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The South American genus Caenocrypticoides (Pimeliinae: Caenocrypticini) comprises five species distributed in western South America. A new species from western Argentina, the first record of the tribe east of the high Andes mountains, Caenocrypticoides triplehorni sp. nov., is described and included in the most recent key for the genus. Distributional and habitat records, SEM, and habitus photographs for this new species are included. A phylogeny of the five species of the genus is proposed, based on 19 morphological characters. The cladistic analysis provides one most parsimonious cladogram showing that four unambiguous synapomorphic characters of external morphology support the monophyly of Caenocrypticoides. Sexual dimorphism is for the first time reported for the genus and is present in all five species of the genus. A discussion on the biogeographic implications of the discovery of this new species east of the Andean mountains is presented, which also includes adding accurate data records and habitat associations for the Chilean species of the genus.
A cladistic reconstruction of phylogenetic relationships between species of the feather mite family Syringobiidae was carried out. The maximum parsimony and neighbor-joining analyses were based on 201 external morphological characters of 65 syringobiid species (two species represented by 2 morphotypes each) and 4 species of pterolichid and ptiloxenid outgroups. The MP analysis produced 2 equally most parsimonious trees that were phylogenetically consistent and topologically very similar to the single tree reconstructed by NJ procedure. The results confirmed the monophyly of the family and monophyly of most syringobiid genera. The generic status of Limosilichus was weakly supported. Intergeneric relationships were most stable and well supported in the basal part of the tree (Plutarchusia-Paidoplutarchusia, Leptosyringobia, Grenieria, Thecarthra) with the exception of the position of the genus Raineria. All remaining species were placed in a large monophyletic clade with weaker statistical support for its internal composition. The present studies revealed the Magimeliinae as a sistergroup of Syringobiidae, a relationship that is discordant with the hitherto prevailing hypothesis. The cospeciation hypothesis was strongly supported statistically as one of the main factors in the current distribution of syringobiid mites on the hosts. However, other evolutionary events including at least four instances of host-switching have also contributed into the contemporary observed host-syringobiid associations. Only among the Laridae have all lineages of Syringobiidae diverged in parallel with host birds and represent members of the original acarofauna. In contrast, most of the syringobiid acarofauna of shore birds (Scolopacida and Charadrioidea) had ancestors on the Laridae and secondarily cospeciated after switching from this host group onto new hosts. The reconciliation results for syringobiid mites were compared with the patterns shown by other commensal mites inhabiting the same hosts - subfamily Avenzoariinae. In Syringobiidae the number of cospeciations was significantly smaller and the contribution of sorting events was significantly greater than in Avenzoariinae. Differences in distribution patterns on hosts (prevalence and density) of these two taxa were probably responsible for the significant differences in importance of particular evolutionary events observed in both taxa. The differences in distribution patterns of Syringobiidae and Avenzoariinae may be related to different degrees of virulence of each taxon. The cospeciation analysis has also allowed reinterpretation of morphological features occurring in many Syringobiidae that are typical of mites inhabiting the vane’s surface. The adaptations are most probably apomorphic reversals due to these syringobiids secondarily reoccupying this microhabitat from the quill environment.
The monotypie genus Dasytomima (type species: D. rachelae sp. nov.) from southeastern Australia is described and illustrated, and its relationship to the Neotropical genus Polypria Chevrolat, 1874 is discussed. A cladistic analysis of these two taxa, nine exemplar genera of Oedemeridae, one genus each of Synchroidae and Stenotrachelidae, with 37 adult characters using Winclada/Nona produced two shortest trees, in which Calopus+Sparedrus, Dasytomimus+Polypria and the remaining oedemerid taxa form three monophyletic groups. Based on this analysis, Dasytomima and Polypria are placed in Polypriinae, subfam. nov., Calopodinae is recognized at the subfamily level, and all other oedemerid genera are placed in Oedemerinae; the monophyly of Nacerini+Ditylini is not supported.
The phylogeny and classification of the superfamily Plectoidea Örley, 1880 is revised on the basis of published and updated morphological data for 35 ingroup and 2 outgroup species. The following features are here considered to support the monophyletic origin of the superfamily: 1) stegostom developed and differentiated into two sections; 2) dorsal gland orifice opening into the second stegostom section; 3) pharynx cylindrical, with distinct subdivision into corpus and postcorpus by the orifices of the subventral pharyngeal glands and a discontinuity in the muscular pharyngeal tissue; 4) corpus cylindrical, with subdivision into procorpus and metacorpus homologues; 5) pharyngeal radii of the corpus with prominent pharyngeal tubes along the procorpus; 6) cuticular lumen of the basal part of postcorpus (within basal bulb if latter is present) is modified to form a valvular apparatus. In addition the inner labial sensilla open inside the cheilostom. New data on postembryonic development of Anaplectus grandepapillatus (Ditlevsen, 1928), Plectus parietinus Bastian, 1865, P. decens Andrássy, 1985 and P. communis Bütschli, 1873 are given and supplemented with a discussion of the phylogenetic significance of the ontogeny in Plectoidea. Following the proposal of a phylogeny, some key events in the evolution of Plectidae Örley, 1880 are discussed. It is suggested that the superfamily Plectoidea includes four families: Pakiridae Inglis, 1983, Chronogastridae Gagarin, 1975, Metateratocephalidae Eroshenko, 1973 and Plectidae. Plectolaimus supplementatus Keppner, 1988 is transferred to the genus Caribplectus Andrássy, 1973. The genus Keralanema Siddiqi, 2003 is considered a junior synonim of Chronogaster Cobb, 1913. The genus Chiloplectus Andrássy, 1984 is considered a junior synonim of Plectus Bastian, 1865. The family Anaplectidae Zell, 1993 is downgraded to the subfamily level.
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