PAPER SESSION I: BIOLOGY AND DIVERSITY OF THE ACARI
CHAIRPERSON: Dr. E.A. Ueckermann
PAPER 1
SOIL MITE (MESOSTIGMATA) FAUNA
OF THE
A.K. Bhattacharyya
Desert Regional Station, Zoological
Survey of
The Thar Desert of India
covers four Indian states viz., Rajasthan,
PAPER 2
Ptyctimous mites (Acari, Oribatida) of
W. Niedbała
Department of Animal Taxonomy and Ecology,
In the
PAPER 3
PRESENT STATE OF
A.K. Bhattacharyya
Desert Regional Station,
Zoological Survey of
Ascid mites being highly specialised
inhabit almost all the zoogeographical regions of the world. The global ascid
fauna is represented by around 1000 species distributed over 34 genera. In
spite of varied ecological nature, the Indian ascid fauna has failed to draw
the proper attention of the ascidologists. So far, only 13 species were known
from the Indian region. During a five-year long study the author studied Indian
ascid mites and recorded 79 species belonging to 12 genera. Of the 12 genera so
far encountered in
PAPER 4
J.G. Palacios-Vargas, R.
Iglesias & G. Castano
Lab. Ecología y Sistemática de Microartrópodos, Depto. Biología, Fac. Ciencias, UNAM, México, D.F. 04510, Mexico, E-mail: gcm@hp.fciencias.unam.mx
Mites are very small, but they occupy diverse biological niches. On trees, some are associated with suspended soils, while others live in epiphytic plants, moss, lichens, bark crevices or even on leaves and flowers. They are known to live in a diverse number of habitats, those free living are better represented in soil and litter, where they can have huge populations in a few square centimetres. Only recently they were collected in big numbers from tropical tree canopies, where they can be predators, scavengers, grazers, or associated with any animal or plant. The five localities of the oak species studied were at the states of Mexico (Cahuacán, Juchitepec, Villa del Carbón), Distrito Federal (Milpa Alta), and Hidalgo State (Santiaguito). All the foggings were individual trees and with triplicates. Foggings were employed to obtain the arthropods living on the canopy of the oak trees. Specimens were taken from two collections made by Tovar (1999) in February and August 1997. He used a natural pyrethrum in aqueous solution, to fog three isolated trees of each of six selected oak species (Quercus castanea, Q. crassifolia, Q. crassipes, Q. greegii, Q. laeta and Q. rugosa) and put 10 square spans (0.99 m2 in surface) under each tree. All specimens were stored in 70% alcohol. Mites were sorted, counted and mounted in Hoyer’s solution, in order to identify the different taxa. The total amount of mites obtained with the two foggings was 6,256 specimens. Most of them (95%) were collected during the rainy season, and only about 5% during the dry season. The Mesostigmata were represented by 194 specimens, Prostigmata by 849 and the Cryptostigmata or Oribatids were by far the most abundant, with a total of 5,212 specimens. Only the 4% of the Oribatids were collected in the dry season and 96% during the rainy season. The oak species with most oribatid mites during the dry season were: Quercus crassipes (92), Q. castanea (35), Q. crassifolia and Q. rugosa (33), Q. laeta (13) and Q. greggii (9). The species with highest abundance during the rainy season were: Q. crassipes (2,094), Q. castanea (1,054), Q. laeta (979), Q. crassifolia (514), Q. rugosa (247), Q. greggii (235). The mite taxa we have found are represented by the following groups of Oribatid mites, Camisiidae: Camisia ca. segnis, Camisia sp.; Trhypochthoniidae: Trhypochthonius ca. tectorun; Liodidae: Platyliodes; Damaeidae: Belba sp.; Carabodidae: Carabodes sp., Tectocepheidae: Tectocepheus ca. elegans; Oppiidae: Striatoppia sp.; Cymbaeremaeidae: Scapheremaeus volcanicus, S. palaciosi; Oribatulidae: Zigoribatula sp.; Scheloribatidae: Cryptozetes usnea, Scheloribates sp.; Oripodidae: Oripoda ca. cubana, Parapirnodus ca. longus; Ceratozetidae: Ceratozetes sp.We present the inventory of the species found on each oak tree and the differences during the dry and rainy seasons.
PAPER 5
The functional micromorphology of the spiracles of the tortoise tick Amblyomma marmoreum.
E.D. Green1, F.C. Clarke2 & C. Baker3
1Department of Anatomy, 2Dept. of Biology and 3Electron Microscope Unit, Medical University of Southern Africa, Box 139, Medunsa, 0204, South Africa. E-mail: clark@medunsa.ca.za
Spiracles in ticks control both respiratory gas exchange and tracheal water loss. The large size of the spiracles of A. marmoreum makes them suitable for morphological studies to investigate how the spiracles may control these processes. Larvae and nymphs were fixed directly in 70% ethanol. 50% of the flat and engorged adult ticks were euthanased in CO2 in an attempt to cause the spiracles to open before fixation, while the remaining adults were fixed directly in 70% ethanol. Spiracles were carefully dissected and routinely processed for scanning electron microscopy (SEM) and viewed in a Leica Stereoscan 420 SEM at 5 to 7 kV. The external morphology revealed a spiracular plate with a porous comma-shaped outer margin perforated by many small aeropyles, surrounding a macula with a central ostium plugged by a valve-like lip. The spiracular plates of the nymphs and adults differed in size and shape of the macula and distribution of aeropyles. The interpedicellar space consists of a labyrinth of pedicels, which connect the spiracular plate to the thick base plate, which forms the floor of the subostial space. The pedicels are arranged in groups forming tubular chambers, many of which open to the atmosphere through the aeropyles. All chambers interconnect by means of slit-like fenestrations between the pedicles to allow respiration. The subostial space leads into the atrial chamber from which the main tracheal trunks arise. The thick lateral wall of the atrial chamber has a distinctive circular internal rim against which the thin medial wall may evert, to form a valve-like mechanism. This may close off the atrial chamber and trachea from the subostial chamber, and thus limit tracheal water loss through the open aeropyles when the spiracles are closed during interrespiratory intervals. The dense arrangement of pedicles and the closely spaced small aeropyles may further increase the resistance to transpiration and reduce the airflow, thereby reducing the water vapour loss from the spiracles.