Distribution and diversity of mtDNA lineages among southern right whales (Eubalaena australis) from Australia and New Zealand

Using a biopsy dart system, samples of skin tissue were collected from southern right whales (Eubalaena australis) in 1995 on two wintering grounds, southwest Australia (n = 20) and the Auckland Islands of New Zealand (n = 20); and on offshore feeding grounds at Latitudes 40 to 43°, south of Western Australia (n = 5). A variable section of the mitochondrial DNA control-region (289 nucleotides) was amplified and sequenced from these 45 individuals (21 males, 20 females and 4 of unknown sex), distinguishing a total of seven unique sequences (i.e. mtDNA haplotypes). Two haplotypes were found on both wintering grounds (including a common type representing 45% of each sample), and five types were unique to only one wintering ground. An analysis of variance adapted for molecular information revealed significant genetic differentiation between the two wintering grounds (p = 0.017). The feeding-ground sample was too small for statistical comparison with the wintering grounds, but included two haplotypes found only in the Auckland Islands as well as the common haplotype found on both wintering grounds. The nucleotide diversity and differentiation of mtDNA among the right whales was similar to that among humpback whales (Megaptera novaeangliae) from the same regions (Baker et al. 1998), but haplotype diversity was significantly reduced, perhaps as a result of more intensive hunting during the last century and continued illegal hunting during this century. Received: 16 March 1998 / Accepted: 18 December 1998     

Contrast in the importance of arrow squid as prey of male New Zealand sea lions and New Zealand fur seals at The Snares,subantarctic New Zealand

New Zealand sea lions (Phocarctos hookeri) are threatened by incidental bycatch in the trawl fishery for southern arrow squid (Nototodarus sloanii). An overlap between the fishery and foraging sea lions has previously been interpreted as one piece of evidence supporting resource competition for squid. However, there is currently no consensus about the importance of squid in the diet of New Zealand sea lions. Therefore, we investigated this importance independently of spatial and temporal differences in squid availability through a simultaneous study with sympatric New Zealand fur seals (Arctocephalus forsteri), a species known to target arrow squid. Diet sampling at The Snares (48°01′S 166°32′E), subantarctic New Zealand, in February 2012 coincided with peak annual catch in the nearby squid fishery. Diets were deduced by analyses of diagnostic prey remains from scats (faeces) and casts (regurgitations). The contribution of each prey species to the diet was quantified using the per cent index of relative importance (% IRI) that combined frequency of occurrence, mass and number of prey items. Arrow squid was a minor component in sea lion scats (2 % IRI), and none was found in their casts. In contrast, arrow squid was the major component in fur seal scats and casts (93 and 99 % IRI, respectively). This study found that New Zealand sea lions ate minimal squid at a time when squid was clearly available as evidenced by the diet of New Zealand fur seals; hence, there was no indication of resource competition between sea lions and the squid fishery.     

Stable isotopes in southern right whale (Eubalaena australis) baleen as indicators of seasonal movements,feeding and growth

Ratios of stable carbon and nitrogen isotopes were examined in the baleen of 11 southern right whales originating from South Africa, including one neonate, six juveniles and four adults. Oscillations in carbon isotope ratios were marked, and indicated feeding north of or at the Subtropical Convergence (STC) alternating with feeding south of the STC. There was an inverse relationship in juveniles between the periodicity of the oscillations and the length of the baleen plate, indicating a reduction in baleen growth with age. The size of the periodicity predicted for the smallest juvenile plate was equivalent to the length of the baleen at 1 yr of age as estimated from the rate of baleen growth in calves, suggesting that the oscillations in carbon isotope ratios were annual events. On this assumption, the timing of the formation of the most recent carbon enrichment peak could be calculated for each individual, given the date of death and the rate of baleen growth in the preceding year; formation occurred over a period of 100 d from January to April (mean in February). A similar analysis indicated that valleys in the nitrogen isotope ratios were formed between January and June (mean in April), and enrichment peaks between August and May (mean in December). These patterns were not inconsistent with previous scenarios of southern right whale migration, if the enrichment peaks in carbon isotopes were taken to represent feeding just north of the STC, the subsequent decline in enrichment levels to represent feeding south of the STC in autumn, and the persistence of an isotopic signature characteristic of high latitude plankton throughout the winter and early spring to indicate that feeding essentially ceased when the northern migration began, and did not resume until the southern migration was under way. The oscillations in nitrogen isotope ratios would support this interpretation, if they were assumed to represent cycles of starvation and recovery. A comparison with baleen growth rates for bowhead whales allowed the ages of the six juveniles to be assessed. Their size at age, when compared to the lengths and growth rates of calves measured photogrammetrically, suggested that growth in body length of southern right whales slows markedly between weaning and 1 yr, and may be almost negligible from 1 to 4 yr of age.     

Reproduction in the seagrass Zostera novazelandica on intertidal platforms in southern New Zealand

This study investigates the reproductive periodicity and reproductive output of the seagrass Zostera novazelandica on two intertidal reefs. Peak numbers of flowering shoots occurred during March (late summer) of two years at both sites and no flowering shoots occurred during the winter months of July to September. There were greater numbers of flowering shoots in seagrass patches in the low intertidal zone (up to an average of 55 per 0.1 m²) compared to the middle (up to 20 per 0.1 m²) and upper (up to 9 per 0.1 m²) zones, and about three times greater reproductive output in patches associated with tidepools compared to those not bordering tidepools. The average number of inflorescences per shoot was 3.1 (±0.25) at one site vs 1.2 (±0.08) at the other, and showed a progressive decrease from the lower shore to the upper shore. Patches associated with tidepools had twice the number of inflorescences per shoot (2.8 ± 0.24) than patches not bordering tidepools (1.5 ± 0.16). The number of flowering shoots was highly correlated with leaf width, leaf length, and ramet density, while the leaf-area index decreased from the lower shore to the upper shore. The reproductive effort of plants, as measured by the percent biomass invested in flowering shoots during peak reproduction, was significantly different between sites, tidepool associations, and shore level. For all the variables measured, there was considerable spatial variation, with significant interaction terms between most factors investigated. In laboratory experiments, more inflorescences were produced at light intensities of 30 and 300 μE m⁻² s⁻¹ than at 100 μE m⁻² s⁻¹. At a salinity of 17‰, 1.5 × the number of flowers was produced than at 33‰, while none was formed at 70‰. Plants cultured at 5 °C had about three times the number of inflorescences than those at 15 °C, while none was formed at 25 °C. Received: 25 June 1997 / Accepted: 24 September 1997     

Abundance,distribution and prey composition of scyphomedusae in the southern North Sea

The annual cycle of abundance and distribution of the scyphozoan medusae Aurelia aurita, Cyanea lamarckii, C. capillata and Chrysaora hysoscella were studied in the southern North Sea in 2004 and 2005. Three different patterns of seasonal occurrence of medusae were distinguished: (1) the early occurring C. lamarckii (February–August), (2) C. capillata and A. aurita (April–August) and (3) the late appearing C. hysoscella (July/August–September). Cyanea lamarckii was the most frequently encountered species in this study; its highest mean abundance was 1.8 ± 2.7 ind. 100 m⁻³. The prey spectra of C. lamarckii, C. capillata and C. hysoscella contained several copepod and other crustacean species and thus make them potential competitors with fish larvae. Medusae in this study also consumed fish eggs and larvae, including clupeids, in all months analysed. Although peak spawning of sprat (Sprattus sprattus) coincides with the maximum abundance of medusae (May–June) the relative low abundance of all medusae species in this study makes jellyfish predation unlikely to be a factor controlling sprat recruitment in the time frame investigated.     

Effects of Spatially Extensive Control of Invasive Rats on Abundance of Native Invertebrates in Mainland New Zealand Forests

Predation on native fauna by non‐native invasive mammals is widely documented, but effects of predation at the population level are rarely measured. Eradication of invasive mammals from islands has led to recovery of native biota, but the benefits of controlling invasive mammal populations in settings where eradication is not feasible are less understood. We used various combinations of aerially delivered toxic bait and control measures on the ground to reduce abundances of invasive rats (Rattus rattus) to low levels over large areas on mainland New Zealand and then monitored the abundance of invertebrates on replicated treatment sites to compare with abundances on similar nontreatment sites. We also assessed rat diet by examining stomach contents. Abundance of the rats’ most‐consumed invertebrate prey item, the large‐bodied Auckland tree weta (Hemideina thoracica), increased 3‐fold on treatment sites where we maintained rats at <4/ha for approximately 3 years, compared with the nontreatment sites. Auckland tree weta also increased in abundance on sites where rats were controlled with a single aerial‐poisoning operation, but rat abundance subsequently increased on these sites and tree weta abundance then declined. Nevertheless, our data suggest that biennial reduction of rat abundances may be sufficient to allow increases in tree weta populations. Other invertebrates that were consumed less often (cave weta [Rhaphidophoridae], spiders [Araneae], and cockroaches [Blattodea]) showed no systematic changes in abundance following rat control. Our results suggest that the significant threat to recruitment and individual survival that predation by rats poses for tree weta can be mitigated by wide‐scale aerial pest control. Efectos del Control Extensivo Espacial de Ratas Invasoras sobre la Abundancia de Invertebrados Nativos en Bosques de Nueva Zelanda     

A demographic study of a subtidal population of the New Zealand articulate brachiopod Terebratella inconspicua

Size-frequency distributions from subtidal populations of Terebratella inconspicua (Sowerby, 1846) consistently display prominent modes at 18 to 22 mm shell length, representing many years accumulation of non-growing adults. In addition, these distributions contain seasonally variable modes made up of new recruits which are present in very high numbers towards the end of the breeding season, but are reduced to very low numbers by the end of their first year of life. Growth of recruits follows a sigmoid curve with considerable variability between individuals. Some adults survive at least 14 years. Females are 2 years old before they breed. Larvae are brooded internally by the parent and spawned in autumn and spring. The density of recruitment is positively correlated with the density of residents. Larvae commonly settle on the shells of large brachiopods; these recruits can survive to breed, but their survivorship as adults is lower than that of conspecifics attached to rock. Total mortality in the population is size (=age)-dependent; the mean life expectancy of a new recruit is 0.54 years compared with 2.57 years for a 1 year-old. Sources of mortality are considered.     

A spatially explicit estimate of the prewhaling abundance of the endangered North Atlantic right whale

The North Atlantic right whale (NARW) (Eubalaena glacialis) is one of the world's most threatened whales. It came close to extinction after nearly a millennium of exploitation and currently persists as a population of only approximately 500 individuals. Setting appropriate conservation targets for this species requires an understanding of its historical population size, as a baseline for measuring levels of depletion and progress toward recovery. This is made difficult by the scarcity of records over this species’ long whaling history. We sought to estimate the preexploitation population size of the North Atlantic right whale and understand how this species was distributed across its range. We used a spatially explicit data set on historical catches of North Pacific right whales (NPRWs) (Eubalaena japonica) to model the relationship between right whale relative density and the environment during the summer feeding season. Assuming the 2 right whale species select similar environments, we projected this model to the North Atlantic to predict how the relative abundance of NARWs varied across their range. We calibrated these relative abundances with estimates of the NPRW total prewhaling population size to obtain high and low estimates for the overall NARW population size prior to exploitation. The model predicted 9,075–21,328 right whales in the North Atlantic. The current NARW population is thus <6% of the historical North Atlantic carrying capacity and has enormous potential for recovery. According to the model, in June–September NARWs concentrated in 2 main feeding areas: east of the Grand Banks of Newfoundland and in the Norwegian Sea. These 2 areas may become important in the future as feeding grounds and may already be used more regularly by this endangered species than is thought.     

A model for energetics and bioaccumulation in marine mammals with applications to the right whale.

We present a dynamic energy budget (DEB) model for marine mammals, coupled with a pharmacokinetic model of a lipophilic persistent toxicant. Inputs to the model are energy availability and lipid-normalized toxicant concentration in the environment. The model predicts individual growth, reproduction, bioaccumulation, and transfer of energy and toxicant from mothers to their young. We estimated all model parameters for the right whale; with these parameters, reduction in energy availability increases the age at first parturition, increases intervals between reproductive events, reduces the organisms' ability to buffer seasonal fluctuations, and increases its susceptibility to temporal shifts in the seasonal peak of energy availability. Reduction in energy intake increases bioaccumulation and the amount of toxicant transferred from mother to each offspring. With high energy availability, the toxicant load of offspring decreases with birth order. Contrary to expectations, this ordering may be reversed with lower energy availability. Although demonstrated with parameters for the right whale, these relationships between energy intake and energetics and pharmacokinetics of organisms are likely to be much more general. Results specific to right whales include energy assimilation estimates for the North Atlantic and southern right whale, influences of history of energy availability on reproduction, and a relationship between ages at first parturition and calving intervals. Our model provides a platform for further analyses of both individual and population responses of marine mammals to pollution, and to changes in energy availability, including those likely to arise through climate change.     

Early development and estimated life cycle of the mesopelagic copepod Pareuchaeta elongata in the southern Japan Sea

Life cycle of the mesopelagic copepod Pareuchaeta elongata was investigated combining laboratory rearing data on the eggs, nauplii, and early copepodites with field growth data on the late copepodites. Examination and incubation at near the in situ temperature (0.5°C) of egg sacs collected from the field indicated that the clutch size was 13 to 24 eggs (mean: 20), hatching time was 39.4d (mean), and hatchability was low (mean: 28.5%). The development time at 0.5°C was 2.4 d for Nauplius Stage 1 (N1), 4.6 d for N2, 6.2 d for N3. 7.4 d for N4, 7.1 d for N5, 20.8 d for N6, 36.7 d for Copepodite Stage 1 (C1) and 65.3 d for C2. From the numerical analysis of seasonal samples collected from the field, the development time was estimated as 1 mo for C3, 2 mo for C4 and 2.5 mo for C5. Thus, the egg hatching time plus the integrated development time by stage was 355 d or nearly 1 yr (i.e. span of one life cycle). Duration of the C6 (adult) was estimated as>2.5 mo. Combining the present data on development times of each stage with published data on the major spawning season (August to October) and ontogenetic migration, a schematic representation of the life cycle of this copepod was developed. Between-stage comparison of wet, dry, and ash-free dry weights of all developmental stages of preserved wild specimens revealed that there is almost no gain in weight during naupliar stages, and the greatest weight increment over the life cycle was during the C4 stage. The present results are compared with those for the same and related species living in other regions.     

Systematic status of two oyster populations of the genus Tiostrea from New Zealand and Chile

A systematic examination of Tiostrea chilensis endemic to the Pacific coast of South America and of T. lutaria endemic to new Zealand was conducted using protein-gel electrophoresis. Also, ecological and life-history traits were compared between these two documented species. Our study revealed that although three different ecomorphs could be distinguished from various environmental and ecological conditions, the life-history traits between the two species were remarkably similar. Estimates were made of levels of genetic variation and similary based on 29 structural loci among individuals from each documented species. The percentage of loci polymorphic was estimated at 17.2 and 17.6, while the percentage of loci heterozygous was 2.1 and 6.7 for T. chilensis and T. lutaria, respectively. The genetic similarity between the two species was computed as 0.991, where 1.0 indicates no genetic difference among structural loci. The overwhelming evidence of this study indicates that T. chilensis and T. lutaria are different geographical populations of one species and by priority this species should be T. chilensis.     

Cephalopod remains from the stomach of a sperm whale stranded off Patagonia

The stomach of a male sperm whale (Physeter macrocephalus) stranded near Comodoro Rivadavia, Argentina, on 21 March 1986, contained 247 cephalopod beaks (128 upper and 119 lower). The lower beaks were identified, their rostral lengths were measured and used to estimate the mantle lengths and wet weight of the representatives of each cephalopod taxon. Fifteen species from nine families were represented. The most numerous species, in order of decreasing abundance, were the large cranchiidMesonychoteuthis hamiltoni (32.8% of total numbers),Mastigoteuthis sp. A (16.0%), andKondakovia longimana andHistioteuthis atlantica (both 13.5%). Almost 85% of the estimated total weight was contributed by two species,Mesonychoteuthis hamiltoni (61.6%) andK. longimana (23.1%). The presence of beaks fromK. longimana, Alluroteuthis antarcticus andM. hamiltoni, which are all thought to be restricted to the Antarctic, suggests that the whale had migrated North prior to stranding.     

Genetic population structure of the southern oyster drillStramonita (=Thais)haemostoma

Nine collections in the southeastern USA of the thaidid molluscStramonita haemastoma, comprising 963 individuals, were made between June 1988 and November 1989, and examined for allozyme variation at 18 electrophoretically-detected loci. Two genetically-differentiated groups were identified and are referred to ascanaliculata-like andfloridana-like snails, based on previously-described subspecies ofS. haemastoma. The two groups were differentiated genetically at a level that is characteristic of congeneric species in other molluscan taxa. The two groups maintained their genetic differences in areas of sympatry, although rare hybrid individuals occurred (about 1.2% of the total set). Shell and radular characters showed little variation within or between the two groups. Within each group, allozyme allele frequencies showed little geographic variation across distances as great as 1 500 km. This result is consistent with the suggestion that species with planktonic larvae (such asS. haemastoma) should have higher rates of gene flow than related brooding species.     

Allometry and growth of the green-lipped mussel Perna canaliculus in New Zealand

Length is the most precise (and the most practical) linear measurement for predicting total weight (r>0.98 at P=0.001) in the green-lipped mussel Perna canaliculus Gmelin. The allometry varies with the environmental conditions under which the mussels grow, resulting in morphologically distinct forms of raft- and shore-grown mussels. Mussels grown intertidally are wider, less high and heavier than mussels of similar length grown in suspension. Increase in length and total weight of P. canaliculus grown in suspended cultivation was recorded at 8 experimental sites around New Zealand, during 1973–1975. Comparisons are drawn with growth on an intertidal mussel bed, where length increase was less than half that in the same period in suspension. The growth rate of mussels transferred from intertidal to suspended conditions depends on the size at transfer. Close similarity in growth rate occurred at the majority of sites in spite of a direct correlation between water temperature and length increment and substantial, differences in temperature between sites. Reasons for the uniformity are suggested. Average values for growth at sites over the northern half of New Zealand were 73 mm length (32.5 g weight) after 12 months, 113 mm (110 g) after 2 years. Growth continued throughout the year, highest growth rates corresponding to highest water temperatures. Variation due to depth was not significant. Larger mussels grew more slowly. P. canaliculus can be grown in suspended cultivation in New Zealand at a rate comparable to that in other commercial mussel-farming areas.     

Time series analysis of elemental and isotopic data from biomineralized whale tissue

A temporal record of environmental conditions is often contained within accretionary biological tissue. These records can provide knowledge of the environmental conditions that existed at the time the tissue was formed. In this study, we look at trace element concentrations and isotopic ratios of carbon and nitrogen as contained in baleen from bowhead whales in the eastern and western Arctic Ocean. Time series techniques, including maximum likelihood method and likelihood ratio tests, are applied to analysis of data and inference about their mean structures.     

Lessons in Ecosystem Management from Management of Threatened and Pest Loranthaceous Mistletoes in New Zealand and Australia

Loranthaceous mistletoes are interesting because of their complex dependence on suitable host trees and avian dispersers and because of their patchy distribution at the landscape level. Although their over- and under-abundance in Australia and New Zealand have been widely documented, little attention has been given to the need for an ecosystem approach to their management. Although the current status of mistletoes is very different in Australia and New Zealand, some of the causal factors and the long-term effects of changes in mistletoe abundance are similar in the two countries. We suggest that mistletoe abundance in pre-European landscapes was dependent on a series of evolutionary and environmental filters relating to host specificity, pollination, dispersal, infection, environmental habitat quality, predation, and disturbance. European settlement modified these filters in a number of ways, resulting in either increases or decreases in mistletoe abundance. The three broad groups of changes that have occurred with European settlement involve fragmentation, predation, and altered disturbance regimes. Although managers have usually addressed mistletoe over- or under-abundance with short-term solutions (e.g., pruning infected trees), we suggest that management must address the underlying causes of the problems involving mistletoes. This requires an ecosystem approach to management that addresses both the direct and indirect causes of the current status of mistletoes.     

Condition cycle of the green-lipped mussel Perna canaliculus in New Zealand

The condition of the green-lipped mussel Perna canaliculus (Gmelin) from 7 sites around the northern half of New Zealand was determined monthly between December 1973 and February 1975. Seven separate estimates of condition were calculated for each sample; 4 condition indices, 2 percentage glycogen analyses and 1 estimate of percentage solids. All showed a similar annual cycle, with minimum values in winter (June/ August) rising to peak levels in spring (October/ December). The 7 sites were divided into 3 groups, (i) a central New Zealand group, characterised by high levels of condition index (CI) throughout most of the year >10 CI_weight for 8 to 11 months, average to high percentage glycogen (annualmeans 25 to 35% dry weight), and high percentage solids (annual means > 20% dry weight); (ii) an intertidal group, having low levels of CI (<10 CI_weight for 10 to 11 months), low percentage glycogen(mean <20%), and low percentage solids (mean <18%); and (iii) a northern group, showing intermediate values for each of the estimates of condition. Difficulties in defining the causes of changes in the condition cycle are discussed. There is an inverse relationship between CI and mussel size, resulting from changes in body proportions. An inverse relationship is also suggested between CI and water temperature. A precise index, $$CI_{weight} = \frac{{100 \times dry meat weight}}{{whole{\text{ weight - shell weight}}}}$$ is recommended for biological studies on mussels and a rapid simple index, $$CI_{commercial} = \frac{{100 \times wet meat weight}}{{whole{\text{ (live) weight}}}}$$ for use in the field and in mussel farming practice.