Introduction to Simulink with Engineering Applications 2nd Edition Steven T. Karris - The ebook is ready for download with just one simple click
Introduction to Simulink with Engineering Applications 2nd Edition Steven T. Karris - The ebook is ready for download with just one simple click
com
https://ebookname.com/product/introduction-to-simulink-with-
engineering-applications-2nd-edition-steven-t-karris/
OR CLICK HERE
DOWLOAD EBOOK
https://ebookname.com/product/signals-and-systems-with-matlab-
computing-and-simulink-modeling-4th-edition-steven-t-karris/
https://ebookname.com/product/numerical-analysis-using-matlab-
and-spreadsheets-2nd-edition-steven-t-karris/
https://ebookname.com/product/numerical-analysis-using-matlab-
and-spreadsheets-2nd-ed-edition-steven-t-karris/
https://ebookname.com/product/the-agile-startup-quick-and-dirty-
lessons-every-entrepreneur-should-know-1st-edition-richter-sand/
Small Firms in Tourism International Perspectives
Advances in Tourism Research 1st Edition Rhodri Thomas
https://ebookname.com/product/small-firms-in-tourism-
international-perspectives-advances-in-tourism-research-1st-
edition-rhodri-thomas/
https://ebookname.com/product/bovine-genomics-1st-edition-james-
womack/
https://ebookname.com/product/the-ethics-of-war-second-edition-a-
j-coates/
https://ebookname.com/product/the-twitter-book-1st-edition-tim-
oreilly/
World Civilizations 4th Edition Philip J. Adler
https://ebookname.com/product/world-civilizations-4th-edition-
philip-j-adler/
Introduction to Simulink
with Engineering Applications
Second Edition
Steven T. Karris
Orchard Publications
www.orchardpublications.com
Introduction to Simulink®
with Engineering Applications
Second Edition
Steven T. Karris
Orchard Publications
www.orchardpublications.com
Introduction to Simulink ® with Engineering Applications, Second Edition
Copyright ©2008 Orchard Publications. All rights reserved. Printed in the United States of America. No part of this
publication may be reproduced or distributed in any form or by any means, or stored in a data base or retrieval system,
without the prior written permission of the publisher.
Product and corporate names are trademarks or registered trademarks of The MathWorks™, Inc. They are used only
for identification and explanation, without intent to infringe.
ISBN-10: 1-934404-10-1
ISBN-13: 978-1-934404-10-2
TXu 1−303-668
Disclaimer
The author has made every effort to make this text as complete and accurate as possible, but no warranty is implied.
The author and publisher shall have neither liability nor responsibility to any person or entity with respect to any loss
or damages arising from the information contained in this text.
Preface
This text is an introduction to Simulink ®, a companion application to MATLAB ®. It is written
for students at the undergraduate and graduate programs, as well as for the working professional.
The author claims no originality of the content, and the description of the Simulink blocks is
extracted from The MathWorks™ documentation without intent to infringe. The intent is to
provide a complete reference text, and whenever necessary, the author refers the reader to The
MathWorks™ documentation. Whenever there is a conflict between this text and The
MathWorks™ documentation, the latter takes precedence.
Although some previous knowledge of MATLAB would be helpful, it is not absolutely necessary;
Appendix A of this text is an introduction to MATLAB to enable the reader to begin learning
both MATLAB and Simulink simultaneously, and to perform graphical computations and
programming.
Chapters 2 through 19 describe the blocks in all Simulink Version 7.1 libraries. Their application
is illustrated with Simulink models that contain the pertinent blocks, and some are supplemented
with MATLAB functions, commands, and statements. Some background information is provided
for lesser known definitions and topics. Chapters 1 and 20 contain several Simulink models to
illustrate various applied math and engineering applications. Appendix B is an introduction to
masked subsystems, and Appendix C introduces the reader to random generation procedures.
Appendix D is an introduction to Weighted Moving Averages.
This text supplements our Numerical Analysis Using MATLAB and Excel, ISBN 978−1−934404−
03−4. It is self-contained; the blocks of each library are described in an orderly fashion that is
consistent with Simulink’s documentation. This arrangement provides insight into how a model is
used and how its parts interact with each another.
Like MATLAB, Simulink can be used with both linear and nonlinear systems, which can be
modeled in continuous time, sample time, or a hybrid of these. Examples are provided in this text.
Most of the examples presented in this book can be implemented with the Student Versions of
MATLAB and Simulink. A few may require the full versions of these outstanding packages, and
these examples may be skipped. Some add−ons, known as Toolboxes and Blocksets can be
obtained from The MathWorks,™ Inc., 3 Apple Hill Drive, Natick, MA, 01760-2098, USA,
www.mathworks.com.
To get the most out of this outstanding application, it is highly recommended that this text is used
in conjunction with the MATLAB and Simulink User’s Guides. Other references are provided in
the reference section of this text.
This is the second edition of this title, and although every effort was made to correct possible
typographical errors and erroneous references to figures and tables, some may have been
overlooked. Accordingly, the author will appreciate it very much if any such errors are brought to
his attention so that corrections can be made for the next edition.
The author wishes to express his gratitude to the staff of The MathWorks™, the developers of
MATLAB® and Simulink® for the encouragement and unlimited support they have provided me
with during the production of this text.
Our heartfelt thanks also to Mr. Howard R. Hansen, and Dr. Niel Ransom, former CTO of
Alcatel, for bringing some errors on the first print to our attention.
Orchard Publications
www.orchardpublications.com
info@orchardpublications.com
Table of Contents
1 Introduction to Simulink 1−1
1.1 Simulink and its Relation to MATLAB ....................................................................1−1
1.2 Simulink Demos ......................................................................................................1−20
1.3 Summary ..................................................................................................................1−28
1.4 Exercises ..................................................................................................................1−29
1.5 Solutions to End−of−Chapter Exercises ..................................................................1−30
The word pupa is from the Latin meaning baby. Linnæus gave it
this name from its resemblance to a baby which has been swathed or
bound up, as is still the custom in Southern Europe. The term pupa
should be restricted to the resting inactive stage of the
holometabolous insects.
Lamarck’s term chrysalis was applied to the complete or obtected pupa of
Lepidoptera and of certain Diptera, and mumia, a mummy, to the pupæ of
Coleoptera, Trichoptera, and most Hymenoptera. Latreille (1830) also restricted
the term pupa to the “oviform nymph,” or puparium, of Diptera. Brauer applies the
term nymph to the pupa of metabolous insects.
The typical pupa is that of a moth or butterfly,
popularly called a chrysalis. A lepidopterous pupa
in which the appendages are more or less folded
close to the body and soldered to the integument,
was called by Linnæus a pupa obtecta; and when
the limbs are free, as in Neuroptera, Mecoptera,
Trichoptera, and the lepidopterous genus
Micropteryx it is called a pupa libera (Fig. 579).
When the pupa is enclosed in the old larval skin, Fig. 578.—Pupa
which forms a pupal covering (puparium), the obtecta: a, of
pupa was said by Linnæus to be coarctate. The Sesia, with its
pupa of certain Diptera, as that of the cocoon-cutterthe head; b, of
on
orthoraphous families, is nearly as much obtected Tortrix
as that of the tineoid families of moths, especially vacciniivorana.
as regards the appendages of the head; the legs
being more as in pupæ liberæ (Fig. 580).
The male Coccid anticipates the metabolous insects in passing
through a quiescent state, when, as Westwood states, it is “covered
by the skin of the larva, or by an additional pellicle.” The body
appears to be broad and flat, the antennæ and fore legs resting under
the head, while the two hinder pairs of legs are appressed to the
under side of the body. There is but a slight
approach to the pupa libera of a metabolous
insect.
Riley states that the male larva of Icerya purchasi
forms a cocoon waxy in character, but lighter, more
flossy, and less adhesive than that of the female egg-
cocoon. It melts and disappears when heated, proving
its entirely waxy nature. When the mass has reached
the proper length, the larva casts its skin, which
remains in the hind end of the cocoon, and pushes itself
forward into the middle of the cocoon. The pupa (Fig.
581) is of the same general form and size as the larva.
Fig. 579.—Pupa libera of All the limbs are free and slightly movable, so that they
neuropterous insects a, vary in position, though ordinarily the antennæ are
Corydalus cornutus; b, pressed close to the side, as are the wing-pads; the front
Sialis; c, Hemerobius. pair of legs are extended forward. “If disturbed, they
twist and bend their bodies quite vigorously.” The pupa
state lasts two or three weeks. A similar pupa is that of
Icerya rosæ. (Riley and Howard.)
The metamorphosis of
Aspidiotus perniciosus is of
interest. The male nymph
differs much after the first
moult from the female, having
large purple eyes, while the
female nymph loses its eyes
entirely. It passes into what
Riley terms the pro-pupa (Fig.
Fig. 580.—Pupa obtecta of 582, b), in which the wing-pads
Diptera: a, Ptychoptera; b, are present, while the limbs are
Tabanus atratus; c, short and thick. The next stage Fig. 581.—
Proctacanthus philadelphicus; d, is the “true pupa” (Fig. 582, c, Pupa libera
Midas clavatus. d), in which the antennæ and of Icerya
legs are much longer than purchasi,
before. There is no waxy ventral
cocoon, but only a case or scale composed of the shed larval skin, i.e. view.—After
“with the first moult the shed larval skin is retained beneath the Riley, Insect
scale, as in the case of the female; with the later moultings the shed Life.
skins are pushed out from beneath the scale,” and when they
transform into the imago they “back out from the rear end of their
scale.”
Fig. 582.—Aspidiotus perniciosus, development of
male insect: a, ventral view of larva after first moult;
b, the same, after second moult (pro-pupa stage); c
and d, true pupa, ventral and dorsal views. All
greatly enlarged.—After Riley.
In Myrmeleon the pupa pushes its way half out of the cocoon, and
then remains, while the imago ruptures the skin and escapes (Fig.
589, a).
Thus in the Neuroptera and Trichoptera we have already
established the more fundamental methods of escape from the
cocoon, which we see carried out in various ways in the more
generalized or primitive Lepidoptera.
The most primitive method in the Lepidoptera of escaping from
the cocoon seems to be that of Micropteryx.
Fig. 589.—Larva of Myrmeleon
with (a) its cocoon and cast
pupa-skin.
“In this genus,” says Chapman, “though it is nominally the pupa that escapes
from the cocoon, it is in reality still the imago, the imago clothed in the effete pupal
skin. To rupture the cocoon it uses not its own jaws, but those of the pupal skin,
energizing them, however, in some totally different way from ordinary direct
muscular action, their movements being the result of the vermicular movements of
the pupa, acting probably by fluid pressure on the articular structure of the jaws,
by some arrangement not altogether different perhaps from the frontal sac of the
higher Diptera. In the Micropteryges the jaws of the pupa not only rupture the
cocoon, but appear to be the most active agents in dragging the pupa through the
opening in the cocoon and through any superincumbent earth, being merely
assisted by the vermicular action of the abdominal segments, and we find in
accordance with this circumstance that the pupal envelope is still very thin and
delicate, and has little or no hardening or roughness by which to obtain a leverage
against the walls of the channel of escape.” (Trans. Ent. Soc. London, 1896, pp.
570, 571.)
Some sort of a beak or hard process, more or less developed,
according to Chapman, adapted for breaking open the cocoon exists
in nearly all the Lepidoptera with incomplete pupæ (pupæ
incompletæ), except the limacodid and nepticulid section. “In all
these instances the pupa emerges from the cocoon precisely as in the
Micropteryges, that is, the moth it really is that emerges, but does so
encased in the pupal skin. To achieve this object, it seems to have
been found most efficient to have three, four, or five abdominal
segments capable of movement, but to have the terminal sections
(segments) soldered together.”
This cocoon-breaker, as we may call it, is especially developed in
Lithocolletis hamadryadella. As described by Comstock, it forms a
toothed crest on the forehead which enables it to pierce or saw
through the cocoon.
“Each pupa first sawed through the cocoon near its juncture with the
leaf and worked its way through the gap, by means of the minute
backward-directed spines upon its back, until it reached the upper
cuticle of the leaf. Through this cuticle it sawed in the same way that it
did through the cocoon. The hole was in each case just large enough to
permit the chrysalis to work its way out, holding it firmly when partly
emerged. When half-way out it stopped, and presently the skin split
across the back of the neck and down in front along the antennal
sheaths, and allowed the moth to emerge.”[104]
We have observed and figured the cocoon-breaker in
Bucculatrix, Talæporia (Fig. 590, a), Thyridopteryx, and
Œceticus, and rough knobs or slight projection answering
the purpose in Hepialidæ, Megalopyge, Zeuzera, and in
Datana.[105] See also the spine on the head of Sesia
Fig. 590. tipuliformis (Fig. 578).
—Pupa of The imago of the attacine moths cuts or saws through its
Talæpori
a: a,
cocoon by means of a pair of large, stout, black spines
cocoon- (sectores coconis), one on each side of the thorax at the
cutter; base of the fore wings (Fig. 591), and provided with five or
with six teeth on the cutting edge (C, D).
vestiges Our attention[106] was drawn to this subject by a rustling, cutting,
of four and tearing noise issuing from a cocoon of Actias luna. On
pairs of examination a sharp black point was seen moving to and fro, and then
abdomin another, until both points had cut a rough irregular slit, through which
al legs, the shoulder of the moth could be seen vigorously moving from side to
and the side. The hole or slit was made in one or two minutes, and the moth
cremaste worked its way at once out of the slit. The cocoon was perfectly dry.
r. The cocoon-cutter occurs in all the American genera, in Samia
cynthia, and is large and well marked in the European Saturnia
pavonia-minor and Endromis versicolora. In Bombyx mori the spines
are not well marked, and they are quite different from those in the Attaci. There
are three sharp points, being acute angles of the pieces at the base of the wing, and
it must be these spines which at times perform the cutting through of the threads
of the cocoon described by Réaumur, and which he thought was done by the facets
of the eyes. It is well known that in order to guard against the moths cutting the
threads, silkraisers expose the cocoon to heat sufficient to destroy the enclosed
pupa. In Platysamia the cocoon-cutters, though well developed, do not appear to
be used at all, and the pupa, like that of the silkworm and other moths protected by
a cocoon, moistens the silk threads by a fluid issuing from the mouth, which also
moistens the hairs of the head and thorax, together with the antennæ. It remains to
be seen whether these structures are only occasionally used, and whether the
emission of the fluid is not the usual and normal means of egress of the moth from
its cocoon. Dr. Chapman remarks
that throughout the obtected
moths “there are many devices for
breaking through the cocoon:
specially constructed weak places
in the cocoon, softening fluid,
applied by the moth, assisted by
special appliances of diverse sorts,
[107] and
Fig. 591.—Cocoon- such as in Hybocampa
cutter of the Luna Attacus,” etc.
moth: front view of As to the fluid mentioned
the moth with the above, Trouvelot states that it is
shoulders elevated secreted during the last few days Fig. 592.—Larva and
and the rudimentary of the pupa state, and is a pupa of a wood-wasp
wings hanging down: dissolvent for the gum so firmly (Rhopalum),
s, cocoon-cutter; p, uniting the fibres of the cocoon. enlarged: h,
patagium. B, “This liquid is composed in great temporary locomotive
represents another part of bombycic acid.” (Amer. tubercles on head of
specimen with fully Naturalist, i, p. 33.) pupa.—Trouvelot del.
developed wings: ms, The pupa of the dipterous genus
scutum; st, scutellum Sciara (S. ocellaris O. S.)
of the mesothoracic resembles a tineid pupa, and before transforming emerges
segment; s, cocoon- for about two-thirds of its length from the cocoon; the
cutter, which is pupa-skin remaining firmly attached in this position.[108]
evidently a Certain hymenopterous pupæ are provided with
modification of one temporary deciduous conical processes. Thus we have
of the pieces at the observed in the pupa of Rhopalum pedicellatum two very
base of the fore prominent acute tubercles between the eyes (h, Fig. 592).
wings; it is As the cocoon is very slight, these may be of use either in
surrounded by extracting itself from the silken threads or in pushing its
membrane, allowing way along before emerging from the tunnel in the stem of
free movement. C plants. (See also p. 611.)
and D, different
views of the spine,
magnified, showing
the five or six
c. The cremaster
irregular teeth on the
cutting edge. Although this structure is in general confined
to lepidopterous pupæ, and is not always present
even in them, since it is purely adaptive in its
nature, yet on account of its singular mode of development from the
larval organs, and the accompanying changes in the pupal abdomen,
it should be mentioned in this connection. The cremaster is the stout,
triangular, flattened, terminal spine of the abdomen, which aids the
pupa in working its way out of the earth when the pupa is
subterranean, or in the pupa of silk-spinning caterpillars its
armature of secondary hooks and curved setæ enables it to retain its
hold on the threads of the interior of its cocoon after the pupa has
partially emerged from the cocoon, restraining it, as Chapman well
says, “at precisely that degree of emergence from the cocoon that is
most desirable.” He also informs us that while in the “pupæ
incompletæ the cremaster is attached to an extensible cable, which
always allows some emergence of the pupa, in the pupæ obtectæ
there is no doubt but that in such cases as the Ichthyuræ, Acronyctæ,
and many others, it retains the pupal case in the same position
within the cocoon that the living pupa occupied; this is also very
usually the case in the Geometræ and in the higher tineids (my
pyraloids).”
In many of the more generalized moths there is no cremaster (Micropteryx,
Gracilaria, Prodoxus, Tantura, Talæporia, Psychidæ, Hepialidæ, Zeuzera, Nola,
Harrisina), though in Tischeria and Talæporia (Fig. 590, but not in Solenobia) and
Psychidæ, two stout terminal spines perform the office of a cremaster, or there are
simply curved setæ on the rounded, unarmed end of the abdomen, as in Solenobia.
In the obtected Lepidoptera, for example in such a group as the Notodontidæ,
where the cremaster is present, though variable in shape, it may from disuse,
owing to the dense cocoon, be without the spines and hooks in Cerura, or the
cremaster itself is entirely wanting in Gluphisia, and only partially developed in
Notodonta. In the butterflies whose pupæ are suspended (Suspensi), the cremaster
is especially well developed. Reference might here be made to the temporary pupal
structures in certain generalized moths, which take the place of a cremaster, such
as the transverse terminal row of spines in Tinea, the two stout spines in Tischeria,
and the dense rough integument and thickened callosities of the pupal head and
end of abdomen of Phassus, which bores in trees with very hard wood; also the
numerous stout spines at the end and sides of the abdomen in Ægerians. These
various projections and spines, besides acting as anchors and grappling hooks, in
some cases serve to resist strains and blows, and have undoubtedly, like the
armature in the larvæ and imagines of other insects, arisen in response to
intermittent or occasional pressure, stresses, and impacts.
Mode of formation of the cremaster and suspension of
the chrysalis in butterflies.—We are indebted to Riley[109] for an
explanation of the way the cremaster has originated, his observations
having been made on species of over a dozen genera of butterflies
(Suspensi).
He shows that the cremaster is the homologue of the suranal plate
of the larva.[110] The preliminary acts of the larva have been observed
by various authors since the days of Vallisneri, i.e. the larva hanging
by the end of the abdomen, turning up the anterior part of the body
in a more or less complete curve, and the skin finally splitting from
the head to the front edge of the metathoracic segment, and being
worked back in a shrivelled mass toward the point of attachment.
The critical feat, adds Riley, which has most puzzled naturalists, is
the independent attachment of the chrysalis and the withdrawal
from and riddance of the larval skin which such attachment implies.
Réaumur explained this in 1734 by the clutching of the larval skin
between sutures of the terminal segments of the chrysalis, and this is
the case, though the sutures act in a somewhat different way.
Before pupation the larva spins a mass or heap of silk, the shape of which is like
an inverted settee or a ship’s knee, and “one of the most interesting acts of the
larva, preliminary to suspension, is the bending and working of the anal parts in
order to fasten the back of the (suranal) plate to the inside of the back of the settee,
while the crotchets of the legs are entangled in the more flattened position or seat.”
In shedding the larval skin, the following parts are also shed, and have some part
to play in the act of suspension: i.e. 1st, the tracheal ligaments (Fig. 593, tl), or the
shed tracheæ from the last or 9th pair of spiracles; 2d, the rectal ligament (Fig.
593, rl), or shed intestinal canal; 3d, the Osborne or retaining membrane
(membrana retinens, Fig. 593, mr), which is the stretched part of the membrane
around the rectum and in the anal legs, and which is intimately associated with the
rectal ligament.
Fig. 593.—Shrunken larval skin
of Vanessa antiopa, cut open
from the back and showing (mr)
the retaining membrane, (rl)
the rectal ligament, and (tl) the
tracheal ligaments.
The structures in the chrysalis are, first, the cremaster, with its dorsal (Fig. 594,
dcr) and ventral (vcr) ridges, and the cremastral hook-pad (chp), said by Riley to
be “thickly studded with minute but stout hooks, which are sometimes compound
or furnished with barbs, very much as are some of our fishing-hooks, and which
are most admirably adapted to the purpose for which they are intended.”
Secondly, there are the other structures, viz., the sustainers (sustentors), two
projections which Riley states “homologize with the soles (plantæ) of the anal
prolegs, which take on various forms (3), but are always directed forward so as
easily to catch hold of the retaining membrane.” These sustentors are, however, as
Jackson[111] has shown, and as we are satisfied, the vestiges of the anal legs.
Fig. 595.—Anal parts
Fig. 594.—Ideal of chrysalis of Vanessa
representation of antiopa, just prior to
the anal subjoint of final extraction from
Vanessa antiopa, shrunken larval skin:
from behind, with c, cremaster; chp,
the spines cremastral hook-pad;
removed, and all h, one of the hooks,
parts forced apart more enlarged; vcr,
by pressure so as to ventral cremastral
show the ridge; dcr, dorsal
homologies of the cremastral ridge; lr,
parts in the larval rectum; pr,
chrysalis which are pupal rectum; rp,
concerned in rectal plate; sr,
pupation: sustentor ridges; mr,
homologies membrana retinens;
indicated by rl, rectal ligament; tl,
corresponding tracheal ligament; the
letters in Fig. 595, 11th or last spiracle-
except that r (the bearing joint and the
rectum) 12th joint being
corresponds with numbered.
pr in Fig. 595.
Fig. 596.—A, chrysalis of Terias. B,
posterior end of chrysalis of Paphia.
C, posterior end of chrysalis of
Danais. E, one of the sustainers of
Terias, greatly enlarged to show its
hooked nature. All the parts of
subjoint lettered to correspond with
Fig. 595.
Thirdly, the sustentor ridges, which, as Riley states, may be more or less obsolete
in some forms, in Paphia (Fig. 596, B) and Limenitis form “quite a deep notch,
which doubtless assists in catching hold of the larval skin in the efforts to attach
the cremaster.”
Fig. 597.—Pupation of butterflies: a,
attachment of larva of Danais archippus;
p, attachment of larva of Paphia
glycerium; b, ideal larva soon after
suspension; d, ideal larva a few hours later,
the needle (n) separating the forming
membrane from the sustainers; l, ideal
larva just before splitting of larval skin,
with retaining membrane loosened from
the sustainers and showing its connection
both with the larval and pupal rectum. In
all the figures the joints of the body are
numbered; the forming chrysalis is shaded
in transverse lines; the intervening space
between it and larval skin is dotted: h, is
the hillock of silk; hl, hooks of hind legs;
ap, anal plate; lr, larval rectum; pr, pupal
rectum; mr, retaining membrane; c,
cremaster; s, sustainers.—This and Figs.
593–596 after Riley.
“It is principally,” adds Riley, “by the leverage obtained by the hooking of the
sustainers in the retaining membrane, which acts as a swimming fulcrum, that the
chrysalis is prevented from falling after the cremaster is withdrawn from the larval
skin. It is also principally by this same means that it is enabled to reach the silk
with the cremastral hook-pads.”
“Dissected immediately after suspension, the last abdominal segment of the
larva is found to be bathed, especially between the legs and around the rectum, in
an abundance of translucent, membranous material.”
“An hour or more after suspension the end of the forming chrysalis begins to
separate from the larval skin, except at the tip of the cremaster (Fig. 597, b).
Gradually the skin of the legs and of the whole subjoint (10th segment) stretches,
and with the stretching, the cremaster elongates, the rectal piece recedes more and
more from the larval rectum, and the sustentor ridges diverge more and more from
the cremaster, carrying with them, on the sustainers, a part of the soft membrane.”
The rectal ligament will sustain at least 10 or 12 times the weight of the chrysalis.
That of Apatura seems to rely almost entirely on the rectal ligament, assisted by the
partial holding of the delicate larval skin.
FORMATION OF THE PUPA AND IMAGO IN
THE HOLOMETABOLOUS INSECTS (THE
DIPTERA EXCEPTED)
a. The Lepidoptera
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