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2 results for “Marimermithidae”

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zenodo32/100

Figure 1. Cavitary marine nematodes. A in Paraphyly of Marimermithida refines primary routes of transition to parasitism in roundworms

Figure 1. Cavitary marine nematodes. A, Marimermis maritima: 1, live specimens exposed in open host, sea urchin Strongylocentrotus polyacanthus; 2, 3, cephalic end apically and laterally, respectively, scanning electron microphotograph; pharyngeal gland outlets on lips, abundant irregular somatic setae; 4, generalized anterior ends juxtaposed in M. maritima [modified from Tchesunov (1997a)] and Thoracostomopsis barbata (Enoplida: Thoracostomopsidae) [modified from Lorenzen (1994)]. B, Aborjinia sp.: 1, juvenile occupying introvert of Priapulus caudatus (photograph courtesy of Dr A. S. Maiorova, NSCMB FEB RAS); 2, generalized anterior ends juxtaposed in Aborjinia sp. and Leptosomatum sp. (Enoplida: Leptosomatidae); 3, anterior body with two-celled ventral secretory-excretory gland, a distinctive genus feature [redrawn and modified from Miljutin (2003)]. C, Nematimermis enopliƲora: 1, two mature parasitoid individuals within host body of nematode Enoplus communis (Enoplida: Enoplidae); 2, 3, anterior body and head of immature parasitoid retrieved from body cavity of E. communis; 4, 5, anterior and tail regions of mature parasitoid from E. communis; trophosome resorbed, embryos with larval stylet inside egg cases, nested retained exuvia (old moulted cuticles) [all drawings modified from Tchesunov & Spiridonov (1993)]. (See also Fig. S1.) Key: a, amphid; emb ova, embryonated eggs; ep g, epidermal glands; ils, inner labial sensilla; ols + cs, joint crown of outer labial and cephalic setae; paras ind, parasitoid individuals; ph g, pharyngeal glands; ph t, pharyngeal tube; ss, somatic setae; stylet, spear-shaped armature; tr, trophosome; vgc, ventral gland cells.

opennotspecifiedMar 2023View details →
zenodo32/100

Figure 2 in Paraphyly of Marimermithida refines primary routes of transition to parasitism in roundworms

Figure 2. Bayesian tree of Nematoda based on concatenated rDNA data. Gene sampling maximizes the available coverage of SSU, 5.8S and LSU genes (accession IDs for each taxon correspond either to individual genes available, full cistrons or eDNA samples). The data covers the three major clades (Enoplia, Dorylaimia and Chromadoria), with extended sampling of marine Enoplia, and a selection of representative host-associations (in bold) for the clades. Parasitism-relevant life traits are mapped as pictograms, explained in the legend and addressed in the following discussion section. Traits apply either to a particular sampled species or more broadly to the subclade it represents (according to general knowledge of typical large subclades). Pictogram series denote the co-occurrence of traits either within subclade or individual life cycle. The habitat is colour-coded to generally typify subclades (e.g. as per Holterman et al., 2019), blue – marine; yellow – brackish/ limnic/terrestrial. Marine animal parasites/associates are listed in dark blue, brackish/limnic/terrestrial in red, while plant parasites/associates are shown in green. Nodes mismatched in BI and ML topologies are unlabelled. Otherwise, labels contain BI posterior probabilities (left) and ML bootstrap support (right). Values <0.7/70 are replaced with dashes (–). Bipartitions with support>0.95/95 dotted (●). BI posterior probabilities are calculated across GTR+Г parameter space in 3 M generations, ML bootstrap support estimated under GTR+F+G16 model in 100 replicates. NCBI accessions appended to taxon names, original sequences and assemblies marked with asterisk (*). Scale bar: substitutions per site. See also Supporting Information, Figure S2 (for an ML tree) and Supporting Information, Table S1 (for details on gene sampling, data origin and accession IDs).

opennotspecifiedMar 2023View details →

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