A large dacitic lava flow in northern chile

A dacitic lava flow with a volume of about 24 km³ is described. This flow is the largest of three of this type which were erupted in the youngest phase of volcanism in one part of the Andes of northern Chile. The majority of volcanoes erupted during this phase are more andesitic in composition and are made up of small flows and pyroclastic materials.     

Monte Vulture Volcano (Basilicata,Italy): an analysis of morphology and volcaniclastic facies

The earliest activity of Monte Vulture, central Italy, included ignimbrites but the bulk of the volcano was built up by plinian airfall deposits. Contemporaneous remobilisation of these deposits formed an apron of lahars around the base of the main cone. The volcano was constructed on a ridge; the valley to the east and tributaries to the north and south became sediment traps for volcaniclastic materials emplaced by fluvial reworking and directly from volcanic activity. To the west the valley was swept clear by active downcutting. Instability of the west flank as a result of this erosion was probably a contributory cause of major gravitational sector collapse on the volcano's flank, terminating the main cone-building phase. The resultant scar is an amphitheatre-shaped hollow called here the Valle dei Grigi. Previous workers have attributed this feature to coalescing calderas formed by engulfment. The last volcanic phase was the production of the Monticchio calderas and associated phreatomagmatic explosions producing airfall and surge deposits. Because most of the activity at Vulture has been repeated plinian eruptions producing similar assemblages of products, detailed stratigraphy of the volcano is difficult to accomplish. To characterise Vulture in terms of its products, various facies are identified and interpreted in relation to volcanic processes, distance from vent and environmental conditions.     

The evolution of lava flow-fields: observations of the 1981 and 1983 eruptions of Mount Etna,Sicily

The eruptions of Mount Etna in 1981 on the north flank and 1983 on the south flank of the volcano were of strikingly different character. The former was a short duration, high effusion rate eruption producing for the most part a simple flow-field; the latter was of relatively long duration and low effusion rate, producing a compound flow-field of overlapping flows.Despite the differences between the eruptive behaviour of these two events and the way in which the flow-field developed, both the flow-fields achieved about the same maximum length. This is considered fortuitous. The evidence suggests that the main 1981 flow stopped because the lava supply ceased and was thus volume controlled. The 1983 flow-field had a more complex history of branching, but in this case it appears that, for the longest individual flow, cooling played an important role in controlling the maximum extent of the flows.     

Lava tubes,terraces and megatumuli on the 1614–24 pahoehoe lava flow field,Mount Etna,sicily

The 1614–1624 lava flow of Mt. Etna was formed during a long-duration flank eruption involving predominantly pahoehoe flows which produced unusual surface features including mega-tumuli (here defined) and terraces. Detailed mapping of the flow units, surface features, and associated tubes reveals a complex sequence of emplacement for the field. The stair-stepped terraces appear to have been formed as a consequence of self-damming of tube-fed flows which developed «perched» ponds of lava. Surges of lava through tubes elevated sections of crusted lava at the distal ends of the flow to generate tumuli, some as high as 130 m, as a consequence of pressure via «hydrostatic head» conditions within the tube. Although pahoehoe lavas and the related features described here are atypical of Mt. Etna, they may reflect styles of eruption and lava emplacement found on volcanoes elsewhere.     

The ISOCAM/LW Detector Dark Current Behaviour

We describe the calibration, measurements and data reduction, ofthe dark current of the ISOCAM/LW detector. We point-out theexistence of two significant drifts of the LW dark-current, onethroughout the ISO mission, on a timescale of days, another within each single revolution, on a timescale of hours. We alsoshow the existence of a dependence of the dark current on thetemperature of the ISOCAM detector.By characterizing all these effects through polynomial fittings,we build a model for the LW calibration dark, that depends onthe epoch of observation (parametrized with the revolutionnumber and the time elapsed in that given revolution since theactivation) and on the temperature of the ISOCAM detector. Themodel parameters are tuned for each of ISOCAM/LW pixel.We show that the modelling is very effective in taking intoaccount the dark-current variations and allows a much cleanerdark subtraction than using a brute average of severalcalibration dark images.The residuals of the LW model-dark subtraction are, on average,similar to the pre-launch expectation.     

Genetic improvement of New Zealand aquaculture species: programmes,progress and prospects

Aquaculture, like terrestrial farming, cannot achieve economic and sustainable production without high performing genetic stocks tailored to the conditions under which they are grown. It is essential, therefore, that aquaculture investment includes genetics and biotechnology to adapt marine livestock to the novel conditions of intensive aquaculture and to the demanding markets into which they are sold. The return on investment in well-structured breeding programmes can be very high, and significant performance and economic gains have been demonstrated in multiple species. Many factors must be considered in designing a genetic improvement programme, including the reproductive biology of the species and the identification of realistic and commercially relevant breeding goals based on the resources and facilities available. This paper reviews the options available to aquaculturists and provides examples of how these are being applied to six aquaculture species in New Zealand: king salmon, hāpuku, kingfish, Greenshell^TM mussels, Pacific oysters and pāua (abalone).