Biochemical Investigation on the Edible Molluscs of Kerala. 3. a Study on the Nutritional Value of Some Gastropods and Cephalopo

Total Page:16

File Type:pdf, Size:1020Kb

Biochemical Investigation on the Edible Molluscs of Kerala. 3. a Study on the Nutritional Value of Some Gastropods and Cephalopo CORE Metadata, citation and similar papers at core.ac.uk Provided by Aquatic Commons PART II SCIENTIFIC AND TECHNICAL IOC E l VESTIGATI s 0 E EDI lE llUSCS f lie STUDY ON THE UTRITIONAL VALUE OF SO E GASTROPODS D CEPHALOPODS H. SURYANARAYANAN, R. SHYLAJA KUMARI AND K. M. ALEXANDER Department of Zoology, University of Kera/a, Kariavottom-P. 0., Trivondrum, india Data on the biochemical composition and food value of the edible portions of two gastropods, Pila virens and Achatina fulica and two cephalopods, Sepiella inermis and Loigo indica have been presented. These molluscs posses nutritive meat very rich in protein and mine­ rals, which compare favourably with popular food fishes in caloric value. The significance of the variations met with in the bioche­ mical constituents of the different species has been di~cussed. INTRODUCTION inland waters and west c:;ast of Kerala would provide valuable data regarding Apart from prawns and shrimps, their nutritional value aad pave way for various molluscs such as squids, mussels, better exploitation and utilization of the oysters and clams comprise the major part molluscan fisheries of Kerala. The present of shell fishery. As a matter of fact these report, dealing with the nutritional value molluscs constitute a comparatively unex­ of certain edible gastropods and cephalopods ploited fishery resource of great promise is the continuation of an earlier publication by virtue of their high productivity and on the edible bivalves (Suryanarayanan natural abundance (Jones, 1968). Despite and Alexander, 1972). the considerable data available on the biochemical aspects of fishes of India MATERIAL AND METHODS (Saha and Guha, 1938; Giri et, al, 1944: Venkitaraman and Chari, 1955: Alexander, Adult specimens of the fresh water 1955, 56) investigations on the edible moll­ gastropod, Pila virens, the terrestrial pul­ uscs have been rather few (Joshi and Bal, monate, Achatina fttlica and two cephalo­ 1968; Chinnamma et al, 1970; Pandit and pods, Loligo indica and Sepiella inermis Magar, 1972). Hence it was thought that were collected from their natural habitats a study of the various biochemical constitu­ and were brought to the laboratory in live ents of the edible molluscs found in the condition. They were later killed and their 100 FISHERY TECHNOLOGY Suryanarayanan, Sllylaja 'Kumari & Alexander: 13iocftemical investigations on tfte edi5le molluscs of 'Kerala. II- A study on tfl.e nutritional value of some gastropods and cepfwlopods edible portions were analysed for moisture of 0.53% (Sepiella inermis) and 0.61% content, total proteins, free amino acids, ( Loligo indica). total lipids, glycogen, iron, phosphorus and ash content employing standard analytical All molluscs investigated revealed a techniques (Suryanarayrnan and Alexander, fairly high percentage of lipids, 5.56% in 1972). The food value was calculated Sepiella inermis, 5.4% in Loligo indica, 4.4% using Rubner's (1901) Table. in Pi/a virens and 10.8% in Achatinafulica. The highest value for iron content is RESULTS shown by Achatinafulica (153.8mg%) while The data obtained for the various Pila virens has a lower value of I24.4mg%. biochemical constituents of these edible Relatively very low percentages, 16.64 mg% molluscs are given in Table I and II. in Loligo indjca and 12.88mg% in Sepiella inermis) have been observed. The p~rcentage of edible portions is· comparatively high in cephalopods ranging The phosphorus content of cephalopods from 68.5% (sepiel!a inermis) to 71.38% is rather high (138.0mg% in Sepiella i~termis (Loligo indica) whereas the gastropods, and 145.0mg% in Loligo indica) whereas Pila virens and Achatina fulica have only both gastropods have much lower values 29.08% and 24.7% respectively. (62.5mg% in Achatina fulica and 83.0mg% in Pila virens). The moisture content in the cephalo­ pods is rather low being 74. 78% in Sepiella Sepiella inermis and Loligo indica inermis and 75.05% in Loligo ·indica. Of the showed a comparatively higher percentage two gastropods studied, Pila virens has a of ash content, 13.42%, 12.5% respectively moisture content of 78.87% and Achatina than Pita virens (10.96%) and Achatina fulica, 75.5%. fulica (6.3%). Relatively, the cephalopods have the The ener_gy content of these molluscs highest protein content of 83.49% in Loligo range from 453.42 calories in Achatina indica and 81.49% in Sepiella inermis. fulica, 379.83 calories in Pila virens, 395.05 The gastropod pila virens has only 75.32% calories in Loligo indica to 387.99 calories and Achatina fulica, 76.2% . in Sepiella inermis. The edible portions of the molluscs DISCUSSION investigated appeared to possess aU or most of the following amino acids namely, The data suggest that' among the arginine, cysteine, glutamic acid,_ molluscs studied, the percentage of edible glycine, histidine, isoleucine, leucine portions is rather high in cephalopods ( 68.5% lysine, methionine, phenylalanine, serine to 71.38%) whereas the gastropods possessed threonine, tryptophan, tyrosir:e and valine. only lower percentage (24.7% to 29.08%). Table II shows the free amino acids in the In fact the higher percentage of edihle different animals concernd. portions found in cephalopods could be attributed to their possession of light inter­ Regarding the glycogen content, Acha­ nal shells. Among the two gastropods, tina fulica shows the highest percentage of Achatina fulica has a relatively heavier shell 10.4%and Pila virens 7.2%. Nevertheless, the which would explain its lower percentage cephalopods exihibit only very low values of edible tissue: Since both gastropods and VoL X No. 2 1973 101 0 -N d()') £.~ ... -!':!<.<::: (")"' c;::! TABLE 1. "' c 0 'I BIOCHEMICAL COMPOSITION OF THE EDIBLE PORTIONS OF THE MOLLUSCS STUDIED -c ~II::: (\) c "' ;s Food value o e Animals %of edible Moisture Proteins Lipid Glycogen Phosphorus Iron Ash Calories; ~"N "ry, Portionst content t %* mg%* mg%* %* lOOgm.* * :::~I- 0 Pi/a virens 29.08 78.87 75.32 4.44 7.25 83.0 124.4 10.96 378.83 >-~· ~~ Achatina fulica ::: ::: 24.7 75.50 76.20 10 80 10.4 62.5 153.8 6.30 453.42 0-::l '1::: ""0 Sepiella inermis 68.56 74.78 81.49 5.56 0.53 138.0 12.88 13.42 387.99 0 ... ;:; Loligo indica 71.38 75.05 83.49 5.40 0.61 145.0 16.66 12.50 395.03 .... ;,~ ;::-"'>- !':! '1. ·(Expressed as gms/ 100 gms wet weight. .... x ... c ~Expressed as units/100 gms dry weig~t. E:~ 0 (\) TABLE II. ;s ., !?.:" FREE . AMINO ACIDS IN THE V ARlO US MOLLUSCS STUDIED oti] -o1:1 .... !::! (") Phenyls Gly~ Cyst~ Tyro~ Histi. Vali~ Lysi- Methi- Glutamic Insol~ Leuc- Ser- Trypto- Pro- Arg- Thre ">;:to 0 ~ Animals alanine cine tine sine dine ne ne onine acid eusine ine ine phan line inie onine ...... ;:l ()"' (")... :::-- c "' .... <Q ;:l 0 <;I Pila virens + + + + - + + + + + + + + + + + ~;."'"' O<Q ""O0 .... 0- .... :zl. Loligo indica - + - - + - - tl:l + + + + + + + + tn g l:Il 0 tn l:;!'j ;:l - - 0-0 c; Sepiella inermis+ + + + + + + + + - + + (") ;::! + + "'­ "";:;;.;:.."> ~ + indicate presence 2.."'00., ""OQ'> .... ~ o..­ s0 (1) (\) Cl ><: 8uryararayanan, 811ylaja 'Kumari & Alexander: 13iocfiemical investigations on tfte edi(ile molluscs of 'Kerala. II- A study. on tfie nutritional value of some gastropods and cepfwlopods bivalves possess much heavier shells, they muscular activity (Fields, 1965). In con have comparatively lesser percentage of trast to the low glycogen values of cephalo­ edible portions. pods the gastropods store larger amounts of glycogen in their tissues. Infact glycogen The moisture content of the gastropod, constitutes a major fuel reserve of terrestrial Pi/a virens is 78.87% and Achatina fulica gastropods and is utilized as an energy 75.5%. Comparatively lower values have source during hibernation and aestivation been obtained for the cephalopods, Loligo (Meenaks11i. 1958; Thiele, 1959). indica (75.5%) and Sepiella inermis 74.78 %). The lower moisture content in the terrestri­ The lipids in the body and in the diet al pulmonate, Achatina fulica and in the constitute a concentrated form of energy for marine cephalopods could be attributed to metabolism and storage purposes. Further the osmotic requirements of the habitat fats may serve important non-caloric metabo­ concerned. lic functions also(George and Berger, 1966). Relatively, the cephalopods showed much The cephalopods revealed high protein higher percentages of lipids than glycogen content (83.49% in Loligo indica and (5.56% for Sepi?lla inermis and 5.4% for 81.49% in Sepiella inermis). Similar values Laligo indica). The lipid content reported have been reported by Pandit and Mag3:r by Pandit and Magar (1972) for Sepia (1972) for Sepia orienta/is (80.21 %) and orienta/is (3.9%) and Loligo vulgaris Loligo vulgaris (81.50%). It has been sugg­ (4 %) is 'l little lower than those obtained in ested that since the cephalopods possess our present sfujy. The gastropods invest­ only scant glycogen reserves, their inter­ igated also exhibited high lipid content mediary merabolism may utilize body (10.8% in Achatina fulica and 7.2% in Pila protein to sustain life at times of starvation virens). (Goddard and Martin, 1966). Among the gastropods, Achatina fulica has a slightly The ash content of particular animal higher protein content (76.2%) than Pila indicates the amount of inorganic constitu­ virens (72.32%). ents p:esent in its tissue. No significant variation could be observed in the ash Paradoxically the glycogen reserves content of [he two cephalopods, Sepiella exhibited by cephalopods are significantly inermis (13.42%) and Loligo indica 12.5%). low (0.53% and 0.61 %). The present data Lower values have been obtained for the compares favourably with those obtained gastropods, Pila virens (10.96%) and Achatina by Boyland (1928) for Sepiaelegans 0.037% fulica (6.3%). and Eledone (0.11 %). Studies· on fuel re­ serves of molluscan muscle revealed very Among the molluscs investigated, the low glycogen content for cephalopod mus­ gastropods showed much higher percentage cles (Suryanarayanan and Alexander, 1971).
Recommended publications
  • Is Sepiella Inermis ‘Spineless’?
    IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS) e-ISSN:2278-3008, p-ISSN:2319-7676. Volume 12, Issue 5 Ver. IV (Sep. – Oct. 2017), PP 51-60 www.iosrjournals.org Is Sepiella inermis ‘Spineless’? 1 Visweswaran B * 1Department of Zoology, K.M. Centre for PG Studies (Autonomous), Lawspet Campus, Pondicherry University, Puducherry-605 008, India. *Corresponding Author: Visweswaran B Abstract: Many a report seemed to project at a noble notion of having identified some novel and bioactive compounds claimed to have been found from Sepiella inermis; but lagged to log their novelty scarcely defined due to certain technical blunders they seem to have coldly committed in such valuable pieces of aboriginal research works, reported to have sophistically been accomplished but unnoticed with considerable lack of significant finesse. They have dealt with finer biochemicals already been reported to have been available from S.inermis; yet, to one’s dismay, have failed to maintain certain conventional means meant for original research. This quality review discusses about the illogical math rooting toward and logical aftermath branching from especially certain spectral reports. Keywords: Sepiella inermis, ink, melanin, DOPA ----------------------------------------------------------------------------------------------------------------------------- ---------- Date of Submission: 16-09-2017 Date of acceptance: 28-09-2017 ----------------------------------------------------------------------------------------------------------------------------- ---------- I. Introduction Sepiella inermis is a demersally 1 bentho-nektonic 2, Molluscan, cephalopod ‗spineless‘ cuttlefish species, with invaluable juveniles 3, from the megametrical Indian coast 4-6, as incidental catches in shore seine 7 & 8, as egg clusters 9 from shallow waters 1 after monsoon at Vizhinjam coast 10 and Goa coast 11 of India and sundried, abundantly but rarely 8. II.
    [Show full text]
  • Reproductive Behavior of the Japanese Spineless Cuttlefish Sepiella Japonica
    VENUS 65 (3): 221-228, 2006 Reproductive Behavior of the Japanese Spineless Cuttlefish Sepiella japonica Toshifumi Wada1*, Takeshi Takegaki1, Tohru Mori2 and Yutaka Natsukari1 1Graduate School of Science and Technology, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852-8521, Japan 2Marine World Uminonakamichi, 18-28 Saitozaki, Higashi-ku, Fukuoka 811-0321, Japan Abstract: The reproductive behavior of the Japanese spineless cuttlefish Sepiella japonica was observed in a tank. The males competed for females before egg-laying and then formed pairs with females. The male then initiated mating by pouncing on the female head, and maintained the male superior head-to-head position during the mating. Before ejaculation, the male moved his right (non-hectocotylized) arm IV under the ventral portion of the female buccal membrane, resulting in the dropping of parts of spermatangia placed there during previous matings. After the sperm removal behavior, the male held spermatophores ejected through his funnel with the base of hectocotylized left arm IV and transferred them to the female buccal area. The spermatophore transfer occurred only once during each mating. The female laid an egg capsule at average intervals of 1.5 min and produced from 36 to more than 408 egg capsules in succession during a single egg-laying bout. Our results also suggested one female produced nearly 200 fertilized eggs without additional mating, implying that the female have potential capacity to store and use active sperm properly. The male continued to guard the spawning female after mating (range=41.8-430.1 min), and repeated matings occurred at an average interval of 70.8 min during the mate guarding.
    [Show full text]
  • Bioaccumulation of Heavy Metals in Cuttlefish Sepiella Inermis from Visakhapatnam Coastal Waters
    International Journal of Science and Research (IJSR) ISSN: 2319-7064 Index Copernicus Value (2016): 79.57 | Impact Factor (2017): 7.296 Bioaccumulation of Heavy Metals in Cuttlefish Sepiella Inermis from Visakhapatnam Coastal Waters R.Rekha1, B. Ganga Rao2 1Department of Foods, Nutrition & Dietetics, Andhra University, Visakhapatnam-530 003, India 2Professor, Department of Pharmaceutical Sciences, Andhra University, Visakhapatnam-530 003, India Abstract: This study investigates 9 elements both essential (Cr, Cu, Zn, Fe, Mn and Ni) and non essential (Cd, Hg and Pb) in the tissues and whole of the cuttlefish Sepiella inermis caught off Visakhapatnam coast (east coast of India, Bay of Bengal). The level of elements was determined by atomic absorption spectrophotometry (AAS). The concentration ranges found for these heavy metals, expressed on a wet weight basis, were as follows: Hg, Cd, Pb, Cu, Zn, Fe, Mn, Cr, and Ni concentrations in cuttlefish muscle samples were 0.01 - 0.07, 0.11-0.67, 0.11-1.14, 0.52-6.08, 4.82-19.32, 0.08-5.84, 0-0.49 and 0-2.11, 0-0.92 ppm respectively. As for other cephalopod species, the liver showed the highest concentrations of many elements highlighting their role in bioaccumulation and detoxification processes. The mean values of highly hazardous metals in the muscle of the Sepiella inermis, were: Hg = 0.04, Cd = 0.481, Pb = 0.525, Cr = 0.662, all within the international safety limits. The level of contamination in Sepiella inermis by these heavy metals is compared to those studied in other parts of the world and the legal standards set by international legalizations.
    [Show full text]
  • Combining Disparity with Diversity to Study the Biogeographic Pattern of Sepiidae
    Coleoid cephalopods through time (Warnke K., Keupp H., Boletzky S. v., eds) Berliner Paläobiol. Abh. 03 189-197 Berlin 2003 COMBINING DISPARITY WITH DIVERSITY TO STUDY THE BIOGEOGRAPHIC PATTERN OF SEPIIDAE P. Neige Centre des Sciences de la Terre & UMR CNRS 5561 Biogéosciences, Université de Bourgogne, 6 bd Gabriel, F-21000, Dijon, France, [email protected] ABSTRACT Diversity and disparity metrics of recent cuttlefishes are studied at the macroevolutionary scale to establish the geographical biodiversity patterns of these cephalopods at species level and to explore the relationship between these two metrics. One hundred and eleven species distributed in 17 biogeographic areas serve as basic units to explore these complementary biodiversity metrics in space. Landmarks describe cuttlebones; differences between shapes are quantified using relative warp analyses. Relative warps are used as the morphological axis to construct morphospaces whose characteristics are described with total variance as a disparity index. Disparity is analysed and then compared with diversity (i.e. species richness). Results show the peculiarity of southern African coasts (high disparity level with low or high species richness) and the low disparity level of the “East Indies” area associated with high species richness. The particular pattern of southern Africa may have been caused by paleogeographical changes since the Eocene whereas that of the “East Indies” may indicate that this area could have acted as a centre of origin. The number of species in a given area does not predict the level of disparity, which suggests the need for both diversity and disparity metrics to be explored when studying biogeography. INTRODUCTION opportunity to search for evolutionary mechanisms at macroevolutionary scale (Foote 1993, Jablonski 2000).
    [Show full text]
  • BEIIAVIOLIR of Jiwenile CEPIIALOPODS: PREFERENCE for TEXTI,]RE AI\D BRIGIITNESS of SI.]BSTRA
    Phuhet Marine Biological Center Special Publication 21(1): 103-112 (2000) 103 BEIIAVIOLIR OF JIwENILE CEPIIALOPODS: PREFERENCE FOR TEXTI,]RE AI\D BRIGIITNESS OF SI.]BSTRA. TA Jaruwat Nabhitabhata & Pitiporn Nilaphat Rayong Coastal Aquaculture Station, Ta-pong, Changwat Rayong 2100, Thailand. ABSTRACT strata is referred to as epipsammon (on Behavioural preference for different types and sand) or epipelos (on mud). An important levels of brightness of substrata was studied in property for the inhabiting animals is the cultured, juvenile sepiid cuttlefish, Sepia suitability to move upon and to burrow in pharaonis and Sepiella inermis. Sand, muddy the soft substrata. Substrata affect metabo- sand and mud represented types ofbenthic sub- lism and activity of the animals via their stratum. Both species ofcuttlefish preferred sand physico-chemical properties, particularly to mud in long term studies (24 hrs). White, grey and black plastic plates were used as substrata their resistance to animal activities such as representing high, medium and low levels of Iocomotion, respiratory ventilation, and bur- brightness. The cuttlefish preferred medium level rowing in benthic cephalopods. Exposure ofbrightness during the early phase (up to 3 hrs) and water movement influences properties of the experiment. The degree of preference for of soft substrata. Therefore, habitat selec- substratum was higher in Sepia, living in the tion of aquatic animals is essentially the re- open sea, compared to the estuafine Sepiella. Iationship between behaviour and environ- Cuttlefish selected substrata in relation to ben- ment (Meadows & Campbell 1972). The ani- efrts, which we suggest are facilitated respira- mals are not able to differentiate between tion, crypsis, and energy conservation.
    [Show full text]
  • Recent Cephalopoda Primary Types
    Ver. 2 March 2017 RECENT CEPHALOPOD PRIMARY TYPE SPECIMENS: A SEARCHING TOOL Compiled by Michael J. Sweeney Introduction. This document was first initiated for my personal use as a means to easily find data associated with the ever growing number of Recent cephalopod primary types. (Secondary types (paratypes, etc) are not included due to the large number of specimens involved.) With the excellent resources of the National Museum of Natural History, Smithsonian Institution and the help of many colleagues, it grew in size and became a resource to share with others. Along the way, several papers were published that addressed some of the problems that were impeding research in cephalopod taxonomy. A common theme in each paper was the need to locate and examine types when publishing taxonomic descriptions; see Voss (1977:575), Okutani (2005:46), Norman and Hochberg (2005b:147). These publications gave me the impetus to revive the project and make it readily available. I would like to thank the many individuals who assisted me with their time and knowledge, especially Clyde Roper, Mike Vecchione, Eric Hochberg and Mandy Reid. Purpose. This document should be used as an aid for finding the location of types, type names, data, and their publication citation. It is not to be used as an authority in itself or to be cited as such. The lists below will change over time as more research is published and ambiguous names are resolved. It is only a search aid and data from this document should be independently verified prior to publication. My hope is that this document will make research easier and faster for the user.
    [Show full text]
  • ICES STATUTORY MEETING 1993 Shellfish Committea K:39 RANG
    • ICES STATUTORY MEETING 1993 Shellfish Committea K:39 SIZE SELECTION OF OCTOPUS VULGARIS CUVIER, SEPIA OFFICINALIS HIERREDDA RANG AND SEPIELLA ORNATA RANG IN BOTTOM TRAWLS OFF THE COAST OF GUINEA-BISSAU. by Joäo M. da F. Pereira • Instituto Nacional de Investiga<;äo das Pescas, Av. de Brasnia - 1400 Lisboa, Portugal. ABSTRACT The results presented refer to three species of cephalopod caught in two consecutive bottom trawl hauls, shot off the coast of Guinea-Bissau, during a research cruise of the portuguese RN "NORUEGA", in June 1991. Selectivity experiments were performed using the covered cod-end method, with a 61.4 mm cod-end mesh size. The selection factors (SF) estimated for the two species of Sepiidae (0.85 and 0.84) fall between the • range of values found in the literature for fish and crustaceans. The values of L50'l' were, respectively, 55.5 and 54.5 for Sepia officinalis hierredda and Sepiella omara. The characteristics of the size selection observed in the two species of Sepiidae and the lack of size selection obtained for the Octopodid (Ocropus vulgaris) suggest a behaviour­ dependent selection which departs from the pattern usually found in fish. Kay words: Cephalopods, trawling, selectivity, selection factor, Octopus vulgaris, Sepia officinalis hierredda, Sepiella amata. 2 INTRODUCTION In the context of the scientific assistance programme which INIP has undergone in the waters of Guinea-Bissau since 1988, selectivity experiments have taken place, which aimed to identify the characteristics of the size selection of a cod-end similar in construction material and mesh size to the ones used commercially in bottom trawl nets in this country.
    [Show full text]
  • Cephalopod Guidelines
    Reference Resources Caveats from AAALAC’s Council on Accreditation regarding this resource: Guidelines for the Care and Welfare of Cephalopods in Research– A consensus based on an initiative by CephRes, FELASA and the Boyd Group *This reference was adopted by the Council on Accreditation with the following clarification and exceptions: The AAALAC International Council on Accreditation has adopted the “Guidelines for the Care and Welfare of Cephalopods in Research- A consensus based on an initiative by CephRes, FELASA and the Boyd Group” as a Reference Resource with the following two clarifications and one exception: Clarification: The acceptance of these guidelines as a Reference Resource by AAALAC International pertains only to the technical information provided, and not the regulatory stipulations or legal implications (e.g., European Directive 2010/63/EU) presented in this article. AAALAC International considers the information regarding the humane care of cephalopods, including capture, transport, housing, handling, disease detection/ prevention/treatment, survival surgery, husbandry and euthanasia of these sentient and highly intelligent invertebrate marine animals to be appropriate to apply during site visits. Although there are no current regulations or guidelines requiring oversight of the use of invertebrate species in research, teaching or testing in many countries, adhering to the principles of the 3Rs, justifying their use for research, commitment of appropriate resources and institutional oversight (IACUC or equivalent oversight body) is recommended for research activities involving these species. Clarification: Page 13 (4.2, Monitoring water quality) suggests that seawater parameters should be monitored and recorded at least daily, and that recorded information concerning the parameters that are monitored should be stored for at least 5 years.
    [Show full text]
  • Cephalopod Ink: Production, Chemistry, Functions and Applications
    Mar. Drugs 2014, 12, 2700-2730; doi:10.3390/md12052700 OPEN ACCESS marine drugs ISSN 1660-3397 www.mdpi.com/journal/marinedrugs Review Cephalopod Ink: Production, Chemistry, Functions and Applications Charles D. Derby Neuroscience Institute and Department of Biology, Georgia State University, P.O. Box 5030, Atlanta, GA 30302-5030, USA; E-Mail: [email protected]; Tel.: +1-404-413-5393 Received: 14 March 2014; in revised form: 10 April 2014 / Accepted: 14 April 2014 / Published: 12 May 2014 Abstract: One of the most distinctive and defining features of coleoid cephalopods—squid, cuttlefish and octopus—is their inking behavior. Their ink, which is blackened by melanin, but also contains other constituents, has been used by humans in various ways for millennia. This review summarizes our current knowledge of cephalopod ink. Topics include: (1) the production of ink, including the functional organization of the ink sac and funnel organ that produce it; (2) the chemical components of ink, with a focus on the best known of these—melanin and the biochemical pathways involved in its production; (3) the neuroecology of the use of ink in predator-prey interactions by cephalopods in their natural environment; and (4) the use of cephalopod ink by humans, including in the development of drugs for biomedical applications and other chemicals for industrial and other commercial applications. As is hopefully evident from this review, much is known about cephalopod ink and inking, yet more striking is how little we know. Towards closing that gap, future directions in research on cephalopod inking are suggested. Keywords: Cephalopoda; cuttlefish; funnel organ; ink; ink sac; melanin; neuroecology; octopus; predator-prey; squid 1.
    [Show full text]
  • 4. List of Nominal Species
    Cephalopods of the World 213 4. LIST OF NOMINAL SPECIES The following list gives information (horizontally) in the order (i) the scientific name as it originally appeared, in alphabetical order according to the specific name; (ii) the author(s); (iii) date of publication; and (iv) present allocation. NOMINAL SPECIES PRESENT ALLOCATION NAUTILIDAE Nautilus belauensis Saunders, 1981 Nautilus belauensis Nautilus macromphalus Sowerby, 1849 Nautilus macromphalus Nautilus perforatus Conrad, 1847 Allonautilus perforatus Nautilus pompilius Linnaeus (1758) Nautilus pompilius Nautilus repertus Iredale, 1944 Nautilus repertus Nautilus scrobiculatus Lightfoot, 1786 Allonautilus scrobiculatus Nautilus stenomphalus Sowerby, 1849 Nautilus stenomphalus SEPIIDAE Acanthosepion whitleyana Iredale, 1926 Sepia whitleyana Arctosepia limata Iredale, 1926 Sepia limata Arctosepia rhoda Iredale, 1954 Sepia rhoda Blandosepia bartletti Iredale, 1954 Sepia bartletti Blandosepia baxteri Iredale, 1940 Sepia baxteri Doratosepion trygoninum Rochebrune, 1884 Sepia trygonina Glyptosepia opipara Iredale, 1926 Sepia opipara Hemisepius typicus Steenstrup, 1875 Sepia typica Rhombosepion hieronis Robson, 1924a Sepia hieronis Rhombosepion robsoni Massy, 1927 Sepia robsoni Sepia aculeata Van Hasselt, 1835 Sepia aculeata Sepia acuminata Smith, 1916 Sepia acuminata Sepia adami Roeleveld, 1972 Sepia adami Sepia andreana Steenstrup, 1875 Sepia andreana Sepia angulata Roeleveld, 1972 Sepia angulata Sepia apama Gray, 1849 Sepia apama Sepia appellofi Wülker, 1910 Sepia appellofi Sepia
    [Show full text]
  • Amanda Reid Publications to 2010 Refereed
    Amanda Reid Publications to 2010 Refereed papers as sole author Reid, A. (2009). Sepioloidea magna sp. nov.: a new bottletail squid (Cephalopoda : Sepiadariidae) from northern Australia. The Beagle. Records of the Museums and Art Galleries of the Northern Territory 25: 103–109. Reid, A.L. (2002). Western Australian Onychophora (Peripatopsidae): a new genus, Kumbadjena, for a southern species-complex. Records of the Western Australian Museum 21: 129–155. Reid, A.L. (2001). Sepia hedleyi Berry, 1918 (Cephalopoda: Sepiidae): a complete description and clarification of the status of S. dannevigi Berry, 1918 and S. rex (Iredale, 1926). Records of the South Australian Museum 34(2): 79–97. Reid, A.L. (2001). A new cuttlefish, Sepia grahami, sp. nov. (Cephalopoda: Sepiidae) from eastern Australia. Proceedings of the Linnean Society of New South Wales. 123: 159–172. Reid, A.L. (2000). Descriptions of Lathropatus nemorum, gen. et sp. nov., and six new Ooperipatus Dendy (Onychophora : Peripatopsidae) from south-eastern Australia. Proceedings of the Royal Society of Victoria. 112(2): 153–184. Reid, A. (2000). Eight new Planipapillus (Onychophora: Peripatopsidae) from southeastern Australia. Proceedings of the Linnean Society of New South Wales 122: 1–32. Reid, A.L. (2000). Australian cuttlefishes (Cephalopoda, Sepiidae) : the ‘doratosepion’ species complex, with descriptions of three new species. Invertebrate Taxonomy 14(1): 1–76. Reid, A.L. (1998). A complete description of Sepia mira (Cotton, 1932) (Cephalopoda: Sepiidae) from Eastern Australia. Proceedings of the Linnean Society of New South Wales 119: 155–171. Reid, A.L. (1996). A review of the Peripatopsidae (Onychophora) in Australia, with descriptions of new genera and species, and comments on Peripatopsid relationships.
    [Show full text]
  • Using Molluscan Eye Diversity to Understand Parallel and Convergent Evolution
    Evo Edu Outreach (2008) 1:439–447 DOI 10.1007/s12052-008-0084-1 ORIGINAL SCIENTIFIC ARTICLE Charting Evolution’s Trajectory: Using Molluscan Eye Diversity to Understand Parallel and Convergent Evolution Jeanne M. Serb & Douglas J. Eernisse Published online: 25 September 2008 # Springer Science + Business Media, LLC 2008 Abstract For over 100 years, molluscan eyes have been muscular foot common in other molluscan lineages. The used as an example of convergent evolution and, more largest classes by far are Gastropoda (snails, slugs; 60,000 recently, as a textbook example of stepwise evolution of a species) and Bivalvia (clams, oysters, mussels; 10,000 complex lens eye via natural selection. Yet, little is known species). Polyplacophora (chitons) and Cephalopoda (squids, about the underlying mechanisms that create the eye and octopuses) are smaller classes, each containing nearly 1,000 generate different morphologies. Assessing molluscan eye species. Of the seven molluscan classes, it is these four classes diversity and understanding how this diversity came about that possess eyes. will be important to developing meaningful interpretations Molluscan eyes are extremely varied, ranging from a of evolutionary processes. This paper provides an introduc- simple eye cup or pit eye that is open to the environment to tion to the myriad of eye types found in molluscs, focusing closed lens eyes much like those seen in fish (Fig. 1), on some of the more unusual structures. We discuss how compound eyes that superficially resemble the eyes of flies, molluscan eyes can be applied to the study of evolution by pinhole eyes, and eyes with mirrors. In fact, molluscs have examining patterns of convergent and parallel evolution and some of the greatest morphological diversity of eye types provide several examples, including the putative convergence among all animals, with seven to 11 different lineages of the camera-type eyes of cephalopods and vertebrates.
    [Show full text]