Noctuidonema dibolia n. sp. (Aphelenchida: Acugutturidae), an Ectoparasite of the moth Mocis latipes (Lepidoptera: Noctuidae) 1

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Journal of Nematology 27(3):387-394. 1995. The Society of Nematologists 1995. Noctuidonema dibolia n. sp. (Aphelenchida: Acugutturidae), an Ectoparasite of the moth Mocis latipes (Lepidoptera: Noctuidae) 1 O. G. MARTI, JR, AND C, E. ROGERS 2 Abstract: Noctuidonema dibolia n. sp., an ectoparasite of adults of the noctuid moth Mocis latipes (Guen6e) is described. The differentiating characters are a club-shaped body with a subterminal vulva in the female, spicules with a reduced matrix and sheath and closely apposed dorsal and ventral arms in the male, very long styler and conus, moderately prominent stylet knobs, a bluntly rounded head, and a large renette cell in both sexes. Lateral fields, rectum, anus, bursa, and gubernaculum are absent. Noctuidonema dibolia differs from the other species of the subfamily Noctuidonematinae in the size and robustness of the body, the length of the stylet and conus, the length of the tail, and the shape of the spicules. Key words: ectoparasite, insect parasite, Lepidoptera, Mocis latipes, moth, nematode, Noctuidae, Noctuidonema dibolia n. sp., taxonomy. Surveys of Lepidoptera in French Guiana (9,12), the tropical Americas (11,12), and the southeastern United States (10) documented the widespread occurrence of an ectoparasitic nematode, Noctuidonema guyanense Remillet and Silvain, particularly among moths in the family Noctuidae. Noctuidonema Remillet and Silvain is of interest because it is one of only a few known metazoan parasites of adult moths (3) and is currently under study as a possible biological control agent for the fall armyworm moth, Spodoptera frugiperda (J. E. Smith), a serious pest of corn, sorghum, and pasture grasses (12,13). Mocis latipes (Guen6e), whose larvae are known as striped grass loopers, is primarily a pest of pasture grasses (5,12). Specimens of the genus Noctuidonema, collected from M. latipes in Tift County, Georgia, were examined and found to differ from N. guyanense, Vampyronema daptria (Anderson and Laumond) (2,7), and the related genus Acugutturus Hunt (6), and are here described as a new species, N. dibolia. The specific name 'dibolia' is taken from Greek (= pointed at both ends). Received for publication 19 September 1994. i Mention of a trade name, warranty, proprietary product, or vendor does not constitute an endorsement of a product and does not imply its approval to the exclusion of other products or vendors that may also be suitable. Microbiologist and Research Entomologist, USDA, ARS, Insect Biology and Population Management Research Laboratory, P.O. Box 748, Georgia Coastal Plain Experiment Station, Tifton, GA 31793. MATERIALS AND METHODS Mocis latipes adults were collected from 1991-93 in a walk-in ultraviolet light trap located on a research farm near Tifton, Georgia. The external surfaces of the moth abdomens were examined with a stereoscopic microscope for the presence of nematodes. Infested moths were placed into a 15-ml cup containing 2 ml of water plus a few drops of Tween 80 (polyoxyethylenesorbitan monooleate) and shaken for a few seconds to dislodge nematodes. Nematodes were concentrated by sedimentation in distilled water, examined live or killed in hot water (60 C), and fixed and stored in TAF (Triethanolamine-Formalin-Water 7:2:91) (4) until processed through an alcohol series to glycerin. The nematodes were then mounted on glass slides and examined with differential interference contrast or phase contrast optics. Drawings are based on microscopic examination and photographs of living as well as processed specimens. Values in the text are expressed as: range in p~m (mean in txm -+ SD). SYSTEMATICS Noctuidonema dibolia n. sp. (Figs. 1A-C;2A-E) Holotype ~emale): Length = 522 Ixm; maximum width = 57 Ixm; width at vulva = 44 i~m; anterior end to excretory pore 387

388 Journal of Nematology, Volume 27, No. 3, September 1995 = 22 ixm; anterior end to nerve ring = 137 Ixm; stylet length = 108 ~m; styler conus length = 91 p.m; metacorpus length = 28 Ixm; metacorpus width = 23 ~xm; ovary length = 225 p.m; tail length = 66 /~m. Allo~pe (male): Length = 464 p~m; maximum width = 41 ixm; width at cloaca = 16 ~m; anterior end to excretory pore = 25 >m; anterior end to nerve ring = 118 ~m; stylet length = 89 p.m; stylet conus length = 73 Ixm; metacorpus length = 28 Ixm; metacorpus width = 20 p~m; testis length = 225 p~m; tail length = 8 jxm; spicule length = 44 Ixm; rostrum length = 12 ~xm. 7( 5( 2 / Flo. 1. Noctuidonema dibolia n. sp. A) Female. B) Male. C) Spicules.

Noctuidonema dibolia n. sp.: Marti and Rogers 389 / a ~ V ii ', ~ C 60um A 10urn B 10um C,25urn D 30um E FIG. 2. Noctuidonema dibolia n. sp. A) Fourth-stage juvenile. B) Head end of female. C) Head end of male. D) Newly hatched second-stage juvenile. E) Embryonated egg with fully formed juvenile. Paratypes: Measurements of 39 females and 16 males in Tables 1-4. Description Female: Measurements in Tables 1-3. Body club-like, slightly arcuate ventrally. Annules continuous, 1.0-1.6 wide (1.3 -+ 0.2) at midbody, anastomoses common. Lateral fields absent. Lip region low, bluntly rounded, not strongly set off. Styler flexible, delicate, elongate, representing 19-22% of total body length. Conus representing 80-82% of total stylet length. Conus midpoint diameter 0.8-1.0

390 Journal of Nematology, Volume 27, No. 3, September 1995 TABLE 1. Measurements of 14 small paratype (<500 p.m body length), non-gravid female Noctuidonema dibolia n. sp. from Tift County, Georgia. Character ~ Mean SD Range Measurements (p,m) Body length 455 37.2 396-495 Maximum body width 54 7.3 44-67 Body width at nerve ring 36 3.1 32-41 Body width at vulva 41 5.9 34-54 Body width at anterior 36 3.1 32-41 end of intestine Anterior end to base 120 9.8 105-140 of bulb Metacorpus length 27 2.0 23-31 Metacorpus width 23 1.8 20-26 Excretory pore to 18 2.9 15-23 anterior end Stylet total length 99 6.1 83-108 Stylet conus length 81 5.3 69-89 Stylet shaftqength 18 3.0 15-23 Head width 9 0.8 7-10 Head length 4 0.5 3-4 Ovary length 200 37.4 149-262 Vulva to end of tail 53 7.4 42-70 Vulva to anterior end 402 33.4 346-433 Vagina depth 24 4.1 18-31 Anterior end to 129 25.4 85-187 anterior ovary Ratios and Percentages a 8.5 0.7 7-10 b 3.8 0.4 3-5 c 8.6 1.0 7-11 c' 1.3 0.2 1-2 V 88.3 1.3 86-91 M 82.0 2.6 76-86 G 59.7 6.8 48-70 Ovary, % of body length 43.7 5.9 36-53 Stylet, % of body length 21.8 2.3 17-26 a a = body length/greatest body width; b = body length/ distance from anterior end to junction of esophagus and intestine; c = body length/tail length; c' = tail length/body width at vulva; V = distance of vulva from anterior end x 100/body length; M = conus length x 100/stylet length; G = distance from vulva to anterior end of ovary x 100/body length. (1.0 -+ 0.1). Shaft diameter 1.0-1.6 (1.4 + 0.3). Styler knobs rounded with concave anterior surfaces, 4.0-5.0 (4.6 + 0.4) wide, 6.0-20.0 (12.9 ± 4.9) from guide ring. Procorpus strongly reflexed at level of metacorpus when stylet is retracted. Metacorpus ovoid, with a sclerotized valve slightly offset posteriorly. Nerve ring immediately posterior to metacorpus. Hemizonid position variable, 0-23.4 (10.4 ± 8.4) posterior to nerve ring in gravid females. Intestinal contents usually yellow, depend- ing on host diet, containing amorphous ingesta, crystalline inclusions, and bacteria. Intestine ending in a blind, rounded sac extending posterior to vulva. Esophageal glands 45.3-65.7 long (59.7 +- 6.1) in small non-gravid females, 43.8-77.4 long (66.7 -+ 8.8) in large non-gravid females, and 62.8-81.8 (72.8 +- 6.8) in large gravid females. Ovary outstretched,.rarely reflexed, frequently extending anterior to metacorpus in large specimens. Rachis present in large specimens. Oocytes progressively larger in posterior ovary, usually not more than one TABLE 2. Measurements of 13 large paratype (>500 ~m body length), non-gravid female Noctuidonema dibolia n. sp. from Tiff County, Georgia. Character a Mean SD Range Measurements (~m) Body length 526 25.7 501-568 Maximum body width 57 6.6 44---67 Body width at nerve ring 36 4.6 28--44 Body width at vulva 44 6.7 32-54 Body width at anterior 36 5.3 26~4 end of intestine Anterior end to bulb base 125 13.6 96-143 Metacorpus length 28 2.8 20-31 Metacorpus width 24 1.9 20-26 Excretory pore to 19 2.5 15-23 anterior end Stylet total length 100 6.8 92-114 Stylet conus length 81 4.6 73-88 Head width 9 0.9 7-10 Head length 4 1.3 3-7 Ovary length 214 54.3 117-306 Vulva to end of tail 62 8.7 47-79 Vulva to anterior end 467 23.8 435-505 Vagina depth 27 5.4 15-34 Anterior end to 136 28.6 67-175 anterior ovary Ratios and Percentages a 9.3 1.0 8-11 b 4.2 0.4 4-5 c 8.7 1.1 7-11 c' 1.5 0.3 1-2 V 88.7 1.8 86-92 M 81.1 4.7 73-89 G 62.6 5.6 54-75 Ovary, % of body length 40.9 10.9 21-61 Styler, % of body length 18.9 0.9 17-20 a = body length/greatest body width; b = body length/ distance from anterior end to junction of esophagus and intestine; c = body length/tail length; c' = tail length/body width at vulva; V = distance of vulva from anterior end x 1001body length; M = conus length x 100/styler length; G = distance from vulva to anterior end of ovary x loo/hody length.

Noctuidonema dibolia n. sp.: Marti and Rogers 391 TAaLE 3. Measurements of 12 gravid paratype female Noctuidonema dibolia n. sp. from Tift County, Georgia. Character ~ Mean SD Range Measurements (p.m) Body length 541 54.4 451-640 Maximum body width 67 11.3 53-88 Body width at nerve ring 40 4.8 31--47 Body width at vulva 52 8.5 42-67 Body width at anterior 40 4.8 31-47 end of intestine Anterior end to bulb base 132 9.6 117-143 Metacorpus length 28 2.8 23-32 Metacorpus width 23 2.0 19-26 Excretory pore to 21 3.0 15-25 anterior end Stylet total length 102 7.0 91-114 Stylet cone length 82 3.3 76-86 Stylet shaft length 20 6.0 10-31 Head width 9 1.5 6-10 Head length 4 1.0 3-6 Ovary length 258 38.2 198-320 Vulva to end of tail 68 5.4 60-79 Vulva to anterior end 474 52.1 388-562 Vagina depth 30 7.3 20--45 Intrauterine egg length 86 8.5 66-98 Intrauterine egg width 30 2.5 26-35 Anterior end to 95 38.1 60-175 anterior ovary Ratios and Percentages a 8.2 1.1 7-10 b 4.1 0.3 4-5 c 8.0 0.7 7-10 c' 1.3 0.2 1-2 V 87.6 1.3 86-90 M 80.7 4.7 73-89 G 69.7 6.3 57-77 Ovary, % of body length 47.8 3.7 41-54 Stylet, % of body length 18.9 2.1 14-21 a a = body length/greatest body width; b = body length/ distance from anterior end to junction of esophagus and intestine; c = body length/tail length; c' = tail length/body width at vulva; V = distance of vulva from anterior end x 100/body length; M = conus length x 100/stylet length; G = distance from vulva to anterior end of ovary x 100/body length. mature egg in uterus. Bacteria frequently present, particularly in anterior ovary, and sometimes seen in intestinal epithelial cells, intestinal lumen, and eggs. Uterine glands not seen. Spermatheca ovoid, thick-walled, usually containing sperm. Intrauterine eggs 30 x 86 p,m, usually in 1-8 cell stage. Excretory pore 14-25 p.m from anterior end. Renette cell large, about 20 x 60 jxm, consisting of a loosely coiled tubule extending anteriorly to the excretory pore and posteriorly toward the tail. Renette cell nucleus large, 7.3-10.2 (8.8 + 1.2) in gravid females, irregular in outline in fixed specimens, smooth in live specimens. Tail shape conical, with mucro small or absent. Anus not visible with light microscopy. Vulva subterminal (V = 88%), transverse, with overlapping anterior lip. One pair of prevulval and one pair of postvulval papillae. Males: Measurements in Table 4. Body hook-shaped, tapering gradually at ante- TABLE 4. Measurements of 16 paratype male Noctuidonema dibolia n. sp. from Tift County, Georgia. Character ~ Mean SD Range Measurements (v.m) Body length 422 48.6 343-524 Maximum body width 42 3.1 38-51 Body width at nerve ring 31 2.5 28-35 Body width at cloaca 14 2.3 10-18 Body width at anterior 31 2.5 28-35 end of intestine Anterior end to base 106 14.0 77-126 of bulb Metacorpus length 26 1.5 23-28 Metacorpus width 20 2.1 16-23 Excretory pore to 21 4.2 15-31 anterior end Stylet total length 86 4.4 76-93 Styler cone length 68 4.8 61-82 Stylet shaft length 18 5.1 16-26 Head width 8 1.0 7-10 Head length 4 0.9 3-6 Testis length 144 47.5 85-233 Spicule length 48 3.5 41-53 Spicule rostrum length 12 1.2 10-13 Cloaca to end of tail 9 1.1 6-10 Cloaca to anterior end 413 49,0 333-515 Anterior end to 132 21.8 98-174 anterior testis Ratios and Percentages a 10.0 1.1 8--12 b 4.0 0.3 3-5 c 50.8 1 I. 1 34-80 c' 0.7 0.2 0-1 V 98.0 0.4 97-99 M 78.7 5.5 70-93 T 66.6 4.4 60-74 Testis, % of body length 34.6 12.1 21-56 Stylet, % of body length 20.7 2.1 17-24 a = body length/greatest body width; b = body length/ distance from anterior end to junction of esophagus and intestine; c = body length/tail length; c' = tail length/body width at cloaca; V = distance of cloaca frmn anterior end x 100/body length; M = conus length x 100/stylet length; T = distance from cloaca to anterior end of testis x 100/body length.

392 Journal of Nematology, Volume 27, No. 3, September 1995 rior end, with posterior half strongly arcuate ventrally. Annules continuous, 1.2-1.8 wide (1.4 +- 0.2) at midbody, anastomoses common. Lateral field absent. Lip region low, bluntly rounded, not strongly set off, similar to female. Stylet flexible, delicate, elongate, attenuated at tip, 17-24% of total body length. Conus representing about 79% of total stylet length. Stylet knobs rounded, with concave anterior surfaces. Stylet conus diameter 0.7-1.0 (0.9 + 0.1), shaft diameter 1.0-1.6 (1.2 +- 0.2), knob width 2.6-5.0 (3.8 -+ 0.8). Knobs to guide ring 6.8-17.0 (13.9 -+ 3.0). Metacorpus ovoid, with a sclerotized valvular apparatus offset slightly posteriorly. Procorpus strongly flexed at level of metacorpus. Esophageal glands 36.5-71.5 (58.1 + 11.38) long, overlying anterior intestine. Nerve ring immediately posterior to metacorpus. Hemizonid position variable, 7.3-33.6 (15.9 -+ 8.5) posterior to nerve ring. Intestine a blind sac, terminating well anterior to cloaca. Intestinal contents usually yellow, similar to female. Tail short, blunt, with one pair of precloacal and one pair of postcloacal papillae. Tail mucro absent or low. Spicules paired, sclerotized, nearly equal in size and shape, ventrally arcuate, with dorsal and ventral arms not well separated, ending in fine points closely apposed at tips. Matrix and sheath present, but greatly reduced. Rostrum slender, arcuate, distal end slightly enlarged. Manubria well developed, wedge-shaped, with right slightly more rounded than left. Gubernaculum and bursa absent. Cloacal cylinder thin-walled, projecting 4-6 Ixm nearly perpendicular to tail axis during spicule protraction. Testis single, outstretched anteriorly, without rachis. Anterior end of testis usually not extending anterior to metacorpus. Seminal vesicle containing spermatids and set off from remainder of testis by a moderate constriction. Bacteria commonly present in testis. Excretory pore 15-30 ~m from anterior end. Renette cell large, about 20 50 txm, similar to female. Renette cell nucleus 4.4-10.2 (7.6 +- 1.7), similar to female. Type Host and Locality Ectoparasitic on adults of Mocis latipes (Guen6e) (Lepidoptera: Noctuidae), particularly on intersegmental membranes of the abdomen. Type locality is the Belflower Farm, located 5 km NNW of Tifton, Tift County, Georgia. Type Designations Holotype (female) (slide T-519t), allotype (male) (slide T-520t), 5 paratype slides (slides T-4526p-T-4530p), and one vial of paratypes in glycerin (vial T-370p) deposited in the U.S. Department of Agriculture Nematode Collection, Nematology Laboratory, USDA ARS, BARC-West, Beltsville, Maryland 20705. Four paratype slides deposited at each of the following: Museum National d'histoire Naturelle, Laboratoire des Vers, Paris, France; Instituut voor Dierkunde, Gent, Belgium; Biosystematics Research Centre, Canadian National Collection of Nematodes, Canada Agriculture, Ottawa, Ontario, Canada; Rothamsted Experimental Station, Nematode Collection, Entomology and Nematology Department, Harpenden, Herts, United Kingdom. Diagnosis All stages of N. dibolia n. sp. are ectoparasitic on adult Mocis latipes. Stylet length is 83-114 Ixm in females, 76-93 ~m in males, with a conus 73-89% of total styler length in females and 70-93% in males. Cephalic end similar in males and females. Tail length is 42-79 ixm in females and 6-10 txm in males. Spicules have dorsal and ventral arms closely apposed, not separated; the matrix and sheath are present but much reduced. A large renette cell is present in both sexes. Relationships Males of N. dibolia n. sp. are smaller and more slender than those of N. guyanense, have shorter stylets and shorter styler coni,

Noctuidonema dibolia n. sp.: Marti and Rogers 393 and have spicules that differ in size and structure. The spicules of N. dibolia n. sp. are smaller and simpler than those of N. guyanense and have a greatly reduced matrix and sheath. In N. dibolia n. sp., the spicules have well-developed, wedgeshaped manubria, not reduced as in V. daptria, and have dorsal and ventral arms closely apposed, not widely separated as in V. daptria. Males ofn. dibolia n. sp. are similar in size to V. daptria males, but have longer stylets and longer styler coni. Female N. dibolia n. sp. are smaller and more slender than those of N. guyanense and have a shorter stylet, shorter stylet conus, and longer tail. Female N. dibolia n. sp. differ from those of V. daptria in having a longer stylet, longer styler cone, and shorter tail. The excretory pore is farther from the anterior end in N. dibolia than in V. daptria. DISCUSSION Hunt (7) erected the family Acugutturidae to include the genera Acugutturus, Noctuidonema, and the new genus Vampyronema. Remillet and Silvain (8) placed Noctuidonema in the subfamily Acugutturinae and distinguished it from Acugutturus by differences in body shape, stylet length, shape of head and tail, position of the excretory pore, shape and size of the spicules, and presence of a bursa. Anderson and Laumond (2) described Noctuidonema daptria, which Hunt (7) later redescribed as Vampyronema and placed with Noctuidonema in the newly created subfamily Noctuidonematinae. Hunt (7) noted that basal swellings and knobs were absent on the stylet in A. parasiticus, and Remillet and Silvain (8) reported that stylet knobs were present in N. guyanense. Anderson and Laumond (1) provided more details on the morphology of the spicule and redescribed the male of N. guyanense. However, they also reported that the basal part of the styler of N. guyanense is uniformly tubular, without swellings or knobs. Anderson and Laumond (2) also reported the presence of stylet knobs in N. daptria. Stylet knobs are present in N. dibolia. We examined Noctuidonema specimens from several species of Spodoptera (S. frugiperda, S. ornithogalli, S. latifascia, and S. androgea) from the United States and French Guiana and found that styler knobs were present in all Noctuidonema specimens examined. During processing of N. dibolia specimens for this report, we observed that the basal part of the styler frequently becomes transparent, rendering the knobs difficult to see. However, the knobs are easily visible in living specimens. Our observations indicate that stylet knobs are present in all species of Noctuidonema and that this feature unites the known species of the subfamily Noctuidonematinae and aids in differentiating them from Acugutturus. Spicule structure in N. guyanense and N. dibolia are similar enough to justify grouping them within a single genus, and different enough to identify them as separate species and separate them from the related genus Vampyronema. LITERATURE CITED 1. Anderson, R. V., and C. Laumond. 1990. Noctuidonema guyanense Remillet & Silvain, 1988: Morphologie du spicule, redescription du mille et diagnose amend6e du genre Noctuidonema. Revue de N6matologie 13:433---436. 2. Anderson, R. V., and C. Laumond. 1992. Noctuidonema daptria, n. sp. (Nematoda:Aphelenchoididae), an ectoparasite of the moth Lesmone porcia (Stoll). Journal of Nematology 24:16-22. 3. Ashley, T. R. 1979. Classification and distribution of fall armyworm parasites. Florida Entomologist 62:114-123. 4. Courtney, W. D., D. Polley, and V. L. Miller. t955. TAF, an improved fixative in nematode technique. Plant Disease Reporter 39:570-571. 5. Dean, T.W. 1985. Behavioral biology of the striped grass looper, Mocis latipes (Guen6e), in northcentral Florida. Ph.D. dissertation, University of Florida, GainesviUe. 6. Hunt, D.J. 1980. Acugutturus parasiticus n. g., n. sp., a remarkable ectoparasitic aphelenchoid nematode from Periplaneta americana (k.), with proposal of Acugutturinae n.subf. Systematic Parasitology 1:167-170. 7. Hunt, D.J. 1993. Aphelenchida, Longidoridae, and Trichodoridae: Their systematics and bionomics. CAB International, Wallingford, UK. 8. Remillet, M., and J.-F. Silvain. 1988. Noc-

394 Journal of Nematology, Volume 27, No. 3, September 1995 tuidonema guyanense n. g., n. sp., (Nematoda: Aphelenchoididae) ectoparasite de noctuelles du genre Spodoptera (Lepidoptera: Noctuidae). Revue de Nfmatologie 11:21-24. 9. Rogers, C. E., O. G. Marti, A. M. Simmons, and J.-F. Silvain. 1990. Host range of Noetuidonema guyanense (Nematoda: Aphelenchoididae): An ectoparasite of moths in French Guiana. Environmental Entomology 19:795-798. 10. Rogers, C. E., A. M. Simmons, and O.G. Marti. 1990. Parasitism of Lepidoptera adults by Noctuidonema guyanense Remillet and Silvain (Nematoda: Aphelenchoididae) in southeastern United States. Journal of Agricultural Entomology 7:241-245. 11. Simmons, A. M., and C. E. Rogers. 1990. Distribution and prevalence of an ectoparasitic nematode, Noctuidonema guyanense, on moths of the fall armyworm (Lepidoptera: Noctuidae) in the tropical Americas. Journal of Entomological Science 25:510-518. 12. Silvain, J.-F. 1984. Premihres observations sur l'4cologie de Spodopterafrugiperda (J. E. Smith) et Mocis latipes (Guen4e), noctuelles d4pr4datrices des gramin6es fourraghres en Guyane frangaise. Prairies guyanaises et elevage bovin. Les Colloques de I'INRA 24:243-272. 13. Sparks, A. N. 1979. A review of the biology of the fall armyworm. Florida Entomologist 62:82-87.