http://hdl.handle.net/10125/3329 Wed, 22 May 2013 13:02:01 GMT 2013-05-22T13:02:01Z http://hdl.handle.net/10125/7851 Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7851 1967-10-01T00:00:00Z http://hdl.handle.net/10125/7850 Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7850 1967-10-01T00:00:00Z Eldredge, LG http://hdl.handle.net/10125/7849 Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7849 1967-10-01T00:00:00Z Nelson, Gareth J http://hdl.handle.net/10125/7848 Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7848 1967-10-01T00:00:00Z Adegoke, Oluwafeyisola S http://hdl.handle.net/10125/7847 Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7847 1967-10-01T00:00:00Z Stone, Benjamin C http://hdl.handle.net/10125/7846 Specimens from the heartwood of 2-5 trees of each of 25 species of Fijian rain forest timbers were tested by the laboratory soil-block method against two white-rot fungi , Fomes lividus (Kalch.) Sacc. and Pycnoporus coccineus (Fr.) Bond. and Sing., syn. Coriolus sangutneus (L. ex Fr.) G. H. Cunn.; and against two brown-rot fungi, Lenzites trabea Pers. ex Fr. and Coniophora olivacea (Fr.) Karst. The species most resistant to decay were Palaquium hornei, Intsia bijuga, Fagraea gracilipes, Syzygium spp. complex, and Dacrydium elatum. Most of the species tested were highly susceptible to decay. There was a tendency, both among species and with in species, for the denser and less water-absorbent wood to be more resistant to decay. Also, the outer heartwood was, in general, more resistant to decay than inner heartwood. Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7846 1967-10-01T00:00:00Z Osborne, Lynette http://hdl.handle.net/10125/7845 Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7845 1967-10-01T00:00:00Z Hohl, Hans R; Hamamoto, Susan T http://hdl.handle.net/10125/7844 Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7844 1967-10-01T00:00:00Z St. John, Harold http://hdl.handle.net/10125/7843 Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7843 1967-10-01T00:00:00Z St. John, Harold http://hdl.handle.net/10125/7842 Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7842 1967-10-01T00:00:00Z St. John, Harold http://hdl.handle.net/10125/7841 Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7841 1967-10-01T00:00:00Z Burch, John Q; Burch, Rose L http://hdl.handle.net/10125/7840 Three marine species of Plotosidae are found along the coastlines of the Indian and Pacific oceans, but the other 25 species occur exclusively in the Australian region. The majority of the Plotosidae are freshwater inhabitants, some of which are indigenous to both Australia and New Guinea. The marine members of the family and two freshwater members possess a dendritic organ. It is suggested that this organ has an osmoregulatory function. Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7840 1967-10-01T00:00:00Z Lanzing, WJR http://hdl.handle.net/10125/7839 Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7839 1967-10-01T00:00:00Z Gooding, Reginald M; Magnuson, John J http://hdl.handle.net/10125/7838 Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7838 1967-10-01T00:00:00Z Alvarino, Angeles http://hdl.handle.net/10125/7837 Larvae were reared under various temperature conditions. Those maintained at 15°C were unable to moult to the second instar although some individuals lived as long as 35 days after hatching. At 20°C some individuals were able to reach fifth instar, but glaucothoes were obtained only at 25°C, 33-52 days after hatching. Effects of starvation and temperature on larval survival are discussed. The number of zoeal stages in the development of this species is variable, as it is in other diogenids which have been studied in the laboratory, glaucothoes of this species being obtained after four or five zoeal instars. Descriptions and illustrations of the zoeal stages and the glaucothoe are presented. No other larvae of this genus have been described and intra-generic comparisons of larval morphology were not possible, but a comparison was made of the zoeal and glaucothoe stages of this species with those of others in the family. Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7837 1967-10-01T00:00:00Z Provenzano, Anthony J JR http://hdl.handle.net/10125/7836 Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7836 1967-10-01T00:00:00Z Brusca, Gary J http://hdl.handle.net/10125/7835 A general aspect of the daytime surface swarming of Euphausia pacifica in Japanese nearshore waters is described in connection with the water temperature. Swarming usually starts with a local minimum temperature around 7°C and terminates with a temperature just below 16°C. The swarming season is essentially in spring, from February through May, with little difference among regions. The main swarming areas are on the Pacific coast around Kinkazan, and on the coast of the Sea of Japan around Sadogashima, in Wakasawan and its vicinity, around Oki, and on the east side of the Tsushima Gunto. It is shown that the swarming is closely related to cold water masses, and that the approach of offshore cold water masses to the nearshore areas and the mixing process in the coastal areas may provide favorable conditions for swarming . Swarming of E. pacifica is a phenomenon that occurs at the margins of the cold water bodies, and is related to the seasonal change in the geographical distribution of those euphausiids. A uniformly low water temperature profile must be the necessary condition for swarming, but other possible factors stimulating euphausiids to swarm are enumerated. Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7835 1967-10-01T00:00:00Z Komaki, Yuzo http://hdl.handle.net/10125/7834 Sun, 01 Oct 1967 00:00:00 GMT http://hdl.handle.net/10125/7834 1967-10-01T00:00:00Z