The Deep-sea Genus Coronarctus (Tardigrada, Arthrotardigrada) in Brazil, South-Western Atlantic Ocean, with the Description of Three New Species

: Three new marine tardigrade species from the deep-sea genus Coronarctus are described from the South-Western Atlantic Ocean: Coronarctus dissimilis sp. nov., C. neptunus sp. nov., and C. yurupari sp. nov. These, and C. laubieri Renaud-Mornant, 1987, are the first records of deep-sea tardigrades from this marine region. Specimens of those species were collected from two localities of the Brazilian continental slope (Potiguar and Campos basins) at depths comprised between 150 and 3000 m. Specimens of the three new species have short cephalic appendages and heteromorphic claws, belonging to the, here designated, C. tenellus group of species. Each of the new species can be distinguished from all the other species of the group by their peculiar-shaped secondary clavae and claws. The most relevant morphological characters used for the taxonomy of the genus: shape of cephalic cirri, shape of secondary-clavae, size and number of accessory spines on claws, and shape of seminal receptacles, are discussed and an identification key to all ten known Coronarctus species is provided.


Introduction
Tardigrades (phylum Tardigrada) are micrometazoans that occur worldwide in terrestrial, freshwater, and marine environments. Marine tardigrades are present in all oceans, ranging from the intertidal zone to abyssal depths, inhabiting a great diversity of sediments from fine mud to coarse sand, rocks, algae, and some benthic fauna [1][2][3].
About 220 species and subspecies of Arthrotardigrada, the order that includes almost all the marine tardigrades, had been described until now [4][5][6]. However, Bartels et al. [7] estimated that this number would likely exceed 1000, which demonstrates the paucity of knowledge about the biology of marine tardigrades. This problem is particularly severe in the Southern hemisphere, namely in poorly surveyed, deep sublittoral, and abyssal zones [4].
For nature management purposes, the need for meiofauna species inventories is especially justified in order to evaluate the environmental effects of human activities [17][18][19], for example oil extraction, which the Brazilian coast is strongly subjected to. Thus, in the frame of a project aiming to assess the impact of this activity on natural resources and marine communities, specimens of the deep-sea tardigrade genus Coronarctus Renaud-Mornant, 1974 were recorded from two localities in the major oil extraction basins in Brazil (Campos and Potiguar basins).
After the description of C. tenellus, the type species of the genus, recorded from abyssal sediments (1600-4700 m deep) in several localities of the Somalian coast in the Indian Ocean, six other species were assigned to this genus. Although, still remaining restricted, the geographic distribution of the species of the genus Coronarctus was extended to the Canal de Mozambique in the Indian Ocean [20]; the Namibian coast in the South-Eastern Atlantic Ocean as referred above [12]; France, Faroe Bank, and Spain in the North-Eastern Atlantic Ocean [20][21][22][23]; U.S.A. and the Gulf of Mexico [20,24] in the North-Western Atlantic, and Japan in the Pacific Ocean [25].
In this study, we provide the description of three new species to science: Coronarctus dissimilis sp. nov., C. neptunus sp. nov., and C. yurupari sp. nov., and a new record, C. laubieri Renaud-Mornant, 1987, from the Brazilian coast, South-Western Atlantic Ocean. Additionally, based mainly on new types of secondary clavae and claws observed in the new species, a dichotomous key to the identification of all Coronarctus species is also provided.

Materials and Methods
Tardigrades were collected from deep-sea sediments obtained from two localities of the Brazilian continental slope (South-Western Atlantic Ocean), at the interference zone of two relevant oil extraction basins: Campos Basin (21°55'-23°56' S; 39°55'-45°55' W), Rio de Janeiro State, at 150-3000 m in depth, and Potiguar Basin (4°36'-4°46' S; 36°05'-36°31' W), Rio Grande do Norte State, at 900-2500 m in depth ( Figure 1). Both sites are characterized by the presence of submarine canyons and the sediments are predominantly constituted of fine muds. Samples were obtained in 2009, via a box corer (50 × 50 cm), during the oceanographic campaigns (Environmental Characterization Project of the Continental Slope in the Potiguar Basin, and Environmental Characterization Project of the Campos Basin) developed by PETROBRAS (Petróleo Brasileiro SA). Then sediment subsamples were taken with 10 cm long PVC cores (diameter 3.7 cm) and fixed in 4% buffered formaldehyde.
At the laboratory sediments were washed and sieved using a 30 µm mesh sieve. Tardigrades were sorted under a dissecting microscope and transferred to microslides with coverslips. Specimens were permanently mounted in pure glycerin with formalin (ca. 1%) and sealed with nail paraffin. Animals were examined, measured (all measurements in micrometers-µm) and microphotographed under 1000x oil immersion, with a Leica DM 2500 Phase Contrast Microscopes (Leica Microsystems, Wetzlar, Germany) and a Zeiss Axioimager 2 Differential Interference Contrast Microscope (ZEISS Microscopy, Jena, Germany), both equipped with digital cameras and imaging software (Leica Application Suite V4.9 and Zen Imaging Software for Leica and Zeiss microscopes respectively). All photomicrographs were made under DIC, and structures were measured only if they were undamaged and if their orientation was suitable. When symmetrical structures were measured, the larger value was recorded when different values were obtained. Identifications were based on Fontoura et al. [2] and on original species descriptions in the literature [20,22,24,26,27].

Diagnosis
Coronarctus with reduced leaf-like cephalic appendages. Median cirrus inserted at the rear of the head, near the posterior edges of secondary clavae. Subspherical primary clavae. Flattened secondary clavae with two dorsal lobes and two ventral lobes each. The anterior dorsal lobe located far ahead; the second dorsal lobe located in a medial position. The posterior ventral lobes are closely jointed and separated from the anterior lobes by a deep indentation. Cuticle smooth. Sensory organs present on each pair of legs and additional flexible spine-like processes on legs IV. Heteromorphic claws: claws of legs IV much longer than claws of the first three pairs of legs. External claws slightly shorter than internal claws. All claws with apical accessory spines.

Type Locality
Campos Basin, Rio de Janeiro State, Brazil; specimens were collected from the Brazilian continental slope at 1300 m below sea level, in a submarine canyon, at two sampling points (21°55' S, 39°55' W and 21°55' S, 45°55' W). The sediment type is fine mud.

Etymology
From the Latin dissimilis (= dissimilar, unequal) as the two most external claws of the new species are considerably thinner than the two most internal claws on each leg I-III.

Description of Holotype
Adult female 350 µm long and 86.1 µm wide (Figures 2A,3A). The body, cylindrical and elongated, is covered by a smooth and transparent cuticle with metameric folds. Coelomocytes and other globular bodies (about 5 µm in diameter) are present in the body cavity. The head, narrower than the body, is made of two parts bearing short leaf-like cephalic cirri: the first conical part bears the paired internal (4.4 µm long) and external cirri (7.3 µm long), and the unpaired median cirrus (2.6 µm); the posterior second part bears the subspherical primary clavae and the leaf-like lateral cirri A ( Figures 2B-C,3B). Primary clavae (6.2 µm in diameter) are embedded into a socket and separated from the short lateral cirri A (5.2 µm) ( Figure 3B).
The flattened secondary clavae have two dorsal lobes and two ventral lobes each. The anterior dorsal lobe is located far ahead and can be easily overlooked; the posterior dorsal lobes are very wide and located in a medial position ( Figures 2B,3C). The posterior lobes are closely jointed. After the insertion of the external cephalic cirri, the anterior ventral lobes display a small projection that when deformed by the slide mounting process can be easily confused with a third ventral lobe (see Figure  2C). The anterior ventral lobes are separated from the posterior lobes by a deep indentation ( Figures  2C,3D). The posterior ventral lobes of secondary clavae are closely jointed. The median cirrus is inserted in the rear of the head, after the posterior dorsal lobes and near the posterior edges of the secondary clavae ( Figures 2B,3C).
Trunk cirri B (5.1 µm long), C (23.6 µm long), and E (20.6 µm long) are present as typical of the genus. Each trunk cirrus consists of a very short cirrophore, accordion-like scapus and tubular flagellum which is very short on cirrus B, tapering into a blunt tip.
The legs are short and stout. Legs IV are longer than the first three leg pairs. Sensory organs are present on all legs, very short on legs I-III (2.2, 3.4, and 5.3 µm long, respectively) and longer on legs IV (6.7 µm long). Sensory organs consist of a needle-like structure partly embedded into a conical base. On legs IV the needle-like structure is shorter, ending in a blunt apex ( Figure 4A). A flexible spine-like process (10.7 µm long) is inserted dorsally in the coxa of legs IV, above the sensory organ ( Figure 4A).
The claws, supplied with basal spurs and connected by a membrane, display heteromorphy: claws on the legs IV (external claws 27.4 and 31.2; internal claws 37.1 and 35.7 µm long) are much longer than claws on the first three leg pairs (on legs I: external claws 19.4 and 18.6; internal claws 24.4 and 24.5 µm long) (Figures 2A,D,3A). On all legs, external claws are slightly shorter than internal claws (see Table S1 for measurements). Claws on legs I are more robust than claws on legs II and III.
On the first three leg pairs and particularly on legs I, the two most external claws are considerably thinner than the two most internal claws ( Figures 3B,4B). All claws with apical short accessory spines ( Figures 2D,4D).
The mouth opening is terminal and surrounded by cuticular folds. Details of the buccal apparatus were not observed.
The ovary is odd and dorsal. Two pear-shaped seminal receptacles, with ducts directed frontwards, are present next to the rosette-like gonopore ( Figure 4E). The distance between gonopore and anus, a fissure surrounded by a wrinkled cuticle, is 15.7 µm.

Remarks
The observed male does not display external sexual dimorphism, except for the gonopore that is a slit on the top of a cylindrical cuticular fold. However, this assumption needs to be confirmed, particularly for morphometric data, with the examination of additional material to increase the sample size.
The two-clawed larvae lack gonopore and anus and the most external claw on legs I are particularly thin ( Figure 4F). As in adults, the claws also have short apical accessory spines. In larvae sensory organs were not observed on legs I-III probably due to their small size. For the other characters, larvae are similar to adults.

Differential Diagnosis
Currently, seven species are assigned to the genus Coronarctus. Based on the relative size of claws and length of cephalic appendages, which are considered as reliable taxonomic characters [20,22,24], two main groups can be recognized. Four species, exhibit claw heteromorphy (i.e., claws on legs IV much longer than claws of legs I-III) and have short cephalic appendages (<10 µm long): C. tenellus, C. disparilis Renaud-Mornant, 1987, C. laubieri and C. mexicus Romano III, Gallo, D'Addabbo, Accogli, Baguley and Montagna, 2011. Three other species, C. stylisetus Renaud-Mornant, 1987, C. fastigatus Renaud-Mornant, 1987 and C. verrucatus Hansen, 2007, display claw homomorphy (claws on all legs similar in length) and long (>10 µm) cephalic appendages. From now on these two groups will be designated as C. tenellus group of species and C. stylisetus group of species, respectively, referring to the two first described species within each group.
Coronarctus dissimilis sp. nov., in having short leaf-like cephalic appendages and claws displaying heteromorphy, belongs to the C. tenellus group. Within this group, only one described species, C. laubieri, also has the median cirrus inserted at the rear of the conical part of the head and secondary clavae with the posterior ventral lobes separated from the anterior ventral lobes by a deep indentation (see Figure 11). The new species can be clearly distinguished from C. laubieri in having differently shaped secondary clavae: in the new species, the posterior dorsal lobes are located at a medial position, before the insertion of the median cirrus, while in C. laubieri they are located at the rear, and the median cirrus is inserted between them (see Figure 11). Additionally, in C. dissimilis sp. nov. external claws on legs IV are just slightly shorter than internal claws (mean values of external claw length/mean values of internal claw length = 0.77-0.82, assessed in 7 adult specimens with the 4 claws measured) and all claws have well-visible dorsal accessory spines. On the contrary, in C. laubieri external claws are markedly shorter than internal claws (in the holotype external claw length / internal claw length = 0.40) and minute apical accessory spines are present on internal claws only. Moreover, in comparison with C. laubieri, in C. dissimilis sp. nov. the two most external claws on each leg I-III are particularly thin when compared with the two most internal claws.

Material Examined
Seven specimens (two females, 244 and 395 µm long, one male 259 µm long, one specimen of unknown gender 362 µm long and a two-clawed larva 256 µm long) were collected from the Potiguar Basin (4°36'-4°46' S; 36°05'-36°31' W), Rio Grande do Norte State, Brazil, in the Brazilian continental slope between 1985 and 2500 m below sea level; and two specimens (female 445 µm long and specimen of unknown gender 294 µm long) were collected from Campos Basin (22°10' S; 40°20' W), Rio de Janeiro State, Brazil, in the Brazilian continental slope between 2500 and 3000 m below sea level (see table S2 for measurements and Figures S1 and S2). At both sampling sites the sediment type is fine grain.

Remarks
Accessory spines on claws were not observed on the examined specimens. For all the other characters the specimens perfectly match the description of the species in Renaud-Mornant [20]. Up until now, this species was recorded in the North Atlantic only at depths of between 625 and 4190 m below sea level [4]: five records [20] from St. KG 215, terra typica (47°35'65'' N; 9°39'9'' W), one record [30] from France, Bay of Biscay (46°18'68'' N; 12°33'90'' W), and one record [24] from U.S.A., Gulf of Mexico (27°07' N; 92°20' W). This is the first record of this species from the South-Western Atlantic Ocean. Table S3 3.

Diagnosis
Coronarctus with reduced cephalic cirri, each with annulated scapus and flagellum. Spherical primary clavae. Flattened secondary clavae with two ventral lobes, the posterior ones jointed. Dorsally, the internal edges of secondary clavae, diverging posteriorly, are almost rectilinear, not displaying evident lobes. Median cirrus inserted at about equal distance from the mouth opening and the posterior edges of secondary clavae. Cuticle smooth. Sensory organs present on each pair of legs. The leg sensory organ on legs I-III consists of a needle-like structure, protruding from a wrinkled broad cylindrical basal portion, in which it is partly embedded. The wrinkled basal portion is conical on legs IV with the embedded needle-like structure slightly protruding. Similar spine-like processes are present on the coxa of legs IV. Heteromorphic claws (claws of legs IV much longer than claws of the first three pairs of legs) with very robust basal spurs. Internal claws on legs IV with a pair of apical spines; on external claws IV a robust spine is present mediodorsally. Minute accessory spines are present on legs I-III.

Etymology
The epithet is inspired by the trident used by Neptuno, the Roman god of the sea, as an allusion to the long and sharp spines of the claws of the new species.

Description of Holotype
Adult female with an elongated cylindrical body (about 216 µm long and 75.8 µm wide) with a constriction between each pair of legs ( Figures 5A,6A). Cuticle smooth and transparent.
A full set of short cephalic appendages is inserted into a conical head (Figures 5B-C,6B-C). Divided lateral cirri A (11.1 µm), each consisting of an annulated scapus followed by a smooth flagellum, ending in a spherical tip, are located in the posterior portion of the head and inserted separately but at the same time closely to the spherical and not pedunculated primary clavae (5.6 µm) ( Figures 5B,6C-D). Short median cephalic cirrus (4.0 µm) is inserted at about equal distance from the anterior head margin (17 µm) and the posterior edges of secondary clavae (15 µm) ( Figure 5C). Dorsal internal and ventral external cephalic cirri are short, similar in length (5.5 and 6.1 µm long respectively), and inserted anteriorly, close to the mouth opening ( Figures 5B,6B). The cephalic cirri end forming a blunt tip and the division into annulated scapi and flagella, although not confirmed, is likely. The flattened secondary clavae have two ventral lobes, the posterior ones jointed ( Figures  5B,6B). Dorsally the internal edges of secondary clavae are almost rectilinear, not displaying evident lobes; left and right edges, which are very closely jointed anteriorly, diverging backwards gradually ( Figures 5C,6C).  The legs, particularly the first three pairs, are short and stumpy. The hind legs are slightly longer. Sensory organs present on all pairs of legs. Leg sensory organs on legs I-III ( Figure 7A,B) consist in a needle-like structure (about 2.0 µm long), partly embedded into a wrinkled broad cylindrical basal portion and partly protruding (basal portion is 4.0, 8.0, and 8.0 µm long in legs I, II, and III, respectively). On legs IV sensory organs (not measured in the holotype) are similar but the wrinkled basal portion is more conical and the protruding needle-like structure is relatively smaller. A refractive organ is present at the apex of the basal portion. Similar spine-like processes (16.0 µm long) are present on the coxa of the hind legs ( Figure 7D).
Each leg has four claws with robust basal spurs. Claws exhibit marked heteromorphy: on the claws of the fourth pair of legs (external and internal claws are 39.2/39.7 and 43.0/44.5 µm, respectively) are much longer than claws on the first three pairs of legs (on legs I external claws are 22.0 µm, internal claws 27.0 µm long); on all legs internal and external claws are similar in size or internal claws are slightly longer than external claws (see Table S3 for measurements, Figures  5A,D,6A,7A-C). Minute accessory spines were observed on several (but not all) internal and external claws on legs I-III. The small size of accessory spines and the orientation of claws are a probable reason for not having observed accessory spines on all claws. Therefore, the presence of accessory spines on all claws on legs I-III is likely. All claws on legs IV (Figures 5A,D,7C) are slightly bent and have very long sharp basal spurs (14.0 and 7.0 µm on external and internal claws respectively) and strong and long accessory dorsal spines: a single robust spine, about 4.6 µm, located far from the claw tip (about 10 µm, i.e., 1/3 of the claw length) on external claws, and a pair of slightly shorter (3.4 µm) but evident spines located in a more apical position (about 6.7 µm far from the claw tip) on internal claws (Figures 5B,7C). The mouth is subterminal and surrounded by cuticular folds. The spherical pharyngeal bulb is about 22 µm in diameter. Other structures of the buccal apparatus (buccal tube, stylets, and placoids) were not observed.
The reproductive structures consist of a dorsal ovary and two pear-shaped seminal receptacles (each 12.1 µm long) with straight duct directed backwards and curving anteriorly in the terminal portion only. Seminal ducts openings are located laterally at about 18 µm from the rosette-like gonopore (Figures 5A,7E). The anus, 14.5 µm distant from the gonopore, is a short fissure surrounded by a wrinkled cuticle.

Remarks
The allotypic male does not display external sexual dimorphism, except for the gonopore that is a circular slit located at the top of a cylindrical cuticular fold, 7 µm from the anus ( Figure 7F). Twoclawed larvae were not found.

Differential Diagnosis
In Coronarctus neptunus sp. nov., secondary clavae do not display evident dorsal lobes and the edges jointed anteriorly, diverge backwards. Within the genus Coronarctus, this kind of dorsal-shaped secondary clavae is present in C. stylisetus only (see Figure 11). However, contrary to C. neptunus sp. nov., this species has long cephalic appendages and the claws display homomorphy (C. stylisetus group of species). In having short cephalic appendages and heteromorphic claws, the new species belongs to the C. tennellus group of species. In this group and similarly to C. neptunus sp. nov., only C. mexicus has annulated cephalic cirri and wrinkled leg sensory organs. In addition to the very differently shaped secondary clavae (dorsal edges diverging backwards and two ventral lobes in the new species, whereas the two dorsal lobes are described as very closely jointed and three ventral lobes are present in C. mexicus, see Figure 11), the two species can be clearly distinguished by another relevant taxonomic character, the claws. In the new species, claws IV are less curved, with long and sharp basal spurs, twin accessory spines on internal claws and a robust spine mediodorsally located (all claws more curved and with single apical accessory spines in C. mexicus). Moreover, in C. mexicus claws on legs I-III are thick and external and internal claws are not equal in size (16 and 23 µm respectively in the holotype, which has a 294 µm long body, i.e., the external/internal claws ratio is about 0.70), while in C. neptunus sp. nov. the claws of the three first leg pairs are longer, much thinner and much more similar in length (external/internal claws ratio > 0.74, n = 5; in the 216 µm long holotype this ratio is 0.81). The two species also differ in the relative size of sensory organs and coxal spine-like processes on the hind legs that are equal in size in C. mexicus, while sensory organs are much smaller than coxal spine-like processes in C. neptunus sp. nov. The new species also differs from all the known species of the genus in having straight seminal ducts directed backwards and curving anteriorly in the terminal portion only. In the other Coronarctus species the seminal duct curves immediately after the seminal receptacle, pointing anteriorly in six species and posteriorly in C. stylisetus 3.4. Coronarctus yurupari sp. nov. Table 4 3. 4

.1. Diagnosis
Coronarctus species with reduced leaf-like cephalic cirri. Spherical, pedunculated primary clavae. Flattened and strongly punctated secondary clavae with posterior ventral and dorsal lobes closely jointed. Cuticle smooth. Sensory organs present on each pair of legs. Small spine-like process on legs IV. Heteromorphic claws: claws of legs IV much longer than claws of the first three pairs of legs. All claws (internal and external) with a short apical accessory spine. On claws of legs IV an additional spine is present mediodorsally.

Etymology
The specific epithet yurupari refers to Yurupari, a demon in the mythology of some South American indigenous communities (namely the Mawé), considered the lord of darkness. The specific epithet alludes to the dark ocean depths where the new species was found.

Description of the Holotype
Adult male with a cylindrical and elongated body is 485 µm long and 107 µm wide ( Figures  8A,9A). The cuticle, with metameric folds, is smooth and transparent. Coelomocytes and other globular bodies (about 5.2 µm in diameter) are present in the body cavity. The head is welldifferentiated and narrower than the body, bearing short leaf-like cephalic cirri ( Figures 8B-C,9B). The anterior conical part of the head bears the external (6.8 µm) and internal cirri (6.0 µm), median cirrus (4.7 µm) and the secondary clavae. The posterior cylindrical part of the head bears the primary clavae (7.8 µm) and lateral cirri A (5.0 µm) ( Figure 8A-C). The spherical, finely punctated primary clavae are pedunculated and inserted separately from the shorter lateral cirri A. A very small constriction is present on the top of primary clavae ( Figures  9D,10A). The secondary clavae are flattened and strongly punctated ( Figures 8B-C,9C). Secondary clavae with two dorsal and two ventral lobes each. The dorsal and ventral posterior lobes are closely jointed ( Figure 9C-D). Posterior dorsal end ventral edges of secondary clavae with a poorly marked indentation. The median cirrus is inserted between the anterior and the posterior dorsal lobes at about equal distance from the mouth opening and the posterior edge of secondary clavae.  The legs, particularly the first three pairs, are short and retractile. The hind legs, slightly longer and slender, have a spine-like process (8.4 µm) inserted on the coxa ( Figure 10B, black arrowhead). Each leg has four claws. Claws display marked heteromorphy: on the fourth pair of legs, claws are much longer than claws on the first three pairs of legs (on legs IV external claws are 49.3 and 52.3 and internal claws are 63.5 and 67.2 µm long, on legs I the only external claw measured is 27.2 and internal claws are 34.0 and 38.0 µm long); on all legs internal claws are slightly longer than external claws (see Table S4 for measurements, Figures 8A,D,9A,D,10C). The claws are curved, supplied with basal spurs and are connected to the leg by a membrane. All claws have an apical accessory spine ( Figures  8D,10C). Claws IV have an additional minute spine, located mediodorsally, very difficult to see (Figures 8D).
The mouth opening is terminal and surrounded by cuticular folds. The buccal tube is 70.0 µm long, ending into large droplet-shaped apophyses (well visible in a paratype, Figure 10D). The oval pharyngeal bulb (33.0 µm long and 27.0 µm wide) is devoided from placoids. Stylet supports are not perceptible in the holotype, in a paratype (body 352 µm long; buccal tube 69.0 µm) the stylets ( Figure  10D), without stylet supports, are 61.0 µm long, ending into elongated bulbous furcae.
The gonopore is a circular slit located at the top of a cylindrical cuticular fold, 9.0 µm distant from the anus ( Figure 10E). The anal fissure is surrounded by three lobes of wrinkled cuticle.

Remarks
Although only based on the examination of one female, except for her larger size, sexual dimorphism was not observed on external somatic structures. The female has two pear-shaped seminal receptacles, each consisting of a pouch (11.0 µm long x 9.0 wide µm) and a curving duct (about 33 µm long) bending frontwards ( Figure 10F). The duct opening is located at the same height as the rosette-like gonopore, which is 15.0 µm distant from the anus. The ovary is seen dorsally.
The claws on the two-clawed larvae, lacking gonopore and anus, all have a short apical spine. The additional spine located mediodorsally was not perceptible on claws IV. All the other characteristics are the same as the adult.

Differential Diagnosis
As with the new species, belonging to the C. tennellus group of species, the other six described Coronarctus species also exhibit claw heteromorphy and have short cephalic appendages: C. tennellus, C. disparilis, C. laubieri, C. mexicus and the above newly described species C. dissimilis sp. nov. and C. neptunus sp. nov. Coronarctus yurupari sp. nov. has leaf-like cephalic cirri and the median cirrus inserted at equal distance from the posterior and anterior edges of secondary clavae and can be easily distinguished from C. laubieri and C. dissimilis (both with the median cirrus inserted posteriorly at the level of posterior edges of secondary clavae, see Figure 11) and from C. mexicus and C. neptunus sp. nov. (both species display cephalic cirri with accordion-like scapi). Moreover, C. yurupari sp. nov., differ from C. laubieri and C. dissimilis in lacking a deep indentation between the two ventral lobes of secondary clavae. The new species and C. mexicus exhibit different-shaped secondary clavae: two ventral lobes, from which the posterior lobe is jointed, are present in C. yurupari sp. nov., while three ventral lobes from which the posterior lobe is slightly separated are present in C. mexicus (see Figure  11). Coronarctus yurupari sp. nov. differs from the most similar species C. tenellus and C. disparillis by the claws, as follows: -From C. tenellus, since C. yurupari has coxal spine-like processes on legs IV (absent in C. tenellus) and apical accessory spines on internal and external claws on all legs and additional mediodorsal spine on claws of legs IV (apical accessory spines on external claws and the additional spine are absent in C. tenellus); -From C. disparilis, since C. yurupari has the additional spine on legs IV located mediodorsally, while in C. disparilis it is located on the ventral side of the claws. Apical accessory spines are present on all claws of legs I-III in the new species while lacking on external claws in C. disparilis. Moreover, the primary clavae are pedunculated in C. yurupari sp. nov. and subspherical in C. disparilis. The two species also differ in the shape of internal edges of the posterior lobes of secondary clavae that are circular in the new species and squarish in C. disparilis (Figure 11).

Discussion
Following this study, the number of Coronarctus species increases to ten. This diversity within the genus is supported by the specific variability of some relevant taxonomic morphological characters, such as the shape and development of cephalic cirri; the shape of secondary clavae; the claws, namely the size and number of accessory spines, and the shape of seminal receptacles, as recognized in previous studies, not only for the general taxonomy of marine tardigrades (for a review see [2,29]), but also for the particular case of Coronarctus [20,22,24,27].
The separation of Coronarctus species in two main groups, according to the size of cephalic appendages and relative size of claws on legs I-III and claws IV, was introduced by Renaud-Mornant [20], who provided the description of C. stylisetus and C. fastigatus, both species with long cephalic cirri and homomorphic claws, which were considered plesiomorphic characters. Renaud-Mornant [20], hypothesized that the reduction of cephalic cirri and claw heteromorphy observed in the other three Coronarctus species known at that time (C. tenellus, C. disparilis, and C. laubieri), could represent an apomorphic condition related to the adaptation to abyssal depths. This hypothesis was supported by Hansen [22], with the description of C. verrucatus, the third species with long cephalic cirri and claw homomorphy. Thus, according to these authors, C. stylisetus, C. fastigatus, (despite also being recorded at abyssal depths), and C. verrucatus belong to an evolutionary line, showing a tendency of bathyal distribution (recorded from depths comprised between 40-439 m; 675-2400 m, and 249-260 m, respectively, including the record of C. stylisetus from the Pacific Ocean by Noda [25]). By contrast C. tenellus, C. disparilis, and C. laubieri, from another evolutionary line, show a tendency towards an abyssal distribution (recorded from 1630-4690 m; 3400 m, and 3600-4190 m, respectively). However, in addition to C. fastigatus, other species also overlap bathyal and abyssal depths in their bathymetric distribution. This is the case of C. mexicus, the last described species within the genus by Romano III et al. [24] before this study, which was recorded from 625-3250 m in depth, C. disparilis (763-3000 m) and C. laubieri (625-3250 m), all from the Gulf of Mexico and all with short cephalic appendages [24]. In this study, taking into account their short cephalic appendages and heteromorphic claws, all species should have shown a tendency towards an abyssal distribution. This was the case of C. laubieri (collected from 1985-3000 m), C. dissimilis sp. nov. (1300 m) and C. yurupari sp. nov. (991-2159 m). On the contrary, the distribution of depth of C. neptunus sp. nov., ranging from 150 to 1300 m deep, shows that the species, although found in considerably deep waters, can colonize shallower zones too. In our opinion, the records of C. fastigatus from abyssal depths and C. disparilis, C. laubieri (considering that identifications of these two species in the Gulf of Mexico were correct), C. mexicus and C. neptunus sp. nov from bathyal depths, do not mean that the aforementioned hypothesis should be rejected, but that other unknown factors can influence the distribution of Coronarctus species in ocean depths. In order to facilitate the terminology to be used in future research, in this study the two evolutionary lines are named according to the first described species on each line: the C. tenellus group of species (with short cephalic appendages and heteromorphic claws) and the C. stylisetus group of species (with long cephalic cirri and homomorphic claws).
Which homomorphic and heteromorphic claws are displayed by each of the species of the genus that justify its assignment to one or the other of the evolutionary lineages mentioned above is a question that also needs clarification. As such, claws on legs I-III are compared with claws on legs IV and, if they are similar in size, a species is considered as displaying homomorphic claws. On the contrary, if claws on legs I-III are smaller than claws on legs IV, the species is considered as displaying heteromorphy. This should not be confused with different claw size exhibited between claws on the same leg. With the exception of C. laubieri, which displays much smaller external claws on legs IV than the internal claws, the two internal claws are about the same size or slightly longer than the two external claws for all the other species. Such kind of claw arrangement patterns, together with other aspects of claws, such as the number and size of accessory spines on each claw, express interspecific variability and are, consequently, very relevant for distinguishing species. It must be stressed, that accessory spines were not observed in the specimens identified as C. laubieri collected in this study from the South-Western Atlantic. Although all other characteristics perfectly match the description of this species, the eventual occurrence of cryptic speciation in this genus cannot be neglected as it also occurs in other marine tardigrade genera [31][32][33][34]. We presume that, with molecular data, this problem will be solved in the near future.
Novelties in the shape of secondary clavae on Coronarctus were also found in this study, confirming that interspecific variability can be translated by the number, size, and shape of dorsal and ventral lobes and punctuation, recommending a careful observation of this character in future identifications and species descriptions. The different shape patterns of secondary clavae displayed by all species are represented in Figure 11. Four main types can be recognized: (1) Two dorsal and two ventral lobes and posterior lobes jointing posteriorly (C. tenellus, C. disparillis, and C. yurupari sp. nov.); (2) Two dorsal lobes and two ventral lobes, the posterior ventral lobes separated from the anterior lobes by a deep indentation (in C. dissimilis sp. nov. and C. laubieri the median cirrus is inserted at the rear of the head); (3) Dorsal lobes poorly marked or absent, with dorsal edges of secondary clavae diverging posteriorly (C. fastigatus, also with divergent ventral lobes, C. neptunus sp. nov., C. stylisetus, and C. verrucatus, species with jointed posterior ventral lobes); (4) Three ventral lobes (C. mexicus, in the original description of this species the presence of two very close dorsal lobes is indicated but not illustrated). On the other hand, secondary clavae are described as strongly punctated in C. mexicus, C. verrucatus and C. yurupari. However, this character was not clearly described by Renaud-Mornat [20,26,27], who referred to the presence of slightly punctated secondary clavae in C. tenellus. However, despite the subjectivity of the terminology used, in our opinion it was illustrated as strongly punctated [26,27]. Coronarctus disparillis and C. fastigatus were described as having thicker (without mention of punctuation) secondary clavae [20]. Therefore, it cannot be assumed that all the other species have smooth or finely punctated secondary clavae and this character needs to be confirmed.
The importance of female genital structures, namely the morphology of seminal receptacles as relevant taxonomic characters was highlighted for other tardigrade genera such as the Stygarctidae [35] and Archechiniscidae [36]. The reduction of seminal duct length in Coronarctus was previously referred to by Renaud-Mornant [20] as an apomorphic character. This author also noted that C. stylisetus was the only species within the genus with seminal ducts leaving the seminal receptacles by the anterior margin, curving immediately in a backwards direction. On the contrary, in all the other species the seminal ducts leave the seminal receptacles by the posterior margin and immediately loop in a frontward direction. In this study, the interspecific variability of the morphology of seminal ducts is increased with the discovery of a new pattern in C. neptunus sp. nov. In this species, the seminal ducts leave the seminal receptacles by the posterior margin and, without curving, direct backwards to the gonopore (a short curve directing the duct frontwards occurs near the seminal opening only).
Based on the description of the three new species that brought new insights to the taxonomy of the genus, as discussed above, a dichotomous key to the identification of all Coronarctus species is provided in this paper. It is also expected that these new insights could be pivotal to our understanding of the phylogeny of the genus.
As further concluding remarks, it is important to note that these are the first records of abyssal tardigrades from the South-Western Atlantic Ocean, contributing to the enhancement of our knowledge about the distribution and biogeography of the genus, confirming the uniqueness of this area and supporting the need for more extensive and deeper surveys. Figure 11. Drawings of secondary clavae of all Coronarctus species (C. tennellus, redrawn from Renaud-Mornant [26]; C. disparilis, C. fastigatus, C. laubier,i and C. stylisetus, redrawn from Renaud-Mornant [20]; C. mexicus, redrawn from Romano [24], dorsal view not provided, C. verrucatus redrawn from Hansen [22]; C. dissimilis, C. neptunus, and C. yurupari are original drawings).

Conflicts of Interest:
The authors declare no conflict of interest.