identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
0C1087D5FFB2FFF7CCD854B4FBA47063.text	0C1087D5FFB2FFF7CCD854B4FBA47063.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Cylindridia	<div><p>C y lin d rid ia C a s e y</p><p>Limnobaris auct., not B e d e l 1885-183. C a s e y 1892.</p><p>Cylindridia C a se y 1920-493. Type species Centrinusprolixus L e C o n t e (by original designation).</p><p>Recognition: Species of Cylindridia can be recognized by the following character states and biological data: (1) body shape elongate, slender and parallel-sided, Fig. 1-3; (2) pygidium covered by elytral apices; (3) rostrum sexually dimorphic in terms of length and width, Fig. 21-28; (4) male with deep pectoral cavity and pair of slender, anteriorly projecting prosternal spines usually visible from above, both structures reduced or entirely absent in depauperate specimens; (5) fore tibia in both sexes with ventrodistal spur not larger than tarsal claw; (6) claws curved and separate at base; (7) larval development in pith of flowering culms of Cyperaceae.</p><p>Discussion: C ylindridia is a genus with peculiar, anteriorly projecting prosternal spines that seemed to be restricted to the Nearctic region, whereas this character state occurs rather frequently in Neotropical genera. The southward extension of the range now adds to a geographically more consistent distribution of these weevils.</p><p>Species of Cyperaceae are the host of Cylindridia and numerous other genera in temperate (B o v in g 1924, Sa t t e r t h w a it 1942, P a l m 1957, D ie c k m a n n 1991, Y o s h ih a r a &amp; M o r im o t o 1994) and tropical regions (P a r n e l l 1970, A n d e r s o n &amp; P e c k 1994, Yo s h ih a r a &amp; M o r im o t o 1997). Relatively few of them have the above mentioned spines. The most likely candidate to be confused with Cylindridia is Sibariops C a sey, species of which are less elongate and almost always (indistinct in a Costa Rican population of the S. confusus complex) possess a greatly enlarged, anteriorly directed spur at the apex of the fore tibia of the male. A future taxonomic revision of this genus shall explore its distinctiveness to Cylindridia based on representative material of the diverse South American fauna. The separation of the various genera becomes less clear, when the prosternal spines are disregarded in their classification. As this character state is extremely variable and its phylogenetic value remains unexplored, a concise diagnosis of Cylindridia is not possible at this stage and should be targeted in a comprehensive study of all relevant taxa, which are assigned to no less than three tribes at present.</p><p>Distribution: Neotropical (Mexico, Costa Rica, Brazil; new records) and Nearctic regions (U.S.A. and southern Canada, east of Rocky Mountains)</p><p>Life H istory [based on C. rubripes and C.Juscipes]: The female visits newly emerged culms of large-sized species of Carex, Rhynchospora and possibly other Cyperaceae, where it deposits single eggs in the lowest accessible, unsheathed portion of the apical internode. One to several males may congregate nearby, often in the inner angle of the adjacent leaf or in the developing inflorescence. Any usage of their prosternal spines, such as for ritual fighting over females as reported for Parisoschoenus expositus by E b e r h a r d &amp; G a r c ia -C. (2000), has not been observed. The next oviposition on the same culm occurs, when new non-infested substrate of the old internode or a new unsheathed internode has grown basally. It appears, that the female probes whether or not sufficient non-infested tissue is available. Large culms may contain up to five specimens of different developmental stages, with the oldest specimen found in the apical section, the next-younger specimen boring in the basally adjacent 10-15 cm long section, and so on. The larva tunnels down part of the pithy interior of the culm, where it pupates among yellowish frass without preparing a cocoon. The host plant shows no evidence of physical damage or grossly impaired production of seeds, probably because the vascular system remains largely unaffected. The adult exits the now desiccated culm through a self-made spherical hole. Parasitic wasps were not encountered while rearing immatures from approximately 25 culms of Carex donnell-smithii and Rhynchospora ruiziana collected at two locations. Other weevils observed on the same hosts were Cholusfoveolatus C h a m p io n, Molytini (up to three larvae in the short, succulent stem from where basal leaves and culm emerge; INBC) and an unidentified species of Macroscytalus B r o u n, Cossonini (larvae possibly in the seeds as suggested by exit-holes; JPPC).</p><p>Key to the species of C ylindridia occurring in North and Middle America</p><p>1 Derm aeneous, rarely with slight bluish or greenish metallic luster, flanks ofpronotum and abdomen with white hairs; low and mid-elevations in United States and southern Canada (Nova Scotia, Québec, Ontario, Manitoba) east of Rocky Mountains.................................. .................................................................................................................... C. prolixa (L e C o n t e)</p><p>Derm dark green to cupreous, with strong metallic luster, body glabrous, without discernable hairs; Middle America, high elevations between 2000-3100 m.............................................2</p><p>2 Antennal club compact, approximately as long as distal four funicular segments combined (Fig. 21); femora dark metallic, tibiae and tarsi red; southern Mexico................................... ......................................................................................................................... C. propinqua sp. n.</p><p>Antennal club more elongate, at least as long as distal five funicular segments combined (Fig. 23); legs of uniform color, either dark metallic or reddish; Costa Rica (and probably western Panama)............................................................................................................................. 3</p><p>3 Legs red; elytral stria 10 not impressed subdistally; rostrum as long as or longer than pronotum; male without angularly projecting lamellar process ventrad of antennal insertion; female with rostrum weakly curved throughout (Fig. 23)........................ C. rubripes sp. n.</p><p>Legs dark metallic; elytral stria 10 impressed subdistally; rostrum shorter than pronotum; male with angularly projecting lamellar process ventrad of antennal insertion; female with rostrum notably curved in distal one-third (Fig. 25)................................. C. fuscipes sp. n.</p></div>	https://treatment.plazi.org/id/0C1087D5FFB2FFF7CCD854B4FBA47063	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.		Plazi	Prena, Jens	Prena, Jens (2006): A preliminary study Cylindridia with descriptions of new species from Middle America (Coleóptera: Baridinae). Beiträge Zur Entomologie = Contributions to Entomology 56 (1): 189-198, DOI: 10.21248/contrib.entomol.56.1.189-198, URL: http://dx.doi.org/10.21248/contrib.entomol.56.1.189-198
0C1087D5FFB0FFF0CCDE5478FC04716A.text	0C1087D5FFB0FFF0CCDE5478FC04716A.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Cylindridia prolixa (L e C o n t e)	<div><p>Cylindridia prolixa (L e C o n t e)</p><p>Centrinus prolixus L e C o n t e 1876-317. C a s e y 1892-643 (placed in Limnobaris)-, C a s e y 1920-493 (placed in Cylindridia)</p><p>Limnobaris nitidissima C a s e y 1892-644. C a s e y 1920-493 (placed in Cylindridia)-, new synonymy Cylindridia perexilis C a s e y 1920-493. C a s e y 1892-644 (specimen mentioned under L. prolixa)-, new synonymy</p><p>C ylindridia sim ulator C a s e y 1920-493. C a s e y 1892-644 (specimens mentioned under L. prolixa); new synonymy</p><p>Redescription: Fig. 4-8. Total length 2.3-4.1 mm, standard length 2.2-3.8 mm, derm dark aeneous (occasionally bluish or greenish iridescent), with light-colored hairs particularly on flank, antenna and tarsi often (legs and rostrum occasionally) more-or-less brown, male with prosternai spines red; rostrum as long as (male) or longer (female) than pronotum, evenly curved in both sexes, lamellar process ventrad of antennal insertion not angularly projecting; antennal club moderate, approximately as long as distal five funicular segments combined; pronotum almost as long as wide, sides subparallel, constricted apically and tubulate in front; sides of aedeagus convex, apex blunt, body of aedeagus and apodemes of equal length, internal sac finely asperate, 1.5x longer than apodemes, minute basal sclerite present as lateral reinforcement of duct, tegmen with parameres slightly shorter than basal apodem; male sternite 9 with distal appendices moderately unequal.</p><p>Distribution: United States and adjacent southern Canada (Nova Scotia, Québec, Ontario, Manitoba) east of Rocky Mountain range [based on C h a g n o n (1917), O ’B r i e n &amp; W ib m e r (1982), M a jk a et al. (ms) and material of CM NC, CNCI, CW OB, JPPC, NMNH, N SM C, QMOR]</p><p>Plant association: Cyperaceae: Carex sp. (Observations: A s k e v o l d in Manitoba, P r e n a in Vermont); occasionally visiting flowers of dicotyledonous plants, such as Eupatorium perfoliatum and Taenidia integerrima (H il t y 2005)</p><p>Discussion: M y study of more than 100 specimens (CM NC, CNCI, CW OB, JPPC, NMNH) from numerous collecting sites showed, that dry-mounted material looses its metallic sheen over time and exhibits generally a dull brownish tinge instead. This circumstance may explain partially the 1892 establishment of C. nitidissima (1 female) from Galveston, Texas. More recently collected material from Texas (CM N C, coll. R. A n d e r s o n) corroborates the synonymy with C. prolixa. Cylindridia similis (1 male, 3 females) and C. parexilis (1 female) were described from a single series collected by W ic k h a m at Greeley, Colorado (C a s e y 1920, p. 6 4 4), and lie within the variability of the material from elsewhere. The length of the male prosternai spines is variable and probably affected by the conditions imposed by the host plant and the environmental settings.</p></div>	https://treatment.plazi.org/id/0C1087D5FFB0FFF0CCDE5478FC04716A	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.		Plazi	Prena, Jens	Prena, Jens (2006): A preliminary study Cylindridia with descriptions of new species from Middle America (Coleóptera: Baridinae). Beiträge Zur Entomologie = Contributions to Entomology 56 (1): 189-198, DOI: 10.21248/contrib.entomol.56.1.189-198, URL: http://dx.doi.org/10.21248/contrib.entomol.56.1.189-198
0C1087D5FFB7FFF1CCBA5586FBDC749A.text	0C1087D5FFB7FFF1CCBA5586FBDC749A.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Cylindridia propinqua	<div><p>Cylindridia propinqua sp. n.</p><p>Holotype male, Mexico, labeled: “7000', 32mi. S.I Valle Nacional,/ Oax. Mex. V.21-24,/ 1971 H. Howden” (CMNC).</p><p>Paratypes 3 (1 male, 2 females), Mexico, same label as holotype (CMNC 1, JPPC 2).</p><p>Description: Fig. 9-11, 21, 22. Total length 4.5-5.5 mm, standard length 4.2-5.2 mm; derm dark green with metallic luster, glabrous, tibiae and tarsi red; rostrum as long as (male) or longer (female) than pronotum, evenly curved in both sexes, lamellar process ventrad of antennal insertion not angularly projecting; antennal club compact, approximately as long as distal four funicular segments combined; pronotum almost as long as wide, sides slightly rounded, constricted apically and tubulate in front; sides of aedeagus convex, apex blunt, body of aedeagus shorter than apodemes, internal sac slightly longer than apodemes, with asperities coarse in basal one-third and finer distally, basal sclerite consisting of short flagellum with pair of slender hook-like appendages, tegmen with parameres shorter than basal apodem; male sternite 9 with distal appendices very unequal.</p><p>Distribution: Mexico, Oaxaca, approximately 2150 m elevation</p><p>Plant associations: Unknown</p><p>Epithet: The name is a Latin adjective meaning “related”.</p><p>Discussion: This is the only known record for a species of Cylindridia from Mexico. W ithout dissection, the most obvious difference to the otherwise very similar Costa Rican C. rubripes is the compact antennal club and the metallic color of the femora. However, several details of the male genitalia differ significantly from those of the Costa Rican species, while agreeing much better with those of the North American C. prolixa.</p></div>	https://treatment.plazi.org/id/0C1087D5FFB7FFF1CCBA5586FBDC749A	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.		Plazi	Prena, Jens	Prena, Jens (2006): A preliminary study Cylindridia with descriptions of new species from Middle America (Coleóptera: Baridinae). Beiträge Zur Entomologie = Contributions to Entomology 56 (1): 189-198, DOI: 10.21248/contrib.entomol.56.1.189-198, URL: http://dx.doi.org/10.21248/contrib.entomol.56.1.189-198
0C1087D5FFB6FFF3CCD850F6FD10749F.text	0C1087D5FFB6FFF3CCD850F6FD10749F.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Cylindridia rubripes	<div><p>Cylindridia rubripes sp. n.</p><p>Holotype male (dissected), Costa Rica, labeled: “COSTA RICA: Prov. Heredia:/ 6km ENE Vara Blanca, 1950-/ 2050m, 10T 1 'N 84°07 W/ leg. J. Prena, 21.-25.4.2004/ INBio-OET-ALAS transect ” (INBC) .</p><p>Paratypes 202 (92 males, 110 females), Costa Rica, labeled: as holotype (JPPC 13); same data except 20.4.2002, 20/RG/RVC/011, INB0003230282 (INBC 1); same data except 15.111.2002,20/RG/DBM/007 (INBC 1); same data except 14.IV.2002, 20/RG/DBM/011 (INBC 1); “ COSTA RICA: Heredia / Cerro Chompipe / 10°05/20"N, 84°04'30"W/ ca. 2km. N. Monte de la/ Cruz, 2000 m, 12.VI.1997/ R. Anderson, cloud forest/ 97-012-X, on Cyperaceae.” (CMNC 18); “ COSTA RICA, Prov. Limon:/ P.N. La Amistad, Valle del/ Silencio, 10km NE Altamira,/ 2500 m, 9°07'N 82°58' W,/ 24.2.-26.2.2005, leg. J. Prena ” (JPPC 13, MNHN 2); “ COSTA RICA, Cart. Rd./ to Biol. Sta. Cuerisi [ Cuerici],/ 2600 m. VTII-28-1998/ C.W. &amp; L.B. O’Brien ”, “on/ Cyperaceae ” (CWOB 10); “ COSTARICA, Cart./ Biol. Sta. Cuerisi [ Cuerici],/ 2600m. VIIT28-1998/ C.W. &amp; L.B. O’Brien ”, “on/ Cyperus ” (CWOB 11); “ COSTARICA: Prov. San José:/ R.F. Los Santos, Villa Mills, La/ Georgina, Hwy. km 95, 2900-/ 3000 m, 9°34'N 83°45,W/ 3.3.2000, leg. K. Nishida ” (JPPC); same data except last line “3.-6.3.2005, leg. J. Prena ” (JPPC 72, MNHN 2); “ COSTA RICA, Cart. Cer-/ ro de la Muerte, Villa/ Mills, 3000m. VII-IX-1990,/ malaise trap, P. Hanson ” (CWOB 1); “ COSTA RICA, S.J.,/ 26mi.N. [on highway from] San Isidro/ del General, 10,500 7 VI-23-1974”, “ C.W. &amp; L.B. O’Brien / &amp; G.B. Marshall ” (CWOB 1); “ COSTA RICA, S.J.,/ 29mi.N. [on highway from] San Isidro/ del General, 110007 VI-23-1974”, “on Carexl lehm anniand', “ C.W. &amp; L.B. O’Brien / &amp; G.B. Marshall ” (CWOB 43); same data except “ex Carex / sp.” (CWOB 2); “ COSTA RICA, S.J./ 29mi.N. [on highway from] San Isidro/ del General, 110007 VII-10-1974”, “ C.W. &amp; L.B. O’Brien / &amp; G.B. Marshall ”, “on Chusqueal subtesselata (CWOB 5); same data without plant association (CWOB 2); “ COSTA RICA, S.J./ 33mi.N. [on highway from] San Isidro/ del General, 105007 VII-10-1974”, “C.W &amp; L.B. O’Brien / &amp; G.B. Marshall ” (CWOB 2); “ COSTA RICA, S.J.,/ 32mi.N. [on highway from] San Isidro/ del General, 10,500 7 VI-22-1974 C.W. Sc L./ O’Brien &amp; Marshall” (CWOB 1) .</p><p>Description: Fig. 1, 12-15, 23, 24. Total length 2.4-5.8 mm, standard length 2.3- 5.6 mm; derm dark green with metallic luster, glabrous, legs red, rostrum and antenna fuscous to partially red (&gt;2500 m elevation); rostrum approximately as long as or longer than pronotum, curved basally in male, nearly straight in female, lamellar process ventrad of antennal insertion not angularly projecting; antennal club elongate, at least as long as distal five funicular segments combined; sides of aedeagus subparallel, apex pointed or round (small specimens at 3000 m elevation), body of aedeagus and apodemes of subequal length, internal sac as long as apodemes, with complex blade-like basal sclerite, tegmen with parameres slightly shorter than basal apodem; male sternite 9 with distal appendices very unequal.</p><p>Distribution: Costa Rica (with one site near Panamanian border), Cordilleras Central and Talamanca, 2000-3100 m elevation.</p><p>Plant associations: I reared 11 specimens from Carex donnell-smithii in Valle del Silencio, O ’B r ie n collected two specimens ex Carex sp. in Villa M ills. Adult weevils were collected from Carex lem anniana (O ’B r i e n &amp; M a r s h a l l 43), Carex sp. (P r e n a 2), Cyperus sp. (O ’B r i e n 11), Rhyncbospora ruiziana (P r e n a 8 8), unidentified Cyperaceae (A n d e r s o n 17, O ’B r i e n 10) and Chusquea subtesselata (O ’B r i e n 5). H ie latter association, with a species of Poaceae, might be accidental.</p><p>Epithet: The name is a compound Latin noun referring to red legs.</p><p>Discussion: I include under C. rubripes specimens with reddish legs and a characteristic blade-like basal sclerite in the male (Fig. 15). However, their morphological range is noteworthy. An analysis of the meristic data reveals statistically significant differences between local populations: (1) the length-width ratio of the pronotum decreases linearly with increasing altitude, (2) the standard length decreases exponentially with increasing altitude, and (3) the length of the ante-antennal portion of the rostrum differs from site to site without obvious altitudinal effect. A gradual transition is apparent in the length-width ratio of the body of the aedeagus over the entire altitudinal range, while the apical shape changes at approximately 2500 m from triangularly pointed (Fig. 12) to round (Fig. 13); the shape is intermediate in specimens from Cuerici. At 3000 m, male specimens consistently exhibit greatly reduced prosternai spines. For distinction from the other Costa Rican species, C. fuscipes, see discussion there.</p></div>	https://treatment.plazi.org/id/0C1087D5FFB6FFF3CCD850F6FD10749F	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.		Plazi	Prena, Jens	Prena, Jens (2006): A preliminary study Cylindridia with descriptions of new species from Middle America (Coleóptera: Baridinae). Beiträge Zur Entomologie = Contributions to Entomology 56 (1): 189-198, DOI: 10.21248/contrib.entomol.56.1.189-198, URL: http://dx.doi.org/10.21248/contrib.entomol.56.1.189-198
0C1087D5FFB4FFFCCCD850F1FDD67463.text	0C1087D5FFB4FFFCCCD850F1FDD67463.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Cylindridia fuscipes sp. n.	<div><p>Cylindridia fuscipes sp. n.</p><p>Holotype male (dissected), Costa Rica, labeled: “COSTA RICA, Prov. San José, R. F J Rio Macho, Est. Ojo de Agua./ Alrededor de la Estación . 3000m. 27/ ABR 1997. B. Gamboa. Red de Golpe / L_S_396500_ 482050 #46760”, CRI002 565388 (INBC) .</p><p>Paratypes 26 (12 males, 14 females), Costa Rica, labeled: “COSTA RICA. Prov. San José, R.F./ Los Santos, Centro turístico Mirador de/ Quetzales, Send. Mirador de Quetzales,/ 2755 m, 1 MAY 2002, R. González,/ Golpe, L__S_398799_479741 #69451”, INB0003484893 (INBC 1); “ COSTARICA: Prov. San José:/ R.F. Los Santos, Fea. E./ Serrano, Hwy. km 70, 2600-/ 2700 m, 9°38'N 83°51'W/ leg. J. Preña, 13.-16.5.2004” (JPPC 5); “ COSTA RICA: Prov. San José:/ R.F. Los Santos, Villa Mills, La/ Georgina, Hwy. km 95, 2900-/ 3000 m, 9°34'N 83°45 'W / 3.-6.3.2005, leg. J. Preña ” (JPPC 8); “ COSTARICA, S.J.,/ 26mi.N. [on highway from] San Isidro/ del General, 10,500'/ VI-23-1974”, “ C.W. &amp; L.B. O’Brien/ &amp; G.B. Marshall ” (CWOB 1); “ COSTA RICA, Prov. Limón:/ P .N. La Amistad, Valle del/ Silencio, 10km NE Altamira,/ 2500 m, 9“07'N 82°58' W,/ 24.2.-26.2.2005, leg. J. Prena ” (JPPC 8); “ COSTA RICA: Prov. Heredia:/ 6km ENE Vara Blanca, 1950-/ 2050m, 10°11 'N 84°07'W/ leg. J. Prena, 21.-25.4.2004/ INBio-OET-ALAS transect” (JPPC 1); same label except line 4 “9.4.2002”, “20/M/04/064” (INBC 1); “ COSTA RICA: Heredia/ Cerro Chompipe / 10°05'20"N, 84°04'30"W/ ca. 2km. N. Monte de la/ Cruz, 2000 m, 12.VI.1997/ R. Anderson, cloud forest/ 97-012-X, on Cyperaceae “ (CMNC 1) .</p><p>Description: Fig. 2, 16-20, 25, 26. Total length 3.3-4.9 mm, standard length 3.2-4.7 mm, derm dark green (occasionally bluish iridescent) with metallic luster, glabrous, rostrum and legs fuscous with metallic luster, antenna fuscous; both sexes with rostrum shorter than pronotum, curved in apical one-third (female) or throughout (male), male with angularly projecting lamellar process ventrad of antennal insertion; antennal club elongate, at least as long as distal five funicular segments combined; pronotum longer than wide, sides subparallel, constricted apically and tubulate in front; sides of aedeagus bisinuate, apex sinuate, dorsum with 2-layered proximal lobe on each side, apodemes shorter than body of aedeagus, internal sac short, basal sclerite absent, tegmen with parameres and basal apodem of subequal length, male sternite 9 with distal appendices very unequal.</p><p>Distribution: Costa Rica (with one site near Panamanian border), Cordilleras Central and Talamanca, 2000-3100 m elevation</p><p>Plant associations: I reared two specimens from Carex d o n n ell-sm ith ii and five specimens from R hynchospora ru izian a in Villa Mills. Adult weevils were collected from Carex d o n ­ n ell-sm ith ii (P r e n a 7), R hynchospora ruiziana (P r e n a 1) and unidentified Cyperaceae (A n d e r s o n 1).</p><p>Epithet: The name is a compound Latin noun referring to dark legs.</p><p>Discussion: Cylindridiafuscipes occurs together with C. rubripes, and both species can be found even on the same individual plant. In almost all cases (I noticed one exception in 230 specimens), they can be distinguished by the color of the legs as indicated by the epithets. The outer elytral stria of C. fuscipes generally is impressed near the apex, but not so in C. rubripes. Further useful character states for separating the two species are, for females, the curvature of the rostrum and, for males, the presence of an angular lamellar process below the antennal insertion.</p></div>	https://treatment.plazi.org/id/0C1087D5FFB4FFFCCCD850F1FDD67463	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.		Plazi	Prena, Jens	Prena, Jens (2006): A preliminary study Cylindridia with descriptions of new species from Middle America (Coleóptera: Baridinae). Beiträge Zur Entomologie = Contributions to Entomology 56 (1): 189-198, DOI: 10.21248/contrib.entomol.56.1.189-198, URL: http://dx.doi.org/10.21248/contrib.entomol.56.1.189-198
