The family Austropanorpidae (Mecoptera) was described by Willmann in 1977 from the Eocene of Australia, based on one genus and species, Austropanorpa australis Riek, 1952. During a restudy of the collection of the Paleontological Institute, Russian Academy of Sciences in Moscow, a second and much older representative of this family was found. This specimen, described as Orthophlebia martynovae Sukatsheva, 1985 from Siberia (Russia), was considered until now to be a member of family Orthophlebiidae. We transfer this species to the Austropanorpidae, extending the age of this family back to the Early Jurassic. An updated diagnoses of the family Austropanorpidae and genus Austropanorpa are presented here.

Clavate (club-shaped) structures rimming mid-Cretaceous Burmese amber from Myanmar, previously misdiagnosed as fungal sporocarps, are shown to be domichnia (crypts) of martesiine bivalves (Pholadidae: Martesiinae). They are similar in form to Teredolites clavatus Leymerie, 1842 and Gastrochaenolites lapidicus Kelly & Bromley, 1984; however, the former identification is preferable, given that they are martesiine crypts in amber as opposed to a lithic substrate. Cross-cutting relationships between the clavate features and inclusions in the amber demonstrate that the features post-date hardening of the resin. The fills of the crypts are variable, including sand grade sediment of very fine to coarse sand grainsize, and sparry calcite cements. In some cases, the articulated valves of the pholadid bivalve responsible are visible inside the borings. However, one remarkable specimen contains two pairs of articulated shells ‘floating’ in amber, not associated with crypts; an observation that suggests that the resin was still liquid or soft when the bivalves were trapped in the resin. One individual is associated with an irregular sediment-filled feature and shows shell breakage. Formation of a solid rim around a liquid central volume has been documented in subaqueous bodies of resin in modern swamp forests, and argues for a close proximity between the amber-producing trees and a brackish water habitat for the bivalves. The presence of pyrite as thin films and crystal groups within Burmese amber is further consistent with such a depositional environment. Comparison of the size of pholadid body fossils with growth rates of modern equivalents allows the duration of boring activities to be estimated and suggests that small fossil pholadids in Burmese amber became trapped and died within 1–2 weeks of having settled on the resin. Larger examples present within well-formed domichnia formed in hardened resin. Since ‘hardground’ describes early lithified sediment as a substrate and ‘woodground’ describes wood as a substrate, the term ‘amberground’ is used here to described borings in an amber substrate.

The Family Orthophlebiidae ranges from the Middle Triassic to the Early Cretaceous. The Wealden Mecoptera have added to our knowledge of the Mecoptera from the Early Cretaceous of southern England, but have been comparatively little studied. Here we present the description of the first orthophlebiid from the Wealden of England. Mesopanorpa brooksorum sp. nov. from England is the earliest Cretaceous representative of this genus.

A new family, Worcestobiidae fam. nov., is established for two Triassic fossil species of Mecoptera removed from the family Orthophlebiidae: Orthophlebia gigantea Tillyard, 1933 and O. haradai Ueda, 1991. A new genus, Worcestobia gen. nov., is erected and both species are transferred to this genus. The new taxa were established as a result of ongoing taxonomic work on Orthophlebiidae, one of the most problematic families within fossil Mecoptera, considered to be a paraphyletic group of species.

The family Achilidae (Hemiptera, Fulgoromorpha, commonly called planthoppers) is one of the least known and least understood groups, due to their cryptic lifestyle. They appear in the fossil record in the Lower Cretaceous, with a single genus and two species from the Crato Formation of Brazil. The oldest amber inclusion is reported from the earliest Late Cretaceous amber of Burma. Surprisingly, Achilidae are relatively common among the larger inclusions that can be found in Eocene Baltic amber. The first description of a fossil species was in the mid-19th Century. Currently, there are 13 genera and 16 species known from fossils, of which nine genera and 11 species are from Baltic amber. However, many of them need reconsideration, revisionary studies and placement in the phylogenetic context of the family. Former studies on inclusions in this amber revealed several unique forms (extinct tribes Ptychoptilini and Waghildini), or taxa ascribable to the sparse Recent tribe Achilini. This paper provides an overview of the knowledge of fossil Achilidae, particularly those from Baltic amber. The Eocene appears to be the heyday of the family; however, this hypothesis should be tested with further detailed studies.

We present the first specific record of a chironomid of the tribe Tanytarsini from early Eocene Cambay amber, India (52–53 Ma). The oldest known extinct tanytarsine genus, Gujaratomyia Giłka & Zakrzewska, gen. nov., is described on the basis of adult males of G. miripes Giłka & Zakrzewska, sp. nov. The species displays an unusual leg structure with unique leg ratios and tibial armature. The combination of the head and genital apparatus characters supports the hypothesis that Gujaratomyia and Cladotanytarsus are members of a common group within the subtribe Tanytarsina.

Abundant insect fossils have been recorded from the Lower Cretaceous of the Jiuquan Basin, but very few odonatans have been recorded. In this paper, a new damsel-dragonfly, Cretastenophlebia jiuquanensis sp. nov., is described from the Lower Cretaceous Zhonggou Formation in the Hanxiagou outcrop, Jiuquan Basin, northwestern China. This is the second species of the genus Cretastenophlebia Fleck et al., 2003. Cretastenophlebia jiuquanensis sp. nov. differs from Cretastenophlebia mongolica Fleck et al., 2003 in the presence of a broad discoidal triangle, a basally straight IR1 and less cells along the posterior wing margin between IR2 and RP2. Cretastenophlebia has been previously reported from the Lower Cretaceous of Bon-Tsagaan, central Mongolia. The new discovery expands the record of Cretastenophlebia to the Jiuquan Basin in Albian.

A small fossil insect with scales on the wings and body was identified as a representative of Aphiesmenoptera from Burmese amber. The species is introduced here as Tarachocelis microlepidopterella (†). The insect is described in detail, and photos and line drawings are provided for wing venation, head, mouthparts, scales, legs and abdomen. All characters shared with primitive Lepidoptera and Trichoptera are symplesiomorphies or groundplan traits of Amphiesmenoptera. In addition, the Burmese fossil has a number of remarkable autapomorphies, giving it an appearance that deviates clearly from known families of Lepidoptera and Trichoptera. The species, representing a family of its own, Tarachocelidae, is considered a separate and unique taxon in the stem-group of Amphiesmenoptera and is provisionally placed as Amphiesmenoptera incertae sedis.*

*NB: See Note Added in Proof (Section 4).

A new species of the genus Dicranomyia Stephens, 1829 (Diptera: Limoniidae) from Baltic amber is characterised, illustrated and described. This finding represents the second fossil of the subgenus Melanolimonia. The morphological features of the new species and the morphology comparison with its closest fossil relatives are discussed.

Based on two well-preserved specimens from late Eocene Baltic amber, a new fossil species belonging to the family Trogossitidae, Seidlitzella hoffeinsorum sp. nov., is described. This is the second known fossil species of the tribe Gymnochilini and the second known species of the genus Seidlitzella. The systematic and biogeographical relations of the genus to other members of the Gymnochilini are discussed. It is hypothesised that the extant eastern Mediterranean species Seidlitzella procera may be phylogenetically related to the genus Phanodesta, today distributed in New Zealand, New Caledonia, Lord Howe Island, Juan Fernandez Island and Sulawesi.

Dermaptera (earwigs) are described from the Triassic of Australia and England, and from the Jurassic and Cretaceous of England. Phanerogramma heeri (Giebel) is transferred from Coleoptera and it and Brevicula gradus Whalley are re-described. Seven new taxa are named based on tegmina: Phanerogramma australis sp. nov. and P. dunstani sp. nov. from the Late Triassic of Australia; P. gouldsbroughi sp. nov. from the Triassic/Jurassic of England; Brevicula maculata sp. nov. and Trivenapteron moorei gen. et sp. nov. from the Early Jurassic of England; and Dimapteron corami gen et sp. nov. and Valdopteron woodi gen. et sp. nov. from the Early Cretaceous of England. Phanerogramma, Dimapteron and Valdopteron are tentatively placed in the family Dermapteridae, and Trivenapteron is incertae sedis. Most of the specimens of Phanerogramma heeri are from the Brodie Collection and labelled ‘Lower Lias'; however, some were collected from the underlying Penarth Group, thus this species spans the Triassic/Jurassic boundary. The palaeobiogeography of the Late Triassic and Early Jurassic of England is discussed.

Arthropods were the first known animals to colonise land habitats, with myriapods and arachnids having done so at least by the Silurian. Much later, several lineages of Pancrustacea (hexapods and the paraphyletic crustaceans) also ventured onto land; the hexapods by the Early Devonian, and later at least four other groups of crustaceans, namely isopods, amphipods, ostracods and decapods, most of which generally colonised the continental water bodies. All faced a series of challenges (in particular: gas exchange; desiccation; reproduction; osmoregulation; and exposure to ultraviolet radiation), resulting in many morphological, physiological and ecological adaptations. Nonetheless, whether they reached land via saltwater or freshwater remains poorly documented, mainly because relevant localities are few. The Famennian (Late Devonian) Strud locality in Belgium provided an exceptional source of information on early aquatic continental ecosystems and their plant, vertebrate and arthropod colonisers at a crucial step in the terrestrialisation process. Here, we review and update its crustacean fauna, which inhabited floodplain and temporary pool waters. New anatomical details of the notostracan Strudops goldenbergi Lagebro et al., 2015, as well as a new genus and species of spinicaudatan, are described. We also discuss the ecology of this unique, early continental ecosystem and the insights it gives into the terrestrialisation process.

The genus Orthobittacus was established by Willmann (1989) and is characterised by a long Sc vein and the unusually developed medial sector for the Bittacidae. Four Jurassic species have been described in this genus to date: O. abshiricus (Martynova, 1951) from Kirgizia; O.desacuminatus (Bode, 1953) from Braunschweig (Germany); O. polymitus Novokshonov, 1996 from Karatau (Kazakhstan); and O. maculosus Liu, Shih, Bashkuev & Ren, 2016 from the Jiulongshan Formation of Daohugou (China). The fifth congeneric and second species from China, O. suni sp. nov., is described herein. The importance of the genus Orthobittacus for the phylogeny of Bittacidae, as the most plesiomorphic genus, is discussed.

Fossil tree resins preserve a wide range of animals, plants, fungi and microorganisms in microscopic fidelity. Fossil organisms preserved in an individual piece of amber lived at the same time in Earth history and mostly even in the same habitat, but they were not necessarily parts of the same interacting community. Here, we report on an in situ preserved corticolous community from a piece of Miocene Dominican amber which is composed of a lichen, a moss and three species of leafy liverworts. The lichen is assigned to the extant genus Phyllopsora (Ramalinaceae, Lecanoromycetes) and is described as P.magna Kaasalainen, Rikkinen & A. R. Schmidt sp. nov. The moss, Aptychellites fossilis Schäf.-Verw., Hedenäs, Ignatov & Heinrichs gen. & sp. nov., closely resembles the extant genus Aptychella of the family Pylaisiadelphaceae. The three leafy liverworts comprise the extinct Lejeuneaceae species Cheilolejeunea antiqua (Grolle) Ye & Zhu, 2010 and Lejeunea miocenica Heinrichs, Schäf.-Verw., M. A. M. Renner & G. E. Lee sp. nov. and the extinct Radulaceae species Radula intecta M. A. M. Renner, Schäf.-Verw. & Heinrichs sp. nov. The presence of five associated extinct cryptogam species, four of which belong to extant genera, further substantiates the notion of a stasis in morphotype diversity, but a certain turnover of species, in the Caribbean since the early Miocene.

At least since the Cretaceous Terrestrial Revolution, the geographical distribution of aphids, particularly in the Northern Hemisphere, has been strongly affected by the low thermal tolerance of their obligatory bacterial symbiont, Buchnera aphidicola, which was why the aphids switched to obligate parthenogenesis in low latitudes. Hormaphidids and greenideids penetrated into the tropics only after the Oligocene strengthening of climate seasonality, and specialisations of the tropical representatives of these families did not allow them to spread further south (in the case of cerataphidines), or only allowed in few cases (in the case of greenideids).

Aphids suffered from the Mesozoic–Cenozoic boundary extinction event much more strongly than other insects. The extinction was roughly coincidental with the establishment of the tight symbiosis of aphids with formicine and dolichoderine ants, which was accompanied by the flourishing of all three groups.

In the Cretaceous, all of the representatives of extant and subfamilies occupied positions that were subordinate to Armaniinae and Sphecomyrminae. Prior to large ant colonies evolving their efficient ant–aphid mutualism, the aphids remained unprotected before the growing ant predation. The origin of the aphid trophobiosis with large colonies of Formicinae and Dolichoderinae has resulted in the steep decline of aphids left beyond that ant–aphid symbiotic network. By at least the basal Eocene (unlike the Late Cretaceous), ant proportions in the entomofauna increased sharply, and evident dominants emerged. Even now, aphid milkers from small colonies (hundreds of specimens) never protect their symbionts, and homopteran-tending ants are more likely to be dominant, with large colonies of 104–105 workers.

The mutualistic ant–aphid system failed to cross the tropical belt during the Cenozoic because of Buchnera's low heat tolerance. As a result, the native southern temperate aphid fauna consists now of seven genera only, five of which are Late Cretaceous relicts. Some of them had relatives in Late Cretaceous amber of the Northern Hemisphere.

Twelve specimens of early Toarcian Mecoptera and Diptera from the vicinity of Wolfsburg were investigated for the present study. The material was found during house building activities in the 1980s at the locality Große Kley in Mörse, an urban district of the city of Wolfsburg, Lower Saxony, Germany. The specimens were found in calcareous nodules of the Harpoceras falciferum Zone that occur within the Liassic black shales (Posidonia shale). Six specimens of Mecoptera, five belonging to the family Orthophlebiidae and one belonging to the Bittacidae, and six representatives of the following Diptera families were identified: Ptychopteridae, Limoniidae, Anisopodidae and the superfamily Mycetophiloidea. The fossil fauna of Wolfsburg is similar to that of other early Toarcian sites in Germany, described by Handlirsch (1906, 1939), Bode (1905, 1953) and Ansorge (1996) from Braunschweig, Dobbertin and Grimmen. Two new species are described, Mesorhyphusulrichi sp. nov. (Anisopodidae) and Archipleciomima germanica sp. nov. (Mycetophiloidea).

The Middle Jurassic is a poorly sampled time interval for non-pelagic neosuchian crocodyliforms, which obscures our understanding of the origin and early evolution of major clades. Here we report a lower jaw from the Middle Jurassic (Bathonian) Duntulm Formation of the Isle of Skye, Scotland, UK, which consists of an isolated and incomplete left dentary and part of the splenial. Morphologically, the Skye specimen closely resembles the Cretaceous neosuchians Pachycheilosuchus and Pietraroiasuchus, in having a proportionally short mandibular symphysis, shallow dentary alveoli and inferred weakly heterodont dentition. It differs from other crocodyliforms in that the Meckelian canal is dorsoventrally expanded posterior to the mandibular symphysis and drastically constricted at the 7th alveolus. The new specimen, together with the presence of Theriosuchus sp. from the Valtos Formation and indeterminate neosuchians from the Kilmaluag Formation, indicates the presence of a previously unrecognised, diverse crocodyliform fauna in the Middle Jurassic of Skye, and Europe more generally. Small-bodied neosuchians were present, and ecologically and taxonomically diverse, in nearshore environments in the Middle Jurassic of the UK.