Asphondylia monacha Osten Sacken, 1869: 299 Taxonomy and phylogeny of the Asphondylia species (Diptera: Cecidomyiidae) of North American goldenrods: challenging morphology, complex host associations, and cryptic speciation Dorchin, Netta Joy, Jeffrey B. Hilke, Lukas K. Wise, Michael J. Abrahamson, Warren G. Zoological Journal of the Linnean Society 2015 2015-06-30 174 2 265 304 HDBH OSTEN SACKEN, 1869 Osten Sacken 1869 [186,716,1588,1610] Insecta Cecidomyiidae Asphondylia Animalia Diptera 8 273 Arthropoda species monacha      Asphondylia monacha Osten Sacken, 1869: 299.   Hosts plants   Solidago juncea,  S. erecta,  S. uliginosa(summer generation), and  S. altissima(spring generation).  Gall and biology This species has two generations a year that induce distinct bud galls on different  Solidagospecies.The early-spring generation was found only on  S. altissimain April–May. Galls were discovered accidentally in early April while digging out rhizomes, as they developed in buds that grew from the rhizomes and were barely visible above ground ( Fig. 1). Galled buds were wider and felt harder to the touch than normal buds, were 5 cmlong and 2 cmwide, and contained a single chamber, the internal walls of which were lined by a thick layer of white mycelium. Each gall contained a single larva or pupa. In May, some galls were found in much longer sprouts (∼ 15 cmlong) that still appeared stunted and somewhat thicker than normal sprouts ( Fig. 2). The larval chamber in these galls was situated at the very tip of the shoot. Adults of the spring generation emerged in May. The much more conspicuous summer-generation gall of this species on  S. juncea(the host was incorrectly identified as  S. canadensisin the original description) is a rosette bud gall that is found in great numbers ( Fig. 3). The galls become apparent in mid-June and reach their final size while the larvae inside them are still tiny first instars. They are usually composed of 15–30 individual units, each with a single larval chamber that is surrounded by shortened leaves and lined internally by white mycelium. These units form a spherical structure on shoot tips that is 4–7 cmin diameter and can be spotted from a distance. Adults of the summer generation emerged in late August to mid-September. Although it was not observed, we assume that adults of the autumn generation lay their eggs in plant tissue close to the ground and the hatching first-instar larvae overwinter next to dormant buds in the rhizomes. Old galls turn black and may remain on dry shoots of  S. junceathroughout winter and into the next spring. Galls of similar structure were found on  S. erecta( Fig. 4) and  S. uliginosa, and our molecular analysis indicates that they are all induced by  A. monacha. No morphological differences were found among adults from these three host plants.  Asphondylia monachagalls superficially resemble those of  Rhopalomyia solidaginison  S. altissima, but they are not as wide and flat as the  Rhopalomyiagalls, are never found on  S. altissima, and their structure is different, as indicated by Osten Sacken (1869)in his original description of  A. monacha.   Figures 7–14.Galls: 7, 8,  Asphondylia solidaginissnap galls on  Solidago altissima; 9,  Asphondylia solidaginissnap galls on  Solidago gigantea; 10,  Asphondylia solidaginispupa in snap gall on  Solidago altissima– gall was cut open to show pupa in fungus-lined chamber; 11, 12,   Asphondylia rosulata sp. nov.snap galls on  Solidago rugosa; 13,  Asphondylia solidaginisrosette gall on  Solidago altissima; 14,   Asphondylia rosulata sp. nov.rosette gall on  Solidago rugosa.   Figures 15–22.Galls: 15,   Asphondylia pseudorosa sp. nov.inflorescence gall on  Euthamia graminifolia; 16,   Asphondylia pseudorosa sp. nov.snap gall on  Euthamia graminifolia; 17,   Asphondylia pseudorosa sp. nov.rosette galls on  Euthamia graminifolia; 18,  Asphondyliasp.from  Solidagosp.(photo: Tom Murray); 19, 20,   Asphondylia silva sp. nov.galls on  Solidago caesia; 21,   Clinodiplosis comitis sp. nov.larvae around   Asphondylia pseudorosa sp. nov.bud gall; 22,  Galeopsomia haemon‘internal galls’ inside   Asphondylia pseudorosa sp. nov.bud gall.  Adult General colour black.  Head:Eye facets round. Palpus three-segmented, segments successively longer, with several strong setae and otherwise covered by microtrichia. Labella slightly pointed, with numerous strong setae on lateral surface.  Antenna:Scape and pedicel with long, dark setae. Male flagellomeres cylindrical, flagellomere 1 slightly longer than succeeding flagellomere, apical flagellomere slightly shorter than preceding flagellomere, all covered by anastomosing loops of circumfila, numerous strong setae, and microtrichia ( Fig. 23); flagellomere 1/ flagellomere 5 ratio = 1.13–1.34 ( N= 23). Female flagellomeres 1–9 cylindrical with well-developed circumfila, with two transverse connections, numerous strong setae, and otherwise covered by microtrichia ( Fig. 24); flagellomere 1 conspicuously longer than succeeding flagellomere, flagellomere 1/flagellomere 5 ratio = 1.41–1.62 ( N= 38); flagellomeres 7 and onwards successively shorter; flagellomeres 10–12 with two whorls of circumfila and several longitudinal connections, numerous strong setae, and otherwise covered by microtrichia ( Fig. 25); flagellomere 10 slightly longer than wide; flagellomere 11 slightly wider than long; flagellomere 12 rudimentary.  Thorax:Legs: densely covered by black scales other than a patch of white scales from apical part of femur to base of tibia, and from base of tarsomere 1 to first third of tarsomere 2; ventral part with silvery hairlike scales, coxae with long black setae. Tarsal claws thick, evenly curved; empodia longer than bend in claw. Wing: dark grey, densely covered by dark hair-like microtrichia ( Fig. 18); length 2.00– 2.80 mmin males ( N= 41) and 2.01–3.30 mmin females ( N= 57) of summer generation, 2.91–3.11 mmin males ( N= 2) and 3.29–3.59 mmin females ( N= 5) of spring generation; R1 joins C proximal to mid-length of wing, R5 joins C posterior to wing apex, M weak, CuA forked into CuA1 and CuA2.  Female abdomen ( Fig. 26):Dorsum covered by black scales, pleuron and venter with silvery hair-like scales. Tergites 1–7 rectangular, with posterior one or two rows of strong setae and otherwise evenly covered by scales; tergite 8 narrower than preceding tergite, saddlelike, without setae. Sternites 2–6 with posterior row of setae and several setae on mid part; sternite 7 much longer than preceding sternite, narrowed posteriorly, with group of strong setae on posterior half. Ovipositor relatively long: sclerotized part 1.96–3.04 times as long as sternite 7 ( N= 55) in summer-generation females, 2.62–3.25 times as long in spring-generation females ( N= 6).  Male abdomen ( Fig. 27):Colour pattern as in female. Tergite 1 narrow, band-like, without setae; tergites 2–7 rectangular, with posterior row of strong setae, few setae on basal area, and evenly scattered scales; tergite 7 more setose than preceding tergite; tergite 8 narrow, band-like, without setae. Sternites 2–6 rectangular, with posterior row of strong setae and several strong setae medially, otherwise evenly covered by scales. Sternite 7 more setose than preceding sternite. Sternite 8 with small but strongly setose sclerotized area.  Male terminalia ( Figs 28–30):Gonocoxite compact, wide, and short, with short apical projection extending medially; bearing numerous strong setae and evenly setulose. Gonocoxal apodeme extending on both sides of aedeagus to form complex, strongly sclerotized structure ( Figs 28, 30). Gonostylus round–ovoid, with numerous strong setae and otherwise evenly setulose, bearing crescent-shaped apical tooth. Aedeagus wide at base, tapered towards rounded apex, curved anteriorly in lateral view ( Fig. 30). Hypoproct wide at base, deeply divided into two lobes apically, setose and setulose, with two longer setae apically on each lobe. Cerci completely or almost completely separated, bulbous, strongly setose and setulose throughout.  Larva (third instar) ( Fig. 31) Orange; integument covered by spicules. Length 2.06– 2.84 mm( N= 6). Antennae about 1.5 times as long as wide; cephalic apodeme as long as head capsule. Spatula shape variable ( Figs 32–37): lateral teeth slightly or conspicuously longer and more pointed than median teeth, gap between median teeth slightly or clearly deeper than gaps between lateral and median teeth, shaft thick and well-sclerotized in summer-generation larvae ( Figs 35–37), thinner and less sclerotized in spring-generation larvae ( Figs 32–34).   Figures 23–27.  Asphondylia monacha: 23, male flagellomere 5; 24, female flagellomere 5; 25, female flagellomeres 10– 12; 26, female abdomen; 27, male abdomen. Scale bars: 0.1 mm.  Pupa ( Figs 62–65) The pupae of the summer and spring generations differ from each other in the shape of the antennal horns. In summer-generation pupae antennal horns are robust, wide at base, slightly arched ( Fig. 65), with apices flat and finely serrated in frontal view ( Fig. 64); in springgeneration pupae antennal horns are longer, more slender ( Fig. 63), and are tapered at apex in frontal view ( Fig. 62). Other attributes are similar in pupae of both generations, as follows. Cephalic seta minute. Upper facial horn divided into two apices separated by shallow, curved notch. Lower facial horn curved dorsally at apex, on each side with two papillae, one bearing a relatively long seta. Frons on each side with three lateral papillae: one setose and two asetose. Prothoracic spiracle long and slender, with widened base; trachea ends at apex. Abdominal segments, except for first, each with posterior straight row and two or three anterior less ordered rows of spikes.   Figures 28–30.  Asphondylia monacha, male terminalia: 28, dorsal; 29, ventral; 30, lateral. Scale bars: 0.1 mm.  Notes We could not find any substantial morphological differences among populations from  S. juncea,  S. erecta, and  S. uliginosa, and our molecular analysis indicates that all belong to  A. monacha. The galls on  S. uliginosaare somewhat smaller than those on the other two host plants, and were also found in lateral buds, whereas galls on  S. junceaand  S. erectaalmost always develop in apical buds. Adults reared from galls on  S. uliginosawere likewise smaller than those from the two other hosts. Additional molecular work on the  S. uliginosapopulation may show that it represents a separate species. Adults of the spring generation that develop on  S. altissimaare clearly bigger than those of the summer generation. Based on the collection date, one individual from the Felt collection represents the spring generation of  A. monacha, but the host from which it was reared is not indicated. It is possible that the spring generation of  A. monachainduces galls on other  Solidagospeciesin areas where  S. altissimais uncommon, but such galls have not been found in the present study. Aggregated bud galls that are very similar to those of  A. monachaare also found on  S. sempervirens( Fig. 5) and  S. bicolor( Fig. 6), and although we could not find morphological differences between  A. monachaand individuals from these populations, our molecular analysis indicates that the latter belong to one or more undescribed species. There are additional  Solidagospecieson which similar composite galls have been observed, and further molecular study will probably be necessary to determine whether they belong to  A. monachaor to undescribed species. Felt (1908, 1916) attributed rosette and inflorescence galls on  Euthamia‘ lanceolata’, as well as leaf galls on  S. giganteaor  S. Canadensis, to  A. monacha, but these galls belong to different species discussed in the present paper.  Material examined  Spring generation (from S. altissima bud galls): 4♀, 1 exuviae,  3 larvae, USA, PA, Route642 ( 40°59.114′N 76°38.567′W),  28 April 2005, N. Dorchin;  3♀, 2 exuviae, USA, PA, Montour Environmental Preserve,  25 May 2007, N. Dorchin;  1 larva, USA, PA, Bucknell University Chillisquaque Creek Natural Area,  1 May 2005, N. Dorchin;  1♂, 2 exuviae, USA, PA, Bucknell University Chillisquaque Creek Natural Area,  13 May 2005, N. Dorchin;  5 pupae, USA, PA, multiple localities,  May 2005–2007, N. Dorchin(on SEM stubs).   Figures 31–37.  Asphondylia monacha, larva: 31, head and prothorax; 32–34, spatula of spring-generation larvae; 35– 37, spatula of summer-generation larvae. Scale bars: 0.1 mm.  Material from Felt collection with no indication of host:  1♀, USA, NJ,  Orange Mountain,  May 1907? (Felt no. 813; USNM).  From S. juncea: Gall( syntype), USA, NY, near Brooklyn, 1867 ( USNM);  2 larvae, USA, MD,  Wheaton Park,  22 August 1976, R. J. Gagné( USNM);  1 larva, USA, PA,  Pittsburgh,  13 August 1991, J. Plakidas( USNM);  1♂, USA, PA,  Warrendale,  30 August 1991, J. Plakidas( USNM);  1♂, 1♀, 3 larvae, USA, PA,  Lewisburg,  22 August 2005, N. Dorchin;  1♂, 2♀, USA, PA,  Route642 ( 40°59.114′N 76°38.567′W), 16 Spetember2005, N. Dorchin;  1♂, USA, PA,  Mauses Creek,  16 September 2005, N. Dorchin;  3♂, 12♀, 7 exuviae, USA, PA,  Lewisburg,  23 August 2007, N. Dorchin;  1♂, USA, PA,  Lewisburg,  30 August 2007, N. Dorchin;  12♂, 11♀, USA, VA,  Bedford, Sharp-top, 15 Spetember 2012, M.J. Wise;  9 pupae, USA, PA, multiple localities, August– September 2005–2007, N. Dorchin (on SEM stubs).   From S. erecta: 4♂, 3♀, 2 exuviae,  1 larva, USA, VA, Roanoke,  28 August 2010, N. Dorchinand M.J. Wise;  3♂, 5♀, USA, VA, Roanoke, Spetember2010, M.J. Wise;  3♂, 9♀, USA, VA, Roanoke, Havens,  5 September 2012, M.J. Wise;  3♂, 3♀, USA, VA, Roanoke, Forest Acre Trail,  9 September 2012, M.J. Wise;  12 pupae, USA, VA, Roanoke,  August–September 2010, 2012, M.J. Wise(on SEM stubs).  From  S. uliginosa: 7♂, 6♀, USA, ME, Winter Harbor,  7 September 2007, R.  J. Gagné( USNM).  Material from Felt collection with no indication of host and collector (recognized by Felt as A. monacha; all in    USNM): 1♀,  USA, NY, Albany,  11 June 1906(Felt no. 208); 1♀,  USA, NY, Albany,  20 July 1906(Felt no. 650a); 1♀, 1♂,  USA, NY, Karner,  5 August 1906(Felt no. 1583); 1 exuviae,  USA, NY, Albany,  4 September 1906(Felt no. 1200); 1♀,  USA, NY, Albany,  21 August 1906(Felt no. 761); 1♂,  USA, NY, Nassau,  17 September 1906(Felt no. 1336); 1♀,  USA NY, Albany,  20 July 1907(Felt no. 1568a); 1♂,  USA, NY, Bath,  24 July 1907(Felt no. 1568a); 1 larva,  USA, NY, Albany,  24 July 1907(Felt no. 1583); 1♀,  USA, NY, Bath,  16 July 1907(Felt no. 1568a); 1♂,  USA, NY, Nassau,  7 August 1907(Felt no. 1583a); 1♀, 1 exuviae, USA  NY, Bath,  18 July 1907(Felt no. 1268); 1♂,  USA, MA, Magnolia,  11 August 1908(Felt no. 1879). 2005-04-28 PA N. Dorchin United States of America 14 279 40.985233 Route 1 -76.642784 13 278 3 3 2007-05-25 PA N. Dorchin United States of America Montour Environmental Preserve 14 279 3 3 2005-05-01 PA N. Dorchin United States of America Bucknell University Chillisquaque Creek Natural Area 14 279 1 1 2005-05-13 PA N. Dorchin United States of America Bucknell University Chillisquaque Creek Natural Area 14 279 1 1 2005-05 PA Dorchin United States of America USA 14 279 5 5 [144,310,1572,1594] NJ United States of America USA 14 279 1 1 1907-05 USNM United States of America Orange Mountain 14 279 1 USNM Brooklyn 14 279 1 [362,579,1697,1719] MD United States of America USA 14 279 2 2 1976-08-22 R United States of America Wheaton Park 14 279 1 [355,551,1728,1750] USNM United States of America Gagne 14 279 1 [563,754,1728,1750] PA United States of America USA 14 279 1 1 [144,701,1758,1780] 1991-08-13 USNM J. Plakidas United States of America Pittsburgh 14 279 1 PA United States of America USA 14 279 1 1 1991-08-30 USNM J. Plakidas United States of America Warrendale 14 279 1 [262,609,1819,1841] PA United States of America USA 14 279 5 1 3 1 2005-08-22 N. Dorchin United States of America Lewisburg 14 279 1 [475,680,1850,1872] PA United States of America USA 14 279 3 2 1 Spetember & N. Dorchin United States of America 40.985233 Route 1 -76.642784 14 279 1 [946,1103,1234,1256] PA United States of America USA 14 279 1 1 2005-09-16 N. Dorchin United States of America Mauses Creek 14 279 1 [1063,1417,1264,1287] PA United States of America USA 14 279 15 12 3 [806,1252,1295,1317] 2007-08-23 N. Dorchin United States of America Lewisburg 14 279 1 [1263,1418,1295,1317] PA United States of America USA 14 279 1 1 [806,1233,1326,1348] 2007-08-30 N. Dorchin United States of America Lewisburg 14 279 1 VA United States of America USA 14 279 23 11 12 [853,1417,1356,1378] M. J. Wise United States of America Bedford Sharp-top 14 279 1 [806,1047,1387,1409] PA United States of America USA 14 279 9 9 2010-08-28 VA N. Dorchin & M. J. Wise United States of America Roanoke 14 279 1 1 [806,1418,1541,1563] VA Roanoke & Spetember & M. J. Wise United States of America USA 14 279 8 5 3 2012-09-05 VA M. J. Wise United States of America Roanoke Havens 14 279 12 9 3 2012-09-09 VA M. J. Wise United States of America Roanoke Forest Acre Trail 14 279 6 3 3 2010-08 2010-09-31 2010-08 VA M. J. Wise United States of America Roanoke 14 279 12 12 [876,1236,1756,1779] ME United States of America USA 14 279 13 6 7 2007-09-07 R United States of America 14 279 1 [1055,1262,1788,1810] USNM J. Gagne United States of America 14 279 1 [164,308,197,219] USNM 15 280 1 1 1906-06-11 NY United States of America Albany 15 280 1 1 1906-07-20 NY United States of America Albany 15 280 2 1 1 1906-08-05 NY United States of America USA 15 280 1 1906-09-04 NY United States of America Albany 15 280 1 1 1906-08-21 NY United States of America Albany 15 280 1 1 1906-09-17 NY United States of America Nassau 15 280 1 1 1907-07-20 NY United States of America Albany 15 280 1 1 1907-07-24 NY United States of America Bath 15 280 1 1 1907-07-24 NY United States of America Albany 15 280 1 1 1907-07-16 NY United States of America Bath 15 280 1 1 1907-08-07 NY United States of America Nassau 15 280 1 1 1907-07-18 NY United States of America Bath 15 280 1 1 1908-08-11 MA United States of America USA 15 280 1