Professional Documents
Culture Documents
(download pdf) How Humans Evolved 7th Edition Boyd Test Bank full chapter
(download pdf) How Humans Evolved 7th Edition Boyd Test Bank full chapter
Test Bank
Go to download the full and correct content document:
https://testbankfan.com/product/how-humans-evolved-7th-edition-boyd-test-bank/
More products digital (pdf, epub, mobi) instant
download maybe you interests ...
https://testbankfan.com/product/lifespan-development-7th-edition-
boyd-test-bank/
https://testbankfan.com/product/c-how-to-program-7th-edition-
deitel-test-bank/
https://testbankfan.com/product/lifespan-development-6th-edition-
boyd-test-bank/
https://testbankfan.com/product/lifespan-development-5th-edition-
boyd-test-bank/
Dental Instruments 6th Edition Boyd Test Bank
https://testbankfan.com/product/dental-instruments-6th-edition-
boyd-test-bank/
https://testbankfan.com/product/lifespan-development-
canadian-5th-edition-boyd-test-bank/
https://testbankfan.com/product/lifespan-development-
canadian-6th-edition-boyd-test-bank/
https://testbankfan.com/product/c-how-to-program-7th-edition-
deitel-solutions-manual/
https://testbankfan.com/product/c-how-to-program-late-objects-
version-7th-edition-deitel-test-bank/
CHAPTER 7: The Evolution of Cooperation
MULTIPLE CHOICE
4. Two unrelated male baboons work together to guard a female in estrus to keep away a more dominant
male. This is an example of
a. mutualism. c. reciprocal altruism.
b. altruism. d. kin selection.
ANS: A DIF: Easy REF: Mutualism
OBJ: Understand why altruism is unlikely to evolve in most circumstances.
MSC: Applying
5. Mutualistic behaviors
a. are common in nature when animals work together.
b. are rare because “slacking” is often profitable for individuals, not groups.
c. involve only kin and never unrelated individuals.
d. are profitable for the actor but not the recipient.
ANS: B DIF: Medium REF: Mutualism
OBJ: Understand why altruism is unlikely to evolve in most circumstances.
MSC: Understanding
6. Coalitions among male baboons
a. allow middle-ranking, cooperative males a chance to gain access to receptive females.
b. are an example of mutualistic behavior as all males get equal mating opportunities.
c. do not allow lower-ranking males to outcompete higher-ranking males.
d. can predict male grooming relationships.
ANS: A DIF: Hard REF: Mutualism
OBJ: Understand why altruism is unlikely to evolve in most circumstances.
MSC: Understanding
7. Group selection
a. is likely to occur in primates because they live in well-established social groups.
b. is likely to occur in primates because certain behaviors benefit the whole group.
c. is unlikely to occur in primates because certain behaviors may benefit the group to the
detriment of the actor.
d. is unlikely to occur in primates because it is a theoretically unsound principle.
ANS: C DIF: Hard REF: The Problem with Group-Level Explanations
OBJ: Understand why altruism is unlikely to evolve in most circumstances.
MSC: Understanding
8. Although alarm calling benefits the whole group, it cannot be explained by group selection because
a. callers make themselves conspicuous to the predators, but calling costs little in terms of
individual fitness.
b. calling reduces the risk of mortality for everyone who hears the call, changing the
frequency of callers and noncallers in the population, because everyone benefits.
c. noncallers benefit from the alarm call and will have higher fitness than the callers, so
selection will suppress alarm calling.
d. callers and noncallers have the same relative fitness.
ANS: C DIF: Hard REF: The Problem with Group-Level Explanations
OBJ: Understand how evolution can favor altruism through the processes of kin selection and
reciprocal altruism. MSC: Understanding
17. Imagine that an alarm caller sacrifices its life to save other conspecifics. According to Hamilton’s rule,
how many full siblings would it have to save for the behavior to be favored?
a. at least 1. c. at least 3.
b. at least 2. d. Hamilton’s rule cannot be satisfied.
ANS: C DIF: Medium REF: Kin Selection
OBJ: Understand how evolution can favor altruism through the processes of kin selection and
reciprocal altruism. MSC: Applying
18. Imagine a caregiver who helps raise a conspecific’s offspring. Such caregiving reduces her fitness by
50% and increases the fitness of the conspecific by 50%. According to Hamilton’s rule, in which of the
following scenarios could this behavior evolve?
a. Groups of full siblings c. Both types of groups
b. Groups of half siblings d. Neither type of group
ANS: D DIF: Medium REF: Kin Selection
OBJ: Understand how evolution can favor altruism through the processes of kin selection and
reciprocal altruism. MSC: Applying
19. Imagine a caregiver who helps raise a conspecific’s offspring. Such caregiving reduces her fitness by
10% and increases the fitness of the recipient by 25%. According to Hamilton’s rule, in which of the
following scenarios could this behavior evolve?
a. Groups of full siblings c. Both types of groups
b. Groups of half siblings d. Neither type of group
ANS: A DIF: Medium REF: Kin Selection
OBJ: Understand how evolution can favor altruism through the processes of kin selection and
reciprocal altruism. MSC: Applying
20. If the coefficient of relatedness between two individuals is zero (r = 0), then
a. altruism can evolve if c > b.
b. altruism can evolve if c < b.
c. altruism cannot evolve via kin selection.
d. altruism will sometimes evolve regardless of the values of c and b.
ANS: C DIF: Medium REF: Kin Selection
OBJ: Understand how evolution can favor altruism through the processes of kin selection and
reciprocal altruism. MSC: Applying
25. Recent studies on kin recognition have found that age may provide a good proxy measure of paternal
kinship in
a. monogamous species.
b. species where one male dominates mating activity in a group.
c. groups with polygynous mating strategies.
d. polyandrous groups.
ANS: B DIF: Medium REF: Kin Recognition
OBJ: Discuss the mechanisms that allow primates to recognize their relatives.
MSC: Remembering
30. Kin selection combined with females remaining in their natal group, in many primate species, has led
to
a. mutualistic behavior.
b. asymmetrical behavior.
c. the transmission of rank laterally from sister to sister.
d. the transmission of rank from mothers to offspring.
ANS: D DIF: Medium REF: Kin Biases in Behavior
OBJ: Explain how kinship influences the distribution of altruism in primate groups.
MSC: Remembering
31. The apparent stability in female dominance relationships in female-bonded primates may be due to
a. abundant food supply. c. sexual selection.
b. kin selection. d. habitat seasonality.
ANS: B DIF: Medium REF: Kin Biases in Behavior
OBJ: Explain how kinship influences the distribution of altruism in primate groups.
MSC: Understanding
32. Which of the following is usually more common among kin than among nonkin in primate groups?
a. Aggression c. Alarm calling
b. Foraging d. Coalition formation
ANS: D DIF: Easy REF: Kin Biases in Behavior
OBJ: Explain how kinship influences the distribution of altruism in primate groups.
MSC: Remembering
33. Which of the following describes maternal rank and matrilineages in macaque, vervet, and baboon
groups?
a. Maternal rank is transferred to offspring, particularly daughters.
b. Maternal kin occupy dissimilar ranks in the dominance hierarchy.
c. Ranking within matrilineages is usually laterally transferred.
d. Female dominance relationships are unstable over time.
ANS: A DIF: Medium REF: Kin Biases in Behavior
OBJ: Explain how kinship influences the distribution of altruism in primate groups.
MSC: Remembering
34. Which of the following statements do studies of macaques, vervets, and baboons support?
a. Maternal rank is not a good predictor of a daughter’s rank.
b. Matrilineages rank above or below all members of other matrilineages.
c. The stability of female dominance relationships is not a result of kin-based alliances.
d. Females inherit patrilineal rank.
ANS: B DIF: Medium REF: Kin Biases in Behavior
OBJ: Explain how kinship influences the distribution of altruism in primate groups.
MSC: Remembering
36. The cooperative breeding system of primates such as marmosets and tamarins can be explained by
a. chimerism, which increases fraternal twins’ inclusive fitness when they help raise one
another’s offspring.
b. helpers who care for the offspring of the breeding pair, although the helpers are usually
not related to them.
c. the fact that mothers sometimes allow their daughters to breed.
d. mutualism between the nonbreeding helpers.
ANS: A DIF: Hard REF: Kin Biases in Behavior
OBJ: Explain how kinship influences the distribution of altruism in primate groups.
MSC: Understanding
39. Which of the following is predicted to occur after conflict results in violence as a way to mend
relationships?
a. Huddling c. Coalition formation
b. Reconciliation d. Altruism
ANS: B DIF: Easy REF: Kin Biases in Behavior
OBJ: Explain how kinship influences the distribution of altruism in primate groups.
MSC: Applying
40. Monkey A lives in a group with full siblings. Monkey B lives in a group with half siblings. Monkey C
lives in a group with cousins. And monkey D lives in a group with its grandparents. For which monkey
in which group is altruistic behavior most likely to occur?
a. A c. C
b. B d. D
ANS: A DIF: Medium REF: Hamilton’s Rule
OBJ: Understand why altruism is unlikely to evolve in most circumstances.
MSC: Applying
41. Of the following, which is the most certain way to identify kin in primates?
a. Phenotypic matching c. Proximity/context
b. Age/cohort d. Reconciliation
ANS: C DIF: Easy REF: Kin Recognition
OBJ: Discuss the mechanisms that allow primates to recognize their relatives.
MSC: Understanding
43. Even primate “friends” sometimes come into conflict. Their aggressive interactions may not have a
detrimental effect on social cohesion if there is
a. kin selection. c. grooming.
b. altruism. d. reconciliation.
ANS: D DIF: Easy REF: Kin Biases in Behavior
OBJ: Explain how kinship influences the distribution of altruism in primate groups.
MSC: Applying
44. In most promiscuously mating primate species that live in multimale, multifemale groups, mothers
share 50% of their genes with their offspring. Different offspring of the same female are likely to share
what percentage of their genes with each other?
a. 0% c. 50%
b. 25% d. 100%
ANS: B DIF: Medium REF: Parent–Offspring Conflict
OBJ: Explain how kinship influences the distribution of altruism in primate groups.
MSC: Applying
49. Reconciliatory contact between opponents immediately following an aggressive encounter can reduce
rates of self-scratching, an indicator of stress. If no reconciliation is attempted, then we can assume
that
a. rates of self-scratching drop back to baseline, regardless of stress level.
b. rates of self-scratching remain above baseline, indicating high stress levels.
c. only one opponent experiences high stress levels.
d. the opponent will have high rates of aggression between them in the future.
ANS: B DIF: Medium REF: Reciprocal Altruism
OBJ: Evaluate arguments about the importance of reciprocal altruism in primate groups.
MSC: Applying
ESSAY
1. Compare altruism and mutualism in terms of the fitness effects on actors and recipients.
ANS:
Altruistic acts provide fitness benefits to the recipient but at a fitness cost to the actor. Mutualistic acts
provide fitness benefits to both the recipient and the actor but only under strict conditions that prevent
slackers or cheaters from benefiting at the expense of the other party. Cooperative action by both
individuals must be required for success.
2. What is altruism? Why was it a puzzle for evolutionary biology before Hamilton?
ANS:
Altruism is behavior that benefits another at a cost to the actor. As students have learned so far, natural
selection will favor only traits that benefit the individual actor, and therefore, since these acts are a
detriment to the actor’s reproductive success, they never should evolve and should in fact be selected
against. Hamilton demonstrated how these behaviors could be selected for if they are directed toward
kin because they share some percentage of each other’s genes. It would have been nice if the authors
had actually introduced the term “inclusive fitness” here, and instructors may wish to do so.
3. What is group selection? Why do evolutionary biologists believe that individual selection will be more
powerful than group selection when the two are in conflict?
ANS:
Group selection is the idea that behaviors that benefit the group as a whole will be selected even if
they result in declines in fitness for the actor. This concept is problematic for evolutionary biologists
for several reasons. First, a behavior that benefits the group but to the detriment of the actor could
theoretically disappear, as those that have risky behaviors have reduced reproductive success and
therefore have fewer offspring who will perform that behavior in the next generation. Thus, selection
at the level of the individual should be stronger. Furthermore, for group selection to work, there would
need to be extensive variation between groups, as there is for individuals, but that does not appear to
be the case.
4. What is Hamilton’s rule? What are the two fundamental predictions of Hamilton’s rule? Devise a
primate scenario in which these two predictions of Hamilton’s rule would be satisfied.
ANS:
Hamilton’s rule is the mathematical model that helps predict whether altruistic behaviors will be
selected for. The equation rb > c specifies that an altruistic behavior will be selected for when r, the
coefficient of relatedness (the likely proportion of genes shared between two individuals), multiplied
by b, the fitness benefits for the recipients of such behavior, is greater than c, the fitness cost to the
actor. The two predictions that follow from Hamilton’s rule are that (a) altruism should be directed to
kin only because r = 0 for nonkin and (b) closer kinship allows for more costly altruism because r is
higher and can offset greater costs to the actor. There is extensive evidence within primates that known
or supposed kin, but especially known maternal kin, perform more altruistic behaviors such as
grooming, supporting each other in coalitions, food sharing, cooperative defense of territories and
groups, and helping for cooperatively breeding species.
5. Construct a hypothetical example to illustrate how a gene causing altruism in an individual could
increase in frequency through kin selection.
ANS:
The example used repeatedly in the book is the clearest illustration of how a gene causing altruism in
an individual could increase in frequency through kin selection. Imagine a monkey species that has a
special alarm call for birds of prey. This alarm call is genetically determined, so individuals who carry
the “raptor alarm call gene” warn their group that there is predation threat. Since they share genes with
their kin, including the “raptor alarm call gene,” if they reside in a group with kin they help them
survive when they call, even though they make themselves more obvious to the bird of prey. As
generations go by, the genes shared by relatives keep being passed on and in this way may spread.
6. What is the evidence for maternal and paternal kin recognition? Illustrate your answer with examples.
ANS:
Maternal kin selection is straightforward: Individuals can learn by proximity and familiarity that the
offspring of their mother are their kin. In primates, maternity is the one certainty. Therefore, it is not
surprising to find evidence of nepotism in female primates that reside in their natal groups with their
mothers, such as baboons, macaques, and vervet monkeys: Female kin inherit their rank from their
mother, have adjacent rank to their sisters, form matrilines that allow these large-scale coalitions to
compete with other such matrilines within their group, and groom each other more frequently.
Paternity is harder to determine in primates in promiscuously mating species. There do seem to be
some trends, however. Dominant males tend to sire more of the offspring in multimale, multifemale
groups, and so paternity can be assumed. For these species, age may be a proxy for paternity. But even
so, some species, such as macaques, seem to have preferences for paternal kin. Female macaques have
more affiliative interactions with paternal half siblings so they may be able not only to distinguish age
but also to use some other cue, perhaps a phenotypic one. Male primates may also be able to recognize
siblings, as the example of red howler males cooperatively defending groups demonstrates.
7. Conflict and aggression are a large part of group life for many primate species, which would seem
disruptive to social bonds. What, then, keeps social groups cohesive?
ANS:
Social cohesion in primate groups is achieved through affiliative interactions. Grooming is the number
one social currency in primates. It establishes social bonds and keeps individuals in proximity to one
another. It also functions to decrease the physiological effects of stress. But just because there are
affiliative behaviors does not mean that aggression does not occur. It has been documented that
reconciliation after aggression helps several haplorrhine species maintain positive affiliative
interactions and maintain social cohesion even after aggressive interactions. Furthermore, at least one
sex often resides in a group with kin, and kin selection may also influence social bonds to some
degree. Although the text does not specifically point this out, a student would not be incorrect to draw
on this information, as it is discussed for the majority of the chapter.
8. What evidence exists for reciprocal altruism in primates? Why would reciprocal altruism be common
for primates but not for other animals?
ANS:
Reciprocal altruism would be likely for primates but not other animals because it requires advanced
cognitive skills that may be absent in other species. Relative brain size, our proxy for cognitive skills,
is also large in only a few other mammals. Evidence from primates includes grooming and food
sharing in chimpanzees, vervet coalitionary support and grooming, male chimpanzee coalitionary
support, and food sharing.
9. Explain the phenomenon of genetic chimeras and how it relates to kin selection in cooperatively
breeding marmoset groups.
ANS:
Genetic chimerism is a rare phenomenon in nature, but it occurs in marmosets, who frequently give
birth to fraternal twins. Chimerism occurs when each twin carries its own DNA in addition to its
twin’s DNA, thus having two complete sets within its own body. The chimerism extends to all bodily
tissues, including gametes, so that each twin could pass along the genetic material of itself or its twin
to offspring, effectively increasing relatedness among nonbreeding helpers and infants. This could be
the reason we see this kind of cooperation in marmosets.
10. Interpret the following inequality as it pertains to parent–offspring conflict. Apply Hamilton’s rule,
from the current infant’s perspective, assuming a gene expressed by the current infant increases
maternal investment by a small amount.
ANS:
In the top position is the infant in question, who is related to itself (1.0) and to its sibling in the bottom
position (0.5). Kin selection will increase investment by the mother until the incremental advantage of
another unit of investment in the current infant is twice the cost to future full siblings of the fetus (four
times the cost for half siblings). Asymmetries in genetic expression then lead to a conflict of interest
between mothers and their offspring. Selection favors mothers that provide less investment than their
infants desire, and selection favors offspring that demand more investment than their mothers are
willing to give. This conflict of interest manifests in weaning tantrums and sibling rivalries.
F I N I S.
An A C C O U N T of
RICHARD OF C I R E N C E S T E R,
M O N K of W E S T M I N S T E R,
I.
To the Right Honourable the Lord WILUGHBY of Parham,
President of the Antiquarian Society.
But, to leave this, we will recite what we find of our author’s works.
Thus Gerard John Vossius, de historicis Latinis, L. III. quarto, p.
532, englished: “About the year 1340, lived Richard of Cirencester,
an Englishman, monk of Westminster, Benedictine. He used much
industry in compiling the history of the Anglo-Saxons, in five books of
Chronica: that work begins from the arrival of Hengist the Saxon into
Britain, A. D. 448. thence, through a series of nine centuries, he
ends at the year 1348, 32 Ed. III. and this work is divided into two.
The first part begins,”
Post primum Insulæ Brittaniæ regem, &c. This is called by the
author Speculum historiale, and contains four books.
The other part is called Anglo-Saxonum Chronicon, L. V. is a
continuation of the former part, Prudentiæ Veterum mos inolevit—it
was John Stow’s, says a manuscript note of Joscelin, in a
manuscript in the Cotton library, Nero C. iii. A manuscript of both
parts is found in the public library, Cambridge, among the
manuscripts, fol. contains pages 516, and four books; ends in 1066.
(248.) in the catalogue of manuscripts mentioned p. 168, No 2304.
(124.) It begins,
Brittannia insularum optima, &c. in the end (says Dr. James,
librarian in A.D. 1600.) are these words,
Reges vero Saxonum Gulielmo Malmsburiensi et Henrico
Huntendoniensi permitto: quos de regibus Britonum tacere jubeo,
&c.
Vossius says, there is in Bennet-College library, Cambridge, a
manuscript epitome Chronicorum, which acknowledges our Richard
for its author, in the title.
There is in the Arundel library of the Royal Society, among the
manuscripts, p. 137, mentioned this. Britonum, Anglorum et
Saxonum historia, to the reign of Hen. III. said to be of this author.
Dr. Stanley, in his catalogue of the manuscripts in Bennet-College
library aforesaid, p. 22. G. VIII. mentions this. Ricardi Cicestrii
Speculum historiale, vel Anglo-Saxonum Chronicon, ab anno 449.
ad H. III.
In the printed catalogue of manuscripts, p. 134. No 1343. (66.)
Epitome Chronicorum Angliæ, L. 1, 2. Epitome Chronicorum Ric.
Cic. Monachi Westmonasterii.
There is a work of our Richard’s in the Lambeth library, among the
Wharton manuscripts, L. p. 59. and the late Dr. Richard Rawlinson
bought a manuscript of his, at Sir Joseph Jekyl’s sale; which is now
at Oxford.
Our author was not eminent solely in this kind of learning; but we
find likewise the traces of other works of his, in his clerical character.
Thus, in a volume of St. Jerom’s ad Eugenium, 19. 9. a manuscript
in Bennet-College library, is mention of Tractatus mag. magistri
Ricardi Cirencestre, super symbolum majus et minus.
There is likewise, in the library of Peterburgh, T. IV. a work of his,
de Officiis Ecclesiasticis, L. VII. begins Officium ut—This is
mentioned by William Wydeford, and attributed to our Richard, in his
determination against the trialogue of Wicliff, artic. 1. fol. 96. likewise
by Richard Wych, who says he flourished A. D. 1348.
Thus much we have to say concerning our author’s life and works.
But let us reflect on what Dr. Nicolson says, in reciting what he had
wrote of the Saxon history; adding, but it seems, he treated too of
much higher times. Here he must at least mean his British history, or
that from the time of the Romans; and perhaps that description of
Roman Britain, which we are now treating off: but what reasons were
suggested to him about it, we cannot guess; and in our manuscript
we observe it begins with p. xxii. as appears from a scrip I desired
my friend Bertram to send me, of the manner of the writing: therefore
some other work of our Richard’s was probably contained in those
22 pages.
However these matters may have been, we must justly admire our
author’s great capacity, in compiling the history of his country from
first to last, as far as he could gather it, from all the materials then to
be found in all the considerable libraries in England, and what he
could likewise find to his purpose in foreign parts. Whether he found
our map and manuscript in our monastic libraries at home, or in the
Vatican, or elsewhere abroad, we cannot determine: he himself gives
us no other light in the case, than that it was compiled from memoirs
a quodam Duce Romano consignatis, et posteritati relictis, which I
am persuaded is no other than Agricola, under Domitian.
But, above all, we have reason to congratulate ourselves, that the
present work of his is happily rescued from oblivion, and, most likely,
from an absolute destruction.
I shall now concisely recite the history of its discovery.
In the summer of 1747, June 11, whilst I lived at Stamford, I
received a letter from Charles Julius Bertram, professor of the
English tongue in the Royal Marine Academy of Copenhagen, a
person unknown to me. The letter was polite, full of compliments, as
usual with foreigners, expressing much candor and respect to me;
being only acquainted with some works of mine published: the letter
was dated the year before; for all that time he hesitated in sending it.
Soon after my receiving it, I sent a civil answer; which produced
another letter, with a prolix and elaborate Latin epistle inclosed, from
the famous Mr. Gramm, privy-counsellor and chief librarian to his
Danish Majesty; a learned gentleman, who had been in England,
and visited our universities. (Mr. Martin Folkes remembered him.) He
was Mr. Bertram’s great friend and patron.
I answered that letter, and it created a correspondence between
us. Among other matters, Mr. Bertram mentioned a manuscript, in a
friend’s hands, of Richard of Westminster, being a history of Roman
Britain, which he thought a great curiosity; and an ancient map of the
island annexed.
In November, that year, the Duke of Montagu, who was pleased to
have a favor for me, drew me from a beloved retirement, where I
proposed to spend the remainder of my life; therefore wondered the
more, how Mr. Bertram found me out: nor was I sollicitous about
Richard of Westminster, as he then called him, till I was presented to
St. George’s church, Queen-square. When I became fixed in
London, I thought it proper to cultivate my Copenhagen
correspondence; and I received another Latin Letter from Mr.
Gramm; and soon after, an account of his death, and a print of him in
profile.
I now began to think of the manuscript, and desired some little
extract from it; then, an imitation of the hand-writing, which I showed
to my late friend Mr. Casley, keeper in the Cotton library, who
immediately pronounced it to be 400 years old.
I pressed Mr. Bertram to get the manuscript into his hands, if
possible; which at length, with some difficulty, he accomplished; and,
on my sollicitation, sent to me in letters a transcript of the whole; and
at last a copy of the map, he having an excellent hand in drawing.
Upon perusal, I seriously sollicited him to print it, as the greatest
treasure we now can boast of in this kind of learning. In the mean
time, I have here extracted some account of the Treatise, for your
present entertainment, as I gave it to Dr. Mead, and to my very
worthy friend Mr. Gray of Colchester, some time past, at their
request.
Municipia II.
Verolanium, Verlam cester, St. Alban’s.
Eboracum, York; olim Colonia, legio Sexta.
Colonies IX.
Londinium Augusta, London.
Camulodunum: legio gemina Martia xiv. Colchester.
Rhutupis, Sandwich. Richborough.
Therma, Aquæ Solis, Bath.
Isca Silurum, legio secunda, Augusta, Britannica,
Caerleon, Wales.
Deva, legio Cretica, xx. v. v. West Chester.
Glevum, legio Claudia, vii. Gloucester.
Lindum colonia, Lincoln.
Camboritum, Chesterford, Cambridgeshire.
Civitates Latio jure donatæ X.
Durnomagus, Caster by Peterborough.
Cataracton, Catteric, Yorkshire.
Cambodunum, Alkmundbury, Yorkshire.
Coccium, Burton, north of Lancaster.
Lugubalia, Carlisle.
Pteroton, Alata castra, Inverness.
Victoria, Perth.
Theodosia, Dunbriton.
Corinium Dobunorum, Cirencester.
Sorbiodunum, Old Sarum.
Stipendiariæ XII.
Venta Silurum, Caerwent.
Venta Belgarum, Wintchester.
Venta Icenorum, Caster by Norwich.
Segontium, Carnarvon.
Muridunum, Seaton, Dorsetshire.
Ragæ Coritanorum, Ratæ, Leicester.
Cantiopolis, Durovernum, Canterbury.
Durinum, Dorchester.
Isca Dumnoniorum, Exeter.
Bremenium, Ruchester.
Vindonum, Silchester.
Durobrovis, Rochester.