Behaviour of the Koala, Phascolarctos cinereus (Goldfuss), in CAptivity V*. Sexual Behaviour

1980 ◽  
Vol 7 (1) ◽  
pp. 41 ◽  
Author(s):  
M Smith

At the height of the breeding season male koalas frequently attempted copulation. These attempts were often apparently spontaneous, but many followed bellowing or agonistic interactions. Sexual behaviour began at 3 y old in males, except for penile erections, which sometimes occurred in younger males. Males performed no courtship behaviour. Behavioural oestrus was brief, and consisted of four distinct types of activity: jerking, bellowing, mild aggression towards the male, and pseudomale behaviour. Oestrous females could become very excited by the presence of a male, and the four activities were very flexible in their expression. Copulation itself was quite brief and consisted of mounting, thrusting, convulsions, and disengagement. The pair were always in a vertical position in a tree, the male grasping the female's neck in his jaws.

1980 ◽  
Vol 7 (2) ◽  
pp. 177 ◽  
Author(s):  
M Smith

'In a colony of captive koalas, all aggressive behaviour was a variation on the single motor pattern of throwing a foreleg around an opponent and biting. Squabbles (the most common aggressive behaviour) were brief, low level interactions usually arising from the efforts of one koala to climb past or over another. Minor fghts involved only single bites and the combatants stayed in the same place; major ,fights involved multiple bites and changes of position. Dependent young were seldom involved in aggression. Between males. minor fights were essentially intensified squabbles, but major fights involved wrestling and chasing; they were more likely between males unfamiliar with each other, or those already aroused by, e.g., other aggressive interactions. Females became aggressive especially during pregnancy and at the end of lactation. At such times they stood their ground and vocalized at other koalas, especially males, but attacked only if the opponent came within reach. Although the opponent usually withdrew. sometimes a male seemed provoked to attack. Males sometimes attacked females without obvious provocation. Aggression was slightly more common in than outside the breeding season. Competition for females or food, dominance hierarchies, appeasement, and the defence of young were not seen.


Behaviour ◽  
1979 ◽  
Vol 70 (1-2) ◽  
pp. 1-116 ◽  
Author(s):  
I. Bossema

AbstractThe European jay (Garrulus g. glandarius) strongly depends on acorns for food. Many acorns are hoarded enabling the jay to feed upon them at times of the year in which they would otherwise be unavailable. Many of the hoarded acorns germinate and become seedlings so that jays play an important role in the dispersal of acorns and the reproduction of oaks (in this study: Quercus robur, the pedunculate oak). These mutual relationships were analysed both with wild jays in the field (province of Drente, The Netherlands) and with tame birds in confinement. Variation in the composition of the food throughout the year is described quantitatively. Acorns were the stock diet of adults in most months of the year. Leaf-eating caterpillars predominantly occurring on oak were the main food items of nestlings. Acorns formed the bulk of the food of fledglings in June. A high rate of acorn consumption in winter, spring and early summer becomes possible because individual jays hoard several thousands of acorns, mainly in October. In experiments, acorns of pedunculate oak were not preferred over equal sized acorns of sessile oak (which was not found in the study area). Acorns of pedunculate oak were strongly preferred over those of American oak and nuts of hazel and beech. Among acorns of pedunculate oak, ripe, sound, long-slim and big ones were preferred. Jays collect one or more (up to six) acorns per hoarding trip. In the latter case, the first ones are swallowed and the last one is usually carried in the bill. For swallowing the dimensions of the beak imposed a limit on size preference; for bill transport usually the biggest acorn was selected. The greater the number of acorns per trip, the longer was the transportation distance during hoarding. From trip to trip jays dispersed their acorns widely and when several acorns were transported during one trip, these were generally buried at different sites. Burial took place by pushing acorns in the soil and by subsequent hammering and covering. Jays often selected rather open sites, transitions in the vegetation and vertical structures such as saplings and tree trunks, for burial of acorns. In captivity jays also hoarded surplus food. Here, spacing out of burials was also observed; previously used sites usually being avoided. In addition, hiding along substrate edges and near conspicuous objects was observed. Jays tended to hide near sticks presented in a horizontal position rather than near identical ones in vertical position, especially when the colour of the sticks contrasted with the colour of the substrate. Also, rough surfaced substrate was strongly preferred over similar but smooth surfaced substrate. Successful retrieval of and feeding on hoarded acorns were observed in winter even when snow-cover had considerably altered the scenery. No evidence was obtained that acorns could be traced back by smell. Many indications were obtained that visual information from near and far beacons, memorized during hiding, was used in finding acorns. The use of beacons by captive jays was also studied. Experiments led to the conclusion that vertical beacons are more important to retrieving birds than identical horizontal ones. The discrepancy with the jay's preference for horizontal structures during hiding is discussed. Most seedlings emerge in May and June. The distribution pattern of seedlings and bill prints on the shells of their acorns indicated that many seedlings emerged from acorns hidden by jays in the previous autumn. The cotyledons of these plants remain underground and are in excellent condition in spring and early summer. Jays exploited acorns by pulling at the stem of seedlings and then removing the cotyledons. This did not usually damage the plants severely. Jays can find acorns in this situation partly because they remember where they buried acorns. In addition, it was shown that jays select seedlings of oak rather than ones of other species, and that they preferentially inspected those seedlings that were most profitable in terms of cotyledon yield and quality. Experiments uncovered some of the visual cues used in this discrimination. The effects of hoarding on the preservation of acorns were examined in the field and the laboratory. Being buried reduced the chance that acorns were robbed by conspecifics and other acorn feeders. Scatter hoarding did not lead to better protection of buried acorns than larder hoarding, but the spread of risk was better in the former than the latter. It was concluded that the way in which jays hoard acorns increases the chance that they can exploit them later. In addition, the condition of acorns is better preserved by being buried. An analysis was made of the consequences of the jay's behaviour for oaks. The oak does incur certain costs: some of its acorns are eaten by jays during the dispersal and storage phase, and some seedlings are damaged as a consequence of cotyledon removal. However, these costs are outweighed by the benefits the oak receives. Many of its most viable acorns are widely dispersed and buried at sites where the prospects for further development into mature oak are highly favourable. The adaptiveness of the characters involved in preferential feeding on and hoarding of acorns by jays is discussed in relation to several environmental pressures: competition with allied species; food fluctuations in the jay's niche; and food competitors better equipped to break up hard "dry" fruits. Reversely, jays exert several selective pressures which are likely to have evolutionary consequences for oaks, such as the selection of long-slim and large acorns with tight shells. In addition, oak seedlings with a long tap root and tough stem are selected for. Although other factors than mutual selective pressures between the two may have affected the present day fit between jays and oaks it is concluded that several characters of jays and oaks can be considered as co-adapted features of a symbiotic relationship.


Author(s):  
M.C.P. Amorim ◽  
A.S.M. Neves

Gobies emit sounds during different stages of reproduction, including courtship, pre-spawning events (in the nest) and spawning. The breeding sounds of the painted goby Pomatoschistus pictus and associated courtship behaviour were recorded in captivity and described for the first time. Males emitted thump-like sounds mainly when displaying alone in the nest and produced drumming sounds outside the nest. Thumps have never been reported for other species of the genus Pomatoschistus. Thumps were short (~80 ms) very-low frequency (below 100 Hz) non-pulsed sounds, whereas drums were longer (hundreds of ms) and consisted of low frequency (~300 Hz) pulse trains. Thump characteristics varied significantly among males but also showed high within-male variability. The frequency of thump emissions and courtship behaviour (total number of courtship displays, lead and nest display) were positively correlated with male size but not with male somatic condition. Thump bursts emitted during nest displays were significantly longer than when emitted with other behaviours. These results suggest that larger males courted females more intensively, both with visual and acoustic displays, than smaller ones.


2006 ◽  
Vol 84 (6) ◽  
pp. 887-894 ◽  
Author(s):  
J.D. Rodríguez-Teijeiro ◽  
A. Barroso ◽  
S. Gallego ◽  
M. Puigcerver ◽  
D. Vinyoles

The directional movements of the male European Quail, Coturnix coturnix (L., 1758), during the breeding season and autumn migration were studied using Emlen orientation cages. The characteristics and evolution of the habitat in which males were captured and the sexual behaviour shown at capture indicate that these birds move in search of mating partners rather than of suitable habitats. These displacements are known as “gypsy movements” but are better described, as argued in this paper, as “movements in search of females”. A majority of caged birds (59%) showed a preferred direction (α = 238.5°), which coincided almost exactly with that observed in recoveries of ringed birds during autumn migration (α = 251.3°) but not with results from cage experiments during the same migratory period (α = 187.8°). Therefore, we conclude that displacements of the male European Quail, as shown in ringing recoveries, are much more influenced by “movements in search of females” than by migration. These movements are clearly towards the southwest, the males taking short flights towards suitable breeding grounds and driven by river-course habitats. In addition, we confirm that Emlen funnels are suitable for controlled experiments on the orientation of males in demes of European Quail.


1999 ◽  
Vol 21 (1) ◽  
pp. 139
Author(s):  
I.G. McLean ◽  
N.T. Schmitt

While preparing a review of published descriptions of copulatory behaviour in macropod marsupials (McLean, Lundie-Smith and Jarman 1993), we were surprised to find no description for one of the most studied species, the quokka (Setonix brachyurus, e.g. see Bradshaw 1983). Copulating quokkas have been seen previously by researchers (e.g. Kitchener 1970), but no account was given. Here we provide descriptions of copulatory behaviour in quokkas, and comment on levels of sexual behaviour and activity by quokkas in the wild and in captivity.


1979 ◽  
Vol 6 (2) ◽  
pp. 131 ◽  
Author(s):  
M Smith

2. Young koalas (Phascolarctos cinereus) began to eat leaves after they left the pouch but before they left the mother's back. The oldest seen sucking was about 13 months old and small for its age. Young koalas still in or returning to the pouch, one of them 240 days old, were seen to eat faeces directly from the mother; adults did not practise coprophagy.


1980 ◽  
Vol 28 (1) ◽  
pp. 33 ◽  
Author(s):  
DM Stoddart

Bandicoots (Marsupialia : Peramelidae) of the genera Isoodon, Perameles and Macrotis possess either subauricular or interauricular cephalic skin gland complexes. The pig-footed bandicoot Chaeropus is the only genus apparently lacking cephalic skin glands. Skin gland complexes consist of enlarged sebaceous acini and sudoriferous tubules. though the latter are less apparent in Macrotis than the other genera. The surface of the gland complex has a pockmarked appearance with a small depression surrounding each guard hair shaft. The complex increases in activity very markedly during the breeding season in both sexes. but particularly in males. The most noticeable aspect of the pre-breeding hypertrophy is an expansion of the sebaceous element, which presses the sudoriferous element down into the deeper layers of the dermis. It is suggested that the pungent odour secreted by these complexes plays a calming and reassuring role in the courtship behaviour of these solitary and pugnacious small marsupials.


2018 ◽  
Vol 7 (1) ◽  
pp. 81-85
Author(s):  
Md Abraharul Islam ◽  
Monirujjaman ◽  
Rasel Ahammed ◽  
Mahruma Aktar

Abstract not availableJahangirnagar University J. Biol. Sci. 7(1): 81-85, 2018 (June)


1979 ◽  
Vol 6 (2) ◽  
pp. 117 ◽  
Author(s):  
M Smith

1. Feeding behaviour of koalas (Phascolarctos cinereus) was observed at a sanctuary near Brisbane, Australia. They fed sporadically throughout the day, for a total of at least 19 h daily, on leaves; they ingested soil and gravel, and drank water when it was provided, but infrequently. Young were seen to leave the pouch at 220 days old and to eat leaves at 217 days old. None under 10 months old was seen to pull leaves forward before biting them.


Author(s):  
Junaid Naseer ◽  
Khalid Mahmood Anjum ◽  
Muhammad Asif Munir ◽  
Muhammad Awais Nazir ◽  
Muhammad Zubair Yousaf ◽  
...  

Present research was planned to evaluate the breeding and feeding behaviour of Indian peafowl reared in captivity at Zoological Gardens of Government and Private Sector. For feeding behaviour, a total of fifty pairs (n=100) of Pavo cristatus at both Government Zoological Gardens (n=25pairs) and Private Sectors (n=25pairs) were observed on daily basis. The breeding season of Indian peafowl is not fixed but mostly it breeds in rainy season from April to August. It was observed that most of birds at Government Zoological Gardens breed in month of May, while most of birds at Private Sectors breed in the month of August. For feeding behaviour a total of 200 faecal samples per week were collected for six weeks, out of which 100 samples per week were randomly selected for further analysis. Faecal analysis technique showed that dietary components of Indian peafowl were covered by plant contents following by animal sources. Among the plants components grass seeds were predominant followed by dicotyledon and fruits with least portion of monocotyledons. Among animal components, ants, grasshopper, earthworms, spider and unidentified bones were present. Faecal analysis indicated the presence of some non-food items such as sand and gravel.


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