Butterflies and moths share ancient ‘blocks’ of DNA
Butterflies and moths share “blocks” of DNA dating back more than 200 million years, new research shows.
Scientists from the Universities of Exeter (UK), Lübeck (Germany) and Iwate (Japan) devised a tool to compare the chromosomes (DNA molecules) of different butterflies and moths.
They found blocks of chromosomes that exist in all moth and butterfly species, and also in Trichoptera – aquatic caddisflies that shared a common ancestor with moths and butterflies some 230 million years ago.
Moths and butterflies (collectively called Lepidoptera) have widely varying numbers of chromosomes – from 30 to 300 – but the study’s findings show remarkable evidence of shared blocks of homology (similar structure) going back through time.
“DNA is compacted into individual particles or chromosomes that form the basic units of inheritance,” said Professor Richard ffrench-Constant, from the Centre for Ecology and Conservation on Exeter’s Penryn Campus in Cornwall.
“If genes are on the same ‘string’, or chromosome, they tend to be inherited together and are therefore ‘linked’.
“However, different animals and plants have widely different numbers of chromosomes, so we cannot easily tell which chromosomes are related to which.
“This becomes a major problem when chromosome numbers vary widely – as they do in the Lepidoptera.
“We developed a simple technique that looks at the similarity of blocks of genes on each chromosome and thus gives us a true picture of how they change as different species evolve.
“We found 30 basic units of ‘synteny’ (literally meaning ‘on the same string’ where the string is DNA) that exist in all butterflies and moths, and go back all the way to their sister group the caddisflies or Trichoptera.”
Butterflies are often seen as key indicators of conservation, and many species worldwide are declining due to human activity.
However, this study shows that they are also useful models for the study of chromosome evolution.
The study improves scientific understanding of how moth and butterfly genes have evolved and, importantly, similar techniques may also provide insights about the evolution of chromosomes in other groups of animals or plants.
The paper, published in the journal G3: Genes, Genomes, Genetics, is entitled: “Lepidopteran Synteny Units (LSUs) reveal deep chromosomal conservation in butterflies and moths.”
JOURNAL
G3 Genes Genomes Genetics
SUBJECT OF RESEARCH
Animals
ARTICLE TITLE
Lepidopteran Synteny Units reveal deep chromosomal conservation in butterflies and moths
ARTICLE PUBLICATION DATE
13-Jun-2023
Small-winged and lighter colored butterflies likely to be at greatest threat from climate change
The family, wing length and wing color of tropical butterflies all influence their ability to withstand rising temperatures, say a team led by ecologists at the University of Cambridge.
Peer-Reviewed PublicationImages and paper available at: https://drive.google.com/drive/folders/18XRYP9dHcC1Z8lc3B86j3k6BzgIesqUS?usp=sharing
Small-winged and lighter coloured butterflies likely to be at greatest threat from climate change
The family, wing length and wing colour of tropical butterflies all influence their ability to withstand rising temperatures, say a team led by ecologists at the University of Cambridge. The researchers believe this could help identify species whose survival is under threat from climate change.
Butterflies with smaller or lighter coloured wings are likely to be ‘losers’ when it comes to climate change, with the Lycaenidae family, which contains over 6,000 species of butterflies, the majority of which live in the tropics, found to be particularly vulnerable.
Butterflies with larger or darker coloured wings are likely to fare better under increasing temperatures, but only to a point. Researchers say these butterflies could still experience dramatic declines if there were sudden heatwaves or if cool microclimates were lost through deforestation.
The results are published today in the Journal of Animal Ecology.
Butterflies rely on the sun’s warmth to give them the energy they need to function. They use ‘thermoregulation’ strategies to maintain a balanced body temperature against changing air temperatures.
Generally, strategies to keep cool involve adaptive behaviours like flying to a shady spot or angling wings away from the sun (thermal buffering). But when this is not possible or temperatures become too hot, species have to rely on physiological mechanisms such as the production of heat shock proteins to withstand high temperatures (thermal tolerance). Both of these strategies are needed to cope with climate change.
Researchers collaborated with the Smithsonian Tropical Research Institute (STRI) to study the thermal buffering and thermal tolerance strategies of tropical butterflies. They collected data from multiple habitats in Panama.
Equipped with hand-held nets, ecologists took the temperature of over 1,000 butterflies using a tiny thermometer-like probe. They compared each butterfly’s temperature to that of the surrounding air or the vegetation it was perched on. This gave a measurement of thermal buffering – the ability to maintain a steady body temperature against fluctuating air temperatures.
A second experiment was conducted at STRI Gamboa facilities and involved assessing butterflies’ thermal tolerance – their ability to withstand extreme temperatures, such as those they may experience during a heatwave. This was assessed by capturing a subset of butterflies and placing them in glass jars within a water bath – the temperature of which was steadily increased. Thermal tolerance was assessed as the temperature at which butterflies could no longer function.
Butterflies that had large wings tended to have greater thermal buffering ability but less thermal tolerance than smaller butterflies. Indeed, in a further study conducted by the same research team, butterflies with larger, longer and narrower wings were found to be better at thermal buffering.
Thermal buffering abilities were found to be stronger in darker-winged butterflies who could also tolerate higher temperatures than paler-winged butterflies.
Butterflies from the Lycaenidae family which have small, bright, and often iridescent, wings had the poorest thermal buffering and low thermal tolerance. If temperatures continue to rise at the current rate, forests continue to be cut down, and cool microclimates are lost, there is a very real threat that we could lose many species in this family in the future, say the researchers.
A trade-off in terms of butterflies’ cooling strategies was observed: those that were good at thermal buffering were less good at thermal tolerance and vice versa.
Scientists say this suggests that tropical butterflies have evolved to cope with temperature changes using one of these strategies at the expense of the other, and that this is likely to be due to selective pressures.
Lead author Esme Ashe-Jepson, a PhD student at Cambridge’s Department of Zoology, said: “Butterflies with physical characteristics that may help them to avoid the sun’s heat, like having large wings that enable them to fly quickly into shade, rarely experience high temperatures, and so have not evolved to cope with them. On the other hand, species which can cope with higher temperatures physiologically have experienced less selective pressure to evolve heat-avoiding behaviours.
“As temperatures continue to rise, and forest fragments get smaller and further apart because of deforestation, butterflies which rely on their surroundings to avoid high temperatures may not be able to travel between forest fragments, or cope with increasingly common heatwaves.”
The researchers say this means that species with large dark wings that are good at thermal buffering may initially be unaffected by warming temperatures, as they can continue to thermoregulate effectively using behaviour and microclimates, but their survival could be at risk if there are sudden heatwaves, or they can no longer escape to cool vegetation.
“Ultimately all insects, including butterflies, the world over are likely to be affected by climate change,” said Ashe-Jepson. “Adaptation to climate change is complex and can be impacted by other factors such as habitat destruction. We need to address these two global challenges together.”
Further research is needed to investigate the effect a warming climate may have on other life stages of butterflies, such as caterpillars and eggs, and other insect groups.
Senior author Greg Lamarre, at the Czech Academy of Science and Research Associate at STRI said: “Worldwide, most entomologists are observing drastic declines in insect biodiversity. Understanding the causes and consequences of insect decline has become an important goal in ecology, particularly in the tropics, where most of terrestrial diversity occurs.”
The research was funded by the GACR Czech Science Foundation, an ERC Starting Grant, a Smithsonian Tropical Research Institute short-term fellowship, and the Sistema Nacional de Investigación (SENACYT), Panama.
ENDS.
Esme Ashe-Jepson conducing fieldwork in Panama, with a butterfly from the Calephelis genus in the Riodinidae family.
Esme Ashe-Jepson conducing fieldwork in Panama, with a Juditha caucana butterfly from the Riodinidae family.
Esme Ashe-Jepson conducing fieldwork in Panama, with a Juditha caucana butterfly from the Riodinidae family.
CREDIT
Esme Ashe-Jepson
Esme Ashe-Jepson
Reference:
Esme Ashe-Jepson et al. Tropical butterflies use thermal buffering and thermal tolerance as alternative strategies to cope with temperature increase. Journal of Animal Ecology DOI: 10.1111/1365-2656.13970
Contact details:
Charis Goodyear, University of Cambridge: Charis.Goodyear@admin.cam.ac.uk
Esme Ashe-Jepson, University of Cambridge: ea483@cam.ac.uk
About the University of Cambridge
The University of Cambridge is one of the world’s leading universities, with a rich history of radical thinking dating back to 1209. Its mission is to contribute to society through the pursuit of education, learning and research at the highest international levels of excellence.
Cambridge was second in the influential 2023 QS World University Rankings, the highest rated institution in the UK.
The University comprises 31 autonomous Colleges and over 100 departments, faculties and institutions. Its 20,000 students include around 9,000 international students from 147 countries. In 2022, 72.5% of its new undergraduate students were from state schools and more than 25% from economically disadvantaged backgrounds.
Cambridge research spans almost every discipline, from science, technology, engineering and medicine through to the arts, humanities and social sciences, with multi-disciplinary teams working to address major global challenges. In the Times Higher Education’s rankings based on the UK Research Excellence Framework, the University was rated as the highest scoring institution covering all the major disciplines.
The University sits at the heart of the ‘Cambridge cluster’, in which more than 5,200 knowledge-intensive firms employ more than 71,000 people and generate £19 billion in turnover. Cambridge has the highest number of patent applications per 100,000 residents in the UK.
JOURNAL
Journal of Animal Ecology
SUBJECT OF RESEARCH
Animals
ARTICLE TITLE
Tropical butterflies use thermal buffering and thermal tolerance as alternative strategies to cope with temperature increase
ARTICLE PUBLICATION DATE
13-Jul-2023
Butterfly species’ big brains adapted giving them a survival edge, study finds
Heliconius butterflies’ brains grew as they adopted a novel foraging behaviour, scientists at the University of Bristol have found.
A region of their brain, known as the mushroom body due to its shape, are two to four times larger than those of their close relatives.
The findings, published today in Nature Communications, suggest that the structure and function of the nervous system are closely linked to an organism's ecological niche and behaviour.
Dr Stephen Montgomery of Bristol’s School of Biological Sciences explained: “Heliconius are the only butterflies known to collect and digest pollen, which gives them an adult source of protein, when most other butterflies exclusively obtain protein as caterpillars.
“This shift in diet allows Heliconius to live much longer lives, but they seemingly only collect pollen from specific plant species that occur at low densities.
“Learning the location of these plants is therefore a critical behaviour for them, but to do so they must presumably invest more in the neural structures and cells that support spatial memory.”
The team focused on the relationship between mushroom body expansion, sensory specialization and the evolutionary innovation of pollen feeding.
The study involved a unique synthesis of comparative data on large-scale brain structure, cellular composition and connectivity in the brain, and studies of behaviour across species.
They built 3D models of the brain in 30 pollen-feeding species of Heliconius, and 11 species from closely related genera, collected from across Central and South America.
The volume of different brain areas was measured and mapped over phylogenetic (family) trees to estimate where major evolutionary changes in brain composition occurred.
They then investigated changes in neural circuitry by quantifying in the number of neurons in the mushroom bodies and the density of their connections, as well as sensory specialisation by tracing neural inputs from brain areas that process visual information and smell before sending it to the central brain.
Finally, in partnership with the Smithsonian Tropical Research Institute in Panama, they conducted behavioural experiments in key species to assess whether the observed expansion of the mushroom body correlated with improved visual learning and memory.
One striking result is the remarkable range of variation in mushroom body size observed among these closely-related species within a relatively short evolutionary timeframe. Across the whole dataset mushroom body size varies by 25-fold.
This provides a compelling example of how specific brain structures can vary independently over evolutionary time, known as mosaic evolution, when under strong selective constraints for behavioural adaptation.
Dr Montgomery added: “We identified that changes in mushroom body size are due to an increased number of ‘Kenyon cells’, the neurons that form the majority of the mushroom body and whose interactions are thought to be the basis of memory storage, as well as increased inputs from the visual system.
“This expansion and visual specialization of the mushroom bodies were accompanied by enhanced visual learning and memory abilities. Through this synthesis of data types, we provide a clear example of a novel foraging behaviour coinciding with adaptations in the brain and associated cognitive shifts.”
Co-lead author, Bristol’s Dr Antoine Couto, said: “"The study reveals how brain structure of Heliconius butterflies, specifically the mushroom bodies, has undergone remarkable changes that are tightly linked to their specialized foraging behaviours.
“These butterflies have evolved larger mushroom bodies with enhanced visual processing abilities, allowing them to discriminate complex visual patterns and retain visual memories over extended periods. These findings highlight the fascinating connection between brain evolution and behavioural adaptations in the natural world."
Dr Fletcher Young, also co-lead author, added: “This study provides a rare combination of neurobiological and behavioural data across closely related species, revealing a clear example of marked evolutionary changes in the brain over a relatively short time scale coinciding with improved visual learning and memory abilities. Identifying such relationships between brain adaptations and behavioural shifts are crucial to our understanding of cognitive evolution.”
Dr Montgomery concluded ““We provide evidence that brain structure can vary in striking ways between even closely related species that live in the same habitats.
“In this example, the innovation of one suite of behaviours has led to a dramatic expansion of critical learning and memory centres in the brain, and we show these neural changes co-occur with substantial enhancements in cognitive ability.
“We hypothesise that these behavioural differences reflect either a direct response to selection on foraging behaviour, and the information the butterflies are extracting for the environment around them to guide their behaviour”
Understanding the relationship between brain anatomy, sensory processing, and foraging behaviour in Heliconius butterflies could also provide insights into the evolution of learning and memory mechanisms in not only insects, but other animals as the function and circuitry of mushroom bodies share some similarities with vertebrate brains. Hence these butterflies provide an excellent system in which to explore the neural basis of learning and memory with widespread relevance.
Paper:
‘Rapid expansion and visual specialisation of learning and memory centers in the brains of Heliconiini butterflies’ in by Stephen Montgomery et al in Nature Communications.
Mushroom body calyx in Eueides isabella showing the segregation of areas that receive information about olfactory (green) and visual (magenta) stimuli. In Heliconius the expansion of the mushroom bodies is particularly linked to increases in visual areas.
CREDIT
Antoine Couto et al – linked to the paper
Dryas iulia (non-pollen feeder) and Heliconius sara (pollen feeder)
A Heliconius erato with a pollen load on the proboscis
Heliconius melpomene with a pollen load on the proboscis
CREDIT
Sebastián Men
JOURNAL
Nature Communications
METHOD OF RESEARCH
Computational simulation/modeling
SUBJECT OF RESEARCH
Animals
ARTICLE TITLE
Rapid expansion and visual specialisation of learning and memory centers in the brains of Heliconiini butterflies
ARTICLE PUBLICATION DATE
7-Jul-2023
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