Soft–part preservation in heteromorph ammonites from the Cenomanian–Turonian Boundary Event (OAE 2) in north–west Germany

Abstract: From thinly laminated marlstones of the Hesseltal Formation, representing the Late Cenomanian Oceanic Anoxic Event (OAE) 2, at Lengerich in the Teutoburger Wald (Westfalen, north‐west Germany), 17 sediment‐compacted baculitid ammonites with carbonised and partially phosphatised soft parts are recorded. Some preserve remains of the buccal mass, including jaws (occasionally articulated) and radulae, as well as of the cephalic cartilage, such as eye capsules. Such have not yet been recorded previously for the order Ammonoidea. In addition, originally unmineralised parts found preserved in these specimens include extensive portions of the digestive tract, the siphonal tube, false colour patterns (megastriae), as well as traces of what would appear to be the oviduct. At the same levels, patches with numerous isolated horny upper and rarer lower jaws as well as radulae occur; these may represent regurgitates or faeces of larger predators. The cephalopod remains described were deposited in an epicontinental setting, possibly at palaeodepths between 200 and 600 m. In this particular Late Cretaceous fossil Lagerstätte, upper jaws and anaptychi of ammonites rank among the commonest fossils.     

Generalist predation on forest tent caterpillar varies with forest stand composition: an experimental study across multiple life stages

1. Generalist enemies can regulate low‐density forest insect populations, and are widely considered to cause greater mortality in more diverse habitats. Forest tent caterpillars (Malacosoma disstria Hübner; FTC) are a major defoliator of aspen (Populus tremuloides Micheaux) in the boreal forest, a region with a mosaic of forest stand types. This heterogeneity may influence FTC outbreaks if generalist predation or parasitism differs among stands of different tree composition. 2. Using exclusion experiments we estimate predation and parasitism of FTC across multiple life‐history stages in low‐density populations occupying both aspen (low diversity) and mixedwood stands (high diversity). 3. Arthropod and avian generalist predators were responsible for most natural enemy‐caused mortality of immature FTC, but their relative impacts varied among FTC life‐history stages. Contrary to expectation, predation on late instar larvae and pupae was higher in the less diverse aspen stands and early instar mortality did not differ. 4. By considering multiple life‐history stages, our results provide a more comprehensive view of natural enemy‐caused morality of immature FTC. Because generalist predation on FTC was higher in aspen than in mixedwood stands, we suggest that FTC populations may be slower to reach outbreak levels in aspen stands.     

Some Notes on the Morphology of an Aberrant Actinian (Hexacorallia, Actiniaria) Associated with the Glaucothoe of the Hermit Crab Paguropsis typica Henderson (Anomura, Paguridae)

The planktonic glaucothoe of the Indo-West Pacific hermit crab Paguropsis typica Henderson has an aberrant anthozoan polyp, identified as a nynanthean actinian, attached to the underside of its thorax. The morphology of the anemone is described. The scapus is dumb-bell shaped and exhibits a slit-like mouth opening oriented transverse to the animal's siphonoglyphal plane. The gonads are very well developed, whereas tentacle-like structures or retractor muscles of certain septa are reduced. In the adult stage, Paguropsis typica is associated with the zoanthidean Epizoanthus paguropsides . It is assumed that the actinian is lost at the ecdysis leading to the first "hermit stage" and that P. typica might possibly seize a free Epizoanthus colony and adapt it to its body.     

A field technique for the determination of zooplankton grazing on natural bacterioplankton

SUMMARY. 1. A method for the determination of zooplankton community grazing rates on natural populations of bacteria is described.
2. Undisturbed zooplankton samples were incubated with ³H-thymidine-labelled bac teriioplankton, and animals and their food subsequently separated by size.
3. Prehandling of zooplankton by concentration before incubation reduce the grazing rates by a factor ranging from three to four.
4. Time series experiments showed that appropriate incubation periods ranged from 40 min at 14°C to 60 min at 10°C.
5. Spatial variability in the zooplankton was the main source of the overall standard error. This was considerably reduced by using composite samples.