纤恙螨属恙螨一新种：蜱螨亚纲：恙螨科

从采自新疆博乐县阿拉山口(海拔290 m)室内灰仓鼠伏龙芝亚种 Cricetulus migratorius caesius耳壳内的一批纤恙螨标本鉴定中发现中国新记录亚属——爱柯纤恙螨亚属 Ericotrombidium中的一个新种,定名为博乐纤恙螨 Leptotrombidium (E.) bolei sp.nov.,它与美丽纤恙螨L.(E.)pulchrum(Sosnina,1950)及索氏纤恙螨L.(E.)sokolovi Kudryshova,1984比较近似,但本新种IP及盾板量度除 AM外均较大,PW-SB≥PL,可与前者区别;IP较小,平均787,幅度763—821,DS较少,排列规则:2+8.6.6.4.2=28,可与后者区别。     

珠恙螨属一新种：真螨目：恙螨科

本文描述1个珠恙螨属 Doloisia一新种,采自广东省罗定县社鼠 Rattus confucianus 鼻内,其感器双角状,盾板后侧毛的分枝长密,前侧毛光裸;足指数795。     

纤恙螨属一新种：真螨目：恙螨科

本文报道1983年采自吉林省和龙县棕背(鼠平) Clethrionomys rufocanus 体上的一种新恙螨,棕(鼠平)纤恙螨 Leptotrombidium rufoconum sp.nov,模式标本分别存放福建医学院寄生虫学教研室和沈阳军区后勤部军事医学研究所。     

中国真棒恙螨属一新种：蜱螨亚纲：恙螨科

潍坊真棒恙螨,新种Euschōengastia weifangensis sp.nov.采自山东省潍坊地区褐家鼠Ratius norvegicus 的耳壳。正模♀保存于山东中医学院寄生虫学教研室。     

春川恙螨属一新种：蜱螨亚纲：恙螨科

本文描述春川恙螨属Ｓｈｕｎｓｅｎｎｉａ Ｊａｍｅｓｏｎ ｅｔ Ｔｏｓｈｉｏｋａ一新种,即叉毛春川恙螨Ｓ．ｆｕｒｃｏｓｅｔａ ｓｐ．ｎｏｖ．,模式标本采自青海省化隆回簇自治区的大林姬鼠Ａｐｏｄｅｍｕｓ ｓｐｅｃｉｏｓｕｓ Ｔｅｍｍｉｎｃｋ,１８４５体长,文内量度单位均为μｍ。标本存放在青海省地方病防治研究所。     

同鞭恙螨亚属的修订和一新种恙螨的记述：蜱螨亚纲：恙螨科

本文对同鞭恙螨亚属Synlorillatum Zhao,1985的亚属征作了补充和修订,并探讨了通什长鞭恙螨Lorillatum(S.)tungshihensis Hsu & Chen,1964的分类地位问题。此外,记述了采自鼠耳蝠Myotis sp.的一个恙螨新种——鞭感长鞭恙螨Lorillatum(Synlorillatum)flagellasensilla sp.nov.     

昆明西山纤恙螨一新种：真螨目：恙螨科

1958年在昆明西山采得1种恙螨,经鉴定系1新种,定名为昆西纤恙螨,标本保存在昆明军事医学研究所。昆西纤恙螨Leptotrombidlum(L.)kunxi Xiang et Wen,新种(图1-6) 标本:正模、幼虫,昆明西山,海拔2110m,1958-Ⅸ-26,向容炯、陈祖武采,宿主为普通树鼩中华亚种Tupaia glis chinenis,寄生在肛门周围。 鉴别:本新种与纤恙螨属的Leptotrombidium(L.)pesudofulmentum V.-G.et     

纤恙螨属一新种（蜱螨亚纲：恙螨科）

本文描述纤恙螨属,１９１６,一新种,五角纤恙螨,标本采自青海省玉树藏族自治州称多县。     

青海禽棒恙螨属一新种：蜱螨亚纲：恙螨科

本文记述从朱雀Garpodacus erythrinus(Pallas)体上采到的禽棒恙螨属Ornithogastia Vercammen-Grandjean,1960,一新种,朱雀禽棒恙螨Ornithogastia erythinae sp.nov.标本采自青海省海南藏族自冶州贵南县。     

Electron microscopic observations of the embryo Leptotrombidium (Leptotrombidium) pallidum naturally infected with Rickettsia tsutsugamushi

Embryos of Leptotrombidium (Leptotrombidium) pallidum mites naturally infected with Rickettsia tsutsugamushi were examined by electron microscopy. Rickettsiae were not found in eggs just after oviposition, but were easily detected in cells at the various parts of the embryos just before hatching, indicating that the rickettsiae are surely vertically transmitted from infected adult mites to the larvae through embryos, and the rickettsiae may multiply in situ during the developing process of the embryo.     

Mouthparts in Leptotrombidium larvae (Acariformes: Trombiculidae)

Mouthparts of Leptotrombidium larvae (Acariformes: Trombiculidae), potential vectors of tsutsugamushi disease agents, were studied in detail using light microscopy, scanning electron microscopy, and transmission electron microscopy. The mouthparts incorporated within the pseudotagma gnathosoma are composed of the infracapitulum ventrally and the chelicerae dorsally. The ventral wall of the infracapitulum is formed by a wide mentum posteriorly and a narrowed malapophysis anteriorly. The malapophysis firmly envelops the distal cheliceral portions by its lateral walls. The lateral lips of the malapophysis are flexible structures hiding the cheliceral blades in inactive condition and turning back forming a type of temporary sucker closely applied to the host skin during feeding. The roof of the infracapitulum is formed by a weakly sclerotized labrum anteriorly and a cervix with the capitular apodemes extending posteriorly. The labral muscles are lacking. The capitular apodemes serve as origin for pharyngeal dilators running to the dorsal wall of the pharynx fused with the bottom of the infracapitulum. The basal cheliceral segments are separated from each other besides the very posterior portions where they are movably joined by the inner walls. The sigmoid pieces serve for insertion of the cheliceral elevators originating at the posterior portions of the basal segments. The movable digits reveal the solid basal sclerite and the cheliceral blade curved upward with a tricuspid cap on its tip. Dendrites of nerve cells run along the digits to their tips. The ganglia are placed within the basal segments just behind the movable digits. The chelicerae also reveal well developed flexible fixed digits overhanging the basal portions of the blades. The gnathosoma possesses several sets of extrinsic muscles originating at the scutum and at the soft cuticle behind it. Laterally, the gnathosoma bears five‐segmented palps with a trifurcate palpal claw. J. Morphol. 277:424–444, 2016. © 2016 Wiley Periodicals, Inc.     

浙江省发现地里恙虫的报告

地里恙虫是已知东南亚地区恙虫病的主要传播媒介。近年来,在我国广东、广西、云南、福建、海南岛等省均已先后有发现,并经研究证实是当地恙虫病的主要传播媒介。我们于1957—1958年曾在浙江省沿海地区进行了一些初步调查,也发现了地里恙虫。活的地里恙虫均呈橘红色,其形态与各部测量数字与甘怀杰民(1953)、陈心陶、徐秉锟二氏(1955)等所报告者相符,惟在临海县所发现部分标本的盾片前缘形态稍有不同。甘氏等     

Stylostome organization in feeding Leptotrombidium larvae (Acariformes: Trombiculidae)

The stylostome of larvae of the trombiculids Leptotrombidium scutellare (Nagayo et al.), Leptotrombidium fletcheri (Womersley et Heaslip) and Leptotrombidium deliense (Walch) was studied experimentally at different time intervals after larval attachment using the histological method. The stylostome of these species has the same organization and belongs to the epidermal combined with the mixed type, developing more in width than in length. Neither transverse nor conspicuous longitudinal layers are present within the stylostome walls, which stain predominantly in red with Azan, also showing longitudinal portions with blue staining. Larvae tend to attach closely to each other and scabs, consisting of the hyperkeratotic epidermal layers fusing with migrating inflammatory cells, develop around the attachment sites. The dermis shows inflammatory foci with dilated capillaries and inflammatory cells inserting in the connective tissue layer underneath the stylostome. The feeding cavity, which is moderately expressed, may be found either in the epidermis or in the dermis. It contains inflammatory cells and their debris in the liquefied host tissues. The stylostome length depends on the character of the attachment site (the thicker epidermis or scab the longer the stylostome), and does not directly correspond to the stages of larval feeding. Nevertheless, at the 48-h time interval, nearly all attached larvae are found to be fully fed and their midgut cells are filled with nutritional globules.     

Transovarial Transmission of Orientia tsutsugamushi in Leptotrombidium palpale (Acari: Trombiculidae)

Transovarial transmission of Orientia tsutsugamushi in colonies of Leptotrombidium palpale was studied in the parent and F₁ and F2 generations. Both transovarial transmission and filial infection rates were 100% in the parent and F₁ generations of Leptotrombidium palpale. The filial infection rate in the F₁ generation was 100%, but it declined to 94.3% in the F₂ progeny. The sex ratio of the F₁ generation from infected L. palpale was 1∶0.8 (male:female) and the proportion of males was relatively high. This study is the first to report on the transovarial transmission of O. tsutsugamushi in L. palpale. High transovarial transmission rates in L. palpale suggest that this species might be one of the major vectors of tsutsugamushi disease in Korea.     

Stylostome formation by Leptotrombidium mites (Acari: Trombiculidae).

The modes of stylostome formation by larvae (chiggers) of Leptotrombidium intermedium, L. fletcheri, L. arenicola, and L. deliense in parasitized mouse skin were studied histologically in relation to their capacity to transmit Rickettsia tsutsugamushi. Three types of stylostome formation were recognized among the different species: the epidermal stylostome formed by the larva of L. intermedium; the mesenchymal stylostome formed by the larva of L. fletcheri; and, the mixed stylostome formed by the larva of both L. arenicola and L. deliense. Dermal inflammations related to the three types of stylostomes were histologically defined. The possible importance of stylostome characteristics to the transmission of rickettsial organisms is discussed.     

Comparative ultrastructure of coxal glands in unfed larvae of Leptotrombidium orientale (Schluger, 1948) (Trombiculidae) and Hydryphantes ruber (de Geer, 1778) (Hydryphantidae)

Coxal glands of unfed larvae Leptotrombidium orientale (Schluger, 1948) (Trombiculidae), a terrestrial mite parasitizing vertebrates, and Hydryphantes ruber (de Geer, 1778) (Hydryphantidae), a water mite parasitizing insects were studied using transmission electron microscopy. In both species, the coxal glands are represented by a paired tubular organ extending on the sides of the brain from the mouthparts to the frontal midgut wall and are formed of the cells arranged around the central lumen. As in other Parasitengona, the coxal glands are devoid of a proximal sacculus. The excretory duct, joining with ducts of the prosomal salivary glands constitutes the common podocephalic duct, opening into the subcheliceral space. The coxal glands of L. orientale are composed of a distal tubule with a basal labyrinth, an intermediate segment without labyrinth, and a proximal tubule bearing tight microvilli on the apical cell surface and coiled around the intermediate segment. The coxal glands of H. ruber mainly consist of the uniformly organized proximal tubule with apical microvilli of the cells lacking the basal labyrinth. This tubule shows several loops running backward and forward in a vertical plane on the side of the brain. In contrast to L. orientale , larvae of H. ruber reveal a terminal cuticular sac/bladder for accumulation of secreted fluids. Organization of the coxal glands depends on the ecological conditions of mites. Larvae of terrestrial L. orientale possess distal tubule functioning in re‐absorption of ions and water. Conversely, water mite larvae H. ruber need to evacuate of the water excess, so the filtrating proximal tubule is prominent.     

Variability in Leptotrombidium europaeum and two new related chigger mite species (Acari: Trombiculidae) from Caucasus

Two new chigger mite species closely related to Leptotrombidium europaeum (Daniel et Brelih, 1959) are described from small mammals collected in Caucasus and Transcaucasia. L. alanicum sp. n. differs from L. europaeum in having shorter legs (TaIII = 61-81, Ip = 734-927 versus 72-90, and 855-1017), shorter scutal and idiosomal setae (D(min) = = 30-45, D(max) = 48-67, H = 59, PL = 58 versus 40-52, 54-69, 64, 63), slightly smaller scutum (AP = 25, SD = 47, PW = 89 versus 28, 50, 91), and more numerous idiosomal setae (87 versus 81). L. montanum sp. n. differs from L. europaeum in having more numerous idiosomal setae (102 versus 81), longer scutal and idiosomal setae (AM = 61, AL = 44, H = 68, D(max) = 66 versus 56, 41, 64, 62), thicker legs (TaW = 19 versus 18), and broader scutum (PW = 95 versus 91). Exact identification of both new species is possible only using classification functions constructed by means of discriminant analysis. These three Leptotrombidium species expose sympatric distribution in Daghestan (Eastern Caucasus). L. alanicum and L. montanum also occurred together in Krasnodar Territory (Western Caucasus). Each of these species includes a number of local geographical forms precisely distinguished from each other. Morphometric differences between L. alanicum and L. montanum agree with eco-geographical rules being previously found in chigger mites from other genera. However, differences between local forms of these species show other tendencies directed controversially in part. Therefore it is probable that interspecific differences in this case correspond to the variability which took place in the process of speciation.     

Ultrastructural organization of hypodermis and formation of cuticle in pharate larva of Leptotrombidium orientale (Acariformes: Trombiculidae)

The ultrastructural organization of hypodermis and the process of cuticle deposition is described for the pharate larvae of a trombiculid mite, Leptotrombidium orientale, being under the egg-shell and prelarval covering. The thin single-layered hypodermis consists of flattened epithelial cells containing oval or stretched nuclei and smooth basal plasma membrane. The apical membrane forms short scarce microvilli participating in the cuticle deposition. First of all, upper layers of the epicuticle, such as cuticulin lamella, wax and cement layers, are formed above the microvilli with plasma membrane plaques. Cuticulin layer is seen smooth at the early steps of this process. Very soon, however, epicuticle starts to be curved and forms particular high and tightly packed ridges, whereas the surface of hypodermal cells remains flat. Then a thick layer of the protein epicuticle is deposited due to secretory activity of hypodermal cells. Nearly simultaneously the thick lamellar procuticle starts to form through the deposition of their microfibrils at the tips of microvilli of the apical plasma membrane. Procuticle, as such, remains flat, is situated beneath the epicuticular ridges and contains curved pore canals. Cup-like pores in the epicuticle provide augmentation of the protein epicuticle mass due to secretion of particular substances by cells and to their transportation through the pore canals towards these epicuticular pores. The very beginning of the larval cuticle formation apparently indicates the starting point of the larval stage in ontogenesis, even though it remains for some time enveloped by the prelarval covering or sometimes by the egg-shell. When all the processes of formation are over, hungry larvae with a fully formed cuticle are actively hatched from two splitted halves of prelarval covering.     

Isolation of Orientia tsutsugamushi from Leptotrombidium fuji and its characterization

In our attempts to isolate Orientia tsutsugamushi from trombiculid mites, a strain was successfully isolated from Leptotrombidium fuji collected in Aichi Prefecture, Japan. This is the first case of isolation of O. tsutsugamushi from L. fuji. A phylogenetic analysis based on the base-sequence homology of the 56-kDa type-specific antigen-gene indicated that the strain is a new type which is not closely related to any strains analyzed previously. Three strains isolated from Leptotrombidium pallidum harvested at the same area were identified as being closely related to the JP-2 type (subtype-2 of Karp type in Japan) by phylogenetic analysis.