中国食甜螨属一新种记述（蜱螨亚纲：食甜螨科）

本文记述从江西省余江倒的混合饲料中采得食甜螨科,食甜螨属一新种,余江食甜螨,模式标本保存在江西大学生物学系标本室。     

The efficacy of Dryacide, an inert dust, against two species of Astigmatid mites, Glycyphagus destructor and Acarus siro, at nine temperature and moisture content combinations on stored grain

Dryacide, an inert silicaceous dust, was tested for efficacy on wheat after 14 and 28 days exposure against the mites Acarus siro and Glycyphagus destructor at doses of 1, 3 and 5 g kg–1, moisture contents (MCs) of 14.5, 15.5 and 16.5% and temperatures of 10, 17.5 and 25°C. After 28 days at 10°C, all doses were effective against A. siro with the exception of the lowest dose at the highest MC, but against G. destructor complete control only occurred at 3 g kg–1 and 14.5% MC and at 5 g kg–1 and 14.5 and 15.5% MC. After 28 days at 17.5°C, the dust was fully effective against A. siro at 3 and 5 g kg–1 but only at 14.5% MC. Glycyphagus destructor was only completely controlled after 28 days at 5 g kg–1 and 14.5% MC. After 14 days at 25°C, A. siro was completely controlled at 3 and 5 g kg1 and 14.5% MC as was G. destructor after 28 days. Neither species appeared to ingest the dust but considerable quantities adhered to their cuticles. The high mortalities observed under the range of experimental conditions, particularly the lowest temperature, suggest that a dose of 3 g kg–1 may be effective as a replacement for organo-phosphorous (OP) pesticide surface treatments in an integrated storage strategy based on grain cooling. © Rapid Science Ltd. 1998     

上海市区屋尘螨区系和季节消长的观察

在上海市区的居民家庭和旅店中,用吸尘器从床褥、枕头、沙发、毛衣和地板上采集屋尘样本。区系观察表明上海有4亚目9科21种螨,其中户尘螨为优势种,其次为舍赫尘螨、隐秘甘食螨、粉尘螨、埋内欧尘螨。户尘螨主要集聚于枕头、沙发、床褥和毛衣的样本中,隐秘甘食螨多见于地板上。螨种数以8月份最多(17种),冬季最少。全年的季节消长观察显示:屋尘螨活螨的单位面积密度高峰出现于5—6月间,最高达103只/m~2,而以1—2月间最低。死螨的密度以冬季为最高。屋尘螨密度的变化与大气的温度变化有关。     

Mites from house dust in Glasgow

Glasgow's mild, high-rainfall climate, combined with a deteriorating quality of housing and low standards of living in many parts of the city, makes it a particularly suitable place for thriving populations of house dust mites. The acarofauna in 124 samples of house dust from beds and carpets in seventy-four homes in Glasgow, Scotland, comprised thirty-one species of which the most abundant were Dermatophagoides pteronyssinus (Trouessart) (64.3%), Glycyphagus domesticus (De Geer) (16.7%), Euroglyphus maynei (Cooreman) (11.6%), Tarsonemus sp. (1.6%), Cheyletus eruditus (Schrank) (1.5%), C. trouessarti Oudemans (0.9%), Tarsonemus fusarii Cooreman (0.8%) and Glycyphagus destructor (Schrank) (0.7%). Mites were present in all the homes surveyed and the mean population density was found to be 97/100 mg of dust (range 2-1210). Over 47% of homes visited showed signs of disrepair associated with damp, especially unmodernized flats in old tenement buildings and 1960s council housing stock, many of which contain deprived occupants. There was a high incidence of hygrophilic species such as Glycyphagus spp., Tarsonemus spp. and Euroglyphus maynei in such homes. Samples from homes of atopic asthmatics were found to contain significantly fewer mites than those from normal volunteers (chi 2 = 54.7). This was partly due to the use of house dust mite avoidance measures (e.g. regular vacuum cleaning of mattresses as well as carpets) by some of the asthmatics.     

Mite species identification in the production of allergenic extracts for clinical use and in environmental samples by ribosomal DNA amplification

The identification of allergy‐causing mites is conventionally based on morphological characters. However, molecular taxonomy using ribosomal DNA (rDNA) may be particularly useful in the analysis of mite cultures and purified mite fractions in the production of allergenic extracts. Full‐length internal transcribed spacers (ITS1 and ITS2) were obtained from Dermatophagoides farinae, Dermatophagoides pteronyssinus, Dermatophagoides microceras and Euroglyphus maynei (Astigmata: Pyroglyphidae), Glycyphagus domesticus and Lepidoglyphus destructor (Astigmata: Glycyphagidae), Tyrophagus fanetzhangorum, Tyrophagus putrescentiae, Tyrophagus longior, Tyrophagus neiswanderi, Acarus farris and Acarus siro (Astigmata: Acaridae), and Blomia tropicalis (Astigmata: Echymopodidae), using mite‐specific primers. Polymerase chain reaction (PCR) products were digested with HpaII and RsaI restriction enzymes in order to produce species‐specific PCR restricted fragment length polymorphism (RFLP) profiles. A semi‐nested re‐amplification step was introduced before the RFLP in order to apply the method to environmental samples. Results demonstrate that rDNA sequences can be used for the unambiguous identification of mite species. The PCR–RFLP system allows the identification of species in purified mite fractions when the availability of intact adult mite bodies for morphological identification is limited. This reliable and straightforward PCR–RFLP system and the rDNA sequences obtained can be of use in the identification of allergy‐causing mite species.