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Harriet Lambert

@hcslambert.bsky.social

Investigating plant-pollinator interactions Evolution | Ecology | Bumblebees Lecturer in #BehaviouralEcology at Wageningen University and Research @hcs_lambert on Twitter

756 Followers  |  475 Following  |  70 Posts  |  Joined: 20.11.2024  |  2.6486

Latest posts by hcslambert.bsky.social on Bluesky

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Bumble bees damage plant leaves and accelerate flower production when pollen is scarce Bumble bees manipulate plants to bring about earlier flowering.

Facing a scarcity of pollen, bumblebees will nibble on the leaves of flowerless plants, causing intentional damage in a way that speeds up the production of flowers, according to a Science study from 2020.

Learn more on #WorldBeeDay: scim.ag/45hwgqy

20.05.2025 19:46 โ€” ๐Ÿ‘ 168    ๐Ÿ” 38    ๐Ÿ’ฌ 6    ๐Ÿ“Œ 9
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Leaf-damaging behavior by queens is widespread among bumblebee species - Communications Biology Experiments with captive and wild queens show that leaf-damaging behavior is widespread among bumblebee species and can accelerate plant flowering.

Incredible: New proof that #bumblebee queens destroy leafs (probably helping to found new colonies)! This again can accelerate flowering :)
From researchers @ethzurich.bsky.social
www.nature.com/articles/s42...

14.03.2025 16:25 โ€” ๐Ÿ‘ 12    ๐Ÿ” 7    ๐Ÿ’ฌ 0    ๐Ÿ“Œ 0

yes, of course. Welcome aboard! ๐Ÿ

02.12.2024 13:54 โ€” ๐Ÿ‘ 0    ๐Ÿ” 0    ๐Ÿ’ฌ 0    ๐Ÿ“Œ 0

Thanks for sharing! Such an interesting questionโ€”We're currently funded by an SNF Advanced Grant (data.snf.ch/grants/grant...) to explore the molecular mechanisms, adaptive significance, and ecological implications. ๐Ÿ

28.11.2024 15:10 โ€” ๐Ÿ‘ 2    ๐Ÿ” 0    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0

Thanks so much for your kind words. Stay tuned to pending updates on bumble bee behaviour and fitness! ๐Ÿ˜Š

28.11.2024 13:44 โ€” ๐Ÿ‘ 1    ๐Ÿ” 0    ๐Ÿ’ฌ 0    ๐Ÿ“Œ 0

Stay tuned for upcoming research how this impacts bumblebee performance and fitness!

28.11.2024 13:42 โ€” ๐Ÿ‘ 1    ๐Ÿ” 0    ๐Ÿ’ฌ 0    ๐Ÿ“Œ 0

Great questions! Not all damage triggers early floweringโ€”mechanical damage, for instance, doesnโ€™t have the same effect. We're currently exploring the effects of leaf damage on the regulation of flowering time, as well as the proximate cues mediating plant responses to bumble bee damage.

28.11.2024 13:41 โ€” ๐Ÿ‘ 2    ๐Ÿ” 0    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0

Thank you so much for your kind words! I paint simply to relax and unwind, and bumblebees are the perfect little musesโ€”they never stop inspiring me!

28.11.2024 13:34 โ€” ๐Ÿ‘ 1    ๐Ÿ” 0    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0
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Pollen deprivation stimulates Honeybees Apis mellifera to induce early flowering in tomato plants The intricate relationship between flowering Plants and pollinators is fundamental to crop production and ecosystem health. In the present study, we iโ€ฆ

Great point! This study suggests they can: www.sciencedirect.com/science/arti.... I don't personally work with honey bees, but itโ€™s fascinating to think about how pollination patterns could impact flowering and nectar availability. ๐Ÿ

27.11.2024 13:06 โ€” ๐Ÿ‘ 3    ๐Ÿ” 1    ๐Ÿ’ฌ 0    ๐Ÿ“Œ 0
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17/17 This paper wouldnโ€™t have been possible without my co-authors Foteini, Thomas, Mark & Consuelo and the whole #biocommunication group
@usyseth.bsky.social.
Thanks for reading & follow for updates coming soon!
Research group: biocommunication.ethz.ch
Paper link: www.science.org/doi/10.1126/...

27.11.2024 10:59 โ€” ๐Ÿ‘ 18    ๐Ÿ” 0    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0
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The secret lives of bees as horticulturists? Pollen-starved bumble bees may manipulate plants to fast-forward flowering

16/17 Although these findings open many more questions, particularly in regard to the adaptive nature of bee damaging, I will leave you with this; maybe bees are acting as horticulturists after all?
Thanks for the great perspective by @larschittka.bsky.social
science.sciencemag.org/content/368/...

27.11.2024 10:59 โ€” ๐Ÿ‘ 25    ๐Ÿ” 5    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 1
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15/17 We show that #Bumblebees engage in a remarkable behaviour to accelerate flower production when pollen is urgently needed. This strategy may also help them adapt to the challenges of environmental change.
#PhenologicalMismatch

27.11.2024 10:59 โ€” ๐Ÿ‘ 15    ๐Ÿ” 0    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0
Waletcolour illustration of bombus pratorum worker visiting a snowdrop plant. Illustration by Harriet Lambert.

Waletcolour illustration of bombus pratorum worker visiting a snowdrop plant. Illustration by Harriet Lambert.

14/17 We observed wild workers from other bumble bee species damaging flowerless plant patches, demonstrating that this behaviour occurs in nature and isnโ€™t limited to domesticated Bombus terrestris.

27.11.2024 10:59 โ€” ๐Ÿ‘ 16    ๐Ÿ” 0    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0
Fig. 4 Daily measurements of damage (total number of new leaf holes) by B. terrestris workers in two outdoor experiments.
(A) 2018 experiment with queenless microcolonies. In phase 1, only flowerless plants were present locally. In phase 2, 100 plants in flower were placed adjacent to the focal patch of flowerless plants. Colors indicate individual bee colonies. Damage by bees was significantly higher in phase 1 [generalized linear mixed model fit by maximum likelihood, term = phase, df = 1, F = 712.70, P < 0.001, Akaike information criterion (AIC) 1660.9]. Dots indicate days on which weather prevented data collection. The black line represents a 7-day centered moving average of new bee holes per day. Six flowerless plant species, 36 flowerless plants per bee colony, and five bee colonies (180 flowerless plants in total). (B) 2019 experiment with queenright colonies. Colonies in both treatments were placed adjacent to focal patches of flowerless plants. Colonies in the flowering treatment also had access to 30 plants in flower, placed adjacent to the focal patch, as well as a rooftop garden planted with wildflowers. On 2 days, indicated by triangles, all colonies were given access to sugar solution for 24 hours to mitigate effects of adverse weather conditions. Damage by bees was significantly higher in the flowerless treatment (GLM fit by maximum likelihood, term = treatment, df = 1, F = 5217.7, P < 0.001, AIC 2049.3). Damage levels on roof 2 increased significantly in the month after the wildflower garden was mown (df = 30, P โ‰ค 0.001, AIC 2960.4, GLM). Seven flowerless plant species, 600 flowerless plants per treatment, and eight bee colonies per treatment.

Fig. 4 Daily measurements of damage (total number of new leaf holes) by B. terrestris workers in two outdoor experiments. (A) 2018 experiment with queenless microcolonies. In phase 1, only flowerless plants were present locally. In phase 2, 100 plants in flower were placed adjacent to the focal patch of flowerless plants. Colors indicate individual bee colonies. Damage by bees was significantly higher in phase 1 [generalized linear mixed model fit by maximum likelihood, term = phase, df = 1, F = 712.70, P < 0.001, Akaike information criterion (AIC) 1660.9]. Dots indicate days on which weather prevented data collection. The black line represents a 7-day centered moving average of new bee holes per day. Six flowerless plant species, 36 flowerless plants per bee colony, and five bee colonies (180 flowerless plants in total). (B) 2019 experiment with queenright colonies. Colonies in both treatments were placed adjacent to focal patches of flowerless plants. Colonies in the flowering treatment also had access to 30 plants in flower, placed adjacent to the focal patch, as well as a rooftop garden planted with wildflowers. On 2 days, indicated by triangles, all colonies were given access to sugar solution for 24 hours to mitigate effects of adverse weather conditions. Damage by bees was significantly higher in the flowerless treatment (GLM fit by maximum likelihood, term = treatment, df = 1, F = 5217.7, P < 0.001, AIC 2049.3). Damage levels on roof 2 increased significantly in the month after the wildflower garden was mown (df = 30, P โ‰ค 0.001, AIC 2960.4, GLM). Seven flowerless plant species, 600 flowerless plants per treatment, and eight bee colonies per treatment.

13/17 But how would this work outside the lab?
For two years, we repeated semi-natural experiments on roofs at @ethzurich.bsky.social. We found that bumble bee colonies always made more damage when flowers were limited.

27.11.2024 10:59 โ€” ๐Ÿ‘ 15    ๐Ÿ” 0    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0
Fig. 3 Leaf damage by pollen-satiated and pollen-deprived bumble bees.
(A) Experimental setup: Two colonies were used in parallel for each trial, one of which was initially โ€œpollen satiatedโ€ (PS) and then switched to โ€œpollen deprivedโ€ (PD), while the other experienced the same treatments in the reverse order. Asterisks indicate days (1 and 8) when hives were weighed and new diet treatments were implemented. Adjustment (โ€œAโ€) periods (days 2 to 4 and days 9 to 11) allowed colonies to acclimate to treatments. (B) Bees from pollen-deprived colonies inflicted higher levels of damage on plant leaves [F value (F) = 258, df = 32, R2 = 0.8801, P < 0.001, GLM], regardless of the order of the treatment. Additionally, the observed effects did not differ significantly among colonies (F = 258, df = 32, P = 0.732, GLM). Boxes represent the first to third quartile of the interquartile range, horizontal lines within boxes are medians, and the whiskers are the minimum and maximum values. Six hives, three replicates, and 72 plants. ***P โ‰ค 0.001; ns, not significant.

Fig. 3 Leaf damage by pollen-satiated and pollen-deprived bumble bees. (A) Experimental setup: Two colonies were used in parallel for each trial, one of which was initially โ€œpollen satiatedโ€ (PS) and then switched to โ€œpollen deprivedโ€ (PD), while the other experienced the same treatments in the reverse order. Asterisks indicate days (1 and 8) when hives were weighed and new diet treatments were implemented. Adjustment (โ€œAโ€) periods (days 2 to 4 and days 9 to 11) allowed colonies to acclimate to treatments. (B) Bees from pollen-deprived colonies inflicted higher levels of damage on plant leaves [F value (F) = 258, df = 32, R2 = 0.8801, P < 0.001, GLM], regardless of the order of the treatment. Additionally, the observed effects did not differ significantly among colonies (F = 258, df = 32, P = 0.732, GLM). Boxes represent the first to third quartile of the interquartile range, horizontal lines within boxes are medians, and the whiskers are the minimum and maximum values. Six hives, three replicates, and 72 plants. ***P โ‰ค 0.001; ns, not significant.

12/17 We assigned colonies either a โ€œpollen satiatedโ€ or โ€œpollen deprivedโ€ diet. Halfway through the experiment, we switched the diets to see the effect of pollen access on damaging.
Result? Hungry bees consistently made more damage.

27.11.2024 10:59 โ€” ๐Ÿ‘ 17    ๐Ÿ” 0    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0
photo of microscopic pollen grains

photo of microscopic pollen grains

11/17 We suspected this behaviour was related to a shortage of pollen inside the nest, the only source of protein for #bumblebees.
We started devising experiments to test whether multiple colonies would damage leaves in predictable ways.

27.11.2024 10:59 โ€” ๐Ÿ‘ 12    ๐Ÿ” 1    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0
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10/17 Tomato plants came into flower a month sooner than would normally be expected ๐Ÿ˜ฎ๐Ÿ๐Ÿ…

27.11.2024 10:59 โ€” ๐Ÿ‘ 25    ๐Ÿ” 1    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0
Fig. 2 Effects of bee damage on flowering time. Flowering time of Solanum lycopersicum and Brassica nigra plants subjected to three treatments: (i) bee damage, (ii) mechanical damage, and (iii) no damage (control). Bars represent least squares means ยฑ confidence intervals. Data were converted to a binary response variable (flowering or not flowering, for each plant on each day), and treatment effects were analyzed using generalized additive models (GAMs), avoiding assumptions of linearity. Interactions between โ€œtime since damageโ€ and plant were modeled by smooth functions (table S1). (A) S. lycopersicum: All treatments had highly significant effects on flowering time (bee damage: P < 0.001, estimate = 13.697; mechanical damage: P < 0.001, estimate = 9.131; control: P < 0.001, estimate = โˆ’24.279). The interaction between time and plant (smooth term) was also significant: P < 0.001, estimated degrees of freedom (edf) = 0.974, Chi square (Chi.sq) = 39.49. GAM explained 77% of deviance, with coefficient of determination (R2) = 0.794 over 4800 observations. n = 20 plants per treatment. (B) B. nigra: All treatments had highly significant effects on flowering time (bee damage: P < 0.001, estimate = 2.955; mechanical damage: P < 0.001, estimate = 2.601; control: P < 0.001, estimate = โˆ’5.747). The interaction between time and plant (smooth term) was also significant: P < 0.001, edf = 0.994, Chi.sq = 181.9. GAM explained 48% of the deviance, with R2 = 0.532 over 1200 observations. n = 10 plants per treatment. On the right is a figure legend showing watercolour illustrations of the three treatments: bee damage, mechanical damage, undamaged control).

Fig. 2 Effects of bee damage on flowering time. Flowering time of Solanum lycopersicum and Brassica nigra plants subjected to three treatments: (i) bee damage, (ii) mechanical damage, and (iii) no damage (control). Bars represent least squares means ยฑ confidence intervals. Data were converted to a binary response variable (flowering or not flowering, for each plant on each day), and treatment effects were analyzed using generalized additive models (GAMs), avoiding assumptions of linearity. Interactions between โ€œtime since damageโ€ and plant were modeled by smooth functions (table S1). (A) S. lycopersicum: All treatments had highly significant effects on flowering time (bee damage: P < 0.001, estimate = 13.697; mechanical damage: P < 0.001, estimate = 9.131; control: P < 0.001, estimate = โˆ’24.279). The interaction between time and plant (smooth term) was also significant: P < 0.001, estimated degrees of freedom (edf) = 0.974, Chi square (Chi.sq) = 39.49. GAM explained 77% of deviance, with coefficient of determination (R2) = 0.794 over 4800 observations. n = 20 plants per treatment. (B) B. nigra: All treatments had highly significant effects on flowering time (bee damage: P < 0.001, estimate = 2.955; mechanical damage: P < 0.001, estimate = 2.601; control: P < 0.001, estimate = โˆ’5.747). The interaction between time and plant (smooth term) was also significant: P < 0.001, edf = 0.994, Chi.sq = 181.9. GAM explained 48% of the deviance, with R2 = 0.532 over 1200 observations. n = 10 plants per treatment. On the right is a figure legend showing watercolour illustrations of the three treatments: bee damage, mechanical damage, undamaged control).

9/17 To find out, we started tracking the effect of bee damage on flower emergence.
Even with a small number of holes, plants consistently flowered earlier compared to mechanical or undamaged controls.

27.11.2024 10:59 โ€” ๐Ÿ‘ 27    ๐Ÿ” 1    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 1
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8/17 Using their mouthparts and mandibles, workers consistently made holes in multiple plant species. Each hole took a few seconds, but bees didnโ€™t seem to be collecting tissue or getting anything from the leaf.
Why were they doing this?
Photo credit: bit.ly/hannier_pulido

27.11.2024 10:59 โ€” ๐Ÿ‘ 29    ๐Ÿ” 2    ๐Ÿ’ฌ 2    ๐Ÿ“Œ 0
Gif of a buff-tailed bumble bee worker crawling along a tomato leaf. As she crawls towards the base of the leaf, she uses her mandibles to cut a typical crescent-shaped hole in the leaf.

Gif of a buff-tailed bumble bee worker crawling along a tomato leaf. As she crawls towards the base of the leaf, she uses her mandibles to cut a typical crescent-shaped hole in the leaf.

7/17 We noticed bumble bees behaving very strangely in the lab. Foraging workers were deliberately making holes in the leaves of flowerless plants given to them.

27.11.2024 10:59 โ€” ๐Ÿ‘ 21    ๐Ÿ” 0    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0

6/17 Understanding how bumble bees adapt to ongoing environmental change is more important than ever, particularly in these vulnerable early stages.
What if bumble bees could play an active role in shaping their environment? ๐ŸŒ

27.11.2024 10:59 โ€” ๐Ÿ‘ 19    ๐Ÿ” 1    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0
Fig. 1 Change in community-averaged measures from the baseline (1901โ€“1974) to the recent period (2000โ€“2015).
Local changes in (A) thermal indices are shown. Increases indicate warmer or wetter regions and that, on average, species in a given assemblage are closer to their hot or wet limits than they have been historically. Declines indicate cooling or drying regions and that, on average, species in a given assemblage are closer to their cold or wet limits than they have been historically.

Fig. 1 Change in community-averaged measures from the baseline (1901โ€“1974) to the recent period (2000โ€“2015). Local changes in (A) thermal indices are shown. Increases indicate warmer or wetter regions and that, on average, species in a given assemblage are closer to their hot or wet limits than they have been historically. Declines indicate cooling or drying regions and that, on average, species in a given assemblage are closer to their cold or wet limits than they have been historically.

5/17 Climate change is also driving global bumble bee declines. Increasing weather events and extreme temperatures help push bees out of sync with flowers, which explains some of the dramatic losses. @tnewbold31.bsky.social

27.11.2024 10:59 โ€” ๐Ÿ‘ 21    ๐Ÿ” 1    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 1
Comparison between daily nectar supply and daily demand of three common bumblebee species present on 1 km2 of farmland on: (a) Birches Farm 2016, (b) Birches Farm 2017, (c) Eastwood Farm 2017 and (d) Elmtree Farm 2017. Black lines show grams of sugar available each day on 1 km2 farmland, divided by the number of common bumblebees present on the landscape at that time that is, sugar available per individual bee (ยฑSE). The red line shows the estimated mean daily sugar requirement of a Bombus terrestris individual at each point in the year (ยฑSE), from Rotheray et al. (2017). Note that energy demand per individual is highest in early spring when queens are foraging and establishing colonies. Shaded regions highlight periods of nectar deficit where demand (red line) exceeds supply (black line). Note the y-axis is plotted on a log10 scale

Comparison between daily nectar supply and daily demand of three common bumblebee species present on 1 km2 of farmland on: (a) Birches Farm 2016, (b) Birches Farm 2017, (c) Eastwood Farm 2017 and (d) Elmtree Farm 2017. Black lines show grams of sugar available each day on 1 km2 farmland, divided by the number of common bumblebees present on the landscape at that time that is, sugar available per individual bee (ยฑSE). The red line shows the estimated mean daily sugar requirement of a Bombus terrestris individual at each point in the year (ยฑSE), from Rotheray et al. (2017). Note that energy demand per individual is highest in early spring when queens are foraging and establishing colonies. Shaded regions highlight periods of nectar deficit where demand (red line) exceeds supply (black line). Note the y-axis is plotted on a log10 scale

4/17 Coordinated timing or #phenology between bumble bees and flower emergence are tightly associated.
However, scientists observe increasing โ€˜hunger gapsโ€™ owing to habitat modification and loss.
@TomTimberlake92 on X

27.11.2024 10:59 โ€” ๐Ÿ‘ 20    ๐Ÿ” 0    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0
Watercolour illustration of a buff-tailed bumble bee queen incubating her first clutch of eggs. Illustration by Harriet Lambert.

Watercolour illustration of a buff-tailed bumble bee queen incubating her first clutch of eggs. Illustration by Harriet Lambert.

3/17 When the young queen emerges, she must rapidly establish a new nest. The failure rate of colonies is very high during early development, so having a succession of suitable flowers available is CRUCIAL.
See Bumblebees: their behaviour and ecology by
@davegoulson.bsky.social

27.11.2024 10:59 โ€” ๐Ÿ‘ 26    ๐Ÿ” 0    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0
Watercolour illustration of a buff-tailed bumble bee queen sitting in her burrow under a layer of snow at the end of winter (illustration by Harriet Lambert)

Watercolour illustration of a buff-tailed bumble bee queen sitting in her burrow under a layer of snow at the end of winter (illustration by Harriet Lambert)

2/17 #Bumblebees are exceptional pollinators for many fruits and vegetables.
Unlike honey bees, bumble bee colonies are seasonal. In autumn, the colony dies off, leaving only the young, mated queens to hibernate. Come spring, these queens awaken to start new nests and the cycle begins anew.

27.11.2024 10:59 โ€” ๐Ÿ‘ 25    ๐Ÿ” 2    ๐Ÿ’ฌ 2    ๐Ÿ“Œ 0
Graphical abstract of science paper 'bumble bee damage plant leaves and accelerate flower production' with a list of the authors on a grey background. On the left is a watercolour illustration of a bumble bee damaging a plant leaf with the description 'when hungry for pollen, bumble bees use their mouthparts and mandibles to damage plant leaves'. this illustration is connected by a orange arrow to a watercolour drawing of a flowering yellow black mustard plant with a bumble bee. This has the description: 2) the damage inflicted by bees causes plants to flower earlier than paired control plants.

Graphical abstract of science paper 'bumble bee damage plant leaves and accelerate flower production' with a list of the authors on a grey background. On the left is a watercolour illustration of a bumble bee damaging a plant leaf with the description 'when hungry for pollen, bumble bees use their mouthparts and mandibles to damage plant leaves'. this illustration is connected by a orange arrow to a watercolour drawing of a flowering yellow black mustard plant with a bumble bee. This has the description: 2) the damage inflicted by bees causes plants to flower earlier than paired control plants.

๐ŸŒŸ Throwback to my 2020 research published in @science.org ๐ŸŒผ๐Ÿ We showed how bumble bees actively shape their environmentโ€”making plants flower earlier to meet their needs. Natureโ€™s engineers in action! ๐Ÿงช๐ŸŒ
Sharing this for anyone who missed itโ€”letโ€™s dive in! [1/17] ๐Ÿ‘‡

27.11.2024 10:59 โ€” ๐Ÿ‘ 237    ๐Ÿ” 90    ๐Ÿ’ฌ 8    ๐Ÿ“Œ 13
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17/17 This paper wouldnโ€™t have been possible without my fantastic co-authors Foteini, Thomas, Mark & Consuelo and the whole #biocommunication group.
Thanks for reading & follow me for more!
Research group: biocommunication.ethz.ch
Paper link: science.sciencemag.org/content/368/...

26.11.2024 16:10 โ€” ๐Ÿ‘ 0    ๐Ÿ” 0    ๐Ÿ’ฌ 0    ๐Ÿ“Œ 0
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The secret lives of bees as horticulturists? Pollen-starved bumble bees may manipulate plants to fast-forward flowering

16/17 Although these findings open many more questions, particularly in regard to the adaptive nature of bee damaging, I will leave you with this; maybe bees are acting as horticulturists after all?
Thanks for the great perspective by @larschittka.bsky.social

science.sciencemag.org/content/368/...

26.11.2024 16:10 โ€” ๐Ÿ‘ 0    ๐Ÿ” 0    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0
photo of a bumble bee bottom poking out of a purple flower as it forces itself in to collect pollen

photo of a bumble bee bottom poking out of a purple flower as it forces itself in to collect pollen

15/17 We show that #Bumblebees engage in a remarkable behaviour to accelerate flower production when pollen is urgently needed. This strategy may also help them adapt to the challenges of environmental change.
#PhenologicalMismatch

26.11.2024 16:10 โ€” ๐Ÿ‘ 0    ๐Ÿ” 0    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0
watercolour illustration of a bumble bee approaching a snowdrop plant

watercolour illustration of a bumble bee approaching a snowdrop plant

14/17 We observed wild workers from other bumble bee species damaging flowerless plant patches, demonstrating that this behaviour occurs in nature and isnโ€™t limited to domesticated Bombus terrestris.

26.11.2024 16:10 โ€” ๐Ÿ‘ 1    ๐Ÿ” 0    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0

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