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Interpreting Subsurface
Seismic Data
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Interpreting Subsurface
Seismic Data
Edited by
Rebecca Bell
Department of Earth Science and Engineering, Imperial College London, London, United Kingdom
David Iacopini
DISTAR, Universitá di Napoli Federico II, Napoli, Italy
Mark Vardy
SAND Geophysics, Southampton, United Kingdom
Elsevier
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The Boulevard, Langford Lane, Kidlington, Oxford OX5 1GB, United Kingdom
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Copyright © 2022 Elsevier Inc. All rights reserved.
No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical,
including photocopying, recording, or any information storage and retrieval system, without permission in writing from
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found at our website: www.elsevier.com/permissions.
This book and the individual contributions contained in it are protected under copyright by the Publisher (other than as
may be noted herein).
Notices
Knowledge and best practice in this field are constantly changing. As new research and experience broaden our
understanding, changes in research methods, professional practices, or medical treatment may become necessary.
Practitioners and researchers must always rely on their own experience and knowledge in evaluating and using any
information, methods, compounds, or experiments described herein. In using such information or methods they should
be mindful of their own safety and the safety of others, including parties for whom they have a professional responsibility.
To the fullest extent of the law, neither the Publisher nor the authors, contributors, or editors, assume any liability for any
injury and/or damage to persons or property as a matter of products liability, negligence or otherwise, or from any use or
operation of any methods, products, instructions, or ideas contained in the material herein.
ISBN: 978-0-12-818562-9
CONTRIBUTORS .............................................................................................. xi
ABOUT THE EDITORS ....................................................................................xiii
v
vi Contents
REBECCA BELL
Rebecca Bell has 18 years of experience in the interpretation of seismic reflection data. She is currently a
Senior Lecturer at Imperial College London and teaches Seismic Techniques to undergraduates and MSc
students. She has worked on a wide range of academic and industry 2D and 3D seismic datasets
working on scientific problems from “how do rift zones initiate?” to “what controls the style of
earthquake behavior at subduction zones?” She also has experience in collection of field data optimal
for full-waveform inversion techniques and is interested in the application of machine learning and
artificial intelligence to aid seismic interpretation.
DAVID IACOPINI
David Iacopini is currently an Associate Professor at the University of Naples Federico II. He teaches
Marine Geology and Subsurface Geology Techniques. In the past, he has worked in Pisa and Aberdeen
University where he coordinated the Integrated Petroleum Geology MSc course and contributed to
establish the Geophysics MSci course. His scientific interests range from basin analysis to marine ge-
ology including reservoir characterization for storage technology, using 2D and 3D seismic interpre-
tation, boreholes, and image processing techniques. He acted as research consultant for various O&G
industries, mainly on deep water structures, pre-salt reservoir characterization, and subsurface fault
characterization.
MARK VARDY
Mark Vardy has 14 years of experience in the acquisition, processing, and interpretation of seismic
reflection data. He is currently Head of R&D at SAND Geophysics and holds a Visiting Researcher
position at the University of Southampton, where he has taught Seismic Processing and Interpretation
Methods at undergraduate and postgraduate levels. He has contributed to a wide range of academic and
industry projects, working with data at all scales (engineering to crustal), 2D and 3D, and in a broad
range of environments (both deep and shallow water). However, his primary focus is on quantitative
imaging/inversion at engineering scales.
xiii
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CHAPTER 1
Introduction
Rebecca Bell1, David Iacopini2 and Mark Vardy3
1
Department of Earth Science and Engineering, Imperial College London, United Kingdom;
2
DISTAR, Università di Napoli Federico II, Napoli, Italy; 3SAND Geophysics, Southampton,
United Kingdom
subsurface data still requires a good balance between geological and geophys-
ical knowledge coupled with a certain dose of creative interpolation. Seismic
interpretation could, in fact, be defined as the thoughtful procedure of sepa-
rating the continuity and variability of reflections (related to the geologic struc-
ture, stratigraphy fluids, and reservoir fabric) from the recorded seismic wavelet
(ideally the pulse of seismic energy defined as the minimum phase of some fre-
quency bandwidth) and the noise of various kinds and image artifacts (Brown,
2011). In order to constrain and integrate information out of the reflective
signal, seismic data characterization often requires the combination of bore-
hole and microseismicity data. Prior to the advent of digital data in the
1980s, seismic interpretation was predominantly done on paper. The subse-
quent replacement of paper by digital data on computer devices has led to
an interpretative approach adopting more and more image processing methods
(Liner, 2008). Nowadays the use of virtual data enhancement (Purves et al.,
2016; Rashed and Atef, 2020) and deep learning approaches (Waldeland
et al., 2018) is providing the seismic interpreter with the addition of more inter-
active advanced computational approaches to add to their traditional tool kit.
Alongside this rapidly developing process, which has seen the evolution of dig-
ital tools to visualize, interpret, and manipulate the reflective and diffractive
data from the subsurface, there has been a detailed pathway of digital tech-
niques which have changed our capabilities to extract and invert petrophysical
and geological information out of the reflective seismic surveys (Chopra and
Marfurt, 2005). The introduction of the principles of seismic stratigraphy by
Peter Vail and others in 1977 (Vail et al., 1977) provided a framework to
define, explore for, and exploit stratigraphic traps in a time where most of
the seismic data were 2D and interpreted in pencil (Claerbout, 1992). Early
interactive workstations started with variable area and then wiggle-trace dis-
plays. The uses of color bar (eight colors in the late 1970s, with the Genisco
providing 16 colors in the mid-1980s; see, Chopra and Marfurt, 2005) to
map and estimate relative acoustic impedance changed dramatically our abil-
ity to apply recursive inversion to extract wave form properties (amplitude
phase and frequency). Seismic attribute analysis, including acoustic imped-
ance (Lavergne, 1975; Lindseth, 1976, 1979) and complex trace attributes,
such as the envelope, instantaneous phase, and instantaneous frequency
(Taner et al., 1979; Bodine, 1984), became crucial and routinely applied to
map seismic properties from stacked data. The concepts of bright spots and
Amplitude Variation with Offset (AVO) were also introduced in the 1980s
and 1990s. With the assimilation of 3D seismic volumes that provide data
at fine spatial sampling leading to more accurate 3D representations of the
subsurface reflectivity and advance the use of single trace seismic attributes
with the introduction of horizon dip azimuth attributes (Daley et al., 1989),
the use of coherence (Bahorich and Farmer, 1995), spectral decomposition
4 CHAPTER 1: Introduction
2. Book overview
Within this book, we seek to provide an overview of how seismic reflection data
is currently being used to image the subsurface, combining nine papers that
delve into different aspects of data processing, reprocessing, and/or interpreta-
tion. These papers are collected into three sections, each dealing with a different
aspect of the overall process.
Cook and Portnov give us an introduction to natural gas hydrate systems and
the famous “‘bottom simulating reflection’” (BSR) and explain cases where the
BSR breaks the rules of the original definition by Shipley et al. (1979). The BSR
is another example of the great importance of seismic data. The BSR was hy-
pothesized to relate to free gas in 1974 before being confirmed by IODP dril-
ling two decades later in 1995. Dissociating gas hydrates may play a critical
role in climate change and acidification and oxygen depletion in the oceans.
This contribution explains why it is still challenging to quantify gas hydrate us-
ing seismic data and describes the prospecting tools currently available to iden-
tify natural gas hydrate systems in seismic reflection data.
A potential cause of gas hydrate dissociation is slope failure, which can also
lead to destruction of seabed infrastructure and tsunamis. Scarselli et al. use
seismic reflection data to reveal slope collapse systems in the Exmouth Plateau,
NW Australia, and discuss their potential as petroleum systems. This contribu-
tion provides a masterclass in the interpretation and characterization of slope
failure deposits and their sources using 3D seismic reflection images and root
mean square amplitude (RMS) attributes. Modern-day analogs have been
used for the reader to put into context the features interpreted from seismic
data (Fig. 1.1). The paper argues that thick, stacked talus wedges with reservoir
potential in the hanging walls of normal faults, whose slip in earthquakes likely
trigger footwall slope failure, may diversify potential play types in rifted
margins.
Alvarenga et al. take on the notoriously difficult challenge of interpreting pre-
salt carbonates. These deposits in areas like the Campos and Santos basin,
South Atlantic, have not been well imaged by 3D seismic volumes, so their
interpretation relies on grids of 2D seismic profiles. In this study Alvarenga
et al. used core data to develop a supervised seismic facies analysis to identify
carbonates in the Campos basin, utilizing RMS, cosine of phase, and relative
acoustic impedance. Their analysis results in the identification of 10 carbonate
“geobodies” mapped across the 2D seismic network. They find that some of
these carbonates are likely in situ and others resedimented. All of the likely rese-
dimented carbonates occur during a time of high tectonic activity dsupporting
a tectonic trigger for collapse and resedimenation.
One of the first things we learn as seismic interpreters is that there is consider-
able uncertainty in our interpretations, and interpreters must employ heuristics
(“rules of thumb”). Alcade and Bond, using powerful everyday examples,
explain that these heuristics lead to unwanted, and often unknown, cognitive
biases that influence our interpretations. Alcade and Bond describe four of
the key biases in seismic interpretation. (1) Anchoring dwhen an individual
is fixed on an initial concept or idea it affects all subsequent decisions. (2)
Availability bias dwhen easily retrievable information is used more frequently
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immediately. Ten days’ starvation appeared to weaken the venom,
for a bird bitten by a spider fasting for that period recovered after an
indisposition of six hours.
Most Arachnologists have recorded experiments with regard to the
venom of the commoner European species, with equally conflicting
results. Blackwall came to the conclusion that loss of blood, and not
poison, caused the death of spider-bitten insects. He could not
himself distinguish a spider bite from the prick of a needle inflicted
upon his hand at the same time. Bees, wasps, and grasshoppers
survived the bite about as long as other insects of the same species
outlived a needle-prick in the same part of the body. Walckenaer’s
experience was of the same nature. Bertkau, however, when bitten in
the hand, felt clear indications of an irritant poison in the wound.
The hairs of some of the large hairy species of the Aviculariidae
possess poisonous properties. They are readily parted with, and
when the animal is touched by the hand considerable irritation is set
up.
Fertility of Spiders.—Spiders vary greatly in the average
number of eggs laid by different species, and within the limits of each
species there is a very considerable variation in fertility. As a rule it
appears that the large and vigorous spiders are more prolific than the
smaller and weaker members of the order. Were all the facts before
us, however, we should no doubt find that the number of eggs laid
bore a direct proportion, not to the size of the species, but to the
dangers to which the young of that species are exposed. Where the
total numerical strength of a species is fairly stationary, such a
proportion must of course exist. Some species, no doubt, are tending
to become extinct, while others are increasing in numerical
importance. As a general rule, however, it is safe to infer that, if a
species is especially prolific, special dangers attend the rearing of the
young. The largest of North American Epeirids, Argiope cophinaria,
[287]
constructs a cocoon containing, on an average, 1150 eggs. As
many as 2200 have been counted in exceptional cases. Even this
number is exceeded in the case of some of the great Aviculariidae.
Theraphosa leblondi deposits as many as 3000 eggs. The large
European Epeirids, E. quadrata and E. diademata, lay about 600
eggs, those of Lycosa narbonensis reaching about the same number.
Those American spiders which have been described as stringing up a
series of cocoons in their webs usually attain about the same
aggregate, the eggs being less numerous in each cocoon.
These are examples of fairly large and fertile spiders. In the case of
other species the number of eggs laid is exceedingly small. Ero
furcata makes a single cocoon containing six eggs. Synageles picata,
an ant-like Attid, lays only three. Oonops pulcher constructs several
cocoons, but each contains only two eggs. The eggs of Cave-spiders,
and such as live in dark and damp places, are generally few in
number. Anthrobia mammouthia, for example, an inhabitant of the
great American caves, deposits only from two to five eggs.
Our knowledge of the special perils which beset particular species
is so incomplete that we are often at a loss for the reason of this great
inequality in fertility. For instance, how does Synageles picata
maintain its numerical strength by laying only three eggs, when, as
M‘Cook points out, its resemblance to the ant, though advantageous
to the adult spider, affords no protection to the egg? Our knowledge
must be greatly extended before we are able to account for particular
cases. Many influences hostile to spiders as a group are, however,
well known, and we may here enumerate them.
Natural Enemies.—The precautions taken by the mother in
constructing the cocoon render the inclemency of the weather very
much less destructive to the eggs than to the newly-hatched young.
Nevertheless, among spiders inhabiting swampy regions great havoc
is wrought by the occasional wholesale swamping of the cocoons by
floods. Professor Wilder considers the great fertility of Nephila
plumipes necessary to counterbalance the immense destruction
worked by the heavy rains upon their cocoons, which are washed in
great numbers from the trees, to the leaves of which they are
attached. But such exposed situations are avoided by many species,
and their eggs, enclosed in their silken envelope, are well protected
against the severities of the weather.
A more universal enemy to the egg is found in Ichneumon flies. On
examining the cocoons of almost any species of spider, a large
proportion are almost certain to be found to contain Ichneumon
larvae. Mr. F. Smith, in the Transactions of the Entomological
Society for 1860, describes two species, Hemeteles fasciatus and H.
formosus, which are parasitic on the eggs of Agelena brunnea. They
are figured in Mr. Blackwall’s book on British Spiders. Pezomachus
gracilis attacks the cocoons of many kinds of American spiders,
appearing to have no special preference for any particular species,
while Acoloides saitidis seems to pay special attention to the eggs of
certain of the Jumping-spiders, and particularly of Saitis pulex.
The Ichneumons which thus regard the Spider’s eggs as
convenient food for their own larvae are probably very numerous.
Nor are they themselves always free from parasites. Occasionally the
larvae of minute Hymenopterous insects are found to be parasitic
upon the eggs of an Ichneumon which have been laid in a Spider’s
cocoon.
It sometimes happens that the development of the young spiders
has so far advanced at the time of the Ichneumon’s intrusion that the
latter’s intention is frustrated, and its offspring, instead of devouring,
are themselves devoured. Again, some few of the eggs in an infested
cocoon occasionally escape the general destruction and reach the
adult condition, but there can be no doubt that Ichneumons are
largely instrumental in keeping down the numbers of most species of
spiders. The perils which attend the Spider after leaving the cocoon
are no less formidable, and much more numerous. The whole newly-
hatched brood may be destroyed by a heavy rain-storm. If there is
not a sufficient supply of food suitable to their feeble digestive
powers they perish of inanition, or eat one another. This
cannibalistic propensity is a considerable factor in the mortality
among young spiders, and the adult animals frequently prey upon
one another.
Argyrodes piraticum, in California, invades the webs of larger
spiders of the family Epeiridae, which it seizes and devours. A.
trigonum, common in the eastern states of North America, has the
same habit.[288] Hentz found in Alabama a spider, which he named
Mimetus interfector, of still more ferocious and piratical habits. Its
special quarry is Theridion tepidariorum. Sometimes the Theridion
overcomes the invader, and one case was observed in which a second
Mimetus was devouring a Theridion beside the dead body of its
predecessor, who had come off the worse in the combat.
The eggs of Theridion tepidariorum are also sometimes devoured
by this spider, and a similar propensity has been observed in some
English species, for Staveley[289] states that it is common to see
certain spiders of the genus Clubiona feeding upon the eggs which
have been laid by their neighbours. The larvae of some
Hymenopterous insects are parasitic upon Spiders themselves, and
not upon their eggs. Blackwall found this to be the case with the
larvae of Polysphincta carbonaria, an Ichneumon which selects
spiders of the genera Epeira and Linyphia on which to deposit its
eggs.[290] The spider thus infested does not moult, and is soon
destroyed by the parasite which it is unable to dislodge from its back.
Menge, in his Preussische Spinnen, enumerates several cases of
parasitism in which the larva, as soon as it has developed from the
egg, enters the spider’s body, there to continue its growth. Spiders
are also subject to the attack of a parasitic worm, Gordius (cf. vol. ii.
p. 173).
Some of the most deadly foes of Spiders are the Solitary Wasps.
There are many species of Pompilus (vol. vi. p. 101), which, having
excavated holes in clay banks, store them with spiders or other
creatures which they have paralysed by their sting. They then deposit
an egg in the hole, and immediately seal up the orifice. This habit is
found to characterise the solitary wasps of all parts of the world.
Belt[291] relates the capture of a large Australian spider by a wasp.
While dragging its victim along, it was much annoyed by the
persistent presence of two minute flies, which it repeatedly left its
prey to attempt to drive away. When the burrow was reached and the
spider dragged into it, the two flies took up a position on either side
of the entrance, doubtless with the intention of descending and
laying their own eggs as soon as the wasp went away in search of a
new victim. Fabre[292] gives an interesting account of one of the
largest European Pompilidae, Calicurgus annulatus, which he
observed dragging a “Tarentula” to a hole in a wall. Having with
great difficulty introduced its burden into the cavity, the wasp
deposited an egg, sealed up the orifice, and flew away. Fabre opened
the cell and removed the spider, which, though completely paralysed,
lived for seven weeks.
The same indefatigable observer describes the method adopted by
the comparatively small Pompilus apicalis in attacking the
formidable Wall-spider, Segestria perfida. The combatants are well
matched, and the issue of the battle would be doubtful if the wasp
did not have recourse to stratagem. Its whole energies are directed
towards forcing the spider away from its web. At home, it is
confident and dangerous; when once dislodged, it appears
bewildered and demoralised. The wasp darts suddenly towards the
spider and seizes it by a leg, with a rapid effort to jerk it forth,
releasing its hold before the enemy has had time to retaliate. The
spider, however, as well as being anchored by a thread from its
spinnerets, is clinging to its web with its hind legs, and if the jerk is
not sufficiently energetic, it hastily scrambles back and resumes its
defensive position. Before renewing the attack the wasp gives the
spider time to recover from the excitement of the first onset, seeking,
meanwhile, the retreats of other victims. Returning, it succeeds, by a
more skilful effort, in drawing the spider from its retreat and hurling
it to the ground, where, terrified and helpless, it falls an easy prey.
Should the insect bungle in its first attack and become entangled in
the web, it would itself become the victim. Certain wasps thus appear
to seek out particular species of spiders as food for their larvae.
Others are less discriminate in their tastes. Again, some, as in the
cases cited above, store their egg-nest with a single spider, while
others collect many for the purpose.
The American “blue digger wasp” (Chlorion caeruleum) excavates
its nest in the ground, and inserts a single large spider of any species.
[293]
Another wasp, of the genus Elis, selects the Wolf-spiders, and
especially Lycosa tigrina, for the use of its larvae, while Priocnemus
pomilius shows a preference for the Crab-spiders, or Thomisidae.
One of the most remarkable instances is that of Pepsis formosa,
which preys upon the gigantic spider Eurypelma hentzii, wrongly
styled in America the “tarantula,” but really belonging to an entirely
different family, the Aviculariidae.
Fabre’s most interesting researches have established the fact that
the instinct of the wasp leads it to sting the spider in a particular
spot, so as to pierce the nerve-ganglion in the thorax. The precision
with which this is effected is absolutely necessary for the purpose of
the insect. If stung elsewhere, the spider is either incompletely
paralysed, or it is killed outright, and thus rendered useless as food
for the future larvae of the wasp. On the one hand, therefore, the
Tarantula has acquired the habit of striking the wasp in the only
point where its blow is instantaneously fatal, while on the other the
wasp, with a different object in view, has been led to select the
precise spot where its sting will disable without immediately
destroying the spider. The latter case is, if anything, the more
extraordinary, as the insect can hardly have any recollection of its
larval tastes, and yet it stores up for progeny, which it will never see,
food which is entirely abhorrent to itself in its imago state.
Spiders taken from the egg-nests of wasps by M‘Cook survived, on
the average, about a fortnight, during which period they remained
entirely motionless, and would retain any attitude in which they were
placed.
There are many animals which either habitually or occasionally
feed upon spiders. They are the staple food of some hummingbirds,
and many other birds appear to find in them a pleasing variation on
their customary insect diet. These creatures, moreover, are
destructive to spiders in another way, by stealing the material of
their webs, and especially the more closely textured silk of their egg-
cocoons, to aid in the construction of their nests. M‘Cook has
observed this habit in the case of Vireo noveborocensis, and he
states, on the authority of others, that the “Plover” and the “Wren”
are addicted to it. The smaller species of monkeys are extremely fond
of spiders, and devour large numbers of them. They are said,
moreover, to take a mischievous delight in pulling them in pieces.
Armadillos, ant-eaters, snakes, lizards, and indeed all animals of
insectivorous habit, draw no distinction between Insecta and
Arachnida, but feed upon both indiscriminately. The army ants, so
destructive to insect life in tropical countries, include spiders among
their victims. These formidable insects march along in vast hordes,
swarming over and tearing in pieces any small animal which lies in
their path. They climb over intervening obstacles, searching every
cranny, and stripping them bare of animal life. Insects which attempt
to save themselves by flight are preyed upon by the birds, which are
always to be seen hovering above the advancing army. The spider’s
only resource is to hang from its thread in mid-air beneath the
branch over which the ants are swarming, for the spider line is
impracticable to the ant. Belt[294] has observed a spider escape the
general destruction by this means.
Protective Coloration.—Examples are numerous in which the
spider relies upon the inconspicuousness not of its nest, but of itself,
to escape its natural foes. Its general hues and markings are either
such as to render it not readily distinguishable among its ordinary
surroundings, or the principle has been carried still further, and a
special object has been “mimicked” with more or less fidelity.
This country is not rich in the more striking mimetic forms, but
the observer cannot fail to notice a very general correspondence in
hue between the spiders of various habits of life and their
environment. Those which run on the ground are usually dull-
coloured; tree-living species affect grey and green tints, and those
which hunt their food amongst sand and stones are frequently so
mottled with yellow, red, and grey, that they can scarcely be
recognised except when in motion.
A few of our indigenous species may be mentioned as especially
protected by their colour and conformation. Tibellus oblongus is a
straw-coloured spider with an elongated body, which lives among
dry grass and rushes. When alarmed it clings closely to a dry stem,
remains motionless, and escapes observation by its peculiarity of
colour and shape. Misumena vatia, another of the Thomisidae or
Crab-spiders, approximates in colour to the flowers in which it is
accustomed to lurk on the watch for prey. It is of a variable hue,
generally yellow or pink, and some observers believe that they have
seen it gently waving its anterior legs in a way which made them
easily mistaken for the stamens of the flower stirred by the breeze.
Its purpose appears to be to deceive, not its enemies, but its victims.
It seems to be partial to the blooms of the great mullein (Verbascum
thapsus), and Pickard-Cambridge has more than once seen it seize
and overcome a bee which had visited the flower in search of honey.
He has also observed it in the blossoms of rose and furze bushes.[295]
An Epeirid (Tetragnatha extensa) resembles Tibellus in its
method of concealing itself when alarmed. It also possesses an
elongated abdomen, of a grey-green tint, which it closely applies to
one of the twigs among which it has stretched its net, at the same
time extending its four long anterior legs straight before it, and in
this position it lies perdu, and is very easily overlooked. Another
Orb-weaver, Epeira cucurbitina, is of an apple-green colour, which is
admirably calculated to conceal it among the leaves which surround
its snare.
Most of our English Attidae, or Jumping-spiders, imitate closely
the prevailing tone of the surfaces on which they are accustomed to
hunt. This will be recognised in the familiar striped Wall-spider,
Salticus scenicus, and we may also mention the grey Attus
pubescens, which affects stone walls, and the speckled Attus saltator,
which is hardly distinguishable from the sand which it searches for
food.
Examples may also be found among the Lycosidae or Wolf-spiders.
Of the prettily variegated Lycosa picta, Pickard-Cambridge says:
“Much variation exists in the extent of the different portions of the
pattern and in their depth of colouring, these often taking their
prevailing tint from the colour of the soil in which the spider is
found. The best marked, richest coloured, and largest examples are
found on sandy and gravelly heaths, where there is considerable
depth and variety of colouring.... But on the uniformly tinted greyish-
yellow sandhills between Poole and Christchurch I have found a
dwarf, pale yellow-brown variety, with scarcely any dark markings on
it at all, the legs being of a uniform hue, and wholly destitute of dark
annuli.”[296]
Mimicry.—In the island of Portland, a locality remarkable for the
number of species peculiar to itself, there is found a spider, Micaria
scintillans, very closely resembling a large blackish ant which
frequents the same neighbourhood. Its movements, moreover, are
exceedingly ant-like, as it hurries along in a zigzag course, frequently
running up and down grass stems after the manner of those insects.
It is a great lover of sunshine, and disappears as soon as the sun is
obscured by a passing cloud.
Such resemblances, obvious enough in nature, and heightened by
the behaviour of the mimetic form, are often by no means striking in
the cabinet. In some American species of spiders, however, imitation
of the ant has passed beyond the stage of a general resemblance as
regards size and colour and method of progression. The head of the
ant is well marked off from the body, and the thorax is frequently
divided into distinct regions. These peculiarities are imitated by
constrictions in the cephalothorax of mimetic spiders. The
resemblance, moreover, is much increased by their habit of using but
six legs for locomotion, and carrying the second pair as ants do their
antennae. The best known examples of these spiders are Synageles
picata and Synemosyna formica (see Fig. 215, C, p. 420), and even
more striking resemblances have been observed among some
undescribed South American species.
The object of such mimicry seems to vary in different cases.
Sometimes the spider preys upon the ant which it resembles.
Sometimes, again, by its disguise, it escapes the notice of the ant
which would otherwise feed upon it. More often spider and ant are
neutral as regards each other, but, under cover of its resemblance,
the Arachnid is enabled to approach an unsuspecting victim to which
the ant is not a terror. Again, the unpleasantly acid taste of ants is
unpalatable to most birds, though not to all, and the increased
danger from specially ant-eating birds may be more than
counterbalanced by the immunity they acquire from other birds.
There is quite a large class of Spiders of nocturnal habits, whose
only precaution by day is to sit perfectly still and be mistaken for
something else. We have referred to the adaptation in colour of our
English species, Misumena vatia, to the flowers in which it lies in
wait for prey. Bates[297] mentions exotic examples of the same family
which mimic flower-buds in the axils of leaves. Herbert Smith says of
a spider which sits upon a leaf waiting for prey: “The pink three-
lobed body appears just like a withered flower that might have fallen
from the tree above; to the flies, no doubt, the deception is increased
by the strong sweet odour, like jasmine.”
Trimen[298] describes a Cape Town species which is of the exact
rose-red of the flower of the oleander. “To more effectually conceal it,
the palpi, top of the cephalothorax, and four lateral stripes on the
abdomen are white, according remarkably with the irregular white
markings so frequent on the petals of Nerium.”
The same observer, approaching a bush of the yellow-flowered
Senecio pubigera, noticed that two of the numerous butterflies
settled upon it did not fly away with their companions. Each of these
he found to be in the clutches of a spider, whose remarkable
resemblance to the flower lay not only in its colour, but in the
attitude it assumed. “Holding on to the flower-stalk by the two
hinder pairs of legs, it extended the two long front pairs upward and
laterally. In this position it was scarcely possible to believe that it was
not a flower seen in profile, the rounded abdomen representing the
central mass of florets, and the extended legs the ray florets; while, to
complete the illusion, the femora of the front pair of legs, adpressed
to the thorax, have each a longitudinal red stripe which represents
the ferruginous stripe on the sepals of the flower.”
Cambridge found in Palestine some species of Thomisidae which,
when at rest, were indistinguishable from bits of coarse fleecy wool,
or the rough seeds of some plant.
There is perhaps no more curious case of mimicry than that of a
spider, Phrynarachne (= Ornithoscatoides) decipiens, which Forbes
discovered in Java while butterfly-hunting. It appears that butterflies
of the Family Hesperidae have a custom of settling, for reasons best
known to themselves, upon the excreta of birds, dropped upon a leaf.
Forbes noticed one in this position. Creeping up, he seized the
butterfly, but found it mysteriously glued by the feet. On further
investigation the “excreta” proved to be a spider. So accurate was the
mimicry that he was again completely deceived by the same species
in Sumatra. Its habit is to weave upon a leaf a small white patch of
web, of a shape which greatly assists the deception, and in the midst
of this it lies on its back, holding on by the spines with which its legs
are furnished. It then folds its legs over its thorax, and waits for some
insect to settle upon it.
In rare cases spiders have come to resemble their enemies the
Ichneumon flies. A frequent habit of these insects is to deposit their
eggs in the newly-formed cocoon of the spider. The Ichneumon eggs
are the first to hatch, and the larvae have a convenient food-supply at
hand. Sometimes, however, they adopt another method, and insert
their eggs into the body of the spider itself. It is probably in order to
avoid this unpleasant contingency that the spider has evinced
towards the Ichneumon the sincerest form of flattery.