We analyze a sample of galaxies chosen to have F 24 μm > 0.5 mJy and satisfy a certain IRAC color criterion. Infrared Spectrograph (IRS) spectra yield redshifts, spectral types, and polycyclic aromatic hydrocarbons (PAH) luminosities, to which we add broadband photometry from optical through IRAC wavelengths, MIPS from 24-160 μm, 1.1 mm, and radio at 1.4 GHz. Stellar population modeling and IRS spectra together demonstrate that the double criteria used to select this sample have efficiently isolated massive star-forming galaxies at z ∼ 1.9. This is the first starburst (SB)-dominated ultraluminous infrared galaxies (ULIRG) sample at high redshift with total infrared luminosity measured directly from FIR and millimeter photometry, and as such gives us the first accurate view of broadband spectral energy distributions for SB galaxies at extremely high luminosity and at all wavelengths. Similar broadband data are assembled for three other galaxy samples-local SB galaxies, local active galactic nucleus (AGN)/ULIRGs, and a second 24 μm-luminous z ∼ 2 sample dominated by AGN. L PAH /L IR for the new z ∼ 2 SB sample is the highest ever seen, some three times higher than in local SBs, whereas in AGNs this ratio is depressed below the SB trend, often severely. Several pieces of evidence imply that AGNs exist in this SBdominated sample, except two of which even host very strong AGN, while they still have very strong PAH emission. The Advanced Camera for Surveys images show that most objects have very extended morphologies in the restframe ultraviolet band, thus extended distribution of PAH molecules. Such an extended distribution prevents further destruction PAH molecules by central AGNs. We conclude that objects in this sample are ULIRGs powered mainly by SB; and the total infrared luminosity density contributed by this type of objects is 0.9-2.6 × 10 7 L Mpc −3 .

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A total of 2,718 bp of DNA fragment was amplified from the C-KCE strain of duck enteritis virus (DEV) genome using thermal asymmetric interlaced PCR. This newly identified viral DNA fragment contained two non-overlapping open reading frames (ORFs) oriented from the 5' to 3' direction. The first ORF was comprised of 43.5% G + C and contained the full-length genomic sequence of the UL44 gene (1,296 bp) encoding 431 amino acid residues of DEV glycoprotein C (gC). The second ORF encoded a partial peptide of the UL43 gene. The sequences of DNA and deduced amino acids of the DEV gC gene shared high homology with other members of known herpesviruses, supporting the classification of DEV. Phylogenetic analysis of the DEV gC gene revealed that the gC gene had a close evolutionary relationship with the subfamily of Alphaherpesvirinae.

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