Oxygen consumption in the epilimnia and hypolimnia of two eutrophic,warm‐monomictic lakes

Oxygen consumption was estimated for two eutrophic New Zealand lakes using a simple 2‐layer model, from estimates of net changes in oxygen, phytoplankton photosynthesis, inflow and outflow, diffusion, eddy diffusion, and changes in the depth of the thermocline. Of the total oxygen consumption, 75–85% occurred in the epilimnia. Epilimetic oxygen consumption per m³ and per m² in Lake Johnson were higher than in Lake Hayes, reflecting known differences in the trophic status of the lakes, but estimates for the hypolimnia of the two lakes were similar. Daily hypolimnetic areal deficits were sensitive to both the depths and time intervals chosen.

In the epilimnia, monthly oxygen production by photosynthesis averaged 1.1 and 1.8 times the initial oxygen content in Lakes Hayes and Johnson respectively. Diffusion appeared to be of similar magnitude to photosynthesis in the isothermal period, but was less important during stratification. Losses to the hypolimnia by eddy diffusion were less than 10% of photosynthesis. Photosynthesis in the hypolimnia contributed 30–40% of the oxygen consumed there and eddy diffusion supplied a further 20%.

In Lake Johnson a 3–5 m stratum of water in the metalimnion became anoxic for 2–3 months each summer while there were still up to 5.2 g.rer³ of oxygen remaining in the hypolimnion. Metalimnetic anoxia is attributed largely to oxygen consumption in situ, resulting from the highly eutrophic state of the lake and intense thermal stratification. Zooplankton respiration accounted for less than 10% of the maximum net decline in metalimnetic oxygen in 1970–71, but was more important in the other 2 years.

Changes in the oxygen content of the hypolimnion indicate that Lake Hayes has become more eutrophic since 1954–55. In Lake Johnson low oxygen concentrations at the autumn overturn (<5 g.m^‐3) represent a threat to the trout population.     

A new species of Plaxiphora (Mollusca: Polyplacophora) from southern New Zealand

Plaxiphora boydeni n.sp. from wave‐exposed rocky shores of southern New Zealand is described and illustrated. This is the first published record of the genus from the New Zealand mainland. P. boydeni is readily distinguished from the 2 other New Zealand species of the genus, which occur in the subantarctic region, by the absence of bristle‐tufts on the girdle.     

The effect of membrane filtration on estimates of microbial ATP in New Zealand freshwaters

Concentrations of microbial ATP in 15 New Zealand lakes were determined using 2 extraction techniques. ATP was found in both the paniculate (>0.45 μm) and dissolved (<0.45 μm) fractions of the water samples. Higher concentrations of paniculate ATP were obtained when ATP was extracted directly from freshwater samples rather than following pre‐concentration on to membrane filters. Recovery of particulate ATP declined with increasing volumes of sample filtered. The magnitude of the filtration effect varied unpredictably between lakes and within lakes with time. Corrections for the presence of dissolved ATP were necessary before estimates of particulate ATP could be made by the direct extraction technique. Concentrations of dissolved ATP up to 1.2 μg L^‐1 were observed. The direct extraction technique is recommended for more accurate determination of particulate ATP in New Zealand freshwaters.     

Burrowing behaviour of the paddle crab Ovalipes catharus (White, 1843) (Brachyura: Portunidae)

The burrowing behaviour of Ovalipes catharus (White, 1843) is described and compared with that of some other burrowing crabs. O. catharus is a fast, back burrowing crab which makes temporary burrows in soft sand. The average time from initiation of burrowing to complete submergence was 6.5 s, there was no difference between males and females but burrowing time increased significantly with crab size. Similar morphological adaptations are required for burrowing and swimming: streamlined body shape, smooth lightly constructed exoskeleton, and flattened legs. O. catharus has a reversed respiratory current like O. guadulpensis but it differs in its burrowing behaviour. Compared to some other crabs, burrowing in O. catharus is rapid.     

Two acoustic surveys of pelagic fish in Hawke Bay,New Zealand, 1980

The design and execution of two acoustic surveys of Hawke Bay in February and September/October 1980 are described. Though the resulting acoustic data were, for technical reasons, of limited value, they illustrate the information which may be drawn from acoustic surveys. Fish distributions may be rapidly mapped, not only by area, but throughout most of the water column and over time. Qualitative observations on fish distribution may be quantified. The estimation of variance in acoustic surveys is discussed in detail with particular emphasis on the problems of systematic surveys. The role of replicate observations is stressed. Coefficients of variation for relative fish density estimates from the two surveys probably lie between 5 and 30%.     

Diet of landlocked sockeye salmon (Oncorhynchus nerka) and trout in the Waitaki lakes,New Zealand

Landlocked sockeye salmon (Oncorhynchus nerka), ranging in fork length (FL) from 105 to 313 mm, were captured in fine‐mesh gill nets set in the limnetic zone of the Waitaki hydro lakes (44° 30′ S, 170° 10’ E) in the South Island, New Zealand. A total of 443 stomachs was examined and the frequency of occurrence, volume and weight of prey items calculated. In the Ahuriri Arm of Lake Benmore the principal food (54% by weight) was zooplankton (Boeckella dilatata) whereas in the Haldon Arm of Lake Benmore it was larval and juvenile common bullies (Gobiomorphus cotidi‐anus) (73% by volume). In Lake Waitaki in winter, salmon had eaten insects (43% by volume) with smaller amounts of snails (Potamopyrgus antipo‐darum, 23%) and bullies (24%). In Lake Ohau adult insects may be an important food. There were also variations in diet with season and fish size. The stomachs of 147 brown trout (Salmo trutta) and 181 rainbow trout (S. gairdnerii) caught in the same gill nets were also examined. In contrast to sockeye salmon stomachs they contained negligible amounts of zooplankton (< 1% by weight) and large amounts of aquatic insects (50–58% by weight in the Ahuriri Arm of Lake Benmore). Comparisons with juvenile sockeye salmon and kokanee in North American lakes are made. The impact of introductions of sockeye salmon into other New Zealand lakes is discussed.     

Insights into zooplankton‐cyanobacteria interactions derived from enclosure studies

Few workers have used enclosures specifically to study interactions between zoo‐plankton and cyanobacteria. Differences among studies in enclosure size, nutrient level, plankton abundance and species composition, presence or absence of fish, and length of experiments make generalisations difficult. Zooplankton had no direct effect on the growth of ungrazed cyanobacteria (Anabaena flos‐aquae, Aphanizomenon flos‐aquae, large Microcystis colonies) in short‐term (<5 days) and long‐term (> 1 month) enclosure studies. When large cyanobacteria were abundant, some Daphnia spp. snowed reduced reproduction and development. When large grazers were abundant they suppressed the growth of edible, colonial cyanobacteria (Aphanizomenon elenkinii, small Microcystis colonies). By altering the ambient light and nutrient environment, large zooplankton may suppress cyanobacteria; evidence for the importance of grazers in promoting cyanobacterial dominance by removing competing phytoplankton species is equivocal. Zooplankton may suppress nitrogen fixation by cyanobacteria through ammonia excretion and may promote a change in dominance from diatoms to cyanobacteria through recycling phosphorus but not silicon.     

Book review

Nga tini a Tangaroa, a Maori‐English, English‐Maori dictionary offish names. By R. R. Strickland. New Zealand fisheries occasional publication 5. 1990. 64 unnumbered pages, ISSN 0113–227X. Available from Primedia Bookshop, P.O. Box 2526, Wellington, New Zealand. Price: $26.95.     

Biochemical‐genetic and meristic evidence that blue and copper moki (Teleostei: Latridae: Latridopsis) are discrete species

Specimens of blue moki Latridopsis ciliaris (Forster in Bloch & Schneider, 1801) from New Zealand were shown to differ from specimens of copper moki Latridopsis forsteri (Castelnau, 1872) using two genetic methods—allozymes and muscle proteins. Allozyme techniques revealed fixed differences between blue and copper moki at 4 out of 15 loci. There was a genetic distance of 0.31–0.34 between population samples of the two colour morphs. The two morphs were also distinguished by iso‐electric focusing of muscle proteins. Meristic characters, counted in the specimens studied with genetic markers, revealed diagnostic markers in tubed lateral line scales and scales in the lower transverse series. It is concluded that specimens of blue moki from New Zealand and copper moki from New Zealand and Tasmania are valid species.     

Growth and survival of early juvenile trumulco snail Chorus giganteus (Gastropoda: Muricidae) fed two prey species

Comparative data were obtained on the growth and survival of early juveniles of the trumulco snail Chorus giganteus from settlement to an age of 4 months when fed either of the mussel species Semimytilus algosus or Perumytilus purpuratus. Growth of the snails after 4 months was significantly greater when fed S. algosus, ending with a mean size of 6162 μm compared with 5192 μm with P. purpuratus. Survival between the two fed groups was not prey‐specific. Survival of the unfed control group was significantly lower beginning at 14 days post‐metamorphosis. After 63 days, survival within the fed groups was 63.2% and only 16.5% in the unfed control group. The similarity of growth and survival of these juveniles during the first 2 months in culture suggested that both prey species had the same food value. The energy cost to the snails of penetrating the different prey species diverged after the second month, as the shells of P. purpuratus became thicker and thus more difficult to penetrate than those of S. algosus. This was reflected as differences in growth rates for snails fed the 2 species in the following 2 months of the experiment. Unfed snails grew by 107 μm in average during the first 2 weeks of the experiment and then ceased demonstrating the importance of nutritional reserves carried by the larva from hatching through early benthic survival.