Rahul Sharma (Editor)

Acochlidiacea

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Kingdom
  
Animalia

Class
  
Gastropoda

Phylum
  
Mollusca

Acochlidiacea

Acochlidiacea, common name acochlidians, are a taxonomic clade of very unusual sea snails and sea and freshwater slugs, aquatic gastropod mollusks within the large clade Heterobranchia. Acochlidia is a variant spelling.

Contents

Description

These are mostly very small animals, without a shell or gills, distinguished by the visceral mass being sharply set off from the rest of the body.

Being a small group with only 30 species worldwide known in 2010, and 32 species described in 2011, and 33 in 2012 (+9 undescribed Pontohedyle species), these slugs are morphologically and biologically highly aberrant and diverse, comprising a series of unusual characters (e.g. secondary gonochorism, lack of copulatory organs, asymmetric radulae). Most acochlidians live interstitially in marine sands, while some have conquered limnic systems (uniquely within opisthobranch gastropods).

Taxonomy

Nils Hjalmar Odhner established this taxon as a family in 1937, when he created the families Microhedylidae and Acochlidiidae. In 1939, he treated this taxon as an order.

Rankin (1979) treated this taxon as an order, the order Acochlidioidea.

Salvini-Plawen (1983) wrote this taxon as Acochlidiomorpha.

Anderson (1992) treated this taxon as the order Acochlidiida.

Burn in Beesley et al. (1998), wrote this taxon as the order Acochlidea.

Wawra (1987) and various authors (2007–2010) spelled this taxon as Acochlidia.

Three families (Hedylopsidae, Microhedylidae and Acochlidiidae) are classically recognized. Two controversial classifications (Rankin 1979, Starobogatov 1983) have been proposed recently, but they have not been evaluated since.

An alternative classification by Burn (in Beesley et al., 1998) for the Australian species recognizes 2 superfamilies and 5 families.

The Acochlidia, a traditional "order" of the Opisthobranchia since their establishment by Odhner have formed one of the unsolved mysteries within Euthyneura. Their monophyly is widely accepted especially since a proposed sister group relationship of the acochlidian family Ganitidae with Sacoglossa (based on the dagger-shaped radula teeth) could be rejected based on a comprehensive parsimony analysis of morphological characters. During the last years a series of studies have redescribed key acochlidian taxa in great detail, including 3D reconstructions, and added considerably to the morphological and biological knowledge of this previously little understood group.

Most recent morphological analyses suggested a common origin with either the equally enigmatic Rhodopemorpha, the diaphanid cephalaspidean Toledonia, or with runcinid or philinoid cephalaspideans. Molecular markers independent from direct ecological pressures suggested an unresolved basal opisthobranch origin for Acochlidia (based on nuclear 18S rRNA and 28S rRNA) (Vonnemann et al. 2005). A first combined multi-gene dataset led to the surprising result of Acochlidia clustering in a pulmonate relationship, united in a clade with Pyramidelloidea, Amphiboloidea and Eupulmonata. However, only three derived acochlids were included into analysis prior to 2010, with partially missing data.

2005 taxonomy

The taxonomy of Bouchet & Rocroi (2005) tentatively follows Starobogatov (1983), but they have downgraded his taxonomic ranks (suborders to superfamilies, superfamilies to families). The group Acochlidiacea is arranged as follows:

  • Superfamily Acochlidioidea
  • Family Acochlidiidae
  • Superfamily Hedylopsoidea
  • Family Hedylopsidae
  • Family Ganitidae
  • Family Livorniellidae
  • Family Minicheviellidae
  • Family Parhedylidae
  • Family Tantulidae
  • Superfamily Palliohedyloidea
  • Family Palliohedylidae
  • Superfamily Strubellioidea
  • Family Strubelliidae
  • Family Pseudunelidae
  • 2010 taxonomy

    A first comprehensive cladistic analysis of their phylogeny has been established by Schrödl & Neusser (2010), but the identity of their sister group remained uncertain. Morphology-based analyses by Schrödl & Neusser, demonstrated that Acochlidia usually group with other mesopsammic (they live in interstitial spaces of marine sands) taxa, if any were included (i.e. with the sacoglossan Platyhedyle, the rhodopemorph Rhodope or the cephalaspideans Philinoglossa or Philine exigua). Thus, it is likely that convergent adaptations to the interstitial habitat mask the truly phylogenetic signals.

    Schrödl & Neusser (2010) split Acochlidiacea into two (unranked) taxa and into six families like this:

    Hedylopsacea

    Hedylopsacean Acochlidiacea, whose evolution involves several habitat shifts from marine interstitial to amphibious or freshwater benthic habitats, possess complex excretory and reproductive systems.

    (unranked) Hedylopsacea has no superfamilies defined:

  • Acochlidiidae: Acochlidium, Palliohedyle, including Strubellia
  • Pseudunelidae: with the only genus Pseudunela
  • Hedylopsidae: with the only genus Hedylopsis
  • Tantulidae: with the only species Tantulum elegans
  • Microhedylacea

    Microhedylacean Acochlidiacea are exclusively found in interstitial spaces in sediment, and show a tendency toward reduction of complexity in major organ systems.

    (unranked) Microhedylacea has no superfamilies defined:

  • Asperspinidae: with the only genus Asperspina – junior synonym: Minicheviellidae
  • Microhedylidae s.l.: Pontohedyle, Parhedyle, Microhedyle – including Ganitidae: Ganitus and Paraganitus. Inclusion of Ganitidae within Microhedylidae requires further research and higher statistical support.
  • A multi-locus molecular study by Jörger et al. (2010), included six out of seven acochlidian families. It confirmed Acochlidiacea in a pulmonate relationship, as sister to Eupulmonata. Euthyneura, Opisthobranchia and Pulmonata as traditionally defined were found non-monophyletic. The enigmatic amphibious and insectivorous Aitengidae clusters within Acochlidiacea, as sister to meiofaunal and brackish Pseudunelidae and limnic Acochlidiidae. Inclusion of this small acochlidian group resulted in redefinition of major groups within Heterobranchia, that has led to creation of the new clades Euopisthobranchia and Panpulmonata.

    Phylogeny

    There is no fossil record of Acochlidiacea. Application of a molecular clock allowed estimation of divergence times for these groups. The split between Eupulmonata and Acochlidiacea took place in the Mesozoic, between the Triassic and Jurassic periods. The diversification of Acochlidia is estimated to have happened in the Jurassic with the split between Hedylopsacea and Microhedylacea.

    Cladogram

    A cladogram showing phylogenic relations of some genera and species within Acochlidiacea:

    Ecology

    The life cycle of Acochlidiacea is poorly known. With a typically low reproductive output in Acochlidiacea (max. of 40 eggs in Pontohedyle milaschewitchii), free veliger larvae are assumed to stay in the interstices of the sand grains rather than entering the water column thereby avoiding long distance dispersal. Fertilized eggs are attached to sand grains and might promote dispersal via current driven sediment transport along shorelines.

    Overview of species

    1. Hedylopsis spiculifera (Kowalevsky, 1901) (Hedylopsidae)
    2. Hedylopsis ballantinei Sommerfeldt & Schrödl, 2005 (Hedylopsidae)
    3. Pseudunela cornuta (Challis, 1970) (Pseudunelidae) – marine and temporary brackish
    4. Pseudunela eirene Wawra, 1988 (Pseudunelidae) – marine
    5. Pseudunela espiritusanta Neusser & Schrödl, 2009 (Pseudunelidae) – in brackish water
    6. Pseudunela marteli Neusser, Jörger & Schrödl, 2011 (Pseudunelidae) – marine
    7. Pseudunela viatoris Neusser, Jörger & Schrödl, 2011 (Pseudunelidae) – marine
    8. Aiteng ater Swennen & Buatip, 2009 (Aitengidae) – marine (and brackish)
    9. Aiteng mysticus Neusser, Fukuda, Jörger, Kano & Schrödl, 2011 (Aitengidae) – from Japan
    10. Strubellia paradoxa (Strubell, 1892) (Acochlidiidae) – freshwater
    11. Acochlidium amboinense (Strubell, 1892) (Acochlidiidae) – freshwater
    12. Acochlidium bayerfehlmanni Wawra, 1980 (Acochlidiidae) – freshwater
    13. Acochlidium fijiiensis Haynes & Kenchington, 1991 (Acochlidiidae) – freshwater
    14. Palliohedyle sutteri (Wawra, 1979) (Acochlidiidae) – freshwater
    15. Palliohedyle weberi (Bergh, 1895) (Acochlidiidae) – in brackish waters
    16. Tantulum elegans Rankin, 1979 (Tantulidae) – freshwater
    17. Asperspina brambelli (Swedmark, 1968) (Asperspinidae)
    18. Asperspina murmanica (Kudinskaya & Minichev, 1978) (Asperspinidae)
    19. Asperspina rhopalotecta Salvini-Plawen, 1973 (Asperspinidae)
    20. Asperspina loricata (Swedmark, 1968) (Asperspinidae)
    21. Asperspina riseri (Morse, 1976) (Asperspinidae)
    22. Microhedyle glandulifera (Kowalevsky, 1901) (Microhedylidae)
    23. Microhedyle nahantensis (Doe, 1974) (Microhedylidae)
    24. Microhedyle odhneri (Ev. Marcus & Er. Marcus, 1955) (Microhedylidae)
    25. Microhedyle remanei (Er. Marcus, 1953) (Microhedylidae)
    26. Ganitus evelinae Marcus, 1953 (Microhedylidae s.l. / Ganitidae)
    27. Paraganitus ellynnae Challis, 1968 (Microhedylidae s.l. / Ganitidae)
    28. Parhedyle cryptophthalma (Westheide & Wawra, 1974) (Microhedylidae)
    29. Parhedyle tyrtowii (Kowalevsky, 1900) (Microhedylidae)
    30. Parhedyle gerlachi (Ev. Marcus & Er. Marcus, 1959) (Microhedylidae)
    31. Pontohedyle brasilensis (Rankin, 1979) (Microhedylidae)
    32. Pontohedyle milaschewitchii (Kowalevsky, 1901) (Microhedylidae)
    33. Pontohedyle verrucosa (Challis, 1970) (Microhedylidae)
    34. Pontohedyle sp. 1 - Pontohedyle sp. 9

    References

    Acochlidiacea Wikipedia