| 1 | ! ================================================================================================================================= |
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| 2 | ! MODULE : stomate_data |
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| 3 | ! |
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| 4 | ! CONTACT : orchidee-help _at_ listes.ipsl.fr |
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| 5 | ! |
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| 6 | ! LICENCE : IPSL (2006) |
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| 7 | ! This software is governed by the CeCILL licence see ORCHIDEE/ORCHIDEE_CeCILL.LIC |
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| 8 | ! |
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| 9 | !>\BRIEF "stomate_data" module defines the values about the PFT parameters. It will print |
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| 10 | !! the values of the parameters for STOMATE in the standard outputs. |
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| 11 | !! |
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| 12 | !!\n DESCRIPTION: None |
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| 13 | !! |
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| 14 | !! RECENT CHANGE(S): Sonke Zaehle: Reich et al, 1992 find no statistically significant differences |
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| 15 | !! between broadleaved and coniferous forests, specifically, the assumption that grasses grow |
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| 16 | !! needles is not justified. Replacing the function with the one based on Reich et al. 1997. |
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| 17 | !! Given that sla=100cm2/gDW at 9 months, sla is: |
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| 18 | !! sla=exp(5.615-0.46*ln(leaflon in months)) |
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| 19 | !! |
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| 20 | !! REFERENCE(S) : None |
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| 21 | !! |
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| 22 | !! SVN : |
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| 23 | !! $HeadURL: svn://forge.ipsl.jussieu.fr/orchidee/branches/ORCHIDEE_2_2/ORCHIDEE/src_stomate/stomate_data.f90 $ |
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| 24 | !! $Date: 2017-10-18 11:15:06 +0200 (Wed, 18 Oct 2017) $ |
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| 25 | !! $Revision: 4693 $ |
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| 26 | !! \n |
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| 27 | !_ ================================================================================================================================ |
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| 28 | |
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| 29 | MODULE stomate_data |
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| 30 | |
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| 31 | ! modules used: |
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| 32 | |
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| 33 | USE constantes |
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| 34 | USE time, ONLY : one_day, dt_sechiba, one_year |
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| 35 | USE pft_parameters |
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| 36 | USE defprec |
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| 37 | |
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| 38 | |
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| 39 | IMPLICIT NONE |
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| 40 | |
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| 41 | INTEGER(i_std),ALLOCATABLE,SAVE,DIMENSION(:) :: hori_index !! Move to Horizontal indices |
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| 42 | !$OMP THREADPRIVATE(hori_index) |
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| 43 | |
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| 44 | INTEGER(i_std),ALLOCATABLE,SAVE,DIMENSION(:) :: horipft_index !! Horizontal + PFT indices |
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| 45 | !$OMP THREADPRIVATE(horipft_index) |
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| 46 | |
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| 47 | ! Land cover change |
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| 48 | |
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| 49 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: horip10_index !! Horizontal + P10 indices |
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| 50 | !$OMP THREADPRIVATE(horip10_index) |
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| 51 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: horip100_index !! Horizontal + P100 indice |
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| 52 | !$OMP THREADPRIVATE(horip100_index) |
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| 53 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: horip11_index !! Horizontal + P11 indices |
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| 54 | !$OMP THREADPRIVATE(horip11_index) |
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| 55 | INTEGER(i_std), ALLOCATABLE, SAVE, DIMENSION(:) :: horip101_index !! Horizontal + P101 indices |
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| 56 | !$OMP THREADPRIVATE(horip101_index) |
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| 57 | |
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| 58 | INTEGER(i_std),SAVE :: itime !! time step |
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| 59 | !$OMP THREADPRIVATE(itime) |
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| 60 | INTEGER(i_std),SAVE :: hist_id_stomate !! STOMATE history file ID |
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| 61 | !$OMP THREADPRIVATE(hist_id_stomate) |
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| 62 | INTEGER(i_std),SAVE :: hist_id_stomate_IPCC !! STOMATE history file ID for IPCC output |
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| 63 | !$OMP THREADPRIVATE(hist_id_stomate_IPCC) |
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| 64 | INTEGER(i_std),SAVE :: rest_id_stomate !! STOMATE restart file ID |
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| 65 | !$OMP THREADPRIVATE(rest_id_stomate) |
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| 66 | |
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| 67 | REAL(r_std),PARAMETER :: adapted_crit = 1. - ( 1. / euler ) !! critical value for being adapted (1-1/e) (unitless) |
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| 68 | REAL(r_std),PARAMETER :: regenerate_crit = 1. / euler !! critical value for being regenerative (1/e) (unitless) |
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| 69 | |
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| 70 | |
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| 71 | ! private & public routines |
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| 72 | |
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| 73 | PUBLIC data |
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| 74 | |
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| 75 | CONTAINS |
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| 76 | |
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| 77 | !! ================================================================================================================================ |
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| 78 | !! SUBROUTINE : data |
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| 79 | !! |
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| 80 | !>\BRIEF This routine defines the values of the PFT parameters. It will print the values of the parameters for STOMATE |
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| 81 | !! in the standard outputs of ORCHIDEE. |
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| 82 | !! |
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| 83 | !! DESCRIPTION : This routine defines PFT parameters. It initializes the pheno_crit structure by tabulated parameters.\n |
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| 84 | !! Some initializations are done for parameters. The SLA is calculated according *to* Reich et al (1992).\n |
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| 85 | !! Another formulation by Reich et al(1997) could be used for the computation of the SLA. |
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| 86 | !! The geographical coordinates might be used for defining some additional parameters |
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| 87 | !! (e.g. frequency of anthropogenic fires, irrigation of agricultural surfaces, etc.). \n |
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| 88 | !! For the moment, this possibility is not used. \n |
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| 89 | !! The specifc leaf area (SLA) is calculated according Reich et al, 1992 by : |
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| 90 | !! \latexonly |
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| 91 | !! \input{stomate_data_SLA.tex} |
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| 92 | !! \endlatexonly |
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| 93 | !! The sapling (young) biomass for trees and for each compartment of biomass is calculated by : |
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| 94 | !! \latexonly |
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| 95 | !! \input{stomate_data_sapl_tree.tex} |
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| 96 | !! \endlatexonly |
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| 97 | !! The sapling biomass for grasses and for each compartment of biomass is calculated by : |
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| 98 | !! \latexonly |
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| 99 | !! \input{stomate_data_sapl_grass.tex} |
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| 100 | !! \endlatexonly |
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| 101 | !! The critical stem diameter is given by the following formula : |
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| 102 | !! \latexonly |
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| 103 | !! \input{stomate_data_stem_diameter.tex} |
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| 104 | !! \endlatexonly |
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| 105 | !! |
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| 106 | !! RECENT CHANGE(S): Sonke Zaehle: Reich et al, 1992 find no statistically significant differences |
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| 107 | !! between broadleaved and coniferous forests, specifically, the assumption that grasses grow |
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| 108 | !! needles is not justified. Replacing the function with the one based on Reich et al. 1997. |
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| 109 | !! Given that sla=100cm2/gDW at 9 months, sla is: |
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| 110 | !! sla=exp(5.615-0.46*ln(leaflon in months)) |
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| 111 | !! \latexonly |
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| 112 | !! \input{stomate_data_SLA_Reich_97.tex} |
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| 113 | !! \endlatexonly |
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| 114 | !! |
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| 115 | !! MAIN OUTPUT VARIABLE(S): |
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| 116 | !! |
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| 117 | !! REFERENCE(S) : |
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| 118 | !! - Reich PB, Walters MB, Ellsworth DS, (1992), Leaf life-span in relation to leaf, plant and |
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| 119 | !! stand characteristics among diverse ecosystems. Ecological Monographs, Vol 62, pp 365-392. |
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| 120 | !! - Reich PB, Walters MB, Ellsworth DS (1997) From tropics to tundra: global convergence in plant |
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| 121 | !! functioning. Proc Natl Acad Sci USA, 94:13730 13734 |
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| 122 | !! |
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| 123 | !! FLOWCHART : |
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| 124 | !! \n |
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| 125 | !_ ================================================================================================================================ |
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| 126 | |
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| 127 | SUBROUTINE data (npts, lalo) |
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| 128 | |
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| 129 | |
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| 130 | !! 0. Variables and parameter declaration |
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| 131 | |
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| 132 | |
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| 133 | !! 0.1 Input variables |
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| 134 | |
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| 135 | INTEGER(i_std), INTENT(in) :: npts !! [DISPENSABLE] Domain size (unitless) |
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| 136 | REAL(r_std),DIMENSION (npts,2), INTENT (in) :: lalo !! [DISPENSABLE] Geographical coordinates (latitude,longitude) |
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| 137 | |
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| 138 | !! 0.4 Local variables |
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| 139 | |
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| 140 | INTEGER(i_std) :: j !! Index (unitless) |
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| 141 | REAL(r_std) :: alpha !! alpha's : (unitless) |
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| 142 | REAL(r_std) :: dia !! stem diameter (m) |
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| 143 | REAL(r_std) :: csa_sap !! Crown specific area sapling @tex $(m^2.ind^{-1})$ @endtex |
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| 144 | |
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| 145 | !_ ================================================================================================================================ |
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| 146 | |
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| 147 | !- pheno_gdd_crit |
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| 148 | pheno_gdd_crit(:,1) = pheno_gdd_crit_c(:) |
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| 149 | pheno_gdd_crit(:,2) = pheno_gdd_crit_b(:) |
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| 150 | pheno_gdd_crit(:,3) = pheno_gdd_crit_a(:) |
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| 151 | ! |
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| 152 | !- senescence_temp |
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| 153 | senescence_temp(:,1) = senescence_temp_c(:) |
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| 154 | senescence_temp(:,2) = senescence_temp_b(:) |
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| 155 | senescence_temp(:,3) = senescence_temp_a(:) |
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| 156 | ! |
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| 157 | !- maint_resp_slope |
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| 158 | maint_resp_slope(:,1) = maint_resp_slope_c(:) |
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| 159 | maint_resp_slope(:,2) = maint_resp_slope_b(:) |
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| 160 | maint_resp_slope(:,3) = maint_resp_slope_a(:) |
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| 161 | ! |
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| 162 | !-coeff_maint_zero |
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| 163 | coeff_maint_zero(:,ileaf) = cm_zero_leaf(:) |
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| 164 | coeff_maint_zero(:,isapabove) = cm_zero_sapabove(:) |
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| 165 | coeff_maint_zero(:,isapbelow) = cm_zero_sapbelow(:) |
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| 166 | coeff_maint_zero(:,iheartabove) = cm_zero_heartabove(:) |
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| 167 | coeff_maint_zero(:,iheartbelow) = cm_zero_heartbelow(:) |
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| 168 | coeff_maint_zero(:,iroot) = cm_zero_root(:) |
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| 169 | coeff_maint_zero(:,ifruit) = cm_zero_fruit(:) |
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| 170 | coeff_maint_zero(:,icarbres) = cm_zero_carbres(:) |
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| 171 | |
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| 172 | |
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| 173 | IF ( printlev >= 2 ) WRITE(numout,*) 'data: PFT characteristics' |
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| 174 | |
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| 175 | DO j = 2,nvm ! Loop over # PFTS |
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| 176 | |
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| 177 | IF ( printlev >= 2 ) WRITE(numout,'(a,i3,a,a)') ' > PFT#',j,': ', PFT_name(j) |
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| 178 | |
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| 179 | ! |
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| 180 | ! 1 tree? (true/false) |
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| 181 | ! |
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| 182 | IF ( printlev >= 2 ) WRITE(numout,*) ' tree: (::is_tree) ', is_tree(j) |
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| 183 | |
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| 184 | ! |
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| 185 | ! 2 flamability (0-1, unitless) |
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| 186 | ! |
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| 187 | |
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| 188 | IF ( printlev >= 2 ) WRITE(numout,*) ' litter flamability (::flam) :', flam(j) |
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| 189 | |
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| 190 | ! |
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| 191 | ! 3 fire resistance (unitless) |
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| 192 | ! |
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| 193 | |
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| 194 | IF ( printlev >= 2 ) WRITE(numout,*) ' fire resistance (::resist) :', resist(j) |
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| 195 | |
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| 196 | ! |
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| 197 | ! 4 specific leaf area per mass carbon = 2 * sla / dry mass (m^2.gC^{-1}) |
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| 198 | ! |
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| 199 | |
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| 200 | ! S. Zaehle: Reich et al, 1992 find no statistically significant differences between broadleaved and coniferous |
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| 201 | ! forests, specifically, the assumption that grasses grow needles is not justified. Replacing the function |
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| 202 | ! with the one based on Reich et al. 1997. Given that sla=100cm2/gDW at 9 months, sla is: |
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| 203 | ! sla=exp(5.615-0.46*ln(leaflon in months)) |
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| 204 | |
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| 205 | ! Oct 2010 : sla values are prescribed by values given by N.Viovy |
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| 206 | |
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| 207 | ! includes conversion from |
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| 208 | !! sla(j) = 2. * 1e-4 * EXP(5.615 - 0.46 * log(12./leaflife_tab(j))) |
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| 209 | !!\latexonly |
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| 210 | !!\input{stomate_data_SLA.tex} |
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| 211 | !!\endlatexonly |
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| 212 | ! IF ( leaf_tab(j) .EQ. 2 ) THEN |
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| 213 | ! |
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| 214 | ! ! needle leaved tree |
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| 215 | ! sla(j) = 2. * ( 10. ** ( 2.29 - 0.4 * LOG10(12./leaflife_tab(j)) ) ) *1e-4 |
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| 216 | ! |
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| 217 | ! ELSE |
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| 218 | ! |
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| 219 | ! ! broad leaved tree or grass (Reich et al 1992) |
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| 220 | ! sla(j) = 2. * ( 10. ** ( 2.41 - 0.38 * LOG10(12./leaflife_tab(j)) ) ) *1e-4 |
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| 221 | ! |
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| 222 | ! ENDIF |
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| 223 | |
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| 224 | !!!$ IF ( leaf_tab(j) .EQ. 1 ) THEN |
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| 225 | !!!$ |
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| 226 | !!!$ ! broad leaved tree |
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| 227 | !!!$ |
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| 228 | !!!$ sla(j) = 2. * ( 10. ** ( 2.41 - 0.38 * LOG10(12./leaflife_tab(j)) ) ) *1e-4 |
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| 229 | !!!$ |
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| 230 | !!!$ ELSE |
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| 231 | !!!$ |
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| 232 | !!!$ ! needle leaved or grass (Reich et al 1992) |
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| 233 | !!!$ |
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| 234 | !!!$ sla(j) = 2. * ( 10. ** ( 2.29 - 0.4 * LOG10(12./leaflife_tab(j)) ) ) *1e-4 |
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| 235 | !!!$ |
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| 236 | !!!$ ENDIF |
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| 237 | !!!$ |
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| 238 | !!!$ IF ( ( leaf_tab(j) .EQ. 2 ) .AND. ( pheno_type_tab(j) .EQ. 2 ) ) THEN |
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| 239 | !!!$ |
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| 240 | !!!$ ! summergreen needle leaf |
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| 241 | !!!$ |
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| 242 | !!!$ sla(j) = 1.25 * sla(j) |
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| 243 | !!!$ |
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| 244 | !!!$ ENDIF |
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| 245 | |
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| 246 | IF ( printlev >= 2 ) WRITE(numout,*) ' specific leaf area (m**2/gC) (::sla):', sla(j), 12./leaflife_tab(j) |
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| 247 | |
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| 248 | ! |
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| 249 | ! 5 sapling characteristics |
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| 250 | ! |
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| 251 | |
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| 252 | IF ( is_tree(j) ) THEN |
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| 253 | |
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| 254 | !> 5.1 trees |
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| 255 | |
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| 256 | !!\latexonly |
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| 257 | !!\input{stomate_data_sapl_tree.tex} |
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| 258 | !!\endlatexonly |
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| 259 | |
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| 260 | alpha = alpha_tree |
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| 261 | |
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| 262 | bm_sapl(j,ileaf,icarbon) = & |
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| 263 | & ((bm_sapl_leaf(1)*pipe_tune1*(mass_ratio_heart_sap *bm_sapl_leaf(2)*sla(j)/(pi*pipe_k1)) & |
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| 264 | & **bm_sapl_leaf(3))/sla(j))**bm_sapl_leaf(4) |
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| 265 | |
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| 266 | IF ( pheno_type(j) .NE. 1 ) THEN |
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| 267 | ! not evergreen |
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| 268 | bm_sapl(j,icarbres,icarbon) = bm_sapl_carbres * bm_sapl(j,ileaf,icarbon) |
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| 269 | ELSE |
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| 270 | bm_sapl(j,icarbres,icarbon) = zero |
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| 271 | ENDIF ! (pheno_type_tab(j) .NE. 1 ) |
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| 272 | |
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| 273 | csa_sap = bm_sapl(j,ileaf,icarbon) / ( pipe_k1 / sla(j) ) |
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| 274 | |
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| 275 | dia = (mass_ratio_heart_sap * csa_sap * dia_coeff(1) / pi ) ** dia_coeff(2) |
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| 276 | |
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| 277 | bm_sapl(j,isapabove,icarbon) = & |
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| 278 | bm_sapl_sapabove * pipe_density * csa_sap * pipe_tune2 * dia ** pipe_tune3 |
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| 279 | bm_sapl(j,isapbelow,icarbon) = bm_sapl(j,isapabove,icarbon) |
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| 280 | |
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| 281 | bm_sapl(j,iheartabove,icarbon) = bm_sapl_heartabove * bm_sapl(j,isapabove,icarbon) |
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| 282 | bm_sapl(j,iheartbelow,icarbon) = bm_sapl_heartbelow * bm_sapl(j,isapbelow,icarbon) |
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| 283 | |
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| 284 | ELSE |
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| 285 | |
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| 286 | !> 5.2 grasses |
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| 287 | |
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| 288 | !!\latexonly |
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| 289 | !!\input{stomate_data_sapl_grass.tex} |
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| 290 | !!\endlatexonly |
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| 291 | |
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| 292 | alpha = alpha_grass |
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| 293 | |
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| 294 | IF ( natural(j) ) THEN |
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| 295 | bm_sapl(j,ileaf,icarbon) = init_sapl_mass_leaf_nat / sla(j) |
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| 296 | ELSE |
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| 297 | bm_sapl(j,ileaf,icarbon) = init_sapl_mass_leaf_agri / sla(j) |
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| 298 | ENDIF |
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| 299 | |
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| 300 | bm_sapl(j,icarbres,icarbon) = init_sapl_mass_carbres *bm_sapl(j,ileaf,icarbon) |
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| 301 | |
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| 302 | bm_sapl(j,isapabove,icarbon) = zero |
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| 303 | bm_sapl(j,isapbelow,icarbon) = zero |
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| 304 | |
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| 305 | bm_sapl(j,iheartabove,icarbon) = zero |
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| 306 | bm_sapl(j,iheartbelow,icarbon) = zero |
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| 307 | |
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| 308 | ENDIF !( is_tree(j) ) |
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| 309 | |
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| 310 | bm_sapl(j,iroot,icarbon) = init_sapl_mass_root * (1./alpha) * bm_sapl(j,ileaf,icarbon) |
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| 311 | |
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| 312 | bm_sapl(j,ifruit,icarbon) = init_sapl_mass_fruit * bm_sapl(j,ileaf,icarbon) |
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| 313 | |
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| 314 | IF ( printlev >= 2 ) THEN |
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| 315 | WRITE(numout,*) ' sapling biomass (gC):' |
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| 316 | WRITE(numout,*) ' leaves: (::bm_sapl(j,ileaf,icarbon))',bm_sapl(j,ileaf,icarbon) |
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| 317 | WRITE(numout,*) ' sap above ground: (::bm_sapl(j,ispabove,icarbon)):',bm_sapl(j,isapabove,icarbon) |
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| 318 | WRITE(numout,*) ' sap below ground: (::bm_sapl(j,isapbelow,icarbon))',bm_sapl(j,isapbelow,icarbon) |
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| 319 | WRITE(numout,*) ' heartwood above ground: (::bm_sapl(j,iheartabove,icarbon))',bm_sapl(j,iheartabove,icarbon) |
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| 320 | WRITE(numout,*) ' heartwood below ground: (::bm_sapl(j,iheartbelow,icarbon))',bm_sapl(j,iheartbelow,icarbon) |
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| 321 | WRITE(numout,*) ' roots: (::bm_sapl(j,iroot,icarbon))',bm_sapl(j,iroot,icarbon) |
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| 322 | WRITE(numout,*) ' fruits: (::bm_sapl(j,ifruit,icarbon))',bm_sapl(j,ifruit,icarbon) |
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| 323 | WRITE(numout,*) ' carbohydrate reserve: (::bm_sapl(j,icarbres,icarbon))',bm_sapl(j,icarbres,icarbon) |
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| 324 | ENDIF |
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| 325 | |
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| 326 | ! |
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| 327 | ! 6 migration speed (m/year) |
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| 328 | ! |
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| 329 | |
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| 330 | IF ( is_tree(j) ) THEN |
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| 331 | |
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| 332 | migrate(j) = migrate_tree |
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| 333 | |
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| 334 | ELSE |
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| 335 | |
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| 336 | ! can be any value as grasses are, per *definition*, everywhere (big leaf). |
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| 337 | migrate(j) = migrate_grass |
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| 338 | |
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| 339 | ENDIF !( is_tree(j) ) |
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| 340 | |
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| 341 | IF ( printlev >= 2 ) WRITE(numout,*) ' migration speed (m/year): (::migrate(j))', migrate(j) |
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| 342 | |
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| 343 | ! |
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| 344 | ! 7 critical stem diameter: beyond this diameter, the crown area no longer |
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| 345 | ! increases (m) |
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| 346 | ! |
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| 347 | |
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| 348 | IF ( is_tree(j) ) THEN |
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| 349 | |
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| 350 | !!\latexonly |
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| 351 | !!\input{stomate_data_stem_diameter.tex} |
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| 352 | !!\endlatexonly |
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| 353 | |
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| 354 | maxdia(j) = ( ( pipe_tune4 / ((pipe_tune2*pipe_tune3)/(maxdia_coeff(1)**pipe_tune3)) ) & |
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| 355 | ** ( un / ( pipe_tune3 - un ) ) ) * maxdia_coeff(2) |
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| 356 | cn_sapl(j) = cn_sapl_init !crown of individual tree, first year |
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| 357 | |
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| 358 | ELSE |
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| 359 | |
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| 360 | maxdia(j) = undef |
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| 361 | cn_sapl(j)=1 |
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| 362 | |
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| 363 | ENDIF !( is_tree(j) ) |
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| 364 | |
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| 365 | IF ( printlev >= 2 ) WRITE(numout,*) ' critical stem diameter (m): (::maxdia(j))', maxdia(j) |
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| 366 | |
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| 367 | ! |
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| 368 | ! 8 Coldest tolerable temperature (K) |
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| 369 | ! |
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| 370 | |
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| 371 | IF ( ABS( tmin_crit(j) - undef ) .GT. min_stomate ) THEN |
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| 372 | tmin_crit(j) = tmin_crit(j) + ZeroCelsius |
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| 373 | ELSE |
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| 374 | tmin_crit(j) = undef |
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| 375 | ENDIF |
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| 376 | |
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| 377 | IF ( printlev >= 2 ) & |
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| 378 | WRITE(numout,*) ' coldest tolerable temperature (K): (::tmin_crit(j))', tmin_crit(j) |
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| 379 | |
|---|
| 380 | ! |
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| 381 | ! 9 Maximum temperature of the coldest month: need to be below this temperature |
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| 382 | ! for a certain time to regrow leaves next spring *(vernalization)* (K) |
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| 383 | ! |
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| 384 | |
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| 385 | IF ( ABS ( tcm_crit(j) - undef ) .GT. min_stomate ) THEN |
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| 386 | tcm_crit(j) = tcm_crit(j) + ZeroCelsius |
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| 387 | ELSE |
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| 388 | tcm_crit(j) = undef |
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| 389 | ENDIF |
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| 390 | |
|---|
| 391 | IF ( printlev >= 2 ) & |
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| 392 | WRITE(numout,*) ' vernalization temperature (K): (::tcm_crit(j))', tcm_crit(j) |
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| 393 | |
|---|
| 394 | ! |
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| 395 | ! 10 critical values for phenology |
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| 396 | ! |
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| 397 | |
|---|
| 398 | ! 10.1 model used |
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| 399 | |
|---|
| 400 | IF ( printlev >= 2 ) & |
|---|
| 401 | WRITE(numout,*) ' phenology model used: (::pheno_model(j)) ',pheno_model(j) |
|---|
| 402 | |
|---|
| 403 | ! 10.2 growing degree days. What kind of gdd is meant (i.e. threshold 0 or -5 deg C |
|---|
| 404 | ! or whatever), depends on how this is used in stomate_phenology. |
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| 405 | |
|---|
| 406 | |
|---|
| 407 | IF ( ( printlev >= 2 ) .AND. ( ALL(pheno_gdd_crit(j,:) .NE. undef) ) ) THEN |
|---|
| 408 | WRITE(numout,*) ' critical GDD is a function of long term T (C): (::gdd)' |
|---|
| 409 | WRITE(numout,*) ' ',pheno_gdd_crit(j,1), & |
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| 410 | ' + T *',pheno_gdd_crit(j,2), & |
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| 411 | ' + T^2 *',pheno_gdd_crit(j,3) |
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| 412 | ENDIF |
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| 413 | |
|---|
| 414 | ! consistency check |
|---|
| 415 | |
|---|
| 416 | IF ( ( ( pheno_model(j) .EQ. 'moigdd' ) .OR. & |
|---|
| 417 | ( pheno_model(j) .EQ. 'humgdd' ) ) .AND. & |
|---|
| 418 | ( ANY(pheno_gdd_crit(j,:) .EQ. undef) ) ) THEN |
|---|
| 419 | CALL ipslerr_p(3,'stomate_data','problem with phenology parameters, critical GDD. (::pheno_model)','','') |
|---|
| 420 | ENDIF |
|---|
| 421 | |
|---|
| 422 | ! 10.3 number of growing days |
|---|
| 423 | |
|---|
| 424 | IF ( ( printlev >= 2 ) .AND. ( ngd_crit(j) .NE. undef ) ) & |
|---|
| 425 | WRITE(numout,*) ' critical NGD: (::ngd_crit(j))', ngd_crit(j) |
|---|
| 426 | |
|---|
| 427 | ! 10.4 critical temperature for ncd vs. gdd function in phenology (C) |
|---|
| 428 | |
|---|
| 429 | IF ( ( printlev >= 2 ) .AND. ( ncdgdd_temp(j) .NE. undef ) ) & |
|---|
| 430 | WRITE(numout,*) ' critical temperature for NCD vs. GDD (C): (::ncdgdd_temp(j))', & |
|---|
| 431 | ncdgdd_temp(j) |
|---|
| 432 | |
|---|
| 433 | ! 10.5 humidity fractions (0-1, unitless) |
|---|
| 434 | |
|---|
| 435 | IF ( ( printlev >= 2 ) .AND. ( hum_frac(j) .NE. undef ) ) & |
|---|
| 436 | WRITE(numout,*) ' critical humidity fraction: (::hum_frac(j))', & |
|---|
| 437 | & hum_frac(j) |
|---|
| 438 | |
|---|
| 439 | |
|---|
| 440 | ! 10.6 minimum time elapsed since moisture minimum (days) |
|---|
| 441 | |
|---|
| 442 | IF ( ( printlev >= 2 ) .AND. ( hum_min_time(j) .NE. undef ) ) & |
|---|
| 443 | WRITE(numout,*) ' time to wait after moisture min (d): (::hum_min_time(j))', & |
|---|
| 444 | & hum_min_time(j) |
|---|
| 445 | |
|---|
| 446 | ! |
|---|
| 447 | ! 11 critical values for senescence |
|---|
| 448 | ! |
|---|
| 449 | |
|---|
| 450 | ! 11.1 type of senescence |
|---|
| 451 | |
|---|
| 452 | IF ( printlev >= 2 ) & |
|---|
| 453 | WRITE(numout,*) ' type of senescence: (::senescence_type(j))',senescence_type(j) |
|---|
| 454 | |
|---|
| 455 | ! 11.2 critical temperature for senescence (C) |
|---|
| 456 | |
|---|
| 457 | IF ( ( printlev >= 2 ) .AND. ( ALL(senescence_temp(j,:) .NE. undef) ) ) THEN |
|---|
| 458 | WRITE(numout,*) ' critical temperature for senescence (C) is' |
|---|
| 459 | WRITE(numout,*) ' a function of long term T (C): (::senescence_temp)' |
|---|
| 460 | WRITE(numout,*) ' ',senescence_temp(j,1), & |
|---|
| 461 | ' + T *',senescence_temp(j,2), & |
|---|
| 462 | ' + T^2 *',senescence_temp(j,3) |
|---|
| 463 | ENDIF |
|---|
| 464 | |
|---|
| 465 | ! consistency check |
|---|
| 466 | |
|---|
| 467 | IF ( ( ( senescence_type(j) .EQ. 'cold' ) .OR. & |
|---|
| 468 | ( senescence_type(j) .EQ. 'mixed' ) ) .AND. & |
|---|
| 469 | ( ANY(senescence_temp(j,:) .EQ. undef ) ) ) THEN |
|---|
| 470 | CALL ipslerr_p(3,'stomate_data','Problem with senescence parameters, temperature. (::senescence_type)','','') |
|---|
| 471 | ENDIF |
|---|
| 472 | |
|---|
| 473 | ! 11.3 critical relative moisture availability for senescence |
|---|
| 474 | |
|---|
| 475 | IF ( ( printlev >= 2 ) .AND. ( senescence_hum(j) .NE. undef ) ) THEN |
|---|
| 476 | WRITE(numout,*) ' max. critical relative moisture availability for' |
|---|
| 477 | WRITE(numout,*) ' senescence: (::senescence_hum(j))', & |
|---|
| 478 | & senescence_hum(j) |
|---|
| 479 | END IF |
|---|
| 480 | |
|---|
| 481 | ! consistency check |
|---|
| 482 | |
|---|
| 483 | IF ( ( ( senescence_type(j) .EQ. 'dry' ) .OR. & |
|---|
| 484 | ( senescence_type(j) .EQ. 'mixed' ) ) .AND. & |
|---|
| 485 | ( senescence_hum(j) .EQ. undef ) ) THEN |
|---|
| 486 | CALL ipslerr_p(3,'stomate_data','Problem with senescence parameters, humidity.(::senescence_type)','','') |
|---|
| 487 | ENDIF |
|---|
| 488 | |
|---|
| 489 | ! 14.3 relative moisture availability above which there is no moisture-related |
|---|
| 490 | ! senescence (0-1, unitless) |
|---|
| 491 | |
|---|
| 492 | IF ( ( printlev >= 2 ) .AND. ( nosenescence_hum(j) .NE. undef ) ) THEN |
|---|
| 493 | WRITE(numout,*) ' relative moisture availability above which there is' |
|---|
| 494 | WRITE(numout,*) ' no moisture-related senescence: (::nosenescence_hum(j))', nosenescence_hum(j) |
|---|
| 495 | END IF |
|---|
| 496 | ! consistency check |
|---|
| 497 | |
|---|
| 498 | IF ( ( ( senescence_type(j) .EQ. 'dry' ) .OR. & |
|---|
| 499 | ( senescence_type(j) .EQ. 'mixed' ) ) .AND. & |
|---|
| 500 | ( nosenescence_hum(j) .EQ. undef ) ) THEN |
|---|
| 501 | CALL ipslerr_p(3,'stomate_data','Problem with senescence parameters, humidity. (::senescence_type)','','') |
|---|
| 502 | ENDIF |
|---|
| 503 | |
|---|
| 504 | ! |
|---|
| 505 | ! 12 sapwood -> heartwood conversion time (days) |
|---|
| 506 | ! |
|---|
| 507 | |
|---|
| 508 | IF ( printlev >= 2 ) & |
|---|
| 509 | WRITE(numout,*) ' sapwood -> heartwood conversion time (d): (::tau_sap(j))', tau_sap(j) |
|---|
| 510 | |
|---|
| 511 | ! |
|---|
| 512 | ! 13 fruit lifetime (days) |
|---|
| 513 | ! |
|---|
| 514 | |
|---|
| 515 | IF ( printlev >= 2 ) WRITE(numout,*) ' fruit lifetime (d): (::tau_fruit(j))', tau_fruit(j) |
|---|
| 516 | |
|---|
| 517 | ! |
|---|
| 518 | ! 14 length of leaf death (days) |
|---|
| 519 | ! For evergreen trees, this variable determines the lifetime of the leaves. |
|---|
| 520 | ! Note that it is different from the value given in leaflife_tab. |
|---|
| 521 | ! |
|---|
| 522 | |
|---|
| 523 | IF ( printlev >= 2 ) & |
|---|
| 524 | WRITE(numout,*) ' length of leaf death (d): (::leaffall(j))', leaffall(j) |
|---|
| 525 | |
|---|
| 526 | ! |
|---|
| 527 | ! 15 maximum lifetime of leaves (days) |
|---|
| 528 | ! |
|---|
| 529 | |
|---|
| 530 | IF ( ( printlev >= 2 ) .AND. ( leafagecrit(j) .NE. undef ) ) & |
|---|
| 531 | WRITE(numout,*) ' critical leaf age (d): (::leafagecrit(j))', leafagecrit(j) |
|---|
| 532 | |
|---|
| 533 | ! |
|---|
| 534 | ! 16 time constant for leaf age discretisation (days) |
|---|
| 535 | ! |
|---|
| 536 | |
|---|
| 537 | leaf_timecst(j) = leafagecrit(j) / REAL( nleafages,r_std ) |
|---|
| 538 | |
|---|
| 539 | IF ( printlev >= 2 ) & |
|---|
| 540 | WRITE(numout,*) ' time constant for leaf age discretisation (d): (::leaf_timecst(j))', & |
|---|
| 541 | leaf_timecst(j) |
|---|
| 542 | |
|---|
| 543 | ! |
|---|
| 544 | ! 17 minimum lai, initial (m^2.m^{-2}) |
|---|
| 545 | ! |
|---|
| 546 | |
|---|
| 547 | IF ( is_tree(j) ) THEN |
|---|
| 548 | lai_initmin(j) = lai_initmin_tree |
|---|
| 549 | ELSE |
|---|
| 550 | lai_initmin(j) = lai_initmin_grass |
|---|
| 551 | ENDIF !( is_tree(j) ) |
|---|
| 552 | |
|---|
| 553 | IF ( printlev >= 2 ) & |
|---|
| 554 | WRITE(numout,*) ' initial LAI: (::lai_initmin(j))', lai_initmin(j) |
|---|
| 555 | |
|---|
| 556 | ! |
|---|
| 557 | ! 19 maximum LAI (m^2.m^{-2}) |
|---|
| 558 | ! |
|---|
| 559 | |
|---|
| 560 | IF ( printlev >= 2 ) & |
|---|
| 561 | WRITE(numout,*) ' critical LAI above which no leaf allocation: (::lai_max(j))', lai_max(j) |
|---|
| 562 | |
|---|
| 563 | ! |
|---|
| 564 | ! 20 fraction of primary leaf and root allocation put into reserve (0-1, unitless) |
|---|
| 565 | ! |
|---|
| 566 | |
|---|
| 567 | IF ( printlev >= 2 ) & |
|---|
| 568 | WRITE(numout,*) ' reserve allocation factor: (::ecureuil(j))', ecureuil(j) |
|---|
| 569 | |
|---|
| 570 | ! |
|---|
| 571 | ! 21 maintenance respiration coefficient (g/g/day) at 0 deg C |
|---|
| 572 | ! |
|---|
| 573 | |
|---|
| 574 | IF ( printlev >= 2 ) THEN |
|---|
| 575 | |
|---|
| 576 | WRITE(numout,*) ' maintenance respiration coefficient (g/g/day) at 0 deg C:' |
|---|
| 577 | WRITE(numout,*) ' . leaves: (::coeff_maint_zero(j,ileaf))',coeff_maint_zero(j,ileaf) |
|---|
| 578 | WRITE(numout,*) ' . sapwood above ground: (::coeff_maint_zero(j,isapabove)) ',& |
|---|
| 579 | & coeff_maint_zero(j,isapabove) |
|---|
| 580 | WRITE(numout,*) ' . sapwood below ground: (::coeff_maint_zero(j,isapbelow)) ',& |
|---|
| 581 | & coeff_maint_zero(j,isapbelow) |
|---|
| 582 | WRITE(numout,*) ' . heartwood above ground: (::coeff_maint_zero(j,iheartabove)) ',& |
|---|
| 583 | & coeff_maint_zero(j,iheartabove) |
|---|
| 584 | WRITE(numout,*) ' . heartwood below ground: (::coeff_maint_zero(j,iheartbelow)) ',& |
|---|
| 585 | & coeff_maint_zero(j,iheartbelow) |
|---|
| 586 | WRITE(numout,*) ' . roots: (::coeff_maint_zero(j,iroot))',coeff_maint_zero(j,iroot) |
|---|
| 587 | WRITE(numout,*) ' . fruits: (::coeff_maint_zero(j,ifruit)) ',coeff_maint_zero(j,ifruit) |
|---|
| 588 | WRITE(numout,*) ' . carbohydrate reserve: (::coeff_maint_zero(j,icarbres)) ',& |
|---|
| 589 | & coeff_maint_zero(j,icarbres) |
|---|
| 590 | |
|---|
| 591 | ENDIF !( printlev >= 2 ) |
|---|
| 592 | |
|---|
| 593 | ! |
|---|
| 594 | ! 22 parameter for temperature sensitivity of maintenance respiration |
|---|
| 595 | ! |
|---|
| 596 | |
|---|
| 597 | IF ( printlev >= 2 ) THEN |
|---|
| 598 | WRITE(numout,*) ' temperature sensitivity of maintenance respiration (1/K) is' |
|---|
| 599 | WRITE(numout,*) ' a function of long term T (C): (::maint_resp_slope)' |
|---|
| 600 | WRITE(numout,*) ' ',maint_resp_slope(j,1),' + T *',maint_resp_slope(j,2), & |
|---|
| 601 | ' + T^2 *',maint_resp_slope(j,3) |
|---|
| 602 | END IF |
|---|
| 603 | ! |
|---|
| 604 | ! 23 natural ? |
|---|
| 605 | ! |
|---|
| 606 | |
|---|
| 607 | IF ( printlev >= 2 ) & |
|---|
| 608 | WRITE(numout,*) ' Natural: (::natural(j))', natural(j) |
|---|
| 609 | |
|---|
| 610 | ! |
|---|
| 611 | ! 24 Vcmax et Vjmax (umol.m^{-2}.s^{-1}) |
|---|
| 612 | ! |
|---|
| 613 | |
|---|
| 614 | IF ( printlev >= 2 ) & |
|---|
| 615 | WRITE(numout,*) ' Maximum rate of carboxylation: (::Vcmax_25(j))', vcmax25(j) |
|---|
| 616 | ! |
|---|
| 617 | ! 25 constants for photosynthesis temperatures |
|---|
| 618 | ! |
|---|
| 619 | |
|---|
| 620 | IF ( printlev >= 2 ) THEN |
|---|
| 621 | |
|---|
| 622 | |
|---|
| 623 | ! |
|---|
| 624 | ! 26 Properties |
|---|
| 625 | ! |
|---|
| 626 | |
|---|
| 627 | WRITE(numout,*) ' C4 photosynthesis: (::is_c4(j))', is_c4(j) |
|---|
| 628 | WRITE(numout,*) ' Depth constant for root profile (m): (::1./humcste(j))', 1./humcste(j) |
|---|
| 629 | |
|---|
| 630 | ENDIF |
|---|
| 631 | |
|---|
| 632 | ! |
|---|
| 633 | ! 27 extinction coefficient of the Monsi and Saeki (1953) relationship |
|---|
| 634 | ! |
|---|
| 635 | IF ( printlev >= 2 ) THEN |
|---|
| 636 | WRITE(numout,*) ' extinction coefficient: (::ext_coeff(j))', ext_coeff(j) |
|---|
| 637 | ENDIF |
|---|
| 638 | |
|---|
| 639 | ! |
|---|
| 640 | ! 30 fraction of allocatable biomass which is lost as growth respiration (0-1, unitless) |
|---|
| 641 | ! |
|---|
| 642 | IF ( printlev >= 2 ) & |
|---|
| 643 | WRITE(numout,*) ' growth respiration fraction: (::frac_growthresp(j))', frac_growthresp(j) |
|---|
| 644 | |
|---|
| 645 | ENDDO ! Loop over # PFTS |
|---|
| 646 | |
|---|
| 647 | ! |
|---|
| 648 | ! 29 time scales for phenology and other processes (in days) |
|---|
| 649 | ! |
|---|
| 650 | |
|---|
| 651 | tau_longterm_max = coeff_tau_longterm * one_year |
|---|
| 652 | |
|---|
| 653 | IF ( printlev >= 2 ) THEN |
|---|
| 654 | |
|---|
| 655 | WRITE(numout,*) ' > time scale for ''monthly'' moisture availability (d): (::tau_hum_month)', & |
|---|
| 656 | tau_hum_month |
|---|
| 657 | WRITE(numout,*) ' > time scale for ''weekly'' moisture availability (d): (::tau_hum_week)', & |
|---|
| 658 | tau_hum_week |
|---|
| 659 | WRITE(numout,*) ' > time scale for ''monthly'' 2 meter temperature (d): (::tau_t2m_month)', & |
|---|
| 660 | tau_t2m_month |
|---|
| 661 | WRITE(numout,*) ' > time scale for ''weekly'' 2 meter temperature (d): (::tau_t2m_week)', & |
|---|
| 662 | tau_t2m_week |
|---|
| 663 | WRITE(numout,*) ' > time scale for ''weekly'' GPP (d): (::tau_gpp_week)', & |
|---|
| 664 | tau_gpp_week |
|---|
| 665 | WRITE(numout,*) ' > time scale for ''monthly'' soil temperature (d): (::tau_tsoil_month)', & |
|---|
| 666 | tau_tsoil_month |
|---|
| 667 | WRITE(numout,*) ' > time scale for ''monthly'' soil humidity (d): (::tau_soilhum_month)', & |
|---|
| 668 | tau_soilhum_month |
|---|
| 669 | WRITE(numout,*) ' > time scale for vigour calculations (y): (::tau_longterm_max / one_year)', & |
|---|
| 670 | tau_longterm_max / one_year |
|---|
| 671 | |
|---|
| 672 | ENDIF |
|---|
| 673 | |
|---|
| 674 | IF (printlev >= 4) WRITE(numout,*) 'Leaving stomate_data' |
|---|
| 675 | |
|---|
| 676 | END SUBROUTINE data |
|---|
| 677 | |
|---|
| 678 | END MODULE stomate_data |
|---|
