Gomphidae is a cosmopolitan insect family of Odonata (dragonflies and damselflies) with over 980 species (Dijkstra et al., 2013). The family is diverse in streams and rivers, but also has several species that inhabit lentic environments (e.g., ponds, lakes) (Garrison, von Ellenrieder & Louton, 2006). Taxonomically, the adults in this group of dragonflies have been well-studied, although new species are frequently described. In contrast, and similar to most insect groups, the immature stages are poorly known. Garrison, von Ellenrieder & Louton (2006) report 255 species of gomphids for the New World, with only 177 of them known as larvae (69%). This lack of knowledge of the larval stages greatly limits our ability to understand the ecological role of insects in their ecosystems.
The genus Epigomphus is a poorly-known group of gomphids that inhabits small streams and rivers in the neotropics. Epigomphus comprises 28 species (Garrison, von Ellenrieder & Louton, 2006), but only six are known as larvae (larval descriptions in parentheses): E. paludosus Hagen in Selys, 1854 (Martins, 1968); E. echeverrii Brooks, 1989, E. subobtusus Selys, 1878, E. subsimilis Calvert, 1920 (all three by Ramírez, 1996); E. hylaeus Ris, 1918 (Fleck, 2002); and E. crepidus Kennedy, 1936 (Novelo-Gutiérrez, Gómez-Anaya & Smith-Gómez, 2015). In this paper, a detailed description and illustrations of the larvae of E. jannyae Belle and E. tumefactus Calvert are provided, based upon a specimen found emerging at the field, and reared larvae, respectively. Both species have restricted distributions and have been reported from a single country, E. jannyae is endemic to Panama and E. tumefactus to Costa Rica.
Materials & Methods
Epigomphus larvae were collected in Panama and Costa Rica. Larvae were collected from the stream bottom and transported alive to the laboratory. Individuals emerging in the field were also collected. The male exuvia of E. jannyae was preserved in 96% ethanol while the teneral imago was maintained alive for a couple of days before it died and then preserved in ethanol. A couple of last instars (i.e., F–0) larvae of E. tumefactus were reared until emergence; another two F–0 larvae die and were preserved in ethanol. Emerged adults were identified using original descriptions and comparisons with identified specimens deposited at the Instituto de Ecología, A.C., Xalapa, Mexico.
Mandible nomenclature follows Watson (1956); labium nomenclature follows Corbet (1953). Photographs were obtained with a CANON PowerShot G10 digital camera mounted on a stereomicroscope ZEISS Stemi 2000-C. Measurements (in mm) were made with a calibrated ocular micrometer as follows: Head width, across compound eyes; total length, dorsally from anterior-most margin of labrum to tips of caudal appendages; abdomen length, ventrally from anterior margin of segment 1 to posterior margin of segment 10; hind femur, along midline of external surface. S1–10 = abdominal segments 1–10.
Epigomphus jannyae Belle
Material. One exuvia (male, emerged in the field). PANAMA: Panamá Oeste Province, Capira District, Altos de Campana Park, Sendero Panamá, stream (08°41.033N; 79°55.528 W, 835 masl), 25 April 2015 (1 male exuvia, emerged around noon), D. Delgado, A. Ramírez, R. Novelo leg. Deposited in the Colección Entomológica del Instituto de Ecología, A.C., Xalapa (IEXA).
Description. Medium-sized exuvia, body robust, antennae, legs, sides of thorax and abdomen setose, gently tapering caudad, body light yellow-brown and lacking any particular pattern (Fig. 1).
Head: Wider than long, even wider than pro- and mesothorax and basal abdomen (Fig. 1A). Labrum 0.6 mm long, mostly bare, anterior border with dense brush of golden setae, flattened ventrally; anteclypeus bare; postclypeus, frons, vertex and occiput finely granulose; a tuft of long, upturned, golden setae on fronto-lateral margins of frons; occiput mostly granulose with some bare, irregular areas and with long, golden setae on occipital lobes, anterior margin of frons concave. Antennae 4-segmented (Figs. 1A and 2A), covered with some sparse granuli on dorsum; scape globose, pedicel subglobose, both with abundant, small, scale-like setae on apical margin; 3rd antennomere largest, claviform, flattened dorso-ventrally, 1.6 times longer than its widest part, lateral and apical margins beset with abundant, small, scale-like setae, tightly packed on apical margin; dense rows of long, yellowish setae on lateral margins, those on external margins longest, those on internal margins stiff, with small, regularly spaced, circular structures close to the borders; 4th antennomere a small sphere; scape, pedicel and 3rd antennomere yellow brown, 4th antennomere reddish-brown, length proportions: 0.34, 0.15, 1.0, 0.06. Occipital lobes rounded, bulging; a well-developed longitudinal carina beset with small, stiff setae on each side of ventral surface of head (Fig. 1B). Mandibles (Fig. 3) with molar crest, formula: L 1234 0 a(m1,2,3,4b)/R 1234 y a(m1,2)b, in both mandibles tooth a > b. Maxillae: Galeolacinia (Fig. 4) with seven moderately incurved teeth; three dorsal teeth more or less of same length and robustness and four ventral teeth of different size, apical one largest; maxillary palp thick and robust. Ventral pad of hypopharynx pentagonal, whitish, soft, with a row of antero-ventral, subapical, long, stiff setae and a latero-basal triangular-shaped sclerite to each side of midline. Labium: Prementum-postmentum articulation reaching posterior margin of procoxae (Fig. 1B). Prementum reddish-yellow, subquadrate, as long as its widest part (Fig. 5A); lateral margins with long whitish setae, slightly sinuate at apical 0.60, slightly sinuate and moderately convergent on basal 0.40; basal margin sinuate, without a longitudinal, central sulcus on ventral surface (Fig. 5A); a small, shallow, concavity just below ligula beset with some long setae (Fig. 5B). Ligula poorly developed (Fig. 5B), apical margin slightly convex, with a ventral row of 10 reddish-brown, short, truncate teeth on middle and a dorsal row of short, stout piliform setae. Labial palp stout (Figs. 5A–5B), reddish-brown, with abundant, long delicate, whitish setae on external surface; apical lobe stout, tip rounded and smooth, internal margin concave with 10–12 small teeth, the basal 6–7 teeth truncate and very close each other, remaining 4–5 teeth acutely pointed and more separate each other; external margin gently convex and smooth; movable hook reddish-brown, almost as long as palp, sharp and moderately incurved.
Thorax: Pro- and mesothorax slightly narrower than head, setose on inferior border of pro-and mesopleura. Anterior margin of pronotum straight, lateral margins convex and bulging (similar to Fig. 7), posterior margin convex; a large, subquadrate glabrous area on each side of midline, remainder of pronotum granulose. Meso and metathorax granulose, some tufts of long, curled setae on inferior borders of meso- and metapleura, meso- and metaspiracles evident. Legs short (e.g., when fully extended, hind legs scarcely reaching posterior margin of abdominal segment 7), strongly setose (Fig. 1), with long, yellow-brown, delicate setae mainly on sides and shorter, stiff, reddish setae mainly on anterior surfaces of tibiae and tarsi; burrowing hooks moderately developed (Fig. 1); dorsal margins of metafemora the same length as metatibiae; tarsal formula 2-2-3, claws simple, with a pulvilliform empodium. Wing sheaths reaching posterior margin of S3, strongly divergent (Fig. 1A), mostly granulose, with abundant long, delicate setae on borders.
Abdomen: Yellow-brown; light reddish-brown on middle third of tergites 8–9, and the whole surface of S10 (Figs. 1 and 6A–6B); more or less spindle-shaped, ventral surface flat, dorsal surface convex, lacking dorsal protuberances, widest on S5–6; lateral margins of S1–7 with long, stiff yellowish setae, shorter on S8–10; lateral margins of S5–9 serrate (Figs. 1 and 6A), serrations on S5 very small and only visible in lateral and ventral views, serrations on S6–9 short and stout, dark reddish-brown; S6–9 ending in short (very small on S6 and only visible ventrally), triangular, divergent spines increasing in size and robustness posteriorly, those on S9 slightly upturned (Fig. 6A); tergites 2–10 granulose, with long, delicate setae mainly on the latero-dorsal margins, covering the lateral third of the sternite. Sternites following the same color pattern as tergites (Fig. 1B); sternites 3–8 divided into five plates, sternites 2 and 9 divided into three plates, ventral sutures parallel on 2–3, moderately divergent on 4–8, strongly divergent on 9. Male gonapophyses lacking. Caudal appendages pyramidal, obtusely pointed (Figs. 1 and 6B), epiproct and paraprocts reddish-brown, cerci dark reddish-brown, granulose on external surfaces, small, delicate, white setae on internal surfaces; male’s epiproct with a pair of dorsal tubercles at basal 0.66 rounded apically and divergent; cerci and paraprocts, in dorsal view, mostly convergent except for the extreme tips of cerci, which are suddenly and strongly outcurved; dorsal and ventral margins of paraprocts ridged; paraprocts the shortest, epiproct the longest.
Measurements. Exuvia (N = 1): Total length 25.3; abdomen 16; maximum width of head 5.5; hind femur (lateral) 4.3; maximum width of abdomen (ventral) 6.5; epiproct 1.3, cerci 1.1, paraprocts 1.0; lateral spines on S6 0.10, on S7 0.12, on S8 0.20, on S9 0.4.
Habitat. A transforming individual was found in a small, shallow creek of 1st order, emerging on a small rock located close to the margin in a shady area. Emergence was horizontal, on a flat rock surface and lasted for more 40 min.
Epigomphus tumefactus Calvert
Material. Two exuviae (male and female reared), 2 F–0 larvae (male, female). COSTA RICA: Heredia; Horquetas, Finca El Plástico, (10°17.0N; 84°01.60W, 700 masl), 25 March 1995 (4 F–0 specimens: 1 male and 1 female F–0 emerged, 1 male and 1 female larvae F–0 preserved in ethanol), A. Ramírez leg. Deposited in IEXA and in the Museo de Zoologia, Universidad de Cosa Rica (MZUCR).
Description. Medium-sized larvae, body robust, integument finely and abundantly granular, antennae, legs, sides of thorax and abdomen setose, gently tapering caudad, body yellow-brown lacking any defined pattern (Fig. 8).
Head: As described for E. jannyae except: Labrum 0.7 mm long; occiput mostly finely granulose with some bare, irregular areas (Fig. 7). Antennae yellow brown (Figs. 2B and 8), 3rd antennomere spindle-shaped, 2.3 times longer than its widest part, 4th antennomere a subconical rudiment, length proportions: 0.30, 0.14, 1.0, 0.10. Mandibles: L 1234 0 a(m1,2,3)b / R 1234 y a(m1,2or1,2,3)b, in both mandibles tooth a > b. Prementum yellow, subquadrate, slightly wider than long, lateral margins smooth and slightly sinuate. Ligula (Fig. 5C) with a ventral row of 6–7 (usually 7) reddish-brown, short, truncate teeth on middle, and a dorsal row of short, stout piliform setae; apical lobe of labial palp stout, tip acute and finely serrate, internal margin concave with 9–11 large, truncate teeth, the 2–3 most apical teeth acutely pointed, external margin strongly convex and smooth (Fig. 5C); movable hook slightly shorter than palp.
Thorax: As described for E. jannyae (Fig. 7).
Abdomen: As described for E. jannyae except: Yellowish-brown to light brown (Fig. 8), reddish-brown to dark brown on middle third of tergites 8–9, and the whole surface of S10; lateral margins of S1–6 with long, stiff, yellowish setae, shorter on S7–10, lateral margins of S6–9 serrate, serrations on S6 very small and only visible in lateral and ventral view (absent in one exuvia), serrations on S7–9 short and acute (Figs. 6C and 8), light brown to brown, S7–9 ending in sharply pointed spines, divergent on S7–8, parallel on S9 and increasing in size and robustness posteriorly (Fig. 6C), those on S9 slightly upturned. Caudal appendages pyramidal (Fig. 6C), sharply pointed, reddish-brown to dark brown, subequal in length; male’s epiproct with a pair of dorsal tubercles at basal 0.50, widely convex apically and divergent (Fig. 6C); tips of cerci slightly divergent, tips of paraprocts parallel, dorsal and ventral margin of paraprocts carinated.
Measurements. Exuviae (N = 2): Total length 27.4–29.6; abdomen 16.3–17.7; hind femur 4.8–4.9; maximum width of abdomen (ventral) 6.9–7.2; caudal appendages 1.3–1.4; lateral spines on S7 0.4, on S8 0.6, on S9 0.6–0.7. Larvae (N = 2): Total length 26.7–28.6; abdomen 17.4–17.8; maximum width of head 5.6–6.0; hind femur 4.9; maximum width of abdomen (ventral) 7.2–7.5; caudal appendages 1.3; lateral spines on S7 0.4–0.5, on S8 0.6–0.7, S9 0.7–0.8.
Habitat. E. tumefactus larvae were collected in 1st order streams draining mature forest. Larvae emerged on top of flat rocks on the channel margin.
The larva of Epigomphus jannyae is similar to larvae of other described Epigomphus species, although they can be separated by the following features (in parentheses those of other species, including E. tumefactus above described): Integument abundantly granular (not granular but covered with minute, scale-like setae, E. crepidus, E. echeverrii, E. subobtusus, E. subsimilis); third antennomere claviform, 1.6 times longer than its widest part (spindle-shaped, 2 times longer or more than its widest part, E. crepidus, E. echeverrii, E. subobtusus, E. subsimilis, E. tumefactus); third antennomere with small, regularly spaced, circular structures close to borders (lacking such structures, E. crepidus); lateral margins of prementum slightly sinuate at apical 0.60 (lateral margins slightly convex, E. crepidus, E. echeverrii, E. subobtusus, E. subsimilis; straight and parallel at apical half, E. hylaeus); tip of palpal lobe rounded and smooth (tip of palpal lobe rounded and finely serrate, E. crepidus, E. echeverrii, E. subobtusus, E. subsimilis; tip of labial palp acute and finely serrate, E. tumefactus); movable hook almost as long as palp (as long as palp, E. hylaeus, E. subsimilis); lateral margins of S5 finely serrate (not serrated, E. crepidus, E. hylaeus, E. echeverrii, E. subobtusus, E. subsimilis, E. tumefactus); lateral margins of S6 serrate (no serrate, E. crepidus, E. hylaeus, E. echeverrii, E. subobtusus, E. subsimilis); lateral spines on S6–9 obtusely pointed (lateral spines on S7–9 sharply pointed, all other species); extreme tips of cerci suddenly and strongly out-turned (extreme tips of cerci slightly divergent, all other species).
The shape and length/width ratio of the 3rd antennomere and the rounded, smooth tip of the labial palp makes the larva of E. jannyae most similar to that of E. hylaeus. However, they differ by the larger stature of E. jannyae as well as the presence of serrations on the lateral margins of S5–9 and the obtusely pointed lateral spines on S6–9 of this species. Likewise, by the shape and length/width ratio of the 3rd antennomere, the larva of E. tumefactus appears related to crepidus, echeverrii, subobtusus, and subsimilis, differing from all these species by the acute tips of its labial palps. In this last feature it could be related to E. paludosus, according with the drawing provided by Martins (1968).
The descriptions here provided would shed light on the relationship of Epigomphus with other genera of Gomphidae. Several authors have tried to relate Epigomphus to other genera based mainly on adult morphology (e.g., Williamson, 1920), while others have included some larval characters (Carle, 1986; Belle, 1996). According to our present knowledge of the larvae, we think that Carle’s (1986) classification best reflects the relationships among the genera that he placed in the subfamily Epigomphinae, excepting the Macrogomphini (Macrogomphus only), whose larvae more resemble those of Carl’s tribe Gomphoidini. Epigomphus is probably closely related to the oriental Leptogomphus (tribe Leptogomphini) by the following combination of features: antennae with abundant scale-like setae, dual shape of 3rd antennomere; molar lobe of right mandible with formula a(m1−2)b; shape of prementum, ligula poorly developed and slightly convex; lateral margins of S6–9 serrate, with lateral spines on S7–9; anal pyramid short; sternum 3 divided in 5 sternites; the last 3 features are also shared with the larvae of Heliogomphus, which also belongs to the Leptogomphini (sensu Carle, 1986). However, there are two striking differences between Leptogomphus and Epigomphus—the presence in the former of a ventral, longitudinal, median sulcus on prementum, and abdominal dorsal protuberances.
The larvae of E. jannyae and E. tumefactus would fit in the key provided by Novelo-Gutiérrez, Gómez-Anaya & Smith-Gómez (2015), after the following modifications:
|1. Third antennomere claviform (length/width proportion l.6:1); tip of labial palp rounded and smooth||2.|
|1′. Third antennomere spindle-shaped (length/width proportion ≥ 2:1); tip of labial palp rounded or acute and finely serrate||3.|
|2. Lateral margins of prementum slightly sinuate; lateral margins of S5–9 serrate; lateral spines on S6–9 triangular, obtusely pointed (very small on S6, visible only in ventral view); extreme tips of cerci suddenly and strongly out-turned; total length more than 23 mm||jannyae.|
|2′. Lateral margins of prementum straight and parallel on apical half; lateral margins of S7–9 serrate; lateral spines on S7–9 sharply pointed; tips of cerci slightly divergent; total length less than 23 mm||hylaeus.|
|3. Tip of labial palp acute; ligula with 6–7 teeth; lateral margins of S6 serrate||tumefactus.|
|3′. Tip of labial palp rounded; ligula with 8 or more teeth; lateral margins of S6 no serrate||4 (continues in original key).|
Epigomphus continues to be a poorly known group, only eight of the 28 species are known as larvae. However, descriptions here provided and comparisons with the literature allow for the assessment of important larval characters useful for the separation of species.