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Introduction to quantum physics and information
processing 1st Edition Vathsan Digital Instant Download
Author(s): Vathsan, Radhika
ISBN(s): 9781482238129, 1482238128
Edition: 1
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Year: 2015
Language: english
Physics
w w w. c rc p r e s s . c o m
INTRODUCTION to
QUANTUM PHYSICS and
INFORMATION PROCESSING
INTRODUCTION to
QUANTUM PHYSICS and
INFORMATION PROCESSING
Radhika Vathsan
BITS Pilani K.K. Birla Goa Campus
India
CRC Press
Taylor & Francis Group
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Boca Raton, FL 33487-2742
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Preface ix
I Preliminaries 1
1 Introduction 3
1.1 Bits and Qubits . . . . . . . . . . . . . . . . . . . . . . . . . 6
1.2 Properties of Qubits . . . . . . . . . . . . . . . . . . . . . . . 9
1.3 Practical Considerations . . . . . . . . . . . . . . . . . . . . 11
1.4 References for Further Reading . . . . . . . . . . . . . . . . . 13
II Theoretical Framework 31
3 The Essentials of Quantum Mechanics 33
3.1 The State Space . . . . . . . . . . . . . . . . . . . . . . . . . 33
3.1.1 Basis states . . . . . . . . . . . . . . . . . . . . . . . . 36
3.1.2 Inner product . . . . . . . . . . . . . . . . . . . . . . . 37
3.1.2.1 Meaning of inner product . . . . . . . . . . . 39
3.1.3 Phases . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
v
vi Contents
3.2 Observables . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
3.2.1 Operators . . . . . . . . . . . . . . . . . . . . . . . . . 41
3.2.2 Self-adjoint operators . . . . . . . . . . . . . . . . . . 43
3.2.3 Basis transformation . . . . . . . . . . . . . . . . . . . 43
3.2.4 Outer product representation for operators . . . . . . 46
3.2.5 Functions of operators . . . . . . . . . . . . . . . . . . 48
3.3 Measurement . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
3.4 Evolution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
3.4.1 Continuous time evolution . . . . . . . . . . . . . . . . 55
3.4.1.1 Schrödinger viewpoint . . . . . . . . . . . . . 56
3.4.1.2 Heisenberg viewpoint . . . . . . . . . . . . . 56
3.5 Composite Systems . . . . . . . . . . . . . . . . . . . . . . . 57
4 Properties of Qubits 63
4.1 The Bloch Sphere Representation of a Qubit . . . . . . . . . 63
4.2 Cloning and Deleting . . . . . . . . . . . . . . . . . . . . . . 65
4.3 Distinguishability of Qubit States . . . . . . . . . . . . . . . 67
4.4 Entanglement . . . . . . . . . . . . . . . . . . . . . . . . . . 67
4.4.1 Quantum vs. classical correlations . . . . . . . . . . . 70
4.4.2 The EPR paradox . . . . . . . . . . . . . . . . . . . . 71
4.4.3 Bell’s inequalities and non-locality . . . . . . . . . . . 73
Bibliography 237
Index 243
Preface
ix
x Preface
Acknowledgments
A work of this nature is simply not possible without the inspiration, guid-
ance, help, and cooperation of numerous people. I would first like to dedicate
this book to the memory of Prof. Suresh Ramaswamy whose encouragement
was the inspiration to start on this project. Thanks are due to my faculty col-
leagues who provided guidance, to the many enthusiastic students who took
my course on quantum information and computation at the BITS Pilani Goa
Campus, which formed the base on which this book was built, and to the
kind cooperation of the Raman Research Institute, Bangalore, for extending
its hospitality during a sabbatical period in 2013 during which part of this
work was completed.
I would like to individually thank my students Aarthi Sundaram, Anu-
pam Mitra, Arunav Sanyal, Bharath Srivathsan, Mayank Jog, Milind Shyani,
Nisheeth Bandaru, Pratik Mallya, Shubhanshu Tiwari, Tarik Gupta, and
many others for vital class discussions that made me eagerly look forward
to the pleasure of their class, and for helping produce solutions to problems.
I’d like to thank my colleagues Andal Narayanan, Anu Venugopalan, Tabish
Qureshi, Joseph Samuel, Supurna Sinha, A. R. Usha Devi, Sumati Surya and
Urbasi Sinha, for stimulating discussions. Thanks are due to Dhavala Suri, a
graduate student in our department, for proofreading the material and offering
to help with the clarity and effectiveness of the delivery.
I am greatly indebted to the creators and improvers of the fantastic type-
setting environment of LATEX, which was one of the inducements for writing
this book! Referring to Leslie Lamport’s LATEX and Mittelbach and Goossen’s
Preface xi
The LATEXCompanion made designing the book layout great fun. The quan-
tum circuit diagrams in this book owe their neatness and ease of typesetting to
the wonderful LATEXpackage QCircuit designed by Steve Flammia and Bryan
Eastin. I owe a lot to the Inkscape vector graphics package for making the
illustrations a pleasure to design and draw.
I am indebted to the CRC team starting with my editor, Aastha Sharma,
for encouraging me to bring these notes out in book form, to the anonymous
referees for insightful comments, and to Karen Simon for the fine editing.
Finally, I owe much to my mother, who inculcated in me a sense of per-
fectionism, aesthetic sensibility, and a never-say-die attitude (and provided a
lot of training in copy editing!), my father who introduced me to Feynman’s
legendary lecture notes at a young age and spurred my dream of being a
theoretical physicist, my sister whose sense of humor and support carried me
through many dark moments, and of course to Kshipra who put up with my
many moods and late timings while amma’s book was being put together.
List of Figures
xiii
xiv List of Figures
xvii
List of Boxes
xix
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17. Uzel states that what is regarded as the ligula of Campodea is formed from
the sternite of the first maxillary segment; while the two parts regarded as
paraglossæ grow out from the sternite of the mandibular segment, and these three
structures together he regards as the hypopharynx. (Zool. Anzeiger, July 5, 1897, p.
234.)
18. See, also, Breithaupt, Ueber die Anatomie und die Functionen der
Bienenzunge, 1886. It confirms and extends Cheshire’s work.
22. In his account of his studies on the locomotion of insects, De Moor states
that he obtained the track of each of the feet in different colors by coating them
with different pigments; the insect, as it moved, left its track on a strip of paper.
(Archives de Biologie, Liège, 1890.)
23. Carlet and also De Moor (1890) confirm Graber’s statement that in beetles
the first and last appendages on the same side are in contact with the ground, while
the middle one is raised. On the other side of the body the middle appendage is on
the ground and the first and last one raised.
25. Proc. Ent. Soc. London. Feb. 19, 1896. Heymons also shows that the germs
of the elytra of the larva of Tenebrio molitor in the prepupal stage are like those of
other insects. (Sitzungs-Ber. Gesell. natur f. Freunde zu Berlin, 1896, pp. 142–144.)
28. See our Guide to the Study of Insects, p. 66, Figs. 65, 66.
32. Pancritius, who also adopted Müller’s views, lays much stress on the fact
that in larvæ of some orders the tracheæ do not enter the rudimentary wings until
the end of larval life, and hence the wings have not originated from tracheal gills,
but were originally “perhaps only protective covers for the body.”
34. Von Lendenfeld, however, points out the fact that Straus-Durckheim
proved that the wings of beetles are moved by a complicated system of numerous
muscles. “In the Lepidoptera I have never found less than six muscles to each wing,
as also in the Hymenoptera and Diptera.” “The motions of the wings of Libellulidæ
are the combined working of numerous muscles and cords, and of a great number
of chitinous pieces connected by joints.”
35. Heymons, however, denies that the so-called cerci in Odonata are such,
and claims that they are the homologues of the “caudal processes” (superior
terminal appendages of Calvert), because they arise from the tenth abdominal
segment.
40. This has been shown to be the case by Michels, who states that each
commissure is formed of three parallel bundles of elementary nerve-fibres, which
pass continuously from one end of the ventral or nervous cord to the other. “The
commissures take their origin neither out of a central punctsubstanz (or
marksubstanz), nor from the peripheral ganglion-cells of the several ganglia, but
are mere continuations of the longitudinal fibres which decrease posteriorly in
thickness, and extend anteriorly through the commissures, forming the
œsophageal ring, to the brain.”
41. The following extract from Newton’s paper shows, however, that the infra
or subœsophageal ganglion, according to Faivre, has the power of coördinating the
movements of the body; still, it seems to us that the brain is primarily concerned in
the exercise of this power, as the nerves from the subœsophageal ganglion supply
only the mouth-parts. “The physiological experiments of Faivre in 1857 (Ann. des
Sci. Nat. tom. viii, p. 245), upon the brain of Dyticus in relation to locomotion, are
of very considerable interest, showing, as they appear to do, that the power of
coördinating the movements of the body is lodged in the infraœsophageal
ganglion. And such being the case, both the upper and lower pairs of ganglia ought
to be regarded as forming parts of the insect’s brain.”—Quart. Jour. Micr. Sc., 1879,
p. 342.
43. Viallanes’ assertion that the instincts of the horse-flies and dragon-flies are
“lower” than those of the locusts, may, it seems to us, well be questioned.
44. A. S. Packard, Experiments on the vitality of insects, Psyche, ii, 17, 1877.
46. J. Müller, Physiology of the Senses. Trans. by Baly, copied from Lubbock,
p. 176.
47. Hauser here uses the word taster, but this means palpus or feeler. It is
probably a lapsus pennæ for teeth (Kegeln).
48. In 1870 I observed these sense-pits in the antennæ and also in the
cercopoda of the cockroach (Periplaneta americana). I counted about 90 pits on
each cercus. They are much larger and much more numerous than similar pits in
the antennæ of the same insect. I compared them to similar pits in the antennæ of
the carrion-beetles, and argued that they were organs rather of the smelling than
hearing. (Amer. Nat., iv., Dec. 1870.) Organs of smell in the flies (Chrysopila) and
in the palpi, both labial and maxillary, of Perla were described in the same journal
(Fig. 270). Compare Vom Rath’s account of the organs in the cercopods of Acheta
(Fig. 271); also the singular organ discovered by him on the end of the palpus of
butterflies, in which a number of hair-like rods (sh) are seated on branches of a
common nerve (n, Fig. 272).
49. Forel, however (Recueil Zoologique Suisse, 1887), denies that these
tympanic organs are necessarily ears, and thinks that all insects are deaf, with no
special organs of hearing, but that sounds are heard by their tactile organs, just as
deaf-mutes perceive at a distance the rumbling of a carriage. But he appears to
overlook the fact that many Crustacea, and all shrimps and crabs, as well as many
molluscs, have organs of hearing. The German anatomist Will believes that insects
hear only the stridulation of their own species. Lubbock thinks that bees and ants
are not deaf, but hear sounds so shrill as to be beyond our hearing.
51. Plateau (1877) states that the digestive fluid of insects, as well as of
Arachnids, Crustaceans, and Myriopods, has no analogy with the gastric juice of
vertebrates; it rather resembles the pancreatic sugar of the higher animals. The
acidity quite often observed is only very accessory in character, and not the sign of
a physiological property. “Farther, I have found it in insects; Hoppe-Seyler has
demonstrated in the Crustacea, and I have proved in the spiders, that the ferment
causing the digestion of albuminoids is evidently quite different from the gastric
pepsine of vertebrates; the addition of very feeble quantities of chlorhydric acid, far
from promoting its action, retards or completely arrests it.” (Bull. Acad. roy.
Belgique, 1877, p. 27.)
52. The word grès we translate as the layer of gum. Not sure of the English
equivalent for grès, I applied to Dr. L. O. Howard, U. S. Entomologist, who kindly
answers as follows: “I have consulted Mr. Philip Walker, a silk expert, who writes
me the following paragraph: ‘Grès, as I understand it, is the gum of the silk fibre,
hence the French name for raw silk, grèye, which is in distinction to the silk that
has been boiled out in soap after twisting, or throwing, as it is called. As I
understand it, the silk fibre is composed of the grès and fibroin. The former is
soluble in alkali, like soap water, and the latter is not.’” While Blanc considers the
grès as the product of a special secretion of the wall of the reservoir, Gilson regards
its production as simultaneous with that of the silk or of the fibroin (l.c. 1893, p.
74).
54. See also Giard, Bull. Soc. Ent. France, p. viii, 1894.
55. “The contents of the Malpighian tubules may be examined by crushing the
part in a drop of dilute acetic acid, or in dilute sulphuric acid (10 per cent). In the
first case a cover-slip is placed on the fluid, and the crystals, which consist of
oblique rhombohedrons or derived forms, are usually at once apparent. If
sulphuric acid is used, the fluid must be allowed to evaporate. In this case they are
much more elongated, and usually clustered. The murexide reaction does not give
satisfactory indications with the tubules of the cockroach.” (Miall and Denny, The
cockroach, p. 129, footnote.)
56. “There is a curious analogy between the excretory organs of these insects
and the mesonephros of some vertebrates, where a second, third, etc., generation
of tubules is added to the primitive metameric series. When the embryonic number
of Malpighian vessels persists in insects, the demand for greater excreting surface
is supplied by a lengthening of the individual vessels.”
57. For the mode of adhesion of Cynips eggs, see Adler in Deutsche Ent. Zeits.
1877, p. 320.
60. These midges owe their phosphorescence to bacteria in their bodies during
disease.
61. Untersuchungen zur Anatomie und Histologie der Tiere, 1884, p. 72.
62. Zelle und Gewebe, 1885, p. 43. (See also our p. 217.)
63. Studien über die Lampyriden, Zeits. für wiss. Zool., xxxvii, 1882. Both
Wielowiejski and M. Wistinghausen have completely disproved the view of
Schultze, that the tracheæ end in star-like cells, where respiration takes place, as
the “star-like cells” are simply net-like expansions of the peritoneal membrane of
the tracheæ.
64. The following summary compiled from Krancher, is translated, with some
minor changes, from Kolbe’s work.
65. Miall and Denny state that in the cockroach the abdominal spiracles are
permanently open, owing to the absence of a valve, but communication with the
tracheal trunk may be cut off at pleasure by an internal occluding apparatus.
66. Zur Entwicklungsgeschichte der Biene, Zeitschr. wissens. Zoologie, xx, p.
519, 1870.
67. Die Entwicklung der Dipteren im Ei, Zeitschr. wissens. Zoologie, xiii, 1863.
73. In the Hymenoptera the two pairs on the meso- and metathoracic
segments are open in the Aculeata, also in the Siricidæ, among which sometimes
that on the third segment is closed. In Pimpla and Microgaster (fully grown larvæ)
only the mesothoracic stigmata are open.
Palmén adds that most dipterous larvæ are amphipneustic; Cecidomyia, the
Mycetophilidæ, Bibionidæ, and Stratiomys are typically peripneustic. (p. 92.)
Moreover, a single insect, as Sialis, may be apneustic as a larva, peripneustic
as a pupa, and holopneustic in the imago stage.
74. Mr. J. W. Folsom, who has made the accompanying sketch of the nymph of
Euphæa splendens in the Cambridge Museum, finds only seven pairs of gills, there
being no traces of them on segments 1, 9, and 10. A stout trachea, he writes us,
enters the base of each gill, and subdivides into several long branches, which
course along the periphery. Hagen in his original account said there were eight
pairs on segments 1–8 respectively.
76. Nusbaum’s view has been questioned by Heymons, who, from his studies
on the embryology of the cockroach (Periplaneta and Phyllodromia), Forficula, and
Gryllus, concludes that the ectodermal ends of the sexual outlets owe their origin
to an unpaired median hypodermal invagination, and that it is quite doubtful
whether the ectodermal portions of the sexual passages of insects were ever paired
(p. 104). On the other hand he appears, even throwing out the case of Ephemera, to
have overlooked Nassonow’s discovery of paired outlets in the young of Lepisma.
77. Acta Acad. German., xxxiii, 1867, No. 2, p. 81. Quoted by Dr. Sharp,
Insecta, p. 142.
79. Proc. Boston Soc. Nat. Hist., xi, pp. 88, 89.
81. Korschelt and Heider state that no cellular embryonal membranes are
present in Synaptera, Uljanin finding none in the Podurids. In the embryo of
Isotoma walkerii we, however, observed a membrane which we compared to the
larval skin of many Crustacea, and both Sommer and Lemoine have detected in
eggs of the same group a cuticular larval skin which is provided with spines for
rupturing the chorion. The amnion is also wanting in Proctotrupids (Ayers), and is
rudimental in Muscidæ (Kowalevsky, Graber), in viviparous Cecidomyidæ,
according to Metschnikoff, who also states that in certain ants of Madeira the
envelopes are represented only by a small mass of cells in the dorsal region.
82. In Diptera the stomodæum may be dorsal, Dr. Pratt tells us.
84. The description perhaps applies not only to the cockroaches, but, as seen
from the similar but fragmentary notices of Heider and of Wheeler on the
Coleoptera, may be common to insects in general.
85. Report on the Rocky Mountain locust, etc. Ninth Annual Report U. S.
Geol. and Geogr. Survey of the Territories for 1875, pp. 633, 634.
87. In his Für Darwin (1863), Fritz Müller gives his reasons for the opinion
that the so-called “complete metamorphosis” of insects was not inherited from the
primitive ancestor of all insects, but acquired at a later period.
88. For further details see the 1st Report of the U. S. Entomological
Commission, 1878, pp. 279–281.
89. See Köppen ueber die Heuschrecken in Südrussland, 1862, pp. 22, 23.
90. In Samouelle’s The Entomologist’s Useful Compendium, 1819. See
Westwood’s Class. Insects, i, p. 2; Leach’s Ametabolia comprised the Thysanura
(Synaptera) and the lice.
93. At the same date (March, 1869) we independently suggested that the
insects had originated from some form like the hexapodous young of Pauropus and
Podura. In November, 1870, we suggested that the Thysanura and the hexapodous
Leptus may have descended from some Peripatus-like worm. Afterwards (1871) we
proposed for the ancestral form the term leptiform, which was later abandoned for
Brauer’s term Campodea-form.
96. Trans. Ent. Soc. London, iii, p. xv. See also Ashton, R. J., Trans. Ent. Soc.
London, iii, 1841–43, pp. 157–159.
98. See Max Braun’s article entitled Ueber die histologischen Vorgange bei der
Hautung von Astacus fluviatilis, with a full bibliography, in Semper’s Arbeiten aus
dem Zool. zoot. Institut in Würzburg, ii, pp. 121–166. Also Semper’s Animal Life, p.
20. Trouvelot also discovered the moulting fluid. (Amer. Nat., i, p. 37.)
103. Butterflies, their structure, changes, and life-histories. New York, 1881,
pp. 37–42. Butterflies of the Eastern United States and Canada, 1888, 1889. Also,
Frail children of the air, 1895, pp. 232, 233 a. Dr. Chapman, however, finds that
this piece in micropupæ has no connection whatever with the head or eye, but
belongs rather with the prothoracic segment. (Trans. Ent. Soc. London, 1893, p.
102.) We have been able to confirm his statements, but still this piece is peculiar to
the pupal state.
104. Rep. Ent. U. S. Dept. Agr., 1879, pp. 228, 229, Pl. IV, Fig. 4.
105. Monograph of bombycine moths, Pt. I, 1897. Figs. 24, 28, 29, 33, 34, 40,
77.
107. Hybocampa milhauseni, Dr. Chapman tells me, has a pupal spine
(imperfectly present in Cerura) with which it cuts out a lid of the cocoon.
110. The homology of the suranal plate of the larva with the cremaster of the
pupa, established by Riley in 1880, is also affirmed by Jackson (1888) and by
Poulton, and for some years we have been satisfied that this is the correct view;
Professor Hatchett-Jackson discovered it, he states, in 1876.
112. We copy from Kirby and Spence their abstract of Herold’s conclusions:
“The successive skins of the caterpillar, the pupa-case, the future butterfly, and its
parts or organs, except those of sex, which he discovered in the newly excluded
larva, do not preëxist as germs, but are formed successively from the rete
mucosum, which itself is formed anew upon every change of skin, from what he
denominates the blood, or the chyle after it has passed through the pores of the
intestinal canal into the general cavity of the body, where, being oxygenated by the
air-vessels, it performs the nutritive functions of blood. He attributes these
formations to a vis formatrix (bildende Kraft).
“The caul or epiploon (fett-masse), the corps graisseux of Réaumur, etc.,
which he supposes to be formed from the superfluous blood, he allows, with most
physiologists, to be stored up in the larva, that in the pupa state it may serve for the
development of the imago. But he differs from them in asserting that in this state it
is destined to two distinct purposes: first, for the production of the muscles of the
butterfly, which he affirms are generated from it in the shape of slender bundles of
fibres; and, secondly, for the development and nutrition of the organs formed in
the larva, to effect which, he says, it is dissolved again into the mass of blood, and
being oxygenated by the air-vessels, becomes fit for nutrition, whence the epiploon
appears to be a kind of concrete chyle.” (Entwickelungsgeschichte der
Schmetterlinge, pp. 12–27.) It seems that Herold was right in deriving the pupa
and imago from the hypodermis (his rete mucosum), but wrong in denying that the
germs did not preëxist in the young caterpillar, and wrong in supposing that the
latter originated from the blood, also in supposing that the muscles owe their
origin to the fat-body. Swammerdam, and also Kirby and Spence, were correct in
supposing that the imago arose from “germs” in the larva, though wrong in
adopting the “emboîtement” theory.
113. In the regions where the imaginal buds are not present (dorsal aspect of
the prothorax, and abdomen), the epithelium (hypodermis) may proliferate
independently of these buds.
114. We shall translate portions and, when the text allows, make an abstract of
parts of Gonin’s clear and excellent account, often using his own words.
117. Miall, Natural History of Aquatic Insects, pp. 136–138. Also Trans. Linn.
Soc. London, V, Sept., 1892.
118. This account is translated from Korschelt and Heider, with some
omissions and slight changes.
119. Westwood in his excellent account of this group remarks: “Hence, as well
as from the account given by Jurine, it is evident that the pupa of the Stylops is
enclosed in a distinct skin, and is also in that state enveloped by the skin of the
larva, contrary to the suggestion of Mr. Kelly.” (Class. Insects, II. 297.) This is all
we know about the supernumerary larval stages.
120. Some facts towards a life history of Rhipiphorus paradoxus. Annals and
Magazine of Natural History for October, 1870.
TRANSCRIBER’S NOTES
P. 316, changed “abdominal cells” to “absorbent cells”.
Silently corrected typographical errors and variations in
spelling.
Archaic, non-standard, and uncertain spellings retained as
printed.
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