The last voyage of Capt. Sir John Ross ... to the Arctic regions for the discovery of a north west passage : performed in the years 1829-30-31-32 and 33 : to which is prefixed an abridgement of the former voyages of Captns. Ross, Parry & other celebrated navigators to the northern latitudes : compiled from authentic information and original documents transmitted by an officer attached to the last expedition ; illustrated by engravings from drawings taken on the spot /

"On the position of the north magnetic pole. (Supplement)": 44 p. at end.

Éloge de Mr.Marcot,lu dans une séance particulière de la Société royale des sciences,le 6 juillet 1769.

Mode of access: Internet.

Organizational maintenance manual : radio sets AN/VRC-24 and AN/TRC-68.

"9 June 1960."

Organizational maintenance repair parts and special tools lists for radio set AN/GRC-165 (NSN 5820-00-935-8038).

Includes index.

Hand receipt covering contents of Components of End Item (COEI), Basic Issue Items (BII), and Additional Authorization Lists (AAL) for teletypewriter operations, central, AN/MGC-19A (NSN 5815-01-041-5104).

"1 October 1980."

Tong an shi hui : 10 juan /

T.p. title: Shi ji hui zuan.

Fen lei yun jin : [12 juan] : fu lu [1 juan] /

Block print.

Qing hui zeng yan : 10 juan, fu lu 1 juan /

An ci shu wei Hui xian sheng suo ji dang dai ju gong sheng liu suo wei shi ruo wen yi yi zhe ye.

Shan dai ge ji : san shi san juan /

Xu hou juan "Jinling Liu Wenkai jia juan.

Meng you lu : 1 juan /

Double leaves, oriental style, in case.

Xiang su shan guan quan ji /

Each section has special t.p.

Tian jue lu : 4 juan /

An ci shu yi Ru Shi Dao san jiao wei zong, yi sheng xian fo san men wei ju, huo ji qi xing ming, huo xiang qi gong xing ... huo zheng qi li dai zhi feng hao deng.

Shan you shi ke cong bian : Si shi juan (juan 26 - chuan 40) /

Reissued: 2 ban ; Tai bei : Xin wen feng chu ban gong si, Min'guo 71 [1982]

Experimental analysis of the influence of pest management practice on the efficacy of an endemic arthropod natural enemy complex of the diamondback moth.

Maximizing the contribution of endemic natural enemies to integrated pest management (IPM) programs requires a detailed knowledge of their interactions with the target pest. This experimental field study evaluated the impact of the endemic natural enemy complex of Plutella xylostella (L.) (Lepidoptera: Yponomeutidae) on pest populations in commercial cabbage crops in southeastern Queensland, Australia. Management data were used to score pest management practices at experimental sites on independent Brassica farms practicing a range of pest management strategies, and mechanical methods of natural enemy exclusion were used to assess the impact of natural enemies on introduced cohorts of P. xylostella at each site. Natural enemy impact was greatest at sites adopting IPM and least at sites practicing conventional pest management strategies. At IPM sites, the contribution of natural enemies to P. xylostella mortality permitted the cultivation of marketable crops with no yield loss but with a substantial reduction in insecticide inputs. Three species of larval parasitoids (Diadegma semiclausum Hellen [Hymenoptera: Ichneumonidae], Apanteles ippeus Nixon [Hymenoptera: Braconidae], and Oomyzus sokolowskii Kurdjumov [Hymenoptera: Eulophidae]) and one species of pupal parasitoid Diadromus collaris Gravenhorst (Hymenoptera: Ichneumonidae) attacked immature P. xylostella. The most abundant groups of predatory arthropods caught in pitfall traps were Araneae (Lycosidae) > Coleoptera (Carabidae, Coccinelidae, Staphylinidae) > Neuroptera (Chrysopidae) > Formicidae, whereas on crop foliage Araneae (Clubionidae, Oxyopidae) > Coleoptera (Coccinelidae) > Neuroptera (Chrysopidae) were most common. The abundance and diversity of natural enemies was greatest at sites that adopted IPM, correlating greater P. xylostella mortality at these sites. The efficacy of the natural enemy complex to pest mortality under different pest management regimes and appropriate strategies to optimize this important natural resource are discussed.

Development of an oligonucleotide-based SNP detection method on lateral flow strips using hexapet tages

Detection of point mutations or single nucleotide polymorphisms (SNPs) is important in relation to disease susceptibility or detection in pathogens of mutations determining drug resistance or host range. There is an emergent need for rapid detection methods amenable to point-of-care applications. The purpose of this study was to reduce to practice a novel method for SNP detection and to demonstrate that this technology can be used downstream of nucleic acid amplification. The authors used a model system to develop an oligonucleotide-based SNP detection system on nitrocellulose lateral flow strips. To optimize the assay they used cloned sequences of the herpes simplex virus-1 (HSV-1) DNA polymerase gene into which they introduced a point mutation. The assay system uses chimeric polymerase chain reaction (PCR) primers that incorporate hexameric repeat tags ("hexapet tags"). The chimeric sequences allow capture of amplified products to predefined positions on a lateral flow strip. These "hexapet" sequences have minimal cross-reactivity and allow specific hybridization-based capture of the PCR products at room temperature onto lateral flow strips that have been striped with complementary hexapet tags. The allele-specific amplification was carried out with both mutant and wild-type primer sets present in the PCR mix ("competitive" format). The resulting PCR products carried a hexapet tag that corresponded with either a wild-type or mutant sequence. The lateral flow strips are dropped into the PCR reaction tube, and mutant sequence and wild-type sequences diffuse along the strip and are captured at the corresponding position on the strip. A red line indicative of a positive reaction is visible after 1 minute. Unlike other systems that require separate reactions and strips for each target sequence, this system allows multiplex PCR reactions and multiplex detection on a single strip or other suitable substrates. Unambiguous visual discrimination of a point mutation under room temperature hybridization conditions was achieved with this model system in 10 minutes after PCR. The authors have developed a capture-based hybridization method for the detection and discrimination of HSV-1 DNA polymerase genes that contain a single nucleotide change. It has been demonstrated that the hexapet oligonucleotides can be adapted for hybridization on the lateral flow strip platform for discrimination of SNPs. This is the first step in demonstrating SNP detection on lateral flow using the hexapet oligonucleotide capture system. It is anticipated that this novel system can be widely used in point-of-care settings.