Thursday, 14 May 2026

Refuting Creationism - Rapidly-Evolving Cacti


The phylogeny (V1), showing estimated speciation rate variation in one method (BAMM).

The cactus on your desk is an evolution speed machine - University of Reading

Contrary to half a century of creationist assurances that biologists are about to abandon ‘Darwinism’ and adopt creationism, two biologists from the School of Biological Sciences, University of Reading, UK, have done what scientists actually do: they used evolutionary theory to investigate why cacti have speciated so rapidly. Their conclusion was not that supernatural magic was involved, but that the tempo of evolution itself appears to be a major factor.

Taking their cue from a line of thinking that goes back to Charles Darwin’s work on orchids — including his famous prediction that a then unknown moth, with an exceptionally long proboscis would be found to pollinate a highly specialised Madagascan orchid (subsequently discovered and named Xanthopan praedicta) — botanists had reason to expect cactus diversification to follow a similar pattern. If specialised flowers drive speciation, then cactus speciation should correlate with flower length, especially where long, tubular flowers are associated with particular pollinators.

But that is not what Dr Jamie B. Thompson and Professor Chris Venditti found. They studied flower-length data for more than 750 cactus species in 107 genera, covering a 185-fold range in size, from just 2 mm to 37 cm. Despite that extraordinary variation, flower length itself was only weakly related to how fast cactus lineages split into new species. What mattered was not having a particular flower size, but how rapidly floral morphology — measured here through flower length — was evolving. In other words, faster-speciating cacti had faster-evolving flowers. Their findings have recently been published in the Royal Society’s Biology Letters.

The research was made possible by a new Open Access database called CactEcoDB, created by Jamie Thompson and ten colleagues. This database brings together cactus traits, spatial distributions, environmental variables, range estimates, speciation rates and evolutionary relationships for more than 1,000 cactus species. The result is a major new resource for studying cactus ecology, evolution, biogeography and conservation, and reflects seven years of work compiling and checking data on one of the world’s most distinctive and threatened plant families.

Background: What Are Cacti? Cacti are flowering plants in the family Cactaceae, part of the order Caryophyllales. They are mostly native to the Americas, from Canada to Patagonia, with particularly high diversity in Mexico and other arid or seasonally dry regions. One unusual exception is Rhipsalis baccifera, a mistletoe cactus whose native range also includes parts of tropical Africa and Sri Lanka. [1]

Although cacti are often thought of simply as “desert plants”, the family is much more varied than that. Some are the familiar columnar or barrel-shaped plants of deserts and semi-deserts; others are sprawling prickly pears, small globular species, tree-like forms, or epiphytes that grow on trees in tropical forests. What unites them is not just succulence, but the presence of specialised structures called areoles — the tiny pads from which spines, flowers and new shoots arise. These are a defining feature of true cacti, and help distinguish them from unrelated succulent plants that may look cactus-like because they have evolved similar adaptations to dry conditions.

Most cacti have greatly reduced or absent leaves. Instead, their thick green stems have taken over the job of photosynthesis, while also storing water. The spines are modified leaves and serve several purposes: they discourage herbivores, reduce air movement close to the plant surface, provide a little shade, and in some species may help condense moisture from fog or dew. Many cacti also have shallow, wide-spreading roots, allowing them to absorb water quickly from brief or infrequent rainfall. [2])

A key adaptation in many cacti is crassulacean acid metabolism, or CAM photosynthesis. Instead of opening their stomata during the heat of the day, when water loss would be greatest, CAM plants open them mainly at night, take in carbon dioxide, and store it chemically until daylight, when photosynthesis can proceed with the stomata closed. This is a highly effective water-saving strategy, although it usually comes at the cost of slower growth. [3]

Cactus flowers are often large, showy and highly specialised. Depending on the species, they may be adapted for pollination by bees, moths, bats, birds or other animals. This close relationship between floral form and pollinator behaviour has long made cacti an attractive group for studying evolutionary diversification. The new work from Reading University adds an important refinement: it is not simply the possession of longer or shorter flowers that appears to matter most, but the speed at which floral traits evolve.

Cacti are also a useful reminder that spectacular evolutionary success does not make a group secure. A global assessment found that 31% of evaluated cactus species were threatened with extinction, with pressures including habitat loss, agriculture, development and illegal collection for the horticultural trade. So this is a family that illustrates both evolutionary innovation and modern vulnerability. [4]
The two papers are accompanied by a news release from Reading University:
The cactus on your desk is an evolution speed machine
The cactus on your windowsill may grow slowly, but new research shows that cacti are surprisingly fast at creating new species.
Biologists have long thought that pollinators and specialised flowers drive the formation of new plant species. But scientists at the University of Reading found that in cacti, the secret lies in how quickly flowers change shape, rather than how big the flowers grow or which animal pollinates them.

Researchers studied flower length data for more than 750 cactus species, covering a 185-fold range in size from just 2mm to 37cm. Despite this variation, flower length had almost no relationship with how fast a species split into new ones. Instead, species whose flowers were evolving most rapidly were also the most likely to branch into new species, an effect that held across both recent and deep evolutionary history.

Their study, published today (Wednesday, 18 March) in Biology Letters, challenges ideas going back to Charles Darwin, who studied orchids and suggested that specialised flower forms drove the creation of new plant species.

People may think of cacti as tough, slow-growing plants, but our research shows that the cactus family is one of the fastest-evolving plant groups on Earth. Knowing how fast cacti evolve reveals that deserts, often seen as harsh and unchanging, are actually hotbeds of rapid natural change. We expected cacti with longer, more specialised flowers to be the ones creating the most new species. Instead, flower size made almost no difference. What matters is how quickly flowers change shape. Cacti whose flowers evolve rapidly are far more likely to split into new species than those whose flowers stay the same, however elaborate they are.

This result has real implications for conservation. Since flower evolution has helped generate cactus species over millions of years, evolutionary pace should become part of conservation efforts. Although being able to rapidly evolve does not guarantee resilience, especially as the planet is changing faster than most cacti can keep up, it could help predict which species need the most help. Rather than searching for a single trait that predicts which cacti are most at risk, conservationists may need to look at how fast a species is evolving instead.

Dr. Jamie B. Thompson, lead author
School of Biological Sciences
University of Reading
Reading, Berkshire, UK.

Mapping the cactus family tree

The cactus family contains around 1,850 species and is one of the fastest-expanding plant groups on Earth, spreading across the Americas over the past 20 to 35 million years.

This research was made possible by anew Open Access database called CactEcoDB, created by lead author Jamie Thompson and developed in collaboration with ten coauthors from three continents, including six from the University of Reading. Published this month in Nature Scientific Data, it brings together seven years of work compiling cactus traits, habitats, and evolutionary relationships. With nearly a third of cacti threatened with extinction, the database provides a shared resource for scientists worldwide, to study their biodiversity, conservation and future under climate change, for the first time.

Publications:


Abstract
The rise of biodiversity is shaped by variation in speciation rates. Across many taxonomic groups, both trait values and the rates at which traits evolve have been proposed to influence diversification, but these factors can act independently. Here, we test two competing hypotheses in the cactus family, that speciation depends on flower length variation or on the rate of evolutionary change in flower length. Across >750 species in 107 genera, we find that flower length is only weakly related to speciation, whereas the rate of flower-length evolution is a strongly positive predictor. Moreover, flower length and rate of evolutionary change in flower length are only weakly correlated, indicating that rapid change, rather than any particular floral morphology, underlies cactus diversification. These results challenge expectations that specialized morphologies accelerate diversification, suggesting instead that in cacti, it is the tempo of floral change, rather than any particular floral form, that explains their extraordinary diversity.



Abstract
Integrated datasets linking traits, spatial distributions, environmental variables and phylogenies are essential for comparative research, but remain limited for many plant taxa, including those which are most threatened. Cactaceae are a morphologically and ecologically diverse succulent family that are iconic components of ecosystems across the Americas, and face high extinction risk. To support future comparative research, we present CactEcoDB (The Cactus Ecological Database), an Open Access dataset of curated spatial, ecological, trait, phylogenetic, and diversification data for over 1,000 cactus species. CactEcoDB includes species-level trait data, geographic occurrence records, environmental variables, range size estimates, speciation rates, and the largest time-calibrated phylogeny of cacti to date. By integrating these diverse data in a single and accessible platform, CactEcoDB is intended as a community resource for ecological, evolutionary, biogeographic, and conservation-focussed studies involving cacti, one of the most celebrated yet threatened plant families.
Fig. 1
The phylogeny (V1), showing estimated speciation rate variation in one method (BAMM). Phylogenetic branches in phylogeny V110 are coloured according to speciation rates estimated with BAMM97, and vary 32-fold. Arc segments of median speciation rate for thirteen morphologically varied cactus genera are indicated. This figure and figure legend is reproduced with permission from10. Cactus images are used under Creative Commons with modifications allowed. From left to right: images 1, 3, 8, 11, 12, and 13 used photos taken by Amante Darmanin, Forest & Kim Starr, John Tann, Renee Grayson, and Wendy Cutler, which are licensed under a Creative Commons Attribution 2.0 License (https://creativecommons.org/licenses/by/2.0/). Image 2 used a photo marked as being in the Public Domain (https://creativecommons.org/publicdomain/mark/1.0/). Images 4 and 10 used photos taken by Leonora Enking and Lyubo Gadzhev, which are licensed under a Creative Commons Attribution-ShareAlike 2.0 License (https://creativecommons.org/licenses/by-sa/2.0/). Images 5, 7 and 9 used photos marked as being in the Public Domain using the CC0 1.0 Universal Public Domain Dedication (https://creativecommons.org/publicdomain/zero/1.0/). Image 6 used a photo taken by Christer Johansson, which is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/deed.en).

Fig. 2
The distribution of species coverage by variable. Speciation rate estimates, growth form and plant size (maximum height or length) have highest coverage (1,063-982, 1,061 and 937 species, respectively), and the spatial environmental variables sample 904 species. We only calculated range size for those species in IUCN, given the occurrence scarcity in GBIF for the remaining species. Pollinator and chromosome count have lower coverage with 327 and 378 species, respectively. We compare the species coverage for variables in CactEcoDB against those in the largest previous dataset10.

Fig. 3
Examples of each growth form in CactEcoDB. (a) Rhipsalis baccifera, an epiphytic cactus. (b) Echinocactus grusonii, a barrel cactus. (c) Cephalocereus columna-trajani, a columnar cactus. (d) Mammillaria tetrancistra, a globose solitary species. Note that we have not shown a globose caespitose species, which appears as clusters of globose solitary species. (e) Maihuenia poeppigii, a cushion-forming species. (f) Opuntia microdasys, a shrubby species. (g) Ariocarpus fissuratus, a geophyte. (h) Pachycereus pringlei, an arborescent species. Cactus images are used under Creative Commons licenses with modifications allowed. Image (a) used a photo taken by Maria Vorontsova, which is licensed under the Creative Commons CC0 1.0 Universal Public Domain Dedication (https://creativecommons.org/publicdomain/zero/1.0/). Images (b) and (g) used photos taken by Dr. Hans-Günter Wagner, which are licensed under a Creative Commons Attribution-ShareAlike 2.0 License (https://creativecommons.org/licenses/by-sa/2.0/). Images (c) and (h) used photos taken by Amante Darmanin, which are licensed under a Creative Commons Attribution 2.0 License (https://creativecommons.org/licenses/by/2.0/). Image (d) used a photo taken by Jesse Pluim (BLM), which is marked as being in the Public Domain using the Public Domain Mark 1.0 (https://creativecommons.org/publicdomain/mark/1.0/). Image (e) used a photo taken by Laurent Houmeau, and image (f) used a photo taken by Sergio Niebla; both are licensed under a Creative Commons Attribution-ShareAlike 2.0 License (https://creativecommons.org/licenses/by-sa/2.0/).

Fig. 4
The distribution of plant height, speciation rate, growth form, chromosome count, and pollinator. (a) Cactus size (height or length) is bimodal, which is shaped by underlying growth form variation10. (b) Tip speciation rate is mostly relatively slow, with fewer relatively faster species. (c) The most common growth form is globose solitary, followed by globose caespitose and shrubby. The least common growth forms are cushion forming, geophytic and barrel. 222 species are polymorphic, which mostly consists of species which are both globose solitary and globose caespitose (154 species), or both arborescent and shrubby (50 species). (d) Most species have the base number of 11 chromosomes, and most chromosome count variation is known to be generated by polyploidy74, reflected in the distribution (e.g. 22, 33, 44, 55). (e) Species are classified into ancestral (bee) and derived (bat, bird, moth, other insect) pollination categories following51.

Fig. 5
The spatial distribution of cactus richness and tip speciation rates. (a) Species richness is plotted per grid cell (~50*50 miles), and shows Mexican, Eastern Brazilian and Andean richness hotspots. (b) Median tip speciation rate per grid cell, based on BAMM_V1 estimates from Thompson et al.10 and mapped using the spatial data assembled here. This figure is adapted from supplementary materials in Thompson et al.10, but uses updated spatial data and is presented at higher spatial resolution.

Here, then, is another example of science doing what creationism cannot do: taking observable facts, testing expectations, and refining understanding in the light of evidence. The expectation that cactus speciation might be driven simply by flower length was reasonable. It was based on real evolutionary thinking, on known relationships between flowers and pollinators, and on a Darwinian tradition of using natural selection to make testable predictions. But when the evidence showed that flower length itself was not the main factor, the scientists did not discard evolution. They used it to ask a better question.

And the answer was still an evolutionary one. The important factor was not a fixed floral form, but the rate at which floral traits were changing. That is exactly the kind of result evolutionary biology is equipped to explain: variation, ecological interaction, selection, divergence, and the splitting of lineages over time. Cacti did not diversify because an invisible designer tinkered with them in ways that conveniently left no evidence of design. They diversified through natural processes acting on inherited variation, shaped by ecology, geography, pollinators, climate, and time.

Creationism, by contrast, contributes nothing to this understanding. It could not have predicted this result, cannot explain why closely related cactus lineages differ in their rates of floral evolution, and offers no useful framework for investigating why some groups diversify rapidly while others do not. “The designer did it” is not an explanation; it is the abandonment of explanation. It tells us nothing about mechanisms, makes no useful predictions, and provides no research programme.

What this research shows instead is the continuing strength of evolutionary theory. More than 160 years after Darwin, it is still the framework that enables scientists to make sense of life’s diversity — not as a set of disconnected miracles, but as the result of natural processes that can be investigated, measured and understood. The cactus on the windowsill, far from being a token of supernatural manufacture, is part of a vast evolutionary story: one in which changing flowers, changing environments and changing lineages have produced one of the most distinctive plant families on Earth.




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