Category: student blog

  • The odd-shaped claw… is alone no more

    The odd-shaped claw… is alone no more

    I think most of us at some point in our lives experience loneliness. Even we as a species are alone, having separated from our closest relatives, chimps, several million years ago. We are also alone in our genus with the last of our Homo siblings species having gone extinct roughly 10 – 40 thousand years ago. Now, there is only us, Homo sapiens.

    For the Gradungulidae family of New Zealand’s spiders shared the same story until recently.

    Gradungulidae, the large clawed or odd-clawed spiders, is a family of spiders endemic to New Zealand and Australia. Gradungulids are identified by their asymmetrically large claws on the 1st and 2nd legs that they use to capture prey(giving rise to their ‘odd-clawed’ name).

    Until recently there were only three species of Gradungulidae found in New Zealand; Gradungula sorenseni, Pianoa isolata, and Spelungula cavernicola.

    Granungula sorenseni, Forster, 1955. Photo: Sebastian Doak.
    Photo taken 18 August 2021, sourced from Wikimedia Commons. Cc-by-4.0 license.
    https://commons.wikimedia.org/wiki/File:Gradungula_sorenseni_-_Sebastian_Doak_-_151718791.jpeg

    Gradungula sorenseni has the widest distribution across NZ, in forests stretching from Nelson and Marlborough in the north, to western Southland and across the Foveaux Strait into Stewart Island in the south.

    Pianoa isolata is found only within the native beech (Nothofagaceae) forest of Waikaia Forest in central north Southland, where it gets its common name Piano Flat spider, named for a series of flats along the Waikaia River.

    Piano Flat spider, Pianoa isolata, Forster, 1987. Photo: Steve Kerr.
    Photo taken 11 February 2014, sourced from Wikimedia Commons. Cc-by-4.0 license.
    https://commons.wikimedia.org/wiki/File:Piano-flat-spider-steve-kerr-cc-by-01.jpg

    Spelungula cavernicola, has a more limited distribution, and is one of only two legally protected spiders, the other being the Katipo spider (Latrodectus katipo). Spelungula cavernicola is found, as its name implies, primarily in caverns or cave systems. It is present in the Oparara cave system north of Karamea on the upper west coast of the South Island, caves along the Heaphy River, and in the Motupipi cave region of Golden Bay.

    One of New Zealand’s two legally protected spiders, the Nelson Cave Spider, Spelungula cavernicola, Forster, 1987. Photo: Mark Anderson.
    Photo taken 15 July 2017, sourced from Wikimedia Commons. Cc-by-4.0 license.
    https://commons.wikimedia.org/wiki/File:P1150023-001.jpg

    All of these species of New Zealand’s Gradungulids were described by New Zealand’s most accomplished arachnologist, Dr Ray Forster. While describing these species Dr Forster suspected that the actual diversity of the Gradungulids was much greater but he could not gather sufficient samples to captures this within his lifetime.

    This extra diversity has continued amongst New Zealand’s subsequent arachnologists. Over the last 20 years Gradungulids specimens have been diligently collected across their distributions to fill this gap within Grandungulid taxonomy (including The following people collected specimens over 20 years: Peter Michalik , Cor Vink , Martin Ramírez , Danilo Harms and Stephen Pawson).

    In 2015 a photo was uploaded by Andy MacDonald to iNaturalist of an unidentified species of Pianoa found in Mount Richmond Forest Park, Marlborough. This site is 600 km away from the known population of Pianoa isolata in Waikaia Forest! This find led to the discovery of another population of a different Pianoa species near Rarangi, Marlborough by Patrick Miller. Both of these discoveries were made by amateur naturalists, making this an amazing win for citizen science!

    .

    Unidentified Pianoa sp. (sp. means an unidentified species in the Pianoa genus) in Mount Richmond Forest Park. Photo: Andy MacDonald.
    Photo taken 17 October 2015, sourced from INaturalist. Creative Commons copyright. https://www.inaturalist.org/observations/2148126

    All of this research and specimen collection over the last 20 years has resulted in the discovery of two new species of Gradungulidae, with there likely being more!

    Specimens from Spelungula, Pianoa, and Gradungula were analysed using both DNA and traditional taxonomic methods and confirmed that there was enough difference in populations of Pianoa, and Gradungula to constitute different species!

    These two new species have been named Gradungula kahurangi sp. nov. (sp. nov. means new species) and Pianoa civis sp. nov. There are also likely to be another species of Pianoa and another two species of Gradungula, but these were unable to be confirmed due to a lack of adult specimens (where species differences are most obvious).

    The populations of Spelungula cavernicola found in the Oparara and Takaka cave systems were not found to be different enough to be two separate species, despite these two cave systems not being connected and roughly 70 km apart!

    This suggests that historically, and even currently, there may be travel of Spelungula cavernicola between cave systems, likely using the isolated caves of the Heaphy Valley. This is a rather impressive feat for a cave spider!

    This lines up with present research on Spelungula cavernicola being troglophiles (species that can live both in cave, but also on the surface) rather than troglobites (species that live exclusively in the permanent darkness of underground habitats, such as caves).

    Pianoa isolata, and Gradungula sorenseni now have new siblings, likely with more on the way! However, Spelungula cavernicola is still alone, an impressive testament to their ability to travel outside their cave systems which they depend on!

    Diversity of New Zealand Gradungulids appears to be concentrated in the northern part of the South Island. Research is ongoing, with potentially three more species to be described. Citizen science has played a crucial part in the discovery of these new species! So, get out there and get involved.

    Who knows there may be a new species out there waiting for you to find it!

    This blog was created by BSc (honours) student Max Singers as part of an assignment for ECOL608 and was based on the 2025 paper “Alone no more—Integrative taxonomy of New Zealand odd‐clawed spiders challenges the monotypy of Pianoa and Gradungula ( Araneae: Gradungulidae )” published in Systematic Ecology.

  • Is nitrogen the only driver of freshwater eutrophication?

    Is nitrogen the only driver of freshwater eutrophication?

    Imagine a typical stream or river running through farmland. It looks clear enough at first glance, but you start to notice something is not right. Algae begins appearing over time. The water quality gradually declines. Something is leaking into the ecosystem and altering the natural environment.

    So the question becomes: what is responsible?

    For a long time, scientists suspected a single culprit. But, in the early 2000s, soil scientist Andrew Sharpley and his colleagues, including Lincoln University researcher Professor Richard McDowell, set out to investigate why water quality problems persisted even when nutrient management practices were in place.

    Their research, published in Plant and Soil (Sharpley et al.,2001), revealed that nutrient loss from farms to freshwater was far more complicated than previously thought.

    Instead of one obvious offender, the evidence pointed towards two main suspects: nitrogen and phosphorus.

    Solving this mystery changed how we manage nutrients within agricultural landscapes.

    Scoping the area over Waitaki River at Ikawai, Canterbury. Photo taken by author. CC-BY-NC

    Suspect #1: Nitrogen- a.k.a ‘the quiet traveler’

    Nitrogen moves easily through soil, making it difficult to trace back to its source.

    Unlike phosphorus, which tends to stick to soil particles, nitrogen is highly mobile. It likes to dissolve in water and travels easily through the soil profile into groundwater systems, ultimately reaching streams and rivers. Because of this MO (Method of Operation/ Modus Operandi), nitrogen losses often occur out of sight below the surface, making them harder to catch and manage.

    For a long time, nutrient management strategies focused heavily on the reduction of nitrogen loss. That made sense. If nitrogen moved easily through soil and into waterways, then controlling it should have solved the problem, right?

    Well it didn’t.

    Even when nitrogen losses were reduced and put under house arrest, freshwater quality issues often remained. This meant something else was involved… nitrogen had an apprentice picking up the slack.

    Suspect #2: Phosphorus- a.k.a ‘the one hiding in plain sight’

    Phosphorus has a different MO to nitrogen. Instead of traveling through groundwater channels, phosphorus often attaches itself to soil and sediment particles and is transported during rainfall and runoff events. Although dissolved phosphorus can also contribute to eutrophication, most phosphorus losses are strongly linked to surface processes, such as erosion and overland flow. It, essentially, disguises its movements during significant events, helping to evade detection.

    Sharpley and colleagues showed that this difference between nutrients matters. Managing nitrogen alone was not enough, because phosphorus followed different pathways through the landscape.

    Even more interestingly, strategies that were designed to reduce nitrogen loss sometimes came with unintended consequences. In some cases, the application of manure that was applied based on the crops nitrogen requirements, had repercussions that caused phosphorus to accumulate in soils, increasing the risk of phosphorus loss during runoff events.

    So the investigation suddenly became more complicated.

    It wasn’t just about catching one suspect anymore.

    An event that our suspect uses to disguise its movements while being attached to soil particles. This example is the Leith River, Otago, in flood. Photo taken by author. CC-BY-NC

    A breakthrough clue: location matters more than we thought

    By this point, researchers realised that nitrogen and phosphorus behave differently, travel through landscapes in different ways, and require different management strategies.

    One of the most important insights from this research was that nutrient loss doesn’t happen evenly across farms. Instead, it tends to occur in specific areas where high nutrient availability overlaps with the active transport pathways, such as runoff.

    These are known as Critical source areas.

    Think of them as the crime scene hotspots.

    Not every paddock contributes equally to nutrient loss. Some areas of the farm are more prone to loss than others, especially where saturated soils, slopes or drainage pathways allow for nutrients to move quickly into waterways.

    This changed the way scientists and researchers approached nutrient management. Instead of trying to control the nutrients everywhere at once, the attention shifted towards identifying the places where interventions would make the biggest difference.

    Following the evidence: the phosphorus index

    Once researchers realised that location played such an important role, they needed a way to identify where losses were most likely to occur. This led to the development of tools like the phosphorus index.

    Rather than simply measuring how much phosphorus was present in the soil, the phosphorus index combines information about soil phosphorus levels with landscape features, such as slope, runoff risk and transport pathways. Together, these factors help identify where phosphorus is most likely to leave the farm and enter waterways.

    Instead of treating entire farms the same way, the phosphorus index helps target management practices to the places that matter most.

    Almost like predicting the potential next target location.

    Example of potential critical source area where nutrient runoff and drainage pathways overlap. Photo CC BY-SA 2.0 by Doug Kerr.

    Plot twist: solving one problem can create another

    One of the most interesting outcomes from this research was the discovery that managing nitrogen and phosphorus separately can sometimes create trade-offs between them.

    Practices that were designed to reduce nitrogen losses can increase phosphorus accumulation in soils simultaneously. At the same time, strategies that reduce phosphorus runoff can increase nitrogen losses through drainage pathways.

    This meant nutrient management couldn’t focus on just one suspect anymore. Both needed to be considered together.

    That shift in thinking helped to reshape how scientists and land managers approach water quality protection today.

    Despite these advantages, the case is far from closed. Excess nitrogen and phosphorus continue to enter waterways in New Zealand and around the world, contributing to algal blooms, reduced water clarity, oxygen depletion and the degradation of freshwater ecosystems. While researches now have better tools to identify and manage nutrient losses, protecting water quality remains an ongoing challenge.

    Why does this case still matter?

    The work by Sharpley and colleagues helped move nutrient management away from simple nutrient solutions towards more integrated approaches that recognise how nitrogen and phosphorus interact across landscapes.

    Instead of asking how many nutrients are present, researchers began asking: Where are they most likely to move to?

    That question led to better tools, better targeting of mitigation strategies and a stronger understanding of how agricultural systems influence freshwater quality.

    By recognising that both nitrogen and phosphorus contribute to eutrophication through different pathways, scientists and land managers are better equipped to reduce excessive algal growth and protect the health of rivers, streams and lakes.

    The mystery of nutrient loss is far from completely solved. But thanks to research, we now know where to look and which suspects deserve the most attention.

    This article was prepared by Master of Science student Emma Meikle as part of the ECOL608 Research Methods in Ecology course.

    • Sharpley, A. N., McDowell, R. W., & Kleinman, P. J. A. (2001). Phosphorus loss from land to water: integrating agricultural and environmental management. Plant and Soil, 237(2), 287–307. https://doi.org/10.1023/a:1013335814593
  • Could spiders be our crop protectors?

    Could spiders be our crop protectors?

    We are currently living in the sixth mass extinction event. Human activities are driving a global reduction of species and a rapid loss of natural biodiversity. One of the significant contributors to this crisis is the intensification of agriculture, as farmers have resorted to chemical inputs to increase their yields. This approach is not environmentally or economically sustainable, with one million species facing extinction in the coming decade.

    But hope is far from lost. In order to combat this decline, there is a growing transition to Integrated Pest Management (IPM). IPM applies a strategic approach to pest control, integrating knowledge of plant-pest interactions and a combination of biological, cultural, and chemical methods.

    IPM enables natural ecosystems to function alongside, or within, productive food systems. Recent research suggests that spiders could play a key role in IPM, acting as a natural defence against pests in horticulture systems, reducing the need to rely on harmful chemicals.

    Spider feasting on its prey (ABCDee David, 2023)
    Spider feasting on its prey (ABCDee David, CC BY-NC 2.0, 2023)

    Since the end of World War II, the area of land used for agriculture has plateaued, yet the global population has continued to increase. In order to support the growing demand for food, agricultural systems have utilised chemical inputs, such as fertilisers, pesticides, and herbicides, to increase yields. But this efficiency has come at a cost.

    “Crop Spraying – Harvington” (by Mike Finn CC BY 2.0)

    Pesticides are different types of poison applied in agriculture and horticulture to treat pests, diseases, and weeds. Their application is not, typically, exclusive to a target, resulting in unintended harm to other species. The use of pesticides to increase efficiency has come at the expense of declining species and biodiversity, as well as our own health as humans.

    Despite the associated negative impacts, maintaining a productive agriculture and horticulture industry is critical for national food security, ensuring a reliable food supply to sustain the health and wellbeing of the population. In Aotearoa New Zealand, we are reliant on domestic production, for approximately 99% of our fresh vegetable supply, due to the perishable nature of vegetables and our distance from export markets.

    Horticulture also supports our economic well-being through significant export earnings, contributing $6.85 billion for the 2025 export season.

    DES Daughter, CC BY-NC-SA 2.0
    The use of pesticides in food production has the potential to poison our food (by DES Daughter, CC BY-NC-SA 2.0)

    How, then, do we ensure the success of our horticulture industry without jeopardising natural ecosystems and biodiversity?

    The answer to this question may be hidden in our childhood favourites. From the treacherous Shelob residing in the mountains near Mordor (Lord of the Rings), to Aragog and his kin haunting Hogwarts from the Forbidden Forest (Harry Potter), or the talented weaver Arachne embedded in Greek mythology. What all these characters have in common is: (1) they are spiders, and (2) they are infamous villains. Spiders have a reputation for being an enemy. This perception may actually be their greatest advantage.

    A team from Lincoln University and Plant and Food Research recently published a paper in the New Zealand Journal of Ecology (June 2025), reviewing the current literature available, on the use of spiders in pest management in Aotearoa New Zealand. The lead author, Nicola Sullivan, told Radio New Zealand (RNZ) that “Spiders are the most diverse and most abundant generalist predators in horticultural systems that have been seen overseas.”

    “Aragog” from Harry Potter (by Dellboyy Art, CC BY-NC-SA 2.0)

    International research shows that spiders, as per their reputation, are great natural predators against pests in horticulture systems. Spiders are generalist predators, preying on a range of species at different levels of the food chain and across all stages of life. Spiders are versatile, and able to live in a range of different environments. In order to capture prey spiders, deploy diverse hunting strategies, often killing prey in excess, capturing non-target species, or wounding prey.

    These traits increase the effectiveness of spiders in pest management by reducing the number of pests in the ecosystem that eat and damage crops.

    The world’s population of spiders, weighs 25 million tonnes, and are collectively responsible for hunting and eating between 400–800 million tonnes of insects annually. To put this into perspective, that is the equivalent of spiders eating the weight of 80–160 million elephants annually.

    The spiders’large appetite shows the potential benefits that they could provide if harnessed for pest management. In addition to being great predators, they are also an important food source to other predators, helping to support a thriving ecosystem.

    So, is the ancient proverb correct, is the enemy of my enemy my friend? Sadly, this question remains largely unanswered in New Zealand, with only eight studies focused on spiders in agroecosystems. None of these eight focus on the opportunities that spiders can provide for ecosystem functioning. This highlights a significant gap in our knowledge and the need for research in this critical subject area.

    “Spider” (by sama093, CC BY-NC 2.0)

    A few of the many benefits that spiders can provide in agroecosystems are demonstrated by the research of Hooks et al. (2003), who reported an 89% reduction in plant damage, and Zhang (1992), who successfully used spiders to control aphid populations.

    We must move fast to protect the endangered species, ecosystems, and the health of consumers. Future research should first look at understanding which species are present in New Zealand horticultural systems and in what quantities.

    This foundation would enable further research into how effective spiders are as a biological control agent, what factors influence their control effectiveness, whether they reduce the need for chemical inputs, and how their presence impacts other species in the ecosystem?  

    Today, I leave you to ponder if maybe spiders are not the villains we perceive them to be. Is it possible that the perseverance shown by the Incy Wincy Spider is exactly what the horticulture industry needs to protect our declining biodiversity?

    This blog was prepared by Brehana Venimore, a Master of Bioprotection student at Lincoln University, as part of an assignment for ECOL608 Research Methods in Ecology.

    Paper Reference: Sullivan, N. J., Stringer, L. D., Black, A., & Vink, C. (2025). Harnessing spider biodiversity for sustainable horticulture: A call for research and conservation in Aotearoa New Zealand. New Zealand Journal of Ecology, 49(1), 3600. https://doi.org/10.20417/nzjecol.49.3600

  • A fiery topic: shining light on the  acacia understorey

    A fiery topic: shining light on the acacia understorey

    The story of the understorey

    New Zealand is home to thousands of native plant species, of which a whopping 80% of these trees, flowering plants and, ferns are endemic – found only in Aotearoa and nowhere else!

    A thousand years ago the forests of NZ were comprised of only natives. Since then exotic plants have made their way here – crossing the great seas on waka and sailing ships and riding the air in jets to beautify the human gardens of tomorrow. Sometimes these exotics do more than beautifying modern gardens, they expand and conquer, alongside the human colonists.

    Plant invasions pose one of the most large-scale threats to the conservation of biodiversity worldwide. This issue is only getting worse with climate issues allowing for more habitats and niches to be exploited by plant invaders that were previously unavailable.

    Acacia is a plant genus that is notorious for enacting the invade and conquer regime, often considered a problematic and invasive weed, with wanted posters in multiple regions of the world. Acacia are also well known by their street name: wattles.

    Figure 1. Photo of Acacia dealbata. Image from Donald Holbern (CC-BY-SA-2.0)

    But why is acacia considered an invasive weed?

    Wattle is a grade-A problem maker, changing ecosystem structures and soiling the soil. It achieves these feats by changing the composition of the forest, altering the variety of species present in the forest and changing the microbiome of the soil (all the little bacteria and microscopic life we can’t see with the human eye). It also likes to participate in, and encourage, arson for its own benefit.

    You can read more about how acacia messes with ecosystems and soils soil here:

    Ecosystems -> https://repositorio.uchile.cl/bitstream/handle/2250/154809/art04.pdf?sequence=3
    (Disclaimer – Requires translation from Spanish unable to provide pre-translated copy)

    Soiled soils -> https://doi.org/10.1371/journal.pone.0086560

    Acacia and fire

    So, why does acacia love fire so much?

    As Acacia benefits from fire. Wattles are light loving, early successional plants. They survive after fires through regeneration from seed. This means that after a fire, when there is lots of available light, the Acacia species is one of the first woody plants to start growing and can dominate the scene.

    The Acacia genus is also a major fire hazard due to its leaf litter and twig structure increasing the flammability of the fuel giving the genus a moderate/high flammability. This means they catch fire relatively quickly and are able to sustain it as well.

    This flammability creates a lovely little loop of increasing fire risk – fire burns acacia, acacia seedlings profit from the fire that opens up the canopy and grows like crazy, Acacia then dominate, increasing risk of fire once more.

    Wildfires are an increasing risk as climate issues intensify, making wildfire management a more pressing topic. So, if we think of wildfire management in forests in New Zealand, we could expect that forests with high proportions of acacia to be at a high risk for wildfire.

    Figure 2. Illustration of Acacia melanoxylon by Rosa Fiveash

    The burning question

    So, will Acacia remain present once it’s entered a forest scene, especially if its dominant there? Will it keep coming back, continuing to invade and conquer the forest?

    Well…

    Some scientists from Lincoln University (Tim Curran, Jon Sullivan and Azhar Alam) wanted to know exactly that. Heading off to investigate the story of the understorey of an wattle dominated forest.

    The hot and heavy science:

    The study was done in sunny Picton, Marlborough, in a forest found in Picton Bay. The forest was a mixture of native and exotic woody plants where the Acacia species were the most common.

    Tim, Jon and Azhar devised 24 random 10×10 m plots that were about 3 km apart. These plots had two main acacia species invaders: Acacia dealbata and Acacia melanoxylon, with A. dealbata being the main invader and common canopy species in these plots. The plots were sampled by measuring the abundance of each species present in different height categories:

    <0.3m, 0.3-2m, 2-5m, 5-12m, 12-25m.

    To measure flammability, 70 cm offcuts were abducted from 8 mature and healthy acacia trees between the two species in the plots and sealed in black plastic bags and chilled.

    Offcuts were then subjected to burning where their flammability was measured in four categories:

    Ignitability: How many of the samples ignited per species,
    Combustibility: The max temperature reached during burning,
    Sustainability: How long the offcut burnt for after the source of the fire was removed,
    Consumability: How much burnt after the flame stopped.

    Figure 3. Demonstration of the plant BBQ being used to measure flammability (Video by Fire Emergency NZ | YouTube)

    You can read more detailed versions of the methods and stats-> https://doi.org/10.1016/j.foreco.2023.121671

    Methods for flammability -> https://doi.org/10.1071/WF15047

    What was hot:

    So, what did they find? How does a forest respond when it’s dominated by acacia? Do Acacia species continue to invade and conquer or…
    Enter the underdogs of the acacia forest: the NATIVES!

    The study found that in an Acacia dominated forest where disturbances, like landslides and fires, were not common that the Acacia seedlings did not survive beneath their own canopy. Instead the understorey was populated and dominated by native forest species! But why?

    Well, the Acacia species is a light loving genus of plant, sunbathing is a favorite hobby. When there is a forest with a dense canopy you get shade. Shade is something that the Acacia species do not cope with.

    But what does cope with shade you ask?

    Well, none other than NZ natives of courses.

    That doesn’t mean that Acacia species were absent in the understorey. The Acacia species dominated the height category of <0.3 m, making up most of the seedlings present. Native plant species dominated every other height category.

    If the forest environment was to remain undisturbed then the next generation of forest species would be dominated by NZ native plants. The abundance of Acacia would also slowly decline over time.

    This is great as we regain native forest. Another win is that a majority of Aotearoa’s native plants, such as broadleaf (Griselinia littoralis), have low flammability, meaning that they don’t catch fire very easily. Overall, this would likely lower the forest’s wildfire risk – YAY.

    However, that is the future. For now, the forest still has an increased fire risk. Acacia dealbata was the 5th most flammable plant species in the plot and the most dominant.

    A single fire could still change the entire game, causing a great forest reset due to this high flammability from the presence of the Acacia species. This is also a long-term risk as once A. dealbata is present in an ecosystem they tend to persist, even under native canopies.

    “This is fine” meme, edited in imgflip by the author

    All it would take is a fire, or another large-scale disturbance, for the Acacia species to dominate once more, due to the existing canopy being cleared and the light-loving Acacia seedlings skyrocketing up to form the new canopy. Like a good villain, they can always come back.

    The author, Kayley Wiffen, is a postgraduate student in the Postgraduate Diploma of Applied Science at Te Whare Wānaka o Aoraki Lincoln University. This article was written as an assessment for ECOL 608 Research Methods in Ecology.

    ​Paper Reference: Alam, M. A., Curran, T. J., & Sullivan, J. J. (2024). Variation in understorey floristic composition regeneration and fire hazard under Acacia invaded forest canopy in New Zealand. Forest Ecology and Management, 554, Article 121671. https://doi.org/10.1016/j.foreco.2023.121671

  • New beetle reveals New Zealand origin story

    New beetle reveals New Zealand origin story

    Beginning the journey

    Just before Christmas in 1999, Dr. Eric Scott collected an unusual ground beetle from the Wangapeka Track, in Kahurangi National Park. His wife also suffered a broken arm after a bad fall along the track and Eric safely supported her through the tough walk out for medical care. You will also be pleased to know that the beetle specimen was safely delivered to the Entomology Research Museum at Lincoln University. All in a day’s work for an entomologist!

    At that time, no one knew that this tiny beetle would become crucial evidence in a controversial biogeographical debate years later.

    Classification work

    The scientific name of this newly discovered ground beetle species was Orthoglymma wangapeka (there is no common name). This species belongs to the ground beetle family (Carabidae, Coleoptera). It is quite small, with a body length about the size of a fingernail. The beetle is elongated and narrowed at the ‘neck’ position. Its entire body is covered in a dark brown, polished exoskeleton.

    It looks like a normal brown beetle at first glance. However, careful examination of both its external structure and internal reproductive organs, led an international research team, including John Marris and Rowan Emberson from Lincoln University, to discover that this was a new species, different from any other known Orthoglymma species.

    Dorsal View of Orthoglymma wangapeka, Scale bar: 1 mm.
    Photo Citation: Lincoln University Living Heritage: Tikaka Tuku Iho (6th Mar 2023). Coleoptera Orthoglymma wangapeka Holotype. In Website Lincoln University Living Heritage: Tikaka Tuku Iho. Retrieved 17th Apr 2026 12:00, from https://livingheritage.lincoln.ac.nz/nodes/view/36272, used under CC BY 3.0 NZ

    The research team placed the newly named Orthoglymma (from Ancient Greek for straight carved lines – referring to the lined on the abdomen) wangapeka (from the locality of collection) in a tribe called Broscini.

    They obtained data on 73 physical traits and compared with closely related beetles. The closest relatives of this species are all found only in New Zealand, Australia, and southern South America. This suggests that the ancestor of these Orthoglymma species was found in these areas. Fossil evidence of Broscini ground beetles in other research suggests that this group originated before the Gondwana breakup.

    Ancient biota debate

    What is the Gondwana breakup? Based on earth science research, Gondwana was a supercontinent that formed around 600 million years ago. It included many of the current continents, such as South America, Africa, Antarctica, Australia, and our homeland, New Zealand. The supercontinent Gondwana began to break apart around 180 million years ago.

    The continent of Zealandia started separating from Gondwana about 85 million years ago, becoming isolated around 70 million years ago, leading to the formation of the Tasman Sea.

    The long process of the fragmentation is known as the Gondwana breakup. This history explains why New Zealand’s biology shares high similarities with other southern landmasses, like Australia, South America, and Southern Africa, which were also part of the original landmass and neighbours to New Zealand.

    A map of the supercontinent Gondwana. At this stage in the earth’s history, Zealandia had not formed a distinct continent yet.
    Photo Citation: Mikocheung, CC BY-SA 4.0, via Wikimedia Commons

    A second critical event occurred in New Zealand after the Gondwana breakup. New Zealand experienced a significant rise in sea level due to the sinking of the Zealandia continent around 25 million years ago. This is known as the ‘Oligocene Drowning’ theory.

    There has been a heated debate about the extent of this drowning in the academic world. Some experts argue that New Zealand was completely submerged under the ocean during the Oligocene Drowning, which would cause all local terrestrial organisms to go extinct. From this perspective, our current animals and plants would have had to colonise New Zealand by crossing the sea after the drowning. On the other hand, the opposing experts claim that parts of New Zealand must have remained above the ocean, providing a refuge for ancient species to survive.

    Beetles and land

    Orthoglymma wangapeka is a tiny ground beetle that belongs to an ancient branch that evolved before the Gondwana breakup began. These beetles are flightless, lacking the obvious ability to disperse long distances across oceans. Their ancestors almost certainly were present in the pre-break up New Zealand region of the supercontinent Gondwana. Their presence is a powerful piece of evidence suggesting that New Zealand was not completely submerged in the ocean during the Oligocene Drowning.

    The area where Orthoglymma wangapeka was collected belongs to the Buller Terrane, which is one of the oldest rock formations in New Zealand and originated on the eastern margin of Gondwana. The species may be a Gondwanan relict, a survivor of extreme environmental change in this area.

    Other ‘living fossil’ are also found in this area suggesting that the Nelson area might have been an island that provided insects, including ground beetles, wētā, and micropterigid moths, with dry land to avoid extinction during the Oligocene Drowning.

    View of Wangapeka Track, where Orthoglymma wangapeka was collected.
    Photo Citation: Michal Klajban, CC BY-SA 4.0, via Wikimedia Commons

    Summary

    As an ecology student, I am deeply drawn to this story because it is remarkable that a newly discovered species could play a vital role in a long-standing unsolved debate in earth science.

    It fascinates me how a tiny organism can carry such a wealth of information about our country’s ancient past. This case demonstrates how biodiversity research connects with other subjects and provides a priceless value in broadening knowledge and highlights the importance of environmental conservation.

    Without conservation of the habitat, this new species could have gone extinct before it was collected, and we would have missed a critical piece to the puzzle to understand the ancient geographical secrets of our country.

    Next time you walk a trail in New Zealand (first watch where you are walking – don’t break and arm!), keep in mind that everything that exists in the environment might carry some undiscovered secrets of the earth’s history, even a tiny ground beetle.

    This article was prepared by Master’s of Bioprotection student, Ethan Harland, as part of the ECOL608 Research Methods in Ecology course.

    References

    Liebherr, J. K., Marris, J. W. M., Emberson, R. M., Syrett, P., & ROIG‐JUÑENT, S. (2011). Orthoglymma wangapeka gen.n., sp.n. (Coleoptera: Carabidae: Broscini): a newly discovered relict from the Buller Terrane, north‐western South Island, New Zealand, corroborates a general pattern of Gondwanan endemism. Systematic Entomology, 36, 395-414. https://doi.org/10.1111/j.1365-3113.2011.00569.x

    Matt McGlone, Evolution of plants and animals, Te Ara – the Encyclopedia of New Zealand, https://teara.govt.nz/en/evolution-of-plants-and-animals (accessed 23 April 2026). Story by Matt McGlone, published 1 March 2009.

    Mildenhall, D. C., Mortimer, N., Bassett, K. N., & Kennedy, E. M. (2014). Oligocene paleogeography of New Zealand: maximum marine transgression. New Zealand Journal of Geology and Geophysics, 57(2), 107-109. https://doi.org/10.1080/00288306.2014.904387

  • The war beneath your feet: soil decides the fate of plants

    The war beneath your feet: soil decides the fate of plants

    You stride through lush grasslands. The scenery seems perfect. But lurking just below your feet is a battlefield.

    It’s not an obvious one, of course. There are no bombs going off or explosions or yelling; but there are millions of tiny creatures locked in battle for resources and life. And whoever wins determines whether the plant life above it survives.

    This blog post has been inspired by research published in 2015 by scientists of Lincoln University, AgResearch, and their international colleagues. They examined whether soils from different pastures in New Zealand naturally inhibit soil-borne plant pathogens.

    Figure 1. Grass roots penetrating the soil. The majority of activities that affect plants occur below ground level. Source: iStock/Getty Images

    The Invisible Threat

    Many important plant diseases originate underground rather than from the aerial parts of plants, such as leaves. They attack plant roots and stems before visible symptoms appear above ground. By the time one notices any symptoms of disease, the damage may already have been done.

    And here is the scary part: these silent killers can reduce pasture productivity by 40–50%. Can you imagine how devastating it is to lose nearly half of your production to something unseen? Such is the case in pastures where crop rotation and chemical controls cannot always solve the problem.

    Instead of asking the conventional question, scientists started to wonder:

    What if the soil could defend itself?

    Soil Is Not Just Dirt

    It is easy to think of the soil as lifeless material, but this is far from the truth. Soil is one of the most biologically diverse ecosystems on Earth. A complete microbiota lives within it: bacteria, fungi, and other microorganisms interact continuously. While some assist plants in absorbing nutrients, others … kill them.

    Some soils inhibit diseases. Such soils are referred to as disease-suppressive soils, and their action falls into two categories:

    General suppression: the microbiota competes with the pathogen,
    Specific suppression: some microbiota attack the pathogen itself.

    Soils with high plant diversity likely contain more diverse microbiotas, which suggests a high disease-suppression capacity.

    But how can one measure such a phenomenon?

    A Clever Way to Test Soil

    The researchers developed an interesting experiment to test the soil under examination. Rather than using conventional grass or legumes that can be found on pastures, they opted for something completely out of the ordinary: kale.

    And why kale? This plant is not usually used on pastures. If disease does not occur, then it shows that the soil is pathogen-resistant in general.

    Furthermore, they exposed the plants to a well-known pathogenic fungus named Rhizoctonia solani. And this one leads to a specific disease called damping-off. Plants affected by the disease exhibit dark lesions near the base of the stem which cause plants to fall, like broken wires.

    So, basically, the process works as follows:
    Introduce the same plant into different soils;
    Infect the plant with the same pathogen;
    Observe the results.

    Figure 2. Seedling damping off showing dark spots on stem bases. Seedling damping off may result in death of the seedling before establishment. Image credit: AA Seif and AM Varela, icipe. Source: CABI PlantwisePlus Knowledge Bank.

    All Soils Are Not Equal

    The experiment was conducted using four New Zealand pasture soils, including Lincoln, Eyrewell, Rotorua, and Kurow soils.

    Same plant. Same pathogen. Entirely different results.

    Some soils promoted rapid spread of pathogens; others reduced their effect considerably. There were significant differences between disease levels in the various soils.

    • Final disease levels were highest in Rotorua soil.
    • Disease progression rate was highest in Kurow soil.
    • Lincoln soil displayed maximum resistance, with minimal disease levels in the control.

    Same experiment. Different soil. Entirely different results.

    And here comes the moment when it all becomes evident:

    Soil is not just a neutral element. It actively influences the experiment.

    If a soil keeps plants healthy, it’s suppressive. If plants collapse… not so much.

    Figure 3. Sampling the soil is essential for research purposes on the properties and disease suppression abilities of soils. Image credit: William, Adobe Stock. Source: Farmers Weekly.

    The Twist: Some Soils Had Been Infected Already

    Without even having introduced the pathogen, some soils exhibited symptoms of infection. For instance, in Kurow soils, damping-off disease symptoms appeared in the control group as well. This indicated that the pathogen was already present but dormant until the required environmental conditions prevailed.

    It could be termed an underlying threat embedded in the soil. Furthermore, pathogens, such as Rhizoctonia solani, can survive between successive cropping seasons, affecting both pastures and future agricultural crop growth.

    It’s Not Only “How Many” but Also “How Quickly”

    Besides assessing how many of the plants became diseased, the authors also took into account the dynamics of disease development. Why does this matter?

    This is important because a slowly developing disease will allow the plants to develop properly before being affected. The faster moving disease will kill them much earlier.

    Two metrics were used to assess this:
    Disease Incidence (DI) – number of infected plants at the end;
    Area Under Disease Progress Curve (AUDPC) – a measure of disease development over time.
    Imagine that:
    DI is the final result
    AUDPC is the whole game
    And often, their narratives may be very different.

    Why It All Matters

    It isn’t just scientific research for research’s sake. With knowledge of how soils resist disease, we could:

    • Improve our soil management techniques,
    • Cut down on chemical use,
    • Increase productivity from our crops and pastures,
    • Create a more sustainable agricultural process.

    Rather than battling pathogens directly, we could fortify our soil against disease.

    That’s where it gets revolutionary.

    The Bigger Picture

    Agriculture of the future may rely less on adding things to soil…
    And more on what is already thriving beneath its surface.

    When you look at a flourishing farm, remember this:
    It is not only the plants that prosper. There is an entire ecosystem underground, sustaining all life. And in this unseen world, each microbe counts in the battle beneath our feet.

    This blog was prepared by Vikram Shankar Malagi, a Master of Bioprotection student at Lincoln University, as part of an assignment for ECOL608 Research Methods in Ecology.

    References:

    Dignam, B. E. A., O’Callaghan, M., Condron, L. M., Raaijmakers, J. M., Kowalchuk, G. A., & Wakelin, S. A. (2015). A bioassay to compare the disease suppressive capacity of pasture soils. New Zealand Plant Protection, 68, 151–159.

    http://www.nzpps.org/nzpp_abstract.php?paper=681510



  • Bellbird Babel: Dialect differences in NZ bellbirds

    Bellbird Babel: Dialect differences in NZ bellbirds

    Bellbirds love to sing; they sing for everything that they do. Communicating, courtship, foraging, defending their homes, it’s almost like they’re living in a musical. I’ve always been captivated by the song of bellbirds. Whether I’m on a walk in the Port Hills, or at Willowbank Wildlife Reserve looking at the capybara and otters, I hear bellbirds singing in the background.

    The New Zealand Bellbird, or Anthornis melanura, is a honeyeater species and a close relative of New Zealand’s Tūī (Prosthemadera novaeseelandiae). They have a variable diet, feeding primarily on nectar, but also fruits, insects, and scale insect honeydew. In Christchurch, bellbirds spend their summers in the Port Hills, feeding from the large nectar supplies that come from flowering native vegetation. Then, in the winter, some move to the city, where urbanisation creates a warmer environment, and sugar feeders and exotic plantings provide food.

    In 2019, PhD student Jennifer Dent studied foraging and migratory patterns of bellbirds in Christchurch for her thesis, using their calls to determine where different groups were. Bellbirds in different areas make different calls, basically a different accent, language, or singing a song in a different key, and this is referred to as dialect.

    New Zealand Bellbird. Photo CC0 Max G.W. Verheij. https://www.inaturalist.org/observations/162255122

    For this, Jennifer placed DOC AR4 audio recorders at 59 locations. 29 locations were in the Port Hills, where recording took place in autumn. Sites were everywhere from Rapanui Bush in the east to Ahuriri Reserve in the west, totalling 15 km around the Port Hills. The other 30 recording locations were in Christchurch city during winter, from as far north as the Groynes, as far east as Sumner, and as far west and south as Lincoln. From this, Jennifer matched dialects in the Port Hills in autumn to those recorded in Christchurch city in winter.

    Christchurch dialects

    Jennifer found four different bellbird dialects in Christchurch.

    Dialect A was the most common dialect. It was spread across the northern region of the Port Hills, as well as in more central areas, such as the Botanic Gardens.

    Dialect B was the next most common. In the Port Hills, it was found in Kennedy’s Bush, and in the city, it was in south-western areas, such as Halswell and Hoon Hay.

    Dialect C was the least common dialect that Jennifer observed. In the Port Hills, it was found in Omahu Bush, and in Christchurch, it was found outside of the city, but only as far as Tai Tapu and Lincoln.

    Dialect D was the last dialect. This pattern is unusual because it was not found in the autumn Port Hills recordings, but was found in the winter Christchurch recordings around the eastern and northern parts of Christchurch, such as Sumner, the Groynes, and Riccarton Bush, but because it was not found in the autumn recordings, it is not known where they went after winter.

    Map of Dialect Locations in Christchurch. Photo CC-BY Jennifer Dent https://researcharchive.lincoln.ac.nz/server/api/core/bitstreams/82c22265-dec3-419b-8880-4eb37f1aaee2/content

    Why don’t the dialects overlap?

    It’s surprising that four different dialects were found both so close together and with very little overlap, especially since there are no geographic barriers stopping members of one group from flying to another. Jenny suggested that there could be two main reasons for this: limited dispersal and vocal imitation.

    Limited dispersal, or philopatry, is the theory that states that birds remain in the areas where they were born and raised perhaps because it is harder to survive outside their own groups. A second theory is that vocal imitation by bellbirds occurs when birds move between groups, but we don’t notice it because they are so quick to pick up on the new dialect. It is possible that both of these theories are occurring simultaneously.

    Following bellbirds into the city

    The presence of all Port Hills dialects in the Christchurch recordings suggests that seasonal dispersal from the Port Hills to Christchurch is a shared behaviour among all populations. Furthermore, as shown by the map, dispersing to the nearest suitable location rather than spreading across all of Christchurch also seems to be a shared behaviour.

    Bellbirds in Christchurch likely remember foraging areas for different times of the year, but rather than remembering many locations across Christchurch, they remember only a few patches that are close together. This is referred to as patch-scale resource tracking, and it has been shown to be a low-work, high-reward technique for foraging by bellbirds.

    Next time you hear a bellbird singing, you aren’t just hearing background noise, you’re hearing a local neighbour. That bellbird might be a Cashmere regular or a member of the Tai Tapu community. It makes Christchurch a more lively city, as it’s not only just a place for us, but for birds following their own routines, singing their songs as they go about their day.

    This article was prepared by Master of Science student Max Mulvihill as part of the ECOL608 Research Methods in Ecology course.

    Paper reference: Dent, J. M. (2019). Information use during foraging by New Zealand bellbirds (Anthornis melanura) : A thesis submitted in partial fulfilment of the requirements for the Degree of Doctor of Philosophy at Lincoln University. Lincoln University. https://researcharchive.lincoln.ac.nz/server/api/core/bitstreams/82c22265-dec3-419b-8880-4eb37f1aaee2/content

  • The pines are invading! Planting non-native species increases re-invasion

    The pines are invading! Planting non-native species increases re-invasion

    Soil is life

    I’m not sure if you’re aware, as I was not aware of this before coming to Lincoln University, but soil is very much alive. There are millions of organisms in a single handful of soil. These critters perform the majority of the ecosystem services provided by soils.

    In New Zealand, these organisms range from burrowing animals, to soil-dwelling invertebrates, to fungi, to microscopic bacteria and much more. So next time you walk on soil, think about how much life is beneath your feet.

    For plants, a major component of successful growth and survivability is the soil microbiota, such as bacteria, fungi, viruses, nematodes (tiny worms), and many more. I have much love for fungi in the soil microbiota, especially mycorrhizal fungi that are essential for plant growth.

    Mycorrhizal fungi form mutualistic relationships (beneficial for both organisms) with plant roots. The fungi extend their network to increase the nutrient intake in exchange for carbohydrates that the fungi cannot produce itself.

    There are two major types of mycorrhizal fungi, ectomycorrhizal fungi, which infect the outside of plant roots, and arbuscular mycorrhizal fungi (AMF or endomycorrhizal), which infect the inside of plant roots.

    I did a project on ectomycorrhizal fungi abundance on red beech tree roots for SCIE393 where I took this photo of an ectomycorrhizal fungal fruiting body (mushroom) under the microscope (which I thought was very cool). This is really where my love for mycorrhizal fungi started to blossom.

    Ectomycorrhizal fruiting body under the microscope – Photo by Lucas Watkin (CC-BY-NC)

    Exotic plants are strong invaders

    That’s enough about me for now, time to talk about invasions from non-native plants. As I’m sure everyone who lives in New Zealand is aware, we live in an invaded country, full of exotic predators, pests, and weeds.

    While everyone tends to think of the worst invaders are pests like possums and mustelids, the worst invaders are actually the weeds. Approximately half of all the vascular plants in the wild in New Zealand are non-native. There are around 25,000 exotic plant species that have been introduced to New Zealand, with around 2,700 of these becoming wild. Compared to around 2,500 native plants, this is an insane numbers of exotic plants and so to conserve our native species, we must do something about all of these exotic species.

    From grassland to pineland: The rapid invasion of black pine into well grazed high country pasture – Photo by Jon Sullivan (CC BY-NC 2.0)

    One of the worst exotic plant species are wilding pines, such as lodgepole pine and radiata pine. Lodgepole pine was introduced into New Zealand in 1880 to combat erosion. Burning of forests, overgrazing, and introduced browsers, such as deer, goats and rabbits, were clearing the hillsides of our native plants, leading to more slips. The New Zealand government decided to plant exotic plants, specifically Douglas-fir and lodgepole pine to cover the hillsides and reduce erosion.

    These pines did stop the erosion, however, what was not anticipated was the enormous dispersal ability of these wilding pines. Seeds of wilding pines can survive for a decade in their cones, grow roughly anywhere, and can travel kilometers from their parent. There is now roughly 800,000 hectares of wilding exotics in the South Island alone, two thirds of which is lodgepole pine!

    Wilding pines of Flock Hill Station: The very many wilding pines coming out from the experimental forestry plots in adjacent Craigieburn Forest Park – Photo by Jon Sullivan (CC BY-NC 2.0)

    Be careful what you plant!

    This paper headed by Joanna Green has contributions from my lovely thesis supervisor Lauren Waller. In it they describe the effects of planting non-native plants on the soil microbiota, and how that can impact what grows there afterwards. They were specifically looking at how well lodgepole pines grow in soils that have been used and conditioned by exotic plant species.

    Joanna and Lauren started by using soils that had already been conditioned by 19 native and 20 exotic plant species from another two experiments by Warwick Allen and Lauren Waller. The soil microbiota, the nutrients in the soil, and other factors, like the pH of the soil, had been changed to best suit the plant that had been grown in that soil.

    An example of part of the soil microbiota that was conditioned were the ectomycorrhizal fungi. These fungi are required for successful growth by some of our native species, such as our beech, mānuka, and kānuka species. However, exotic species use different species of ectomycorrhizal fungi than our native species. Therefore, when exotic species are grown in soil they will grow well with their species of ectomycorrhiza.

    Basically, think of it like this. If you owned a garden and really liked roses, you would grow a lot of roses. You might grow some other plants but the focus of the garden would be on roses. Now, if someone else came in and took over the garden for themselves, they might not like roses as much but might really like petunias. They will then plant petunias in place of where the roses used to be, altering the state of that garden.

    In terms of ectomycorrhiza, they require associations to survive, so the native ectomycorrhiza species that were in the soil will die after their native plant partners are gone. Exotic ectomycorrhiza species associated with exotic plant species will then survive. Due to this, it will become a lot more difficult for our native species to grow back in that soil due to a lack of ectomycorrhiza that they can grow with. Conversely, it will be a lot easier for exotic plant species to grow in partnership with a large number of exotic ectomycorrhiza.

    Anyway, back to the paper. The researchers found that lodgepole pine grew better in soils that had been conditioned by exotic species, such as black alder, cocks-foot, spear thistle, gorse, and many more. And this was regardless of whether pines had been planted there or not! Lodgepole pine will have a much easier time establishing and invading into areas that have previously had exotic species growing there.

    Lodgepole pine tree near Lake Benmore – Photo by abcdefgewing (CC-BY-NC)

    So why does this matter?

    To conserve our native plants, sometimes we must plant them in areas that have previously grown exotic species. Joanna and Lauren’s research shows that the soil will be conditioned to favour growth of exotic species, and so growing native plants will be more difficult. It will also be a lot easier for exotic species, such as lodgepole pine, to re-invade and take over the conservation site. Therefore, conservation managers must be aware of this soil legacy and decisions must be made in order to manage this re-invasion potential.

    So, next time you want to plant an exotic plant, think about the soil, and whether you would rather plant a native instead.

    This article was prepared by postgraduate student Lucas Watkin, Master of Science in Conservation and Ecology, for an assignment in ECOL608 Research Methods in Ecology.

    Green, J. L., Waller, L. P., Allen, W. J., Orwin, K. H., Pelser, P. B., Smaill, S., & Dickie, I. A. (2025). Plant-soil feedback from non-native communities increases pine invasion and re-invasion potential. Plant Soil, 514(2), 2461-2474. https://doi.org/10.1007/s11104-025-07528-x

    Featured image: Did somebody order pines? The rapid invasion of black pine into well grazed high country pasture – Photo by Jon Sullivan (CC BY-NC 2.0)

  • Wasps aren’t all aggressive, just misunderstood

    Wasps aren’t all aggressive, just misunderstood

    Uncategorized, behaviour, conservation, entomology, student blog, wildlife management

    If you had asked me four years ago where I would be today, I would not have said ‘planning to study wasps’, and I would NOT have said ‘New Zealand’! But here I am and that’s what I’m doing.

    My interest in this field originates from my research on ants, and more specifically their unique behaviour. Ants belong to the order Hymenoptera, the same order as bees and wasps.

    Just like humans, wasps can be social creatures, and just like humans they display different levels of aggression (although most types of wasps are not social). Despite there being around 100,000 described wasp species, only around 1,000 of them are social. Which seems crazy, because when you see one wasp, you always seem to see more.

    Vespula wasps are what’s called eusocial, this means that they are organised into groups and all work together under a single queen. Eusociality is impressively efficient. E.O Wilson, a famed ant biologist, once said that humans display a weak form of eusociality, and I have to say I agree with him.

    Now, back to how wasps display different levels of aggression. Have you ever noticed that when you walk past a nest or sit near a wasp sometimes you will be harassed while other times they will completely ignore you? That’s because different colonies of wasps display their own levels of aggression!

    Vespula germanica, David Nicholls, Ratby garden, 22 April 2016

    There are many reasons why wasps may vary in aggression. Some may be more aggressive to drive away predators or outcompete other colonies. Others may be more passive to hide from mammals who could destroy their nests.

    A group of brave researchers, including Mateus Detoni from Lincoln University, put themselves in harm’s way to determine what factors cause wasps to display varying levels of aggression.

    One hypothesis that they developed was that foraging and temperature could increase aggression because that is when wasps are the most active. The methods used for testing the aggression of the wasps included a target made from two black plastic plates that had been clasped together and a black cloth. Inside the plates was an omnidirectional microphone that had been connected to a camera.

    As you may know, wasps are a super invasive pest species in New Zealand. Since the early 1900s they have been having a devastating impact on the beech forests and the native ecosystem as a whole. There are two species in New Zealand Vespula vulgaris and Vespula germanica, both having colonised from Europe in the 20th Century.

    To survive, wasps need sugars and protein, so they go hunting. The main thing wasps are foraging for, especially in beech forests, is honeydew. This is a type of sugar that has been pooped out by scale insects, which live on and inside beech trees. The main source of protein for wasps is, well, anything that is soft enough for them to bring back to their nest.

    Wasp foraging for honey dew on a southern beech tree. Image from Adrian Paterson.

    The study found that, surprisingly, neither foraging activity nor temperature seemed to have any role in indicating whether a colony would be particularly more aggressive than another. So, the researchers turned to the next question, could it have something to do with nest and colony size? Unfortunately, this lead was also a bust. Yes, the larger colony size did allow for higher foraging activity but there was still no indication that a larger nest and colony would increase aggression.

    Did aggression have something to do with the age of wasps? Eusocial insect colonies span generations of individuals meaning there are both juvenile and mature workers alive simultaneously. This was a topic that Mateus had previously studied. Age can play a role in aggression, as the older wasps have more experience defending the nest, which can cause them to have a more aggressive response when agitated.

    Vespula wasp colonies were observed through their life, and it was concluded that the behaviour on a colony level is consistent throughout development. However, one key thing was noted “behaviour can change as an individual, or colony develops” and “consistent differences within a population can still be observed”.

    Aggressiveness could depend on the ratio of aggressive to nonaggressive individuals in the colony. Wasps having their own individual personalities is not something that most people consider, as they are often thought of as all being worker drones. But I guess a lot of that can be attributed to the media shaping how we view wasps, bees, and ants.

    In Europe, wasps have predators that both keep the population in check and give them a reason to be aggressive. The researchers suggested that external pressures may cause certain behaviour to be passed down through generations. In a place where they do not have predators, such as New Zealand, they can learn to pass on behaviour that is less aggressive.

    Wasps are insects that have individual personalities influencing the aggression levels of the colonies that they live in. Eusociality truly is one of the most interesting concepts in the animal kingdom.

                    This article was prepared by Postgraduate Diploma in Applied Science student Jack Gregorian as part of the ECOL608 Research Methods in Ecology course.

    Reference:

    Jandt, J. M., Detoni, M., Loope, K. J., & Santoro, D. (2020). Vespula wasps show consistent differences in colony-level aggression over time and across contexts. Insectes Sociaux, 67(3), 367–381. https://doi.org/10.1007/s00040-020-00768-3

  • If friend-shaped, why not friend?

    If friend-shaped, why not friend?

    It’s a fair question.

    If an animal looks soft, furry, and, let’s be honest, kind of adorable… why wouldn’t we treat it like a friend? Picture a common brush-tailed possum, fluffy and wide-eyed, or a spiky little hedgehog snuffling through the undergrowth, both undeniably friend-shaped. They don’t exactly look like villains. In fact, they look like animals we might want to protect.

    But here’s the uncomfortable truth: in Aotearoa/New Zealand, these “friend-shaped” animals are responsible for some of the most devastating environmental damage across the country.

    A curious little hedgehog (Erinaceus europaeus). It doesn’t look dangerous, but they are surprisingly harmful predators.
    Copyright CC BY-SA 3.0, by Tony Willis, from Wikimedia Commons

    Early in my veterinary career, I realised just how complicated it can be to care about the environment. I’d signed up to help animals, not to think about how their populations should be controlled. But here in Aotearoa, even the cutest animals can be a big environmental problem.

    The scale of the problem means pest management is essential. Conservationists must find a balance between the effectiveness of pest control techniques and animal welfare. This article explores how emerging technologies may help meet this challenge.

    Cute… but catastrophic

    Aotearoa’s wildlife is unique because it evolved for millions of years without land mammals. The only land mammals native to Aotearoa are, in fact, two species of bats. This isolation means many native birds nest on the ground, can’t fly well, and have limited natural defences against mammalian predators.

    When humans arrived, they brought mammals, like hedgehogs, rats, stoats, and possums, with them. This is when everything changed. A stoat might seem sweet and harmless, but it will kill more than it needs. Possums, while wide-eyed and cuddly, can change the types of trees in native forests.

    The stoat (Mustela erminea) is an adorable but efficient killer.
    Copyright CC BY-SA, 2.0 by Soumyajit Nandy, from Wikimedia Commons

    Introduced mammals have had a significant impact, contributing to widespread loss of biodiversity (variety of animals and plants) across Aotearoa. They have had a hand to play in the extinction of many native bird species and continue to threaten many more.

    So, while these mammals might look adorable and harmless, their impact is anything but. It’s not that these animals are bad, they’re just in the wrong place.

    Why we can’t just leave them alone

    It’s tempting to think, “can’t we just let nature take its course?” The problem is, this isn’t how nature originally worked here. These species were suddenly introduced by humans, and native birds didn’t have time to adjust. So the decline in bird species isn’t natural, it’s our fault, and without intervention, many more native species will be lost.

    The huia (Heteralocha acutirostris). A bird now extinct, lost in part to predation by introduced mammal predators.
    Copyright public domain (CC0-style, no known copyright restrictions in place), by Johannes Keulemans, from Wikimedia Commons

    This is why pest control is necessary. It’s not because we don’t like these animals, but rather we are trying to protect something even more vulnerable and important to Aotearoa’s history.

    The challenges of traditional methods

    Traditionally, pest control has relied on traps and toxins. While these methods are effective, they are not without their downsides. They can be costly, need regular checking and resetting, and pests often return quickly once control efforts stop.

    These methods have been under scrutiny for several reasons. One concern is how humane these methods are. Animal welfare remains an important consideration even when trying to reduce or eliminate pest populations. There are also concerns about their environmental impact, including whether the toxins are retained in the soil and waterways. In addition, is the risk of harm to non-target animals, including native birds and other wildlife not intended to be affected.

    Traditional DOC 200 trap. Using traditional traps requires substantial staff time, meaning that ongoing funding is needed to maintain them.
    Copyright CC BY-SA 4.0, by Kimberley Collins, from Wikimedia Commons

    Looking for better solutions

    The good news is that things are changing in some really exciting ways! A 2014 study by Dr Helen Blackie and her team reviewed a range of emerging technologies and research for long-term mammalian pest management, several of which are discussed below. The team brought together scientists, university researchers, commercial pest management organisations and iwi (indigenous Māori tribal groups) who worked collaboratively to design new tools that are more humane, better targeted to specific pest species, and more effective over long timeframes.

    Helen and her team develop new toxins to minimise animal distress. Some are even based on natural toxins derived from native plants, blending science with mātauranga Māori (traditional knowledge).

    Highly poisonous Tutu plant (Coriaria arborea) has been investigated as a potential source of new toxins.
    Copyright CC BY-SA 3.0 by Rudolph89, from Wikimedia Commons

    Another innovation presented in the study is “set and forget” traps. While these devices have existed for some time. Newer versions use artificial intelligence (AI) to ensure only target pest species activate them. Once installed, these traps can remain in place for long periods without the need for frequent checks or bait replacement, a big advantage over traditional traps.

    Smart trap that uses AI to target pest species while avoiding non-target species.
    Photograph by Dr Helen Blackie, used with permission.

    In the study, the group also helped develop traps that utilise new toxins in a clever way. When the specific pest interacts with the trap, a small dose of toxin is placed onto its coat. The animal then ingests it through grooming, reducing the risk of environmental contamination.

    In addition, the group is learning more about pest behaviour, specifically how animals move, feed, and interact at different population numbers. This helps determine the best places for traps, increasing the likelihood that pests will interact with them.

    People power in action

    As this study has shown, pest control isn’t just about technology. It’s about how people work together to protect the environment. In Aotearoa, pest control programmes rely on collaboration between iwi, conservation groups, and scientists. Each group brings different expertise to the work, from scientific knowledge to local and cultural understanding.

    When I discussed the new innovations with Dr Helen Blackie, she highlighted that some of the most successful pest control initiatives come from community-led groups. She emphasised that even though these groups may have fewer resources than larger programmes, they are still often highly effective. They work closely together with a strong commitment, enabling them to share ideas and adapt their approaches as needed. At the end of the day, pest control only works if people are willing to take part!

    So…why not friend?

    It’s okay to think these introduced mammals are cute, and the instinct to care about all animals is a good one. But, in Aotearoa, protecting native birds and plants requires managing introduced mammals. Not because they’re bad, not because they don’t deserve compassion, but because the balance has already been tipped, and without action, the consequences could be irreversible.

    With better tools, smarter strategies, and more collaboration, we’re moving toward a future where pest control is more effective, more humane, and more sustainable.

    And maybe that’s the real answer to the question, “if friend-shaped, why not friend?” Because sometimes, protecting one part of nature means making hard choices about another.

    Tough decisions need to be made in order to protect tiny native birds like the titipounamu (Acanthisitta chloris).
    Copyright CC BY-SA 4.0  by Melissa Boardman, from Wikimedia Commons

    How can you help?

    Looking after our environment is a shared effort, the more each of us does, the bigger the impact we can make. If you’re keen to take it further, organisations like Predator Free 2050, Department of Conservation, and Forest & Bird offer opportunities to get involved right across the country. Tools like Trap.NZ can also help you protect your own backyard and track your impact. Karawhiua!

    Written by veterinarian and animal lover, Kim Telford, a student at Te Whare Wānaka o Aoraki/Lincoln University. Inspired by a curiosity for how humans and animals intersect, as part of the ECOL 608 Research Methods in Ecology course.

    Explore the science: Blackie H, M., MacKay J.W., Allen W.J., Smith D.H., Barrett B., Whyte B.I., Murphy E.C., Ross J., Shapiro L., Ogilvie S., Sam S., MacMorran D., Inder S., Eason C.T. (2014) Innovative developments for long-term mammalian pest control. Pest Management Science, 70(3), 345-51. doi: 10.1002/ps.3627.