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 | CCC $Header$ |
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7 | SUBROUTINE p3zbio |
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8 | #if defined key_passivetrc && defined key_trc_p3zd |
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9 | CCC ------------------------------------------------------------------ |
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10 | CCC |
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11 | CCC ROUTINE p3zbio |
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12 | CCC ****************** |
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13 | CCC |
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14 | CCC |
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15 | CC |
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16 | CC PURPOSE. |
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17 | CC -------- |
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18 | CC *P3ZBIO* MODELS PRODUCTION OF BIOGENIC MATTER (POC '' SOFT |
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19 | CC TISSUE'' AND CACO3 PARTICLES ''HARD PARTS'') |
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20 | CC AND ITS DISTRIBUTION IN WATER COLUMN |
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21 | CC |
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22 | CC METHOD. |
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23 | CC ------- |
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24 | CC IN THE SURFACE LAYER POC IS PRODUCED ACCORDING TO |
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25 | CC NURTRIENTS AVAILABLE AND GROWTH CONDITIONS. NUTRIENT UPTAKE |
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26 | CC KINETICS FOLLOW MICHAELIS-MENTON FORMULATION. PROPORTIONAL |
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27 | CC TO THE AMOUNT OF ORGANIC MATTER, CACO3 HARD PARTS ARE PRODUCED. |
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28 | CC THE TOTAL PARTICLE AMOUNT PRODUCED, IS DISTRIBUTED IN THE WATER |
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29 | CC COLUMN BELOW THE SURFACE LAYER. |
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30 | CC |
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31 | CC EXTERNALS. |
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32 | CC ---------- |
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33 | CC NONE. |
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34 | CC |
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35 | CC REFERENCE. |
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36 | CC ---------- |
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37 | CC |
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38 | CC BACASTOW, R., AND E. MAIER-REIMER (1985) |
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39 | CC CIRCULATION MODEL OF THE OCEAN CARBON CYCLE. |
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40 | CC 1. DESCRIPTION OF THE MODEL, PP. 224-232. |
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41 | CC 2. COMPARISON OF THE MODEL RESULTS WITH OBSERVATIONAL DATA, |
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42 | CC PP. 233-240. |
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43 | CC IN: "ATMOSPHERIC CARBON DIOXIDE - ITS SOURCES, SINKS, AND |
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44 | CC GLOBAL tranSPORT", KANDERSTEG, 2 TO 6 SEPTEMBER 1985, |
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45 | CC COMMISSION ON ATMOSPHERIC CHEMISTRY AND GLOBAL POLLUTION, |
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46 | CC INTERNATIONAL ASSOCIATION OF METEOROLOGY AND ATMOSPHERIC PHYSICS. |
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47 | CC |
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48 | CC DUGDALE. R.C. (1967) |
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49 | CC NUTRIENT LIMITATION IN THE SEA: DYNAMICS, IDENTIFICATION |
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50 | CC AND SIGNIFICANCE. |
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51 | CC LIMNOLOGY AND OCEANOGRAPHY, VOL.12, 685-695. |
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52 | CC |
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53 | CC PARSONS, T.R., AND M. TAKAHASHI (1973) |
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54 | CC BIOLOGICAL OCEANOGRAPHIC PROCESSES. |
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55 | CC PERGAMON PRESS, 186 PP. |
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56 | CC |
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57 | CC MODIFICATIONS: |
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58 | CC -------------- |
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59 | CC original : 1998 O. Aumont |
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60 | CC modifications : 1999 C. Le Quere |
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61 | CC modifications : 1999 O. Aumont |
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62 | CC modifications : 2001 O. Aumont |
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63 | CC ---------------------------------------------------------------- |
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64 | CC parameters and commons |
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65 | CC ====================== |
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66 | C DIR$ NOLIST |
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67 | USE oce_trc |
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68 | USE trp_trc |
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69 | USE sms |
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70 | IMPLICIT NONE |
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71 | C DIR$ LIST |
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72 | CC----------------------------------------------------------------- |
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73 | c ----- |
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74 | CC local declarations |
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75 | CC ================== |
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76 | C |
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77 | INTEGER ji, jj, jk |
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78 | INTEGER kmin(jpi,jpj) |
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79 | |
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80 | REAL silpot, expofa |
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81 | REAL calpot, silfra |
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82 | REAL remip,remik |
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83 | C |
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84 | REAL dipnmoy(jpi,jpj),zmeu(jpi,jpj) |
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85 | REAL orem(jpi,jpj,jpk),olimi(jpi,jpj,jpk),intpz(jpi,jpj) |
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86 | REAL phosph2,zoo2,oxygen2 |
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87 | REAL phyto2,poc212 |
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88 | REAL compaph(jpi,jpj,jpk),compaz |
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89 | C |
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90 | REAL parlux |
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91 | REAL graze,prefc,prefp |
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92 | C |
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93 | C SET HALF PRECISION CONSTANTS |
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94 | C----------------------------- |
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95 | C |
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96 | e1 = 0. |
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97 | e2 = 0. |
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98 | zero = 0. |
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99 | one = 1. |
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100 | two = 2. |
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101 | parlux = 0.21 |
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102 | |
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103 | intpz = 0. |
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104 | C |
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105 | C Initialisation of variables used to compute PAR |
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106 | C ----------------------------------------------- |
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107 | C |
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108 | dipnmoy = 0. |
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109 | etot = 0. |
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110 | C |
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111 | C Light penetration in the water column |
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112 | C ------------------------------------- |
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113 | DO jj = 1,jpj |
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114 | DO ji = 1,jpi |
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115 | e1(ji,jj,1)=parlux*qsr(ji,jj) |
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116 | e2(ji,jj,1)=parlux*qsr(ji,jj) |
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117 | etot(ji,jj,1)=e1(ji,jj,1)+e2(ji,jj,1) |
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118 | END DO |
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119 | END DO |
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120 | |
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121 | DO jk = 1,16 |
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122 | DO jj = 1,jpj |
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123 | DO ji = 1,jpi |
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124 | IF (tmask(ji,jj,jk).NE.0) THEN |
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125 | C |
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126 | C Separation in two light bands: red and green |
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127 | C -------------------------------------------- |
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128 | C |
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129 | e1(ji,jj,jk+1) = e1(ji,jj,jk)* |
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130 | & exp(-(ekw1+ekc*trn(ji,jj,jk,jpphy)*12e6 |
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131 | & /dipn(ji,jj,jk))*e3t(jk)/2.) |
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132 | e2(ji,jj,jk+1) = e2(ji,jj,jk)* |
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133 | & exp(-(ekw2+ekc*trn(ji,jj,jk,jpphy)*12e6 |
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134 | & /dipn(ji,jj,jk))*e3t(jk)/2.) |
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135 | etot(ji,jj,jk) = e1(ji,jj,jk+1)+e2(ji,jj,jk+1) |
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136 | C |
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137 | C Computation of irradiance below level T |
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138 | C --------------------------------------- |
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139 | C |
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140 | e1(ji,jj,jk+1)=e1(ji,jj,jk+1)* |
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141 | $ exp(-(ekw1+ekc*trn(ji,jj,jk,jpphy)*12e6 |
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142 | $ /dipn(ji,jj,jk))*e3t(jk)/2.) |
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143 | e2(ji,jj,jk+1)=e2(ji,jj,jk+1)* |
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144 | $ exp(-(ekw2+ekc*trn(ji,jj,jk,jpphy)*12e6 |
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145 | $ /dipn(ji,jj,jk))*e3t(jk)/2.) |
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146 | C |
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147 | C Computation of C/Chl ratio (doney et al., 1996) |
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148 | C ----------------------------------------------- |
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149 | C |
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150 | dipn(ji,jj,jk)=trn(ji,jj,jk,jppo4) |
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151 | $ /(trn(ji,jj,jk,jppo4)+conc0) |
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152 | $ *(2.5-1.5*MIN(etot(ji,jj,jk)/90.,1.))/7.6/12. |
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153 | $ +1.E-30 |
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154 | dipn(ji,jj,jk)=MIN(150.,1./dipn(ji,jj,jk)) |
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155 | ENDIF |
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156 | END DO |
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157 | END DO |
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158 | END do |
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159 | C |
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160 | C Initialisation of the euphotic depth |
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161 | C |
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162 | DO jj = 1,jpj |
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163 | DO ji = 1,jpi |
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164 | kmin(ji,jj)=1 |
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165 | zmeu(ji,jj)=gdept(16) |
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166 | END DO |
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167 | END DO |
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168 | C |
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169 | C Computation of the euphotic depth |
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170 | C --------------------------------- |
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171 | C |
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172 | DO jk = 2,16 |
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173 | DO jj = 1,jpj |
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174 | DO ji = 1,jpi |
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175 | IF (etot(ji,jj,jk).GE.0.0045*qsr(ji,jj)) THEN |
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176 | zmeu(ji,jj) = gdept(jk) |
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177 | IF (gdept(jk).LE.hmld(ji,jj)) THEN |
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178 | kmin(ji,jj)=jk |
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179 | ENDIF |
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180 | ENDIF |
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181 | END DO |
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182 | END DO |
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183 | END DO |
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184 | |
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185 | |
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186 | DO jk = 1,16 |
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187 | DO jj = 1,jpj |
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188 | DO ji = 1,jpi |
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189 | IF (jk.LE.kmin(ji,jj)) THEN |
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190 | C |
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191 | C C/CHL ET PAR MOYENS SUR LA COUCHE DE MELANGE |
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192 | C |
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193 | dipnmoy(ji,jj)=dipnmoy(ji,jj)+dipn(ji,jj,jk)/ |
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194 | $ (float(kmin(ji,jj))+1.E-15) |
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195 | ENDIF |
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196 | END DO |
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197 | END DO |
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198 | END DO |
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199 | |
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200 | |
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201 | DO jk = 1,jpkb |
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202 | DO jj = 1,jpj |
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203 | DO ji = 1,jpi |
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204 | IF (jk.LE.kmin(ji,jj)) THEN |
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205 | dipn(ji,jj,jk)=dipnmoy(ji,jj) |
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206 | ENDIF |
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207 | C |
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208 | # if defined key_trc_dia3d |
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209 | trc3d(ji,jj,jk,1) = dipn(ji,jj,jk) |
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210 | # endif |
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211 | END DO |
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212 | END DO |
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213 | END DO |
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214 | |
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215 | # if defined key_diatrdtrc |
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216 | DO jj = 1,jpj |
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217 | DO ji = 1,jpi |
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218 | trc2d(ji,jj,11) = dipnmoy(ji,jj) |
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219 | END DO |
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220 | END DO |
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221 | # endif |
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222 | |
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223 | C |
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224 | DO jk = 1,jpkb |
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225 | DO jj = 1,jpj |
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226 | DO ji = 1,jpi |
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227 | IF (tmask(ji,jj,jk).NE.0) THEN |
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228 | C |
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229 | C Computation of phyto development constant |
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230 | C ----------------------------------------- |
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231 | C |
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232 | prbio(ji,jj,jk) = 0.6/rjjss*(1.066)**(tn(ji,jj,jk)) |
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233 | C |
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234 | C Computation of production function |
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235 | C ---------------------------------- |
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236 | C |
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237 | prbio(ji,jj,jk) = prbio(ji,jj,jk)*(1.-exp(-pislope/rjjss* |
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238 | & etot(ji,jj,jk)/prbio(ji,jj,jk)))*exp(-betslope/rjjss* |
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239 | & etot(ji,jj,jk)/prbio(ji,jj,jk)) |
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240 | # if defined key_off_degrad |
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241 | & *facvol(ji,jj,jk) |
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242 | # endif |
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243 | C |
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244 | C Mixed-layer effect on production |
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245 | C -------------------------------- |
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246 | C |
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247 | IF (hmld(ji,jj).ge.2*zmeu(ji,jj)) THEN |
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248 | prbio(ji,jj,jk) = prbio(ji,jj,jk)*0.5 |
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249 | |
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250 | ELSEIF (hmld(ji,jj).le.zmeu(ji,jj)) THEN |
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251 | prbio(ji,jj,jk) = prbio(ji,jj,jk) |
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252 | ELSE |
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253 | prbio(ji,jj,jk) = prbio(ji,jj,jk)*(1.- |
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254 | & 0.5*(hmld(ji,jj)/zmeu(ji,jj)-1)) |
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255 | ENDIF |
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256 | ENDIF |
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257 | ENDDO |
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258 | ENDDO |
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259 | |
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260 | C |
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261 | DO jj = 1,jpj |
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262 | DO ji = 1,jpi |
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263 | IF (tmask(ji,jj,jk).ne.0) THEN |
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264 | C |
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265 | C Exsudation of Zoo towards DOC |
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266 | C ----------------------------- |
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267 | C |
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268 | compaz = max((trn(ji,jj,jk,jpzoo)-0.01E-6),0.) |
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269 | compaph(ji,jj,jk) = max((trn(ji,jj,jk,jpphy)-0.01E-6), |
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270 | $ 0.) |
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271 | respz(ji,jj,jk) = resrat/rjjss*trn(ji,jj,jk,jpzoo)/ |
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272 | & (1.E-6+trn(ji,jj,jk,jpzoo))*rfact*compaz* |
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273 | $ tmask(ji,jj,jk) |
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274 | # if defined key_off_degrad |
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275 | & *facvol(ji,jj,jk) |
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276 | # endif |
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277 | c |
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278 | C |
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279 | C Computation of the fast remineralised fraction as a function of nutrients |
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280 | C ------------------------------------------------------------------------- |
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281 | C |
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282 | eps1(ji,jj,jk) =epsbio+0.*7.6e-6/(7.6e-6+ |
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283 | $ trn(ji,jj,jk,jppo4)) |
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284 | C |
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285 | C Squared mortality of Phyto similar to a sedimentation term during |
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286 | c blooms |
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287 | C (Doney et al. 1996) |
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288 | C |
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289 | respp(ji,jj,jk) = wchl/rjjss*1e6* |
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290 | $ trn(ji,jj,jk,jpphy)**2*rfact |
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291 | & *tmask(ji,jj,jk) |
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292 | # if defined key_off_degrad |
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293 | & *facvol(ji,jj,jk) |
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294 | # endif |
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295 | C |
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296 | C Phytoplankton mortality |
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297 | C ----------------------- |
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298 | C |
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299 | tortp(ji,jj,jk) = mprat/rjjss*trn(ji,jj,jk,jpphy) |
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300 | $ /(1.e-6+trn(ji,jj,jk,jpphy)) |
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301 | & *compaph(ji,jj,jk)*rfact*tmask(ji,jj,jk) |
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302 | # if defined key_off_degrad |
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303 | & *facvol(ji,jj,jk) |
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304 | # endif |
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305 | C |
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306 | C Zooplankton mortality |
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307 | C --------------------- |
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308 | C |
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309 | tortz(ji,jj,jk) = mzrat/rjjss*trn(ji,jj,jk,jpzoo) |
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310 | $ /(1.E-6+trn(ji,jj,jk,jpzoo)) |
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311 | & *compaz*rfact*tmask(ji,jj,jk) |
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312 | # if defined key_off_degrad |
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313 | & *facvol(ji,jj,jk) |
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314 | # endif |
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315 | C |
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316 | C Zooplankton grazing |
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317 | C ------------------- |
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318 | C |
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319 | graze = grazrat/rjjss*rfact*tmask(ji,jj,jk) |
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320 | # if defined key_off_degrad |
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321 | & *facvol(ji,jj,jk) |
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322 | # endif |
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323 | C |
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324 | C Preference of zooplankton for Phyto and POC (Fasham et al. 1990) |
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325 | C |
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326 | prefc = xprefc*trn(ji,jj,jk,jpphy)/ |
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327 | $ (xprefc*trn(ji,jj,jk,jpphy) |
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328 | & +xprefp*trn(ji,jj,jk,jppoc)+1E-15) |
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329 | |
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330 | prefp = xprefp*trn(ji,jj,jk,jppoc)/ |
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331 | $ (xprefc*trn(ji,jj,jk,jpphy) |
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332 | & +xprefp*trn(ji,jj,jk,jppoc)+1E-15) |
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333 | |
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334 | grazp(ji,jj,jk) = graze*prefc*compaph(ji,jj,jk)/ |
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335 | $ (xkgraz+prefc*trn(ji,jj,jk,jpphy)+prefp* |
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336 | & trn(ji,jj,jk,jppoc))*trn(ji,jj,jk,jpzoo) |
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337 | |
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338 | |
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339 | grazpoc(ji,jj,jk) = graze*prefp*trn(ji,jj,jk,jppoc)/ |
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340 | & (xkgraz+prefc*trn(ji,jj,jk,jpphy)+prefp* |
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341 | & trn(ji,jj,jk,jppoc))*trn(ji,jj,jk,jpzoo) |
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342 | C |
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343 | C |
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344 | C Sedimentation of Phyto and POC |
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345 | C ------------------------------ |
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346 | C |
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347 | sinking(ji,jj,jk+1) = wsbio/rjjss*trn(ji,jj,jk,jppoc) |
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348 | & *rfact*tmask(ji,jj,jk+1) |
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349 | # if defined key_off_degrad |
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350 | & *facvol(ji,jj,jk) |
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351 | # endif |
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352 | nu(ji,jj,jk+1) = smax/rjjss*(1.-tanh(conc0*0.0481e12* |
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353 | & trn(ji,jj,jk,jppo4)))*trn(ji,jj,jk,jpphy)*rfact* |
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354 | & tmask(ji,jj,jk+1) |
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355 | # if defined key_off_degrad |
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356 | & *facvol(ji,jj,jk) |
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357 | # endif |
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358 | C |
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359 | C Remineralization of DOC and POC |
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360 | C |
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361 | remik=1.64*SPOCRI*(1.-tmask(ji,jj,jk+1))+xremik |
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362 | remik=remik/rjjss*rfact*tmask(ji,jj,jk) |
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363 | & *trn(ji,jj,jk,jppo4)/(trn(ji,jj,jk,jppo4)+32.E-6) |
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364 | & *trn(ji,jj,jk,jpdoc)/(trn(ji,jj,jk,jpdoc)+15.E-6) |
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365 | # if defined key_off_degrad |
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366 | & *facvol(ji,jj,jk) |
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367 | # endif |
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368 | remip=xremip/rjjss*rfact*tmask(ji,jj,jk) |
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369 | # if defined key_off_degrad |
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370 | & *facvol(ji,jj,jk) |
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371 | # endif |
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372 | olimi(ji,jj,jk)=remik*trn(ji,jj,jk,jpdoc) |
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373 | orem(ji,jj,jk)=remip*trn(ji,jj,jk,jppoc) |
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374 | ENDIF |
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375 | END DO |
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376 | END DO |
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377 | END DO |
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378 | C |
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379 | DO jk = 1,jpkb |
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380 | DO jj = 1,jpj |
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381 | DO ji = 1,jpi |
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382 | IF (tmask(ji,jj,jk).NE.0) THEN |
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383 | C |
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384 | C Computation of Primary Production |
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385 | C --------------------------------- |
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386 | C |
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387 | prorca(ji,jj,jk) = prbio(ji,jj,jk)*trn(ji,jj,jk,jppo4)* |
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388 | & trn(ji,jj,jk,jpphy)/(conc0+trn(ji,jj,jk,jppo4))* |
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389 | & rfact |
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390 | C |
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391 | C Evolution of PO4 |
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392 | C ---------------- |
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393 | C |
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394 | phosph2 = trn(ji,jj,jk,jppo4)-prorca(ji,jj,jk) |
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395 | & +eps1(ji,jj,jk)*tortz(ji,jj,jk) |
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396 | & +olimi(ji,jj,jk) |
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397 | C |
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398 | C Nullity test for PO4 |
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399 | C -------------------- |
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400 | C |
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401 | prorca(ji,jj,jk)=prorca(ji,jj,jk) |
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402 | & *(0.5+sign(0.5,phosph2)) |
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403 | |
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404 | C |
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405 | C Evolution of Phyto |
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406 | C ------------------ |
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407 | C |
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408 | phyto2 = trn(ji,jj,jk,jpphy)+prorca(ji,jj,jk)* |
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409 | & (1.-excret)-(tortp(ji,jj,jk)+ |
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410 | & respp(ji,jj,jk))-grazp(ji,jj,jk)+ |
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411 | & (nu(ji,jj,jk)-nu(ji,jj,jk+1))/e3t(jk) |
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412 | C |
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413 | C Nullity test for Phyto |
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414 | C ---------------------- |
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415 | C |
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416 | tortp(ji,jj,jk)=tortp(ji,jj,jk) |
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417 | $ *(0.5+sign(0.5,phyto2)) |
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418 | respp(ji,jj,jk)=respp(ji,jj,jk) |
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419 | $ *(0.5+sign(0.5,phyto2)) |
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420 | grazp(ji,jj,jk)=grazp(ji,jj,jk) |
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421 | $ *(0.5+sign(0.5,phyto2)) |
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422 | prorca(ji,jj,jk)=prorca(ji,jj,jk) |
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423 | $ *(0.5+sign(0.5,phyto2)) |
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424 | nu(ji,jj,jk+1)=nu(ji,jj,jk+1) |
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425 | $ *(0.5+sign(0.5,phyto2)) |
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426 | C |
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427 | C Evolution of detritus |
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428 | C --------------------- |
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429 | C |
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430 | poc212 = trn(ji,jj,jk,jppoc)-grazpoc(ji,jj,jk)+unass* |
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431 | & (grazp(ji,jj,jk)+grazpoc(ji,jj,jk))+ |
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432 | & (1.-eps1(ji,jj,jk))*tortz(ji,jj,jk)+ |
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433 | & tortp(ji,jj,jk)+respp(ji,jj,jk) + |
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434 | & (sinking(ji,jj,jk)-sinking(ji,jj,jk+1))/e3t(jk) |
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435 | & -orem(ji,jj,jk) |
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436 | C |
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437 | C Nullity test for POC |
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438 | C -------------------- |
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439 | C |
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440 | grazpoc(ji,jj,jk)=grazpoc(ji,jj,jk) |
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441 | & *(0.5+sign(0.5,poc212)) |
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442 | sinking(ji,jj,jk+1)=sinking(ji,jj,jk+1) |
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443 | & *(0.5+sign(0.5,poc212)) |
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444 | orem(ji,jj,jk)=orem(ji,jj,jk) |
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445 | & *(0.5+sign(0.5,poc212)) |
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446 | C |
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447 | C Evolution of Zooplankton |
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448 | C ------------------------ |
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449 | C |
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450 | zoo2 = trn(ji,jj,jk,jpzoo)+ |
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451 | & (1-unass)*(grazp(ji,jj,jk)+grazpoc(ji,jj,jk)) |
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452 | & -(tortz(ji,jj,jk)+respz(ji,jj,jk)) |
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453 | C |
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454 | C |
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455 | C Nullity test for Zooplankton |
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456 | C ---------------------------- |
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457 | C |
---|
458 | tortz(ji,jj,jk)=tortz(ji,jj,jk) |
---|
459 | & *(0.5+sign(0.5,zoo2)) |
---|
460 | respz(ji,jj,jk)=respz(ji,jj,jk) |
---|
461 | & *(0.5+sign(0.5,zoo2)) |
---|
462 | grazp(ji,jj,jk)=grazp(ji,jj,jk) |
---|
463 | & *(0.5+sign(0.5,zoo2)) |
---|
464 | grazpoc(ji,jj,jk)=grazpoc(ji,jj,jk) |
---|
465 | & *(0.5+sign(0.5,zoo2)) |
---|
466 | C |
---|
467 | C Evolution of O2 |
---|
468 | C --------------- |
---|
469 | C |
---|
470 | oxygen2 = trn(ji,jj,jk,jpoxy)+o2ut* |
---|
471 | & (prorca(ji,jj,jk)-eps1(ji,jj,jk)*tortz(ji,jj,jk) |
---|
472 | & -olimi(ji,jj,jk)) |
---|
473 | C |
---|
474 | tortz(ji,jj,jk)=tortz(ji,jj,jk) |
---|
475 | & *(0.5+sign(0.5,oxygen2)) |
---|
476 | olimi(ji,jj,jk)=olimi(ji,jj,jk) |
---|
477 | & *(0.5+sign(0.5,oxygen2)) |
---|
478 | C |
---|
479 | ENDIF |
---|
480 | END DO |
---|
481 | END DO |
---|
482 | END DO |
---|
483 | C |
---|
484 | C Determination of tracers concentration as a function of |
---|
485 | C biological sources and sinks |
---|
486 | C -------------------------------------------------------- |
---|
487 | C |
---|
488 | DO jk = 1,jpkb |
---|
489 | DO jj = 1,jpj |
---|
490 | DO ji = 1,jpi |
---|
491 | C |
---|
492 | IF (tmask(ji,jj,jk).NE.0) THEN |
---|
493 | C |
---|
494 | C Evolution of PO4 |
---|
495 | C ---------------- |
---|
496 | C |
---|
497 | trn(ji,jj,jk,jppo4) = trn(ji,jj,jk,jppo4)- |
---|
498 | & prorca(ji,jj,jk)+olimi(ji,jj,jk)+ |
---|
499 | & eps1(ji,jj,jk)*tortz(ji,jj,jk) |
---|
500 | prodt(ji,jj,jk) = prorca(ji,jj,jk) |
---|
501 | & -eps1(ji,jj,jk)*tortz(ji,jj,jk) |
---|
502 | & -olimi(ji,jj,jk) |
---|
503 | C |
---|
504 | C Evolution of Phytoplankton |
---|
505 | C -------------------------- |
---|
506 | C |
---|
507 | C |
---|
508 | trn(ji,jj,jk,jpphy) = trn(ji,jj,jk,jpphy)+ |
---|
509 | & prorca(ji,jj,jk)*(1.-excret)- |
---|
510 | & (tortp(ji,jj,jk)+respp(ji,jj,jk))- |
---|
511 | & grazp(ji,jj,jk)+ |
---|
512 | & (nu(ji,jj,jk)-nu(ji,jj,jk+1))/e3t(jk) |
---|
513 | C |
---|
514 | C Evolution of Zooplankton |
---|
515 | C ------------------------ |
---|
516 | C |
---|
517 | trn(ji,jj,jk,jpzoo) = trn(ji,jj,jk,jpzoo)+ |
---|
518 | & (1-unass)*(grazp(ji,jj,jk)+grazpoc(ji,jj,jk)) |
---|
519 | & -(tortz(ji,jj,jk)+respz(ji,jj,jk)) |
---|
520 | C |
---|
521 | C Evolution of DOC |
---|
522 | C ---------------- |
---|
523 | C |
---|
524 | trn(ji,jj,jk,jpdoc) = trn(ji,jj,jk,jpdoc) |
---|
525 | & +respz(ji,jj,jk)+orem(ji,jj,jk) |
---|
526 | & +excret*prorca(ji,jj,jk)-olimi(ji,jj,jk) |
---|
527 | C |
---|
528 | C Evolution of Detritus |
---|
529 | C --------------------- |
---|
530 | C |
---|
531 | C |
---|
532 | trn(ji,jj,jk,jppoc) = trn(ji,jj,jk,jppoc)- |
---|
533 | & grazpoc(ji,jj,jk)+unass* |
---|
534 | & (grazp(ji,jj,jk)+grazpoc(ji,jj,jk))+ |
---|
535 | & (1.-eps1(ji,jj,jk))*tortz(ji,jj,jk)+ |
---|
536 | & tortp(ji,jj,jk)+respp(ji,jj,jk) |
---|
537 | & +(sinking(ji,jj,jk)-sinking(ji,jj,jk+1))/e3t(jk) |
---|
538 | & -orem(ji,jj,jk) |
---|
539 | C |
---|
540 | C Evolution of O2 |
---|
541 | C --------------- |
---|
542 | C |
---|
543 | trn(ji,jj,jk,jpoxy)=trn(ji,jj,jk,jpoxy)+ |
---|
544 | & o2ut*(prorca(ji,jj,jk)-olimi(ji,jj,jk)- |
---|
545 | & eps1(ji,jj,jk)*tortz(ji,jj,jk)) |
---|
546 | C |
---|
547 | C Vertical integral of phyto and zooplanton concentrations |
---|
548 | C used to compute calcite production |
---|
549 | C |
---|
550 | ENDIF |
---|
551 | END DO |
---|
552 | END DO |
---|
553 | END DO |
---|
554 | |
---|
555 | DO jk=1,jpk |
---|
556 | DO jj=1,jpj |
---|
557 | DO ji=1,jpi |
---|
558 | IF (tmask(ji,jj,jk).NE.0.) then |
---|
559 | intpz(ji,jj)=intpz(ji,jj)+(trn(ji,jj,jk,jpphy) |
---|
560 | & +trn(ji,jj,jk,jpzoo))*e3t(jk)*tmask(ji,jj,jk) |
---|
561 | ENDIF |
---|
562 | END DO |
---|
563 | END DO |
---|
564 | END DO |
---|
565 | |
---|
566 | C |
---|
567 | C Evolution of calcite and silicates as a function of the two tracers |
---|
568 | C ------------------------------------------------------------------- |
---|
569 | C |
---|
570 | DO jk = 1,jpkb |
---|
571 | DO jj = 1,jpj |
---|
572 | DO ji = 1,jpi |
---|
573 | IF (tmask(ji,jj,jk).ne.0) THEN |
---|
574 | C |
---|
575 | C potential production of calcite and biogenic silicate |
---|
576 | C ------------------------------------------------------ |
---|
577 | C |
---|
578 | silpot = grosip*trn(ji,jj,jk,jpsil)/ |
---|
579 | & (trn(ji,jj,jk,jpsil)+xksi1) |
---|
580 | expofa=EXP(0.1*tn(ji,jj,jk)-10.) |
---|
581 | calpot=expofa/(1.+expofa) |
---|
582 | calfra=caco3r*calpot |
---|
583 | silfra=silpot*(1.-calpot)/0.75 |
---|
584 | C |
---|
585 | C in situ production of calcite and biogenic silicate |
---|
586 | C ---------------------------------------------------- |
---|
587 | C |
---|
588 | prcaca(ji,jj,jk)=calfra*(sinking(ji,jj,11) |
---|
589 | & +nu(ji,jj,11))*(trn(ji,jj,jk,jpphy)+ |
---|
590 | & trn(ji,jj,jk,jpzoo))*tmask(ji,jj,1) |
---|
591 | & /(intpz(ji,jj)+1.E-15) |
---|
592 | silpro(ji,jj,jk)=sicmax*silfra* |
---|
593 | & (unass*(grazp(ji,jj,jk)+grazpoc(ji,jj,jk)) |
---|
594 | & +tortp(ji,jj,jk)+respp(ji,jj,jk)) |
---|
595 | C |
---|
596 | C Compute variable Si/C ratio. Very simple formulation |
---|
597 | C based on the assumption that this ratio decreased with |
---|
598 | C decreasing in situ Si concentrations |
---|
599 | C -------------------------------------------------------- |
---|
600 | C |
---|
601 | silpro(ji,jj,jk)=silpro(ji,jj,jk)*trn(ji,jj,jk,jpsil) |
---|
602 | & /(trn(ji,jj,jk,jpsil)+xksi2) |
---|
603 | C |
---|
604 | C Account for changes in total co2, alkalinity and [po4] |
---|
605 | C due to uptake by poc-/caco3 producing organismS |
---|
606 | C ------------------------------------------------------ |
---|
607 | C |
---|
608 | C Evolution of silicates |
---|
609 | C ---------------------- |
---|
610 | C |
---|
611 | silpro(ji,jj,jk)=amin1(silpro(ji,jj,jk), |
---|
612 | & (trn(ji,jj,jk,jpsil)-0.05E-6)) |
---|
613 | trn(ji,jj,jk,jpsil) =trn(ji,jj,jk,jpsil) |
---|
614 | $ -SILPRO(ji,jj,jk) |
---|
615 | C |
---|
616 | C Consumption of Total (12C)O2 |
---|
617 | C ---------------------------- |
---|
618 | C |
---|
619 | trn(ji,jj,jk,jpdic) = trn(ji,jj,jk,jpdic) |
---|
620 | & -prodt(ji,jj,jk)-prcaca(ji,jj,jk) |
---|
621 | C |
---|
622 | # if defined key_trc_biohamocc13 |
---|
623 | C Consumption of Total (13C)O2 |
---|
624 | C ---------------------------- |
---|
625 | trn(ji,jj,jk,jp13c) = trn(ji,jj,jk,jp13c)- |
---|
626 | & pdb*plafr13*prodt(ji,jj,jk) |
---|
627 | & -pdb*prcaca(ji,jj,jk) |
---|
628 | # endif |
---|
629 | C |
---|
630 | C Consumption of alkalinity due to ca++ uptake and increase |
---|
631 | C of alkalinity due to nitrate consumption during organic |
---|
632 | C soft tissue production |
---|
633 | C --------------------------------------------------------- |
---|
634 | C |
---|
635 | trn(ji,jj,jk,jptal) = trn(ji,jj,jk,jptal)+ |
---|
636 | & rno3*prodt(ji,jj,jk)-two*prcaca(ji,jj,jk) |
---|
637 | C |
---|
638 | ENDIF |
---|
639 | END DO |
---|
640 | END DO |
---|
641 | ENDDO |
---|
642 | C |
---|
643 | #endif |
---|
644 | C |
---|
645 | RETURN |
---|
646 | END |
---|
647 | |
---|
648 | |
---|
649 | |
---|