Pinna carnea
| Pinna carnea | |
|---|---|
 | |
| Scientific classification | |
| Kingdom: | Animalia |
| Phylum: | Mollusca |
| Class: | Bivalvia |
| Order: | Pterioida |
| Family: | Pinnidae |
| Genus: | Pinna |
| Species: | P. carnea |
| Binomial name | |
| Pinna carnea Gmelin, 1791 [1] | |
| Synonyms[1] | |
| |
Pinna carnea, commonly called the amber pen shell, is a species of bivalve mollusc in the family Pinnidae.
Description
The amber pen shell has a pair of long, thin translucent valves held together by ligaments that run along the entire dorsal side of the bivalve. The bivalve is triangular with eight to 12 low ribs radiating from the pointed anterior end (or umbo) to the large posterior edge. The exterior of the shell is usually a dull orange amber-like color and may have fragile, scale-like spines that often become eroded over time. The anterior end is usually buried and attached by byssal threads, whereas its wider posterior gaping end extends above the sea bottom surface to facilitate filter-feeding. Algae (e.g. Lobophora variegata) and invertebrates such as sponges and encrusting corals tend to grow on the exposed part of the shell and camouflage it very well.
Distribution and habitat
The amber pen shell can be found in coastal western Atlantic waters, ranging from southern Florida across the Caribbean and the West Indies to Brazil.[2][3][4][5]
The amber pen shell is benthic and usually occurs in medium to coarse sand or mixed substrata (sand, gravel, rocks), in fine calcareous sandy mud of eelgrass (e.g. Zostera spp.), in sandy substrata of turtle grass (e.g. Thalassia spp.) and other mixed-species seagrass meadows at depths usually between 2 and 15 metres (6 ft 7 in and 49 ft 3 in).[6][7][8]
Filter-feeding
The amber pen shell burrows as it grows, but the wide posterior end of the shell always remains exposed so water from above the seafloor can be drawn through the inhalent chamber of the mantle cavity. Typical of bivalves, water is drawn over gills or ctenidium by the beating of cilia where oxygen from the water is absorbed. Suspended food and other water-borne nutrients also become trapped in mucus, which is then transported to the mouth, digested and expelled as feces. Unique gutter-like waste canals in the viscera of the inhalent chamber also help to keep gills and other organs clear from silt and other unwanted water-borne particules by expelling these as pseudofeces.[6]
Growth and predation
The amber pen shell may reach 30 cm (12 in) in length [6] with shell growth being extremely rapid after settlement (up to 2.2 mm (0.087 in) in length/day) and growth slowing down as shells get large and attain a refuge in size (at around 15 cm (5.9 in)).[7] The exposed valves of amber penshells are subject to frequent damage as they often show breaks and scars. While its half-buried position facilitates filtering water from above silty bottoms, it also increases exposure to predators. Octopuses are likely important predators of amber pen shells.[9]
Reproduction and settlement
The amber pen shell is a hermaphrodite, the gonads producing both sperm and ova. The larvae are planktonic and drift with the currents. The shells of the planktonic larvae are transparent, pale golden or amber in color, and also triangular. Larvae likely settle anywhere they can attach byssal threads.[7] The larval shells are quickly eroded after settlement and byssal attachment, with few adult shells ever found with remains of their larval shell stage.[10] Amber pen shells are sessile and remain in the same spot for the rest of their lives, although dislodged individuals can re-establish themselves.[6]
Symbiosis
The amber pen shell may host a number of symbionts in its mantle cavity. Shrimp Pontonia mexicana, cardinalfish Astrapogon stellatus, pea crabs (Pinnotheridae) and sea anemones (Actiniaria) have all been found sheltered inside its shell.[11]
References
- 1 2 WoRMS (2010). "Pinna carnea Gmelin, 1791". World Register of Marine Species. Retrieved 2012-09-11.
- ↑ Abbott, R.T. & Morris, P.A. A Field Guide to Shells: Atlantic and Gulf Coasts and the West Indies. New York: Houghton Mifflin, 1995. 23.
- ↑ Lodeiros, Cesar., Marín, Baumar. y Prieto, Antulio 1999: Catálogo de moluscos marinos de las costas nororientales de Venezuela: Clase Bivalvia. Asociación de Profesores de la Universidad de Oriente. Cumaná - Venezuela. Pp:25.
- ↑ Macsotay, O. & R. Campos. 2001. Moluscos representativos de la plataforma de Margarita, Venezuela. Editora Rivolta. Valencia, Venezuela, 279 pp. ISBN 980-328-808-3
- ↑ Turner, R. D. and J. Rosewater (1958). "The family Pinnidae in the western Atlantic". Johnsonia 3: 285–327.
- 1 2 3 4 Yonge, C. M. (1953). "Form and Habit in Pinna carnea Gmelin". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 237 (648): 335–374. doi:10.1098/rstb.1953.0006. JSTOR 92484.
- 1 2 3 Aucoin, S. and Himmelman, J. H. (2011). "Factors determining the abundance, distribution and population size-structure of the penshell Pinna carnea". Journal of the Marine Biological Association of the United Kingdom 91: 593–606. doi:10.1017/S0025315410001360.
- ↑ Urban H. J. (2001). "Reproductive strategies in tropical bivalves (Pteria colymbus, Pinctada imbricata and Pinna carnea): temporal coupling of gonad production and spat abundance related to environmental variability". Journal of Shellfish Research 20: 1127–1134.
- ↑ Anderson, R. C., Wood, J. B., and J. A. Mather (2008). "Octopus vulgaris in the Caribbean is a specializing generalist.". Marine Ecology Progress Series 371: 191–201. doi:10.3354/meps07649.
- ↑ J.A Allen (2011). "On the functional morphology of Pinna and Atrina larvae (Bivalvia: Pinnidae) from the Atlantic.". Journal of the Marine Biological Association of the United Kingdom 91: 823–829. doi:10.1017/s0025315410001694.
- ↑ Aucoin, S. and Himmelman, J. H. (2010). "A first report on the shrimp Pontonia sp. and other potential symbionts in the mantle cavity of the penshell Pinna carnea in the Dominican Republic". Symbiosis 50: 135–141. doi:10.1007/s13199-010-0050-x.