Upper Cambrian agnostoid trilobites from the Machari Formation, Yongwol, Korea

The Middle to Upper Cambrian Machari Formation in Korea is well known for abundant and diverse trilobites along with other invertebrate fossils. Based on recent reappraisal on the trilobites of the Machari Formation, eight trilobite zones have been proposed for the Upper Cambrian sequence: i.e., in ascending order the Glyptagnostus stolidotus, Glyptagnostus reticulatus, Proceratopyge tenuis, Hancrania brevilimbata, Eugonocare longifrons, Eochuangia hana, Agnostotes orientalis and Pseudoyuepingia asaphoides zones. Trilobites from the lower five zones and part of the Pseudoyuepingia asaphoides Zone have been already published elsewhere. In this paper, we describe the agnostoid trilobites of the upper three zones, Eochuangia hana, Agnostotes orientalis and Pseudoyuepingia asaphoides zones, of the Machari Formation. These comprise 24 species belonging to 13 genera, including one new genus (Yongwolagnostus) and ten new species (Homagnostus? sulcatus, Ivshinagnostus alatus, Ivshinagnostus quadratus, Yongwolagnostus stenorhachis, Yongwolagnostus dubius, Nahannagnostus pratti, Pseudagnostus? dividuus, Pseudagnostus medius, Pseudorhaptagnostus? urceus and Ammagnostus serus). These biozones correlate well with middle Upper Cambrian zones established in South China, Australia, Kazakhstan, Siberia, and Canadian Rocky Mountains.     

Head segmentation of trilobites

Although trilobites have provided research subjects for more than two centuries, their head segmentation has remained unresolved. Four glabellar furrows (SO and S1–S3) marking the segmental boundaries are generally present in the cephalic axis, but there are trilobites with one more pair of furrows, the so‐called S4, in the cephalic axis, causing confusion in understanding trilobite head segmentation. Recent advances in developmental biology and palaeontology have shed light on the arthropod head problem, and thus, trilobite head segmentation can be reviewed in the light of this knowledge. Based on the information from the anatomy of exceptionally preserved trilobites and artiopodans closely related to trilobites, it is inferred that trilobite head contains five segments: the anteriormost ocular segment potentially associated with the hypostome, the antennal segment and the following three segments with walking legs. When present, the S4 furrows are situated where the eye ridges meet the cephalic axis of trilobites, indicating that the furrows are incised ‘within’ the anteriormost segment in trilobites with an anteriorly enlarged frontal lobe. Trilobites of the Order Redlichiida, the most primitive stock, show variable conditions in the frontal glabellar conditions, while in other more derived groups, the condition is rather constant. The frontal glabellar condition, therefore, could provide a clue to elucidate the unresolved Cambrian trilobite phylogeny and the Cambrian roots of the post‐Cambrian trilobites.     

Gut evolution in early Cambrian trilobites and the origin of predation on infaunal macroinvertebrates: evidence from muscle scars in Mesolenellus

Trilobites are particularly common Cambrian fossils, but their trophic impact on the rapidly evolving marine ecosystems of that time is difficult to assess, due to uncertainties on how diverse their feeding habits truly were. Gut anatomy might help to constrain inferences on trilobite feeding ecology, but preservation of digestive organs is exceedingly rare. Muscle scars on the glabella, known as ‘frontal auxiliary impressions’ (FAIs), have been interpreted as evidence of the evolution of a pouch‐like organ with powerful extrinsic muscles (i.e. a crop) in some trilobites. Here we describe FAIs in Mesolenellus hyperboreus from Cambrian Stage 4 strata of North Greenland, which represents the oldest example of such structures and their first report in the Suborder Olenellina. Mesolenellus FAIs suggest that the crop in trilobites was clearly differentiated from the rest of the digestive tract, and essentially located under a hypertrophied glabellar frontal lobe. Reviews of the digestive anatomy of trilobite sister‐taxa and the glabellar morphology of the oldest‐known trilobites suggest that the gut of the trilobite ancestor was an essentially simple tract (i.e. no well‐differentiated crop) flanked laterally by numerous midgut glands. A crop first evolved in the Cambrian in groups like olenelloids and (later) paradoxidoids. Using ichnological evidence, we hypothesize that the emergence of olenelloids yields evidence for the evolution of predatory inclinations in a group of arthropods originally dominated by surface‐deposit‐feeders. By allowing the exploitation of a rapidly developing food source, infaunal animals, the diversification of feeding strategies in trilobites might partially explain their unparalleled evolutionary success.     

Cambrian biostratigraphy of the Bowers back-arc basin,Northern Victoria Land,Antarctica — A review

The Bowers Mountains in Northern Victoria Land contain the richest Cambrian Series 3 (Miaolingian, middle Cambrian) and Cambrian Series 4 (Furongian, late Cambrian) fossiliferous successions in Antarctica. Almost all the fossils are found within the Bowers Supergroup, which outcrops within the Bowers Terrane, a fault-bounded northwest-southeast oriented strip in Northern Victoria Land. The fossils provide the main age control on the history and evolution of the Bowers volcanic arc and back-arc basin. The great bulk of the fossils occur within the Spurs Formation. The fossil assemblages are dominated by agnostoids and polymerid trilobites with most ranging in age from Drumian to Paibian, although one fauna is of Jiangshanian age. Over 40 agnostoid taxa and over 100 polymerid trilobite taxa have been recorded from the rocks of the Bowers Supergroup. The youngest fauna occurs within the adjacent Robertson Bay Terrane, where a limited fauna of polymerid trilobites and conodonts from within a limestone olistolith have a very late Cambrian or early Ordovician age. Faunal affinities are mainly with Australia, New Zealand, North and South China and the Himalaya with lesser ties to Iran, Kazakhstan, Siberia and Laurentia.     

The Cambrian radiation of bilaterians: Evolutionary origins and palaeontological emergence; earth history change and biotic factors

Evidence from a variety of research areas, including phylogenetic palaeobiogeographic studies of trilobites, indicates that there may be a fuse to the Cambrian radiation, with a duration on the order of 20–70 myr. Evolution in trilobites appears to have been powerfully influenced by the tectonic changes occurring at the end of the Neoproterozoic: especially the breakup of Pannotia. This continental fragmentation may have also elevated opportunities for vicariance and speciation in trilobites, and other metazoans, given that speciation rates at this time period were high, though not phenomenally so. This provides clear evidence that abiotic factors played an important role in motivating evolution during this key episode in the history of life; biotic factors probably also played a role. The evidence for the role of biotic factors is considered in light of information from some problematic Cambrian taxa. These may show affinities with modern problematic pseudocoelomate phyla, although Cambrian and modern exponents differ dramatically in body size.     

A tiny eye indicating a planktonic trilobite

Abstract: Cambrian trilobites mainly lived on the sea floor, and up till now few, if any, unequivocally planktonic trilobites have been reported from earlier than the Ordovician. The late Cambrian (Furongian) to late Ordovician olenids are a distinctive group of benthic (sea‐floor dwelling) or nekto‐benthic trilobites. Here we show, however, that one recently described, miniaturized and very spiny olenid species, Ctenopyge ceciliae must have been planktonic (passively drifting or feebly swimming in the upper waters of the sea). This interpretation is based not only upon body form but also on the analysis of its visual system and may be one of the earliest records of the planktonic realm being invaded by trilobites.     

Cambrian agnostid communities in Tasmania

Jago, J. B.: Cambrian agnostid communities in Tasmania.
Two or possibly three different agnostid trilobite assemblages can be distinguished in the late Middle and early Upper Cambrian sequences of northern and western Tasmania. This is significant because in recent years agnostid trilobites have been widely used in local and international correlations of Middle and Upper Cambrian rocks. The three assemblages recognized are (1) an agnostid assemblage in which polymerid trilobites are abscnt, rare or present as thanatocoenotic fossils, (2) a ptychagnostid-non-nepeid assemblage, and (3) a nepeid-clavagnostid-peronopsid assemblage in which non-agnostid trilobites are abundant but ptychag-nostids are absent. It is proposed that assemblage (1) represents an open sea fauna, with assemblages (2) and (3) occurring in progressively shallower water.     

Abnormalities in early Paleozoic trilobites from central and eastern China

Malformations are common in trilobites, but the majority of described specimens are from Europe and North America. Only a few abnormal trilobites have been reported from China. Ten abnormal trilobites from Cambrian, Ordovician and Silurian strata in central and eastern China are documented. The abnormal Ordovician trilobites are found for the first time in China. All malformations occur in the thoraxes and pygidia, and were caused by a sub-lethal predatory attack, genetic or embryological malfunction, or injury sustained during molting. It is difficult to identify the predators of the six injured trilobites, but potential predators include Cambrian non-trilobite arthropods, Ordovician cephalopods, and Silurian eurypterids, chondrichthyes or cephalopods, even cannibalistic trilobites. Abnormal specimens caused by sub-lethal predatory attacks mainly occur in Cambrian strata in China and other areas in the world, and are rare in post-Cambrian strata. This pattern may reflect the rise of predators and increased predation in the post-Cambrian, which led to an increased trilobite fatality rate, thus reducing the probability that injured specimens would become fossilized.     

朝鲜南部的Pseudogl yptagnostus(三叶虫)并论朝鲜寒武纪斜坡相的意义

朝鲜南部Ｍａｃｈａｒｉ组Ｏｌｅｎｏｉｄｅｓ带的Ａｇｎｏｓｔｕｓ（Ｐｔｙｃｈａｇｎｏｓｔｕｓ？）ｏｒｉｅｎｔａｌｉｓ Ｋｏｂａｙａｓｂｈｉ一种应归于Ａｇｎｏｓ－ｔｏｔｅｓ（Ｐｓｅｕｄｏｇｌｙｐｔａｇｎｏｓｔｕｓ）Ｌｕ,１９６４一属,时代是晚寒武世长山期,不是早期中寒琥世,小林贞一的Ｏｌｅｎｏｉｄｅｓ带是中及晚寒武三叶虫混杂在一起的一个化石带。他建立的该组５个化石带也有问题。Ｃｏｒｅｏｌｅｎｕｓ,Ｃｈ     

Reappraising the early evidence of durophagy and drilling predation in the fossil record: implications for escalation and the Cambrian Explosion

The Cambrian Explosion is arguably the most extreme example of a biological radiation preserved in the fossil record, and studies of Cambrian Lagerstätten have facilitated the exploration of many facets of this key evolutionary event. As predation was a major ecological driver behind the Explosion – particularly the radiation of biomineralising metazoans – the evidence for shell crushing (durophagy), drilling and puncturing predation in the Cambrian (and possibly the Ediacaran) is considered. Examples of durophagous predation on biomineralised taxa other than trilobites are apparently rare, reflecting predator preference, taphonomic and sampling biases, or simply lack of documentation. The oldest known example of durophagy is shell damage on the problematic taxon Mobergella holsti from the early Cambrian (possibly Terreneuvian) of Sweden. Using functional morphology to identify (or perhaps misidentify) durophagous predators is discussed, with emphasis on the toolkit used by Cambrian arthropods, specifically the radiodontan oral cone and the frontal and gnathobasic appendages of various taxa. Records of drill holes and possible puncture holes in Cambrian shells are mostly on brachiopods, but the lack of prey diversity may represent either a true biological signal or a result of various biases. The oldest drilled Cambrian shells occur in a variety of Terreneuvian‐aged taxa, but specimens of the ubiquitous Ediacaran shelly fossil Cloudina also show putative drilling traces. Knowledge on Cambrian shell drillers is sorely lacking and there is little evidence or consensus concerning the taxonomic groups that made the holes, which often leads to the suggestion of an unknown ‘soft bodied driller’. Useful methodologies for deciphering the identities and capabilities of shell drillers are outlined. Evidence for puncture holes in Cambrian shelly taxa is rare. Such holes are more jagged than drill holes and possibly made by a Cambrian ‘puncher’. The Cambrian arthropod Yohoia may have used its frontal appendages in a jack‐knifing manner, similar to Recent stomatopod crustaceans, to strike and puncture shells rapidly. Finally, Cambrian durophagous and shell‐drilling predation is considered in the context of escalation – an evolutionary process that, amongst other scenarios, involves predators (and other ‘enemies’) as the predominant agents of natural selection. The rapid increase in diversity and abundance of biomineralised shells during the early Cambrian is often attributed to escalation: enemies placed selective pressure on prey, forcing phenotypic responses in prey and, by extension, in predator groups over time. Unfortunately, few case studies illustrate long‐term patterns in shelly fossil morphologies that may reflect the influence of predation throughout the Cambrian. More studies on phenotypic change in hard‐shelled lineages are needed to convincingly illustrate escalation and the responses of prey during the Cambrian.     

Sphaeroidal enrolment in middle Cambrian solenopleuropsine trilobites

Esteve, J., Zamora, S., Gozalo, R. & Liñán, E. 2010: Sphaeroidal enrolment in middle Cambrian solenopleuropsine trilobites. Lethaia, 10.1111/j.1502‐3931.2009.00205.x Fifty specimens belonging to species of Solenopleuropsis and Pardailhania from Spain and France demonstrate sphaeroidal enrolment in Cambrian trilobites for the first time. These solenopleuropsines show novel coaptative structures in different regions of the exoskeleton: in the cephalon there are vincular furrows and notches; in the thorax an articulating facet is developed at the pleural margins, with a ball and socket connection on the adaxial most portion, and an articulating half‐ring axially; the pygidium possesses an articulating facet. The interaction of these coaptative structures resulted in a sphaeroidal enrolment that was a progressive act from the first articulation between the occipital ring and the first segment to the pygidial articulating facet. A similar type of sphaeroidal enrolment is observed in the Devonian trilobite Phacops. Both Cambrian and Devonian trilobites developed a vincular furrow in the ventral surface of the cephalon to close their bodies tightly. In both cases, this is probably a convergent adaptation to protect against predators and obrution. Indeed, the enrolled trilobites are very common in obrution deposits restricted to shallow and soft muddy substrates. □Coaptative structures, convergence, Murero Formation, Pardailhania, Solenopleuropsinae, Solenopleuropsis.     

Moulting,ontogeny and sexual dimorphism in the Cambrian ptychopariid trilobite Strenuaeva inflata from the northern Swedish Caledonides

Abstract: Three thousand seven hundred disarticulated remains together with several articulated specimens of the Cambrian Series 2 ptychopariid trilobite Strenuaeva inflata Ahlberg and Bergström, 1978 have been collected from the Torneträsk area, northern Sweden. The material provides significant new data on the morphology, ontogeny, moulting and enrolment of the species. Two distinct morphotypes, possibly an expression of sexual dimorphism, are recognized. The morph with a pair of bulbs in the frontal area, interpreted as brood pouches, is considered to represent females. Statistical treatment of the length/width ratio in cranidia reveals isometric growth during ontogeny for both morphotypes. The transition from the meraspid to holaspid ontogenetic period has been established through recognition of the successive development of the number of thoracic segments in articulated late meraspides. Throughout its life cycle, S. inflata went through 11 meraspid degrees and at least 17 holaspid growth stages. Inferred moult ensembles and exuviae reveal the successive opening of cephalic sutures and the function of the rostral plate during exuviation. As in other ellipsocephalid trilobites in which enrolment is known, the pygidium and two or three thoracic segments of S. inflata are concealed beneath the cephalon (spiral enrolment) during complete enrolment.     

贵州剑河中寒武世中期甲劳组水母状化石的发现

贵州剑河革东镇八郎村南甲劳组中部钙质白云岩中新近发现的具有粗强放射状辐管的水母状化石和其下凯里组中具细辐管及同心环的拟轮盘水母(Pararotadiscus)有明显区别,属于伊尔东钵科(Eldoniidae)。其层位晚于中寒武世早期凯里生物群中拟轮盘水母(Pararotadiscus)层位1个化石带,属中寒武世中期,是该类化石在中国的最高层位,相当于北美布尔吉斯页岩生物群中Eldonia化石层位。     

Trilobite faunal successions across the base of the Furongian Series in the Taebaek Group, Taebaeksan Basin, Korea

The base of the Furongian Series in the Sino-Korean Block has not been clearly defined due to the lack of the index taxon, Glyptagnostus reticulatus. The Sesong Formation of the Taebaek Group, Taebaeksan Basin, Korea, has been known to range from the Guzhangian Stage of the Cambrian Series 3 to the middle Furongian Series, hence embracing the base of the Furongian Series. Silicified polymerid trilobites were recovered from the middle part of the Sesong Formation. Described are a total of 18 polymerid species of 13 genera: Neodrepanura sp. 1, Teinistion sp. 1, Huzhuia sp. 1, Huzhuia sp. 2, Liostracina simesi, Liostracina sp. 1, Parachangshania monkei, Parachangshania rectangularis nov. sp., Placosema bigranulosum, Fenghuangella laevis nov. sp., Baikadamaspis jikdongensis nov. sp., Baikadamaspis sp. 1, Prochuangia mansuyi, Maladioides coreanicus, Alataspis sesongensis nov. gen., nov. sp., Chuangia sp. 1, and ceratopygids genus and species indeterminate 1 and 2. The stratigraphic occurrence of these trilobites provides a basis for recognition of five zones across the base of the Furongian Series (in ascending order): the Neodrepanura, Liostracina simesi, Fenghuangella laevis, Prochuangia mansuyi, and Chuangia zones. The Neodrepanura and Chuangia zones are provisionally adopted from the previous biostratigraphic scheme, while the three other ones are newly proposed. The recommended base of the Furongian Series in the Taebaek Group of Korea coincides with the base of the Fenghuangella laevis Zone, which appears to represent an episode of profound trilobite faunal turnover.     

DENSITY-DEPENDENT SEXUAL SELECTION IN THE FUNGUS BEETLE,BOLITOTHERUS CORNUTUS

The hypothesis that population density can affect sexual selection on male horn size was tested in a three-year study of a fungus beetle, Bolitotherus cornutus. Males of this species have horns that vary greatly in length. These horns are used in fights over females; longer-horned males win the majority of fights, regardless of population density. However, density does affect the relationship between horn length and access to females. In six populations of naturally and experimentally varying densities, longer-horned males gained a greater advantage in access to females in low-density populations than at high density. This increase in access to females causes an increase in the number of females inseminated by longer-horned males; thus, sexual selection for longer horns is stronger at lower densities.     

THE LOWER CAMBRIAN EODISCOID TRILOBITE CALODISCUS LOBATUS FROM SWEDEN: MORPHOLOGY, ONTOGENY AND DISTRIBUTION

Abstract:  Several thousand disarticulated remains together with a few complete enrolled specimens of the lower Cambrian eodiscoid trilobite Calodiscus lobatus ( Hall, 1847 ) have been collected at two outcrop areas in Sweden. The material reveals new details of morphology and morphogenesis during ontogenetic development. Size-frequency analyses show that the material from the Fånån rivulet in Jämtland, central Sweden, represents a natural population dominated by juveniles, whereas the material from Gislövshammar in Scania, southern Sweden, has been sorted during postmortem transport. Three stages of protaspid development can be traced and defined as well as all subsequent ontogenetic stages for the cephalon, hypostome and pygidium. The early meraspid pygidium has a pronounced larval notch, which persists, though becoming progressively less distinct in later meraspides. The number of axial rings in the transitory pygidium increases throughout meraspid development until a third and final thoracic segment is liberated. During ontogeny the articulating half-rings are strongly developed, and both meraspides and holaspides were capable of full sphaeroidal enrollment and outstretched postures. The hypostome undergoes some dramatic modifications; in M0 the anterior margin is axe-shaped, by M1 the area of attachment greatly decreases and the hypostome becomes more elongated and pear-shaped, before attaining its adult form, which has an overall resemblance to that of polymerid trilobites. During ontogeny, the hypostome changes from a conterminant attachment to a natant condition, thereby mirroring hypostomal evolution within trilobites generally. The morphology, ontogeny, enrollment, hypostomal development and the presence of calcified protaspides suggest polymerid rather than agnostoid affinities of the eodiscoids.     

Cambrian (Series 2 to Miaolingian) platform facies from central Sonora,Mexico and the regional correlation

This study provides new insights about depositional paleoenvironments through siliciclastic microfacies, carbonate microfacies, and biofacies analysis from sedimentary formations of the lower and middle Cambrian (Stage 4–Wuliuan), exposed in central Sonora, northern Mexico. Results of the petrographic analysis of 48 samples revealed the following lithologies: quartzarenite, oncolytic rudstone, grainstone-packstone, wackestone, mudstone, and to a lesser extent sandy limestone. Two siliciclastic microfacies were identified: (A) quartzarenite with cross-bedded and horizontal stratification deposited in an intertidal and supratidal environment; and (B) massive quartzarenite with Skolithos ichnofacies deposited in subtidal and intertidal environments. Four carbonate microfacies were identified: microfacies 1 is a sandy limestone with trilobite fragments; microfacies 2 is a grainstone with intraclasts, salterellids, hyolithids, trilobites, and echinoderms plates; microfacies 3 is an oncolytic rudstone consisting of microbes and abundant echinoderms plates; and microfacies 4 is a packstone-grainstone with abundant ooids, trilobite fragments, and echinoderm plates. Two biofacies were identified: Agnostid-polymeroid biofacies with predominance of the trilobites Pentagnostus, Bathyuriscus, Oryctocephalites, and Elrathina; and Pagetia biofacies with abundant trilobites of the genera Pentagnostus, Pagetia and Elrathina. It is concluded by the sedimentation model that changes in sea level is the most important parameter in determining the siliciclastic microfacies, carbonate microfacies and biofacies; as well as the depositional environments that vary from the coastline (subtidal to supratidal) to shallow-water open circulation marine platform with low and high energy waters. The Cambrian deposits of northern Mexico are correlated with the deposits of California and Nevada (USA), as well as to the Precordillera (Argentina), where the species in common show a strong affinity.     

The eyes of trilobites: The oldest preserved visual system

The oldest preserved visual systems are to be found in the extinct trilobites, marine euarthropods which existed between about 520 and 250 million years ago. Because they possessed a calcified cuticle, they have a good fossil record, and commonly the lens-bearing surfaces of their paired compound eyes are well preserved. The sublensar structures, however, remain unknown. Three kinds of eyes have been distinguished. Holochroal eyes, apomorphic for trilobites, typically have many contiguous small lenses, set on a kidney-shaped visual surface. Lens optics, angular range of vision, and ontogeny have been established for many compound eyes. Some pelagic trilobites have enormous eyes, subtending a panoramic field of view. Schizochroal eyes are found only in one group, the phacopids (Ordovician to Devonian). These have large lenses, separated from each other by cuticular material, and the lenses have a complex doublet or triplet internal structure, which could focus light sharply. The optics of phacopid eyes are becoming increasingly well known despite the fact that there are no direct counterparts in any living arthropods today. Schizochroal eyes are apomorphic for phacopids and were derived by paedomorphosis from a holochroal precursor. Abathochroal eyes are confined to a short-lived Cambrian group, the eodiscids (of which most representatives were blind). Less is known about them than other trilobite eyes and their origins remain obscure. Some trilobite groups had no eyes, but had other kinds of sensory organs. In Upper Devonian times several groups of trilobites independently underwent progressive eye-reduction leading to blindness, related to prevailing environmental conditions of the time. The last trilobites (of Carboniferous and Permian age), however, had normal holochroal eyes, which persisted until the final extinction of trilobites at the end of the Permian.