Larvae and relationships of the Calymenina (Trilobita)

1990 ◽  
Vol 64 (2) ◽  
pp. 255-277 ◽  
Author(s):  
B. D. E. Chatterton ◽  
D. J. Siveter ◽  
G. D. Edgecombe ◽  
A. S. Hunt

Up to four discrete protaspid larval stages are described for calymenid trilobites of Ordovician to Devonian age. The earliest growth stages are nonadult-like planktonic protaspides; later protaspides are adult-like and benthonic. In contrast, the related homalonotid trilobites apparently lack planktonic protaspides, but have up to two large benthonic protaspid stages that are similar in form to calymenid benthonic protaspides. These differences in life history patterns between these families are reflected in their paleobiogeographic distributions. Calymenids werre widely dispersed from Ordovician to Devonian times, both being common in warm, low latitude provinces (particularly from the Late Ordovician onwards) and well represented in cooler, higher latitude regions. The paleogeographic distribution of the homalonotids during the Ordovician (Arenig to the Ashgill) was concentrated in high paleolatitudes, with only a few forms occurring at low paleolatitudes (often in deeper, cooler environments?). Both families survived the Ordovician–Silurian mass extinction, with the calymenids again being widely dispersed but the homalonotids being best represented in the cool-water Malvinokaffric Province and in other regions where they are largely restricted to clastic facies.So few complete growth series of calymenine trilobites are known that it is unlikely that the ontogenies of taxa that form parts of ancestor–descendant clades can be identified. However, some evidence for heterochronic, particularly paedomorphic (neotenic), evolution is suggested for larval stages of members of both the Calymenidae and the Homalonotidae. Such possible neotenic evolution leading to very large planktonic larval stages of calymenid trilobites during the Devonian could have enhanced dispersal during a period of widespread warm and equable climates. Comparisons of homalonotid protaspides with equivalent stages of calymenids support the close relationship of these families within the Calymenina. A data matrix based upon characters of protaspides of two calymenine trilobites (Flexicalymene Shirley, 1936, and Brongniartella Reed, 1918) and eight other trilobites, belonging to the Phacopina (Calyptaulax), Cheirurina (Physemataspis and Hyrokybe), Proetida (Scharyia), Lichida (Acanthopyge), Odontopleurida (Diacanthaspis), Corynexochida (Bathyuriscus), and Ptychopariida (Crassifimbra) was subjected to cladistic analysis using the parsimony program “Hennig 86.” The shortest length cladogram produced is consistent with the inclusion of the Homalonotidae in the Calymenina, and inclusion of the Calymenina in the order Phacopida. “Cheirurina” is the paraphyletic “stem group” of Phacopina. The hypothesis that Lonchocephalidae is most closely related to part of post-Cambrian Phacopida is poorly supported by protaspid characters.

1997 ◽  
Vol 71 (3) ◽  
pp. 419-433 ◽  
Author(s):  
Gregory D. Edgecombe ◽  
Brian D. E. Chatterton ◽  
Norberto E. Vaccari ◽  
Beatriz G. Waisfeld

Silicified material from the Early Caradoc part of the Las Aguaditas Formation in San Juan Province, Argentina, includes a nearly complete growth series for a new species of the tropidocoryphid Stenoblepharum Owens, 1973. Cladistic analysis of Stenoblepharum species indicates that S. astinii new species is most closely allied to the Early Caradoc S. strasburgense (Cooper, 1953) from Virginia. Chinese species of Stenoblepharum are sister group to a Baltic/Laurentian clade. A single adult-like protaspid stage occurs in the life cycle of S. astinii, closely resembling the protaspis of Decoroproetus. It is preceded by a non-adult-like first protaspid instar that appears to be characteristic of Proetoidea in general but contrasts markedly with the early larval stages of other taxa in Proetida.


2006 ◽  
Vol 37 (3) ◽  
pp. 257-279 ◽  
Author(s):  
William Wolfe ◽  
Kelly Miller ◽  
Olof Biström

AbstractThe phylogeny of the Hydroporinae is investigated in a cladistic analysis emphasizing placement of the genus Peschetius Guignot, historically placed in the tribe Hydroporini. Sixty-nine adult and larval morphological characters were coded for 61 species of Hydroporinae representing eight of the nine tribes. Cladistic analysis of the data resulted in 396 most parsimonious cladograms (length = 176, CI = 46, RI = 80). The results indicate that the genus Peschetius is the sister group to the tribe Bidessini based mainly on an unambiguous character, the presence of a prominent internal spermathecal spine, and several other more ambiguous or homoplasious characters. The tribe Bidessini is expanded to include the genus Peschetius, and it is formally transferred from the tribe Hydroporini. Other results indicating interesting relationships of tribes and genera within Hydroporinae are also discussed. Results include; 1) a dramatically paraphyletic Hydroporini with Laccornellus Roughley and Wolfe, Canthyporus Zimmermann and Hydrocolus Roughley and Larson in basal positions within the phylogeny, 2) Hydrovatus Motschulsky and Queda Sharp resolved as sister groups and not closely related to Methlini van den Branden, 3) support for close relationship of Pachydrus Sharp (Pachydrini Biström, Nilsson and Wewalka) with Hyphydrini Sharp, 4) paraphyly of Hygrotus Stephens sensu lato with the relationship H. (Coelambus) Thomson + (Hygrotus sensus stricto + Hydrovatini)) suggesting recognition of Coelambus and Hygrotus as separate genera, 5) close relationship between the Australian genera of Hydroporini and Hyphydrini and 6) the nesting of Vatellini within a group of Hydroporini.


Zootaxa ◽  
2020 ◽  
Vol 4722 (2) ◽  
pp. 129-156
Author(s):  
LUIS E. ACOSTA ACOSTA

A new genus of Gonyleptidae Pachylinae, Qorimayus gen. nov., is described to place the high-altitude species originally named Parabalta alticola Ringuelet, endemic to Sierra de Famatina, western Argentina. While classical exomorphological features do not separate this new genus from Parabalta Roewer or Pachyloides Holmberg (to which the species was formerly combined), male genitalic features, especially the shape of the ventral process of stylus, differ clearly. In turn, penis morphology suggests the systematic relationship of Qorimayus gen. nov. with the Chilean genera Metabalta Roewer and Nanophareus Roewer. A cladistic analysis was performed to test the phylogenetic affinities of the new genus; 28 terminals were used, comprising selected species of Parabalta, Pachyloides, Metabalta and Nanophareus, as well as other Gonyleptidae to represent the ‘subtropical’ and the ‘Chilean’ opiliofaunistic elements; the most external outgroups included one cosmetid, one metasarcid and one nomoclastid. Results supported the recognition of Qorimayus as an independent genus, and its close relationship with the Chilean genera Metabalta and Nanophareus. A detailed redescription of Qorimayus alticola comb. nov., along with some habitat notes are given. The presumed zoogeographical links of this endemic species with the central Chilean opiliofauna are briefly discussed. 


1950 ◽  
Vol 41 (2) ◽  
pp. 395-413 ◽  
Author(s):  
Joan F. Basden

The different instars of Agriotes sputator larvae cannot be distinguished by measurements of total length or of various parts of the wireworm.The number of teeth on the mesothoracic and abdominal spiracles increases with age, and an examination of 700 wireworms showed that the average numbers of teeth on the two thoracic or on all the abdominal spiracles fell into eight groups. These criteria were valid for populations collected at different times of the year.The number of teeth on the thoracic spiracles of a larva in any particular group approximates to that on the abdominal spiracles of a larva in the next larger group.The eight groups formed by counting either the thoracic or the abdominal spiracle teeth represent growth stages and not necessarily instars.The larvae may sometimes moult without growth, a phenomenon probably caused by an inadequate supply of food. At such an ecdysis the number of spiracle teeth does not increase.The larvae pupate after attaining an optimum size, and reach this size in seven or eight growth stages.A quick method of determining the growth stage to which a larva belongs is given, whereby more than 80 per cent, of the larvae are placed in their correct growth stages by counting the teeth on one spiracle only ; for less than 1 per cent, of the larvae is it necessary to examine as many as five spiracles ; an accuracy of more than 97 per cent, can be maintained.The possibility of determining the relationship of growth stage and age is discussed.The division of the larvae into those which will pupate after seven, and those which will pupate after eight growth stages is apparent at a very early stage in the life history. One larva was found which appeared to be in its ninth growth stage.The cause of this difference in growth stage number is unknown. It may be due to the size of the egg, to the time of the year at which hatching occurs, or to heredity.


2002 ◽  
Vol 39 (12) ◽  
pp. 1755-1765 ◽  
Author(s):  
Sean P Modesto ◽  
Bruce S Rubidge ◽  
Johann Welman

Two fragmentary skulls from the Upper Permian Tapinocephalus Assemblage Zone (Abrahamskraal Formation, Beaufort Group) in Eastern Cape Province, South Africa, represent a new dicynodont taxon. Lanthanocephalus mohoii gen. et sp. nov. is distinguished from other dicynodonts by the presence of a conspicuous laterally facing excavation on the dorsal surface of the postfrontal, by dorsal expansions of the supraoccipital that contact the parietals, and by extensive ossification of the lateral wall of the braincase. Lanthanocephalus features several characters that are suggestive of a close relationship with Endothiodon. These include a transversely narrow intertemporal region, the presence of a pineal boss, and the presence of a distinct boss on the ventral margin of the jugal. Cladistic analysis of a modified data matrix from the literature supports the hypothesis of a sister-group relationship between Lanthanocephalus and Endothiodon. However, this grouping and most others found in the analysis collapse with one extra step, weaknesses that underscore the need for further research on dicynodonts and other non-mammalian synapsids.


PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e9192 ◽  
Author(s):  
Thomas D. Carr

Background During the growth of complex multicellular organisms, chronological age, size and morphology change together in a hierarchical and coordinated pattern. Among extinct species, the growth of Tyrannosaurus rex has received repeated attention through quantitative analyses of relative maturity and chronological age. Its growth series shows an extreme transformation from shallow skulls in juveniles to deep skulls in adults along with a reduction in tooth count, and its growth curve shows that T. rex had a high growth rate in contrast to its closest relatives. However, separately, these sets of data provide an incomplete picture of the congruence between age, size, and relative maturity in this exemplar species. The goal of this work is to analyze these data sets together using cladistic analysis to produce a single hypothesis of growth that includes all of the relevant data. Methods The three axes of growth were analyzed together using cladistic analysis, based on a data set of 1,850 morphological characters and 44 specimens. The analysis was run in TNT v.1.5 under a New Technology search followed by a Traditional search. Correlation tests were run in IBM SPSS Statistics v. 24.0.0.0. Results An initial analysis that included all of the specimens recovered 50 multiple most parsimonious ontograms a series of analyses identified 13 wildcard specimens. An analysis run without the wildcard specimens recovered a single most parsimonious tree (i.e., ontogram) of 3,053 steps. The ontogram is composed of 21 growth stages, and all but the first and third are supported by unambiguously optimized synontomorphies. T. rex ontogeny can be divided into five discrete growth categories that are diagnosed by chronological age, morphology, and, in part, size (uninformative among adults). The topology shows that the transition from shallow to deep skull shape occurred between 13 and 15 years of age, and the size of the immediate relatives of T. rex was exceeded between its 15th and 18th years. Although size and maturity are congruent among juveniles and subadults, congruence is not seen among adults; for example, one of the least mature adults (RSM 2523.8) is also the largest and most massive example of the species. The extreme number of changes at the transition between juveniles and subadults shows that the ontogeny of T. rex exhibits secondary metamorphosis, analogous to the abrupt ontogenetic changes that are seen at sexual maturity among teleosts. These results provide a point of comparison for testing the congruence between maturity and chronological age, size, and mass, as well as integrating previous work on functional morphology into a rigorous ontogenetic framework. Comparison of the growth series of T. rex with those of outgroup taxa clarifies the ontogenetic trends that were inherited from the common ancestor of Archosauriformes.


1938 ◽  
Vol 70 (11) ◽  
pp. 230-232 ◽  
Author(s):  
C. Stuart Walley

The following notes were assembled in arranging the Protarchoides material in the National Collection. In establishing the identity of Protarchoides mellipes (Prov.) it has been found necessary to synonymize one species. A species allied to mellipes is described as new and a table is provided for the separation of the four known North American species. The recording of Trichiosoma as host for a member of this genus is further evidence of the close relationship of the genus with Protarchus Foer.


2007 ◽  
Vol 44 (3) ◽  
pp. 120-125 ◽  
Author(s):  
B. Zheng ◽  
L. Xiao ◽  
X. Wang ◽  
D. Li ◽  
Y. Lu ◽  
...  

AbstractTo study the function of the 49 kDa excretory-secretory (ES) protein gene (P49) of Trichinella, the genes was amplified by RT-PCR from RNA of Trichinella spiralis and Trichinella nativa and several Chinese Trichinella isolates of domestic animals, and sequenced after being cloned. The amplified products of these parasites produced bands of about 950 bp. The 97.2 % to 100 % nucleotides identity and 94.3 % to 100 % identity of deduced amino acids among P49 gene of these Trichinella strains showed the close relationship of these parasites. The P49 gene of T. nativa was cloned into the BamHI site of the prokaryotic expression vector pET-30a, and the recombinant vector was expressed. The expressed product was 40.8 kDa in size. In Western blot analysis, the expressed product was reactive to sera of mice infected with T. nativa, T. spiralis and their Chinese geographical strains.


1991 ◽  
Vol 82 (2) ◽  
pp. 143-181 ◽  
Author(s):  
Lars Ramsköld

ABSTRACTThe systematics of parts of the Odontopleuridae are revised using character analyses tracing homologous structures, and a computerised cladistic analysis. The choice of outgroup is shown to affect the result of the analysis. Several synapomorphies place Selenopeltis, the type genus of the Selenopeltinae Hawle & Corda, 1847 as sister genus to Dicranurus. The latter's close relationship to Miraspis, type genus of the Miraspidinae Richter & Richter, 1917 is confirmed. The Selenopeltinae therefore becomes a senior subjective synonym of the Miraspidinae. The Selenopeltinae includes about 90 of the over 380 named odontopleurid species known to date (excluding accepted synonyms). The Ceratocephalinae is recognised, including about 30 species. The paired, large pygidial border spines present in most odontopleurids are in some species not homologous, and a falsifiable hypothesis is proposed for the homology of the ‘true major border spines’. This structure is the posterior pleural spine of the tenth postcephalic segment in selenopeltines, ceratocephalines and odontopleurines, and in acidaspidines and apianurines it is the serially homologous spine of the eleventh postcephalic segment. The spine belongs to the first pygidial segment in all taxa except ceratocephalines, where it is on the last thoracic segment. The homology in selenopeltines of the progressive restructuring of the cheek border is reviewed, explaining the supramarginal appearance of the genal spine. The presence and homology of the sublobation of L1 in odontopleurids is discussed, and it may be homologous with the sublobation in lichids. The strongly differentiated thoracic segmental lengths (exsag.), with maximum length reached in the anterior part of thorax, and the much reduced length of the posterior segments, are aspects of a single character-complex, uniquely derived within the Selenopeltinae. The ontogenetic origin of the anterior and posterior pleural spines is reviewed. The presence in Ceratocephala of two instars in one meraspid degree is discussed. A cladistic analysis of selenopeltine and ceratocephaline genera does not entirely resolve the topology of the phylogenetic tree of these taxa, but it confirms Selenopeltis as sister taxon to Dicranurus. These two genera belong in a clade also including Miraspis, Selenopeltoides, and Ceratonurus. Two new genera are erected, Ceratocara and Archaeopleura, the latter with type species A. kazakhensis sp. nov.


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