Botrylloides crystallinus, Bay-Nouailhat & Bay-Nouailhat & Gasparini & Brunetti, 2020

Bay-Nouailhat, Anne, Bay-Nouailhat, Wilfried, Gasparini, Fabio & Brunetti, Riccardo, 2020, Botrylloides crystallinus n. sp., a new Botryllinae Adams & Adams, 1858 (Ascidiacea) from Mediterranean Sea, Zoosystema 42 (9), pp. 131-138 : 132-137

publication ID	https://doi.org/ 10.5252/zoosystema2020v42a9
publication LSID	urn:lsid:zoobank.org:pub:9C563B0B-3756-422D-80CD-C75A113626E6
DOI	https://doi.org/10.5281/zenodo.3811002
persistent identifier	https://treatment.plazi.org/id/0B70F962-A46C-FFC7-FC38-FE74FEA56707
treatment provided by	Felipe
scientific name	Botrylloides crystallinus
status	sp. nov.

Treatment

Botrylloides crystallinus View in CoL n. sp.

( Figs 2-5 View FIG View FIG View FIG View FIG )

urn:lsid:zoobank.org:act:4EC1BFD5-51F8-4BC1-BC1E-7B36B56E1E4F

TYPE LOCALITY. — France, Carro , North Tyrrhenyan See.

TYPE MATERIAL. — Syntypes. France • 4 colonies (Bc1, Bc2, Bc3 and BcA); Carro, North Tyrrhenyan See; 43°19’42”N, 5°2’42”E; 9.V.2018; depth 5 -11 m; sea water temperature 16°C; MNHN- IT-2018-3 , MNHN-IT-2018-4 , MNHN-IT-2018 -5, MNHN- IT-2018-6 GoogleMaps . [Part of the syntype named BcA (MNHN-IT-2018-6) was not anaesthetised and directly fixed in ethanol instead of formalin and sent to Prof. Carmela Gissi at the University of Bari who is working on the phylogeny of Botryllinae ].

DISTRIBUTION. — Mediterranean French coasts ( Fig. 1A View FIG ), from the east of the Rhone delta up to the Italian coasts.

ETYMOLOGY. — Crystalline, name based on the transparent aspect of the colonies, from Latin crystallus.

DIAGNOSIS. — Globular colonies with a thick tunic. Zooids with spoon-shaped oral tentacles ( Fig. 3G View FIG ). Internal longitudinal branchial vessels extending anteriorly up to the pre-pharyngeal ring and getting in touch with it ( Fig. 3A, B, H, I View FIG ); stomach with nine folds and with a triangular space between a tiny typhlosole and the last fold ( Fig. 4D View FIG ); pyloric caecum long about half of the stomach length; rotation of the intestine in the second curve of intestinal loop ( Fig. 4A View FIG ).

DESCRIPTION

Colonies

Globular, usually up to 3 cm in diameter, or massive with several rounded lobes and reaching 7-8 cm thick. Adhering to solid substrata by an attaching surface without marginal expanded ampullae. Zooids, arranged in leachii - type systems ( Brunetti 2009), and perpendicularly ordered at the surface of the colony with their buds ( Fig. 2C View FIG ) that lie, immerged in the tunic, below the filtering zooid level (see below in “Zooids ” subsection). Tunic always very thick, up to several times the height of the filtering zooids, and crossed by a network of very thin colonial blood vessels connecting zooids and buds. Tunic soft and sticky, making the extraction of zooids and buds difficult. Colonial vessels ending with very small spherical ampullae. Larger ampullae present only at colony surface. Tunic crystalline, transparent and white to diaphanous pale yellow; thin white lines highlighting the tunic from the base of oral siphon to the rim of dorsal lip and atrial aperture, drawing on the surface of the colony a thin branched pattern of lines running through the zooids up to the rim of the common cloacal opening ( Fig. 2A View FIG ). White longitudinal lines also present in branchial sac: two large ones emphasizing the endostyle and the dorsal lamina, and six thin ones highlighting the internal longitudinal vessels. White pigment present in all these structures. In fixed animals, orange pigmentation present in cell islands close to the endostyle (see below), and around stomach and the first curve of intestinal loop ( Fig. 2B View FIG ).

Zooids

Up to 3-4 mm long. Body wall with a faintly visible network of very fine muscles, making circular bands only at siphon apertures. Size, distribution and number of the tentacles strongly variable in zooids of the same colony ( Fig. 3 View FIG B-E). In general, tentacles not very long; longest tentacles spoon-shaped when observed at high magnification, with the concavity toward the outside ( Fig. 3G View FIG ). Contrary to some other Botryllinae species (e.g. B. schlosseri , see Brunetti et al. 2017), vascular lacunae at tentacle bases without masses of haematic cells. Branchial sac with usually 12 rows of stigmata, the second one dorsally incomplete ( Fig. 3A View FIG ) and the last one (often difficult to see) with small stigmata. Branchial sac cylindrical ( Fig. 2A View FIG ), with about 18 stigmata in the first half row and about 14 in the 11th half row. Ventral “cell islands” (as defined by Manni et al. 2014) present on both sides of the endostyle, at the level of the rows of stigmata ( Figs 2B View FIG ; 3A View FIG ). Each internal longitudinal vessel rising apically to form a lamina; its diameter just a little larger than the diameter of interstigmatic vessels. Internal longitudinal vessels developing anteriorly to the first stigmata row, reaching and touching, but not fusing with, the pre-pharyngeal ring ( Fig. 3A, B View FIG ). Therefore, each branchial sector of the first stigmata row is protruding centripetally in the body between the two delimiting vessels, and the row appears wavy, a feature visible both in living and fixed specimens ( Fig. 3H, I View FIG ). Dorsal and ventral sectors equal in width and wider than lateral sectors. Branchial formula at about half of pharynx length usually DL 5.4. 4.5 E. Few, thin muscle fibres along the transversal branchial vessels. Atrial opening exposing 6-7 rows of branchial stigmata ( Figs 2B View FIG ; 3A View FIG ), and with a dorsal languet more or less developed according to the position of the zooid in the system.

Stomach arranged almost completely posteriorly to branchial sac; axis of well-relaxed zooid inclined at an angle of about 135° compared to anterior-posterior axis of the zooid ( Figs 2B View FIG ; 3A View FIG ). Almost cylindrical in shape with cardiac end slightly larger than pyloric end; with 9 slightly spiralized folds ( Fig. 4 View FIG D- F); a broad smooth triangular space present between the typhlosole and the last fold ( Fig. 4D View FIG ) (note that gastric folds, observed from the cardiac end, are numbered clockwise from the typhlosole). A pyloric caecum rising from posterior part of a tiny typhlosole; about half as long as stomach length (see Fig. 4D, F View FIG ), slightly tilted back and with a slightly swollen tip. Intestinal loop moderately curved. Rectus running along the dorsal edge of the branchial sac; the two structures connected through two trabeculae, at level of the transversal vessel between stigmata rows 9 and 10 ( Fig. 3F View FIG ). A smooth edge anus opening at stigmata row 8: three rows of stigmata anteriorly to oesophageal opening, located at the level of stigmata last row ( Fig. 3A, F View FIG ). Anal opening not lobed, ( Fig. 4A, B View FIG ) but sometimes looking outward ( Fig. 4C View FIG ). Intestine with two

grooves along its ventral and dorsal sides, the first the most evident. Two grooves also present along the two sides of the oesophagus. Second curve of intestinal loop accompanied by a rotation of intestine ( Fig. 4A View FIG ), as in Botrylloides israeliensis Brunetti, 2009 : as a consequence, in gut loop terminal tract, dorsal side of intestine distanced from the dorsal edge of branchial sac; ventral side of intestine by contrast close to the branchial sac dorsal edge, and connected to it by two trabeculae, as described above. Buds connected through blood vessels to parental zooids, not leaning but outdistanced from them ( Fig. 2C View FIG ); this disposition probably takes place during the change of generation when the zooids regress and are substituted by first order buds.

Gonads

No gonads observed in zooids, but oocytes present posteriorly and closed to testis primordia in first order buds of same colonies.

ECOLOGY

The species, locally common along the French Mediterranean coasts ( Fig. 1A View FIG ), lives in shaded areas fixed on vertical side of rocks and overhangs, from 5 to more than 30 meters deep. All samples were collected the 9 May 2018 (water temperature 16°C); many of them were in full activity with filtering zooids but others presented some zooids in regression ( Fig. 5A View FIG ). In spring when temperature rises to summer values ( Fig. 1B View FIG ), the number of regressing zooids increased, the regression moved from the base of the colony to its top ( Fig. 5B, C View FIG ) until all zooids are regressed ( Fig. 5D View FIG ). The regression concerns also the buds and the colony is reduced to a collection of tiny round bodies ( Fig. 5E View FIG ); during the following July (mean water temperature 21°C) almost all colonies (not collected) appear as gelatinous masses with only tiny whitish ampullae at their surface ( Fig. 5F View FIG ). Finally, during scuba diving of August 10 and 17, after a period of high temperature with values up to 28°C, no colonies were detected.

Our observations, although not covering a full annual period, suggest that the species presents a seasonal cycle with a preference for the lower temperature of winter. During the summer, when water temperature is constantly above 20°C ( Fig. 1B View FIG ), probably there is a high mortality that would explain the ostensible absence of the species.

REMARKS

Beside its phenotypic appearance, the species is characterised by the anterior terminal part of the internal longitudinal branchial vessels and the undulating surface of branchial wall at the level of the first row of stigmata. This characteristic was never reported until now in Botryllidae species, but a similar condition seems to be present in some species of the genus Symplegma Herdman, 1886 ( Styelidae , Polyzoinae) although it was not quoted among its generic characters ( Monniot & Monniot 1972). So in S. reptans (Oka, 1927) Kott (1985: 259 , fig. 127) quotes “[…]internal longitudinal vessels extend the whole length of the branchial sac.” and in the figure 127 these vessels extend an unperforated space coming up to the prepharyngeal ring; and in Monniot (2018) the photos in fig. 10 regarding S. brakenhielmi (Michaelsen, 1904) clearly show the vessels going over the first stigmata row and ending in an unperforated space anterior to it, close to the pre-pharyngeal ring.

Also, the folding of the intestinal loop is an unusual character mentioned only in Botrylloides israeliensis Brunetti (2009) , from which however B. crystallinus n. sp. differs in many other characters such as the shape of the stomach the number of stigmata rows, and the incompleteness of the second row.

Among the European species ( Brunetti & Mastrototaro 2017) only B. leachii , B. giganteus (Pérès, 1949) and B. diegensis Ritter & Forsyth, 1917 present some resemblance with the here described species, mainly in stomach shape with a smooth rhomboid area between the typhlosole and the last fold. Only B. leachii has the same number of stomach folds, but its stomach has a more campanulate shape and overall a clear swelling of the cardiac ends of folds and a pyloric caecum shorter than half of the stomach length. Moreover the B. leachii has smaller zooids. Finally, in B. leachii the tunic is strongly thinner than B. crystallinus n. sp. A comparison among the main morphological traits of these species are reported in Table 1 View TABLE .

The seasonal cycle of B. crystallinus n. sp., with a regression stage during summer, recalls the seasonal cycle described in Botrylloides leachii ( Brunetti 1976) in the lagoon of Venice. Total or partial regression phase was reported for many colonial ascidians ( Millar 1971); this is usually named aestivation or hibernation depending on whether it takes place during winter or summer, which may suggest that the cause of the phenomenon is the change in temperature. When the regression concerns only a particular organ of the zooid it may be interpreted as a renewal of organs damaged by an intense metabolic activity ( Turon 1992). In botryllids an aestivation with a total regression, was first described by Bancroft (1903) on colonies of Botrylloides gascoi Della Valle, 1877 (presently junior synonym of B. leachii ) which at the end of June (in Naples) completely degenerated zooids and buds living only the test vascular system. The same phenomenon was described for B. leachii ( Brunetti 1976) in the lagoon of Venice where the difference from winter and summer temperature is stronger ( Brunetti & Canzonier 1973): when sea water temperature drops below 10°C the zooids and their buds undergo a general regression and the colonies, devoid of filtering zooids, appear as a carpet of vascular ampullae mainly crowded of macrophages. In spring, with temperature increase, some zooids originate by vascular budding ( Burighel et al. 1976) giving rise to new systems. At present material do not allow to know if a similar process happens also in the here studied species, that is if the observed regression of zooids and their buds is followed by the development of new buds which rebuild the colony.