Introduction
The Gulf of California is a hydrographically complex region. It possesses strong environmental gradients and latitudinally is associated with convergence in its central region, which results in highly diverse environments due to the mix of temperate, subtropical, and tropical species in a relatively small area (Riginos, 2005). With its high number of microhabitats, the region also has a high number of endemic marine species (Briggs, 1974, Brinton & Towsend, 1980; Brusca & Findley, 2005). For poorly known groups the possibility of finding new species increases, such in the case of gymnosomatous pteropods.
The Gymnosomata is one of two groups within Pteropoda (Jörger et al., 2010, Schrödl et al., 2011) that has adapted for pelagic life (Lalli & Gilmer, 1989): The Gymnosomata, which have no shells, and the Thecosomata, most of which have shells. The division between these two holoplanktonic groups of molluscs is justified by other anatomical characteristics as well (Pelseneer, 1887). The absence of a shell in gymnosomes results in most of the specimens contracting into indistinguishable forms after preservation and all taxonomic features are altered. Despite this problem, the Gymnosomata include about 47 valid species contained in four families (Gofas, 2018). Pneumodermatidae (Pelseneer, 1857) is the most specious with 18 species worldwide (5 Pneumoderma, 13 Pneumodermopsis) (Spoel et al., 1997, Bouchet & Gofas, 2018a, b). The distinctive characteristics of Pneumodermatidae are the presence of suckers on the ventral side of the protrustile on the anterior portion of the buccal cavity, a lateral gill on the right side of the body, a jaw and pigmented skin (Pelseneer, 1887). Only four species are registered in the Gulf of California, one belonging to the genus Pneumoderma (Cuvier, 1805). These are Pneumoderma pacificum Dall, 1871 and three belong to Pneumodermopsis Keferstein, 1862, i.e., Pneumodermopsis canephora Pruvot-Fol, 1924, Pneumodermopsis ciliata (Gegenbaur, 1855) and Pneumodermopsis macrochira Meisenheimer, 1905 (Angulo-Campillo et al., 2011).
Zooplankton tows in the Gulf of California were performed to obtain a collection of specimens of Gymnosomata with morphologic characteristics that did not belong to any species previously described. Two new species of gymnosomes collected from the central portion of the Gulf of California, Mexico, were described here based on radular characteristics.
Materials and methods
Ten specimens of Gymnosomata were obtained from the central region of the Gulf of California during an oceanographic survey in January 2007. The specimens were captured using oblique tows with Bongo nets of 505 μm mesh. Tows were made at a maximum depth of 200 m. The specimens were preserved in 95% ethanol and deposited at the Department of Invertebrate Zoology and Geology of the California Academy of Sciences, San Francisco (CASIZ). The external features were examined and drawn using a dissecting microscope with a camera lucida. All the organisms described here were identified as adult stages using as indicative the presence of a well-developed lateral gill as well as the presence of a developed gonad. Three specimens were dissected, two specimens for Pneumoderma cicimarensis sp. nov. and one for Pneumodermopsis tacoi sp. nov. The buccal mass was removed and dissolved in 10% sodium hydroxide until the radula was isolated from the surrounding tissue (Geiger et al., 2007); later, the radula was mounted for scanning electron micrographs (SEMs) produced on a Hitachi S-3000N scanning electron microscope at CIBNOR.
Results
Family Pneumodermatidae Pelseneer, 1857
Genus Pneumoderma Cuvier, 1805
Pneumoderma cicimarensis sp. nov. (Figs 1a-f)
Type Species: Pneumodermon pacificum Dall, 1871: 139; 37°8’ N 136°10’ W, Coll.: Dall, reg. no. 301.
Previous references: Pneumoderma sp. Angulo-Campillo et al., 2011.
Etymology: The specific name cicimarensis is taken from the acronym CICIMAR (Centro Interdisciplinario de Ciencias Marinas), which refers to the institution where the authors completed their Ph.D.
Type Material: Holotype: Central portion of the Gulf of California (27°49’22” N, 111°24’4” W), 4.3 mm body length, collected by Orso Angulo and Gerardo Aceves, 21 January 2007. (CASIZ 178438).
Paratypes: two specimens, 4.2 and 2.8 mm body length (CASIZ 178439), central portion of the Gulf of California (26°45’2” N, 110° 53’4” W), one specimen 3.1 mm body length, collected by Orso Angulo and Gerardo Aceves, 22 January 2007. (CASIZ 178440).
Additional material: two specimens 3.1 and 3.0 mm (dissected), collected on 22 January 2007 from near shore waters west of Santa Rosalía, Baja California Sur, Mexico (26°25’22” N, 110°32’12” W), by Orso Angulo and Francisco Dominguez.
Type locality: Central portion of the Gulf of California (27°49’22” N, 111°24’4” W), caught in tows made between 200 m depth and the sea surface.
Geographic distribution: Known only to inhabit in the Gulf of California.
Description: External morphology: Body color: translucent; head: cream colored. Visceral mass: dark. Body: cylindrical; rounded anteriorly when extended, and barrel shaped when contracted (Fig. 1a). Head differentiated from the body. Wings subquadrate, slightly notched at their inner posterior edge with one lobe on the median portion of the wing (Fig. 1b). Small chromatophores in the head. Two lateral arms with two suckers each on the mouth region. Lateral footlobes short, reaching 1/4 length of the median footlobe, which is long and pointed when extended, reaching one third the length of the trunk. The viscera can be seen through the body walls, reaching two-thirds the length of the trunk. A long lateral gill with a dorsal spot situated on the upper portion. The lateral gill extends up to two thirds the length of the body where it reaches the margin of the posterior gill, which is simple (without ornamentations) and fringed, well-marked regular undulations (Figs 1c-d). Radula (Figs 1e-f): The radula formula is 3.0.3 with nine rows (Fig. 1e). The radular teeth have a large, curved, and pointed central cusp. On each side of the central cusp there are 11 to 13 smooth, shorter denticles (Fig. 1f). Denticles are slightly curved inwards, with long ridges that extend to the base of the central cusp.
Remarks: The placement of Pneumoderma cicimarensis sp. nov. in the Pneumodermatidae is based on the presence of a lateral gill, differentiation of the cephalic region and presence of chromatophores, while the presence of a dorsal glandular spot is characteristic of the genus (Pelseneer 1857). The other four species are not found in the eastern Pacific and they do not have a wing lobe (Table 1). P. cicimarensis sp. nov. is unique within the genus with the presence of one lobe on each wing; this characteristic has not been described in any other member of the family or gymnosome. Another characteristic feature is the absence of chromatophores on the trunk. P. pacificum differs from P. cicimarensis sp. nov. in coloration; P. pacificum is purple, and chromatophores extend through the entire body. In addition, the form of the teeth and radula formulae is different; in P. cicimarensis sp. nov. the radula formula is 3.0.3 and teeth are hook-shaped with serrated edges that extend to the base of the central cusp, while in P. pacificum it is 4.0.4, and teeth are also hook-shaped, but slender with no serrations or edges (Spoel et al., 1997) (Table 1).
Species | Lt | Lam | RF | HH | Chr | Wl | Distribution |
---|---|---|---|---|---|---|---|
P. cicimarensis sp. nov | 45 | 2 | 3-0-3 | p | p | p | Gulf of California |
P. pacificum (Dall, 1871)* | 25 | 50 | 4-0-4 | ? | p | a | Cosmopolitan of warm waters |
P. violaceum d´Orbigny, 1834* | 7 | 40 | ? | ? | a | a | Warm waters Atlantic and Mediterranean |
P. degraaffiSpoel & Pafort-van Lersel, 1982 | 12 | 6-8 | 3-0-3 | 200 | p | a | N Atlantic |
P. heronensisNewman & Spoel, 1989 | 11 | 12 | 6-0-6 | 100 | p | a | Australia |
P. mediterraneum Van Beden, 1838* | 20 | 7 | 7-0-7 | 40 | p | a | Atlantic, Mediterranean, Indo-Pacific |
*Data obtained from Spoel et al. (1997), number of valid species based from Bouchet and Gofas (2018a).
Genus Pneumodermopsis Keferstein, 1862
Pneumodermopsis tacoi sp. nov. (Figs 2a-d)
Type species: Pneumodermon ciliatum Gegenbaur, 1855: 74. Type locality: not located.
Previous references: Pneumodermopsis sp. Angulo-Campillo et al., 2011, Moreno-Alcántara et al., 2014.
Etymology: The specific name tacoi is given in honor to Enrique González, teacher and mentor of both authors, who is known among his friends as Taco.
Type Material: Holotype: northwest of Guaymas, Sonora (27°29’42” N, 111°24’38” W), 3.1 mm body length, collected by Orso Angulo and Francisco Domínguez. January 21, 2007. (CASIZ 178441).
Paratypes: two specimens, 2.9 mm and 2.6 mm body length (CASIZ 178442), same locality as the holotype.
Additional material: one specimen 2.5 mm body length (dissected), same locality.
Type locality: Northwest of Guaymas, Sonora (27°29’42” N, 111°24’38” W), caught in tows made between 200 m deep and the sea surface.
Geographic distribution: Know in the Gulf of California and Gulf of Tehuantepec
Description: External morphology: Body color: cream, semi-translucent. Visceral mass: brown. Body cylindrical and barrel shaped (Fig. 2a). Head differentiated from the body. Small wings. Small chromatophores in the head. Two lateral suckers arms. Lateral footlobes: short, reaching 1/4 the length of the median footlobe, which is long and thick. Viscera visible through the body wall. A well-developed lateral gill present with a dorsal spot situated on the upper portion. Posterior gill: simple and clearly fringed (Fig. 2b). Radula (Figs 2c-d): The radula formula 3.1.3 (in 13 rows). Lateral teeth: long, slender, and hook-shaped (Fig. 2c). Median teeth: bicuspid (Fig. 2d); base: simple with no ornamentations.
Remarks: The placement of Pneumodermopsis tacoi sp. nov. in the Pneumodermatidae is based on the presence of a lateral gill, differentiation of the cephalic region and presence of chromatophores. Due to preservation effects, it was impossible to determine the number of suckers on the lateral arms, thus the description is based on the radula formula. Presence of central teeth accommodates within the Pneumodermopsis. A previous report of Pneumodermopsis from the North Pacific includes P. ciliata and P. paucidens (Boas, 1886) (Spoel et al., 1997). In P. ciliata the number of lateral teeth varies from 5.1.5 to 6.1.6, with 18 to 25 rows, and with tricuspid median teeth (Spoel & Pafort-Van Lersel, 1982). The teeth shape of P. paucidens is similar to that of P. tacoi sp. nov., both species have bicuspid median teeth without a central cusp. However, the radula of P. paucidens as illustrated in Spoel et al. (1997) compared with the radula of P. tacoi sp. nov. shows differences between them since the lateral teeth in P. tacoi sp nov. are larger and slender, and the bicuspid teeth are larger. In addition, P. paucidens has only a median arm with a large sucker, whereas P. tacoi sp. nov. has two lateral arms with small suckers. Remaining species of this genus have a higher number of lateral teeth, except P. polycotyla (Boas, 1886) and P. spoeli Newman & Greenwood, 1988, which have 2 lateral teeth. However, P. spoeli has 24 lateral arms suckers and P. polycotyla is distributed only in the Atlantic and Mediterranean (Table 2).
Species | Lt | Lg | Pg | Lam | RF | HH | Distribution |
---|---|---|---|---|---|---|---|
P. tacoi sp. nov. | 3 | p | p | 2 | 3-1-3 | - | Gulf of California, Gulf of Tehuantepec |
P. brachialis Minichev, 1976* | 15 | a | p | 12 | 4-1-4 | 40 | Antarctic |
P. canephora Pruvot-Fol, 1924* | 12 | p | a | 1 | 5-1-5 | 30-60 | Atlantic, Mediterranean, Indo-Pacific, |
P. ciliata (Gegenbaur, 1855)* | 15 | p | a | 7-8 | 7-1-7 | 30-40 | N-Atlantic, Mediterranean, N-Pacific |
P. macrochira (Meisenheimer, 1905)* | 8 | p | p | 55 | 6-1-6 | 16-20 | N-Atlantic, N-Pacific and Tasman Sea |
P. macrocotyla Zhang, 1964* | 8 | p | a | 4 | 7-17 | 40 | China Sea and Yellow Sea |
P. michaelsarsi Bonnevie, 1913* | 11 | p | p | 8 | 6-1-6 | 20-50 | N-Antarctic |
P. minutaPelseneer, 1887 | 3 | p | a | 8 | ? | ? | Tropical Pacific |
P. paucidens (Boas, 1886)* | 5 | p | p | 10-12 | 2-3-1-2-3 | 5-6 | Indo & N-Pacific, Atlantic, Mediterranean |
P. polycotyla (Boas,1886)* | 5 | p | p | ? | 2-1-2 | 6 | Atlantic and Mediterranean |
P. pupula Pruvot-Fol, 1926* | 2 | a | a | 5 | 8-1-8 | 12 | Atlantic and Mediterranean |
P. simplex (Boas, 1886)* | 5 | p | a | - | 6-1-6 | 40-50 | South Atlantic |
P. teschi Spoel, 1973 | 9 | p | a | 12-20 | 3-7-1-3-7 | 10 | NE-Atlantic and Mediterranean |
P. spoeli Newman & Greenwood, 1988 | 27 | a | p | 24 | 2-1-2 | 6 | Great Barrier Reef, Australia |
* Data obtained from Spoel et al. (1997), number of valid species based from Bouchet and Gofas (2018b).