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1. Life-history theory predicts that individual birds should invest in reproduction according to their current body condition and the future prospects for survival and reproduction. Thus, it could be expected that current adult body condition should significantly influence food provisioning rates, food loads and concurrent chick growth in the Antarctic petrel. 2. In order to study the significance of parental body condition I correlated meal sizes, feeding frequencies and chick growth with the body condition of the parents. 3. There was a strong correlation between the average meal size delivered to a chick and its growth rate. Adult body condition at the time of hatching was strongly correlated with the average size of meals delivered to individual chicks. Male and female body condition at the time of hatching and average body condition of the pair at the first incubation shift and at hatching significantly influenced the body mass of the chick on day 30. Male body condition and the average body condition of the pair correlated significantly with the growth rate of the chick. 4. The difference in body mass at the age of 30 days of chicks from parents with good body condition compared with chicks from parents with poorer body condition was nearly double that expected. 5. The results strongly suggest that the effort spent during the chick-rearing period, and thus reproductive success, is regulated by the body condition of the parents.

We present data on sexual dimorphism in some morphological measurements (wing length, head length, bill depth and bill length) in the Antarctic Petrel Thalassoica antarctica. Males were on average larger than females for all measurements. Sexual dimorphism was on average largest for bill depths whereas wing lengths discriminated least between the sexes. A discriminant function including bill depth, head length and wing length correctly sexed 92% of the sample. Due to between-measurer variation it is recommended that morphometric measurements obtained by others on sexed birds are compared with ours before proceeding with the use of the discriminant function on unsexed individuals.

Antarctic Petrel Thalassoica antarctica incubation and brooding effort was studied at Svarthamaren, Dronning Maud Land, during the austral summer of 1991-1992. The females probably left the nest site shortly after egg laying. The duration of incubation and brooding shifts as well as the daily weight loss (absolute and proportionate) were comparable with those of other similar-sized procellariform species. Males spent more time incubating and brooding than did females, suggesting higher female energy stress due to egg laying, Incubating birds which were below average weight were likely to desert the nests before their mates returned from feeding trips. Both males and females lost approximately one-fifth of their body-weight during their first incubation shifts. Nevertheless, they increased their initial weights from egg laying to hatching and had their highest initial weights when they returned to start the shift during which the egg hatched. No factors related to adult body-weight explained the duration of the incubation shifts, Both males and females gained weight at a higher rate when at sea than they lost it during incubation, and it is suggested that factors unrelated to food availability or individual feeding skills may be important in regulating the duration of the incubation shifts and the stay at sea.

The diet of the Antarctic petrel Thalassoica antarctica was studied during two seasons at Svarthamaren, an inland colony in Dronning Maud Land, Antarctica, and in the pack ice off the coast of Svarthamaren. The most important food (wet mass) at Svarthamaren was crustaceans (67%), fish (29%) and squid (5%); however, individuals collected in the pack ice took mostly fish (87%). The prey composition and lengths of prey are comparable to what has been documented in other studies on this species. Estimates of food consumption by birds breeding at Svarthamaren (ca. 250,000 pairs) suggest that approximately 6500 tonnes of crustaceans, 2800 tonnes of fish and 435 tonnes of squid are consumed during the breeding season. The annual consumptions of these birds are estimated to be 34,100 tonnes of crustaceans, 14,700 tonnes of fish, and 2300 tonnes of squid. Satellite telemetry data indicate that Antarctic petrels from Svarthamaren may fly more than 3000 km during one foraging trip, and thus may cover a huge ocean area to obtain their prey.

A large number of studies have reported a positive relationship between the egg size of birds and the subsequent growth and/or survival of nestlings, but such effects may partly be due to confounding variables, e.g. parental quality. In order to evaluate the potential effects of egg size, and of parental quality, on early nestling growth in the Antarctic petrel, we performed an experiment in which eggs of different size were swapped between nests. 2. From a sample of 300 nests with eggs of known size, we selected eggs belonging to the lower quartile (small eggs), and those belonging to the upper quartile (large eggs), with respect to volume. Half of the small eggs were exchanged with small eggs from other nests, and the other half with large eggs. A similar procedure was used for large eggs. Growth and survival of the nestlings were recorded until 12 days old. 3. Hatching success was positively related to egg size. 4. Egg size influenced nestling body mass until the age of 3 days, and tarsus length was affected until 12 days old. However, these effects were not due to an effect of egg size on growth rates, but reflected instead the influence of egg size on hatchling size. 5. In contrast to most previous studies, we found no effect of parental quality (as reflected in the size of own eggs) on foster nestling size or growth until 12 days old. This could be because egg size does not reliably reflect parental quality in the species, or because parental effects become evident only at later nestling stages. 6. We discuss why egg size variation is maintained in this and other species where egg size influences parental fitness through the survival of eggs or nestlings.

Considerable interspecific variation exists in the frequency of extrapair fertilizations (EPFs) in birds. In general, EPFs are more common and occur at higher frequencies in passerines than in nonpasserines (Westneat and Sherman 1997). Lower rates of EPFs are typical for territorial nonpasserines as well as those that breed colonially (Westneat and Sherman 1997). This seems to contradict Birkhead and Møller's (Birkhead and Møller 1992, Møller and Birkhead 1993) hypothesis of intense sperm competition in colonial birds. Their arguments were based on the assumption that the need for nest defense in dense aggregations restricts the ability of males to guard their mates, and that the high number of potential extrapair mates available in colonies selects for a high rate of extrapair copulations (EPCs). In contrast, Westneat and Sherman (1997) found no correlation across species between the frequency of EPFs and nesting dispersion, local breeding density, or breeding synchrony, although EPFs were related to nesting density within species. This suggests that EPC rates are not informative regarding EPF rates in colonial birds (Westneat and Sherman 1997), or that the pattern reported by Møller and Birkhead (1993) does not hold true when more species are included. The conflicting evidence regarding the relationship between extrapair activities and breeding density calls for more empirical studies, especially among colonial nonpasserines. Social monogamy is the predominant mating system in the Procellariiformes (Warham 1990). Several aspects of their breeding biology may, however, provide favorable opportunities for extrapair sexual activity. First, colonial breeding provides ample opportunities for EPCs because many potential partners are available at close range (Birkhead and Møller 1992, Møller and Birkhead 1993). Second, when the sexes are spatially and/or temporally separated, as may be the case in procellariiforms where adults seek food far from the colony, males have few cues to assess whether their mates have been unfaithful. Hence, few reasons exist to expect a facultative decrease in male parental investment if cuckolded, in contrast to the case for many territorial species where a male may have more reliable cues to his mate's unfaithfulness (e.g. female disappearance, high intrusion rate, etc.). Accordingly, colonial breeding may facilitate EPCs for both sexes, and colonial species may be expected to display high rates of EPC. Paternity studies require error-free sex determination of adults. This is straightforward for clearly dimorphic species, or if sex determination can be done from genitalia during the fertile period. But if fieldwork can be performed only during the nestling period, sex determination may be problematic for largely monomorphic species, and indirect methods must be used. In the Antarctic Petrel (Thalassoica antarctica), the two sexes differ slightly in mean body size. Lorentsen and Røv (1994) used this difference to determine the sex of Antarctic Petrels by discriminant function analysis (DFA). The procedure correctly determined the sex of 92% of the birds in a sample from the same year. This does not necessarily imply a similar resolution if the discriminant function is adopted for samples from other years, or if data are collected by other observers. Moreover, although useful for many purposes, 92% resolution in sex determination is insufficient for paternity studies. Therefore, we performed molecular sexing of all breeding adults according to the PCR-based method of Griffiths et al. (1998). The main aim of our study was to analyze whether extrapair paternity occurs in a colonial procellariiform, the Antarctic Petrel. We also tested the robustness of morphological sex determination (from DFA) across seasons relative to that obtained from molecular techniques.

We examined how variation in parental quality influences the reproductive success of a long-lived seabird, the Antarctic Petrel (Thalassoica antarctica). In particular, we focused on how quality of parents can interact with and influence the effects of stochastic variation in the environment due to varying climatic conditions. Large annual variation was found in reproductive success. However, body mass of individual chicks at the end and be­ ginning of the nestling period was strongly correlated in two of the study years, suggesting consistent variation among parents in their ability to feed offspring. Furthermore, chick mass was related both to overall body size and to body mass of their parents. Short brooding-shift intervals also were important for growth and survival of chicks. The probability of chick survival to the age of 30 days (ca. two weeks before fledging) was strongly correlated with chick mass when the chick was left unattended. However, the relative importance of different parental characteristics differed between years. These results show that reproductive success of the Antarctic Petrel is influenced by stochastic variation in the environment, probably re­ lated to climatic conditions. Effects of this stochastic variation may depend on body mass and/ or body condition of the parents.

Kommersielle fiskerier kan påvirke marine økosystemer og bestander av topp-predatorer som sjøfugl. I Sørishavet foregår et ekstensivt fiske etter Antarktisk krill (Euphausia superba), og dette er antatt å øke. En sammenligning av fordeling og uttak hos fiskeriene og tilsvarende hos topp-predatorene er nødvendig for å forutsi fiskerirelaterte påvirkninger på krillavhengige predatorer. I dette studiet kartla vi næringssøksområdene hos Antarktispetrell (Thalassoica antarctica) som hekker i verdens største koloni (Svarthammaren, Dronning Maud land) over en treårsperiode. Vi fant at det romlige overlappet mellom krillfiskerier og næringssøkende Antarktispetrell generelt var lite. Konkurranse mellom Antarktispetrell og krill-fiskerier er for tiden neglisjerbart, men kan øke hvis fiskeriet etter krill øker.