Hyperspectral Imaging

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I

Introduction to
T Introduction to Hyperspectral Imaging
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Hyperspectral
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page 1
Introduction to Hyperspectral Imaging

Before Getting Started


For much of the past decade, hyperspectral imaging has been an area of active
research and development, and hyperspectral images have been available only to
researchers. With the recent appearance of commercial airborne hyperspectral
imaging systems, hyperspectral imaging is poised to enter the mainstream of
remote sensing. Hyperspectral images will find many applications in resource
management, agriculture, mineral exploration, and environmental monitoring. But
effective use of hyperspectral images requires an understanding of the nature
and limitations of the data and of various strategies for processing and interpret-
ing it. This booklet aims to provide an introduction to the fundamental concepts
in the field of hyperspectral imaging.
Sample Data Some illustrations in this booklet show analysis results for a hyper-
spectral scene of Cuprite, Nevada. This scene was acquired using the Airborne
Visible/Infrared Imaging Spectrometer (AVIRIS), which is operated by the NASA
Jet Propulsion Laboratory. The same scene is used in the exercises in the com-
panion tutorial booklet Analyzing Hyperspectral Images. You can download this
scene in the TNTmips Project File format (along with associated sample data)
from the MicroImages web site or contact MicroImages to obtain the data on a
free CD-R.
More Documentation This booklet is intended only as a general introduction to
hyperspectral imaging. In TNTmips, hyperspectral images can be processed and
analyzed using the Hyperspectral Analysis process (choose Raster / Hyperspectral
Analysis from the TNTmips menu). For an introduction to this process, consult
the tutorial booklet entitled Analyzing Hyperspectral Images. Additional back-
ground information can be found in the booklet Introduction to Remote Sensing
of Environment (RSE).
TNTmips® and TNTlite® TNTmips comes in two versions: the professional ver-
sion and the free TNTlite version. This booklet refers to both versions as
“TNTmips.” If you did not purchase the professional version (which requires a
hardware key), TNTmips operates in TNTlite mode, which limits object size and
does not allow preparation of linked atlases.
Randall B. Smith, Ph.D., 14 July 2006
©MicroImages, Inc., 1999-2006

It may be difficult to identify the important points in some illustrations without a


color copy of this booklet. You can print or read this booklet in color from
MicroImages’ web site. The web site is also your source for the newest Getting
Started booklets on other topics. You can download an installation guide, sample
data, and the latest version of TNTlite.
http://www.microimages.com

page 2
Introduction to Hyperspectral Imaging

Welcome to Hyperspectral Imaging


Multispectral remote sensors such as the Landsat The technologi-
cal background
Thematic Mapper and SPOT XS produce images
of hyperspectral
with a few relatively broad wavelength bands. Hy- sensors is
perspectral remote sensors, on the other hand, collect discussed on page 4.
image data simultaneously in dozens or hundreds of Pages 5-10 introduce the
concepts of spectral
narrow, adjacent spectral bands. These measure-
reflectance of natural
ments make it possible to derive a continuous materials, spectra as
spectrum for each image cell, as shown in the illus- vectors in n-dimensional
tration below. After adjustments for sensor, spectral space, and
spectral mixing. Factors
atmospheric, and terrain effects are applied, these
contributing to the
image spectra can be compared with field or labo- measured radiance values
ratory reflectance spectra in order to recognize and in an image are detailed
map surface materials such as particular types of on pages 11-13, followed
by methods for converting
vegetation or diagnostic minerals associated with ore
from radiance to reflec-
deposits. tance on pages 14-15.
Strategies for analyzing
Hyperspectral images contain a wealth of data, but hyperspectral images are
interpreting them requires an understanding of ex- discussed on pages 16 -
actly what properties of ground materials we are 21, and a list of literature
trying to measure, and how they relate to the mea- references is provided on
pages 22-23.
surements actually made by the hyperspectral sensor.

Images acquired simultaneously in Set of brightness values for a single


many narrow, adjacent wavelength raster cell position in the
bands. hyperspectral image.

A plot of the brightness values


versus wavelength shows the
continuous spectrum for the
image cell, which can be used
to identify surface materials.
Relative Brightness

0.6
Spectral
Plot
0.4

0.2

0.0
0.7 1.2 1.7 2.2
Wavelength (micrometers)

page 3
Introduction to Hyperspectral Imaging

The Imaging Spectrometer


Hyperspectral images are produced by instruments called imaging spectrometers.
The development of these complex sensors has involved the convergence of two
related but distinct technologies: spectroscopy and the remote imaging of Earth
and planetary surfaces.
Spectroscopy is the study of light that is emitted by or reflected from materials
and its variation in energy with wavelength. As applied to the field of optical
remote sensing, spectroscopy deals with the spectrum of sunlight that is diffusely
reflected (scattered) by materials at the Earth’s surface. Instruments called spec-
trometers (or spectroradiometers) are used to make ground-based or laboratory
measurements of the light reflected from a test material. An optical dispersing
element such as a grating or prism in the spectrometer splits this light into many
narrow, adjacent wavelength bands and the energy in each band is measured by
a separate detector. By using hundreds or even thousands of detectors, spec-
trometers can make spectral measurements of bands as narrow as 0.01 micrometers
over a wide wavelength range, typically at least 0.4 to 2.4 micrometers (visible
through middle infrared wavelength ranges).
Remote imagers are designed to focus and measure the light reflected from many
adjacent areas on the Earth’s surface. In many digital imagers, sequential mea-
surements of small areas are made in a consistent geometric pattern as the sensor
platform moves and subsequent processing is required to assemble them into an
image. Until recently, imagers were restricted to one or a few relatively broad
wavelength bands by limitations of detector designs and the requirements of data
storage, transmission, and processing. Recent advances in these areas have al-
lowed the design of imagers that have spectral ranges and resolutions comparable
to ground-based spectrometers.

Scan Mirror and


Other Optics λ

Dispersing
Element Imaging
Light from Optics Detectors
a single
ground- Schematic diagram of the basic
resolution elements of an imaging spec-
cell. trometer. Some sensors use
multiple detector arrays to mea-
sure hundreds of narrow
wavelength (λλ ) bands.

page 4
Introduction to Hyperspectral Imaging

Spectral Reflectance
In reflected-light spectroscopy the fundamental property that we want to obtain
is spectral reflectance: the ratio of reflected energy to incident energy as a func-
tion of wavelength. Reflectance varies with wavelength for most materials because
energy at certain wavelengths is scattered or absorbed to different degrees. These
reflectance variations are evident when we compare spectral reflectance curves
(plots of reflectance versus wavelength) for different materials, as in the illustra-
tion below. Pronounced downward deflections of the spectral curves mark the
wavelength ranges for which the material selectively absorbs the incident energy.
These features are commonly called absorption bands (not to be confused with
the separate image bands in a multispectral or hyperspectral image). The overall
shape of a spectral curve and the position and strength of absorption bands in
many cases can be used to identify and discriminate different materials. For
example, vegetation has higher reflectance in the near infrared range and lower
reflectance of red light than soils.
1 2 3
SPOT XS Multispectral Bands
1 2 3 4 5 7
Landsat TM Bands
Near Infrared Middle Infrared
Blue

Red
Grn

Reflected Infrared
60
Vegetation
Dry soil
(5% water)
Reflectance (%)

40
Wet soil
(20% water)

20
Clear lake water
Turbid river water
0
0.4 0.6 0.8 1.0 1.2 1.4 1.6 1.8 2.0 2.2 2.4
Wavelength (micrometers)
Representative spectral reflectance curves for several common Earth surface ma-
terials over the visible light to reflected infrared spectral range. The spectral bands
used in several multispectral satellite remote sensors are shown at the top for
comparison. Reflectance is a unitless quantity that ranges in value from 0 to 1.0,
or it can be expressed as a percentage, as in this graph. When spectral measure-
ments of a test material are made in the field or laboratory, values of incident
energy are also required to calculate the material’s reflectance. These values are
either measured directly or derived from measurements of light reflected (under
the same illumination conditions as the test material) from a standard reference
material with known spectral reflectance.

page 5
Introduction to Hyperspectral Imaging

Mineral Spectra
In inorganic materials such as minerals, chemical composition and crystalline
structure control the shape of the spectral curve and the presence and positions of
specific absorption bands. Wavelength-specific absorption may be caused by the
presence of particular chemical elements or ions, the ionic charge of certain ele-
ments, and the geometry of chemical bonds between elements, which is governed
in part by the crystal structure.
The illustration below shows spectra of some common minerals that provide
examples of these effects. In the spectrum of hematite (an iron-oxide mineral), the
strong absorption in the visible light range is caused by ferric iron (Fe+3). In
calcite, the major component of limestone, the carbonate ion (CO3-2) is respon-
sible for the series of absorption bands between 1.8 and 2.4 micrometers (µm).
Kaolinite and montmorillonite are clay minerals that are common in soils. The
strong absorption band near 1.4 µm in both spectra, along with the weak 1.9 µm
band in kaolinite, are due to hydroxide ions (OH-1), while the stronger 1.9 µm band
in montmorillonite is caused by bound water molecules in this hydrous clay. In
contrast to these examples, orthoclase feldspar, a dominant mineral in granite,
shows almost no significant absorption features in the visible to middle infrared
spectral range.

Visible Near Infrared Middle Infrared


100
Calcite
Orthoclase Feldspar
80
Kaolinite
Reflectance (%)

60
Montmorillonite

40

Hematite
20

0
0.4 0.6 0.8 1.0 1.2 1.4 1.6 1.8 2.0 2.2 2.4
Wavelength (micrometers)
Reflectance spectra of some representative minerals (naturally occurring chemical
compounds that are the major components of rocks and soils).

page 6
Introduction to Hyperspectral Imaging

Plant Spectra
The spectral reflectance curves of healthy green plants also have a characteristic
shape that is dictated by various plant attributes. In the visible portion of the
spectrum, the curve shape is governed by absorption effects from chlorophyll
and other leaf pigments. Chlorophyll absorbs visible light very effectively but
absorbs blue and red wavelengths more strongly than green, producing a charac-
teristic small reflectance peak within the green wavelength range. As a
consequence, healthy plants appear to us as green in color. Reflectance rises
sharply across the boundary between red and near infrared wavelengths (some-
times referred to as the red edge) to values of around 40 to 50% for most plants.
This high near-infrared reflectance is primarily due to interactions with the inter-
nal cellular structure of leaves. Most of the remaining energy is transmitted, and
can interact with other leaves lower in the canopy. Leaf structure varies signifi-
cantly between plant species, and can also change as a result of plant stress. Thus
species type, plant stress, and canopy state all can affect near infrared reflectance
measurements. Beyond 1.3 µm reflectance decreases with increasing wavelength,
except for two pronounced water absorption bands near 1.4 and 1.9 µm.
At the end of the growing season leaves lose water and chlorophyll. Near infra-
red reflectance decreases and red reflectance increases, creating the familiar yellow,
brown, and red leaf colors of autumn.

Visible Near Infrared Middle Infrared


Chlorophyll Cell Structure Water Water

Grass
Walnut tree canopy
60
Reflectance (%)

Fir tree

40

Dry, yellowed
20 grass

0
0.4 0.6 0.8 1.0 1.2 1.4 1.6 1.8 2.0 2.2 2.4
Wavelength (micrometers)
Reflectance spectra of different types of green vegetation compared to a spectral
curve for senescent (dry, yellowed) leaves. Different portions of the spectral curves
for green vegetation are shaped by different plant components, as shown at the top.

page 7
Introduction to Hyperspectral Imaging

Spectral Libraries
Several libraries of reflectance spectra of natural and man-made materials are
available for public use. These libraries provide a source of reference spectra
that can aid the interpretation of hyperspectral and multispectral images.
ASTER Spectral Library This library has been made available by NASA as part
of the Advanced Spaceborne Thermal Emission and Reflection Radiometer (AS-
TER) imaging instrument program. It includes spectral compilations from NASA’s
Jet Propulsion Laboratory, Johns Hopkins University, and the United States Geo-
logical Survey (Reston). The ASTER spectral library currently contains nearly
2000 spectra, including minerals, rocks, soils, man-made materials, water, and
snow. Many of the spectra cover the entire wavelength region from 0.4 to 14 µm.
The library is accessible interactively via the Worldwide Web at http://
speclib.jpl.nasa.gov. You can search for spectra by category, view a spectral plot
for any of the retrieved spectra, and download the data for individual spectra as
a text file. These spectra can be imported into a TNTmips spectral library. You can
also order the ASTER spectral library on CD-ROM at no charge from the above
web address.
Sample spectra
80 Visible Near Infrared from the ASTER
Middle Infrared
Spectral Library.
ASTER will be one
Granite
Reflectance (%)

60 of the instruments
on the planned
Concrete EOS AM-1
40 satellite, and will
Asphalt roof shingles record image data
in 14 channels
20 Basalt from the visible
through thermal
infrared wavelength
0 regions as part of
0.4 0.6 0.8 1.0 1.2 1.4 1.6 1.8 2.0 2.2 2.4 NASA’s Earth
Wavelength (micrometers) Science Enterprise
program.

USGS Spectral Library The United States Geological Survey Spectroscopy


Lab in Denver, Colorado has compiled a library of about 500 reflectance spectra
of minerals and a few plants over the wavelength range from 0.2 to 3.0 µm. This
library is accessible online at
http://speclab.cr.usgs.gov/spectral.lib04/spectral-lib04.html.
You can browse individual spectra online, or download the entire library. The
USGS Spectral library is also included as a standard reference library in the
TNTmips Hyperspectral Analysis process.

page 8
Introduction to Hyperspectral Imaging

Plotting Spectra in Spectral Space


The spectral plots on the previous pages provide a convenient way to visualize
the differences in spectral properties between different materials, especially when
we are comparing only a few spectra. Spectral plots are an important tool to use
when you explore a hyperspectral image. But to understand how a computer
compares and discriminates among a large number of spectra, it is useful to con-
sider other conceptual ways of representing spectra.
A reflectance spectrum consists of a set of reflectance values, one for each spec-
tral channel (band). Each of these channels can be considered as one dimension
in a hypothetical n-dimensional spectral space, where n is the number of spectral
channels. If we plot the measured reflectance value for each spectral channel on
its respective coordinate axis, we can use these coordinates to specify the loca-
tion of a point in spectral space that
Point representing
mathematically represents that particular
Reflectance in Band

spectrum (0.8, 0.7)


spectrum. A simple two-band example is
0.7 shown in the illustration. The designated point
g
n t in can also be treated mathematically as the end
e se point of a vector that begins at the origin of
r
r ep r u m the coordinate system. Spectra with the same
r t
c to
p ec shape but differing overall reflectance (al-
Ve s
2

bedo) plot as vectors with the same orientation


0.8
but with endpoints at different distances from
the origin. Shorter spectral vectors represent
Reflectance in Band 1
darker spectra and longer vectors represent
N-dimensional plot of a reflectance brighter spectra.
spectrum for a hypothetical 2-band
case (n = 2). It may be difficult to visualize such a plot for
an image involving more than three wave-
length bands, but it is mathematically possible to construct a hyperdimensional
spectral space defined by dozens or hundreds of mutually-perpendicular coordi-
nate axes. Each spectrum being considered occupies a position in this
n-dimensional spectral space. Similarity between spectra can be judged by the
relative closeness of these positions (spectral distance) or by how small the angle
is between the spectral vectors.
The spectral reflectance curves shown on the previous pages for various materi-
als represent “averages” or “typical examples”. All natural materials exhibit
some variability in composition and structure that results in variability in their
reflectance spectra. If we obtain spectra from a number of examples of a mate-
rial, the resulting spectral points will define a small cloud in n-dimensional spectral
space, rather than plotting at one single location.

page 9
Introduction to Hyperspectral Imaging

Spatial Resolution and Mixed Spectra


An imaging spectrometer makes spectral measurements of many small patches of
the Earth’s surface, each of which is represented as a pixel (raster cell) in the
hyperspectral image. The size of the ground area represented by a single set of
spectral measurements defines the spatial resolution of the image and depends
on the sensor design and the height of the sensor above the surface. NASA’s
Airborne Visible/Infrared Imaging Spectrometer (AVIRIS), for example, has a
spatial resolution of 20 meters when flown at its typical altitude of 20 kilometers,
but a 4-meter resolution when flown at an altitude of 4 kilometers.
60
When the size of the ground C = 60% A + 40% B
resolution cell is large, it is B
Reflectance (%)

more likely that more than 40


C
one material contributes to
an individual spectrum mea- A
20
sured by the sensor. The
result is a composite or
mixed spectrum, and the 0
0.4 0.6 0.8 1.0 1.2 1.4 1.6 1.8 2.0 2.2 2.4
“pure” spectra that contrib-
Wavelength (micrometers)
ute to the mixture are called
Example of a composite spectrum (C) that is a linear
endmember spectra. mixture of two spectra: A (dry soil) and B (green vegeta-
Spectral mixtures can be tion).
macroscopic or intimate. In a macroscopic mixture each reflected photon inter-
acts with only one surface material. The energy reflected from the materials
combines additively, so that each material’s contribution to the composite spec-
trum is directly proportional to its area within the pixel. An example of such a
linear mixture is shown in the illustration
Spectrum A
above, which could represent a patchwork
Reflectance in Band 2

of vegetation and bare soil. In spectral space


each endmember spectrum defines the end
Mixing
of a mixing line (for two endmembers) or
space
the corner of a mixing space (for greater num-
bers of endmembers). Later we will discuss
Spectrum C
Spectrum B how the endmember fractions can be calcu-
lated for each pixel. In an intimate mixture,
Reflectance in Band 1 such as the microscopic mixture of mineral
N-dimensional plot of three end-
particles found in soils, a single photon in-
member spectra for a hypothetical teracts with more than one material. Such
2-band case. All spectra that are mixtures are nonlinear in character and there-
mixtures of A, B, and C alone must fore more difficult to unravel.
lie within the mixing space.

page 10
Introduction to Hyperspectral Imaging

Radiance and Reflectance


From the discussions on the preceding pages, it should be clear that spectral
reflectance is a property of ground features that we would like to be able to mea-
sure precisely and accurately using an airborne or satellite hyperspectral sensor.
But look at the brightness spectrum in the illustration below. This is the average
of 25 image spectra measured by the AVIRIS sensor over a bright dry lake bed
surface in the Cuprite, Nevada scene. The input spectra have been adjusted for
sensor effects using on-board calibration data, but no other transformations have
been applied.
Relative Brightness at Sensor

Averaged measured
brightness for a portion
of playa surface (red
square at right).

0.5 1.0 1.5 2.0 2.5


Wavelength, (micrometers)

This spectrum does not bear much resemblance to the reflectance spectra illus-
trated previously. This is because the sensor has simply measured the amount of
reflected light reaching it in each wavelength band (spectral radiance), in this
case from an altitude of 20 kilometers. The spectral reflectance of the surface
materials is only one of the factors affecting these measured values. The spectral
reflectance curve for the sample area is actually relatively flat and featureless.
In addition to surface reflectance, the spectral radiance measured by a remote
sensor depends on the spectrum of the input solar energy, interactions of this
energy during its downward and upward passages through the atmosphere, the
geometry of illumination for individual areas on the ground, and characteristics
of the sensor system. These additional factors not only affect our ability to re-
trieve accurate spectral reflectance values for ground features, but also introduce
additional within-scene variability which hampers comparisons between individual
image cells. These factors are discussed in more detail on the next two pages.

page 11
Introduction to Hyperspectral Imaging

Illumination Factors
Source Illumination The figure below shows a typical solar irradiance curve
for the top of the Earth’s atmosphere. The incoming solar energy varies greatly
with wavelength, peaking in the range of visible light. The spectrum of incoming
solar energy at the time an image was acquired must be known, assumed, or
derived indirectly from other measurements in order to convert image radiance
values to reflectance.
2.5

2.0
(kilowatts / m2 • µ m)
Spectral Irradiance

Solar energy arriving at the


1.5 top of the atmosphere

1.0

0.5

0 0.5 1.0 1.5 2.0 2.5 3.0


Wavelength (micrometers, µm)
Illumination Geometry The amount of energy reflected by an area on the ground
depends on the amount of solar energy illuminating the area, which in turn de-
pends on the angle of incidence: the angle between the path of the incoming
energy and a line perpendicular to the ground surface. Specifically, the energy
received at each wavelength (Eg) varies as the cosine of the angle of incidence
(θ): Eg = Eo x cos θ, where Eo is the amount of incoming energy. The energy
received by any ground area therefore varies as the sun’s height changes with
time of day and season. If the terrain is not flat, the energy received also varies
instantaneously across a scene because
θ of differences in slope angle and direc-
θ
tion.
C
B Shadowing The amount of illumina-
A tion received by an area can also be
reduced by shadows. Shadows cast by
Illumination differences can arise from topographic features or clouds can af-
differing incidence angles (θθ ) as for A
and B, or from shadowing (C).
fect areas including many contiguous
image cells. Trees, crop rows, rock out-
crops, or other small objects can also cast shadows that are confined to an individual
image cell. Both types of shadows have the effect of lowering the measured
brightness across all wavelengths for the affected pixels.

page 12
Introduction to Hyperspectral Imaging

Atmospheric and Sensor Effects


Atmospheric Effects Even a relatively clear atmosphere interacts with incom-
ing and reflected solar energy. For certain wavelengths these interactions reduce
the amount of incoming energy reaching the ground and further reduce the amount
of reflected energy reaching an airborne or satellite sensor. The transmittance of
the atmosphere is reduced by absorption by certain gases and by scattering by gas
molecules and particulates. These effects combine to produce the transmittance
curve illustrated below. The pronounced absorption features near 1.4 and 1.9
µm, caused by water vapor and carbon dioxide, reduce incident and reflected
energy almost completely, so little useful information can be obtained from im-
age bands in these regions. Not shown by this curve is the effect of light scattered
upward by the atmosphere. This scattered light adds to the radiance measured by
the sensor in the visible and near-infrared wavelengths, and is called path radi-
ance. Atmospheric effects may also differ between areas in a single scene if
atmospheric conditions are spatially variable or if there are significant ground
elevation differences that vary the path length of radiation through the atmo-
sphere.
Visible Near Infrared Middle Infrared
1.0
H2O H2O,
O2 CO2 CO2
0.8 H2O
O3 O2 H2O,
Transmittance

O2 CO2 CO2
0.6
H2O
0.4 H2O
CO2
H2O
0.2

0
0.5 1.0 1.5 2.0 2.5
Wavelength (micrometers)
Plot of atmospheric transmittance versus wavelength for typical atmospheric con-
ditions. Transmittance is the proportion of the incident solar energy that reaches the
ground surface. Absorption by the labeled gases causes pronounced lows in the
curve, while scattering is responsible for the smooth decrease in transmittance with
decreasing wavelength in the near infrared through visible wavelength range.

Sensor Effects A sensor converts detected radiance in each wavelength channel


to an electric signal which is scaled and quantized into discrete integer values
that represent “encoded” radiance values. Variations between detectors within
an array, as well as temporal changes in detectors, may require that raw measure-
ments be scaled and/or offset to produce comparable values.

page 13
Introduction to Hyperspectral Imaging

Reflectance Conversion I
In order to directly compare hyperspectral image spectra with reference reflec-
tance spectra, the encoded radiance values in the image must be converted to
reflectance. A comprehensive conversion must account for the solar source spec-
trum, lighting effects due to sun angle and topography, atmospheric transmission,
and sensor gain. In mathematical terms, the ground reflectance spectrum is mul-
tiplied (on a wavelength per wavelength basis) by these effects to produce the
measured radiance spectrum. Two other effects contribute in an additive fashion
to the radiance spectrum: sensor offset (internal instrument noise) and path radi-
ance due to atmospheric scattering. Several commonly used reflectance conversion
strategies are discussed below and on the following page. Some strategies use
only information drawn from the image, while others require varying degrees of
knowledge of the surface reflectance properties and the atmospheric conditions
at the time the image was acquired.
Flat Field Conversion This image-based method requires that the image in-
clude a uniform area that has a relatively flat spectral reflectance curve. The
mean spectrum of such an area would be dominated by the combined effects of
solar irradiance and atmospheric scattering and absorption The scene is con-
verted to “relative” reflectance by dividing each image spectrum by the flat field
mean spectrum. The selected flat field should be bright in order to reduce the
effects of image noise on the conversion. Since few if any materials in natural
landscapes have a completely flat reflectance spectrum, finding a suitable “flat
field” is difficult for most scenes. For desert scenes, salt-encrusted dry lake beds
present a relatively flat spectrum, and bright man-made materials such as con-
crete may serve in urban scenes. Any significant spectral absorption features in
the flat field spectrum will give rise to spurious features in the calculated relative
reflectance spectra. If there is significant elevation variation within the scene,
the converted spectra will also incorporate residual effects of topographic shad-
ing and atmospheric path differences.
Average Relative Reflectance Conversion This method also normalizes image
spectra by dividing by a mean spectrum, but derives the mean spectrum from the
entire image. Before computing the mean spectrum, the radiance values in each
image spectrum are scaled so that their sum is constant over the entire image.
This adjustment largely removes topographic shading and other overall bright-
ness variations. The method assumes that the scene is heterogeneous enough that
spatial variations in spectral reflectance characteristics will cancel out, produc-
ing a mean spectrum similar to the flat field spectrum described above. This
assumption is not true of all scenes, and when it is not true the method will
produce relative reflectance spectra that contain spurious spectral features.

page 14
Introduction to Hyperspectral Imaging

Reflectance Conversion II
The image-based conversion methods discussed on the previous page only ac-
count for multiplicative contributions to the image spectra. Most studies that
have used these methods have focused on mapping minerals using shortwave
infrared spectra (2.0 to 2.5 µm) for which the additive effect of atmospheric path
radiance is minimal. If the spectra to be analyzed include the visible and near
infrared ranges, however, path radiance effects should not be neglected. If the
scene includes dark materials or deep topographic shadows, an approximate cor-
rection can be made by determining (for each band) the minimum brightness
value (or the average value of a shadowed area) and subtracting it from each pixel
in the band.
Empirical Line Method Field researchers using hyperspectral imagery typically
use field reflectance measurements from the image area to convert the image data
to reflectance. Field reflectance spectra must be acquired from two or more uni-
form ground target areas. Target areas should have widely different brightness
and be large enough to recognize in the image. Using the image radiance and
ground reflectance values for the target areas, a linear equation relating radiance
to reflectance can be derived for each image band.
Bright target
In a plot of radiance versus reflectance, the slope of
the calculated line quantifies the combined effects Slope = gain
Radiance

of the multiplicative radiance factors (gain), while


the intercept with the radiance axis represents the
additive component (offset). These values are then Dark target
used to convert each image band to apparent reflec-
tance. The final values should be considered Intercept = offset
“apparent” reflectance because the conversion does Reflectance
not account for possible effects of topography Reflectance conversion
within the scene (shading and atmospheric path parameters for a single
length differences). image band using known
target reflectance values.
Modeling Methods Radiative-transfer computer
models start with a simulated solar irradiance spectrum, then compute the scene
radiance effects of solar elevation (derived from the day and time of the scene)
and atmospheric scattering and absorption. In the absence of measurements of
actual atmospheric conditions, the user must estimate some input parameters,
such as amount and distribution of scattering agents. Absorption by well-mixed
gases (CO2 and O2) is assumed to be uniform across a scene but absorption due
to water vapor is often variable. Water vapor absorption effects can be estimated
and corrected individually for each image pixel using portions of the spectra that
include water absorption bands. The final apparent reflectance values may still
incorporate the effects of topographic shading, however.

page 15
Introduction to Hyperspectral Imaging

Strategies for Image Analysis


The table below lists some of the imaging spectrometers currently being operated
for research or commercial purposes. The hyperspectral images produced by
these sensors present a challenge for the analyst. They provide the fine spectral
resolution needed to characterize the spectral properties of surface materials but
the volume of data in a single scene can seem overwhelming. The difference in
spectral information between two adjacent wavelength bands is typically very
small and their grayscale images therefore appear nearly identical. Much of the
data in a scene therefore would seem to be redundant, but embedded in it is
critical information that often can be used to identify the ground surface materi-
als. Finding appropriate tools and approaches for visualizing and analyzing the
essential information in a hyperspectral scene remains an area of active research.
Most approaches to analyzing hyperspectral images concentrate on the spectral
information in individual image cells, rather than spatial variations within indi-
vidual bands or groups of bands. The statistical classification (clustering) methods
often used with multispectral images can also be applied to hyperspectral images
but may need to be adapted to handle their high dimensionality (Landgrebe, in
press). More sophisticated methods combine both spectral and spatial analysis.
The following pages detail some of the popular methods of analyzing the spectral
content of hyperspectral images.

A Sample of Research and Commercial Imaging Spectrometers

N u m b e r Wa v e l e n g t h
Sensor Or g a n iz a tio n C o u n try
o f B a n d s R a n g e (µ m )

U ni t e d
AV IRIS NA S A 224 0 .4 - 2 .5
S ta te s

A IS A S p e c t r a l Im a g i ng L t d . F i nl a nd 286 0 .4 5 - 0 .9

CASI It r e s Re s e a r c h C a na d a 288 0 .4 3 - 0 .8 7

D A IS U ni t e d
GE R C o rp . 2 11 0 .4 - 1 2 .0
2 11 5 S ta te s

Int e g r a t e d S p e c t r o ni c s
HYM A P A us t r a l i a 128 0 .4 - 2 .4 5
P ty L td

E a r t h S e a r c h S c i e nc e s U ni t e d
P ROB E - 1 128 0 .4 - 2 .4 5
Inc . S ta te s

page 16
Introduction to Hyperspectral Imaging

Match Each Image Spectrum


One approach to analyzing a hyperspectral image is to attempt to match each
image spectrum individually to one of the reference reflectance spectra in a spec-
tral library. This approach requires an accurate conversion of image spectra to
reflectance. It works best if the scene includes extensive areas of essentially pure
materials that have corresponding reflectance spectra in the reference library. An
observed spectrum will typically show varying degrees of match to a number of
similar reference spectra. The matching reference spectra must be ranked using
some measure of goodness of fit, with the best match designated the “winner.”
Spectral matching is compli- 1.0 Image
cated by the fact that most
Reflectance
hyperspectral scenes include 0.8
many image pixels that repre- 0.6
Library
sent spatial mixtures of different
materials (see page 10). The re- 0.4
sulting composite image
0.2
spectra may match a variety of 2.1 2.2 2.3 2.4
“pure” reference spectra to Wavelength (micrometers)
varying degrees, perhaps in- Sample image spectrum and a matched spectrum
cluding some spectra of of the mineral alunite from the USGS Spectral
Library (goodness of fit = 0.91).
materials that are not actually
present. If the best-matching reference spectrum has a sufficient fit to the image
spectrum, then this material is probably the dominant one in the mixture and the
pixel is assigned to this material. If no reference spectrum achieves a sufficient
match, then no endmember dominates, and the pixel should be left unassigned.
The result is a “material map” of the image that portrays the dominant material
for most of the image cells, such as the example shown below. Sample mixed
spectra can be included in the library to improve the mapping, but it is usually not
possible to include all possible mixtures (and all mixture proportions) in the ref-
erence library.
Minerals
Alunite
Mineral map for part of the
Cuprite AVIRIS scene,
Kaolinite created by matching
image spectra to mineral
spectra in the USGS
Alunite + Kaolinite
Spectral Library. White
areas did not produce a
Montmorillonite sufficient match to any of
the selected reflectance
spectra, and so are left
Chalcedony
unassigned.

page 17
Introduction to Hyperspectral Imaging

Spectral Matching Methods


The shape of a reflectance spectrum can usually be broken down into two com-
ponents: broad, smoothly changing regions that define the general shape of the
spectrum and narrow, trough-like absorption features. This distinction leads to
two different approaches to matching image spectra with reference spectra.
Many pure materials, such as minerals, can be recognized by the position, strength
(depth), and shape of their absorption features. One common matching strategy
attempts to match only the absorption features in each candidate reference spec-
trum and ignores other parts of the spectrum. A unique set of wavelength regions
is therefore examined for each reference candidate, determined by the locations of
its absorption features. The local position and slope of the spectrum can affect
the strength and shape of an absorption feature, so these parameters are usually
determined relative to the continuum: the upper limit of the spectrum’s general
shape. The continuum is computed for each wavelength subset and removed by
dividing the reflectance at each spectral channel by its corresponding continuum
value. Absorption features can then be matched using a set of derived values
(including depth and the width at half-depth), or by using the complete shape of
the feature. These types
of procedures have been 1.0 C
organized into an expert
system by researchers at 0.8
Reflectance

the U.S. Geological Sur- 0.6


vey Spectroscopy Lab B
(Clark and others, 1990). 0.4

Many other materials, 0.2 A


such as rocks and soils, 0
may lack distinctive ab- 0.5 1.0 1.5 2.0 2.5
sorption features. These Wavelength (µµ m)
spectra must be character- Reflectance spectrum for the mineral gypsum (A) with
ized by their overall shape. several absorption features. Curve B shows the
continuum for the spectrum, and C the spectrum after
Matching procedures uti- removal of the continuum.
lize full spectra (omitting
noisy image bands severely affected by atmospheric absorption) or a uniform
wavelength subset for all candidate materials. One approach to matching seeks
the spectrum with the minimum difference in reflectance (band per band) from the
image spectrum (quantified by the square root of the sum of the squared errors).
Another approach treats each spectrum as a vector in spectral space and finds
the reference spectrum making the smallest angle with the observed image spec-
trum.

page 18
Introduction to Hyperspectral Imaging

Linear Unmixing
Linear unmixing is an alternative approach to simple
spectral matching. Its underlying premise is that a scene
includes a relatively small number of common materi-
als with more or less constant spectral properties.
Furthermore, much of the spectral variability in a scene
can be attributed to spatial mixing, in varying propor-
tions, of these common endmember components. If
we can identify the endmember spectra, we can math- Portion of an AVIRIS
ematically “unmix” each pixel’s spectrum to identify scene with forest, bare
the relative abundance of each endmember material. and vegetated fields,
and a river, shown with
The unmixing procedure models each image spectrum a color-infrared band
as the sum of the fractional abundances of the combination (vegetation
is red). Fraction images
endmember spectra, with the further constraint that the from linear unmixing are
fractions should sum to 1.0. The best-fitting set of frac- shown below.
tions is found using the same spectral-matching
procedure described on the previous page. A fraction
image for each endmember distills the abundance in-
formation into a form that is readily interpreted and
manipulated. An image showing the residual error for
each pixel helps identify parts of the scene that are not
adequately modeled by the selected set of endmembers.
The challenge in linear unmixing is to identify a set of Vegetation fraction
spectral endmembers that correspond to actual physi-
cal components on the surface. Endmembers can be
defined directly from the image using field information
or an empirical selection technique such as the one
outlined on the next page can be used. Alternatively,
endmember reflectance spectra can be selected from a
reference library, but this approach requires that the
image has been accurately converted to reflectance.
Water / shade fraction
Variations in lighting can be included directly in the
mixing model by defining a “shade” endmember that
can mix with the actual material spectra. A shade spec-
trum can be obtained directly from a deeply shadowed
portion of the image. In the absence of deep shadows,
the spectrum of a dark asphalt surface or a deep water
body can approximate the shade spectrum, as in the
example to the right.
Soil fraction

page 19
Introduction to Hyperspectral Imaging

Defining Image Endmembers


When spectral endmembers are defined from a hyperspectral image, each image
endmember should have the maximum abundance of the physical material that it
represents. (Ideally, each endmember would be a single pure material, but “pure”
pixels of each endmember may not be present in the image). If image spectra are
represented as points in an n-dimensional scatterplot, the endmembers should
correspond to cusps at the edge of the cloud of spectral points.
One common procedure for isolating candidate image endmembers involves sev-
eral steps. Because of the high degree of correlation between adjacent spectral
bands, the dimensionality of the dataset first can be reduced by applying the
Minimum Noise Fraction (MNF) transform and retaining the small number of
noise-free components. The MNF transform (Green et al. 1988) is a noise-ad-
justed principal components transform that estimates and equalizes the amount
of noise in each image band to ensure that output components are ordered by
their amount of image content. Second, an automated procedure is applied to the
MNF components to find the extreme spectra around the margins of the n-dimen-
sional data cloud. One such procedure is the Pixel Purity Index (PPI). It examines
a series of randomly-oriented directions radiating outward from the origin of the
coordinate space. For each test direction, all spectral points are projected onto
the test vector, and the extreme spectra (low and high) are noted. As directions
are tested, the process tallies the number of times each image cell is found to be
extreme. Pixels with high values in the resulting PPI raster should correspond
primarily to the edges of the MNF data cloud. In the third step, the PPI raster is
used to select pixels from the MNF dataset for viewing in a rotating n-dimen-
sional scatterplot (using a tool such as the
n-Dimensional Visualizer in the TNTmips Extreme spectra
MNF Component 2

Hyperspectral Analysis process). By


viewing the PPI spectral cloud from vari-
ous directions, the analyst can identify
significant directions, mark the spectral
points that are extreme in those directions,
and save an image of the marked cells.
Finally, the marked cell image is overlaid
on the original hyperspectral image and MNF Component 1
used as a guide to select and examine the Simple two-component plot showing
one of the random vector directions
image spectra. The best candidate (arrow) tested by the Pixel Purity In-
endmember spectra are then saved in a dex procedure. All spectral points are
spectral library for use in unmixing the hy- projected to each test vector, and ex-
perspectral image. treme points are noted.

page 20
Introduction to Hyperspectral Imaging

Partial Unmixing
Some hyperspectral image applications do not require finding the fractional abun-
dance of all endmember components in the scene. Instead the objective may be
to detect the presence and abundance of a single target material. In this case a
complete spectral unmixing is unnecessary. Each pixel can be treated as a poten-
tial mixture of the target spectral signature and a composite signature representing
all other materials in the scene. Finding the abundance of the target component
is then essentially a partial unmixing problem.
Methods for detecting a target spectrum against a background of unknown spec-
tra are often referred to as matched filters, a term borrowed from radio signal
processing. Various matched filtering algorithms have been developed, includ-
ing orthogonal subspace projection and constrained energy minimization (Farrand
and Harsanyi, 1994). All of these approaches perform a mathematical transfor-
mation of the image spectra to accentuate the contribution of the target spectrum
while minimizing the background. In a geometric sense, matched filter methods
find a projection of the n-dimensional spectral space that shows the full range of
abundance of the target spectrum but “hides” the variability of the background.
In most instances the spectra that contribute to the background are unknown, so
most matched filters use statistical methods to estimate the composite background
signature from the image itself. Some methods only work well when the target
material is rare and does not contribute significantly to the background signature.
A modified version of matched filtering uses derivatives of the spectra rather
than the spectra themselves, which improves the matching of spectra with differ-
ing overall brightness.

Fraction images produced by Matched Filtering (left) and Derivative Matched


Filtering (right) for a portion of the Cuprite AVIRIS scene. The target image
spectrum represents the mineral alunite. Brighter tones indicate pixels with
higher alunite fractions. The image produced by Derivative Matched Filtering
shows less image noise, sharper boundaries, and better contrast between
areas with differing alunite fractions.

page 21
Introduction to Hyperspectral Imaging

References
General
Kruse, F.A. (1999). Visible-Infrared Sensors and Case Studies. In Renz, Andrew
N. (ed), Remote Sensing for the Earth Sciences: Manual of Remote Sens-
ing (3rd ed.), Vol 3. New York: John Wiley & Sons, pp. 567-611.
Landgrebe, David (1999). Information Extraction Principles and Methods for Mul-
tispectral and Hyperspectral Image Data. In Chen, C.H. (ed.), Information
Processing for Remote Sensing. River Edge, NJ: World Scientific Publish-
ing Company, pp. 3-38.
Vane, Gregg, Duval, J.E., and Wellman, J.B. (1993). Imaging Spectroscopy of the
Earth and Other Solar System Bodies. In Pieters, Carle M. and Englert,
Peter A.J. (eds.), Remote Geochemical Analysis: Elementatl and Miner-
alogic Composition. Cambridge, UK: Cambridge University Press, pp.
121-143.
Vane, Gregg, and Goetz, A.F.H. (1988). Terrestrial Imaging Spectroscopy. Re-
mote Sensing of Environment, 24, pp. 1-29.
Spectral Reflectance Signatures
Ben-Dor, E., Irons, J.R., and Epema, G.F. (1999). Soil Reflectance. In Renz, Andrew
N. (ed), Remote Sensing for the Earth Sciences: Manual of Remote Sens-
ing (3rd ed.), Vol 3. New York: John Wiley & Sons, pp. 111-188.
Clark, Roger N. (1999). Spectroscopy of Rocks and Minerals, and Principles of
Spectroscopy. In Renz, Andrew N. (ed), Remote Sensing for the Earth
Sciences: Manual of Remote Sensing (3rd ed.), Vol 3. New York: John
Wiley & Sons, pp. 3-58.
Ustin, S.L., Smith, M.O., Jacquemoud, S., Verstraete, M., and Govaerts, Y. (1999).
Geobotany: Vegetation Mapping for Earth Sciences. In Renz, Andrew N.
(ed), Remote Sensing for the Earth Sciences: Manual of Remote Sensing
(3rd ed.), Vol 3. New York: John Wiley & Sons, pp. 189-248.
Reflectance Conversion
Farrand, William H., Singer, R.B., and Merenyi, E., 1994, Retrieval of Apparent
Surface Reflectance from AVIRIS Data: A Comparison of Empirical Line,
Radiative Transfer, and Spectral Mixture Methods. Remote Sensing of
Environment, 47, 311-321.

page 22
Introduction to Hyperspectral Imaging

References
Goetz, Alexander F.H., and Boardman, J.W. (1997). Atmospheric Corrections:
On Deriving Surface Reflectance from Hyperspectral Imagers. In Descour,
Michael R. and Shen, S.S. (eds.), Imaging Spectrometry III: Proceedings
of SPIE, 3118, 14-22.
van der Meer, Freek (1994). Calibration of Airborne Visible/Infrared Imaging
Spectrometer Data (AVIRIS) to Reflectance and Mineral Mapping in
Hydrothermal Alteration Zones: An Example from the “Cuprite Mining
District”. Geocarto International, 3, 23-37.
Hyperspectral Image Analysis
Adams, John B., Smith, M.O., and Gillespie, A.R. (1993). Imaging Spectros-
copy: Interpretation Based on Spectral Mixture Analysis. In Pieters, Carle
M. and Englert, Peter A.J. (eds.), Remote Geochemical Analysis:
Elementatl and Mineralogic Composition. Cambridge, UK: Cambridge
University Press, pp. 145-166.
Clark, R.N., Gallagher, A.J., and Swayze, G.A. (1990). Material absorption band
depth mapping of imaging spectrometer data using a complete band shape
least-squares fit with library reference spectra. Proceedings of the Sec-
ond Airborne Visible/Infrared Imaging Spectrometer (AVIRIS) Workshop,
JPL Publication 90-54, pp. 176-186.
Cloutis, E.A., (1996). Hyperspectral Geological Remote Sensing: Evaluation of
Analytical Techniques. International Journal of Remote Sensing, 17, 2215-
2242.
Farrand, William H., and Harsanyi, J.C. (1994). Mapping Distributed Geologi-
cal and Botanical Targets through Constrained Energy Minimization.
Proceedings of the Tenth Thematic Conference on Geological Remote
Sensing, San Antonio, Texas, 9-12 May 1994, pp. I-419 - I-429.
Green, Andrew A., Berman, M., Switzer, P., and Craig, M.D. (1988). A Trans-
formation for Ordering Multispectral Data in Terms of Image Quality with
Implications for Noise Removal. IEEE Transactions on Geoscience and
Remote Sensing, 26, 65-74.
Mustard, John F., and Sunshine, J.M. (1999). Spectral Analysis for Earth Sci-
ence: Investigations Using Remote Sensing Data. In Renz, Andrew N.
(ed), Remote Sensing for the Earth Sciences: Manual of Remote Sensing
(3rd ed.), Vol 3. New York: John Wiley & Sons, pp. 251-306.

page 23
I
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Introduction to Hyperspectral Imaging T
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Index
absorption spectral radiance.........................................11
bands..................................................5-7 spectral reflectance.................................5-11
atmospheric...................................13,18 converting image to.........................14-15
atmosphere curve See spectrum
absorption by...........................13,18 defined.................................................5
scattering by.................................13 spectral space..............................................9
continuum.......................................18 spectrometer..................................................4
illumination..........................................11,12 spectroscopy.........................................4,5
imaging spectrometer........................4,10,16 spectrum (spectra)
irradiance, solar.........................................12 endmember....................................19,20
linear unmixing....................................19-21 image....................................3,17-20
matched filtering.......................................21 in library.........................................8
matching, spectral................................17,18 mineral......................................6
minimum noise fraction transform............20 mixed.................................................10
pixel purity index......................................20 plant.....................................................7
resolution, spatial......................................10 plotting.................................................9
scattering.............................................4,5,13 reflectance.......................................5-11
sensor effects.............................................13 soil.......................................................5
shadowing.................................................12 solar...................................................12
spectral libraries..........................................8 water....................................................5

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