Metadata record for data from ASAC Project 257 See the link below for public details on this project. From the abstracts of some of the referenced papers: Anatomical and physiological studies of southern elephant seals (Mirounga leonina), particularly in the post-natal period, raise questions of relative musculature growth, control of metabolism, circulation and temperature regulation, which could be important in our understanding of these processes in mammals and of their contribution to adaptation to environmental extremes. The diving behaviour of 14 adult southern elephant seals was investigated using time depth recorders. Each of the seals performed some dives that were longer than its theoretical aerobic dive limit. Forty-four percent of all dives made by post-moult females exceeded the calculated limit compared with 7% of those made by postbreeding females and less than 1% of those made by adult males. The extended dives displayed characteristics that suggested they were predominantly foraging dives, although some were apparently rest dives. Dives longer than the calculated aerobic limits often occurred in bouts; the longest consisted of 63 consecutive dives and lasted 2 days. Postmoult females performed longer bouts of extended dives than postbreeding females. Extended surface periods (longer than 30 min) were not related to the occurrence of extended dives or bouts of extended dives. The possible physiological mechanisms that permit such prolonged continuous dives are discussed. Southern elephant seals may increase the aerobic capacity of dives by lowering their metabolism to approximately 40% of the resting metabolic rate on long dives. There is substantial interseal variability in the methods used to cope with long dives. Some animals appear to use phsyiological strategies that allow them to prolong the time available to them at the bottom of a dive, while others use alternative strategies that may limit the time available at the bottom of their dives. Fourteen time-depth-temperature recorders were recovered from adult southern elephant seals (Mirounga leonina) returning to Macqaurie Island to breed or moult. The resulting temperature/depth profiles indicated that all four males spent most of their time in waters lying over the Antarctic Continental Shelf, whereas only one of the ten females spent any time there. Five of the females foraged just off the Antarctic Continental Shelf, and the other five remained near the Antarctic Polar Front. 1) Mark-resight data were analysed for thirteen cohorts from a declining population of southern elephant seals branded at Macquarie Island between 1951 and 1965. 2) First year survival was essential stable during the 1950s at about 46% for females and 42% for males. There was a dramatic fall in first year survival during the 1960s, declinging to less than 2% for both sexes in 1965. Post-year-1 survival did not change between the 1950s and the 1960s. 3) Comparisons with a stable population of southern elephant seals at South Georgia indicated that both first year and adult survival were lower in the Macquarie Island population. There were no changes in the age at first breeding of the Macquarie Island seals during the study, but this was on average 1 year later than at South Georgia. 4) It is hypothesised that the current decline in elephant seal numbers at several of their major breeding islands is due to the populations returning to pre-sealing levels after they had risen to abnormally high levels with the end of commercial exploitation early this century. 5) Possible tests of the hypothesis include studying the diet and foraging behaviour of southern elephant seals to gain an understanding of the predator-prey relationships, continuing to census the Macquarie Island population to determine if the population levels out at around the estimated pre-sealing levels, and monitoring northern elephant seal populations which were also severely exploited but are currently increasing

At Heard Island, Southern Indian Ocean, seals were branded between 1949-1953. Seal length was measured in feet and inches. Recaptures of seals were made up until 1955, and growth and age-specific survival was calculated.

Taken from the report prepared by R Kenny: In this report our comparatively brief knowledge of the Elephant Seal at Macquarie Island (based only on one year's observations) have been augmented by abstracting notes from "The Natural History of the Elephant Seal" by L. Harrison Matthews Discovery Reports, vol. 1 p. 233. 1929., based on observations at South Georgia. The Elephant Seal herds at the two islands are comparable - at South Georgia the animals had been overfished almost to the point of extinction by 1885, but were then not hunted for many years, and by 1929 had "increased in numbers till at the present time they are probably as numerous as ever", and are now fished under Government regulation to prevent extermination; the Macquarie Island herd has a similar history.

Elephant seals use a suite of physiological and behavioural mechanisms to maximise the time they can be submerged. Of these hypo-metabolism is one of the most important, so this study quantified maximum O2 consumptions relative to dove depth and swim speed. From the abstract of the referenced paper: The ability of air-breathing marine predators to forage successfully depends on their ability to remain submerged. This is in turn related to their total O2 stores and the rate at which these stores are used up while submerged. Body size was positively related to dive duration in a sample of 34 adult female southern elephant seals from Macquarie Island. However, there was no relationship between body size and dive depth. This indicates that smaller seals, with smaller total O2 stores, make shorter dives than larger individuals but operate at similar depths, resulting in less time being spent at depth. Nine adult female elephant seals were also equipped with velocity time depth recorders. In eight of these seals, a plot of swimming speed against dive duration revealed a cloud of points with a clear upper boundary. This boundary could be described using regression analysis and gave a significant negative relationship in most cases. These results indicate that metabolic rate varies with activity levels, as indicated by swimming speed, and that there are quantifiable limits to the distance that a seal can travel on a dive of a given swimming speed. However, the seals rarely dive to these physiological limits, and the majority of their dives are well within their aerobic capacity. Elephant seals therefore appear to dive in a way that ensures that they have a reserve of O2 available. Data were collected on Time Depth Recorders (TDRs), and stored in hexadecimal format. Hexadecimal files can be read using 'Instrument Helper', a free download from Wildlife Computers (see the url given below). Data for this project is the same data that was collected for ASAC projects 857 and 589 (ASAC_857 and ASAC_589).

This dataset contains the results from studies of the Elephant Seal (Mirounga leonina) at Macquarie Island. Results from branding surveys and photographs from 1985 onwards are reported. Numbers, life stage, sex, moult stage and migration patterns have been reported. Currently some 2000 pups a year are branded and the dataset includes birth dates, weights at birth and weaning and at 6, 12 and 18 months. This work was completed as part of ASAC (AAS) project 2265 (ASAC_2265). Objectives: To prepare research papers, from the extensive southern elephant seal dataset, that deal with key demographic parameters of the population such as size, age specific survivorship, fecundity, recruitment into the breeding population, age specific growth rates, and intrinsic rate of change of the population. In addition, later papers will investigate interannual variability in these parameters, how these relate to changing environmental conditions, and the effects of this on long term population fluctuations. To analyse and compare stable isotope ratios in the facial vibrissae of the seals and the hard parts of their prey to determine the geographical positions of the major foraging grounds of the seals. The isotope values will also allow the food webs, that support the seals, to be better defined. To measure the growth rates of elephant seal vibrissae so that changing isotope values, related to the prey and foraging areas, can be referred to particular foraging periods. Elephant seals characteristically have two separate periods of foraging: one in summer and one in winter. The positions of these episodes on a vibrissa can be identified once the growth rates of vibrissae are known. Taken from the progress report for the 2009-2010 season: Progress against objectives: 1. One paper published from the elephant seal dataset. Two papers also published during 2009/10 using data collected opportunistically during the life of this project. PhD student Andrea Walters continues to analyse the results of the whisker analyses. She has presented some of her results at the AMSA 2009 marine connectivity conference in Adelaide. An honours student has been engaged (start date March 2010) to analyse the squid component of the seals' diet. John van den Hoff spent the early summer at Macquarie Island finalising the collection of the demographic data. 2154 tag/brand resights were recorded. Collection of the data has continued on the island by Chris Oosthuizen, Ben Arthur and Iain Field since John returned to Australia. When those field workers return data collection will cease.

This dataset is a document describing the Ctenophores of the Southern Ocean. It lists all the known species and with illustrated diagrams provides a guide to their taxonomic identification. The document is available for download as a pdf from the provided URL.

Metadata record for data from ASAC Project 2184 See the link below for public details on this project. The objectives of this project were: To characterise the mating system of the Weddell seal by: 1) acoustically tracking males under the ice during the breeding season, 2) measuring changes in health and condition of individual males over the breeding season, 3) determining whether vocalisations are used as advertisements of individual quality to attract females, and/or in male-male competition, 4) develop and use a combination of microsatellite loci tests to assign paternity to newborn pups, and then use these results to determine whether the variance in male mating success is related to territory size, tenure and/or individual characteristics. A large number of collected data files are available for download. Many files are in an unknown format, but will open with a standard text editor. See below for summaries of the two seasons of fieldwork. 1997/1998 Season: In November/December 1997, we conducted a pilot study at the Turtle Rock colony (77.727S, 166.85E) in McMurdo Sound. All of the techniques outlined in the proposal were successfully trialled. Acoustic pingers were attached to seven males and five females for a total deployment of 104 seal days and mass and morphometrics obtained for each animal. Preliminary analysis of male movements indicate that males held adjacent yet non-overlapping territories on the southern side of Turtle Rock, along a major ice crack and where the congregation of females was highest. Both the size and shape of the males territories, and the evidence from the vocalisation data show that we captured the dominant males at the site. Both males and females were immobilised using Ketamine/Diazepam with no loss of an animal, nor signs of respiratory depression. Vocalisations were recorded from all territory holding males, and both behavioural and vocal responses of both male and female seals to familiar and unfamiliar calls were observed. We bleach marked all animals to which we attached pingers and these markings were visible on our under-ice video - with which we also recorded behavioural responses to both animals and our under-ice speaker during playback experiments. We conducted a daily census of all animals at Turtle Rock and above-ice movements were recorded. Skin samples were taken from 24/25 males seen at the site and 43/45 mother-pup pairs (One male was only seen on a single occasion at the colony, though sighted elsewhere, and two females disappeared shortly after our arrival at the colony). Significant findings Dominant males hold under-ice territories which are adjacent yet non-overlapping - however territory boundaries change considerably over the course of the breeding season. Males respond to playbacks of their own and others calls as do females. Females towards the end of lactation will visit each males territories. Whether to assess individual males or not is yet to be determined. 1998/1999 Season Between October 29 through December 10 1998, the behaviour of male and female weddell seals at the Turtle Rock colony (77.727S, 166.85E) were monitored both above and below the ice. This season, we switched from the seal sled method of capture and restraint (see K027 report 1997) to the use of a pole net and tripod. Seals were bagged by placing a seal hood over their head and then a 3m pole net (consisting of two, 3m long poles connected by a 2m wide, 2.5cm mesh, net , was placed over them and the poles tied tightly at both ends, leaving them constrained within the netting bag. The pole net was then hoisted under a tripod (built by Antarctica New Zealand) using a chain block suspended from the head of the tripod, and the animal weighed using electronic scales. For attachment of instruments, animals were immobilised with an intra-muscular injection of Ketamine/Diazepam at a dose rate of approximately 2.0mg/100 kg Ketamine, 0.4mg/100 kg Diazepam as was used successfully in 1997. Animals were

Elephant seals use a suite of physiological and behavioural mechanisms to maximise the time they can be submerged. Of these hypo-metabolism is one of the most important, so this study quantified maximum O2 consumptions relative to dove depth and swim speed. From the abstract of the referenced paper: Heart rate, swimming speed, and diving behaviour were recorded simultaneously for an adult female southern elephant seal during her postbreeding period at sea with a Wildlife Computers heart-rate time depth recorder and a velocity time depth recorder. The errors associated with data storage versus real-time data collection of these data were analysed and indicated that for events of short duration (i.e., less than 10 min or 20 sampling intervals) serious biases occur. A simple model for estimating oxygen consumption based on the estimated oxygen stores of the seal and the assumption that most, if not all, dives were aerobic produced a mean diving metabolic rate of 3.64 mL O2 kg-1, which is only 47% of the field metabolic rate estimated from allometric models. Mechanisms for reducing oxygen consumption while diving include cardiac adjustments, indicated by reductions in heart rate on all dives, and the maintenance of swimming speed at near the minimum cost of transport for most of the submerged time. Heart rate during diving was below the resting heart rate while ashore in all dives, and there was a negative relationship between the duration of a dive and the mean heart rate during that dive for dives longer than 13 min. Mean heart rates declined from 40 beats min-1 for dives of 13 min to 14 beats min-1 for dives of 37 min. Mean swimming speed per dive was 2.1 m s-1, but this also varied with dive duration. There were slight but significant increases in mean swimming speeds with increasing dive depth and duration. Both ascent and descent speeds were also higher on longer dives. Data were collected on Time Depth Recorders (TDRs), and stored in hexadecimal format. Hexadecimal files can be read using 'Instrument Helper', a free download from Wildlife Computers (see the provided URL). Data for this project is the same data that was collected for ASAC projects 769 and 589 (ASAC_769 and ASAC_589).

These notes present a summary of observations on seabirds, seals and plankton conducted from the vessel Kyo Maru No 27 during the seventh International Decade of Cetacean Research Southern Hemisphere Minke Whale Assessment cruise. The cruise was conducted under the auspices of the International Whaling Commission (IWC) to whom Paul Ensor was contracted as a consultant. The information presented here are personal observations only; recorded outside normal research hours or in such a manner that his participation in the cetacean research was not compromised.