Liaghinella heldamariae, Castro-Huertas & Forero, 2017
publication ID |
https://doi.org/ 10.11646/zootaxa.4277.3.5 |
publication LSID |
lsid:zoobank.org:pub:D8DB26BA-0646-48B4-8F1B-A63F6B77E2F6 |
DOI |
https://doi.org/10.5281/zenodo.6020774 |
persistent identifier |
https://treatment.plazi.org/id/333587E1-D14C-FFCF-FF64-E6CEC5BC729B |
treatment provided by |
Plazi |
scientific name |
Liaghinella heldamariae |
status |
sp. nov. |
Liaghinella heldamariae View in CoL , sp. nov., Castro-Huertas & Forero
( Figs. 1 View FIGURE 1 , 2 View FIGURE 2 , 7 View FIGURE 7 )
Holotype: Female. COLOMBIA. Cundinamarca, Páramo de Monserrate, 3,230 m, 6 ii 1968, Sturm leg. / En hojas muertas de Espeletia grandiflora [in fallen leaves of Espeletia grandiflora ] / Liaghinella heldamariae sp. nov. Castro-Huertas & Forero 2017 ( ICN) . Paratypes: Female : Boyacá, Villa de Leyva, 30 dic 2003 / MUPJ _ ENT 0 0 41140 ( MPUJ) .
Other specimens examined: 2 nymphs, same locality data as holotype ( ICN).
Diagnosis. Recognized by a pair of medial spines on the posterior margin of the pronotum ( Fig. 1 View FIGURE 1 C‒E), clypeus with an anteriad projected sharp spine ( Fig. 1 View FIGURE 1 F), posterolateral angles of dorsal laterotergites flat ( Fig. 1 View FIGURE 1 B), and caudal margin of tergite 9 rounded ( Fig. 2 View FIGURE 2 C).
Description. Male: unknown.
Apterous female (total length, holotype 13.1 mm; head length, 1.6 mm; prothorax length, 2.1 mm; meso- and metathorax length, 2.2 mm; abdomen length, 7.2 mm).
Color. Head: Dorsally pale brown, ventrally dark brown ( Fig. 1 View FIGURE 1 F). Clypeus spine pale brown, second (first visible) and third (second visible) segments of the labium basally dark brown and apically whitish, third segment of the labium dark brown. Scapus pale brown, apically dark brown, flagellomeres dark brown. Thorax: dark brown with the posterior margin of the prothorax reddish ( Fig. 1 View FIGURE 1 D); coxal cavities dark brown; procoxae, protrochanter and profemur dark brown; protibia pale brown, distally dark brown; protarsus dark brown; meso- and meta coxae and trochanters dark brown, meso- and metafemur dark brown, meso- and meta tibiae pale brown with a dark brown narrow bands on sub-basal and apical regions, meso-and metatarsi dark brown. Abdomen: Dark brown, dorsally with a medial longitudinal darker band; medially interrupted in the tergites 1 and 2 and entire in the rest of tergites ( Fig. 1 View FIGURE 1 A).
Vestiture. Body covered with numerous setiferous tubercles. Head: Dorsally with setiferous tubercles, ventrally with sparse setae; antennal scapus with numerous, short setae; labium glabrous. Male genitalia: Gonapophysis 8 (gap8) with some sparse setae medially. Structure. Head: Elongated, interocular sulcus deep, clypeus with a projected sharp spine; eyes globose in dorsal view, ovoid in lateral view ( Fig. 1 View FIGURE 1 F); antenna slender, scapus the longest, first flagellomere the shortest; second (first visible) labial segment short, third (second visible) labial segment swollen basally, about as long as second, fourth (third visible) segment slender, about twice the length of the third segment. Thorax: Pronotum longer than wide, about as long as meso- and metanotum together; lateral angles of anterior margin with rounded tubercles, posterior margin with a pair of conspicuous medial spiniform process projected upward ( Figs. 1 View FIGURE 1 C‒E); meso- and metanotum flat, posterior margin of metanotum with a pair of short tubercles; stridulitrum narrow. Legs: Proleg distinctly wider and shorter than meso- and metalegs; procoxa elongate, profemur about three times as long as the protibia, wider profemur with posteroventral series composed by spiniform process and setae, and located near to the base of article ( Fig. 1 View FIGURE 1 D), anteroventral series composed by a row of setae, protibia ventrally with a row of triangular denticles, protibial comb present; protarsus one-segmented, about as long as protibia, with two claws; meso- and metalegs longer and slender than proleg. Abdomen: elongate, abdominal tergites I‒VI not produced on posterior margin ( Figs. 1 View FIGURE 1 A‒B), dorsal laterotergites with short projections on lateroposterior margin, not produced dorsad; posteromedial margin with an acute projection. Female genitalia ( Fig. 2 View FIGURE 2 ): Tergite 8 (T8) rectangular, with caudal margin (mpm8) rounded, medially flat ( Fig. 2 View FIGURE 2 C); tergite 9 (T9) nearly rectangular with the caudal margin (mpm9) entire and rounded ( Fig. 2 View FIGURE 2 C); gonocoxa 8 (gcx8) nearly quadrangular, short and wide, with the lateral anterior area produced into a prolongation (lap) nearly straight apically ( Fig. 2 View FIGURE 2 D); gonapophysis 8 (gap8) nearly triangular ( Fig. 2 View FIGURE 2 A); gonocoxa 9 (gcx9) elongated; gonapophysis 9 (gap9) small and elongated ( Fig. 2 View FIGURE 2 B); gonoplac (gpl) rounded, fused medially, with a subapical ventral projection and longer setae on the apical margin ( Fig. 2 View FIGURE 2 A, B); bursa copulatrix (bc) elongate, ventral medial surface of bursa copulatrix transversely striated, with ring gland (gr) present, situated transverse across the bursa ( Fig. 2 View FIGURE 2 A).
Etymology. This species is dedicated in memory of Mrs. Helda María Castro Moreno, V. Castro-Huertas´s grandmother (1936-2015). Thanks for to be an inspiration.
Biology. One of the examined specimens was collected on fallen leaves of Espeletia grandiflora Humboldt & Bonpland (1809) (Asteraceae) , a typical paramo species.
Distribution. Found on Monserrate, adjacent to Bogotá (Cundinamarca), and Villa de Leyva (Boyacá), Colombia.
Discussion. Despite having only female specimens, we are confident in considering this taxon as a new species, mainly by differences in the morphology of the genitalia, particularly in the structure of tergites 8 and 9.
The holotype was found with two immature specimens. The nymphs do not show any process on the posterior margin of the pronotum as in the adult, in contrast to what happens in L. tuberculata sp. nov. (see below), in which nymphs do exhibit a pair of tubercles on the posterior margin of the pronotum. We tentatively attribute these two examined nymphs to L. heldamariae sp. nov., at least until a greater series of immature specimens are examined and more accurately collected specimens where adults and positively associated nymphs become available. Forero (2007) examined a nymph of Liaghinella from Villa de Leyva that he attributed to L. andina . Nonetheless, given the problematic association of nymphs with adults and the scant information on the ontogenesis of these species, we regard the record of L. andina from Villa de Leyva dubious, until adults of this species are found.
Liaghinella heldamariae View in CoL sp. nov. and L. tuberculata View in CoL sp. nov. are further records of species of Liaghinella View in CoL in the Colombian high Andes View in CoL , in the remnants of Andean montane forests adjacent to urban areas, in contrast to L. farri View in CoL , known from Jamaica at approximately 900 meters of altitude ( Wygodzinsky 1966; Forero 2007). Liaghinella heldamariae View in CoL sp. nov. is the first record of this genus at altitudes over 3,000 meters. It is interesting to note that the type locality of L. heldamariae View in CoL sp. nov. is relatively close to the type locality of L. andina View in CoL , being only five kilometers apart ( Fig. 7 View FIGURE 7 ), whereas both localities of L. heldamariae View in CoL sp. nov. are set apart for about 150 km. The locality of Villa de Leyva is ambiguous with respect to the altitude. Villa de Leyva is at about 2,100 meter, although nearby are high mountains in which several habitats reach well beyond 3,000 meters, where paramo is found. It is probable that this specimen was collected at a higher altitude (see also below for discussion) similar to the altitude in which the holotype was found, but only further careful collecting will allow testing this idea.
Emesella nebulosa Dohrn, 1860 View in CoL , is another Metapterini View in CoL recorded from Bolivia and Colombia at remarkable high altitudes. Wygodzinsky (1966) mentioned as diagnostic characters for this species: the dorsal process of the pronotum, nodulose meso- and metalegs and the unique structure of prolegs. Because of the high altitude in which L. heldamariae View in CoL sp. nov. was found and the particular structure of the posterior margin of the pronotum with a pair of processes, Emesella View in CoL could be confused with L. heldamariae View in CoL sp. nov. or L. tuberculata View in CoL sp. nov. Nonetheless, there are morphological characters that allow separating Emesella View in CoL from Liaghinella View in CoL , such as the nodulose mid and hind legs present in Emesella View in CoL , or the particular structure of the prolegs as found in Liaghinella View in CoL .
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.
Kingdom |
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Class |
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Order |
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Family |
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SubFamily |
Emesinae |
Genus |
Liaghinella heldamariae
Castro-Huertas, Valentina & Forero, Dimitri 2017 |
Liaghinella heldamariae
Castro-Huertas & Forero 2017 |
L. tuberculata
Castro-Huertas & Forero 2017 |
Liaghinella heldamariae
Castro-Huertas & Forero 2017 |
L. heldamariae
Castro-Huertas & Forero 2017 |
L. heldamariae
Castro-Huertas & Forero 2017 |
L. heldamariae
Castro-Huertas & Forero 2017 |
L. heldamariae
Castro-Huertas & Forero 2017 |
L. tuberculata
Castro-Huertas & Forero 2017 |
L. andina
Forero 2007 |
Andes
Armenteras et al. 2003 |
Liaghinella
Wygodzinsky 1966 |
L. farri
Wygodzinsky 1966 |
Liaghinella
Wygodzinsky 1966 |
Liaghinella
Wygodzinsky 1966 |
Emesella nebulosa
Dohrn 1860 |
Emesella
Dohrn 1860 |
Emesella
Dohrn 1860 |
Emesella
Dohrn 1860 |