Aptychen als Kieferelemente der Ammoniten

The jaws of the ammonite generaEleganticeras, Hildoceras, Normannites, Scaphites, Physodoceras, andQuenstedtoceras (ofQuenst. lower jaws only) are described. Lower jaws and aptychi of these genera are shown to be identical. They consist of an inner layer of organic material, which corresponds to the complete anaptychi of liassic ammonites, and an outer layer of calcitic material deposited on both flancs of the lower jaw, giving rise, after decay of the organic layer, to the aptychi. Previously published interpretations of aptychi as opercula or hoods are discussed and rejected. It is concluded that they certainly functioned as jaws or possibly shovel-like devices.     

Double function of aptychi (Ammonoidea) as jaw elements and opercula

Lehmann, U. & Kulicki, C. 1990 10 15: Double function of aptychi (Ammonoidea) as jaw elements and opercula. Lethaia , Vol. 23, pp. 325–331. Oslo. ISSN 0024–1164.
Aptychi are calcitic coverings on the outer surface of organic ammonite lower jaws. They are similar in shape to that of the corresponding ammonite apertures. This observation and additional features of many aptychi are in harmony with their former interpretation as protective opercula. We suggest that they served as opercula in addition to functioning as jaws. The primary function of the lower jaws was thus secondarily extended to that of protective shields when they acquired their calcitic covering, while as lower jaws their importance dwindled to that of a more passive abutment. Phylogenetically, this seems to have started slowly in some anaptychi and became obvious with the first aptychi. ▭ Ammonites, aptychus, operculum, jaw apparatus, evolution, function .     

Aptychi microstructure in Late Cretaceous Ancyloceratina (Ammonoidea)

The microstructure of aptychi (bivalved calcareous coverings on lower jaws) of three genera of Late Cretaceous Ancyloceratina, Baculites, Polyptychoceras and Jeletzkytes is described for the first time on the basis of well-preserved and in situ material from the Western Interior of the USA and Hokkaido, Japan. Optical and scanning electron microscope observations of aptychi on polished median and cross-sections reveal some variation in their relative size, shape and microstructure among the three genera. The aptychus of Baculites is composed of two calcitic layers: one with tilted lamellae and the other one with horizontal lamellae, whereas those of Polyptychoceras and Jeletzkytes consist of a thin layer with horizontal lamellae. Comparison with aptychi (e.g. Laevaptychus) of Jurassic Ammonitina shows that the aptychi of Ancyloceratina differ from those of Jurassic Ammonitina in the smaller number of layers and the absence of a sponge-like structure. We propose for the first time growth models for a sponge-like aptychus of Jurassic Ammonitina and the lamellar aptychus of Cretaceous Ancyloceratina. The remarkable microstructural variation of aptychi observed in Mesozoic Ammonoidea is probably related to the diversity of their modes of feeding and the secondary function of the lower jaws as opercula.     

Biological and stratigraphical significance of the Silurian nautiloid Aptychopsis

Turek, Vojtach 1978 04 15: Biological and stratigraphical significance of the Silurian nautiloid
Circular or elliptical structures described as the genus Aptychopsis Barrande 1872 (and mostly referred to the Crustacea) represent the opercula of a specialized group of orthoceratids. Their morphology bears a considerable resemblance to the structure of the lower jaws (aptychi) of some Mesozoic ammonoids, particularly of the genus Physodoceras . Because of its size and structure, however, Aptychopsis cannot have functioned as a jaw apparatus. Observation of an operculumin siru supports this assumption as regards its functional and systematic position. The classification of the genus Aptychopsis as given by Jones and Woodward (1872–1893) is purely typological and hardly applicable in palaeobiology. Continuous gradations exist between the various morphological types. The lack of systematically distinctive features explains the unsuitability of Aptychopsis for biostratigraphical use. Aptychopsids occur in the Silurian of Central Bohemia between the Spirograprus turriculatus Zone and the Neodiversograptus nilssoni Zone, inclusive, with maximum frequency in the uppermost Wenlockian.     

贵州剑河寒武系凯里组脊状单臂螺(Haplophrentis carinatus)埋藏特征及与始海百合共生关系探讨

贵州剑河寒武系凯里组软舌螺化石丰富、埋藏形式多样,其中以脊状单臂螺Haplophrentis carinatus化石数量最多、保存最为完整。过去有关学者对凯里组单臂螺化石的研究主要集中在化石分类学方面,对脊状单臂螺埋藏特征及与其他生物共生关系缺乏深入探讨。本文对324块脊状单臂螺化石标本进行系统研究对比后发现,凯里组脊状单臂螺口盖化石埋藏形式有四类:口盖单独保存、口盖以内模或外模化石形式保存、口盖与锥壳完全绞合保存、口盖与锥壳不完全绞合保存;附肢保存较少;锥壳多以内模化石形式保存;脊状单臂螺内模化石与印痕化石上普遍出现类似软体保存形成的三分叉结构,这类三分叉结构属于后期埋藏因素造成的次生结构。文中还对脊状单臂螺与始海百合共生关系进行探讨,并将二者共生关系归为偏害共生。     

Phylogeny of the aptychi-possessing Neoammonoidea (Aptychophora nov., Cephalopoda)

The different forms of the aptychi (opercula, homologous with lower jaws) of the Ammonoidea are used for the first time in a phylogenetic analysis of part of the classic Ammonoidea phylogeny. The results indicate that the aptychi-possessing ammonoids form a monophylum for which we propose the informal name Aptychophora nov. Among the Jurassic ammonoids, it is possible to recognize several monophyletic groups. In part, our results support existing superfamilies (e.g. Hildocerataceae, Haplocerataceae) by new synapomorphies. However, the Perisphinctaceae can now be much more clearly differentiated than in the previously established phylogenetic tree. The Upper Cretaceous ammonoid superfamilies cannot be derived from the Haplocerataceae, but are descendants of a 'primitive' perisphinctacean possessing a praestriaptychus. Nor can they be derived from the 'higher' perisphinctaceans (family Perisphinctidae) because that clade is characterized by granulaptychi. The consequence of these results is that the quadrilobate primary suture of the 'Ancyloceratina' must have evolved more than once by reduction from an ancestral quinquelobate primary suture. The Ancyloceratidae have praestraptychi or aptychi types which can be derived from praestriaptychi, whereas the Crioceratitinae have longitudinally striated anaptychi.     

Size and function of ammonite aptychi in comparison with buccal masses of modern cephalopods

Morton, Nicol & Nixon, Marion 1987 07 15: Size and function of ammonite aptychi in comparison with buccal masses of modem cephalopods.
Previous impressions that the size of ammonite aptychi is unusually large, thereby posing a problem to their interpretation as part of the jaw apparatus, are shown to be incorrect. The relative length of the aptychus for at least the Jurassic ammonite groups studied, at approximately 15% of the length of the body chamber, is remarkably constant in different taxonomic groups and sizes. This is well within the range for buccal mass length as percentage of mantle length of living cephalopods, being most similar to Octopus and Sepia and much smaller than Nautilus. The height and width of aptychi relative to whorl height and width are larger but again ammonites are probably not significantly different from modern cephalopods. The size and design, with no obvious structures for biting or crushing, suggest that ammonites were adapted to a particular type of relatively unspecialised feeding in which mostly small animals were ingested, possibly with some external digestion. The large shovel-like lower jaw may have functioned like a scoop for collecting large quantities of water and small prey, and movement of the buccal complex with the upper jaw almost closed against the lower jaw could have expelled water while retaining captured prey. Calcification of aptychi may have been protective, but more likely acted to weight the buccal mass for nektobenthic feeding and to make it more rigid.     

Operculum regeneration following failed predation in the Silurian gastropod Oriostoma

Regeneration of the calcareous rigiclaudent operculum following severe, non‐lethal, predatory attacks is described in two specimens of the characteristic Silurian gastropod Oriostoma from the English Midlands. This is the first record of the regeneration of opercula in Palaeozoic gastropods and of opercula conjoined with shells that have been repaired after significant, failed, durophagous attacks. In one specimen, a series of repaired injuries culminates in a repaired aperture closed by the operculum. In the second specimen, new shell growth has failed to recover the full extent of the original broken whorl, and the new aperture and operculum, though well developed, are smaller than the originals. Both opercula are unusually thin centrally when compared to other, strongly domed, Oriostoma opercula.     

Über Nahrung und Ernährungsweise von Ammoniten

Until only a few years ago, the majority of ammonites were considered to have been rather swift nectonic swimmers of little ecologic bondage. About their food, nothing was known with certainty. Comparison with recent Coleoids and withNautilus suggests, however, that most ammonoids were poor swimmers. It is not even certain that the hyponome was used for locomotion as much as inNautilus. Slow locomotion made it impossible for ammonites to hunt for fish or other highly agile prey. Their lower jaws, which are identical to the structures known as aptychi and anaptychi (formerly considered to be opercula), are like shovels and make it impossible for their bearers actually to bite and cut with them. Consequently the structure of their jaws also prevented their hunting large and active prey. Their jaws were probably actually used like shovels along the bottom of the sea. They may have gathered small or slow benthonic organisms like foraminifers, ostracodes, small crustaceans, young brachiopods, corals, bryozoa, but also drifting or slowly swimming and dead organisms. Several unusually well preserved stomachs of ammonites contained foraminifers, ostracodes, crinoids, smaller ammonites, and possibly inarticulate brachiopods. It is concluded that, ecologically, ammonites inhabited the place of modern bottom-feeding gastropods.     

Taphonomic differentiation of Oxfordian ammonites from the Cracow Upland, Poland

Taphonomic analysis of Lower and Middle Oxfordian ammonites from the Cracow Upland, southern Poland (localities at Pod???e, Zalas, M?ynka) revealed differences in ammonite preservation. The studied ammonites, usually termed as external and internal moulds, show a more complex state of preservation. In the Middle Oxfordian glauconitic marls, ammonites are preserved as internal moulds with neomorphic calcite shells showing relics of the original internal structure. In the Middle Oxfordian platy peloidal limestones, ammonites are preserved mostly as external moulds, without septal suture, however under microscope might show relics of internal whorls and septa and/or subtle differences in sediment filling phragmocone chambers. In sponge–microbial bioherms and biostromes, ammonite internal moulds have shells, which in contrast to ammonites from glauconitic marls are not strictly neomorphic ones, but originated by shell dissolution and subsequent filling of moldic porosity by calcite cement. In sponge–microbial nodular limestones, the ammonites are strongly deformed and the outer wall is usually removed by dissolution under pressure. Other important taphonomic differences include the rate of compaction (highest in platy limestones), sedimentary infillings, microborings, encrustations and preservation of siphuncular tubes. The majority of the ammonites appear to be phragmocones; aptychi in all facies are rare. Siphuncular tubes are fossilized exclusively in oppeliids, only in specimens from glauconitic marls and platy limestones, although their other taphonomic attributes are different. Tubes seem to have fossilized due to microbially mediated phosphatization that could be favoured by a set of parameters which operated rather at the scale of ammonoid carcasses: closed, poorly oxygenated conditions, and reduced pH. Taphonomic processes were controlled by the sedimentary environment (fragmentation, sedimentary filling, phosphatization of siphuncular tubes), as well as by early and late diagenesis (neomorphic transformation, dissolution, cementation, compaction) influenced by lithology.     

First direct evidence of ammonoid ovoviviparity

Ammonoids had high evolutionary rates and diversity throughout their entire history and played an important role in the high‐resolution sub‐division of the Mesozoic, but much of their palaeobiology remains unclear, including the brooding habitat. We present our study of the first recorded ammonite embryonic shell clusters preserved with calcified embryonic aptychi in situ within the body chambers of mature macroconch shells of the Early Aptian (Early Cretaceous) ammonite Sinzovia sazonovae. The following support the idea that the clusters are egg masses, which developed inside ammonite body chambers: the absence of post‐embryonic shells and any other fossils in these clusters, the presence of the aptychi in all embryonic shell apertures and peculiarities of adult shells preservation. These facts confirm earlier speculations that at least some ammonoids could have been ovoviviparous and that, like many modern cephalopods, they could have reproduced in mass spawning events. The aptychi of ammonite embryonic shells are observed here for the first time, indicating that they were already formed and calcified before hatching. Our results are fully congruent with the peculiar modes of ammonoid evolution: quick recovery after extinctions, distinct evolutionary rates, pronounced sexual dimorphism and the nearly constant size of embryonic shells through ammonoid history. We assume that adaptation to ovoviviparity may be the reason for the presence of these features in all post‐Middle Devonian ammonoids.     

Ammonite aptychi: Functions and role in propulsion

Seven previous proposals of aptychus (sensu stricto) function are reviewed: lower mandible, protection of gonads of females, protective operculum, ballasting, flushing benthic prey, filtering microfauna and pump for jet propulsion. An eighth is introduced: aptychi functioned to actively stabilize the rocking produced by the pulsating jet during forward foraging and backward swimming. Experiments with in-air models suggest that planispiral ammonites could lower their aperture by the forward shift of a mobile cephalic complex. In the experiments, the ventral part of the peristome is lowered from the lateral resting (neutral) position by the added “ballast” of a relatively thin Laevaptychus to an angle < 25° from horizontal with adequate stability to withstand the counter-force produced by the jet of the recurved hyponome. However, of the shell forms tested, only brevidomes with thick aptychi, e.g., the Upper Jurassic Aspidoceratidae with Laevaptychus and average whorl expansion rates, were stable enough to swim forward by jet propulsion at about Nautilus speed (∼ 25 cm/s). We propose that aptychus function most commonly combined feeding (jaw, flushing, filtering) with protection (operculum), and, more rarely, with locomotion (ballast, pump, diving and stabilizing plane). Aptychi may thus have been multi-functional.     

Densely packed concentrations of sessile barnacles (Cirripedia: Sessilia) from the Early Pliocene of SE Spain

Sessile barnacle assemblages, dominated by Concavus concavus (Bronn) and Balanus perforatus Bruguière, are very abundant in the Lower Pliocene deposits of the Almería-Níjar and Carboneras basins (southeastern Spain). They occur in shallow-coastal siliciclastic and mixed siliciclastic-carbonate sediments, forming dense concentrations in two contexts: (1) sheltered shallow-marine depressions and (2) the mouth of distributary channels feeding a delta lobe. Extensive colonization took place during periods of quiescence with a high nutrient and food supply inducing the formation of hummocks. Crowding of high morphotypes was presumably triggered by a high larval supply and recruitment rate. The barnacles are exceptionally well preserved, often as in situ clusters, many with opercula, and include a range of ontogenetic stages with some specimens preserving original colouration. Good preservation is probably due to sudden burial without further reworking.     

Microstructure of aptychi of Upper Jurassic (Upper Oxfordian) ammonites from Central Russia

To date, bivalve calcitic plates which cover the outer chitinous lamella of the lower jaws of Jurassic and Cretaceous ammonoids (aptychi sensu stricto) have been classified into several morphotypes (form genera) based on shape, surface sculpture and internal microstructure. However, previous works on aptychi microstructure focused mainly on thick morphotypes (e.g. Laevaptychus and Lamellaptychus), whereas little was investigated for thin Praestriaptychi. In this study, the microstructure of Praestriaptychi of Upper Oxfordian Perisphinctes and of recently discovered aptychi of aspidoceratid microconch Mirosphinctes (both belonging to the superfamily Perisphinctoidea) is described. These aptychi are compared with Laevaptychi of Upper Oxfordian macroconchs Euaspidoceras (a dimorphic counterpart of Mirosphinctes). This study demonstrated that the aptychi of Perisphinctes and Mirosphinctes differ from each other and from Laevaptychi in their microstructure, number of calcitic layers and in growth patterns. The aptychi of both aspidoceratid dimorphs are similar in terms of growth pattern, but differ in microstructure and the number of calcitic layers. Neither aptychi of Perisphinctes nor of Mirosphinctes have a tubular layer with a honeycomb surface pattern, which is typical for Laevaptychus. This indicates that aptychi were extremely diverse and their microstructure varied significantly not only within the superfamily, but even within a dimorphic pair of aspidoceratid ammonites. A lack of a tubular layer in Praestriaptychus indicates that it developed independently in Lamellaptychus of Haploceratoidea and Laevaptychus of Aspidoceratidae.     

The tübingen fossil collections of Werner Quenstedt (1893–1960): Mesozoic cephalopod jaws (Rhyncholites,Aptychi) from the achensee area (Tyrol,Austrian Alps)

The size, state, and depository of the important Alpine rhyncholite and aptychi collection of Werner Quenstedt, compiled during 30 years of bed-by-bed collecting from the Aalenian-Valanginian deposits of the Achental area (Tyrol, Austria), are presented. Preparation and investigation of the rhyncholite collection (approximately 700 specimens) has been done in 1985 by one of the present authors. A short outline of the life and scientific work of Werner Quenstedt (1893–1960), geologist and palaeontologist, lecturer and associate professor at the universities of Berlin and Munich, is also given and his scientific diaries (more than 6500 pages) are summarized.     

Allocrioceras from the Cenomanian (mid-Cretaceous) of the Lebanon and its bearing on the palaeobiological interpretation of heteromorphic ammonites

Specimens of the mid-Cretaceous heteromorphic ammonite Allocrioceras cf. annulatum (Shumard, 1860) from the Upper Cenomanian lithographic limestones of the Lebanon provide an in situ record of aptychi and interpreted remnants of internal soft tissue and stomach content. Based on this exceptionally well-preserved material, Allocrioceras is interpreted as a pelagic, aperture-upwards drifter that probably fed on comatulid crinoids.     

A revision of Holm's Early and early Mid Cambrian hyoliths Of Sweden

ABSTRACT. Re-examination of type specimens of Early Cambrian and early Mid Cambrian hyoliths from Sweden confirms placement of Hyolithes teretiusculus Linnarsson in Hexitheca Syssoiev, and reassignment to the order Hyolithida rather than Orthothecida. Inclusion of Hyolithes affinis Holm within Decoritheca Syssoiev is re-confirmed, and Hyolithes socialis Linnarsson is now referred to Nevadotheca Malinky and Slapylites Marek. An operculum included under Hyolithes oelandicus Holm is transferred provisionally to Maxilites Marek, and conchs of that species are placed under Tulenicornus Val'kov with question. No other hyolith species of Holm can be definitely assigned to genus. The rarity of well preserved opercula is a major impediment to recognizing hyolith taxa confidently, and we follow Holm in attributing the comparative rarity of opercula to the fact that in some hyolith taxa the operculum may have been composed of a different, and perhaps less stable, material than the rest of the conch.     

中华鲱鲇年龄鉴定及生长特征

对2009-2010年采自澜沧江下游的188尾中华鲱鲇(Clupisoma sinensis)进行了年龄与生长的研究.采用耳石、脊椎骨、鳃盖骨、胸鳍棘4种材料对全部样本进行年龄鉴定,耳石年龄鉴定最为准确,4-5月是年轮形成高峰期.渔获种群由1-6龄共6个龄组组成,以1-4龄个体为主.体长与耳石半径呈线性函数关系.体长与...     

Sources and sinks of diversification and conservation priorities for the Mexican tropical dry forest

Elucidating the geographical history of diversification is critical for inferring where future diversification may occur and thus could be a valuable aid in determining conservation priorities. However, it has been difficult to recognize areas with a higher likelihood of promoting diversification. We reconstructed centres of origin of lineages and identified areas in the Mexican tropical dry forest that have been important centres of diversification (sources) and areas where species are maintained but where diversification is less likely to occur (diversity sinks). We used a molecular phylogeny of the genus Bursera, a dominant member of the forest, along with information on current species distributions. Results indicate that vast areas of the forest have historically functioned as diversity sinks, generating few or no extant Bursera lineages. Only a few areas have functioned as major engines of diversification. Long-term preservation of biodiversity may be promoted by incorporation of such knowledge in decision-making.     

The <Emphasis Type="Italic">Karsteniceras</Emphasis> level: Dysoxic ammonoid beds within the Early Cretaceous (Barremian,Northern Calcareous Alps,Austria)

Summary An Early Cretaceous mass-occurrence of ammonites in the Ternberg Nappe of the Northern Calcareous Alps (Upper Austria) is described for the first time. The mass-occurrence (section KB1-B=Klausrieglerbach 1, section B) dominated by Karsteniceras ternbergense Lukeneder is of Early Barremian age (Moutoniceras moutonianum Zone). The Karsteniceras mass-occurrence comprises eight different genera, each apparently represented by a single species, of which four are identified to species level. About 300 specimens of K. ternbergense between 5 and 37 mm in diameter were investigated. Two groups showing thick main ribs but different maximum size are distinguishable. The latter parameters are suggested to reflect sexual dimorphism within K. ternbergense, a condition that is most probably applicable to the whole leptoceratoid group. The geochemical results indicate that the Karsteniceras mass-occurrence within the described Lower Cretaceous succession was deposited under intermittent oxygen-depleted conditions associated with stable, salinity-stratified water masses. The rhythmicity of laminated black-marly lime-stone layers and light-grey bioturbated, organic-poor lime-stones suggests that the oxic and dysoxic conditions underwent highly dynamic changes. The deposition of the limestones in this interval occurred in an unstable environment and was controlled by short- and long-term fluctuations in oxygen levels. Karsteniceras inhabited areas of stagnant water with low dissolved oxygen; it showed peak abundance during times of oxygen depletion, which partially hindered other invertebrates from settling in such environments. The autochthonous Karsteniceras mass-occurrence can be assigned to the deposition-type of ‘Konservat Lagerst?tte’, which is indicated by the preservation of phosphatic siphuncle structures and proved by the in situ preservation of aptychi within Karsteniceras ternbergense. Based on lithological and geochemical analysis combined with in vestigations of trace fossils, microfossils and macrofossils, an invasion of an opportunistic (r-strategist) Karsteniceras biocoenosis during nonfavorable conditions over the sea bed during the Lower Barremian is proposed for the KB1-B section.