Microdajus sp.
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publication ID |
https://doi.org/ 10.1590/2358-2936e2021005 |
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publication LSID |
lsid:zoobank.org:pub:B11C7CED-041A-4D9F-BDF0-3C95B4A34975 |
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DOI |
https://doi.org/10.5281/zenodo.10910343 |
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persistent identifier |
https://treatment.plazi.org/id/9A098782-0E2B-AD6C-FBBA-FA37FE9E78DC |
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treatment provided by |
Felipe |
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scientific name |
Microdajus sp. |
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( Figs. 1–2 View Figure 1 View Figure 2 )
Material examined (measured specimens so noted). Early expanded tantulus larva bearing trunk sac (108 µm)attached to antennule of neuter Typhlotanais sp. (1.2 mm) (on SEM stub; USNM 1640971, Fig. 2A, B View Figure 2 ), 26.9997, -87.9967, Gulf of Mexico, 2767 m, coll. R / V Gyre, 20 Sept 2010. Head of tantulus larva (body lost) (24 µm head length; ca. 58 µm total length), attached to left side of body between second and third pereomeres of neuter Typhlotanais sp. (877 µm), same collection data as above (on SEM stub; USNM 1640972, Fig. 1E, F View Figure 1 ). Expanded tantulus larva with developing male (245 µm) attached to right pereopod 1 of neuter Typhlotanais sp. (1.0 mm) (on SEM stub; USNM 1640973, Fig.2C–F View Figure 2 ),28.4479, -89.6719, Gulf of Mexico, 684 m,coll. R / V Gyre, 13 Oct 2010.Expanded tantulus larva with developing male (330 µm total length) and tantulus larva with very early trunk sac(90 µm), attached to left first pereopod of male Typhlotanais sp. (1.5 mm), 28.4479, -89.6719, Gulf of Mexico, 684 m, coll. R / V Gyre, 13 Oct 2010 ( USNM 1640974, photographic specimens 2671.1, 2671.2, Fig. 1A–D View Figure 1 ). Expanded tantulus larva with developing male, attached to right pereopod of male Typhlotanais sp. , Gulf of Mexico (precise locality unknown) (photographic specimen 2672). Expanded tantulus larvae with early parthenogenetic sac, attached to right antennule of neuter Typhlotanais sp. , Gulf of Mexico (precise locality unknown) (photographic specimen 2673). Tantulus larva, attached to right antennule of neuter Typhlotanais sp. , Gulf of Mexico (precise locality unknown) (photographic specimen 2675).
Description of tantulus larva. Body comprised of cephalon, 6 limb-bearing thoracic segments, and two-segmented urosome ( Fig. 1E View Figure 1 ). Total length 58 µm for tantulus larva prior to development of trunk sac ( Fig. 1E View Figure 1 ). Cephalon triangular, tapering anteriorly, ~24 µm long × 18 µm wide ( Fig. 1E View Figure 1 ). Cephalic shield smooth, with two long mediodorsal longitudinal lamellae ( Fig. 1E View Figure 1 ). Cephalic pore formula A I, L I; both sets of pores bearing setae; A I setae more than twice as long as L I setae ( Fig.1E, F View Figure 1 ). Ventral surface of cephalon without pores, smooth. Trunk segments 1–7 with distinct tergites ( Fig. 1E View Figure 1 ) lacking ornamentation. First tergite narrow, almost entirely concealed under cephalic shield ( Fig. 1E View Figure 1 ), more visible in metamorphosed tantulus containing developing male ( Fig. 1B, C View Figure 1 ). Tergite 2 widest, width of the following tergites gradually decreasing posteriorly until tergite 6, tergite 7 (first segment of urosome) approximately half the width of preceding tergite. Urosome consisting of two unequal segments (2 µm and 6 µm long) ( Fig. 1E View Figure 1 ). First segment (seventh trunk segment) smooth, without ornamentation; approximately half width of tergite 6 ( Fig. 1E View Figure 1 ). Second segment (abdomen) dorsally smooth. Furcal rami each with one terminal seta, longer than wide ( Fig. 1E View Figure 1 ), length subequal to length of terminal urosome segment (two outer lateral setae not visible in light micrographs).
Description of tantulus larva with early parthenogenetic sac. ( Figs. 1D View Figure 1 , 2A, B View Figure 2 ). Body comprised of smooth, triangular cephalon ( Fig. 2A, B View Figure 2 ) and rounded trunk; trunk 2–3 times longer than cephalon, with wrinkled appearance ( Fig. 2A, B View Figure 2 ). 90 µm total length of tantulus larva with very early trunk sac ( Fig. 1D View Figure 1 ); 108 µm for tantulus larva with early trunk sac ( Fig. 2A View Figure 2 ). Cephalic shield as in tantulus larva; other segments lacking.
Description of tantulus larva with early male sac. ( Fig. 2C–F View Figure 2 ). Cephalon as described above, trunk expanded toward posterior end (approximately 2 times wider at distal end than base), rounded posterior end, lacking wrinkled appearance of early parthenogenetic sac ( Fig. 2C View Figure 2 ); 250 µm total length. Thoracic segments 1–6 bearing biramous thoracopods without medial endites ( Fig. 2D–F View Figure 2 ). Thoracopods 1–5 subequal in size and shape; protopods subrectangular, wider than long, each extending to acute point on lateral margin; rami situated on mesial side of protopods; each a small, stub-shaped segment bearing single elongate serrate seta; endopodal and exopodal setal length and width subequal, each endopodal seta of thoracopods 2–5 with large, mesial spine one-third of distance from base of seta ( Fig. 2D–F View Figure 2 ). Thoracopod 6 with cylindrical protopod, ramal segments reduced, exopod more than twice as long and wide as endopod, each endopod with one seta ( Fig. 2D–F View Figure 2 ). Urosome of two unequal segments; first segment (seventh trunk segment) minute; second segment (abdomen) cylindrical with smooth surface, approximately twice the size of thoracopod 6 ( Fig. 2D–F View Figure 2 ). Furcal rami distinct, longer than wide, each bearing one short smooth terminal seta with truncate distal margin and two lateral serrate tapering setae, larger seta greater than three times as long as smaller seta ( Fig. 2D–F View Figure 2 ).
Description of male ( Fig. 1A–C View Figure 1 ). All studied males were inside trunk sacs; length of complete specimens (cephalothorax and trunk sac) measured to 330 µm ( Fig. 1A View Figure 1 ), total body length of male inside sac approximately285 µm (if straightened).Trunk sac with developing male formed posterior to sixth thoracic tergite ( Fig. 1A–C View Figure 1 ). Larval tergites separated from appendages by slight thoracic expansion, abdomen def lected ventrally ( Fig. 1A, B View Figure 1 ). Male inside sac connected to host via umbilical cord passing through attached larva ( Fig.1C View Figure 1 ). Cephalothorax(129 µm long) includes first and second limb-bearing segments, followed by four free limb-bearing thoracic and two abdominal segments ( Fig. 1A, B View Figure 1 ). Cephalic shield smooth, with seven pairs of pits containing from one to two setae ( Fig. 1C View Figure 1 ) arranged in five anterior (A1– A5) and two posterior (P1, P2) pairs; A1, A2 setal counts indeterminate, A3, A4 with one seta each, A5, P1, P2 with two setae each. Cephalothorax with aesthetascs at anterior margin; other appendages lacking. First two thoracic segments fused with cephalon, bearing two pairs of biramous thoracopods. Tergites of following thoracic segments each with two lineae across surface ( Fig. 1B View Figure 1 ). Thoracopods 1–3 each comprised of large unsegmented protopod and one-segmented ramus; thoracopod 1 exopod slightly longer than endopod. Thoracopods 4 and 5 each with two-segmented protopod comprised of small basis and larger coxa ( Fig. 1C View Figure 1 ). Thoracopod 6 uniramous, with unsegmented protopod; distal segment (exopod?) with long subequal terminal setae and shorter outer seta. All thoracopods with long terminal setae; precise setal counts unclear. First abdominal segment approximately 17 µm long.Second abdominal segment (telson; 26 µm long) bearing furcal rami approximately 37 µm long ( Fig. 1B View Figure 1 ). Penis approximately 38 µm long, recurved.
Remarks. Due to the lack of adequate specimens, we cannot describe the present material as a new species, although it is likely to be so. However, sufficient characters were examined in the photomicrographs and in the extant specimens that we can make comparisons with the described species of Microdajus . We have identified these specimens as belonging to Microdajus because all species in this genus have one or two anterior cephalic pores, whereas the sole species of Xenalytus Huys, 1991 has three anterior pores.
The tantulus larvae of Microdajus sp. from the Gulf of Mexico differ from four of the other five described species in the genus in having a total of two cephalic pores: A I and L I. The only other species with so few pores is Microdajus aporosus Grygier and Sieg, 1988 , which likewise has A I and L I. Grygier and Sieg (1988: fig.9)included arrows pointing to pores at the anterior margin and ventral posterior corners of the carapace of M. aporosus , indicating that these pores are indeed A I and L I, not D I and L I as stated by Kolbasov and Savchenko (2010). Microdajus sp. differs from M. aporosus in having a long seta arising from each A I pore(pore without long seta in M. aporosus ). However,the position of the anterior pore is different in these species, being positioned considerably farther from the anterior end and more laterally on the cephalon in Microdajus sp. than in M. aporosus , where it is nearly at the tip and more dorsally positioned (compare Fig.1E, F View Figure 1 herein with Grygier and Sieg, 1988:figs.6, 9); this suggests than these “A I ” pores may not be homologous in the two species.
Microdajus sp. is most similar to M. aporosus View in CoL and Microdajus tchesunovi Kolbasov and Savchenko, 2010 in View in CoL having an endopodal seta on each of the sixth thoracopods; the other three species in Microdajus View in CoL lack endopodal setae. The present material is also similar to M. aporosus View in CoL , M. tchesunovi View in CoL , and Microdajus gaelicus Boxshall and Lincoln, 1987 in View in CoL lacking medial endites on the thoracopods; the other two species in the genus possess endites (see table 1 in Kolbasov and Savchenko, 2010). The abdomen of Microdajus sp. does not appear to bear any denticles whereas that of M. tchesunovi View in CoL bears minute, irregular denticles; the other species in the genus either have long patterned denticles or the character state is unknown (see table 1 in Kolbasov and Savchenko, 2010).
The male of Microdajus sp. can only be compared to that of the four species where males are known: M. aporosus View in CoL , Microdajus langi Greve, 1965 View in CoL , Microdajus pectinatus Boxshall, Huys and Lincoln, 1989 View in CoL , and M. tchesunovi View in CoL . The present material and M. tchesunovi View in CoL are the only species known to have males with unsegmented protopods of thoracopod 6; the other species have two-segmented protopods on this thoracopod. However, protopods1–5of Microdajus sp. extend to an acute point on their lateral margins, whereas they are rounded in M. tchesunovi View in CoL . The anterior and posterior pits on the cephalothorax of the male of Microdajus sp. show the same pattern as in M. tchesunovi View in CoL but the number of setae in each pit is fewer in the former species than the latter.
In addition to the differences noted previously, the tantulus larva of Microdajus sp. appears to be the smallest recorded in this genus or of any tantulocaridan species (see Kolbasov and Savchenko, 2010; Petrunina and Huys, 2020). The total length for the tantulus larvae of Gulf of Mexico species is estimated based on a combination of directly measured material (head, SEM preparation) and photographic images (body), the approximate length of approximately 58 µm suggests that these larvae are the smallest ever recorded for any species of tantulocaridan. However, recollection and measurement of an intact tantulus larva is necessary to confirm this potential size record.
The tantulus larvae ( Figs. 1D View Figure 1 , 2A, B View Figure 2 ) lack all trunk segments and appendages and are likely developing the early parthenogenetic sacs; however, it is possible that the sacs will develop females inside them, as the trunk segments are lost in larvae in both developmental pathways (see Huys et al., 1993). The complete life cycle of tanulocaridans is in need of investigation and in some ways still remains hypothetical, with details such as metamorphosis of tantulus larvae into adult sexual females and sexual reproduction never having been observed ( Mohrbeck et al., 2010; Martinez Arbizu and Petrunina, 2017; Petrunina et al., 2018).
Most species of Microdajus are known from European waters(north-east Atlantic,Mediterranean), with one species being found in the nearby White Sea ( Kolbasov and Savchenko, 2010). Only one species was previously known outside this region: M. aporosus from the Ross Sea ( Grygier and Sieg, 1988). Microdajus sp. is the first material referable to this genus to be reported from the western Atlantic and the first tantulocaridan to be described from the Gulf of Mexico or the northwestern Atlantic. In terms of depth distribution, Microdajus sp. was collected from 684–2767 m, which is similar to the ranges for two other Microdajus species: M. gaelicus (897–2884 m) and M. pectinatus (540–2175 m). Most tantulocaridans are from deep sea habitats (see review in Mohrbeck et al., 2010); however, Microdajus sp. represents one of the deepest records for a species in the genus. The deepest record was reported by Mohrbeck et al. (2010) for an unidentified species of Microdajus collected at 5194 m off King George Island, Southern Ocean (see their table 2).
The hosts for Microdajus sp. are specimens of an apparently undescribed species of typhlotanaid, similar in morphology to Typhlotanais kussakini Kudinova-Pasternak, 1970 and T. williamsae Dojiri and Sieg, 1997 (M. Błażewicz, pers. communication). A lthough other epibionts and parasites (e.g., protozoans, nematodes) are sometimes found associated with tanaids, tantulocaridans have been most commonly reported ( Błażewicz et al., 2020) and they are almost always on the front of the host body, possibly due to the tubiculous lifestyle of the hosts ( Boxshall and Lincoln, 1987). Typhlotanaids are relatively poorly calcified, which may make them preferred hosts for tantulocaridans ( Błażewicz et al., 2020) and these parasites may be more readily observed on tanaids than hosts with more heavily calcified exoskeletons such as isopods ( Boxshall and Lincoln, 1987).
| USNM |
Smithsonian Institution, National Museum of Natural History |
| R |
Departamento de Geologia, Universidad de Chile |
| V |
Royal British Columbia Museum - Herbarium |
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