1 | |
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2 | CCC $Header$ |
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3 | CCC TOP 1.0 , LOCEAN-IPSL (2005) |
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4 | C This software is governed by CeCILL licence see modipsl/doc/NEMO_CeCILL.txt |
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5 | C --------------------------------------------------------------------------- |
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6 | SUBROUTINE trcbio(kt) |
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7 | #if defined key_passivetrc && defined key_trc_lobster1 |
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8 | CCC--------------------------------------------------------------------- |
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9 | CCC |
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10 | CCC ROUTINE trcbio |
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11 | CCC ******************* |
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12 | CCC |
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13 | CCC PURPOSE : |
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14 | CCC --------- |
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15 | CCC compute the now trend due to biogeochemical processes |
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16 | CCC and add it to the general trend of passive tracers equations. |
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17 | CCC |
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18 | CCC Three options: |
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19 | CCC Default option : no biological trend |
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20 | CCC IF 'key_trc_lobster1' : LOBSTER1 model |
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21 | CCC |
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22 | CC METHOD : |
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23 | CC ------- |
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24 | CC each now biological flux is calculated in FUNCTION of now |
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25 | CC concentrations of tracers. |
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26 | CC depending on the tracer, these fluxes are sources or sinks. |
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27 | CC the total of the sources and sinks for each tracer |
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28 | CC is added to the general trend. |
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29 | CC |
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30 | CC tra = tra + zf...tra - zftra... |
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31 | CC | | |
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32 | CC | | |
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33 | CC source sink |
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34 | CC |
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35 | CC |
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36 | CC IF 'key_trc_diabio' key is activated, the biogeochemical |
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37 | CC trends for passive tracers are saved for futher diagnostics. |
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38 | CC |
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39 | CC multitasked on vertical slab (jj-loop) |
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40 | CC |
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41 | CC ----- |
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42 | CC argument |
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43 | CC ktask : task identificator |
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44 | CC kt : time step |
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45 | CC COMMON |
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46 | CC /comcoo/ : orthogonal curvilinear coordinates |
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47 | CC and scale factors |
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48 | CC depths |
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49 | CC /cottrp/ : present and next fields for passive |
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50 | CC : tracers |
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51 | CC /comtsk/ : multitasking |
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52 | CC /comtke/ : emin, en() |
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53 | CC /cotbio/ : biological parameters |
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54 | CC |
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55 | CC OUTPUT : |
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56 | CC ------ |
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57 | CC COMMON |
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58 | CC /cottrp/ tra : general tracer trend increased by the |
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59 | CC now horizontal tracer advection trend |
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60 | CC /cottbd/ trbio : now horizontal tracer advection trend |
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61 | CC (IF 'key_trc_diabio' is activated) |
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62 | CC |
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63 | CC WORKSPACE : |
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64 | CC --------- |
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65 | CC local |
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66 | CC zdet,zzoo,zphy,znh4,zno3,zdom : now concentrations |
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67 | CC zlt,zlno3,zlnh4,zle : limitation terms for phyto |
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68 | CC zfno3phy and so on.. : fluxes between bio boxes |
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69 | CC zphya,zzooa,zdeta, ... : after bio trends |
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70 | CC zppz, zpdz, zpppz, zppdz, zfood : preferences terms |
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71 | CC zfilpz, zfilpd : filtration terms |
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72 | CC COMMON |
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73 | CC |
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74 | CC EXTERNAL : no |
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75 | CC -------- |
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76 | CC |
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77 | CC REFERENCES : no |
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78 | CC ---------- |
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79 | CC |
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80 | CC MODIFICATIONS: |
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81 | CC -------------- |
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82 | CC original : 99-07 (M. Levy) |
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83 | CC 00-12 (E. Kestenare): assign a parameter |
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84 | CC to name individual tracers |
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85 | CC 01-03 (M. Levy) LNO3 + dia2d |
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86 | CC---------------------------------------------------------------------- |
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87 | CC---------------------------------------------------------------------- |
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88 | USE oce_trc |
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89 | USE trp_trc |
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90 | USE sms |
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91 | USE lbclnk |
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92 | IMPLICIT NONE |
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93 | CC local declarations |
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94 | CC ================== |
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95 | INTEGER kt |
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96 | INTEGER ji,jj,jk,jn |
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97 | REAL ztot(jpi) |
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98 | #if defined key_trc_diaadd |
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99 | REAL ze3t(jpi,jpj,jpk) |
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100 | endif |
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101 | REAL zdet,zzoo,zphy,zno3,znh4,zdom,zlno3,zlnh4,zle,zlt |
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102 | REAL zno3phy, znh4phy, zphynh4, zphydom, zphydet, zphyzoo, zdetzoo |
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103 | $ ,zzoonh4, zzoodom, zzoodet, zdetnh4, zdetdom, znh4no3, zdomnh4 |
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104 | $ ,zppz,zpdz,zpppz,zppdz,zfood,zfilpz,zfildz,zphya,zzooa,zno3a |
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105 | $ ,znh4a,zdeta,zdoma, ztra, zzoobod, zboddet, zdomaju |
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106 | |
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107 | CC---------------------------------------------------------------------- |
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108 | CC statement functions |
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109 | CC =================== |
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110 | CDIR$ NOLIST |
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111 | #include "domzgr_substitute.h90" |
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112 | CDIR$ LIST |
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113 | CCC--------------------------------------------------------------------- |
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114 | CCC OPA8, LODYC (07/99) |
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115 | CCC--------------------------------------------------------------------- |
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116 | C | --------------| |
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117 | C | LOBSTER1 MODEL| |
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118 | C | --------------| |
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119 | |
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120 | #if defined key_trc_diaadd |
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121 | C convert fluxes in per day |
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122 | ze3t(:,:,:) = 0. |
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123 | DO jk=1,jpkbm1 |
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124 | DO jj = 2, jpjm1 |
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125 | DO ji = 2, jpim1 |
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126 | ze3t(ji,jj,jk)=fse3t(ji,jj,jk)*86400. |
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127 | END DO |
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128 | END DO |
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129 | END DO |
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130 | #endif |
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131 | C |
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132 | C vertical slab |
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133 | C ============= |
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134 | C |
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135 | DO 1000 jj = 2,jpjm1 |
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136 | C |
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137 | C 1. biological level |
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138 | C =================== |
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139 | C |
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140 | DO ji = 2,jpim1 |
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141 | fbod(ji,jj)=0. |
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142 | #if defined key_trc_diaadd |
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143 | DO jn=1,jpdia2d |
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144 | trc2d(ji,jj,jn)=0. |
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145 | END DO |
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146 | #endif |
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147 | END DO |
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148 | |
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149 | DO jk=1,jpkbm1 |
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150 | DO ji = 2,jpim1 |
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151 | C |
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152 | C |
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153 | C 1.1 trophic variables( det, zoo, phy, no3, nh4, dom) |
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154 | C --------------------------------------------------- |
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155 | C |
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156 | C negative trophic variables DO not contribute to the fluxes |
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157 | C |
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158 | zdet = max(0.,trn(ji,jj,jk,jpdet)) |
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159 | zzoo = max(0.,trn(ji,jj,jk,jpzoo)) |
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160 | zphy = max(0.,trn(ji,jj,jk,jpphy)) |
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161 | zno3 = max(0.,trn(ji,jj,jk,jpno3)) |
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162 | znh4 = max(0.,trn(ji,jj,jk,jpnh4)) |
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163 | zdom = max(0.,trn(ji,jj,jk,jpdom)) |
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164 | C |
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165 | C |
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166 | C 1.2 Limitations |
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167 | C ---------------- |
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168 | C |
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169 | zlt = 1. |
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170 | zle = 1. - exp( -xpar(ji,jj,jk)/aki/zlt) |
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171 | C psinut,akno3,aknh4 added by asklod AS Kremeur 2005-03 |
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172 | zlno3 = zno3* exp(-psinut*znh4) / (akno3+zno3) |
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173 | zlnh4 = znh4 / (znh4+aknh4) |
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174 | |
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175 | C |
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176 | C |
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177 | C 1.3 sinks and sources |
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178 | C --------------------- |
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179 | C |
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180 | C |
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181 | C 1. phytoplankton production and exsudation |
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182 | C |
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183 | zno3phy = tmumax * zle * zlt * zlno3 * zphy |
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184 | znh4phy = tmumax * zle * zlt * zlnh4 * zphy |
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185 | |
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186 | C fphylab added by asklod AS Kremeur 2005-03 |
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187 | zphydom = rgamma * (1 - fphylab) * (zno3phy + znh4phy) |
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188 | zphynh4 = rgamma * fphylab * (zno3phy + znh4phy) |
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189 | |
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190 | C |
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191 | C 2. zooplankton production |
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192 | C |
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193 | C preferences |
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194 | C |
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195 | zppz = rppz |
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196 | zpdz = 1. - rppz |
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197 | zpppz = ( zppz * zphy ) / |
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198 | $ ( ( zppz * zphy + zpdz * zdet ) + 1.e-13 ) |
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199 | zppdz = ( zpdz * zdet ) / |
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200 | $ ( ( zppz * zphy + zpdz * zdet ) + 1.e-13 ) |
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201 | zfood = zpppz * zphy + zppdz * zdet |
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202 | C |
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203 | C filtration |
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204 | C |
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205 | zfilpz = taus * zpppz / (aks + zfood) |
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206 | zfildz = taus * zppdz / (aks + zfood) |
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207 | C |
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208 | C grazing |
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209 | C |
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210 | zphyzoo = zfilpz * zphy * zzoo |
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211 | zdetzoo = zfildz * zdet * zzoo |
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212 | C |
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213 | C 3. fecal pellets production |
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214 | C |
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215 | zzoodet = rpnaz * zphyzoo + rdnaz * zdetzoo |
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216 | C |
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217 | C 4. zooplankton liquide excretion |
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218 | C |
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219 | zzoonh4 = tauzn * fzoolab * zzoo |
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220 | zzoodom = tauzn * (1 - fzoolab) * zzoo |
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221 | C |
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222 | C 5. mortality |
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223 | C |
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224 | C phytoplankton mortality |
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225 | C |
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226 | zphydet = tmminp * zphy |
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227 | C |
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228 | C |
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229 | C zooplankton mortality |
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230 | c closure : flux fbod is redistributed below level jpkbio |
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231 | C |
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232 | zzoobod = tmminz * zzoo * zzoo |
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233 | fbod(ji,jj) = fbod(ji,jj) |
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234 | $ + (1-fdbod) * zzoobod * fse3t(ji,jj,jk) |
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235 | zboddet = fdbod * zzoobod |
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236 | C |
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237 | C |
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238 | C 6. detritus and dom breakdown |
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239 | C |
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240 | C |
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241 | zdetnh4 = taudn * fdetlab * zdet |
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242 | zdetdom = taudn * (1 - fdetlab) * zdet |
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243 | |
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244 | zdomnh4 = taudomn * zdom |
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245 | C |
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246 | C flux added to express how the excess of nitrogen from |
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247 | C PHY, ZOO and DET to DOM goes directly to NH4 (flux of ajustment) |
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248 | zdomaju = (1 - redf/reddom) * (zphydom + zzoodom + zdetdom) |
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249 | C |
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250 | C 7. Nitrification |
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251 | C |
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252 | znh4no3 = taunn * znh4 |
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253 | C |
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254 | C |
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255 | C |
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256 | C 1.4 determination of trends |
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257 | C --------------------------- |
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258 | C |
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259 | C total trend for each biological tracer |
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260 | C |
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261 | zphya = zno3phy + znh4phy - zphynh4 - zphydom - zphyzoo |
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262 | $ - zphydet |
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263 | zzooa = zphyzoo + zdetzoo - zzoodet - zzoodom - zzoonh4 |
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264 | $ - zzoobod |
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265 | zno3a = - zno3phy + znh4no3 |
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266 | znh4a = - znh4phy - znh4no3 + zphynh4 + zzoonh4 + zdomnh4 |
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267 | $ + zdetnh4 + zdomaju |
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268 | zdeta = zphydet + zzoodet - zdetzoo - zdetnh4 - zdetdom + |
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269 | $ zboddet |
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270 | zdoma = zphydom + zzoodom + zdetdom - zdomnh4 - zdomaju |
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271 | C |
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272 | #if defined key_trc_diabio |
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273 | trbio(ji,jj,jk,1) = zno3phy |
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274 | trbio(ji,jj,jk,2) = znh4phy |
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275 | trbio(ji,jj,jk,3) = zphynh4 |
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276 | trbio(ji,jj,jk,4) = zphydom |
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277 | trbio(ji,jj,jk,5) = zphyzoo |
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278 | trbio(ji,jj,jk,6) = zphydet |
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279 | trbio(ji,jj,jk,7) = zdetzoo |
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280 | trbio(ji,jj,jk,9) = zzoodet |
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281 | trbio(ji,jj,jk,10) = zzoobod |
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282 | trbio(ji,jj,jk,11) = zzoonh4 |
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283 | trbio(ji,jj,jk,12) = zzoodom |
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284 | trbio(ji,jj,jk,13) = znh4no3 |
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285 | trbio(ji,jj,jk,14) = zdomnh4 |
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286 | trbio(ji,jj,jk,15) = zdetnh4 |
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287 | #endif |
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288 | #if defined key_trc_diaadd |
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289 | trc2d(ji,jj,1)=trc2d(ji,jj,1)+zno3phy*ze3t(ji,jj,jk) |
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290 | trc2d(ji,jj,2)=trc2d(ji,jj,2)+znh4phy*ze3t(ji,jj,jk) |
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291 | trc2d(ji,jj,3)=trc2d(ji,jj,3)+zphydom*ze3t(ji,jj,jk) |
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292 | trc2d(ji,jj,4)=trc2d(ji,jj,4)+zphynh4*ze3t(ji,jj,jk) |
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293 | trc2d(ji,jj,5)=trc2d(ji,jj,5)+zphyzoo*ze3t(ji,jj,jk) |
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294 | trc2d(ji,jj,6)=trc2d(ji,jj,6)+zphydet*ze3t(ji,jj,jk) |
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295 | trc2d(ji,jj,7)=trc2d(ji,jj,7)+zdetzoo*ze3t(ji,jj,jk) |
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296 | c trend number 8 is in trcsed.F |
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297 | trc2d(ji,jj,9)=trc2d(ji,jj,9)+zzoodet*ze3t(ji,jj,jk) |
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298 | trc2d(ji,jj,10)=trc2d(ji,jj,10)+zzoobod*ze3t(ji,jj,jk) |
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299 | trc2d(ji,jj,11)=trc2d(ji,jj,11)+zzoonh4*ze3t(ji,jj,jk) |
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300 | trc2d(ji,jj,12)=trc2d(ji,jj,12)+zzoodom*ze3t(ji,jj,jk) |
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301 | trc2d(ji,jj,13)=trc2d(ji,jj,13)+znh4no3*ze3t(ji,jj,jk) |
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302 | trc2d(ji,jj,14)=trc2d(ji,jj,14)+zdomnh4*ze3t(ji,jj,jk) |
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303 | trc2d(ji,jj,15)=trc2d(ji,jj,15)+zdetnh4*ze3t(ji,jj,jk) |
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304 | |
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305 | trc2d(ji,jj,16)=trc2d(ji,jj,16)+(zno3phy+znh4phy-zphynh4 |
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306 | $ -zphydom-zphyzoo-zphydet)*ze3t(ji,jj,jk) |
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307 | trc2d(ji,jj,17)=trc2d(ji,jj,17)+(zphyzoo+zdetzoo-zzoodet |
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308 | $ -zzoobod-zzoonh4-zzoodom) *ze3t(ji,jj,jk) |
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309 | trc2d(ji,jj,18)=trc2d(ji,jj,18)+zdetdom*ze3t(ji,jj,jk) |
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310 | c trend number 19 is in trcexp.F |
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311 | trc3d(ji,jj,jk,1)= zno3phy *86400 |
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312 | trc3d(ji,jj,jk,2)= znh4phy *86400 |
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313 | trc3d(ji,jj,jk,3)= znh4no3 *86400 |
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314 | #endif |
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315 | C |
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316 | C tracer flux at totox-point added to the general trend |
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317 | C |
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318 | tra(ji,jj,jk,jpdet) = tra(ji,jj,jk,jpdet) + zdeta |
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319 | tra(ji,jj,jk,jpzoo) = tra(ji,jj,jk,jpzoo) + zzooa |
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320 | tra(ji,jj,jk,jpphy) = tra(ji,jj,jk,jpphy) + zphya |
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321 | tra(ji,jj,jk,jpno3) = tra(ji,jj,jk,jpno3) + zno3a |
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322 | tra(ji,jj,jk,jpnh4) = tra(ji,jj,jk,jpnh4) + znh4a |
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323 | tra(ji,jj,jk,jpdom) = tra(ji,jj,jk,jpdom) + zdoma |
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324 | C |
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325 | END DO |
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326 | END DO |
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327 | C |
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328 | C 2. under biological level |
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329 | C ========================= |
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330 | C |
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331 | DO jk = jpkb,jpk |
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332 | C |
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333 | C 2.1 compute the remineralisation of all quantities towards nitrate |
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334 | C ------------------------------------------------------------------ |
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335 | C |
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336 | DO ji = 2,jpim1 |
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337 | C |
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338 | C 2.1.1 trophic variables( det, zoo, phy, no3, nh4, dom) |
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339 | C ----------------------------------------------------- |
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340 | C |
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341 | C negative trophic variables DO not contribute to the fluxes |
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342 | C |
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343 | zdet = max(0.,trn(ji,jj,jk,jpdet)) |
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344 | zzoo = max(0.,trn(ji,jj,jk,jpzoo)) |
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345 | zphy = max(0.,trn(ji,jj,jk,jpphy)) |
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346 | zno3 = max(0.,trn(ji,jj,jk,jpno3)) |
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347 | znh4 = max(0.,trn(ji,jj,jk,jpnh4)) |
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348 | zdom = max(0.,trn(ji,jj,jk,jpdom)) |
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349 | CC |
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350 | CC 2.1.2 Limitations |
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351 | CC ---------------- |
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352 | CC |
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353 | zlt = 0. |
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354 | zle = 0. |
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355 | zlno3 = 0. |
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356 | zlnh4 = 0. |
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357 | CC |
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358 | CC |
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359 | CC 2.1.3 sinks and sources |
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360 | CC --------------------- |
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361 | CC |
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362 | CC |
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363 | CC 1. phytoplankton production and exsudation |
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364 | CC |
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365 | zno3phy = 0. |
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366 | znh4phy = 0. |
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367 | C |
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368 | zphydom = 0. |
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369 | zphynh4 = 0. |
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370 | CC |
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371 | CC 2. zooplankton production |
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372 | CC |
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373 | CC grazing |
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374 | CC |
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375 | zphyzoo = 0. |
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376 | zdetzoo = 0. |
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377 | CC |
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378 | CC 3. fecal pellets production |
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379 | CC |
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380 | zzoodet = 0. |
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381 | CC |
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382 | CC 4. zooplankton liquide excretion |
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383 | CC |
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384 | zzoonh4 = tauzn * fzoolab * zzoo |
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385 | zzoodom = tauzn * (1 - fzoolab) * zzoo |
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386 | CC |
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387 | CC 5. mortality |
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388 | CC |
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389 | CC phytoplankton mortality |
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390 | CC |
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391 | zphydet = tmminp * zphy |
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392 | CC |
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393 | CC |
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394 | CC zooplankton mortality |
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395 | Cc closure : flux fbod is redistributed below level jpkbio |
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396 | CC |
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397 | zzoobod = 0. |
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398 | zboddet = 0. |
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399 | CC |
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400 | CC |
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401 | CC 6. detritus and dom breakdown |
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402 | CC |
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403 | zdetnh4 = taudn * fdetlab * zdet |
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404 | zdetdom = taudn * (1 - fdetlab) * zdet |
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405 | C |
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406 | zdomnh4 = taudomn * zdom |
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407 | zdomaju = (1 - redf/reddom) * (zphydom + zzoodom + zdetdom) |
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408 | CC |
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409 | CC 7. Nitrification |
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410 | CC |
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411 | znh4no3 = taunn * znh4 |
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412 | CC |
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413 | CC |
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414 | CC 2.1.4 determination of trends |
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415 | CC --------------------------- |
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416 | CC |
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417 | CC total trend for each biological tracer |
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418 | CC |
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419 | zphya = zno3phy + znh4phy - zphynh4 - zphydom - zphyzoo |
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420 | $ - zphydet |
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421 | zzooa = zphyzoo + zdetzoo - zzoodet - zzoodom - zzoonh4 |
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422 | $ - zzoobod |
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423 | zno3a = - zno3phy + znh4no3 |
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424 | znh4a = - znh4phy - znh4no3 + zphynh4 + zzoonh4 + zdomnh4 |
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425 | $ + zdetnh4 + zdomaju |
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426 | zdeta = zphydet + zzoodet - zdetzoo - zdetnh4 - zdetdom + |
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427 | $ zboddet |
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428 | zdoma = zphydom + zzoodom + zdetdom - zdomnh4 - zdomaju |
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429 | CC |
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430 | #if defined key_trc_diabio |
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431 | trbio(ji,jj,jk,1) = zno3phy |
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432 | trbio(ji,jj,jk,2) = znh4phy |
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433 | trbio(ji,jj,jk,3) = zphynh4 |
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434 | trbio(ji,jj,jk,4) = zphydom |
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435 | trbio(ji,jj,jk,5) = zphyzoo |
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436 | trbio(ji,jj,jk,6) = zphydet |
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437 | trbio(ji,jj,jk,7) = zdetzoo |
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438 | trbio(ji,jj,jk,9) = zzoodet |
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439 | trbio(ji,jj,jk,10) = zzoobod |
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440 | trbio(ji,jj,jk,11) = zzoonh4 |
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441 | trbio(ji,jj,jk,12) = zzoodom |
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442 | trbio(ji,jj,jk,13) = znh4no3 |
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443 | trbio(ji,jj,jk,14) = zdomnh4 |
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444 | trbio(ji,jj,jk,15) = zdetnh4 |
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445 | #endif |
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446 | #if defined key_trc_diaadd |
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447 | trc2d(ji,jj,1)=trc2d(ji,jj,1)+zno3phy*ze3t(ji,jj,jk) |
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448 | trc2d(ji,jj,2)=trc2d(ji,jj,2)+znh4phy*ze3t(ji,jj,jk) |
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449 | trc2d(ji,jj,3)=trc2d(ji,jj,3)+zphydom*ze3t(ji,jj,jk) |
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450 | trc2d(ji,jj,4)=trc2d(ji,jj,4)+zphynh4*ze3t(ji,jj,jk) |
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451 | trc2d(ji,jj,5)=trc2d(ji,jj,5)+zphyzoo*ze3t(ji,jj,jk) |
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452 | trc2d(ji,jj,6)=trc2d(ji,jj,6)+zphydet*ze3t(ji,jj,jk) |
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453 | trc2d(ji,jj,7)=trc2d(ji,jj,7)+zdetzoo*ze3t(ji,jj,jk) |
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454 | Cc trend number 8 is in trcsed.F |
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455 | trc2d(ji,jj,9)=trc2d(ji,jj,9)+zzoodet*ze3t(ji,jj,jk) |
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456 | trc2d(ji,jj,10)=trc2d(ji,jj,10)+zzoobod*ze3t(ji,jj,jk) |
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457 | trc2d(ji,jj,11)=trc2d(ji,jj,11)+zzoonh4*ze3t(ji,jj,jk) |
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458 | trc2d(ji,jj,12)=trc2d(ji,jj,12)+zzoodom*ze3t(ji,jj,jk) |
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459 | trc2d(ji,jj,13)=trc2d(ji,jj,13)+znh4no3*ze3t(ji,jj,jk) |
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460 | trc2d(ji,jj,14)=trc2d(ji,jj,14)+zdomnh4*ze3t(ji,jj,jk) |
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461 | trc2d(ji,jj,15)=trc2d(ji,jj,15)+zdetnh4*ze3t(ji,jj,jk) |
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462 | |
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463 | trc2d(ji,jj,16)=trc2d(ji,jj,16)+(zno3phy+znh4phy-zphynh4 |
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464 | $ -zphydom-zphyzoo-zphydet)*ze3t(ji,jj,jk) |
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465 | trc2d(ji,jj,17)=trc2d(ji,jj,17)+(zphyzoo+zdetzoo-zzoodet |
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466 | $ -zzoobod-zzoonh4-zzoodom) *ze3t(ji,jj,jk) |
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467 | trc2d(ji,jj,18)=trc2d(ji,jj,18)+zdetdom*ze3t(ji,jj,jk) |
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468 | |
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469 | trc3d(ji,jj,jk,1)= zno3phy *86400 |
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470 | trc3d(ji,jj,jk,2)= znh4phy *86400 |
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471 | trc3d(ji,jj,jk,3)= znh4no3 *86400 |
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472 | #endif |
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473 | CC |
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474 | CC tracer flux at totox-point added to the general trend |
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475 | CC |
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476 | tra(ji,jj,jk,jpdet) = tra(ji,jj,jk,jpdet) + zdeta |
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477 | tra(ji,jj,jk,jpzoo) = tra(ji,jj,jk,jpzoo) + zzooa |
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478 | tra(ji,jj,jk,jpphy) = tra(ji,jj,jk,jpphy) + zphya |
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479 | tra(ji,jj,jk,jpno3) = tra(ji,jj,jk,jpno3) + zno3a |
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480 | tra(ji,jj,jk,jpnh4) = tra(ji,jj,jk,jpnh4) + znh4a |
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481 | tra(ji,jj,jk,jpdom) = tra(ji,jj,jk,jpdom) + zdoma |
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482 | CC |
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483 | END DO |
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484 | END DO |
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485 | |
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486 | |
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487 | |
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488 | |
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489 | c$$$ DO jk = jpkb,jpk |
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490 | c$$$C |
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491 | c$$$C 2.1 Old way to compute the remineralisation : asklod AS Kremeur (before 2005-03) |
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492 | c$$$C ------------------------------------------------------------------ |
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493 | c$$$C |
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494 | c$$$ DO ji=2,jpim1 |
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495 | c$$$ ztot(ji) = 0. |
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496 | c$$$ END DO |
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497 | c$$$ DO jn=1,jptra |
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498 | c$$$ IF (ctrcnm(jn).NE.'NO3') THEN |
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499 | c$$$ DO ji=2,jpim1 |
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500 | c$$$ ztra = remdmp(jk,jn) * trn(ji,jj,jk,jn) |
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501 | c$$$ tra(ji,jj,jk,jn) = tra(ji,jj,jk,jn) - ztra |
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502 | c$$$ ztot(ji) = ztot(ji) + ztra |
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503 | c$$$ END DO |
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504 | c$$$ ENDIF |
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505 | c$$$ END DO |
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506 | c$$$ DO jn=1,jptra |
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507 | c$$$ IF (ctrcnm(jn).EQ.'NO3') THEN |
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508 | c$$$ DO ji=2,jpim1 |
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509 | c$$$ tra(ji,jj,jk,jn) = tra(ji,jj,jk,jn) + ztot(ji) |
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510 | c$$$ END DO |
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511 | c$$$#if defined key_trc_diabio |
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512 | c$$$ trbio(ji,jj,jk,1)=ztot(ji) |
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513 | c$$$#endif |
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514 | c$$$ ENDIF |
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515 | c$$$ END DO |
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516 | c$$$ END DO |
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517 | |
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518 | C |
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519 | C |
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520 | C END of slab |
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521 | C =========== |
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522 | C |
---|
523 | 1000 CONTINUE |
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524 | |
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525 | #if defined key_trc_diaadd |
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526 | |
---|
527 | C Lateral boundary conditions on trc2d |
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528 | DO jn=1,jpdia2d |
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529 | CALL lbc_lnk(trc2d(:,:,jn),'T',1. ) |
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530 | END DO |
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531 | |
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532 | C Lateral boundary conditions on trc3d |
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533 | DO jn=1,jpdia3d |
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534 | CALL lbc_lnk(trc3d(:,:,1,jn),'T',1. ) |
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535 | END DO |
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536 | |
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537 | #endif |
---|
538 | |
---|
539 | #if defined key_trc_diabio |
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540 | C Lateral boundary conditions on trcbio |
---|
541 | DO jn=1,jpdiabio |
---|
542 | CALL lbc_lnk(trbio(:,:,1,jn),'T',1. ) |
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543 | END DO |
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544 | #endif |
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545 | |
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546 | # else |
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547 | C |
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548 | C no biological model |
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549 | C |
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550 | # endif |
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551 | |
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552 | C |
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553 | C |
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554 | RETURN |
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555 | END |
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