12 research outputs found

    The efficacy of a slow-release albendazole capsule against <i>Haemonchus contortus</i> with known resistance to albendazole

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    Controlled-release albendazole capsules (CRCs) are currently registered for use in Australia and New Zealand as anthelmintic treatment in sheep. However, reports on the efficacy of such products on resistant parasite populations are sometimes controversial. This is the first study to report on the efficacy of such products under South African field conditions in sheep harbouring a population of Haemonchus contortus with known multiple anthelmintic resistance, including to albendazole. Treatment groups were comprised of CRC-treated and single dose albendazole-treated sheep, as well as negative controls. Groups were compared by using faecal egg count reduction tests, FAMACHA© anaemia scoring, conception rates and comparative weight gains over three and a half months. Based on a comparison of faecal egg counts, no advantage could be found using CRCs. Moreover, the use of the product actually decreased weight gain when compared with the control group animals

    On reconstructing Giraffa sivalensis, an extinct giraffid from the Siwalik Hills, India

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    Giraffa sivalensis occurred during the Plio-Pleistocene and represents the terminal species of the genus in southern Asia. The holotype is a cervical vertebra of disputed anatomical location. Although there is also uncertainty as to this animal’s size, other specimens have been assigned to this species including fragments of two humeri, a radius, metacarpi and teeth. We estimated G. sivalensis neck length, leg length and body mass using interspecific and, unusually, ontogenetic allometry of extant giraffe skeletal parameters. The appropriateness of each equation to estimate body mass was evaluated through the prediction error incurred in both extant giraffes and okapis. It followed that the equations with the lowest prediction error in both species were considered robust enough to use in G. sivalensis. The size of G. sivalensis, based on the holotype, is proposed as 400 kg (range 228 kg - 575 kg), with a neck length of about 147 cm and a height of 390 cm. The molar lengths of tooth specimens considered agree with this size estimate. The humerus was the most appropriate long bone to establish body mass which estimates a heavier animal of ca 790 kg. The discrepancy with the vertebral body weight estimate might indicate sexual dimorphism. Radial and metacarpal specimens estimate G sivalensis to be as heavy as extant giraffes. This may indicate that the radius and metacarpus are unsuitable for body mass predictions in Giraffa spp. Alternatively, certain long bones may have belonged to another long legged giraffid that occurred during the same period and locality as G. sivalensis. We have concluded that if sexual dimorphism was present then males would have been about twice the size of females. If sexual dimorphism was not present and all bones were correctly attributed to this species, then G sivalensis had a slender neck with a relatively stocky body.Poster presented at the University of Pretoria, Faculty of Veterinary Science Faculty Day, August 20, 2015, Pretoria, South Africa.Created in CoralDRAW X5 on 2015/07/22. PDF size: 12.32 MB.ab201

    The digestive morphophysiology of wild, free-living, giraffes

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    We have measured rumen-complex (rumen, reticulum, omasum, abomasum) and intestine (small and large combined) mass in 32 wild giraffes of both sexes with body masses ranging from 289 to 1441 kg, and parotid gland mass, tongue length and mass, masseter and mandible mass in 9 other giraffes ranging in body mass from 181 to 1396 kg. We have estimated metabolic and energy production rates, feed intake and home range size. Interspecific analysis of mature ruminants show that components of the digestive system increase linearly (Mb1) or positively allometric (MbN1)with bodymasswhile variables associatedwith feed intake scalewithmetabolic rate (Mb.75). Conversely, in giraffes ontogenetic increases in rumen-complex masswere negatively allometric (Mbb1), and increases in intestine mass, parotid gland mass, masseter mass, and mandible mass were isometric (Mb1). The relative masseter muscle mass (0.14% of Mb) and the relative parotid mass (0.03% of Mb) are smaller than in other ruminants. Increases in tongue length scale with head length0.72 andMb.32 and tongue mass with Mb.69. Absolute mass of the gastrointestinal tract increased throughout growth but its relative mass declined from 20% to 15% of Mb. Rumen-complex fermentation provides ca 43% of daily energy needs, large intestine fermentation 24% and 33% by digestion of soluble carbohydrates, proteins, and lipids. Dry matter intake (kg) was 2.4% of body mass in juveniles and 1.6% in adults. Energy requirements increased from 35 Mj/day to 190 Mj/day. Browse production rate sustains a core home range of 2.2–11.8 km2.Don Craib Trust and the University of Wyoming.http://www.elsevier.com/locate/cbpa2016-09-30hb201

    Scaling of the appendicular skeleton of the giraffe (Giraffa camelopardalis)

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    Giraffes have remarkably long and slender limb bones, but it is unknown how they grow with regard to body mass, sex and neck length. In this study we measured the length, medio-lateral diameter (ML), cranio-caudal diameter (CC) and circumference of the humerus, radius, metacarpus, femur, tibia and metatarsus in 10 fetuses, 21 females and 23 males of known body masses. Allometric exponents were determined and compared. We found the average bone length increased from 340±50mm at birth to 700±120mm at maturity, while average diameters increased from 30±3mm to 70±11mm. Fetal bones increased with positive allometry in length (relative to body mass) and in diameter (relative to body mass and length). In postnatal giraffes bone lengths and diameters increased iso- or negatively allometric relative to increases in body mass, except for the humerus CC diameter which increased with positive allometry. Humerus circumference also increased with positive allometry, that of the radius and tibia isometrically and the femur and metapodials with negative allometry.Relative to increases in bone length, both the humerus and femur widened with positive allometry. In the distal limb bones ML diameters increased isometrically (radius, metacarpus) or positively allometric (tibia, metatarsus) while the corresponding CC widths increased with negative allometry and isometrically respectively. Except for the humerus and femur, exponents were not significantly different between corresponding front and hind limb segments. We concluded that the patterns of bone growth in males and females are identical. In fetuses the growth of the appendicular skeleton is faster than it is after birth which is a pattern opposite to that reported for the neck. Allometric exponents seemed unremarkable compared to the few species described previously, and pointed to the importance of neck elongation rather than leg elongation during evolution. Nevertheless, the front limb bones and especially the humerus may show adaptation to behaviors such as drinking posture.http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-46872016-05-31hb201

    Demography of giraffe deaths in a drought

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    Darwin’s theory for the evolution of the long neck of giraffes is that height confers access to browse free of competition from smaller browsers. The theory predicts that survivors of a drought will be the tallest animals in a population. All studies so far have tested this hypothesis by analysis of feeding patterns and behaviour.We have studied it by analysing the demography of deaths in a drought. Using skeletal material from 26 giraffes that died as a result of a drought in southeastern Zimbabwe in 2008, we established the body mass, height, and age of the dead giraffes using allometric equations developed from culled animals. Typical giraffe populations consist of 55% adults (>6 years old), 15% young adults (3–6 years old), 15% juveniles (1–3 years old), and 15% neonates (<1 year old). Skeletons came from 54% adults, 14% young adults, and 32% juveniles. No neonatal skeletons were found. More juveniles died than expected because they have to compete with other browsers for nutrients. Most adult deaths occurred in the tallest and largest males because their daily requirements for browse are highest and could not be met by the amounts available at any level. Thus the survivors of this drought were young adults, a finding contrary to the predictions of Darwin’s feeding hypothesis.The Don Craib Trust (JDS), the University of Wyoming (GM), and the University of Pretoria (SvS).http://www.informaworld.commn201

    Growth patterns and masses of the heads and necks of male and female giraffes

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    We have analyzed the growth patterns of the head and neck of 65 male and 71 female giraffes from two different populations of giraffes, and also the dimensions of 19 different components of the head and neck in 8 female and 13 male giraffes, to establish if they showed sexual dimorphism and if sexual selection for a weapon was a possible origin of the long neck of giraffes. We found that in both genders, the rate of increase in head mass was hypoallometric with respect to body mass. The rate of increase in neck length was similar in both genders and faster than the rate of increase in body mass. Increases in neck mass tend to be isometric relative to increases in body mass in both genders before puberty (c. 650 kg body mass in male and 700 kg in female giraffes), but in giraffes of greater body mass increases in neck mass are iso- to hyperallometric in both genders, with final neck, body and head mass being greater in male giraffes. The only significant gender difference we found for the dimensions of the 19 different head and neck components was that ossicones and skulls were heavier in mature male than in mature female giraffes, but increases in skull mass did not alter the growth pattern of head mass significantly. These data suggest that the morphology and growth patterns of the heads and necks of male and female giraffes are similar, that sexual dimorphism of the head and neck is minimal and can be attributed to secretion of sex steroids. We have concluded that there is no evidence that sexual selection was a factor in the evolution of giraffe morphology and that the long neck of giraffes did not evolve as a weapon in males. The more likely selective advantage of a long neck was improvement of access to high-level browse.The Bubye Valley Conservancy, Zimbabwe.The Don Craib Trust (JDS), from a personal research grant (JDS) and the University of Wyoming (GM).http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1469-7998hb2013mn201

    Orbit orientation and eye morphometrics in giraffes (Giraffa camelopardalis)

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    Giraffe are thought to have excellent vision.We measured eye size, orbit orientation and retina surface area in 27 giraffes of both sexes ranging in age from neonates to mature adults (>10 yrs), to assess how it changes with growth, whether their eye anatomy correlates with their apparently excellent vision and lifestyle, and we have compared our findings with those for other large mammals to assess whether giraffe eye anatomy is unique.We found that giraffe eye volume increases from 33 cm3 at birth to approximately 65 cm3 in adults. The focal (axial) length increases from c. 40 to 48 mm in adults and retina surface area from c. 3000 mm2 at birth to 4320 mm2 in adults. The orbital axis angle at birth is c. 73° and the horizontal visual field mainly monocular and panoramic.With age the axis angle becomes more acute to c. 50° in adults and the visual field more binocular, changes that occur concurrently with increasing neck length. These results show that the giraffe eye and retinal surface area are larger than in all other ungulates, and their visual fields more binocular, attributes which are consistent with the idea that they have excellent vision.The Don Craib Trust (J.D.S.), from a personal research grant (J.D.S.) and the University of Wyoming (G.M.). S.J.v.S. is in receipt of the Maberly Memorial Scholarship and a University of Pretoria study bursary.http://africanzoology.journals.ac.za/am2014mn201

    Occurrence of African horse sickness in a domestic dog without apparent ingestion of horse meat

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    This is the first case of African horse sickness (AHS) in a dog where there was no apparent ingestion of horse meat. Significantly, the dog was part of a colony that resides in a Good Clinical Practice and Good Laboratory Practice accredited facility where complete history, weather and feeding records are maintained. The dog died after a week-long illness despite therapy. The principal post-mortem findings were severe hydrothorax and pulmonary consolidation (red hepatisation of the lungs). Histopathology revealed severe oedema and congestion of the lungs, hyaline degeneration of the myocardium and congestion of the liver sinusoids. Immunohistochemistry detected AHS-positive staining granules in the myocardium, whilst a real-time reverse transcription quantitative Polymerase chain reaction assay of tissue samples was strongly positive for African horse sickness virus nucleic acid. Other dogs on the property showed a 43% seroconversion rate to AHS.The National Veterinary Clinicians Group of the South African Veterinary Associationhttp://www.jsava.co.zaam2014ab201

    On reconstructing Giraffa sivalensis, an extinct giraffid from the Siwalik Hills, India

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    Giraffa sivalensis occurred during the Plio-Pleistocene period and probably represents the terminal species of the genus in Southern Asia. The holotype is an almost perfectly preserved cervical vertebra of disputed anatomical location. Although there is also uncertainty regarding this animal’s size, other specimens that have been assigned to this species include fragments of two humeri, a radius, metacarpi and teeth. Here we estimate neck length, leg length and body mass using interspecific and, unusually, ontogenetic allometry of extant giraffe skeletal parameters. The appropriateness of each equation to estimate body mass was evaluated by calculating the prediction error incurred in both extant giraffes (G. camelopardalis) and okapis (Okapia johnstoni). It followed that the equations with the lowest prediction error in both species were considered robust enough to use in G. sivalensis. The size of G. sivalensis, based on the holotype, is proposed as 400 kg (range 228 kg–575 kg), with a neck length of approximately 147 cm and a height of 390 cm. The molar lengths of tooth specimens considered agree with this size estimate. The humerus was the most appropriate long bone to establish body mass, which estimates a heavier animal of ca 790 kg. The discrepancy with the vertebral body weight estimate might indicate sexual dimorphism. Radial and metacarpal specimens estimate G. sivalensis to be as heavy as extant giraffes. This may indicate that the radius and metacarpus are unsuitable for body mass predictions in Giraffa spp. Alternatively, certain long bones may have belonged to another long legged giraffid that occurred during the same period and locality as G. sivalensis. We have concluded that if sexual dimorphism was present then males would have been about twice the size of females. If sexual dimorphism was not present and all bones were correctly attributed to this species, then G. sivalensis had a slender neck with a relatively stocky body

    The structure and function of giraffe jugular vein valves

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    When a giraffe (Giraffa camelopardalis) lowers its head to drink, blood could enter the jugular vein from the inferior vena cava or regurgitate from the jugular veins into the cranial veins. We investigated the anatomy of jugular valves in giraffes to establish if they could prevent either of these regurgitations. Jugular vein length and intervalve distances of 396 valves (192 left, 204 right) were measured in 60 veins from 25 adult (11 males and 14 females) and five foetal giraffes. The average number of valves in the left jugular veins was 6.4 ± 2.7 (mean ± S.D.; range = 2-13) and in the right was 6.8 ± 2.1 (range = 3-12). Male giraffes had 7.3 ± 2.7, females 5.9 ± 2.1, and foetuses 7.0 ± 2.1 valves per vein. None of these differences was statistically significant (t-test; P > 0.05). Most valves (88%) were bicuspid in structure. Their position in the veins was irregular. Most (36.1%) were located in the first 500mm of vein. The relative distribution of foetal valves was not significantly different from that in adult giraffes (X2 = 0.274, P > 0.05). We concluded that the main function of the jugular vein valves is to prevent regurgitation of blood from the inferior vena cava and right atrium into the jugular vein and that the number of valves is fixed in utero
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