Kunstidamaeus tecticola ( Michael, 1888 )
publication ID |
https://doi.org/ 10.5281/zenodo.202939 |
DOI |
https://doi.org/10.5281/zenodo.5621001 |
persistent identifier |
https://treatment.plazi.org/id/647F87A1-6D5A-FFBC-B8C7-BE30F3652A58 |
treatment provided by |
Plazi |
scientific name |
Kunstidamaeus tecticola ( Michael, 1888 ) |
status |
|
Kunstidamaeus tecticola ( Michael, 1888) View in CoL
( Figs. 8 View FIGURE 8 C, 10B, 11B, 15B, 16–19)
Damaeus tecticola Michael, 1888 View in CoL .
Oribata tecticola: Kulczyński 1902 .
Damaeus (Spatiodamaeus) tecticola: Bulanova-Zachvatkina 1957a View in CoL . Spatiodamaeus tecticola: Bulanova-Zachvatkina 1967, 1975 ; Schatz 1983; Olszanowski et al. 1996. Epidamaeus tecticola: Luxton 1989 ; Subías 2004.
Kunstidamaeus tecticola: Miko 2006 View in CoL .
Diagnosis. Mite of medium size (630–810 μm), brown, with arched, almost spherical notogaster ( Fig. 16 View FIGURE 16 ), cerotegument filamentous, mainly in dorsosejugal area. Setae in and ex nearly as long as seta c 1 ( Table 1), sensillus approximately twice as long as seta c 1. Apophysis Sa larger than P, apophysis Ba larger than La, apophysis Sp and discidium well-developed; all rounded. Spinae adnatae directed anteroventrally ( Fig. 10 View FIGURE 10 B), sometimes curved laterally. Notogastral setae relatively short, anterior pair directed anteriorly, other pairs strongly curved outside. Coxisternal apophysis E2a well-developed, rounded, other apophyses weakly developed. Anal setae located on anterior part of anal plates ( Fig. 11 View FIGURE 11 B). Formulae of leg setae and solenidia given in Table 2, dorsal coupled seta d lost on tibiae I–IV. Legs monodactylous.
Juveniles elongated, unpigmented, with darker legs, approximately as long as body ( Table 1). Seta in slightly shorter than c 3, sensillus long, but shorter than seta c 1. Most dorsal gastronotal setae long, curved, finely barbed, inserted on large apophyses, and flagellate in distal parts; seta h 3 present. Posterior excrescence with two pairs of setae; long pair h 1, directed posteriorly, and shorter pair p 1, directed posterolaterally. Prodorsum and gastronotum with granular cerotegument, cornicle long, between setae lp, exuviae usually without adherent debris.
Description of juvenile stages. Larva elongated ( Fig. 17 View FIGURE 17 ), unpigmented. Prodorsum triangular, with four rather long pairs of setae: ro and le curved, finely barbed; le strongly curved, longer and inserted more than twice as far apart as pair ro. Bothridium rather large, rounded, protruding from surface, with funnel-like rim; sensillus setiform, long, usually with cerotegument in distal half. Prodorsum covered with granular cerotegument.
Gastronotum of larva with 12 pairs of setae, including h 2 and h 3, inserted lateral to posterior part of anal opening ( Fig. 18 View FIGURE 18 A). All gastronotal setae long ( Table 1), curved, erected, finely barbed, inserted on large apophyses and distally flagellate, except for shorter setae c 3, h 2 and h 3; h 3 shorter than h 2; all setae finely barbed. Paraproctal valves (segment PS) bare. Cupule ia, im, ip and ih, and gland opening (gla) located similar as in D. onustus . Gastronotum with granular cerotegument.
Nymphs slightly slimmer than larva, with relatively longer legs, and unpigmented. Gastronotum of protonymph with 12 pairs of setae, as three pairs of pseudanal setae appear (p 1– p 3), and remain in successive instars, but setae of d -series lost, leaving central part of gastronotum bare. Other numerical changes of setae in successive nymphs, including tritonymph ( Fig. 18 View FIGURE 18 B) as in D. onustus . Anogenital region with granular cerotegument.
Prodorsum of nymphs relatively shorter than in larva; triangular, lateral part with depression above leg I. Prodorsal setae of tritonymph long ( Fig. 19 View FIGURE 19 ), setae ro and le curved, finely barbed; le longer and more widely spaced than ro; in nearly as long as ro, and barbed, ex shorter. Bothridium large, rounded, protruding from surface, with funnel-like rim; sensillus setiform, long, finely barbed, and covered with cerotegument in distal half. Prodorsum with granular cerotegument.
Exuviae of previous instars usually without adherent debris, and only weakly connected to gastronotum ( Fig. 15 View FIGURE 15 B). With exuviae removed, centrodorsal part bare, with rather long cornicle situated midway between setal pair lp. Gastronotal setae rather long, inserted on large apophyses on lateral and posterior parts of gastronotum, leaving dorsocentral part bare except for cornicle; all setae strongly curved posteromedially, erected, distally pliable. Gastronotum of nymphs with well formed posterior excrescence bearing two pairs of setae: long pair h 1, directed posteriorly, and shorter pair p 1, directed posterolaterally. Cupules ia, im, ip, iad, ips and ih, and gland opening (gla) located as in D. clavipes . Gastronotum with granular cerotegument.
Tarsus I of tritonymph long and thin, with two solenidia, ω1 longer and thicker than ω2 ( Fig. 8 View FIGURE 8 C). Tibia I with two solenidia, φ1 long, with rather long coupled seta d, φ2 rather short.
Summary of ontogenetic transformations. Prodorsal setae rather long in all instars, but setae ro are inserted closer to the rostrum in the juveniles than in the adult. The bothridium is rather large, rounded in all instars, with funnel-like rim; the sensillus is setiform, and long in all instars (in the adult nearly twice longer than seta c 1).
The larva has 12 pairs of gastronotal setae, but in the protonymph setae of p -series appear and setae of d -series are lost, such that 12 pairs remain in all nymphs. The adult loses seta c 3, such that 11 pairs of notogastral setae remain. The formula of gastronotal setae in K. tecticola is 12-12-12-12 -11 (larva to adult), while those of coxisternal, genital, aggenital, segments PS −AN, and paraproctal setae are as in D. onustus ( Table 3 View TABLE 3 ).
Distribution and ecology. Kunstidamaeus tecticola is considered a European species ( Subías 2004; Miko 2006). In Poland it was recorded only from southern parts of country ( Olszanowski et al. 1996).
This species occurs usually in mosses, and sometimes in dry habitat ( Miko 2006), while Mahunka and Mahunka-Papp (2006) found it in beech litter. In Botanical Garden on the campus of the University of Life Sciences in Ås ( Norway) it was rather abundant in spruce litter. Schatz (1983) considered this species myrmecophilous and xerophilous.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
Kingdom |
|
Phylum |
|
Class |
|
Order |
|
Family |
|
Genus |
Kunstidamaeus tecticola ( Michael, 1888 )
Seniczak, Stanisław & Seniczak, Anna 2011 |
Kunstidamaeus tecticola:
Miko 2006 |
Epidamaeus tecticola:
Luxton 1989 |
Spatiodamaeus tecticola:
Bulanova-Zachvatkina 1967 |
Damaeus (Spatiodamaeus) tecticola:
Bulanova-Zachvatkina 1957 |
Oribata tecticola: Kulczyński 1902
Kulczynski 1902 |
Damaeus tecticola
Michael 1888 |