Latitudinal and seasonal effects on growth of the Australian eastern king prawn (Melicertus plebejus)

2012 ◽  
Vol 69 (9) ◽  
pp. 1525-1538 ◽  
Author(s):  
Luke R. Lloyd-Jones ◽  
You-Gan Wang ◽  
Anthony J. Courtney ◽  
Andrew J. Prosser ◽  
Steven S. Montgomery
Keyword(s):  
Growth Rate ◽  
Shape Parameter ◽  
New South ◽  
Seasonal Effects ◽  
Seasonal Effect ◽  
Model Framework ◽  
Mark Recapture ◽  
South Wales ◽  
Males And Females ◽  
Latitudinal Effect

The growth of the Australian eastern king prawn ( Melicertus plebejus ) is understood in greater detail by quantifying the latitudinal effect. The latitudinal effect is the change in the species’ growth rate during migration. Mark–recapture data (N = 1635, latitude 22.21°S–34.00°S) presents northerly movement of the eastern king prawn, with New South Wales prawns showing substantial average movement of 140 km (standard deviation: 176 km) north. A generalized von Bertalanffy growth model framework is used to incorporate the latitudinal effect together with the canonical seasonal effect. Applying this method to eastern king prawn mark–recapture data guarantees consistent estimates for the latitudinal and seasonal effects. For M. plebejus, it was found that growth rate peaks on 25 and 29 January for males and females, respectively; is at a minimum on 27 and 31 July, respectively; and that the shape parameter, k (per year), changes by –0.0236 and –0.0556 every 1 degree of latitude south increase for males and females, respectively.

Estimating brush-tailed rock-wallaby population size using individual animal recognition

2011 ◽  
Vol 33 (2) ◽  
pp. 228
Author(s):  
Karl Vernes ◽  
Stuart Green ◽  
Piers Thomas
Keyword(s):  
Population Size ◽  
National Park ◽  
New South ◽  
Morphological Characters ◽  
Population Estimates ◽  
Individual Animal ◽  
Mark Recapture ◽  
South Wales ◽  
North Eastern ◽  
Estimate Population Size

We undertook surveys of brush-tailed rock-wallabies (Petrogale penicillata) at four colonies in Oxley Wild Rivers National Park, north-eastern New South Wales, with the aim of developing a technique based upon individual animal recognition that could be used to obtain robust population estimates for rock-wallaby colonies. We identified individuals on the basis of distinct morphological characters in each colony using visual observations, and used the data within a ‘mark–recapture’ (or sight–resight) framework to estimate population size. More than 37 h of observations were made over 10 sampling days between 18 May and 9 June 2010. We could identify 91.7% of all rock-wallabies that were independently sighted (143 of 156 sightings of 35 animals). A small percentage of animals could not be identified during a visit because they were seen only fleetingly, were in dense cover, or were partly obscured by rock. The number of new animals sighted and photographed declined sharply at the midpoint of the survey, and there was a corresponding increase in resighting of known individuals. Population estimates using the mark–recapture methodology were nearly identical to estimates of total animals seen, suggesting that this method was successful in obtaining a complete census of rock-wallabies in each colony.

A Decade of Mark-Recapture of Platypuses on The Duckmaloi River: Any New Insights into Population Dynamics?

1998 ◽  
Vol 20 (2) ◽  
pp. 302
Author(s):  
D. Goldney
Keyword(s):  
Sex Ratio ◽  
New South ◽  
First Year ◽  
Mark Recapture ◽  
South Wales ◽  
Adult Status ◽  
Second Year ◽  
Gill Netting ◽  
Population Numbers

A long-term mark-recapture program has been carried out on the Duckmaloi Weir (near Oberon, New south Wales) and associated river over the period 1986 to the present. The pipehead weir creates a long shallow ·pool' about 2.5 ha in area, ideal for gill-netting platypuses. One hundred and eighty-two (182) individual animals have been captured in excess of 500 times. The majority of animals have been captured in the weir pool. A very dynamic situation exists with new adults and juveniles being captured on a regular basis and conversely captured animals "disappearing" on a regular basis from the system. Some individuals exhibit both transience and site attachment characteristics. However, relatively few animals remain site attached for long periods of time. Sixty nine percent of individuals are captured two or fewer times. Band loss cannot account for this phenomenon. Of the captured animals, 11.3% have been caught more than 5 times. The sex ratio of the population favours females in first capture adults (1:1.72) but males in first capture juveniles (1:0.73). Females are more likely to be recaptured than males. The sex ratio of juveniles varies significantly from year to year. The period between recaptures varies greatly and can be up to 6 years. Four animals have been captured over nine years (3 females/1 male) but no animal has been captured every year of the study. Recruitment has occurred at levels able to maintain the current population numbers. Thirty percent of available adults have been found lactating, including second year females. Seventy one percent of first year capture juveniles and 89.9% of first capture adults "disappear" within two years of first capture. Forty two percent of juvenile animals reach adult status before "disappearing".

Seasonal Field Energetics of the Rufous Rat-Kangaroo (Aepyprymnus-Rufescens)

1992 ◽  
Vol 40 (3) ◽  
pp. 279 ◽  
Author(s):  
IR Wallis ◽  
B Green
Keyword(s):  
New South ◽  
Water Flux ◽  
Behavioural Ecology ◽  
Free Living ◽  
Doubly Labelled Water ◽  
South Wales ◽  
Poor Understanding ◽  
Males And Females ◽  
The Mean ◽  
The Difference

Water flux and field metabolic rate (FMR) were measured by the doubly labelled water (DLW) method in free-living male and female rufous rat-kangaroos Aepyprymnus rufescens near Drake in northern New South Wales. The mean FMR of 499 kJ kg-1 day-1 was similar in winter and summer even though the difference in mean minimum temperatures between the two seasons was 20-degrees-C. Furthermore, we did not find any differences in FMR between males and females even though several females carried large pouch young or had young-at-foot. A poor understanding of the diet and the behavioural ecology of A. rufescens makes ft difficult to explain the similarities between sexes and seasons.

The dynamics of B chromosomes in populations of the Australian plague locust, Chortoicetes terminifera (Walker)

1984 ◽  
Vol 26 (2) ◽  
pp. 194-208 ◽  
Author(s):  
P. C. Gregg ◽  
G. C. Webb ◽  
M. A. Adena
Keyword(s):  
New South ◽  
Female Parent ◽  
B Chromosome ◽  
Average Frequency ◽  
B Chromosomes ◽  
Banding Patterns ◽  
South Wales ◽  
Random Fashion ◽  
Accumulation Mechanism ◽  
Males And Females

The B chromosomes of Chortoicetes terminifera possess an accumulation mechanism. B chromosomes were transmitted at a rate of 0.766 in one B(♂) × zero B(♀) crosses and 0.477 in zero B(♂) one × B(♀) crosses. In crosses where the female had a B chromosome, there were significant differences in transmission rates between pods, but these were not related to differences in G-banding patterns of the B chromosomes involved. In crosses where either the male or female parent had two B chromosomes the B chromosomes did not segregate perfectly, nor did they segregate in a random fashion. The closest resemblance to the behaviour of normal bivalents occurred when the two B chromosomes were of the same, rather than different, G-banding variants, and when they were present in the male rather than the female parent. B chromosomes occurred at eight localities scattered throughout New South Wales. No locality was found where they were not present. The average frequency of B chromosomes was 14.0% for one-B individuals and 0.8% for two-B individuals. There were no significant differences in B-chromosome frequency between males and females. Of the eight localities, only one had a B-chromosome frequency significantly different from any other locality. This relatively uniformity of B-chromosome distribution is interpreted as a consequence of the migratory nature of C. terminifera. A model was constructed to simulate the dynamics of B chromosomes in locust populations. Three main dynamic patterns were recognized, and these were related to differences in the fitness of one-B and two-B individuals. It was concluded that the B chromosome of C. terminifera is probably parasitic, although the simulation model revealed some difficulties which suggest that caution should be applied to the description of any B chromosome as purely parasitic.Key words: B chromosomes, locust, meiotic drive, G-banding, fitness. Chortoicetes terminifera (Walker).

Revision of the Australian wolf spider genus Anomalosa Roewer, 1960 (Araneae: Lycosidae)

Zootaxa ◽  
2006 ◽  
Vol 1304 (1) ◽  
pp. 1 ◽  
Author(s):  
VOLKER W. FRAMENAU
Keyword(s):  
New South ◽  
South Australia ◽  
Wolf Spider ◽  
Original Description ◽  
Morphological Evidence ◽  
Pitfall Traps ◽  
Systematic Revision ◽  
South Wales ◽  
As Species ◽  
Males And Females

The wolf spider genus Anomalosa Roewer, 1960 is revised with Anomalosa kochi (Simon, 1898) as type species. Anomalosa includes a further Australian species, A. oz sp. nov. Representatives of Anomalosa are small, elongated lycosids with a longitudinal light median band on the dorsal shield of the prosoma and on the opisthosoma, the latter being particularly distinct in males. They are closely related to Venonia Thorell, 1894. Similar to Venonia, males have a bipartite prolateral tegular lobe on the pedipalp, but it is much larger than in Venonia and, in contrast to Venonia, larger than the membranous tegular apophysis. Anomalosa kochi has only been found in Queensland, whereas the distribution of A. oz sp. nov. includes New South Wales, South Australia and Victoria. This allopatric distribution coincides with the McPherson Range as a biogeographical border. Although most males and females of Anomalosa have been caught in pitfall traps or running freely in moderately moist habitats, such as near creeks and dams, there is evidence that representatives of this genus build sheet-webs similar to Venonia. This behaviour is supported by morphological evidence as species of Anomalosa have elongated posterior spinnerets. The original description of A. harishi (Dyal, 1935) from Panjab, India, does not match the diagnosis of Anomalosa. Consequently, I reject the inclusion of A. harishi in Anomalosa and re-transfer it to its original genus Anomalomma Simon, 1890, Anomalomma harishi Dyal, 1935, pending a systematic revision of this genus.

Factors affecting pre-weaning growth and weaning conformation of Angus cattle

1978 ◽  
Vol 29 (2) ◽  
pp. 359
Author(s):  
R Barlow ◽  
EB Dettmann ◽  
LG Williams
Keyword(s):  
Least Squares ◽  
New South ◽  
Average Daily Gain ◽  
Factors Affecting ◽  
Angus Cattle ◽  
South Wales ◽  
Weaning Age ◽  
Males And Females ◽  
Main Effects ◽  
Daily Gain

Weaning weight (ww) and conformation score (cs) records from Angus calves in five New South Wales herds were analysed by least-squares procedures to assess the nature and magnitude of variation. Herd, year, age of dam and sex were considered as main effects. Covariates included in the models were weaning age (WA) for ww and average daily gain (ADG), and both WA and ww for cs. Male calves (steers and bulls) were 16.6 kg heavier at weaning than female calves. Dams that were 5-8 years of age weaned calves that were 30.1 kg, 15.4 kg and 6.7 kg heavier than 2-, 3- and 4-year-old dams respectively. When ww was not included as a covariate in the model, age of dam effects on cs reflected those on ww, and there was little difference in cs between males and females. When adjusted for differences in ww, males had poorer cs than females, and calves from 3-year-old dams, and from dams over 8 years old, had poorer cs than those from dams of all other ages. Partial regressions of ww and ADG on WA, and of cs on ww, varied considerably between herd/year/sex subgroups.

Validation of the formation and appearance of annual marks in the otoliths of yellowtail (Trachurus novaezelandiae) and blue mackerel (Scomber australasicus) in New South Wales

1999 ◽  
Vol 50 (5) ◽  
pp. 389 ◽  
Author(s):  
John Stewart ◽  
Douglas J. Ferrell ◽  
Neil L. Andrew
Keyword(s):  
Growth Rate ◽  
Age Estimation ◽  
New South ◽  
New South Wales ◽  
Early Summer ◽  
Age Class ◽  
South Wales ◽  
In Captivity

Yellowtail (Trachurus novaezelandiae) and blue mackerel (Scomber australasicus) were captured off the coast of New South Wales, marked with oxytetracycline, and kept in captivity for 1 year. The fish were periodically sampled to validate the use of their otoliths for age estimation. Opaque marks were formed during the year in the otoliths of yellowtail apparently aged 0 to 7 years and in apparently 1-year-old blue mackerel. These marks were formed in winter for both species, but did not become visible until early summer in some fish. There was an association between the growth rate of the otolith and the detection of opaque marks. Within an age class, fish with the fastest growing otoliths tended to have their most recently formed opaque marks visible earliest. These relationships between growth rate and the probability of correctly assigning an age class have important implications for ageing fish. Extra keyword: ageing

Australian trends in mortality by socioeconomic status using NSW small area data, 1970–89

1995 ◽  
Vol 27 (4) ◽  
pp. 409-419 ◽  
Author(s):  
Susan Quine ◽  
Richard Taylor ◽  
Lillian Hayes
Keyword(s):  
Socioeconomic Status ◽  
Local Government ◽  
Census Data ◽  
New South ◽  
Common Trend ◽  
South Wales ◽  
Males And Females ◽  
Socioeconomic Differentials ◽  
Industrialised Countries ◽  
The Relationship

SummaryThis ecological study examines trends in socioeconomic differentials in mortality in New South Wales, Australia, over a 20-year period (1970–89). The proportion unskilled was used as the indicator of socioeconomic status and its selection justified. Using census data aggregated by Local Government Area, the relationship between mortality and socioeconomic status was examined using quintiles based on the proportion unskilled in the population. Local Government Areas were also sorted into quintiles using mortality rates (0–74 years) to describe change in mortality differentials over time. Socioeconomic differentials were more evident in the relatively homogeneous Local Government Areas within the Sydney Statistical Division than in the remaining NSW Statistical Divisions which are more heterogeneous and predominantly rural. Although there has been an overall decline in mortality for males and females, and for high and low status groups, over this period the relative socioeconomic differentials have not declined. For the most recent period (1985–89) there appears to be some widening of differentials for males. The NSW state trends are generally similar to those reported for Britain and for other industrialised countries, suggesting that this is a common trend and that policies to reduce inequalities have not been effective.

Studies on Age, Growth, and Life History of the Pilchard, Sardinops neopilchardus (Steindachner), in Southern and Western Australia

1950 ◽  
Vol 1 (2) ◽  
pp. 221 ◽  
Author(s):  
JM Blackburn
Keyword(s):  
Growth Rate ◽  
Western Australia ◽  
New South ◽  
New South Wales ◽  
South Australia ◽  
The Body ◽  
Fish Length ◽  
Linear Type ◽  
Spawning Period ◽  
South Wales

The biology of the unexploited Australian pilchard, Sardinops neopilchardus (Steindachner), was studied from a limited material available from Victorian, Tasmanian, South Australian, and Western Australian waters. This completes the preliminary study of the species over almost the whole of its sub-continental range. In Victorian waters, the surface shoaling season is spring and summer, in South Australia, summer and autumn, and in southern Western Australia, autumn and winter; these are the spawning seasons for the respective areas. In New South Wales and Queensland waters, the shoaling season is autumn to spring, which is again a spawning period. The situation in Tasmania, where the species is rare, is probably similar to that in Victoria. On the west coast of Australia, where the species extends northward to the Tropic of Capricorn (as it also does in the east) the seasonal distribution is not clear. In all these areas pilchard occurrences are virtually limited to the bay and neritic waters. Victorian pilchards attain mean standard lengths of about 8.0, 10.5, 12.5, 14.0, and 15.5 cm. at the ages of one, two, three, four, and five years respectively. This growth rate is considerably lower than that in New South Wales. In southern Western Australia the growth rate is intermediate between the other two, but in South Australia it was not established. The average size of pilchards in the seasonal shoals appears to be greater in Western Australia than elsewhere, but no fish over 19.5 cm. standard length (9.0 in. total length) has been encountered in any of the current Australian investigations. Sexual maturity occurs earlier in Victoria than in New South Wales, sometimes at one year of age. The ring pattern of Australian pilchard scales is complex, involving yearly, spawning, and secondary rings. A hypothesis to account for the formation of spawning rings is outlined, and an earlier hypothesis relating to yearly rings is abandoned. Secondary rings occur on most scales from the same fish. In all waters the season of ring formation coincides with that of surface availability of fish, but in Victoria it is also the growing season, which makes age determination particularly difficult. The fish-length/scale-length relationship for Victorian material is of the same linear type as for New South Wales, but there are differences in the size of scales taken from the same area of the body. The possible influences of distribution, size, and condition of fish on future economic exploitation are discussed.

Reproduction of Pseudomys novaehollandiae (Muridae) in the Wild

1980 ◽  
Vol 7 (3) ◽  
pp. 385 ◽  
Author(s):  
CM Kemper
Keyword(s):  
Breeding Season ◽  
New South ◽  
Reproductive Organs ◽  
First Year ◽  
Reproductive Condition ◽  
South Wales ◽  
In The Wild ◽  
Males And Females ◽  
Preputial Glands ◽  
Breeding Seasons

A total of 291 P. novaehollandiae were observed during a 4-y study in the Nelson Bay and Smith Lake regions of New South Wales. Reproductive organs were examined from males and females, May 1972-May 1974; reproductive condition of females was noted during a CMR study, August 1974-July 1976. Breeding seasons (conceptions and births) occurred between August and early January (4-5 months) in the first 3 years and between September and March (7 months) in the last year. Second-year females produced three or four litters in short seasons, four or five litters in the long season and up to 20 offspring per season. First-year females produced one litter in short seasons and one or two litters in the long season. Mean litter size was 4.56 (2-6). Ovarian follicles were largest in September and smallest in May. Small, inactive CL persisted in parous females until May. Placental scars were present in all sampled months. Vaginae remained closed during the non-breeding season. In mature males testes and epididymides contained sperm from July to March. Vesicular, prostate and preputial glands were enlarged and secretory from September to December. Testes were smallest and least developed in May and June. Males were divided into five categories depending on age and overall reproductive condition. Sexual maturity was reached in the breeding season of birth by some males (33%) and females (13-88%). More females matured early when population density was low. Food abundance and quality may have been important variables in regulating the timing of the breeding season.

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