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Estuarine Mixing
Estuarine Mixing
η(t)
2ao
Tt
Head
2ξo
ao = tidal amplitude
Mouth
2ao = tidal range
Gravitational and centrifugal
Tt = tidal period acceleration (E with M & S)
2ξo = tidal excursion Ocean range ~ 0.5 m
Coastal waters may have
much larger ranges
Equilibrium tide; moon only
Low
Water surface
M High E High
Low
Lunar
29.5d month
S 27.3d
13.6d
20.5d
Sun and moon aligned (full and new moon) => spring tide;
Sun and moon opposed (1st and 3rd quarters) => neap tide
Because the earth revolves, period of spring-neap cycle =
365d/[(365/27.3)-1] = 29.5 days
E 24 h M
Moon Phase
Los Angles, California
(outer harbor)
Tidal displacement above reference
o o
33 43' N, 118 16' W
12.4 hr
5 10 15 20 25 30
Date in July 1963 Ippen, 1969
Figure by MIT OCW.
Idealized (linear) tidal motion
η(t)
Qf
2ξο(x)
High Tide
Vu(x)
Low Tide
2ξ(x)
Pu(x)
0 x L
Now introduce salinity
River Estuary Ocean
Tidal, Salinity
Qf Freshwater Intrusion
+ + +
10 20 30
S=0 S=35 psu
⎡ T + 288.9414 ⎤
ρ (T ) = 1000⎢1 − (T − 3.9863) 2 ⎥
⎣ 508929.2(T + 68.12963) ⎦
∆ρ ( S ) = AS + BS 3 / 2 + CS 2
⎡ 1 ⎤
∆ρ (TSS ) = TSS ⎢1 − x10 −3
⎣ SG ⎥⎦
48
-10
Fischer, et al. (1979)
44 -8
40 -6
-4 σt = 1000*(ρ-1)
36 -2
0 (ρ in g/cm3)
32 2
Temperature (oC)
28 6
8
10
24
12
14
20 16
18
16 20
22
12 24
26
8 28
30
0
0 4 8 12 16 20 24 28 32 36 40
SALINITY (% )
Figure by MIT OCW.
Seawater Density ( σ1 Units )
48
-10
Example:
44 -8
-4
36 -2
32 2
Ocean salinity
Temperature (oC)
28 6
8
~ 35 psu
24
10
12
Freshwater salinity
0 psu
14
20 16
18
16
Temperatures 0 to 30C
20
22
12
∆ρ o ρ = [28-0]/1000=0.028
24
26
8 28
30 (0C)
4
= [22-(-4)]/1000=0.026
0
0 4 8 12 16 20 24 28 32 36 40 (30C)
SALINITY (% )
2
Pt Fd Pt = tidal prism; Q f = freshwater flow rate;
Ed =
Q f Tt Tt = tidal period
∆ρ o gQ f / W
R= W = estuary width;
ρu t 3
−1
u t = RMS tidal velocity ≅ 0.71u o
~ Ed
R ~ potential energy rate/kinetic energy rate
Example later
Estuary classification, cont’d
The definitions are related
3
ut
E d ~ R −1 ~ 2
u f ud
2 Semi-empirical
-1
10
x
1
Predicts
3.3
-1
P=
< - Salinity stratification
10
=
P
salinity stratification
10 -2
x
-1
3
3.
-3
Fm = 10
-2
δS -1
δS S o = ( S b − S s ) S
=
Fm = 10
-2
P
10
S0 10
Fm = 10
=
P
Fm = 1
-3
Increases w/ P, decreases w/ Fm
10
-4
-4
-3
x
Fm = 10
10
3
10
3.
Velocity stratification
x
=
=
3
P
P
3.
10-2
=
P
10-3 2 3
Decreases w/ Fm
us
1 10
uf
10 10
uf uf
Velocity stratification ->
P= ; Fm =
ut ud
Figure by MIT OCW.
Tide resolving models
Well-mixed (1-D) estuary
∂c ∂c 1 ∂ ⎛ ∂c ⎞ q L (c L − c ) ′
+ u (t ) = ⎜ AE L (t ) ⎟ + + ∑ ri + ∑ re
∂t ∂x A ∂x ⎝ ∂x ⎠ A
Look at 2) first
Characteristic dispersion time scales
(Fischer et al., 1979)
EL ~ Uc2Tc ~ u*2Tc
For rivers, two possible time scales, Tc:
Ttm ~ B2/ET and Tvm ~ h2/Ez
Ttm >> Tvm => EL ~ u*2 Ttm
(after transverse mixing)
For estuaries, additional possibility: Tc = Tt/2
Ttm >> Tt/2 ~ Tvm => EL ~ u*2 Ttm or u*2 Tt/2
“narrow” channel
B
t=0 Tc=Ttm 0.5Tt
2
u* B 2
Dispersion governed by Ttm, EL ~
ET
Dispersion in reversing flow, cont’d
“narrow” channel
B
t=0 Ttm 2
0.5Tt
2
u* B
Dispersion governed by Ttm, E L ~
ET
“wide” channel
B
l ~ ET Tc
Tc = 0.5Tt
t=0 2 2 2
2⎛ l ⎞ u* ET Tt
Dispersion governed by Tt, E ~ u * ⎜ ⎟ t
T ~
L
⎝ ⎠
B B2
Effects of reversing u(t)
Mass continuously injected at x = 0
C
land ocean
High Low
tide tide
x
0
2ξo
An actual simulation Harleman, 1971
1.0
H.W.S L.W.S
N = 30.0 N = 30.5
0.0
-2.0 -1.5 -1.0 -0.5 0.0 0.5 1.0 1.5 2.0
x / 2ξ o
Continuous injection at x = 0; output after 30, 400 tidal
periods (high slack) and 30.5 and 400.5 tidal cycles (low slack)
Tidal-average models
Perhaps we don’t care to resolve intra-
tidal time-dependence
Strong non-uniformities prevent
resolution of intra-tidal variability
Long term calculations more efficient
with tidal-average time step
However, averaging obscures physics
Tidal-average models, cont’d
Analogous, in principle, to time and cross-sectional averaging
u = u + u ′′′
Triple bars imply tidal average
c = c + c ′′′
∂c ∂ c 1 ∂ ⎛⎜ ∂ c ⎞⎟ Structurally similar to
+u = ⎜ AE L ⎟ + ∑ ri + ∑ re equation for river
∂t ∂x A ∂x ⎜ ∂x ⎟ transport => similar
⎝ ⎠
solutions
Tidal average Tidal average
velocity disp coef
Tidal average dispersion
Tidal pumping (shown)
Asymmetric ebb (a) & flood (b)
Tidal averaging => mean
Ebb velocity (c)
Trans mixing + trans velocity
gradients => dispersion!
Similar drivers
Flood Tidal trapping
Coriolis + density
Depth-dependent tidal reversal
Net
EL ~ (2ξo)2/Tt
General result
A B C
c
Conservative Tracer;
3 injection locations
x
c
Non-conservative
tracer; middle location
x
c
Non-conservative
tracer; 3 locations
x
Comments
For conservative tracer, c(x)
Is independent of xd for x > xd
Decrease with xd for x < xd
If you must pollute, do it downstream
(more discussion later)
Several specific solutions in notes
Conclusion applies loosely even if not 1-D
Signell, MWRA
(1999)
One example q" =
m&
A
Rectangular channel; no through flow
d ⎛ dc ⎞
0= ⎜ E L ⎟ − kc
dx ⎝ dc ⎠
E L ~ ( 2ξ o ) 2 / Tt = αx 2
dc 2
2d c
0 xd L x
0 = 2αx + αx − kc
dx 2
dx
Solution
q ′′ ⎡ x −1 2−κ 2 x −1 2+κ 2 ⎤
c + ( x, x d ) − c L = ⎢ 1 2−κ 2 − κ 1 2−κ 2 ⎥ x > xd
ακ ⎣ x d L xd ⎦
κ = 1 + 4k / α
q " ⎡ x −1 2+κ 2 x −1 2+κ 2 ⎤
c _( x, x d ) − c L = ⎢ 1 2+κ 2 − κ 1 2−κ 2 ⎥ x < xd
ακ ⎣ x d L xd ⎦
WE4-1 Proposed relocation of
Gillette’s Intake
Proposal to shorten Fort Point Channel
as part of the Big Dig threatened to limit
Gillette’s cooling water source
Details
Boston Harbor
1700m 1700m
2ao=2.9 m;
h=6 m;
k=0.1 day-1
Qo = 1.4 m3/s;
∆To = 6C
0
2.5
Existing
Mod Chan
Temperature (C)
2
MC + Disch
1.5
0.5
xd
0
0 400 m 500 1000 1500 2000
Distance (m)
Pn f n
= Qf fn = “freshness” =(So-Sn)/So
Tt
Pn cn
= m& mass injected continuously upstream of
Tt section n (behaves like freshwater)
m& Tt
cn =
Pn
Comments
Modified Tidal Prism Method has been
modified and re-modified many times
Ad-hoc assumption => not always
agreement with data
Non-conservative contaminates reduced in
concentration by χ
r
χ=
1 − (1 − r )e − kTt
r = 2a / h
Salinity as tracer to measure EL
Steady, tidal average flow
d
(u f AS ) = d ( AE L dS )
dx dx ds
Integrate with
S = dS/dx at head, x=0
uf S
EL =
dS / dx
C&D
3.0 3.0
Cheater
Cheater
6 14 18
10 22
4.0 4.0 2
26
5.0 2.0
6.0 10.0 14.0 18.0 22.0 26.0 5.0 4 20
8
PRESSURE (db)
4.0 16
PRESSURE (db)
6.0 8.0 12.0 12 24
16.0
20.0
6.0
24.0 28.0
7.0 7.0
8.0 8.0
9.0 9.0
10.0 10.0
11.0 11.0
12.0 12.0
140.0 120.0 100.0 80.0 60.0 40.0 20.0 0.0 100.0 40.0 20.0 0.0
Salinity profiles show
140.0 120.0 80.0 60.0
DISTANCE FROM BAY MOUTH (km) DISTANCE FROM BAY MOUTH (km)
74.6
DRBC RIVER MILES
55.9 37.3 18.8 0.0 74.6
DRBC RIVER MILES
55.9 37.3 18.8 0.0
Should it be?
2.0 2.0
3.0
Cheater
3.0
Cheater
8
12 16 24 12
20
4.0 2 4.0
16
22
5.0 4
26 5.0
10 26
4
PRESSURE (db)
22 2
PRESSURE (db)
6.0 6 6.0 18
18
14 24
7.0 14 7.0
6 10
8.0 8.0
20
9.0 9.0
10.0 10.0 8
28.0
11.0 11.0
12.0 12.0
140.0 120.0 100.0 80.0 60.0 40.0 20.0 0.0 140.0 120.0 100.0 80.0 60.0 40.0 20.0 0.0
DISTANCE FROM BAY MOUTH (km) DISTANCE FROM BAY MOUTH (km)
Figure by MIT OCW.
C&D
3.0
Cheater
8
12 16 20 24
4.0 2
5.0 4
26
10
22
PRESSURE (db)
6.0 6 18
7.0 14
11.0
uf S (Q f / A) S
EL = ≅ Qf = 260 m3/s; A = 1.5x104 m2;
dS / dx ∆S / ∆x
(260)(8) S = 8 psu (80 km);
≅
(1.5 x10 4 )(8) / 20000) ∆S/∆x = (12-4) psu/20 km (70-90 km)
≅ 350 m 2 / s
Should river be well-mixed?
∆ρ Qf
g
ρ W
R= 3
ut
(0.025)(10)(260) / 4000
≅ 3
≅ 0.02 < 0.08 Yes!
1
Box models
Qf Qf Qf Qf
c1 c2 c3 c4
Q f + f 2 Q1, 2 = f 1 (Q1, 2 + Q f )
f1 (Q1, 2 + Q f ) + f 3 Q2,3 = f 2 (Q1, 2 + Q2,3 + Q f )
f 2 (Q2,3 + Q f ) + f 4 Q2,3 = f 3 (Q2,3 + Q3, 4 + Q f )
Qf x
0 xd L
S/So
1 S/So
0
0 xd L
Qf x
0 xd L
1 f S/So
0
0 xd L
Qf x
0 xd L
E L A df
Qeff = Q f − dx Qeff really accounts for both
f advection and dispersion
Qf x
0 xd L
1 f S/So
2
0 0
0 xd L
Qf x
0 xd L
cx m&
=
fx Qf
Concentration at xd
⎛ So − S x ⎞ m& ⎛ So − Sd ⎞ m&
c x = ⎜⎜ ⎟⎟ c d = ⎜⎜ ⎟⎟
⎝ So ⎠ Qf ⎝ So ⎠ Qf
Qf x
0 xd L
1 f S/So
2
0 0
0 xd L
Qf x
0 xd L
cx S x
=
cd S d
S o − S d m& S x
cx =
So Q f Sd
cd
Qf x
0 xd L
c 4
1 f S/So
2
0 0
0 xd L
(Conservative) Mixing Diagrams
Concentration of
c conservative contaminant
discharged at head (using
cmax freshness as tracer)
⎛ So − S x ⎞ m&
c x = ⎜⎜ ⎟⎟
⎝ So ⎠ Qf
x
c x = a − bS x
m&
0 S a= = c max
So
Qf
0
aka C-S (or T-S, etc.) diagram, or property-salinity diagram
Uses for Property-S diagrams
Determine end-member concentration
and loading (So, Qf known, but not m
& )
Identify extraneous sources (we think
we know m& = Q f co but cmax > co)
Distinguish different water masses
Predict quality of mixed water masses
Detect non-conservative behavior
Determining end member c
1) Extrapolate to get cmax
c
2) m& = Q f c max
0
0 So
Distinguishing water masses
0 S
0 So
Non-conservative
c
behavior
cmax
+
-
0 S
0 So
Non-conservative
c
behavior
cmax
+
-
0 S
0 So
Note that conservative mixing curve is only linear if
conditions are steady and there is a single source
Two conservative sources look
like one NC source
2
0
0 So
Two conservative sources look
like one NC source
1 1+2
2
0
0 So
Transient Conditions
200 WE4-2 Nitrate-Salinity
100
X Fall diagrams in Delaware R
200
Ciufuentes, et al. (1990)
Summer
100
Solid lines are predictions for
conservative tracer & salinity at 4
Nitrate (µM)
200
Spring times (not linear because river flow
100 varies in space and time)
200
Symbols are data for nitrate &
Water salinity
100
Why the discrepancy in fall, spring?
0 16 32
Salinity (% )
∫ cdV
t res = 0
m&
=
M
m&
m&
SS inventory over renewal rate;
heuristic interpretation
Types of Tracers
m&
Advantages and Disadvantages of each
∫ fdV
t res = 0
Qf
WE 4-4 Trace metals to calculate
residences times for Boston Harbor
Residence Time in Boston Harbor 3.4 Days
2500
10 Days
Zn
2000
Cu
1500
Cr
2 Days
1000
Ni
500 Pb
Cd
PCB PAH
0
0 Hg 20 40 60 80 100 120 140 160 180
cV
t res = Total Load to Harbor (kg/yr)
m& (Thousands)
∫ cdV M
c t res = 0
=
m& m&
x
c
x
Instantaneous Release; c(x,y,z,t)
monitored over time
Unit mass
m& m* f*
1
1
0 t 0 t 0 t
Rate of injection Mass remaining in system Mass leaving rate
∞
dm *
f * (t ) = −
dt ∫ f * (t )dt = 1
0
Instantaneous release, cont’d
f* is also distribution of residence times (mass leaving no longer
resides). By definition, tres is mean (first temporal moment) of f*
∞ ∞ ∞
dm& ∞
t res = ∫ f *tdt − ∫ tdt = −m * t 0 + ∫ m * (t )dt
0 0
dt 0
N Boston
Inner Harbor
18
ft
18
ft Northern Ave.
Congress St.
Summer St.
18
ft
Gillette
Dorchester Ave.
Broadway Meters
Adams, et al. (1998) Dye 100 0 500
BOS 070
12
10
Total Mass of Dye (Kg)
8 ∞
6
∫ M (t )dt
4
t res = 0
≅ 2.7 day
2 Mo
0
0 20 40 60 80 100 120
TIME (Hours after injection)
tres
Adams, et al. (1998)
Comments
f(t) can be obtained from time rate of
change of M(t); or from measurements
of mass leaving (at mouth)
Residence times for continuous and
instantaneous releases are equivalent
f(t) of f*(t) conveniently used to assess
first order mass loss.
∞
F = ∫ f * (t )e − kt dt F = total fraction of mass that leaves
0
WE 4-6 Residence time of bacteria in CSO
effluent in Fort Point Channel (Adams et al., 1995)
40 1.6
35 1.4
1.2
Residence time distributions f(t)
Mass loss from FPC (%/10hrs)
30
f*(t) 1990 determined from distributions of
1
25
m(t).
20 0.8
0.6
Indicator bacteria “disappear”
15
1
(die or settle) at rates of 0.25
10 0.4
0.25
to 2 d-1
5 0.5 0.2
2
0 What fraction of bacteria would
0 50 100
Time (h)
150 200
disappear for 1990 conditions?
t t V
Instantaneous Instantaneous Continuous
∞ V
∞
=⎡ ⎤ e − kt
M nc M nc
M c ⎢⎣ M c ⎥⎦ o
WE 4-7 Fort Point Channel again
2 R Best-fitted line
Fluorescent pigment
1.8
1.6
particles (yellow DayGlo
1.4 paint) were injected with
1.2
1
dye. Pigment particles
0.8
settle as well as flush.
R
0.6 k3 = 0.25 d-1 R = (Mp/Mpo)/(Md/Mdo)
0.4
k = ksettle = 0.25 d-1
k = ws/h
0.2
ws = kh = (0.25d-1)(6m)
0 20 40 60 80
Time (hr) =1.5 m d-1
More in Chapter 9
Figure by MIT OCW.