Crepidula plana, SAY 1822

Strong, Ellen E., 2003, Refining molluscan characters: morphology, character coding and a phylogeny of the Caenogastropoda, Zoological Journal of the Linnean Society 137 (4), pp. 447-554 : 464-466

publication ID

https://doi.org/ 10.1046/j.1096-3642.2003.00058.x

persistent identifier

https://treatment.plazi.org/id/03B6B923-EE27-FFF1-8C88-66C33A1B6B0D

treatment provided by

Carolina

scientific name

Crepidula plana
status

 

CREPIDULA PLANA SAY 1822 View in CoL

Material Examined

Cape Henlopen, Virginia ( USNM 890937).

External anatomy and mantle cavity

Foot narrow anteriorly, broadly rounded posteriorly. Duct of pedal gland opening to shallow propodial groove. Head flattened dorso-ventrally. Mantle cavity extending down left side of visceral mass. Hypobranchial gland large and well developed. Mantle edge folded anteriorly to form food pouch. Gill filaments long and slender with skeletal rods. Ctenidial axis glandular, forming endostyle.

Reproductive system

Protandrous hermaphrodites. In male phase, testis lying alongside tubules of digestive gland, extending down sides of visceral mass. Testis opening anteriorly to broad and tightly coiled seminal vesicle lying just behind base of mantle cavity. Short vas deferens emerging from seminal vesicle, opening to seminal groove ( Fig. 3C View Figure 3 , sg) at base of mantle cavity. Prostate (pr) small, comprising small region of glandular cells at base of mantle cavity, extending short distance along seminal groove. Prostatic tissue forming two distinct concentric layers of basophilic cells. Seminal groove extending down neck and along ventral surface of elongate, narrow penis (pe) with curved terminal papilla.

Ovary dorsally overlying digestive gland. Broad renal oviduct opening to approximately four or five small seminal receptacles ( Fig. 2B View Figure 2 , rcs) with narrow ducts. Gonopericardial canal absent. Oviduct opening to short, compact pallial oviduct comprising closed albumen (ag) and capsule (cg) glands. Long vagina (v) emerging from capsule gland, terminating in narrow, elongate female opening (fo).

Alimentary system

Foregut. Paired jaw weakly developed at anterior ends of dorsal folds; jaw composed of rods with laterally overlapping homogeneous layer. Subradular membrane incompletely covering odontophore. Small subradular organ present ( Fig. 5E View Figure 5 , sro) in shallow sublingual cavity. Long, tubular salivary glands ( Fig. 6E View Figure 6 , sgl) by-passing circum-oesophageal nerve ring. Short mid-ventral fold ( Fig. 9F View Figure 9 , vf) and flanking ventro-lateral folds (vlf) present in anterior oesophagus. Mid-oesophagus uniformly folded; septate oesophageal gland absent ( Fig. 11D View Figure 11 , me).

Midgut. Midgut occupying apex of visceral mass. Oesophagus opening mid-ventrally ( Fig. 14B, e View Figure 14 ), near distal end of ventro-lateral gastric shield (gs). Sorting area (sa) well developed anterior to oesophageal aperture. Ciliary currents flowing toward intestinal groove within sorting area. Ciliated fold (cf) extending posteriorly from proximal end of minor typhlosole, passing to left of oesophageal aperture. Glandular pad (gp) extending posteriorly from gastric shield, paralleling ciliated fold to posterior end of midgut. Folds terminating within small caecum (c) on right behind gastric shield. Paired digestive gland ducts (dgd) opening at proximal end of major typhlosole (t1). Style sac region characterized by horizontally folded epithelium bearing differentiated cilia. Raised tract of cilia (ctr) present on both typhlosoles (t1, t2). Crystalline style present. Ciliary currents flowing clockwise within style sac region when viewed from behind.

Hindgut. Intestine exiting style sac and extending from left to right, looping broadly and slightly posteriorly around kidney, then turning anteriorly.

Reno-pericardial system

Kidney anteriorly surrounding pericardium, slightly overhanging pallial cavity. Afferent renal vessel entering kidney floor anteriorly, just in front of renopericardial duct, supplying excretory tissue along floor. Excretory tissue ramifying dorsally within roof and along walls. Nephridial gland present.

Nervous system and sensory structures

Nervous system epiathroid, right zygoneurous, left dialyneurous ( Fig. 24C View Figure 24 ). Supra-oesophageal (sp) and sub-oesophageal (sb) connectives extremely short. Circum-oesophageal nerve ring ( Fig. 6E View Figure 6 , nr) lying well posterior to buccal mass. Tentacular nerve (tn) splitting upon entering tentacle into two nerves of equal size. Visceral loop short bearing two small visceral ganglia (vg) straddling oesophagus. Statocysts with statoliths ( Fig. 24C View Figure 24 , sc) present on dorso-lateral surfaces of pedal ganglia. Osphradium unipectinate ( Fig. 6E View Figure 6 , os).

Remarks

In a series of papers on development of the sex organs, emphasizing the transformations that occur during sex change, Gould (1917, 1949, 1952) provided the essential features of reproductive anatomy for Crepidula plana which are congruent with those provided above. This includes the presence of a tightly coiled seminal vesicle, seminal groove and penis behind the right cephalic tentacle in males and, in females, the presence of the gonopericardial canal, the presence of the seminal receptacle, and the absence of the bursa copulatrix. However, the detailed morphology of neither the seminal receptacles nor glandular pallial oviduct was described. In contrast to Gould (1917), the presence of a gonopericardial canal could not be confirmed in the present study.

Discussion

The mantle cavity and mechanism of ciliary suspension feeding in the Calyptraeidae has been well studied (e.g. Orton, 1912, 1913; Yonge, 1938; Werner, 1953). Calyptraeids possess a triangular mantle cavity extending over an elongate neck and along the left side of a flattened visceral mass; a large gill bearing skeletal rods is present, with an elaborate mucusproducing ‘endostyle’ along its axis ( Orton, 1912, 1913; Kleinstüber, 1913; Yonge, 1938; Graham, 1952). Members of the family are unique among ciliary feeders because they obtain food particles from a food groove on the right side of the neck, in addition to a food pouch that collects particles at the anterior edge of the mantle skirt via a modification of the rejection current of other caenogastropods ( Yonge, 1938).

Calyptraeids typically possess seminal receptacles at or near the junction of the renal and pallial oviducts; the number of receptacles and the nature of their connection to the oviduct can vary (single duct or one per receptacle). A gonopericardial canal is present only in females and generates during the transition between male and female phases ( Giese, 1915; Ishiki, 1939; Graham, 1952; Fretter & Graham, 1962; Yipp, 1983). The pallial oviduct of calyptraeids is characterized by the absence of a bursa copulatrix and a narrow vagina that can vary greatly in length ( Kleinstüber, 1913; Fretter & Graham, 1962; Yipp, 1983). The pallial vas deferens lacks prostatic development ( Graham, 1952; Yipp, 1983), but rudiments of female glands in the male phase may have a prostatic function ( Giese, 1915; Graham, 1952).

Midgut features are conservative among described calyptraeids, including the development and position of sorting areas, the extension of the minor typhlosole and parallel glandular pad across the midgut floor, the presence of a caecum, the position of the gastric shield, and the concavity of the major typhlosole ( Fretter & Graham, 1962; Yipp, 1980; pers. obs.). One variable feature includes the position and number of digestive gland ducts. Graham (1939) found four ducts within the midgut of Crepidula fornicata and Calyptraea chinensis ; two opening at the proximal end of the major typhlosole, and two opening within the caecum. Development of the major typhlosole terminal lappet also varies between species ( Fretter & Graham, 1962; pers. obs.). In addition, the ciliary tract on the minor typhlosole, present in Crepidula plana , is lacking in C. fornicata (pers. obs.).

Calyptraeid nervous systems have been described as right zygoneurous and left dialyneurous ( Graham, 1952). A notable exception is Crepidula fornicata , which has a connection between the left dialyneury and a nerve from the left visceral ganglion, in addition to a dialyneurous connection between nerves from the right visceral and the sub-oesophageal ganglia (Graham). Crepidula plana lacks secondary connections involving nerves from the visceral ganglia. Bouvier (1887) reported the presence of a left zygoneury in C. fornicata ?. This could not be confirmed by Graham.

USNM

Smithsonian Institution, National Museum of Natural History

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