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Neelides folsomi

Neelides folsomi

Caroli, 1912

GBIF:4537267

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PROFILE

Species Profile

Habitat

Terrestrial

ABOUT

Descriptions(4)

Description. Adult (Figs 1 a, 2 A, 3 A, 4 A 5, 9 A, 22 – 31). Size. Length from labrum to anus of the biggest specimens ~ 600 µm. Pigmentation. Dorsal pigmentation from blue-gray to deep black, spotted with small patches of bright yellow and with a pale yellow dorso-median line from thorax to middle of the abdominal area. Ventral side pale yellow. Body shape and segmentation. Habitus as in Fig. 22 A, B. Orthognathous. Head rather round and short, ratio height: length ~ 0.67 (Fig. 22 A – D). Antennae pointed anteriorly, with four distinct antennomeres, with an internal curve and abrupt narrowing between Ant. III and IV (Figs 22 A – D, 27 A, B). Total length of antenna ~ 77.6 µm; max width (Ant. III) ~ 20 µm; ratio width: length ~ 0.25; ratio length of Ant. I: Ant. II: Ant. III: Ant. IV ~ 0.26: 0.60: 0.92: 1. Th. I diameter reduced, with steep curves between head – Th. I and Th. I – II (Fig. 22 A, B, E). Connection of Th. I with head as a well-developed neck (Fig. 22 A, B, E, F). Insertion of the neck on head moved ventrally creating a posterior apex of the vertex. Th. I with a posterior transversal fold subdivided laterally in two folds respectively reaching the anterior and posterior limits of the subcoxa; neck with a pair of slanted folds connected laterally with the posterior folds and converging dorsally toward the head (Fig. 22 E, F). Terga from Th. II to Abd. VI completely fused, with no other delimitation marks than legs insertions. Trunk bumpy (observed on specimens dryed for SEM, Fig. 22 B, E), with slight folds but no marks of segmentation. Dorso-median line as a slight crest well defined on Th. I, becoming more and more indistinct until Th. III (Fig. 22 B, E). Posterior granule T of the line missing. Precoxal areas of Th. II and III each with a pair of large lobes which cover the subcoxae anteriorly (Figs 22 A, B, E, 28 A, 29 F). Each coxa long and bended (Figs 22 A, B, 29 A, C, F). On legs I length of coxa> tibiotarsus> femur ~ trochanter. On leg II and III length of coxa> tibiotarsus ~ femur ~ trochanter. All sterna fused together except Abd. VI sternum. Abd. VI sternum clearly separated posteriorly from Abd. VI tergum by anal aperture; separated anteriorly from Abd. V sternum by a steep curve (Fig. 24 A, B); fused laterally with the great abdomen without any distinction in the integumentary granulation (Fig. 24 A, B). Abd. V sternum with genital plate cryptic, enclosed deeply between Abd. IV and Abd. VI sterna. Abd. IV sternum enlarged forming a large ventro-posterior side bearing the furca (Fig. 22 A, B). Abd. I – III sterna reduced with tenaculum being stuck to ventral tube (Fig. 31 I). Ratio length of head: length of thorax (distance from anterior insertion point of subcoxa I to posterior insertion point of subcoxa III): length of abdomen (distance from posterior insertion point of subcoxa III to anus) = 1.1: 1.8: 1. Manubrium / dens articular processes: strong, with a concave tip on manubrium; as a cavity (external side) sided with a small convex process (internal side) on dens (Figs 24 B, 31 G). Dens with a proximal part (dp) wider than the distal part (dd) (Figs 24 B, 31 G). No suture or articular process between dp and dd but dens flexible at this point (fixed specimens often exhibit a flexion of the dens between dp and dd with subsequent folds in the integument, Fig. 24 B). Length of manubrium: dp: dd: mucro ~ 0.33: 0.56: 1: 0.78. Granulation. Primary granulation made of ordinary hexagonal pattern (six primary granules connected with bridges). Three morphological variations of primary granules pattern observed: (i) ordinary; (ii) thickening of all the granules of the hexagon — width increased but not height, bridges shortened and visible surface of the base of the integument reduced — occurs on the labrum around m- and p-rows of chaetae (Fig. 23 A, C); (iii) enlargement of only a few granules of the hexagon — width and height increased, those granules being brighter than the other in SEM and visible as dark dots in light microscopy (= secondary granules sensu Dallai 1979). Enlarged granules with two kinds of pattern. First kind is a random distribution of two or three enlarged granules by hexagon, such pattern occurs on clypeus (Fig. 23 A – C), distal part of Ant. III, anal valves (Fig. 31 C), most of Ant. IV sternum (Fig. 24 A – C), posterior side of manubrium and dens (Fig. 24 B), and moderately on leg. Second kind is a new hexagonal (sometimes pentagonal) pattern of enlarged granules, the center of those hexagons devoid of primary granules but the base of the integument bears about seven small protuberances (six around a central one, also see the accurate description of Dallai 1979), this pattern covers the head dorsally and laterally with an anterior limit matching the position of the unpaired chaeta of cl. p-row (Figs 3 A, 22 D), the whole trunk terga (e. g. Fig. 23 E, F), the Abd. VI sternum (Fig. 24 A, B), the basal part of the legs down to basal part of coxae and Ant. I – III. Enlarged granules with random pattern being larger than those with hexagonal pattern. Presence of dermastra typical of the genus (e. g. Fig. 23 E, F). From the commonest dermastra with five edges, up to eight edges can be observed. The areas of repartition of the dermastra perfectly match the areas of repartition of the hexagonal pattern of enlarged granules. Integumentary channels. Presence of a simple integumentary channel surrounding the head in the clypeal area, connecting linea ventralis at the base of basomedian fields of labium (Figs 23 B, D, 26 A – C). A pair of fingershaped cuticular processes cover the channel at basolateral fields of labium level (Figs 23 B, D, 26 A, C). The bed of the channel is devoid of granulation and shallow (as deep as a the height of a primary grain), the channel edges are thin and smooth, without granule (Fig. 23 D). Integumentary channels absent on posterior part of head and on trunk. Chaetae. Eight morphological variations of chaetae on head and trunk: (i) ordinary chaetae mostly found on antennae, ventrally and laterally on head, dorsally and laterally on forehead and legs (e. g. Fig. 1 c); (ii) setulae, peculiarly thin variety of microchaetae (4 – 6 µm), weakly contrasted in light microscopy mostly found on the vertex of the head and dorsally on trunk (e. g. Figs 1 a, 28 B); (iii) s-chaetae, short and swollen special chaetae (s 1 – s 5) found on trunk (e. g. Fig. 23 F); (iv) τ-chaetae, flexible mesochaetae (~ 10 µm) with rounded apex, basal ring implanted in a small depression of the integument, weakly contrasted in light microscopy, found on trunk (Figs 23 E, 28 D); (v) primary wax secretory rods (WR) (~ 6 µm); (vi) secondary wax secretory rods (wr), (~ 3 µm); (vii) tertiary wax secretory rods (from 2 to 4 µm); (viii) neosminthuroid chaetae (Figs 24 C, 28 F) (from 8 to 10 µm). Wax secretory rods. Presence of three kinds of chaetae associated with the secretion of rods (putatively wax): primary (WR), secondary (wr) and tertiary rods. The primary rods (WR) are straight mesochaetae (~ 6 µm) with a round apex and with a basal ring implanted in a small depression of the integument. The depression is surrounded with an integumentary bulge on which lies an orifice (putative pore of a secretory gland according to Dallai 1979). The secondary wax rods are similar to the primary wax rods but shorter and thinner (~ 3 µm), with a more conical shape. The basal ring is not so deep in the integument than for the primary rods. The integumentary bulge is either weak or not visible but a secretory pore is apparently present. A primary rod is generally associated with one or more secondary rods (Figs 25 C, 28 A). The tertiary rods are very short, conical microchaetae with a round apex (Fig. 28 C). The basal ring is only weakly sunk in the integument, there is no integumentary bulge nor visible secretory pore. There is some small variation in size and thickness among the numerous tertiary rods of a same specimen (from 2 to 4 µm). Sensory fields. Four pairs of sensory fields can be recognized, three on head and one on Th. II, being depressions with more or less clear edges, each with a patch devoid of dermastra and associated with one primary rod. Each preantennal field with primary rod on posterior edge, the latter creating a cornice that overhang a flat area devoid of secondary hexagons, this area as a cliff in the slope of the forehead (Fig. 25 A). Postantennal anterior fields as simple depressions, edge marked only on the dorsal side (Fig. 25 B). Postantennal posterior fields as simple depressions with no clear edge. Fields on Th. II with no clear edge, with three secondary wax rods in addition to the primary wax rods (Fig. 25 C). Mouth parts. Left mandibula with about five apical teeth (Fig. 25 D), right mandibula with six teeth and two processes between apex and molar plate (Fig. 25 E). Molar plate with anterior process bearing teeth (Fig. 25 D – F). Maxilla with five lamellae. Labium. Basomedian field with three mesochaetae, basolateral field with two ventral mesochaetae and a dorsal mesochaeta on tubercle (Figs 23 D, 26 A). Basomedian field separated from basolateral field by a furrow (Fig. 23 D). Palp with three strong chaetae in proximal field (Fig. 25 H) and four strong papillate chaetae (H, B, D, E). B, D, E each with three guard mesohairs, H with two guard mesohairs (Fig. 25 I). The papilla B in anterior position in regard to the hypostomal papilla (H). Chaeta H is long, with a curved an pointed apex (Fig. 25 I). Maxillary outer lobe and oral fold. Maxillary palp with a mesochaeta (12 µm) in the sub-basal papilla, a strong, straight macrochaeta (20 µm) in the apical papilla (Fig. 25 J). Apical papilla with a strong hair (8 – 9 µm) in sub-apical, dorso-lateral position (Fig. 25 J). Sublobal plate with a micro-hair on a small papilla (Fig. 25 J). Oral fold with two mesochaetae (Figs 23 D, 26 A). Labrum. Labrum rather plane despite some bumps on which the chaetae of the a-, m and p-rows are implanted (Figs 2 E, 23 A – C, 25 J). a-row with two pairs of mesochaetae (a 1, a 2), sub-apical and in dorsal position. a 1, a 2 around 10 µm. m- and p-rows each with two pairs of mesochaetae (respectively m 1, 2 and p 1, 2) and an unpaired mesochaeta (respectively m 0 and p 0). Chaetae p 0 – p 2 and m 0 – m 2 curved with tip pointed upward, subtlety longer than chaetae a 1, 2. Chaetae a 1, a 2 clearly thicker than m 0 – m 2, m 0 – m 2 slightly thicker than p 0 – p 2, all of them with smooth edges. Labral ridge sclerotized, bearing two rows of apical hairs, the dorsal row apparently made of a lateral pair of finger-shaped hairs, an axial pair of hand-shaped hairs (large body with around five fingers) and an unpaired forked hair (Fig. 25 K), the ventral row apparently as a comb of simple, thin hairs (Fig. 25 L). Head chaetotaxy. Postero-dorsal area with 13 + 13 setulae, an unpaired setula and two pairs of primary rods (sensory fields). Postero-lateral area with 1 + 1 setulae and 5 + 5 mesochaetae (Figs 3 A, 26 C). Antero-dorsal area with a pair of setulae (inter-antennal position, Fig. 26 C), eight pairs of mesochaetae, two unpaired mesochaetae and a pair of primary rods (sensory fields). Antero-lateral area with five pairs of mesochaetae (Figs 3 A, 26 A – C). Ventral area with 1 + 1 post-labial mesochaetae (Figs 4 A, 26 A). Antenna chaetotaxy. Ant. I with a setula on antero-dorsal side (Fig. 27 B). Ant. II with four mesochaetae in a whorl, dorsal side (Fig. 27 A, B). Ant. III with 14 mesochaetae in three rough whorls (repartition from base to apex: 3, 4 and 7 chaetae); with five apical S-chaetae (S 1 – S 5), S 1 and S 4 long and tubular, S 2 and S 3 as two short bulbs, S 5 short and flam-shaped (Fig. 27 A, B). Ant. IV with 22 chaetae, size decreasing from the basal mesochaetae (10 µm) to the apical microchaetae (4 µm), whorls unclear; with seven S-chaetae, five long (8 – 10 µm), one short (6 µm) and thicker than the other (Sy), another shorter than the other (5 µm) (Sx); with seven sensory rods with truncated apex in apical (a) and sub-apical position (sa), one of which half as long as the others (6 µm and 3 µm); sub-apical organite short (1 – 2 µm), in basal position to the rods sa, and apical position to the S-chaeta Sx (Fig. 27 A – C). S-chaetae of Ant. III and IV without ornamentation. Th. II – Abd. V terga chaetotaxy. Th. II – Abd. V terga with a total of 23 + 23 setulae, 7 + 7 mesochaetae, 20 + 20 τ-chaetae all in the thoracic region, 7 + 7 s-chaetae (s 1, s 2, s 3, s 3 ’, s 3 ”, s 4, s 5), 9 + 9 primary rods (WR), 21 + 21 secondary rods (wr) including 2 + 2 rather large (Figs 9 A, 28 A – E). Dorso-lateral area of Th. II with: 8 + 8 setulae; 11 + 11 τ-chaetae; 2 + 2 primary rods, dorsal and lateral, attended respectively by 3 + 3 and 2 + 2 secondary rods (Figs 9 A, 28 A); 1 + 1 s-chaetae s 1 (Fig. 28 E), next to the lateral rods. Precoxal areas of Th. II with 2 + 2 mesochaetae, 1 + 1 τ-chaetae, 1 + 1 primary rods and 1 + 1 secondary rods (Figs 9 A, 28 A). Dorso-lateral area of Th. III – anterior abdomen with 8 + 8 setulae, 7 + 7 τ-chaetae, 4 + 4 primary rods, 11 + 11 secondary rods and 4 + 4 s-chaetae (s 3, s 3 ’, s 3 ”, s 5; Figs 9 A, 28 A); all wax rods, τ- and s-chaetae restricted to the lateral part of the area (i. e. far from dorsal axis). Position of primary rods and number of associated secondary rods as follows: (i) anterodorsal with four secondary rods, (ii) antero-ventral with one secondary rod, (iii) postero-dorsal with three secondary rods and (iv) postero-ventral with one secondary rod (Figs 9 A, 28 A). Precoxal areas of Th. III with 5 + 5 mesochaetae, 1 + 1 τ-chaetae, 1 + 1 s-chaetae s 4, 1 + 1 primary rods and 1 + 1 secondary rods (Figs 9 A, 28 A). Posterior region of the abdomen (until Abd. V included) with 7 + 7 setulae, 1 + 1 primary rods, 3 + 3 secondary rods, about 31 + 31 tertiary rods and 1 + 1 s-chaetae (s 2; Figs 9 A, 28 A). The primary rods, one of the pair of secondary rods, s 2 and one of the pair of setulae are positioned at the limit of Abd. VI tergum and sternum (Figs 9 A, 24 A, 28 A). s 1 and s 5 tubular with apex cut on a slant (Fig. 28 E), s 5 flam-shaped, s 2, s 3, s 3 ’ and s 3 ” beanshaped (Figs 23 F, 24 A). Legs chaetotaxy. On leg I: subcoxa 1, subcoxa 2 and coxa each with a mesochaeta (Fig. 29 A); trochanter with two proximal microchaetae and two distal mesochaetae (Fig. 29 A); femur with seven chaetae with strong base (a microchaeta, six mesochaetae) and three s-chaetae that differ from the other in shape and light refraction — a thicker s-chaeta (5 µm) with rounded apex in postero-median position, a thinner (5 µm) with pointed apex and a short one (1 µm) both in postero-distal position (Fig. 29 B); tibiotarsus with 21 chaetae with strong base in four whorls distributed from the most proximal to the most distal as 2, 5, 5, 9, size ranging from 4 to 10 µm (Fig. 29 B). On leg II: subcoxa 1, subcoxa 2 each with a mesochaeta (Fig. 29 C); coxa with three chaetae (two mesochaetae proximal and median, a median microchaeta, Fig. 29 C); trochanter with five mesochaeta (2 proximal, 1 median, 2 distal, Fig. 29 D); femur with 10 micro / mesochaetae (3 median, 7 distal, Fig. 29 D); tibiotarsus with 20 chaetae with strong base in three whorls distributed from the most proximal to the most distal as 5, 6, 9, size ranging from 4 to 10 µm (Fig. 29 D). On leg III: subcoxa 1 with two chaetae (a microchaeta and an anterior mesochaeta, Fig. 29 F); subcoxa 2 with a microchaeta (Fig. 29 F); coxa with a proximal mesochaeta and a median microchaeta (Fig. 29 F); trochanter with five chaetae (two proximal microchaetae, three distal mesochaetae with strong base, Fig. 29 F); femur with 11 chaetae with strong base (4 median, 7 distal, Fig. 29 G); tibiotarsus with 18 chaetae in three whorls distributed from the most proximal to the most distal as 4, 5, 9 size ranging from 4 to 10 µm (Fig. 29 G). See Tables 9, 10, 11 for a summary. Claws. Each pretarsus bearing two microchaetae with strong base, one on anterior side and one on posterior side (Figs 29 B, E, H, 30 A, B). Unguis: lamellae L, la and lp each with a strong smooth edge (Fig. 30 A). The smooth edges of la and lp are fused together at the base, remain close to the body of the unguis in external position and fit closely the smooth edge of L (Fig. 30 A), with which they can easily be mistaken in light microscopy. Lamella Bp reduced to a small tooth implanted on the internal edge of the main lamella (Fig. 30 A, B). The smooth edge of the main lamella is ornamented with a pair of small teeth near the tip (Fig. 30 A). Unguiculus: basal tubercle with a bulk anterior process and a flatten posterior process perpendicular to the claw (Fig. 30 A, B), this three layers structure visible in light microscopy (Fig. 29 B, E, H). Unguiculal lamella with posterior crest Cp (Fig. 30 A), without anterior crest. Claw I and II similar (Fig. 29 B, E), claw III shorter with its lateral-basal part particularly protruding from tibiotarsus edge and with a strong unguiculus (Fig. 29 H). Abd. VI. Three regions with different integuments can be observed: (i) with dermastra in anterior regions of the tergum and sternum, (ii) without dermastra, with enlarged primary granules in region of anal valves, (iii) without primary granulation on anal aperture edges and inner integument (Fig. 31 C). Anterior region of the tergum with a pair of secondary wax rods, one anterior row of 2 + 2 mesochaetae (10 µm) and one posterior row of 2 + 2 macrochaetae (17 µm), the lateral pair of chaetae on the anterior row in a more lateral position than the lateral pair of chaetae on the posterior row (Fig. 31 A). Dorsal anal valve with 1 + 1 microchaetae µ. av (1 – 2 µm) and an unpaired mesochaeta av (6 - 7 µm) (Fig. 31 A, C). Ventral pair of anal valves with 2 + 2 lateral microchaetae µ. av and 1 + 1 axial microchaetae av (Fig. 31 B, C). Anterior region of sternum with 3 + 3 axial macrochaetae and 3 + 3 lateral mesochaetae (Fig. 31 B). Genital plate. Female with 4 + 4 mesochaetae (Fig. 31 D). Male unknown. Abd. IV sternum. With 1 + 1 macrochaetae, 1 + 1 mesochaetae (Figs 28 A, 31 B, G) and a variable number of neosminthuroid chaetae (ns, Fig. 28 A). This number is probably correlated to the age: in the same population, I observed from 3 + 3 to 5 + 5 neosminthuroid chaetae in adult or at least sub-adult specimens, the biggest specimens having the greatest number. Neosminthuroid chaetae rather short, clothed with spicules on the whole length (Figs 24 C, 28 F). Abdominal appendages. Manubrium with 3 + 3 posterior mesochaetae aligned in parallel with the axis of symmetry, the proximal pair longer than the others and with 1 + 1 neosminthuroid chaetae in lateral position (Figs 28 F, 31 E, G). Dens proximal part with a posterior mesochaeta (Fig. 31 E, G); distal part with a basal, posteroexternal spine (E 3), three median spines (anterior A 2, postero-external E 2 and postero-internal J 2), five apical spines (three anterior AE 1, A 1, AJ 1, one postero-external E 1 and one postero-internal J 1) and one apical, posterior strong and short chaeta (P 1) almost spine-like (Fig. 31 E – H). All spines with a basal ring. Mucro’s body almost perfectly conical with a slight constriction at 3 / 5 from the base, lamellae thin and about 12 teeth on both posterior lamellae (Figs 24 D, 31 G). Tenaculum with two median lobes without chaeta, 2 + 2 apical teeth, basal tubercles as small, hardened bumps on each side (Fig. 31 I, J). Ventral tube with a posterior lobe and 2 + 2 apical mesochaetae (Fig. 31 I). Juvenile (Figs 3 A, 4 A, 5, 9 B, 32 – 35). Size. Length from labrum to anus ~ 250 µm. Pigmentation. Dorsally with pale blue-gray, ventrally whitish (in ethanol). Body shape and segmentation. Habitus as in Fig. 32. Orthognathous, ratio height of head: length of head ~ 0.65. Total length of antenna ~ 54.5 µm; max width (Ant. III) ~ 15 µm; ratio width: length ~ 0.28; ratio length of Ant. I: Ant. II: Ant. III: Ant. IV ~ 0.33: 0.55: 1: 1. Th. I not so reduced in regard to head and rest of the trunk, neck not perceptible. Precoxal areas not so prominent. On leg I length of coxa> tibiotarsus> femur ~ trochanter. On legs II and III length of coxa> tibiotarsus ~ femur ~ trochanter. Abd. IV sternum not so enlarged. Ratio length of head: length of thorax (distance from anterior insertion point of subcoxa 1 I to posterior insertion point of subcoxa 1 III): length of abdomen (distance from posterior insertion point of subcoxa 1 III to anus) ~ 1.8: 1.7: 1. Length of manubrium: dp: dd: mucro ~ 0.9: 0.5: 1: 0.85. Granulation. Dermastra present. Integumentary channels. Similar to the adult (Fig. 33 C). Chaetae. Five morphological variations of chaetae on head and trunk: (i) ordinary chaetae; (ii) s-chaetae, short and swollen chaetae with rounded apex (s 1 – s 5) found on trunk; (iii) τ-chaetae, conical and well contrasted in light microscopy; (iv) primary wax secretory rods (WR), (v) secondary wax secretory rods (wr). Absence of the ‘ setula’ morphology, ordinary, well contrasted microchaetae observed instead (Figs 33 A – C, 34 A). Pairs of mesochaetae in precoxal area of Th. II and precoxal area of Th. III with contrast similar to s-chaetae under light microscopy (Figs 34 A, 35 A, B). Wax secretory rods and sensory fields. Primary rods stronger than secondary rods. The primary rods of each sensory field reported in the adult are present but the depression and edge of the fields are not perceptible in light microscopy. Labium, maxilla outer lobe, oral fold, labrum. Labrum apparently with only one range of apical hairs, being a comb of simple hairs (Fig. 33 A). Rest of the chaetotaxy similar to the adult (Fig. 33 A, C). Head chaetotaxy. Postero-dorsal area with five pairs of microchaetae, an unpaired microchaeta and two pairs of primary rods. Postero-lateral area with five microchaetae (Fig. 33 B, C). Antero-dorsal area with seven pairs of microchaetae, two unpaired microchaetae and a pair of primary rods. Antero-lateral area with four pairs of microchaetae (Fig. 33 A, C). Ventral area with 1 + 1 post-labial microchaetae (Fig. 33 C). E — I J 50 Μm 50 Μm Antenna chaetotaxy. Ant. I with a microchaeta on anto-dorsal side (Fig. 34 C). Ant. II with four microchaetae in a whorl, dorsal side (Fig. 34 B, C). Ant. III with 14 microchaetae in three rough whorls (repartition from base to apex: 3, 4 and 7 chaetae); with five apical S-chaetae (S 1 – S 5), S 1 and S 4 long and tubular, S 2 and S 3 as two short bulbs, S 5 short and flam-shaped (Fig. 34 B, C). Ant. IV with 22 microchaetae, proximal chaetae longer, distal chaetae shorter, in four rough whorls; with four S-chaetae, one of which clearly thicker than the others (Sy), another shorter than the others (Sx); with six sensory rods with truncated apex in apical (a) and sub-apical position (sa), one of which two times shorter than the others; sub-apical organite present (Fig. 34 B, C). Th. II – Abd. V terga chaetotaxy. Th. II – Abd. V terga with a total of 33 + 33 ordinary chaetae (30 + 30 microchaetae and 3 + 3 mesochaetae), 19 + 19 τ-chaetae all in the thoracic region, 7 + 7 s-chaetae (s 1, s 2, s 3, s 3 ’, s 3 ”, s 4, s 5), 7 + 7 primary rods (WR), 5 + 5 secondary rods (wr) (Figs 9 B, 34 A). Dorso-lateral area of Th. II with: 5 + 5 microchaetae (more dorsal) and 1 + 1 mesochaetae (more lateral); 11 + 11 τ-chaetae; 2 + 2 primary rods dorsal and lateral, the latters accompanied by 1 + 1 secondary rods; 1 + 1 s-chaetae s 1, next to the lateral rods (Figs 9 B, 34 A). Precoxal areas of Th. II with 1 + 1 mesochaetae, 1 + 1 primary rods and 1 + 1 τ-chaetae (Figs 9 B, 34 A). Dorso-lateral area of Th. III – anterior abdomen with 16 + 16 microchaetae, 7 + 7 τ-chaetae, 2 + 2 primary rods, 2 + 2 secondary rods and 4 + 4 s-chaetae (s 3, s 3 ’, s 3 ”, s 5); wax rods, τ- and s-chaetae restricted to the lateral part of the area (Figs 9 B, 34 A). Precoxal areas of Th. III with 1 + 1 mesochaetae, 1 + 1 s-chaetae s 4, 1 + 1 primary rods (Figs 9 B, 34 A). Posterior area of the abdomen (until Abd. V included) with 9 + 9 microchaetae, 1 + 1 primary rods, 2 + 2 secondary rods, and 1 + 1 s-chaetae (s 2), tertiary rods absent (Figs 9 B, 34 A). s 1, s 4 and s 5 tubular with rounded apex, flam-shaped, s 2, s 3, s 3 ’ and s 3 ” shaped as bulbs (Fig. 34 A). Legs chaetotaxy. Legs clothed with microchaetae (with variations from 1 µm to 6 µm, Fig. 35 A – C). in regard to adult: coxa II missing two chaetae, coxa III missing a chaeta; trochanter I, II and III each missing a chaeta; femur I missing the three special chaetae, femur III missing three chaetae; tibiotarsus I missing five chaetae, tibiotarsus II missing four chaetae and tibiotarsus III missing three chaetae (Fig. 35 A – C). Claws morphology. Tooth Bp missing on each claw, otherwise similar to the adult (Fig. 35 B – D). Abd. VI. Tergum with one anterior row of 3 + 3 microchaetae and one posterior row of 2 + 2 microchaetae (Fig. 34 A). Dorsal anal valve with 1 + 1 microchaetae (µ. av) and an unpaired microchaeta (av; Fig. 34 A). Ventral pair of anal valves with 2 + 2 lateral microchaetae (µ. av) and 1 + 1 axial microchaetae (av). Anterior region of the sternum with 5 + 5 chaetae (micro- / mesochaetae; Fig. 34 A). 50 µm B, C 50 µm 25 µm Abd. IV sternum. With 2 + 2 microchaetae (Fig. 34 A). Neosminthuroid chaetae absent. Abdominal appendages. Manubrium with 3 + 3 posterior chaetae, neosminthuroid chaetae absent (Fig. 34 A, D, E). Dens proximal part with a posterior chaeta; postero-external spine (E 3) absent (Fig. 34 D, E). Tenaculum with 2 + 2 apical teeth (Fig. 34 D). Ventral tube with 1 + 1 apical microchaetae (Fig. 34 D).
Morphological review of the order Neelipleona (Collembola) through the redescription of the type species of Acanthoneelidus, Neelides and Neelus
Diagnosis. Pigmentation black and deep blue-gray with yellow patches. Body length up to 600 µm. Labrum with ordinary chaetae in m-row. Ant. II without ventral lobe. Ventral tube with posterior lobe. Dens with strong spines. Mucro with serrate posterior lamellae.
Morphological review of the order Neelipleona (Collembola) through the redescription of the type species of Acanthoneelidus, Neelides and Neelus
Discussion. The specimens of Neelides folsomi from France match with the description of the Italian specimens of Caroli (1912) and Dallai (1979) and the Scandinavian specimens of Fjellberg (2007) (the latters named Neelides minutus). Fjellberg (2007) drew 5 + 5 neosminthuroid chaetae from his Scandinavian specimens and Dallai (1979) reported 4 + 4 for the Italian specimens, I could check that this number is variable at the population level. The specimen described by Yosii (1965) differs from the present description in 4 + 4 chaetae on the manubrium, it is possible that the lateral pair of chaetae reported by Yosii is in fact the neosminthuroid chaetae. The only known distinction with the original Neelides minutus would be the presence of a ventral lobe on Ant. II in the latter species (Folsom 1901). Neelides folsomi differs from Neelides dianae in the shape of the posterior lamellae of the mucro (serrate vs smooth, Christiansen & Bellinger 1981), and from Neelides bisetosus by the number of chaetae in the basomedian field of the labium. The juvenile of Neelides folsomi is very similar to Neelides snideri, described by Bernard (1975) only from juvenile (Christiansen & Bellinger 1981). The juveniles of those two species differ in the number of sensory rods (a, sa) on Ant. IV (six in Neelides folsomi, two in Neelides snideri) and the number of wax rods on the posterior part of head (2 + 2 in Neelides folsomi, 1 + 1 in Neelides snideri). However, it is possible that those two characters were described from an earlier instar than those I have at disposal. Neelides minutus and Neelides snideri must be redescribed. The necessity of a new genus for Neelides snideri and Neelides dianae (Bretfeld & Trinklein 2000) does not exist.
Morphological review of the order Neelipleona (Collembola) through the redescription of the type species of Acanthoneelidus, Neelides and Neelus
Material examined. 15 ♀, 5 juveniles on slides (MNHN-EA 040190 – 209), France, Moselle, near Remilly, 49 ° 00 ' 07 " N 6 ° 25 ' 43 " E, 06. iii. 2011, extracted with Berlese-Tullgren funnel from soil and litter, L. Marchal leg., [MNHN]. 1 ♀ on slide (MNHN-EA 040189), 2 spm (sex unknown) on mount for SEM (MNHN-EA 041009), France, Haute-Garonne, near Arbas, 42 ° 58 ' 52 " N 0 ° 53 ' 44 " E, 26. vii. 2010, extracted with Berlese-Tullgren funnel from litter, L. Deharveng leg., [MNHN]. 1 juvenile on slide (MNHN-EA 040188), France, Loire, near La Tuilière, 45 ° 59 ' 01 " N 3 ° 50 ' 45 " E, 16. iv. 2011, extracted with Berlese-Tullgren funnel from peat, G. Charrier leg., [MNHN].
Morphological review of the order Neelipleona (Collembola) through the redescription of the type species of Acanthoneelidus, Neelides and Neelus

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Mediterranean
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FIGURE 1. Chaetae on posterior part of head, shape and size. (A) Chaetae on the same scale, (B) chaetae with length normalized; setulae: (a) Neelides folsomi, (b) Neelus murinus; mesochaetae: (c) Neelides folsomi, (d) Megalothorax rapoporti, (e, f) Megalothorax granulosus, (g) Megalothorax svalbardensis, (h) Megalothorax perspicillum, (i) Megalothorax willemi, (j) Megalothorax nigropunctatus; macrochaetae: (k) lanceolate, Megalothorax potapovi, (l) cylindro-conical, Acanthoneelidus pratensis, (m, n) ordinary and gladiuform, Megalothorax massoudi.

Imageimage/png© Schneider, ClémentMorphological review of the order Neelipleona (Collembola) through the redescription of the type species of Acanthoneelidus, Neelides and Neelus

FIGURE 2. External morphology of the mouth region. From labrum to labium (A) Neelides folsomi (simplified), (B) Megalothorax perspicillum and (C) Sphaeridia pumilis. Labium (D) Parisotoma sp. ventral side. Labrum (E) without anterior process, (F) with anterior process. Legend: blf = basolateral field of labium; blf tub. = tubercle of the basolateral field; bmf = basomedian field of labium; mol = maxilla outer lobe; of = oral fold; * indicates in Sphaeridia pumilis the chaeta putatively homologous with the chaeta on tubercle of basolateral field in Neelipleona.

Imageimage/png© Schneider, ClémentMorphological review of the order Neelipleona (Collembola) through the redescription of the type species of Acanthoneelidus, Neelides and Neelus

FIGURE 3. Diagram of the dorsal chaetotaxy of the head. (A) Neelides folsomi; (B) Acanthoneelidus pratensis; (C) Neelus murinus; (D) Megalothorax nigropunctatus; (E) Megalothorax perspicillum; (F) Megalothorax granulosus, integumentary channels not represented. In gray, chaetae absent in juvenile.

Imageimage/png© Schneider, ClémentMorphological review of the order Neelipleona (Collembola) through the redescription of the type species of Acanthoneelidus, Neelides and Neelus

FIGURE 4. Diagram of the ventral chaetotaxy of the head. (A) Neelides folsomi; (B) Acanthoneelidus pratensis; (C) Neelus murinus; (D) Megalothorax nigropunctatus; (E) Megalothorax minimus; (F) Megalothorax granulosus.

Imageimage/png© Schneider, ClémentMorphological review of the order Neelipleona (Collembola) through the redescription of the type species of Acanthoneelidus, Neelides and Neelus

FIGURE 9. Diagram of the chaetotaxy of the trunk. Neelides folsomi, (A) adult, (B) juvenile.

Imageimage/png© Schneider, ClémentMorphological review of the order Neelipleona (Collembola) through the redescription of the type species of Acanthoneelidus, Neelides and Neelus

FIGURE 22. Neelides folsomi. (A, B) Whole body, lateral view; (C) head, lateral view; (D) head, dorsal view; (E) focus on Th. I and II, lateral view; (F) organization of Th. I with pattern of folds in gray. Legend: 1 = precoxal area II; 2 = precoxal area III. Scale bars (B) = 100 µm; (C, D, E) = 50 µm.

Imageimage/png© Schneider, ClémentMorphological review of the order Neelipleona (Collembola) through the redescription of the type species of Acanthoneelidus, Neelides and Neelus

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GBIF Backbone Taxonomy

GBIF Backbone Taxonomy

checklist

The GBIF Backbone Taxonomy is a single, synthetic management classification with the goal of covering all names GBIF is dealing with. It's the taxonomic backbone that allows GBIF to integrate name based information from different resources, no matter if these are occurrence datasets, species pages, names from nomenclators or external sources like EOL, Genbank or IUCN. This backbone allows taxonomic search, browse and reporting operations across all those resources in a consistent way and to provide means to crosswalk names from one source to another.

It is updated regulary through an automated process in which the Catalogue of Life acts as a starting point also providing the complete higher classification above families. Additional scientific names only found in other authoritative nomenclatural and taxonomic datasets are then merged into the tree, thus extending the original catalogue and broadening the backbones name coverage. The GBIF Backbone taxonomy also includes identifiers for Operational Taxonomic Units (OTUs) drawn from the barcoding resources iBOL and UNITE.

International Barcode of Life project (iBOL), Barcode Index Numbers (BINs). BINs are connected to a taxon name and its classification by taking into account all names applied to the BIN and picking names with at least 80% consensus. If there is no consensus of name at the species level, the selection process is repeated moving up the major Linnaean ranks until consensus is achieved.

UNITE - Unified system for the DNA based fungal species, Species Hypotheses (SHs). SHs are connected to a taxon name and its classification based on the determination of the RefS (reference sequence) if present or the RepS (representative sequence). In the latter case, if there is no match in the UNITE taxonomy, the lowest rank with 100% consensus within the SH will be used.

The GBIF Backbone Taxonomy is available for download at https://hosted-datasets.gbif.org/datasets/backbone/ in different formats together with an archive of all previous versions.

The following 105 sources have been used to assemble the GBIF backbone with number of names given in brackets:

  • Catalogue of Life Checklist - 4766428 names
  • International Barcode of Life project (iBOL) Barcode Index Numbers (BINs) - 635951 names
  • UNITE - Unified system for the DNA based fungal species linked to the classification - 611208 names
  • The Paleobiology Database - 212054 names
  • World Register of Marine Species - 188857 names
  • The Interim Register of Marine and Nonmarine Genera - 183894 names
  • The World Checklist of Vascular Plants (WCVP) - 131891 names
  • GBIF Backbone Taxonomy - 114350 names
  • TAXREF - 109374 names
  • The Leipzig catalogue of vascular plants - 75380 names
  • ZooBank - 73549 names
  • Integrated Taxonomic Information System (ITIS) - 68377 names
  • Plazi.org taxonomic treatments database - 61346 names
  • Genome Taxonomy Database r207 - 60545 names
  • International Plant Names Index - 52329 names
  • Fauna Europaea - 45077 names
  • The National Checklist of Taiwan (Catalogue of Life in Taiwan, TaiCoL) - 36193 names
  • Dyntaxa. Svensk taxonomisk databas - 35892 names
  • The Plant List with literature - 32692 names
  • United Kingdom Species Inventory (UKSI) - 29643 names
  • Artsnavnebasen - 29208 names
  • The IUCN Red List of Threatened Species - 21221 names
  • Afromoths, online database of Afrotropical moth species (Lepidoptera) - 13961 names
  • Brazilian Flora 2020 project - Projeto Flora do Brasil 2020 - 13829 names
  • Prokaryotic Nomenclature Up-to-Date (PNU) - 10079 names
  • Checklist Dutch Species Register - Nederlands Soortenregister - 8814 names
  • ICTV Master Species List (MSL) - 7852 names
  • Cockroach Species File - 6020 names
  • GRIN Taxonomy - 5882 names
  • Taxon list of fungi and fungal-like organisms from Germany compiled by the DGfM - 4570 names
  • Catalogue of Afrotropical Bees - 3623 names
  • Catalogue of Tenebrionidae (Coleoptera) of North America - 3327 names
  • Checklist of Beetles (Coleoptera) of Canada and Alaska. Second Edition. - 3312 names
  • Systema Dipterorum - 2850 names
  • Catalogue of the Pterophoroidea of the World - 2807 names
  • The Clements Checklist - 2675 names
  • Taxon list of Hymenoptera from Germany compiled in the context of the GBOL project - 2496 names
  • IOC World Bird List, v13.2 - 2366 names
  • Official Lists and Indexes of Names in Zoology - 2310 names
  • National checklist of all species occurring in Denmark - 1922 names
  • Myriatrix - 1876 names
  • Database of Vascular Plants of Canada (VASCAN) - 1822 names
  • Taxon list of vascular plants from Bavaria, Germany compiled in the context of the BFL project - 1771 names
  • Orthoptera Species File - 1742 names
  • A list of the terrestrial fungi, flora and fauna of Madeira and Selvagens archipelagos - 1602 names
  • Aphid Species File - 1565 names
  • World Spider Catalog - 1561 names
  • Taxon list of Jurassic Pisces of the Tethys Palaeo-Environment compiled at the SNSB-JME - 1270 names
  • Backbone Family Classification Patch - 1143 names
  • GBIF Algae Classification - 1100 names
  • International Cichorieae Network (ICN): Cichorieae Portal - 975 names
  • Psocodea Species File - 803 names
  • New Zealand Marine Macroalgae Species Checklist - 787 names
  • Annotated checklist of endemic species from the Western Balkans - 754 names
  • Taxon list of animals with German names (worldwide) compiled at the SMNS - 503 names
  • Catalogue of the Alucitoidea of the World - 472 names
  • Lygaeoidea Species File - 462 names
  • Catálogo de Plantas y Líquenes de Colombia - 422 names
  • GBIF Backbone Patch - 317 names
  • Phasmida Species File - 259 names
  • Cortinariaceae fetched from the Index Fungorum API - 234 names
  • Coreoidea Species File - 233 names
  • GTDB supplement - 139 names
  • Mantodea Species File - 119 names
  • Endemic species in Taiwan - 93 names
  • Taxon list of Araneae from Germany compiled in the context of the GBOL project - 88 names
  • Species of Hominidae - 78 names
  • Taxon list of Sternorrhyncha from Germany compiled in the context of the GBOL project - 77 names
  • Taxon list of mosses from Germany compiled in the context of the GBOL project - 75 names
  • Mammal Species of the World - 73 names
  • Plecoptera Species File - 71 names
  • Species Fungorum Plus - 64 names
  • Catalogue of the type specimens of Cosmopterigidae (Lepidoptera: Gelechioidea) from research collections of the Zoological Institute, Russian Academy of Sciences - 47 names
  • Species named after famous people - 41 names
  • Dermaptera Species File - 36 names
  • Taxon list of Trichoptera from Germany compiled in the context of the GBOL project - 34 names
  • True Fruit Flies (Diptera, Tephritidae) of the Afrotropical Region - 33 names
  • Range and Regularities in the Distribution of Earthworms of the Earthworms of the USSR Fauna. Perel, 1979 - 32 names
  • Taxon list of Diplura from Germany compiled in the context of the GBOL project - 30 names
  • Lista de referencia de especies de aves de Colombia - 2022 - 24 names
  • Taxon list of Auchenorrhyncha from Germany compiled in the context of the GBOL project - 20 names
  • Catalogue of the type specimens of Polycestinae (Coleoptera: Buprestidae) from research collections of the Zoological Institute, Russian Academy of Sciences - 19 names
  • Taxon list of Thysanoptera from Germany compiled in the context of the GBOL project - 19 names
  • Lista de especies de vertebrados registrados en jurisdicción del Departamento del Huila - 18 names
  • Taxon list of Microcoryphia (Archaeognatha) from Germany compiled in the context of the GBOL project - 15 names
  • Catalogue of the type specimens of Bufonidae and Megophryidae (Amphibia: Anura) from research collections of the Zoological Institute, Russian Academy of Sciences - 12 names
  • Grylloblattodea Species File - 11 names
  • Coleorrhyncha Species File - 9 names
  • Taxon list of liverworts from Germany compiled in the context of the GBOL project - 9 names
  • Embioptera Species File - 7 names
  • Taxon list of Pisces and Cyclostoma from Germany compiled in the context of the GBOL project - 6 names
  • Taxon list of Pteridophyta from Germany compiled in the context of the GBOL project - 6 names
  • Taxon list of Siphonaptera from Germany compiled in the context of the GBOL project - 5 names
  • The Earthworms of the Fauna of Russia. Perel, 1997 - 5 names
  • Taxon list of Zygentoma from Germany compiled in the context of the GBOL project - 4 names
  • Asiloid Flies: new taxa of Diptera: Apioceridae, Asilidae, and Mydidae - 3 names
  • Taxon list of Protura from Germany compiled in the context of the GBOL project - 3 names
  • Taxon list of hornworts from Germany compiled in the context of the GBOL project - 2 names
  • Chrysididae Species File - 1 names
  • Taxon list of Dermaptera from Germany compiled in the context of the GBOL project - 1 names
  • Taxon list of Diplopoda from Germany in the context of the GBOL project - 1 names
  • Taxon list of Orthoptera (Grashoppers) from Germany compiled at the SNSB - 1 names
  • Taxon list of Pscoptera from Germany compiled in the context of the GBOL project - 1 names
  • Taxon list of Pseudoscorpiones from Germany compiled in the context of the GBOL project - 1 names
  • Taxon list of Raphidioptera from Germany compiled in the context of the GBOL project - 1 names

GBIF Secretariat (2023). GBIF Backbone Taxonomy. Checklist dataset https://doi.org/10.15468/39omei accessed via GBIF.org on 2026-06-15.

CC BYPublished 8/28/2023View dataset
GBIF Usage Key
4537267
Dataset Key
d7dddbf4-2cf0-4f39-9b2a-bb099caae36c
Origin
source
Backbone Key
4537267
Taxon ID
gbif:4537267
Last Crawled
8/22/2023
Last Interpreted
8/22/2023