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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;