Decapod crustacean material collected recently from the lower Callovian (Middle Jurassic) in Maine-et-Loire (north-west France) comprises two new species of prosopid and one new species of tanidromitid crabs, of the genera Nodoprosopon and Tanidromites, respectively. Also represented in this faunule is a probable paguroid anomuran, in the form of isolated chelae here assigned to the genus Orhomalus, as well as appendicular remains of unknown affinity; some of the latter might belong to prosopid crabs. These anomurans and brachyurans co-occur with a diverse benthic fauna in limestones with abundant iron ooids; their main interest lies in the fact that they add valuable data to the rather poor record of Middle Jurassic decapod crustaceans.
Dans la région de Montreuil-Bellay (Maine-et-Loire), de nombreuses coupes ont été réalisées au passage Callovien moyen-Callovien supérieur. Le premier banc attribué au Callovien supérieur a été daté de l'horizon à Leckenbyi. Il a fourni une très importante faune ammonitique (N=3125), dans laquelle les Perisphinctidae représentent 51% de l'effectif. À côté de formes plus ou moins bien connues comme Pseudopeltoceras leckenbyi (BEAN), Orionoides pseudorion (WAAGEN), Subgrossouvria famulum (BEAN) et S. crassa GÉRARD et CONTAUT, on trouve une espèce qui n'a jamais été ni décrite ni figurée : cette espèce fait l'objet du présent article. Choffatia isabellae n. sp. se distingue sans aucune ambiguité des Perisphinctidae contemporains par : 1) un long stade juvénile lisse, 2) une costulation habituellement ténue, 3) l'absence de formations paraboliques et 4) la très grande fréquence des constrictions. Comme cette espèce est inconnue dans les faunes de l'extrême sommet du Callovien moyen, nous pensons qu'elle a colonisé, avec beaucoup d'autres espèces, dont Peltoceras marysae BONNOT et alii, via la marge sud de la Téthys, la plate-forme nord-ouest européenne à la faveur de l'intervalle transgressif qui débute à l'extrême base du Callovien supérieur. Apparue brutalement à la base de l'horizon à Leckenbyi, cette nouvelle espèce possède son acmé dans la partie médiane de l'horizon, où elle peut représenter la moitié des Perisphinctidae, avant de devenir rare dans la partie supérieure de l'horizon, puis très rare dans l'horizon à Athleta.
Résumé : À Montreuil-Bellay (Maine-et-Loire, France), le premier banc d'âge Callovien supérieur (Horizon à Leckenbyi) a fourni une très abondante faune ammonitique (N=3275). Dans la famille des Perisphinctidae, à côté de Choffatia isabellae BONNOT et al. et Thanks to the abundance and quality of the material, it was possible to describe and figure macroconchs and microconchs of these three species, including adult specimens with preserved peristome. The stratigraphical ranges of these taxa are also specified and their potential descendants can be considered. These species are unknown in the uppermost Middle Callovian, and we assume that they colonized the northwestern part of the European platform via the southern margin of the Tethys, as did Peltoceras marysae BONNOT et al. and Choffatia isabellae BONNOT et al.
Background Expression of sexual dimorphism is recognised in various fossil groups of molluscs such as the Ammonoidea, an extinct group of shelled cephalopods. During the Mesozoic, the best-documented sexual dimorphic examples are seen in the Jurassic superfamily Perisphinctoidea. It is usually expressed by distinct adult size and apertural modifications between the antidimorphs. Putative males (otherwise referred to as microconch) are small in size and develop lappets at the end of the shell while the females (macroconch) are larger and bear a simple peristome. Dubious cases are, however, known in that superfamily, which often relate to taxonomic biases or lack of diagnostic characters, and some others expose ontogenetic anomalies illustrated by ‘sex reversals’ in the shell morphology and ornamentation. Results The discovery of two specimens of the Callovian Aspidoceratidae Peltoceras athleta (Phillips), having both female and male features, questions the significance and causes of ‘sex reversals’ in the Ammonoidea. The two specimens have started with the macroconch ontogeny of Peltoceras athleta and show an apparent change toward maleness in the adult, as illustrated by their rounded whorl section, ribs retroversion, fading of the tubercles and lappets typical of the microconchs. Few other cases of female-to-male, as well as male-to-female ‘sex reversal’, are known in the fossil record, all belonging to the Jurassic Perisphinctoidea (families Perisphinctidae or Aspidoceratidae). Since all Jurassic Perisphinctoidea are strictly gonochoristic, these ‘sex reversals’ are pathological in nature and are herein referred to as a new forma-type pathology: namely “forma hermaphrodita”. Conclusions In the absence of any clear evidence of injury or parasitism, we hypothesize that such “forma hermaphrodita” individuals illustrate pathologic cases of intersexuality. Little is known about the ammonoid soft parts, and it is not possible to determine which internal sexual organs occur in specimens having both male and female external shell features. Abnormal feminisation and/or masculinisation also occur in modern cephalopods, the latter also grouping only gonochoric species. This phenomenon is similarly illustrated by a change in the adult body size and a mixing of both female and male structures. In that case, intersexuality is either advantageous in the population or caused sterility. The causes of intersexuality are not clearly established but environmental pollutants are evoked in modern cephalopods because they act as endocrine disrupters. ‘Sex reversals’ and/or non-functional reproductive abnormalities have also been caused by endocrine disrupters in various gonochoric gastropods species, but infestation, genetic abnormalities, temperature fluctuations or viruses are multiple causes, which can stimulate or inhibit neural-endocrinal activity by direct gonadal influence, and ultimately lead to feminisation or masculinisation in fishes, isopods, crustaceans, and gastropods as well. Regardless of whether “forma hermaphrodita” is due to an exogenic or endogenic cause, the record of intersex Perisphinctoidea in the Jurassic can be explained by the ready recognition of dimorphic pairs, and the easy collection of large and sufficiently preserved fossil palaeopopulations in which intersex specimens have statistically more chance to be found.
Background: Expression of a sexual dimorphism is recognised in various fossil groups of molluscs such as the Ammonoidea, an extinct group of shelled cephalopods. During the Mesozoic, the best documented sexual dimorphic examples are seen in the Jurassic superfamily Perisphinctoidea. It is most usually expressed by distinct adult size and apertural modifications between the antidimorphs. Putative males (otherwise referred to as microconch) are small in size and develop lappets at the end of the shell while the females (macroconch) are larger and bear a simple peristome. Dubious cases are, however, known in that superfamily. They most often relate to taxonomic biases or lack of diagnostic characters, and some others expose ontogenetic anomalies illustrated by ‘sex reversals’ in the shell morphology and ornamentation. Results: The discovery of two specimens of the Callovian Aspidoceratidae Peltoceras athleta (Phillips), having both female and male features, questions the significance and causes of ‘sex reversals’ in the Ammonoidea. The two specimens have started with the macroconch ontogeny of Peltoceras athleta, and show an apparent change toward maleness in the adult, as illustrated by their rounded whorl section, ribs retroversion, fading of the tubercles and lappets typical of the microconchs. Few other cases of female-to-male ‘sex reversal’, as well as male-to-female ones, are known in the fossil record, all belonging to the Jurassic Perisphinctoidea (families Perisphinctidae or Aspidoceratidae). Since all Jurassic Perisphinctoidea are strictly gonochoristic, these ‘sex reversals’ are pathological in nature and are herein referred to as a new forma-type pathology: namely “forma hermaphrodita”.Conclusions: In the absence of any clear evidence of injury or parasitism, we hypothesize that such “forma hermaphrodita” individuals illustrate pathologic cases of intersexuality. Little is known about the ammonoid soft parts, and it is not possible to determine which internal sexual organs occur in specimen having both male and female external shell features. Abnormal feminisation and/or masculinisation also occur in modern cephalopods; the latter also grouping only gonochoric species. This phenomenon is similarly illustrated by a change in the adult body size and a mixing of both female and male structures. In that case, intersexuality is either advantageous in the population or caused sterility. The causes of intersexuality are not clearly established but environmental pollutants are evoked in modern cephalopods because they act as endocrine disrupters. ‘Sex reversals’ and/or non-functional reproductive abnormalities have also been caused by endocrine disrupters in various gonochoric gastropods species, but infestation, genetic abnormalities, temperature fluctuations or viruses are multiple causes which can stimulate or inhibit neural-endocrinal activity by direct gonadal influence, and ultimately lead to feminisation or masculinisation in fishes, isopods, crustaceans, and gastropods as well. Regardless of whether “forma hermaphrodita” is due to an exogenic or endogenic cause, the high frequency of intersex Perisphinctoidea in the Jurassic can be explained by the readily recognition of dimorphic pair, and the easy collection of large and sufficiently preserved fossil palaeopopulations in which intersex specimens have statistically more chance to be found.
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