Lepidocyrtus bilobatus, Mateos, Eduardo, 2008
publication ID |
https://doi.org/ 10.5281/zenodo.184638 |
DOI |
https://doi.org/10.5281/zenodo.5687726 |
persistent identifier |
https://treatment.plazi.org/id/038C0943-FFCD-FFB8-FF21-FF746FDF55FF |
treatment provided by |
Plazi |
scientific name |
Lepidocyrtus bilobatus |
status |
sp. nov. |
Lepidocyrtus bilobatus sp. nov.
Figs 2–20 View FIGURES 2 – 10 View FIGURES 11 – 13 View FIGURES 14 – 15 View FIGURE 16 View FIGURES 17 – 20 , Tab. 1 View TABLE 1
Type material. Spain, Salamanca (LOC139, see Tab. 1 View TABLE 1 and Fig. 1 View FIGURE 1 ), on herbaceous vegetation along the Alayón river, 2.viii.2007, E.Mateos coll. Holotype: female ( CRBA 1272) on 1 slide, paratypes: lot LP175 (unpigmented specimens) composed by 11 specimens prepared on slides and 80 specimens in alcohol, lot LP176 (pigmented and unpigmented specimes) composed by 4 specimens mounted on slides and 16 specimens in alcohol. Holotype and 7 paratypes mounted on slides deposited at the Centre de Recursos de Biodiversitat Animal, Faculty of Biology, University of Barcelona (http://www.crba.ub.edu): Slide CRBA 1341 with one pigmented specimen, slides CRBA 1342 and CRBA 1343 with one unpigmented specimen each, slide CRBA 1344 with two pigmented and two unpigmented specimens. Other paratypes deposited in the E. Mateos collection.
Etymology. The species name refers to the bilobed morphology of the ant. IV apical bulb, which is a diagnostic character for the new species within the European Lepidocyrtus fauna.
Description. Holotype body length (without head nor furca) 1 mm, paratypes 0.7–1.0 mm. Holotype body unpigmented; paratypes body color highly variable with yellow-white (form A) and purple (form B) specimens present in the same population ( Figs 2–3 View FIGURES 2 – 10 ); all specimens with purple pigment on anterior region of the head and ant. II–IV. Ocular areas densely black pigmented. Antenna, legs, and dorsal side of manubrium without scales. Body dorsoventrally compressed; mesothorax not projecting over the head.
Ratio antenna:cephalic diagonal = 1.5 for holotype, for paratypes 1.4–1.7; ant. I:II:III:IV = 1:1.9:2.1:3.6. Basis of ant. I dorsally with three microchaetae arranged in triangle. Ant. III organ as in Fig. 4 View FIGURES 2 – 10 . With bilobed nonretractile ant. IV apical bulb ( Fig. 5 View FIGURES 2 – 10 ). 8+8 eyes of equal size.
Smooth prelabral and labral setae in typical number 4/554; prelabral setae ciliated; the four labral setae of the third row are shorter, more curved, and with more developed insertion than setae of the other two rows; inverted U-shaped labral apical intrusion; with four rounded labral papillae ( Fig. 6 View FIGURES 2 – 10 ). Subapical seta of outer maxillary palp smooth and slightly longer than or subequal to apical seta, with three smooth setae on sublobular plate ( Fig. 7 View FIGURES 2 – 10 ). Outer differentiated seta of labial appendage curved, tip almost reaching the apex of the papilla ( Fig. 8 View FIGURES 2 – 10 ).
Labium anterior row (a1–a5) formed by smooth setae; posterior row formed by ciliated setae (M2R*EL1L2), with R half in length on seta M2 (marked as R*) ( Fig. 9 View FIGURES 2 – 10 ). Ventral cephalic groove with 3+3 ciliated macrochaetae and 2+2 scales.
The dorsal macrochaetae formula is R0R1R2STSo/10/0301+3, with a pair of supplementary macrochaetae R1s between R0 and R1 ( Fig. 10 View FIGURES 2 – 10 ). Maximum number of macrochaetae A on the head 9+9 ( Fig. 11 View FIGURES 11 – 13 ). Interocular chaetotaxy with s, t, r, q, p ciliated setae, without scales ( Fig. 12 View FIGURES 11 – 13 ). The th. II dorsal macrochaeta correspond to p3 ( Fig. 13 View FIGURES 11 – 13 ). Abd. II–III chaetotaxy as in Figs 14–15 View FIGURES 14 – 15 ; abd. II setae a2, m3 and m3e ciliated macrochaetae, seta a2p absent; abd. III seta m7a acuminate thin ciliated macrochaeta. Abd. IV chaetotaxy as in Fig. 16 View FIGURE 16 -A; trichobothrium T2 without accessory seta s; seta D1p ciliated and double in length than other setae of the trichobothrial complex ( Fig. 17 View FIGURES 17 – 20 ); seta Fe4 can be thin ciliated macrochaeta or smooth mesochaeta depending on the specimens ( Fig. 16 View FIGURE 16 -B). Bilateral asymmetries can be observed in some specimens in which Fe4 is thin ciliated macrochaeta on one side and smooth mesochaeta on the other; without correlation between the morphology of seta Fe4 and other characters like size, color pattern nor locality. Three posterior smooth mesochaetae on abd. IV present. All setae associated with the trichobothria on abd. II–IV are acuminate and strongly ciliate, except pi and pe on abd. IV which are fan-shaped.
V-shaped trochanteral organ formed by 6–8 smooth straight setae ( Fig. 18 View FIGURES 17 – 20 ). Unguis with basal pair teeth at 46 % of the inner edge, and with two inner teeth at 66 % (the bigger) and 83 % of the inner edge respectively; unguiculus lanceolate with finely serrated outer margin; spatulate tibiotarsal tenent hair ( Fig. 19 View FIGURES 17 – 20 ).
Ratio manubrium: dens: mucro = 23:21:1. Manubrial plate with 2 inner setae and 4–5 external setae ( Fig. 20 View FIGURES 17 – 20 ).
Ecology and distribution. All the individuals were obtained beating the herbaceous vegetation along the Alayón river.
Discussion. The bilobed antennal apical bulb is a diagnostic character that separates L. bilobatus sp. nov. from all other European species. The new species is very close to L. lusitanicus and L. selvaticus , from which it can be differentiated by abd. IV chaetotaxy: In L. bilobatus sp. nov. setae E1, De1 and E4p are ciliated macrochaetae ( Fig. 16 View FIGURE 16 ), whereas in the other two species are smooth mesochaetae ( Fig. 27 View FIGURES 26 – 27 ). The new species also differs from L. selvaticus by the presence of labial seta R (absent in L. selvaticus ) and by having 3+3 ciliated setae along ventral cephalic groove (2+2 ciliated and 1+1 smooth in L. selvaticus , see: Fig. 29 View FIGURES 28 – 29 ). As L. lusitanicus , the new species has high color pattern variability, with white ( L. bilobatus form A) and purple pigmented specimens ( L. bilobatus form B) living in the same population. The fact that specimens with different color pattern live together in the same population, suggests that body pigment distribution cannot be considered a good subspecific character in L. bilobatus sp. nov.; for this reason L. bilobatus form A and form B have been described as color forms and not as subspecies.
ref | code locality | province country | lat | long | elev date | method | species |
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a | LOC137 Bandeira | Coimbra Portugal | 40.2016 | -8.8798 | 241 29-07-07 | v | 1, 5 |
b | LOC126 Arrimal | Leiria Portugal | 39.4995 | -8.8712 | 320 12-07-07 | v | 4 |
c | LOC129 Pragais | Leiria Portugal | 39.5785 | -8.8221 | 308 18-07-07 | v | 1 |
d | LOC125 Mira | Coimbra Portugal | 40.4457 | -8.7988 | 13 08-07-07 | v | 5 |
e | LOC131 San Jacinto | Aveiro Portugal | 40.6706 | -8.7252 | 9 21-07-07 | v | 1, 2 |
f | LOC134 Arzila | Coimbra Portugal | 40.1830 | -8.5462 | 120 26-07-07 | v | 1, 2 |
g | LOC133 Taveiro | Coimbra Portugal | 40.2013 | -8.5376 | 4 26-07-07 | v | 3 |
h | LOC124 Curia | Coimbra Portugal | 40.4260 | -8.4655 | 42 08-07-07 | v | 2 |
i | LOC132 Coimbra | Coimbra Portugal | 40.2231 | -8.4458 | 34 25-07-07 | v | 1, 5, 3 |
j | LOC123 Buçaco | Coimbra Portugal | 40.3796 | -8.3763 | 243 08-07-07 | v | 1, 2 |
k | LOC135 Coimbra | Coimbra Portugal | 40.2227 | -8.3349 | 9 28-07-07 | v | 1, 3 |
l | LOC136 Casal de Santo Amaro | Coimbra Portugal | 40.2845 | -8.3046 | 165 28-07-07 | v | 2 |
m | LOC127 Gerês | Braga Portugal | 41.7371 | -8.1579 | 465 14-07-07 | v | 1 |
n | LOC128 Gerês | Braga Portugal | 41.7507 | -8.1528 | 720 14-07-07 | v | 1 |
o | LOC052 Pardieiros | Coimbra Portugal | 40.2168 | -7.9096 | 600 22-07-07 | v | 1 |
p | LOC138 El Casarito | Salamanca Spain | 40.5218 | -6.1382 | 1065 02-08-07 | v | 1, 4 |
q | LOC139 Sotoserrano | Salamanca Spain | 40.4110 | -6.0535 | 364 02-08-07 | v | 7 |
r | LOC120 Pina de Ebro | Zaragoza Spain | 41.4793 | -0.2415 | 400 31-05-07 | s | 3 |
s | LOC091 Vall d'Aran | Lleida Spain | 42.7755 | 0.7851 | 1450 17-07-06 | v | 1 |
t | LOC097 Taull | Lleida Spain | 42.5102 | 0.8779 | 1800 20-07-06 | s | 1 |
u | LOC108 Montsant | Tarragona Spain | 41.2370 | 0.8843 | 385 17-02-07 | v | 3 |
v | LOC156 Vila-seca | Lleida Spain | 41.6850 | 0.9434 | 230 29-05-08 | v | 3 |
w | LOC102 Prades | Tarragona Spain | 41.3594 | 1.0804 | 990 03-01-07 | v | 1 |
x | LOC101 Viladecavalls | Barcelona Spain | 41.5469 | 1.9601 | 200 25-10-06 | v | 6 |
y | LOC144 Blanes | Girona Spain | 41.6867 | 2.8165 | 2 28-02-08 | v | 6 |
z | LOC143 Tossa de Mar | Girona Spain | 41.7190 | 2.9028 | 2 21-02-08 | v | 6 |
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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