Invasive insects can be vectors of diseases, cause damage to agriculture and forestry, and threaten native biodiversity. Recognising this dramatic impact, the open-access journal Alpine Entomology, published by Pensoft on behalf of the Swiss Entomological Society, opened a dedicated topical collection that is already accepting submissions.
Impacts of alien insects in the Alpine ecosysteminvites scientists working on invasive species and plant-insect interactions in Alpine regions to openly publish their research articles, review articles, and short communications on, among others, trends or changes in biogeography of emblematic species, shifts in current distributions, or niche replacement.
The new article collection will be edited by Oliver Martin of ETH Zürich, subject editor and editorial board member at Alpine Entomology, Stève Breitenmoser, and Dominique Mazzi.
“Recent years have seen a worldwide increase in invasions by alien species, especially plants and insects, mostly due to trade and climate change,” they explain, noting that although numerous studies exist on the topic, few of them focus on the Alpine areas.
“With this collection we hope to generate exciting discussions and exchange within the scientific community interested in this very particular and sensitive ecosystem,” the editors say, inviting authors to submit their manuscripts assessing the possible impacts of invasive insects on mountain areas.
The collection will remain open for submissions for the next two years. In the meantime, the accepted manuscripts will be published on a rolling basis, as soon as they are ready for publication.
Guest blog post by Harry E. Clarke, Independent Researcher
5th instar Swallowtail larvae feeding on Milk-parsley.
Many books on butterflies publish lists of their larval foodplants. However, many of these lists of larval foodplants have been copied from previous lists, which in turn have been copied from previous lists. Consequently, errors have crept in, and many plant names have long been superseded. This can result in duplicates in the list, with the same plant being given two different names. Most plant lists do not include the authority, which can make it difficult or impossible to identify which plant is being referred to. Some of these plants may not be used by butterflies in Europe, but elsewhere in their range. Or the plants may have been used in breeding experiments, but not used by the butterflies in the wild.
Many of these publications providing the larval foodplants of butterflies only provide the binomial name, without specifying the author. This can create problems in knowing which species of plant is being used, as the same plant name has been used in the past by different authors to describe different species. In some cases, distribution can be used to determine the correct species, but plants can often have similar distributions. For example, in the World Checklist of Vascular Plants, there are 40 entries for the plant with the scientific name Centaurea paniculata, which refer to thirteen different accepted species, depending on authors, subspecies, and variety or form.
Not quite so simple: updating the current lists of larval foodplants
With climate change and habitat loss threatening numerous species, the conservation of butterflies (and other animals) is becoming more important. Whilst many factors determine the distribution of butterflies, such as temperature and rainfall, their survival depends solely on the kinds of plants their larvae eat. Accurate lists of larval foodplants are therefore important to find out where to direct limited conservation resources for the best result.
What started out as a straightforward job of updating the existing lists of larval foodplants with currently accepted names turned out to be a far bigger job. Many of the lists are incomplete, and may vary throughout the range of the butterfly. Here, errors have crept in too. Many references provide incomplete, unverifiable information. Many species of butterfly lay their eggs off-host, rather than on the host plant. For example, the Silver-washed Fritillary (Argynnis paphia)oviposits on tree trunks above where Viola species are growing. Consequently, oviposition records need to be treated with caution, depending on the species.
What do butterfly larvae eat, and why does it matter?
Butterfly larvae can be very fussy about which plants they can use. 20% of European butterfly larvae are monophagous, feeding on just one species of plant. 50% are oligophagous, feeding on a few different closely related plants, whilst 30% are polyphagous feeding on plants in many different families. The Holy Blue (Celastrina argiolus) can utilise plants in an astonishing 19 different families.
The oligophagous butterflies can be divided into two groups:
Oligophagous-monophagous (OM) – feeding on one plant species in one region, and another species in another region.
Oligophagous-polyphagous (OP) – feeding on several closely related species of plants throughout their range, usually in the same genus, or a closely related genus.
4th instar Small Tortoiseshell feeding on Common Nettle.
Plant preferences are only known for a few species of butterflies. For example, the English race of the Swallowtail (Papilio machaon) feeds on Milk-parsley (Peucedanum palustre), whereas in the rest of Europe it has been recorded on 62 other plants. The main larval foodplant of the Small Tortoiseshell (Aglais urticae) is Common Nettle(Urtica dioica), although it will occasionally use other plants.
The survivability of larvae on different plants is largely unknown, except in a few cases where the butterfly species has been studied in detail. There are plants that larvae may be able to eat, but that would likely not help them survive to pupation.
Two species are known to switch their larval foodplant during their second year of development. The Scarce Fritillary (Euphydryas maturna),for example, switches from Ash (Fraxinus excelsior) to Guelder-rose (Viburnum opulus). The Northern Grizzled Skipper (Pyrgus centaureae) switches from Dwarf birch (Betula nana) to Cloudberry (Rubus chamaemorus).
The most delicious plants
For the first time, a list of the current accepted plant names utilised by 471 European butterfly larvae is presented, with references. Where possible, errors in previous lists have been removed. The list of larval foodplants doubled compared to previous published lists. This has resulted in a list of 1506 different plant species in 72 different families. 86 plant records are only known at the generic level. Larval foodplants of 25 butterfly species are currently unknown, which are mostly the “Browns” (Satyrinae), which probably feed on grasses (Poaceae), or possibly sedges (Cyperaceae).
Whilst most plant families are utilised by less than six butterfly species, a few plant families are particularly favoured, with grasses (Poaceae) and legumes (Fabaceae) being the most popular. Similarly, most plant species are only utilised by a few butterfly species, but the fine grasses Sheep’s Fescue (Festuca ovina) and Red Fescue (Festuca rubra) are favoured by a large number of butterfly species.
Taxonomic splits create problems. Where cryptic species are allopatric, records can be allocated on the basis of their distribution. But where cryptic species are sympatric, this will require a resurvey to determine the larval foodplants. It cannot be assumed that two cryptic butterfly species use the same plants, as something has to become different for them to evolve into separate species.
Looking forward
Future publications should ensure that old and ambiguous plant names are not used. Plant names should be specified with their full scientific name, as specified by the International Code of Nomenclature for algae, fungi, and plants. The World Checklist of Vascular Plants should be checked to ensure the currently accepted plant name is being used.
Fully documented records are needed of what larval foodplants butterfly larvae are utilising in the wild. To get a better understanding of usage, full details need to be recorded, including date, location, altitude, abundance, and larval stage. Abundance will help in the understanding of preferences. To allow records to be properly verified, evidence should be provided on how the larvae and plants were identified. Regional lists are also important – to help direct conservation efforts to the plants being used locally, rather than elsewhere. This list of larval foodplants is provided as a step towards a fully justified database, which will be updated as and when corrections are found. It highlights those 25 butterfly species whose larval foodplants are currently unknown.
Clarke HE (2022) A provisional checklist of European butterfly larval foodplants. Nota Lepidopterologica 45: 139-167. https://doi.org/10.3897/nl.45.72017
African Invertebrates invites any submissions linked to Jason, new species descriptions, revisions of taxa he has worked on, or any work based on specimens he collected.
From 1976 to 1994, Jason Londt was Assistant Director at the Natal Museum (now KwaZulu-Natal Museum) in South Africa, publisher of the African Invertebratesjournal. Then, he became Director before retiring in 2003.
During his career at the Museum and well after that, Jason described more than 570 species and 46 genera of insects from the Afrotropics. While the majority of his work was on the robber fly family (Asilidae), Jason also worked on hangingflies (Bittacidae) and ticks. He was also a prolific collector of many other insects, still kept in the collection of the KwaZulu-Natal Museum.
Dr Jason Gilbert Hayden Londt
Jason’s fieldwork was extensively targeting the diverse habitats in South Africa: from the subtropical coast of KwaZulu-Natal, the grasslands in the Midlands around Pietermaritzburg – where the museum is based – and further north in the Highveld, to the higher elevations of the Drakensberg Mountains bordering Lesotho, and from the Succulent and Nama Karoo, to the diverse Fynbos habitats along the south-western coast of South Africa. Additional major fieldwork took place in Namibia, Kenya, Malawi, and to a lesser extent: Eswatini (Swaziland) and Cote d’Ivoire. In addition to utilising the collected material for taxonomic work, Jason also used his field trips to publish behavioural observations and prey selection of Asilidae species.
To celebrate Jason’s career achievements and his 80th birthday, African Invertebrates will be publishing a Festschrift in his honour in April 2023. We invite any submissions linked to Jason, new species descriptions, revisions of taxa he has worked on, or any work based on specimens collected by Jason.
The insect, described as Mantispa? damzenogedanica, helped reveal important insights into the morphology of these fascinating insects and how it changed through history
Lacewings (Neuroptera) are mostly known for representatives such as green lacewings or antlions, which are distinguished by their appearance – large eyes and four long wings – but also by their predatory larvae, which play an important role as pest control agents in agriculture. But few non-specialists know that some lacewings can look a lot like praying mantises.
Mantispa? damzenogedanica, general overview. Photo by V. Baranov
Mantis lacewings (Mantispida) are among the most charismatic, though rather poorly known representatives of the true lacewings. They look like small- to medium-sized praying mantises. Mantis lacewing are 5-47 mm long, and all of them have prominent grasping (also called raptorial) legs. This superficial resemblance is due to the convergent evolution of the shape in true mantises and mantis lacewings. Convergent evolution is a process of organisms evolving similar traits, due to their adaptation to the similar conditions – i.e. hummingbirds and sunbirds live on different continents but look very similar due to their similar lifestyle. This type of evolution has led to the similar shape of the grasping legs, which act as a couple of snap traps for unsuspecting prey.
Going back to the Cretaceous, Mantis lacewings have a long geological record. There are plenty of Mesozoic records of them and their relatives, such as thorny lacewings (Rachiberothidae) and beaded lacewings (Berothidae), totalling 105 recorded specimens. Curiously, there is a clear gap in mantis lacewings records from the Cainozoic.
Until recently, no adult mantis lacewings had been recorded from Baltic amber. In a single case, fossil parasitoid larvae of mantis lacewings were found attached to their host, a spider.
This changed last year, when a beautiful specimen of the mantis lacewing, almost 2 cm long, was brought to our attention by a private amber collector and esteemed supporter of palaeoentomology research – Jonas Damzen from Vilnus, Lithuania. The specimen was found at the Yantarny mine in Kaliningrad oblast, Russia.
By analysing the morphology of this beautiful specimen, we found out that it is closely related to the extant genus Mantispa. However, it was impossible to conclusively corroborate its affinity, because important characters such as rear wing venation and genitalia were obscured by so called “verlummung” – a white film, which covers many of the fossils in Baltic amber.
Morphospace plot showing changes in the diversity of raptorial appendages over geological time. Image credit J. Haug/ V. Baranov
So, to deal with this uncertainty, we designated this specimen as “probable Mantispa” (Mantispa?). In our research article published in the journal Fossil Record, we gave it the name Mantispa? damzenogedanica. The specific epithet is a combination of ‘Damzen’, honouring Jonas Damzen, who found, prepared, and made the specimen available, and ‘gedanicum’, relative to one of the Latin names for Gdańsk, Poland, where the specimen is housed in the Museum of Gdańsk.
Except for being an impressive, large, imposing insect fossil of the mantis lacewing, and the first one in Baltic amber at that, M.? damzenogedanica also present an intriguing question: why are so few mantis lacewings recorded from this fossil deposit, which is among the best-studied in the world?
Baltic amber deposits were formed in the mid-to-late Eocene epoch (38-33.9 MYA) in Northern Europe. Current consensus on the climate of the area at the time stands that it was not dissimilar to the south of the North American eastern seaboard, for example the Carolinas or Florida’s Panhandle: it was warm-temperate. Such climate is in fact perfect for extant mantis lacewings, so it is logical to suggest that unsuitable climate was not the main reason for the rarity of these animals in Baltic amber.
Analysing the diversity of the shape of mantis lacewings, we found a surprising trend – since the Cretaceous, the diversity in the shape of their legs has decreased. While the shape of the raptorial legs in the Cretaceous was characterised by eclectic, amazing diversity, later mantis lacewings have a rather uniform shape of raptorial legs.
We are not sure what may have caused this decrease. We think that drastic biotic changes after the Cretaceous-Paleogene extinction event (the mass extinction that killed the dinosaurs) may have led to the environment becoming less conductive to mantis lacewings, which in turn decreased their diversity. Thus, it is likely that the rarity of mantis lacewings is simply a reflection of the decline in their diversity and abundance after the Cretaceous-Paleogene extinction.
Younger amber deposits (i.e. Dominican amber), and, of course, extant fauna display significant species diversity, but the diversity of shape never recovered after the Cretaceous. This new mantis lacewing from Baltic amber offers us a rare glimpse into a time when, in the world after dinosaurs, lacewings got a little less diverse and charismatic.
Research article: Baranov V, Pérez-de la Fuente R, Engel MS, Hammel JU, Kiesmüller C, Hörnig MK, Pazinato PG, Stahlecker C, Haug C, Haug JT (2022) The first adult mantis lacewing from Baltic amber, with an evaluation of the post-Cretaceous loss of morphological diversity of raptorial appendages in Mantispidae. Fossil Record 25(1): 11-24. https://doi.org/10.3897/fr.25.80134
New Research Idea, published in RIO Journal presents a promising machine-learning ecosystem to unite experts around the world and make up for lacking taxonomic expertise.
In their Research Idea, published in Research Ideas and Outcomes (RIO Journal), Swiss-Dutch research team present a promising machine-learning ecosystem to unite experts around the world and make up for lacking expert staff
Guest blog post by Luc Willemse, Senior collection manager at Naturalis Biodiversity Centre (Leiden, Netherlands)
Imagine the workday of a curator in a national natural history museum. Having spent several decades learning about a specific subgroup of grasshoppers, that person is now busy working on the identification and organisation of the holdings of the institution. To do this, the curator needs to study in detail a huge number of undescribed grasshoppers collected from all sorts of habitats around the world.
The problem here, however, is that a curator at a smaller natural history institution – is usually responsible for all insects kept at the museum, ranging from butterflies to beetles, flies and so on. In total, we know of around 1 million described insect species worldwide. Meanwhile, another 3,000 are being added each year, while many more are redescribed, as a result of further study and new discoveries. Becoming a specialist for grasshoppers was already a laborious activity that took decades, how about knowing all insects of the world? That’s simply impossible.
Then, how could we expect from one person to sort and update all collections at a museum: an activity that is the cornerstone of biodiversity research? A part of the solution, hiring and training additional staff, is costly and time-consuming, especially when we know that experts on certain species groups are already scarce on a global scale.
We believe that automated image recognition holds the key to reliable and sustainable practises at natural history institutions.
Today, image recognition tools integrated in mobile apps are already being used even by citizen scientists to identify plants and animals in the field. Based on an image taken by a smartphone, those tools identify specimens on the fly and estimate the accuracy of their results. What’s more is the fact that those identifications have proven to be almost as accurate as those done by humans. This gives us hope that we could help curators at museums worldwide take better and more timely care of the collections they are responsible for.
However, specimen identification for the use of natural history institutions is still much more complex than the tools used in the field. After all, the information they store and should be able to provide is meant to serve as a knowledge hub for educational and reference purposes for present and future generations of researchers around the globe.
This is why we propose a sustainable system where images, knowledge, trained recognition models and tools are exchanged between institutes, and where an international collaboration between museums from all sizes is crucial. The aim is to have a system that will benefit the entire community of natural history collections in providing further access to their invaluable collections.
We propose four elements to this system:
A central library of already trained image recognition models (algorithms) needs to be created. It will be openly accessible, so any other institute can profit from models trained by others.
Mock-up of a Central Library of Algorithms.
A central library of datasets accessing images of collection specimens that have recently been identified by experts. This will provide an indispensable source of images for training new algorithms.
Mock-up of a Central Library of Datasets.
A digital workbench that provides an easy-to-use interface for inexperienced users to customise the algorithms and datasets to the particular needs in their own collections.
As the entire system depends on international collaboration as well as sharing of algorithms and datasets, a user forum is essential to discuss issues, coordinate, evaluate, test or implement novel technologies.
How would this work on a daily basis for curators? We provide two examples of use cases.
First, let’s zoom in to a case where a curator needs to identify a box of insects, for example bush crickets, to a lower taxonomic level. Here, he/she would take an image of the box and split it into segments of individual specimens. Then, image recognition will identify the bush crickets to a lower taxonomic level. The result, which we present in the table below – will be used to update object-level registration or to physically rearrange specimens into more accurate boxes. This entire step can also be done by non-specialist staff.
Mock-up of box with grasshoppers mentioned in the above table
Results of automated image recognition identify specimens to a lower taxonomic level.
Another example is to incorporate image recognition tools into digitisation processes that include imaging specimens. In this case, image recognition tools can be used on the fly to check or confirm the identifications and thus improve data quality.
Mock-up of an interface for automated taxon identification.
Using image recognition tools to identify specimens in museum collections is likely to become common practice in the future. It is a technical tool that will enable the community to share available taxonomic expertise.
Using image recognition tools creates the possibility to identify species groups for which there is very limited to none in-house expertise. Such practises would substantially reduce costs and time spent per treated item.
Image recognition applications carry metadata like version numbers and/or datasets used for training. Additionally, such an approach would make identification more transparent than the one carried out by humans whose expertise is, by design, in no way standardised or transparent.
Greeff M, Caspers M, Kalkman V, Willemse L, Sunderland BD, Bánki O, Hogeweg L (2022) Sharing taxonomic expertise between natural history collections using image recognition. Research Ideas and Outcomes 8: e79187. https://doi.org/10.3897/rio.8.e79187
While scrolling through iNaturalist – a social network where professional and citizen scientists share their photographs, in order to map biodiversity observations from across the globe – a group of students from Croatia discovered a couple of curious pictures, taken in 2008 in the Peruvian rainforest and posted in 2018. What they were looking at was a pygmy grasshopper sporting a unique pattern of lively colors. The motley insect was nothing they have so far encountered in the scientific literature.
While scrolling through iNaturalist – a social network where professional and citizen scientists share their photographs, in order to map biodiversity observations from across the globe – a group of students from Croatia discovered a couple of curious pictures, taken in 2008 in the Peruvian rainforest and posted in 2018. What they were looking at was a pygmy grasshopper sporting a unique pattern of lively colors. The motley insect was nothing they have so far encountered in the scientific literature.
The scientist and photographer Roberto Sindaco, Museo Civico di Storia naturale (Torino, Italy) graciously shared his camera roll with Niko Kasalo, Maks Deranja, and Karmela Adžić, graduate students under the mentorship of Josip Skejo, all currently affiliated with University of Zagreb, Faculty of Science, Croatia. Together, they published a paper describing the yet to be named insect in the open-access scientific journal Journal of Orthoptera Research.
Typically, new species are described from specimens collected from their natural habitats and then deposited in a museum to be preserved for future reference. The authors, possessing several high-quality photographs, decided to challenge the norm and name the new species based on photographs only. The paper was initially rejected, but a compromise was reached—it could be published with the species name removed.
The International Code of Zoological nomenclature is a document that contains regulations for proper scientific naming of animal species. It allows naming species from photographs, but the practice is generally looked down upon. Thus, the authors decided to use the nameless species to draw attention to this problem and bring more clarity. Names in zoology consist of two words: the genus name and the species name. As the species name was denied, the grasshopper is now mysteriously referred to as „the nameless Scaria“.
Another important message of this paper is how citizen science portals, such as iNaturalist, allow everybody interested in nature to contribute to ‘real’ scientific work by posting their findings online.
The authors believe that including laypeople in the scientific process can help bridge the communication gap between scientists and the general population, dissipating the growing suspicion towards science. The researchers urge everybody to engage with nature around them and capture its beauty with their camera lens.
“Only by interacting with nature can we truly feel how much we might lose if we do not take care of it, and care is urgently needed,”
said the authors of the study.
Male of the nameless Scaria species Photo by Roberto Sindaco
Original source:
Kasalo N, Deranja M, Adžić K, Sindaco R, Skejo J (2021) Discovering insect species based on photographs only: The case of a nameless species of the genus Scaria (Orthoptera: Tetrigidae). Journal of Orthoptera Research 30(2): 173-184. https://doi.org/10.3897/jor.30.65885
A new species of parasitoid wasp that constructs remarkable star-shaped cocoon masses is reported from the biodiversity hot spot Ryukyu Islands. Japanese researchers observed how the wasps construct “stars” after making their way out of the moth larvae they inhabit during their own larval stage. In their study, published in the open-access journal Journal of Hymenoptera Research, the team discuss the ecological significance of the cocoon mass and the evolution of this peculiar structure.
The new parasitoid wasps, Meteorus stellatus. Photo by Fujie S
Parasitoid wasps parasitize a variety of organisms, mostly insects. They lay eggs in the host, a larva of hawk moth in this case, where the wasp larvae later hatch. After eating the host from the inside out, the larvae spin threads to form cocoons, in which they pupate, and from which the adult wasps eventually emerge.
The larvae of Meteorus stellatus emerging from a host moth. Photo by Tone K
Larvae of the newly discovered parasitoid wasp form star-shaped masses of cocoons lined up in a spherical pattern, suspended by a thread that can reach up to 1 meter in length. The structure, 7 to 14 mm wide and 9 to 23 mm long, can accommodate over 100 cocoons.
The star-shaped cocoon mass and the cable of the new parasitoid wasps. Photo by Shimizu S
Despite its peculiarity, the wasp species constructing these masses had not been previously described: morphological observation and molecular analysis revealed that it was new to science. The authors aptly called it Meteorus stellatus, adding the Latin word for “starry” to its scientific name.
Thanks to the recent publication, we now have the first detailed report about the construction of such a remarkable cocoon mass in parasitoid wasps. We can also see what the process looks like, as the researchers were able to film the wasps escaping from the moth larvae and forming the star-shaped structure.
Why does M. stellatus form cocoons in such a unique structure?
The authors of the study believe this unique structure helps the wasps survive through the most critical time, i.e. the period of constructing cocoons and pupating, when they are exposed to various natural enemies and environmental stresses. The star shape most likely reduces the exposed area of individual cocoons, thus increasing their defense against hyper-parasitoids (wasps attacking cocoons of other parasitoid wasps), while the long thread that suspends the cocoon mass protects the cocoons from potential enemies like ants.
“How parasitoid wasps have evolved to form such unique masses instead of the common individual cocoons should be the next thing on our ‘to-research’ list,” say the authors.
Research article:
Fujie S, Shimizu S, Tone K, Matsuo K, Maeto K (2021) Stars in subtropical Japan: a new gregarious Meteorus species (Hymenoptera, Braconidae, Euphorinae) constructs enigmatic star-shaped pendulous communal cocoons. Journal of Hymenoptera Research 86: 19-45. https://doi.org/10.3897/jhr.86.71225
Discovery of the first moth species to mine the leaves of the highly poisonous Alpine rose
Rust-red alpine rose, one of the most popular alpine plants. Photo by Ingrid Huemer
An Austrian-Swiss research team was able to find a previously unknown glacial relic in the Alps, the Alpine rose leaf-miner moth. It is the first known species to have its caterpillars specializing on the rust-red alpine rose, a very poisonous, widely distributed plant that most animals, including moths and butterflies, strictly avoid. The extraordinary record was just published in the peer-reviewed scientific journal Alpine Entomology.
Poisonous host plant
The rust-red alpine rose (Rhododendron ferrugineum) is among the best-known and most attractive plants due to its flowering splendor – at least for humans. It is, in fact, a highly poisonous plant, strictly avoided by grazing animals. For insects, the alpine rose is attractive at most as a nectar plant; insect larvae, on the other hand, develop on it only in exceptional cases. This also applies to Alpine butterflies and moths, which leave Alpine roses largely untouched despite their wide distribution. Therefore, the discovery of a highly specialized species in the Alps came as a complete surprise.
Chance find
Alpine rose leaf-miner moth adults resting on leaves of the host-plant in Ardez, Graubünden, Switzerland. Photos by Jürg Schmid
Since alpine roses are unattractive to caterpillars and no insect the entire Alpine region was previously known to specialize on them, butterfly and moth experts had considered them rather uninteresting and ignored them in their research. The discovery of the alpine rose leaf-miner wasn’t the result of a targeted search: it was a pure stroke of luck.
During a cloudy spell in July this year, researchers surveying the butterflies in Ardez in the Engadine valley, Switzerland, happened to take a break exactly at an infested alpine rose bush.
“The accidental sighting of the first caterpillar in an alpine rose leaf was an absolute adrenaline rush, it was immediately clear that this must be an extraordinary species,”
Peter Huemer, researcher and head of the natural sciences department of the Tyrolean State Museums
Peter Huemer, researcher and head of the natural sciences department of the Tyrolean State Museums, and Swiss butterfly and moth expert Jürg Schmid came back in late July and early August to look for caterpillars and pupae and find out more about this curious insect. The extended search yielded evidence of a stable population of a species that was initially a complete enigma.
Life in the leaf
Leaf-mines of the alpine rose leaf-miner moth on Rhododendron ferrugineum in Ardez, Graubünden, Switzerland. Photos by Peter Huemer
The alpine rose leaf-miner moth drills through the upper leaf skin and into the leaf interior immediately after the caterpillar hatches. The caterpillar then spends its entire life until pupation between the intact leaf skins, eating the leaf from the inside. Thanks to this behavior, the caterpillar is just as well protected from bad weather as from many predators such as birds, spiders, or some carnivore insects. The feeding trail, called a leaf mine, begins with a long corridor and ends in a large square-like mine section. The feces are deposited inside this mine. When the time comes for pupation, the caterpillar leaves the infested leaf and makes a typical web on the underside or a nearby leaf. With the help of several fine silk threads, it produces an elaborate “hammock”, in which the pupation finally takes place. In the laboratory, after about 10 days, the successful breeding to a moth succeeded, with a striking result.
Enigmatic glacial relic
Final instar larva of the alpine rose leaf-miner moth on Rhododendron ferrugineum in Ardez, Graubünden, Switzerland. Photo by Jürg Schmid
Huemer and Schmid were surprised to find out that the moths belonged to a species that was widespread in northern Europe, northern Asia and North America – the swamp porst leaf-miner butterfly Lyonetia ledi. By looking at its morphological features, such as wing color and pattern, and comparing its DNA barcodes to those of northern European specimens, they were able to confirm its identity.
Habitat of the alpine rose leaf-miner moth in Engadine/Switzerland with Rhododendron ferrugineum. Photo by Jürg Schmid
The Engadine population, however, is located more than 400 km away from the nearest other known populations, which are on the border of Austria and the Czech Republic. Furthermore, the species lives in northern Europe exclusively on swamp porst and Gagel bush – two shrubs that are typical for raised bogs and absent from the Alps. However, the researchers suggest that in earlier cold phases – some 22,000 years ago – the swamp porst and the alpine rose did share a habitat in perialpine lowland habitats north of the Alps. It is very likely that after the last cold period and the melting of the glaciers, some populations of the species shifted their host preference from the swamp porst to the alpine rose. The separation of the distribution areas of the two plants caused by subsequent warm phases inevitably led to the separation of the moth populations.
Extinction risk
Characteristic cocoon with final instar larva and pupa of the alpine rose leaf-miner moth on Rhododendron ferrugineum in Ardez, Graubünden, Switzerland. Photos by Jürg Schmid
The Alpine Rose Leaf-miner Moth is so far only known from the Lower Engadine. It lives in a steep, north-exposed, spruce-larch-pine forest at about 1,800 m above sea level. The high snow coverage in winter and the largely shady conditions in summer mean that alpine roses don’t get to bloom there. The scientists suspect that the moth species can still be discovered in places with similar conditions in the northern Alps, such as in neighboring Tyrol and Vorarlberg. Since the moth is likely nocturnal and flies late in the year, probably hibernating in the adult stage, the search for the caterpillars and pupae is more promising. However, the special microclimate of the Swiss location does not suggest that this species, which has so far been overlooked despite 250 years of research, is widespread. On the contrary, there are legitimate concerns that it could be one of the first victims of climate change.
Research article:
Huemer P, Schmid J (2021) Relict populations of Lyonetia ledi Wocke, 1859 (Lepidoptera, Lyonetiidae) from the Alps indicate postglacial host-plant shift to the famous Alpenrose (Rhododendron ferrugineum L.). Alpine Entomology 5: 101-106. https://doi.org/10.3897/alpento.5.76930
… and 27 other new species of beetles discovered on Sulawesi Island
Many curious animals can be found on the Indonesian Island of Sulawesi – such as the deer-hog and the midget buffalo. But the island’s tropical forests hide a diversity of tiny insects that still remains largely unexplored. Museum scientists from Indonesia and Germany have just discovered 28 new species of beetles, all belonging to the weevil genus Trigonopterus.
Twenty-four newly discovered species of the genus Trigonopterus from Sulawesi. Image by Alexander Riedel
Most of the new species were collected by Raden Pramesa Narakusumo, curator of beetles at the Museum Zoologicum Bogoriense, from two localities of Central Sulawesi Province: Mt. Dako and Mt. Pompangeo. In fact, the forests on their slopes had never been searched for small weevils before.
A view from a ridge over the cloudy slopes of Mt. Pompangeo. Photo by Raden Pramesa Narakusumo
His research partner, Alexander Riedel of the Natural History Museum Karlsruhe, had been studying this genus for the past 15 years and was planning for a research trip to Papua New Guinea, when the COVID-19 pandemic hit. Finding himself grounded, he decided to work on the specimens from Sulawesi together with Narakusumo instead.
After diagnosing the new species, it was a challenge to find suitable names for them. One obvious choice was Trigonopterus corona, which reflects the large impact of the COVID-19 pandemic on this project. However, T. corona is by far not the first insect species with a pandemic-inspired name. In the last year, we’ve seen the species descriptions of the caddisfly Potamophylax coronavirus and the wasps Stethantyx covida and Allorhogas quarentenus.
Trigonopterus corona.
Trigonopterus ewok.
While some of the newly described species go by rather ‘standard’ names that derive from either the localities they have been collected from or their distinct characters, others were given a free pass to the Hall of Fame. Two of them were named after Indonesian movie characters (T. gundala and T. unyil), while T. ewok is another addition based on the Star Wars universe – perfectly in line with T. chewbacca, T. yoda and T.porg, all described between 2016 and 2019 by teams involving Riedel. The two-millimeter-long, rust-coloured Trigonopterus ewok was found at 1900–2000 m on Mt Pompangeo, hiding among the leaf litter in the forest.
But how come the critters have remained overlooked for so long? Almost all of these beetles measure only 2-3 millimeters, while most entomologists have a preference for the larger and strikingly looking stag beetles or jewel beetles.
A second factor is the superficial resemblance of many species: they are most easily diagnosed by their DNA sequences. Besides the publication in the open-access journal ZooKeys, high-resolution photographs of each species were uploaded to theSpecies ID website, along with a short scientific description. This provides a face to the species name, an important prerequisite for future studies.
R.P. Narakusumo during fieldwork at the top of Mt. Dako. Photo by Raden Pramesa Narakusumo
This is the duo’s second published paper on Trigonopterus weevils from Sulawesi – the first one describing the whopping 103 new species from the area. Currently, the known Trigonopterus species on the island amount to 132, which is likely a mere fraction of the real diversity. The numerous mountains of Sulawesi have a distinct fauna of endemics that have evolved over the past millions of years, and these wingless, flightless weevils, highly isolated in their habitats, are a good example of this diversification. Their evolution is interwoven with the island´s geological history. Riedel wants to increase the number of sampled localities:
“Once we have enough locality coverage and understand the weevils’ evolution, we can draw conclusions on the geological processes that formed the island of Sulawesi. This is a fascinating subject, because this island was formed by the fusion of different fragments millions of years ago.” The new species thus fill an important gap required for solving the island´s geological puzzle.
For the Indonesian side, it is equally important to obtain an inventory of species: “A large percentage of Indonesian biodiversity is yet unknown and we need names and diagnoses of species, so we can use these in further studies on conservation and bioprospecting,” says R. Pramesa Narakusumo. “Two of the newly described species came from our museum collection, and this underlines the importance of museums as a source for biological discoveries,” he added.
With many more new species of this genus to be expected, it is a lucky coincidence that the number of Star Wars characters is equally long. May the Force be with these researchers!
Research article:
Narakusumo RP, Riedel A (2021) Twenty-eight new species of Trigonopterus Fauvel (Coleoptera, Curculionidae) from Central Sulawesi. ZooKeys 1065: 29-79.https://doi.org/10.3897/zookeys.1065.71680
“Trends in Arthropods of Alpine Aquatic Ecosystems” is the first topical collection for the journal of the Swiss Entomological Society
The open-access, peer-reviewed scholarly journal Alpine Entomology, published by Pensoft on behalf of the Swiss Entomological Society, announced its very first topical collection of articles, which will be focusing on arthropods associated with aquatic ecosystems in mountainous regions.
The journal is currently inviting scientists, working on aquatic fauna from alpine habitats, to openly publish their research articles and short notices that provide evidence how arthropods’ biogeography, species communities, distribution, behaviour and morphology have changed in recent times.
“Aquatic invertebrates are key indicators of global or local changes. Furthermore, many aquatic ecosystems are closely linked to mountains because they originate in them. Many valuable unpublished datasets on aquatic arthropod fauna may therefore be available from mountainous regions,”
The aim of the “Trends in Arthropods of Alpine Aquatic Ecosystems” collection is to bring together data and findings about what many agree is the most impacted type of environment on Earth: aquatic ecosystems, especially running waters.
The collection will remain open for submissions for the next two years. In the meantime, the accepted manuscripts will be published on a rolling basis, as soon as they are ready for publication.
