1 | ! establishment routine |
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2 | ! Suppose seed pool >> establishment rate. |
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3 | ! |
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4 | !< $HeadURL$ |
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5 | !< $Date$ |
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6 | !< $Author$ |
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7 | !< $Revision$ |
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8 | ! IPSL (2006) |
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9 | ! This software is governed by the CeCILL licence see ORCHIDEE/ORCHIDEE_CeCILL.LIC |
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10 | ! |
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11 | MODULE lpj_establish |
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12 | |
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13 | ! modules used: |
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14 | |
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15 | USE ioipsl |
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16 | USE stomate_data |
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17 | USE constantes |
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18 | |
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19 | IMPLICIT NONE |
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20 | |
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21 | ! private & public routines |
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22 | |
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23 | PRIVATE |
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24 | PUBLIC establish,establish_clear |
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25 | |
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26 | ! first call |
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27 | LOGICAL, SAVE :: firstcall = .TRUE. |
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28 | CONTAINS |
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29 | |
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30 | |
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31 | SUBROUTINE establish_clear |
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32 | firstcall = .TRUE. |
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33 | END SUBROUTINE establish_clear |
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34 | |
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35 | SUBROUTINE establish (npts, dt, PFTpresent, regenerate, & |
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36 | neighbours, resolution, need_adjacent, herbivores, & |
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37 | precip_annual, gdd0, lm_lastyearmax, & |
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38 | cn_ind, lai, avail_tree, avail_grass, npp_longterm, & |
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39 | leaf_age, leaf_frac, & |
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40 | ind, biomass, age, everywhere, co2_to_bm,veget_max, woodmass_ind) |
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41 | ! |
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42 | ! 0 declarations |
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43 | ! |
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44 | |
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45 | ! 0.1 input |
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46 | |
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47 | ! Domain size |
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48 | INTEGER(i_std), INTENT(in) :: npts |
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49 | ! Time step of vegetation dynamics (days) |
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50 | REAL(r_std), INTENT(in) :: dt |
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51 | ! Is pft there |
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52 | LOGICAL, DIMENSION(npts,nvm), INTENT(in) :: PFTpresent |
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53 | ! Winter sufficiently cold |
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54 | REAL(r_std), DIMENSION(npts,nvm), INTENT(in) :: regenerate |
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55 | ! indices of the 8 neighbours of each grid point (1=N, 2=NE, 3=E, 4=SE, 5=S, 6=SW, 7=W, 8=NW) |
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56 | INTEGER(i_std), DIMENSION(npts,8), INTENT(in) :: neighbours |
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57 | ! resolution at each grid point in m (1=E-W, 2=N-S) |
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58 | REAL(r_std), DIMENSION(npts,2), INTENT(in) :: resolution |
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59 | ! in order for this PFT to be introduced, does it have to be present in an |
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60 | ! adjacent grid box? |
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61 | LOGICAL, DIMENSION(npts,nvm), INTENT(in) :: need_adjacent |
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62 | ! time constant of probability of a leaf to be eaten by a herbivore (days) |
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63 | REAL(r_std), DIMENSION(npts,nvm), INTENT(in) :: herbivores |
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64 | ! annual precipitation (mm/year) |
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65 | REAL(r_std), DIMENSION(npts), INTENT(in) :: precip_annual |
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66 | ! growing degree days (C) |
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67 | REAL(r_std), DIMENSION(npts), INTENT(in) :: gdd0 |
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68 | ! last year's maximum leaf mass, for each PFT (gC/(m**2 of ground)) |
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69 | REAL(r_std), DIMENSION(npts,nvm), INTENT(in) :: lm_lastyearmax |
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70 | ! crown area of individuals (m**2) |
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71 | REAL(r_std), DIMENSION(npts,nvm), INTENT(in) :: cn_ind |
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72 | ! leaf area index OF AN INDIVIDUAL PLANT |
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73 | REAL(r_std), DIMENSION(npts,nvm), INTENT(in) :: lai |
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74 | ! space availability for trees |
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75 | REAL(r_std), DIMENSION(npts), INTENT(in) :: avail_tree |
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76 | ! space availability for grasses |
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77 | REAL(r_std), DIMENSION(npts), INTENT(in) :: avail_grass |
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78 | ! longterm NPP, for each PFT (gC/(m**2 of ground)) |
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79 | REAL(r_std), DIMENSION(npts,nvm), INTENT(in) :: npp_longterm |
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80 | ! "maximal" coverage fraction of a PFT (LAI -> infinity) on ground |
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81 | REAL(r_std), DIMENSION(npts,nvm), INTENT(inout) :: veget_max |
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82 | |
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83 | ! 0.2 modified fields |
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84 | |
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85 | ! leaf age (days) |
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86 | REAL(r_std), DIMENSION(npts,nvm,nleafages), INTENT(inout) :: leaf_age |
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87 | ! fraction of leaves in leaf age class |
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88 | REAL(r_std), DIMENSION(npts,nvm,nleafages), INTENT(inout) :: leaf_frac |
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89 | ! Number of individuals / m2 |
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90 | REAL(r_std), DIMENSION(npts,nvm), INTENT(inout) :: ind |
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91 | ! biomass (gC/(m**2 of ground)) |
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92 | REAL(r_std), DIMENSION(npts,nvm,nparts), INTENT(inout) :: biomass |
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93 | ! mean age (years) |
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94 | REAL(r_std), DIMENSION(npts,nvm), INTENT(inout) :: age |
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95 | ! is the PFT everywhere in the grid box or very localized (after its introduction) |
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96 | REAL(r_std), DIMENSION(npts,nvm), INTENT(inout) :: everywhere |
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97 | ! biomass uptaken (gC/(m**2 of total ground)/day) |
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98 | !NV passage 2D |
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99 | REAL(r_std), DIMENSION(npts,nvm), INTENT(inout) :: co2_to_bm |
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100 | ! woodmass of the individual, needed to calculate crownarea in lpj_crownarea |
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101 | REAL(r_std), DIMENSION(npts,nvm), INTENT(inout) :: woodmass_ind |
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102 | |
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103 | ! 0.3 local |
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104 | |
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105 | ! time during which a sapling can be entirely eaten by herbivores (d) |
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106 | REAL(r_std) :: tau_eatup |
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107 | ! new fpc ( foliage protected cover: fractional coverage ) |
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108 | REAL(r_std), DIMENSION(npts,nvm) :: fpc_nat |
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109 | ! maximum tree establishment rate, based on climate only |
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110 | REAL(r_std), DIMENSION(npts) :: estab_rate_max_climate_tree |
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111 | ! maximum grass establishment rate, based on climate only |
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112 | REAL(r_std), DIMENSION(npts) :: estab_rate_max_climate_grass |
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113 | ! maximum tree establishment rate, based on climate and fpc |
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114 | REAL(r_std), DIMENSION(npts) :: estab_rate_max_tree |
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115 | ! maximum grass establishment rate, based on climate and fpc |
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116 | REAL(r_std), DIMENSION(npts) :: estab_rate_max_grass |
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117 | ! total natural fpc |
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118 | REAL(r_std), DIMENSION(npts) :: sumfpc |
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119 | ! total fraction occupied by natural vegetation |
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120 | REAL(r_std), DIMENSION(npts) :: fracnat |
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121 | ! total woody fpc |
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122 | REAL(r_std), DIMENSION(npts) :: sumfpc_wood |
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123 | ! for trees, measures the total concurrence for available space |
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124 | REAL(r_std), DIMENSION(npts) :: spacefight_tree |
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125 | ! for grasses, measures the total concurrence for available space |
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126 | REAL(r_std), DIMENSION(npts) :: spacefight_grass |
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127 | ! change in number of individuals /m2 per time step (per day in history file) |
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128 | REAL(r_std), DIMENSION(npts,nvm) :: d_ind |
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129 | ! biomass increase (gC/(m**2 of ground)) |
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130 | REAL(r_std), DIMENSION(npts) :: bm_new |
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131 | ! stem diameter (m) |
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132 | REAL(r_std), DIMENSION(npts) :: dia |
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133 | ! temporary variable |
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134 | REAL(r_std), DIMENSION(npts) :: b1 |
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135 | ! new sap mass (gC/(m**2 of ground)) |
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136 | REAL(r_std), DIMENSION(npts) :: sm2 |
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137 | ! woodmass of an individual |
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138 | REAL(r_std), DIMENSION(npts) :: woodmass |
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139 | ! carbon mass in youngest leaf age class (gC/m**2 PFT) |
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140 | REAL(r_std), DIMENSION(npts) :: leaf_mass_young |
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141 | ! ratio of hw(above) to total hw, sm(above) to total sm |
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142 | REAL(r_std), DIMENSION(npts) :: sm_at |
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143 | ! reduction factor for establishment if many trees or grasses are present |
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144 | REAL(r_std), DIMENSION(npts) :: factor |
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145 | ! Total carbon mass for all pools |
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146 | REAL(r_std), DIMENSION(npts) :: total_bm_c |
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147 | ! Total sappling biomass for all pools |
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148 | REAL(r_std), DIMENSION(npts) :: total_bm_sapl |
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149 | ! from how many sides is the grid box invaded |
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150 | INTEGER(i_std) :: nfrontx |
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151 | INTEGER(i_std) :: nfronty |
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152 | ! daily establishment rate is large compared to present number of individuals |
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153 | !LOGICAL, DIMENSION(npts) :: many_new |
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154 | ! flow due to new individuals |
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155 | ! veget_max after establishment, to get a proper estimate of carbon and nitrogen |
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156 | REAL(r_std), DIMENSION(npts) :: vn |
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157 | ! lai on each PFT surface |
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158 | REAL(r_std), DIMENSION(npts) :: lai_ind |
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159 | |
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160 | ! indices |
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161 | INTEGER(i_std) :: i,j,k,m |
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162 | |
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163 | ! ========================================================================= |
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164 | |
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165 | IF (bavard.GE.3) WRITE(numout,*) 'Entering establish' |
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166 | |
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167 | ! |
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168 | ! 1 messages and initialization |
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169 | ! |
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170 | tau_eatup = one_year/2. |
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171 | |
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172 | IF ( firstcall ) THEN |
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173 | |
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174 | WRITE(numout,*) 'establish:' |
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175 | |
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176 | WRITE(numout,*) ' > time during which a sapling can be entirely eaten by herbivores (d): ', & |
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177 | tau_eatup |
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178 | |
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179 | firstcall = .FALSE. |
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180 | |
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181 | ENDIF |
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182 | |
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183 | |
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184 | IF (control%ok_dgvm) THEN |
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185 | ! |
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186 | ! 2 recalculate fpc |
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187 | ! |
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188 | |
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189 | ! |
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190 | ! 2.1 Only natural part of the grid cell |
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191 | ! |
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192 | |
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193 | fracnat(:) = un |
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194 | do j = 2,nvm |
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195 | IF ( .NOT. natural(j) ) THEN |
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196 | fracnat(:) = fracnat(:) - veget_max(:,j) |
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197 | ENDIF |
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198 | ENDDO |
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199 | |
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200 | ! |
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201 | ! 2.2 total natural fpc on grid |
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202 | ! |
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203 | sumfpc(:) = zero |
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204 | DO j = 2,nvm |
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205 | |
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206 | IF ( natural(j) ) THEN |
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207 | WHERE(fracnat(:).GT.min_stomate) |
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208 | WHERE (lai(:,j) == val_exp) |
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209 | fpc_nat(:,j) = cn_ind(:,j) * ind(:,j) / fracnat(:) |
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210 | ELSEWHERE |
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211 | fpc_nat(:,j) = cn_ind(:,j) * ind(:,j) / fracnat(:) & |
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212 | * ( un - exp( - lm_lastyearmax(:,j) * sla(j) * ext_coeff(j) ) ) |
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213 | ENDWHERE |
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214 | ENDWHERE |
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215 | |
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216 | WHERE ( PFTpresent(:,j) ) |
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217 | sumfpc(:) = sumfpc(:) + fpc_nat(:,j) |
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218 | ENDWHERE |
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219 | ELSE |
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220 | |
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221 | fpc_nat(:,j) = zero |
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222 | |
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223 | ENDIF |
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224 | |
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225 | ENDDO |
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226 | |
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227 | ! |
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228 | ! 2.3 total woody fpc on grid and number of regenerative tree pfts |
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229 | ! |
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230 | |
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231 | sumfpc_wood(:) = zero |
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232 | spacefight_tree(:) = zero |
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233 | |
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234 | DO j = 2,nvm |
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235 | |
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236 | IF ( tree(j) .AND. natural(j) ) THEN |
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237 | |
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238 | ! total woody fpc |
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239 | |
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240 | WHERE ( PFTpresent(:,j) ) |
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241 | sumfpc_wood(:) = sumfpc_wood(:) + fpc_nat(:,j) |
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242 | ENDWHERE |
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243 | |
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244 | ! how many trees are competing? Count a PFT fully only if it is present |
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245 | ! on the whole grid box. |
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246 | |
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247 | WHERE ( PFTpresent(:,j) .AND. ( regenerate(:,j) .GT. regenerate_crit ) ) |
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248 | spacefight_tree(:) = spacefight_tree(:) + everywhere(:,j) |
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249 | ENDWHERE |
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250 | |
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251 | ENDIF |
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252 | |
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253 | ENDDO |
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254 | |
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255 | ! |
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256 | ! 2.4 number of natural grasses |
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257 | ! |
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258 | |
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259 | spacefight_grass(:) = zero |
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260 | |
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261 | DO j = 2,nvm |
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262 | |
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263 | IF ( .NOT. tree(j) .AND. natural(j) ) THEN |
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264 | |
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265 | ! how many grasses are competing? Count a PFT fully only if it is present |
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266 | ! on the whole grid box. |
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267 | |
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268 | WHERE ( PFTpresent(:,j) ) |
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269 | spacefight_grass(:) = spacefight_grass(:) + everywhere(:,j) |
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270 | ENDWHERE |
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271 | |
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272 | ENDIF |
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273 | |
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274 | ENDDO |
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275 | |
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276 | ! |
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277 | ! 3 establishment rate |
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278 | ! |
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279 | |
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280 | ! |
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281 | ! 3.1 maximum establishment rate, based on climate only |
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282 | ! |
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283 | |
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284 | WHERE ( ( precip_annual(:) .GE. precip_crit ) .AND. ( gdd0(:) .GE. gdd_crit_estab ) ) |
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285 | |
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286 | estab_rate_max_climate_tree(:) = estab_max_tree |
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287 | estab_rate_max_climate_grass(:) = estab_max_grass |
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288 | |
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289 | ELSEWHERE |
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290 | |
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291 | estab_rate_max_climate_tree(:) = zero |
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292 | estab_rate_max_climate_grass(:) = zero |
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293 | |
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294 | ENDWHERE |
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295 | |
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296 | ! |
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297 | ! 3.2 reduce maximum tree establishment rate if many trees present. |
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298 | ! In the original DGVM, this is done using a step function which yields a |
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299 | ! reduction by factor 4 if sumfpc_wood(i) .GT. fpc_crit - 0.05. |
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300 | ! This can lead to small oscillations (without consequences however). |
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301 | ! Here, a steady linear transition is used between fpc_crit-0.075 and |
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302 | ! fpc_crit-0.025. |
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303 | ! |
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304 | |
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305 | ! factor(:) = 1. - 15. * ( sumfpc_wood(:) - (fpc_crit - 0.075) ) |
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306 | ! factor(:) = MAX( 0.25_r_std, MIN( un, factor(:) ) ) |
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307 | |
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308 | !SZ modified according to Smith et al. 2001, 080806 |
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309 | factor(:)=(un - exp(- establish_scal_fact * (un - sumfpc_wood(:))))*(un - sumfpc_wood(:)) |
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310 | |
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311 | estab_rate_max_tree(:) = estab_rate_max_climate_tree(:) * factor(:) |
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312 | |
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313 | ! |
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314 | ! 3.3 Modulate grass establishment rate. |
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315 | ! If canopy is not closed (fpc < fpc_crit-0.05), normal establishment. |
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316 | ! If canopy is closed, establishment is reduced by a factor 4. |
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317 | ! Factor is linear between these two bounds. |
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318 | ! This is different from the original DGVM where a step function is |
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319 | ! used at fpc_crit-0.05 (This can lead to small oscillations, |
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320 | ! without consequences however). |
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321 | ! |
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322 | |
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323 | ! factor(:) = 1. - establish_scal_fact * ( sumfpc(:) - (fpc_crit - 0.05) ) |
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324 | ! factor(:) = MAX( 0.25_r_std, MIN( un, factor(:) ) ) |
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325 | ! estab_rate_max_grass(:) = estab_rate_max_climate_grass(:) * factor(:) |
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326 | |
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327 | !SZ modified to true LPJ formulation, grasses are only allowed in the |
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328 | !fpc fraction not occupied by trees..., 080806 |
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329 | !NVmodif estab_rate_max_grass(:)=MAX(0.98-sumfpc(:),zero) |
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330 | estab_rate_max_grass(:) = MAX(MIN(estab_rate_max_climate_grass(:), max_tree_coverage - sumfpc(:)),zero) |
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331 | |
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332 | ! SZ: longterm grass NPP for competition between C4 and C3 grasses |
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333 | ! to avoid equal veget_max, the idea is that more reestablishment |
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334 | ! is possible for the more productive PFT |
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335 | factor(:) = min_stomate |
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336 | DO j = 2,nvm |
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337 | IF ( natural(j) .AND. .NOT.tree(j)) & |
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338 | factor(:) = factor(:) + npp_longterm(:,j) * & |
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339 | lm_lastyearmax(:,j) * sla(j) |
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340 | ENDDO |
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341 | ! |
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342 | ! |
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343 | ! |
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344 | ! 4 do establishment for natural PFTs |
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345 | ! |
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346 | |
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347 | d_ind(:,:) = zero |
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348 | |
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349 | DO j = 2,nvm |
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350 | |
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351 | ! only for natural PFTs |
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352 | |
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353 | IF ( natural(j) ) THEN |
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354 | |
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355 | ! |
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356 | ! 4.1 PFT expansion across the grid box. Not to be confused with areal |
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357 | ! coverage. |
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358 | ! |
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359 | |
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360 | IF ( treat_expansion ) THEN |
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361 | |
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362 | ! only treat plants that are regenerative and present and still can expand |
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363 | |
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364 | DO i = 1, npts |
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365 | |
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366 | IF ( PFTpresent(i,j) .AND. & |
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367 | ( everywhere(i,j) .LT. un ) .AND. & |
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368 | ( regenerate(i,j) .GT. regenerate_crit ) ) THEN |
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369 | |
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370 | ! from how many sides is the grid box invaded (separate x and y directions |
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371 | ! because resolution may be strongly anisotropic) |
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372 | ! |
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373 | ! For the moment we only look into 4 direction but that can be extanded (JP) |
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374 | ! |
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375 | nfrontx = 0 |
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376 | IF ( neighbours(i,3) .GT. 0 ) THEN |
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377 | IF ( everywhere(neighbours(i,3),j) .GT. 1.-min_stomate ) nfrontx = nfrontx+1 |
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378 | ENDIF |
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379 | IF ( neighbours(i,7) .GT. 0 ) THEN |
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380 | IF ( everywhere(neighbours(i,7),j) .GT. 1.-min_stomate ) nfrontx = nfrontx+1 |
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381 | ENDIF |
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382 | |
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383 | nfronty = 0 |
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384 | IF ( neighbours(i,1) .GT. 0 ) THEN |
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385 | IF ( everywhere(neighbours(i,1),j) .GT. 1.-min_stomate ) nfronty = nfronty+1 |
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386 | ENDIF |
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387 | IF ( neighbours(i,5) .GT. 0 ) THEN |
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388 | IF ( everywhere(neighbours(i,5),j) .GT. 1.-min_stomate ) nfronty = nfronty+1 |
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389 | ENDIF |
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390 | |
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391 | everywhere(i,j) = & |
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392 | everywhere(i,j) + migrate(j) * dt/one_year * & |
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393 | ( nfrontx / resolution(i,1) + nfronty / resolution(i,2) ) |
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394 | |
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395 | IF ( .NOT. need_adjacent(i,j) ) THEN |
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396 | |
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397 | ! in that case, we also assume that the PFT expands from places within |
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398 | ! the grid box (e.g., oasis). |
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399 | |
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400 | everywhere(i,j) = & |
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401 | everywhere(i,j) + migrate(j) * dt/one_year * & |
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402 | 2. * SQRT( pi*everywhere(i,j)/(resolution(i,1)*resolution(i,2)) ) |
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403 | |
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404 | ENDIF |
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405 | |
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406 | everywhere(i,j) = MIN( everywhere(i,j), un ) |
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407 | |
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408 | ENDIF |
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409 | |
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410 | ENDDO |
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411 | |
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412 | ENDIF ! treat expansion? |
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413 | |
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414 | ! |
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415 | ! 4.2 establishment rate |
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416 | ! - Is lower if the PFT is only present in a small part of the grid box |
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417 | ! (after its introduction), therefore multiplied by "everywhere". |
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418 | ! - Is divided by the number of PFTs that compete ("spacefight"). |
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419 | ! - Is modulated by space availability (avail_tree, avail_grass). |
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420 | ! |
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421 | |
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422 | IF ( tree(j) ) THEN |
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423 | |
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424 | ! 4.2.1 present and regenerative trees |
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425 | |
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426 | WHERE ( PFTpresent(:,j) .AND. ( regenerate(:,j) .GT. regenerate_crit ) ) |
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427 | |
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428 | |
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429 | d_ind(:,j) = estab_rate_max_tree(:)*everywhere(:,j)/spacefight_tree(:) * & |
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430 | avail_tree(:) * dt/one_year |
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431 | |
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432 | ENDWHERE |
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433 | |
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434 | ELSE |
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435 | |
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436 | ! 4.2.2 present and regenerative grasses |
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437 | |
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438 | WHERE ( PFTpresent(:,j) .AND. ( regenerate(:,j) .GT. regenerate_crit ) & |
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439 | .AND.factor(:).GT.min_stomate .AND. spacefight_grass(:).GT. min_stomate) |
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440 | |
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441 | d_ind(:,j) = estab_rate_max_grass(:)*everywhere(:,j)/spacefight_grass(:) * & |
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442 | MAX(min_stomate,npp_longterm(:,j)*lm_lastyearmax(:,j)*sla(j)/factor(:)) * fracnat(:) * dt/one_year |
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443 | |
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444 | ENDWHERE |
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445 | |
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446 | ENDIF ! tree/grass |
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447 | |
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448 | ENDIF ! if natural |
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449 | ENDDO ! PFTs |
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450 | |
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451 | ELSE ! lpj establishment in static case, SZ 080806, account for real LPJ dynamics in |
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452 | ! prescribed vegetation, i.e. population dynamics within a given area of the |
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453 | ! grid cell |
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454 | |
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455 | d_ind(:,:) = zero |
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456 | |
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457 | DO j = 2,nvm |
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458 | |
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459 | ! only for natural PFTs |
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460 | |
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461 | WHERE(ind(:,j)*cn_ind(:,j).GT.min_stomate) |
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462 | lai_ind(:) = sla(j) * lm_lastyearmax(:,j)/(ind(:,j)*cn_ind(:,j)) |
---|
463 | ELSEWHERE |
---|
464 | lai_ind(:) = zero |
---|
465 | ENDWHERE |
---|
466 | |
---|
467 | IF ( natural(j) .AND. tree(j)) THEN |
---|
468 | |
---|
469 | fpc_nat(:,j) = MIN(un, cn_ind(:,j) * ind(:,j) * & |
---|
470 | MAX( ( un - exp( - ext_coeff(j) * lai_ind(:) ) ), min_cover ) ) |
---|
471 | !fpc_nat(:,j) = max(fpc_nat(:,j),1.-exp(-0.5*sla(j) * lm_lastyearmax(:,j))) |
---|
472 | |
---|
473 | |
---|
474 | WHERE (veget_max(:,j).GT.min_stomate.AND.ind(:,j).LE.2.) |
---|
475 | |
---|
476 | ! only establish into growing stands, ind can become very |
---|
477 | ! large in the static mode because LAI is very low in poor |
---|
478 | ! growing conditions, favouring continuous establishment. To avoid this |
---|
479 | ! a maximum IND is set. BLARPP: This should be replaced by a |
---|
480 | ! better stand density criteria |
---|
481 | ! |
---|
482 | factor(:)=(un - exp(-establish_scal_fact * (un - fpc_nat(:,j))))*(un - fpc_nat(:,j)) |
---|
483 | |
---|
484 | estab_rate_max_tree(:) = estab_max_tree * factor(:) |
---|
485 | ! |
---|
486 | ! 4 do establishment for natural PFTs |
---|
487 | ! |
---|
488 | d_ind(:,j) = MAX( zero, estab_rate_max_tree(:) * dt/one_year) |
---|
489 | |
---|
490 | ENDWHERE |
---|
491 | |
---|
492 | !SZ: quickfix: to simulate even aged stand, uncomment the following lines... |
---|
493 | !where (ind(:,j) .LE. min_stomate) |
---|
494 | !d_ind(:,j) = 0.1 !MAX( 0.0, estab_rate_max_tree(:) * dt/one_year) |
---|
495 | |
---|
496 | WHERE (veget_max(:,j).GT.min_stomate .AND. ind(:,j).EQ.zero) |
---|
497 | d_ind(:,j) = ind_0_estab |
---|
498 | ! elsewhere |
---|
499 | !d_ind(:,j) =0.0 |
---|
500 | ENDWHERE |
---|
501 | |
---|
502 | ELSEIF ( natural(j) .AND. .NOT.tree(j)) THEN |
---|
503 | |
---|
504 | WHERE (veget_max(:,j).GT.min_stomate) |
---|
505 | |
---|
506 | fpc_nat(:,j) = cn_ind(:,j) * ind(:,j) * & |
---|
507 | MAX( ( un - exp( - ext_coeff(j) * lai_ind(:) ) ), min_cover ) |
---|
508 | |
---|
509 | d_ind(:,j) = MAX(zero , (un - fpc_nat(:,j)) * dt/one_year ) |
---|
510 | |
---|
511 | ENDWHERE |
---|
512 | |
---|
513 | WHERE (veget_max(:,j).GT.min_stomate .AND. ind(:,j).EQ. zero) |
---|
514 | d_ind(:,j) = ind_0_estab |
---|
515 | ENDWHERE |
---|
516 | |
---|
517 | ENDIF |
---|
518 | |
---|
519 | ENDDO |
---|
520 | |
---|
521 | ENDIF ! DGVM OR NOT |
---|
522 | |
---|
523 | DO j = 2,nvm |
---|
524 | |
---|
525 | ! only for natural PFTs |
---|
526 | |
---|
527 | IF ( natural(j) ) THEN |
---|
528 | |
---|
529 | ! |
---|
530 | ! 4.3 herbivores reduce establishment rate |
---|
531 | ! We suppose that saplings are vulnerable during a given time after establishment. |
---|
532 | ! This is taken into account by preventively reducing the establishment rate. |
---|
533 | ! |
---|
534 | |
---|
535 | IF ( ok_herbivores ) THEN |
---|
536 | |
---|
537 | d_ind(:,j) = d_ind(:,j) * EXP( - tau_eatup/herbivores(:,j) ) |
---|
538 | |
---|
539 | ENDIF |
---|
540 | |
---|
541 | ! |
---|
542 | ! 4.4 be sure that ind*cn_ind does not exceed 1 |
---|
543 | !SZ This control is now moved to lpj_cover.f90 |
---|
544 | !SZ |
---|
545 | |
---|
546 | !The aim is to control for sum(veget)=1., irrespective of ind*cnd (crowns can overlap as long as |
---|
547 | ! there is enough light |
---|
548 | ! |
---|
549 | !SZ: This could be part of the dynamic vegetation problem of Orchidee |
---|
550 | !in conjunction with the wrong formulation of establishment response |
---|
551 | !to tree fpc above... |
---|
552 | ! WHERE ( ( d_ind(:,j) .GT. zero ) .AND. & |
---|
553 | ! ( (ind(:,j)+d_ind(:,j))*cn_ind(:,j) .GT. un ) ) |
---|
554 | ! |
---|
555 | ! d_ind(:,j) = MAX( 1._stnd / cn_ind(:,j) - ind(:,j), zero ) |
---|
556 | ! |
---|
557 | ! ENDWHERE |
---|
558 | |
---|
559 | ! |
---|
560 | ! 4.5 new properties where there is establishment ( d_ind > 0 ) |
---|
561 | ! |
---|
562 | |
---|
563 | ! 4.5.1 biomass. |
---|
564 | ! Add biomass only if d_ind, over one year, is of the order of ind. |
---|
565 | ! (If we don't do this, the biomass density can become very low). |
---|
566 | ! In that case, take biomass from the atmosphere. |
---|
567 | |
---|
568 | ! compare establishment rate and present number of inidivuals |
---|
569 | !many_new(:) = ( d_ind(:,j) .GT. 0.1 * ind(:,j) ) |
---|
570 | |
---|
571 | ! gives a better vectorization of the VPP |
---|
572 | |
---|
573 | !IF ( ANY( many_new(:) ) ) THEN |
---|
574 | |
---|
575 | ! save old leaf mass to calculate leaf age |
---|
576 | leaf_mass_young(:) = leaf_frac(:,j,1) * biomass(:,j,ileaf) |
---|
577 | ! total biomass of existing PFT to limit biomass added from establishment |
---|
578 | total_bm_c(:) = zero |
---|
579 | |
---|
580 | DO k = 1, nparts |
---|
581 | total_bm_c(:)=total_bm_c(:)+biomass(:,j,k) |
---|
582 | ENDDO |
---|
583 | IF(control%ok_dgvm) THEN |
---|
584 | vn(:) = veget_max(:,j) |
---|
585 | ELSE |
---|
586 | vn(:) = un |
---|
587 | ENDIF |
---|
588 | total_bm_sapl(:)=zero |
---|
589 | DO k = 1, nparts |
---|
590 | WHERE(d_ind(:,j).GT.min_stomate.AND.vn(:).GT.min_stomate) |
---|
591 | |
---|
592 | total_bm_sapl(:) = total_bm_sapl(:) + & |
---|
593 | bm_sapl(j,k) * d_ind(:,j) / vn(:) |
---|
594 | ENDWHERE |
---|
595 | ENDDO |
---|
596 | |
---|
597 | IF(control%ok_dgvm) THEN |
---|
598 | ! SZ calculate new woodmass_ind and veget_max after establishment (needed for correct scaling!) |
---|
599 | ! essential correction for MERGE! |
---|
600 | IF(tree(j))THEN |
---|
601 | DO i=1,npts |
---|
602 | IF((d_ind(i,j)+ind(i,j)).GT.min_stomate) THEN |
---|
603 | |
---|
604 | IF((total_bm_c(i).LE.min_stomate) .OR. (veget_max(i,j) .LE. min_stomate)) THEN |
---|
605 | |
---|
606 | ! new wood mass of PFT |
---|
607 | woodmass_ind(i,j) = & |
---|
608 | & (((biomass(i,j,isapabove) + biomass(i,j,isapbelow) & |
---|
609 | & + biomass(i,j,iheartabove) + biomass(i,j,iheartbelow))*veget_max(i,j)) & |
---|
610 | & + (bm_sapl(j,isapabove) + bm_sapl(j,isapbelow) & |
---|
611 | & + bm_sapl(j,iheartabove) + bm_sapl(j,iheartbelow))*d_ind(i,j))/(ind(i,j) + d_ind(i,j)) |
---|
612 | |
---|
613 | ELSE |
---|
614 | ! new biomass is added to the labile pool, hence there is no change in CA associated with establishment |
---|
615 | woodmass_ind(i,j) = & |
---|
616 | & (biomass(i,j,isapabove) + biomass(i,j,isapbelow) & |
---|
617 | & +biomass(i,j,iheartabove) + biomass(i,j,iheartbelow))*veget_max(i,j) & |
---|
618 | & /(ind(i,j) + d_ind(i,j)) |
---|
619 | |
---|
620 | ENDIF |
---|
621 | |
---|
622 | ! new diameter of PFT |
---|
623 | dia(i) = (woodmass_ind(i,j)/(pipe_density*pi/4.*pipe_tune2)) & |
---|
624 | & **(1./(2.+pipe_tune3)) |
---|
625 | vn(i) = (ind(i,j) + d_ind(i,j))*pipe_tune1*MIN(dia(i),maxdia(j))**pipe_tune_exp_coeff |
---|
626 | |
---|
627 | ENDIF |
---|
628 | ENDDO |
---|
629 | ELSE ! for grasses, cnd=1, so the above calculation cancels |
---|
630 | vn(:) = ind(:,j) + d_ind(:,j) |
---|
631 | ENDIF |
---|
632 | ELSE ! static |
---|
633 | DO i=1,npts |
---|
634 | IF(tree(j).AND.(d_ind(i,j)+ind(i,j)).GT.min_stomate) THEN |
---|
635 | IF(total_bm_c(i).LE.min_stomate) THEN |
---|
636 | |
---|
637 | ! new wood mass of PFT |
---|
638 | woodmass_ind(i,j) = & |
---|
639 | & (((biomass(i,j,isapabove) + biomass(i,j,isapbelow) & |
---|
640 | & + biomass(i,j,iheartabove) + biomass(i,j,iheartbelow))) & |
---|
641 | & + (bm_sapl(j,isapabove) + bm_sapl(j,isapbelow) & |
---|
642 | & + bm_sapl(j,iheartabove) + bm_sapl(j,iheartbelow))*d_ind(i,j))/(ind(i,j)+d_ind(i,j)) |
---|
643 | |
---|
644 | ELSE ! new biomass is added to the labile pool, hence there is no change in CA associated with establishment |
---|
645 | |
---|
646 | woodmass_ind(i,j) = & |
---|
647 | & (biomass(i,j,isapabove) + biomass(i,j,isapbelow) & |
---|
648 | & + biomass(i,j,iheartabove) + biomass(i,j,iheartbelow)) & |
---|
649 | & /(ind(i,j) + d_ind(i,j)) |
---|
650 | |
---|
651 | ENDIF |
---|
652 | ENDIF |
---|
653 | ENDDO |
---|
654 | |
---|
655 | vn(:) = un ! cannot change in static!, and veget_max implicit in d_ind |
---|
656 | |
---|
657 | ENDIF |
---|
658 | ! total biomass of PFT added by establishment defined over veget_max ... |
---|
659 | total_bm_sapl(:) = zero |
---|
660 | DO k = 1, nparts |
---|
661 | WHERE(d_ind(:,j).GT.min_stomate.AND.total_bm_c(:).GT.min_stomate.AND.vn(:).GT.min_stomate) |
---|
662 | |
---|
663 | total_bm_sapl(:) = total_bm_sapl(:) + & |
---|
664 | bm_sapl(j,k) * d_ind(:,j) / vn(:) |
---|
665 | ENDWHERE |
---|
666 | ENDDO |
---|
667 | |
---|
668 | DO k = 1, nparts |
---|
669 | |
---|
670 | bm_new(:) = zero |
---|
671 | |
---|
672 | ! first ever establishment, C flows |
---|
673 | WHERE( d_ind(:,j).GT.min_stomate .AND. & |
---|
674 | total_bm_c(:).LE.min_stomate .AND. & |
---|
675 | vn(:).GT.min_stomate) |
---|
676 | ! WHERE ( many_new(:) ) |
---|
677 | |
---|
678 | !bm_new(:) = d_ind(:,j) * bm_sapl(j,k) / veget_max (:,j) |
---|
679 | bm_new(:) = d_ind(:,j) * bm_sapl(j,k) / vn(:) |
---|
680 | |
---|
681 | biomass(:,j,k) = biomass(:,j,k) + bm_new(:) |
---|
682 | |
---|
683 | co2_to_bm(:,j) = co2_to_bm(:,j) + bm_new(:) / dt |
---|
684 | |
---|
685 | ENDWHERE |
---|
686 | |
---|
687 | ! establishment into existing population, C flows |
---|
688 | WHERE(d_ind(:,j).GT.min_stomate.AND.total_bm_c(:).GT.min_stomate) |
---|
689 | |
---|
690 | bm_new(:) = total_bm_sapl(:) * biomass(:,j,k) / total_bm_c(:) |
---|
691 | |
---|
692 | biomass(:,j,k) = biomass(:,j,k) + bm_new(:) |
---|
693 | co2_to_bm(:,j) = co2_to_bm(:,j) + bm_new(:) / dt |
---|
694 | |
---|
695 | ENDWHERE |
---|
696 | ENDDO |
---|
697 | |
---|
698 | ! reset leaf ages. Should do a real calculation like in the npp routine, |
---|
699 | ! but this case is rare and not worth messing around. |
---|
700 | ! SZ 080806, added real calculation now, because otherwise leaf_age/leaf_frac |
---|
701 | ! are not initialised for the calculation of vmax, and hence no growth at all. |
---|
702 | ! logic follows that of stomate_npp.f90, just that it's been adjusted for the code here |
---|
703 | ! |
---|
704 | ! 4.5.2 Decrease leaf age in youngest class if new leaf biomass is higher than old one. |
---|
705 | ! |
---|
706 | |
---|
707 | !!$ WHERE ( many_new(:) ) |
---|
708 | !!$ leaf_age(:,j,1) = zero |
---|
709 | !!$ leaf_frac(:,j,1) = un |
---|
710 | !!$ ENDWHERE |
---|
711 | !!$ |
---|
712 | !!$ DO m = 2, nleafages |
---|
713 | !!$ |
---|
714 | !!$ WHERE ( many_new(:) ) |
---|
715 | !!$ leaf_age(:,j,m) = zero |
---|
716 | !!$ leaf_frac(:,j,m) = zero |
---|
717 | !!$ ENDWHERE |
---|
718 | !!$ |
---|
719 | !!$ ENDDO |
---|
720 | |
---|
721 | WHERE ( d_ind(:,j) * bm_sapl(j,ileaf) .GT. min_stomate ) |
---|
722 | |
---|
723 | leaf_age(:,j,1) = leaf_age(:,j,1) * leaf_mass_young(:) / & |
---|
724 | ( leaf_mass_young(:) + d_ind(:,j) * bm_sapl(j,ileaf) ) |
---|
725 | |
---|
726 | ENDWHERE |
---|
727 | |
---|
728 | leaf_mass_young(:) = leaf_mass_young(:) + d_ind(:,j) * bm_sapl(j,ileaf) |
---|
729 | |
---|
730 | ! |
---|
731 | ! new age class fractions (fraction in youngest class increases) |
---|
732 | ! |
---|
733 | |
---|
734 | ! youngest class: new mass in youngest class divided by total new mass |
---|
735 | |
---|
736 | WHERE ( biomass(:,j,ileaf) .GT. min_stomate ) |
---|
737 | |
---|
738 | leaf_frac(:,j,1) = leaf_mass_young(:) / biomass(:,j,ileaf) |
---|
739 | |
---|
740 | ENDWHERE |
---|
741 | |
---|
742 | ! other classes: old mass in leaf age class divided by new mass |
---|
743 | |
---|
744 | DO m = 2, nleafages |
---|
745 | |
---|
746 | WHERE ( biomass(:,j,ileaf) .GT. min_stomate ) |
---|
747 | |
---|
748 | leaf_frac(:,j,m) = leaf_frac(:,j,m) * & |
---|
749 | ( biomass(:,j,ileaf) + d_ind(:,j) * bm_sapl(j,ileaf) ) / biomass(:,j,ileaf) |
---|
750 | |
---|
751 | ENDWHERE |
---|
752 | |
---|
753 | ENDDO |
---|
754 | |
---|
755 | !ENDIF ! establishment rate is large |
---|
756 | |
---|
757 | WHERE ( d_ind(:,j) .GT. min_stomate ) |
---|
758 | |
---|
759 | ! 4.5.3 age decreases |
---|
760 | |
---|
761 | age(:,j) = age(:,j) * ind(:,j) / ( ind(:,j) + d_ind(:,j) ) |
---|
762 | |
---|
763 | ! 4.5.4 new number of individuals |
---|
764 | |
---|
765 | ind(:,j) = ind(:,j) + d_ind(:,j) |
---|
766 | |
---|
767 | ENDWHERE |
---|
768 | |
---|
769 | ! |
---|
770 | ! 4.6 eventually convert excess sapwood to heartwood |
---|
771 | ! |
---|
772 | |
---|
773 | !SZ to clarify with Gerhard Krinner: This is theoretically inconsistent because |
---|
774 | ! the allocation to sapwood and leaves do not follow the LPJ logic in stomate_alloc.f90 |
---|
775 | ! hence imposing this here not only solves for the uneveness of age (mixing new and average individual) |
---|
776 | ! but also corrects for the discrepancy between SLAVE and LPJ logic of allocation, thus leads to excess heartwood |
---|
777 | ! and thus carbon accumulation! |
---|
778 | ! should be removed. |
---|
779 | |
---|
780 | IF ( tree(j) ) THEN |
---|
781 | |
---|
782 | !!$ sm2(:) = 0.0 |
---|
783 | !!$ WHERE ( d_ind(:,j) .GT. 0.0 ) |
---|
784 | !!$ |
---|
785 | !!$ ! ratio of above / total sap parts |
---|
786 | !!$ sm_at(:) = biomass(:,j,isapabove) / & |
---|
787 | !!$ ( biomass(:,j,isapabove) + biomass(:,j,isapbelow) ) |
---|
788 | !!$ |
---|
789 | !!$ ! woodmass of an individual |
---|
790 | !!$ |
---|
791 | !!$ woodmass(:) = & |
---|
792 | !!$ ( biomass(:,j,isapabove) + biomass(:,j,isapbelow) + & |
---|
793 | !!$ biomass(:,j,iheartabove) + biomass(:,j,iheartbelow) ) / ind(:,j) |
---|
794 | !!$ |
---|
795 | !!$ ! crown area (m**2) depends on stem diameter (pipe model) |
---|
796 | !!$ dia(:) = ( woodmass(:) / ( pipe_density * pi/4. * pipe_tune2 ) ) & |
---|
797 | !!$ ** ( 1. / ( 2. + pipe_tune3 ) ) |
---|
798 | !!$ |
---|
799 | !!$ b1(:) = pipe_k1 / ( sla(j) * pipe_density*pipe_tune2 * dia(:)**pipe_tune3 ) * & |
---|
800 | !!$ ind(:,j) |
---|
801 | !!$ sm2(:) = lm_lastyearmax(:,j) / b1(:) |
---|
802 | !!$ |
---|
803 | !!$ ENDWHERE |
---|
804 | |
---|
805 | sm2(:) = biomass(:,j,isapabove) + biomass(:,j,isapbelow) |
---|
806 | |
---|
807 | WHERE ( ( d_ind(:,j) .GT. min_stomate ) .AND. & |
---|
808 | ( biomass(:,j,isapabove) + biomass(:,j,isapbelow) ) .GT. sm2(:) ) |
---|
809 | |
---|
810 | sm_at(:) = biomass(:,j,isapabove) / & |
---|
811 | ( biomass(:,j,isapabove) + biomass(:,j,isapbelow) ) |
---|
812 | |
---|
813 | biomass(:,j,iheartabove) = biomass(:,j,iheartabove) + & |
---|
814 | ( biomass(:,j,isapabove) - sm2(:) * sm_at(:) ) |
---|
815 | biomass(:,j,isapabove) = sm2(:) * sm_at(:) |
---|
816 | |
---|
817 | biomass(:,j,iheartbelow) = biomass(:,j,iheartbelow) + & |
---|
818 | ( biomass(:,j,isapbelow) - sm2(:) * (un - sm_at) ) |
---|
819 | biomass(:,j,isapbelow) = sm2(:) * (un - sm_at(:)) |
---|
820 | |
---|
821 | ENDWHERE |
---|
822 | |
---|
823 | ENDIF ! tree |
---|
824 | |
---|
825 | ENDIF ! natural |
---|
826 | |
---|
827 | ENDDO ! loop over pfts |
---|
828 | |
---|
829 | ! |
---|
830 | ! 5 history |
---|
831 | ! |
---|
832 | |
---|
833 | d_ind = d_ind / dt |
---|
834 | |
---|
835 | CALL histwrite (hist_id_stomate, 'IND_ESTAB', itime, d_ind, npts*nvm, horipft_index) |
---|
836 | CALL histwrite (hist_id_stomate, 'ESTABTREE', itime, estab_rate_max_tree, npts, hori_index) |
---|
837 | CALL histwrite (hist_id_stomate, 'ESTABGRASS', itime, estab_rate_max_grass, npts, hori_index) |
---|
838 | |
---|
839 | IF (bavard.GE.4) WRITE(numout,*) 'Leaving establish' |
---|
840 | |
---|
841 | END SUBROUTINE establish |
---|
842 | |
---|
843 | END MODULE lpj_establish |
---|