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981.
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986.
Shallow-water vegetated estuarine habitats, notably seagrass, mangrove and saltmarsh, are known to be important habitats for many species of small or juvenile fish in temperate Australia. However, the movement of fish between these habitats is poorly understood, and yet critical to the management of the estuarine fisheries resource. We installed a series of buoyant pop nets in adjacent stands of seagrass, mangrove and saltmarsh in order to determine how relative abundance of fishes varied through lunar cycles. Nets were released in all habitats at the peak of the monthly spring tide for 12 months, and in the seagrass habitat at the peak of the neap tide also. The assemblage of fish in each habitat differed during the spring tides. The seagrass assemblage differed between spring and neap tide, with the neap tide assemblage showing greater abundances of fish, particularly those species which visited the adjacent habitats when inundated during spring tides. The result supports the hypothesis that fish move from the seagrass to the adjacent mangrove and saltmarsh during spring tides, taking advantage of high abundances of zooplankton, and use seagrass as a refuge during lower tides. The restoration and preservation of mangrove and saltmarsh utility as fish habitat may in some situations be linked to the proximity of available seagrass.  相似文献   
987.
The basic regulation of macromoleoular synthesis in mycelium-forming bacteria is in principle the same as in unicellular bacteria, but modified by morphological peculiarities. The higher the specific growth rate the moreStreptomyces resembles unicellular bacteria.  相似文献   
988.
989.
Species of Elachisina are marine and extend from the Caribbeanand western North and Central America to the Philippines, Hawaiiand New Zealand. The anatomy and other morphological featuresof Elachisina ( = Microdocluis) floridana (Rehder) from theFlorida Keys are described and compared with rissoacean familiesjudged to be most closely allied. This species has a uniquecombination of characters which do not correspond to those character-setsused to define any known rissoacean family. Important featuresinclude a metapodial as well as pallial tentacles, a wide ctenidiumwith low, triangular filaments, an osphradium which is shortrelative to the ctenidium, an S-shaped loop of the intestinewhich extends into the pallial roof, long dorsal folds in themidoesophagus, a rather loosely organised nervous system, anopen prostate gland from which the pallial vas deferens exitsat its anterior extremity, glandular lobes on the penis, a non-glandularfold on the right side of the ventral channel of the capsulegland and a fold on the left side in the posterior end of thechannel, a pair of seminal receptacles lying between the albumenand capsule glands, a bursa which lies alongside the capsulegland and opens posteriorly to the ventral channel and a U-shaped,expanded section of the oviduct proximal to the albumen glandand seminal receptacles. This combination of characters is consideredto be sufficiently distinct to arrant the erection of a newfamily-level taxon to accommodate the small group of speciesjudged to be congeneric with E. floridana. The Elachisinidaeappears to be most closely related to the Rissoidae, Iravadiidaeand Hydrobiidae. (Received 19 October 1983;  相似文献   
990.
Changes are reported of Crataegus-Betula dune woodlands between 1950–1980 from Meijendel, a calcareous coastal dune system near the city of The Hague, The Netherlands, which is used as a water catchment area. It concerns both woodlands in degradation stage and, more common, woodlands on the increase. Changes were recorded with help of successive vegetation maps, air photos and permanent plot observations. Woodland increase usually occurs on places with groundwater at or near the surface, either because of natural circumstances or as a result of artificial groundwater recharge through infiltration as part of the water catchment activities. The management of both types of woodland is discussed.Nomenclature follows Heukels-van der Meijden (1983), Flora van Nederland, 20th ed. Wolters-Noordhoff, Groningen. Nomenclature of mosses follows Margadant & During (1982), Beknopte Flora van Nederlandse Blad- en Levermossen, Thieme, Zutphen.The authors have pleasure in thanking their colleagues from the Dune Water Works who supplied data on hydrology.  相似文献   
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