Sensitivity and cost considerations for the detection and eradication of marine pests in ports

Port surveys are being conducted in Australia, New Zealand and around the world to confirm the presence or absence of particular marine pests. The most critical aspect of these surveys is their sensitivity-the probability that they will correctly identify a species as present if indeed it is present. This is not, however, adequately addressed in the relevant national and international standards. Simple calculations show that the sensitivity of port survey methods is closely related to their encounter rate-the average number of target individuals expected to be detected by the method. The encounter rate (which reflects any difference in relative pest density), divided by the cost of the method, provides one way to compare the cost-effectiveness of different survey methods. The most cost-effective survey method is site- and species-specific but, in general, will involve sampling from the habitat with the highest expected population of target individuals. A case study of Perna viridis in Trinity Inlet, Cairns, demonstrates that plankton trawls processed with gene probes provide the same level of sensitivity for a fraction of the cost associated with the next best available method-snorkel transects in bad visibility (secchi depth=0.72 m). Visibility and the adult/larvae ratio, however, are critical to these arguments. If visibility were good (secchi depth=10 m), the two approaches would be comparable. Diver deployed quadrats were at least three orders of magnitude less cost-effective in this case study. It is very important that environmental managers and scientists perform sensitivity calculations before embarking on port surveys to ensure the highest level of sensitivity is achieved for any given budget.     

Organic sedimentary deposits in Titan’s dry lakebeds: Probable evaporite

We report the discovery of organic sedimentary deposits at the bottom of dry lakebeds near Titan’s north pole in observations from the Cassini Visual and Infrared Mapping Spectrometer (VIMS). We show evidence that the deposits are evaporitic, making Titan just the third known planetary body with evaporitic processes after Earth and Mars, and is the first that uses a solvent other than water.     

Estimating relative abundance of juvenile brown trout in rivers by underwater census and electrofishing

Underwater census and single‐pass electrofishing were compared for estimating relative abundance of juvenile brown trout in the Kakanui River, South Island, NZ. Mean sampling efficiency was lower, and the variability of sampling efficiency was much greater, for underwater census (0+ trout: x = 0.38, s = 0.368; 1+ trout: x = 0.62, s = 0.822) than for single‐pass electrofishing (0+ trout: x = 0.61, s = 0.143; 1+ trout: x = 0.74, s = 0.171). Sampling efficiency of both methods was dependent on temperature. Electrofishing became less efficient at higher temperatures whereas underwater census became less efficient at colder temperatures. The low, and highly variable, sampling efficiency for underwater census of 0+ brown trout was related to substrate hiding behaviour which is dependent on temperature. A ratio method for comparing relative abundance estimates is presented. Minimum significance values for the ratio (R) were derived for 0+ trout using temperature adjusted sampling efficiencies. To be statistically significant, relative abundance estimates made by underwater census had to differ by a factor of 6–7 times, whereas those made by single‐pass electrofishing had to differ only by about 2 times, depending on the number of fish counted. By confining comparisons of relative abundance estimates made by underwater census to the summer period, differences of about 3.5–4 times could be detected statistically. It was concluded that single‐pass electrofishing is superior to underwater census for estimating the relative abundance of juvenile brown trout in shallow (< 1 m) river habitat, especially when temperature varies widely as with season and time of day.     

Intraplate deformation adjacent to the Macquarie Ridge south of New Zealand—The tectonic evolution of a complex plate boundary

The distribution of relocated seismicity and the evolving shape of fracture zones through time in the oceanic crust of the Australian Plate adjacent to the Australia:Pacific plate boundary south of New Zealand are used to constrain the deformation of this region of the Australian Plate, here called the Puysegur Block. Relocated seismicity reveals a broad distribution of earthquakes in the Puysegur Block on both inter- and intraplate structures, including two great (M8+) earthquakes in the region over the past twenty years, one of which occurred over 130 km from the plate boundary. Plate reconstructions from the Late Oligocene through Early–Mid Miocene allow us to determine the undeformed shape of fracture zones in the Puysegur Block, formed during the Paleogene when the plate boundary was dominantly a divergent mid-ocean ridge system. Comparing these reconstructions to the present-day shape of the fracture zones allows us to map the deformation that has occurred within the Puysegur Block since the fracture zones formed. These two sets of independent observations delineate a broad zone of deformation extending ~ 150 km into the plate interior from the Macquarie Ridge Complex, the modern plate boundary structure through the region. The persistence of this deformation through time indicates a link with the evolution of the plate boundary over the past ~ 25 Ma from divergence to translation and subduction of the Australian Plate further north at the Puysegur Trench. We infer that this deformation may be a result of stresses in the Puysegur Block resulting from the impingement of the subducting plate on the thickened lithosphere of southern New Zealand. Such a collision may resist subduction, and if resistance remains substantial, further deformation internal to the Puysegur Block may lead to a southward migration of the Australia:Pacific subduction interface and the capturing of this section of lithosphere onto the Pacific Plate.     

Changes in zooxanthellae density,morphology, and mitotic index in hermatypic corals and anemones exposed to cyanide

Sodium cyanide (NaCN) is widely used for the capture of reef fish throughout Southeast Asia and causes extensive fish mortality, but the effect of NaCN on reef corals remains debated. To document the impact of cyanide exposure on corals, the species Acropora millepora, Goniopora sp., Favites abdita, Trachyphyllia geoffrio, Plerogyra sp., Heliofungia actinformis, Euphyllia divisa, and Scarophyton sp., and the sea anemone Aiptasia pallida were exposed to varying concentrations of cyanide for varying time periods. Corals were exposed to 50, 100, 300, and 600 mg/l of cyanide ion (CN(-)) for 1-2 min (in seawater, the CN(-) forms hydrocyanic acid). These concentrations are much lower than those reportedly used by fish collectors. Exposed corals and anemones immediately retracted their tentacles and mesenterial filaments, and discharged copious amounts of mucus containing zooxanthellae. Gel electrophoreses techniques found changes in protein expression in both zooxanthellae and host tissue. Corals and anemones exposed to cyanide showed an immediate increase in mitotic cell division of their zooxenthellae, and a decrease in zooxanthellae density. In contrast, zooxanthellae cell division and density remained constant in controls. Histopathological changes included gastrodermal disruption, mesogleal degradation, and increased mucus in coral tissues. Zooxanthellae showed pigment loss, swelling, and deformation. Mortality occurred at all exposure levels. Exposed specimens experienced an increase in the ratio of gram-negative to gram-positive bacteria on the coral surface. The results demonstrate that exposure cyanide causes mortality to corals and anemones, even when applied at lower levels than that used by fish collectors. Even brief exposure to cyanide caused slow-acting and long-term damage to corals and their zooxanthellae.