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A length–frequency sample (n = 295) from a fossil population of the Ordovician trilobite Triarthrus eatoniHall, 1838, assembled and analyzed by J. L. Cisne in 1973 is here reexamined using methods of length–frequency analysis commonly used in fishery science and marine biology. Theoretical considerations and the empirical data at hand suggest that the growth of T. eatoni was not “linear,” but asymptotic, as is the growth of most Recent marine invertebrates. The parameters of the von Bertalanffy growth function (L∞ = 41 mm, K = 0.29 yr–1) suggest that T. eatoni, which apparently lived in a challenging environment, grew somewhat more slowly than the extant marine isopod Ceratoserolis trilobitoides (Eights, 1833), used here as Recent analogue to T. eatoni. This trilobite probably lived up to 10 years, rather than the suggested 4 years, and its mortality rate was 15%–20% per year rather than 30%–40% per year. These represent the first estimates of trilobite absolute growth characteristics using methods known to accurately model growth in extant water-breathing ectotherms. These provide a baseline for trilobite growth that can be used to make inferences about growth in other species. The approach used here may also be applied to other trilobites for which suitable length–frequency data exist.

Efficient extraction of oxygen from ambient waters played a critical role in the development of early arthropods. Maximizing gill surface area enhanced oxygen uptake ability but, with gills necessarily exposed to the external environment, also presented the issue of gill contamination. Here we document setae inserted on the dorsal surface of walking legs of the benthic-dwelling middle Cambrian Olenoides serratus and on the gill shaft of the Late Ordovician Triarthrus eatoni. Based on their physical positions relative to gill filaments, we interpret these setae to have been used to groom the gills, removing particles trapped among the filaments. The coordination between setae and gill filaments is comparable to that seen among modern crustaceans, which use a diverse set of setae-bearing appendages to penetrate between gill filaments when grooming. Grooming is known relatively early in trilobite evolutionary history and would have enhanced gill efficiency by maximizing the surface area for oxygen uptake.

Traditionally, the distinction between meraspis and holaspis among trilobites has been based on the achievement of the full adult complement of thoracic segments. Using a large sample (over 700 specimens collected from a single bed) we explore the utility of employing the ontogenetic trajectory of the cranidium as an alternative means to differentiate trilobite growth stages. This method is particularly useful for species represented solely by exuviae and disarticulated individuals. We use geometric morphometrics to examine shape change among cranidia ranging in size from 0.9 mm to 11.6 mm in cephalic length. The 114 measured specimens exhibit a rather continuous gradation in size in which no distinct instars are evident. The meraspid and holaspid specimens exhibit allometry when partial warp scores and uniform components of shape derived from thin-plate spline analysis are regressed onto log centroid size. To describe allometric shape change, deformation vectors from the smallest to the largest specimen in both ontogenetic stages are presented in three different superimposition settings by using a new software program. We have concluded that a new superimposition method (the Sliding Baseline Registration) is a useful tool for visualizing allometry in organisms that contain an axis of symmetry. As a result, we conclude that allometry is evident in meraspides and holaspides, but the degree of allometry in holaspides is very small relative to that in meraspides. The boundary between meraspis and holaspis in Triarthrus becki appears to correspond to a large change in the rate of ontogenetic change, but neither to a change in the direction of that trajectory nor to a cessation of ontogenetic change. This boundary also corresponds to a cranidium centroid size that matches well previous determinations that holaspis begins at about 2.8 mm in cephalic length.

Olenid trilobites are characteristic of low-oxygen environments in the early Paleozoic, and researchers have proposed that olenids may have harbored chemoautotrophic symbionts, allowing them to live in borderline sulfidic environments. Beds with soft-tissue preservation at the Beecher's Trilobite Bed site in the Frankfort Shale and the Martin Quarry in the Whetstone Gulf Formation (both Ordovician, New York State) are dominated by the olenid Triarthrus. A bed-by-bed analysis of the sedimentology, taphonomy, paleoecology, and ichnology demonstrates that the exceptionally preserved organisms did not undergo extensive transport, and that the intervals bearing Triarthrus accumulated predominantly in the lower part of the dysaerobic zone. These intervals contain a low-diversity benthic fauna occurring in relatively low abundance, and consisting primarily of small brachiopods and trilobites. The taphonomy, in particular localized pyritization, the associated fauna, and the distribution of Triarthrus elsewhere in the Taconic foreland basin demonstrate that the environments in which Triarthrus lived were not sulfidic, and that these trilobites were unlikely to have adopted a chemoautotrophic mode of life.

Traditionally, the distinction between meraspis and holaspis among trilobites has been based on the achievement of the full adult complement of thoracic segments. Using a large sample (over 700 specimens collected from a single bed) we explore the utility of employing the ontogenetic trajectory of the cranidium as an alternative means to differentiate trilobite growth stages. This method is particularly useful for species represented solely by exuviae and disarticulated individuals. We use geometric morphometrics to examine shape change among cranidia ranging in size from 0.9 mm to 11.6 mm in cephalic length. The 114 measured specimens exhibit a rather continuous gradation in size in which no distinct instars are evident. The meraspid and holaspid specimens exhibit allometry when partial warp scores and uniform components of shape derived from thin-plate spline analysis are regressed onto log centroid size. To describe allometric shape change, deformation vectors from the smallest to the largest specimen in both ontogenetic stages are presented in three different superimposition settings by using a new software program. We have concluded that a new superimposition method (the Sliding Baseline Registration) is a useful tool for visualizing allometry in organisms that contain an axis of symmetry. As a result, we conclude that allometry is evident in meraspides and holaspides, but the degree of allometry in holaspides is very small relative to that in meraspides. The boundary between meraspis and holaspis in Triarthrus becki appears to correspond to a large change in the rate of ontogenetic change, but neither to a change in the direction of that trajectory nor to a cessation of ontogenetic change. This boundary also corresponds to a cranidium centroid size that matches well previous determinations that holaspis begins at about 2.8 mm in cephalic length.

Middle and Upper Ordovician Triarthrinae from the Precordillera of San Juan, Argentina, include the Whiterock/Llanvirn Porterfieldia turneri (Baldis and Pöthe, 1995) and P. acava new species, and the early Caradoc Triarthrus jachalensis (Harrington and Leanza, 1957). Each of these species is described based on silicified material, including ontogenies, from the Las Aguaditas Formation. Porterfieldia maanssonae new species from the lower member of the Gualcamayo Formation (late Arenig) at Río Gualcamayo, San Juan Province, and Río Guandacol, La Rioja Province, is closely allied to P. turneri. Two protaspid stages are present in Porterfieldia, whereas mineralized protaspid stages are apparently lacking in Triarthrus jachalensis. Triarthrus jachalensis was capable of sphaeroidal enrollment by meraspid degree 2. Precordilleran species bear closest comparison to others from Spitsbergen (Porterfieldia acava n. sp. and P. parapunctata) and Sweden/Norway (Triarthrus jachalensis and T. linnarssoni).

Fossils of trilobites were discovered at a New York quarry named Beecher's Trilobite Bed. These creatures were of a family of invertebrates that flourished during much of the Paleozoic era. Mineral pyrite formed on these animals reveals them to shine against their bed of black shale.