Ventilatory accommodation of oxygen demand and respiratory water loss in kangaroos from mesic and arid environments, the eastern grey kangaroo (Macropus giganteus) and the red kangaroo (Macropus rufus)

We studied ventilation in kangaroos from mesic and arid environments, the eastern grey kangaroo (Macropus giganteus) and the red kangaroo (Macropus rufus), respectively, within the range of ambient temperatures (T(a)) from -5 degrees to 45 degrees C. At thermoneutral temperatures (Ta=25 degrees C), there were no differences between the species in respiratory frequency, tidal volume, total ventilation, or oxygen extraction. The ventilatory patterns of the kangaroos were markedly different from those predicted from the allometric equation derived for placentals. The kangaroos had low respiratory frequencies and higher tidal volumes, even when adjustment was made for their lower basal metabolism. At Ta>25 degrees C, ventilation was increased in the kangaroos to facilitate respiratory water loss, with percent oxygen extraction being markedly lowered. Ventilation was via the nares; the mouth was closed. Differences in ventilation between the two species occurred at higher temperatures, and at 45 degrees C were associated with differences in respiratory evaporative heat loss, with that of M. giganteus being higher. Panting in kangaroos occurred as a graded increase in respiratory frequency, during which tidal volume was lowered. When panting, the desert red kangaroo had larger tidal volumes and lower respiratory frequencies at equivalent T(a) than the eastern grey kangaroo, which generally inhabits mesic forests. The inference made from this pattern is that the red kangaroo has the potential to increase respiratory evaporative heat loss to a greater level.     

Free-ranging heart rate, body temperature and energy metabolism in eastern grey kangaroos (Macropus giganteus) and red kangaroos (Macropus rufus) in the arid regions of South East Australia

Eastern grey kangaroos (Macropus giganteus) are generally regarded as mesic inhabitants. Even though access to drinking water in permanent stock watering troughs is commonly available, these animals are still found in only low densities in arid pastoral areas. We hypothesised that the differential success of red and grey kangaroos in the arid zone may be due to higher energy requirements of M. giganteus with a concomitant need for increased food, rather than limitations imposed by inadequate water access. We set out to test this by indirectly measuring energy expenditure through the monitoring of heart rate by radio telemetry in semi-free-ranging eastern grey and red kangaroos (Macropus rufus). Radio telemetry measurements of heart rate were calibrated against oxygen consumption and were used in the assessment of energy expenditure of animals maintained in an 8-ha enclosure in the arid zone of southeast Australia. Heart rate provided a reliable estimate of oxygen consumption. This well-correlated relationship was curvilinear and was established for each individual. Behavioural observations revealed that both kangaroo species spent most of the day in low energy demanding activities. M. rufus were more active at night whilst M. giganteus were more active in the early mornings and late afternoons. Like other marsupials, both species had low field metabolic rates (FMRs). However, M. giganteus in keeping with their mesic history had higher FMRs than the more arid-adapted M. rufus, particularly during water restriction. Body temperature telemeters revealed a further species difference in that under hot conditions when water is freely available, M. rufus exhibits a higher and more labile daytime body temperature than M. giganteus. During the hottest part of the day M. giganteus maintain body temperature, relying upon increased evaporative cooling mechanisms, such as licking. Indeed, only when access to drinking water was restricted was thermolability evident in M. giganteus. Differences in behaviour and concomitant energy expenditure may thus contribute substantially to the divergent distribution and abundance of these two kangaroo species.     

"Whey" proteins of milk of the red (Macropus rufus) and eastern grey (Macropus giganteus) kangaroo

1. A comparison is made of gel electrophoretic patterns of the "whey" proteins of the milk of red (Macropus rufus) and eastern grey (Macropus giganteus) kangaroos at various stages of lactation. Qualitative and quantitative changes occur with time during the mature phase of lactation of both types. Their onset is related solely to the stage of lactation. "Whey" proteins are isolated and characterised and the nature of protein changes determined for the first time. 2. The anodic electrophoretic pattern is divided into 6 main zones (designated A F in order of decreasing mobility) and 2 cathodic zones (G and H) that are only detected in the milk of M. giganteus. 3. Zones A, B and C are milk specific. Zone B is present throughout lactation in both species and is an alpha-lactalbumin. Zones A and C are present only in late lactation, zone C, usually, but not always, appearing first. Zone A is an alpha-lactalbumin in M. giganteus, but is not an alpha-lactalbumin in M. rufus. Zone C appears to be the same protein in both species and is possibly a beta-lactoglobulin. 4. Zone D is kangaroo serum albumin and zone E is possibly a beta 2-microglobulin. Zone F contains three main iron (III) binding bands whose relative intensity varies with stage of lactation. Their intensity differs from the corresponding blood serum transferrin bands. 5. Zone H of Macropus giganteus is a lysozyme. 6. Lactose is present in the milk, but is not the principal sugar. 7. The significance of the results is discussed.     

A new species of Cryptosporidium (Apicomplexa: Cryptosporidiidae) from eastern grey kangaroos (Macropus giganteus)

Cryptosporidium macropodum n. sp is described. Oocysts of C. macropodum from the feces of kangaroos (Macropus spp.) are morphologically indistinguishable from other mammalian Cryptosporidium species, including C. parvum, C. hominis, C. suis, and C. canis. The oocysts are fully sporulated on excretion, lack sporocysts, and have an average width of 4.9 microm (4.5-6.0), a length of 5.4 microm (5.0-6.0), and a length:width ratio of 1.1. Phylogenetic analyses of the 18S ribosomal RNA, actin, and heat shock protein 70 (HSP70) loci demonstrate that C. macropodum is genetically distinct from all described Cryptosporidium species, including others found in marsupials. The parasite seems to be highly host-specific, because it has been found only in marsupials to date. Therefore, based on biological and molecular data, we consider C. macropodum a new species.     

Tooth wear in eastern grey kangaroos (Macropus giganteus) and western grey kangaroos (Macropus fuliginosus), and its potential influence on diet selection, digestion and population parameters

As teeth wear in eastern and western grey kangaroos, the pattern of enamel ridges changes. This affects the amount of available cutting edges and consequently the masticatory efficiency. These kangaroos also have molar progression. There is evidence for the independence of rates of tooth wear and molar progression, and variation is found in the maximum amount of wear attained by teeth both within and between populations. This variation has the potential to affect diet selection, digestion and population parameters.     

Foraging behaviour and dispersion of eastern grey kangaroos (Macropus giganteus) in an ideal free framework

Ideal free distribution (IFD) theory predicts that animals in competitive situations should distribute themselves among available habitat patches according to the density of conspecifics and its regulatory effect on resources. To investigate the applicability of IFD models to free-ranging herbivores, we quantified the dispersion and foraging behaviour of eastern grey kangaroos Macropus giganteus among habitat patches of differing suitability, within and outside a reservoir catchment in southern Victoria, Australia. Kangaroo densities within the catchment had a regulatory effect on resource density, while surrounding farmland maintained a higher standing crop despite higher densities of competitors. This difference was slight in autumn, however, when the system was apparently close to equilibrium. Gross bite rates of individuals foraging in farmland were lower than for individuals foraging within the catchment, and vigilance behaviour occurred more frequently in farmland habitat than any other, decreasing time devoted to feeding. Interference competition occurred in only 1.9% of focal samples, although competitive differences based on phenotype were observed. Although resource gains by individual kangaroos are likely to be influenced by other factors, including resource dynamics, predation risk and phenotypic differences, IFD theory provides a valuable analytical framework for this herbivore foraging system.     

Thermoregulation in juvenile red kangaroos (Macropus rufus) after pouch exit: higher metabolism and evaporative water requirements.

The population dynamics of red kangaroos (Macropus rufus) in the Australian arid zone is tightly linked with environmental factors, which partly operate via the survival of juvenile animals. A crucial stage is the young-at-foot (YAF) stage when kangaroos permanently exit the pouch. We have examined the thermal biology of YAF red kangaroos during ages from permanent pouch exit until weaning. Over a wide range of environmental temperatures (ambient temperature [T(a)] -5 degrees to 45 degrees C), YAF red kangaroos had a mass-specific metabolism that was generally twice that of adults, considerably higher than would be expected for an adult marsupial of their body size. The total energy requirements of YAF red kangaroos were 60%-70% of those of adult females, which were three times their size. Over the same range in T(a), YAF red kangaroos also had total evaporative water losses equal to those of adult females. At the highest T(a) (45 degrees C), differences were noted in patterns of dry heat loss (dry conductance) between YAF red kangaroos and adult females, which may partially explain the relatively high levels of evaporative cooling by YAF. By weaning age, young kangaroos showed little change in their basal energy and water requirements (at T(a) 25 degrees C) but did show reduced mass-specific costs in terms of energy and water use at extremes of T(a) (-5 degrees and 45 degrees C, respectively). In their arid environment, typified by unpredictable rainfall and extremes of T(a), young red kangaroos may need to remain close to water points, which, in turn, may restrict their ability to find the high-quality forage needed to meet their high energy demands.     

Competition between red kangaroos (Macropus rufus) and sheep (Ovis aries) in the arid rangelands of Australia

Abstract Competition between red kangaroos and sheep in the more arid areas of Australia was examined by means of a large-scale manipulative experiment incorporating two replicates of each of three treatments: sheep-only, kangaroo-only and a sheepAangaroo mixture. The study was conducted over two years during which time pasture conditions varied markedly. Competition was intermittent, occurring only during a period of climatically related food depletion (semi-drought). At this time there was a large increase in kangaroo densities due to an influx of kangaroos from neighbouring areas. Competition reduced live-weight in sheep but had no significant impact on wool production. This effect was linked to diet selection. Competition caused red kangaroos to favour paddocks destocked of sheep but had no detectable effect on the condition of kangaroos.     

The dietary overlap between red kangaroos (Macropus rufus) and sheep (Ovis aries) in the arid rangelands of Australia

Abstract The interaction between red kangaroos and sheep in the more arid areas of Australia was examined by means of a large-scale manipulative experiment. The diets of red kangaroos and sheep grazing together and separately in large paddocks were studied to assess whether competition for food might influence diet selection in these species. Diets and the amount of intra- and interspecific dietary overlap varied in accordance with pasture conditions. At pasture biomasses ranging from 50 to 200 g m^?2 (dry weight [wt]), the diets of red kangaroos and sheep overlapped by 58–73%, with forbs and grasses being the major items in the diets of both species. The diets of both sheep and red kangaroos under different experimental regimes were similar. In dry times (pasture biomass 40–50 g m^?2 (dry wt) more shrubs were eaten by both species and the amount of dietary overlap tended to be lower (52–66%). The diets of kangaroos were similar between paddocks. However, in paddocks containing both species sheep consumed proportionately more chenopodaceous shrubs and fewer grasses than those in ‘kangaroo-free’ paddocks.     

Repertoires of social behaviour in captive and free-ranging grey kangaroos, Macropus giganteus and Macropus fuliginosus (Marsupialia: Macropodidae)

The eastern grey kangaroo, Macropus giganteus , and the western grey kangaroo, M. fuliginosus , are sibling species. The behaviour of 48 eastern grey kangaroos and 15 western grey kangaroos was observed for 249 h at Melbourne Zoo. Up to 31 eastern grey kangaroos and 38 western grey kangaroos were observed for 305 h where they occurred syntopically in the Grampians National Park.
In total, 46 social acts were identified in four social contexts between conspecifics. All but one of the acts were performed by both species in captivity, whereas fewer were seen performed by either species in the field. Five general acts were performed by all age/sex classes, and 10 acts occurred in mother-young contexts. High-intensity agonistic acts and all sexual acts were performed exclusively by adult males. In captivity, western grey males performed a truncated range of sexual acts directed at eastern grey females, but no interspecific sexual acts were performed by males of either species in the field, supporting the distinctiveness of the two species. The close evolutionary relationship between the two species was confirmed by high degree of concordance between their behavioural repertories, which differed only in the structure of the isolation call given by large pouch young.     

A trichoepithelioma in a wild eastern grey kangaroo (Macropus giganteus)

The gross and microscopic pathology of a neoplastic skin lesion from the chest of a wild adult eastern grey kangaroo (Macropus giganteus) was consistent with the diagnosis of a trichoepithelioma. This was a benign lesion of the epithelial cells of the hair follicle and is the second type of skin neoplasm reported from macropodids.     

Endogenous nitrogen excretion by red kangaroos (Macropus rufus): effects of animal age and forage quality

Red kangaroos (Macropus rufus) are large (>20 kg) herbivorous marsupials common to arid and semiarid Australia. The population dynamics of red kangaroos are linked with environmental factors, operating largely through juvenile survival. A crucial period is the young-at-foot (YAF) stage, when juveniles have permanently left the mother's pouch but still take milk from a teat in the pouch. Forage quantity and quality have been implicated in drought-related mortalities of juvenile kangaroos. Here we compared how forage quality affected nitrogen (N) intake and excretion by YAF, weaned, and mature, nonlactating female red kangaroos. On high-quality forage (chopped lucerne hay, Medicago sativa) low in neutral-detergent fiber (43%+/-1%) and high in N (2.9%+/-0.1%), YAF and weaned kangaroos had ideal growth rates and retained 460-570 mg dietary N kg(-0.75) d(-1). But on poor-quality forage (chopped oaten hay, Avena sativa) high in neutral-detergent fiber (64%+/-1%) and low in N (0.9%+/-0.1%), YAF and weaned kangaroos could not sustain growth and were in negative N balance at -103+/-26 mg and -57+/-31 mg N kg(-0.75) d(-1), respectively. Notably, the YAF kangaroos excreted 64% of their truly digestible N intake from forage as nondietary fecal N (NDFN). By weaning age, the situation had improved, but the juveniles still lost 40% of their truly digestible N intake as NDFN compared with only 30% by the mature females. Our findings support field observations that forage quality, and not just quantity, is a major factor affecting the mortality of juvenile red kangaroos during drought.     

Structure and function of the eastern grey kangaroo (Macropus giganteus) foot thump

Most species of the family Macropodidae (kangaroos and wallabies) make a distinctive foot thump by striking the ground with their hind feet when they detect potential danger. I used the eastern grey kangaroo Macropus giganteus as a model to examine (1) the acoustic characteristics and structure of the thump, (2) the social context in which free-ranging kangaroos thumped when approached by a human observer on foot and (3) the intended recipient of the signal. Thumps were about two-thirds of a second in length, generally composed of two noisy pulses, and had the majority of the signal energy below 7 kHz. Only adult kangaroos, of both sexes, were observed to thump. A higher proportion of solitary kangaroos thumped than grouped kangaroos, and a higher proportion of kangaroos thumped when visibility was poor, either because of habitat type or low light levels. Given the context in which thumps were given, the foot thump appears to be a signal to a potential predator with three possible functions: to startle, signal detection or deter pursuit.     

Intraspecific variation,sex-biased dispersal and phylogeography of the eastern grey kangaroo (Macropus giganteus)

Genetic information has played an important role in the development of management units by focusing attention on the evolutionary properties and genetics of populations. Wildlife authorities cannot hope to manage species effectively without knowledge of geographical boundaries and demic structure. The present investigation provides an analysis of mitochondrial DNA and microsatellite data, which is used to infer both historical and contemporary patterns of population structuring and dispersal in the eastern grey kangaroo (Macropus giganteus) in Australia. The average level of genetic variation across sample locations was one of the highest observed for marsupials (h=0.95, HE=0.82). Contrary to ecological studies, both genic and genotypic analyses reveal weak genetic structure of populations, where high levels of dispersal may be inferred up to 230 km. The movement of individuals was predominantly male-biased (average Nem=22.61, average Nfm=2.73). However, neither sex showed significant isolation by distance. On a continental scale, there was strong genetic differentiation and phylogeographic distinction between southern (TAS, VIC and NSW) and northern (QLD) populations, indicating a current and/or historical restriction of gene flow. In addition, it is evident that northern populations are historically more recent, and were derived from a small number of southern founders. Phylogenetic comparisons between M. g. giganteus and M. g. tasmaniensis indicated that the current taxonomic status of these subspecies should be revised as there was a lack of genetic differentiation between the populations sampled.     

Similarities and differences in activities and agonistic behavior of male Eastern grey kangaroos (Macropus giganteus) in captivity and the wild

The behavior of free-ranging and captive Eastern grey kangaroos Macropus giganteus, was observed by the same observers, with similar methods and under similar vegetational/climatic conditions in a 4.2-ha enclosure at Neuwied Zoo, Germany and at Grampians National Park, Victoria, Australia. Data were collected from a zoo group of 56 animals and a free-ranging mob of 50 to 60 animals. Males were individually identified and observed: 3 large males, 9 medium males, and 10 small males in the zoo, and 8 large, 9 medium, and approximately 10 small males in the National Park were present. Activities in both situations were very similarly distributed: Feed took up less time in the zoo, resting was almost similar in both situations, alert behavior was significantly different for small and medium males, locomotor activities were similar in large males and females, autogrooming occurred significantly more in the zoo only for females. Frequencies of social interactions were slightly greater for large males and females in the zoo. Agonistic behavior in males was more frequent in the zoo situation, except for ritualized fights. Sequences of agonistic behavior were more predictable in the zoo. No differences in escalation tendencies toward potentially injurious fighting could be found. Zoo Biol 19:529-539, 2000. Copyright 2000 Wiley-Liss, Inc.     

Predation by red foxes limits recruitment in populations of eastern grey kangaroos

We investigated the impact of red fox (Vulpes vulpes Linnaeus 1758) predation on juvenile eastern grey kangaroos (Macropus giganteus Shaw 1790) using a replicated predator removal experiment. In two sites in Namadgi National Park, south‐eastern Australia, a persistent 1080 poisoning campaign over 18 months reduced fox density by more than 85%, and to less than 10% of the fox density in two other sites with no fox baiting. Changes in the mother : young ratios and densities of kangaroo populations were monitored twice monthly along 2‐km transects in each site from July 1993 to February 1995. Compared to nonremoval sites, where foxes were controlled, 25–40% more females retained juveniles over the period when these young became emergent from the pouch. This higher survival of emergent pouch young resulted in a significantly higher proportion of juveniles in kangaroo populations at fox control sites, which resulted in a significantly higher annual growth rate. We conclude that predation upon juveniles is an important limiting factor for kangaroo populations in Namadgi NP.     

Water use and the thermoregulatory behaviour of kangaroos in arid regions: insights into the colonisation of arid rangelands in Australia by the Eastern Grey Kangaroo (Macropus giganteus)

The Eastern Grey Kangaroo (Macropus giganteus) occurs mostly in the wetter regions of eastern Australia. However, in the past 30–40 years it has moved into more arid regions (rainfall<250 mm), thus increasing its overlap zone with the xeric adapted Red Kangaroo (Macropus rufus). An increased access to water (supplied for domestic stock) may explain this range extension, but changes in the availability of preferred feed could also be involved. The water use, drinking patterns and thermoregulatory behaviour of these two species of kangaroo have been examined in a semi-free range study, during summer at an arid rangeland site. Foraging was largely nocturnal in both species and during the day they behaved to reduce heat loads. This was especially so for M. giganteus, which showed greater shade seeking. However, it still used more water (72±2.6 mL kg⁻¹ day⁻¹, mean ± SE) than M. rufus (56±7.6 mL kg⁻¹ day⁻¹) and drank twice as frequently. Although M. giganteus produced a less concentrated urine (1422±36 mosmol kg⁻¹) than M. rufus (1843±28 mosmol kg⁻¹), kidney physiology did not explain all of the differences in water metabolism between the species. Water from the feed and faecal water retention also appear to be involved. Broadly, a better access to reliable water and the utilisation of mesic microhabitats has enabled M. giganteus to make inroads into the changing rangelands of eastern Australia. However, changes in the vegetation, due to stock grazing, have also favoured M. giganteus, which is a grass eating specialist.     

The effect of carbonic anhydrase inhibitors on secretion by the parotid and mandibular glands of red kangaroos Macropus rufus

Summary The effects of carbonic anhydrase inhibitors on secretion by macropodine parotid and mandibular glands were investigated using anaesthetized red kangaroos. In the parotid gland, acetazolamide (500 mol·l^-1) reduced a stable acetylcholine-evoked, half-maximal flow rate of 2.02±0.034 to 0.27±0.023 ml·min^-1 (87% reduction). Concurrently, salivary bicarbonate concentration and secretion fell (129.4±1.46 to 80.9±1.63 mmol·l^-1 and 264.8±7.96 to 22.3±2.30 mol·min^-1, respectively), phosphate and chloride concentrations rose (14.0±0.79 to 27.6±0.85 mmol·l^-1 and 5.6±0.25 to 27.5±1.32 mmol·l^-1, respectively), sodium concentration and osmolality were unaltered, and potassium concentration fell (8.8±0.33 to 6.4±0.29 mmol·l^-1). High-rate cholinergic stimulation during acetazolamide blockade was unable to increase salivary flow beyond 11±0.9% of that for equivalent unblocked control stimulation. However, superimposition of isoprenaline infusion on the acetylcholine stimulation caused a three-fold increase in the blocked flow rate. These treatments were accompanied by small increases in salivary phosphate and chloride concentrations but not bicarbonate concentration. Methazolamide infusion caused similar changes in parotid secretion. In the mandibular gland, acetazolamide infusion had no effect on salivary flow rate during either low- or high-level acetylcholine stimulation. Acetazolamide caused no alterrations in salivary electrolyte secretion at low flow rates, but curtailed the rise in bicarbonate concentration associated with high-level acetylcholine stimulation. Acetazolamide administration did not affect the increase in salivary flow rate associated with isoprenaline infusion, but did block the concomitant increase in bicarbonate concentration and secretion substantially. It was concluded that neither cholinergic nor adrenergic stimulation of mandibular fluid secretion depends on secretion of bicarbonate derived from catalysed hydration of CO₂, but a substantial proportion of the increase in bicarbonate secretion during isoprenaline administration, which is probably ductal in origin, is so dependent. In contrast to other salivary glands, including the ovine parotid, fluid secretion by the kangaroo parotid gland during cholinergic stimulation is largely dependent (about 90%) on secretion of bicarbonate derived from hydration of CO₂ catalysed by glandular carbonic anhydrase. Fluid secretion during adrenergic stimulation is not bicarbonate dependent.Abbreviations b.w. body weight - PAH p-aminohippurate - PCO₂ partial pressure carbon dioxide - PCO₂ partial pressure of oxygen