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A New Endemic Species of Lambis Röding, 1798 From the Philippines (Mollusca:
Neostromboidae: Strombidae)
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Dekkers, A. M., & Maxwell, S. J. (2022). A New Endemic Species of Lambis Röding, 1798 From the Philippines (Mollusca: Neostromboidae:
Strombidae). European Journal of Applied Sciences, 10(1). 393-400.
Supplementary Diagnosis: Ovoid, large and sturdy shells with digitations on the edge of the
outer lip. The number of digitations is usually 6 and a “7th” false digitation is the prolongation
of the anterior canal. Typical Lambis species have a smooth columella lacking spiral lirae and
with hardly any lirae on the inside of the labrum. Also, species occur with strong lirae on the
columella and inside of the labrum.
Remarks: Historically the species with strong lirae used to be included in the subgenus Millepes
Mörch, 1852; however more recently, authors have synonymized Millepes with Lambis [8,9].
For the Indian Ocean species with strong lirae, raised callus on the columella and a bifurcated
first digitation, Ophioglossolambis Dekkers, 2012 was introduced [8,9].
Lambis vertriesti n. sp.
Figures 2 and 3
Type Material: Holotype - Nocnocan Island, Bohol, Philippines, 2019, 146.1 mm (MNHN-IM-
2000-37203); Paratype 1 - Banacon Island, Bohol, Philippines 2019, 118 mm (SMC 111.001);
Paratype 2 - Banacon Island, Bohol, Philippines 2019, 127 mm (SMC 111.002); Paratype 3 -
Nocnocan, Bohol, Philippines, 2019, 134.8 mm (GVC A); B) Paratype 4 - Nocnocan, Bohol,
Philippines, 2019, 131.7 mm (GVC C); Paratype 5 - Nocnocan, Bohol, Philippines, 2019, 144.4
mm (GVC D); Paratype 6 - Bohol, Philippines, 2018, 154.5 mm (GVC H); Paratype 7 - Bohol,
Philippines, 2006. 144 mm (AMD STR1458); Paratype 8 - Bohol, Philippines, 2006, 127.5 mm
(AMD STR1601); Paratype 9 - Panglao, Bohol, Philippines, 2007, 113 mm (AMD STR1605);
Paratype 10 - Inabanga, Bohol, Philippines (GVC I); Paratype 11 - Banacon Island, Bohol,
Philippines, 2020, 125 mm (SMC 111.003).
Type Location: Bohol Island, Philippines.
Description: Shell typical ovoid form for a Lambis species, with relative short digits, solid and
heavy. Shell height with posterior spine up to 140 mm, without the posterior spine around 110
mm. Shell bears normally 6 spines on the apertural rim. Anterior spine (anterior channel) ca.
20-25 mm and bending to the left seen dorsally; first thick and quickly turning to slim and
bending like a hook. First digit bends to the right leaning against the apex. The second digit
straight forward or slightly to the left, forming the largest interdigitalis distance with the first
digit and often have a slight ‘V ’ form together. Third digit bends to the left and adapical and
thus forming a 3-dent fork with the first and the second digit. The 4th, 5th and 6th digit relatively
short, evenly spaced and bending to the left and adapical. Dorsally bearing strong ridges with
strong knobs, of which the first ends in the first digit. The second and strongest splits beyond
the whorl into the second, third and fourth digit. The other digits have a ridge each. In between
the primary strong ridges multiple secondary spiral ridges of which some are a bit stronger and
those are ending in a pseudo digit. Strombiodal notch present and on both sides reinforced with
a ridge ending in a small spine. In between the strombiodal notch and the anterior channel a
downward flap with 4-5 fingers. The apex is sharp pointed. The early whorl rapidly widens.
Spire whorls bearing minute spiral lines and axial growth lines; the bottom of each whorl has a
raised ridge with knobs that in the adult stage becomes the ridge to the second, third and fourth
digit. Digits at the underside (ventral side) with a cut in the middle following the length of the
digit; the mark of the retreating mantel that formed the digit. The base of the digit is overgrown
with callus that is put on by the mantel when getting the full adult stage, in lobes form. Only
URL: http://dx.doi.org/10.14738/aivp.101.11712 395
European Journal of Applied Sciences (EJAS) Vol. 10, Issue 1, February-2022
with the first and second digit a gutter is still visible in the aperture. The slightly bent columella
is bearing a callus pad at the bottom half, normally ca. 1.5 to 2 cm. The upper part of the
columella is decorated with strong lirae. Shorter lirae also in the lower part running from the
callus pad into the aperture. Inside of the labrum with many strong lirae, the ones at the
adapical and the abapical end the strongest. Deeper inside the shell smooth and cream
coloured; before that entrance of the shell a band of about 1 cm of a bit of orange colour. Base
colour of the shell cream-brownish, but darker to almost black is not uncommon; often with
irregular brown flecks. The underside of the digits often light coloured to whiteish. Operculum
as in Lambis lambis: not serrated, dark brown and smooth.
Etymology: The species is named after Goran Vertriest who donated the type material and
offered a number of specimens for examination.
Comparison and Remarks: Lambis lambis is always without lirae in the aperture. This
common species of the genus can also grow much larger, even over 200 mm. Lambis lambis has
two main forms which are sex related: females have a larger and often broader shell with the
digits strongly curving up dorsally; males typically have smaller shell with the digits
horizontally levelled. The new species never has upward curved digits. Lambis lambis typically
has 6 digits.
Lambis millepeda generally bears 9 digits, that are always short especially along the side of the
aperture, and strongly adapical curved. The inside of the aperture is full of lirae, purplish
coloured in freshly caught specimens with often black in between the lirae. The black colour is
always missing in the new species; instead, L. millepeda gets darker purple to blackish. The
purple colour in L. milepeda often loses quickly the bright purple colour and fades to pinkish or
light brown.
DISCUSSION
The Lambis is known to have a number of regional species, and L. vertriesti n. sp. is also highly
localised being from the central Philippines. The Philippines is a hotspot for Lambis with six of
the eleven known species frequenting the region. The small range of the new species highlights
the importance of the central Philippines as a biodiversity hotspot for a wide range of unique
organisms both marine and terrestrial [9-11].
There are two main biogeographic hypotheses seek to explain the high level of biodiversity
[12]: the centre of origin theory; and the centre of accumulation theory. The central Philippines,
has remained relatively stable in terms of land sea boundaries during interglacial fluctuations,
and with many regional currents dominating the archipelago, leading to a centre of regional
maximum diversity, indicating that the centre of accumulation theory may best explain the high
level of biodiversity in the central Philippine region [13,14]. The central Philippines is an
archipelago that is subjected to a number of inflows, from the western Pacific currents and the
South China Sea, with the primary outflow through the Sulu Sea. The inflows into Indonesia
remained relatively stable with changes in sea level, leading to a high degree of shared taxa
having first arisen from that area as exemplified by the new species herein, and supporting it
as a centre of origin on a regional scale [13-15].
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Services for Science and Education – United Kingdom
Dekkers, A. M., & Maxwell, S. J. (2022). A New Endemic Species of Lambis Röding, 1798 From the Philippines (Mollusca: Neostromboidae:
Strombidae). European Journal of Applied Sciences, 10(1). 393-400.
ACKNOWLEDGEMENTS
We thank Goran Vertriest, Belgium, for donating the holotype and collection information.
References
[1]. Abbott, R.T., The genus Lambis in the Indo-Pacific. Indo-Pacific Mollusca, 1961. 1: p. 147-174.
[2]. Dekkers, A.M., Revision of the family Strombidae (Gastropoda) on the supra specific level. Part1. De Kreukel,
2008. 44: p. 35-64.
[3]. Liverani, V., The superfamily Stromboidea. Addenda and corrigenda. In A Conchological Iconography, Poppe,
G.T., Groh, K., Renker, C., Eds.; Conchbooks: Harxheim, Germany, 2014. 54 pp.
[4]. Shikama, T., On some noteworth marine gastropoda from southwest Japan (III). Science Reports of the
Yokahama National University, 1971. 18: p. 27-35.
[5]. Maxwell, S.J. & A.M. Dekkers, A newname for Altivasum typicum Hedley, 1916 fide Dekkers and Maxwell, 2018
and the description of Altivasum clarksoni nov. sp.. The Festivus, 2019, 51(2): p. 171-176.
[6]. Maxwell, S.J., et al., Defining and bringing relevance of meaning to species group level taxa. Proceedings of the
Biological Society of Washington, 2021. 134: p. 27-28.
[7]. Röding, P.F., Museum Boltenianum sive Catalogus Cimeliorum e Tribus Regnis Naturæ quæ Olium Collegerat
Jon. Fried Bolten, M.D.p.d. per X: Pars Secunda Continens Conchylia sive Testacea Univalvia, Bivalvia and
Multivalvia. Typis Johan. Christi. Trappii; Hamburgi, Germany, 1798. 199 pp.
[8]. Dekkers A.M., A new genus related to the genus Lambis Röding, 1798 (Gastropoda: Strombidae) from the Indian
Ocean. Gloria Maris, 2012, 51 (2-3): 68-74. [8 April 2012; title page erroneously dated 11 March].
[9]. Damaška, A.F., D.J. Mohagan, and M. Fikácek, Moss-inhabiting flea beetles in the Philippines (Coleoptera,
Chrysomelidae, Alticinae). ZooKeys, 2020. 960: p. 125–142.
[10]. Maxwell, S.J., et al., Studies in Canarium urceus (Linné, 1758) Part 2: Strombus anatellus Duclos, 1844,
Strombus crassilabrum Anton, 1839, Strombus incisus Wood, 1828 and Strombus ustulatus form laevis Dodge, 1946
(Neostromboidae: Strombidae). The Festivus, 2020. 52(4): p. 335-344.
[11]. Supsup, C.E., et al., Variation in species richness, composition and herpetological community structure across a
tropical habitat gradient of Palawan Island, Philippines. Herpetozoa (Wien), 2020; 33: p. 95-11.
[12]. Gaither, M.R. and L.A. Rocha, Origins of species richness in the Indo-Malay-Philippine biodiversity hotspot:
evidence for the centre of overlap hypothesis. Journal of Biogeography, 2013. 40(9): p. 1638–1648.
[13]. DeVantier, L. and E. Turak, Species Richness and Relative Abundance of Reef-Building Corals in the Indo-West
Pacific. Diversity, 2017. 9(3): 25.
[14]. Yang, Y., et al., Ancient geographical barriers drive differentiation among Sonneratia caseolaris populations
and recent divergence from S. lanceolata. Frontiers in Plant Science, 2016. 7: 1618.
[15]. Carpenter, K.E., et al., Comparative phylogeography of the Coral Triangle and Implications for Marine
Management. Journal of Marine Biology, 2011. 2011: 396982.
Figure 1: Lectotypes from the Linnean Collection, London: A) Lambis lambis (Linné, 1758) (G-M
0010148 Strombus lambis); B) Lambis millepeda (Linné, 1758) (G-M 0010272 Strombus
millepeda) (https://www.linnean.org/research-collections/linnaean-collections)
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Services for Science and Education – United Kingdom
Dekkers, A. M., & Maxwell, S. J. (2022). A New Endemic Species of Lambis Röding, 1798 From the Philippines (Mollusca: Neostromboidae:
Strombidae). European Journal of Applied Sciences, 10(1). 393-400.
Figure 2 : Lambis vertriesti n. sp. : A) Holotype - Nocnocan Island, Bohol, Philippines, 2019,
146.1 mm (MNHN-IM-2000-37203); B) Paratype 1 - Banacon Island, Bohol, Philippines 118 mm
(SMC 111.001); C) Paratype 2 - Banacon Island, Bohol, Philippines 127 mm (SMC 111.002)
Figure 3: Lambis vertriesti n. sp.: A) Paratype 3 - Nocnocan, Bohol, Philippines, 2019, 134.8 mm
(GVC A); B) Paratype 4 - Nocnocan, Bohol, Philippines, 2019, 131.7 mm (GVC C); C) Paratype 5 -
Nocnocan, Bohol, Philippines, 2019, 144.4 mm (GVC D); D) Paratype 6 - Bohol, Philippines,
2018, 154.5 mm (GVC H); E) Paratype 7 - Bohol, Philippines, 2006, 144 mm (AMD STR1458); F)
Paratype 8 - Bohol, Philippines, 2006, 127.5 mm (AMD STR1601); G) Paratype 9 - Panglao,
Bohol, Philippines, 2007, 113 mm (AMD STR1605); H) Paratype 10 - Inabanga, Bohol,
Philippines (GVC I); I) Paratype 11 - Banacon Island, Bohol, Philippines 125 mm (SMC 111.003)
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