Milnesium guanyinensis, Yuan & Liu & Wang & Liu & Chen & Li, 2023
publication ID |
https://doi.org/ 10.11646/zootaxa.5249.3.4 |
publication LSID |
lsid:zoobank.org:pub:A20B0FA1-0BA8-4BB9-B166-7FE56991ECB9 |
DOI |
https://doi.org/10.5281/zenodo.7691089 |
persistent identifier |
https://treatment.plazi.org/id/03DAFC21-105F-7871-FF5B-50EEFC15FD2E |
treatment provided by |
Plazi |
scientific name |
Milnesium guanyinensis |
status |
sp. nov. |
Milnesium guanyinensis sp. nov.
Fig. 2–8 View FIGURE 2 View FIGURE 3 View FIGURE 4 View FIGURE 5 View FIGURE 6 View FIGURE 7 View FIGURE 8 , Table 1–2 View TABLE 1 View TABLE 2
Description of the new species
Animals (measurements and statistics in Table 1 View TABLE 1 and Table 2 View TABLE 2 )
Adults and juveniles (from the second instar onwards; morphometrics and holotype measurements in Table 1 View TABLE 1 .) Body brownish and slender ( Fig. 2B View FIGURE 2 , 3B View FIGURE 3 ). Eyes present in living specimens, quickly dissolving after fixation in Hoyer’s medium. In juveniles, cuticle with a robust reticular design with thick reticulum and pit-shaped meshes (the krzysztofi type) on the whole dorsum except for the head ( Fig. 6B, E View FIGURE 6 ). In adults, the reticulum is weakly developed, thus it may not be visible under PCM ( Fig. 6C View FIGURE 6 ), although it is always identifiable in SEM. Reticulum mesh reaches 0.50–0.70 μm in diameter. The species is characterised by numerous pseudoplates ( Fig. 3B–C View FIGURE 3 ) arranged in nine transverse rows, which are visible both in PCM and UVM. Some of the pseudoplates are difficult to observe (marked with dotted line in Fig. 3C View FIGURE 3 ); the exact arrangement is as follow: (I) situated anteriorly to legs I; central rectangular pseudoplate (divided longitudinally) + two smaller roundish lateral pseudoplates; (II) situated in line with legs I, large rectangular pseudoplate (divided into four uneven portions, with the anterior ones being smaller) + two smaller lateral rectangular pseudoplates; (III) situated between legs I and II, large central elliptical pseudoplate (divided longitudinally) + two lateral about elliptical pseudoplates; (IV) situated in line with legs II, central, undivided rectangular pseudoplate with poorly visible anterior portion + a pair of lateral roundish pseudoplates; (V) situated between legs II and III, central, rectangular pseudoplate (divided longitudinally) + a pair of lateral roundish pseudoplates; (VI) situated in line with legs III, large central trapezoid pseudoplate (divided into six roughly equal potions) + a pair of lateral roundish pseudoplates; (VII) situated just posterior to legs III, central rectangular pseudoplate (divided longitudinally) with poorly visible posterior portion + a pair of lateral roundish pseudoplates, each with poorly visible pair of roundish anterior pseudoplates; (VIII) the largest, most complex, trapezoid pseudoplate (divided into eight parts: a central triangle and seven quadrangles) + two roundish lateral pseudoplates; (IX) four pseudoplates arranged transversally (internal trapezoid and the lateral roundish).
Buccal apparatus of the Milnesium type ( Fig. 4B – C View FIGURE 4 , 5A–D View FIGURE 5 ). Buccal tube in adults and juveniles wide and short (standard width on average 39% of its length) and cylindrical, wider anteriorly (posterior diameter on average 95% of the anterior diameter); Six peribuccal papillae and six peribuccal lamellae around the mouth opening present ( Fig. 5A – D View FIGURE 5 ). Two cephalic papillae positioned laterally. The peribuccal papillae usually longer than the cephalic ones. Pharyngeal bulb elongated and pear-shaped, without placoids or septulum.
Claws of the Milnesium type ( Fig. 7C – F View FIGURE 7 , 8C – D View FIGURE 8 ). Primary branches with thin accessory points; claw bases with rounded basal thickenings; the CC in adults and juveniles is [2-3]-[3-2] ( Fig. 5C–F, I–J View FIGURE 5 ). A long cuticular bar present under the claws I–III ( Fig. 5A, C, E View FIGURE 5 ).
Hatchlings (morphometrics and measurements in Table 2 View TABLE 2 .) Morphologically similar to adults and juveniles, but with a better developed dorsal reticulation (denser and more visible; meshes 0.65–0.90 μm in diameter; Fig. 6A, D View FIGURE 6 ) and a more vaguely outlined dorsal pseudoplates ( Fig. 2A View FIGURE 2 , 3A View FIGURE 3 ). Buccal tube in hatchlings is more slender (standard width on average 34% of its length) and cylindrical, slightly wider anteriorly (posterior diameter on average 88% of the anterior diameter). The [2-2]-[2-2] CC was observed in hatchlings ( Fig. 7A–B View FIGURE 7 , 8A–B View FIGURE 8 ). Other qualitative traits as in adults and juveniles.
Ontogenetic variability. Based on the relationship between buccal tube and body length, the type series of Milnesium guanyinensis sp. nov. comprises hatchlings, juveniles and adults ( Fig. 9 View FIGURE 9 ). The new species exhibits developmental changes in three crucial taxonomic traits: cuticular sculpturing, buccal tube shape and CC. The dorsal cuticle sculpturing becomes less clear in later life stages. Particularly, in PCM, the reticulum is most clearly visible in hatchlings, marginally less developed in juveniles, and it can be indistinct in adults or even not visible at all in large adults. In SEM, the dorsal cuticle sculpturing also fades with consecutive instars, but it is visible in all life stages ( Fig. 6 View FIGURE 6 ). The buccal tube in hatchings is more slender than in adults and juveniles. The CC changes from [2-2]-[2-2] in hatchlings to [2-3]-[3-2] in juveniles and adults, i.e. the new species exhibits an early positive CC change.
Remarks. Several irregular cuticular depressions present in the dorsal cuticle are present, with the most caudal one being always the largest ( Fig. 6F View FIGURE 6 ).
Eggs. Oval, yellow, smooth and laid in the exuviae; up to 7 in a single clutch were found in exuviae.
Type locality. 23º2'52"N, 102º49'34"E; 2 300 m asl: Guanyinshan , Ailao Mountains, Yuannan Province, China; habitat: forest; substrate: mosses on a rock. GoogleMaps
Etymology. The new species is named after the Guanyinshan district of Yunnan, China, where it was discovered.
Type depositories. The series consists of the holotype (adult, GY050116) and 37 paratypes, 29 on microscope slides (GY050101–15, GY050117–20, GY050201–10) and 8 on an SEM stub (22.02 and 22.06). All slides and the SEM stub are deposited at Xiaochen Li’s tardigrade collection, Molecular Ecology, Department of Biology, College of Life Sciences of Shaanxi Normal University, China.
Adults and juveniles differential diagnosis. Milnesium guanyinensis sp. nov. is characterised by six peribuccal lamellae, fine reticular design of dorsal cuticle and a [2-3]-[3-2] CC in adults. Thus, the new species is similar to five other species but differs specifically from:
• M. cassandrae Moreno-Talamantes et al., 2019 ( Mexico) , by cuticle with fine reticular design (adults cuticle sculptured with pseudopores, sparsely distributed and not forming a reticular design in M. cassandrae ); by a lower pt of the standard buccal tube width (37.5–41.5 in the new species vs 41.6–67.2 in M. cassandrae ).
• M. decorum Morek et al., 2022 ( Portugal) , by cuticular bars under claws I–III present (cuticular bars under claws I–III absent in the majority of specimens in M. decorum ); by a higher pt of stylet supports inserted on buccal tube (65.5–69.3, mean 66.8, in the new species vs 59.2–65.6, mean 62.9, in M. decorum , t 16 =-5.17, p <0.001).
• M. krzysztofi Kaczmarek & Michalczyk, 2007 ( Costa Rica), by eyes present and body brownish (eyes absent and body white in M. krzysztofi ); by the relatively shorter posterior primary branch on claws IV (51.7–57.1, mean 53.7 in the new species vs 56.9–66.5, mean 62.1 in M. krzysztofi , t 12 =-5.92, p<0.001); by the relatively longer posterior spur on claws IV (10.1–15.0, mean 12.1 in the new species vs 8.0–10.1, mean 9.1 in M. krzysztofi , t 12 =- 3.15, p<0.01).
• M. pacificum Sugiura et al., 2020 ( Japan) by the brownish body and the reticulum mesh is sunken (body creamy white and the reticulum is tuberculate in M. pacificum ); by the relatively longer spurs on claws III (12.6– 15.5 in the new species vs 7.5–12.4 in M. pacificum ).
• M. pelufforum Rocha et al., 2022 ( Argentina) by the brownish body (body reddish in M. pelufforum ); no spurs present on claws (small basal spurs present in M. pacificum ); by a lower pt of the standard buccal tube width (37.5–41.5 in the new species vs 55.2–64.0 in M. pelufforum ).
Hatchlings differential diagnosis. Milnesium guanyinensis sp. nov. first instar specimens are characterised by fine reticular design and a [2-2]-[2-2] CC, the new species is similar to four other congeners but differs specifically from:
• M. cassandrae by eyes present and body brownish (eyes absent and white or transparent with light yellow brownish tones before fixation in M. cassandrae ); by a higher pt of stylet supports inserted on buccal tube (67.1–72.1, mean 69.1 in the new species vs 56.5–70.5, mean 66.3 in M. cassandrae , t 31 =- 3.36, p<0.01).
• M. katarzynae Kaczmarek et al., 2004 ( China) by eyes present and body brownish (eyes absent and body white in M. katarzynae ), a higher pt of the standard buccal tube width (28.4–39.6 in the new species vs 21.7–26.6 in M. katarzynae ) and a lower pt of stylet supports inserted on buccal tube (67.1–72.1 in the new species vs 73.3–78.3 in M. katarzynae ).
• M. pacificum by the brownish body and the reticulum mesh is shallow (body creamy white and the reticulum is tuberculate in M. pacificum ).
• M. pelufforum by the brownish body (body reddish in M. pelufforum ); by a lower pt of the standard buccal tube width (28.4–39.6 in the new species vs 43.7–52.1 in M. pelufforum ).
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
Kingdom |
|
Phylum |
|
Class |
|
Order |
|
Family |
|
Genus |