@article {64,
	title = {Mantophasmatodea and phylogeny of the lower neopterous insects},
	journal = {Cladistics},
	volume = {21},
	year = {2005},
	month = {2005/06//},
	pages = {240 - 257},
	url = {http://doi.wiley.com/10.1111/j.1096-0031.2005.00062.x},
	author = {Terry, Matthew D and Whiting, Michael F}
}
@article {74,
	title = {New Damselflies (Odonata : Synlestidae , Hemiphlebiidae) from the Mesozoic Transbaikalian Locality of Chernovskie Kopi},
	journal = {Paleontological Journal},
	volume = {39},
	year = {2005},
	month = {2005///},
	pages = {280 - 283},
	abstract = {Two new genera and two new species, Gaurimacia sophiae gen. et sp. nov. (Synlestidae) and Mersituria ludmilae gen. et sp. nov. (Hemiphlebiidae), are described from the Mesozoic locality of Chernovskie Kopi in eastern Transbaikalia. The Odonata assemblage of Chernovskie Kopi is analyzed.},
	keywords = {chernovskie kopi, damselflies, Hemiphlebiidae, insecta, mesozoic, new species and genera, ODONATA, Synlestidae, transbaikalia},
	author = {Vasilenko, D.V.}
}
@article {53,
	title = {Phylogeny of Ephemeroptera (mayflies) based on molecular evidence.},
	journal = {Molecular phylogenetics and evolution},
	volume = {37},
	year = {2005},
	month = {2005/12//},
	pages = {625 - 43},
	abstract = {This study represents the first molecular phylogeny for the Order Ephemeroptera. The analyses included 31 of the 37 families, representing approximately 24\% of the genera. Fifteen families were supported as being monophyletic, five families were supported as nonmonophyletic, and 11 families were only represented by one species, and monophyly was not testable. The suborders Furcatergalia and Carapacea were supported as monophyletic while Setisura and Pisciforma were not supported as monophyletic. The superfamilies Ephemerelloidea and Caenoidea were supported as monophyletic while Baetoidea, Siphlonuroidea, Ephemeroidea, and Heptagenioidea were not. Baetidae was recovered as sister to the remaining clades. The mayfly gill to wing origin hypothesis was not supported nor refuted by these data. Mandibular tusks were supported as having at least one loss in Behningiidae and, together with the burrowing lifestyle, possibly two origins. The fishlike body form was supported as plesiomorphic for mayflies with multiple secondary losses. Topological sensitivity analysis was used as a tool to examine patterns concerning the stability of relationships across a parameter landscape, providing additional information that may not have been acquired otherwise.},
	keywords = {Animals, Base Sequence, DNA Primers, Insects, Insects: anatomy \& histology, Insects: classification, Insects: genetics, Molecular Sequence Data, PHYLOGENY, Sequence Analysis, DNA, Species Specificity},
	url = {http://www.ncbi.nlm.nih.gov/pubmed/16214375},
	author = {Ogden, T Heath and Whiting, Michael F}
}
@article {56,
	title = {Austroperilestidae, a new family of Damselflies from early Eocene of Argentina (Insecta: Odonata). Phylogenetic relationships within Odonata},
	journal = {Journal of Paleontology},
	volume = {79},
	year = {2005},
	month = {2005///},
	pages = {658 - 662},
	author = {Petrulevi{\v c}ius, Julian F and Nel, Andr{\'e}}
}
@article {28,
	title = {Phylogenetic relationships, divergence time estimation, and global biogeographic patterns of calopterygoid damselflies (odonata, zygoptera) inferred from ribosomal DNA sequences.},
	journal = {Systematic biology},
	volume = {54},
	year = {2005},
	month = {2005/06//},
	pages = {347 - 62},
	abstract = {The calopterygoid superfamily (Calopterygidae + Hetaerinidae) is composed of more than twenty genera in two families: the Calopterygidae (at least 17) and the Hetaerinidae (at least 4). Here, 62 calopterygoid (ingroup) taxa representing 18 genera and 15 outgroup taxa are subjected to phylogenetic analysis using the ribosomal 18S and 5.8S genes and internal transcribed spacers (ITS1, ITS2). The five other families of calopterid affinity (Polythoridae, Dicteriadidae, Amphipterygidae, Euphaeidae, and Chlorocyphidae) are included in the outgroup. For phylogenetic inference, we applied maximum parsimony, maximum likelihood, and the Bayesian inference methods. A molecular phylogeny combined with a geographic analysis produced a well-supported phylogenetic hypothesis that partly confirms the traditional taxonomy and describes distributional patterns. A monophyletic origin of the calopterygoids emerges, revealing the Hetaerinid clade as sister group to the Calopterygidae sensu strictu. Within Calopterygidae, seven clades of subfamily rank are recognized. Phylogenetic dating was performed with semiparametric rate smoothing by penalized likelihood, using seven reference fossils for calibration. Divergence time based on the ribosomal genes and spacers and fossil constraints indicate that Calopteryginae (10 genera, approximately 50\% of all Calopterygid taxa studied here), Vestalinae (1 genus), and Hetaerinidae (1 genus out of 4 studied here) started radiating around 65 Mya (K/T boundary). The South American Iridictyon (without distinctive morphology except for wing venation) and Southeast Asian Noguchiphaea (with distinctive morphology) are older (about 86 My) and may be survivors of old clades with a Gondwanian range that went extinct at the K/T boundary. The same reasoning (and an even older age, ca. 150 My) applies to the amphipterygids Rimanella and Pentaphlebia (South America-Africa). The extant Calopterygidae show particular species and genus richness between west China and Japan, with genera originating between the early Oligocene and Pleistocene. Much of that richness probably extended much wider in preglacial times. The Holarctic Calopteryx, of Miocene age, was deeply affected by the climatic cooling of the Pliocene and by the Pleistocene glaciations. Its North American and Japanese representatives are of Miocene and Pliocene age, respectively, but its impoverished Euro-Siberian taxa are late Pliocene-Pleistocene, showing reinvasion, speciation, and introgression events. The five other calopterid families combine with the Calopterygidae and Hetaerinidae to form the monophyletic cohort Caloptera, with Polythoridae, Dicteriadidae, and Amphipterygidae sister group to Calopterygoidea. The crown node age of the latter three families has an age of about 157 My, but the Dicteriadidae and Polythoridae themselves are of Eocene age, and the same is true for the Euphaeidae and Chlorocyphidae. The cohort Caloptera itself, with about 197 My of age, goes back to the early Jurassic.},
	keywords = {Animals, Base Sequence, Bayes Theorem, Demography, DNA, DNA Primers, Evolution, Genetic, Geography, Insects, Insects: genetics, Likelihood Functions, Models, Molecular, Molecular Sequence Data, PHYLOGENY, Ribosomal, Ribosomal: genetics, Sequence Analysis},
	url = {http://www.ncbi.nlm.nih.gov/pubmed/16012103},
	author = {Dumont, Henri J and Vanfleteren, Jacques R and De Jonckheere, Johan F and Weekers, Peter H}
}
@article {35,
	title = {A simple synthesis of Caribbean geology},
	journal = {Caribbean Journal of Earth Science},
	volume = {39},
	year = {2005},
	month = {2005///},
	pages = {69 - 82},
	url = {http://www.caribphilanthropy.org.jm/geoggeol/JamGeolSoc/CJES Web page/CJESpdf/CJES 39-07 - James - model.pdf},
	author = {James, K H}
}
