identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
F82587D8FFD92C75FF56FDBDFC2756F7.text	F82587D8FFD92C75FF56FDBDFC2756F7.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Puri	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Puri gen. nov.</p>
            <p> Type species.  Puri aleca sp. nov. Cardoso-Costa, Azevedo &amp; Ferreira-Jr </p>
            <p>Generic characters. Male: antennae subserrate, short, less than ½ length of forewing; wings alternating dark and pale venation; forewings with crossvein between 1A and 2A placed between footstalks of 1A and 2A; hindwings with basal r-m crossvein reconnected to M by an additional short branch; dorsally, ninth tergum anteriorly truncate and, laterally, ventral margin acutely produced; ninth sternum with membranous apical process; proximal margin of tenth tergum vertical; laterally tenth gonocoxite with bifurcation indistinct; lateral lobes connected by a broad and feebly sclerotized plate.</p>
            <p> Etymology. This new genus is named in honor of the native Indian tribe “  Puri ” that inhabited the region of Mantiqueira Mountain Range of southeastern Brazil. </p>
            <p> Taxonomic notes. In the male, the short antennae and dorsally the proximal inner portion of tenth tergum strongly sclerotized allies  Puri with  Anachauliodes Kimmins ,  Chauliodes ,  Ctenochauliodes Weele ,  Neochauliodes Weele ,  Nigronia and  Sinochauliodes Liu &amp; Yang. However the new genus can be distinguished from these Nearctic and Oriental genera by the ninth tergum anteriorly truncate. This latter characteristic allies  Puri to the fishfly genera  Archichauliodes ,  Platychauliodes Esben-Petersen ,  Madachauliodes Paulian ,  Dysmicohermes ,  Orohermes ,  Neohermes ,  Protochauliodes ,  Nothochauliodes and  Taeniochauliodes Esben-Petersen. The 2A sessile in forewing and the broad plate between lateral lobes allies  Puri to  Ctenochauliodes , but the tenth gonocoxite is not bifuricate and the subserrate antennae of the male differentiate the new genus. </p>
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	https://treatment.plazi.org/id/F82587D8FFD92C75FF56FDBDFC2756F7	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Cardoso-Costa, Gil;Azevêdo, Carlos Augusto Silva De;Ferreira-Jr, Nelson	Cardoso-Costa, Gil, Azevêdo, Carlos Augusto Silva De, Ferreira-Jr, Nelson (2013): New genus and new species of Chauliodinae (Insecta: Megaloptera: Corydalidae) from Brazil. Zootaxa 3613 (4): 391-399, DOI: 10.11646/zootaxa.3613.4.6
F82587D8FFD92C73FF56FAB6FA9055C6.text	F82587D8FFD92C73FF56FAB6FA9055C6.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Puri aleca	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Puri aleca sp. nov.</p>
            <p>(Figs. 1–5)</p>
            <p>Description. Holotype male: total length (mandible to genitalia) 44 mm; maximum width 5 mm; maximum length of the head 6 mm; maximum width of the head 5 mm; maximum length of the antennae 23 mm; maximum length of the pronotum 5 mm; maximum width of the pronotum 3 mm; maximum length of the forewings 53 mm; maximum length of the hindwings 42 mm.</p>
            <p>Body densely setose, reddish brown. Head subtriangular and robust, with short and golden filiform setae, long and yellowish filiform setae and dark spiniform setae. Compound eyes prominent. Antennae subserrate, short, less than one half of forewing.</p>
            <p>Prothorax subcylindrical, longer than wide; meso- and metathorax distinctly robust, wider than long. Legs with long and yellowish filiform setae and spiniform setae dark brown setae; tarsal claws simple. Wings hyaline with dark macula, veins alternating dark and pale. Forewing longer than hindwings; SC fused with R on the rear quarter of the wing; with three crossveins between R and Rs; Rs four branched, anterior branch trifurcated, posterior branch simple; three crossveins between Rs and M; M trifurcated, MA simple, MP two branched; three crossveins between MA e MP; one basal crossvein between M and Cu; three crossveins between posterior branch of MP and Cu; two crossveins between basal CuA and CuP; one crossvein between CuA1 and CuA2; two crossvein between Cu and 1A; 1A two-branched; 2A with anterior branch not fused to 1A; one crossvein between 1A and 2A placed between footstalks of 1A and 2A; 2A strongly sinuated (Fig. 2 a). Hindwing with MA simple; basal r-m crossvein reconnects to M by an additional short branch (Fig. 2 b).</p>
            <p>Ninth tergum anterior and posteriorly truncate, and wider than long, in dorsal view; with ventral margin acutely produced, in lateral view. Ninth sternum as long as ninth tergum; connected by a membrane to basal portion of tenth gonocoxite. Ninth gonocoxite and gonostylus reduced and absent, respectively. Tenth tergum as long as or longer than ninth tergum; narrowing towards apex; with spinous setae feebly modified; without strongly sclerotized distal claws; with proximal inner portion strongly sclerotized, in dorsal view; with base narrower than one-half of ninth tergum and proximal margin oblique and in lateral view; cercus distinctly prominent and fused to base of tenth tergum (Figs. 3 &amp; 4). Tenth gonocoxite not bifurcated, with apex incised; mostly visible, curved dorsally and with distal half feebly widened, in lateral view; with lateral arm longer than one-half of the median plate; with median plate longer than wide (Fig. 5). Lateral lobes present, separated from tenth gonocoxite; connected by a broad and feebly sclerotized plate.</p>
            <p>Variation. Body measurements variable in total length 35–45 mm; maximum length of the head 5–6 mm; maximum width of the head 4–5 mm; maximum length of the antennae 23 mm; maximum length of the pronotum 4–5 mm; maximum width of the pronotum 3–4 mm; maximum length of the forewing 43–53 mm; maximum length of the hindwing 41–42 mm.</p>
            <p>Female: Unknown.</p>
            <p>Type material. Holotype male (DZRJ500), BRAZIL, Minas Gerais, Itamonte, 1st order stream [riacho de primeira ordem], 22°19’38,6’’S 44°40’37,9’’W, 1898m, 09.XII.2005, Jorge Luiz Nessimian leg. Paratypes: BRAZIL, Minas Gerais, Itamonte; 1 male, 2nd order tributary to Aiuruoca River, 22°19’38,6’’S 44°40’37,9’’W, 1898m, 20.XI.2005, J. L. Nessimian &amp; L. L. Dumas legs.; BRAZIL, Minas Gerais, Itamonte; 1 male (DZRJ501), 1st order tributary to Aiuruoca River, 22°21’44,7’’S 44°42’31,5”W, 2297m, 21.XI.2009, B. C. Mattos leg.</p>
            <p> Etymology. The specific epithet is an expression in  Puri language “ah! lekah!” meaning “I live here”. </p>
            <p>Distribution. Itamonte Municipality, Minas Gerais, Brazil.</p>
            <p>Parsimony analysis. A parsimony analysis was performed in PAUP*4b10 (Swofford 2002), with exhaustive search branch-and-bound and characters unordered and of equal weight. Bootstrap values for clades were calculated with 1000 replicates and 100 random stepwise additions of taxa using a general heuristic search Tree bisection and reconnection (TBR). Bremer’s decay index was calculated with TreeRot (Sorenson &amp; Franzosa 2007) and PAUP*4.0b10 and visualized in FigTree (Rambaut 2009).</p>
            <p> Discussion. A phylogeny by Liu &amp; Yang (2006) proposed two main clades in  Chauliodinae : one Eastern/ Northern Clade containing the five Asian and two Nearctic genera (  Ctenochauliodes ((  Anachauliodes ,  Chauliodes ) ((  Neochauliodes ,  Nigronia ) (  Sinochauliodes ,  Parachauliodes Weele )))) and other Western/Southern Clade (  Archichauliodes (  Neohermes ,  Protochauliodes )). However, in this analysis the Afrotropical genera  Madachauliodes ,  Platychauliodes and  Taeniochauliodes and the Nearctic genera  Dysmicohermes ,  Nothochauliodes and  Orohermes were not included. </p>
            <p> A new data matrix was constructed by coding morphological characters of  P. aleca and the new matrix was modified by coding of character states 7, 8, 16, 36 and 44 into Liu &amp; Yang (2006) data matrix, using the character states in Table 1. A parsimony analysis of the new data matrix recovered three most parsimonious trees (L = 101, CI = 0,66, RI = 0,87, RC = 0,58), of which the strict consensus tree was similar to that of Liu &amp; Yang (2006). Differences lie in the inclusion of  Puri as a sister-group to  Ctenochauliodes in the Clade 1 of these authors (Fig. 6, left tree). The clade  Puri +  Ctenochauliodes (supported by bootstrap = 63 and Bremer’s decay = 2) is supported by the unambiguous synapomorphic state of the broad plate between lateral lobes (Liu &amp; Yang (2006) character 52); and the homoplastic states of the ninth tergum in lateral view with ventral margin acutely produced (27), that is shared with the  Neochauliodes lineage, and lateral lobes connected by a sclerotized plate (51), shared with the genus  Nigronia . The character states basal r-m crossvein of hindwings modified (23), tenth tergum narrowing towards apex (31), and lateral lobes present (49) are presented as ambiguous and may represent homoplastic states. In our analysis,  Puri is supported by homoplastic states of the male antenna subserrate (7) shared with  Parachauliodes and  Nigronia serricornis (Say) (Liu &amp; Yang (2006) indicate that the type antenna is an important diagnostic character at the generic level); coloration of veins alternating dark and pale pattern (13), shared with the  Anachauliodes lineage; crossvein between 1A and 2A of forewing placed between footstalks of 1A and 2A (19) and ninth sternum with membranous apical process (29), shared with the  Neochauliodes lineage +  Parachauliodes lineage; ninth tergum in dorsal view anteriorly truncate (25), shared with clade 2; tenth tergum in lateral view with proximal margin vertical (36), shared with  S. fujianensis (Yang &amp; Yang) +  S. maculosus (Liu &amp; Yang) ; tenth sternum without bifurcation distinct (46), shared with  Anachauliodes and with the  Neochauliodes lineage +  Parachauliodes lineage; and the plate between lateral lobes feebly sclerotized (53), shared with  Nigronia . </p>
            <p> A recent phylogeny by Liu et al. (2012), including all extant and fossil fishfly genera using fewer character states and numerous character states left uncoded for some genera, supported Lui &amp; Yang (2006) original Clade 1 with some differences in the relationship between the genera (  Ctenochauliodes ((  Nigronia (  Neochauliodes (  Sinochauliodes ,  Parachauliodes ))) (  Anachauliodes ,  Chauliodes ))). In this analysis, the Lui &amp; Yang (2006) Clade 2 was not supported, with  Archichauliodes (+  Apochauliodes ) more closely related to Lui &amp; Yang (2006) Clade 1 than to (  Neohermes ,  Protochauliodes ). A reanalysis of Liu et al. (2012) data matrix with  Puri included (Table 2) recovered thirty-six equal parsimonious trees (L = 70, CI = 0,60, RI = 0,84, RC = 0,50), which the strict consensus tree presented numerous polytomies, varying from those found by Liu et al. (2012). Our second analysis (Fig. 6, right tree) included  Puri as sister-group to  Anachauliodes lineage +  Neochauliodes lineage (Liu et al. 2012) (supported by bootstrap = 51 and Bremer’s decay = 1) and not closely related to  Ctenochauliodes , as obtained in our analysis of Liu &amp; Yang (2006) modified data matrix. In this analysis,  Puri is supported by ambiguous character states of the forewing with 1A connected by a crossvein at stem of 2A (Liu et al. 2012) character 6, homoplastic states shared with Liu et al. (2012)  Archichauliodes lineage and  Neochauliodes lineage. The Clade  Puri + Liu et al. (2012)  Anachauliodes lineage +  Neochauliodes lineage is supported by the homoplastic states of the male antenna subserrate or pectinate (16), shared with  Ctenochauliodes ; male tenth gonocoxite present as a single sclerite (37), shared with  Madachauliodes and  Neohermes +  Protochauliodes +  Taeniochauliodes . </p>
            <p> 0 1 0 2 0 3 0 4 0 5 0 6 0 7 0 8 0 9 10 11 12 13 14 15 16 17 18 19 20  Puri aleca gen. nov. sp. nov. 2 1 1 1 1 0 0 1 0 0 1 1 0 0 0 1???? </p>
            <p>continued.</p>
            <p> 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41  Puri aleca gen. nov. sp. nov. ?? 0 0 0 0 1 1? 0 0 0 0 0 0 0 1 0??? </p>
            <p> Liu &amp; Yang (2006) proposed monophyly of New World fishfly genera based on the male characters of long filiform antenna, ninth tergum anteriorly truncate and tenth tergum in dorsal view with proximal inner portion almost membranous, and female gonocoxite with lateral sclerotized plate subquadrate. However, this hypothesis was rejected by Lui et al. (2012), demonstrating that the Oriental genera of fishflies,  Anachauliodes ,  Ctenochauliodes ,  Neochauliodes ,  Parachauliodes and  Sinochauliodes and the Nearctic genera  Chauliodes and  Nigronia are probably derived from Gondwanan ancestors. Our analysis indicated a relationship of  Puri to the Nearctic and/or Oriental genera, also rejecting the hypothesis of monophyly of New World fishfly genera. </p>
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	https://treatment.plazi.org/id/F82587D8FFD92C73FF56FAB6FA9055C6	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Cardoso-Costa, Gil;Azevêdo, Carlos Augusto Silva De;Ferreira-Jr, Nelson	Cardoso-Costa, Gil, Azevêdo, Carlos Augusto Silva De, Ferreira-Jr, Nelson (2013): New genus and new species of Chauliodinae (Insecta: Megaloptera: Corydalidae) from Brazil. Zootaxa 3613 (4): 391-399, DOI: 10.11646/zootaxa.3613.4.6
