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WORKING CLASSIFICATION OF THE GASTROPODA 277<br />

substantiate its re-classification in the Ellobioidea. It is<br />

even questionable whether the Cretaceous Chinese<br />

fossils examined by Yu (1987) are really related to the<br />

Jurassic Mesocochliopa from North America.<br />

''33 Moitessieriidae given family rank after Wilke et al. (2001 ).<br />

^^ Classification of Pomatiopsidae after Davis (1979 and<br />

subsequent papers). The family-group name Rehderiellinae<br />

Brandt, 1974 belongs in Pomatiopsidae but it has<br />

not been possible to allocate it to one of the currently<br />

recognized subfamilies<br />

135 Classification after Ponder & Waren (1988)<br />

^^ Classification of Aporrhaidae with data from Korotkov<br />

(1992).<br />

'3' Seraphsidae included in Strombidae by Wells (in<br />

Beesleyetal., 1998).<br />

138 Tylostomatidae placed in Stromboidea after Kollman et<br />

al. (2003).<br />

13^ Classification based on Waren & Bouchet (1990) with<br />

emendations based on Beu (in Beesley et al., 1998).<br />

For an alternative classification, see Bändel & Riedel<br />

(1994b) and Riedel (1995a).<br />

^'^ Contents and classification after Ponder & Waren (1 988)<br />

and Ponder (1998).<br />

"'' Hipponicidae placed in Calyptraeoidea by Bändel &<br />

Riedel (1994b).<br />

^'•2 The position of Omalaxidae is unsettled Because they<br />

resemble planorboid architectonicids, they have been<br />

placed near that family, but the resemblance is very<br />

superficial. Based on the heterostrophy of the protoconch<br />

of species of Anomalorbis. the family Omalaxidae<br />

has been placed in the lower Heterobranchia.<br />

However, the relationship between Anomalorbis and<br />

Omalaxis is not clear. Lozouet (pers. comm.) notes a<br />

resemblance of protoconch and teleoconch characters<br />

with Lyocyclus, and the family Omalaxidae is here ten-<br />

tatively included in Vanikoroidea.<br />

"^ Classification after Ponder & Waren (1988), with adap-<br />

tations from Schilder (1966a) for Triviidae.<br />

i"*^ The position of the Vermetidae has been controversial.<br />

However, sperm ultrastructure (Healy, 1988) and mo-<br />

lecular data (e.g., Colgan et al. 2000) clearly show that<br />

it belongs in the Littorinimorpha although placement in<br />

the Cerithioidea still persist (e.g. Bändel & Kowaike,<br />

1997; Kowaike, 1998; Bändel & Kiel, 2000). Lydeard et<br />

al. (2002) found Campanile and Serpulorbis formed a<br />

clade that was sister to the Cerithioidea but outgroup<br />

sampling in this analysis was limited.<br />

1"^ Allocation of fossil families to SPF questioned by Bändel<br />

(1993b). Xenophoridae placed in Stromboidea by Kiel<br />

&Perrilliat(2001).<br />

^^ Considered paraphyletic or polyphyletic by Ponder &<br />

Lindberg (1997).<br />

'•*' Nystiellidae raised to family rank by Nützel (1998).<br />

^'^^ The position of Aclididae, in Eulimoidea or Epitonioidea,<br />

is uncertain. The protoconch and the presence of a<br />

penis (at least in Costaclis) suggest a closer affinity to<br />

Eulimidae than to Epitoniidae<br />

''^^ Classiftcation partly based on Ponder & Waren (1988)<br />

and Nützel (1998), partly original. For alternative clas-<br />

sification, see Golikov & Starobogatov (1987).<br />

150 Marshall (1980) has showed that dextral "Triforis" has<br />

taenioglossate radula and argued that "Triforidae Jousseaume,<br />

1 884" should be recognized as a separate fam-<br />

ily. The name Triforis Deshayes, 1834 is an incorrect<br />

subsequent spelling of Triphora Blainville, 1828 and "Tri-<br />

foridae Jousseaume" is not an available name. For the<br />

dextral species currently placed in Triforis, Trituba Jousseaume,<br />

1884 is available. However, it is not clear<br />

whether a new family-group name is necessary to classify<br />

Trituba, and it is here tentatively placed in New-<br />

toniellinae<br />

'51 Little is known about Johnwyaíí/ayohnwafí/ Serna, 1979,<br />

from the Paleocene of Colombia, and only known mem-<br />

ber of the family It was described as a member of the<br />

Conoidea but Sysoev (pers. comm.) suggests it is more<br />

likely a member of the Buccinoidea.<br />

'52 Perissityidae included in Tonnoidea by Tracey et al.<br />

(1993).<br />

'53 The families Sarganidae and Pholidotomidae [as<br />

Pyrifusidae] are united by Bändel & Dockery (2001 ) in<br />

a separate superfamily "Pyrifusoidea". Bändel (1999)<br />

suggested that this and Moreinae were stem groups of<br />

the Naticoidea.<br />

'5^ The family Spelghtiidae is traditionally classified near<br />

the "Turridae", but Tracey et al. (1993) noted that "some<br />

if not all of the speightiids may prove to belong in the<br />

Fasciolariidae".<br />

155 Buccinoidea is recognised following Harasewych et al.<br />

(1997) and Riedel (2000).<br />

156 Classification of Buccinidae after Kantor (pers. comm.).<br />

15'' Busyconinae ranked as a subfamily of Buccinidae after<br />

Kosyan & Kantor (in press), while Melongenidae stand<br />

out as a distinct family.<br />

'58 Classification of Columbellidae after Radwin (1977).<br />

153 Classification of Fasciolariidae after Snyder (2003).<br />

"^ Classification of Nassariidae after Alimón (1990).<br />

161 Coralliophilinae given subfamily status within Muncidae<br />

after Oliverio & Mariottini (2001 ).<br />

1^2 Babyloniidae ranked as family after Harasewych &<br />

Kantor (2002). Three family-group names are older than<br />

Babyloniidae. Swainson based his concept of Eburninae<br />

on species of Babylonia, but he misidentified Eburna,<br />

the type species of which belongs to the family Olividae;

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