We have identified cobalt-base superalloys showing a high-temperature strength greater than those of conventional nickel-base superalloys. The cobalt-base alloys are strengthened by a ternary compound with the L1(2) structure, gamma' Co3(Al,W), which precipitates in the disordered gamma face-centered cubic cobalt matrix with high coherency and with high melting points. We also identified a ternary compound, gamma' Ir3(Al,W), with the L1(2) structure, which suggests that the Co-Ir-Al-W-base systems with gamma+gamma' (Co,Ir)3(Al,W) structures offer great promise as candidates for next-generation high-temperature materials.
Phase equilibria between the and 0 phases at 900 C in the Co-(10-70)Ni-Al-W system were determined by electron probe microanalysis (EPMA) and X-ray diffractometry (XRD). It was found that the 0 phase with L1 2 structure continuously exists from the Co side to the Ni side in Co-Ni-Al-W system and that it widens to the low W region with increasing Ni content. The partition of Al into the 0 phase increased with Ni content, while the W changed from a 0 former to a former by increase of Ni content. Differential scanning calorimetry (DSC) measurements also revealed that the 0 solvus temperature increases with Ni content, while the solidus temperature is hardly affected by such content. The lattice parameter of the and 0 phases and the mismatch decreased with increasing Ni content, which caused the morphologic change of the 0 precipitates from cubes to spheres.
Betanodaviruses are the causative agents of viral nervous necrosis (VNN) or viral encephalopathy and retinopathy (VER) in cultured marine fish. A total of 131 apparently healthy fish from 30 species were collected in two geographically remote aquaculture areas, Yashima Bay (Kagawa Prefecture) and Tamanoura Bay (Nagasaki Prefecture), in Japan. The brains of fish were examined by reverse transcriptase-polymerase chain reaction (RT-PCR) and nested PCR to detect the coat protein gene of betanodavirus. In Yashima Bay, two and 13 of 20 cultured fish were positive for nodavirus in RT-PCR and nested PCR, respectively, and four of five wild fish were positive only in nested PCR. In Tamanoura Bay, 28 and 99 of 106 wild fish were positive for the virus in RT-PCR and nested PCR, respectively. All the sequences of the nested PCR products (177 nt) from 27 fish species (10 cultured and 17 wild) were highly homologous to each other (99-100%) and were closely related to that of the known betanodavirus, redspotted grouper nervous necrosis virus (RGNNV). These results illustrate that large populations of cultured and wild marine fish in aquaculture areas are subclinically infected with genetically closely related betanodaviruses, suggesting an importance of such infected fish as a carrier or reservoir of betanodaviruses.
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