
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169 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: alb_leaf_vis !! leaf albedo of vegetation type, visible albedo (unitless) |
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170 | !$OMP THREADPRIVATE(alb_leaf_vis) |
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171 | |
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172 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: alb_leaf_nir !! leaf albedo of vegetation type, near infrared albedo (unitless) |
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173 | !$OMP THREADPRIVATE(alb_leaf_nir) |
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174 | |
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175 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:,:) :: leaf_ssa !! leaf single scattering albedo of all |
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176 | !$OMP THREADPRIVATE(leaf_ssa) |
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177 | |
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178 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:,:) :: leaf_psd !! leaf prefered scattering direction of all |
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179 | !! vegetation types and spectra (unitless) |
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180 | !$OMP THREADPRIVATE(leaf_psd) |
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181 | |
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182 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:,:) :: bgd_reflectance !! background reflectance of all vegetation types and spectra (unitless) |
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183 | !$OMP THREADPRIVATE(bgd_reflectance) |
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184 | |
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185 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: leaf_to_shoot_clumping !! The clumping factor for leaves to shoots in the |
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186 | !! effective LAI calculation...notice this should be |
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187 | !! equal to unity for grasslands/croplands |
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188 | !$OMP THREADPRIVATE(leaf_to_shoot_clumping) |
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189 | |
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190 | |
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191 | !---add by YC ---a constant for tunning the LAI, which coupled with the atmosphere for the transpiaration |
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192 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: tune_coupled !! The coupled factor of LAI for the transpiration |
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193 | !$OMP THREADPRIVATE(tune_coupled) |
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194 | |
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195 | |
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196 | |
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197 | |
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198 | ! NOTE: this next variable originally was a plant-to-stand clumping factor to be used |
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199 | ! in describing how grasses and crops clump together at the plant level (but not trees, |
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200 | ! as their plant-to-stand clumping is calculated directly) to calculate abledo. However, we |
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201 | ! get the effective spectral parameters for the albedo calculation from inverting satelite data, |
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202 | ! which includes all clumping. Therefore we do not wish to account for this effect twice. |
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203 | ! What will be incorrect about our grassland and crop albedo is the lack of management options |
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204 | ! for these PFTs in ORCHIDEE, which will lead to LAI values which are wrong. Thus we |
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205 | ! will include an LAI correction factor in the calculation of the effective LAI which |
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206 | ! allows us to compensate for this via tuning. |
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207 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: lai_correction_factor !! see note above |
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208 | !$OMP THREADPRIVATE(lai_correction_factor) |
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209 | |
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210 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: min_level_sep !! This is used in determining the levels |
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211 | !! for photosynthesis. This is the thinnest |
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212 | !! that the levels are allowed to be, in |
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213 | !! vertical thickness. |
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214 | !! @tex $(m)$ @endtex |
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215 | !$OMP THREADPRIVATE(min_level_sep) |
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216 | |
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217 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: lai_top !! Diffuco.f90 calculates the stomatal conductance of the |
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218 | !! top layer of the canopy. Because the top layer can contain |
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219 | !! different amounts of LAI depending on the crown diameter |
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220 | !! we had to define top layer in terms of the LAI it contains. |
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221 | !! stomatal conductance in the top layer contributes to the |
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222 | !! transpiration (m2 m-2). Arbitrary values. |
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223 | !$OMP THREADPRIVATE(lai_top) |
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224 | |
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225 | |
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226 | |
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227 | ! |
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228 | ! SOIL - VEGETATION |
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229 | ! |
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230 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: pref_soil_veg !! Table which contains the correlation between the soil |
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231 | !! types and vegetation type. Two modes exist : |
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232 | !! 1) pref_soil_veg = 0 then we have an equidistribution |
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233 | !! of vegetation on soil types |
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234 | !! 2) Else for each pft the prefered soil type is given : |
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235 | !! 1=sand, 2=loan, 3=clay |
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236 | !! This variable is initialized in slowproc.(1-3, unitless) |
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237 | !$OMP THREADPRIVATE(pref_soil_veg) |
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238 | |
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239 | ! |
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240 | ! PHOTOSYNTHESIS |
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241 | ! |
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242 | !- |
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243 | ! 1. CO2 |
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244 | !- |
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245 | LOGICAL, ALLOCATABLE, SAVE, DIMENSION(:) :: is_c4 !! flag for C4 vegetation types (true/false) |
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246 | !$OMP THREADPRIVATE(is_c4) |
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247 | |
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248 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: vcmax_fix !! values used for vcmax when STOMATE is not activated |
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249 | !! @tex $(\mu mol.m^{-2}.s^{-1})$ @endtex |
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250 | !$OMP THREADPRIVATE(vcmax_fix) |
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251 | |
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252 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: vjmax_fix !! values used for vjmax when STOMATE is not activated |
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253 | !! @tex $(\mu mol.m^{-2}.s^{-1})$ @endtex |
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254 | !$OMP THREADPRIVATE(vjmax_fix) |
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255 | |
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256 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: co2_tmin_fix !! values used for photosynthesis tmin when STOMATE |
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257 | !! is not activated (C) |
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258 | !$OMP THREADPRIVATE(co2_tmin_fix) |
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259 | |
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260 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: co2_topt_fix !! values used for photosynthesis topt when STOMATE |
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261 | !! is not activated (C) |
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262 | !$OMP THREADPRIVATE(co2_topt_fix) |
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263 | |
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264 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: co2_tmax_fix !! values used for photosynthesis tmax when STOMATE |
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265 | !! is not activated (C) |
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266 | !$OMP THREADPRIVATE(co2_tmax_fix) |
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267 | |
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268 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: downregulation_co2_coeff !! Coefficient for CO2 downregulation (unitless) |
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269 | !$OMP THREADPRIVATE(downregulation_co2_coeff) |
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270 | |
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271 | |
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272 | !- |
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273 | ! 2. Stomate |
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274 | !- |
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275 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: ext_coeff !! extinction coefficient of the Monsi&Saeki relationship (1953) |
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276 | !! (unitless) |
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277 | !$OMP THREADPRIVATE(ext_coeff) |
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278 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: E_KmC !! Energy of activation for KmC (J mol-1) |
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279 | !$OMP THREADPRIVATE(E_KmC) |
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280 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: E_KmO !! Energy of activation for KmO (J mol-1) |
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281 | !$OMP THREADPRIVATE(E_KmO) |
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282 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: E_gamma_star !! Energy of activation for gamma_star (J mol-1) |
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283 | !$OMP THREADPRIVATE(E_gamma_star) |
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284 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: E_Vcmax !! Energy of activation for Vcmax (J mol-1) |
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285 | !$OMP THREADPRIVATE(E_Vcmax) |
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286 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: E_Jmax !! Energy of activation for Jmax (J mol-1) |
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287 | !$OMP THREADPRIVATE(E_Jmax) |
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288 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: aSV !! a coefficient of the linear regression (a+bT) defining the Entropy term for Vcmax (J K-1 mol-1) |
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289 | !$OMP THREADPRIVATE(aSV) |
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290 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: bSV !! b coefficient of the linear regression (a+bT) defining the Entropy term for Vcmax (J K-1 mol-1 °C-1) |
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291 | !$OMP THREADPRIVATE(bSV) |
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292 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: tphoto_min !! minimum photosynthesis temperature (deg C) |
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293 | !$OMP THREADPRIVATE(tphoto_min) |
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294 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: tphoto_max !! maximum photosynthesis temperature (deg C) |
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295 | !$OMP THREADPRIVATE(tphoto_max) |
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296 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: aSJ !! a coefficient of the linear regression (a+bT) defining the Entropy term for Jmax (J K-1 mol-1) |
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297 | !$OMP THREADPRIVATE(aSJ) |
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298 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: bSJ !! b coefficient of the linear regression (a+bT) defining the Entropy term for Jmax (J K-1 mol-1 °C-1) |
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299 | !$OMP THREADPRIVATE(bSJ) |
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300 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: D_Vcmax !! Energy of deactivation for Vcmax (J mol-1) |
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301 | !$OMP THREADPRIVATE(D_Vcmax) |
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302 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: D_Jmax !! Energy of deactivation for Jmax (J mol-1) |
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303 | !$OMP THREADPRIVATE(D_Jmax) |
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304 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: E_Rd !! Energy of activation for Rd (J mol-1) |
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305 | !$OMP THREADPRIVATE(E_Rd) |
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306 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: Vcmax25 !! Maximum rate of Rubisco activity-limited carboxylation at 25°C |
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307 | !! @tex $(\mu mol.m^{-2}.s^{-1})$ @endtex |
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308 | !$OMP THREADPRIVATE(Vcmax25) |
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309 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: arJV !! a coefficient of the linear regression (a+bT) defining the Jmax25/Vcmax25 ratio (mu mol e- (mu mol CO2)-1) |
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310 | !$OMP THREADPRIVATE(arJV) |
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311 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: brJV !! b coefficient of the linear regression (a+bT) defining the Jmax25/Vcmax25 ratio (mu mol e- (mu mol CO2)-1) |
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312 | !$OMP THREADPRIVATE(brJV) |
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313 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: KmC25 !! MichaelisâMenten constant of Rubisco for CO2 at 25°C (ubar) |
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314 | !$OMP THREADPRIVATE(KmC25) |
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315 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: KmO25 !! MichaelisâMenten constant of Rubisco for O2 at 25°C (ubar) |
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316 | !$OMP THREADPRIVATE(KmO25) |
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317 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: gamma_star25 !! Ci-based CO2 compensation point in the absence of Rd at 25°C (ubar) |
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318 | !$OMP THREADPRIVATE(gamma_star25) |
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319 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: a1 !! Empirical factor involved in the calculation of fvpd (-) |
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320 | !$OMP THREADPRIVATE(a1) |
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321 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: b1 !! Empirical factor involved in the calculation of fvpd (-) |
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322 | !$OMP THREADPRIVATE(b1) |
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323 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: g0 !! Residual stomatal conductance when irradiance approaches zero (mol mâ2 sâ1 barâ1) |
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324 | !$OMP THREADPRIVATE(g0) |
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325 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: h_protons !! Number of protons required to produce one ATP (mol mol-1) |
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326 | !$OMP THREADPRIVATE(h_protons) |
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327 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: fpsir !! Fraction of PSII eâ transport rate partitioned to the C4 cycle (-) |
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328 | !$OMP THREADPRIVATE(fpsir) |
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329 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: fQ !! Fraction of electrons at reduced plastoquinone that follow the Q-cycle (-) - Values for C3 platns are not used |
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330 | !$OMP THREADPRIVATE(fQ) |
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331 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: fpseudo !! Fraction of electrons at PSI that follow pseudocyclic transport (-) - Values for C3 platns are not used |
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332 | !$OMP THREADPRIVATE(fpseudo) |
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333 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: kp !! Initial carboxylation efficiency of the PEP carboxylase (mol mâ2 sâ1 barâ1) |
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334 | !$OMP THREADPRIVATE(kp) |
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335 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: alpha !! Fraction of PSII activity in the bundle sheath (-) |
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336 | !$OMP THREADPRIVATE(alpha) |
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337 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: gbs !! Bundle-sheath conductance (mol mâ2 sâ1 barâ1) |
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338 | !$OMP THREADPRIVATE(gbs) |
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339 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: theta !! Convexity factor for response of J to irradiance (-) |
---|
340 | !$OMP THREADPRIVATE(theta) |
---|
341 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: alpha_LL !! Conversion efficiency of absorbed light into J at strictly limiting light (mol eâ (mol photon)â1) |
---|
342 | !$OMP THREADPRIVATE(alpha_LL) |
---|
343 | |
---|
344 | ! |
---|
345 | ! ALLOCATION (stomate) |
---|
346 | ! |
---|
347 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: R0 !! Default root allocation (0-1, unitless) |
---|
348 | !$OMP THREADPRIVATE(R0) |
---|
349 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: S0 !! Default sapwood allocation (0-1, unitless) |
---|
350 | !$OMP THREADPRIVATE(S0) |
---|
351 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: L0 !! Default leaf allocation (0-1, unitless) |
---|
352 | !$OMP THREADPRIVATE(L0) |
---|
353 | |
---|
354 | |
---|
355 | ! |
---|
356 | ! RESPIRATION (stomate) |
---|
357 | ! |
---|
358 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:,:) :: maint_resp_slope !! slope of maintenance respiration coefficient |
---|
359 | !! (1/K, 1/K^2, 1/K^3), used in the code |
---|
360 | !$OMP THREADPRIVATE(maint_resp_slope) |
---|
361 | |
---|
362 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: maint_resp_slope_c !! slope of maintenance respiration coefficient (1/K), |
---|
363 | !! constant c of aT^2+bT+c , tabulated |
---|
364 | !$OMP THREADPRIVATE(maint_resp_slope_c) |
---|
365 | |
---|
366 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: maint_resp_slope_b !! slope of maintenance respiration coefficient (1/K), |
---|
367 | !! constant b of aT^2+bT+c , tabulated |
---|
368 | !$OMP THREADPRIVATE(maint_resp_slope_b) |
---|
369 | |
---|
370 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: maint_resp_slope_a !! slope of maintenance respiration coefficient (1/K), |
---|
371 | !! constant a of aT^2+bT+c , tabulated |
---|
372 | !$OMP THREADPRIVATE(maint_resp_slope_a) |
---|
373 | |
---|
374 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:,:) :: coeff_maint_zero !! maintenance respiration coefficient at 0 deg C, |
---|
375 | !! @tex $(gC.gC^{-1}.day^{-1})$ @endtex |
---|
376 | !$OMP THREADPRIVATE(coeff_maint_zero) |
---|
377 | |
---|
378 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: cm_zero_leaf !! maintenance respiration coefficient at 0 deg C, |
---|
379 | !! for leaves, tabulated |
---|
380 | !! @tex $(gC.gC^{-1}.day^{-1})$ @endtex |
---|
381 | !$OMP THREADPRIVATE(cm_zero_leaf) |
---|
382 | |
---|
383 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: cm_zero_sapabove !! maintenance respiration coefficient at 0 deg C, |
---|
384 | !! for sapwood above, tabulated |
---|
385 | !! @tex $(gC.gC^{-1}.day^{-1})$ @endtex |
---|
386 | !$OMP THREADPRIVATE(cm_zero_sapabove) |
---|
387 | |
---|
388 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: cm_zero_sapbelow !! maintenance respiration coefficient at 0 deg C, |
---|
389 | !! for sapwood below, tabulated |
---|
390 | !! @tex $(gC.gC^{-1}.day^{-1})$ @endtex |
---|
391 | !$OMP THREADPRIVATE(cm_zero_sapbelow) |
---|
392 | |
---|
393 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: cm_zero_heartabove !! maintenance respiration coefficient at 0 deg C |
---|
394 | !! for heartwood above, tabulated |
---|
395 | !! @tex $(gC.gC^{-1}.day^{-1})$ @endtex |
---|
396 | !$OMP THREADPRIVATE(cm_zero_heartabove) |
---|
397 | |
---|
398 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: cm_zero_heartbelow !! maintenance respiration coefficient at 0 deg C, |
---|
399 | !! for heartwood below, tabulated |
---|
400 | !! @tex $(gC.gC^{-1}.day^{-1})$ @endtex |
---|
401 | !$OMP THREADPRIVATE(cm_zero_heartbelow) |
---|
402 | |
---|
403 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: cm_zero_root !! maintenance respiration coefficient at 0 deg C, |
---|
404 | !! for roots, tabulated |
---|
405 | !! @tex $(gC.gC^{-1}.day^{-1})$ @endtex |
---|
406 | !$OMP THREADPRIVATE(cm_zero_root) |
---|
407 | |
---|
408 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: cm_zero_fruit !! maintenance respiration coefficient at 0 deg C, |
---|
409 | !! for fruits, tabulated |
---|
410 | !! @tex $(gC.gC^{-1}.day^{-1})$ @endtex |
---|
411 | !$OMP THREADPRIVATE(cm_zero_fruit) |
---|
412 | |
---|
413 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: cm_zero_carbres !! maintenance respiration coefficient at 0 deg C, |
---|
414 | !! for carbohydrate reserve, tabulated |
---|
415 | !! @tex $(gC.gC^{-1}.day^{-1})$ @endtex |
---|
416 | !$OMP THREADPRIVATE(cm_zero_carbres) |
---|
417 | |
---|
418 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: cm_zero_labile !! maintenance respiration coefficient at 0 deg C, |
---|
419 | !! for the labile pool, tabulated |
---|
420 | !! @tex $(gC.gC^{-1}.day^{-1})$ @endtex |
---|
421 | !$OMP THREADPRIVATE(cm_zero_labile) |
---|
422 | |
---|
423 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: coeff_maint_init !! initial value for maintenance respiration |
---|
424 | !! coefficient at 0 deg C used in functional allocation |
---|
425 | !! @tex $(gC.gC^{-1}.day^{-1})$ @endtex |
---|
426 | !$OMP THREADPRIVATE(coeff_maint_init) |
---|
427 | |
---|
428 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: frac_growthresp !! Fraction of growth respiration expressed as |
---|
429 | !! share of the total C that is to be allocated |
---|
430 | !! (0-1). |
---|
431 | !$OMP THREADPRIVATE(frac_growthresp) |
---|
432 | |
---|
433 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: labile_reserve !! The size of the labile pool as a fraction of the |
---|
434 | !! weekly gpp (-). For example, 3 indicates that the |
---|
435 | !! is 3 times the weekly gpp. |
---|
436 | !$OMP THREADPRIVATE(labile_reserve) |
---|
437 | |
---|
438 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: deciduous_reserve !! Fraction of sapwood mass stored in the reserve pool of deciduous |
---|
439 | !! trees during the growing season (unitless, 0-1) |
---|
440 | |
---|
441 | !$OMP THREADPRIVATE(deciduous_reserve) |
---|
442 | |
---|
443 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: evergreen_reserve !! Fraction of sapwood mass stored in the reserve pool of evergreen |
---|
444 | !! trees (unitless, 0-1) |
---|
445 | |
---|
446 | !$OMP THREADPRIVATE(evergreen_reserve) |
---|
447 | |
---|
448 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: senescense_reserve !! Fraction of sapwood mass stored in the reserve pool of deciduous |
---|
449 | !! trees during senescense(unitless, 0-1) |
---|
450 | |
---|
451 | !$OMP THREADPRIVATE(senescense_reserve) |
---|
452 | |
---|
453 | ! |
---|
454 | ! STAND STRUCTURE (stomate) |
---|
455 | ! |
---|
456 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: pipe_density !! Wood density in @tex $(gC.m^{-3})$ @endtex |
---|
457 | !$OMP THREADPRIVATE(pipe_density) |
---|
458 | |
---|
459 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: pipe_tune1 !! crown area = pipe_tune1*stem diameter**pipe_tune_exp_coeff |
---|
460 | !$OMP THREADPRIVATE(pipe_tune1) |
---|
461 | |
---|
462 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: pipe_tune2 !! height=pipe_tune2 * diameter**pipe_tune3 |
---|
463 | !$OMP THREADPRIVATE(pipe_tune2) |
---|
464 | |
---|
465 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: tree_ff !! Volume reduction factor from cylinder to real tree shape (inc.branches) |
---|
466 | !$OMP THREADPRIVATE(tree_ff) |
---|
467 | |
---|
468 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: pipe_tune3 !! height=pipe_tune2 * diameter**pipe_tune3 |
---|
469 | !$OMP THREADPRIVATE(pipe_tune3) |
---|
470 | |
---|
471 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: pipe_tune4 !! ???needed for stem diameter |
---|
472 | !$OMP THREADPRIVATE(pipe_tune4) |
---|
473 | |
---|
474 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: pipe_k1 !! ??? |
---|
475 | !$OMP THREADPRIVATE(pipe_k1) |
---|
476 | |
---|
477 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: pipe_tune_exp_coeff !! crown area = pipe_tune1*stem diameter**pipe_tune_exp_coeff |
---|
478 | !$OMP THREADPRIVATE(pipe_tune_exp_coeff) |
---|
479 | |
---|
480 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: mass_ratio_heart_sap!! mass ratio (heartwood+sapwood)/heartwood |
---|
481 | !$OMP THREADPRIVATE(mass_ratio_heart_sap) |
---|
482 | |
---|
483 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: lai_to_height !! Covert lai into vegetation height for grasses and crops |
---|
484 | !$OMP THREADPRIVATE(lai_to_height) |
---|
485 | |
---|
486 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: canopy_cover !! Canopy cover - current values are guesses for testing |
---|
487 | !! could tune this variable to match MODIS albedo |
---|
488 | !$OMP THREADPRIVATE(canopy_cover) |
---|
489 | |
---|
490 | |
---|
491 | ! |
---|
492 | ! GROWTH (resource limitation - stomate) |
---|
493 | ! |
---|
494 | |
---|
495 | ! |
---|
496 | ! GROWTH (functional allocation - stomate) |
---|
497 | ! |
---|
498 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: cn_leaf_prescribed !! CN of foliage for allocation, according to stich et al 2003 |
---|
499 | !$OMP THREADPRIVATE(cn_leaf_prescribed) |
---|
500 | |
---|
501 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: fcn_wood !! CN of wood for allocation, relative to leaf CN according |
---|
502 | !! to stich et al 2003 |
---|
503 | !$OMP THREADPRIVATE(fcn_wood) |
---|
504 | |
---|
505 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: fcn_root !! CN of roots for allocation, relative to leaf CN according |
---|
506 | !! to stich et al 2003 |
---|
507 | !$OMP THREADPRIVATE(fcn_root) |
---|
508 | |
---|
509 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: k_latosa_max !! Maximum leaf-to-sapwood area ratio (unitless) |
---|
510 | !$OMP THREADPRIVATE(k_latosa_max) |
---|
511 | |
---|
512 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: k_latosa_min !! Minimum leaf-to-sapwood area ratio (unitless) |
---|
513 | !$OMP THREADPRIVATE(k_latosa_min) |
---|
514 | |
---|
515 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: fruit_alloc !! Fraction of biomass allocated to fruit production (0-1) |
---|
516 | |
---|
517 | !$OMP THREADPRIVATE(fruit_alloc) |
---|
518 | |
---|
519 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: m_dv !! Parameter in the Deleuze & Dhote allocation rule that |
---|
520 | !! relaxes the cut-off imposed by ::sigma. Owing to m_relax |
---|
521 | !! trees still grow a little when their ::circ is below |
---|
522 | !! ::sigma |
---|
523 | !$OMP THREADPRIVATE(m_dv) |
---|
524 | |
---|
525 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: lai_max_to_happy !! Multiplicative factor of lai_max that determines |
---|
526 | !! the threshold value of LAI below which the carbohydrate |
---|
527 | !! reserve is used. |
---|
528 | |
---|
529 | !$OMP THREADPRIVATE(lai_max_to_happy) |
---|
530 | |
---|
531 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: k_root !! Fine root specific conductivity |
---|
532 | !! @tex $(m^{3} kg^{-1} s^{-1} MPa^{-1})$ @endtex |
---|
533 | !$OMP THREADPRIVATE(k_root) |
---|
534 | |
---|
535 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: k_sap !! Sapwood specific conductivity |
---|
536 | !! @tex $(m^{3} kg^{-1} s^{-1} MPa^{-1})$ @endtex |
---|
537 | !$OMP THREADPRIVATE(k_sap) |
---|
538 | |
---|
539 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: k_leaf !! Leaf conductivity @tex $(m s^{-1} MPa^{-1})$ @endtex |
---|
540 | !$OMP THREADPRIVATE(k_leaf) |
---|
541 | |
---|
542 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: phi_leaf !! Minimal leaf water potential @tex $(m s^{-1} MPa^{-1})$ @endtex |
---|
543 | !$OMP THREADPRIVATE(phi_leaf) |
---|
544 | |
---|
545 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: phi_50 !! Sapwood leaf water potential that causes 50% loss of xylem |
---|
546 | !! conductivity through cavitation @tex $(m s^{-1} MPa^{-1})$ @endtex |
---|
547 | !$OMP THREADPRIVATE(phi_50) |
---|
548 | |
---|
549 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: c_cavitation !! Shape parameter for loss of conductance Machado & Tyree, 1994 (unitless) |
---|
550 | !$OMP THREADPRIVATE(c_cavitation) |
---|
551 | |
---|
552 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: phi_soil_tune !! Additive tuning parameter to account for soil-root interaction |
---|
553 | !! @tex $(MPa)$ @endtex |
---|
554 | !$OMP THREADPRIVATE(phi_soil_tune) |
---|
555 | |
---|
556 | ! |
---|
557 | ! PRESCRIBE (stomate) |
---|
558 | ! |
---|
559 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: tune_reserves_in_sapling !! A factor to scale the reserve pool of newly |
---|
560 | !! planted saplings. This is required by some deciduous |
---|
561 | !! trees in order to survive the first year until budburst, |
---|
562 | !! but it has no physical basis. |
---|
563 | !! (unitless) |
---|
564 | |
---|
565 | !$OMP THREADPRIVATE(tune_reserves_in_sapling) |
---|
566 | |
---|
567 | ! |
---|
568 | ! MORTALITY (stomate) |
---|
569 | ! |
---|
570 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) & |
---|
571 | :: death_distribution_factor !! The scale factor between the smallest and largest |
---|
572 | !! circ class for tree mortality in lpj_kill. |
---|
573 | !! (unitless) |
---|
574 | !$OMP THREADPRIVATE(death_distribution_factor) |
---|
575 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) & |
---|
576 | :: npp_reset_value !! The value of the NPP that the long-term value is |
---|
577 | !! reset to after a PFT dies in stomate_kill. This |
---|
578 | !! only seems to be used for non-trees. |
---|
579 | !! @tex $(gC m^{-2})$ @endtex |
---|
580 | !$OMP THREADPRIVATE(npp_reset_value) |
---|
581 | |
---|
582 | ! |
---|
583 | ! WINDFALL (stomate_windfall) |
---|
584 | ! |
---|
585 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: streamlining_c_leaf !! Modulus of Rupture (Pa) |
---|
586 | !$OMP THREADPRIVATE(streamlining_c_leaf) |
---|
587 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: streamlining_c_leafless !! Modulus of Rupture (Pa) |
---|
588 | !$OMP THREADPRIVATE(streamlining_c_leafless) |
---|
589 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: streamlining_n_leaf !! Modulus of Rupture (Pa) |
---|
590 | !$OMP THREADPRIVATE(streamlining_n_leaf) |
---|
591 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: streamlining_n_leafless !! Modulus of Rupture (Pa) |
---|
592 | !$OMP THREADPRIVATE(streamlining_n_leafless) |
---|
593 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: streamlining_rb_leaf !! Modulus of Rupture (Pa) |
---|
594 | !$OMP THREADPRIVATE(streamlining_rb_leaf) |
---|
595 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: streamlining_rb_leafless !! Modulus of Rupture (Pa) |
---|
596 | !$OMP THREADPRIVATE(streamlining_rb_leafless) |
---|
597 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: canopy_density_leaf !! Modulus of Rupture (Pa) |
---|
598 | !$OMP THREADPRIVATE(canopy_density_leaf) |
---|
599 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: canopy_density_leafless !! Modulus of Rupture (Pa) |
---|
600 | !$OMP THREADPRIVATE(canopy_density_leafless) |
---|
601 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: intercept_breadth !! Modulus of Rupture (Pa) |
---|
602 | !$OMP THREADPRIVATE(intercept_breadth) |
---|
603 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: slope_breadth !! Modulus of Rupture (Pa) |
---|
604 | !$OMP THREADPRIVATE(slope_breadth) |
---|
605 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: intercept_depth !! Modulus of Rupture (Pa) |
---|
606 | !$OMP THREADPRIVATE(intercept_depth) |
---|
607 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: slope_depth !! Modulus of Rupture (Pa) |
---|
608 | !$OMP THREADPRIVATE(slope_depth) |
---|
609 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: green_density !! Modulus of Rupture (Pa) |
---|
610 | !$OMP THREADPRIVATE(green_density) |
---|
611 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: modulus_rupture !! Modulus of Rupture (Pa) |
---|
612 | !$OMP THREADPRIVATE(modulus_rupture) |
---|
613 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: f_knot !! Modulus of Rupture (Pa) |
---|
614 | !$OMP THREADPRIVATE(f_knot) |
---|
615 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_free_draining_shallow !! Modulus of Rupture (Pa) |
---|
616 | !$OMP THREADPRIVATE(overturning_free_draining_shallow) |
---|
617 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_free_draining_shallow_leafless !! Modulus of Rupture (Pa) |
---|
618 | !$OMP THREADPRIVATE(overturning_free_draining_shallow_leafless) |
---|
619 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_free_draining_deep !! Modulus of Rupture (Pa) |
---|
620 | !$OMP THREADPRIVATE(overturning_free_draining_deep) |
---|
621 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_free_draining_deep_leafless !! Modulus of Rupture (Pa) |
---|
622 | !$OMP THREADPRIVATE(overturning_free_draining_deep_leafless) |
---|
623 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_free_draining_average !! Modulus of Rupture (Pa) |
---|
624 | !$OMP THREADPRIVATE(overturning_free_draining_average) |
---|
625 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_free_draining_average_leafless !! Modulus of Rupture (Pa) |
---|
626 | !$OMP THREADPRIVATE(overturning_free_draining_average_leafless) |
---|
627 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_gleyed_shallow !! Modulus of Rupture (Pa) |
---|
628 | !$OMP THREADPRIVATE(overturning_gleyed_shallow) |
---|
629 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_gleyed_shallow_leafless !! Modulus of Rupture (Pa) |
---|
630 | !$OMP THREADPRIVATE(overturning_gleyed_shallow_leafless) |
---|
631 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_gleyed_deep !! Modulus of Rupture (Pa) |
---|
632 | !$OMP THREADPRIVATE(overturning_gleyed_deep) |
---|
633 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_gleyed_deep_leafless !! Modulus of Rupture (Pa) |
---|
634 | !$OMP THREADPRIVATE(overturning_gleyed_deep_leafless) |
---|
635 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_gleyed_average !! Modulus of Rupture (Pa) |
---|
636 | !$OMP THREADPRIVATE(overturning_gleyed_average) |
---|
637 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_gleyed_average_leafless !! Modulus of Rupture (Pa) |
---|
638 | !$OMP THREADPRIVATE(overturning_gleyed_average_leafless) |
---|
639 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_peaty_shallow !! Modulus of Rupture (Pa) |
---|
640 | !$OMP THREADPRIVATE(overturning_peaty_shallow) |
---|
641 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_peaty_shallow_leafless !! Modulus of Rupture (Pa) |
---|
642 | !$OMP THREADPRIVATE(overturning_peaty_shallow_leafless) |
---|
643 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_peaty_deep !! Modulus of Rupture (Pa) |
---|
644 | !$OMP THREADPRIVATE(overturning_peaty_deep) |
---|
645 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_peaty_deep_leafless !! Modulus of Rupture (Pa) |
---|
646 | !$OMP THREADPRIVATE(overturning_peaty_deep_leafless) |
---|
647 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_peaty_average !! Modulus of Rupture (Pa) |
---|
648 | !$OMP THREADPRIVATE(overturning_peaty_average) |
---|
649 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_peaty_average_leafless !! Modulus of Rupture (Pa) |
---|
650 | !$OMP THREADPRIVATE(overturning_peaty_average_leafless) |
---|
651 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_peat_shallow !! Modulus of Rupture (Pa) |
---|
652 | !$OMP THREADPRIVATE(overturning_peat_shallow) |
---|
653 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_peat_shallow_leafless !! Modulus of Rupture (Pa) |
---|
654 | !$OMP THREADPRIVATE(overturning_peat_shallow_leafless) |
---|
655 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_peat_deep !! Modulus of Rupture (Pa) |
---|
656 | !$OMP THREADPRIVATE(overturning_peat_deep) |
---|
657 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_peat_deep_leafless !! Modulus of Rupture (Pa) |
---|
658 | !$OMP THREADPRIVATE(overturning_peat_deep_leafless) |
---|
659 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_peat_average !! Modulus of Rupture (Pa) |
---|
660 | !$OMP THREADPRIVATE(overturning_peat_average) |
---|
661 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: overturning_peat_average_leafless !! Modulus of Rupture (Pa) |
---|
662 | !$OMP THREADPRIVATE(overturning_peat_average_leafless) |
---|
663 | |
---|
664 | ! |
---|
665 | ! FIRE (stomate) |
---|
666 | ! |
---|
667 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: flam !! flamability : critical fraction of water holding |
---|
668 | !! capacity (0-1, unitless) |
---|
669 | !$OMP THREADPRIVATE(flam) |
---|
670 | |
---|
671 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: resist !! fire resistance (0-1, unitless) |
---|
672 | !$OMP THREADPRIVATE(resist) |
---|
673 | |
---|
674 | |
---|
675 | ! |
---|
676 | ! FLUX - LUC (Land Use Change) |
---|
677 | ! |
---|
678 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: coeff_lcchange_s !! Coeff of biomass export for the year (unitless) |
---|
679 | !$OMP THREADPRIVATE(coeff_lcchange_s) |
---|
680 | |
---|
681 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: coeff_lcchange_m !! Coeff of biomass export for the decade (unitless) |
---|
682 | !$OMP THREADPRIVATE(coeff_lcchange_m) |
---|
683 | |
---|
684 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: coeff_lcchange_l !! Coeff of biomass export for the century (unitless) |
---|
685 | !$OMP THREADPRIVATE(coeff_lcchange_l) |
---|
686 | |
---|
687 | |
---|
688 | ! |
---|
689 | ! PHENOLOGY |
---|
690 | ! |
---|
691 | !- |
---|
692 | ! 1. Stomate |
---|
693 | !- |
---|
694 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: lai_max !! maximum LAI, PFT-specific @tex $(m^2.m^{-2})$ @endtex |
---|
695 | !$OMP THREADPRIVATE(lai_max) |
---|
696 | |
---|
697 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: pheno_type !! type of phenology (0-4, unitless) |
---|
698 | !! 0=bare ground 1=evergreen, 2=summergreen, |
---|
699 | !! 3=raingreen, 4=perennial |
---|
700 | !! For the moment, the bare ground phenotype is not managed, |
---|
701 | !! so it is considered as "evergreen" |
---|
702 | !$OMP THREADPRIVATE(pheno_type) |
---|
703 | |
---|
704 | !- |
---|
705 | ! 2. Leaf Onset |
---|
706 | !- |
---|
707 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:,:) :: pheno_gdd_crit !! critical gdd,tabulated (C), used in the code |
---|
708 | !$OMP THREADPRIVATE(pheno_gdd_crit) |
---|
709 | |
---|
710 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: pheno_gdd_crit_c !! critical gdd,tabulated (C), |
---|
711 | !! constant c of aT^2+bT+c (unitless) |
---|
712 | !$OMP THREADPRIVATE(pheno_gdd_crit_c) |
---|
713 | |
---|
714 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: pheno_gdd_crit_b !! critical gdd,tabulated (C), |
---|
715 | !! constant b of aT^2+bT+c (unitless) |
---|
716 | !$OMP THREADPRIVATE(pheno_gdd_crit_b) |
---|
717 | |
---|
718 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: pheno_gdd_crit_a !! critical gdd,tabulated (C), |
---|
719 | !! constant a of aT^2+bT+c (unitless) |
---|
720 | !$OMP THREADPRIVATE(pheno_gdd_crit_a) |
---|
721 | |
---|
722 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: ngd_crit !! critical ngd,tabulated. Threshold -5 degrees (days) |
---|
723 | !$OMP THREADPRIVATE(ngd_crit) |
---|
724 | |
---|
725 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: opti_kpheno_crit !! multiplicative factor to use optimised gdd_crit (Natasha MacBean) |
---|
726 | !! (unitless) |
---|
727 | !$OMP THREADPRIVATE(opti_kpheno_crit) |
---|
728 | |
---|
729 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: ncdgdd_temp !! critical temperature for the ncd vs. gdd function |
---|
730 | !! in phenology (C) |
---|
731 | !$OMP THREADPRIVATE(ncdgdd_temp) |
---|
732 | |
---|
733 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: hum_frac !! critical humidity (relative to min/max) for phenology |
---|
734 | !! (0-1, unitless) |
---|
735 | !$OMP THREADPRIVATE(hum_frac) |
---|
736 | |
---|
737 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: hum_min_time !! minimum time elapsed since moisture minimum (days) |
---|
738 | !$OMP THREADPRIVATE(hum_min_time) |
---|
739 | |
---|
740 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: tau_sap !! turnover sapwood -> heartwood conversion time (1/days) |
---|
741 | !$OMP THREADPRIVATE(tau_sap) |
---|
742 | |
---|
743 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: tau_fruit !! fruit turnover (1/days) |
---|
744 | !$OMP THREADPRIVATE(tau_fruit) |
---|
745 | |
---|
746 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: tau_root !! root turnover (1/days) |
---|
747 | !$OMP THREADPRIVATE(tau_root) |
---|
748 | |
---|
749 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: tau_leaf !! leaf turnover (1/years) |
---|
750 | !$OMP THREADPRIVATE(tau_leaf) |
---|
751 | |
---|
752 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: tau_leafinit !! time to attain the initial foliage using the carbohydrate reserve |
---|
753 | !$OMP THREADPRIVATE(tau_leafinit) |
---|
754 | |
---|
755 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: ecureuil !! fraction of primary leaf and root allocation put |
---|
756 | !! into reserve (0-1, unitless) |
---|
757 | !$OMP THREADPRIVATE(ecureuil) |
---|
758 | |
---|
759 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: alloc_min !! NEW - allocation above/below = f(age) - 30/01/04 NV/JO/PF |
---|
760 | !$OMP THREADPRIVATE(alloc_min) |
---|
761 | |
---|
762 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: alloc_max !! NEW - allocation above/below = f(age) - 30/01/04 NV/JO/PF |
---|
763 | !$OMP THREADPRIVATE(alloc_max) |
---|
764 | |
---|
765 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: demi_alloc !! NEW - allocation above/below = f(age) - 30/01/04 NV/JO/PF |
---|
766 | !$OMP THREADPRIVATE(demi_alloc) |
---|
767 | |
---|
768 | |
---|
769 | !- |
---|
770 | ! 3. Senescence |
---|
771 | !- |
---|
772 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: leaffall !! length of death of leaves,tabulated (days) |
---|
773 | !$OMP THREADPRIVATE(leaffall) |
---|
774 | |
---|
775 | CHARACTER(len=6), ALLOCATABLE, SAVE, DIMENSION(:) :: senescence_type !! type of senescence,tabulated (unitless) |
---|
776 | !! List of avaible types of senescence : |
---|
777 | !! 'cold ', 'dry ', 'mixed ', 'none ' |
---|
778 | !$OMP THREADPRIVATE(senescence_type) |
---|
779 | |
---|
780 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: senescence_hum !! critical relative moisture availability for senescence |
---|
781 | !! (0-1, unitless) |
---|
782 | !$OMP THREADPRIVATE(senescence_hum) |
---|
783 | |
---|
784 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: nosenescence_hum !! relative moisture availability above which there is |
---|
785 | !! no humidity-related senescence (0-1, unitless) |
---|
786 | !$OMP THREADPRIVATE(nosenescence_hum) |
---|
787 | |
---|
788 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: max_turnover_time !! maximum turnover time for grasses (days) |
---|
789 | !$OMP THREADPRIVATE(max_turnover_time) |
---|
790 | |
---|
791 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: min_turnover_time !! minimum turnover time for grasses (days) |
---|
792 | !$OMP THREADPRIVATE(min_turnover_time) |
---|
793 | |
---|
794 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: min_leaf_age_for_senescence !! minimum leaf age to allow senescence g (days) |
---|
795 | !$OMP THREADPRIVATE(min_leaf_age_for_senescence) |
---|
796 | |
---|
797 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:,:) :: senescence_temp !! critical temperature for senescence (C), |
---|
798 | !! used in the code |
---|
799 | !$OMP THREADPRIVATE(senescence_temp) |
---|
800 | |
---|
801 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: senescence_temp_c !! critical temperature for senescence (C), |
---|
802 | !! constant c of aT^2+bT+c , tabulated (unitless) |
---|
803 | !$OMP THREADPRIVATE(senescence_temp_c) |
---|
804 | |
---|
805 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: senescence_temp_b !! critical temperature for senescence (C), |
---|
806 | !! constant b of aT^2+bT+c , tabulated (unitless) |
---|
807 | !$OMP THREADPRIVATE(senescence_temp_b) |
---|
808 | |
---|
809 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: senescence_temp_a !! critical temperature for senescence (C), |
---|
810 | !! constant a of aT^2+bT+c , tabulated (unitless) |
---|
811 | !$OMP THREADPRIVATE(senescence_temp_a) |
---|
812 | |
---|
813 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: gdd_senescence !! minimum gdd to allow senescence of crops (days) |
---|
814 | !$OMP THREADPRIVATE(gdd_senescence) |
---|
815 | |
---|
816 | ! |
---|
817 | ! DGVM |
---|
818 | ! |
---|
819 | |
---|
820 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: residence_time !! residence time of trees (y) |
---|
821 | !$OMP THREADPRIVATE(residence_time) |
---|
822 | |
---|
823 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: tmin_crit !! critical tmin, tabulated (C) |
---|
824 | !$OMP THREADPRIVATE(tmin_crit) |
---|
825 | |
---|
826 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: tcm_crit !! critical tcm, tabulated (C) |
---|
827 | !$OMP THREADPRIVATE(tcm_crit) |
---|
828 | |
---|
829 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: mortality_min !! Asymptotic mortality if plant growth exceeds long term |
---|
830 | !! NPP @tex $(year^{-1})$ @endtex |
---|
831 | !$OMP THREADPRIVATE(mortality_min) |
---|
832 | |
---|
833 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: mortality_max !! Maximum mortality if plants hardly grows |
---|
834 | !! @tex $(year^{-1})$ @endtex |
---|
835 | !$OMP THREADPRIVATE(mortality_max) |
---|
836 | |
---|
837 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: ref_mortality !! Reference mortality rate used to calculate mortality |
---|
838 | !! as a function of the plant vigor @tex $(year^{-1})$ @endtex |
---|
839 | !$OMP THREADPRIVATE(ref_mortality) |
---|
840 | |
---|
841 | ! |
---|
842 | ! Seasonal average |
---|
843 | ! |
---|
844 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: tau_hum_growingseason !! Time integral to calculate the mean growingseason |
---|
845 | !! plant available soilmoisture (days) |
---|
846 | !$OMP THREADPRIVATE(tau_hum_growingseason) |
---|
847 | |
---|
848 | |
---|
849 | ! |
---|
850 | ! Biogenic Volatile Organic Compounds |
---|
851 | ! |
---|
852 | |
---|
853 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: em_factor_isoprene !! Isoprene emission factor |
---|
854 | !! @tex $(\mu gC.g^{-1}.h^{-1})$ @endtex |
---|
855 | !$OMP THREADPRIVATE(em_factor_isoprene) |
---|
856 | |
---|
857 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: em_factor_monoterpene !! Monoterpene emission factor |
---|
858 | !! @tex $(\mu gC.g^{-1}.h^{-1})$ @endtex |
---|
859 | !$OMP THREADPRIVATE(em_factor_monoterpene) |
---|
860 | |
---|
861 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: em_factor_ORVOC !! ORVOC emissions factor |
---|
862 | !! @tex $(\mu gC.g^{-1}.h^{-1})$ @endtex |
---|
863 | !$OMP THREADPRIVATE(em_factor_ORVOC) |
---|
864 | |
---|
865 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: em_factor_OVOC !! OVOC emissions factor |
---|
866 | !! @tex $(\mu gC.g^{-1}.h^{-1})$ @endtex |
---|
867 | !$OMP THREADPRIVATE(em_factor_OVOC) |
---|
868 | |
---|
869 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: em_factor_MBO !! MBO emissions factor |
---|
870 | !! @tex $(\mu gC.g^{-1}.h^{-1})$ @endtex |
---|
871 | !$OMP THREADPRIVATE(em_factor_MBO) |
---|
872 | |
---|
873 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: em_factor_methanol !! Methanol emissions factor |
---|
874 | !! @tex $(\mu gC.g^{-1}.h^{-1})$ @endtex |
---|
875 | !$OMP THREADPRIVATE(em_factor_methanol) |
---|
876 | |
---|
877 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: em_factor_acetone !! Acetone emissions factor |
---|
878 | !! @tex $(\mu gC.g^{-1}.h^{-1})$ @endtex |
---|
879 | !$OMP THREADPRIVATE(em_factor_acetone) |
---|
880 | |
---|
881 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: em_factor_acetal !! Acetaldehyde emissions factor |
---|
882 | !! @tex $(\mu gC.g^{-1}.h^{-1})$ @endtex |
---|
883 | !$OMP THREADPRIVATE(em_factor_acetal) |
---|
884 | |
---|
885 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: em_factor_formal !! Formaldehyde emissions factor |
---|
886 | !! @tex $(\mu gC.g^{-1}.h^{-1})$ @endtex |
---|
887 | !$OMP THREADPRIVATE(em_factor_formal) |
---|
888 | |
---|
889 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: em_factor_acetic !! Acetic Acid emissions factor |
---|
890 | !! @tex $(\mu gC.g^{-1}.h^{-1})$ @endtex |
---|
891 | !$OMP THREADPRIVATE(em_factor_acetic) |
---|
892 | |
---|
893 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: em_factor_formic !! Formic Acid emissions factor |
---|
894 | !! @tex $(\mu gC.g^{-1}.h^{-1})$ @endtex |
---|
895 | !$OMP THREADPRIVATE(em_factor_formic) |
---|
896 | |
---|
897 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: em_factor_no_wet !! NOx emissions factor soil emissions and |
---|
898 | !! exponential dependancy factor for wet soils |
---|
899 | !! @tex $(ngN.m^{-2}.s^{-1})$ @endtex |
---|
900 | !$OMP THREADPRIVATE(em_factor_no_wet) |
---|
901 | |
---|
902 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: em_factor_no_dry !! NOx emissions factor soil emissions and |
---|
903 | !! exponential dependancy factor for dry soils |
---|
904 | !! @tex $(ngN.m^{-2}.s^{-1})$ @endtex |
---|
905 | !$OMP THREADPRIVATE(em_factor_no_dry) |
---|
906 | |
---|
907 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: Larch !! Larcher 1991 SAI/LAI ratio (unitless) |
---|
908 | !$OMP THREADPRIVATE(Larch) |
---|
909 | |
---|
910 | ! |
---|
911 | ! INTERNAL PARAMETERS USED IN STOMATE_DATA |
---|
912 | ! |
---|
913 | |
---|
914 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: lai_initmin !! Initial lai for trees/grass |
---|
915 | !! @tex $(m^2.m^{-2})$ @endtex |
---|
916 | !$OMP THREADPRIVATE(lai_initmin) |
---|
917 | |
---|
918 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:,:,:) :: bm_sapl_old !! sapling biomass for the OLD allocation |
---|
919 | !! @tex $(gC.ind^{-1})$ @endtex |
---|
920 | !$OMP THREADPRIVATE(bm_sapl_old) |
---|
921 | |
---|
922 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: migrate !! migration speed @tex $(m.year^{-1})$ @endtex |
---|
923 | !$OMP THREADPRIVATE(migrate) |
---|
924 | |
---|
925 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: maxdia !! maximum stem diameter from which on crown area no longer |
---|
926 | !! increases (m) |
---|
927 | !$OMP THREADPRIVATE(maxdia) |
---|
928 | |
---|
929 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: cn_sapl !! crown of tree when sapling @tex $(m^2$)$ @endtex |
---|
930 | !$OMP THREADPRIVATE(cn_sapl) |
---|
931 | |
---|
932 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: leaf_timecst !! time constant for leaf age discretisation (days) |
---|
933 | !$OMP THREADPRIVATE(leaf_timecst) |
---|
934 | |
---|
935 | ! |
---|
936 | ! FOREST MANAGEMENT |
---|
937 | ! |
---|
938 | |
---|
939 | LOGICAL, ALLOCATABLE, SAVE, DIMENSION(:) :: plantation !! |
---|
940 | !$OMP THREADPRIVATE(plantation) |
---|
941 | |
---|
942 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: fm_allo_a !! |
---|
943 | !$OMP THREADPRIVATE(fm_allo_a) |
---|
944 | |
---|
945 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: fm_allo_c !! |
---|
946 | !$OMP THREADPRIVATE(fm_allo_c) |
---|
947 | |
---|
948 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: fm_allo_d !! |
---|
949 | !$OMP THREADPRIVATE(fm_allo_d) |
---|
950 | |
---|
951 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: fm_allo_p !! |
---|
952 | !$OMP THREADPRIVATE(fm_allo_p) |
---|
953 | |
---|
954 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: fm_allo_q !! |
---|
955 | !$OMP THREADPRIVATE(fm_allo_q) |
---|
956 | |
---|
957 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: allo_crown_a0 !! |
---|
958 | !$OMP THREADPRIVATE(allo_crown_a0) |
---|
959 | |
---|
960 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: allo_crown_a1 !! |
---|
961 | !$OMP THREADPRIVATE(allo_crown_a1) |
---|
962 | |
---|
963 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: allo_crown_a2 !! |
---|
964 | !$OMP THREADPRIVATE(allo_crown_a2) |
---|
965 | |
---|
966 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: h_first !! |
---|
967 | !$OMP THREADPRIVATE(h_first) |
---|
968 | |
---|
969 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: nmaxtrees !! Intial number of seedlings per hectare. Used |
---|
970 | !! in prescribe to initialize the model and after |
---|
971 | !! every clearcut |
---|
972 | !$OMP THREADPRIVATE(nmaxtrees) |
---|
973 | |
---|
974 | ! The following two variables are used to define the range of sapling heights for a newly cleared plot |
---|
975 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: height_init_min !! The minimum height of a tree sapling when a forest |
---|
976 | !! stand is established. Owing to the allometric |
---|
977 | !! relationship this setting determines all |
---|
978 | !! biomass components of a newly establised stand |
---|
979 | !! @tex $(m)$ @endtex |
---|
980 | !$OMP THREADPRIVATE(height_init_min) |
---|
981 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: height_init_max !! The maximum height of a tree sapling when a forest |
---|
982 | !! stand is established. |
---|
983 | !! @tex $(m)$ @endtex |
---|
984 | !$OMP THREADPRIVATE(height_init_max) |
---|
985 | |
---|
986 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: alpha_self_thinning !! Coefficient of the self-thinning relationship D=alpha*N^beta |
---|
987 | !! estimated from German, French, Spanish and Swedish |
---|
988 | !! forest inventories |
---|
989 | !$OMP THREADPRIVATE(alpha_self_thinning) |
---|
990 | |
---|
991 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: beta_self_thinning!! Exponent of the self-thinning relationship D=alpha*N^beta |
---|
992 | !! estimated from German, French, Spanish and swedish |
---|
993 | !! forest inventories |
---|
994 | !$OMP THREADPRIVATE(beta_self_thinning) |
---|
995 | |
---|
996 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: fuelwood_diameter !! Diameter below which the wood harvest is used as fuelwood (m) |
---|
997 | !! Affects the way the wood is used in the dim_product_use |
---|
998 | !! subroutine |
---|
999 | !$OMP THREADPRIVATE(fuelwood_diameter) |
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1000 | |
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1001 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: coppice_kill_be_wood !! Diameter below which the wood harvest is used as fuelwood (m) |
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1002 | !$OMP THREADPRIVATE(coppice_kill_be_wood) |
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1003 | |
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1004 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: thinstrat !! The thinning strategy used for forest management. |
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1005 | !! Comes from Eq. 12 of Bellassen et al (2010) |
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1006 | !! @tex $(unitless)$ @endtex |
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1007 | !$OMP THREADPRIVATE(thinstrat) |
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1008 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: taumin !! Minimum tree death probability. stomate_forest.f90 |
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1009 | !! Comes from Eq. 12 of Bellassen et al (2010) |
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1010 | !! @tex $(unitless)$ @endtex |
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1011 | !$OMP THREADPRIVATE(taumin) |
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1012 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: taumax !! Maximum tree death probability. stomate_forest.f90 |
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1013 | !! Comes from Eq. 12 of Bellassen et al (2010) |
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1014 | !! @tex $(unitless)$ @endtex |
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1015 | !$OMP THREADPRIVATE(taumax) |
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1016 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: alpha_rdi_upper !! Coefficient of the yield-table derived thinning relationship |
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1017 | !! D=alpha*N^beta estimated from JRC yield table database |
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1018 | !$OMP THREADPRIVATE(alpha_rdi_upper) |
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1019 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: beta_rdi_upper !! Coefficient of the yield-table derived thinning relationship |
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1020 | !! D=alpha*N^beta estimated from JRC yield table database |
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1021 | !$OMP THREADPRIVATE(beta_rdi_upper) |
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1022 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: alpha_rdi_lower !! Coefficient of the yield-table derived thinning relationship |
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1023 | !! D=alpha*N^beta estimated from JRC yield table database |
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1024 | !$OMP THREADPRIVATE(alpha_rdi_lower) |
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1025 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: beta_rdi_lower !! Coefficient of the yield-table derived thinning relationship |
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1026 | !! D=alpha*N^beta estimated from JRC yield table database |
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1027 | !$OMP THREADPRIVATE(beta_rdi_lower) |
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1028 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: dens_target !! The minimum density of trees in a stand before |
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1029 | !! they all die off and we replant. This is to prevent |
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1030 | !! the stand from becoming just one large tree. |
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1031 | !! @tex $(trees ha{-1})$ @endtex |
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1032 | !$OMP THREADPRIVATE(dens_target) |
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1033 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: largest_tree_dia !! The diameter at which we decide to clearcut |
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1034 | !! a stand because our equipment cannot handle |
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1035 | !! trees larger than this. |
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1036 | !! @tex $(cm)$ @endtex |
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1037 | !$OMP THREADPRIVATE(largest_tree_dia) |
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1038 | |
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1039 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: branch_ratio !! branches/total aboveground biomass ratio |
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1040 | !! (cf carbofor for CITEPA inventory, these |
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1041 | !! Guerric, Lim 2004, Peischl 2007, |
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1042 | !! Schulp 2008: 15-30% slash after harvest, |
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1043 | !! Zaehle 2007: 30% slash after harvest) |
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1044 | !$OMP THREADPRIVATE(branch_ratio) |
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1045 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: branch_harvest !! The fraction of branches which are harvested |
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1046 | !! during thinning and clearcut operations on |
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1047 | !! forests. 1.0 means all branches are taken offsite, |
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1048 | !! 0.0 means all branches are left onsite and go |
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1049 | !! into the litter pool. This number is not |
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1050 | !! based on any data. |
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1051 | !$OMP THREADPRIVATE(branch_harvest) |
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1052 | |
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1053 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: decl_factor !! Age_decline factor in fraction of vmax decline per year |
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1054 | !! (yield tables > 130 years : inc90=0.8inc50, |
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1055 | !! inc130=0.55inc50, |
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1056 | !! same for broadleaves and coniferous. |
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1057 | !! For temperate pfts, calibration on one site to get a 0.55 |
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1058 | !! increment decrease. |
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1059 | !! For boreal pfts, calibration to get an average 0.55 |
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1060 | !! increment decrease over 25,7 and 2 sites: Adam Wolf dataset) |
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1061 | !$OMP THREADPRIVATE(decl_factor) |
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1062 | |
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1063 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: opt_factor !! Optimisation factor for vcmax and vjmax |
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1064 | !$OMP THREADPRIVATE(opt_factor) |
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1065 | |
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1066 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: coppice_diameter !! The trunk diameter at which a coppice will be cut. |
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1067 | !! @tex $(m)$ @endtex |
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1068 | !$OMP THREADPRIVATE(coppice_diameter) |
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1069 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: shoots_per_stool !! The number of shoots that regrow per stool after |
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1070 | !! the first coppice cut |
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1071 | !! @tex $-$ @endtex |
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1072 | !$OMP THREADPRIVATE(shoots_per_stool) |
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1073 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: src_rot_length !! The number of years between cuttings for short |
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1074 | !! rotation coppices. |
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1075 | !! @tex $-$ @endtex |
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1076 | !$OMP THREADPRIVATE(src_rot_length) |
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1077 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: src_nrots !! The number of rotations for short rotations coppices |
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1078 | !! before the roots are killed and replanted. |
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1079 | !! @tex $-$ @endtex |
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1080 | !$OMP THREADPRIVATE(src_nrots) |
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1081 | |
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1082 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: deleuze_a !! intercept of the intra-tree competition within a stand |
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1083 | !! based on the competion rule of Deleuze and Dhote 2004 |
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1084 | !! Used when n_circ > 6 |
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1085 | !$OMP THREADPRIVATE(deleuze_a) |
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1086 | |
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1087 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: deleuze_b !! slope of the intra-tree competition within a stand |
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1088 | !! based on the competion rule of Deleuze and Dhote 2004 |
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1089 | !! Used when n_circ > 6 |
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1090 | !$OMP THREADPRIVATE(deleuze_b) |
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1091 | |
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1092 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: deleuze_p_all !! Percentile of the circumferences that receives photosynthates |
---|
1093 | !! based on the competion rule of Deleuze and Dhote 2004 |
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1094 | !! Used when n_circ > 6 for FM1, FM2 and FM4 |
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1095 | !$OMP THREADPRIVATE(deleuze_p_all) |
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1096 | |
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1097 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: deleuze_p_coppice !! Percentile of the circumferences that receives photosynthates |
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1098 | !! based on the competion rule of Deleuze and Dhote 2004 |
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1099 | !! Used when n_circ > 6 for FM3 |
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1100 | !$OMP THREADPRIVATE(deleuze_p_coppice) |
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1101 | |
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1102 | |
---|
1103 | ! SAPIENS - CROP MANAGEMENT |
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1104 | |
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1105 | REAL(r_std), ALLOCATABLE, SAVE, DIMENSION(:) :: harvest_ratio !! Share of biomass that is removed from the site during harvest |
---|
1106 | !! A high value indicates a high harvest efficiency and thus a |
---|
1107 | !! input of residuals. (unitless, 0-1). |
---|
1108 | |
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1109 | !$OMP THREADPRIVATE(harvest_ratio) |
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1110 | |
---|
1111 | |
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1112 | ! STOMATE - Age classes |
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1113 | |
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1114 | INTEGER(i_std), SAVE :: nvmap !! The number of PFTs we have if we ignore age classes. |
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1115 | !! @tex $-$ @endtex |
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1116 | !$OMP THREADPRIVATE(nvmap) |
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1117 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: agec_group !! The age class group that this PFT belongs to. |
---|
1118 | !! If you're not using age classes, this will just be |
---|
1119 | !! set to the number of the PFT and should be ignored |
---|
1120 | !! in the code. |
---|
1121 | !! @tex $-$ @endtex |
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1122 | !$OMP THREADPRIVATE(agec_group) |
---|
1123 | ! I do not like the location of these next two variables. They are computed |
---|
1124 | ! after agec_group is read in. Ideally, they would be passed around |
---|
1125 | ! as arguments or in a structure, since they are not really |
---|
1126 | ! parameters read in from the input file. |
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1127 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: start_index !! Gives the index that this real PFT starts |
---|
1128 | !! on, ignoring age classes |
---|
1129 | !! @tex $-$ @endtex |
---|
1130 | !$OMP THREADPRIVATE(start_index) |
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1131 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: nagec_pft !! The number of age classes for each PFT. |
---|
1132 | !! Only 1 or nagec are supported right now. |
---|
1133 | !! @tex $-$ @endtex |
---|
1134 | !$OMP THREADPRIVATE(nagec_pft) |
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1135 | |
---|
1136 | |
---|
1137 | END MODULE pft_parameters_var |
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