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1 chondrial rRNA structures of a hexapod and a chelicerate.
2 erbivores that are very distantly related to chelicerates.
3 inities to pancrustacean WYR was observed in chelicerates.
4 tacea, and an alliance between myriapods and chelicerates.
5 mnants of a much larger diversity of aquatic chelicerates.
6 tream of where they are typically located in chelicerates.
7 ve been analyzed in insects, crustaceans and chelicerates.
8 stral domain similar to that found in modern chelicerates.
9 number of median eyes is two, as retained in chelicerates.
10 as, respectively, stem mandibulates and stem chelicerates.
11 and Sanctacarididae has been that of a basal chelicerate,(2) stemward of Leanchoiliidae, whose neurom
12 chelate first appendage is consistent with a chelicerate affinity for the pycnogonids.
13 d it shows a combination of primitive marine chelicerate and derived arachnid characteristics.
14            Of note, other arthropods such as chelicerates and crustaceans express two dsx genes, both
15 round patterns characterizing onychophorans, chelicerates and mandibulates are likely to have diverge
16 gnized that extant arthropods are split into chelicerates and mandibulates, and relationships within
17 pond to neuromeres defining brains of living chelicerates and mandibulates.
18 debate was stimulated recently by studies in chelicerates and myriapods that show that neural precurs
19     In the remaining euarthropod groups, the chelicerates and myriapods, a single-minded homologue ha
20 ed in insects and several representatives of chelicerates and myriapods, while data on crustaceans ar
21 many cases intermediate between those of the chelicerates and those of the insects and crustaceans, c
22 umber of studies in insects, crustaceans and chelicerates, and is important for the correct reconstru
23                                              Chelicerates are a diverse group of arthropods, represen
24 .(1) Two mid-Cambrian genera claimed as stem chelicerates are Mollisonia and Sanctacaris, defined by
25 n segment (protocerebrum) of mandibulate and chelicerate arthropods and the nonganglionic brains of p
26 hat a true biramous limb was once present in chelicerates as well as in the mandibulates.
27 genetic relationships have been proposed for chelicerates based on both morphological and molecular d
28                                          The chelicerate body plan is distinguished from other arthro
29 s); in the remaining euarthropod groups, the chelicerates (e.g. spiders) and myriapods (e.g. milliped
30 ed by segmental stripes, while myriapods and chelicerates exhibit segmental stripes that form early i
31 between these taxa and the horseshoe crab, a chelicerate from the sister group to arachnids.
32 nguish some groups of arachnids, distinguish chelicerates from other arthropods, and further clarify
33  and lateral eye neuropils, respectively, of chelicerate groups like spiders and horseshoe crabs.
34 ore the last common ancestor of these marine chelicerates >135 million years ago.
35 mology of these rami between crustaceans and chelicerates has, however, been challenged by data from
36 fied in the spider Achaearanea tepidariorum (chelicerate), however, the gene is not expressed in the
37 the affinities of megacheirans as stem-group chelicerates, in line with recent paleoneurological foss
38 ifferent from the pattern in all other known chelicerates, including the horseshoe crab Limulus polyp
39                                          The chelicerate Limulus polyphemus, all isopod crustaceans t
40 nd the longest contiguous fragments with the chelicerate Limulus polyphemus.
41 a single group represent the most biodiverse chelicerate lineage.
42                                              Chelicerate mites diverged from other arthropod lineages
43 the central nervous system of the stem-group chelicerate Mollisonia symmetrica from the mid-Cambrian
44 tin was not identified in representatives of chelicerates, myriapods, or any species outside Pancrust
45 ucial step in the evolution of Euarthropoda (chelicerates, myriapods, pancrustaceans) was the transit
46 s (insects/crustaceans) or precursor groups (chelicerates/myriapods) per hemi-segment.
47 ancestor or whether myriapods group with the chelicerates (Myriochelata).
48 tionship to 46 other insect, crustacean, and chelicerate opsin sequences.
49 rown-group euarthropods near the ancestry of chelicerates, or a segmented ecdysozoan lineage with con
50 studies have examined its variability within chelicerate orders including Scorpiones.
51 able confidence, whereas relationships among chelicerate orders remain poorly resolved.
52 are observed in both our fossil and outgroup chelicerate orders.
53 he shared neural characters of myriapods and chelicerates represent derived characters that support t
54  two cucumber (Cucumis sativus) genotypes to chelicerate spider mites (Tetranychus urticae) during th
55 rpret as evidence of mosaic evolution in the chelicerate stem-lineage.
56  pair-rule patterning in either myriapods or chelicerates, suggesting that the early pair-rule expres
57 that differs in location from those of other chelicerates, suggesting that these translocations occur
58 covery of a protein (S-CAP) in Myriapods and Chelicerates that contains a motif similar to the Su(H)-
59 he development of mechanosensory organs in a chelicerate, the spider Cupiennius salei.
60  most basally branching arthropod clade, the chelicerates (which includes spiders, scorpions, and hor
61                        Spiders belong to the chelicerates, which is an arthropod group that branches
62        Horseshoe crabs are archetypal marine chelicerates with a fossil record extending from the Low