By Ralph O. Brinkhurst (auth.), Giuliano Bonomi, Christer Erséus (eds.)

At the 1st overseas Symposium on Aquatic Oligochaete Biology in Sidney, B. C. , the recommendation used to be made to carry the second one in Pallanza, on Lake Maggiore, on the C. N. R. -Istituto Italiano di Idrobiologia. while it was once made up our minds that there could be a symposium each 3rd yr. The association of the symposium was once made significantly more uncomplicated by means of the Senior Editor's having been in own touch with a number of Russian colleagues (courtesy of a type invitation from the U. S. S. R. Academy of Sciences), the 'Hamburg staff' and the Junior Editor. Correspondence with a number of scholars of Oligochaeta additionally supplied many beneficial feedback. the second one foreign Symposium on Aquatic Oligochaete Biology used to be for this reason held in Pallanza in overdue September 1982 and used to be attended via fifty three scientists from sixteen international locations in Europe, North the United States, Asia and Australia. No assessment papers have been officially invited as this had already been performed on the first symposium: the entire papers have been hence dispensed a similar time for oral presentation. those lawsuits comprise all papers Hrabe and Slepukhina, which have been given in absentia, because it offered on the symposium, together with these by way of used to be very unlikely for the authors to hitch the gang. the most themes have been taxonomy and evolution of Oligo chaeta, life-cyle and inhabitants reviews, the function of Oligo chaeta in assessing water toxins, physiolog­ ical stories, group and distribution experiences. unique taxonomic workshops happened within the evenings.

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Extra resources for Aquatic Oligochaeta: Proceedings of the Second International Symposium on Aquatic Obligochaete Biology, held in Pallanza, Italy, September 21–24, 1982

Example text

These problems also tainted the earlier views of simultaneous evolution of the coelom and segmentation, whereas such pitfalls were avoided by Clark (1946). His brilliant exposition of the independent origin of both leads us to the presumption of a simplified ancestor to both oligochaetes and polychaetes with earthworm-like anatomy apart from its reproductive system (Brinkhurst, 1982). Evolution within the Tubificida It is necessary to touch on one or two implications of this theory to the evolution of the various families within the Tubificida.

1984). 1I'd/Or ESTUARIES schemes accept the Haplotaxidae as ancestors of the Lumbricida. The ancestor of the Lumbricomorpha postulated by Timm must be rather similar to my protohaplotaxid ancestor, which I also see as giving rise to the Lumbriculidae. g. Yamaguchi, 1953), depends upon undue focus on a few parthenogenetic species in the former and misunderstanding of the latter (see Brinkhurst, 1982; Jamieson, 1977). , Clark, 1969), in contrast to their position in Timm's scheme. They have recently been classified as Hirudinoidae (Richardson, 1970).

R. Baker, 1979. A review ofthe marine Tubificidae (Oligochaeta) of North America. Can. J. Zoo!. 57: 1553-1569. Brinkhurst, R. O. & W. Fulton, 1979. Some aquatic Oligochaeta from Tasmania. Rec. Queen Vict. Mus. 64: \-8. Brinkhurst, R. O. & B. G. M. Jamieson, 1971. Aquatic Oligochaeta of the world. Oliver & Boyd, Edinburgh. 860 pp. Cook, D. G. & J. K. Hiltunen, 1975. Phallodrilus hallae, a new tubificid oligochaete from the St. Lawrence Great Lakes. Can. J. Zoo!. 53: 934-941. , 1979. Taxonomic revision of the marine genus Bathydrilus Cook and Macroseta Erseus (Oligochaeta, Tubificidae), with descriptions of six new species and SUbspecies.

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