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International Journal of Marine Science 2015, Vol.5, No.32, 1-3
http://ijms.biopublisher.ca
1
A Letter Open Access
Note on the Genus maretia gray, 1855 and Description of Maretia planulata
(Lamarck, 1816) (Echinoidea, Spatangoida), off Thoothukudi Coast of Gulf of
Mannar, India (08º 35’22.5” N 78º 27’40.9 E) – (310 M)
T. Vaitheeswaran , T. Rajasekaran, S. Balasubramani
Rarbio Energies Private Limited, Department of New Drug Discovery (Marine Division), #311/2, Vellalar Street, Mel Ayanambakkam, Chennai- 600 95, Tamil
Nadu, India
Corresponding author email: fdre@rarbio.com
International Journal of Marine Science, 2015, Vol.5, No.32 doi: 10.5376/ijms.2015.05.0032
Received: 20 Mar., 2015
Accepted: 06 May., 2015
Published: 20 May., 2015
Copyright © 2015 Vaitheeswaran et al., This is an open access article published under the terms of the Creative Commons Attribution License, which permits
unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Preferred citation for this article:
Vaitheeswaran et al., 2015, Note on the Genus maretia gray, 1855 and Description of Maretia planulata (Lamarck, 1816) (Echinoidea, Spatangoida), off
Thoothukudi Coast of Gulf of Mannar, India (08º 35’ 22.5” N 78º 27’ 40.9 E) – (310 M), International Journal of Marine Science, Vol.5, No.32 1-3 (doi:
10.5376/ijms.2015.05.0032)
Abstract Heart sea-urchin was collected from Thoothukudi coast of Gulf of Mannar, Southeast coast of India on April 11, 2014.
This specimen was classified as Maretia planulata (Lamarck, 1816) belonging to the family Spatangidae. The most speciose echinoid
orders, Spatangoida and Clypeasteroida, are abundant in the Indo-West Pacific and Caribbean. This genus and species are newly
recorded in two distinct Indo-Pacific marine zones. One specimen was caught at the depth of 310 m as an incidental by-catch. It was
found in tropical waters from about 08º 35’ 22.5”N 78º 27’ 40.9 E/310 m from Thoothukudi fishing harbour, southeast coast of India.
This species inhabits tropical waters and usually distributed over the West Pacific from southern Japan to Australia.
Keywords Spatangidae; Maretia planulata; First record; Thoothukudi coast; Gulf of Mannar
Introduction
The genus Hemipatagus was established in 1858 by
Desor for the species Spatangus hoffmanni Goldfuss,
1829. Subsequently, Agassiz (1873) placed
Hemipatagus is synonymy with Maretia Gray, 1855.
Heart sea-urchins represent the largest group of
irregular echinoids. There are well over 200 living
species assigned to some 60 genera representative of
10 families, occurs in the Indo-West Pacific. Heart
sea-urchin is capable of burrowing and living within
most sediments, hence their worldwide distribution
(Joe Chiold, 2013). Individual geographic ranges
worldwide are illustrated in map form for 414
echinoid species. Few forms show widespread ranges,
the exceptions being Metalia sternalis, Brissopsis
luzonica, Brissus latecarinatus, Metalia spatangus,
Maretia planulata, and Echinocardium cordatum (Joe
Chiold, 2013). The East Indian Ocean harbors a rich
array of heart sea-urchin forms. Thirty-five or more
species occur here representing over 20 genera from
seven families.
Mortensen (1951) noted that the presence of ampullae
was not verified in the type species of Hemipatagus.
The other two features listed by him were: 1. a more
heart shaped outline with deeper frontal notch. 2. The
broader, bilobed subanal fasciole in Hemipatagus.
Smith (2004) noted the high similarity between
Hemipatagus and Lovenia and proposed its inclusion
in the Loveniidae. Apparently there are no records
from Western India, Pakistan, the Persian Gulf or the
Indian coast of the Arabian Peninsula. In view of this
the colouration differences noted by Mortensen (1951)
may be more meaningful than he considered they were.
He described a whitish to yellow colouration in Indian
Ocean populations, verus Malayan specimens, which
are usually dark.
Spatangoids are echinoids characterized by their
bilaterally summetrical corona and highly modified
ambulacra forming a complex respiratory apparatus.
They are well adapted to a life as burrowers and
ploughers in mobile sediments, exploiting organic
detritus as their prime food resource. Indeed,
spatangoid phylogeny and higher-rank taxonomy
has been heavily reliant on fascioles. These are
narrow bands of small ciliate spines secreting
mucus that consolidated the walls of their burrows
and protects the respiratory tube feet from fine mud
(Lawrence, 1987).
International Journal of Marine Science 2015, Vol.5, No.32, 1-3
http://ijms.biopublisher.ca
2
Spatangus planulatus Lamarck, 1816, p. 326
Spatangus (Maretia) perornatus Schaffer, 1912: 190-1;
pl. 59, fig. 4-6
Maretia perornata, Schaffer, 1912: 596; pl. 1, fig. 5-6
M. planulata Ali, 1985: 294-295; figs 12 A-B
M. ranjitpurensis Jain, 2002: 130-132; pl. 6, figs. 11-14
M. carolinensis Kier, 1997: 11-13; fig. 6; pl. 9, figs
8-9; pl. 10, figs. 1-7; pl. 11, figs. 1-2
1 Material
Measuring 8.3 cm total length and 15 g weight (Figure
1 and 2)
2 Locality
08º 35’ 22.5”N 78º 27’ 40.9 E off Thoothukudi coast
of Gulf of Mannar, Southeast coast of India; depth at
trawling 310 m.
3 Description
Maretia planulata, the frontal sinus is shallower and
often indistinct 2. The labrum is much narrower and
more elongated 3. The Posterior end is bluntly pointed
not transversely truncated 4. Even in large specimens
the primary tubercles do not develop true ampullae or
strongly sunken areoles. Especially not on the oral
surface 5. The plastron is much more strongly
constricted between the first and second pair of
episternal plates (Figure 1) 6. The outline of the test is
oval, antero-posteriorly elongated, not cordiform 7.
The subanal fasciole is oval and rather high instead of
bilobed, very wide and low 8. The labrum and the
primordial plates of the interambulacra extend much
further 9. There are phyllodal pores (14-15) in
ambulacra II and IV (only 6-7 in H. hoffmanni) 10.
Figure 1 Dorsal view – Maretia planulata
Ambulacra II and IV are only slightly constricted
ambitally, whereas they are strongly constricted in H.
hoffmanni.
4 Remarks
Extant species of Maretia, principally M. planulata,
are currently considered to occur in two distinct
Indo-Pacific marine zones. Maretia differs by
possessing an extremely shallow frontal notch, the
distribution of the aboral primary tubercles (primary
tubercle reach the tips of the posterior pairedpetals), the
lack of strongly sunken areoles or camellate aboral and
oral primary tubercles, the strongly crenulate nature of
the aboral primary tubercles, the lack of a conspicuous
field of coarse tubercles in adapical interambulacral
columns 2b and 3a, its oval ‘t’ shield-shaped subanal
fasciole, the longer primordial plates of the paired
interabulacra (Figure 1 and 2) which extend to the third
or fourth ambulacral plates of the adjacent ambulacra
in Maretia, while they do not extend the second
ambulacral plate in (Hemipatagus or Lovenia), the
labrum which extends to the third or fourth ambulacral
plate (not extending beyond) the second ambulacral
plate in Hemipatagus and Lovenia and the less
constricted adoral ambulacra 2 and 3 (Figure 1).
5 Distribution
Extant species of Maretia, principally M. planulata,
are currently considered to occur in two distinct
Indo-Pacific marine zones: From southern India and
Figure 2 Ventral view – Maretia planulata
International Journal of Marine Science 2015, Vol.5, No.32, 1-3
http://ijms.biopublisher.ca
3
Sri Lanka, eastwards across the Indo-Malayan
Archipelago, Indonesia, the Philippines, Papua New
Guinea, north and east Australia, and western Pacific
Islands from Japan in the north to Fiji and New
Caledonia in the south, and as far east as Hawaii. This
latter species is the most widely distributed of the
spatangoids; it can be found in nearly all major oceans,
but it is absent from the mid-Atlantic, North Australia,
and the East Indies. A little over half of the Indo-West
Pacific species are endemic. This is true particularly
among the families Brissidae, Spatangidae, Lovenidae
and Pericosmidae. M. planulata Indonesia (Mortensen,
1951), M. planulata Papua New Guinea (Lindley,
2003), M. planulata South Sea Islands (Nisiyama,
1968), Maretia sp. New Zealand (Henderson, 1975),
Agassizia aequipetala United Kingdom (Gregory,
1891).
Author’s Contribution
Vaitheeswaran Thiruvengadam have been collected and
identification of specimen and took photograph of specimen
and reference collection. Rajsekaran T, Managing Director of
RARBIO Energies Pvt Ltd, Financial support of Marine
Invertebrate Division and Marine Pharma division, Chennai,
India. Balasubramani S, Director of RARBIO Energies Pvt Ltd.,
conceived of the study, help and support of Fishing landing
centre, Chennai, India.
References
Agassiz, 1873, Revision of the Echini. Memoirs of the Museum of
Comparative Zoology at Harward College. III: pt.3:379-628 +1.
Pls.50-77
Ali M.S.M., 1985, On some Pliocene echinoids from the area north of
Mersa Alam, Red Sea coast, Egypt. Paldontologische Zeitschrift 59:
277-300
http://dx.doi.org/10.1007/BF02988814
Henderson R.A., 1975, Cenozoic spatangoid echinoids from New Zealand.
New Zealand Geological Survey Paleontological Bulletin 46: 1-128
Gregory J.W., 1891, A revision of the British Fossil Cainozoic Echinoidea.
Proceedings of the Geologists Association 12(1): 16–60, pls 1-2
Jain R.L., 2002, Echinoids from the Gaj Formation (early and middle
Miocene) of Kathiawar, Gujarat, India. Journal of the Paleontological
Society of India 47: 107-135
Joe Chiold, 2013, Species distributions of irregular echinoids. Biological
Oceanography. Vol. 6, pp. 79-162
Kier P.M., 1997, Oligocene echinoids of North Carolina. Smithsonian
Contributions to Paleobiology. 55: 1-336, 90 pls
Mortensen T., 1951, A monograph of the Echinoidea 5(2). Spatangoida 2.
Amphisternata 2. Spatangidae. Loveniidae, Pericosmidae, Schizasteridae,
Brissidae. C. A. Reitzel: Copenhagen. 593 pp. + separate atlas 30 pp.,
64 pls
Nisiyama S., 1968, The echinoid fauna from Japan and adjacent regions.
Part 2. Palaeontological Society of Japan Special Papers 13: 1-495, pls.
19-30
Lam Lamarck J.B.P.M.D., 1816, Histoire Naturelle des Animaux
sansVert`ebres, pr´esentant Lcaract`eres g´en´eraux et particuliers de
cesanimaux, leur distribution, leur classes, leurs familles, leurs genres,et
le citation des principales esp`eces qui s’y rapportent pr´ ec´ed´eed’
uneIntroductionoffrantla D´ eterminationdescaract eresessentiellesde
l’animal, sa distinction du v´ eg´etal et des autres corps naturels,enfin,
l’Exposition des Principes fondamentaux de la Zoologie. Tome
Troisi`eme. Verdi`ere, Paris, 586 pp
Lawrence J.M., 1987, A functional biology of Echinoderms. Croom Helm
Ltd. Publishers, Kent, 352 pp
Lindley I.D., 2003, Echinoids of the Kairuka Formation (Lower Pliocene),
Yule Island, Papua New Guinea: Spatangoida. Proceedings of the
Linnean Society of New South Wales 124: 153-162
Smith A.B., 2004, The Echinoid Directory. World Wide Web electronic
publication. Available at:
http://www.nhm.ac.uk.science-projects/echinoids
Schaffer F.X., 1912, Die Echiniden der Mioc¨anbildung von Eggen-burg
Abhandlungen der Geologischen Reichsanstalt. 22 (2): 187–192, pls
58-60

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  • 1. International Journal of Marine Science 2015, Vol.5, No.32, 1-3 http://ijms.biopublisher.ca 1 A Letter Open Access Note on the Genus maretia gray, 1855 and Description of Maretia planulata (Lamarck, 1816) (Echinoidea, Spatangoida), off Thoothukudi Coast of Gulf of Mannar, India (08º 35’22.5” N 78º 27’40.9 E) – (310 M) T. Vaitheeswaran , T. Rajasekaran, S. Balasubramani Rarbio Energies Private Limited, Department of New Drug Discovery (Marine Division), #311/2, Vellalar Street, Mel Ayanambakkam, Chennai- 600 95, Tamil Nadu, India Corresponding author email: fdre@rarbio.com International Journal of Marine Science, 2015, Vol.5, No.32 doi: 10.5376/ijms.2015.05.0032 Received: 20 Mar., 2015 Accepted: 06 May., 2015 Published: 20 May., 2015 Copyright © 2015 Vaitheeswaran et al., This is an open access article published under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Preferred citation for this article: Vaitheeswaran et al., 2015, Note on the Genus maretia gray, 1855 and Description of Maretia planulata (Lamarck, 1816) (Echinoidea, Spatangoida), off Thoothukudi Coast of Gulf of Mannar, India (08º 35’ 22.5” N 78º 27’ 40.9 E) – (310 M), International Journal of Marine Science, Vol.5, No.32 1-3 (doi: 10.5376/ijms.2015.05.0032) Abstract Heart sea-urchin was collected from Thoothukudi coast of Gulf of Mannar, Southeast coast of India on April 11, 2014. This specimen was classified as Maretia planulata (Lamarck, 1816) belonging to the family Spatangidae. The most speciose echinoid orders, Spatangoida and Clypeasteroida, are abundant in the Indo-West Pacific and Caribbean. This genus and species are newly recorded in two distinct Indo-Pacific marine zones. One specimen was caught at the depth of 310 m as an incidental by-catch. It was found in tropical waters from about 08º 35’ 22.5”N 78º 27’ 40.9 E/310 m from Thoothukudi fishing harbour, southeast coast of India. This species inhabits tropical waters and usually distributed over the West Pacific from southern Japan to Australia. Keywords Spatangidae; Maretia planulata; First record; Thoothukudi coast; Gulf of Mannar Introduction The genus Hemipatagus was established in 1858 by Desor for the species Spatangus hoffmanni Goldfuss, 1829. Subsequently, Agassiz (1873) placed Hemipatagus is synonymy with Maretia Gray, 1855. Heart sea-urchins represent the largest group of irregular echinoids. There are well over 200 living species assigned to some 60 genera representative of 10 families, occurs in the Indo-West Pacific. Heart sea-urchin is capable of burrowing and living within most sediments, hence their worldwide distribution (Joe Chiold, 2013). Individual geographic ranges worldwide are illustrated in map form for 414 echinoid species. Few forms show widespread ranges, the exceptions being Metalia sternalis, Brissopsis luzonica, Brissus latecarinatus, Metalia spatangus, Maretia planulata, and Echinocardium cordatum (Joe Chiold, 2013). The East Indian Ocean harbors a rich array of heart sea-urchin forms. Thirty-five or more species occur here representing over 20 genera from seven families. Mortensen (1951) noted that the presence of ampullae was not verified in the type species of Hemipatagus. The other two features listed by him were: 1. a more heart shaped outline with deeper frontal notch. 2. The broader, bilobed subanal fasciole in Hemipatagus. Smith (2004) noted the high similarity between Hemipatagus and Lovenia and proposed its inclusion in the Loveniidae. Apparently there are no records from Western India, Pakistan, the Persian Gulf or the Indian coast of the Arabian Peninsula. In view of this the colouration differences noted by Mortensen (1951) may be more meaningful than he considered they were. He described a whitish to yellow colouration in Indian Ocean populations, verus Malayan specimens, which are usually dark. Spatangoids are echinoids characterized by their bilaterally summetrical corona and highly modified ambulacra forming a complex respiratory apparatus. They are well adapted to a life as burrowers and ploughers in mobile sediments, exploiting organic detritus as their prime food resource. Indeed, spatangoid phylogeny and higher-rank taxonomy has been heavily reliant on fascioles. These are narrow bands of small ciliate spines secreting mucus that consolidated the walls of their burrows and protects the respiratory tube feet from fine mud (Lawrence, 1987).
  • 2. International Journal of Marine Science 2015, Vol.5, No.32, 1-3 http://ijms.biopublisher.ca 2 Spatangus planulatus Lamarck, 1816, p. 326 Spatangus (Maretia) perornatus Schaffer, 1912: 190-1; pl. 59, fig. 4-6 Maretia perornata, Schaffer, 1912: 596; pl. 1, fig. 5-6 M. planulata Ali, 1985: 294-295; figs 12 A-B M. ranjitpurensis Jain, 2002: 130-132; pl. 6, figs. 11-14 M. carolinensis Kier, 1997: 11-13; fig. 6; pl. 9, figs 8-9; pl. 10, figs. 1-7; pl. 11, figs. 1-2 1 Material Measuring 8.3 cm total length and 15 g weight (Figure 1 and 2) 2 Locality 08º 35’ 22.5”N 78º 27’ 40.9 E off Thoothukudi coast of Gulf of Mannar, Southeast coast of India; depth at trawling 310 m. 3 Description Maretia planulata, the frontal sinus is shallower and often indistinct 2. The labrum is much narrower and more elongated 3. The Posterior end is bluntly pointed not transversely truncated 4. Even in large specimens the primary tubercles do not develop true ampullae or strongly sunken areoles. Especially not on the oral surface 5. The plastron is much more strongly constricted between the first and second pair of episternal plates (Figure 1) 6. The outline of the test is oval, antero-posteriorly elongated, not cordiform 7. The subanal fasciole is oval and rather high instead of bilobed, very wide and low 8. The labrum and the primordial plates of the interambulacra extend much further 9. There are phyllodal pores (14-15) in ambulacra II and IV (only 6-7 in H. hoffmanni) 10. Figure 1 Dorsal view – Maretia planulata Ambulacra II and IV are only slightly constricted ambitally, whereas they are strongly constricted in H. hoffmanni. 4 Remarks Extant species of Maretia, principally M. planulata, are currently considered to occur in two distinct Indo-Pacific marine zones. Maretia differs by possessing an extremely shallow frontal notch, the distribution of the aboral primary tubercles (primary tubercle reach the tips of the posterior pairedpetals), the lack of strongly sunken areoles or camellate aboral and oral primary tubercles, the strongly crenulate nature of the aboral primary tubercles, the lack of a conspicuous field of coarse tubercles in adapical interambulacral columns 2b and 3a, its oval ‘t’ shield-shaped subanal fasciole, the longer primordial plates of the paired interabulacra (Figure 1 and 2) which extend to the third or fourth ambulacral plates of the adjacent ambulacra in Maretia, while they do not extend the second ambulacral plate in (Hemipatagus or Lovenia), the labrum which extends to the third or fourth ambulacral plate (not extending beyond) the second ambulacral plate in Hemipatagus and Lovenia and the less constricted adoral ambulacra 2 and 3 (Figure 1). 5 Distribution Extant species of Maretia, principally M. planulata, are currently considered to occur in two distinct Indo-Pacific marine zones: From southern India and Figure 2 Ventral view – Maretia planulata
  • 3. International Journal of Marine Science 2015, Vol.5, No.32, 1-3 http://ijms.biopublisher.ca 3 Sri Lanka, eastwards across the Indo-Malayan Archipelago, Indonesia, the Philippines, Papua New Guinea, north and east Australia, and western Pacific Islands from Japan in the north to Fiji and New Caledonia in the south, and as far east as Hawaii. This latter species is the most widely distributed of the spatangoids; it can be found in nearly all major oceans, but it is absent from the mid-Atlantic, North Australia, and the East Indies. A little over half of the Indo-West Pacific species are endemic. This is true particularly among the families Brissidae, Spatangidae, Lovenidae and Pericosmidae. M. planulata Indonesia (Mortensen, 1951), M. planulata Papua New Guinea (Lindley, 2003), M. planulata South Sea Islands (Nisiyama, 1968), Maretia sp. New Zealand (Henderson, 1975), Agassizia aequipetala United Kingdom (Gregory, 1891). Author’s Contribution Vaitheeswaran Thiruvengadam have been collected and identification of specimen and took photograph of specimen and reference collection. Rajsekaran T, Managing Director of RARBIO Energies Pvt Ltd, Financial support of Marine Invertebrate Division and Marine Pharma division, Chennai, India. Balasubramani S, Director of RARBIO Energies Pvt Ltd., conceived of the study, help and support of Fishing landing centre, Chennai, India. References Agassiz, 1873, Revision of the Echini. Memoirs of the Museum of Comparative Zoology at Harward College. III: pt.3:379-628 +1. Pls.50-77 Ali M.S.M., 1985, On some Pliocene echinoids from the area north of Mersa Alam, Red Sea coast, Egypt. Paldontologische Zeitschrift 59: 277-300 http://dx.doi.org/10.1007/BF02988814 Henderson R.A., 1975, Cenozoic spatangoid echinoids from New Zealand. New Zealand Geological Survey Paleontological Bulletin 46: 1-128 Gregory J.W., 1891, A revision of the British Fossil Cainozoic Echinoidea. Proceedings of the Geologists Association 12(1): 16–60, pls 1-2 Jain R.L., 2002, Echinoids from the Gaj Formation (early and middle Miocene) of Kathiawar, Gujarat, India. Journal of the Paleontological Society of India 47: 107-135 Joe Chiold, 2013, Species distributions of irregular echinoids. Biological Oceanography. Vol. 6, pp. 79-162 Kier P.M., 1997, Oligocene echinoids of North Carolina. Smithsonian Contributions to Paleobiology. 55: 1-336, 90 pls Mortensen T., 1951, A monograph of the Echinoidea 5(2). Spatangoida 2. Amphisternata 2. Spatangidae. Loveniidae, Pericosmidae, Schizasteridae, Brissidae. C. A. Reitzel: Copenhagen. 593 pp. + separate atlas 30 pp., 64 pls Nisiyama S., 1968, The echinoid fauna from Japan and adjacent regions. Part 2. Palaeontological Society of Japan Special Papers 13: 1-495, pls. 19-30 Lam Lamarck J.B.P.M.D., 1816, Histoire Naturelle des Animaux sansVert`ebres, pr´esentant Lcaract`eres g´en´eraux et particuliers de cesanimaux, leur distribution, leur classes, leurs familles, leurs genres,et le citation des principales esp`eces qui s’y rapportent pr´ ec´ed´eed’ uneIntroductionoffrantla D´ eterminationdescaract eresessentiellesde l’animal, sa distinction du v´ eg´etal et des autres corps naturels,enfin, l’Exposition des Principes fondamentaux de la Zoologie. Tome Troisi`eme. Verdi`ere, Paris, 586 pp Lawrence J.M., 1987, A functional biology of Echinoderms. Croom Helm Ltd. Publishers, Kent, 352 pp Lindley I.D., 2003, Echinoids of the Kairuka Formation (Lower Pliocene), Yule Island, Papua New Guinea: Spatangoida. Proceedings of the Linnean Society of New South Wales 124: 153-162 Smith A.B., 2004, The Echinoid Directory. World Wide Web electronic publication. Available at: http://www.nhm.ac.uk.science-projects/echinoids Schaffer F.X., 1912, Die Echiniden der Mioc¨anbildung von Eggen-burg Abhandlungen der Geologischen Reichsanstalt. 22 (2): 187–192, pls 58-60