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Scaling of the Appendicular Skeleton of the Giraffe (Giraffa camelopardalis)

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, mediolateral (ML) diameter, craniocaudal (CC) diameter 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 ± 50 mm at birth to 700 ± 120

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Urinary steroid evaluations to monitor ovarian function in exotic ungulates: II. Comparison between the giraffe (giraffa camelopardalis) and the okapi (okapia johnstoni)

Ovarian activity in the female giraffe was evaluated during the nonfertile ovarian cycle and during the terminal stages of gestation. Progesterone metabolites, in the form of pregnanediol‐3‐glucuronide (PdG), were measured in daily random urine samples collected from four adult parous giraffes. The follicular phase averaged 4.0 ± 0.1 days in length (N = 12; range 3–5 days) and peak PdG levels in the postovulatory period averaged 30.9 ± 1.7 ng/mg Cr (N = 12). PdG levels during the latter half

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Physiological cross-sectional area of the masticatory muscles in the giraffe (Giraffa camelopardalis)

Numerous studies have investigated how the skeletal morphology is related to feeding behaviour (Christiansen and Adolfssen 2005; Wroe et al. 2005; Christiansen and Wroe 2007; Ellis et al. 2009; Koyabu and Endo 2009; Koyabu et al. 2009; Koyabu and Endo 2010), although remarkably few studies have focused on the architecture of masticatory muscles from which bite forces are produced. In this regard, the quantification of physiological cross-sectional areas (PCSA) of muscle is critical for estimation of bite forces. PCSA is

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Are giraffes pollinators or flower predators of Acacia nigrescens in Kruger National Park, South Africa?

We examined the relationship between giraffes (Giraffa camelopardalis) and Acacia nigrescens in Kruger National Park, South Africa, to determine whether these tall ungulates may be providing a pollination service for the trees, or are simply flower predators. We quantified florivory and subsequent fruit set in the presence and absence of giraffes. Acacia nigrescens flowers are clearly a substantial dietary component for giraffes. Although A. nigrescens flowers contain almost three times as much condensed tannin as leaves, giraffes consume large quantities

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The diet of a small group of extralimital giraffe

Giraffe are extralimital in the Eastern Cape Province, South Africa where recent local introductions have persisted despite limited research into their impact on the indigenous flora. The diet of 15 giraffe at the Shamwari Game Reserve was recorded by direct observation during summer (March/April) and winter (July/August) 2001, quantifying diet by frequency of occurrence (individual records scored and expressed as a percentage of the total). Preference indices were also calculated. Habitat use was measured by the number of hours giraffe

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Colonic obstruction in three captive reticulated giraffe (Giraffa camelopardalis reticulata)

Fatal colonic obstructions were diagnosed in three captive, adult, reticulated giraffe (Giraffa camelopardalis reticulata). Clinical presentations varied, but all cases displayed decreased activity, anorexia, and considerably decreased fecal production, consistent with intestinal obstruction. Case 1 was diagnosed at necropsy with a phytobezoar obstructing the spiral colon. Case 2 was diagnosed at necropsy with a fecal impaction of the colon. Case 3 was diagnosed during surgery with colonic ileus. Cases 2 and 3 underwent surgical intervention but were markedly compromised by

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Large predators and their prey in a southern African savanna: a predator’s size determines its prey size range

A long‐term (13‐year) data set, based on > 4000 kills, was used to test whether a sympatric group of large predators adheres to the theoretical predictions that (1) mean prey body size and (2) prey diversity increase as functions of predator body size. All kills observed by safari guides are documented routinely in Mala Mala Private Game Reserve, South Africa. We analysed these records for lion (Panthera leo, Linnaeus), leopard (Panthera pardus, Linnaeus), cheetah (Acinonyx jubatus, Schreber) and African wild dog (Lycaon

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Development of 11 microsatellite markers for Giraffa camelopardalis through 454 pyrosequencing, with primer options for an additional 458 microsatellites

Many wild giraffe populations are declining across Africa, with two subspecies listed by the IUCN as Endangered in the past 4 years. We developed 11 microsatellite markers from Giraffa camelopardalis angolensis in Etosha National Park, Namibia using 454 sequencing. In 70 individuals, the loci showed 2–4 alleles per locus and expected heterozygosities of 0.082–0.711. There were no significant deviations from Hardy–Weinberg equilibrium for any of the loci. Null allele frequencies were low (<3 %) across all loci. We present primer options for

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Identification of novel Babesia and Theileria species in South African giraffe (Giraffa camelopardalis, Linnaeus, 1758) and roan antelope (Hippotragus equinus, Desmarest 1804)

Blood specimens were received from five cases in which young adult giraffe, from different geographic origins in South Africa, showed sudden onset of disease and subsequently died. Additional specimens from two translocated giraffe, as well as one specimen from a roan antelope, were also included in the study. Blood slides from some of these animals showed the presence of piroplasms. DNA was extracted; the V4 hypervariable region of the 18S rRNA gene amplified and analyzed using the Reverse Line Blot

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Extensive population genetic structure in the giraffe

Background: A central question in the evolutionary diversification of large, widespread, mobile mammals is how substantial differentiation can arise, particularly in the absence of topographic or habitat barriers to dispersal. All extant giraffes (Giraffa camelopardalis) are currently considered to represent a single species classified into multiple subspecies. However, geographic variation in traits such as pelage pattern is clearly evident across the range in sub-Saharan Africa and abrupt transition zones between different pelage types are typically not associated with extrinsic barriers

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