hydrogeophysical methods at the test-site nauen ......2 basics and theory of used measurement...
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Hydrogeophysical Methods at the Test-site Nauen -
Evaluation and Optimisation
Jeanette Goldbeck
Diplomarbeit January 2002
Technical University Berlin
Institute of Applied Geosciences
Department of Applied Geophysics
Ackerstraße 71 – 76
13355 Berlin
Content
Abstract 3
Introduction 4
1 The test-site Nauen 5
1.1 Location............................................................................................................................ 5
1.2 Regional geological background...................................................................................... 5
2 Basics and Theory of used measurement methods 6
2.1 DC Geoelectrics ............................................................................................................... 6
2.2 Ground Penetrating Radar (GPR) .................................................................................... 8
2.3 Refraction seismics ........................................................................................................ 10
2.4 Petrophysical properties ................................................................................................. 11
2.5 Nuclear Magnetic Resonance......................................................................................... 14
2.6 Electric conductivity and Archie exponents................................................................... 18
3 Field measurements and results 19
3.1 General information ....................................................................................................... 19
3.2 DC Geoelectrics ............................................................................................................. 19
3.3 Ground Penetrating Radar .............................................................................................. 25
3.4 Refraction seismics ........................................................................................................ 29
3.5 Well logging................................................................................................................... 30
3.6 Induced Polarisation....................................................................................................... 32
3.7 Surface Nuclear Magnetic Resonance (SNMR)............................................................. 33
1
4 Laboratory measurements and results 35
4.1 General information ....................................................................................................... 35
4.2 Grain Size Analysis ........................................................................................................ 35
4.3 Rock density and porosity .............................................................................................. 37
4.4 Specific internal surface ................................................................................................. 37
4.6 Electric conductivity and Archie exponents................................................................... 46
5 Interpretation 50
5.1 Hydrological stratigraphy............................................................................................... 50
5.2 Evaluation and effectiveness of used methods............................................................... 53
6 Conclusion 56
7 Outlook 57
Bibliography 58
Acknowledgements 59
Appendix 60
2
Abstract
3
Abstract
Hydrogeophysical Methods at the Test-site Nauen – Evaluation and Optimisation
Goldbeck, J., 2000, Diplomarbeit, Technical University Berlin
During the last few years a geophysical test-site to the northwest of Berlin was established by
the Department of Applied Geophysics of the Technical University Berlin in cooperation with
the Berlin Office of the Federal Institute for Geosciences and Natural Resources (BGR). Basic
geological and widely known hydrogeological conditions form a good fundament for testing
geophysical techniques.
Extensive measurements, using various geophysical techniques, have been carried out at the
test-site earlier. Within this thesis these were completed by additional surface geophysical
measurements such as 2D geoelectrics, Ground Penetrating Radar and refraction seismics. A
continuously cored and logged 60m borehole is available for purposes of calibration. Detailed
laboratory measurements of core samples took place to complement the field measurements.
Special attention was turned to petrophysical measurements such as determination of density
and porosity, laboratory NMR and determination of geoelectrical parameters through Spectral
Induced Polarisation.
By comparing laboratory specific values to borehole logs and surface geophysical data it was
analysed in what way a characterisation of the subsoil in regard to petrophysical and hydraulic
properties is possible. Furthermore an optimisation of results could be achieved by suitably
combining the various techniques.
Introduction
4
Introduction
For the last few years a site to the northwest of Berlin has been used be by members of this
department to test and evaluate different hydrogeophysical techniques. Based on these
measurements a fundamental geologic and hydrologic stratigraphy could be defined for this
test-site.
During the course of this thesis the following additional surface geophysical measurements
have been carried out to deepen the general geophysical information about the test-site:
Ground Penetrating Radar , 2D DC geoelectrics and refraction seismics. The objective was to
characterise the hydrologic structures above the first aquiclude.
These will be related to earlier results and can be calibrated with newly accessible borehole
data. Further on core samples are available for detailed laboratory investigations. In this
context special importance has been attached to hydrologically relevant petrophysical
parameters such as permeability and porosity which can be determined by laboratory Nuclear
Magnetic Resonance. This is a recent field of research for this department and the
transferability of laboratory parameters to respective field measurements shall be verified.
Additionally electric parameters such as conductivity, Archie parameter and formation factor
can be used to determine rock characteristics.
As a variety of techniques were used to obtain the different parameters, it will be evaluated in
what way they can be utilised to complement each other and the field measurements.
Limitations of these methods, in a hydrogeophysical sense, shall be pointed out and proposals
for optimisation will be made.
A short geographic and regional geologic background on the test-site will be given in
chapter 1. In the following section the basics of used techniques will be illustrated, theoretic
elaborations will nevertheless be restricted to direct applications. Chapters 3 and 4 display the
actual measured data from field and laboratory including a brief description of measurement
sequence and instrument as well as a short evaluation of each individual method. The
combination and evaluation of all results, based on the intention of this thesis, will take place
in chapter 5. Conclusions will be given in chapter 6 and an outlook to possible future projects
will be presented in chapter 7.
1 The test-site Nauen
5
1 The test-site Nauen
1.1 Location
The test-site Nauen is located to the
northwest of Berlin, about 20 km west of
Nauen. Directly to the south of the village
Barnewitz a field path branches off the main
road, reaching the edge of woods after about
300m.
test-site
The site, covering an area of roughly
60000m², consists mainly of an untilled
field surrounded by woods to the south and
east and bordered by the road to the west
and by the field track to the north.
The topography is overall plane, though
there are small unevenness’ and the terrain
rises for approximately 1m in the woods to
the east and south. Fig. 1.1. Map selection from topographic map: region
Barnewitz
1.2 Regional geological background
Due to 3 major ice advances during the last 650000 years, the Brandenburg geology consists
nearly solely of quaternary sediments.
The prequarternary set-up correlates to the eastern branch of the North German depression
including variscan blocks and marginal deposits of the Mesozoic.
Today’s structure and morphology though is predominated be the latest Weichsel Glacial
Period about 16 – 20000 years ago. It left glacial sediments and surface forms with slight
relief.
The region to the west and north of Berlin is subdivided into tabular plates and partially water
filled low grounds, which have been glaziofluvially buried. Valley sands and gravels form the
principal sedimentary structure for those filled morphologic depressions.
The test-site is situated at the southern brink of the Nauen plate. The transition from solid
glacial till in the north of the site to sandy material to the south is recognizable. The valley
sands form an excellent aquifer with a base of glacial till.
2 Basics and Theory of used measurement methods
6
2 Basics and Theory of used measurement methods
2.1 DC Geoelectrics
In DC geoelectrics a direct current is applied to the subsoil and the resulting difference in
potential is measured.
There is a linear relation between generated current density j and electric field intensity E:
Ej ⋅= σ (2.1)
In an isotropic homogeneous medium the conductivity σ is a scalar. The reciprocal of σ is
called resistivity ρ.
With Ohm’s law the electrical resistance R can be calculated from electric current I and
voltage U as:
IUR = (2.2)
Additionally resistance can be determined from a samples’ material properties:
ALR ⋅= ρ (2.3)
where L is the samples’ length and A is the cross-section. Following equation (2.2) and (2.3)
the resistivity ρ can calculated as:
LA
IU
⋅=ρ (2.4)
If the point electrode delivering I is located at the surface of a homogeneous isotropic medium
(ρ=constant) the potential V can be calculated in dependence to distance r of the point
electrode (the return current electrode is at a great distance):
rIV
⋅⋅
=π
ρ2
(2.5)
When the distance between two current electrodes is finite, the potential at any surface point
N will be affected by both electrodes
⋅⋅
⋅=
BNAN rrIPV 112
)(πρ (2.6)
with rAN and rBN being the distances electrode A – point N and electrode B – point N.
When adding a second potential electrode at a point M the difference in potential between N
and M will be (M, N: potential electrodes; A, B: current electrodes)[Telford et al. 1990]:
2 Basics and Theory of used measurement methods
7
+−−
⋅=−==∆
BNANBMAM rrrrINVMVUV 11112
)()(πρ (2.7)
Electrode positions and distances are summarized into the geometry factor k:
+−−=
BNANBMAM rrrrk 1111
21π
(2.8)
So resistivity ρ can be calculated from:
IUk ⋅=ρ (2.9)
Several different electrode arrays or spreads are known in today’s geophysics. Generally the
electrodes don’t have to be arranged in a certain geometry or linear spread (equation (2.7))
though interpretation becomes more and more complicated the more complex the electrode
layout is.
One of the most commonly used electrode arrays is the Wenner-spread where all electrodes
are spaced in line and equidistant. With unit electrode spacing a, equation (2.9) changes into:
IUa ⋅⋅= πρ 2 (2.10)
Fig. 2.1. Scheme of Wenner-section [RES2DINV Manual]
As the medium is not homogeneous under most geophysical conditions the measured apparent
resistivity is an integral value of individual layer or object resistivities. Through inversion and
2 Basics and Theory of used measurement methods
8
modelling during data-processing this apparent resistivity can be counted back to original
resistivities or resistivity distributions.
Two different inversion programs where used to model resistivity data during this thesis:
RES2DINV and RESIX IP2DI.
RES2DINV is a so called “Smooth-Inversion” program based on the smoothness-constrained
least-squares method. The optimisation method basically tries to reduce the difference
between the calculated and measured apparent resistivity values by adjusting the resistivity of
the model blocks. A measure of this difference is given by the root-mean-squared (RMS)
error. However the model with the lowest possible RMS error can sometimes show large and
unrealistic variations in the model resistivity values and might not always be the "best" model
from a geological perspective. The users influence to the inversion routine is minimal which
is the major drawback of that program. On the other hand RES2DINV enables a quick first
overview of the acquired dataset and it’s resistivity distribution.
RESIX IP2DI is block-inversion program based “ridge-regression” which is a variation of
least square inversion. The subsoil is subdivided into discrete cells whose form and
distribution can be influenced directly by the user. This default distribution is used for
forward modelling. As the main difference to RES2DINV the user can now influence the
inversion routine directly by restricting or enabling the different body or layer parameters.
Higher RMS errors from RESIX IP2DI are due to threshold values which are difficult to
model exactly.
2.2 Ground Penetrating Radar (GPR)
GPR or Georadar is an electromagnetic method based on radiation and reception of short
electromagnetic pulses.
Electromagnetic pulses of short wavelengths are emitted in to the subsoil where they are
reflected or dispersed from boundaries or objects underground back to the receiver.
Propagation velocities depend on the dielectric constant ε of the medium, while the resistivity
ρ controls damping and therefore the penetration depth.
Electromagnetic wave propagation is based on the Maxwell equations from which the wave
equations for electric and magnetic fields can be derived as:
Et
Et
E rrr
rrr2
2
0002
δδεεµµ
δδσµµ +=∇ (2.11)
2 Basics and Theory of used measurement methods
9
Ht
Ht
H rrr
rrr2
2
0002
δδεεµµ
δδσµµ +=∇ (2.12)
To solve these equations plane-waves, spreading in z direction, may be used:
)(0
kztieEE +⋅= ωrr (2.13)
k is called complex wave number and can be calculated from:
σωµµωεεµµ 02
002
rrr ik −= (2.14)
or
βα ik −= (2.15)
If eq.(2.13) is solves with this approach, then:
)(0
aztiz eeEE +⋅⋅= ωβrr (2.16)
The result is a damping term (involving β) and a wave propagation term (involving α).
Additionally it can be stated that damping is frequency and resistivity dependent. The later is
the reason for poor resolution in or below high conductivity layers (e.g. aquifers).
From the wave equation and it’s solution, α and β can be derived directly as:
+
+⋅= 11
2
2
0
00ωεε
σεεµµωα
r
rr (2.17)
−
+⋅= 11
2
2
0
00ωεε
σεεµµωβ
r
rr (2.18)
In the so-called radar case, if measuring with high frequencies, conductivity σ is very low
compared to εω. In that case eq. 2.17 and 2.18 can be developed to:
00 εεµµωα rr= (2.19)
0
02 εε
µµσβr
r= (2.20)
For non-magnetic media (µr=1) and ε0µ0=c (velocity of light) phase velocities merge to
propagation velocities:
vcvrr
p ====εεεµα
ω
00
1 (2.21)
2 Basics and Theory of used measurement methods
10
2.3 Refraction seismics
Like most geophysical methods refraction seismics aims for identifying structures and
physical properties of the underground from above ground level. In this case seismic waves
refracted along boundaries are used. Refracted waves traverse the underground primarily
horizontal and are therefore observed farther from the source point then for instance reflected
seismic waves.
Wave propagation is based on Snell’s law:
.sinsin 2
2
1
1 consti
vi
v== (2.22)
This means there is a critical
angle ic where the angle of
emergence will be 90°, so that
the refracted wave will propagate
along the boundary in the lower
layer, where head waves are
generated. Based on the
Huygens’ principle every point
on a wavefront can be regarded
as a new source of waves. These
will superpose to form a new
wavefront arriving at the surface
under the critical angle. At the
crossover-distance the refracted
wave will overtake the direct
ground wave. This can be seen as
a break in traveltime curves. Fig.2.2 Timetravel curves for reflected and refrac ted seismic waves
Seismic velocities can be determined successively from the first arrivals of the seismogram,
the slope is inversely proportional to the traversed layer’s velocity.
2 Basics and Theory of used measurement methods
11
2.4 Petrophysical properties
2.4.1 Density
The quotient of a samples mass m and it’s volume V is defined as the samples density ρ. The
SI-unit of density is kg m-3, but g cm-3 is more commonly used.
Additionally it is necessary to distinguish between different densities that describe the various
aspects of the material [Schön 1996]:
- bulk density: mean density including all components of the analysed sample volume
- individual rock component density: in sandstones e.g. quartz
- mean density of the pore filling (fluid or gas)
- mean density of the solid matrix with out pores.
2.4.2 Porosity and Saturation
For any material the porosity Φ describes the volume fraction of voids, e.g. pores, relative to
the complete sample volume:
sample
poreVV
=Φ (2.23)
To further characterize the pores the saturation S related to the pore fluid is defined as the
ratio of the fluid volume to the pore volume [Schön 1996].
Porosity is especially influenced by grain properties as grain size, sorting and grain shape.
0.2
0.3
0.4
0.5
0.6
0.01 0.1 1 10
medium grain size [mm]
med
ium
por
osity
Fig. 2.3. Medium porosity versus grain size for Nauen samples
2 Basics and Theory of used measurement methods
12
Porosity will increase with increasing degrees of sorting and shows a tendency to decrease
with growing grain size (see figure 2.3.). Different grain shapes change the packing structure
of materials and consequently it’s porosity.
2.4.3 Specific Internal Surface
The specific internal surface forms the interface of pores and matrix. Similar to the
description of density it is advisable to distinguish between different types of specific internal
surfaces, relating the surface area of pores to:
- the total rock volume Stot
- the pore volume Spor
- the volume of the solid matrix Sm
- the mass of the dry rock Sma [Schön 1996]
The SI unit of Stot, Spor and Sm is m2 m-3=m-1. More commonly µm-1 is used. The SI unit of
Sma is m2 g-1.
2.4.4 Permeability
The fluid flow through porous media can be described using the permeability k to characterise
the material and the fluid.
puk
∇⋅−= η (2.24)
with u: volume flow density, η: dynamic viscosity of the fluid, p: fluid pressure
Permeability depends on porosity and pore space geometries. The SI unit is m2=10-12d.
If the streaming fluid is water the hydraulic conductivity coefficient kf can be used instead,
which is defined only for the constant viscosity and density of the medium water. The relation
between permeability k and hydraulic conductivity kf is as follows: 1−⋅⋅⋅= ηρ gkk flf (2.25)
where ρfl is the density of the streaming fluid (rH2O=1 g cm-3), g is the gravity acceleration and
η is the dynamic viscosity of water (η=10.02kg m-1 s-1 (20°C)). Usually it is sufficient to use
the relation that a permeability of 105d corresponds to a kf of 1m s-1.
2 Basics and Theory of used measurement methods
13
Different estimations exist to calculate permabilities or hydraulic conductivities. For this
thesis 4 of them were used:
- from grain size analysis the kf value can be calculated by using Beyer’s equation: 2
10dCk f ⋅= (2.26)
where d10 is the grain size (mm) of 10 percentile from the grain size distribution and
the coefficient C is a function of U=d60/d10 [Hölting 1996]
- the PARIS equation is a modification of the Kozeny-Carman equation [Schön 1996]
and links permeability to specific internal surfaces and formation factors derived from
electrical measurements:
1085.3
1475][porSF
dk⋅
⋅= (2.27)
- to estimate permeability from NMR decay times and porosity the following equation
can be used [Kenyon, 1997]: 42][][ Φ⋅⋅= imsTCmdk i=1,2 (2.28)
The factor C is a rock parameter which is about 4.5 for sediments and sedimentary
rocks.
- instead of porosity in the above equation the formation factor calculated from
electrical measurements can be used if Φ4 is replaced by an approximation of F-2. 22][][ −⋅⋅= FmsTCmdk i i=1,2 (2.29)
2 Basics and Theory of used measurement methods
14
2.5 Nuclear Magnetic Resonance
2.5.1 Basic concept
Magnetic resonance is a phenomenon related to any
magnetic system possessing an angular momentum.
Elementary particles such as protons and neutrons
possess a spin. Spin comes in multiples of ½ and can be
positive or negative. Unpaired protons, neutrons and
electrons all possess a spin of ½. Two or more particles
with spins having opposite signs can pair up to eliminate
the observable manifestations of spin. In nuclear
magnetic resonance, it is unpaired nuclear spins that are
of importance.
A nucleus rotating about it’s spin axis generates a
magnetisation along the same axis. If it is placed in an
external static magnetic field B0 having a different
orientation, the nucleus will precess along the orientation axis of B0 with Lamor frequency ω0.
B0
spinning
proton
Fig. 2.4. Precessing nucleus
00 B⋅= γω (2.30)
γ is the gyromagnetic ratio, characteristic to each isotope. For hydrogen, γ= 42.58 MHz / T.
There are two different energy states the nucleus can align with: a stable, low energy state
parallel to B0 and an instable high energy state antiparallel to B0. The particle can undergo a
transition between the two energy states by the absorption of a photon. A particle in the lower
energy state absorbs a photon and ends up in the upper energy state. The energy of this photon
must exactly match the energy difference between the two states and is related to the
frequency ω0 by Plank's constant (h = 6.626x10-34 J s).
hE ⋅= 0ω (2.31)
2.5.2 Decay times
At equilibrium, the net magnetisation vector lies along the direction of the applied magnetic
field B0 and is called the equilibrium magnetisation M0. In this configuration, the z component
of magnetisation MZ equals M0. MZ is referred to as the longitudinal magnetisation.
It is possible to change the net magnetisation by exposing the nuclear spin system to energy of
a frequency equal to the energy difference between the spin states. The time constant which
2 Basics and Theory of used measurement methods
15
describes how MZ returns to its equilibrium value is called the spin lattice relaxation time
(T1). The equation governing this behaviour as a function of the time t after its displacement
is:
)1( 1/0
Ttz eMM −−= (2.32)
T1 is therefore defined as the time required to change the z component of magnetisation by a
factor of e.
If the net magnetisation is placed in the xy plane it will rotate about the z axis at a frequency
equal to the frequency of the photon which would cause a transition between the two energy
levels of the spin. The time constant which describes the return to equilibrium of the
transverse magnetisation, MXY, is called the spin-spin relaxation time, T2.
2/0
Ttxyxy eMM −⋅= (2.33)
T2 is always less than or equal to T1.
2.5.3 Pulse sequences
Three pulse sequences were uses for this thesis: FID to obtain T2*, CPMG for T2 and
INVREC for T1.
For the FID (Free Induction Decay) pulse sequence, net magnetisation is rotated down into
the xy plane with a 90o radio frequency pulse (RF). The net magnetisation vector begins to
precess about the z axis. After the pulse the relaxation process starts and in the coil producing
the pulse a current is induced due to the precessing moving charges. The received signal is
called FID and it’s amplitude is proportional to the number of protons causing the signal.
Fig. 2.5. Signal versus time for FID sequence Fig. 2.6. Signal versus time for spin-echo pulse sequence
2 Basics and Theory of used measurement methods
16
Another commonly used pulse sequence is the spin-echo pulse sequence (e.g. CPMG). Here a
90o pulse is first applied to the spin system. The 90o degree pulse rotates the magnetisation
down into the xy plane. At some point in time after the 90o pulse, a 180o pulse is applied. This
pulse rotates the magnetisation by 180o about the x axis and causes the magnetisation to
produce a signal called an echo.
An inversion recovery pulse sequence (INVREC) can also be used to record an NMR
spectrum. In this sequence, a 180o pulse is first applied. This rotates the net magnetisation
down to the -z axis. The magnetisation undergoes spin-lattice relaxation and returns toward its
equilibrium position along the +z axis. Before it reaches equilibrium, a 90o pulse is applied
which rotates the longitudinal magnetisation into the xy plane. Once magnetisation is present
in the xy plane it rotates about the z axis and gives a FID. The amplitude of the FID is
correlated to the time difference between the 180° and the 90° pulses.
2.5.4 Petrophysical parameters from NMR relaxation
The amplitude of an NMR signal is proportional to the number of the signal producing
protons. Referring to a calibration sample with known water content, the water content of any
sample can be calculated from:
ncalibratio
onOcalibratiHsampleamplitude
VamplitudeOsampleHV 2
2
⋅= (2.34)
When measured with full saturation and the sample’s volume is known, the sample’s porosity
can be deduced from:
lV
V
tota
por=Φ (2.35)
This porosity is sometimes called NMR or effective porosity. It depends on measurement
resolution especially for very low relaxation times. In laboratory NMR studies capillary water
will be registered and can be distinguished from free / mobile water by characteristic (material
related) cutoff values.
In addition to porosity and internal surface, pore radii can be used to characterise pore
structure. Due to surface relaxation effects water inside pores will relax a lot faster than for
instance water in a test-tube [Kenyon 1997]. The surface / volume ratio of a specific pore is
proportional to the relaxation time constant, small pores will result in faster relaxation thus
lower decay times. The distribution of pore radii can therefore be demonstrated as summation
2 Basics and Theory of used measurement methods
17
of single pore size relaxation constants. These can be displayed as a discrete spectrum, where
the amplitude of each pore (~size) is assigned to it’s respective relaxation time. Nevertheless a
direct conversion of relaxation times to exact pore sizes has not been attempted for this thesis.
Additionally permeability can be estimated from decay times. Various assumptions exist, 2 of
the were used for this thesis. They are discussed in more detail in chapter 2.4.4.
2 Basics and Theory of used measurement methods
18
2.6 Electric conductivity and Archie exponents
Conductivity is a physical property of rocks and sediments and can be explained by 3
individual mechanisms which add linearly:
- matrix or metallic conductivity σm
- electrolytic conductivity σe
- excess or interface conductivity σq.
The matrix conductivity of most minerals except metals is small. Mean values are in the range
of 10-14 to 10-10Sm-1[Knödel 1997]. That means σm can mostly be neglected.
The electrolytic conductivity of saturated rocks is controlled by the electrical conductivity of
the fluid i.e. ion concentration, by the amount of fluid i.e. porosity and saturation and by the
connectivity of the pores i.e. pore structure.
Interface conductivity results mainly from the electric bilayer at the grain boundaries and
includes all conductivity mechanisms that are not matrix or electrolytic dependent [Knödel
1997]. This is a special characteristic of clays or clay containing sediments.
Conductivity of saturated rocks is well described by the empirical equation of Archie:
qwnm SS σσσ ν ⋅+⋅⋅Φ= (2.36)
with: Φ: porosity, S: degree of water saturation (S=Vwater/Vpore), σw: conductivity of the pore
fluid, σq: interface conductivity, n, ν: saturation exponents and m: Archie exponent.
An additional parameter can be derived from Archie’s 1. equation:
σσ w
mF =
Φ=
1 (2.37)
F is the formation resistivity factor and describes the conductivity change related to the pore
fluid as a result of the presence of a non-conductive matrix. [Schön 1996]
3 Field measurements and results
19
3 Field measurements and results
3.1 General information
The geophysical field measurements were carried out during fall 2001. The following
measuring techniques were used: DC geoelectrics, GP radar and refraction seismics. Most
profiles were aligned on the main profile line (MPL) that crosses the test-site from northeast
to southwest with the origin located to the far northeast. The borehole is located on the MPL
as well, just before it enters the woods to the southwest.
To provide more detailed information about the test-site additional earlier measurements will
be considered. These have been carried out by other members of the department before this
thesis: Induced Polarisation measurements and Surface Nuclear Magnetic Resonance.
Furthermore borehole logs are available as well.
field
woods
grassland
Main profile
GP radar
DC geoelectrics
borehole
seismics
IP
SNMR
0-100-200-300
0
-100
-200
-300
Distance [m]
Dis
tanc
e [m
]
IP3
IP2
IP1
B5
B8
B7
B2
B6
Fig. 3.1. Map of field measurements at Nauen
3 Field measurements and results
20
3.2 DC Geoelectrics
3.2.1 Measuring instrument and method
Measuring instrument during the field work in Nauen was a “Campus Tigre” of the University
of Kassel. It is a multi-electrode resistivity equipment for up to 64 electrodes. For controlling
and data recording a laptop was used.
Fig. 3.2. Outline of geoelectric profiles at the test-site
The used electrode array was a Wenner-spread with an electrode spacing of 3.5m
main3 and 5m for main1 and main6. For profile main1 a roll-along method was u
initial section only a part of the electrodes is moved along the profile and the nex
include only those data points not already covered by the first. As the first step o
the main section and all associated roll-alongs are merged into one file which
processed.
The complete inversion results including measured apparent resistivities can be
appendix.
N
(a=5m)(a=5m)
(a=3.5m)
for profile
sed: after the
t section will
f processing
can now be
found at the
3 Field measurements and results
21
3.2.2 Results
Profile main1
Main1 is the longest of the geoelectric profiles and extends nearly completed across the test-
site. It starts about 80m southwest of the borehole (see figure 3.1.) in the woods and has a
length of 314m with a spacing of 5m. main6 borehole
Fig. 3.3. Smooth inversion results main1
The RES2DINV inversion results show a quite homogenous resistivity distributio
Principally a two to three layered underground can be identified.
The first layer from the ground level to about 2m depth is a high resistivity layer wi
apparent resistivities of approximately 1000 to 4000Ωm. This is the vadose zone above th
first aquifer. The extremely high value from the uttermost southwest to –260m are due to th
high contact resistances in the woods. The coupling of the electrodes to the soil was high
difficult in that area, as the ground is covered with about 0.5 to 1m of underwood.
Below that is a seemingly uniform layer of about 100 to 250Ωm where the resistivity is n
varying much. This can be identified as the first aquifer.
From other measurements, geologic background and borehole measurements it is known th
the first aquiclude, consisting of mainly of silts, should follow the aquifer at a depth of abo
20m near the borehole. Another drop in resistivity can be seen in the lowest levels though th
data basis is to thin to assume a third layer from these measurement alone.
With this background information as a starting model an inversion using RESIX IP2DI w
attempted. During this inversion different parameters were fixed or released in alternation
gain a geological reasonable result. First all parameters were unlocked to get a gener
overview of the resistivity range and the layer distribution. Then the individual resistiviti
were fixed so the error balancing was achieved only through adjusting the position of th
layers.
NE
SWn.
th
e
e
ly
ot
at
ut
e
as
to
al
es
e
3 Field measurements and results
22
As a result the resistivities were set to 3500 Ωm for the weathered zone and 300 Ωm for the
aquifer. The seeming drop of the groundwater table in the woods to the southwest is explained
by a rise in topography of about 1 to 1.5m which was not considered during inversion.
distance [m]
0
20
10
dept
h [m
]
3500 mΩ
SW NE
300 mΩ
90 mΩ
borehole main6
Fig. 3.4.Block inversion model main1, RMS error 24 %
Below 20m again the aquiclude is modelled, though as in the RES2DINV model the data is
stretched quite thin in the lowest levels and the dataset contains no information about the
lower boundary areas.
Profile main3
Main3 is the shortest profile located at the northeast end of the test site (see figure 3.1). The
complete length was 171m with a spacing of 3.5m. The reason for this special spread was the
preliminary geologic information about this area, so a better resolution was wanted for.
SW NE
Fig. 3.5. Smooth inversion results main3
The change from main1 is quite obvious. Although the topmost layer seems identical to the
weathered zone of main1 in resistivity and depth, below that an identification is not so simple.
There seems to be a very low resistivity layer coming from the northeast, which appears to
drop in the middle of the profile and then rises again at the end. The RMS value for this
3 Field measurements and results
23
model is quite low nevertheless it doesn’t seem very reasonable. From the measured data
(figure 3.6) the rise to the southwest is not evident.
SW NE
Fig. 3.6. Apparent resistivity section main3
There it rather seems like the low resistivity layer has an outcrop to the northeast which is
coherent with the already mentioned preliminary information. So the effects to the southwest
are probably artefacts from the inversion process of RES2DINV.
The resistivities from the inversion match the ones from profile main1.
Based on the resistivity values from for the main1-model a block-model was calculated for
main3. As the to profiles lap for about 100m the resistivities should be the same.
distance [m]
3500 mΩ
300 mΩ
90 mΩ
0
20
10
dept
h [m
]
SW NEmain6
Fig. 3.7. Block inversion model main3, RMS error 22 %
The outcrop now is quite obvious, the resistivities match those in main1. It is not explicit from
this model if the outcrop comes though the weathered zone, there are not enough data points
at the far sides. The resistivity of 90Ωm corresponds to the implied aquiclude / silt layer in
main1 but this time it can be modelled quite well even at the lowest level to the southwest.
The lapping area of both models matches perfectly.
Profile main6
Main6 is a cross-profile to main1 and main6 (see figure 3.1). The spacing was 5m, full profile
length is 245m. Main6 crosses the MPL at a length of –100m.
3 Field measurements and results
24
he RES2DINV section of that profile resembles main1 a lot though it is not as undisturbed.
The RESIX IP2DI model was rather difficult to obtain and took longer than both of the other
NW SE
Fig. 3.8. Smooth inversion results main6
T
Especially along the edges the data seems to be a bit unsettled which was obvious during the
field work already, where it resulted in number of necessary repeated measurements. The
measured resistivities again match those of the other profiles with 1000-6000Ωm for the dry
cover and about 50-150Ωm for the lower aquifer. From the RES2DINV model it is possible to
assume that there is another outcrop or at least upward arching of the silt layer. This can be
observed from the measured apparent resistivity section also. distamain1 / main3
0
20
10
dept
h [m
]
3500 mΩ
350 mΩ
70 mΩ
Fig. 3.9. Block inversion model main6, RMS error 28 %
NWnce [m]
SE
models, probably due to the higher noise level in this section. Most of the calculated models
were not reasonable or simply geological nonsense, additionally the resistivity difference
from aquifer to aquiclude could not be modelled without accepting high RMS errors. Figure
3.9 was the only reasonable model for the given conditions, although the resistivities don’t
match to well and the RMS error is above 25 %.
3 Field measurements and results
3.3 Ground Penetrating Radar
3.3.1 Measuring instrument and method
For radar field measurements a RAMAC / GPR instrument of MALA Geoscience was used.
The instrument consists of a processing unit, a receiver and a transmitter antenna and a laptop
for data handling and storing.
For profile measurements the antennas
are arranged at a constant offset. By
moving slowly along the profile
individual traces for each location are
recorded, which can be displayed as
radargrams. They present two-way
traveltimes depending on the location
along the line.
T T T TR R R R
tProfilfortschritprofile line
Fig. 3.10. Scheme of travel-ways for radar profile
To determine propagation velocities the common midpoint (CMP) method is used: receiver
and transmitter are moved apart from a mutual midpoint thus constantly increasing
traveltimes of the transmitted wave in
ε1
ε2
Fig. 3.11. CMP
The main prof
woods to the
0.1m. Due to
restarted from
disturbance of
the same datu
both CMPs a
processed and
For processin
processing flo
were applied.
at balancing t
R
layout
ile was again laid out a
southwest. Antenna f
problems with the equ
this location at a late
layers at this point, w
m point 25m to the no
ppear to be equal in
will be presented here
g and presentation th
w was applied: the fil
The last “technical” co
echnical features of th
T
25
the medium. Velocities for each layer
can be determined based on reflection
curves.
long the MPL (see figure 3.1.), starting about 30m in the
requency was 200MHz and traces were recorded every
ipment the profile had to be interrupted at –100m, it was
r time and both files were merged. The result is a slight
hich will not be interpreted. Two CMPs were realised for
rtheast of the borehole along the MPL. As the results for
data range and content, only one of them was further
.
e program REFLEX was used. The following general
es were start-time corrected, then declipping and dewow
rrection was to subtract the DC shift. These 4 steps aim
e instrument. After this a frequency filter was applied to
3 Field measurements and results
26
suppress unwanted frequency bands. The last processing step was a gain function. To improve
data quality a background removal was attempted, but this proved to be non effective.
Fig. 3.12. Radar CMP measurement Nauen
3.3.1 Results
First the CMP shall be discussed (figure 3.12).
The dent in the direct ground and the air wave is due to irregular movement (trace increment)
during the measurement. Nevertheless the velocities can be adapted to the front part (0 to
20m) of the CMP. Below 200ns the reflections from trees of the nearby wood is very
noticeable. 4 decreasing velocities were adapted, though in my opinion only the first is an
actual boundary, that is the ground water table. All other modelled boundaries rather appear to
“mirror” each other: all modelled layers have the same thickness and velocity difference.
They are in my opinion due to multiples of the ground water table. Overall velocities seem
too low. In my opinion this CMP is rather featureless, maybe because of the wet conditions on
that day. The modelled velocities were not used for depth adjustment of the main profile.
The main radar profile line is displayed in figure 3.13..
The most prominent feature is obviously the descending reflector to the right of the
radargram. For the first about 200ns the descent is quite steep, after that the slope is more
flattened with little depressions along the line. This reflector is interpreted as the outcropping
glacial till.
Apart from this reflector the appearance below the groundwater-table (20ns) is homogeneous,
the layers are horizontally bedded. At about 180ns a “layer” appears to have rather stronger
3 Field measurements and results
27
echoes than the upper horizons. It can be traced along the complete line up to the outcropping
till. From the stratigraphic profile at the borehole (-265m) a gravel layer is known from the
depth of about 12 to 14 m. The transition from overlaying fine sands into the gravel should
produce a rather strong reflector, due to the change in material consistency. That this will not
be as smooth a layer as e.g. the till’s upper boundary is obvious.
To the left of the profile (-270 to –230m) a kind of lineament with a ~45° angle appears. As
the profile run into the woods at –268m to the southwest, these can be interpreted as
reflections from the trees.
For time-depth conversion a medium velocity of 0.15m/ns was used. This value was chosen to
adjust the groundwater table to a depth of about 1.5 to 2m.
3 Field measurements and results
28
Fig. 3.13. Radargram for the MPL Nauen
3 Field measurements and results
29
3.4 Refraction seismics
3.4.1 Measurement instrument and method
For seismic measurements a 12 channel Bison instrument was used. Geophone spacing was
2m along the Main Profile Line. Shots were arranged every 12m, the first shotpoint was set
1m in front of the first geophone. The used source was an accelerated weight drop mounted
on a trailer.
Resulting files were first merged into shot-point-based files, then evaluated and presented
with REFLEX.
3.4.2 Results
Although the measured data appeared to be of good quality during the field day, it wasn’t
possible to evaluate the time-travel curves (they will therefore not be displayed here).
From preliminary information it is known that the velocity of the weathered layer is very low,
with about 150 to 500m/s sometimes even lower than sound velocity. That’s why the
accelerated weight drop was used as a source, to get a distinct signal and improve the signal-
noise ratio. This proved to be unsuccessful, rather the noise seems to have been increased
even more. A velocity analysis was not possible, because shot and reverse shot travel-times
could not be balanced.
From the different seismograms (example figure 3.14.) little information could be gained: as
already known velocities of the first layer (weathered zone) vary between 200 to 450 m/s. For
the second layer velocities of 1000 to 3000m/s can be presumed.
Fig. 3.14. Example seismogram for shot point 191 / Nauen
3 Field measurements and results
30
3.5 Well logging
3.5.1 General information
In January 2001 a 60m bore hole was drilled by an external company at the end of the Main
Profile Line (see figure 3.1). A few days after drilling extensive borehole logs where
recorded, thereafter the well was supported and additional control logs were measured (see
[Richter, 2000]).
The following logging techniques were used:
- Gamma-Ray-Log (before and after support)
- GG-Log (Dual Spacing) (before and after support)
- NN-Log (Dual Spacing) (before and after support)
- FEL (before support)
- Short / Long Normal (Resistivity) (before support)
- Caliber (before support)
- Sal-Temp-Log (before and after support)
- Microlog2 (after support)
- Microcaliber (after support)
Some of those logs will be discussed in detail, all of them are displayed at the appendix.
3.5.2 Resistivity Logs
Normal logs are used for resistivity logging, the configuration being similar to those in
surface resistivity methods (dipole-dipole-configuration). For a short normal log (sondes 16
inch apart) the measured apparent resistivity depends mainly on the beds close to the hole
wall and are influences by the mud in the borehole and penetration of drilling fluid into the
formation. The long normal (sondes 64 inch apart) measures intermediate resistivities,
containing information about the invaded zone resistivities and true formation resistivities.
The third used electric log is a focused current log (FEL). A sharply focused current is used to
measure resistivity with a resolution of few centimetres. The depth of penetration is very
shallow, the device is used to measure the resistivity of the flushed zone.
The normal logs are quite inconspicuous, dropping to a level of about 150 to 200Ωm for long
and 80 to 100Ωm for short below the first aquifer. The only major feature is in my opinion the
3 Field measurements and results
31
rise in resistivity for the short normal at about 20m. This can be probably attributed to the
change in formation from sands to silts. This anomaly is not very prominent though, as it is
covered by the influence of the drilling fluid and mud.
The resistivity distribution for the FEL log is more distinct, with a few noticeable maxima and
jumps. The sand-silt transition at the bottom of the upper aquifer is 2m early and overall the
distribution seems a little erratic.
3.5.3 Gamma Ray Logs
For sediments γ logs reflect mainly shale content as natural radioactive elements tend to
concentrate in clays and shales. γ ray logs are calibrated in API units, shales having average
values of 100API. γ ray logs are used quantitatively to estimate shale / clay content.
Gamma-gamma logs are known as density logs and may be used to determine porosity if
matrix and formation fluid density are known. The detected γ ray intensity is an exponential
function of rock density, with a maximum depth of investigation of about 15cm. [Telford]
The measured gamma ray log shows, as was expected, strong reactions to the different layers
with high clay content. Additionally it displays a maximum for 12-14m which was
interpreted, by the driller, as a mica containing level. From the stratigraphic profile this can
not be verified. Rather it contains a higher fraction of fine material additional to the gravel
fraction, thus also explaining the observed higher bulk
densities. GWT
aquifer
aquiclude
aquifer
aquiclude
aquifer
The resolution of even smallest layers of silt is very good, in
particular notable for the about 1m thick coarse silt layer at 8
– 9m or the small interbedding of silt at 42.5m.
3.5.4 Main stratigraphy from logging
Based on the borehole logs a basic, overall hydrological
stratigraphy was obtained as follows:
- 0 - 21m: aquifer
- 21 – 31m: aquiclude
- 31 – 39m: semi-permeable aquifer
- 39 – 47m: aquiclude
- 47 – 60m: aquifer Fig. 3.15. Hydrological stratigraphy
for borehole Nauen
3 Field measurements and results
32
3.6 Induced Polarisation
During an earlier thesis [Hertrich, 2000]
extended IP measurements were conducted for
3 different locations on and near the test-site.
The first is located in the field to the northeast
of the actual site thus measured results should
be mainly influenced by the solid glacial till.
The second point is right on the field track in
the transition area from till to fluvial sands
and the third is situated farther inside the
measurement field (see figure 3.1).
Figure 3.16. displays inversion results for
resistivity and phase. The complete dataset
can be found at the appendix.
At the southernmost location IP1 the expected
3 layered case can be observed: to a depth of
2m resistivities are very high (~3000Ωm)
which resembles DC geoelectric results
(chapter 3.2) from this campaign, clearly
identifiable a the vadose zone. Below that, to a
depth of about 8m, follows a 300Ωm layer.
Subsequently a very low resistivity layer
(~100Ωm) was modelled. The phase
adjustment is rather poor for this assumed
case, though the general trend matches the
data. The second layer can be identified as the
aquifer followed by the glacial till.
IP3 is located to outside of the actual test-site and is o
Resistivities are below 100Ωm, but surprisingly a segm
a depth of ~6m another drop in resistivity occurs.
Fig. 3.16. IP models for resistivty (left) and
phase (right) / Nauen
verall implicat
entation is vis
The reason fo
IP3
IP2
IP1
ed with undisturbed till.
ible. Near the surface to
r his distribution is not
3 Field measurements and results
33
completely clear. It was assumed, that this implied layer is generated by 3 dimensional
influences due to the large spread. I find this rather hard to accept.
For the upper layers the electrode spread is small thus reducing effects from 3D influences.
The measurement location is about 50m remote of any anticipated changes in stratigraphy and
should therefore display the natural habit of the subsoil to a depth of at least 20m. For lower
depths the model concurs with the properties of the till in the test-site itself and if
discrepancies should appear due to 3D effects I would expect them in those levels.
It is difficult to explain the lower resistivities. The phases match my expectations for loosened
ground due to cultivation. From comparison to laboratory measurement it is known that
phases tend to rise with decreasing consolidation. A depth of 6m may be a bit low but isn’t
totally out of range. Loosening due to constant cultivation may well reach a few meters.
At the middle location IP2 influences of the northern exposed till and of the fluvial sediments
mix. The result is an implied 3 layer case with abrupt resistivity changes for the first 3m.
Below that again the undisturbed till is displayed with resistivities of ~100Ωm and phases of –
0.2 degrees.
3.7 Surface Nuclear Magnetic Resonance (SNMR)
5 SNMR soundings have been conducted along a secondary profile during an earlier
measuring campaign [Hertrich, 2000]. They were arranged linearly with a spacing of 25m
(see figure 3.1).
Similarly to the measurement principle for laboratory NMR an external alternating field with
the Lamor frequency is generated. For surface applications this is realised with an antenna
loop on the ground which, after turning of the external field, will measure the relaxation
signal as well. Again the initial amplitude correlates to the number of excited protons i.e. the
water content and decay times relate to mean pore sizes. Measured ambient noise is used to
examine signal quality and the phase shift between incitement and measured signal contains
information about subsurface electrical conductivity [Hertrich]. In SNMR, contrary to
laboratory NMR, irreducible water will not be detected due to measurement restriction in
early response times. Water content will therefore include only mobile water.
Figure 3.17. displays the water content (from amplitude) and decay times for all 5 locations.
Complete datasets can be found at the appendix.
3 Field measurements and results
34
60
50
40
30
20
10
00 10 20 30 40
de
pth
[m]
watercontent [%]
60
50
40
30
20
10
00 100 200 300 400
de
pth
[m]
decaytime[ms]
60
50
40
30
20
10
00 10 20 30 40
de
pth
[m]
watercontent [%]
60
50
40
30
20
10
00 100 200 300 400
de
pth
[m]
decaytime[ms]
60
50
40
30
20
10
00 10 20 30 40
de
pth
[m]
watercontent [%]
60
50
40
30
20
10
00 100 200 300 400
de
pth
[m]
decaytime[ms]
60
50
40
30
20
10
00 10 20 30 40
de
pth
[m]
watercontent [%]
60
50
40
30
20
10
00 100 200 300 400
de
pth
[m]
decaytime[ms]
60
50
40
30
20
10
00 10 20 30 4
de
pth
[m]
watercontent [%]
60
50
40
30
20
10
00 100 200 300 400
de
pth
[m]
decaytime[ms]
S N
0
B5 B8 B2 B7 B6
Fig. 3.17. Results of SNMR for 5 locations at the test-site Nauen
Inversions show a clear separation of vadose and saturated zone for the upper aquifer for all
soundings. Though the vertical resolution is insufficient the till interface for B8 and B7 can
probably be expected at 15m depth, recognisable from the drop in “free” water content. In
depths below 30m, water volume increases again pointing to the second aquifer. A more
specific segmentation based on water content below that level is not possible because the
vertical resolution is not high enough. From decay times more information can be gained. For
B8 and B7 decay times drop from about 300ms to 100ms in a depth of about 10 to 15m. This
is probably due to the stratigraphic change from medium sands to finer material including silt.
Below the till layer, which at this location should be situated in 10-15m depth, decay times
first rise and then decrease again, pointing to first a sandier (15-30m) and then finer facies
(below 30m). The low free water content is coherent with information from drilling, where a
low-permeable layer is presumed. Below 30m the vertical resolution for water content is to
low to gain additional information.
Inversions show a clear separation of vadose and saturated zone for the upper aquifer for all
soundings. Though the vertical resolution is insufficient the till interface for B8 and B7 can
probably be expected at 15m depth, recognisable from the drop in “free” water content. In
depths below 30m, water volume increases again pointing to the second aquifer. A more
specific segmentation based on water content below that level is not possible because the
vertical resolution is not high enough. From decay times more information can be gained. For
B8 and B7 decay times drop from about 300ms to 100ms in a depth of about 10 to 15m. This
is probably due to the stratigraphic change from medium sands to finer material including silt.
Below the till layer, which at this location should be situated in 10-15m depth, decay times
first rise and then decrease again, pointing to first a sandier (15-30m) and then finer facies
(below 30m). The low free water content is coherent with information from drilling, where a
low-permeable layer is presumed. Below 30m the vertical resolution for water content is to
low to gain additional information.
B6 and B5 are difficult to interpret as the data contradicts the expected structural information.
With the glacial tilt exposed here, low water content would be expected. Actually it is only
low for shallow depth and then rapidly increases to about 30%. This is probably due to the
large sphere of influence for the loop, so that the 3D effect is significant and the high values
are supposed to be caused by the aquifer beside.
B6 and B5 are difficult to interpret as the data contradicts the expected structural information.
With the glacial tilt exposed here, low water content would be expected. Actually it is only
low for shallow depth and then rapidly increases to about 30%. This is probably due to the
large sphere of influence for the loop, so that the 3D effect is significant and the high values
are supposed to be caused by the aquifer beside.
4 Laboratory measurements and results
35
4 Laboratory measurements and results
Depth [m] Facies Sample Name0.7 medium sand B1_011.7 medium sand B1_022.7 medium sand B1_033.7 medium sand B1_04
4.75 fine sand B1_055.6 medium sand B1_066.7 medium sand B1_077.7 fine sand B1_08
8.75 interbed. Fs / Gu B1_099.6 fine sand B1_10
10.7 fine sand B1_1111.7 medium sand B1_1212.7 fine gravel B1_1313.7 fine gravel B1_1414.7 medium sand B1_1515.7 fine sand B1_1616.7 fine sand B1_1717.7 fine sand B1_1818.6 fine sand B1_1919.7 fine sand B1_2020.7 fine sand B1_21
21.45 medium sand B1_2226.2 coarse silt B1_23
31.23 medium sand B1_2436.3 fine sand B1_25
41.45 interbed. Fs / Gu B1_2647.35 medium sand B1_2756.3 fine sand B1_28
Fig. 4.1. Core segment photos
for segment 13 to 14m (left) and
segment 17 to 18m (right)
18m
17
m
14m
13
m
4.1 General information
During the well-logging a continuous drill core was
gained for the 60m-borehole on the test-site. The
individual 1m core segments were photographed to
preserve the in-situ facial character of the layers. Two
examples are displayed in figure 4.1.
For a detailed geological analysis a stratigraphic profile
was compiled by Mr. Jorzig of the Geological Survey
Berlin / Brandenburg. The complete profile can be found
at the appendix.
To gain a better overview the stratigraphic profile was
translated into medium grain sizes for each layer, which
was then displayed versus depth (figure 4.2.).
For all following laboratory analysis’ 28 samples were
taken throughout the core. Table 4.1. presents those
samples with depth and stratigraphical units.
The following laboratory measurements were used and
are described in detail during the next subchapters: grain
size analysis, rock density analysis, determination of
internal surface, laboratory NMR and Spectral Induced
Polarization for the determination of geoelectrical
parameters.
4.2 Grain Size Analysis
The first step for the petrophysical analysis was a grain
size analysis for the individual samples. By that a
classification for the samples can be received which not
only includes grain size distributions but also the
reference values for hydrologic conductivities.
The distribution curves and sum curves for the individual
samples are displayed in the appendix. Table 4.1. Laboratory sample list
4 Laboratory measurements and results
Fig. 4.2. Stratigraphic profile (grain sizes) versus depth after Jorzig, GeologicalSurvey Berlin/Brandenburg (2001)
36
4 Laboratory measurements and results
37
4.3 Rock density and porosity
4.3.1 Measuring instrument and method
The matrix density of the different core samples was analysed with a “micromeritics”
Pycnometer ‘AccuPyc 1330’. The pycnometer determines the volume of a specific sample by
measuring the pressure change of helium in a calibrated volume. From volume density can be
derived directly if the sample weight has been entered. Multiple measurement were carried
out to determine a medium density for each sample.
Additionally the pycnometer measurements allow an estimation of sample porosity by
determining the actual sample volume before pycnometer analysis which then is compared to
the measured matrix volume.
4.3.2 Results
As the measured samples consist mainly of sands and silts the expected grain densities were
in the range of 2.65 to 2.75 g/cm3.
These values were confirmed with a minimum value of 2.67 g/cm3 and the maximum being
2.74 g/cm3. The scattering probably results from temperature differences while measuring
different samples. A calibration for the instrument seems necessary for more extreme
temperature ranges.
Individual sample porosities were also determined from pycnometer analysis. As the material
consists of unconsolidated sediments there can be no exact porosity rather only a plausible
range. The obtained values should be compared to the NMR and log measurements.
Porosities from pycnometer analysis range from a minimum of about 30% for sandy gravel to
nearly 50% for sandy silts.
The exact values for density and porosity can be found at the appendix.
4.4 Specific internal surface
4.4.1 Measuring instrument and method
The specific internal surface in relation to the mass of the dry rock Sma was measured with a
“micromeritics” ‘Gemini 2360 Surface Area Analyser’. It’s primary function is to determine
the surface area of solid samples by measuring the differential pressure between a balanced
4 Laboratory measurements and results
38
tube and a tube containing the sample. As the sample adsorbs the analysis gas the pressure
will drop in the sample tube. By maintaining a constant pressure of gas over the sample and
varying the rate of analysis gas, the rate at which the sample can adsorb the gas can be
determined.
The dry rock specific internal surface
was then calibrated with the
measured matrix density and the
porosity to gain the more commonly
used solid matrix specific internal
surface Sm and the pore specific
internal surface Spor.
4.4.2 Results
Values of internal surfaces can vary
over a wide range of magnitudes and
are directly dependent of
measurement resolution. With higher
resolution the absolute value will
increase, so the gained values can
only be an orientation and should be
used carefully. In general decreasing
grain sizes result in increasing
internal surfaces, which was
confirmed during the measurement
though the exact values seem a bit
low, especially for the sandy silts
(25m–end) were I expected more extreme values. On the other hand the internal surfaces of
the gravel samples (12-14m) are about as high as values for the sands, so the fine grained
fraction seems to balance out the expected low values. Overall the trends for all samples seem
right but the error range for the exact values is assumed to be 30% (due to resolution limits of
the instrument for small surfaces).
0
5
10
15
20
25
0 5 10 15 20
specific internal surface
dept
h [m
]
25
30
35
40
45
50
55
600 5 10 15 20
Sma [m²/g] Sm [1/µm] Spor [1/µm]
Fig. 4.3. Specific internal surface for Nauen samples
4 Laboratory measurements and results
39
4.5 Laboratory NMR
4.5.1 Measurement instrument and method
For all laboratory NMR measurements a Maran2 of Resonance Instruments was used. The
magnetic flux density of the integrated permanent magnet is 0.047T, which corresponds to a
Lamor frequency of 2MHz for protons.
Before starting a measurement cycle a
ll samples were measured in full saturation. To eliminate effects due to ferromagnetic ions
amplitudes and relaxation times
needed. To
4.5.2 Results
careful selection of sequence
parameters is necessary. To receive
comparable results for all samples,
most of the parameters need to be
fixed for a complete sequence. For a
more detailed account on measurement
parameters and necessary adjustments
see [Krüger].
Fig.4.4. NMR instrument Maran2 (Resonance Instruments)
A
of any kind desalted samples were used. Additionally an individual porosity was determined
for each NMR sample to be compared to the measurements.
Two different pulse sequences were used to determine NMR
(see chapter 2.5.3): INVREC for T1 and CPMG, which is a spin-echo pulse sequence, for T2.
At first an FID sequence for measuring T2* was used as well. But the results proved to be
quite unstable, even during a sequence, so I decided to concentrate on T1 and T2.
For determining porosities from maximum amplitudes a calibration sample is
reduce relaxation times for the calibration sample it was mixed with copper sulphate, which is
paramagnetic. Relaxation acceleration will be dependent of the solution’s concentration.
Porosities from amplitudes
ces maximal amplitudes were determined by averaging over the From the two pulse sequen
first 3 measurement points. Based on equations 2.34 and 2.35 those amplitudes were then
converted into sample’s water content and later into NMR porosities. These were compared to
4 Laboratory measurements and results
40
individual and medium porosities. The latter is an average value from all porosity
determinations (except NMR) for the sample material. Results are displayed in figure 4.5.
Measured porosities range from
NMR porosities
compared to medium
consolidated sediments.
ibutions. Generally a cut-off time
20% for the gravel layer (12-
14m), about 30–40% for
medium to fine sands and
nearly 50% for the silty beds.
The match for NMR porosities
to individual sample porosities
is very good.
As expected
tend to be slightly lower then
porosities determined for
individual samples.
Nevertheless the effect is
minimal. Due to the resolution
of the instrument even
irreducible water can be
resolved, one of the main
differences to SNMR, where
main effects result from “free”
water.
When
porosities large differences can
occur. This once again verifies
the importance of specifying
individual sample porosities for un
Irreducible water can be estimated from relaxation time distr
0
5
10
15
20
25
0 0.2 0.4 0.6
porosity
dept
h [m
]
25
30
35
40
45
50
55
600 0.2 0.4 0.6
T1 porosity T2 porosityindiv. porosity med. porosity
Fig. 4.5. Porosities from NMR relaxation amplitudes
of 33ms is assumed, relaxation times faster then that are attributed to adhesive water. A more
detailed description will be delivered by means of examples in the next subchapter.
4 Laboratory measurements and results
41
Pore size distributions from relaxation
As seen in chapter 2.5.4, assumptions can be made about pore size distributions from decay
times. There is a direct relation from grain sizes to pore sizes (see Figure 4.6.). Though there
is no direct conversion, estimations are possible from comparison of different samples.
sand), B1_14 (fine gravel), B1_23 (coarse silt) in relation to grain size distributions.
Figure 4.7. shows the grain size distribution and T2 spectrum for sample B1_06, which is a
very good sorted medium sand. Despite the good sorting the T2 spectrum is not simple, that is
containing only one absolute maximum. Rather it shows 3 partial maxima with the latest at
B1_06 T2 distribution
0
20
40
60
80
100
120
1.E+00 1.E+01 1.E+02 1.E+03 1.E+04 1.E+05 1.E+06 1.E+07tim e [µs]
B1_06 (5.6 m)
0
20
40
60
80
100
0.01 0.1 1 10
grain size [m m ]
Fig. 4.7. Grain size distribution (left) and T2 spectrum (right) for sample B1_06
T1 and T2 spectra for all samples can be found at the appendix. As it would be to extensive to
explain every result in detail, evaluation will be explained for 3 samples: B1_06 (medium
0.010.01 0.1 1 10
medium grain size [mm]
T1 T2
Fig. 4.6. Medium grain sizes versus decay times for Nauen samples
0.1
1
deca
y tim
e [s
]
4 Laboratory measurements and results
432ms (85%) being the overall maximum and the lesser two at 0.3ms (5.7%) and 2.5ms
(9.3%) being about equal. This can be related to effects of packing which obviously results in
To estimate irreducible water any relaxation time amplitudes below the cut-off of 33ms have
to be considered. For B1_06 this would result in an irreducible water saturation of ca. 15%.
7%
about
small
maxim
B1_0
Again
That
usual
“usua
a very low percentage of very small pore radii throughout the sample. This effect is often
observed when good sorting i.e. narrow grain size distributions are involved (see [Krüger]
results for synthetic samples).
B1_14 (13.7 m)
0
20
40
60
80
100
0.01 0.1 1 10
grain size [mm]
mas
s %
B1_14 T2 distribution
01020304050607080
1.E+00 1.E+01 1.E+02 1.E+03 1.E+04 1.E+05 1.E+06 1.E+07time [µs]
re. a
mpl
itude
4
The n
From
for th
6
notice
Fig. 4.8. Grain size distribution (left) and T2 spectrum (right) for sample B1_1
42
es about
of the samples pores and due to the larger grains the pore diameters are wider, as
80ms (22.5%) and at 2ms (9.9%). The later one is very broad, probably including 2
er maxima at about 1 and 4ms. The two (or three, depending on fitting parameters) local
a nevertheless contain a greater percentage of pores than i.e. the smaller ones of
6.
a cut-off value of 33ms is applied to display adhesive water, resulting in about 33%.
means, one third of the pore fluid is immobile. So even if the hydraulic conductivity is
ly higher for gravels, in this special case kf will probably be rather low compared to
l” gravel layers.
ext example displays the grain size and T2 distribution of B1_14, a fine gravel sample.
the grain size distribution the poor sorting is obvious, the curve has two maxima: one
e gravel size and another one for fine sands. The T2 maximum at 742ms includ
able from the higher values of T2 compared to B1_06. There are 2 more maxima: at
4 Laboratory measurements and results
43
The third example is B1_23, a coarse silt sample. The grain sizes are very small, though
60
80
100
B1_23 T2 distribution
120
inside the silty band quite broad. The small dent at 0.045mm might be due to the conversion
from sieving to hydrometer analysis. In this case the T2 relaxation spectrum
straightforward: there is only one maximum at 19ms which of course is very low compared to
B1_06 and B1_14.
40
grain size [m m ] 0
1.E+00 1.E+01 1.E+02 1.E+03 1.E+04 1.E+05 1.E+06 1.E+07tim e [µs]
Fig. 4.9. Grain size distribution (left) and T2 spectrum (right) for sample B1_23
B1_23 (26.2 m)
80
100
0
20
0.01 0.1 1 10 20
40
60
is
If an irreducible water cut-off of 33ms is assumed, B1_23 contains little to no mobile water.
This result was expected as the sample comes from the impermeable bed below the first
aquifer.
For all samples T spectra were determined as well. Although the exact values vary from T
the general distributions compared by sample are about the same. Differences in distribution
(additional or lost peaks) result in my opinion from the algorithm of the fitting program. One
of the main parameters of the program RI WinDXP is the “weight” parameter, which is
difficult to stabilize. I found that especially for T spectra this parameter was hard to maintain
for the complete sequence, resulting in artefacts or lost data. An example for this behaviour is
displayed in figure 4.10, where distribution spectra are compared for sample B1_19 (fine
sand).
1 2
1
B1_19 T1 distribution
50
150
200
0
100
1.E+00 1.E+01 1.E+02 1.E+03 1.E+04 1.E+05 1.E+06 1.E+07
tim e [µs]
B1_19 T2 distribution
150
200
0
50
100
1.E+00 1.E+01 1.E+02 1.E+03 1.E+04 1.E+05 1.E+06 1.E+07
tim e [µs]
Fig. 4.10. T1 (left) and T2 (right) distributions for B1_19
4 Laboratory measurements and results
44
The overall maxima are about the same with 329ms for T1 and 296ms for T2. Nevertheless the
The second non-NMR-related permeability can be estimated from the PARIS equation (eq.
2.27). The values base on formation factors F from laboratory geoelectric measurements (see
chapter 4.6) and specific internal surfaces. The later has major relevance for the result as it is
highly error afflicted
T2 distribution is in my opinion more significant as it wasn’t possible to separate the smaller
maximum from the large without producing a main artefact below 0.1ms for T1.
Permeabilities from decay times
As mentioned in chapter 2.4.4 four different estimations for permeability were used.
From grain size analysis hydrologic conductivities will be calculated from the equation of
Beyer cted method, these
values will be used as reference.
.
s, the second again on formation factors. Additionally this will be a good error
stimation for the laboratory geoelectric measurements because even though the 2 parameters
) are most exemplary for those stratigraphic regions. I was a bit puzzled about the
intermediate region of about 30 to 40m. Stratigraphically this area consist of medium and fine
sands (samples B1_24 (31.2m) and B1_25 (36.3m)), so at least for B1_24 I expected a higher
permeability. But obviously the fine grained ratio is sufficient to lower k to nearly silty levels.
Below the interbedding region the material turns again to medium and fine sands (samples
B1_27 (47.35m) and B1_28 (56.3m)). This time permeability rises as well, resulting in values
equal to the upper aquifer.
(eq. 2.26). As this was the most basic and therefore least error affli
Two equations for NMR permeabilities were used (eq. 2.28 and 2.29) thus resulting in 4
different NMR values (two for each relaxation time). The first is based on individual sample
porositie
e
(porosity and formation factor) are related theoretically they were determined independently.
Permeabilities range from about 5 to 100d for the upper aquifer consisting of primarily
medium sands. There are smaller breaks for finer layers (e.g. 5m or 8-9m) where k drops to 1
to 10d. The gravel layer between 12 and 14m is not exceptionally noticeable, values tend to
be in the higher range but not really far above the medium sands. As expected the lowest
results of 0.01 to 1d were obtained for the silty layers, the samples B1_23 (26.2m) and B1_26
(41.45m
4 Laboratory measurements and results
45
From [Kenyon] it is to be assumed that NMR permeabilities should come into the range of
true permeabilities with a factor of about 3. This comes very close to the results of my
measurements, but as [Kenyon]’s
assumptions were realised for
sandstones rather then unconsolidated
sediments an adjustment of the
atch
n the PARIS
alues. On the other hand
empirical factor C should be allowed. 5
The reference from NMR
permeabilities to “real” (Beyer) values
is surprisingly good, but the best m
was obtained based on a combination
of relaxation times and formation
factor.
The model based o
20
dept
h [m
]
equation seems to be the poorest,
although the results are better for the
layers below 25m. For this region
internal surfaces are higher, thus
probably resulting in more stable
25
30
35
40
50
10
15
25
45
55
k PaRiS from T1 & porosity from T1 & formation f.
Fig. 4.11. Permeabilities based on NMR measurements in
reference to Beyer and PARIS
00.01 0.1 1 10 100 1000
permeability k [d]
v
discrepancies are high for fine
materials at the top (e.g. ~5m or ~9m)
so the results will not simply get better
if the material is finer.
600.01 0.1 1 10 100 1000
k Beyer from T2 & porosity from T2 & formation f.
4 Laboratory measurements and results
46
4.6 Electric conductivity and Archie exponents
4.6.1 Measurement instrument and method
Laboratory measurements for electric cond
1260 Impedance/Gain Phase
Analyzer”.
As the samples consist mainly of
uctivity or resistivity were done with a “Solatron
otential electrodes
meters to be determined to fully describe a samples
- q0
- exponent
-
To gain all 4 parameters with a minimum of
used:
1. interface conductivity
The samples were fully saturated with aqua dest. to exclude electrolytic conductivity. With
S=1 and σw→0
(4.1)
Because of the pore space of the sample is naturally filled with various ions electrolytic
conductivity can never be fully neglected. But it can be reduced to a minimum by desalting
the samples before the measurement process is started. This is a very drawn-out procedure
which can, depending on the sample, well take weeks.
unconsolidated sediments a new
measurement cell had to be designed
to prevent the pore fluid from
leaking. The cell is now completely
self-contained with the 4 connections
for current and p
included. It is well suited to small
sample volumes, containing about
70g of material.
Following equation (2.36) there are 4 para
conductivity:
σ : the interface conductivity
m: Archie exponent or cementation
n, ν: Saturation exponents
Fig. 4.12. Solatron Analyzer with measurement cell (front)
measurements, the following measuring plan was
00 qσσ =
4 Laboratory measurements and results
47
2. Saturation exponent ν
The second step would be to use a partially aqua dest. saturated sample. The conductivity will
etermined from step 1. If the samples saturation S
ill be:
the be determined from:
0qo S σσ ν ⋅= (4.2)
with σq0 being the interface conductivity d
is known ν w
0
0
q )log(log S
=σσ
ν
wm
0
and
)log(log 0 Φ
=
w
mσσ
(4.3)
3. Archie exponent m
To determine m the samples will now be fully saturated with a highly conductive electrolyte
so interface conductivity can be neglected. With S=1:
(4.4) σσ ⋅Φ=
(4.5)
. Saturation exponent n
(4.6)
and
4
If m is known n can be determined from a partially (high conductive) saturated sample: nm Sσ ⋅⋅Φ=0 wσ
)log(log 0 Sn = mw
Φσ
σ (4.7)
4 Laboratory measurements and results
48
4.6.2 Results
Interface or
ple. That is the higher the clay
or silt fraction of a sample is, the higher the
interface conductivity
These assumptions were verified with my
measurements. For the finer and medium sands
conductivity varies in a range of 0.002 - 0.008Sm .
Some samples in the upper layers contain a certain
fraction of finer sometimes even silty materials.
s probably why the conductivity has no
definite value for all t
up and down.
lower layers that consist
conductivity rise
gh this is higher than for the sandy samples it
is still lower than to be expected for silts. But as the
researched samples are o
definition, this had to be expected.
Exact values for individual samples can be found in
the appendix.
Archie exponent
The Archie exponent is an empirical material
constant and is often related to the cementation of
sediments and rocks. It is expected to be in the
range of 1.3 to 1.5 for unconsolidated sediments and
Interface conductivity
0
surface conductivity is phenomenon
that is known to be caused by mainly clay
components of a sam
is expected to be. 20
dept
h [m
]
5
10
15
25
0.001 0.01 0.1
interface conductivity [S/m]
25
35
40
50
55
Fig. 4.13. Interface conductivity for
Nauen samples
-130
45
That’
hose layers, but rather jumps 600.001 0.01 0.1
For the samples from the
primarily of silts and very fine sands the 1 1.5 2
Archie-exponent m
s to about 0.02 to 0.04Sm-1. 0
Thou
nly coarse silt by geologic 10
5
15
20
25
2.5
dept
h [m
]
25
30
35
40
45
50
55
601 1.5 2 2.5
Fig. 4.14. Archie exponent m for Nauen
samples
4 Laboratory measurements and results
49
will rise with cementation to about 2.2 for highly
cemented sandstones [Schön].
values of 1.5 to 1.7 should
Both saturation exponent tend to be quite stable
over the variety of samples with n and ν having a
value of about 1 to 1.5 .
Exact value for individual samples can be found in the
appendix.
nce to porosity:
ified for the Nauen measurements.
here the formation factor varies little for most of
ly the gravel samples with low
porosities show increased values.
Exact value for individual samples can be found in
the appendix.
0
5
10
15
20
25
0.5 1 1.5 2 2
saturation exponents
dept
h [m
]
25
30
35
40
45
50
55
600.5 1 1.5
.5
For the Nauen samples
be expected and most of the values for the sands are
in that range. Nevertheless the overall trend is for
slightly too high values. The m values for the silty
sand is obviously to high though no explanation can
be given.
Exact value for individual samples can be found in
the appendix.
Saturation exponents
Fig. 4.15. Saturation expo
Formation factor F
The formation factor F can be calculated from
individual porosities and the Archie exponent m.
There is a direct inverse depende
0
5
10
15
20
25
2 4 6
formation facto
dept
h [m
]
25
30
35
40
55
602 4 6
Fig. 4.16. Formation facto
samples
45
50
with decreasing porosities F should rise.
This was ver
T
the samples. On
n
ν
2 2.5
s n and ν nent
8
r F
8 10
r for Nauen
10
5 Interpretation
50
5 Interpretation Related to the intention of this thesis there are two objectives for interpretation: first all results
a hydrogeophysical point of view, then
o each other, to effectiveness and to the
esults.
logical stratigraphy
have so far been orientated mainly at the
ing of the borehole to the southwest and the outcropping area of glacial till to
e northeast. These individual areas are linked by the measurements along the main profile
line (radar, DC geoelectrics). A concentration of data exists for both ends of this line. Due to
ssociated core samples a very detailed petrophysical characterisation of
ed on the general geologic structure it
units and therefore their hydrological
n area of the test-site. The stratigraphic profile at the borehole can be
si /
tline.
Starting from the basic model from well logging the following substructure can be assumed:
an open aquifer is followed by a impermeable layer at a depth of ~21m. Situated between this
ifer (31-39m). The third aquifer follows
r boundary can not be set.
edominantly consist of medium grained sands with
an be set at ~1.8 – 2.2m, depending on
rea can be identified by resistivities of
3000-4000 m for the vadose zone and ~400 m below the GWT. The percentage of
irreducible water can be assumed to be about 10-15% of the total water content (based on
laboratory NMR).
From 7 to 11m the aquifer is characterised through fine sands and the first occurrences of
coarse silts. For the latter porosities rise to 40% while at the same time permeabilities
decrease to 5d. The fine sands possess intermediate porosities (35%) and permeabilities of 20-
will brought together to characterise the test-site from
the numerous methods shall be valuated in relation t
possibility of combining them for an optimisation of r
5.1 Hydro
The measurement target-areas for the test-site Nauen
close surround
th
the borehole and the a
the subsurface is possible for the borehole area. Bas
should be possible to trace back the lithological
parameters to the norther
characterised in detail, based on boreholelogs, grain
geologic ou
ze analysis’ and the lithologic
aquiclude and the next at about 39m is the second aqu
from ~48m to the final depth of the borehole, the lowe
The first 7m of the uppermost aquifer pr
porosities of about 30 – 35%. The groundwater table c
season and rainfall. In DC geoelectric sections this a
Ω Ω
5 Interpretation
51
40d. From geoelectrics a medium resistivity of 150Ωm can be assumed for the lower part of
he poor sorting porosity drops to
0% and the increase in permeability is minimal. The rise in γ intensity can not be attributed
to mica, as done by the logger, but has to be ascribed to silt-bearing inclusions.
tom of the first aquifer the facies again changes to fine sands.
ayer from the rest of the aquiclude. The NMR porosities are at ~45% though
ll other laboratory measurements list at least 50%. This discrepancy can not be explained as
re immobile.
rom geoelectrics a medium resistivity of 70-90Ωm is implied.
ot as high as for the upper aquiclude. Laboratory relaxation times propose
this aquifer.
Located underneath to about 14.5m is a layer of fine gravel with medium grain sizes of 2-
4mm. From grain size analysis this layer can be characterised as unevenly grained, as it
contains a 20-30% fraction of fine to medium sands. Due to t
2
Below the gravel layer to the bot
Petrophysical parameters correlate to the upper fine sand layer, including porosities of 35%
and permeabilities of 10-50d.
Summarising the first aquifer consists of medium to fine grained sands with an intermediate
layer of fine gravel. Porosities vary in the range of 30-40%. The aquifer can be characterised
as medium permeable [Hölting], the irreducible water saturation can be assumed to be 15-
25% of total porosity.
The first aquiclude consists of mainly coarse silt with a layer of medium silt at the bottom.
The latter can be clearly distinguished in the γ log, but there is no further information to
differentiate this l
a
yet. Permeability is at the lowest value, 0.07d, corresponding to a hydraulic conductivity
below 10-6ms-1. From a hydrological point of view, this layer can still be considered “low
permeable” [Hölting]. Nevertheless laboratory NMR measurements show, that, due to the
small grains and pore throats, all water is bound to the grain structure and therefo
F
The second aquifer again is made up of mainly fine sands and silts with a layer of medium
sands at the top. Porosities for the fine sands are in the range of 45-50% with a permeability
of only ~0.2d. The percentage of fine grained material is nearly twice as high compared to
resembling sands from the upper aquifer. The irreducible water saturation will probably be
very high, though n
a ratio of about 50%. By hydrological standards this a medium to low permeable aquifer.
5 Interpretation
52
The second aquiclude from 39 to 48m is characterised by an interbedding of primarily coarse
silts with fine sands and silts. The stratigraphic sequence is varying quickly though the finer
s of medium
uifer.
hern part of the test-site, characterised by the outcropping till.
that vertical resolution is too
w for deeper interpretation.
to
5m thus rising with the upper aquifer / aquiclude.
material is concentrated at the top. Porosity and permeability match those of the first
aquiclude although the intermediate sand layers probably rather concur with the second
aquifer. Decay time distributions show a very low percentage of mobile water (~10-30%).
The lowest aquifer again consists of mainly fine sands with a few insertation
sands. Porosities are well in range for this stratigraphy (medium sands: 35%, fine sands 45%)
with an irreducible water content of 25-35%.Permeabilities again are higher (1-5d), qualifying
this as a medium permeable aq
All the above stratigraphical and petrophysical classification is keyed to the borehole and it’s
nearest surrounding area. But the radar and geoelectric profiles allow to link the deduced
information to the nort
For most of the main profile line the stratigraphic sequence is horizontal, only for the last
~100m the lithology is disturbed by the ascending aquiclude.
From the southernmost SNMR sounding the depth of the first aquifer can be seen at 12-15m
as indicated by water content. This concurs with the radar profile along the MPL, for a
location of about –75m. I nevertheless think that rather decay times should be considered as
the vertical resolution seems better. There I would place the till interface at 10-12m which
seems too shallow compared to radar, but is in an acceptable range. From radar no additional
information below this interface can be gained, but decay times place the aquiclude basis at
~18m with the second aquifer following to about 30m. Below
lo
For the next sounding location data of IP3 and SNMR B7 can be taken into account. In the IP
model an interface is displayed for 8m but there is only a small drop in free water content for
B7, rising again below. If decay times are examined the aquifer’s lower boundary can be
placed at again 10m. This difference to IP is within error tolerance due to vertical resolution
of both techniques. Again at radar the interface is a little deeper, so probably a variation
perpendicular to the main profile exists. This time the second aquifer stretches from ~14m
2
5 Interpretation
53
Due to the structural inhomogeneities and 3D effects the SNMR and IP soundings to the north
are difficult to explain and mostly contradict each other. That’s why they are not considered
in detail any further.
The following can be summarised: the rising outcrop of glacial till to the northeast of the test-
ite can be clearly identified as the first aquiclude from the borehole. Furthermore the basis of
5.2 Evaluation and effectiveness of used methods
Various laboratory and field technique have been used to gain as much geophysical and
hydrological information as possible about the test-site. Some have proved to be more
effective than others, some failed completely.
The most information about the lateral extent of hydrogeophysicaly relevant structures still
yields radar. Though it was limited to the upper aquifer and its interface with the till it
nevertheless provided detailed information which can be correlated to the punctual
information of soundings or logs. DC geoelectrics can provide similar details but data point
resolution is lower and needs to be balanced by inversion and modelling. An adequate starting
model e.g. from IP soundings is needed to improve inversion quality.
For this thesis refraction seismics proved to be the least effective method. Despite extensive
field work and data analysis no additional information was received. This might be due to the
s
the aquiclude as well as the second aquifer can be observed. Additionally can be stated that
the thickness of the lower layers is increasing to the southwest.
-250 -200 Borehole
Main Profile Line [m] SW
Fig. 5.1. Hydrogeological out-line of Nauen stratigraphy
0
10
40
]
-150 -100 -50 0
?
?
NE
aquiclude
20
30Dep
th [m
? aquifer
aquiclude
aquifer
50 aquifer
5 Interpretation
54
special circumstances for the test-site (very low velocities for the weathered zone). If
successful, measured seismic velocities can be used to characterise groundwater-bearing
layers in connection to porosity and saturation. The field effort is extensive compared to radar
r geoelectrics that’s why a pure seismic groundwater exploration is in my opinion obsolete
d can be efficiently combined
with lateral techniques. Especially radar and SNMR seem complementary as the general
ctural inf
porosity. From empirical relations an additional estimation of hydraulic permeabilities is
possible which is in general coherent with laboratory data.
reholes and ~logs provide an ional source of vertical structural information and can be
put to an effective use in groundwater exploration. γ gs are a valuable tool concerning
hydrogeological structures as they contain direct information on the percental distribution of
fine grained material (i.e. clay, shale, silt) and can be used to determine formation density and
porosity. If possible a borehole should be included in hydrogeophysical examinations though
is might prove difficult under normal conditions.
Laboratory investigations proved to be more time-consuming than field measurements.
Especially the electric measurement, with desalting, dragged on for more than 2 months.
Moreover, the measurements at partial saturations with low conductivities are highly unstable.
Partial saturations are used to determine saturation exponents, which are not necessarily
needed to access hydrologically relevant parameters. They shouldn’t be measured for large
groups of samples as the prove to be quite stable in value. If they are needed e.g. for new
inversion routines an exemplary determination for few samples might be sufficient.
Sample preparation for NMR is not as time consuming, especially as one sample is sufficient
for any number of pulse sequences. T takes the longest to measure and there is little to no
additional information compared to T . T * should not be used for laboratory evaluation as,
due to instability, results can not be compared to field data.
The measurement of rock density is a presupposition for electric and NMR measurements as
it is needed for porosity determination. The results are quite stable and again exemplary
determinations for the different stratigraphical units should probably be sufficient if no
o
and should be used only when all other lateral methods fail.
Both sounding methods used for this thesis, IP and SNMR, were highly effective. They
provide 1D vertical information about the sounding location an
stru ormation is upgraded with punctual data about stratigraphy (grain sizes) and
Bo addit
lo
th
1
2 2
5 Interpretation
55
material change is suspected (e.g. all samples consist of sands and silts, therefore matrix
densities should all correlate to quartz). For further intensive investigations the instrument
needs a temperature calibrated surrounding.
The determination of specific internal surface proved to be difficult as the surfaces involved
are very small for sands. This leads to unstable results near instrument resolution. The
easurement instrument has special set-ups for these situations, though they don’t seem to
ummarising, for the test-site Nauen the optimal combination of measurement techniques
m
improve data quality much.
The correlation of formation factor and decay times provided the best estimation of hydraulic
conductivities which can be used to specify aquifer properties from SNMR soundings.
Though radar isn’t very effective below the first aquifer, identification of relevant structures is
precise and transferable.
S
seems to be involving Ground Penetration Radar profiling, SNMR sounding and a combined
NMR and electric laboratory analysis.
6 Conclusion
56
6 Conclusion
The intention of this thesis was to evaluate and optimise different geophysical methods
trophysics) were successful and could be integrated into a more
etailed description of the test-site. The earlier stratigraphic model was expanded to the layers
n with SNMR soundings in correlation to laboratory
tudies. For SNMR vertical resolution needs to be improved for depths below 30m, though.
or laboratory measurements I would propose a reduced measurement program. Some of the
arameters determined for the Archie equations are not essential to access rock parameters in
a hydrological sense but nevertheless take the most time to determine. From only 2
measurements the necessary interface conductivity and Archie exponent could be calculated.
Additionally it wouldn’t be obligatory to desalt the samples, thus saving about 3-5 weeks of
measurement time. For laboratory NMR the use of only one pulse sequence seems
appropriate. There is no additional information from analysing both T1 and T2, nevertheless
T2* should be omitted as those decay times seem highly instable in the lab.
related to hydrological problems. These implementations should be based on the
determination of hydrogeophysical properties for the test-site Nauen.
With the exception of seismics, all field (DC geoelectrics, radar, IP, SNMR) and laboratory
measurement (NMR, SIP, pe
d
below the first aquiclude and the hydraulic parameters like porosity, irreducible water
saturation and permeability could be determined for the known 3 aquifers as well as for the
aquicludes. Earlier measurements could be correlated to the new data and interpretation was
improved.
By comparing the results of different techniques conclusions could be drawn about
effectiveness of laboratory and field measurements. Especially promising proves to be a
combination of lateral radar exploratio
s
F
p
7 Outlook
57
7 Outlook
On the subject of the failed seismic exploration, maybe another attempt should be made. The
accelerated weight drop failed to provide an appropriate signal to noise ratio. But within a
smaller scope there have been improved results with a sledgehammer and very high rates of
opographic grid should be established.
stacking. The measurement and evaluation effort for a small layout of maybe 4 shotpoints is
justifiable, even if the results should prove to be as unsuccessful as within this thesis.
To further analyse and model the measured data it seems necessary to improve the
topographic information about the test-site. Even though the field appears to be quite plain,
there are significant depressions and a rise in topography at the margins to the south and east.
A detailed t
Moreover an improved investigation of the area directly to the northeast of the test-site seems
promising. The lower boundary of the glacial till has not been accessed , the same applies to
the second aquifer and aquiclude. As IP or SNMR soundings prove to be difficult in that
region due to 3D effects, a drop-penetration-test might yield additional information.
Bibliography
Bibliography
Hertrich, M., 2000, Joint Inversion of Surface Nuclear Magnetic Resonance and Geoelectric
Sounding, Diplomarbeit, Technical University Berlin.
Kenyon, W. E., 1997, Petrophysical Principles of Applications of NMR Logging: The Log
Analysist.
nödel, K., Krummel, H., Lange, G., 1997, Handbuch zur Erkundung des Untergrundes von
Krüger, U., 2001, Untersuchungen mit der nuklearmagnetischen Resonanz (NMR) an
Gesteinsproben und synthetischen Materialien, Diplomarbeit, Technical University
Berlin.
oke, M. H., 1998, RES2DINV v3.4 Manual.
Richter, C.,2000, Ergebnisbericht zur Anlage und geophysikalischen Vermessung einer
Forschungsbohrung mit Ausbau zur Grundwassermessstelle im Bereich Nauen,
HGN (unpublished report).
Schön, J. H., 1996, Physical Properties of Rocks: Fundamentals and Principles of
Petrophysics.
Telford, W., Geldart, L., Sheriff, R., 1990, Applied Geophysics, Cambridge University Press
Dannowski, G., 1998, Abschätzung hydrologisch relevanter gesteinsphysikalischer Merkmale
durch kombinierte Radar- und Geoelektrikerkundung, Diplomarbeit, Technical
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Hölting, B., 1989, Hydrogeologie, 3-rd edition, Stuttgart.
K
Deponien und Altlasten, Band 3: Geophysik, Springer Verlag.
L
58
Acknowledgements
59
Acknowledgements
constant su
All membe ave been extremely helpful, a special thanks to Mr. Schmarsow
nd Mr. Schenkluhn from the department’s workshop, who supported me in the field and the
laboratory and to Mr. Hertrich, who uncomplainingly answered all my numerous questions
about the test-site and earlier used methods. Additionally a special thanks to Mrs. Krüger who
can never be found in textbooks.
ast but not least I would like to acknowledge my parents for their never-ending support
during the long progression of this study.
First I would like to thank Prof. Yaramanci for introducing me to the topic and for the
pport and encouragement during the course of this work.
rs of the institute h
a
explained NMR and Archie and all those little knacks that
L
Acknowledgements
60
Appendix