! source file: /Users/jfidler/work/UVic_ESCM/2.9/source/common/co2calc.F subroutine co2calc_SWS (t, s, dic_in, ta_in, co2_in, pt_in &, sit_in, atmpres, depth, phlo, phhi, ph &, co2star, dco2star, pCO2, dpco2 &, CO3, Omega_c, Omega_a) !------------------------------------------------------------------------- ! Modified from co2calc.f (RCS version 1.8, OCMIP-2) ! - by A. Mouchet, 2004: ! NOW; "All" constants are given on seawater H scale (hSWS) ! - HOWEVER, dissociation constants for S and F are on the 'free' H scale ! (this is necessary to work with hSWS) ! - this routine corrects for inconsistencies in the previous version. ! - Other changes: ! * use ta_iter_SWS instead of ta_iter_1; ! * hSWS replaces htotal; ! * moved upward the calculation of bt, st and ft ! (needed in evaluation of kb); ! * added various comments and references. ! subroutine CO2CALC_SWS ! PURPOSE ! Calculate delta co2* from total alkalinity and total CO2 at ! temperature (t), salinity (s) and "atmpres" atmosphere total pressure. ! USAGE ! call co2calc_SWS(t,s,dic_in,ta_in,pt_in,sit_in ! & ,phlo,phhi,ph,co2_in,atmpres ! & ,co2star,dco2star,pCO2,dpco2) ! INPUT ! dic_in = total inorganic carbon (mol/m^3) ! where 1 T = 1 metric ton = 1000 kg ! ta_in = total alkalinity (eq/m^3) ! pt_in = inorganic phosphate (mol/m^3) ! sit_in = inorganic silicate (mol/m^3) ! t = temperature (degrees C) ! s = salinity (PSU) ! phlo = lower limit of pH range ! phhi = upper limit of pH range ! co2_in = atmospheric mole fraction CO2 in dry air (ppmv) ! atmpres = atmospheric pressure in atmospheres (1 atm==1013.25mbar) ! depth = ocean depth (m) ! Note: arguments dic_in, ta_in, pt_in, sit_in, and co2_in are ! used to initialize variables dic, ta, pt, sit, and co2. ! * Variables dic, ta, pt, and sit are in the common block ! "species". ! * Variable co2 is a local variable. ! * Variables with "_in" suffix have different units ! than those without. ! pressure dependency added (Millero 1995). ! OUTPUT ! co2star = CO2*water (mol/m^3) ! dco2star = delta CO2 (mol/m^3) ! pco2 = oceanic pCO2 (ppmv) ! dpco2 = Delta pCO2, i.e, pCO2ocn - pCO2atm (ppmv) ! IMPORTANT: Some words about units - (JCO, 4/4/1999) ! - Models carry tracers in mol/m^3 (on a per volume basis) ! - Conversely, this routine, which was written by observationalists ! (C. Sabine and R. Key), passes input arguments in umol/kg ! (i.e., on a per mass basis) ! - I have changed things slightly so that input arguments are in mol/m^3, ! - Thus, all input concentrations (dic_in, ta_in, pt_in, and st_in) ! should be given in mol/m^3; output arguments "co2star" and "dco2star" ! are likewise in mol/m^3. ! FILES and PROGRAMS NEEDED ! drtsafe ! ta_iter_SWS !-------------------------------------------------------------------------- implicit none real permil, pt, pt_in, sit, sit_in, ta, ta_in, dic, dic_in real permeg, co2, co2_in, tk, t, tk100, tk1002, dlogtk, s real sqrtis, s2, sqrts, s15, scl, bt, st, ft, ff, x1, phhi real x2, phlo, xacc, hSWS, drtsafe, hSWS2, co2star, co2starair real atmpres, dco2star, ph, pco2, dpco2, invtk, is, is2 real k0, k1, k12, k2, kw, kb, ks, kf, k1p, k2p, k3p, ksi, C2K real Kspc, Kspa, ca, co3, omega_c, omega_a, depth, pres real t2, dvc, dva, dk, pitkR, p2itkR common /const/ k0, k1, k12, k2, kw, kb, ks, kf, k1p, k2p, k3p common /const/ ksi, ff common /species/ bt, st, ft, sit, pt, dic, ta ! --------------------------------------------------------------------- ! Change units from the input of mol/m^3 -> mol/kg: ! (1 mol/m^3) x (1 m^3/1024.5 kg) ! where the ocean's mean surface density is 1024.5 kg/m^3 ! Note: mol/kg are actually what the body of this routine uses ! for calculations. ! --------------------------------------------------------------------- permil = 1.0 / 1024.5 ! To convert input in mol/m^3 -> mol/kg pt = pt_in*permil sit = sit_in*permil ta = ta_in*permil dic = dic_in*permil C2K = 273.15 pres = depth*0.1 ! [decibars ~ meters of depth to bars] ! --------------------------------------------------------------------- ! Change units from uatm to atm. That is, atm is what the body of ! this routine uses for calculations. ! --------------------------------------------------------------------- permeg = 1.e-6 ! To convert input in uatm -> atm co2 = co2_in*permeg ! --------------------------------------------------------------------- !************************************************************************* ! Calculate all constants needed to convert between various measured ! carbon species. References for each equation are noted in the code. ! Version 2 of "Handbook of Methods for the Analysis of the Various ! Parameters of the Carbon Dioxide System in Seawater", DOE, 1994 ! (SOP No. 3, p25-26). ! Derive simple terms used more than once tk = C2K + t tk100 = tk/100.0 tk1002 = tk100*tk100 invtk = 1.0/tk dlogtk = log(tk) is = 19.924*s/(1000.-1.005*s) is2 = is*is sqrtis = sqrt(is) s2 = s*s t2 = t*t sqrts = sqrt(s) s15 = s**1.5 scl = s/1.80655 pitkR = pres/tk/83.15 ! % 83.15 = the gas constant R in cm3 bar k-1 p2itkR = pres*pitkR !------------------------------------------------------------------------ ! Calculate concentrations for borate, sulfate, and fluoride ! Uppstrom (1974) bt = 0.000232 * scl/10.811 ! Morris & Riley (1966) st = 0.14 * scl/96.062 ! Riley (1965) ft = 0.000067 * scl/18.9984 !------------------------------------------------------------------------ ! f = k0(1-pH2O)*correction term for non-ideality ! Weiss & Price (1980, Mar. Chem., 8, 347-359; Eq 13 with table 6 values) ff = exp(-162.8301 + 218.2968/tk100 + 90.9241*log(tk100) & - 1.47696*tk1002 + s*(.025695 - .025225*tk100 & + 0.0049867*tk1002)) ! K0 from Weiss 1974 !------------------------------------------------------------------------ ! k1 = [H][HCO3]/[H2CO3] ! k2 = [H][CO3]/[HCO3] on hSWS ! Millero p.664 (1995) using Mehrbach et al. data on SEAWATER scale ! (Original reference: Dickson and Millero, DSR, 1987) k1 = 10**(-1.*(3670.7*invtk - 62.008 + 9.7944*dlogtk & - 0.0118*s + 0.000116*s2)) k2 = 10**(-1*(1394.7*invtk + 4.777 - 0.0184*s + 0.000118*s2)) !------------------------------------------------------------------------ ! k1p = [H][H2PO4]/[H3PO4] on hSWS ! Millero p.670 (1995) k1p = exp(-4576.752*invtk + 115.540 - 18.453*dlogtk & + (-106.736*invtk + 0.69171)*sqrts & + (-0.65643*invtk - 0.01844)*s) !------------------------------------------------------------------------ ! k2p = [H][HPO4]/[H2PO4] on hSWS ! Millero p.670 (1995) k2p = exp(-8814.715*invtk + 172.1033 - 27.927*dlogtk & + (-160.340*invtk + 1.3566)*sqrts & + (0.37335*invtk - 0.05778)*s) !------------------------------------------------------------------------ ! k3p = [H][PO4]/[HPO4] on hSWS ! Millero p.670 (1995) k3p = exp(-3070.75*invtk - 18.126 & + (17.27039*invtk + 2.81197)*sqrts & + (-44.99486*invtk - 0.09984)*s) !------------------------------------------------------------------------ ! ksi = [H][SiO(OH)3]/[Si(OH)4] on hSWS ! Millero p.671 (1995) using data from Yao and Millero (1995) ! change to (mol/ kg soln) ! depth dependancy assumed to be the same as boric acid ! typo in Millero 1994 corrected in sign of 0.1622 ksi = exp(-8904.2*invtk + 117.400 - 19.334*dlogtk & + (-458.79*invtk + 3.5913)*sqrtis & + (188.74*invtk - 1.5998)*is & + (-12.1652*invtk + 0.07871)*is2 & + log(1.0-0.001005*s)) !------------------------------------------------------------------------ ! kw = [H][OH] on hSWS ! Millero p.670 (1995) using composite data ! pressure dependancy in Millero 1994 corrected for sea water from ! Millero 1983 kw = exp(-13847.26*invtk + 148.9802 - 23.6521*dlogtk & + (118.67*invtk - 5.977 + 1.0495*dlogtk)*sqrts - 0.01615*s) !------------------------------------------------------------------------ ! ks = [H][SO4]/[HSO4] on free H scale ! Dickson (1990, J. chem. Thermodynamics 22, 113) ! change to (mol/ kg soln) ks = exp(-4276.1*invtk + 141.328 - 23.093*dlogtk & + (-13856*invtk + 324.57 - 47.986*dlogtk)*sqrtis & + (35474*invtk - 771.54 + 114.723*dlogtk)*is & - 2698*invtk*is**1.5 + 1776*invtk*is2 & + log(1.0 - 0.001005*s)) !------------------------------------------------------------------------ ! kf = [H][F]/[HF] on free H scale ! Dickson and Riley (1979) ! change to (mol/ kg soln) kf = exp(1590.2*invtk - 12.641 + 1.525*sqrtis & + log(1.0 - 0.001005*s)) !------------------------------------------------------------------------ ! kb = [H][BO2]/[HBO2] on hSWS ! Dickson p.673 (1990) ! change from htotal to hSWS ! typo in Millero 1994 corrected in sign of 0.1622 kb = exp((-8966.90 - 2890.53*sqrts - 77.942*s & + 1.728*s15 - 0.0996*s2)*invtk & + (148.0248 + 137.1942*sqrts + 1.62142*s) & + (-24.4344 - 25.085*sqrts - 0.2474*s)*dlogtk & + 0.053105*sqrts*tk & + log((1+(st/ks)+(ft/kf))/(1+(st/ks)))) !************************************************************************* ! Calculate [H+] SWS when DIC and TA are known at T, S and 1 atm. ! The solution converges to err of xacc. The solution must be within ! the range x1 to x2. ! If DIC and TA are known then either a root finding or iterative method ! must be used to calculate hSWS. In this case we use the Newton-Raphson ! "safe" method taken from "Numerical Recipes" (function "rtsafe.f" with ! error trapping removed). ! As currently set, this procedure iterates about 12 times. The x1 and x2 ! values set below will accomodate ANY oceanographic values. If an initial ! guess of the pH is known, then the number of iterations can be reduced to ! about 5 by narrowing the gap between x1 and x2. It is recommended that ! the first few time steps be run with x1 and x2 set as below. After that, ! set x1 and x2 to the previous value of the pH +/- ~0.5. The current ! setting of xacc will result in co2star accurate to 3 significant figures ! (xx.y). Making xacc bigger will result in faster convergence also, but this ! is not recommended (xacc of 10**-9 drops precision to 2 significant figures). ! Parentheses added around negative exponents (Keith Lindsay) x1 = 10.0**(-phhi) x2 = 10.0**(-phlo) xacc = 1.e-10 hSWS = drtsafe(x1, x2, xacc) ! Calculate [CO2*] as defined in DOE Methods Handbook 1994 Ver.2, ! ORNL/CDIAC-74, Dickson and Goyet, eds. (Ch 2 p 10, Eq A.49) hSWS2 = hSWS*hSWS co2star = dic*hSWS2/(hSWS2 + k1*hSWS + k1*k2) co2starair = co2*ff*atmpres dco2star = co2starair - co2star ph = -log10(hSWS) ! Add two output arguments for storing pCO2 ! Should we be using K0 or ff for the solubility here? pCO2 = co2star/ff dpCO2 = pCO2 - co2*atmpres ! Calculate [CO3] in mol/kg from co2star and hSWS CO3 = k1*k2*co2star/hSWS2 ! Solubility products of calcite and aragonite at sea level ! (Ksp0) as a function of temperature and salinity. Based on ! Mucci, 1983 as written by Sarmiento and Gruber, 2006 p366 ! Ksp0 for calcite: Kspc = exp(-395.8293 + (6537.773/tk) + 71.595*alog(tk) & - 0.17959*tk + (-1.78938 + (410.64/tk) & + 0.0065453*tk)*s**0.5 - 0.17755*s + 0.0094979*s15) ! Ksp0 for aragonite: Kspa = exp(-395.9180 + (6685.079/tk) + 71.595*log(tk) & - 0.17959*tk + (-0.157481 + (202.938/tk) & + 0.0039780*tk)*s**0.5 - 0.23067*s + 0.0136808*s15) ! Calculate saturation state (Omega) using a fix value ! for [Ca] in mol/kg Ca = 10.28E-3 ! calcite (Omgc) Omega_c = Ca*CO3/Kspc ! aragonite (Omga) Omega_a = Ca*CO3/Kspa ! Convert units of output arguments ! Note: co2star and dco2star are calculated in mol/kg within this routine ! Thus Convert now from mol/kg -> mol/m^3 co2star = co2star/permil dco2star = dco2star/permil CO3 = CO3/permil ! Note: pCO2 and dpCO2 are calculated in atm above. ! Thus convert now to uatm pCO2 = pCO2/permeg dpCO2 = dpCO2/permeg return end real function drtsafe(x1, x2, xacc) implicit none integer maxit, j real x1, fl, df, x2, fh, xl, xh, swap, dxold, dx, f, temp, xacc ! File taken from Numerical Recipes. Modified R.M.Key 4/94 maxit = 100 call ta_iter_SWS (x1, fl, df) call ta_iter_SWS (x2, fh, df) if (fl .lt. 0.0) then xl = x1 xh = x2 else xh = x1 xl = x2 swap = fl fl = fh fh = swap endif drtsafe = 0.5*(x1 + x2) dxold = abs(x2 - x1) dx = dxold call ta_iter_SWS (drtsafe, f, df) do J=1,maxit if (((drtsafe - xh)*df - f)*((drtsafe - xl)*df - f) .ge. 0. & .or. abs(2.0*f) .gt. abs(dxold*df)) then dxold= dx dx = 0.5*(xh-xl) drtsafe = xl + dx if (xl .eq. drtsafe) return else dxold = dx dx = f/df temp = drtsafe drtsafe = drtsafe - dx if (temp .eq. drtsafe) return endif if (abs(dx) .lt. xacc) return call ta_iter_SWS (drtsafe, f, df) if (f .lt. 0.0) then xl = drtsafe fl = f else xh = drtsafe fh = f endif enddo return end subroutine ta_iter_SWS (x, fn, df) implicit none real x2, x, x3, c, st, ft, a, a2, da, b, b2, db, fn, dic, bt real pt, sit, ta, df, ff, k12p, k123p real k0, k1, k12, k2, kw, kb, ks, kf, k1p, k2p, k3p, ksi common /const/ k0, k1, k12, k2, kw, kb, ks, kf, k1p, k2p, k3p common /const/ ksi, ff common /species/ bt, st, ft, sit, pt, dic, ta ! Modified from ta_iter_1.f (RCS version 1.2, OCMIP-2) ! - by A. Mouchet, 2004: ! Fixed Problems w/ version of ta_iter_1.f used in OCMIP-2 (vers. 1.2) ! 1) fixed errors in signs, parenthesis and coefficient c in derivative ! 2) changed from Total to Seawater Scale ! * c defined for seawater H scale; ! * fn and df adapted to KF on free H scale ! * comments have been adapted ! This routine expresses TA as a function of DIC, hSWS and constants. ! It also calculates the derivative of this function with respect to ! hSWS. It is used in the iterative solution for hSWS. In the call ! "x" is the input value for hSWS, "fn" is the calculated value for TA ! and "df" is the value for dTA/dhSWS x2=x*x x3=x2*x k12 = k1*k2 k12p = k1p*k2p k123p = k12p*k3p c = 1.0 + st/ks + ft/kf a = x3 + k1p*x2 + k12p*x + k123p a2=a*a da = 3.0*x2 + 2.0*k1p*x + k12p b = x2 + k1*x + k12 b2=b*b db = 2.0*x + k1 ! fn = hco3+co3+borate+oh+hpo4+2*po4+silicate-hfree-hso4-hf-h3po4-ta !=========================================================================== fn = k1*x*dic/b + & 2.0*dic*k12/b + & bt/(1.0 + x/kb) + & kw/x + & pt*k12p*x/a + & 2.0*pt*k123p/a + & sit/(1.0 + x/ksi) - & x/c - & st/(1.0 + ks/(x/c)) - & ft/(1.0 + kf/(x/c)) - & pt*x3/a - & ta ! df = dfn/dx df = ((k1*dic*b) - k1*x*dic*db)/b2 - & 2.0*dic*k12*db/b2 - & bt/kb/(1.0+x/kb)**2 - & kw/x2 + & (pt*k12p*(a - x*da))/a2 - & 2.0*pt*k123p*da/a2 - & sit/ksi/(1.0+x/ksi)**2 - & 1.0/c - & st *(1.0 + ks/(x/c))**(-2) *(ks*c/x2) - & ft*(1.0 + kf/(x/c))**(-2) *(kf*c/x2) - & pt*x2*(3.0*a-x*da)/a2 return end