1 | MODULE trcbio |
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2 | !!====================================================================== |
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3 | !! *** MODULE trcbio *** |
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4 | !! TOP : LOBSTER |
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5 | !!====================================================================== |
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6 | !! History : - ! 1999-07 (M. Levy) Original code |
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7 | !! - ! 2000-12 (E. Kestenare) assign a parameter to name individual tracers |
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8 | !! - ! 2001-03 (M. Levy) LNO3 + dia2d |
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9 | !! 2.0 ! 2007-12 (C. Deltel, G. Madec) F90 |
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10 | !!---------------------------------------------------------------------- |
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11 | #if defined key_lobster |
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12 | !!---------------------------------------------------------------------- |
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13 | !! 'key_lobster' LOBSTER bio-model |
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14 | !!---------------------------------------------------------------------- |
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15 | !! trc_bio : |
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16 | !!---------------------------------------------------------------------- |
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17 | USE oce_trc ! |
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18 | USE trp_trc ! |
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19 | USE sms_lobster ! |
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20 | USE lbclnk ! |
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21 | USE prtctl_trc ! Print control for debbuging |
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22 | |
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23 | IMPLICIT NONE |
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24 | PRIVATE |
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25 | |
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26 | PUBLIC trc_bio ! called in ??? |
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27 | |
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28 | !!* Substitution |
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29 | # include "domzgr_substitute.h90" |
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30 | !!---------------------------------------------------------------------- |
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31 | !! NEMO/TOP 2.0 , LOCEAN-IPSL (2007) |
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32 | !! $Id: trcbio.F90 777 2007-12-19 18:40:57Z gm $ |
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33 | !! Software governed by the CeCILL licence (modipsl/doc/NEMO_CeCILL.txt) |
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34 | !!---------------------------------------------------------------------- |
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35 | |
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36 | CONTAINS |
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37 | |
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38 | SUBROUTINE trc_bio( kt ) |
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39 | !!--------------------------------------------------------------------- |
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40 | !! *** ROUTINE trc_bio *** |
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41 | !! |
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42 | !! ** Purpose : compute the now trend due to biogeochemical processes |
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43 | !! and add it to the general trend of passive tracers equations |
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44 | !! |
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45 | !! ** Method : each now biological flux is calculated in function of now |
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46 | !! concentrations of tracers. |
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47 | !! depending on the tracer, these fluxes are sources or sinks. |
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48 | !! the total of the sources and sinks for each tracer |
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49 | !! is added to the general trend. |
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50 | !! |
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51 | !! tra = tra + zf...tra - zftra... |
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52 | !! | | |
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53 | !! | | |
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54 | !! source sink |
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55 | !! |
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56 | !! IF 'key_trc_diabio' defined , the biogeochemical trends |
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57 | !! for passive tracers are saved for futher diagnostics. |
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58 | !!--------------------------------------------------------------------- |
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59 | INTEGER, INTENT( in ) :: kt ! ocean time-step index |
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60 | !! |
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61 | INTEGER :: ji, jj, jk |
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62 | REAL(wp) :: zdet, zzoo, zphy, zno3, znh4, zdom ! now concentrations |
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63 | REAL(wp) :: zlno3, zlnh4, zle, zlt ! limitation terms for phyto |
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64 | REAL(wp) :: zno3phy, znh4phy, zphynh4, zphydom |
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65 | REAL(wp) :: zphydet, zphyzoo, zdetzoo |
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66 | REAL(wp) :: zzoonh4, zzoodom, zzoodet, zdetnh4, zdetdom |
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67 | REAL(wp) :: znh4no3, zdomnh4, zppz, zpdz, zpppz, zppdz, zfood |
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68 | REAL(wp) :: zfilpz, zfildz, zphya, zzooa, zno3a |
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69 | REAL(wp) :: znh4a, zdeta, zdoma, zzoobod, zboddet, zdomaju |
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70 | #if defined key_trc_diaadd |
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71 | REAL(wp), DIMENSION(jpi,jpj,jpk) :: ze3t |
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72 | #endif |
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73 | CHARACTER (len=25) :: charout |
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74 | !!--------------------------------------------------------------------- |
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75 | |
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76 | IF( kt == nit000 ) THEN |
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77 | IF(lwp) WRITE(numout,*) |
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78 | IF(lwp) WRITE(numout,*) ' trc_bio: LOBSTER bio-model' |
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79 | IF(lwp) WRITE(numout,*) ' ~~~~~~~' |
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80 | ENDIF |
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81 | |
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82 | #if defined key_trc_diaadd |
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83 | ! convert fluxes in per day |
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84 | ze3t(:,:,:) = 0.e0 |
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85 | DO jk = 1, jpkbm1 |
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86 | ze3t(:,:,jk) = fse3t(:,:,jk) * 86400. |
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87 | END DO |
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88 | #endif |
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89 | |
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90 | fbod(:,:) = 0.e0 |
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91 | #if defined key_trc_diaadd |
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92 | DO ji = 1, jpdia2d |
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93 | trc2d(:,:,ji) = 0.e0 |
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94 | END DO |
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95 | #endif |
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96 | |
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97 | |
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98 | ! ! -------------------------- ! |
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99 | DO jk = 1, jpkbm1 ! Upper ocean (bio-layers) ! |
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100 | ! ! -------------------------- ! |
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101 | DO jj = 2, jpjm1 |
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102 | DO ji = 2, jpim1 !!gm use of fs_2 fs_jpm1 required here |
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103 | |
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104 | ! trophic variables( det, zoo, phy, no3, nh4, dom) |
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105 | ! ------------------------------------------------ |
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106 | |
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107 | ! negative trophic variables DO not contribute to the fluxes |
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108 | zdet = MAX( 0.e0, trn(ji,jj,jk,jpdet) ) |
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109 | zzoo = MAX( 0.e0, trn(ji,jj,jk,jpzoo) ) |
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110 | zphy = MAX( 0.e0, trn(ji,jj,jk,jpphy) ) |
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111 | zno3 = MAX( 0.e0, trn(ji,jj,jk,jpno3) ) |
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112 | znh4 = MAX( 0.e0, trn(ji,jj,jk,jpnh4) ) |
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113 | zdom = MAX( 0.e0, trn(ji,jj,jk,jpdom) ) |
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114 | |
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115 | ! Limitations |
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116 | zlt = 1. |
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117 | zle = 1. - EXP( -xpar(ji,jj,jk) / aki / zlt ) |
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118 | ! psinut,akno3,aknh4 added by asklod AS Kremeur 2005-03 |
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119 | zlno3 = zno3 * EXP( -psinut * znh4 ) / ( akno3 + zno3 ) |
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120 | zlnh4 = znh4 / (znh4+aknh4) |
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121 | |
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122 | |
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123 | ! sinks and sources |
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124 | ! phytoplankton production and exsudation |
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125 | zno3phy = tmumax * zle * zlt * zlno3 * zphy |
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126 | znh4phy = tmumax * zle * zlt * zlnh4 * zphy |
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127 | |
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128 | ! fphylab added by asklod AS Kremeur 2005-03 |
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129 | zphydom = rgamma * (1 - fphylab) * (zno3phy + znh4phy) |
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130 | zphynh4 = rgamma * fphylab * (zno3phy + znh4phy) |
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131 | |
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132 | ! zooplankton production |
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133 | ! preferences |
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134 | zppz = rppz |
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135 | zpdz = 1. - rppz |
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136 | zpppz = ( zppz * zphy ) / ( ( zppz * zphy + zpdz * zdet ) + 1.e-13 ) |
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137 | zppdz = ( zpdz * zdet ) / ( ( zppz * zphy + zpdz * zdet ) + 1.e-13 ) |
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138 | zfood = zpppz * zphy + zppdz * zdet |
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139 | ! filtration |
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140 | zfilpz = taus * zpppz / (aks + zfood) |
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141 | zfildz = taus * zppdz / (aks + zfood) |
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142 | ! grazing |
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143 | zphyzoo = zfilpz * zphy * zzoo |
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144 | zdetzoo = zfildz * zdet * zzoo |
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145 | |
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146 | ! fecal pellets production |
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147 | zzoodet = rpnaz * zphyzoo + rdnaz * zdetzoo |
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148 | |
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149 | ! zooplankton liquide excretion |
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150 | zzoonh4 = tauzn * fzoolab * zzoo |
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151 | zzoodom = tauzn * (1 - fzoolab) * zzoo |
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152 | |
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153 | ! mortality |
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154 | ! phytoplankton mortality |
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155 | zphydet = tmminp * zphy |
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156 | |
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157 | ! zooplankton mortality |
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158 | ! closure : flux fbod is redistributed below level jpkbio |
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159 | zzoobod = tmminz * zzoo * zzoo |
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160 | fbod(ji,jj) = fbod(ji,jj) + (1-fdbod) * zzoobod * fse3t(ji,jj,jk) |
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161 | zboddet = fdbod * zzoobod |
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162 | |
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163 | ! detritus and dom breakdown |
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164 | zdetnh4 = taudn * fdetlab * zdet |
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165 | zdetdom = taudn * (1 - fdetlab) * zdet |
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166 | |
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167 | zdomnh4 = taudomn * zdom |
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168 | |
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169 | ! flux added to express how the excess of nitrogen from |
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170 | ! PHY, ZOO and DET to DOM goes directly to NH4 (flux of ajustment) |
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171 | zdomaju = (1 - redf/reddom) * (zphydom + zzoodom + zdetdom) |
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172 | |
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173 | ! Nitrification |
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174 | znh4no3 = taunn * znh4 |
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175 | |
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176 | ! determination of trends |
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177 | ! total trend for each biological tracer |
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178 | zphya = zno3phy + znh4phy - zphynh4 - zphydom - zphyzoo - zphydet |
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179 | zzooa = zphyzoo + zdetzoo - zzoodet - zzoodom - zzoonh4 - zzoobod |
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180 | zno3a = - zno3phy + znh4no3 |
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181 | znh4a = - znh4phy - znh4no3 + zphynh4 + zzoonh4 + zdomnh4 + zdetnh4 + zdomaju |
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182 | zdeta = zphydet + zzoodet - zdetzoo - zdetnh4 - zdetdom + zboddet |
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183 | zdoma = zphydom + zzoodom + zdetdom - zdomnh4 - zdomaju |
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184 | |
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185 | #if defined key_trc_diabio |
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186 | trbio(ji,jj,jk, 1) = zno3phy |
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187 | trbio(ji,jj,jk, 2) = znh4phy |
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188 | trbio(ji,jj,jk, 3) = zphynh4 |
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189 | trbio(ji,jj,jk, 4) = zphydom |
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190 | trbio(ji,jj,jk, 5) = zphyzoo |
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191 | trbio(ji,jj,jk, 6) = zphydet |
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192 | trbio(ji,jj,jk, 7) = zdetzoo |
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193 | trbio(ji,jj,jk, 9) = zzoodet |
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194 | trbio(ji,jj,jk,10) = zzoobod |
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195 | trbio(ji,jj,jk,11) = zzoonh4 |
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196 | trbio(ji,jj,jk,12) = zzoodom |
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197 | trbio(ji,jj,jk,13) = znh4no3 |
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198 | trbio(ji,jj,jk,14) = zdomnh4 |
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199 | trbio(ji,jj,jk,15) = zdetnh4 |
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200 | #endif |
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201 | #if defined key_trc_diaadd |
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202 | trc2d(ji,jj, 1) = trc2d(ji,jj, 1) + zno3phy * ze3t(ji,jj,jk) |
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203 | trc2d(ji,jj, 2) = trc2d(ji,jj, 2) + znh4phy * ze3t(ji,jj,jk) |
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204 | trc2d(ji,jj, 3) = trc2d(ji,jj, 3) + zphydom * ze3t(ji,jj,jk) |
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205 | trc2d(ji,jj, 4) = trc2d(ji,jj, 4) + zphynh4 * ze3t(ji,jj,jk) |
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206 | trc2d(ji,jj, 5) = trc2d(ji,jj, 5) + zphyzoo * ze3t(ji,jj,jk) |
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207 | trc2d(ji,jj, 6) = trc2d(ji,jj, 6) + zphydet * ze3t(ji,jj,jk) |
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208 | trc2d(ji,jj, 7) = trc2d(ji,jj, 7) + zdetzoo * ze3t(ji,jj,jk) |
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209 | ! trend number 8 is in trcsed.F |
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210 | trc2d(ji,jj, 9) = trc2d(ji,jj, 9) + zzoodet * ze3t(ji,jj,jk) |
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211 | trc2d(ji,jj,10) = trc2d(ji,jj,10) + zzoobod * ze3t(ji,jj,jk) |
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212 | trc2d(ji,jj,11) = trc2d(ji,jj,11) + zzoonh4 * ze3t(ji,jj,jk) |
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213 | trc2d(ji,jj,12) = trc2d(ji,jj,12) + zzoodom * ze3t(ji,jj,jk) |
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214 | trc2d(ji,jj,13) = trc2d(ji,jj,13) + znh4no3 * ze3t(ji,jj,jk) |
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215 | trc2d(ji,jj,14) = trc2d(ji,jj,14) + zdomnh4 * ze3t(ji,jj,jk) |
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216 | trc2d(ji,jj,15) = trc2d(ji,jj,15) + zdetnh4 * ze3t(ji,jj,jk) |
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217 | |
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218 | trc2d(ji,jj,16) = trc2d(ji,jj,16) + ( zno3phy + znh4phy - zphynh4 & |
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219 | & - zphydom - zphyzoo - zphydet ) * ze3t(ji,jj,jk) |
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220 | trc2d(ji,jj,17) = trc2d(ji,jj,17) + ( zphyzoo + zdetzoo - zzoodet & |
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221 | & - zzoobod - zzoonh4 - zzoodom ) * ze3t(ji,jj,jk) |
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222 | trc2d(ji,jj,18) = trc2d(ji,jj,18) + zdetdom * ze3t(ji,jj,jk) |
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223 | ! trend number 19 is in trcexp.F |
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224 | trc3d(ji,jj,jk,1) = zno3phy * 86400 |
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225 | trc3d(ji,jj,jk,2) = znh4phy * 86400 |
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226 | trc3d(ji,jj,jk,3) = znh4no3 * 86400 |
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227 | #endif |
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228 | |
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229 | ! tracer flux at totox-point added to the general trend |
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230 | tra(ji,jj,jk,jpdet) = tra(ji,jj,jk,jpdet) + zdeta |
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231 | tra(ji,jj,jk,jpzoo) = tra(ji,jj,jk,jpzoo) + zzooa |
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232 | tra(ji,jj,jk,jpphy) = tra(ji,jj,jk,jpphy) + zphya |
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233 | tra(ji,jj,jk,jpno3) = tra(ji,jj,jk,jpno3) + zno3a |
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234 | tra(ji,jj,jk,jpnh4) = tra(ji,jj,jk,jpnh4) + znh4a |
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235 | tra(ji,jj,jk,jpdom) = tra(ji,jj,jk,jpdom) + zdoma |
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236 | |
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237 | END DO |
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238 | END DO |
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239 | END DO |
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240 | |
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241 | !!gm do loop until jpkm1 only! |
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242 | ! ! -------------------------- ! |
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243 | DO jk = jpkb, jpk ! Upper ocean (bio-layers) ! |
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244 | ! ! -------------------------- ! |
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245 | |
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246 | DO jj = 2, jpjm1 |
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247 | DO ji = 2,jpim1 !!gm use of fs_2 & fs_jpim1 required |
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248 | |
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249 | ! remineralisation of all quantities towards nitrate |
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250 | |
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251 | ! trophic variables( det, zoo, phy, no3, nh4, dom) |
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252 | ! negative trophic variables DO not contribute to the fluxes |
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253 | zdet = MAX( 0.e0, trn(ji,jj,jk,jpdet) ) |
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254 | zzoo = MAX( 0.e0, trn(ji,jj,jk,jpzoo) ) |
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255 | zphy = MAX( 0.e0, trn(ji,jj,jk,jpphy) ) |
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256 | zno3 = MAX( 0.e0, trn(ji,jj,jk,jpno3) ) |
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257 | znh4 = MAX( 0.e0, trn(ji,jj,jk,jpnh4) ) |
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258 | zdom = MAX( 0.e0, trn(ji,jj,jk,jpdom) ) |
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259 | |
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260 | ! Limitations |
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261 | zlt = 0.e0 |
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262 | zle = 0.e0 |
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263 | zlno3 = 0.e0 |
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264 | zlnh4 = 0.e0 |
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265 | |
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266 | ! sinks and sources |
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267 | ! phytoplankton production and exsudation |
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268 | zno3phy = 0.e0 |
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269 | znh4phy = 0.e0 |
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270 | zphydom = 0.e0 |
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271 | zphynh4 = 0.e0 |
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272 | |
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273 | ! zooplankton production |
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274 | zphyzoo = 0.e0 ! grazing |
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275 | zdetzoo = 0.e0 |
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276 | |
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277 | zzoodet = 0.e0 ! fecal pellets production |
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278 | |
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279 | zzoonh4 = tauzn * fzoolab * zzoo ! zooplankton liquide excretion |
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280 | zzoodom = tauzn * (1 - fzoolab) * zzoo |
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281 | |
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282 | ! mortality |
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283 | zphydet = tmminp * zphy ! phytoplankton mortality |
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284 | |
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285 | zzoobod = 0.e0 ! zooplankton mortality |
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286 | zboddet = 0.e0 ! closure : flux fbod is redistributed below level jpkbio |
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287 | |
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288 | ! detritus and dom breakdown |
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289 | zdetnh4 = taudn * fdetlab * zdet |
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290 | zdetdom = taudn * (1 - fdetlab) * zdet |
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291 | |
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292 | zdomnh4 = taudomn * zdom |
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293 | zdomaju = (1 - redf/reddom) * (zphydom + zzoodom + zdetdom) |
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294 | |
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295 | ! Nitrification |
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296 | znh4no3 = taunn * znh4 |
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297 | |
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298 | |
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299 | ! determination of trends |
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300 | ! total trend for each biological tracer |
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301 | zphya = zno3phy + znh4phy - zphynh4 - zphydom - zphyzoo - zphydet |
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302 | zzooa = zphyzoo + zdetzoo - zzoodet - zzoodom - zzoonh4 - zzoobod |
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303 | zno3a = - zno3phy + znh4no3 |
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304 | znh4a = - znh4phy - znh4no3 + zphynh4 + zzoonh4 + zdomnh4 + zdetnh4 + zdomaju |
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305 | zdeta = zphydet + zzoodet - zdetzoo - zdetnh4 - zdetdom + zboddet |
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306 | zdoma = zphydom + zzoodom + zdetdom - zdomnh4 - zdomaju |
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307 | |
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308 | #if defined key_trc_diabio |
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309 | trbio(ji,jj,jk, 1) = zno3phy |
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310 | trbio(ji,jj,jk, 2) = znh4phy |
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311 | trbio(ji,jj,jk, 3) = zphynh4 |
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312 | trbio(ji,jj,jk, 4) = zphydom |
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313 | trbio(ji,jj,jk, 5) = zphyzoo |
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314 | trbio(ji,jj,jk, 6) = zphydet |
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315 | trbio(ji,jj,jk, 7) = zdetzoo |
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316 | trbio(ji,jj,jk, 9) = zzoodet |
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317 | trbio(ji,jj,jk,10) = zzoobod |
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318 | trbio(ji,jj,jk,11) = zzoonh4 |
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319 | trbio(ji,jj,jk,12) = zzoodom |
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320 | trbio(ji,jj,jk,13) = znh4no3 |
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321 | trbio(ji,jj,jk,14) = zdomnh4 |
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322 | trbio(ji,jj,jk,15) = zdetnh4 |
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323 | #endif |
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324 | #if defined key_trc_diaadd |
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325 | trc2d(ji,jj, 1) = trc2d(ji,jj, 1) + zno3phy * ze3t(ji,jj,jk) |
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326 | trc2d(ji,jj, 2) = trc2d(ji,jj, 2) + znh4phy * ze3t(ji,jj,jk) |
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327 | trc2d(ji,jj, 3) = trc2d(ji,jj, 3) + zphydom * ze3t(ji,jj,jk) |
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328 | trc2d(ji,jj, 4) = trc2d(ji,jj, 4) + zphynh4 * ze3t(ji,jj,jk) |
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329 | trc2d(ji,jj, 5) = trc2d(ji,jj, 5) + zphyzoo * ze3t(ji,jj,jk) |
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330 | trc2d(ji,jj, 6) = trc2d(ji,jj, 6) + zphydet * ze3t(ji,jj,jk) |
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331 | trc2d(ji,jj, 7) = trc2d(ji,jj, 7) + zdetzoo * ze3t(ji,jj,jk) |
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332 | ! trend number 8 is in trcsed.F |
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333 | trc2d(ji,jj, 9) = trc2d(ji,jj, 9) + zzoodet * ze3t(ji,jj,jk) |
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334 | trc2d(ji,jj,10) = trc2d(ji,jj,10) + zzoobod * ze3t(ji,jj,jk) |
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335 | trc2d(ji,jj,11) = trc2d(ji,jj,11) + zzoonh4 * ze3t(ji,jj,jk) |
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336 | trc2d(ji,jj,12) = trc2d(ji,jj,12) + zzoodom * ze3t(ji,jj,jk) |
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337 | trc2d(ji,jj,13) = trc2d(ji,jj,13) + znh4no3 * ze3t(ji,jj,jk) |
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338 | trc2d(ji,jj,14) = trc2d(ji,jj,14) + zdomnh4 * ze3t(ji,jj,jk) |
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339 | trc2d(ji,jj,15) = trc2d(ji,jj,15) + zdetnh4 * ze3t(ji,jj,jk) |
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340 | |
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341 | trc2d(ji,jj,16) = trc2d(ji,jj,16) + ( zno3phy + znh4phy - zphynh4 & |
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342 | & - zphydom - zphyzoo - zphydet ) * ze3t(ji,jj,jk) |
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343 | trc2d(ji,jj,17) = trc2d(ji,jj,17) + ( zphyzoo + zdetzoo - zzoodet & |
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344 | & - zzoobod - zzoonh4 - zzoodom ) * ze3t(ji,jj,jk) |
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345 | trc2d(ji,jj,18) = trc2d(ji,jj,18) + zdetdom * ze3t(ji,jj,jk) |
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346 | |
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347 | trc3d(ji,jj,jk,1) = zno3phy * 86400 |
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348 | trc3d(ji,jj,jk,2) = znh4phy * 86400 |
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349 | trc3d(ji,jj,jk,3) = znh4no3 * 86400 |
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350 | #endif |
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351 | |
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352 | ! tracer flux at totox-point added to the general trend |
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353 | tra(ji,jj,jk,jpdet) = tra(ji,jj,jk,jpdet) + zdeta |
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354 | tra(ji,jj,jk,jpzoo) = tra(ji,jj,jk,jpzoo) + zzooa |
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355 | tra(ji,jj,jk,jpphy) = tra(ji,jj,jk,jpphy) + zphya |
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356 | tra(ji,jj,jk,jpno3) = tra(ji,jj,jk,jpno3) + zno3a |
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357 | tra(ji,jj,jk,jpnh4) = tra(ji,jj,jk,jpnh4) + znh4a |
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358 | tra(ji,jj,jk,jpdom) = tra(ji,jj,jk,jpdom) + zdoma |
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359 | ! |
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360 | END DO |
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361 | END DO |
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362 | END DO |
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363 | |
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364 | #if defined key_trc_diaadd |
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365 | ! Lateral boundary conditions on trc2d and trc3d |
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366 | DO ji = 1, jpdia2d |
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367 | CALL lbc_lnk( trc2d(:,:,ji),'T', 1. ) |
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368 | END DO |
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369 | DO ji = 1, jpdia3d |
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370 | CALL lbc_lnk( trc3d(:,:,1,ji),'T', 1. ) |
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371 | END DO |
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372 | #endif |
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373 | |
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374 | #if defined key_trc_diabio |
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375 | ! Lateral boundary conditions on trcbio |
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376 | DO ji = 1, jpdiabio |
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377 | CALL lbc_lnk( trbio(:,:,1,ji),'T', 1. ) |
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378 | END DO |
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379 | #endif |
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380 | ! |
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381 | IF(ln_ctl) THEN ! print mean trends (used for debugging) |
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382 | WRITE(charout, FMT="('bio')") |
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383 | CALL prt_ctl_trc_info(charout) |
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384 | CALL prt_ctl_trc(tab4d=tra, mask=tmask, clinfo=ctrcnm) |
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385 | ENDIF |
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386 | |
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387 | END SUBROUTINE trc_bio |
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388 | |
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389 | #else |
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390 | !!====================================================================== |
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391 | !! Dummy module : No PISCES bio-model |
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392 | !!====================================================================== |
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393 | CONTAINS |
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394 | SUBROUTINE trc_bio( kt ) ! Empty routine |
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395 | INTEGER, INTENT( in ) :: kt |
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396 | WRITE(*,*) 'trc_bio: You should not have seen this print! error?', kt |
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397 | END SUBROUTINE trc_bio |
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398 | #endif |
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399 | |
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400 | !!====================================================================== |
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401 | END MODULE trcbio |
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