Macrobiotus huziori, Michalczyk & Kaczmarek, 2006
publication ID |
1175-5326 |
publication LSID |
lsid:zoobank.org:pub:68009476-AFD2-4133-A7B5-F7303D38AE2F |
persistent identifier |
https://treatment.plazi.org/id/03C27D02-783F-FF90-5F4D-B5EEFCA413C9 |
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Plazi (2019-04-18 11:38:36, last updated 2019-04-18 11:38:37) |
scientific name |
Macrobiotus huziori |
status |
sp. nov. |
Macrobiotus huziori sp. nov. ( Figs. 1–5, 7–43)
Material examined. 8 adults, 1 infant and 20 eggs (prepared for both, DIC and SEM) from the type locality and from Cartago ( Costa Rica; near the road from Pacayas to Turrialba, 27.5 km before Turrialba; moss from soil; 17.12.2002; leg. Ł. Kaczmarek) .
Description. Adult (measurements of the holotype): Body length 455.0 ( Fig. 1, see also Fig. 2). Body transparent/white, eyes present. Cuticle smooth and without pores. Fine but evident, regular granulation present on all legs but developed better on IV pair ( Figs. 10–11). Granules have a complex structure and with SEM they are visible as aggregations of small granules or cones (2 to 10 granules/cones on each aggregation) ( Fig. 11).
Buccopharyngeal apparatus of Macrobiotus type ( Figs. 3–5). Mouth anteroventral, surrounded by ring of 10 peribuccal lamellae. Oral cavity armature with three bands of teeth ( Figs. 3–4). Teeth of first band are smaller than those of the other two bands and are in the shape of small cones/granules. They are present in anterior portion of oral cavity just behind peribuccal lamellae and on them. This band of teeth is continuous and looks the same on all oral cavity walls. The teeth of the second band are intermediate in size between those of the first band and those of the third band of teeth. They are in the shape of small ridges parallel to the main axis of the buccal tube (ventral teeth are little larger than dorsal). They are positioned in the posterior portion of the oral cavity just behind the ring fold and just before the third band of teeth. The second band of teeth is continuous and arranged in one row. Some of the teeth are uniform and regular, in the shape of ridges but the rest are joined onebyone. Joined teeth are H, V and Wshaped. The teeth of the third band are larger than those in the other two bands and there are usually six. They are in the shape of transverse ridges/baffles. Teeth in this band are positioned in the rear of the oral cavity just behind the second band of teeth and just before the buccal tube opening. Usually this band is not continuous and is divided into two series: ventral and dorsal. Both series consist of one median and two lateral teeth. Dorsal teeth are more barshaped and ventral are more rectangular shaped. Medioventral tooth is very often divided into 2–5 smaller teeth.
of Macrobiotus huziori sp. nov. mounted in Hoyer’s medium (Range refers to the smallest and the
largest structure found among all measured specimens; N, number of specimens/structured
measured, SD, standard deviation).
Buccal tube 54.0 long and 12.0 [22.2] wide with one bend in anterior part of tube
(visible in lateral view). Stylet supports inserted on buccal tube at 42.0 [77.8]. Pharyngeal
bulb slightly oval with apophyses and three macroplacoids ( Figs. 3, 5). Pharyngeal
apophyses distinct, triangular, wider and indented posteriorly. First macroplacoid thinner anteriorly, 9.0 [16.7] long, second oval or rectangular 7.0 [13.0] long, both without constriction (second microplacoid may sometimes have slight constriction in anterior part). Third macroplacoid 12.0 [22.2] long, with constriction in subterminal part. Microplacoid absent, but there are faint cuticular matchlike structures growing out of the posterior ends of the third macroplacoids ( Fig. 6, visible also on Figs. 1–5). These matchlike structures are slightly wider in their terminal parts (see also ‘Differential diagnosis’). Macroplacoid row 31.5 [58.3] long.
Claws of hufelandi type, slender with very narrow bases ( Figs. 8–10). Primary
branches with distinct accessory points. Lunules on all legs smooth, better developed on
IV pair of legs. Primary branch of external claw (pb) of II pair of legs 13.0 [24.1] long,
secondary branch (sb) 10.0 [18.5] long; III pb 13.0 [24.1], sb 10.0 [18.5]; IV pb 16.0
[29.6], sb 12.0 [22.2]. Bars on legs absent but cuticular thickenings below claws present
( Fig. 8).
Eggs. White, laid freely ( Figs. 12–21, see also Fig. 2). Spherical, areolated, with 9–11
processes on circumference. Processes generally in the shape of cones, elongated in
terminal part, however the shape is highly variable ( Figs. 24–36, see also Figs. 12–21).
The elongated terminal part may be missing or be thin and long or split in the end. If the
terminal part is present it is usually covered by irregular tubercles ( Figs. 30–32 and 34–
36). Processes consist of double wall with transverse supporting walls forming ‘cells’
visible in DIC as a dense reticular design (‘reticulation’ slightly elongated vertically) ( Figs. 22–23). External walls of processes smooth or slightly wrinkled (wrinkles in form of rings around a process), without pores. Internal walls strongly porous (visible in SEM only). Surface between processes areolated. Areolation complex ( Figs. 37–44). Areolae in the shape of holes which branch into smaller holes closer to the egg surface (see Figs. 43– 44 and 37–38). This kind of areolation has not been described so far.
(DIC, scale on 23 same as on 22).
Remarks. Adults: Results of simple statistical analysis of measurements and pt values of selected morphological structures for six specimens are given in Table 1. Eggs: Statistics for all measurable eggs are provided in Table 2.
Type locality. Costa Rica, Cartago Province, slope of the Irazu Volcano; Irazu Volcano National Park ; moss from a tree; ca. 3400 m a.s.l.; 17.12.2002; leg. Ł. Kaczmarek.
Type depositories. Holotype and 16 paratypes (6 adults, 1 infant hatching out of egg and 9 eggs) are deposited in the Natural History Collections, Faculty of Biology , A. Mickiewicz University, Umultowska 89, 61–614 Poznań, Poland.
Etymology. The new species was named after the first author’s dear friend Paweł ‘ ihs ’ Huzior.
Differential diagnosis. The eggs of Macrobiotus huziori sp. nov. have a unique, never described before, type of multilevel areolation ( Figs. 37–44) unlike other species’ eggs which have areolation in the form of ovals or polygons with just one bottom (‘one level’ areolation). This character excludes the new species from any of the known species groups within the genus Macrobiotus (like the areolatus group, for example) and makes M. huziori sp. nov. easily distinguishable from all the known species. However, the adults of the new species are similar to Macrobiotus areolatus Murray , Macrobiotus crenatus Maucci, 1991 , Macrobiotus csotiensis Iharos, 1966 and species of the Macrobiotus richtersi group. Also the eggs of these species (except for M. csotiensis ) are similar to the
eggs of M. huziori sp. nov. with the respect to the conical shape of the processes and the presence of areolation between the processes.
Adults of M. huziori sp. nov. are similar to adults of M. areolatus , M. crenatus and M.
csotiensis by the presence of three rodlike macroplacoids and lack of the microplacoid.
However, the adults of the new species differ from M. crenatus and M. areolatus by the
absence of teeth on the lunulae of IV pair of legs. Due to the poor description of M.
csotiensis we were unable to find any differences in the adult morphology, but the eggs of
M. csotiensis are very different from the eggs of the new species (hemispherical
ornamentations positioned very near to each other covered with a hyaline layer, which is
concaved between the processes) ( Iharos 1966). Additionally M. huziori sp. nov. has
larger eggs than M. areolatus (80.0–100.0 in M. areolatus and 120.0–160.0 in the new
species) ( Ramazzotti & Maucci 1983).
while focusing down, see also Figs. 43–44). (DIC, scale on 38 same as on 37).
It is also worth noting that the matchlike structures growing out of the third
macroplacoids in M. huziori sp. nov. and in M. areolatus terminate where the
microplacoid is placed in the species of the Macrobiotus richtersi group (see Figs. 6–7). In the richtersi group the microplacoid is connected with the third macroplacoid by a thin cuticular yarnlike structure. This, and also similarity in the buccal apparatus structure and the egg shell appearance may suggest that both M. huziori sp. nov. and M. areolatus are closely related to the richtersi group but have probably lost the microplacoids and the matchlike structures are the microplacoids remnants.
Iharos, G. (1966) Neue Tardigraden-arten aus Ungarn (Neuere Beitrage zur kenntnis der Tardigraden-Fauna Ungarns, VI.). Acta Zoologica Academiae Scientiarum Hungaricae, XII (1 - 2), 111 - 122.
Maucci, W. (1991) Tre nuove specie di Eutardigradi della Groenlandia Meridionale. Bollettino del Museo Civico di Storia Naturale, Verona, 15, 279 - 289.
Ramazzotti, G. & Maucci, W. (1983) Il Phylum Tardigrada (Translation by C. Beasley). Memorie dell'Istituto Italiano di Idrobiologia, Pallanza, 41, 1 - 1012.
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