Pararhagadochir noronhensis, Costa-Pinto & Olivier & Rafael, 2021

Costa-Pinto, Paula J., Olivier, Renan S. & Rafael, José A., 2021, The first species of Embioptera (Insecta) from the archipelago of Fernando de Noronha (Pernambuco: Brazil), Zootaxa 4941 (1), pp. 142-150 : 143-147

publication ID

https://doi.org/ 10.11646/zootaxa.4941.1.9

publication LSID

lsid:zoobank.org:pub:DF4BB7D3-D0AA-4D35-B5C4-979627FED09F

DOI

https://doi.org/10.5281/zenodo.4594868

persistent identifier

https://treatment.plazi.org/id/F4049A13-904B-9405-FF0D-F908192FF80C

treatment provided by

Plazi

scientific name

Pararhagadochir noronhensis
status

sp. nov.

Pararhagadochir noronhensis sp. nov.

( Figs. 2–6 View FIGURE 2 View FIGURE 3 View FIGURE 4 View FIGURE 5 View FIGURE 6 )

urn:lsid:zoobank.org:act:C168BF4F-1FF9-4103-8E0D-80FED1C2D67F

Pararhagadochir View in CoL sp., Rafael et al. 2020: 16.

Type-series. Holotype Ƌ: Brasil, PE, Fernando de Noronha , Trilha Sancho, 3°51’30’’S – 32°25’50’’W, 20-27.ii.2020, hand-collected, J.A. Rafael, P.C. Grossi, F. Limeira-de-Oliveira GoogleMaps . Paratypes: 4 subadult ♀, 1 subadult Ƌ, 28 nymphs, same data as holotype [ INPA] GoogleMaps .

Etymology. The specific epithet refers to the type locality: Fernando de Noronha, Pernambuco, Brazil.

Diagnosis. Pararhagadochir noronhensis sp. nov. is closest to P. balteata . The male of P. noronhensis sp. nov. is 4.5 mm long, apterous; with antennal setae of uniform size over the entire length of the antennae; submentum quadrate; epiproct large, triangular, entirely sclerotized, extending the full length of the flap; the female is 7 mm long, and has 17 antennal segments. On the other hand, the male of P. balteata is 11 mm long and alate; with very long antennal setae on the basal half of segments and shorter setae on the apical half; submentum with sides caudally divergent to the basal third; epiproct small, not triangular, partially unsclerotized, not extending the full length of the flap; the female is 14 mm long and has 23 antennal segments.

Description. Male (holotype). Color details (based on specimen in alcohol): predominantly chestnut brown, with the exception of two intersomital white bands on thorax ( Fig. 2A, B View FIGURE 2 ). Body length 4.5 mm. Apterous.

Head subhexagonal, as long as wide, anterior region wider than the posterior region due to the small and slightly protruding eyes, occipital margin uniformly rounded ( Fig. 2C View FIGURE 2 ), length = 0.68 mm, width = 0.70 mm, OR = 0.73; two depigmented areas present, slightly visible ( Fig. 2C View FIGURE 2 ); occipital region with maculae indistinct in dorsal view. Antenna (incomplete) with 11–8 segments ( Figs. 2A, B View FIGURE 2 ). Mm visible, sclerotic, but less pigmented than Sm and well separated; submentum sclerotic, quadrangular, wider than long (2:1), anterior margin straight with the edges rounded ( Fig. 2D View FIGURE 2 ).

Hind basitarsus length = 0.16 mm, width = 0.08 mm; setae rows: 2 inner, 2 proximal, 3 outer; medial bladder present, circular, in the middle of the hind basitarsus, length = 0.02 mm, width = 0.02 mm ( Fig. 4A View FIGURE 4 ). Terminalia . 10L subquadrate, 10R wider basally, tapering distally to form the right process ( Fig. 3A View FIGURE 3 ). 10Rp1 prominent, sclerotic talon. MF narrow and arched ( Fig. 3A View FIGURE 3 ). Outer flange of 10Lp entirely translucent, the inner process curved outward and with same length as the outer flange ( Fig. 3A View FIGURE 3 ); Ep present, visible, in the cleft membrane, seemingly attached at the base of the MF. H sclerotic; Hp well developed, central, right curved, with many transverse lines on its anterior margin ( Fig. 3B View FIGURE 3 ); Lpp present, sclerotic ( Fig. 3B View FIGURE 3 ); LC1dp well developed, quadrate, echinulate. Length of the left cercus: LC1 = 0.27 mm, LC2 = 0.29 mm; width of the left cercus: LC1 = 0.09 mm, LC2 = 0.07 mm; length ratio of LC1/LC2 = 0.93.

Female subadult (Paratype). Color details (based on specimens in alcohol): same color pattern as male, but lighter ( Fig. 5A View FIGURE 5 ). Body length 7 mm.

Head circular, as long as wide ( Fig. 5C View FIGURE 5 ), length = 0.85 mm, width = 0.85 mm; eyes small, not protruding, OR = 0.88; three depigmented areas present, sometimes the central one barely discernible ( Fig. 5C View FIGURE 5 ); occipital region with four pairs of maculae visible in dorsal view, two larger lateral maculae reaching half of the head length, median macula smaller, and one contiguous central cordiform macula ( Fig. 5C View FIGURE 5 ); two more pairs of maculae visible in ventral view ( Fig. 5D View FIGURE 5 ). Antennae with 17–17 segments ( Figs. 5A, B View FIGURE 5 ). Mm and Sm slightly sclerotic; Sm quadrangular, wider than long (1.6:1) ( Fig. 5D View FIGURE 5 ).

Hind basitarsus slightly more robust than male, length = 0.19 mm, width = 0.10 mm; setal rows: 1 inner, 2 proximal, 3 outer; medial bladder present, ellipsoid, same position as in male, length = 0.07 mm, width = 0.04 mm ( Fig. 4B View FIGURE 4 ). Terminalia with 1st valvula slightly differentiated from the 8th sternum; 8th sternum with posterior margin uniformly rounded ( Figs. 6A, B View FIGURE 6 ).

Distribution. Brazil: Pernambuco, archipelago of Fernando de Noronha ( Fig. 1 View FIGURE 1 ).

Types condition. Holotype: Good, lacking right hind leg; both antennae missing their distal halves ( Figs. 2A, B View FIGURE 2 ). The four female paratype specimens apparently subadult (5th instar) based on morphological characteristics as some depigmented areas appear reabsorbed such as in the paraproct.

Intraspecific variation. Female paratypes exhibit lighter or darker shades of chestnut brown color, though never so dark as male.

Biology. The holotype male of P. noronhensis sp. nov. is apterous, an unusual characteristic for male webspinners. The reduction or absence of wings is probably induced by the secretion of the juvenile hormone, which is one of the factors responsible for the neotenization ( Iwanaga & Tojo 1986; Ross 2000). The amount and timing of secretion of juvenile hormone during nymphal instars influences directly the development of male wings: complete, when macropterous; partial, when subapterous or micropterous; or none, when apterous. All of these conditions can occur within the same species population. In arid environments, apterous males tend to remain inside the colony, mate with sisters, and consequently increase the probability of new males also being apterous. On the other hand, macropterous males living in more favorable environments can fly from colony to colony and perform random matings, thus decreasing the tendency to apterism ( Ross 2000). For Pararhagadochir the trend towards apterism has been observed at the population level in P. trachelia Navás, 1915 ( Szumik 2004) .

INPA

Instituto Nacional de Pesquisas da Amazonia

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Embioptera

Family

Scelembiidae

Genus

Pararhagadochir

Loc

Pararhagadochir noronhensis

Costa-Pinto, Paula J., Olivier, Renan S. & Rafael, José A. 2021
2021
Loc

Pararhagadochir

Rafael, J. A. & Limeira-de-Oliveira, F. & Hutchings, R. W. & Miranda, G. F. G. & Neto A. M. S. & Somavilla, A. & Camargo, A. & Asenjo, A. & Pinto, A. P. & Bello, A. M. & Dalmorra, C. & Mello-Patiu, C. A. & Carvalho, C. J. B. & Takiya, D. M. & Parizotto, D. R. & Marques, D. W. & Cavalheiro, D. O. & Mendes, D. M. M. & Zeppelini, D. & Carneiro, E. & Lima, E. F. B. & Lima, E. C. A. & Godoi, F. S. P. & Pessoa, F. A. C. & Vaz-de-Mello, F. Z. & Sosa-Duque, F. J. & Flores, H. F. & Fernandes, I. O. & Silva-Junior, J. O. & Gomes, L. R. P. & Monne, M. L. & Castro, M. C. & Silva, M. P. G. & Couri, M. S. & Gottschalk, M. S. & Soares, M. M. M. & Monne, M. A. & Rafael, M. S. & Casagrande, M. M. & Mielke, O. H. H. & Grossi, P. C. & Pinto, P. J. C. & Bartholomay, P. R. & Sobral, R. & Heleodoro, R. A. & Machado, R. J. P. & Correa, R. C. & Hutchings, R. S. G. & Ale-Rocha, R. & Santos, S. D. & Lima, S. & Mahlmann, T. & Silva, V. S. & Fernandes, D. R. R. 2020: 16
2020
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