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Larvae of lacewings (Neuroptera) are known to be fierce predators. According to the morphology of fossil forms thisseems to have been the case already in the Early Cretaceous. While being predators, lacewing larvae are also food itemsfor other organisms. Here we report two pieces of amber from Myanmar providing instances of such cases. In one amberpiece several isolated stylets of lacewing larvae are preserved closely associated together. The most likely interpretationis that a predator preying on lacewing larvae has regurgitated or defecated these non-digestible pieces, yet the identityof the predator remains unclear. The other amber piece preserves a larva resembling modern day larvae of split-footedlacewings (Nymphidae). The larva has projections on its trunk, allowing it to wear a camouflaging cloak. In the headregion, a mite (Acari) is attached to the larva; more precisely, the entire anterior body region of the mite is apparentlyinserted into the lacewing larva. The mite is smaller than the larva. It is known from the modern fauna that stage 1 larvaeof Ascalaphidae can be attacked also by rather small predators, such as ants. The mite can therefore well be interpretedas a true predator instead of a parasite, especially considering the unusual mode of attachment. We briefly review interactionsof lacewing larvae with other organisms represented in amber from Myanmar and add two new pieces to thepuzzle of reconstructing the trophic interactions in the 100-million-year old amber forest.

Neuroptera is one of the smaller ingroups of Holometabola, the ingroup of Insecta characterised by “complete” metamorphosis. Neuroptera comprises about 6000 species in the modern fauna, but appears to have been more diverse in the past. While adults distantly resemble certain moths or damselflies, the larval forms of Neuroptera are mostly fierce predators with prominent venom-injecting stylets. The most well-known of these larvae are probably those of antlions. Antlions and their closer relatives (silky lacewings, split-footed lacewings, ribbon-winged lacewings, spoon-winged lacewings, and owlflies) form a distinct monophyletic ingroup of Neuroptera, Myrmeleontiformia, hence the antlion-like forms. The fossil record of antlion-like larvae dates back far into the Cretaceous; many forms are known by exceptionally wellpreserved specimens entrapped in amber. The oldest fossil record of a neuropteran larva (not an antlion-like form) comes from Lebanese amber. Interestingly, the supposedly oldest record of an antlion-like larva is preserved in rock and comes from the famous Lower Cretaceous Crato Formation. We re-evaluate this fossil based on high-resolution composite photography. Due to the non-availability of many key characters, standard procedures for identifying the specimen to a more narrow ingroup remains challenging. Therefore, we used a morphometric approach. A combination of non-metric multidimensional scaling (NMDS), parallel coordinate plots and discriminant function analysis indicates that the fossil is a representative of the group Ascalaphidae (owlflies) + Myrmeleontidae (antlions). We discuss implications of this result for the fossil record of neuropteran larvae. These include the rather derived morphology of the oldest fossil larva of Myrmeleontiformia in contrast to previous expectations. Furthermore, fossils from soil dwellers can not only be expected to be found in amber, but also as compression fossils.

Achelatan lobsters, also known as spiny and slipper lobsters, develop via a highly specialised larval form. This special larva, phyllosoma, is flat, translucent, possesses elongate legs and can grow to enormous sizes. Although these larvae may appear very fragile, they are well-known as fossils. Thousands of specimens have been found in the lithographic limestone of Southern Germany (Tithonian, Upper Jurassic, about 150 mya). At least three types of fossil, but modern-appearing phyllosoma larvae are known. Additionally, fossil larvae that possess only some of the characters of modern-day phyllosoma larvae are known from the same Lagerstätte, but also from the younger limestone beds of Lebanon. Here we report a new achelatan fossil from the older Posidonia Shale (Toarcian, Lower Jurassic, 175–183 mya). The specimen shows certain characters of a phyllosoma larva, but other characters appear like those of post-phyllosoma stages of achelatan lobsters. This specimen is therefore the oldest occurrence of an achelatan lobster larva. We compare the new specimen with other fossil larvae with such mixed or “intermetamorphic” morphologies.

Dictyoptera, which comprises cockroaches, termites and mantids, is a quite successful group of insects in evolutionary terms with a long fossil record—roachoid insects were already abundant 315 million years ago in the Carboniferous forests. One of the most remarkable autapomorphies of extant dictyopterans, and possibly a major factor for their persisting success, is the ability to produce oothecae. Despite the robustness of this sort of egg package, fossils of oothecae are very rare, the oldest direct evidences being from the Cretaceous Crato Formation in Brazil (115 mya). The ability to produce oothecae is presumably linked to a specific ovipositor morphology, including a significant length reduction. Hence, ovipositor morphology can indirectly inform about the reproductive strategy of a species. Herein we describe the ovipositor morphology of various fossil forms of dictyopteran insects. Early fossil roachoids, in contrast to the modern forms, possessed a very long and prominent ovipositor, reminiscent of the ovipositor in orthopterans (Ensifera), indicating that these forms laid individual, rather small eggs into a substrate. We present examples from different fossil deposits, which show the entire range of ovipositor morphologies, from very long forms over forms with ovipositors partly reduced in length to modern-appearing morphologies. Most remarkably, different shapes of ovipositors seem to be present in roachoids in the fauna of the 115 million years old Crato Formation—species with long prominent ovipositors co-existed with species with a reduced short and broad ovipositor. Additionally, females that carry oothecae attached to their abdomen indicate a third type of ovipositor: a further reduced ovipositor as seen in modern forms, which already allowed the internal production of oothecae.