中国多毛腺水螨亚属两新种记述(蜱螨亚纲,水螨群,腺水螨科)

记述了中国腺水螨科Lebertiidae腺水螨属Lebertia腺水螨亚属Pilolebertia两新种拟刷毛腺水螨Lebertia(Pilole-bertia)pseudociliata sp.nov.和蓖齿毛腺水螨Lebertia( Pilolebertia)pectinata sp.nov.前者体壁具细致刻纹,E1具2毛状表皮突,P-Ⅱ腹毛长以及EpⅣ侧缘弧形等特征将之与其他种明显区分开;后者体壁具细致刻纹和具缘毛的P-Ⅱ腹毛可以将之与其他种类明显区分.文中对其腺毛和眼毛的体位特征做了详细描述.     

伊朗腺水螨总科三新种记述(蜱螨亚纲,水螨群)

记述了采集自伊朗的腺水螨总科Lebertioidea 3新种:光足腺水螨Lebertia(Pseudolebertia)abseta sp.nov.,羽足尼罗螨Nilotonia(Dartia)pinnata sp.nov.,双羽激流水螨Torrenticola(Monoatractides)diploseta sp.nov.光足腺水螨Lebertia(Pseudolebertia)abseta sp.nov.P-Ⅱ羽状腹毛和无游泳毛的各足等形态特征可与其它种类明显区别;羽足尼罗螨Nilotonia(Dartia)pinnata sp.nov.鉴别性特征为O1的位置,P-Ⅱ羽状毛的数量和结构等;双羽激流水螨Torrenticola(Monoatractides)diploseta sp.nov.其P-Ⅱ具2腹毛,其中较为粗壮1毛羽状,此外P-Ⅱ和P-Ⅲ具数量不等的羽状毛等特征可与其他种类区别.同时文中对上述3新种的腺毛和眼毛的体位特征作了详细描述.     

水螨群总科阶元系统发育的支序分析 (蜱螨亚纲：水螨群)

对水螨群9总科进行了系统发育分析,支序分析选用了23个形态学特征和3个生物学特征。据分析结果所揭示的9总科间的系统发育关系和姐妹群关系,将水螨群9总科划分为5类：拟水螨类,含冥绒螨总科;始水螨类,含溪螨总科;真水螨类,含古水螨类和新水螨类;古水螨类,含水螨总科、盾水螨总科和皱喙螨总科;新水螨类,含刺触螨总科、腺水螨总科、湿螨总科和雄尾螨总科。类间姐妹群关系为：拟水螨类与始水螨类+真水螨类为姐妹群,始水螨类与真水螨类(古水螨类+新水螨类)为姐妹群,古水螨类与新水螨类为姐妹群。该文还就所提出的水螨群5类9总科的阶元排列建议与已有的观点进行了比较。     

软滑水螨属中国五新种暨老挝一新种：蜱螨亚纲：湿螨总科：软滑水螨科

本文记述软滑水螨属Ｐｉｏｎａ的中国５种新和老挝１新种：李氏软滑水螨ｐ．ｌｉｉｓｐｎ,ｍ、成都软滑水螨Ｐ．ｃｈｅｎｇｄｕｅｎｓｉｓｓｐ．ｎ．、剌足软滑水螨Ｐ．ｓｐｉｎｉｐｏｄａｓｐ．ｎ．、簇瘤软滑水螨Ｐ．ｔｕｂｅｒｃｕｌｏｓａｓｐ．ｎ、多突软滑水螨Ｐ．ｐａｐｉｌｓａｓｐ．ｎ．和异达氏软滑水螨Ｐ．ａｌｌｄａｄａｙｉｓｐ．ｎ。本文属为老挝水螨区系之新纪录。本文还简记了该属属征和腺毛分布特征,编制了中国珊     

腺水螨属二新种记述(蜱螨亚纲:腺水螨总科:腺水螨科)(英文)

本文记述我国腺水螨科Lebertiidae、腺水螨属Lebertia二新种。该属腺毛分布以E1位移于1基节板前端背方为显著特点,基于对两新种的详细观察,描述了腺毛分布体位。三叉腺水螨Lebertia（Piloleberia）trifurcillaJin,sp．nov．本新种近似于印度种Lebertia（P．）carmamayaCook1967,但其E1具发达的毛状表皮突、殖吸盘板后缘刚毛少而短等特征明显别于后者。刷电腺水螨Lebertia（Pilolebertia）ciliaaJin,sp．nov．本新种近似于非洲种L．algeriensisLundblad1942,其以颚底背突长而尖、腹突尖锐等特征显著别于后者。     

中国腺水螨科一新纪录亚属拟腺水螨亚属及一新纪录种记述(水螨群,腺水螨总科,腺水螨科)

记述了采自中国腺水螨科1新纪录亚属,拟腺水螨亚属Pseudolebertia Thor,1897及1新纪录种,光足腺水螨Lebertia(Pseudolebertia)abseta Guo,Jin et Asadi,2006.检视标本存放于贵州大学昆虫研究所.     

中国新纪录龟水螨亚科及一新种描述(蜱螨亚纲,急流水螨科)

记述了采自贵州茂兰急流水螨科Torrenticolidae中国新纪录亚科龟水螨亚科Testudacarinae 1新种:双瘤须龟水螨Testudacarus binodipalpis sp.nov..新种与美洲龟水螨Testudacarus americanus Marshall很相似,但是新种P-Ⅳ具2瘤突;P-Ⅱ和P-Ⅲ各有1羽状毛;背突和腹突尖端圆滑;E4具1个三角形基座,所有这些特征可以将之与美洲龟水螨明显区分开来.文中对其腺毛和眼毛的体位特征作了详细描述.     

蚌螨腺毛和足爪的亚显微结构观察

利用扫描电镜分别对6种蚌螨的腺毛和足爪结构进行了观察,结果表明蚌螨的腺毛是由腺体、围腺片、刚毛和腺毛板共同构成的复合结构;对弯弓蚌螨的连续切片的观察表明,腺体是从体表延伸至体腔的消化道附近,由此认为蚌螨的腺体是由体壁皮层细胞演化而来。蚌螨足末除了爪外,还观察到跗节端部背面或腹面有体壁突及刚毛,因此,蚌螨足的步行结构不是仅由爪形成的简单结构,而是由爪、跗节末端背突或腹垫和刚毛组成的复合体。     

贵州软滑水螨属二新种记述：（蜱螨亚纲：软滑水螨科）

本文描述软滑水螨科Pionidae二新种。新种多盘软滑水螨Pipma polyacetabula sp.nov.以其两性具极多殖吸盘(雄螨68—72个,雌螨45—50个)为其显著特征。新种宽殖软滑水螨P.platyura sp.nov.两性殖吸盘数目较多(雄螨35—42个,雌螨约48个),两性殖吸盘板宽近与Ⅳ足基节板等宽。两新种间以雄性殖吸盘数差异显著;两新种亦以殖吸盘数与本属已知种有显著差异而易于鉴别。     

中国叶刺瘿螨亚科一新属七新种(真螨目:瘿螨总科)

叶刺瘿螨亚科(Phyllocoptinae)属瘿螨总科(Eriophyoidea),瘿螨科(Eriophyidae)。本文记述了作者于1985年采自福建省的标本,文内长度单位均为微米。模式标本保存于南京农业大学植保系。 新谢氏瘿螨属Neoshevtchenkella新属 体纺锤形。背盾板似三角形,具前叶突,在前叶突的正下方生一明显的尖状突起。背瘤位于盾后缘,背毛斜后指。前基节由腹板线分开,基节刚毛三对。足各节及其刚毛俱     

Anatomy and ultrastructure of dermal glands in an adult water mite,Teutonia cometes (Koch, 1837) (Acariformes: Hydrachnidia: Teutoniidae)

Organization of dermal glands in adult water mites Teutonia cometes (Koch, 1837) was studied using light-optical, SEM and TEM methods for the first time. These glands are large and occur in a total number of ten pairs at the dorsal, ventral and lateral sides of the body. The slit-like external openings of the glands (glandularia) are provided with a cone-shaped sclerite, and are combined with a single small trichoid seta (hair sensillum), which is always situated slightly apart from the anterior aspect of the gland opening. Each gland is formed by an epithelium encompassing a very large lumen (central cavity) normally filled with secretion that stains in varying intensity on toluidine blue stained sections. The epithelium is composed of irregularly shaped secretory cells with an electron-dense cytoplasm and infolded basal portions. The cells possess a large irregularly shaped nucleus and are filled with tightly packed slightly dilated cisterns and vesicles of rough endoplasmic reticulum (RER) with electron lucent contents. Dense vesicles are also present in the apical cell zone. Some cells undergo dissolution, occupy an upper position within the epithelium and have a lighter cytoplasm with disorganized RER. Muscle fibers are regularly present in the deep folds of the basal cell portions and may serve to squeeze the gland and eject the secretion into the external milieu. The structure of these dermal glands is compared with the previously described idiosomal glands of the same species and a tentative correlation with the glandularia system of water mites is given. Possible functions of the dermal glands of T. cometes are discussed.     

Food and water resources used by the Madagascan hissing-cockroach mite,Gromphadorholaelaps schaeferi

We determined the food source and water balance properties of the hissing-cockroach mite, Gromphadorholaelaps schaeferi. The food source for mites was identified using Evans blue dye by direct injection into a fasting host cockroach, Gromphadorhina portentosa, or by incorporation into cockroach food. No coloration was observed in mites on dye-injected cockroaches, but coloration was present in mites when only the food for the cockroaches had been stained. Thus, the mites are scavengers of cockroach food, and are not parasitic as previously thought. Our results demonstrate that the mites can absorb water from the air anywhere between 0.84 and 0.93 a _v (%RH/100), and wax-block experiments revealed that the mouth is the site of uptake. The mites are normally clumped together on the host, typically in between the cockroach's legs and around the spiracles. Water loss rates for mites in groups (0.16% h^-1) were far lower than for isolated mites (0.30% h^-1), suggesting a group effect with regard to water balance. Above the transition temperature of 30°C rate of water loss was rapid. The sites occupied by mites on the cockroach's body seem to be highly specific for feeding and absorption of water vapour.     

Syntheses, structures and bioactivities of silver(I) complexes with dithioether ligands that contain a di- or triethylene glycol chain and different terminal groups

A series of flexible dithioethyl ligands that contain ethyleneoxy segments were designed and synthesized, including bis(2-(pyridin-2-ylthio)ethyl)ether (L¹), 1,2-bis(2-(pyridin-2-ylthio)ethoxy)ethane (L²), bis(2-(benzothiazol-2-ylthio)ethyl)ether (L³) and 1,2-bis(2-(benzothiazol-2-ylthio)ethoxy)ethane (L⁴). Reactions of these ligands with AgNO₃ led to the formation of four new supramolecular coordination complexes, [Ag₂L¹(NO₃)₂]₂ (1), [Ag₂L²(NO₃)₂] (2), [AgL³(NO₃)]_∞ (3) and [AgL⁴(NO₃)] (4) in which the length of the (CH₂CH₂O)_n spacers and the terminal groups of ligands cause subtle geometrical differences. Studies of the inhibitory effect to the growth of Phaeodactylum tricornutum show that all four complexes are active and the compound 4 has the highest inhibitory activity.     

Syntheses, structures, and mesomorphic properties of two series of oxovanadium(IV) salen and salpn complexes with 4-substituted long alkoxy chains

Two series of oxovanadium(IV) salen and salpn complexes containing 4-substituted alkoxy chains of aromatic rings, [VO((4-C_nH_2n+1O)₂salen)] (n = 3 (1), 4 (2), 6 (3), 8 (4), 10 (5), 12 (6), 14 (7), 16 (8), 18 (9), and 20 (10) and salen = N,N′-ethylenebis(salicylideneiminato)), and [VO((4-C_nH_2n+1O)₂salpn)] (n = 8 (11), 10 (12), 12 (13), 14 (14), 16 (15), and 18 (16) and salpn = N,N′-propylenebis(salicylideneiminato)), have been prepared and their mesomorphic properties have been investigated. The crystal structures of 1-9 except for 7 by an X-ray crystallographic analysis have been revealed. Complexes 4-9 in the solid state have been confirmed as novel bilayer crystal structures composed of only the VO(IV) complex without linear chains via the VO units. The VO(IV) complexes with longer alkoxy chains of 8-10 transferred from the bilayer crystal to the bilayer metallomesogens (liquid crystals). Based on the X-ray analyses and the precise extinction rules for 8-10 with the bilayer metallomesogens, complexes 8-10 were identified as the liquid crystalline (M(Pa2₁)) phase derived from 80 layer groups. On the other hand, the 4-alkoxysalpn complexes of 14-16 showed the unusual rectangular columnar mesophase (Col_r) with the linear chain via the VO units supported by the existence of the VO stretching band characteristic of weak linear chain formation via the VO units in the liquid crystal.     

Syntheses, structures and bioactivities of cadmium(II) complexes with a tridentate heterocyclic N- and S-ligand

Four cadmium(II) complexes of the semirigid tridentate ligand 8-[(pyridin-4-yl)methylthio] quinoline (TQMP4, L), namely, [CdL₂](ClO₄)₂ (1), [Cd(L)Br₂] (2), [Cd₂(L)₂(NO₃)₄] (3), and [Cd₂(L)₂I₄] (4), have been prepared by the methods of layering and the diffusing of diethyl ether. The structures of the complexes have been identified by elemental analysis (EA), infrared spectra (IR) and single-crystal diffraction. The different coordination modes of the ligands and counter anions result in a 2D (4, 4) net structure in complex 1, a 1D polymer chain in complex 2, and 0D binuclear rings in complexes 3 and 4. Their antibacterial and antifungal activities were also tested.     

Syntheses, structures, and mesomorphism of a series of Ni(II) salen complexes with 4-substituted long alkoxy chains

A series of nickel(II) salen complexes containing 4-substituted alkoxy chains of aromatic rings, [Ni((4-C_nH_2n + 1O)₂salen)] (n = 3 (1), 4 (2), 6 (3), 8 (4), 10 (5), 12 (6), 14 (7), 16 (8), 18 (9), and 20 (10)), and their parent complex, [Ni((4-HO)₂salen)] (11) (salen = N,N′-ethylenebis(salicylideneiminato)), have been prepared and mesomorphic properties have been investigated. An X-ray crystallographic analysis revealed that complex 11 · 2DMF has one-dimensional stacking structure supported by the π-π interaction between the six-membered chelate and aromatic rings with the NiNi distances of alternatively 3.3957 and 3.7224 Å and that complex 3 is formed by one-dimensional stacking by weak CH?O type hydrogen bonded interaction between the five-membered chelate ring and phenoxo atoms of the dramatically distorted salen moieties with the NiNi distance of 5.994 Å. Complexes 1-6 did not exhibit any mesophases. On the other hand, complexes 7-10 with longer alkoxy chains of n = 14-20 showed an unusual metallomesogen of a lamello-columnar mesophase within the smectic layers with an interlamellar distance of 31.1 Å (7), 33.6 Å (8), 37.1 Å (9), and 39.5 Å (10) and nearly constant stacking distance of 6.19-6.24 Å between the inter-dimers, irrespective of the variation of the alkoxy chain lengths by the X-ray diffraction measurements of the liquid crystal. The relationship between molecular assemblies and mesomorphic properties is discussed.     

Synthesis, spectral characterization, and single crystal X-ray structures of a series of manganese-2,2′-bipyridine complexes derived from substituted aromatic carboxylic acids

Reaction of [Mn(2,2′-bpy)₂(OAc)](ClO₄)(H₂O) with a series of aromatic carboxylic acids yields new Mn(II)carboxylates [Mn(2,2′-bpy)₂(L)](ClO₄)}₂ (1-3), [Mn(2,2′-bpy)₂(L)₂] (4-5) and [Mn(2,2′-bpy)₂(L)(H₂O)](ClO₄) (6) (L = 2-aminobenzoate (2-aba) (1), 4-hydroxybenzoate (4-hba) (2), thiophene-2-carboxylate (2-tca) (3), 2-hydroxynapthoate (2-hnapa) (4), 3,5-diisopropylsalicylic acid (dipsa) (5), 2,4,6-triisopropylbenzoate (tipba) (6)). The new compounds have been characterized with the aid of elemental analysis, spectroscopy, and single-crystal X-ray diffraction studies. Compounds 1-3, which have been synthesized from less bulky carboxylic acids, are dimeric in the solid-state. Compounds 4-6, which are derived from more bulkier aromaric carboxylic acids, exist as monomeric complexes. In the case of 6, where very bulky 2,4,6-triisopropyl benzoic acid is used as the starting material, only one carboxylate ligand binds to the metal, resulting in a cationic complex. Interestingly in all the six complexes, the C-H hydrogen atoms of the 2,2′-bpy ligands are involved in extensive hydrogen bonding with the carboxylate oxygen atoms of the adjacent molecules and hence form non-covalent 1-D or 2-D aggregates in the solid state.     

Syntheses, crystal structure, spectroscopic characterization and antifungal activity of new N-R-sulfonyldithiocarbimate metal complexes

Five new compounds with the general formula of (Bu₄N)₂[M(RSO₂NCS₂)₂], where Bu₄N = tetrabutylammonium cation, (M = Ni, R = 4-FC₆H₄) (1), (M = Zn, R = 4-FC₆H₄, 4-ClC₆H₄, 4-BrC₆H₄, 4-IC₆H₄), (2), (3), (4) and (5), respectively, were obtained by the reaction of the appropriate potassium N-R-sulfonyldithiocarbimate (RSO₂NCS₂K₂) with nickel(II) chloride hexahydrate or zinc(II) acetate dihydrate in metanol:water 1:1. The elemental analyses and the IR data are consistent with the formation of the expected bis(dithiocarbimato)metal(II) complexes. The ¹H and ¹³C NMR spectra showed the signals for the tetrabutylammonium cation and the dithiocarbimate moieties. The compounds 1, 2 and 5 were also characterized by X-ray diffraction techniques. The nickel(II) is coordinated by two N-4-fluorophenylsulphonyldithiocarbimato(2-) ligands forming a planar coordination. The zinc(II) exhibits distorted tetrahedral configuration in compounds 2 and 5 due to the chelation effect of two sulfur atoms of the N-R-sulfonyldithiocarbimate ligands. The antifungal activities of the compounds were tested in vitro against Colletotrichum gloeosporioides, an important fungus that causes the plant disease known as anthracnose in fruit trees. All the complexes were active.     

Syntheses and structure of heterobimetallic helical polymeric Mo-M(II) (M = Mn, Co, Zn, Cd or Ni) complexes using a flexidentate metalloligand

A series of heterobimetallic polymeric complexes of manganese, cobalt, zinc, cadmium and nickel, [M(Mo₂O₅L₂)(MeOH)₂(H₂O)₂]_n·nH₂O {M = Mn (2), n = 1, Co (3), n = 0, Zn (4), n = 1 and Cd (5), n = 1} and [Ni(Mo₂O₅L₂)(MeOH)(H₂O)₃]_n·2H₂O·MeOH (6) have been synthesized form the reaction of [{Na₄(H₂O)₄(μ-H₂O)₂} ⊂ (Mo₂O₅L₂)₂] (1) {LH₂ = 2-(3,5-di-tert-butyl-2-hydroxybenzylamino)acetic acid} with the corresponding metal salts. The complexes have been structurally characterized. The Complexes, 3 and 6 undergo thermal decomposition to afford mixed oxides of the type, MMoO₄·MoO₃ {M = Co or Ni}.