Last week, you could find an enthusiastic subset of our team hanging around suspiciously on the campus of the University Hospital in Antwerp, booklets in hand and an ominous device close by.
This was the kick-off of a new measurement campaign in the framework of ‘De Oorzaak’, our ongoing large-scale citizen science project on urban soundscapes. Our trip to the hospital allowed us to catch multiple birds with one stone.
First of all, we’re out in the real world capturing sounds. We need a whole lot of different sounds, from all kind of sources, to feed in the AI-models that will automatically detect sound sources in our upcoming large-scale measuring campaign. We listen, the sensor records, and we write down exactly what we hear, greatly facilitating manual labelling of the soundbites afterwards.
Second, we are interest in the soundscape on the campus of the university hospital itself. We want to know what sounds patients residing on campus experience, and how that affects their health. And, as we are ecologists at hard, we want to figure out what role a greener hospital campus can play in that regard.
Third, we made use of this trip to start recording bird sounds. We hope to use our extensive sensor network to make a unique spatiotemporal assessment of the distribution of bird sounds in the city. For that, we of course again need to listen to a lot of birds ourselves. Luckily, those were starting to wake up for spring: great tits, blue tits, robins, wrens, ducks, moorhens, even a long-tailed tit: our bird sound dataset is starting to grow!
Finally, we can provide a subjective assessment of that soundscape: how nice was it, how lively, how chaotic? Following standardized terminology, we can create a dataset that links objective sound measurements to our experience of that sound.
Glad this is on a role again, and much more to come!
Major milestone: first of May, The 3D Lab is making a big move to Utrecht University in the Netherlands, and it is doing so following my recent appointment as an assistant professor in the Ecology & Biodiversity-group there. Major milestone, indeed, as this means I have left the realm of temporary postdoc positions, and entered the world of long-term academic security (pending tenure, of course).
I’m very honored to be stepping into the role of ‘assistant professor in ecological scaling,’ a unique title that perfectly aligns with my current and future aspirations. Ecological scaling involves delving into ecological mechanisms at a fine resolution and assessing their validity, robustness, and broader applicability on regional or even global scales. This scaling up of ecology has been at the forefront of my work since my first involvement with the Mountain Invasion Research Network (MIREN), back in the days of my master’s thesis in 2012. Through MIREN, our aim is to delve into the factors driving species redistributions in mountainous regions and understand how these dynamics scale up from specific regional settings to the entire spectrum of mountains worldwide.
Scaling up ecology is also a key component of my work with another project dear to my heart: the SoilTemp network. This initiative aims to extend the understanding of microclimate—a phenomenon inherently local in nature—to broader regional and global contexts. These two networks – SoilTemp and MIREN – will therefore remain core pillars of my future work. With the added security of a long-term position, I am eager to finally stop nibbling and start taking full bites out of my long-term vision to explore the intricate mechanisms governing both microclimate dynamics and species redistributions from local to global scale.
However, I am also eager to push the boundaries further, particularly in unraveling the intricate mechanisms driving biodiversity dynamics. To achieve this, I look forward to collaborating with the exceptional expertise in experimental research within the Ecology & Biodiversity group at Utrecht University. Together, we will tackle the issue of ecological scaling both top-down and bottom-up. A lot of room left for future developments in the area of scaling up experimental findings, for sure. To be continued, so stay tuned for the coming few decades…
‘Ecological scaling’ to me is the perfect blend of theory and practice. It involves a lot of fundamental ecology, yet with the ultimate goal to save the world. I will also make it a crucial point to build that link from theory to practice and work further on the scaling of ecosystem services and ecological management, the way we have for example been working in our citizen science project ‘CurieuzeNeuzen in de Tuin’.
Above all, however, I see this new position as a once-in-a-lifetime opportunity to further expand my role as a mentor. The 3D Lab will continue to evolve into a nurturing environment where aspiring young scientists can learn and thrive as part of a team. While the physical transition to the Netherlands won’t include my team members, our strength in virtual collaboration remains a hallmark of the group. Moreover, I’m committed to leveraging all available resources to enhance opportunities for those working alongside me—a goal that was previously constrained by the uncertainty of my own position.
That mentoring will also expand further as I join the teaching staff for the over 400 biology students in Utrecht. I will take my time – and am extremely grateful for the opportunity – to think critically about what and how we should be teaching the next generation, and if any updates are to be made.
So: are you interested in doing science in the Netherlands, or are eager to forge collaborations on the expansive topics of microclimate, species redistributions, and scaling up ecology, now’s the time to reach out! The opportunities are endless, and I’m excited to explore them together. Let’s embark on this journey of discovery!
Yes, you read that correctly—300% faster! That’s the remarkable leap in speed I’ve experienced in tackling my most common R programming challenges ever since I enlisted the help of a certain robotic companion to think alongside me.
That companion, as you might have guessed, is none other than ChatGPT. It’s become a trusted ally in various aspects of my research. While its prowess in aiding writing tasks has been widely discussed, I stumbled upon its true strength in assisting with my all-to-common R-isuses.
Let me start with a disclaimer: I consider myself fairly decent in R, but I’m perhaps a bit old-fashioned when it comes to embracing new ideas. My focus tends to be on results, sometimes neglecting code cleanliness or efficiency. These days, I find myself using R much less frequently than during my PhD, mainly for data manipulation, while also doing a lot of debugging of student code.
So, what magic does that friendly robot perform for me?
First off, ChatGPT is surprisingly adept at coding. Describe an issue, and it often churns out a correct, clear, and concise solution. For example, filtering a dataset based on specific criteria and then calculating averages across factor levels—a task more proficient R users might do from memory, but one I often find myself looking up the functions for.
Sure, I could turn to traditional help files and forums, but with ChatGPT, everything I need is in one place. I can formulate queries easily and get immediate responses, bypassing the need to scour forums or craft elaborate forum posts myself.
It gets even better when faced with a series of tasks. ChatGPT remembers previous actions within the same conversation, offering suggestions that build upon each other, simplifying code integration throughout a workflow.
When you get a suggestion back from ChatGPT that does not do exactly what you want it to do, you can simply describe where or what is not according to expectations, and ChatGPT immediately provides an alternative. I can even paste error codes directly from R, providing the robot with the context it needs to troubleshoot effectively. This way you can truly get into conversation with the robot, slowly but steadily molding and improving the code into your wishes.
If you provide the dataset and column names in your queries – or even snippets of your own code – the R-code generated by ChatGPT uses these names immediately when generating code, making it much easier to see what goes where.
Many of the tasks I encounter in R are ones I’ve tackled before. But digging through files to find previous solutions takes time, whereas ChatGPT provides guidance swiftly and efficiently.
I’ve noticed my students increasingly relying on ChatGPT as well, empowering them to resolve issues independently, reducing dependency on my assistance and time.
Fabulous, no? To me, this works pretty fluently, and allowed me to effectively speed up some daunting R-tasks, especially regarding data wrangling.
I also see very few drawbacks:
One concern is plagiarism, though in coding, this seems less of an issue compared to academic writing. Personally, I’ve borrowed code snippets without explicit credit before, though I do ensure proper attribution for packages used, so that has not changed much by switching to the robot.
There is a minor drawback that ChatGPT would not include the most recent developments in R. However, for most general tasks, for example regarding data wrangling, it does have access to everything we need.
There’s also the minor drawback of potentially limiting oneself to popular R packages, as ChatGPT may not be well-versed in lesser-known ones. But given my pragmatic approach to coding, as long as I achieve the desired outcomes, this limitation isn’t a major concern to me.
In conclusion, integrating ChatGPT into my coding workflow has streamlined my R programming endeavors, particularly in data wrangling. There might of course be a lot more to say about this, but I thought it might be beneficial to many to at least get the conversation going.
Now, I’m curious—have you used ChatGPT for your coding issues, and if so, what has been your experience? Are there drawbacks that I have – perhaps in my naivety – overlooked?
And now we do that again! This time, for an area that has long been undersampled, but that is extremely important for global biodiversity and ecosystem functioning: tropical forests. As is the case for European forests, we can expect substantial temperature buffering under tropical forest canopies. How much, that has always been hard to say.
Not anymore, as we are proud to introduce a new paper in Nature Communications: patterns of tropical forest understory temperatures. The big thing: we created maps of tropical forest understory temperatures at a resolution of just a few tens of meters for all tropical forests, in South America, Africa, and Oceania!
As expected, forest understories were on average cooler (1.58°C, to be precise) than macroclimatic temperatures, and they were also buffered more (1.72°C lower diurnal – day/night – variation) than macroclimate.
Importantly, however, these averages hide significant spatiotemporal variation in that buffering, driven by patterns in macroclimate, vegetation structure, and topography. This variation holds some important information for understanding of these important ecosystems. For example, temperature buffering is stronger in regions with a distinct dry season. Although reduced rainfall is usually associated with higher temperatures, deep-rooting tropical species can for a long time still access water reserves and keep up their ‘airconditioning’ function, effectively creating a larger difference between understory and free-air temperatures.
The former works as long as these droughts remain within reasonable limits, of course, as climate change might very well push these forests over a threshold, making them lose their airconditioning function and rapidly increasing understory microclimatic temperatures. But that’s a story for another day.
An interesting observation for me is the fact that offsets across these tropical forests are usually not so large. On a daily basis, forest understory temperatures were often less than 1°C cooler than macroclimatic temperatures outside the forests. This was especially true in Indonesia, for example, but large swaths of South American and African rainforests are showing surprisingly small offset values as well.
This phenomenon can be attributed partially to the contrast between daily maximums (which tend to be cooler in forests) and minimums (warmer within forests). However, there might be other contributing factors at play. The high humidity prevalent in tropical regions is likely another significant influencer, dampening the intensity of microclimatic differences.
Nevertheless, despite these seemingly small variations, the consistent stability of temperatures throughout the year results in a cumulative effect. Over time, these incremental differences in temperature do add up, significantly impacting the overall energy input within the ecosystem.
The marked disparities and the crucial spatial diversity present across the pantropical regions underscore the significance of the maps we’ve crafted. These visual representations hold immense importance for anyone delving into the intricate workings of tropical forest understories, spanning from deciphering species distributions to comprehending litter decomposition dynamics. The relevance of such high-resolution microclimate products has already been elegantly demonstrated in understanding the distribution patterns of European forest understory plants. It’s only a matter of time before their paramount significance in tropical ecosystems is similarly illuminated.
The maps are freely available here! For now, at a 300 m-resolution, while we figure out a good way to share the 30-m resolution files open access. The latter are currently available upon request.
With long-term monitoring campaigns focussing on mountain roads and trails, and divergences to railroads and rivers, we are happy to announce that MIREN wants to tackle another – perhaps more unusual – linear disturbance in a new, global survey: rock climbing!
Rock climbing is in many respects similar to mountain roads and trails, with routes serving as linear disturbances and dispersal corridors across elevation gradients, with significant effects on the local vegetation. Nevertheless, cliff vegetation, and the influence of rock climbing on it, is pretty unique: rock faces often cover strong microclimatic gradients, resulting in a unique vegetation of species at either the warm or cool edge of their distribution. This unique vegetation often consists of (locally) rare species with very patchy distribution, and the passage of climbing routes over their habitat might thus have substantial impact. To map that impact, and its interaction with the effects of microclimate and climate change on species redistributions, we launch this new MIREN rock face survey, and you are welcome to join!
Through the MIREN rock face survey we want to learn about global similarities and interregional differences between rock faces. To do this, we will set up permanent vegetation monitoring plots on and adjacent to existing rock climbing routes to monitor local plant species richness and community composition. Wherever possible, we will also measure rock face microclimate in comparison with the microclimate in the environment.
If you are interested in monitoring the vegetation on and along one or a few rock climbing routes in the upcoming summer, express your interest via this form. We are currently developing a standardized protocol that can be applied with minimal effort on any rock climbing route across the globe. If you want to be involved in finalizing that methodology, you can inform us through the same form!
Lake Törnetrask, Abisko Research Station, Abisko, Sweden
Lake Torneträsk, Abisko, Sweden
Trifolium repens
Luscinia svecica, Abisko, Sweden
Luscinia svecica, Abisko, Sweden
Lake Torneträsk
in the Skjomen valley
Norway
Skjomen valley, northern Norway
Abisko, Sweden
Laktatjakka valley
Narvik, Norway
Hair’s tail cotton grass
Saxifraga aizoides, Narvik, Norway
Laktatjakka valley
Narvik, Norway
Common heather
Narvik, Norway
Epilobium angustifolium
Lake Törnetrask, Abisko Research Station, Abisko, Sweden
Lake Torneträsk, Abisko, Sweden
Norway, Narvik
Oenanthe oenanthe, alpine tundra Abisko, Sweden
Phyllodoce caerulea
Angelica archangelica along mountain road in the northern Scandes, Norway
Lake Torneträsk, Abisko, Sweden
Narvik, Norway
Sweden
Narvik, Norway
Oenanthe oenanthe
Diapensia lapponica in one of our plots
Summer in the Skjomen valley, northern Norway
Angelica archangelica
Skjomen valley, northern Norway
Hallerbos 2017
Young bluebell (Hyacinthoides non-scripta) surrounded by flowers of yellow archangel (Lamium galeobdolon)
The common bluebell (Hyacinthoides non-scripta), the signature flower of the Hallerbos
Single bluebell flower surviving on a wetter spot, as indicated by the field of wild garlic (Allium ursinum)
A really wet patch of forest, with giant horsetail (Equisetum telmateia) in a field of wild garlic (Allium ursinum)
Wild garlic (Allium ursinum) in the Hallerbos flowers a bit later than the bluebells, yet this one was already in full bloom
A bumblebee visiting yellow archangel (Lamium galeobdolon)
A bumblebee visiting yellow archangel (Lamium galeobdolon)
Wild garlic (Allium ursinum)
Wild garlic (Allium ursinum)
Weirdly beautiful, the inflorescence of pendulous sedge (Carex pendula), typical for the wettest spots in the forest
Weirdly beautiful, the inflorescence of pendulous sedge (Carex pendula), typical for the wettest spots in the forest
A little stream in the Hallerbos, surrounded by endless fields of wild garlic (Allium ursinum)
The herb-paris (Paris quadrifolia), less common in the forest
Wild garlic (Allium ursinum)
Bluebells (Hyacinthoides non-scripta)
Weirdly beautiful, the inflorescence of pendulous sedge (Carex pendula), typical for the wettest spots in the forest
Another one from the wet plots: large bitter-cress (Cardamine amara)
Another one from the wet plots: large bitter-cress (Cardamine amara)
Young beech leaves, as soon as they are fully grown, spring in the understory is over
A beech forest without understory, most likely too dry and too acid for any survivors
A young beech seedling (Fagus sylvatica), looking nothing like a beech, yet everything like a tiny dancer
Young beech seedling (Fagus sylvatica)
Bluebells (Hyacinthoides non-scripta)
Bluebells (Hyacinthoides non-scripta)
Bluebells (Hyacinthoides non-scripta)
Mountain melick (Melica nutans), a grass in the most amazing green
Bluebells (Hyacinthoides non-scripta) in a rare patch of mountain melick (Melica nutans), a grass in the most amazing green
Bluebells (Hyacinthoides non-scripta)
Bluebells (Hyacinthoides non-scripta)
Montpellier 2017
The entrance to the cathedral of Montpellier
The cathedral of Montpellier
The entrance to the cathedral of Montpellier
The cathedral of Montpellier
Narcissus poetics
The cathedral of Montpellier
The botanical garden of Montpellier
The botanical garden of Montpellier
The botanical garden of Montpellier
Brackish Camargue vegetation
Brackish Camargue vegetation
Brackish Camargue vegetation
A typical lagune
Brackish Camargue vegetation
Camargue horses
Camargue horses
Camargue horses
Brackish Camargue vegetation
Brackish Camargue vegetation
Brackish Camargue vegetation
Camargue horses
Brackish Camargue vegetation
Little egret in the evening sun
Flamingo’s in the evening sun
A typical lagune
Dandelion fuzz
Grass lily
Grass lily
Dandelion fuzz
Veronica in a sea of poplar fluff
Euphorbia in a sea of poplar fluff
Poplar
Gare du Midi, Brussels
Gare du Midi, Brussels
Gare du Midi, Brussels
Gare du Midi, Brussels
Sweden autumn 2016
Autumn in Abisko
Yellow leaves of mountain birch, with lake Torneträsk in the background.
Lapporten, the gate to Lapland, in Abisko
Rain blowing over the Abisko National Park
The colours of the north: red fireweed and yellow mountain birches, with lake Torneträsk on the background
Yellow leaves of mountain birch, with lake Torneträsk in the background.
Rain on the background, the ski lift in Abisko on the foreground
The steep slope of mount Nuolja on a dramatic looking morning
The beautiful colors of lake Torneträsk in Abisko
A little stream on top of the mountain, with a view on Lapporten, the gate to Lapland
Well, that is a beautiful table with a nice view on lake Torneträsk in Abisko
Our little experiment on top of the mountain in Abisko, with a view on Lapporten
Autumn in Abisko is extremely colorfull
The ski lift with a view on Abisko National Park and Lapporten
Hiking dowhill towards lake Torneträsk
This green is greener than the greenest green: moss on top of mount Nuolja
Well, that is a beautiful table with a nice view on lake Torneträsk in Abisko
The ski lift with a view on Abisko National Park and Lapporten
The ski lift with a view on Abisko National Park and Lapporten
The most beautiful hiking trail of the world: Nuolja in Abisko
Angelica archangelica, often the biggest plant of the Arctic
The most beautiful hiking trail of the world: Nuolja in Abisko
Cirsium helenioides, the melancholy thistle
Hiking down mount Nuolja
The steep slope of mount Nuolja on a dramatic looking morning
The colours of the north: red fireweed and yellow mountain birches, with lake Torneträsk on the background
The prettiest yellow and blue: autumn in Abisko
Fireweed, Epilobium angustifolium
Campanula or bellflower, I think ‘uniflora’
Vaccinium myrtillus
Cornus suecica, the prettiest red of the world
Hieracium alpinum, alpine hawkweed
Carex atrata, one of my favourite sedges
Alpine clubmoss, Diphasiastrum alpinum
Agrostis capillaris, bentgrass
Common yarrow (Achillea millefolium)
Anthoxanthum odoratum, sweet vernal grass, fully grown and mature
Snow scooter trail
Our plot in the mids of a field of horsetails (Equisetum pratense)
Equisetum pratense
Cliff overlooking the valley with the road to Norway
Seedling of Taraxacum officinale, the dandelion, after two years of growing in bad conditions
Poa alpina, the alpine meadow-grass, with its viviparous seeds
Massive flowerhead of Angelica archangelica
Angelica archangelica
Blueberry (Vaccinium myrtillus) in autumn
A lowland marsh in Abisko in autumn
Installing the plots of our trail observations on top of mount Nuolja
Installing the plots of our trail observations on top of mount Nuolja
Tanacetum vulgare (Tansy), non-native for the high north
Autumn forest down in the valley
The valley of Nuolja to Björkliden
Summer on the Nuolja-side
A full rainbow behind mount Nuolja in Abisko
It’s raining in the west, clouds trapped behind the mountains
A strong wind blowing rain from behind the mountains to our side
A strong wind blowing rain from behind the mountains to our side
Betula nana, the dwarf birch, mini autumn forest
Betula nana, the dwarf birch, mini autumn forest
The valley of Björkliden in autumn
The valley of Björkliden in autumn
The valley of Björkliden in autumn
The valley of Björkliden in autumn
Sweden spring 2016
A rainy hike
Overlooking the valley of Laktajakka
Eriophorum vaginatum
Bartsia alpina
Salix reticulata
The valley of the lakes
Trifolium repens
Dryas octopetala
Cornus suecica
Oxyria digyna
Melting snowpatch on a lake
Although the alpine zone has been harder for invasives to access than most places, human structures like trails are often an easy gateway for the invaders to get up there. Picture from Abisko, Swedish Lapland.
Ranunculus glacialis
Western European species like the red clover (Trifolium pratense) here are often listed as non-native species in mountain regions.
Ranunculus glacialis
Silene suecica
Silene acaulis
Rubus arcticus
Trifolium pratense
Amiens
Sunny but cold, the Quai Bélu
Enjoying silence and the morning sun
Nice architectural curve
Almost cold enough for ice-skating
Gargoyle planning to eat the cathedral
Colourful mirror
Cathedral with a glimpse of spring
Le Club d’Aviron in winter weather
Cathedral at night
Sun rising above the water
Frozen to the bone
Just outside of Amiens
Maria without a shirt
The southern side
Frozen mirror
House on the square before the cathedral
The museum behind the beautiful gates
Cathedral at night
View from my office window
Cathedral seen from the frozen Parc Saint-Pierre
Amiens is filled with cute little houses
Cold!
Cathedral at night
Sunny but cold, the Quai Bélu
View from my office window
Winter sun on the Place du Don
Cathedral at night
Sweden autumn 2015
Lichen
Sweden summer 2015
View on the 1000 meter plots
Doing research on a cold Arctic morning
Plots flooded by the snowmelt
Flooded by the snowmelt
Meltwater river, racing down the mountain
After a hike, even the most basic house looks cosy. Little hut in the mountains, open for everybody
Snowbridge, maybe don’t cross…
Snowbridge
View from a cliff
Silene acaulis or cushion pink, cutest plant of the Arctic
Two seasons in one image
Steep slope
Hiking down
Narvik Kirche, church of the subarctic
Narvik Kirche
Reindeer on top of the mountain
Narvik Kirche
Summer at the church
Summer flowers
Massive waterfall
Young willow catkins
View from Narvik’s hospital, with lilac flowers
Building a bridge over the fjord will gain al drivers at least an hour
Norwegian fjord
Posing with the water, getting soaked
Minimalistic mountains
Insect investigating our reindeer antler
Catching mosquitoes with our license plate, harvest of the year!
Posing with the plot
Fieldwork on the most beautiful spot of the world
Fieldwork on the most beautiful spot of the world
Summer bridge – still next to the sadly impassable river
Rhinanthus flower in the mountains
Plateau in the valley, beautiful brown
Experimental view from my favourite plot
Salix catkins
Extremely old Betula tree
Waterfall from a cliff
Buttercup is the earliest in spring, here
Rocks!
Alpine views
Views!
Fieldwork
Jumping over rivers
Plot
Golden plover
Angry lemming
Green, the whole north is green!
Snow, so much snow left!
Minimalistic mountain moments
Fieldwork
The research center
Red clover – focal invader
Look at this tiny cute snail!
Massive floods of melting water
Bartsia alpina
Hooray, a toilet!
Dryas octopetala
Lowest elevation plots
Butterball!
That’s a lot of water
Midnight sun is the best
At the lakeside
Beautiful Bistorta vivipara
Don’t fall in the water
Midnight sun
Wild river
Art – made by ages of wild rivers
Baby firework for America’s independence day
Midnight sun at the lake
The Abisko canyon was wilder than ever
That’s a crazy amount of water!
The Abisko canyon was wilder than ever
The Abisko canyon was wilder than ever
Black and white
Stone-man overlooking Abisko
Nothing as soft as a willow catkin
Label and soil temperature sensor attached
I’d drive to the top every day
Reflections
Rocks and clouds
Brave little birch
Brewing our camping poison
Basic camping stuff
Camping in Norway
Home-made temperature houses
Roadside research at its best
Norway is crazy
Horsetail is so funny
Little creek in magical forest
Birches, birches everywhere
Beautiful rock, a gift from the river
Another roadside fellow
Lichen
Ready to rock the summer
Collecting mosses
That’s a crazy old lichen
Tiny tiny piny trees, but old, so old!
Ready to jump into the fjord?
Ready to jump into the fjord?
That’s a spiky stone!
Views on Norwegian fjords
Silene in the mountains
Cute little orchid
Skua
Attacking skua, mind your heads!
Watch out for the attack of the fierce skua!
Black snail
New plot!
Still a lot of snow to melt, but this spot was free for a new plot
Reindeer are better than people
Two seasons in one picture
Let’s see what is happening to the balance in mountains! Is this a starting avalanche, or will it last a bit longer?
Cute little hut
Climbing mountains by car
Softest moss in history
Drosera in the marsh
Hiking in no-man’s land
The clouds are coming
Abisko valley
‘Butterball’
Fieldwork in the tundra
Abisko valley
Little plot
Clouds and sun and mountains
Making soup on a campfire with a view
Little creek on high elevations
Skua on the look-out
Melting snow in a river
Rhodiola rosea and the Törnetrask lake
Beginning of spring
Flooded plots, melting snow, impassible wetness
Ferns and horsetails
Chile 2015
Lunch made by our local colleague, with funny bread (tasty as well!)
Trips to the field sites were sometimes a real adventure, especially right after snowmelt