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The nymph, female imago and egg of Siphluriscus chinensis Ulmer are described and figured in detail for the first time based on associated nymphs and imagos from China. Additional characters of the male imago are described. Based upon imaginal and nymphal characters, Siphluriscidae fam. n. is established in the Siphlonuroidea for Siphluriscus and, provisionally, the Jurassic genus Stackelbergisca Tshernova. Siphluriscus ? davidi Navás, known from one male subimago, is transferred to Siphlonurus davidi comb. n. The family Siphluriscidae is distinguished from all other families of Siphlonuroidea by the presence of coxal gills on the fore and middle legs in all stages and in the nymph by the presence of a basal, moveable, dactyl-like appendage on each claw, and labial and maxillary gills. Characters of the nymphal mouthparts, particularly the mandibles and maxillae, suggest that Siphluriscidae is a sister-group of the family Nesameletidae. However, the majority of character states are considered plesiomorphic in the Ephemeroptera, and may contribute valuable information on the origin, phylogeny and biogeography of Ephemeroptera.

Ephemeroptera (mayflies) are among the oldest orders of insects. The earliest record comes from the Upper Carboniferous (Carpenter 1992; Hubbard 1990; Kukalová-Peck 1983, Kukalová-Peck 1985, Kukalová-Peck 1991; McCafferty 1990; Sinitchenkova 1984), and six extant families have been found from the Jurassic (Hubbard & Savage 1981; Hubbard 1990; McCafferty 1990). Because of fragmentary and incomplete specimens and because usually only one life history stage is known, McCafferty (1990) indicated that among extant families only Siphlonuridae sensu lato is unquestionably represented from the Jurassic.

In 1967, Tshernova established a new genus and species for the Middle Jurassic species Stackelbergisca sibirica based on an imaginal forewing print and relatively well-deposited nymphal parts. Earlier, Ulmer (1920) had described Siphluriscus chinensis from extant male imagos and female subimagos from China. In 1976, Edmunds et al. suggested that Acanthametropus might be the immature stage of Siphluriscus, but this theory was negated by publication of the imago of Acanthametropus by Tshernova et al. (1986). Although Ulmer’s specimens were redescribed by Demoulin (1955) and McCafferty & Wang (1994), the nymph remained unknown until the present. Demoulin (1974) grouped Stackelbergisca and Siphluriscus together based on similarities in the wing and proposed a new unnamed subfamily of Siphlonuridae.

A second species, Siphluriscus ? davidi, was described by Navás (1932), but only a wing fragment was illustrated and the description was inadequate for generic placement. From the distribution (Sichuan province, “Se-Tchouen”), body length, and wing venation, this appears to be a species of Siphlonurus, a genus which the senior author has frequently collected from Sichuan province in western China. Pending its redescription, we treat this species as Siphlonurus davidi (Navás) comb. n.

In 1994, nymphs of an unknown genus of mayflies were collected by the senior author from Zhejiang province, southeastern China, and a male and a female imago of Siphluriscus chinensis were collected from nearby localities in 1993 and 1999. Brief notes on these specimens were published by Gui (1994). Upon further study, we were able to associate the nymphs with imagos based on characters not previously discussed in the literature, particularly the existence of coxal gills on the forelegs and middle legs. In addition, the wing venation and abdominal color pattern were the same as that described by Ulmer (1920). In this paper, we provide additional description of the male imago, describe the female imago, nymph and egg for the first time, establish the new family Siphluriscidae, and discuss its relationship with Stackelbergisca.

Genus Siphluriscus Ulmer, 1920

Nymph [(in alcohol) (Figs. 1-20Fig. 28)]

Head hypognathous, upper portion global (Figs. 1-2). Antennae short, 6-segmented, scape thicker than other segments, apical segment of flagellum hair-like (Figs. 2-3). Clypeus large, lateral margins with indentation (Fig. 2). Mouthparts (Figs. 2-11): labrum with Y-shaped suture on dorsal surface and short setae on margins (Figs. 2, 4). Hypopharynx as in Fig. 5, lingua narrow basally and broadened apically, apical margins of lingua and superlinguae with fine hair. Mandible with large blade-like outer incisor and small spine-like inner incisor; a row of hair between incisor and molar area, and a small tuft of hairs present at apex of mola (Figs. 6-7). Maxillae with distinct galea-lacinia fusion suture; distal portion of galea-lacinia with a row of spines and setae (Figs. 8-9); maxillary palps 3-segmented, basal segment a little longer than 2nd, apical segment small, very short; two tufts of gills on inner and outer basal surface of maxillae (Fig. 8). Labium with long, narrow, unfused glossae and paraglossae, aboral surface with long hair; labial palp 3-segmented, 3rd segment shorter than basal two with small rounded constriction apically (Figs. 10-11); postmentum well-developed, with one pair of gill tufts laterally (Fig. 10). Forelegs and middle legs with coxal gill tufts (Fig. 15); tibia and tarsus of all legs subequal in length, together shorter than femur, apex of femur divided into 3 lobes (Figs. 15-17), each with small, stout spines at apex; tibiae of middle and hind legs with patellar-tibial fusion suture; outer margins of all legs with a row of fine hairs (Figs. 15-17). All claws with a broad-based, movable dactyl-like appendage arising from claw base (Figs. 18-19, Fig. 28), its inner margin with a row of shallow depressions and its apex long, slender and spine-shaped; inner surface of claw with a shallow groove (Fig. 18). Gills present on abdominal segments 1-7, all gills single, oval, with sclerotized fore costae and submesal sclerotized hind costae (Fig. 1, Fig. 12) except costae on first pair of gills small and indistinct (Fig. 14), costae with small blunt setae on surface (Fig. 13); gills 2-7 with small spines apically on anterior margin (Fig. 13); tracheae pigmented. Terga and sterna with very tiny spines on surface, posterior margins of terga with a row of similar spines. Posterolateral projections on abdominal segments 1-9 moderately developed into sharp spines, largest on terga 7-9, tergum 10 with concave posterior margin (Fig. 1). Paraproct with a stout spine on mesal-posterior angle (Fig. 20). Terminal filament shorter than cerci; lateral margins of terminal filament and inner margins of cerci with dense long hairs, each cercus with spines laterally (Fig. 1).

Imago [(in alcohol) (Figs. 21-27)]

As previously described by Demoulin (1955) and McCafferty & Wang (1994) with following additional characters: compound eyes of ♂ contiguous dorsally, divided into dorsal and ventral portions (Fig. 21); eyes of ♀ separated by width of lateral ocellus (Fig. 24). Head with a horseshoe-shaped carina surrounding median ocellus posteriorly and laterally, a median longitudinal carina running from median ocellus to anterior margin of head (Fig. 25), occiput with posterior projection in ♂ (Fig. 21), broad in ♀ (Fig. 24). Furcasternal protuberances of mesothorax separated posteriorly (Fig. 25). Coxae of fore and middle legs with gill remnants at base (Fig. 25); middle and hind legs with distinct patellar-tibial fusion line; apex of femora of all legs subdivided into 3 lobes. Claws of all legs similar, paired; each hooked, acute with opposing hook (Fig. 22). Ninth sternum of ♀ with concave posterior margin (Fig. 26); sternum 7 of ♀ well developed and extended about half length of sternum 8, median portion of sternum 8 pale, more membranous than surrounding exoskeleton (Figs. 26-27). Terminal filament very short, about 1/10 length of cerci (Fig. 26).

Egg [(description from T. Soldán) (Figs. 29-31)]

Oval, about 1.3 times longer than wide, measurements: 243 μm (238-252 μm) × 188 μm (185-200 μm), 16 eggs measured. Approximately 15-24 loose attachment structures irregularly scattered around poles, but absent at the poles (Figs. 29-31). Attachment structures measuring 10-35 m and consisting of two subunits: proximal part elongated, funnel-like, about 3-5 times wider apically than at base; distal part regularly oval or globular, measuring about 7-12 μm in diameter (Fig. 30). Attachment structures similar in length and shape at both poles, but globular distal subunits about twice as wide in diameter on one of the poles. A single micropyle submedial to attachment structures in all eggs examined (Fig. 30). Micropyle roughly oval, bluntly pointed at one side, measuring 10-12 μm × 15-16 m; micropylar rim not developed; sperm guide inconspicuous, connected to bluntly pointed portion of micropyle, measuring about 7.5 μm. Exochorionic surface uniform, consisting of irregular rounded or oval granulation 2.5-4.5 μm in diameter.

Species Included

Siphluriscus chinensis Ulmer.


Siphluriscus is distinguished from all extant genera of Ephemeroptera in the imagos by the combination of straight penes without accessory structures, the deeply divided styliger plate, the ‘siphlonuroid’ forewing with an exceptionally long and narrow cubital field (as in the Middle Jurassic Stackelbergisca), long hind wings (more than half length of forewings), gill remnants on fore and middle coxae, and similar claws. In the nymph, the labial gills, the constricted 3rd segment of the labial palp, and the claws are unique among Ephemeroptera. We believe these characters are sufficiently distinct to follow the recommendation of Demoulin (1974) and establish Siphluriscidae fam. n. [type genus Siphluriscus Ulmer, 1920] for Siphluriscus and, provisionally, the Jurassic Stackelbergisca, although details of Stackelbergisca are not well known (discussed below).

McCafferty & Wang (1994) analyzed relationships between imagos of Siphluriscus, Acanthametropus, Analetris, and Siphlonuridae (in the broad sense), showing that Siphluriscus was not closely related to the specialized genera included in the psammophilous Acanthametropodidae; they considered the deeply forked MA in the hind wing to be an apomorphy of Siphluriscus. Kluge et al. (1995) then summarized relationships of all the family groups where both adults and nymphs were known. Although lacking details of the subimago cuticle, we refer to Kluge et al. (1995) for most comparative data. Siphluriscidae share a few common characters with genera of the Northern Hemisphere Siphlonuridae and Ameletidae. However, the closest relationship would appear to be with the Southern Hemisphere Nesameletidae where at least seven of the character states discussed by Kluge et al. (1995) are of similar structure (elongated mandibles with long incisor, modified setae on apex of maxilla, short third segment of maxillary palp, long and narrow unfused glossae and paraglossae, unpaired projection on occiput of male imago, well developed subgenital plate on female sternum 7, and similar adult claws). Siphluriscus is easily distinguished from all genera of Nesameletidae in imagos by the greater length of the hind wing (>H length of forewing), the deeply divided male styliger plate, penes joined only at base, and the basally forked MA vein in the hind wing; and in the nymph by the presence of well-developed maxillary and labial gills, gills on the pro- and mesothoracic coxae and the unique claw.

Any attempt at cladistic analysis of families within Siphlonuroidea is complicated by the fact that the group as presently defined is distinguished by a complex of plesiomorphies (Kluge et al. 1995). In Siphluriscus, imaginal structures are considered either plesiomorphic, subject to frequent reversal, or derived by reduction or fusion. Based on the work of paleontologists and morphologists (Smith 1969; Kukalová-Peck 1991, Kukalová-Peck 1992; Gaino & Rebora 1995), we know that the penes of insects have evolved through the loss or fusion of what were ancestrally complex structures and the simpler structure of the penes of Siphluriscus would be considered derived, but such reductions are found throughout the order. Similarly, the blade-like outer incisor of the mandible represents a highly specialized algal scraping device found in mayfly nymphs of other families and immature stages of other insect orders; it is considered the most common type of feeding specialization found in immature aquatic insects (Arens 1990). The inner incisor (termed “kinetodontium” by Kukalová-Peck 1991 and Kluge 2000) appears as a spine inserted at the base of the outer incisor (“canine”) and its evolutionary status is unclear. Gills at the base of mouthparts and coxae, sometimes called accessory gills to distinguish them from the plate-like abdominal gills (tergaliae of Kluge et al. 1995), are broadly distributed in Ephemeroptera nymphs and persist into the adult stage of several genera of Ephemeroptera, Plecoptera, Odonata, and Trichoptera (Stys& Soldán 1980). The historical evolution of the paraproct has never been studied in Ephemeroptera, but the paraproct of Siphluriscus is presumably plesiomorphic based on available outgroups because an acute submedial spine or projection is also found in Siphlonuridae, Metretopodidae, Oniscisgastridae and Rallidentidae.

Of the characters discussed in Kluge et al. (1995) and McCafferty & Wang (1994), none will clearly align Siphluriscus with other extant families, although initial analysis (Table 1) shows a potential relationship with Nesameletidae. Table 1 gives a brief summary of characters for which there is general agreement in the literature, and ignores for now the many characters (such as accessory gills) open to more than one interpretation. More detailed analysis is needed to determine if characters such as the structure of apical maxillary setae (Kluge 1998) and the structure of the incisor are synapomorphic. Of all nymphal characters of Siphluriscidae, the most interesting and least understood is the claw. It does not resemble the apically bifurcate foreclaw of Metretopodidae, and only one similar claw is known in Ephemeroptera-that of certain Jurassic nymphs found in association with the imago of Stackelbergisca sibirica.

Stackelbergisca includes the type species S. sibirica described from the holotype wing (indistinguishable from Siphluriscus) and S. shaburensis Sinitshenkova. At least two different nymphal types have been associated with the S. sibirica imago and S. shaburensis is described from nymphs only (Sinitshenkova 1991). Some nymphs (S. sibirica in part) have a dactyl-like appendage basally, and others do not (S. sibirica in part and S. shaburensis), and some have small paired projections on posterior abdominal terga and others do not. The presumed mandibles of Stackelbergisca are also not clearly associated with a specimen (Tshernova 1967). From this, we can only conclude that some nymphs with a second basal dactyl-like appendage are present in the same formation as Stackelbergisca imagos. Although full double claws are clearly the ancestral state in Ephemeroptera (Kukalová-Peck 1968), the illustrated fossil claw of Stackelbergisca does not display enough detail to make any definitive determination of its relationships. Thus, the placement of Stackelbergisca in Siphluriscidae is provisional, a placement first suggested by Demoulin (1974) based only on the imaginal wing. The discovery of the similar nymphal claw which has possibly been retained for more than 100 million years reinforces this placement.

If the relationship between Siphluriscus and Stackelbergisca is correct, we can say that the Siphluriscus lineage arose in the Jurassic, and is a representative of the oldest known extant family with regard to the fossil record. Stackelbergisca is among the oldest fossils of Siphlonuridae sensu lato (Carpenter 1992; Hubbard 1990; McCafferty 1990). However, there are many plesiomorphies in Siphlonuridae sensu stricto (Table 1) and one other genus from the Jurassic (Olgisca Demoulin, 1970, known only from a forewing) is assigned to Siphlonuridae sensu stricto. The Chinese Siphlonuridae have yet to be studied, and discovery of the nymph of species such as Siphlonurus davidi may require a reevaluation of this hypothesis.

Nelson & Platnick (1984) used some mayfly distribution information provided by Edmunds (1981) as evidence to support the geographic congruence between South America, Australia and New Zealand. Kluge et al. (1995) suggested a Northern Hemisphere (Laurasian) origin for the Southern Hemisphere (Gondwanian) Siphlonuroidea. Based upon present findings, their arguments should be qualified because the ancestor of extant Nesameletidae may have had a much broader distribution than previously known. The present distribution [Nesameletidae: Nesameletus (New Zealand), Ameletoides (Australia), Metamonius (Chile, Argentina); Siphluriscidae: Siphluriscus (Southeastern China), Stackelbergisca (Eastern Siberia)] implies that the ancestor of Nesameletidae and Siphluriscidae may have originated in an ancient, continental mass in the paleo-Pacific region and gives support to the hypothesized Pacifica continent proposed by Nur & Ben-Avraham (1977).

The claw could also represent a more recent, independently evolved structure. The limited series of specimens available to us are sufficient for description and diagnosis, but many questions remain. The functional morphology of the claw cannot be studied without fresh or living material, and almost nothing is known of the biology of the species. Further study of Siphluriscus is essential to understand its biology and evolutionary history.

Siphluriscus chinensis Ulmer, 1920

Siphluriscus chinensisUlmer, 1920: 62 (male imago, subimago); Demoulin, 1955:1 (subimago); McCafferty & Wang, 1994: 211 (male imago and subimago).

Male imago [(in alcohol) (Figs. 21-23)]

Body length 23 mm; forewing 23 mm; hind wing 13 mm; foreleg 17 mm; middle leg 10 mm; cerci 40 mm; terminal filament 3.5 mm. Compound eyes with gray to dark gray dorsal portion and brown ventral portions. Head and thorax dark brown. Body dark brown with yellowish marks; abdominal terga 1-8 as in Fig. 23, each tergum with pair of yellowish marks and median dark brown stripes. Wings transparent, veins dark brown; Sc and Rs of forewing with distinct vein bullae. Forelegs light brown to brown, femora paler than tibiae and tarsi; middle and hind legs slightly paler than forelegs, femora almost similar to tibiae and tarsi in color. Tergum 10 with slight concave posterior margin. Terminal filament paler than cerci, all filaments with tiny brown setae on surface.

Female imago [(in alcohol) (Figs. 24-27)]

Body length 24-25 mm; forewing 24-25 mm; hind wing 13.5 mm; foreleg 11.5 mm, middle leg 10.7 mm, hind leg 9.5 mm; cerci 38 mm, terminal filament 3 mm. Similar to male, but body paler, venter and thorax yellowish brown. Terga with similar color pattern as male, but paler. Sterna yellowish, each sternum with a pair of indistinct gray marks on median portion, each mark with pale dots. Last ventral abdominal segments shown in Fig. 26.

Nymph [(in alcohol) (Figs. 1-20Fig. 28)]

Body length 22-24 mm, cerci 7.5 mm, terminal filament 6 mm. General color pale yellowish with indistinct brown marks (in life, yellowish green with reddish stripes). Ocelli gray (Fig. 2). Incisors of mandibles strong, reddish. Apex of tibiae yellowish brown; tarsi with 2 brown bands on basal and distal portions (Figs. 15-16). Each tergum with a pair of pale submedian marks, median area dark, especially on terga 2-3, 6 and 8-9 (Fig. 1). Basal and middle portions of caudal filaments with yellowish brown bands (Fig. 1); apically from basal band, every 4th annulation of cerci with spines on outer lateral margin, 10 of them distinct.


P.R. CHINA: 15 nymphs, Zhejiang Province, Guan-Pu-Yang, Nang-Ju, Long-Quan county (28.04°N, 119.08°E), 600 m, 15-VIII-1994, leg. ZHOU Chang-fa & ZHU Chao-Dong; 1♀, Zhejiang Province, Bai-Shan-Zhu, Qingyuan county (27.37°N, 119.04°E), 20-IX-1993, leg. WU Hong; 1♂, Zhejiang Province, Tian-Mu-Shan mountain (30.26°N, 119.34°E), 2-VI-1999, leg. ZHAO Ming-Shui (13 nymphs, 1♂, 1♀ deposited in Department of Biology, Nanjing Normal University, P.R. China; 2 nymphs in Florida A&M University, USA). Egg from 1♀ collected at light trap, Zhejiang Province, Long-Wan-Shan mountains (30.28°N, 119.22°E), 3-VI-1999, leg. Ignac SIVEC, deposited in the Institute of Entomology, Academy of Sciences of the Czech Republic,CeskéBudejovice.


The nymphs were collected in quiet water of a small mountain stream with a sand and stone substrate. Width of the streambed was between 2 m and 4 m, but at the time of collection the stream was only about 1 m wide and less than 40 mm deep. The stream is in an undisturbed mountainous area with large trees on the bank, and sunlight reaches the water surface only at noon and early afternoon. Living nymphs can jump quickly like small fish when removed from water. They are strong swimmers and can hold tightly to branches or stones with their legs and claws. Gills of observed nymphs did not move. Mayflies collected from the same stream included Vietnamella, Serratella, Isonychia, and some baetid and heptageniid species.


We thank Le-Yi Zheng (Nankai University, China), the major advisor of the senior author, for his review and comments on this manuscript. We would like to acknowledge and sincerely thank Dr. George F. Edmunds, Jr. (Salt Lake City) and the late Dr. William L. Peters (Florida A&M University) who suggested and encouraged this research. Special thanks to Dr. Tomás Soldán (CeskéBudejovice)who generously gave us photographs and information on egg structure based on material provided by Dr. Ignac Sivec (Ljublana), Ms. Carolina Nieto (Tucumán) who prepared Figure 12 and Mr. Ignacio Baez (Florida A&M University) who prepared the Spanish summary. We also thank Dr. M. D. Hubbard and Mr. B. A. Richard (Florida A&M University), Dr. M. Sartori (Lausanne), Dr. J. Kukalová-Peck (Ottawa), Dr. A. H. Stanizcek (Stuttgart), Dr. N. Kluge (St. Petersburg), Dr. T. Soldán, and Dr. E. Bauernfeind (Vienna) for their suggestions and useful discussion. This work was supported by a Ph.D. fellowship awarded to C.-F. Zhou by the Nankai University, a postdoctoral fellowship to C.-F. Zhou by Nanjing Normal University, and the “Education Grant” of National Natural Sciences Foundation of China (No. 108).

References Cited


W. Arens 1990. Wear and tear of mouthparts: a critical problem in stream animals feeding on epilithic algae. Canadian J. Zool. 68:1896–1914. Google Scholar


F. M. Carpenter 1992. Order Ephemeroptera. pp. 19-25. In R. C. Moore and R. L. Kaesler (eds.), Treatise on Invertebrate Paleontology. Arthropoda 4, Vol. 4. Superclass Hexapoda. Geol. Soc. America and Univ. Kansas. Google Scholar


G. Demoulin 1955. Brève note sur la position systématique de Siphluriscus chinensis Ulmer (1920) (Ephemeroptera). Bull. Inst. R. Sci. Nat. Belgique 31:(80). 1–2. Google Scholar


G. Demoulin 1970. Contribution a l’étude morpho logique, systématique et phylogénique des Ephéméroptères Jurassiques d’Europe centrale. V. Hexagenitidae = Paedephemeriae (syn. nov). Bull Inst. R. Sci. Nat. Belgique 46:(4). 1–8. Google Scholar


G. Demoulin 1974. Remarques critiques sur les Acanthametropodinae et sur certaines formes affines (Ephemeroptera: Siphlonuridae). Bull. Inst. R. Sci. Nat. Belgique, Entomol. 50:(2). 1–5. Google Scholar


G. F. Edmunds Jr. 1981. Discussion. pp. 287-297. In G. Nelson and D. E. Rosen (eds.), Vicariance Biogeography: A Critique. Columbia Univ. Press, New York. Google Scholar


G. F. Edmunds Jr., S. L. Jensen, and L. Berner . 1976. The Mayflies of North and Central America. Univ. Minnesota Press, Minneapolis. Google Scholar


E. Gaino and M. Rebora . 1995. Mating apparatus of Leptophlebiidae (Ephemeroptera). Aquatic Insects 17:95–104. Google Scholar


Gui Hong 1994. Chapter 10: Ephemeroptera. pp. 117-134. In J. C. Morse, L.-F. Yang, and L.-X. Tian (eds.), Aquatic Insects of China Useful for Monitoring Water Quality. Hohai University Press, Nanjing, China. Google Scholar


M. D. Hubbard 1990. Mayflies of the World: A Catalog of the Family and Genus Group Taxa. Sandhill Crane Press, Inc. Gainesville, FL. Google Scholar


M. D. Hubbard and H. M. Savage . 1981. The fossil Leptophlebiidae (Ephemeroptera): a systematic and phylogenetic review. J. Paleontol. 55:810–814. Google Scholar


N. Ju Kluge 1998. Phylogeny and higher classification of Ephemeroptera. Zoosyst. Rossica. 7:255–261. Google Scholar


N. Ju Kluge 2000. [Modern Systematics of Insects. Part l]. Lan’, S.-Petersburg. Google Scholar


N. Ju Kluge, D. Studemann, P. Landolt, and T. Gonser . 1995. A reclassification of Siphlonuroidea (Ephe-meroptera). Bull. Soc. Entomol. Suisse 68:103–132. Google Scholar


J. Kukalová-Peck 1968. Permian mayfly nymphs. Psyche 75:310–327. Google Scholar


J. Kukalová-Peck 1983. Origin of the insect wing and wing articulation from the arthropodan leg. Canadian J. Zool. 61:1618–1669. Google Scholar


J. Kukalová-Peck 1985. Ephemeroid wing venation based upon new gigantic Carboniferous mayflies and basic morphology, phylogeny, and metamorphosis of pterygote insects (Insecta, Ephemerida). Canadian J. Zool. 63:933–955. Google Scholar


J. Kukalová-Peck 1991. Fossil history and the evolution of hexapod structures. pp.141-179. In I. D. Naumann (ed.), The Insects of Australia. 2nd ed. Vol. I. CSIRO, Melbourne Univ. Press. Google Scholar


J. Kukalová-Peck 1992. The “Uniramia” do not exist: the ground plan of the Pterygota as revealed by Permian Diaphanopterodea from Russia (Insecta: Paleodictyopteroidea). Canadian J. Zool. 70:236–255. Google Scholar


W. P. McCafferty 1990. Chapter 2. Ephemeroptera. pp. 20-50. In D. A. Grimaldi (ed.), Insects from the Santana Formation, Lower Cretaceous, of Brazil. Bull. American Mus. Nat. Hist. Vol. 195. Google Scholar


W. P. McCafferty and T-Q. Wang . 1994. Relationships of the genera Acanthametropus, Analetris, and Siphluriscus, and re-evaluation of their higher classification (Ephemeroptera: Pisciforma). Great Lakes Entomol. 27:209–215. Google Scholar


L. Navás 1932. Insecta orientalia. Mem. Pont. Accad. Scienze, Nuovi Lincei. 16:921–949. Google Scholar


G. Nelson and N. Platnick . 1984. Biogeography. Carolina Biology Readers 119:1–20. Google Scholar


A. Nur and Z. Ben-Avraham . 1977. Lost Pacifica continent. Nature 270:(5632). 41–43. Google Scholar


N. D. Sinitchenkova 1984. The Mesozoic mayflies (Ephemeroptera) with special reference to their ecology. pp. 61-66. In V. Landa, T. Soldán, and M. Tonner (eds.), Proc. 4th Int. Conf. Ephemeroptera (Bechyne, September 4-10, 1983). Inst. Entomol., Czechoslovak Acad. Sci.,CeskéBudejovice. Google Scholar


N. D. Sinitshenkova 1991. New Mesozoic mayflies from Transbaikalia and Mongolia. Paleontol. Zh. 1991:120–123. Google Scholar


E. L. Smith 1969. Evolutionary morphology of external insect genitalia. 1. Origin and relationships to other appendages. Ann. Entomol. Soc. America 62:1051–1079. Google Scholar


P. Stys and T. Soldán . 1980. Retention of tracheal gills in adult Ephemeroptera and other insects. Acta Univ. Carolinae-Biol. 1978:409–435. Google Scholar


O. A. Tshernova 1967. Mayfly of the recent family in Jurassic deposits of Transbajkalia (Ephemeroptera, Siphlonuridae). Entomol. Obozr. 46:322–326. Google Scholar


O. A. Tshernova, N. Yu Kluge, N. D. Sinitshenova, and V. V. Belov . 1986. Order Ephemeroptera - Mayflies. pp. 99-142. In Keys to Insects of the Far Eastern USSR, Vol. I. Far Eastern Sci. Center, Acad. Sci. USSR, Leningrad. Google Scholar


G. Ulmer 1920. Neue Ephemeropteren. Arch. Naturg. 85:1–80. Google Scholar


Fig. 1.

Siphluriscus chinensis, female nymph (habitus).


Figs. 2-11. Nymph of Siphluriscus chinensis: 2, head (frontal view); 3, antenna; 4, labrum; 5, hypopharynx; 6, left mandible; 7, right mandible; 8, maxilla; 9, distal detail of maxilla; 10, labium (with apex of postmentum); 11, dorsal detail of apex of labial palp segment 3.


Figs. 12-27. Siphluriscus chinensis. Figs. 12-20, nymph: 12-13, gill 4 with apical detail of gill costa (13); 14, gill 1 (tracheation not drawn); 15, foreleg; 16, distal segments of middle leg (ventral); 17, connection between tibia and tarsus of middle leg (dorsal view); 18, apical portion of foreclaw (schematic showing position of groove); 19, detail of dactyl-like appendage of claw; 20, apex of paraproct and margin of tergum 10. Figs. 21-23, male imago: 21, head, dorsal; 22, foreclaw; 23, tergum 2. Figs. 24-27, female imago: 24, head; 25, pro- and mesosternum (arrow points to gill remnant); 26, sterna 7-9 and caudal filaments; 27, lateral view of sterna 7-9.


Figs. 28-31, Siphluriscus chinensis. Fig. 28, nymphal claw. Figs. 29-31, egg: 29-30, polar regions of egg with detail of attachment structures and micropyle (Fig. 30, arrow); 31, whole egg. (SEM scale bar = 100 m in Figs. 28, 31; 10 μm in Figs. 29, 30).


Table 1.

Character states of Siphluriscidae, Siphlonuridae, and Nesameletidae.

Published: 1 September 2003

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