Research Article |
Corresponding author: Boonsatien Boonsoong ( fscibtb@ku.ac.th ) Academic editor: Lyndall Pereira-da-Conceicoa
© 2021 Boonsatien Boonsoong, Chonlakran Auychinda, Michel Sartori, Nuttakun Khanyom.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Boonsoong B, Auychinda C, Sartori M, Khanyom N (2021) First record of Paegniodes Eaton, 1881 (Ephemeroptera, Heptageniidae) from Thailand with description of a new species. ZooKeys 1036: 153-170. https://doi.org/10.3897/zookeys.1036.64880
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A new species of Heptageniidae, Paegniodes sapanensis sp. nov., is described based on larvae, subimagos, eggs, and COI data. The mayfly genus Paegniodes Eaton, 1881 is reported for the first time from Thailand. The larva of the new species can be distinguished from other known Paegniodes species by i) lamellae of gill I ca 1/4 of fibrilliform portion and ii) mandibles and basal segment of maxillary palp without dense setae on margin. The subimago characters useful to distinguish this new species from previously known species are i) the median stripes on abdominal terga and ii) shape of the female subgenital and subanal plates. The genetic distance between the new species and P. cupulatus (Eaton, 1871) was approximately 11%. The morphological characters of the new species are discussed and compared to other known species.
COI, diversity, mayfly, Southeast Asia
The poorly known mayfly genus Paegniodes, established by
In the past decade, knowledge about the diversity of the Heptageniidae in Thailand has continued to increase, and more species have been described and revised (
Here, we describe a new species of Paegniodes based on specimens from Nan province. In addition, the mitochondrial COI sequence data and a distribution map of the genus are provided.
Paegniodes larvae were collected by a hand-picking method from slow-flowing water in Nan Province in northern Thailand. The specimens were fixed and preserved in 95% ethanol for molecular and morphological studies. Mature larvae were reared using earthenware pots connected to an air supply until emergence of winged stages.
Measurements (given in mm) and photographs were taken using a NIKON SMZ800 stereoscopic microscope. For scanning electron microscopy (SEM), eggs were dried in a critical point drier (CPD7501) and coated with gold (Sputter Coater SC7620). The SEM photographs were obtained with a FEI Quanta 450 SEM. Final plates were prepared with Adobe Photoshop CC 2020.
The preserved specimens were dissected for DNA extraction. Total DNA was extracted using a genomic DNA purification kit (NucleoSpin, Macherey-Nagel, Germany), following the manufacturer’s protocol. The COI amplification was performed using LCO1490 and HCO2198 (
Sequenced specimens of the genus Paegniodes (new sequence indicated in bold).
The material is deposited in the collection of the Zoological Museum at Kasetsart University in Bangkok, Thailand (ZMKU) and at the Museum of Zoology in Lausanne, Switzerland (MZL).
Family Heptageniidae
Holotype. 1 female mature larva in alcohol, deposited in ZMKU, Thailand, Nan province, Bo Kluea district, Sapan waterfall, 19°11'25.8"N, 101°11'56.3"E, 800 m, 21.III.2020, B. Boonsoong leg.
Paratypes. 3 larvae in ethanol, deposited in ZMKU, same data as holotype; 2 larvae in ethanol, GBIFCH00834844, deposited in MZL same locality as holotype, 26.XI.2019, B. Boonsoong leg.; 1 male subimago (reared from larva), 2 female subimagos (reared from larvae), 2 larvae, all in ethanol, deposited in ZMKU, same locality as holotype, 29.XI.2020, B. Boonsoong leg.
Body length 16.2 mm (holotype) 10.0–13.5 mm (exuvia) 7.2–11.5 mm (immature), caudal filaments ca 1.5× of body length (immature).
General colouration dark brown with pale markings on tibiae and abdominal tergites.
Colouration
(Figs
Head. Head capsule. Ovoid in shape and flattened, 1.8–2.5 mm in length, 2.5–4.1 mm in width, brown, without distinct markings (Fig.
Antenna
(Figs
Labrum
(Fig.
Left mandible
(Fig.
Right mandible
(Fig.
Hypopharynx
(Fig.
Maxilla
(Fig.
Labium
(Fig.
Thorax. Foreleg (Fig.
Abdomen. Terga (Fig.
Gills
(Fig.
Caudal filaments
(Fig.
The main diagnostic characters are: i) lamellae of gill I ca 1/4 of fibrilliform portion, ii) mandibles without dense hair-like setae on lateral margin, iii) basal segment of maxillary palp without hairlike setae on margins, and iv) apical segment of labial palp slightly pentagonal with broad projection at apex.
Male subimago (in ethanol Fig.
Body length 8.5 mm, cerci 17.5 mm, forewing 10.9 mm, hindwing 1.5 mm.
Colouration
(Fig.
Paegniodes sapanensis sp. nov., male subimago A head and thorax (dorsal view) B forewing C hindwing D head and thorax (ventral view) E foreleg F middle leg G hind leg H abdomen (dorsal view) I abdomen (lateral view) J abdomen (ventral view) K genitalia (dorsal view) L genitalia (ventral view).
Head
(Fig.
Abdomen. Dorsally with ornamentation as in Fig.
Female subimago (in ethanol Fig.
Body length 12.8 mm, cerci 20.0 mm, forewing 14.4 mm, hindwing 2.6 mm.
Colouration
(Fig.
Head
(Fig.
Thorax
(Fig.
Abdomen. Dorsally with ornamentation as in Fig.
(dissected from female subimago). Length ca 155–175 µm, width ca 80–95 µm; elongate and oval in shape (Fig.
The diagnostic characters to distinguish our new species from P. cupulatus are: i) the median stripes on abdominal terga and ii) lateral margins of genital plates slightly concave near apex.
The specific epithet is named for the Sapan waterfall (Bo Kluea district; tourist attraction of Nan province, Thailand), where the holotype is known.
Nan province.
The specimens were collected from tropical mountain streams (Fig.
Two COI sequences of Paegniodes were retrieved from BOLD system and GenBank (Table
In this study, the morphology of the new species showed a close similarity to P. cupulatus (from China) in terms of mandibles, maxillary palp, gill I, and abdominal pattern (Table
Larval characters of Paegniodes sapanensis sp. nov. compared with known species (
Species | P. cupulatus | P. dao | P. sapanensis sp. nov. |
---|---|---|---|
Distribution | China | Vietnam | Thailand |
Mandibles | without dense hairlike setal field on lateral margin | with dense hairlike setal field on lateral margin | without dense hairlike setal field on lateral margin |
Basal segment of maxillary palp | without dense hairlike setal fields on anterior and posterior margins | with dense hairlike setal fields on anterior and posterior margins | without dense hairlike setal fields on anterior and posterior margins |
Number of comb-shape setae on the crown of the galea-lacinia | 9 | unknown | 8 |
Shape of labial palp segment II | apex with broad projection | apically rounded | apex with broad projection |
Number of apical denticles of tarsal claw | 3 | unknown | 2–3 |
Lamellae of gill I | 1/3 | rudimentary | 1/4 |
However, the new species can be separated from Paegniodes cupulatus by the colouration of mature nymphs of P. sapanensis sp. nov. which seem darker than that of P. cupulatus. On the abdominal terga of P. cupulatus, the pale dots are on both side of median stripe (
The molecular analysis clearly supports P. sapanensis sp. nov. as a species separate from P. cupulatus, as the genetic distance between the two species is 11%, which is much higher than the value of 3.5% generally considered to represent the maximum intraspecific divergence (
The combination characteristics of Paegniodes that distinguish it from all other genera in the subfamily Rhithrogeninae include: i) reduced lamellae on the gills I, ii) caudal filaments with interfacing setae, iii) short hindwings (usually less than 1/4 the length of the forewings), and iv) males having widely separated penes with strongly median titillators (
The distribution of the genus Paegniodes is limited to Southeast Asia (Fig.
This research has been supported by the Centre of Excellence on Biodiversity (BDC) Office of Higher Education Commission (BDC-PG2-161004). We are most grateful to our colleagues for assistance during field trips. We would like to thank the Department of Zoology and the Faculty of Science at Kasetsart University in Bangkok for their assistance and use of their facilities.