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Fig. 9 in Early and Middle Frasnian brachiopod faunas and turnover on the South China shelf

Fig. 9. Transverse serial sections of Desquamatia qiziqiaoensis sp. nov. Specimen PUM05017 (24.3 mm wide, 24.6 mm long, and 11.8 mm thick), acetate peel number: 05B, sample QZQ3, Qiziqiao section, Middle Frasnian. Numbers refer to distance in mm from the ventral apex.

Fig. 7 in Early and Middle Frasnian brachiopod faunas and turnover on the South China shelf

Fig. 7. Photographs of acetate peels of Desquamatia cf. kimberleyensis (Coleman, 1951) from the Middle Frasnian of the Panxi section, PUM05008, sample PY4 (same specimen as Fig. 5C). A. Left side at 0.8 mm. B. Left inner socket ridge at 2.2 mm showing combed knots (traces of muscle attachment?). C. Left tooth and socket at 3.2 mm.

Fig. 8 in Early and Middle Frasnian brachiopod faunas and turnover on the South China shelf

Fig. 8. Atrypid Desquamatia qiziqiaoensis sp. nov. from the Middle Frasnian of the Panxi and Qiziqiao sections. A. PUM05012, sample PY5, Panxi section, probably Middle Frasnian, dorsal (A1), ventral (A2), posterior (A3), anterior (A4), and lateral (A5) views showing the general shape of a silicified specimen, 22.2 mm wide, 20.6 mm long, 12.9 mm thick. B. PUM05013, sample PY5, Panxi section, probably Middle Frasnian, ventral view showing nature of ribbing and concentric growth lamellae of a non−silicified specimen, 19.9 mm wide, 19.3 mm long, 11.8 mm thick. C. PUM05014 (holotype), sample QZQ1–3, Qiziqiao section, Middle Frasnian, dorsal (C1), ventral (C2), lateral (C3), posterior (C4), and anterior (C5) views. D. PUM05015, sample QZQ3, Qiziqiao section, Middle Frasnian, posterior (D1), anterior (D2), dorsal (D3), ventral (D4), and lateral (D5) views. E. PUM05016, sample QZQ3, Qiziqiao section, Middle Frasnian, dorsal (E1, E5), ventral (E2, E7), posterior (E3), anterior (E4), and lateral (E6) views.

Fig. 6 in Early and Middle Frasnian brachiopod faunas and turnover on the South China shelf

Fig. 6. Transverse serial sections of Desquamatia cf. kimberleyensis (Coleman, 1951), PUM05008, sample PY4, Panxi section, probably Middle Frasnian, specimen figured in Fig. 5C. Acetate peel number: 05A. Numbers refer to distance in mm from the ventral apex.

Fig. 4 in Early and Middle Frasnian brachiopod faunas and turnover on the South China shelf

Fig. 4. Strophomenid and rhynchonellid brachiopods from the Early and Middle Frasnian of the Panxi and Caiziyan sections. A. Sulcatostrophia? bunapica Veevers, 1959a, PUM05001, sample PY5, Panxi section, Middle Frasnian, dorsal (A1), ventral (A2), area (A3) views, and enlargement of framed area in image A1 (A4). B. Phlogoiderhynchus squamosus (Wang, 1956), PUM05002, sample PY3, Panxi section, Early Frasnian, dorsal (B1), lateral (B2), and posterior (B3) views. C. Phlogoiderhynchus depressus (Wang, 1956), PUM05003, sample PY2, Panxi section, Early Frasnian, dorsal view. D. Pugnax cf. triplicata (Chen in Xu et al. 1978), PUM05004, sample GC20, Caiziyan section, Early Frasnian, lateral (D1: ventral beak broken), dorsal (D2), and anterior (D3: left anterior broken, right lateral anterior slightly broken) views. E. Coeloterorhynchus sp., PUM05005, sample GC21−24, Caiziyan section, Early Frasnian, dorsal (E1: right anterior and right lateral broken), posterior (E2), and lateral (E3) views.

Fig. 3 in Early and Middle Frasnian brachiopod faunas and turnover on the South China shelf

Fig. 3. Brachiopod distribution in the Early and Middle Frasnian of South China. (from Chen 1983; 1984; Hou 1988; Sartenaer and Xu 1991; Ma et al. 2005; this study, and our unpublished data). Species of "Ningbingella" and "Ypsilorhynchus" needs confirmation of their generic status. Abbreviations: K., Klapperina; M. Mesotaxis; Pa., Palmatolepis.

Fig. 2 in Early and Middle Frasnian brachiopod faunas and turnover on the South China shelf

Fig. 2. Stratigraphy and distribution of Early and Middle Frasnian brachiopods in South China. Most but not all known brachiopods are described and illustrated in this paper. For the distribution of atrypids in the Dushan section, for example, see Ma et al. (2005). The stratigraphy of Panxi and the occurrence of Cyrtospirifer sp. are based on Yunnan compiling group (1978) and the occurrence of Stringocephalus in the lower part of the Yidade Formation is as in Xian et al. (1988: 148). The stratigraphy of Dushan and the occurrence of Stringocephalus sp. are as in Liao et al. (1979); the Caiziyan section was re−measured by Long−Ming Wei, Xue−Ping Ma, and Hua Li (personal communication 2005), with coral identifications by Wei−Hua Liao. The stratigraphy of Qiziqiao is based on data of Z.−X. Hu and Z.−Q. Deng in Tan et al. (1987), and the occurrence of Yunnanella sp. is based on Zu−Han Liu (personal communication 2001). Abbreviations: calc., calcareous; argill., argillaceous; C., Cyrtospirifer; Pa., Palmatolepis; Po., Polygnathus; S., Spinatrypina.

Fig. 1 in Early and Middle Frasnian brachiopod faunas and turnover on the South China shelf

Fig. 1. Geographic map of China (A) and locations of the stratigraphic sections (Δ) investigated in this study (B).

Frasnian, lateral (B1), ventral (B2), anterior (B3), posterior (B4), and dorsal (B5) views of a rounded exfoliated shell, 27.7 mm wide, 25.6 mm long, and about 14.5 mm thick. C. PUM05008, sample PY4, Panxi section, probably Middle Frasnian, lateral (C1), dorsal (C2), and ventral (C3) views of the sectioned specimen (Fig. 6). D. PUM05009, sample PY5, Panxi section, probably Middle Frasnian, ventral beak broken, showing small conjunct deltidial plates (note that true foramen (approximately dashed line) takes up only a small part at the bottom of the seen later enlarged hole). E. PUM05010, sample PY5, Panxi section, probably Middle Frasnian, posterior (E1), lateral (E2), anterior (E3), ventral (E4), and dorsal (E5) views, 26.7 mm wide, 27.7 mm long, 18.5 mm thick, adpressed ventral beak. F. PUM05011, sample GC22, Caiziyan section, Early Frasnian, dorsal view. in Early and Middle Frasnian brachiopod faunas and turnover on the South China shelf

Frasnian, lateral (B1), ventral (B2), anterior (B3), posterior (B4), and dorsal (B5) views of a rounded exfoliated shell, 27.7 mm wide, 25.6 mm long, and about 14.5 mm thick. C. PUM05008, sample PY4, Panxi section, probably Middle Frasnian, lateral (C1), dorsal (C2), and ventral (C3) views of the sectioned specimen (Fig. 6). D. PUM05009, sample PY5, Panxi section, probably Middle Frasnian, ventral beak broken, showing small conjunct deltidial plates (note that true foramen (approximately dashed line) takes up only a small part at the bottom of the seen later enlarged hole). E. PUM05010, sample PY5, Panxi section, probably Middle Frasnian, posterior (E1), lateral (E2), anterior (E3), ventral (E4), and dorsal (E5) views, 26.7 mm wide, 27.7 mm long, 18.5 mm thick, adpressed ventral beak. F. PUM05011, sample GC22, Caiziyan section, Early Frasnian, dorsal view.

opencc-by-4.0Dec 2020View details →

Table 3 in Neohexostoma gymnosardae n. sp. (Monogenea, Hexostomatidae), a gill parasite of Gymnosarda unicolor (Valenciennes) (Teleostei, Scombridae) in the South China Sea

Table 3. Measurements of Neohexostoma gymnosardae n. sp. from Gymnosarda unicolor from the South China Sea, and Neohexostoma spp.<table><tbody><tr><th></th><th>N. gymnosardae</th><th>N. mochimae N. kawakawa</th><th>N. thunninae</th><th>N. euthynni</th><th>N. extensicaudum N. robustum</th><th>N. pricei</th></tr></tbody><tbody><tr><th></th><td>n. sp.</td><td>Fuentes-Zambrano,</td><td>Yamaguti,</td><td>(Parona &</td><td>(Meserve,</td><td>(Dawes, 1940)</td><td>Price, 1961</td><td>(Koratha,</td></tr><tr><th></th><td></td><td>1997</td><td>1968</td><td>Perugia,</td><td>1938)</td><td></td><td></td><td>1955)</td></tr><tr><th></th><td></td><td></td><td></td><td>1889)</td><td></td><td></td><td></td><td></td></tr><tr><th>Hosts Gymnosarda unicolor</th><td>Auxis thazard</td><td>Euthynnus</td><td>Thynnus</td><td>Euthynnus alleteratus</td><td>Thunnus thynnus Thunnus obesus Sarda sarda</td></tr><tr><th></th><td></td><td></td><td>yaito</td><td>thunninae</td><td>[Euthynnus lineatus]</td><td></td><td>(Parathynnus</td><td></td></tr><tr><th></th><td></td><td></td><td>Neothunnuus</td><td></td><td></td><td></td><td>sibi)</td><td></td></tr><tr><th></th><td></td><td></td><td>macropterus</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Locality</th><td>South China Sea, P.</td><td>Venezuela, A.</td><td>Hawaii, P.</td><td>Italy, M.</td><td>Galapagos Islands, P.</td><td>English</td><td>Tropical Pacific Texas, A.</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>[Baja California, P.]</td><td>Channel, A.</td><td></td><td></td></tr><tr><th>Source</th><td>Present study</td><td>[35]</td><td>[34]</td><td>[24, 25]</td><td>[20] [21]</td><td>[7]</td><td>[26]</td><td>[17]</td></tr><tr><th>Body length 9660–18800 (13827)</th><td>4444–6166 (5093)</td><td>4900–8400</td><td>11,000–12,000</td><td>5853 [3570–5850]</td><td>11,000</td><td>17,000</td><td>4500</td></tr><tr><th>Body width</th><td>2875–5375(3847)</td><td>874–1160 (1011)</td><td>70–180</td><td>2000</td><td>953 [740–950]</td><td>3300</td><td>4000–4700</td><td>400–850</td></tr><tr><th>Haptor length 1172–1810 (1 446)</th><td>665–1140 (903)</td><td></td><td></td><td>953</td><td></td><td></td><td>440</td></tr><tr><th>Haptor width</th><td>1369–2582 (1827)</td><td>1273–1615 (1444)</td><td>1200–1550</td><td>1500</td><td>1300</td><td></td><td></td><td>750–850</td></tr><tr><th>Clamps</th><td>1st pair: 275–506</td><td>Anterior 3 clamps:</td><td>224–370</td><td>1st pairs:</td><td>203 × 339 [Anterior 3</td><td>0.067**</td><td>1st pair:</td><td>Anterior two pairs:</td></tr><tr><th></th><td>× 505–697</td><td>122–209</td><td>× 200–230</td><td>275 × 220</td><td>clamps:</td><td></td><td>500 × 750</td><td>500 × 340</td></tr><tr><th></th><td>(415 × 594)</td><td>× 200–315</td><td></td><td></td><td>153–255 × 221–403,</td><td></td><td></td><td></td></tr><tr><th></th><td></td><td>(164 × 250)</td><td></td><td></td><td>posterior-most pair:</td><td></td><td></td><td></td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>156–238 × 194–332]</td><td></td><td></td><td></td></tr><tr><th></th><td>2nd pair: 327–477</td><td>Posterior clamp:</td><td></td><td>2nd pairs:</td><td></td><td>0.030***</td><td>2nd pair:</td><td>3rd pair:</td></tr><tr><th></th><td>× 577–713</td><td>94–177 ×</td><td></td><td>225 × 180</td><td></td><td></td><td>600 × 850</td><td>460 × 340</td></tr><tr><th></th><td>(395 × 620)</td><td>117–198 (126 × 166)</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td>3rd pair: 302–455</td><td></td><td></td><td></td><td></td><td></td><td>3rd pair:</td><td>4th pair: 375 × 300</td></tr><tr><th></th><td>× 475–624</td><td></td><td></td><td></td><td></td><td></td><td>500 × 670</td><td></td></tr><tr><th></th><td>(376 × 587)</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td>4th pair: 233–358</td><td></td><td></td><td></td><td></td><td></td><td>4th pair:</td><td></td></tr><tr><th></th><td>× 389–496</td><td></td><td></td><td></td><td></td><td></td><td>350 × 500</td><td></td></tr><tr><th></th><td>(316 × 447)</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Oral sucker</th><td>62–99 ×</td><td>29–30 ×</td><td>28–45*</td><td></td><td>56 × 40[27–56 × 24–40]</td><td>– × 100</td><td></td><td>40 × 30</td></tr><tr><th></th><td>51–102 (83 × 70)</td><td>28–30(30 × 29)</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Pharynx</th><td>63–93 ×</td><td>40–13 ×</td><td>40–58 ×</td><td></td><td>[44–68 × 26–36]</td><td>100 × 70</td><td></td><td>75 × 45</td></tr><tr><th></th><td>49–58 (82 × 55)</td><td>24–29 (42 × 26)</td><td>23–35</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Vagina</th><td>244–359 ×</td><td>10–40 (35)*</td><td>Pads: 60–80</td><td>54*</td><td></td><td>600 × 350</td><td></td><td>Right pad: 55 × 24</td></tr><tr><th>191–250 (302 × 221)</th><td></td><td>× 20–30</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>Left pad: 70 × 24</td></tr><tr><th>Genital atrium 92–321 ×</th><td></td><td>40–70*</td><td></td><td></td><td>600 × 300</td><td></td><td></td></tr><tr><th>112–348 (225 × 228)</th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Large anchor</th><td>43–57 (50)</td><td>34–90(64)</td><td>85–105</td><td>135</td><td>68 [85–120]</td><td>75</td><td>100</td><td>145</td></tr><tr><th>Small anchor</th><td>39–42(41)</td><td>20–31(25)</td><td>20–40</td><td>45</td><td>34 [24 – 34]</td><td>15</td><td>40</td><td></td></tr><tr><th>Eggs</th><td>125–193 ×</td><td>182–196 ×</td><td>180–260 ×</td><td>270 × 91</td><td>168–203 × 72–80</td><td>250 × 150</td><td>220 × 110</td><td></td></tr><tr><th></th><td>91–137 (156 × 114)</td><td>74 (196 × 74)</td><td>70–160</td><td></td><td>[103–221 × 44–105]</td><td></td><td></td><td></td></tr><tr><th>Egg filaments 411–719 (518)</th><td></td><td>up to 200</td><td></td><td>100 [anterior: 100–179,</td><td>250</td><td></td><td></td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>posterior: 100–161]</td><td></td><td></td><td></td></tr><tr><th>Testes number 185–246</th><td>30–35</td><td>13–35</td><td></td><td>26 [32 –40]</td><td></td><td>Numerous</td><td></td></tr></tbody></table>The width of the body given for N. extensicaudum is that of the third region. The data for N. euthynni in square brackets are from Millemann (1956) [21].* Diameter. ** Ratio large clamp/body length. *** Ratio small clamp/body length. A., Atlantic Ocean. M., Mediterranean Sea. P., Pacific Ocean.

opencc-by-4.0Dec 2020View details →

Table 1 in Neohexostoma gymnosardae n. sp. (Monogenea, Hexostomatidae), a gill parasite of Gymnosarda unicolor (Valenciennes) (Teleostei, Scombridae) in the South China Sea

Table 1. Species of monogeneans used in the molecular analyses.<table><tbody><tr><th>Species</th><th>Family</th><th>Accession No.</th><th>Reference</th></tr></tbody><tbody><tr><th>Neohexostoma gymnosardae n. sp.</th><td>Hexostomatidae</td><td>MN242399</td><td>Present study</td></tr><tr><th>Hexostoma thynni (Delaroche, 1811) Rafinesque, 1815</th><td>Hexostomatidae</td><td>EF653383</td><td>[1]</td></tr><tr><th>Diplostamenides sciaenae (Goto, 1894) Mamaev, 1986</th><td>Microcotylidae</td><td>FJ432589</td><td>Direct submission</td></tr><tr><th>“ Cynoscionicola branquialis ”</th><td>Microcotylidae</td><td>AF382050</td><td>[23]</td></tr><tr><th>Diclidophora denticulata (Olsson, 1876) Price, 1943</th><td>Diclidophoridae</td><td>AF382047</td><td>[23]</td></tr><tr><th>Urocotyle nibae Zhang & Xiao in Zhang, Yang & Liu, 2001</th><td>Diclidophoridae</td><td>FJ432588</td><td>Direct Submission</td></tr><tr><th>Gotocotyla bivaginalis (Ramalingam, 1961) Rohde, 1976</th><td>Gotocotylidae</td><td>AF382039</td><td>[23]</td></tr><tr><th>Gotocotyla secunda (Tripathi, 1954)</th><td>Gotocotylidae</td><td>AF382040</td><td>[23]</td></tr><tr><th>Pseudohexabothrium taeniurae Agrawal, Chisholm & Whittington, 1996</th><td>Hexabothriidae</td><td>AF382035</td><td>[23]</td></tr><tr><th>Hypanocotyle bullardi Chero, Cruces, Sáez, Camargo, Santos & Luque, 2018</th><td>Hexabothriidae</td><td>MG591249</td><td>[5]</td></tr><tr><th>Polystoma gallieni Price, 1938</th><td>Polystomatidae</td><td>AF382064</td><td>Direct Submission</td></tr></tbody></table>“ Cynoscionicola branquialis ” was accepted as “ Cynoscionicola branchialis ”, but in a status of taxon inquirendum. Gotocotyla secunda (Tripathi, 1954) was accepted as Gotocotyla acanthura (Parona & Perugia, 1896) Meserve, 1938.

opencc-by-4.0Oct 2024View details →

The in situ Mg/Ca ratios of planktonic foraminifera shells in the northeastern South China Sea: an attempt to get efficient and reliable proxies

Planktonic foraminifera are one of the important carriers of the physico-chemical environments. Nowadays, the development of in situ microanalysis technology provides a new opportunity for further understanding the distribution and variation of trace element concentrations in foraminifera shells. In this study, we focus on the in situ Mg/Ca ratios in four planktonic foraminifera shells from the surface sediments of the northeastern slope of the South China Sea (SCS). The results of electron microprobe mapping indicate that G. ruber had periodic bands of high Mg contents and Mg/Ca ratios, consistent with the results of LA-ICP-MS. In contrast, N. dutertrei, P. obliquiloculata, and G.inflata had thick calcite layer with low Mg contents and Mg/Ca ratios. The Mg/Ca ratios of shells may be attributed to symbionts, but the physiological regulation may also have some contributions. Meanwhile, contaminants may lead to the relatively higher Mg/Ca ratios. Therefore, the large Mg/Ca variations in foraminifera shells are not only affected by the surrounding seawater temperature but also constrained by other factors. At last, we employed this method to reconstruct the Mg/Ca-SST in the northeastern SCS over the past ~3000 years. The similar trend to the previous SST records proves that this method is reliable. We hope that this method can be widely applied in the future due to the efficient, fast, and high spatial resolution with small sample amounts.

opencc-zeroJan 2024View details →

Linked collectors and determiners for: Vascular plants of south-central China.

Natural history specimen data linked to collectors and determiners held within, "Vascular plants of south-central China". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/861f9a3c-f762-11e1-a439-00145eb45e9a">https://bionomia.net/dataset/861f9a3c-f762-11e1-a439-00145eb45e9a</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/861f9a3c-f762-11e1-a439-00145eb45e9a">https://gbif.org/dataset/861f9a3c-f762-11e1-a439-00145eb45e9a</a>. Formatted as a Frictionless Data package.

opencc-zeroJan 2024View details →

Linked collectors and determiners for: The talitrid amphipod genus Talorchestia from the South China Sea to the Indonesian Archipelago (Crustacea, Senticaudata).

Natural history specimen data linked to collectors and determiners held within, "The talitrid amphipod genus Talorchestia from the South China Sea to the Indonesian Archipelago (Crustacea, Senticaudata)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/4b84979a-e3de-4956-b9c7-91e178dd46b1">https://bionomia.net/dataset/4b84979a-e3de-4956-b9c7-91e178dd46b1</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/4b84979a-e3de-4956-b9c7-91e178dd46b1">https://gbif.org/dataset/4b84979a-e3de-4956-b9c7-91e178dd46b1</a>. Formatted as a Frictionless Data package.

FIG. 3. — Sinella colorata n in Two syntopic and remarkably similar new species of Sinella and Coecobrya from South China (Collembola, Entomobryidae)

FIG. 3. — Sinella colorata n. sp.: A, chaetotaxy of Abd. V; B, anterior face and lateral flap of ventral tube; C, posterior face of ventral tube; D, distal part of dens and mucro; A, macrochaetae and large ordinary chaetae represented by their sockets; s-chaetae represented in full. Scale bars: A, D, 25 μm; B, C, 10 μm.

FIG. 4. — Coecobrya mulun n in Two syntopic and remarkably similar new species of Sinella and Coecobrya from South China (Collembola, Entomobryidae)

FIG. 4. — Coecobrya mulun n. sp.: A, lateral process of labial palp; B, maxillary outer lobe; C, chaetae on labium and ventral side of the head; D, dorsal cephalic chaetotaxy; E, thoracic chaetotaxy; F, trochanteral organ; G, hind claw; H-J, abdominal chaetotaxy; H, Abd. I-III; I, Abd. IV; J, Abd. V; K, anterior face and lateral flap of ventral tube; L, posterior face of ventral tube; M, distal part of dens and mucro; D, E, H-J, macrochaetae and large ordinary chaetae represented by their sockets; s-chaetae represented in full. Scale bars: A-C, 10 μm; D, F, G, J-M, 25 μm; E, H, I, 50 μm.

FIG. 2. — Sinella colorata n in Two syntopic and remarkably similar new species of Sinella and Coecobrya from South China (Collembola, Entomobryidae)

FIG. 2. — Sinella colorata n. sp.: A, lateral process of labial palp; B, maxillary outer lobe; C, chaetae on labium and ventral side of the head; D, dorsal cephalic chaetotaxy (eyes are represented by their pigment trace, which has migrated anteriorly during the clearing process); E, thoracic chaetotaxy; F, trochanteral organ; G, hind claw in lateral view, with detail of basal teeth in dorsal view; H, I, abdominal chaetotaxy; H, Abd. I-III; I, Abd. IV; D, E, H, I, macrochaetae and large ordinary chaetae represented by their sockets; s-chaetae represented in full. Scale bars: A, B, 10 μm; C, D, F, G, 25 μm; E, H, I, 50 μm.

FIG. 1 in Two syntopic and remarkably similar new species of Sinella and Coecobrya from South China (Collembola, Entomobryidae)

FIG. 1. — Habitus of Collembola from South China: A, B, two views of Sinella colorata n. sp. (1.2 mm); C, D, two views of Coecobrya mulun n. sp. (1.3 mm).

opencc-by-4.0Jun 2012View details →

Figs. 2–3 in A new species of the flat-footed fly genus Callomyia (Diptera: Platypezidae) from South China

Figs. 2–3. Callomyia triangulata sp. nov., female: 2 – head, anterior view; 3 – antenna, lateral view.