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18 August 2021 Lepidodermella weissi, new species (Gastrotricha: Chaetonotida: Chaetonotidae) from northwestern Oregon, U.S.A. (see erratum)
James J. Kirk
Author Affiliations +
Abstract

A new species of Lepidodermella (Gastrotricha: Chaetonotida: Chaetonotidae) is described from two streams in northwestern Oregon, U.S.A. This is the fourth species of freshwater gastrotrich reported from the Pacific Northwest region of the United States. The dearth of reports appears to be due more to a lack of study rather than a lack of gastrotrichs. Lepidodermella squamata is one of the species already reported from the Pacific Northwest, and occurs sympatrically with the new species described here. No other members of the genus have been reported from the Pacific Northwest. Three species of Lepidodermella have been reported previously from North America. The genus includes one marine species and 14 freshwater species. Lepidodermella weissi, new species, brings the number of freshwater species to 15 and can be distinguished from other freshwater members of the genus by the following characters: absence of parafurcal spines, absence of transverse anterior ventral plates, head width of less than 40 µm, head with five lobes, pharynx length 44 µm or less, adhesive tube length of 5 µm or more, more than 35 scales per middorsal column, presence of seven or fewer posterior midventral columns of scales, presence of a pair of posterior ventral plates, and the presence of several columns of spined scales between the ventral ciliary bands and the smooth scales of dorsum and sides.

Gastrotrichs are small (60–3500 µm), vermiform or tenpin-shaped, acoelomate animals common in most aquatic environments. The Phylum Gastrotricha includes nearly 900 species divided into two orders: Chaetonotida and Macrodasyida. The Order Chaetonotida includes 38 genera and over 470 species, of which just over three-quarters occur in freshwater; the remainder occur in marine or brackish water. For an expanded introduction to the phylum, see Kånneby (2016), Kieneke & Schmidt-Rhaesa (2014), Todaro et al. (2019), and WoRMS (2019).

Some 59 freshwater species have been reported from the United States (Kånneby & Weiss 2016, Kånneby & Kirk 2017), but only three species have been reported from the west coast states of Washington, Oregon, and California: Redudasys neotemperatus Kånneby & Kirk, 2017 was reported from the Little Nestucca River in western Oregon, and Chaetonotus chuni Voigt, 1901 and Lepidodermella squamata Dujardin, 1841 were reported from a pond on the University of Washington campus in Seattle, Washington (Hatch 1939).

Materials and Methods

Sediment and occasional limited samples of aquatic moss were collected more or less throughout the year, depending in part on weather and stream flow (high water limits collecting), during 2015 through 2016. Eighteen collecting trips were made, eight of which (May through October) yielded the new species. Samples were collected by hand, by use of a mosquito larva dipper (350 ml capacity) on an aluminum handle extensible to 1.6 m, by use of a manual, piston-type aquatic sediment sampler with a tube length of 1 m and a bore diameter of 5.6 cm (manufacturer unknown), or by use of a smaller, manual, piston-type aquatic sediment sampler with a tube length of 42 cm, a bore diameter of 4.6 cm, and a plastic sediment collection jar (220 ml capacity) near the lower end of the tube. Sediment or moss samples were placed with water in 1.1 L self-sealing plastic bags in the field, and transferred to 250 ml or 550 ml plastic deli cups in the lab. Subsamples of sediment or mosses with water were drawn from deli cups with a spoon or a disposable plastic syringe with no needle and placed in 100 × 15 mm plastic Petri dishes. Petri dishes were monitored at irregular intervals for up to 8 wk using a Wild M8 stereo microscope. Single specimens usually were anesthetized with 0.5% or 1% magnesium chloride for examination, but occasionally were examined without anesthesia. Specimens were examined using a Leitz Orthoplan, Nikon Optiphot, or Nikon Microphot FXA microscope, all equipped with differential interference contrast optics. Specimens were photographed using a PAXcam5+ or PAXcam2+ dedicated microscope camera and PAX-it! Imaging Software (©2020). Measurements were made on captured images using PAX-it! software. Drawings were made using Inkscape software. The positions of selected morphological features along the longitudinal axis are reported as percentage units (“U”) of the total body length following the convention of Hummon (1974).

This work has been registered in Zoo-Bank with registration number urn:lsid: zoobank.org:act:3AD4AF44-93A4-4784BAED-FF7ABE2F4144.

Results

Systematic Account
Phylum Gastrotricha Metschnikoff, 1865
Order Chaetonotida Remane, 1925
Suborder Paucitubulatina d'Hondt, 1971
Family Chaetonotidae Gosse, 1864 (sensu Garraffoni et al. 2016)
Subfamily Chaetonotinae Kisielewski, 1991
Genus Lepidodermella Blake, 1933
Lepidodermella weissi, new species Figs. 14, Table 1.

  • Type locality.—Sand pockets among boulders in rapids on the Little Nestucca River, near Pacific City, Tillamook County, State of Oregon, United States; (45°06′59″N; 123°51′23″W). The site is shown in Kånneby & Kirk (2017, Fig. 1).

  • Other localities.—Sand pockets among boulders in rapids on the Little Nestucca River, near Pacific City, Tillamook County, Oregon, U.S.A. (45°07′02″N, 123°51′52″W); sand pockets in the Little Nestucca River below the mouth of Hiack Creek, Tillamook County, Oregon, U.S.A. (45°05′13″N, 123°47′27″W); and coarse sand behind a small log jam, Nestucca River, Tillamook County, Oregon, U.S.A. (45°17′19″N, 123°30′13″W).

  • Type material.—Pursuant to Articles 72.5.6 and 73.1.4 of the International Code of Zoological Nomenclature (ICZN), the specimen shown in Figs. 14 is hereby designated as the holotype of Lepidodermella weissi. Other specimens illustrated or described are designated as paratypes. No attempt was made to preserve a specimen as the name-bearing type in part because specimens may be destroyed in the course of examination (e.g., Schwank 1990:22–23), “permanent” microscope slide preparations of freshwater gastrotrichs tend to deteriorate over relatively short periods of time, and modern photomicrography provides high quality images that persist much longer (see Kånneby et al. 2014, Garraffoni et al. 2019, Todaro et al. 2019). In the author's own limited experience, gastrotrichs shipped in ethanol sometimes “disappear” in transit.

  • Etymology.—Named in honor of Dr. Mitchel J. Weiss, longtime student of gastrotrichs, especially Lepidodermella, and mentor to the author upon the latter's entry into the world of gastrotrichs.

  • Diagnosis.—A small Lepidodermella (mean total length = 108 µm; range = 77–143) with a with large head and a stocky body (maximum body width ‚ total length = 0.31). Ventral motor ciliary bands merge anteriorly. Small, keeled, midventral scales in 3–7 longitudinal columns, extending from the pharyngeal area to the posterior ventral plates. Middorsal longitudinal column with 34–42 scales. With 15–24 dorsal plus ventrolateral longitudinal columns of scales. Small, keeled, usually spine-bearing scales in 1–3 ventral longitudinal columns on the trunk, immediately lateral to the ventral motor ciliary bands. Usually with a single pharyngeal tooth. With a single pair of broad, overlapping, posterior ventral plates with offset keels. Without parafurcal spines.

  • Differential diagnosis.—Lepidodermella weissi differs from Lepidodermella acantholepida Suzuki, Maeda & Furuya, 2013 in having: (1) a shorter pharynx (22–33 µm versus 37 µm), (2) no anterior transverse ventral plates, (3) more scales per midventral column (22–28 versus 18), and (4) more columns of dorsal trunk scales (9–15 versus 5–7).

  • Lepidodermella weissi differs from Lepidodermella amazonica in having: (1) a shorter total length (77–143 µm versus 199–200 µm), (2) a shorter pharynx (22–33 µm versus 61–65 µm), (3) no anterior transverse ventral plates, (4) more columns of dorsal trunk scales (9–15 versus 5, (5) more dorsal and lateral columns of trunk scales (15–24 versus 17–19), and (6) shorter adhesive tube length (6–13 µm versus 17–19 µm).

  • Lepidodermella weissi differs from Lepidodermella aspidioformis Sudzuki, 1971 in having: (1) fewer columns of dorsal trunk scales (9–15 versus 16), (2) keeled scales between ventral ciliary bands versus none, and (3) a pair of posterior ventral plates versus no such plates.

  • Lepidodermella weissi differs from Lepidodermella broa Kisielewski, 1991 in having: (1) more scales per middorsal column (34–42 versus 18–19, (2) shorter adhesive tubes (6–13 µm versus 13–15 µm), (3) a narrower cephalion (9–14 µm versus 16–18 µm, (4) midventral scales (absent in L. broa), and (5) more dorsal and lateral columns of trunk scales (15–24 versus 10–12).

  • Lepidodermella weissi differs from Lepidodermella forficulata Schwank, 1990 in having: (1) more dorsal trunk scale columns (9–15 versus 5–7), (2) more dorsal and lateral scale columns (15–24 versus 9–13), (3) shorter adhesive tubes (6–13 µm versus 20–22 µm), (4) shorter furca (11–18 µm versus 30 µm), and (5) parafurcal spines absent versus present.

  • Lepidodermella weissi differs from Lepidodermella intermedia Kånneby, Todaro & Jondelius, 2011 in having: (1) parafurcal spine absent versus present, and (2) interciliary area with elliptical, keeled scales versus round smooth scales.

  • Lepidodermella weissi differs from Lepidodermella limogenum Schrom, 1972 in inhabiting freshwater versus salt water and in having: (1) parafurcal spine absent versus present, (2) interciliary area covered with elliptical, keeled scales versus round, smooth scales, and (3) parafurcal spines absent versus present.

  • Lepidodermella weissi differs from Lepidodermella macrocephala d'Hondt, 1971 in having: (1) a pharynx length of 22–36 µm versus 45 µm, (2) a maximum head width of 22–36 µm versus 45 µm, (3) 9–15 dorsal trunk scale columns versus 8, (4) a furca length of 11–18 µm versus 24 µm, and (5) an adhesive tube length of 6–13 µm versus 18 µm.

  • Lepidodermella weissi differs from Lepidodermella minor chaetifer in having: (1) 34–42 scales per middorsal column versus 30–31, (2) 15–24 dorsal and ventrolateral longitudinal columns versus 13–15, (3) 34–42 scales per middorsal column versus 30–31, and (4) parafurcal spine absent versus present.

  • Lepidodermella weissi differs from Lepidodermella minor minor (Remane, 1936) in having: (1) midventral scales with keels versus without keels, and (2) Kisielewski's (1991) “ratio of scale distribution” of 49% versus 50–63% (number of columns of scales, counted from one ciliary band around the dorsum to the other ciliary band, divided by the number of scales in the median dorsal column, and expressed as a percentage).

  • Lepidodermella weissi differs from Lepidodermella polaris Kolicka, Kotwicki, & Dabert, 2018 in having: (1) no transverse plates posteriolateral to the hypostomium versus having those plates, (2) a single pair of posterior ventral plates versus two pair, and (3) no transverse ventral plates versus transverse ventral plates in the pharyngeal area.

  • Lepidodermella weissi differs from Lepidodermella serratum Sudzuki, 1971 in having keeled midventral scales versus none.

  • Lepidodermella weissi differs from Lepidodermella spinifera Tretjakova, 1991 in having: (1) 3–7 midventral columns of scales versus 8–16, (2) 22–28 scales per midventral column versus 60, (3) adhesive tube length 6–13 µm versus 20–23 µm, (4) furca length 11–18 versus 27, (5) dorsal trunk scales with smooth edges versus jagged lateral edges, (6) parafurcal spines absent versus present, and (7) ventral base of each caudal appendage without a large lamella versus the ventral base of each caudal appendage covered by a large lamella.

  • Lepidodermella weissi differs from Lepidodermella squamata (Dujardin, 1841) in having: (1) 34–42 scales per middorsal column versus 25–30, (2) anterior ventral plates absent versus present, (3) adhesive tube length 6–13 µm versus 13–19 µm, (4) hypostomium not visible or a single transverse bar versus a pair of bumps, (5) furca length 11–18 µm versus 18–27 µm, and (6) 9–15 scales per transverse dorsal trunk row versus 7–9.

  • Lepidodermella weissi differs from Lepidodermella tabulata Preobrajenskaja, 1926 in having: (1) adhesive tube length of 6–13 µm versus 3 µm, (2) 34–42 scales per longitudinal middorsal column versus 50, and (3) furcal scales extending to the base of adhesive tubes versus not extending to the base of adhesive tubes.

  • Lepidodermella weissi differs from Lepidodermella trilobum (Brunson, 1950) in having: (1) pharynx length of 22–33 µm versus 50 µm, (2) head five-lobed with two pairs of anterior sensory cilia tufts versus a three-lobed head with a single pair of anterior sensory cilia tufts, (3) total length 77–143 µm versus 177 µm, (4) prefurcal width of 11–19 µm versus 19 µm, and (5) furca length 11–18 µm versus 20 µm.

  • Lepidodermella weissi differs from Lepidodermella zelinkai (Konsuloff, 1913) in having: (1) visible midventral scales and keels versus only keels visible, (2) 3–7 midventral scale columns versus 20 midventral keel columns, (3) furcal notch broad, shallow, and not sharp anteriorly versus furcal notch deep, narrow, and with a sharp anterior end; (4) spined trunk scales between the ventral cilia bands and ventrolateral smooth scales versus no such spined scales, and (5) posterior ventral plates wide and overlapping versus narrow and not touching.

  • Description.—Morphometrics are described below, and most are summarized in Table 1.

  • I. Head: The maximum head width exceeds the maximum trunk width in some specimens. The head is rounded (virtually a partial circle in a compressed specimen). The hypopleuria (see Figs. 1 and 3) are sometimes difficult to see from above. When measured from above or below, the epipleuria average 8 µm in length (5–10 µm, n = 11), and the hypopleuria also average 8 µm in length (5–13 µm, n = 6). When measured from the side (n = 2), the epipleuria average 8 µm in length (7–10 µm), 9 µm in height (7–11), and 51 µm2 in area (38–64); the hypopleuria average 9 µm in length (6–12), 8 µm in height (5–11), and 58 µm2 in area (27–89). The width of the cephalion and the lengths of the pleuria viewed from above or below vary with the position of the focal plane along the z-axis. Tufts of at least four sensory cilia (see Fig. 1) arise from between the cephalion and each epipleurion, and from between each epipleurion and its associated hypopleurion. Each tuft includes approximately equal numbers of cilia in two size classes: short, averaging 5 µm (4–7), and long, averaging 13 µm (11–15). In a living animal, the long cilia arising between the cephalion and each epipleurion are typically carried extended in a sagittal plane and directed forward at an angle of 5–65° from the animal's extended midline, and those arising between each epipleurion and hypopleurion are typically carried extended slightly forward in the same plane and at an angle of 60–90° from the animal's extended midline.

  • II. Hypostomion: The hypostomion, without stain, appears as a narrow, transverse structure immediately posterior to the mouth. Stained with 2% aceto-orcein (Weiss 2001), the hypostomion is seen to consist of an anterior transverse element, with a longitudinal element extending posteriorly from each end of the transverse element (Fig. 5). In some cases evidence of the longitudinal elements is visible without staining, but the elements are clear only when properly stained (obscured if over-stained). The transverse element is fusiform, straight, and measures about 1.1 × 3.9 µm. The anterior end of each longitudinal element touches a lateral end of the transverse element; each lateral element is fusiform and slightly curved (describing an arc of a circle with its center lateral to the element and a radius of 2–5 µm), and measures about 0.7 × 2.7 µm.

  • III. Dorsal Scales: Dorsal scales (see Figs. 1 and 2) average 13 longitudinal columns on the head (9–17, n = 18), and 11 longitudinal columns on the trunk (9–15, n–16). Dorsal plus ventrolateral trunk scales average 18 longitudinal columns (15–24, n = 18). The number of scales per middorsal longitudinal column, counting posteriorly to the furcal notch, averages 37 µm (34–42, n = 18). Dorsal scale width generally increases from 3–4 µm anteriorly to 4–5 µm posteriorly. Dorsal scale width also increases from 2–3 µm ventrolaterally to 4–5 µm dorsally. Lateral scale length generally increases from 1–3 µm anteriorly to 1–5 µm posteriorly. Measurement of middorsal scale lengths with the scales in place is difficult because the scales overlap and their posterior margins tend to be obscured. However, one image allowed some measurements, which showed that middorsal, midtrunk scales averaged 5.4 µm long (5.0–5.8, n = 6 scales) and 5.0 µm wide (4.8–5.2, n = 6 scales). Dorsal scales are wider than long on the head, but longer than wide on the posterior trunk. The dorsal scales posterior to the transverse row immediately anterior to the double-keeled scales (“posterior dorsal scales”) are arranged in a pattern that differs from the more anterior dorsal scales (Fig. 1) but which is consistent among all individuals in which the posterior dorsal scales could be studied. Whether that scale pattern is unique to this species remains to be seen.

  • IV. Spined Scales: On the trunk, immediately lateral to each ventral band of cilia, is a band of one to three, but usually two, narrow longitudinal columns of small scales that bear keels and spines (Figs. 3, 4). Each band appears to continue posteriorly onto the ventral surface of the base of the furcal branch, which bears two transverse rows of small, keeled and spined scales. In one specimen the scales appeared to be keeled with very short or no spines. The spined scales tend to be larger posteriorly with longer spines, are reduced to a single column on the anterior trunk, and do not extend into the neck constriction. The spined scales in the marginal column tend to be smaller and more rounded than those of the other column(s); the latter resemble smaller, narrower versions of the spineless ventrolateral scales.

  • V. Sensory Cilia: A pair of anterior sensory cilia are located at U28 (U24–U31, n = 9), and a pair of posterior sensory cilia are located on double-keeled scales at U80 (U75–U85, n = 18). The anterior sensory cilia average 10.2 µm in length (4.8–21.1, n = 13); the thicker proximal section averages 6.2 µm in length (5.4–7.6, n = 3). The posterior sensory cilia average 12.7 µm in length (8.2–22.0, n = 14); the thicker proximal section averages 8.0 µm in length (6.0–10.1, n = 2).

  • VI. Pharynx: Pharynx length averages 27 µm (22–33, n = 21). The maximum anterior pharynx width averages 11 µm (8–15, n = 21). The minimum mid-pharynx width averages 10 µm (6–13, n = 21). The maximum posterior pharynx width averages 13 µm (9–17, n = 21). The slight anterior widening and greater posterior widening of the pharynx are consistently present. When stained with 2% aceto-orcein, longitudinal bands are visible in both the posterior and anterior pharyngeal swellings; band length in one specimen averaged 4.1 µm (4.0–4.4) and width averaged 0.6 µm (0.4–0.7). These bands are sometimes faintly visible without staining.

  • VII. Ventral Plates and Scales: A single pair of posterior ventral plates (see Figs. 3 and 4) average 10 µm in length (8–12, n = 14) and 4 µm in width (3–6, n = 12). The plates bear keels and short spines. The plates almost always overlap medially, and the keels are offset so that the distance from keel to margin is greater on the lateral side than on the medial side of each plate. Anterior to the plates are keeled midventral scales which consistently extend anteriorly to the pharyngeal area, and in some specimens can be seen as far forward as just posterior to the hypostomion. The midventral scales are sometimes rounded anteriorly, but are always ellipsoidal on the mid- and posterior trunk. The more anterior midventral scales often lack the distinct keels visible in the more posterior scales. The number of scales in a midventral longitudinal column averages 25 (22–28, n= 5), and the number of columns averages 5 (3–7, n = 13).

  • VIII. Digestive Tract: The pharynx-intestine junction is located at U28 (U22–U35, n = 20). The ventral anus is located at U83 (U79–U86, n = 13). The outside diameter of the subterminal mouth averages 6 µm (3–14, n = 16), and the diameter of the mouth opening averages 4 µm (2–9, n = 16). The average number of folds around the mouth periphery is 21 (20–21, n = 15). A single pharyngeal tooth (Kisielewski 1991) projects from the mouth opening in most individuals.

  • IX. Ventral Cilia: A band of ventral motor cilia originates on each side in the area lateral to the anterior half of the posterior ventral plates, and extends anteriorly into the pharyngeal area, where the band divides into two fingers which extend anteriorly to U9 (U8–U10, n–5). The medial finger of each band arches mediad and merges with the opposite medial finger at the centerline (see Fig. 3). Cilia from the posterior ends of the cilia bands may extend posteriorly and give the appearance of a more posterior origin, but the cilia insertion points are located opposite the anterior half of the posterior ventral plates. In addition to the ventral bands of cilia, patches of cilia are located on either side of the mouth.

  • Fig. 1

    Drawing of dorsal aspect of Lepidodermella weissi holotype. Scale bar = 12 µm.

    img-z3-1_116.jpg

    Fig. 2

    Photomicrograph of dorsal aspect of Lepidodermella weissi holotype showing dorsal scalation typical of the genus Lepidodermella.

    img-z3-6_116.jpg

    Fig. 3

    Drawing of ventral aspect of Lepidodermella weissi holotype. Scale bar = 12 µm. The mouth is the round feature at the anterior end; a pharyngeal “tooth” is visible within the mouth. The cephalion is visible just anterior to the mouth. Epipleuria are lateral to the cephalion. The hypopleuria are the largest plates visible on the head. The hypostomion is a narrow, transverse element in contact with the posterior edge of the mouth. Patches of motor cilia (denoted as dots) are visible on either side of the mouth (longer sensory cilia are not shown but can be seen in Fig. 1). The motor cilia bands divide into two “fingers” at their anterior ends; the medial “fingers” merge medially; the lateral fingers end opposite the hypopleura. Midventral, keeled scales occupy the interciliary field, with keels posteriorly and no or small keels anteriorly. Large keeled terminal plates overlap at the posterior end. One or more narrow columns of keeled, spined scales occur lateral to the motor cilia, and extend from the furcal base to about halfway to the head.

    img-z4-1_116.jpg

    Fig. 4

    Photomicrograph (DIC) of posterior ventral aspect of Lepidodermella weissi holotype: (a) ventrolateral trunk scales, (b) spined, keeled scales medial to ventrolateral trunk scales, (c) keeled midventral scales, and (d) a pair of large, posterioventral plates. Note motor cilia insertion points on the left (specimen's right) side between the spined scales and the keeled, midventral scales.

    img-z5-1_116.jpg

    Table 1

    Morphometrics of Lepidodermella weissi. Measurements in micrometers.

    img-z6-2_116.gif

    Fig. 5

    Photomicrograph (DIC) of ventral aspect of Lepidodermella weissi paratype showing the hypostomion with an anterior transverse element and a pair of lateral longitudinal elements. Specimen stained with 2% aceto-orcein. Without staining, the horizontal element generally appears narrower and the longitudinal elements generally are invisible or barely visible.

    img-z8-1_116.jpg

    Acknowledgments

    Thanks to Dr. Mitch J. Weiss and Dr. Malgorzata Kolicka for helpful comments. Thanks also to two anonymous reviewers whose suggestions improved the manuscript.

    Literature Cited

    1.

    Blake, C. H. 1933. Nomenclatural notes on Gastrotricha. Science, New Series 77(2008):606. Google Scholar

    2.

    Brunson, R. B. 1950. An introduction to the taxonomy of the Gastrotricha with a study of eighteen species from Michigan. Transactions of American Microscopical Society 69(4):325–352. Google Scholar

    3.

    Dujardin, F. 1841. Observations Zoologiques. Histoire Naturelle des Zoophytes, Infusoires. Librairie Encyclopedique de Roret, Paris, 684 p. Google Scholar

    4.

    Garraffoni, A. R. S., T. Q. Araújo, A. P. Lourenço, L. Guidi, & M. Balsamo. 2019. Integrative taxonomy of a new Redudasys species (Gastrotricha: Macrodasyida) sheds light on the invasion of fresh water habitats by macrodasyids. Scientific Reports 9(2067):1–15 Google Scholar

    5.

    Gosse, P. H. 1864. The natural history of the hairy-backed animalcules (Chaetonotidae). The Intellectual Observer 5:387–406. Google Scholar

    6.

    Hatch, M. H. 1939. Notes on two species of Gastrotricha from Washington. American Midland Naturalist 21:257–258. Google Scholar

    7.

    d'Hondt, J. L. 1971. Note sur quelques Gastrotriches Chaetonotidae. Bulletin de la Société Zoologique de France 96:215–235. Google Scholar

    8.

    Hummon, W. D. 1974. Intertidal marine Gastrotricha from Columbia. Bulletin of Marine Science 24(2):396–408. Google Scholar

    9.

    ICZN. 1999. International Code of Zoological Nomenclature, 4th ed. The International Trust for Zoological Nomenclature, London, 306 pp.  https://www.iczn.org. (Last accessed 22 June 2021.) Google Scholar

    10.

    Kånneby, T. 2016. Phylum Gastrotricha. Pp. 115–130 in J. H. Thorp & D. C. Rogers, eds., Keys to Nearctic Fauna. Thorp and Covich's Freshwater Invertebrates – Volume II, Fourth Edition. Elsevier Inc., xxi + 740 pp. Google Scholar

    11.

    Kånneby, T., & J. J. Kirk. 2017. A new species of Redudasys (Gastrotricha: Macrodasyida: Redudasyidae) from the United States. Proceedings of the Biological Society of Washington 130:128–139. Google Scholar

    12.

    Kånneby, T., & M. J. Weiss. 2016. U.S. freshwater Gastrotricha. 9 pp.  http://www.gastrotricha.unimore.it/USAfreshwater.pdf. (Last accessed 22 June 2021.) Google Scholar

    13.

    Kånneby, T., S. Atherton, & R. Hochberg. 2013 [2014]. Two new species of Musellifer (Gastrotricha: Chaetonotida) from Florida and Tobago and the systematic placement of the genus within Paucitubulatina. Marine Biology Research 10:983–995. Google Scholar

    14.

    Kånneby, T., M. A. Todaro, & U. Jondelius. 2011 [2012]. A phylogenetic approach to species delimitation in freshwater Gastrotricha from Sweden. Hydrobiologia 683(1):185–202. Google Scholar

    15.

    Kieneke, A., & A. Schmidt-Rhaesa. 2014. Gastrotricha. Pp 1–134 in A. Schmidt-Rhiaesa, ed., Handbook of Zoology. Vol. 3 Gastrotricha and Gnathifera. De Gruyter, Berlin, Boston. Google Scholar

    16.

    Kisielewski, J. 1991. Inland-water Gastrotricha from Brazil. Annales Zoologici 43(Suppl. 2):1–168. Google Scholar

    17.

    Kolicka, M., L. Kotwicki, & M. Dabert. 2018. Diversity of Gastrotricha on Spitsbergen (Svalbard Archipelago, Arctic) with a description of seven new species. Annales Zoologici (Warszawa) 68(4):609–739. Google Scholar

    18.

    Konsuloff, S. 1913. Notizen über die Gastrotrichen Bulgariens. Zoologischer Anzeiger 43:255–260. Google Scholar

    19.

    Metschnikoff, E. 1865. Über einige wenig bekannte Thierformen. Zeitschrift für wissenschaftliche Zoologie 15:450–463. Google Scholar

    20.

    Preobajenskaja, E. N. 1926. Zur Verbreitung der Gastrotrichen in den Gewässern der Umgebung von Kossino. Arbeiten der Biologischen Station zu Kossino (Moskau) 4:3–14. Google Scholar

    21.

    Remane, A. 1925. Organisation und systematische Stellung der aberranten Gastrotrichen. Verhandlungen der deutschen zoologischen Gesellschaft 30:121–128. Google Scholar

    22.

    Remane, A. 1935–1936. Gastrotricha and Kinorhyncha. In H. G. Bronns, ed., Klassen und Ordungen des Tierreichs, volume 4, section 2, book 1, part 2, numbers 1–2, p. 71, 194. Akademie Verlagsgesellschaft, Leipzig 1–385. Google Scholar

    23.

    Schrom, H. 1972. Nordadriatische Gastrotrichen. Helgoländer wissenschaftliche Meeresunters 23:286–351. Google Scholar

    24.

    Schwank, P. 1990. Gastrotricha. In: J. Schwoerbel, & P. Zwick, eds., Süsswasserfauna von Mitteleuropa. Volume 3, Part 1: xvii + 252. Google Scholar

    25.

    Sudzuki, M. 1971. Die das Kapillarwasser des Lückensystems bewohnenden Gastrotrichen Japans II. Bulletin of the Biogeographical Society of Japan 27(5):37–41. Google Scholar

    26.

    Suzuki, T. G., M. Maeda, & H. Furuya. 2013. Two new Japanese species of Gastrotricha (Chaetonotida, Chaetonotidae, Lepidodermella and Dichaeturidae, Dichaetura), with comments on the diversity of gastrotrichs in rice paddies. Zootaxa 3691(2):229–239. Google Scholar

    27.

    Todaro, M. A., J. A. Sibaja-Cordero, O. A. Segura-Bermúdez, G. Coto-Delgado, N. Goebel-Otárola, J. D. Barquero, M. Cullell-Delgado, & M. Dal Zotto. 2019. An introduction to the study of Gastrotricha, with a taxonomic key to families and genera of the group. Diversity 2019; 11(7):117. 25 p. Google Scholar

    28.

    Tretjakova, E. I. 1991. Lepidodermella spinifera –new species of gastrotrich (Gastrotricha) with traits of an intermediate genus. Byulleten' Moskovskogo obshchestva ispytatelei prirody Otdel biologicheskii 96(2):79–85. Google Scholar

    29.

    Voigt, M. 1901. Mitteilungen aus der Biologischen Station zu Plön, Holstein. Über einige bisiher unbekannte Susswasserorganismen. Zoologischer Anzeiger 24:191–195. Google Scholar

    30.

    Weiss, M. J. 2001. Widespread hermaphroditism in freshwater gastrotrichs. Invertebrate Zoology 120(4):308–341. Google Scholar

    31.

    WoRMS. 2019. Gastrotricha.  http://www.marinespecies.org/aphia.php?p=taxdetails& id=2078. (Last accessed 22 June 2021.) Google Scholar
    James J. Kirk "Lepidodermella weissi, new species (Gastrotricha: Chaetonotida: Chaetonotidae) from northwestern Oregon, U.S.A. (see erratum)," Proceedings of the Biological Society of Washington 134(1), 116-126, (18 August 2021). https://doi.org/10.2988/0006-324X-134.1.116
    Published: 18 August 2021
    KEYWORDS
    freshwater streams
    morphology
    Pacific Northwest
    speciation
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