Nodocepheus, Hammer, 1958

Colloff, Matthew J., 2022, First records of Tumerozetidae and Nodocepheidae from Australia, with descriptions of new taxa and a re-assessment of the Polypterozetoidea (Oribatida, Brachypylina), Zootaxa 5194 (1), pp. 33-57 : 44

publication ID

https://doi.org/ 10.11646/zootaxa.5194.1.2

publication LSID

lsid:zoobank.org:pub:7C18727C-3AF0-4BE6-AFBC-EA1AC2F2B926

DOI

https://doi.org/10.5281/zenodo.7141890

persistent identifier

https://treatment.plazi.org/id/03EE7A4D-C90A-FD05-FF5E-FBD4FAC7F836

treatment provided by

Plazi

scientific name

Nodocepheus
status

 

Redefinition of Nodocepheus View in CoL

Definition. Polypterozetoid mites with subcapitulum secondarily anarthric ( Figure 5b View FIGURE 5 ) or diarthric, though the labiogenal articulation may be incomplete ( Figure 7d View FIGURE 7 ); rutellum bifurcate, apex Y-shaped ( Figure 4g View FIGURE 4 ); chelicerae modified: either with digitus fixus pointed, lacking teeth and digitus mobilis comb-like ( Figure 4e View FIGURE 4 ) or both digits with reduced, blunted teeth, offset from each other ( Figure 4l View FIGURE 4 ). With serrated tutorium and cusped sub-tutorium. With short, rounded single-lobed or bilobed humeral processes. With 11 pairs of smooth notogastral setae positioned marginally; c 1 and c 2 marginal, on or near humeral process, sometimes on ventral fold. With five pairs of genital setae. Epimeral setal formula 3-1-3-3. Genital setae 6 pairs; aggenital setae 1 pair, anal setae 2 pairs, adanal setae 3 pairs. Legs monodactylous.

Remarks. The above definition is based on those of Piffl (1972) and Woas (2002). Mahunka (1983) provided a key to the six species of Nodocepheus known at that time, stressing the morphology of the humeral lobe, bothridial seta, tutorium and sub-tutorium.

The presence of Trägårdh’s organ is based on the examination by Piffl (1972) of a single specimen of Nodocepheus dentatus Hammer 1958 in which the chelicerae were damaged. The structure is described as short, broad and thus lacks the characteristic elongated form of this structure. I could not identify a Trägårdh’s organ on the chelicerae Nodocepheus luxtoni sp. nov.

In Nodocepheus dentatus , N. laterodentatus Piffl, 1972 and N. luxtoni sp. nov., setae c l are shifted laterally to the humeral region, positioned on a fold of the humeral process adjacent to setae c 2 ( Piffl 1972, Plate 13 therein; Figure 5a View FIGURE 5 herein). It is likely that N. barbatus Hammer, 1966 (originally described as N. dentatus var. barbatus ) shares this character state, giving a likely notogastral setal complement of 11 pairs (cf. Piffl 1972, p. 292), rather than 9 pairs as illustrated by Hammer (1966, Figure 85 therein). In N. minimus Mahunka, 1985 , setae c 1 appear to be absent and c 2 are apparently reduced to their alveoli, giving a complement of 10 pairs (including c 2). In N. cerebralis Mahunka, 1980 and N. hammerae Balogh, 1961 neither of the c series are illustrated, yet in the figures of the humeral regions of N. baloghi Mahunka, 1983 , N. cerebralis , N. dentatus and N. hammerae by Mahunka (1983, Figures 47-53 therein), c 1 is present on the ventral surface of the median lobe of the humeral process, as illustrated for N. dentatus by Piffl (1972, Plate 13, Figure Nd 3 therein). It seems likely that c 2 is also present in N. cerebralis , N. hammerae , and N. minimus on the anterioventral surface of the rugose lateral lobe of the humeral process, but has been overlooked when viewed dorsally because of its position below the heavily textured surface of the lobe.

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