International Perspectives On Violence Risk Assessment 1st Edition Bjørkly Instant Download
International Perspectives On Violence Risk Assessment 1st Edition Bjørkly Instant Download
https://ebookname.com/product/international-perspectives-on-
violence-risk-assessment-1st-edition-bjorkly/
Get the full ebook with Bonus Features for a Better Reading Experience on ebookname.com
Instant digital products (PDF, ePub, MOBI) available
Download now and explore formats that suit you...
https://ebookname.com/product/handbook-of-violence-risk-
assessment-2nd-edition-kevin-douglas/
https://ebookname.com/product/the-feeling-of-risk-new-
perspectives-on-risk-perception-1st-edition-paul-slovic/
https://ebookname.com/product/rethinking-risk-assessment-the-
macarthur-study-of-mental-disorder-and-violence-1st-edition-john-
monahan/
https://ebookname.com/product/the-last-male-bastion-gender-and-
the-ceo-suite-in-america-s-public-companies-1st-edition-douglas-
m-branson/
Cellulite Pathophysiology and Treatment 1st Edition
Mitchel P. Goldman
https://ebookname.com/product/cellulite-pathophysiology-and-
treatment-1st-edition-mitchel-p-goldman/
https://ebookname.com/product/early-modern-english-news-
discourse-newspapers-pamphlets-and-scientific-news-discourse-1st-
edition-andreas-h-jucker-ed/
https://ebookname.com/product/amorphous-semiconductors-kugler/
https://ebookname.com/product/how-to-create-and-manage-a-hedge-
fund-a-professional-s-guide-1st-edition-stuart-a-mccrary/
https://ebookname.com/product/the-business-meetings-
sourcebook-1st-edition-eli-mina/
Roman Villas in Central Italy A Social and Economic
History Annalisa Marzano
https://ebookname.com/product/roman-villas-in-central-italy-a-
social-and-economic-history-annalisa-marzano/
International Perspectives on Violence Risk Assessment
American Psychology–Law Society Series
Series Editor The Miranda Ruling: Its Past, Present,
Patricia A. Zapf and Future
Editorial Board Lawrence S. Wrightsman
Gail S. Goodman and Mary L. Pitman
Thomas Grisso Juveniles at Risk: A Plea
Craig Haney for Preventive Justice
Kirk Heilbrun Christopher Slobogin
John Monahan and Mark R. Fondacaro
Marlene Moretti The Ethics of Total Confinement
Edward P. Mulvey Bruce A. Arrigo, Heather Y. Bersot,
J. Don Read and Brian G. Sellers
N. Dickon Reppucci
Ronald Roesch International Human Rights and Mental
Gary L. Wells Disability Law
Lawrence S. Wrightsman Michael L. Perlin
Adolescents, Media, and the Law Murder in the Courtroom: The Cognitive
Roger J.R. Levesque Neuroscience of Extreme Violent
Behavior
Oral Arguments Before Brigitte Vallabhajosula
the Supreme Court
Lawrence S. Wrightsman Rational Suicide, Irrational
Laws: Examining Current Approaches
God in the Courtroom to Suicide in Policy and Law
Brian H. Bornstein and Monica K. Miller Susan Stefan
Expert Testimony on the Psychology International Perspectives on Violence
of Eyewitness Identification Risk Assessment
Edited by Brian L. Cutler Edited by Jay P. Singh, Stål Bjørkly,
The Psychology of Judicial and Seena Fazel
Decision-Making
Edited by David Klein
and Gregory Mitchell
International Perspectives
on Violence Risk Assessment
Edited by
Jay P. Singh
Stål Bjørkly
Seena Fazel
1
1
Oxford University Press is a department of the University of Oxford. It furthers
the University’s objective of excellence in research, scholarship, and education
by publishing worldwide. Oxford is a registered trade mark of Oxford University
Press in the UK and certain other countries.
9╇8╇7╇6╇5╇4╇3╇2╇1
Series Foreword xi
Acknowledgments xiii
About the Editors xv
Contributors xvii
Index 373
Series Foreword
xi
xii Series Foreword
Patricia A. Zapf
Series Editor
Acknowledgments
xiii
About the Editors
xv
Contributors
xvii
xviii Contributors
Adam J. E. Blanchard, MA
Department of Psychology
Simon Fraser University
Burnaby, BC, Canada
Seena Fazel, MD
Department of Psychiatry
University of Oxford
Oxford, UK
Meghann Galloway, MS
Department of Psychology
Drexel University
Philadelphia, PA, USA
Natascha Leech, MA
BC Mental Health and Substance Use Services
Forensic Psychiatric Services Commission
Vancouver, Canada
Doron Menashe, JD
Faculty of Law
University of Haifa
Haifa, Israel
Rebecca Newsham, MA
Department of Psychology
Drexel University
Philadelphia, PA, USA
Unnati Patel, BS
Department of Psychology
Drexel University
Philadelphia, PA, USA
John Petrila, JD
Department of Health and Policy Management
University of South Florida
Tampa, FL, USA
Victoria Pietruszka, BA
Department of Psychology
Drexel University
Philadelphia, PA, USA
Kim A. Reeves, MA
Department of Psychology
Simon Fraser University
Burnaby, BC, Canada
Alberta Health Services
Edmonton, AB, Canada
Nicholas Scurich
3
Exploring the Variety of Random
Documents with Different Content
Doomed rivals 313 drive evolution in adaptive directions.
Their claim is simply that a lot of evolutionary change (as a
molecular geneticist sees evolutionary change) is not adaptive.
Dover makes no such modest claims for his theory. He thinks that he
can explain all of evolution without natural selection, although he
generously concedes that there may be some truth in natural
selection as well! Throughout this book, our first recourse when
considering such matters has been to the example of the eye,
although it has, of course, been only a representative of the large
set of organs that are too complex and well designed to have come
about by chance. Only natural selection, I have repeatedly argued,
even comes close to offering a plausible explanation for the human
eye and comparable organs of extreme perfection and complexity.
Fortunately, Dover has explicitly risen to the challenge, and has
offered his own explanation of the evolution of the eye. Assume, he
says, that 1,000 steps of evolution are needed to evolve the eye
from nothing. This means that a sequence of 1,000 genetic changes
were needed to transform a bare patch of skin into an eye. This
seems to me to be an acceptable assumption for the sake of
argument. In the terms of Biomorph Land, it means that the bare-
skin animal is 1,000 genetic steps distant from the eyed animal.
Now, how do we account for the fact that just the right set of 1,000
steps were taken to result in the eye as we know it? Natural
selection's explanation is well known. Reducing it to its simplest
form, at each one of the 1,000 steps, mutation offered a number of
alternatives, only one of which was favoured because it aided
survival. The 1,000 steps of evolution represent 1,000 successive
choice points, at each of which most of the alternatives led to death.
The adaptive complexity of the modern eye is the end-product of
1,000 successful unconscious 'choices'. The species has followed a
particular path through the labyrinth of all possibilities. There were
1,000 branch-points along the path, and at each one the survivors
were the ones that happened to take the turning that led to
improved eyesight. The wayside is littered with the dead bodies of
the failures who took the wrong turning at each one of the 1,000
successive choice points. The eye that we know is the end-product
of a sequence of 1,000 successful selective 'choices'. That was (one
way of expressing) natural selection's explanation of the evolution of
the eye in 1,000 steps. Now, what of Dover's explanation? Basically,
he argues that it wouldn't have mattered which choice the lineage
took at each step: it would retrospectively have found a use for the
organ that resulted. Each step that the lineage took, according to
him, was a random step. At Step 1, for example, a random mutation
spread through the species. Since the newly evolved charac
314 The Blind Watchmaker teristic was functionally random,
it didn't aid the animals' survival. So the species searched the world
for a new place or new way of life in which they could use this new
random feature that had been imposed upon their bodies. Having
found a piece of environment that suited the random part of their
bodies, they lived there for a while, until a new random mutation
arose and spread through the species. Now the species had to scour
the world for a new place or way of life where they could live with
their new random bit. When they found it, Step 2 was completed.
Now the Step 3 random mutation spread through the species, and
so on for 1,000 steps, at the end of which the eye as we know it had
been formed. Dover points out that the human eye happens to use
what we call 'visible' light rather than infrared. But if random
processes had happened to impose an infrared sensitive eye upon
us, we would, doubtless, have made the most of it, and found a way
of life that exploited infrared rays to the full. At first glance this idea
has a certain seductive plausibility, but only at a very brief first
glance. The seductiveness comes from the neatly symmetrical way in
which natural selection is turned on its head. Natural selection, in its
most simple form, assumes that the environment is imposed upon
the species, and those genetic variants best fitted to that
environment survive. The environment is imposed, and the species
evolves to fit it. Dover's theory turns this on its head. It is the nature
of the species that is 'imposed', in this case by the vicissitudes of
mutation, and other internal genetic forces in which he has a special
interest. The species then locates that member of the set of all
environments that best fits its imposed nature. But the
seductiveness of the symmetry is superficial indeed. The wondrous
cloud-cuckooism of Dover's idea is displayed in all its glory the
moment we begin to think in terms of numbers. The essence of his
scheme is that, at each of the 1,000 steps, it didn't matter which
way the species turned. Each new innovation that the species came
up with was functionally random, and the species then found an
environment to suit it. The implication is that the species would have
found a suitable environment, no matter which branch it had taken
at every fork in the way. Now just think how many possible
environments this lets us in for postulating. There were 1,000
branch points. If each branch point was a mere bifurcation (as
opposed to a 3-way or 18-way branch, a conservative assumption),
the total number of livable environments that must, in principle,
exist, in order to allow Dover's scheme to work, is 2 to the power
1,000 (the first branch gives two pathways; then each of those
branches into two, making four in all; then each of these branches,
giving 8; then 16, 32, 64, . . . all the way
Doomed rivals 315 to 21,000). This number may be written
as a 1 with 301 noughts after it. It is far far greater than the total
number of atoms in the entire universe. Dover's alleged rival to
natural selection could never work, not just never in a million years
but never in a million times longer than the universe has existed,
never in a million universes each lasting a million times as long
again. Notice that this conclusion is not materially affected if we
change Dover's initial assumption that 1,000 steps would be needed
to make an eye. If we reduce it to only 100 steps, which is probably
an underestimate, we still conclude that the set of possible livable
environments that must be waiting in the wings, as it were, to cope
with whatever random steps the lineage might take, is more than a
million million million million million. This is a smaller number than
the previous one, but it still means that the vast majority of Dover's
'environments' waiting in the wings would each have to be made of
less than a single atom. It is worth explaining why the theory of
natural selection is not susceptible to a symmetrical destruction by a
version of the 'largenumbers argument'. In Chapter 3 we thought of
all real and conceivable animals as sitting in a gigantic hyperspace.
We are doing a similar thing here, but simplifying it by considering
evolutionary branch points as 2-way, rather than 18-way branches.
So the set of all possible animals that might have evolved in 1,000
evolutionary steps are perched on a gigantic tree, which branches
and branches so that the total number of final twigs is 1 followed by
301 noughts. Any actual evolutionary history can be represented as
a particular pathway through this hypothetical tree. Of all
conceivable evolutionary pathways, only a minority actually ever
happened. We can think of most of this 'tree of all possible animals'
as hidden in the darkness of non-existence. Here and there, a few
trajectories through the darkened tree are illuminated. These are the
evolutionary pathways that actually happened, and, numerous as
these illuminated branches are, they are still an infinitesimal minority
of the set of all branches. Natural selection is a process that is
capable of picking its way through the tree of all conceivable
animals, and finding just that minority of pathways that are viable.
The theory of natural selection cannot be attacked by the kind of
large-numbers argument with which I attacked Dover's theory,
because it is of the essence of the theory of natural selection that it
is continually cutting down most of the branches of the tree. That is
precisely what natural selection does. It picks its way, step by step,
through the tree of all conceivable animals, avoiding the almost
infinitely large majority of sterile branches - animals with eyes
316 The Blind Watchmaker in the soles of their feet, etc. -
which the Dover theory is obliged, by the nature of its peculiar
inverted logic, to countenance. We have dealt with all the alleged
alternatives to the theory of natural selection except the oldest one.
This is the theory that life was created, or its evolution master-
minded, by a conscious designer. It would obviously be unfairly easy
to demolish some particular version of this theory such as the one
(or it may be two) spelled out in Genesis. Nearly all peoples have
developed their own creation myth, and the Genesis story is just the
one that happened to have been adopted by one particular tribe of
Middle Eastern herders. It has no more special status than the belief
of a particular West African tribe that the world was created from
the excrement of ants. All these myths have in common that they
depend upon the deliberate intentions of some kind of supernatural
being. At first sight there is an important distinction to be made
between what might be called 'instantaneous creation' and 'guided
evolution'. Modern theologians of any sophistication have given up
believing in instantaneous creation. The evidence for some sort of
evolution has become too overwhelming. But many theologians who
call themselves evolutionists, for instance the Bishop of Birmingham
quoted in Chapter 2, smuggle God in by the back door: they allow
him some sort of supervisory role over the course that evolution has
taken, either influencing key moments in evolutionary history
(especially, of course, human evolutionary history), or even meddling
more comprehensively in the day-to-day events that add up to
evolutionary change. We cannot disprove beliefs like these,
especially if it is assumed that God took care that his interventions
always closely mimicked what would be expected from evolution by
natural selection. All that we can say about such beliefs is, firstly,
that they are superfluous and, secondly, that they assume the
existence of the main thing we want to explain, namely organized
complexity. The one thing that makes evolution such a neat theory is
that it explains how organized complexity can arise out of primeval
simplicity. If we want to postulate a deity capable of engineering all
the organized complexity in the world, either instantaneously or by
guiding evolution, that deity must already have been vastly complex
in the first place. The creationist, whether a naive Bible-thumper or
an educated bishop, simply postulates an already existing being of
prodigious intelligence and complexity. If we are going to allow
ourselves the luxury of postulating organized complexity without
offering an explanation, we might as well make a job of it and simply
postulate the existence of life as we know it! In short, divine
creation, whether
Doomed rivals 317 instantaneous or in the form of guided
evolution, joins the list of other theories we have considered in this
chapter. All give some superficial appearance of being alternatives to
Darwinism, whose merits might be tested by an appeal to evidence.
All turn out, on closer inspection, not to be rivals of Darwinism at all.
The theory of evolution by cumulative natural selection is the only
theory we know of that is in principle capable of explaining the
existence of organized complexity. Even if the evidence did not
favour it, it would still be the best theory available! In fact the
evidence does favour it. But that is another story. Let us hear the
conclusion of the whole matter. The essence of life is statistical
improbability on a colossal scale. Whatever is the explanation for life,
therefore, it cannot be chance. The true explanation for the
existence of life must embody the very antithesis of chance. The
antithesis of chance is nonrandom survival, properly understood.
Nonrandom survival, improperly understood, is not the antithesis of
chance, it is chance itself. There is a continuum connecting these
two extremes, and it is the continuum from single-step selection to
cumulative selection. Single-step selection is just another way of
saying pure chance. This is what I mean by nonrandom survival
improperly understood. Cumulative selection, by slow and gradual
degrees, is the explanation, the only workable explanation that has
ever been proposed, for the existence of life's complex design. The
whole book has been dominated by the idea of chance, by the
astronomically long odds against the spontaneous arising of order,
complexity and apparent design. We have sought a way of taming
chance, of drawing its fangs. 'Untamed chance', pure, naked chance,
means ordered design springing into existence from nothing, in a
single leap. It would be untamed chance if once there was no eye,
and then, suddenly, in the twinkling of a generation, an eye
appeared, fully fashioned, perfect and whole. This is possible, but
the odds against it will keep us busy writing noughts till the end of
time. The same applies to the odds against the spontaneous
existence of any fully fashioned, perfect and whole beings, including
- I see no way of avoiding the conclusion - deities. To 'tame' chance
means to break down the very improbable into less improbable small
components arranged in series. No matter how improbable it is that
an X could have arisen from a Y in a single step, it is always possible
to conceive of a series of infinitesimally graded intermediates
between them. However improbable a large-scale change may be,
smaller changes are less improbable. And provided we postulate a
sufficiently large series of sufficiently finely graded intermediates, we
shall be able to derive anything from anything else,
318 The Blind Watchmaker without invoking astronomical
improbabilities. We are allowed to do this only if there has been
sufficient time to fit all the intermediates in. And also only if there is
a mechanism for guiding each step in some particular direction,
otherwise the sequence of steps will career off in an endless random
walk. It is the contention of the Darwinian world-view that both
these provisos are met, and that slow, gradual, cumulative natural
selection is the ultimate explanation for our existence. If there are
versions of the evolution theory that deny slow gradualism, and deny
the central role of natural selection, they may be true in particular
cases. But they cannot be the whole truth, for they deny the very
heart of the evolution theory, which gives it the power to dissolve
astronomical improbabilities and explain prodigies of apparent
miracle.
Bibliography 1 . Alberts, B., Bray, D., Lewis, J., Raff, M.,
Roberts, K. & Watson, J. D. ( 1983) Molecular Biology of the Cell.
New York: Garland. 2. Anderson, D. M. (1981) Role of interfacial
water and water in thin films in the origin of life. In J. Billingham
(ed.) Life in the Universe. Cambridge, Mass: MIT Press. 3.
Andersson, M. (1982) Female choice selects for extreme tail length
in a widow bird. Nature, 299: 818-20. 4. Arnold, S. J. (1983) Sexual
selection: the interface of theory and empiricism. In P. P. G. Bateson
(ed.), Mate Choice, pp. 67-107. Cambridge: Cambridge University
Press. 5. Asimov, I. (1957) Only a Trillion. London: Abclard-
Schuman. 6. Asimov, I. (1980) Extraterrestrial Civilizations. London:
Pan. 7. Asimov, I. (1981) In the Beginning. London: New English
Library. 8. Atkins, P. W. (1981) The Creation. Oxford: W. H. Freeman.
9. Attenborough, D. (1980) Life on Earth. London: Reader's Digest,
Collins & BBC. 10. Barker, E. (1985) Let there be light: scientific
creationism in the twentieth century. In J. R. Durant (ed.) Darwinism
and Divinity, pp. 189-204. Oxford: Basil Blackwell. 11. Bowler, P. f.
(1984) Evolution: the history of an idea. Berkeley: University of
California Press. 12. Bowles, K. L. (1977) Problem-Solving using
Pascal. Berlin: SpringerVerlag. 321
322 Bibliography 13. Caims-Smith, A. G. (1982) Genetic
Takeover. Cambridge: Cambridge University Press. 14. Caims-Smith,
A. G. (1985) Seven Clues to the Origin of Life. Cambridge:
Cambridge University Press. 15. Cavalli-Sforza, L. & Feldman, M.
(1981) Cultural Transmission and Evolution. Princeton, N. ].:
Princeton University Press. 16. Cott, H. B. (1940) Adaptive Coloration
in Animals. London: Methuen. 17. Crick, F. (1981) Life Itself. London:
Macdonald. 18. Darwin, C. (1859) The Origin of Species. Reprinted.
London: Penguin. 19. Dawkins, M. S. (1986) Unravelling Animal
Behaviour. London: Longman. 20. Dawkins, R. (1976) The Selfish
Gene. Oxford: Oxford University Press. 21 . Dawkins, R. ( 1982) The
Extended Phenotype. Oxford: Oxford University Press. 22. Dawkins,
R. (1982) Universal Darwinism. In D. S. Bendall (ed.) Evolution from
Molecules to Men, pp. 403-25. Cambridge: Cambridge University
Press. 23. Dawkins, R. & Krebs, J. R. (1979) Arms races between
and within species. Proceedings of the Royal Society of London, B,
205: 489-511. 24. Douglas, A. M. (1986) Tigers in Western Australia.
New Scientist, 110 (1505): 44-7. 25. Dover, G. A. (1984) Improbable
adaptations and Maynard Smith's dilemma. Unpublished manuscript,
and two public lectures, Oxford, 1984. 26. Dyson, F. (1985) Origins
of Life. Cambridge: Cambridge University Press. 27. Eigen, M.,
Gardiner, W., Schuster, P., & Winkler-Oswatitsch. (1981 ) The origin
of genetic information. Scientific American, 244 (4): 88-118. 28.
Eisner, T. (1982) Spray aiming in bombardier beetles: jet deflection
by the Coander Effect. Science, 215: 83-5. 29. Eldredge, N. (1985)
Time Frames: the rethinking of Darwinian evolution and the theory
of punctuated equilibria. New York: Simon & Schuster (includes
reprinting of original Eldredge & Gould paper). 30. Eldredge, N.
(1985) Unfinished Synthesis: biological hierarchies and modern
evolutionary thought. New York: Oxford University Press. 31. Fisher,
R. A. (1930) The Genetical Theory of Natural Selection. Oxford:
Clarendon Press. 2nd edn paperback. New York: Dover Publications.
Bibliography 323 32. Gillespie, N. C. (197 9) Charles Darwin
and the Problem of Creation. Chicago: University of Chicago Press.
33. Goldschmidt, R. B. (1945) Mimetic polymorphism, a controversial
chapter of Darwinism. Quarterly Review of Biology, 20: 147-64 and
205-30. 34. Gould, S. J. (1980) The Panda's Thumb. New York: W.
W. Norton. 35. Gould, S. J. (1980) Is a new and general theory of
evolution emerging? Paleobiology, 6: 119-30. 36. Gould, S. J. (1982)
The meaning of punctuated equilibrium, and its role in validating a
hierarchical approach to macroevolution. In R. Milkman (ed.)
Perspectives on Evolution, pp. 83-104. Sunderland, Mass: Sinauer.
37. Gribbin, J. &. Cherfas, J. (1982) The Monkey Puzzle. London:
Bodley Head. 38. Griffin, D. R. (1958) Listening in the Dark. New
Haven: Yale University Press. 39. Hallam, A. (1973) A Revolution in
the Earth Sciences. Oxford: Oxford University Press. 40. Hamilton,
W. D. & Zuk, M. (1982) Heritable true fitness and bright birds: a role
for parasites? Science, 218: 384-7. 41. Hitching, F. (1982) The Neck
of the Giraffe, or Where Darwin Went Wrong. London: Pan. 42. Ho,
M-W. & Saunders, P. (1984) Beyond Neo-Darwinism. London:
Academic Press. 43. Hoyle, F. & Wickramasinghe, N. C. (1981)
Evolution from Space. London: J. M. Dent. 44. Hull, D. L. (1973)
Darwin and his Critics. Chicago: Chicago University Press. 45. Jacob,
F. (1982) The Possible and the Actual. New York: Pantheon. 46.
Jenson, H. J. (1985) Issues in brain evolution. In R. Dawkins &. M.
Ridley (eds) Oxford Surveys in Evolutionary Biology, 2: 102-34. 47.
Kimura, M. (1982) The Neutral Theory of Molecular Evolution.
Cambridge: Cambridge University Press. 48. Kitcher. P. (1983)
Abusing Science: the case against creationism. Milton Keynes: Open
University Press. 49. Land, M. F. (1980) Optics and vision in
invertebrates. In H. Autrum (ed.) Handbook of Sensory Physiology,
pp. 471-592. Berlin: Springer.
324 Bibliography 50. Lande, R. (1980) Sexual dimorphism,
sexual selection, and adaptation in polygenic characters. Evolution,
34: 292-305. 51. Lande, R. (1981) Models of speciation by sexual
selection of polygenic traits. Proceedings of the National Academy of
Sciences, 78: 3721-5. 52. Leigh, E. G. (1977) How does selection
reconcile individual advantage with the good of the group?
Proceedings of the National Academy of Sciences, 74: 4542-6. 53.
Lewontin, R. C. & Levins, R. (1976) The Problem of Lysenkoism. In
H. & S. Rose (eds) The Radicalization of Science. London: Macmillan.
54. Mackie, J. L. (1982) The Miracle of Theism. Oxford: Clarendon
Press. 55. Margulis, L. (1981) Symbiosis in Cell Evolution. San
Francisco: W. H. Freeman. 56. Maynard Smith, J. (1983) Current
controversies in evolutionary biology. In M. Grene (ed.) Dimensions
of Darwinism, pp. 273-86. Cambridge: Cambridge University Press.
57. Maynard Smith, J. (1986) The Problems of Biology. Oxford:
Oxford University Press. 58. Maynard Smith, J. et al. (1985)
Developmental constraints and evolution. Quarterly Review of
Biology, 60: 265-87. 59. Mayr, E. (1963) Animal Species and
Evolution. Cambridge, Mass: Harvard University Press. 60. Mayr, E.
(1969) Principles of Systematic Zoology. New York' McGraw-Hill. 61.
Mayr, E. (1982) The Growth of Biological Thought. Cambridge, Mass:
Harvard University Press. 62. Monod, J. (1972) Chance and
Necessity. London: Fontana. 63. Montefiore, H. (1985) The
Probability of God. London: SCM Press. 64. Morrison, P., Morrison, P.,
Eames, C. &. Eames, R. (1982) Powers of Ten. New York: Scientific
American. 65. Nagel, T. (1974) What is it like to be a bat?
Philosophical Review, reprinted in D. R. Hofstadter & D. C. Dennett
(eds). The Mind's I, pp. 391-403, Brighton: Harvester Press. 66.
Nelkin, D. (1976) The science textbook controversies. Scientific
American 234 (4): 33-9. 67. Nelson, G. &. Platnick, N. 1. (1984)
Systematics and evolution. In M-W Ho & P. Saunders (eds), Beyond
Neo-Darwinism. London: Academic Press.
Bibliography 325 68. O'Donald, P. (1983) Sexual selection
by female choice. In P. P. G. Bateson (ed.) Mate Choice, pp. 53-66.
Cambridge: Cambridge University Press. 69. Orgel, L. E. (1973) The
Origins of Life. New York: Wiley. 70. Orgel, L. E. (1979) Selection in
vitro. Proceedings of the Royal Society of London, B, 205: 435^-2.
71. Paley, W. (1828) Natural Theology, 2nd edn. Oxford: J. Vincent.
72. Penney, D., Foulds, L. R. & Hendy, M. D. (1982) Testing the
theory of evolution by comparing phylogenetic trees constructed
from five different protein sequences. Nature, 297: 197-200. 73.
Ridley, M. (1982) Coadaptation and the inadequacy of natural
selection. British Journal for the History of Science, 15: 45-68. 74.
Ridley, M. (1986) The Problems of Evolution. Oxford: Oxford
University Press. 75. Ridley, M. (1986) Evolution and Classification:
the reformation of cladism. London: Longman. 76. Ruse, M. (1982)
Darwinism Defended. London: Addison-Wesley. 77. Sales, G. &. Pye,
D. (1974) Ultrasonic Communication by Animals. London: Chapman
& Hall. 78. Simpson, G. G. (1980) Splendid Isolation. New Haven:
Yale University Press. 79. Singer, P. (1976) Animal Liberation.
London: Cape. 80. Smith, J. L. B. (1956) Old Fourlegs: the story of
the Coelacanth. London: Longmans, Green. 81. Sneath, P. H. A. &
Sokal, R. R. (1973) Numerical Taxonomy. San Francisco: W. H.
Freeman. 82. Spiegelman, S. (1967) An in vitro analysis of a
replicating molecule. American Scientist, 55: 63-8. 83. Stebbins, G.
L. (1982) Darwin to DNA, Molecules to Humanity. San Francisco: W.
H. Freeman. 84. Thompson, S. P. (1910) Calculus Made Easy.
London: Macmillan. 85. Trivers, R. L. (1985) Social Evolution. Menlo
Park: BenjaminCummings. 86. Turner, J. R. G. (1983) 'The
hypothesis that explains mimetic resemblance explains evolution':
the gradualist-saltationist schism. In M. Grene (ed.) Dimensions of
Darwinism, pp. 129-69. Cambridge: Cambridge University Press.
326 Bibliography 87. Van Valen, L. (1973) A new
evolutionary law. Evolutionary Theory, 1: 1-30. 88. Watson, J. D.
(1976) Molecular Biology of the Gene. Menlo Park: Benjamin-
Cummings. 89. Williams, G. C. (1966) Adaptation and Natural
Selection. New Jersey: Princeton University Press. 90. Wilson, E. O.
(1971) The Insect Societies. Cambridge, Mass: Harvard University
Press. 91. Wilson, E. O. (1984) Biophilia. Cambridge, Mass: Harvard
University Press 92. Young, J. Z. (1950) The Life of Vertebrates.
Oxford: Clarendon Press.
Index and key to Bibliography This book is meant to be
read from cover to cover. It is not a work of reference. Many items in
the index will mean something only to people that have already read
the book and want to find a particular place again. In such a book,
footnotes are an irritating distraction. The following index, in
addition to performing the normal function of an index, is intended
to replace footnotes by acting as a key to the bibliography. The
numbers in brackets refer to the numbered books or articles in the
bibliography. Other numbers refer to pages in the book. Where an
indexed word recurs on a consecutive series of pages, normally only
the first page, or the page where a definition will be found, is given.
Acquired characteristics, inheritance of, 290,299,(22) Adaptation, 9,
178, 288, (19, 89) Addressing, memory and genes, 1 1 7 Aesop,
191,(21) Altruism, 267, (20, 52) Ambulance Effect, 29 Amniotes,
258, (92) Amoeba, 116,249 Amplifier analogy, 251 Anderson, D. M.,
157,(2) Andersson, M., 213, (3) Angel wings, 309 Anteaters, 105
Antennapaedia, 230 Ants, 106-9, (90) in Panama, 108,195
Archaeopteryx, 262 Archives, DNA, 122 fidelity of, 123 Argument
from Design, 4, 6, (71) from Personal Incredulity, 38, (63) Argyll,
Duke of, 248, (73) Arms race, 178,(21,23) between sexes, 178,185,
(85) cyclical, 213 economic end to, 190 Asdic, 23 Asimov, I., 44-5,
(5) Atkins, P.W., 14,(8) Australian fauna, 100, (78) Australopithecus,
228,231 Bacteria, 116,130,176 Baghdad, walk to, 40 Bateson, W.,
305, (quoted in 22) Bats, 21-37, (38,77) conference of, 35 detector,
25 diversity of, 23 Doppler sensitivity of, 31 ear muscles, 27
economics, 25 frequency modulated cries, 29 327
328 Index lack of angel wings, 309 problems of, 26, 28, 32,
{ 1 9) subjective experience of, 33 Bear, polar, 38, (63) Beaver, 135,
(21) Bee-flower, 61,63 Beetle, bombardier, 86-7, (28) Bennet, G., 39,
(quoted in 63) Bestsellers, 219 Biblical Creation, 251, (quoted in 10)
Biochemical pathway, 171 Biomorphs, 55, 234, 311 Birds,
echolocation by, 95 Birmingham, Bishop of, 37—41, 316, (63)
Blacksmith, 290 Blueprint, theory of embryology, 294 Boeing 747,
random assembly, 7, 234, 248 (43) Brain, evolution of, 188, 215,
228, (46) Caims-Smith, A. G., 148-65, (13, 14) Calluses, 298 Cake,
analogy for development, 297 Carrier frequency, 28 Cataract, 81
Catastrophism, 241 Cheetah, 180 Chemists, 144 Chess, 65
Chimpanzee, 118,263 Chirp radar, 28 Choice discrepancy, 208
Cicadas, periodical, 99-100,(21) Clade, 259,279 Cladism, 258, 276-9,
(75) transformed, 279, 281 Classification, 255-84, (60, 75, 81)
arbitrariness of non-biological, 257 cladistic, 258, 276, (75)
molecular, 269, 274, (37, 72) numerical, 279,(81) 'traditional', 276,
(60) uniqueness of biological, 258, 269 Clay, 150,(13,14) 'power',
153 Clouds, 45, 49 Coadaptation, 169 Coelacanth, 246, (80)
Coincidence, 159, 274 Colour, hypothesis of bat sensation, 35
Combination lock, 7 Compact disc, 112,152 Complexity as
heterogeneity of form, 6 as statistical improbability, 7 but not with
hindsight, 7-8 Computer, explanation of, 12 biomorphs, 50 chess-
playing, 65 disc analogy, 173 games, 62 model, 63 typing
Shakespeare, 47 underestimated, 63, 158 value of, 74 Constant
speedism, 245, 263 Constraints on evolution, 308, (58) Constructive
evolution, 169 Continental drift, 100, (39) Convergence,
evolutionary, 94, (92) by RNA in test-tubes, 133, (27) Copernicus,
252 Costs and benefits, 26,190 Cott, H.B., 188,(16) Covenant, Ark of
the, 109 Creationism, 230, 24 1 , 25 1 , 283, 3 1 6, (10,48,66,76)
smuggled into evolution, 248, 3 1 6 Creator, 14,141,316 Cromwell,
O., 228 Crystal, 150 Cuckoo, 40 Cultural evolution, 216 Cumulative
selection, 45 DC8, stretched, 234, (22) DNA, information technology,
1 1 1-36, (1,57,88) as ROM, 117 computer disc analogy, 1 73
conservatism, 124 origin, 140, 157 selfish, 116,(20,21) Dam beaver,
136,(21) clay, 154 Darwin, C., 3, 305, (11,18,32) and Argument from
Welcome to our website – the ideal destination for book lovers and
knowledge seekers. With a mission to inspire endlessly, we offer a
vast collection of books, ranging from classic literary works to
specialized publications, self-development books, and children's
literature. Each book is a new journey of discovery, expanding
knowledge and enriching the soul of the reade
Our website is not just a platform for buying books, but a bridge
connecting readers to the timeless values of culture and wisdom. With
an elegant, user-friendly interface and an intelligent search system,
we are committed to providing a quick and convenient shopping
experience. Additionally, our special promotions and home delivery
services ensure that you save time and fully enjoy the joy of reading.
ebookname.com