Pancrustacea
| Pancrustacea | |
|---|---|
| Scientific classification | |
| Kingdom: | |
| Phylum: | |
| (unranked): | Pancrustacea Zrzavý & Štys, 1997
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| Subphyla | |
| Synonyms | |
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Tetraconata Dohle, 2001 | |
Pancrustacea is a clade, comprising all crustaceans and hexapods.[1] This grouping is contrary to the Atelocerata hypothesis, in which Myriapoda and Hexapoda are sister taxa, and Crustacea are only more distantly related. As of 2010, the Pancrustacea taxon is considered well accepted.[2] The clade has also been called Tetraconata, referring to the square ommatidia of many of its members.[3] That name is preferred by some scientists as a means of avoiding confusion with the use of "pan-" to indicate a clade that includes a crown group and all of its stem group representatives.[4]
Molecular studies
A monophyletic Pancrustacea has been supported by several molecular studies,[5][6][7][8][9] in most of which the subphylum Crustacea is paraphyletic with regard to insects (that is, that insects are derived from crustacean ancestors).
The evidence for this clade derives from molecular data and morphological characteristics. The molecular data consists of comparisons of nuclear ribosomal RNA genes, mitochondrial ribosomal RNA genes, and protein coding genes. The morphological data consists of ommatidial structures (see arthropod eye), the presence of neuroblasts, and the form and style of axonogenesis by pioneer neurons.[10][11]
Regier et al. (2005)
In 2005 study of nuclear genomes Regier et al. suggest that Hexapoda is most closely related to Branchiopoda and Cephalocarida + Remipedia, thereby hexapods are "terrestrial crustaceans", thus supporting the Pancrustacea hypothesis that maxillopods are not monophyletic (in the following cladograms Maxillopoda subclasses are highlighted). In addition, there appeared some evidence against the Ostracoda monophyly: that Ostracoda subclass Podocopa may form a clade with Branchiura.[5]
| Cladogram following Regier et al. (2005).[5] |
Regier et al. (2010)
2010 study of nuclear genomes (Regier et al.) strongly supports Pancrustacea and strongly favour Mandibulata (Myriapoda + Pancrustacea) over Paradoxopoda (Myriapoda + Chelicerata). According this study, Pancrustacea is divided into four lineages: Oligostraca (Ostracoda, Mystacocarida, Branchiura, Pentastomida), Vericrustacea (Malacostraca, Thecostraca, Copepoda, Branchiopoda), Xenocarida (Cephalocarida, Remipedia) and Hexapoda, with the Xenocarida is a sister group to the Hexapoda (comprising "Miracrustacea").[6]
New proposed by Regier et al. clades are:
- Vericrustacea ("true crustaceans") — Branchiopoda, Copepoda, Malacostraca, Thecostraca;
- Multicrustacea ("numerous crustaceans") — Copepoda, Malacostraca, Thecostraca;
- Communostraca ("common shelled ones") — Malacostraca, Thecostraca;
- Miracrustacea ("surprising crustaceans") — Cephalocarida, Remipedia, Hexapoda;
- Xenocarida ("strange shrimp") — Cephalocarida, Remipedia.
All these proposed clades, except Multicrustacea, were not confirmed in later molecular studies.
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| Cladogram following Regier et al. (2010).[6] |
von Reumont et al. (2012)
In 2012 molecular study von Reumont et al. challenge the monophyly of Vericrustacea: they present four versions of Pancrustacea cladogram (figures 1—4), and in all four figures Remipedia is a sister group to Hexapoda, and Branchiopoda is a sister group to (Remipedia + Hexapoda). Thus, theirs data strongly suggest that Branchiopoda more closely related to Hexapoda and Remipedia than to Multicrustacea. Based on these data, they propose the following scenario of evolution of Branchiopoda, Remipedia and Hexapoda: under the impact of predatory fishes their common ancestors go to the littoral zone, then ancestors of Branchiopoda go to the ephemeral freshwater habitat, whereas ancestors of Remipedia go to the Anchialine cave, and ancestors of Hexapoda go to the land.[12]
Figures 1 and 3
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| Cladogram following von Reumont et al. (2012), figures 1 and 3.[12] |
Figure 2
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| Cladogram following von Reumont et al. (2012), figure 2.[12] |
Figure 4
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| Cladogram following von Reumont et al. (2012), figure 4.[12] |
Jondeung et al. (2012)
Another molecular study (of mitochondrial genomes), conducted in 2012 by Jondeung et al., strongly support monophyletic Pancrustacea and places Malacostraca + Entomostraca and Branchiopoda as the sister clade to Hexapoda and places Cirripedia + Remipedia as a basal lineage of Pancrustacea.[13]
Oakley et al. (2013)
In 2013 combined study of morphology, including fossils, and molecular data, including expressed sequence tag, mitochondrial genome, nuclear genome, and ribosomal DNA data Oakley et al. obtained support for three pancrustacean clades: Oligostraca (Ostracoda, Mystacocarida, Branchiura, Pentastomida), Multicrustacea (Copepoda, Thecostraca, Malacostraca) and a clade they refer to as Allotriocarida (Branchiopoda, Cephalocarida, Remipedia, Hexapoda), as well as for monophyly of Ostracoda. Within Multicrustacea they obtained support for a clade they suggest the name Hexanauplia: Thecostraca + Copepoda. Relations within Allotriocarida remain uncertain: sister taxon to Hexapoda is either Remipedia, or the clade Branchiopoda + Cephalocarida, however, authors are inclined to the first version (see "Conclusion", 4), which is also consistent with von Reumont et al. (2012) results.[14][12]
New proposed by Oakley et al. clades are:
- Hexanauplia (refers to six ("hexa-") naupliar molts) — Copepoda, Thecostraca;
- Allotriocarida ("allotrios" is "strange", "carida" is "shrimp") — Cephalocarida, Branchiopoda, Remipedia, Hexapoda.[14]
Note: Allotriocarida was also proposed in 2005 by Regier et al. as Clade #33,[5] but relations within it were different, and they did not choose a name for it.
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| Cladogram following Oakley et al. (2013)[14] |
Rota-Stabelli et al. (2013)
In 2013 Rota-Stabelli et al. used the signal in the 62 protein-coding genes assembled by Regier et al. in 2010 to improve the knowledge of the internal relationship in the Pancrustacea group. This data set infers a highly supported nucleotide tree that is substantially different to the corresponding, but poorly supported, amino acid one. The discrepancy between the nucleotide-based and the amino acids-based trees is caused by substitutions within synonymous codon families (especially those of serine-TCN and AGY): different arthropod lineages are differentially biased in their usage of serine, arginine, and leucine synonymous codons, and the serine bias is correlated with the topology derived from the nucleotides, but not the amino acids. The authors suggest that a parallel, partially compositionally driven, synonymous codon-usage bias affects the nucleotide topology. As substitutions between serine codon families can proceed through threonine or cysteine intermediates, amino acid data sets might also be affected by the serine codon-usage bias. The analyses suggests that a Dayhoff recoding strategy would partially ameliorate the effects of such bias. Although amino acids provide an alternative hypothesis of pancrustacean relationships, neither the nucleotides nor the amino acids version of this data set bring enough genuine phylogenetic information to robustly resolve the relationships within group, which should still be considered unresolved. However the amino acid tree seems to be the more likelihood since it appears to be free from synonymous codon-family bias affecting the nucleotide one. Most of the inferences based on amino acids sequences support a clade which includes Branchiopoda, Remipedia, Copepoda and Hexapoda (group A). Using the best amino acids substitution model, CATGTR, also Cephalocarida falls inside this group. In all the analyses group A (with or without Cephalocarida) is sister-group of a clade composed by Malacostraca, Oligostraca and Thecostraca (group B).[15]
The following image shows the tree resulting from the Dayhoff recoding.
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Position of Tantulocarida
According to Petrunina A.S. and Kolbasov G.A., the sixth subclass of Maxillopoda Tantulocarida may lie within Thecostraca, forming a clade with thecostracan infraclass Cirripedia (if so, Thecostraca excluding Tantulocarida is paraphyletic):[16][17]
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| Thecostraca cladogram following Petrunina (2012), page 19, picture 8[17] |
See also
References
- ^ J. Zrzavý; P. Štys (1997). "The basic body plan of arthropods: insights from evolutionary morphology and developmental biology". Journal of Evolutionary Biology. 10 (3): 353–367. doi:10.1007/s000360050029.
{{cite journal}}: Unknown parameter|lastauthoramp=ignored (|name-list-style=suggested) (help) - ^ Omar Rota-Stabelli, Ehsan Kayal, Dianne Gleeson, Jennifer Daub, Jeffrey L. Boore, Maximilian J. Telford, Davide Pisani, Mark Blaxter & Dennis V. Lavrov (2010). "Ecdysozoan Mitogenomics: Evidence for a Common Origin of the Legged Invertebrates, the Panarthropoda". Genome Biology and Evolution. 2: 425–440. doi:10.1093/gbe/evq030. PMC 2998192. PMID 20624745.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ W. Dohle (2001). "Are the insects terrestrial crustaceans? A discussion of some new facts and arguments and the proposal of the proper name 'Tetraconata' for the monophyletic unit Crustacea+Hexapoda". Annales de la Société Entomologique de France. 37 (1–2): 85–103.
- ^ Stefan Richter, Ole S. Møller & Christian S. Wirkner (2009). "Advances in Crustacean Phylogenetics" (PDF). Arthropod Systematics & Phylogeny. 67 (2): 275–286.
- ^ a b c d J. C. Regier; J. W. Shultz; R. E. Kambic (2005). "Pancrustacean phylogeny: hexapods are terrestrial crustaceans and maxillopods are not monophyletic". Proceedings of the Royal Society B. 272 (1561): 395–401. doi:10.1098/rspb.2004.2917. PMC 1634985. PMID 15734694.
- ^ a b c Jerome C. Regier, Jeffrey W. Shultz, Andreas Zwick, April Hussey, Bernard Ball, Regina Wetzer, Joel W. Martin & Clifford W. Cunningham (2010). "Arthropod relationships revealed by phylogenomic analysis of nuclear protein-coding sequences". Nature. 463 (7284): 1079–1083. doi:10.1038/nature08742. PMID 20147900.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Jeffrey W. Shultz; Jerome C. Regier (2000). "Phylogenetic analysis of arthropods using two nuclear protein-encoding genes supports a crustacean + hexapod clade" (PDF). Proceedings of the Royal Society B. 267 (1447): 1011–1019. doi:10.1098/rspb.2000.1104. PMC 1690640. PMID 10874751.
{{cite journal}}: Unknown parameter|lastauthoramp=ignored (|name-list-style=suggested) (help) - ^ Gonzalo Giribet; Carles Ribera (2000). "A review of arthropod phylogeny: new data based on ribosomal DNA sequences and direct character optimization". Cladistics. 16 (2): 204–231. doi:10.1111/j.1096-0031.2000.tb00353.x.
{{cite journal}}: Unknown parameter|lastauthoramp=ignored (|name-list-style=suggested) (help) - ^ Francesco Nardi, Giacomo Spinsanti, Jeffrey L. Boore, Antonio Carapelli, Romano Dallai & Francesco Frati (2003). "Hexapod origins: monophyletic or paraphyletic?" (PDF). Science. 299 (5614): 1887–1889. doi:10.1126/science.1078607. PMID 12649480.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Stefan Richter (2002). "The Tetraconata concept: hexapod-crustacean relationships and the phylogeny of Crustacea". Organisms Diversity & Evolution. 2 (3): 217–237. doi:10.1078/1439-6092-00048.
- ^ Casey W. Dunn, Andreas Hejnol, David Q. Matus, Kevin Pang, William E. Browne, Stephen A. Smith, Elaine Seaver, Greg W. Rouse, Matthias Obst, Gregory D. Edgecombe, Martin V. Sørensen, Steven H. D. Haddock, Andreas Schmidt-Rhaesa, Akiko Okusu, Reinhardt Møbjerg Kristensen, Ward C. Wheeler, Mark Q. Martindale & Gonzalo Giribet (2008). "Broad phylogenomic sampling improves resolution of the animal tree of life". Nature. 452 (10): 745–749. doi:10.1038/nature06614. PMID 18322464.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ a b c d e Bjoern M. von Reumont, Ronald A. Jenner, Matthew A. Wills, Emiliano Dell'Ampio, Günther Pass, Ingo Ebersberger, Benjamin Meyer, Stefan Koenemann, Thomas M. Iliffe, Alexandros Stamatakis, Oliver Niehuis, Karen Meusemann & Bernhard Misof (2012). "Pancrustacean phylogeny in the light of new phylogenomic data: support for Remipedia as the possible sister group of Hexapoda". Molecular Biology and Evolution. 29 (3): 1031–1045. doi:10.1093/molbev/msr270. PMID 22049065.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Amnuay Jondeung; Wirangrong Karinthanyakit; Jitlada Kaewkhumsan (2012). "The complete mitochondrial genome of the black mud crab, Scylla serrata (Crustacea: Brachyura: Portunidae) and its phylogenetic position among (pan)crustaceans". Molecular Biology Reports. 39 (12): 10921–10937. doi:10.1007/s11033-012-1992-2. PMID 23053985.
- ^ a b c Todd H. Oakley, Joanna M. Wolfe, Annie R. Lindgren and Alexander K. Zaharoff (2013). "Phylotranscriptomics to bring the understudied into the fold: monophyletic ostracoda, fossil placement, and pancrustacean phylogeny". Molecular Biology and Evolution. 30 (1): 215–233. doi:10.1093/molbev/mss216. PMID 22977117.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Omar Rota-Stabelli, Nicolas Lartillot, Hervé Philippe, Davide Pisani (2013). “Serine Codon-Usage Bias in Deep Phylogenomics: Pancrustacean Relationships as case study”, Systematic Biology 60 (6): 833-844. doi: 10.1093/sysbio/syr064.
- ^ Петрунина А.С., Колбасов Г.А. (2011). "Two species of Tantulocarida from the White Sea: what new could they tell us about morphology, anatomy and phylogeny of these minute parasitic crustaceans?" 11th International Conference on Copepoda.
- ^ a b Петрунина Александра Сергеевна. (2012). Микроскопические ракообразные класса Tantulocarida: морфология, анатомия, систематика и филогения.