革板螨属2新种（蜱螨亚纲：中气门目：派盾螨科）

记述革板螨属2新种：拟变革板螨 Gamasholaspis quasivariabilis sp. nov.和新绒革板螨Gamasholaspis noveothenomydis sp. nov.     

派伦螨属1新种和革板螨属1新种及都匀革板螨雄螨描述(蜱螨亚纲:中气门目:派盾螨科)

记述派伦螨属1新种:遵义派伦螨Parholaspulus zunyiensis sp.nov.和革板螨属1新种:江西革板螨Gamasholaspis jiangxiensissp.nov.,并描述都匀革板螨Gamasholaspis duyunensis Chen,Guo et Gu,1994雄螨.     

亚洲革板螨雄螨和后若螨描述(蜱螨亚纲:中气门目:派盾螨科)

亚洲革板螨(Gamasholaspis asiaticus Petrova,1967)在所查到的文献中仅描述了雌螨[1],本文描述其雄螨和后若螨. 文中测量单位为μm,括号内为测量均值. 亚洲革板螨(Gamasholaspis asiaticus Petrova,1967) 雄螨(图1):体黄色,椭圆形,长宽,一标本为804×540,另一标本为689×425.背板覆盖整个背面,具29对光滑长毛,末端远超过下位毛基部.胸前板1对,发达,楔形.     

中国革板螨属2新种和大陆1新记录（蜱螨亚纲：中气门目：派盾螨科）

记述中国革板螨属2新种：拟翼革板螨Gamasholaspis subaliventroanalis sp．nov．,似林革板螨Gamasholaspis linsimilis sp．nov．和大陆1新记录：柔革板螨Gamasholaspis blandus Tseng,1993。     

革板螨属3新种和派伦螨属1新种（蜱螨亚纲：中气门目：派盾螨科）

记述革板螨属3新种和派伦螨属1新种：井冈山革板螨Gamasholaspis jinggangshanensis sp．nov．,何氏革板螨Gamasholaspis hochyicheni sp．nov．,新阿革板螨Gamasholaspis novakimotoi sp．nov．和沙县派伦螨Parholaspulus shaxianensis sp．nov．     

多变革板螨雄螨及后若螨描述(蜱螨亚纲:革螨股:派盾螨科)

在所查到的献中,多变革板螨(Gamasholaspis variabilis Petrova,1967)已描述了雌螨、前若螨和幼螨,本描述其雄螨和后若螨。中测量单位为μm,括号内为测量均值。     

武夷山革板螨属1新种和拉提螨属1新种（蜱螨亚纲：中气门目：派盾螨科）

记述派盾螨科Parholaspidae 2新种：翼状革板螨Gamasholaspis aliventroanalis sp．nov．和壮距拉提螨Lattinela robustocalearis sp．nov．     

裂缝常革螨形态描述(蜱螨亚纲:革螨股:寄螨科)

裂缝常革螨 Vulgarogamasus lyriformis ( Mc Grow et Farrier,1 96 9)分布于美国、加拿大和前苏联。 2 0 0 0年自朝鲜入境货物中采得该螨。在所查到的文献中 ,仅《ОпределительОбитающихвПочвеКлещеи,М esostigmata》一书有该种的记载 ,但只记载有雌螨胸板、生殖区、头盖和雄螨足 的特征 ,无完整描述。今根据朝鲜标本 ,详细描述其雌螨、雄螨、前若螨和幼螨。文中测量单位为μm,括号内为测量均值。裂缝常革螨 Vulgarogamasuslyriformis (Mc Grow et Farrier,1969)图 1- 6　裂缝常革螨 Vulgarogamasu…     

血革螨属一新种(蜱螨亚纲:厉螨科)

本文记述采自云南剑川县大绒鼠巢中的血革螨属一新种,六毛血革螨Ｈａｅｍｏｇａｍａｓｕｓｓｅｘｓｅｔｏｓｕｓｓｐ．ｎｏｖ．,其背部刚毛呈三叉状,与多齿血革螨Ｈ．ｍｕｌｔｉｄｅｎｔｉｓ较相近,但肛板副毛６根,钳齿毛呈喇叭状,胸部副毛全部光滑,殖腹板较宽大,可与后者相区别。     

单角新革螨雌雄螨描述(蜱螨亚纲:革螨股:寄螨科)

单角新革螨 Neogamasus unicornutus ( Ewing,1 90 9)同物异名为岛屿新革螨 Neogamasusislandicus( Sellnick,1 94 0 ) ,其后若螨 [1 ]、前若螨及幼螨 [2 ]已有较详细描述 ,但雌螨和雄螨在所查到的文献中只记载有个别特征 ,没有完整描述 [1 ,3- 6] 。本文根据采自集安的标本 ,描述其雌螨和雄螨。文中测量单位为 μm,括号内为测量均值。单角新革螨 Neogamasusunicornutus(Ewing,190 9)雌螨 (图 1 - 7)体黄色 ,卵圆形 ,长 6 78- 70 1 ( 6 89) ,宽 36 8- 41 4 ( 394 )。背板几乎覆盖整个背面 ,后部留狭窄裸露区。前背板长 345- 356 ( 349) ,…     

革板螨属1新种和浩伦螨属1新种(蜱螨亚纲:中气门目:派盾螨科)

记述派盾螨科Parholaspidae2新种：拟阿革板螨Gamasholaspis imitakimotoi sp．nov．和福建浩伦螨Holaspulus fujianensis sp．nov．。     

Hormone interactions and regulation of PsPK2::GUS compared with DR5::GUS and PID::GUS in Arabidopsis thaliana

The putative pea PINOID homolog, PsPK2, is expressed in all growing plant parts and is positively regulated by auxin, gibberellin, and cytokinin. Here, we studied hormonal regulation of PsPK2::GUS expression compared with DR5::GUS and PID::GUS in Arabidopsis. PsPK2::GUS, DR5::GUS, and PID::GUS expression in Arabidopsis shoots is mainly localized in the stipules, hydathodes, veins, developing leaves, and cotyledons. Unlike DR5::GUS, PsPK2::GUS, and PID::GUS are weakly expressed in root tips. Both DR5::GUS and PsPK2::GUS are induced by different auxins and are more sensitive to methyl indole acetic acid, 4-chloro-indole acetic acid, and α-naphthalene acetic acid than others. GA(3) has no significant effect on GUS activity in DR5::GUS-transformed seedlings compared to the control, but induction by auxin and gibberellin in combination is synergistic. Cytokinin increases auxin transport in Arabidopsis seedlings. Auxin, gibberellin, and cytokinin all increase GUS activity in shoots of PsPK2::GUS transformed plants compared to the control. However, only auxin and gibberellin increase GUS activity in PID::GUS shoots. In conclusion, auxin, gibberellin, and cytokinin positively regulate PsPK2 expression in shoots, but not in roots. Auxin and gibberellin also upregulate AtPIN1 and LEAFY expression, which is similar to PsPIN1 and Uni in pea. With minor exceptions, the orthologous genes from both species are regulated similarly.     

Platelet adhesiveness and aggregation: the collagen:glycosyl, polypeptide:N-acetylgalactosaminyl and glycoprotein:galactosyl transferases of human platelets

Four glycoprotein:glycosyl transferases were identified, purified, and characterized from human platelets. The enzymes present were collagen:glc, collagen:gal, polypeptide:galNAc, and glycoprotein:gal; the fetuin:glcNAc transferase was absent. Each of the 4 transferases was found to be almost exclusively bound to the platelet plasma membrane. Incubation of platelet homogenates without exogenous acceptors yielded no transfer of monosaccharide, indicating the complete lack of endogenous acceptors. These results lead to the interesting speculation that the transferases may not be responsible in the mature platelet for glycoprotein synthesis at all, but rather that they may function for intercellular adhesion and the primary step in hemostasis, the adhesion of collagen to platelets.     

Photo and thermoluminescence of KMgSO4F: Ce and :Mn phosphors

KMgSO₄F:Ce and KMgSO₄F:Mn phosphors were prepared by a wet chemical method and studied for their photoluminescence (PL) and thermoluminescence (TL) characteristics. PL emission of KMgSO₄F:Ce peaked at around 440 nm for the excitation at 377 nm due to 5d → 4f transition, while KMgSO₄F:Mn had a peak at 540 nm for an excitation at 363 nm and 247 nm due to ⁴T_1g → ⁶A_1g transition. The phosphors also showed good thermoluminescence characteristics when they were exposed to γ‐rays at a 5 Gy dose at the rate of 0.36 kGyh^?1. KMgSO₄F:Ce exhibited a single thermoluminescence (TL) peak at around 167 °C and KMgSO₄F:Mn also exhibited a single TL peak at around 177 °C. Possible trapping parameters such as order of kinetics (b), the geometrical factor (μ_g), the frequency factor (s) and the activation energy were also evaluated by Chen's half width method. This article discusses fundamental PL and TL characteristics in inorganic fluoride material activated by Ce³⁺ and Mn²⁺ ions and prepared by a wet chemical method. Copyright © 2014 John Wiley & Sons, Ltd.