Paranota spinosa ( Boheman, 1854 )
publication ID |
https://doi.org/ 10.1649/0010-065X-68.4.631 |
persistent identifier |
https://treatment.plazi.org/id/360F0904-FFCA-491B-5938-2CE52DE1FBAE |
treatment provided by |
Carolina |
scientific name |
Paranota spinosa ( Boheman, 1854 ) |
status |
|
Paranota spinosa ( Boheman, 1854) View in CoL ( Figs. 69–81 View Figs , 101 View Figs )
Batonota spinosa Boheman 1854: 168, 1856: 95 , 1862: 238; Gemminger and Harold 1876: 3645; Wagener 1881: 45; Spaeth 1914: 67, 1923: 69; Maulik 1916: 583; Węgrzynowicz and Wšsowska 1996: 40.
Dorynota spinosa: Blackwelder 1946: 747 ; Buzzi 1988: 566; Borowiec 1996 a: 182.
Paranota spinosa: Monrós and Viana 1949: 401 View in CoL , 425; Borowiec 1999: 167, 2002 a: 108, 2009f: 692; Flinte et al. 2009: 594.
Diagnosis. Paranota spinosa can be easily distinguished from the other species of the genus by the reddish brown dorsal ground color, anterior margin of pronotum and post-humeral region yellow and disc mottled with reddish brown and yellow, yellow venter, and elytra with rounded anterior angle and humeral ridge absent.
Redescription. Body ( Figs. 69–70 View Figs ) reddish brown dorsally, with anterior margin of pronotum and posthumeral region yellow and disc mottled with reddish brown and yellow, ventrally yellow, except prosternal process, mesosternum, anterior margin of metasternum, and metepimeron black. Head: Interocular distance as wide as widest width of eye. Vertex densely punctate and with long, dense setae; coronal suture deep, glabrous, extending to epistomal suture. Frontoclypeus triangular, swollen, with deep, sparse punctures and discernible, incomplete epistomal suture. Interantennal distance half width of antennal sockets; antennae with length ratio of segments 100: 40: 20: 40: 60: 104: 92: 80: 80: 88: 132. Thorax: Mesosternal process notched medially, 2.5 times shorter than prosternal process, with truncate posterior angle. Metasternum 3.5 times wider than long, smooth and glabrous, 5.3 times longer than mesosternal process. Metepimeron ( Fig. 71 View Figs ) with deep depression apically and smooth surface; elytral disc with confluent, obscured punctation in lateral view; epipleural ridge with sharp, curved denticular expansion projecting over the metepisternum. Elytra with dense, fine, confused punctation clustered at the parascutellar disc; anterior angle rounded; humeral ridge absent; disc with 2 longitudinal ridges, one closer to suture, departing from anterior margin extending to basal third of disc, one departing from humerus, extending to basal third of disc; spinose projection ca. 1.5 times shorter than body. Tarsomere II 2.4 times longer than I; III 2 times longer than II and 1.2 times longer than IV. Internal claw 1.5 times longer than external claw. Male terminalia ( Figs. 72–74 View Figs ): Same as described for P. minima ( Fig. 52–56 View Figs ). Internal sac ( Figs. 75–77 View Figs ) membranous, highly convoluted dorsally, with 2 bags bulging dorsally ( Fig. 77 View Figs ); surface and inner walls armed with spicules, more concentrated distally, with 2 sclerites (sclt) and 1 short, slender flagellum (flg) medially at the apex. Female terminalia ( Figs. 78–81 View Figs ): Same as described for Paranota , except for sternite IX ( Fig. 46 View Figs ) with sclerosed region between the 2 plates; tergite X ( Fig. 45 View Figs ) with sclerosed plates with sinuous anterior margin and posterior margin rounded and expanded.
Measurements. Thirteen males / 41 females: total length: 9.3–10.0 / 10.1–11.5; greatest elytral width: 7.8–8.3 / 8.1–9.4; pronotal length: 2.8–3.0 / 2.9–3.5; greatest pronotal width: 5.1–5.8 / 5.1–6.1.
Host Plants. Recorded on T. aurea ( Fiebrig 1910) and Lecythis pisonis Cambess. (Lecythidiaceae) ( Silva et al. 1968).
Remarks. Boheman (1854) described P. spinosa and compared it with P. ensifera (as B. gregaria ) ( Figs. 35–36 View Figs ) and considered them very similar on the basis of size, prothorax subtly punctate on the sides, anterior angle of elytra prominent, and humeral ridge absent. However, P. ensifera has the anterior angle expanded laterally, forming an oblique angle, and the humeral ridge is poorly marked, whereas P. spinosa has the anterior angle rounded, not expanded laterally, and the humeral ridge is absent.
In his key to the species of Batonota, Wagener (1881) differentiated P. ensifera from P. spinosa by the presence of a carina on elytral disc. However, P. spinosa also has a carina on the disc, though it is less marked than in P. ensifera .
Monrós and Viana (1949) differentiated P. spinosa from P. ensifera by a longer and more convex body, the elytral punctation less coarse, the disc with a brighter spot at the medial region, and the spinose projection not as long as that in P. ensifera . I agree with Monrós and Viana (1949) and add that P. spinosa has the anterior elytral angle rounded, with a ridge not well-marked and incomplete, the elytral disc with two longitudinal ridges, one closer to the suture, departing from the anterior margin, and extending to the basal third of disc and one departing from the humerus and extending to basal third of disc. Paranota ensifera has the anterior elytral angle externally obtuse, with an interrupted and poorly marked ridge, the elytral disc with three longitudinal ridges, two closer to the suture, departing from the anterior margin, and extending to apex, and another departing from the humerus and extending to the basal third of disc. For more comments, see P. ensifera .
Paranota spinosa is quite similar to P. apiculata ( Figs. 82–83 View Figs ). Both have the anterior angle of the elytra rounded and the humeral ridge absent. However, P. spinosa has an elongate body, the prosternum with a vestigial antennal sulcus, the metepimeron with a deep depression apically and smooth surface, the elytral disc with confluent and obscured punctation in lateral view, and the epipleural ridge ( Fig. 71 View Figs ) with a sharp and curved denticular expansion projecting over the metepisternum. Paranota apiculata has a subquadrangular body, the prosternum with a developed antennal sulcus, the metepimeron elevated medially at the apex, with deep punctures close to the anterior margin, the elytral disc with not confluent punctures closely arranged into rows in lateral view, and the epipleural ridge ( Fig. 84 View Figs ) with a blunt denticular expansion projecting over the metepisternum.
Geographic Distribution. R e c o r d e d f r o m Argentina ( Misiones ) , Bolivia, Brazil (Mato Grosso, Minas Gerais, Pará, Rio de Janeiro), and Paraguay (Distrito Capital, Cordillera) (Borowiec and Świętojańska 2014). New state/province records include Goiás and São Paulo in Brazil and Formosa in Argentina ( Fig. 101 View Figs ).
Type Material. Lectotype ( Figs. 69–7 View Figs 0): Brasil // Type // Mhn // Lectotype \ des. L. Borowiec // NHRS-JLKB \ 000020987 ( SMNH) . Paralectotype: Brasil // Type // Mhn // Lectotype \ des. L. Borowiec ( SMNH) .
Other Material Examined (580). (1 female, DZUP); ARGENTINA: Formosa: (1 female, 5 specimen, DZUP); XI.1952, Dirings lgt. (1 male, 1 female, MZUSP); XII.1953, Dirings lgt. (3 specimens, MZUSP); Gran Guardia , XII.1953, A ., Maller lgt. (2 females, 1 specimen, DZUP) ; BOLIVIA: (2 specimens, MNHN); Chiquitos : (1 specimen, DBET) ; BRAZIL: (1 specimen, MMUE); Goiás: C . Elias lgt. (1 specimen, MMUE); Aragarças , I .1955, F. M. Oliveira lgt. (1 female, MNRJ); I .1955, F. M. Oliveira lgt. (1 male, 1 female, DZUP); Bananeiras , X.1938, B . Pohl lgt. (1 specimen, MZUSP); XII.1935, Campinas, Borgmeier & S . Lopes. lgt. (4 specimen, DZUP); XII.1935, Borgmeier and S . Lopes. lgt. (1 female, MNRJ); 1935, R . Spitz lgt. (5 specimen, DZUP); I .1936, Borgmeier and S . Lopes. lgt. (2 specimens, DZUP); I .1939, Dirings lgt. (1 specimen, MZUSP); Corumbá, Faz. Monjolinho , 14. VI .1949, F . Lane lgt. (4 specimens, DZUP); Goiatuba, (1 female, DZUP); Jataí , I .1955, P. Pereira lgt. (1 specimen, DZUP); Donckier lgt. (2 specimens, DBET); Leopoldo Bulhões , XII.1933, R . Spitz lgt. (1 female, 2 specimens, MMUE); XII.1933, R . Spitz lgt. (1 specimen, DZUP); XI.1937, Dirings lgt. (3 specimens, MZUSP); Minaçú , XII.1987, Monné & Roppa lgt. (4 specimens, DZUP); XII.1987, Monné & Roppa lgt. (1 female, DZUP); Mato Grosso: II.1923 (1 female, DZUP); 2.XI.1961, F. M . Oliveira lgt. (1 specimen, DZUP); Barra do Tapirapé , XI.1964, B . Malkin lgt. (2 females, 2 specimens, DZUP); Cáceres , 13.XI.1984, Buzzi, Mielke, Elias & Casagrande lgt. (3 females, DZUP); 9–11.XI.1984, C . Elias lgt. (2 specimens, DZUP); Chapada , (1 female, USNM); 27.X.1961, F. M . Oliveira lgt. (1 female, 1 specimen, DZUP); Corumbá, (2 specimens, DBET); Cuiabá , 26.X.1953, C. R . Gonçalves lgt. (1 specimen, DZUP); Guaicurus, XI.1938 (3 females, 1 specimen, DZUP); Murtinho , XII.1927, W . Meher lgt. (1 specimen, DZUP); XI.1929, R . Spitz lgt. (1 male, 3 females, 4 specimens, DZUP); XII.1939, W . Meher lgt. (3 specimens, DZUP); Porto Velho, Rio Tapirapé , 30.XII.1964, R. T . Lima lgt. (1 specimen, DZUP); Rio Varccaria , XII.1922, Lane lgt. (8 specimens, DZUP); I . 24 (11 males, 11 females, DZUP); Rio Verde (1 female, MNRJ); XI. 1964, A . Maller lgt. (3 specimen, DZUP); XI. 1964, A . Maller lgt. (1 female, MNRJ); X.1965, A . Maller lgt. (1 specimen, DZUP); Rondonópolis , XI.1950, Dirings lgt. (2 specimens, MZUSP); Rosário-Oeste, XI.1970, Dirings lgt. (24 specimens, MZUSP); III– II.1971, Dirings lgt. (259 specimen, MZUSP); XI.1971, Dirings lgt. (31 specimens, MZUSP); I – II.1972, Dirings lgt. (35 specimen, MZUSP); X.1973, Dirings lgt. (41 specimens, MZUSP); II.1974, Dirings lgt. (9 specimens, MZUSP); Minas Gerais: I .1916 (1 specimen, MMUE); Uberaba, (1 specimen, DBET); Pirapora, 1912, Garbe lgt. (1 female, DZUP); Pará: Santarensinho , Rio Tapajós , II.1964, Dirings lgt. (32 specimens, MZUSP); São Paulo: Franca, (1 male, DZUP); Ihering. lgt. (1 specimen, MMUE); XI.1911, Garbe lgt. (7 specimens, DZUP); Mogi Guaçu, Fazenda Campinha, 17–19.1967, H . Reichardt lgt. (2 females, 3 specimen, DZUP) ; PARAGUAY: Bruch lgt. (3 specimens, MMUE) .
R |
Departamento de Geologia, Universidad de Chile |
L |
Nationaal Herbarium Nederland, Leiden University branch |
SMNH |
Department of Paleozoology, Swedish Museum of Natural History |
DZUP |
Universidade Federal do Parana, Colecao de Entomologia Pe. Jesus Santiago Moure |
MZUSP |
Museu de Zoologia da Universidade de Sao Paulo |
A |
Harvard University - Arnold Arboretum |
MNHN |
Museum National d'Histoire Naturelle |
MMUE |
Museum of Manchester University |
C |
University of Copenhagen |
I |
"Alexandru Ioan Cuza" University |
F |
Field Museum of Natural History, Botany Department |
M |
Botanische Staatssammlung München |
MNRJ |
Museu Nacional/Universidade Federal de Rio de Janeiro |
B |
Botanischer Garten und Botanisches Museum Berlin-Dahlem, Zentraleinrichtung der Freien Universitaet |
S |
Department of Botany, Swedish Museum of Natural History |
VI |
Mykotektet, National Veterinary Institute |
P |
Museum National d' Histoire Naturelle, Paris (MNHN) - Vascular Plants |
USNM |
Smithsonian Institution, National Museum of Natural History |
W |
Naturhistorisches Museum Wien |
T |
Tavera, Department of Geology and Geophysics |
H |
University of Helsinki |
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.
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Genus |
Paranota spinosa ( Boheman, 1854 )
Simões, Marianna V. P. 2014 |
Paranota spinosa: Monrós and Viana 1949: 401
Flinte 2009: 594 |
Borowiec & World Catalogue of the Cassidinae & Coleoptera & Chrysomelidae & Biologica Silesiae & Wroclaw & Poland 1999: 167 |
Dorynota spinosa:
Buzzi & Biology of Neotropical Cassidinae 1988: 566 |
Blackwelder 1946: 747 |
Batonota spinosa
Spaeth 1923: 69 |
Maulik 1916: 583 |
Spaeth 1914: 67 |
Boheman & Monographia Cassididarum. Tomo IV & Ex Officina Norstedtiana & Holmie 1862: 238 |
Boheman & Catalogue of Coleopterous Insects in the collection of the British Museum. Part IX & Cassidae. British Museum & Natural History & Dept. of Zoology & London & UK 1856: 95 |
Boheman & Monographia & Ex Officina Norstedtiana & Holmiae 1854: 168 |