Temporal range: Emsian–Carnian
The Bactritida form a small order of more or less straight-shelled (orthoconic) cephalopods that first appeared during the Emsian stage of the Devonian period (390 million years ago) and persisted until the Carnian stage of the Triassic period (235 million years ago). They are considered ancestors of the ammonoids, as well as of the coleoids (octopus, squid, cuttlefish, and the extinct belemnites).
Bactritids are distinguished from the more primitive nautiloids by the small size and globular shape of the protoconch, the so-called embryonic shell. Nautiloids have relatively large embryonic shells, and living species lay a few large eggs. In contrast, bactritids and ammonoids produced large numbers of small eggs, each housing a small embryonic shell .
Classification and description
Bactritida (Erben 1964) are characterized by orthoconic to cyrtochonic shells that may be long or short with a narrow siphuncle invariably in contact with the ventral wall and sutures uniformly with V-shaped ventral lobes. Septal necks are orthochoanitic to cyrtochoanitic, the apical angle may be small or large, and the protoconch is globular to egg-shaped. The Bactritida comprise two families, the Bactritidae and the Parabactritidae.
The Bactritidae (Erben 1964) are characterized by long orthoconic to cyrtochonic shells with a small apical angle (less than 10°) and septal necks that are orthochoanitic. Chamber length is variable. The Bactritidae contain eight recognized genera. Bactrites has the longest range, from the Lower Devonian to the Upper Permian, and even possibly from the Silurian. The Bactritidae gave rise to the Ammonoidea in the Early Devonian starting with an early Bactrites and going with increasingly tight curvature from Lobobactrites to Cyrtobactrites, leading to the gyroconic Anetoceras of the Anarcestida (Ammonoidea) (Erben 1964, Klug and Korn 2004).
The Parabactritidae (Erben 1964) are characterized by orthoconic and breviconic shells with a large apical angle (greater than about 10°) and septal necks that are vary from orthochoanitic or suborthochoanitic to cyrtochoanitic. The Parabactritidae contain some five described genera and are thought to have given rise to the Belemnoidea (Coleoidea).
The Bactritida have their origin in the Orthocerida. Some paleontologists, such as Erben (1964) and Holland (2003), regard Bactroceras (Eobactrites) as a true bactritid because of its spherical apex and ventral siphuncle.
Recent research suggests otherwise, however. The shell of Bactroceras has important differences from those of true bactritids. For instance, the first chamber of Bactroceras resembles that of other Ordovician orthocerids, such as Archigeisonoceras and Hedstroemoceras: it is about 10 mm in diameter, and is short, forming a spherical cap. True bactritids more strongly resemble late Silurian and Devonian orthocerids, whose first chamber is only about 5 mm across. Moreover, there is a large stratigraphic gap of nearly 50 million years between Bactroceras and the next orthocones with a spherical apex and ventral siphuncle.
Paleoecology and lifestyle
Bactritids, especially the Bactritidae, seem to have lived in a vertical orientation, head down, as probably did many of the Orthocerida such as Michelinoceras and Buttsoceras, or these forms without extensive internal ballast may simply have been more flexible in their vertical orientation than the well-ballasted bottom-dwellers such as the actinocerids and endocerids. The ventral siphuncle of the Bactritida would have facilitated chamber dewatering in either horizontal or vertical orientation or in between. A central siphuncle would have made horizontal or near-horizontal dewatering more difficult, on the other hand. (Holland 2003, Klug and Korn 2004) Bactritids, like cephalopods in general, were probably active predators with tentacles of some sort. As with other externally shelled forms, they were probably not active swimmers in the sense of fish or squid. Rather, they were likely stalkers and ambush predators hiding among the sea weeds, snatching prey found below.
- Holland, Charles H. (2003). "Some observations on bactritid cephalopods". Bulletin of Geosciences (Czech Geological Survey) 78 (4): 369–372. ISSN 1214-1119.
- Kröger, B.; Mapes, R. H. (2007). "On the origin of bactritoids (Cephalopoda)". Paläontologische Zeitschrift 81 (3): 316–327. doi:10.1007/BF02990181.
- Erben H.K. 1964; Bactritoidea, in the Treatise on Invertebrate Paleontology Vol K Nautiloidea, K491 –, Teichert, C and Moore R.C. Eds, GSA and Univ Kansas Press.
- Klug, C. and Korn, D. 2004. The origin of ammonoid locomotion. Acta Palaeontologica Polonica 49 (2): 235–242