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Post-10 ka rhyolitic eruptions from the Haroharo linear vent zone, Okataina Volcanic Centre, have occurred from several simultaneously active vents spread over 12 km. Two of the three eruption episodes have tapped multiple compositionally distinct homogeneous magma batches. Three magmas totalling ~8 km3 were erupted during the 9.5 ka Rotoma episode. The most evolved Rotoma magma (SiO2=76.5–77.9 wt%, Sr=96–112 ppm) erupted from a southeastern vent, and is characterised by a cummingtonite-dominant mineralogy, a temperature of 739±14°C, and fO2 of NNO+0.52±0.11. The least evolved (SiO2=75.0–76.4 wt%, Sr=128–138 ppm, orthopyroxene+ hornblende-dominant) Rotoma magma erupted from several vents, and was hotter (764±18°C) and more reduced (NNO+0.40±0.13). The ~11 km3 Whakatane episode occurred at 5.6 ka and also erupted three magmas, each from a separate vent. The most evolved (SiO2=73.3–76.2 wt%, Sr=88–100 ppm) Whakatane magma erupted from the southwestern (Makatiti) vent and is cummingtonite-dominant, cool (745±11°C), and reduced (NNO+0.34±0.08). The least evolved (SiO2=72.8–74.1 wt%, Sr=132–134 ppm) magma was erupted from the northeastern (Pararoa) vent and is characterised by an orthopyroxene+ hornblende-dominant mineralogy, temperature of 764±18°C, and fO2 of NNO+0.40±0.13. Compositionally intermediate magmas were erupted during the Rotoma and Whakatane episodes are likely to be hybrids. A single ~13 km3 magma erupted during the intervening 8.1 ka Mamaku episode was relatively homogeneous in composition (SiO2=76.1–76.8 wt%, Sr=104–112 ppm), temperature (736±18°C), and oxygen fugacity (NNO+0.19±0.12). Some of the vents tapped a single magma while others tapped several. Deposit stratigraphy suggests that the eruptions alternated between magmas, which were often simultaneously erupted from separate vents. Both effusive and explosive activity alternated, but was predominantly effusive (>75% erupted as lava domes and flows). The plumbing systems which fed the vents are inferred to be complex, with magma experiencing different conditions in the conduits. As the eruption of several magmas was essentially concurrent, the episodes were likely triggered by a common event such as magmatic intrusion or seismic disturbance.  相似文献   
2.
A preliminary scuba survey of oligotrophic Lake Rotoma in 1972 revealed a vegetation mainly composed of native hydrophytes in which exotics were at an early stage of colonisation. In 1973 the presence of species was recorded in 5708 quadrats (625 cm2) at 1 m intervals along a total of 50 line transects placed systematically around the lake. Water depth was measured, and quadrat cover and substrate type were subjectively estimated. Species frequency calculations showed that the dominant vegetation pattern was a characean meadow of Chara fibrosa f. acanthopitys (A.Br.) R.D.W., Nitella leptostachys var. leonhardii (R.D.W.) R.D.W., and N. pseudoflabellata var. mucosa (Nordst.) Bailey. The charophytes extended over a depth range of 1–17.5 m on a wide variety of substrates and gradients. Native vascular plants were absent from many transects, and had a depth range only from 0 to 4.5 m, with most occurring above 3.5 m. The Low Mixed Community, found in shallow water less than 1.25 m in depth at the northeast end of the lake, provided this area with a high species diversity. Exotic hydrophytes had established in many areas around the lake. The distribution of Lagarosiphon major (Ridley) Moss and Elodea canadensis Michx. appeared to coincide with boating access and fallen submerged trees over a depth range of 0–6.0 m, although much of the available habitat had not yet been exploited. Emergent species were most abundant within the southwest inlet and also in the lagoons surrounding the lake where sheltered conditions and shallow gradients prevail.  相似文献   
3.
Fluctuations in water level and the growth of the introduced exotic Lagarosiphon major (Ridley) Moss have significantly influenced the submerged vegetation of Lake Rotoma over the period 1973–80. Low lake levels temporarily reduced the proportion of native vascular plants by removing available shallow‐water habitats through erosion, siltation, or desiccation. High lake levels have allowed native vascular plants to re‐establish from seed and rhizomes. Fluctuations in water level appear to have reduced the long‐term replacement of native species by L. major, which has none the less spread progressively around the lake. Water‐level fluctuations enhanced its rate of fragmentation, and thus its dispersal and establishment. The annual increase in the proportion of L. major has been primarily at the expense of the shallow‐water characean algae, but also partly by competitive displacement of native vascular plants. The southwest inlet of Lake Rotoma had an exceptionally high plant density, with up to 3518 g/m2 dry weight of L. major (believed to be a world record for submerged plant biomass); this is attributed to local enrichment and protection from wave exposure.  相似文献   
4.
The presence of suitable gravel size alone can stimulate female rainbow trout (Salmo gairdneri) to excavate nests for spawning on the shores of Lake Rotoma. Emergent fry result from lake‐shore spawning, and could contribute significantly to the trout fishery in Lake Rotoma. Lake‐shore spawning could be enhanced by the use of stable artificial spawning beds that have adequate depth and appropriate sizes of gravel.  相似文献   
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