Blog post by Rodger Caseby – HOPE for the Future Learning Officer
By the end of 2022, the Museum’s HOPE project will have rehoused and documented over one million British insects, restored our historic Westwood Room to create a new multi-purpose public space, and designed and delivered a wide-reaching learning and community programme.
The Crunchy on the outside blog is an exciting part of this community programme, aimed at 10–14 year-olds. For and by young entomologists, we’re not actually asking anyone to sink their teeth into a crispy exoskeleton! Instead, we are keen for young people to get involved in the HOPE project and the fascinating six-legged world of insects.
Natural World posts highlight amazing insects, like this recent piece on the red-tailed bumblebee, or this one on the red-legged shield bug written by young contributor Noah.
Red-legged shield bug
Six Legs of Summer School 2021
People posts featured entomologists and others with an interest in insects. These might be about members of the HOPE team at the Museum, like Collections Manager Amo Spooner, or those working elsewhere, such as Professor Karim Vahed, who studies bush crickets at the University of Derby.
Make & Do posts focus on creativity. They range from this cartooning tutorial from Chris Jarvis to things you can make at home, like this pitfall trap to catch ground-dwelling insects.
Museum posts take a look behind the scenes and also showcase what’s happening here at the museum, such as this post Events 4U in ’22 for the New Year, or our summer school in August.
The blog also features a gallery of insect photography and art created by young people which is continually expanding.
The Crunchy blog is very much by young people as well as for them. We are keen to receive items about insects, or connected to them, and have already published several articles. If you are a young person who is interested in contributing, you can get in touch via the Contact Us page on the blog or by emailing hopelearning@oum.ox.ac.uk. We would also love submissions of insect pictures for inclusion in our gallery!
And if there is a young person in your life who is crazy about creepy crawlies, or interested in science and nature in general, why not get them to take a look at the Crunchy blog? It could be the start of a wonderful journey into natural history.
Sneak peak: Enjoy this excerpt from a Crunchy on the outside blog post by Ben about Raising Moths!
“One morning we found that a lot of the caterpillars were wandering around, banging their heads on the bottom of the tank. They were also turning a darker green which (after a bit of research) we found out meant they needed to bury and become a chrysalis. We put a deep layer of soil into the tank and within minutes they had disappeared. We tucked them up in the shed for winter and waited. After months of hibernation, they started emerging this spring with crumpled wings, looking very like dead leaves.”
Thanks to National Lottery players for their generous support of the HOPE project through the National Lottery Heritage Fund.
We have an ambitious project underway at the Museum, to preserve a unique and scientifically important collection of over one million British insects. It’s called HOPE for the Future, after the Hope Entomological Collections, and we are keen to shout about how these specimens can help us understand biodiversity, habitats and ecologies.
The learning team behind the project are today launching a new blog for young people interested in entomology. Intriguingly, it’s called Crunchy on the Outside, but please don’t confuse this with the similar, but fundamentally different, mid-’90s advertising campaign for the Dime bar.
One of many weird and wonderful specimens from our collection, the Acorn Weevil (Curculio glandium).
Here is a peek at some of the tools of the trade, used to move and mend specimens like this moth.
Crunchy will be crammed full of interesting insect info, fun things to make and do, a peek behind the scenes at the Museum, and news from people, past and present, who work in the field of entomology. The odd bad joke may also worm its way in (What do butterflies sleep on? Cater-pillows).
The blog will also be a platform for young people to have their say, about the topics covered on Crunchy itself, as well as on the activity of the Museum. It will give them first dibs on access to related events too. You can check it out, follow, and share at crunchyontheoutside.com.
This article is taken from European research magazine Horizon as part of our partnership to share natural environment science stories with readers of More than a Dodo.
Armed with sensitive antennae and wide-angled compound eyes, bees have a sophisticated set of senses to help them search out pollen and nectar as they buzz from flower to flower.
But new research is revealing that bumblebees may employ another hidden sense that lets them detect when a flower was last visited by another insect.
Professor Daniel Robert, an expert in animal behaviour and senses at the University of Bristol, UK, has discovered that bumblebees have the ability to sense weak electrostatic fields that form as they fly close to a flower.
‘A bee has a capacity, even without landing, to know whether a flower has been visited in the past minutes or seconds, by measuring the electric field surrounding the flower,’ Prof. Robert explained.
The discovery is one of the first examples of electroreception in air. This sense has long been known in fish such as sharks and rays, which can detect the weak electrical fields produced by other fish in the water. Water-dwelling mammals such as platypus and dolphins have also been found to use electric fields to help them hunt for prey.
But rather than hunting for fish, bees appear to use their ability to sense electrical fields to help them find flowers that are likely to be rich in pollen and nectar.
Charge Bees develop an electrostatic charge because as they fly they lose electrons due to the air rubbing against their bodies, leading to a small positive electric charge. The effect is a bit like rubbing a party balloon against your hair or jumper, except the charge the bees accumulate is around 10,000 times weaker.
Flowers, by comparison, are connected to the ground, a rich source of electrons, and they tend to be negatively charged.
These electrostatic charges are thought to help bees collect pollen more easily. Negatively charged pollen sticks to the positively charged bee because opposite charges attract. Once the pollen sticks to the bee, it too becomes more positively charged during flight, making it more likely to stick to the negatively charged female part of a flower, known as a stigma.
Bees develop a positive electric charge as they fly, which helps them to collect pollen from negatively charged flowers. Image credit – Pxfuel.com/DMCA
But Prof. Robert and his colleagues wondered whether there could be more to this interaction. When they put an electrode in a flower, they detected a current flowing through the plant whenever a bumblebee approached in the air. Their study revealed that the oppositely charged flower and bee generate an electrostatic field between them that exerts a tiny attractive force.
To study whether the bees are aware of this electrostatic field, they then offered bumblebees discs with or without sugar rewards. Those with sugar also had 30 volts of electricity flowing through them to create an electrical field. They showed that the bees could sense electrical field and learn that it was associated with a reward. Without the charge, bees were no longer able to correctly identify the sugary disc.
Research by another group published shortly after Prof. Robert’s own work also showed that honey bees are also able to detect an electrical field. But exactly how the insects were able to do this remained a mystery, leading Prof. Robert to set up the ElectroBee project.
Very few animals have the capacity to read the stars and use it to find, north, south, east or west.
Professor Eric Warrant, Lund University, Sweden
Hairs
He has discovered that fine hairs on the bees’ bodies move in the presence of weak electrical fields. Each of these hairs has nerves at its base that are so sensitive they can detect tiny movements – as little as seven nanometres – caused by the electrical field.
Prof. Robert believes that when a bee visits a flower, it may cancel out some of the negative charge and so reduce the electrostatic field that forms when bees approach. This change in the strength of the electrostatic field could allow other bees flying past to work out whether a flower is worth visiting before they land, helping to save time and energy.
Other signals, such as changes in the colour and smell of flowers, happen in minutes or hours, while switches in electric potential occurs within seconds.
Prof. Robert and his team are now testing their theory that the electric field helps bees know which flowers to visit by counting visits by bumblebees to flowers in a meadow this summer and measuring electric fields around the flowers.
Their findings could help scientists better understand the relationship between plants and pollinating insects, which may prove crucial for improving the production of many vital fruit crops that rely upon bees for pollination.
Prof. Robert is also investigating whether bumblebees use their electrostatic charge to communicate to their nest sisters about the best places to fly for pollen.
But while bumblebees use their extraordinary sensory power to find food just a few kilometres from their nests, another insect is using another hidden sense to make far longer journeys.
The Bogong moth can travel more than 1,000km to hibernate in caves during the Australian summer. Image credit – Lucinda Gibson & Ken Walker, Museum Victoria/Wikimedia, licenced under CC BY-SA 3.0
In Australia, Bogong moths (Agrotis infusa) flitter steadily from various parts of the country and make their way towards the Snowy Mountains in the southeast. They fly for many days or even weeks to reach the high alpine valleys of the highest mountain range in the country, sometimes travelling over 1,000km. Once there, the insects hibernate in caves typically above 1,800m for the Australian summer, before making the return journey.
The only other insect known to migrate so far is the monarch butterfly in North America. But while the monarch butterfly relies in part on the sun’s position for navigation, the moths fly by night. Professor Eric Warrant, a zoologist at Lund University in Sweden, has been fascinated with how these insects, just a couple of centimetres in length, managed such a feat ever since he was a student in Canberra, Australia.
Moth mystery He suspected that the moths might use the Earth’s magnetic field to find their way, so his team tethered moths to a stalk that allowed them to fly and turn in any direction before surrounding them with magnetic coils to manipulate Earth’s magnetic field.
‘It is a little like how we would go hiking,’ said Prof. Warrant, who is trying to unravel how the moths sense the Earth’s magnetic fields in his project MagneticMoth. ‘We’d take a reading from a compass, then look for something to walk towards in that direction, a tree or mountain peak.’
His research has already shown that the moths check their internal compass every two or three minutes and continue to make for a visual cue ahead. But what are the insects able to see at night?
Further research revealed something remarkable. When Prof. Warrant downloaded an open source planetarium programme called Stellarium and projected the Australian night sky above the moths, he discovered they were using the stars.
‘Very few animals have the capacity to read the stars and use it to find, north, south, east or west,’ said Prof. Warrant. ‘We (humans) learnt how to do it. Some birds do it.’
But insect eyes of bogongs mean they don’t simply follow one guiding star. Rather they are sensitive to panoramic scenes.
‘In the southern hemisphere, the Milky Way is much more distinct than it is here in the northern hemisphere,’ said Prof. Warrant. ‘It really is a stripe of pale light in which there are interspersed very bright stars.’ He believes that the moths are at least in part guided to their cool alpine caves by the light of the Milky Way.
Prof. Warrant believes that Bogong moths naviagte in part by using the Milky Way as a guide. Image credit – Dave Young/Flickr, licenced under CC BY 2.0
The discovery could also lead to the development of new types of navigation for our own species too. GPS, for example, relies upon a constellation of satellites that are vulnerable to disruption. Prof. Warrant believes studying an insect capable of flying 1,000km to a cave using a brain the size of a rice grain, could help us find alternatives too.
‘Animals seem to solve complex problems with little material and low amounts of energy,’ Prof Warrant said.
The research in this article was funded by the EU. If you liked this article, please consider sharing it on social media.
Top image: Fine hairs on bees’ bodies can sense tiny changes in electrostatic fields, enabling them to sense whether another bee has visited a flower before them. Image credit – Unsplash/George Hiles, licenced under Unsplash licence
Earwigs are fascinating creatures. Belonging to the order Dermaptera, these insects can be easily recognised by their rear pincers, which are used for hunting, defence, or mating. But perhaps the most striking feature of earwigs is usually hidden – most can fly with wings that are folded to become 15 times smaller than their original surface area, and tucked away under small leathery forewings.
With protected wings and fully mobile abdomens, these insects can wriggle into the soil and other narrow spaces while maintaining the ability to fly. This is a combination very few insects achieve.
I have been working on research led by Dr Kazuya Saito from Kyushu University in Japan, which presents a geometrical method to design earwig wing-inspired fans. These fans could be used in many practical applications, from daily use articles such as fans or umbrellas, to mechanical engineering or aerospace structures such as drone wings, antennae reflectors or energy-absorbing panels!
Dr Saito came to Oxford last year for a six-month research stay at Prof Zhong You’s lab, in the Department of Engineering Science at the University of Oxford. He introduced me to biomimetics, an ever-growing field aiming to replicate nature for a wide range of applications.
Biological structures have been optimised by the pressures of natural selection over tens of millions of years, so there is much to learn from them. Dr Saito had previously worked on the wing folding of beetles, but now he wanted to tackle the insect group that folds its wings most compactly – the earwigs.
He was developing a design method and an associated software to re-create and customise the wing folding of the earwig hind wing, in order to use it in highly compact structures which can be efficiently transported and deployed. Earwigs were required!
Here at the Museum we provided access to our insect collections, including earwig specimens from different species having their hind wings pinned unfolded. These were useful to inform the geometrical method that Saito had been devising.
Dr Saito was also interested in learning about the evolution of earwigs and finding out when in deep time their characteristic crease pattern established. Some fossils of Jurassic earwigs show hints of possessing the same wing structure and folding pattern of their relatives today.
However, distant earwig relatives that lived about 280 million years ago during the Permian, the protelytropterans, possessed a different – yet related – wing shape and folding pattern. That provided the chance to test the potential and reliability of Saito’s geometrical method, as all earwigs have very similar wings due to their specialised function.
The geometrical method turned out to be successful at reconstructing the wing folding pattern of protelytropterans as well, revealing that both this extinct group and today’s earwigs have been constrained during evolution by the same geometrical rules that underpin the new geometrical design method devised by Dr Saito. In other words, the fossils were able to inform state-of-the-art applications: palaeontology is not only the science of the past, but can also be a science of the future!
We were also able to hypothesise intermediate extinct forms – somewhere between protelytropterans and living earwigs – assuming that earwigs evolved from a form closely resembling the protelytropterans.
As a collaboration between engineers and palaeobiologists, this research is a great example of the benefits of a multidisciplinary approach in science and technology. It also demonstrates how even a minute portion of the wealth of data held in natural history collections can be used for cutting-edge research, and why it is so important to keep preserving it for future generations.
Soon these earwig-inspired deployable structures might be inside your backpacks or used in satellites orbiting around the Earth. Nature continues to be our greatest source of inspiration.
Katherine Child, image technician in the Museum’s Life collections, doesn’t just use photography to capture the beauty of specimens. She is also an artist and has been trying out innovative techniques for her paintings. You may remember her amazing moth illustrations created with deposits of verdigris on pinned insects and she’s now using that technique to explore Museum staff’s favourite insect specimens.
Verdigris is a green corrosion often found on old pins within entomology collections (as well as elsewhere, on things like statues and copper pipes). Last year, after learning that the substance was once used as a pigment, I decided to try and make my own paint.
A clearwing moth before conservation, showing verdigris spreading where metal reacts with insect fats, or lipids.
Verdigris forms when copper or a copper alloy reacts with water, oxygen, carbon dioxide or sulphur. While a beautiful shade of green, the substance is damaging in natural history collections, where it can actually develop inside specimens and if left, split them irreversibly. So as part of the conservation of the Hope Entomological Collections, verdigris is removed.
I started to collect up the substance as it was cleaned from specimens and after about three years (you only get a little bit per pin) I was ready to make my paint! After my first moth project, the only question was, what to paint next…?
Byctiscus populi or ‘The Attelabid that changed my life’, chosen by Zoë (collections manager) who said ‘I saw a pink version of this species in the Natural History Museum in London and that’s when I decided I wanted to study entomology’.
With an estimated 6 million insects and arachnids in the entomology collections, it’s very easy to feel overwhelmed. You can pull open any one of thousands of draws and find astonishing specimens. While I have favourites, my first inclinations as to what to paint still felt a little arbitrary. After mulling over various possibilities, I decided to get help!
Chosen by DPhil student Leonidas, Agalmatium bilobum is a little bug which lays its eggs on tree bark, then covers them with mud to protect them.
I asked my co-workers what their favourite insects were, then opened the question out to regular volunteers and visitors of the Life collections. I loved finding out why people chose the things they did. Answers varied from ‘It was the first spider I ever looked at under a microscope aged 12’ to ‘Because they’re cool’ to ‘Because they have an ingenious way of manipulating spiders!’
One of arachnologist Russell’s favourite spiders: Nuctenea umbratica. Though common in the UK, umbratica is Latin for “living in the shadows”, and it often hides away during the day. The slight transparency of the paint lends itself to a spider’s glittering eyes.
Painting this live African Mantis Sphodromantis lineola (chosen by conservator Jackie) was made slightly more challenging by the fact that the subject thought Katherine’s pencil might be tasty.
Most of the subjects I painted were based on specimens from the Museum’s collections or specimens individuals had brought in from their own collections, but one favourite was a live African Mantis, housed in the department to help with education and outreach. When I began to draw her she was intrigued by the movement of my pencil and came to the front of the tank, to follow every mark I made with her intimidating gaze.
A detail from the final painting
Katherine’s fabulous finished painting, which will be framed and displayed in the Life collections department.
Though time consuming, the painting was loads of fun to research and do. It’s fantastic to be surrounded not only by extremely knowledgeable people, but also by people with a genuine passion for what they do and a love for the insects (and spiders) they study.
Since we posted about ten-year-old Sarah’s amazing beetle discovery, we’ve had lots of queries as to why the insect needed to be caught and pinned. It’s a question we’re often asked, so here’s Darren Mann, Head of Life Collections at the Museum, to explain the value of ‘voucher specimens’.
The Museum’s collection houses over five million insect specimens, amassed over the past 300 years. This collection is, in effect, a biodiversity database, but unlike virtual databases, each data point has an associated ‘voucher specimen’ that was caught, pinned and labelled.
Although technical advances in digital macro-photography do reduce the need for some collecting, it is impossible to dissect an image to confirm an identification. So for many groups, even the best photograph in the world is inadequate for identification purposes.
Shingle CrawlerD18 (Psammoporus insularis Pittino, 2006) one of our few endemic insects.
Unlike plants and birds, many insects can only be identified with the aid of a microscope, to study tiny features that distinguish closely-related species. Some groups even require the dissection of minuscule genitalia to really tell them apart.
Entomologists take voucher specimens to enable this correct identification and these are later deposited in museum collections, making them available for further study in years to come. From an entomologist’s point of view, we believe we need to know what a species is, where it occurs and as much about it as possible, so we can inform biodiversity conservation.
The conservation assessment of UK insects by Natural England in their Species Status Reviews has only been possible with the data provided by entomologists, generated from collecting and identifying voucher specimens.
Entomologists follow a Code of Conduct for responsible collecting, which ensures they don’t remove too many species or damage the environment during their work .
There are numerous examples of the value and use of insect collections in contemporary science, including the discovery of previously unknown species in the UK and population genetics for butterfly conservation. Recently a species believed extinct in the UK was rediscovered. This was only made possible by checking the identification of several thousand museum specimens.
Museum collections also contain numerous examples of species now considered extinct in the UK. Without voucher specimens much of this research would be impossible and our understanding of insect distribution patterns, ecology and conservation would be significantly diminished.
Large Tortoiseshell butterflies, now considered to be extinct in the UK. The voucher specimens act as record in time of its occurrence in the UK.
What is rare? Sarah’s False Darkling Beetle (Anisoxya fuscula) has been described as ‘rare’, but what does that mean in reality? For most invertebrates when we talk about a rare species we are not talking about a tiny number of individuals. This conservation status is based on their known distribution and the level of threat they face. A species can be rare if it is only found at one or two locations, but at those locations there may be many thousands of individuals.
The greatest threats to biodiversity are well known and include habitat loss, fragmentation and degradation and pollution, such as pesticides and light. Taking a small number of voucher specimens to confirm the identification of species has negligible impact on its population. But if we don’t know it’s there because we couldn’t identify it, then a housing development destroys its entire habitat… well you get the picture!