Spelling suggestions: "subject:"otomys irroratus"" "subject:"otomys irroratum""
1 |
Phylogeography of the southern African vlei rat, Otomys irroratus, inferred from chromosomal and DNA sequence dataEngelbrecht, Adriaan 12 1900 (has links)
Thesis (MSc)--University of Stellenbosch, 2010. / ENGLISH ABSTRACT: This study examines the phylogeography of the southern African vlei rat, Otomys
irroratus using the mtDNA cyt b gene and chromosomal data derived using G-, and C-banding,
Ag-NOR staining and fluorescence in situ hybridization (FISH using flow sorts of Myotomys
unisulcatus). A total of N = 102 specimens were used from the Western Cape, Eastern Cape,
Northern Cape, Free State, Mpumalanga and KwaZulu-Natal provinces of South Africa. Of the
N = 102, N = 55 comprised fresh material while N = 47 comprises museum material obtained
from the Durban Natural Science Museum of South Africa.
Cytogentic analysis of N = 55 specimens collected from seven localities in South Africa
revealed intra-specific variation resulting from two rearrangements, namely pericentric inversions
and heterochromatin variation. Of the 55 specimens that were analyzed 47% contained
inversions or centromeric shifts on four autosomes (OIR1, OIR4, OIR6 and OIR10) which were
present singly in specimens (i.e. none of the specimens contained all four inversions
concurrently). These inversions were present in both homozygous and heterozygous state over a
wide geographic range suggesting that they are floating polymorphisms. Given the potential role
of inversions in post-mating isolation (through production of aneuploid gametes), the prevalence
of inversions as floating polymorphisms in the vlei rats suggest that they are probably retained in
the population through suppression of recombination in the inverted regions of the chromosomes.
In addition, differences between populations is due to the presence or absence of heterochromatic
arms (and not inversions), which cause variation in the NFa (40 – 49) and supernumerary B
chromosomes, resulting in the variation in diploid number (2n = 28 – 32). Analysis of N = 55
specimens revealed Ag-NORs on 7 autosomal pairs 1, 2, 5, 7, 8 and 9 proximal to the centromere
on the short arm of the chromosome. Pair 8 also displayed Ag-NOR at the distal end of the long
arm of the chromosome in individuals from the Free State province. Pair 3 showed two Ag-
NORs occurring proximal to the centromere on the short arm and on the terminal end of the long
arm, respectively.
I obtained 953bp of mtDNA cyt b from fresh material and 400bp from museum material.
Using maximum parsimony and Bayesian inference two main clades were retrieved. Clade A
specimens occur mainly in the Western and Eastern Cape provinces of South Africa. Clade B
specimens occur in the Eastern Cape, Free State, KwaZulu-Natal, Northern Cape and
Mpumalanga provinces of South Africa. The mean sequence divergence between the main clades
(A and B) is 7.0% and between sub-clades comprising clade B is 4.8%, while within clade A the
sequence divergence was 1.91%. Nested clade analysis revealed allopatric fragmentation within
O. irroratus. Chromosomal characters also support the two evolutionary lineages as clade A has
pericentric inversions which occur as floating polymorphisms which are absent in clade B. Clade
B in turn is fixed for a complex tandem fusion rearrangement which is absent from clade A.
Divergence date estimates indicate that the two clades separated around 1.1 MYA, which
coincides with climate changes since the late Pliocene/Pleistocene epochs. Cladogenesis within
this species complex could therefore have been influenced by habitat fragmentation. A full
taxonomic review of O. irroratus is therefore warranted by this study. / AFRIKAANSE OPSOMMING: Die suider Afrikaanse vlei rot, Otomys irroratus word gekenmerk deur fenotipiese konservatisme
regoor die spesie se verspreiding en het groot chromosomale variasie met diploied chromosoom
getalle wat reeks vanaf 2n = 23 tot 2n = 32. Hierdie variasie binne O. irroratus het gelei tot die
beskrywing van drie chromosomale groupe naamlik die A sitotipe wat gekenmerk word deur 'n
akrosentriese komplement. Die tweede groep wat die B sitotipe genoem word besit ten minste
agt chromosoom pare met heterokromatiese kort arms, onderwyl die derde group (die C sitotipe)
vier chromosoom pare het met heterokromatiese kort arms. Hierdie studie bestudeer die
bevolkings genetika struktuur van O. irroratus deur 102 monsters te analiseer wat gekollekteer
was regoor die spesie se verspreiding binne Suid-Afrika en die mitochondriale merker sitokroom
b sowel as chromosoom fluoressent hibridisasie te gebruik.
Ek het 55 monsters van sewe lokaliteite binne Suid-Afrika sitogeneties geanaliseer deur gebruik
te maak van G- en C-bandbepaling asook die hibridisasie patrone geproduseer deur die vloeisorteerde
chromosoome van Myotomys unisulcatus. Die analise het gewys dat 47% van die
monsters perisentromeriese inversies besit het, wat slegs aangetref was of die outosome OIR1,
OIR4, OIR6 en OIR10. Hierdie inversies was nooit almal teenwoordig binne dieselfde monster
nie en was gevind in beide heterosigotiese en homosigotiese vorm. Die inversies kom ook voor
oor 'n wye verspreiding wat daarop aandui dat dit swerwende polymorfisme is. Omdat inversies
lei tot die produksie van aneuploiede gamete speel hulle 'n belangrike rol in post-parings
reproduktiewe isolasie, die verskyning van swerwende inversies binne vlei rotte dui dus daarop
dat hulle onderhou word binne populasie verband deur die onderdrukking van rekombinasie in
die gedeeltes van die chromosoom. Verdere verskille tussen populasies behels die voorkoms of
afwesigheid van heterochromatiese kort arms wat (nie inversies) wat lei tot die variasies in die
Nfa (40 – 49). Die variasie in diploied getal (2n = 28 – 32) is eksklusief as gevolg van B
chromosoome. Ag-NOR banding het ook gewys dat daar twee evolusionêre lyne binne O.
irroratus voorkom.
Verder het filogenetiese analise van al die monsters verkryg deur volgorde-bepaling met behulp
van maksimale parsimonie en Bayesian afleiding twee klades geidentifiseer. Klade A diere kom
voor in die Wes en Oos-Kaap provinsies van Suid-Afrika terwyl klade B diere voorkom in die
Oos-Kaap, Vrystaat, KwaZulu-Natal, Noord-Kaap en Mpumalanga provinsies onderskeidelik van
Suid-Afrika. Die gemiddelde volgorde-bepalings verskille beloop 7% tussen die twee hoof
klades (A en B) en tussen sub-klades 4.8%, terwyl binne klade A die verskille slegs 1.91%
beloop het. Analise van die verwantskap tussen die klades het gewys dat allopatriese
fragmentasie heel waarskynlik gelei het tot die populasie genetiese struktuur binne O. irroratus.
Chromosoom karakters onderskraag die twee evolusionêre lyne waar klade A slegs perisentriese
inversies besit wat swerwend wat ontbreek in klade B. Klade B op sy beurt besit 'n komplekse
tandemme fusie wat glad nie voorkom in klade A nie. Molekulêre datering het verder gewys dat
die twee klades omtrent 1.1 miljoen jaar gelede versprei het, wat ooreenstem met die klimaats
veranderinge wat sedert die Peioceen en Pleistoceen plaasgevind het. Klade vorming binne die
spesies komples kan daarom as gevolg van habitat fragmentasie plaasgevind het. Hierdie studie
dus noodsaak 'n volle taksonomiese ondersoek van O. irroratus ten einde vas te stel hoeveel
spesies binne die komplex voorkom.
|
2 |
Ecology and life history of the Vlei Rat, Otomys Irroratus (Brants, 1827), on the Van Riebeeck Nature Reserve, PretoriaDavis, Richard Marcy January 1973 (has links)
The ecology and life history of the vlei rat, Otomys irroratus
(Brants, 1827), were studied in a population on the Van Riebeeck
Nature Reserve near Pretoria. Two main procedures were used to collect
the basic information and material for the project. First, a permanent
live-trapping grid was established where 333 animals were captured,
marked, released, and recaptured over a period of 26 months, Second,
snap-trapping and live-trapping were conducted elsewhere in the study
area for supplementary material. Because Otomys angoniensis Wroughton,
1906, a sibling species of 0. irroratus, also occurred in the study area and grid, it was necessary to define the differences in morphology and ecological distribution between the two species.
The ecology and life history of 0. irroratus are described and discussed in regard to the following major topics: taxonomy and morphology, distribution, population dynamics, reproduction, postnatal growth and development, activity, behavior, and economic importance.
In addition to the presently used means of distinguishing 0. irroratus and 0. angoniensis, it was found that the hind foot length of the two species differed, being 29-34 mm in 0. irroratus and 25-28 mm in O. angoniensis. The baculum of the two species was also found to be distinct in both shape and size.
In Southern Africa 0. irroratus occurs primarily in the grassland
subregion of the Southern Savanna biotic zone, while O. angoniensis
occurs primarily in the woodland subregion of the same biotic zone.
The preferred habitats of the two species on the study grid were
determined. There was little overlap of niches and each species had
a high degree of association with a different veld type, O. irroratus
being associated with the more mesic habitat.
The population size of O. irroratus reached a peak in May and a
low in September. The population also fluctuated considerably from
one year to the next, with rainfall possibly being the main contributing cause. The ratio of juveniles, subadults, and adults fluctuated primarily in respect to the season when the young were born. The sex ratio did not depart significantly from 1:1. Males comprised 49,5 per cent of the total and females 50,5 per cent.
The rate of disappearance after one month from first capture was
41 per cent, indicating that a large number of transients and individuals
dispersing from their birth site were involved. The overall rate
of disappearance, excluding the high first month rate of disappearance,
was 3,1 per cent per month.
The mortality rate appeared to be at its highest between August
and September when the food and cover were of very poor quality and
quantity. This was also the period when males demonstrated a significant
loss in body weight. The major factors causing mortality appeared to be flooding of
the habitat and owl predation. Floods not only reduced the population
but significantly interrupted breeding. Otomys irroratus was one of
the most prominent prey species of both barn and grass owls.
The major factors causing mortality appeared to be flooding of
the habitat and owl predation. Floods not only reduced the population
but significantly interrupted breeding. Otomys irroratus was one of
the most prominent prey species of both barn and grass owls.
Recapture data revealed that the mean home range size was 1 443m2, while that of males (1 730 m2) was highly significantly different
(P<O,Ol) from that of females (1 252m2). Home range size decreased
significantly in winter but only slightly in relation to a doubling of the population size. Of 18 individuals recaptured after a flood, 12 (66,7 per cent) had returned to their previously determined home range. Despite a small mean litter size (2,33) and relatively long gestation period (about 40 days), the long breeding season (nine months) and
precocial birth, rapid development, and nipple-clinging behavior of the
young together give O. irroratus a good reproductive potential.
Several litters of young were reared. They are precocial at
birth and development proceeds rapidly. At birth the incisors are
erupted, enabling the young to cling firmly to the nipples of the
mother, thereby reducing mortality losses. Most adult behavior
patterns are developed before weaning at 13 days of age. Sexual maturity
is reached at approximately three months of age. Otomys irroratus is primarily crepuscular, but activity tests conducted in the field and laboratory indicated some activitv throughout the day and night. Individual and social behavior are described and discussed. The
vlei rat is shy and retiring in captivity and in nature is not easily
captured by the use of snap-traps.
Interactions of adults were tested and they were found to be antisocial,
with intrasexual aggression occurring when caged. Complex
threat and communication patterns exist, a feature of asocial behavior.
Mating failed to occur in captivity, probably as a result of their
antisocial nature.
Marking behavior is very distinctive and, combined with urination
and possibly defecation, would appear to be useful in delineating
territories. It would also appear from their social habits, marking
behavior, and considerable overlap of home ranges that their interactions
with conspecifics in nature are represented by a dominance
hierarchy.
The influence of O. irroratus upon the environment was found to
be slight. The species serves as a common prey item for a number of
predators and was found to harbor several endo- and ectoparasites of
public health importance. / Thesis (DSc)--University of Pretoria, 1973. / gm2013 / Zoology and Entomology / Unrestricted
|
Page generated in 0.0596 seconds