Macrobiotus rawsoni Horning, Schuster & Grigarick, 1978
publication ID |
https://doi.org/ 10.11646/zootaxa.4363.1.3 |
publication LSID |
lsid:zoobank.org:pub:B1494311-BF2D-44B4-9107-68930116E97F |
DOI |
https://doi.org/10.5281/zenodo.6041765 |
persistent identifier |
https://treatment.plazi.org/id/03CC8792-5435-FFAD-FF06-FEC8FAFFFE81 |
treatment provided by |
Plazi |
scientific name |
Macrobiotus rawsoni Horning, Schuster & Grigarick, 1978 |
status |
|
Macrobiotus rawsoni Horning, Schuster & Grigarick, 1978 View in CoL
( Tables 3–4, Figs 9–12 View FIGURE 9 View FIGURE 10 View FIGURE 11 View FIGURE 12 )
Macrobiotus rawsoni n.sp. ( Horning, et al. 1978)
Material examined ( Fig. 9 View FIGURE 9 ). Three paratypes (2 animals and 1 egg) on three slides designated as: 1) Macrobiotus rawsoni Horning et al., 1978 [300], PARATYPE, Rangitira Isl., Triang. Station, Chatham Isl., VIII-25-71, D.S. Horning, NZ-891, National Museum, N.Z.; 2) Macrobiotus rawsoni Horning, Schuster & Grigarick, 1978 [340], PARATYPE, Rangatira Isl., Triang. Station, Chatham Isl., VIII-25-71, D.S. Horning, NZ-891, Museum of New Zealand ; 3) Macrobiotus rawsoni Horning et al., 1978 [egg], Museum of New Zealand, PARATYPE, Rangatira Isl. , Triang. Station, Chatham Isl., VIII-25-71, D.S. Horning, NZ-891, National Museum, N.Z.
Type locality. Original coordinates: 44°17'S, 176°10'W, corrected coordinates: 44°21'S, 176°11'W, ca. 150 m asl: Chatham Islands, Rangatira Island (South East Island), Triangulation Station, 400 m SW of Woolshed, in dense bush, moss ( Porotrichum ramulosum (Mitt.) Mitt. ) from rocks.
Re-description (measurements in Tables 3–4). Animals: Body colour unknown, eyes present ( Fig. 10A View FIGURE 10 ). Entire cuticle covered with round or oval cuticular pores, not arranged in bands ( Fig. 11A View FIGURE 11 ). Obvious granulation only present on legs IV ( Fig. 11 View FIGURE 11 ). Bucco-pharyngeal apparatus of the Macrobiotus type, with ventral lamina and ten peribuccal lamellae ( Fig. 10B–D View FIGURE 10 ). Mouth antero-ventral. The oral cavity armature of the maculatus type (see, Kaczmarek & Michalczyk 2017 for details), with only the third band of teeth visible under LM, composed of three dorsal and three ventral teeth in the shape of transverse ridges ( Fig. 10B–C View FIGURE 10 ). Third band of teeth on dorsal and ventral side composed of small singles teeth arranged irregularly. Pharyngeal bulb spherical with triangular apophyses, two rod-shaped macroplacoids and thin microplacoid. Macroplacoid length configuration 2<1. The first macroplacoid with a central constriction. The second macroplacoid without constrictions, but with latero-terminal globular projections ( Fig. 10D View FIGURE 10 ). Claws of the hufelandi type, stout ( Fig. 11A View FIGURE 11 ). Primary branches with distinct accessory points. Lunules on all legs smooth. Thin bars paired under claws I–III present. Other cuticular thickenings on legs absent.
Eggs: Spherical, ornamented and laid freely ( Fig. 12A View FIGURE 12 ), with the chorion surface of the hufelandi type (reticulated; Fig. 12B View FIGURE 12 ). The reticulum well defined, with only a single peribasal ring (i.e. two lines of mesh between neighbouring egg processes). The mesh size uniform (1.8–2.5 µm in diameter). Process trunks concave, wide at the base, terminated with a concave disc ( Fig. 12C View FIGURE 12 ). Disc edges serrated ( Fig. 12B–C View FIGURE 12 ).
Original measurements according to Horning et al. (1978), including the original terminology: Body length excluding legs IV (456 µm); body length including legs IV (490 µm); body width (160 µm); mouth tube length (43 µm); mouth tube width (6 µm, expanding to 9 µm at base); stylet supports attached 11 µm from base; apophysis length (3 µm); I macroplacoid length (11 µm); II macroplacoid length (6 µm); microplacoid length (3 µm); claw length (18 µm), lunules (ca. 3 µm).
Etymology. Although not specified in the original description, the species was almost certainly dedicated to T.W. Rawson (Botany Division of the Department of Scientific and Industrial Research in Lincoln, New Zealand), who was mentioned in the acknowledgements of Horning et al. (1978) as one of two experts who, “provided the determinations of bryophytes and lichens; material from nearly 2000 samples was identified to species for this study, and their prodigious efforts are gratefully acknowledged”.
Type depositories. Holotype, paratypes and the egg are preserved at the Museum of New Zealand Te Papa Tongarewa, Tory Street, PO Box 467, Wellington , New Zealand.
Remarks. Pilato et al. (2006) partially re-described this species, however, they only provided measurements for a few taxonomic characters, and no eggs measurements; which we are now supplementing. While our measurements are in agreement with those given in Pilato et al. (2006), we came to different conclusions regarding the morphology of the oral cavity armature of M. rawsoni . Namely, Pilato et al. (2006) described the oral cavity armature as, “A band of almost invisible teeth and a system of three dorsal and three ventral thin transverse ridges are present in the posterior portion of the buccal cavity. An anterior band of teeth is not visible”, whereas we did not detect the second band of teeth. Thus, whether the oral cavity armature in M. rawsoni is of the maculatus or patagonicus type (see, Kaczmarek & Michalczyk 2017 for details), will remain open until fresh material is available.
Differential diagnosis. Our observations suggest that Macrobiotus rawsoni is characterised by the oral cavity of the maculatus type and eggs of the hufelandi type, and is therefore most similar to the following five species, but can be distinguished specifically from:
M. almadai Fontoura et al., 2008 View in CoL , reported from the type locality in the Azores, by: a higher pt of the buccal tube width (13.4–15.5 in M. rawsoni View in CoL vs. 10.1–11.5 in M. almadai View in CoL ), a higher pt of the stylet support insertion point (77.0– 77.1 in M. rawsoni View in CoL vs. 74.0– 76.8 in M. almadai View in CoL ), and a different parameters of the egg reticulum (one or two lines of mesh between neighbouring processes in M. rawsoni View in CoL vs. three meshes between neighbouring processes in M. almadai View in CoL ).
M. humilis Binda & Pilato, 2001 View in CoL , recorded from the type locality in Sri Lanka, by: the absence of granulation on legs I–III, a higher pt of the buccal tube width (13.4–15.5 in M. rawsoni View in CoL vs. 11.3–11.8 in M. humilis View in CoL ), a higher pt of the stylet support insertion point (77.0– 77.1 in M. rawsoni View in CoL vs. 71.1–71.3 in M. humilis View in CoL ), higher egg processes (5.2–6.3 µm in M. rawsoni View in CoL vs. 4.1–5.1 µm in M. humilis View in CoL ), and a larger diameter of the terminal discs of egg processes (4.9–5.3 µm in M. rawsoni View in CoL vs. 2.9–3.4 µm in M. humilis View in CoL ).
M. madegassus Maucci, 1993 View in CoL , reported from the type locality in Madagascar, by: the absence of teeth on lunules IV, the presence of eyes, a higher pt of the buccal tube width (13.4–15.5 in M. rawsoni View in CoL vs. 7.0– 11.8 in M. madegassus View in CoL ), a higher pt of the stylet support insertion point (77.0– 77.1 in M. rawsoni View in CoL vs. 68.1–71.3 in M. madegassus View in CoL ), and a lower number of processes on the egg circumference (ca. 26 in M. rawsoni View in CoL vs. ca. 30–34 in M. madegassus View in CoL ).
M. martini Bartels et al., 2009 View in CoL , recorded from the type locality in USA (North Carolina), by: the absence of granulation on legs I–III, the absence of teeth on lunules IV, a higher pt of the buccal tube width (13.4–15.5 in M. rawsoni View in CoL vs. 12.5–12.9 in M. martini View in CoL ), a higher pt of the stylet support insertion point (77.0– 77.1 in M. rawsoni View in CoL vs. 72.9–74.3 in M. martini View in CoL ), the presence of teeth on the terminal discs of egg processes (smooth discs in M. martini View in CoL ), and a lower process base/height ratio (96–100% in M. rawsoni View in CoL vs. 117–157% in M. martini View in CoL ).
M. modestus Pilato & Lisi, 2009 View in CoL , reported from the type locality in the Seychelles, by: a higher pt of the buccal tube width (13.4–15.5 in M. rawsoni View in CoL vs. 7.4–7.9 in M. modestus View in CoL ), a higher pt of the stylet support insertion point (77.0– 77.1 in M. rawsoni View in CoL vs. 67.3–69.8 in M. modestus View in CoL ), the absence of teeth on lunules IV, a lower number of processes on the egg circumference (ca. 26 in M. rawsoni View in CoL vs. ca. 32–33 µm in M. modestus View in CoL ), higher egg processes (5.2–6.3 µm in M. rawsoni View in CoL vs. 4.6–5.1 µm in M. modestus View in CoL ), wider bases of the egg processes (5.0–6.3 µm in M. rawsoni View in CoL vs. 4.2–4.9 µm in M. modestus View in CoL ), and a larger diameter of terminal discs of egg processes (4.9–5.3 µm in M. rawsoni View in CoL vs. 2.8–3.6 µm in M. modestus View in CoL ).
SPECIMEN Paratype 300 Paratype 340 CHARACTER µm pt µm pt
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 |
Macrobiotus rawsoni Horning, Schuster & Grigarick, 1978
Kaczmarek, Łukasz & Michalczyk, Łukasz 2017 |
M. martini
Bartels et al. 2009 |
M. modestus
Pilato & Lisi 2009 |
M. modestus
Pilato & Lisi 2009 |
M. modestus
Pilato & Lisi 2009 |
M. modestus
Pilato & Lisi 2009 |
M. modestus
Pilato & Lisi 2009 |
M. modestus
Pilato & Lisi 2009 |
M. modestus
Pilato & Lisi 2009 |
M. almadai
Fontoura et al. 2008 |
M. humilis
Binda & Pilato 2001 |
M. humilis
Binda & Pilato 2001 |
M. humilis
Binda & Pilato 2001 |
M. humilis
Binda & Pilato 2001 |
M. humilis
Binda & Pilato 2001 |
M. madegassus
Maucci 1993 |
M. madegassus
Maucci 1993 |
M. madegassus
Maucci 1993 |
M. madegassus
Maucci 1993 |