Scallop
Scallop | |
---|---|
Argopecten irradians, the Atlantic bay scallop | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Mollusca |
Class: | Bivalvia |
Order: | Pectinida |
Superfamily: | Pectinoidea |
Family: | Pectinidae Wilkes, 1810 |
Genera | |
See text | |
Synonyms | |
Pectenidae |
Scallop (
Scallops are a
Many species of scallops are highly prized as a food source, and some are farmed as aquaculture. The word "scallop" is also applied to the meat of these bivalves, the adductor muscle, that is sold as seafood. The brightly coloured, symmetric, fan-shaped shells of scallops with their radiating and often fluted ornamentation are valued by shell collectors, and have been used since ancient times as motifs in art, architecture, and design.
Owing to their widespread distribution, scallop shells are a common sight on beaches and are often brightly coloured, making them a popular object to collect among beachcombers and vacationers.[2] The shells also have a significant place in popular culture.
Distribution and habitat
Scallops inhabit all the oceans of the world, with the largest number of species living in the
Anatomy and physiology
Very little variation occurs in the internal arrangement of organs and systems within the scallop family, and what follows can be taken to apply to the anatomy of any given scallop species.[4]
Orientation
The shell of a scallop consists of two sides or
Valves
The model scallop shell consists of two similarly shaped valves with a straight hinge line along the top, devoid of teeth, and producing a pair of flat wings or "ears" (sometimes called "auricles", though this is also the term for two chambers in its heart) on either side of its midpoint, a feature which is unique to and apparent in all adult scallops.[7] These ears may be of similar size and shape, or the anterior ear may be somewhat larger (the posterior ear is never larger than the anterior one, an important feature for distinguishing which valve is which). As is the case in almost all bivalves, a series of lines and/or growth rings originates at the center of the hinge, at a spot called the "beak" surrounded by a generally raised area called the "umbo". These growth rings increase in size downwards until they reach the curved ventral edge of the shell. The shells of most scallops are streamlined to facilitate ease of movement during swimming at some point in their lifecycles, while also providing protection from predators. Scallops with ridged valves have the advantage of the architectural strength provided by these ridges called "ribs", although the ribs are somewhat costly in weight and mass. A unique feature of the scallop family is the presence, at some point during the animal's lifecycle, of a distinctive and taxonomically important shell feature, a comb-like structure called a ctenolium located on the anterior edge of the right valve next to the valve's byssal notch. Though many scallops lose this feature as they become free-swimming adults, all scallops have a ctenolium at some point during their lives, and no other bivalve has an analogous shell feature. The ctenolium is found in modern scallops only; both putative ancestors of modern scallops, the entoliids and the Aviculopectinidae, did not possess it.[8]
Muscular system
Like the true oysters (family
Adductor muscles
Scallops possess fast (striated) and slow (smooth) adductor muscles, which have different structures and contractile properties. These muscles lie closely apposed to one another but are divided by a connective tissue sheet. The striated adductor muscle contracts very quickly for swimming, whereas the smooth catch adductor muscle lacks striations, and contracts for long periods, keeping shells closed with little expenditure of energy.[9]
Digestive system
Scallops are
Nervous system
Like all bivalves, scallops lack actual brains. Instead, their nervous system is controlled by three paired ganglia located at various points throughout their anatomy, the cerebral or cerebropleural ganglia, the pedal ganglia, and the visceral or parietovisceral ganglia. All are yellowish. The visceral ganglia are by far the largest and most extensive of the three, and occur as an almost-fused mass near the center of the animal – proportionally, these are the largest and most intricate sets of ganglia of any modern bivalve. From this, radiate all of the nerves which connect the visceral ganglia to the circumpallial nerve ring which loops around the mantle and connects to all of the scallop's tentacles and eyes. This nerve ring is so well developed that, in some species, it may be legitimately considered an additional ganglion.[6]: p.46 The visceral ganglia are also the origin of the branchial nerves which control the scallop's gills. The cerebral ganglia are the next-largest set of ganglia and lie distinct from each other a significant distance dorsal to the visceral ganglia. They are attached to the visceral ganglia by long cerebral-visceral connectives, and to each other via a cerebral commissure that extends in an arch dorsally around the esophagus. The cerebral ganglia control the scallop's mouth via the palp nerves and connect to statocysts which help the animal sense its position in the surrounding environment. They are connected to the pedal ganglia by short cerebral-pedal connectives. The pedal ganglia, though not fused, are situated very close to each other near the midline. From the pedal ganglia, the scallop puts out pedal nerves which control the movement of, and sensation in, its small muscular foot.[6]: pp. 43–47
Vision
Scallops have a large number (up to 200) of small (about 1 mm) eyes arranged along the edge of their mantles. These eyes represent a particular innovation among molluscs, relying on a concave, parabolic mirror of guanine crystals to focus and retro-reflect light instead of a lens as found in many other eye types.[11] Additionally, their eyes possess a double-layered retina, the outer retina responding most strongly to light and the inner to abrupt darkness.[12] While these eyes are unable to resolve shapes with high fidelity, the combined sensitivity of both retinas to light entering the eye and light retro-reflected from the mirror grants scallops exceptional contrast definition, as well as the ability to detect changing patterns of light and motion.[13][14] Scallops primarily rely on their eyes as an 'early-warning' threat detection system, scanning around them for movement and shadows which could potentially indicate predators. Additionally, some scallops alter their swimming or feeding behaviour based on the turbidity or clarity of the water, by detecting the movement of particulate matter in the water column.[15]
Locomotion
Scallops are mostly free-living and active, unlike the vast majority of bivalves, which are mostly slow-moving and infaunal. All scallops are thought to start out with a byssus, which attaches them to some form of substrate such as eelgrass when they are very young. Most species lose the byssus as they grow larger. A very few species go on to cement themselves to a hard substrate (e.g. Chlamys distorta and Hinnites multirigosus).[16]
However, the majority of scallops are free-living and can swim with brief bursts of speed to escape predators (mostly starfish) by rapidly opening and closing their valves. Indeed, everything about their characteristic shell shape – its symmetry, narrowness, smooth and/ or grooved surface, small flexible hinge, powerful adductor muscle, and continuous and uniformly curved edge – facilitates such activity. They often do this in spurts of several seconds before closing the shell entirely and sinking back to the bottom of their environment. Scallops are able to move through the water column either forward/ventrally (termed swimming) by sucking water in through the space between their valves, an area called the gape, and ejecting it through small holes near the hinge line called exhalant apertures, or backward/dorsally (termed jumping) by ejecting the water out the same way it came in (i.e. ventrally). A jumping scallop usually lands on the sea floor between each contraction of its valves, whereas a swimming scallop stays in the water column for most or all of its contractions and travels a much greater distance (though seldom at a height of more than 1 m off the sea bed and seldom for a distance of greater than 5 m).[16] Both jumping and swimming movements are very energy-intensive, and most scallops cannot perform more than four or five in a row before becoming completely exhausted and requiring several hours of rest. Should a swimming scallop land on its left side, it is capable of flipping itself over to its right side via a similar shell-clapping movement called the righting reflex. So-called singing scallops are rumored to make an audible, soft popping sound as they flap their shells underwater (though whether or not this happens is open to some debate).[17] Other scallops can extend their foot from between their valves, and by contracting the muscles in their foot, they can burrow into sand.[18]
Mobility and behavior
Most species of the scallop family are free-living, active swimmers, propelling themselves through the water through the adductor muscles to open and close their shells. Swimming occurs through the clapping of valves for water intake. Closing the valves propels water with a strong force near the hinge via the velum, a curtain-like fold of the mantle that directs water expulsion around the hinge. Scallops swim in the direction of the valve opening unless the velum directs an abrupt change in course direction.[20][21]
Other species of scallops can be found on the ocean floor attached to objects by byssal threads. Byssal threads are strong, silky fibers extending from the muscular foot, used to attach to a firm support, such as a rock. Some can also be found on the ocean floor, moving with an extendable foot between their valves or burrowing themselves in the sand by extending and retracting their feet.[6] Scallops are highly sensitive to shadows, vibrations, water movement, and chemical stimuli.[22] All possess a series of 100 blue eyes, embedded on the edge of the mantle of their upper and lower valves that can distinguish between light and darkness. They serve as a vital defense mechanism for avoiding predators. Though rather weak, their series of eyes can detect surrounding movement and alert precaution in the presence of predators, most commonly sea stars, crabs, and snails.[6] Physiological fitness and exercise of scallops decrease with age due to the decline of cellular and especially mitochondrial function,[23] thus increasing the risk of capture and lowering rates of survival. Older individuals show lower mitochondrial volume density and aerobic capacity, as well as decreased anaerobic capacity construed from the amount of glycogen stored in muscle tissue.[23] Environmental factors, such as changes in oxidative stress parameters, can inhibit the growth and development of scallops.[24]
Seasonal changes in temperature and food availability have been shown to affect muscle metabolic capabilities. The properties of mitochondria from the phasic adductor muscle of Euvola ziczac varied significantly during their annual reproductive cycle. Summer scallops in May have lower maximal oxidative capacities and substrate oxidation than any other time in the year. This phenomenon is due to lower protein levels in adductor muscles.[25]
Lifecycle and growth
The scallop family is unusual in that some members of the family are
Many scallops are hermaphrodites (having female and male organs simultaneously), altering their sex throughout their lives, while others exist as dioecious species, having a definite sex. In this case, males are distinguished by roe-containing white testes and females with roe-containing orange ovaries. At the age of two, they usually become sexually active, but do not contribute significantly to egg production until four. The reproduction process occurs externally through spawning, in which eggs and sperm are released into the water. Spawning typically occurs in late summer and early autumn; spring spawning may also take place in the Mid-Atlantic Bight.[27] The females of scallops are highly fecund, capable of producing hundreds of millions of eggs per year.[27]
Once an egg is fertilized, it is then planktonic, a collection of microorganisms that drift abundantly in fresh or salt water. Larvae stay in the water column for four to seven weeks before dissipating to the ocean floor, where they attach themselves to objects through byssus threads. Byssus is eventually lost with adulthood, transitioning almost all scallop species into free swimmers. Rapid growth occurs within the first several years, with an increase of 50–80 % in shell height and quadrupled size in meat weight, and reaches a commercial size at about four to five years of age.[27] The lifespans of some scallops have been known to extend over 20 years.[28]
Ecology
Scallops are known to be infected by
Mutualism
Some scallops, including Chlamys hastata, frequently carry epibionts such as sponges and barnacles on their shells. The relationship of the sponge to the scallop is characterized as a form of mutualism, because the sponge provides protection by interfering with adhesion of predatory sea-star tube feet,[30][31][32] camouflages Chlamys hastata from predators,[31] or forms a physical barrier around byssal openings to prevent sea stars from inserting their digestive membranes.[32] Sponge encrustation protects C. hastata from barnacle larvae settlement, serving as a protection from epibionts that increase susceptibility to predators. Thus, barnacle larvae settlement occurs more frequently on sponge-free shells than on sponge-encrusted shells.[30]
In fact, barnacle encrustation negatively influences swimming in C. hastata. Those swimming with barnacle encrustation require more energy and show a detectable difference in anaerobic energy expenditure than those without encrustation. In the absence of barnacle encrustation, individual scallops swim significantly longer, travel further, and attain greater elevation.[33]
Taxonomy and phylogeny
Etymology
The family name Pectinidae, which is based on the name of the type genus,
Phylogeny
The fossil history of scallops is rich in species and specimens. The earliest known records of true scallops (those with a ctenolium) can be found from the
The cladogram is based on molecular phylogeny using mitochondrial (12S, 16S) and nuclear (18S, 28S, and H3) gene markers by Yaron Malkowsky and Annette Klussmann-Kolb in 2012.[37]
Pteriomorphia |
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Taxonomic structure
Scallops are the family Pectinidae, marine bivalve molluscs within the superfamily Pectinoidea. Other families within this same superfamily share a somewhat similar overall shell shape, and some species within some of the related families are also commonly referred to as "scallops" (for example, Propeamussiidae, the glass scallops).
The family Pectinidae is the most diversified of the pectinoideans in present-day oceans. It is one of the largest marine bivalve families and contains over 300 extant species in 60 genera. Its origin dates back to the Middle Triassic Period, approximately 240 million years ago;[8] in terms of diversity, it has been a thriving family to the present day.[38]
Evolution from its origin has resulted in a successful and diverse group: pectinids are present in the world's seas, found in environments ranging from the intertidal zone to the hadal depths. The Pectinidae play an extremely important role in many benthic communities and exhibit a wide range of shell shapes, sizes, sculptures, and cultures.[39]
Raines and Poppe
This family's earliest and most comprehensive taxonomic treatments were based on macroscopic morphological characters of the adult shells and represent broadly divergent classification schemes.[42][29] Some level of taxonomic stability was achieved when Waller's studies in 1986, 1991, and 1993 concluded evolutionary relationships between pectinid taxa based on hypothesized morphological synapomorphies, which previous classification systems of Pectinidae failed to do. He created three Pectinidae subfamilies: Camptonectinidae, Chlamydinae and Pectininae.[43][44][45]
The framework of its phylogeny shows that repeated life habit states derive from evolutionary convergence and parallelism.[46][47] Studies have determined the family Pectinidae is monophyletic, developing from a single common ancestor. The direct ancestors of Pectinidae were scallop-like bivalves of the family Entoliidae.[48] Entoliids had auricles and a byssal notch only at youth, but they did not have a ctenolium, a comb-like arrangement along the margins of the byssal notch in Pectinidae. The ctenolium is the defining feature of the modern family Pectinidae and is a characteristic that has evolved within the lineage.[49]
In a 2008 paper, Puslednik et al. identified considerable convergence of shell morphology in a subset species of gliding Pectinidae, which suggests iterative morphological evolution may be more prevalent in the family than previously believed.[50]
There have been a number of efforts to address phylogenetic studies. Only three have assessed more than ten species[51][52][53] and only one has included multiple outgroups.[52] Nearly all previous molecular analyses of the Pectinidae have only utilized mitochondrial data. Phylogenies based only on mitochondrial sequence data do not always provide an accurate estimation on the species tree. Complicated factors can arise due to the presence of genetic polymorphisms in ancestral species and resultant lineage sorting.[54][55]
In molecular phylogenies of the Bivalvia, both the Spondylidae and the Propeamussiidae have been resolved as sister to the Pectinidae.[52][56]
List of subfamilies and genera
The following are recognised in the family Pectinidae:
- Subfamily Camptonectinae Habe, 1977[57]
- Camptonectes Agassiz, 1864
- Ciclopecten Seguenza, 1877
- Delectopecten Stewart, 1920
- Hyalopecten A. E. Verrill, 1897
- Pseudohinnites Dijkstra, 1989
- Sinepecten Schein, 2006
- Subfamily Palliolinae Korbkov in Eberzin, 1960
- Tribe Adamussiini Habe, 1977
- Adamussium Thiele, 1934
- Antarctipecten Beu & Taviani, 2013 †
- Duplipecten Marwick, 1928 †
- Lentipecten Marwick, 1928 †
- Leoclunipecten Beu & Taviani, 2013 †
- Ruthipecten Beu & Taviani, 2013 †
- Tribe Eburneopectinini T. R. Waller, 2006 †
- Eburneopecten Conrad, 1865 †
- Tribe Mesopeplini T. R. Waller, 2006
- Kaparachlamys Boreham, 1965 †
- Mesopeplum Iredale, 1929
- Phialopecten Marwick, 1928 †
- Sectipecten Marwick, 1928 †
- Towaipecten Beu, 1995 †
- Tribe Palliolini Waller, 1993
- Karnekampia H. P. Wagner, 1988
- Lissochlamys Sacco, 1897
- Palliolum Monterosato, 1884
- Placopecten Verrill, 1897
- Pseudamussium Mörch, 1853
- Tribe Serripectinini T. R. Waller, 2006 †
- Janupecten Marwick, 1928 †
- Serripecten Marwick, 1928 †
- Tribe Adamussiini Habe, 1977
- Subfamily Pectininae
- Tribe Aequipectinini F. Nordsieck, 1969
- Aequipecten P. Fischer, 1886
- Argopecten Monterosato, 1889
- Cryptopecten Dall, Bartsch & Rehder, 1938
- Flexopecten Sacco, 1897
- Haumea Dall, Bartsch & Rehder, 1938
- Leptopecten Verrill, 1897
- Volachlamys Iredale, 1939
- Tribe Amusiini Ridewood, 1903
- Amusium Röding, 1798
- Dentamussium Dijkstra, 1990
- Euvola Dall, 1898
- Leopecten Masuda, 1971
- Ylistrum Mynhardt & Alejandrino, 2014
- Tribe Austrochlamydini Jonkers, 2003
- Austrochlamys Jonkers, 2003
- Tribe Decatopectinini Waller, 1986
- Dall, Bartsch & Rehder, 1938
- Antillipecten T. R. Waller, 2011
- Bractechlamys Iredale, 1939
- Decatopecten Rüppell in G. B. Sowerby II, 1839
- Excellichlamys Iredale, 1939
- Glorichlamys Dijkstra, 1991
- Gloripallium Iredale, 1939
- Juxtamusium Iredale, 1939
- Lyropecten Conrad, 1862
- Dall, Bartsch & Rehder, 1938
- Nodipecten Dall, 1898
- Tribe Pectinini Wilkes, 1810
- Annachlamys Iredale, 1939
- †Fascipecten Freneix, Karache & Salvat 1971
- †Gigantopecten Rovereto, 1899
- Minnivola Iredale, 1939
- †Oopecten Sacco, 1897
- †Oppenheimopecten Teppner, 1922
- Pecten Müller, 1776
- Serratovola Habe, 1951
- Tribe Aequipectinini F. Nordsieck, 1969
- Subfamily Pedinae Bronn, 1862
- Tribe Chlamydini von Teppner, 1922
- Austrohinnites Beu & Darragh, 2001 †
- Azumapecten Habe, 1977
- Chesapecten Ward & Blackwelder, 1975 †
- Chlamys Röding, 1798
- Chokekenia Santelli & del Río, 2018 †
- Ckaraosippur Santelli & del Río, 2019 †
- Complicachlamys Iredale, 1939
- Coralichlamys Iredale, 1939
- Dietotenhosen Santelli & del Río, 2019 †
- Equichlamys Iredale, 1929
- Hemipecten A. Adams & Reeve, 1849
- Hinnites Deference, 1821
- Laevichlamys Waller, 1993
- Manupecten Monterosato, 1872
- Moirechlamys Santelli & del Río, 2018 †
- Notochlamys Cotton, 1930
- Pascahinnites Dijkstra & Raines, 1999
- Pixiechlamys Santelli & del Río, 2018 †
- Praechlamys Allasinaz, 1972 †
- Scaeochlamys Iredale, 1929
- Semipallium Jousseaume in Lamy, 1928
- Swiftopecten Hertlein, 1936
- Talochlamys Iredale, 1929
- Veprichlamys Iredale, 1929
- Yabepecten Masuda, 1963 †
- Zygochlamys Ihering, 1907
- Tribe Crassadomini Waller, 1993
- Caribachlamys Waller, 1993
- Crassadoma Bernard, 1986
- Tribe Fortipectinini Masuda, 1963
- Fortipecten Yabe & Hatai, 1940 †
- Kotorapecten Masuda, 1962 †
- Masudapecten Akiyama, 1962 †
- Mizuhopecten Masuda, 1963
- Nipponopecten Masuda, 1962 †
- Patinopecten Dall, 1898
- Tribe Mimachlamydini Waller, 1993
- Mimachlamys Iredale, 1929
- Spathochlamys Waller, 1993
- Tribe PediniBronn, 1862
- PedumBruguière, 1792
- Tribe Chlamydini von Teppner, 1922
- Subfamily incertae sedis
- Agerchlamys Damborenea, 1993 †
- Athlopecten Marwick, 1928 †
- Camptochlamys Arkell, 1930 †
- Indopecten Douglas, 1929 †
- Jorgechlamys del Río, 2004 †
- Lamellipecten Dijkstra & Maestrati, 2010
- Lindapecten Petuch, 1995
- Mixtipecten Marwick, 1928 †
- Pseudopecten Bayle, 1878 †
Seafood industry
Aquaculture
Wild fisheries
The largest wild scallop fishery is for the Atlantic sea scallop (
In the D'Entrecasteaux Channel in the south of Tasmania dredging was banned in 1969, and since then divers have caught them in this area.[59] Attempts to use lighted pots to attract lobster and crab led to the discovery that they were effective in attracting scallops.[60]
Sustainability
The scallop fishery in New Zealand declined from a catch of 1246 tonnes in 1975 to 41 tonnes in 1980, at which point the government ordered the fishery closed.
On the east coast of the United States, over the last 100 years, the populations of bay scallops have greatly diminished due to several factors but probably mostly due to a reduction in seagrasses (to which bay scallop spat attach) caused by increased coastal development and concomitant nutrient runoff. Another possible factor is the reduction of sharks from overfishing. A variety of sharks used to feed on rays, which are the main predator of bay scallops. With the shark population reduced – this apex predator in some places almost eliminated – the rays have been free to feed on scallops to greatly decrease their numbers.[63] By contrast, the Atlantic sea scallop (Placopecten magellanicus) is at historically high levels of abundance after recovery from overfishing.[64]
As food
Scallops are characterized by offering two flavors and textures in one shell: the meat, called "scallop", which is firm and white, and the roe, called "coral", which is soft and often brightly coloured reddish-orange. Sometimes, markets sell scallops already prepared in the shell, with only the meat remaining. Outside the U.S., the scallop is often sold whole. They are available both with and without coral in the UK and Australia.[65]
Scallops without any additives are called "dry-packed", while scallops that are treated with
In
Scallops have lent their name to the culinary term "scalloped", which originally referred to seafood creamed and served hot in the shell.
-
Adductor muscle meat of the giant scallop (seven white circular items) with a large shrimp
-
Dried scallops, also known as conpoy
-
Taiwanese steamed scallops
-
A scallop being grilled next to sausages in Japan
-
Fried scallops on a stick served with rice
-
Pan seared scallops
Pearls
Scallops do occasionally produce
Symbolism of the shell
Shell of Saint James
The scallop shell is the traditional emblem of
Indeed, in French, the mollusc itself – as well as a popular preparation of it in cream sauce – is called coquille St. Jacques. In German they are Jakobsmuscheln – literally "James's shellfish". Curiously the
When referring to St James, a scallop shell valve is displayed with its convex outer surface showing. In contrast, when the shell refers to the goddess Venus (see below), it is displayed with its concave interior surface showing.[73]
Badge
The scallop shell symbol found its way into
Fertility symbol
Throughout antiquity, scallops and other hinged shells have symbolized the feminine principle.[77] Outwardly, the shell can symbolize the protective and nurturing principle, and inwardly, the "life-force slumbering within the Earth",[78] an emblem of the vulva.[79][80]
Many paintings of
One legend of the
Other interpretations
Alternatively, the scallop resembles the setting sun, which was the focus of the pre-Christian Celtic rituals of the area.[
Contemporary art
The beach at Aldeburgh, Suffolk, England, features Maggi Hambling's steel sculpture, The Scallop, erected in 2003 as a memorial to the composer Benjamin Britten, who had a long association with the town.[85]
Scalloped shape
The term "scalloped" is used to designate an decorative pattern, resembling the wavy scallop surface, that is used at the edges of furniture, fabrics, and other items.[86]
See also
Explanatory notes
- ^ Also occasionally written scollop and once spelled scalap, -opp, scalop, skalop, scalepp, -oppe, scalloppe, skallap, -op, scallope, scallap, s(c)kollop, and scollup, -op as well as escallop, escalop, and escollop, though scallop appears to have become the dominant way of spelling the word in English.[1]
- ^ Raines, B. K. & Poppe, G. T. (2006): The Family Pectinidae.[40]
Citations
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- ^ Robinson & Robinson 2000, p. 65.
- ^ Shumway & Parsons 2011, p. 207.
- ^ Shumway & Parsons 2011, p. 124.
- ^ Milsom & Rigby 2009, p. 62.
- ^ a b c d e f g h Drew 1906, pp. 5–6.
- ^ Shumway & Parsons 2011, p. 59.
- ^ S2CID 84457522.
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- ^ "Eyes detect changing movement patterns: queen scallop". asknature.org.
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- ^ a b Shumway & Parsons 2011, pp. 689–690.
- ^ Dore 2013, p. 152.
- ^ Gosling 2015, p. 29.
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- ^ a b c Hart, D.R.; Chute, A.S. (2004). "Essential Fish Habitat Source Document: Sea Scallop, Placopecten magellanicus, Life History and Habitat Characteristics" (PDF). NOAA Tech Memo NMFS NE-189.
- ^ "Scallop Aquaculture" (PDF). College of Marine Science, University of South Florida.
- ^ ISBN 978-0-444-62719-3.
- ^ .
- ^ .
- ^ .
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- ^ Rice 2012, p. 47.
- ^ Waller, T. R. (1993). "The evolution of Chlamys (Mollusca: Bivalvia: Pectinidae) in the tropical western Atlantic and eastern Pacific". American Malacological Bulletin. 10 (2): 195–249.
- ^ Harper et al. 2000, p. 254.
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- ^ Waller, Thomas R. (2006). Shumway, Sandra E. (ed.). New phylogenies of the Pectinidae (Mollusca: Bivalvia): Reconciling morphological and molecular approaches. Amsterdam: Elsevier. pp. 1–44.
{{cite book}}
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ignored (help) - )
- ^ Raines, Poppe & Groh 2006.
- ^ Barucca, M., Olmo, E., Schiaparelli, S. & Canapa, A. (2004): Molecular phylogeny of the family Pectinidae (Mollusca: Bivalvia)
- )
- .
- ^ Waller 1991, pp. 1–73.
- ^ Waller, Thomas R. (1993). "The evolution of "Chlamys" (Mollusca: Bivalvia: Pectinidae) in the tropical western Atlantic and eastern Pacific". American Malacological Bulletin. 10 (2): 195–249.
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- ^ Waller, Thomas R. (1984). "The ctenolium of scallop shells: functional morphology and evolution of a key family-level character in the Pectinacea (Mollusca: Bivalvia)". Malacologia. 25 (1): 203–219.
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- ^ Waller, Thomas R., 1998. Origin of the Molluscan Class Bivalvia and a Phylogeny of Major Groups. Pp. 1–45. In: P.A. Johnston & J.W. Haggart (eds), Bivalves: An Eon of Evolution. Calgary: University of Calgary Press xiv + 461 pp.
- ^ Habe 1977.
- ^ Shumway & Parsons 2011, p. 902.
- ^ Walker, Margaret (1991). "What price Tasmanian scallops? A report of morbidity and mortality associated with the scallop diving season in Tasmania 1990". South Pacific Underwater Medicine Society Journal. 21 (1). Archived from the original on 2013-10-20. Retrieved 2013-07-16.
{{cite journal}}
: CS1 maint: unfit URL (link) - ^ "Orkney part of 'scallop discos' fishing trial". BBC News. BBC. 2022-06-06. Retrieved 2022-06-07.
- ^ a b Arnold, Naomi (July–August 2018). "What we do in the shallows". New Zealand Geographic. 152: 56–73.
- ^ "Scallops". Forest and Bird.
- ^ Pinet 2011, p. 333.
- ^ Granata, Flick & Martin 2012, p. 96.
- ^ Shumway & Parsons 2011, p. 1355.
- ^ Rolnick & Peterson 2014, p. 47.
- ^ Broder, Andy (June 7, 2012). "AndyTalk: Beyond Lox – Smoked Seafood Hold the Bagels". Phoenix New Times. Archived from the original on June 9, 2012. Retrieved January 31, 2017.
- ^ Rombauer & Becker 1964, p. 369.
- ^ Matlins 2001, p. 56.
- ISBN 9780826415257.)
{{cite book}}
: CS1 maint: multiple names: authors list (link - ISBN 9781472410832.
- ^ Starkie 1965, pp. 70–71.
- ^ ISBN 9781472410832.
- ^ St. James Church 1963, p. 22.
- ^ Stix, Stix & Abbott 1968, p. [pages needed].
- ^ "New York State Shell: Bay Scallop". State Symbols USA. Retrieved 2012-05-24.
- ^ Salisbury 2001, p. 11.
- ^ Fontana 1994, pp. 88, 103.
- JSTOR 25010972.
- ^ Johnson 1994, p. 230.
- ^ "Birth of Venus". artble.com. 2017. Retrieved 25 February 2017.
- S2CID 144403461.
- ^ Gauding 2009, p. 169.
- ^ Thomas, Isabella. "Pilgrim's Progress". Europe in the UK. European Commission. Archived from the original on March 23, 2008. Retrieved January 21, 2017.
- ^ Dunford & Lee 2012, p. 486.
- ^ Court of Customs and Patent Appeals Reports. The Court of Customs and Patent Appeals. 1930. Retrieved 2023-11-11.
General bibliography
- Dore, Ian (29 June 2013). The New Fresh Seafood Buyer's Guide: A manual for distributors, restaurants and retailers. Boston, MA: ISBN 978-1-4757-5990-7.
- Drew, Gilman Arthur (1906), The Habits Anatomy, and Embryology of the Giant Scallop: (Pecten Tenuicostatus, Mighels), Orono, Maine, pp. 5–6
{{citation}}
: CS1 maint: location missing publisher (link) - Dunford, Martin; Lee, Phil (13 September 2012). The Rough Guide to Norfolk & Suffolk. Rough Guides. p. 486. ISBN 978-1-4053-9037-8.
- Fontana, David (1994). The secret language of symbols: a visual key to symbols and their meanings. San Francisco: ISBN 978-0-8118-0462-2.
- Gauding, Madonna (2009). The Signs and Symbols Bible: The Definitive Guide to Mysterious Markings. ISBN 978-1-4027-7004-3.
- Gosling, Elizabeth (27 April 2015). Marine Bivalve Molluscs. ISBN 978-1-119-04522-9.
- Granata, Linda Ankenman; Flick, George J. Jr.; Martin, Roy E. (8 February 2012). The Seafood Industry: Species, Products, Processing, and Safety. John Wiley & Sons. p. 96. ISBN 978-1-118-22953-8.
- Habe, Tadashige (1977). "Bivalvia and Scaphopoda". Systematics of mollusca in Japan: Bivalvia and Scaphopoda. Hokuryukan.
- Harper, Elizabeth; Taylor, John David; Crame, J. Alistair; ISBN 978-1-86239-076-8.
- Johnson, Buffie (1994). Lady of the beasts: the Goddess and her sacred animals. Rochester, Vt: Inner Traditions/ISBN 978-0-89281-523-4.
- Matlins, Antoinette, L. (2001). The Pearl Book: The Definitive Buying Guide: how to Select, Buy, Care for & Enjoy Pearls. New York, NY: Gemstone. p. 56. ISBN 978-0-943763-35-4.)
{{cite book}}
: CS1 maint: multiple names: authors list (link - Milsom, Clare; ISBN 978-1-4443-1123-5.
- Pinet, Paul R. (28 December 2011). Invitation to Oceanography. ISBN 978-1-4496-0192-8.
- Rice, Tony (3 December 2012). Can Squid Fly? Can squid fly?: answers to a host of fascinating questions about the sea and sea life. London: ISBN 978-1-4081-5130-3.
- Rolnick, Glenn; Peterson, Chris (November 4, 2014). Carmine's celebrates: classic Italian recipes for everyday feasts. New York: ISBN 978-1-4668-3723-2.
- Raines, Bret K.; Poppe, Guido T.; Groh, Klaus (2006). A conchological iconography. Hackenheim Germany: ConchBooks. p. 402. ISBN 978-3-925919-78-7.
- Robinson, Chuck; Robinson, Debbie (2000). The Art of Shelling: A Complete Guide to Finding Shells and Other Beach Collectibles at Shelling Locations from Florida to Maine. Old Squan Village Publishing. p. 65. ISBN 978-0-9647267-8-9.
- Rombauer, Irma S.; Becker, Marion Rombauer (1964) [1931]. The Joy of Cooking. Indianapolis, Indiana: ISBN 978-0-452-25665-1.
- ISBN 978-1-57607-092-5.
- Shumway, Sandra E.; Parsons, G. Jay, eds. (22 September 2011). Scallops: Biology, Ecology and Aquaculture (2nd ed.). Amsterdam Boston: ISBN 978-0-08-048077-0.
- St. James' Church (Sydney, N.S.W.) (1963). A Short story of historic St. James', Sydney (2nd ed.). The Church. Retrieved 25 September 2023.
- Starkie, Walter (1965) [1959]. The Road to Santiago. Berkeley, Los Angeles: University of California Press. p. 71. Retrieved 20 January 2017.
- Stix, Hugh; Stix, Marguerite; Abbott, Robert Tucker (1968). The Shell: Five Hundred Million Years of Inspired Design (First ed.). New York NY: ISBN 978-0810904750.
- Waller, Thomas R. (1991). "Evolutionary relationships among commercial scallops (Mollusca: Bivalvia: Pectinidae)". In S. E. Shumway (ed.). Scallops: Biology, ecology and aquaculture. New York: Elsevier.
- Willard, Barbara; Owens, Mary B. (1 September 1997). Augustine Came to Kent. Warsaw, N.D.; San Francisco: Bethlehem Books, ISBN 978-1-883937-21-8.
External links
- Mollusca - Bivalvia - Pectinidae at Natural History Museum Rotterdam – photos of Pectinidae shells