We tend to think of ways to categorize animals either by shape (4 legs? 2 legs? no legs?, thin? Fat? big headed? small headed?) or phylogenetic affinities (reptiles? lesser animals? Snakes? Skinks?). But what about ecology?
The many aspects of a species ecological niche are generally quantified singly, or we refer to some abstract “multidimensional niche”, meaning we give up trying to characterize it before we even started. In a paper published recently in the Journal of Biogeography GARDians, led by Enav Vidan and Jonathan Belmaker, tried to define, and numerate, the main types of lizards out there – as reflected in their ecology.

We have selected four traits that we felt define much of the fundamental axes of ecological variation seen in lizards: 1. use of space / microhabitat preference, that defines where in the environment a lizard is active (on the ground? In trees or rocks? Under ground? In water?); 2. Activity times: species active in the same place, or even on the same branch or piece of ground, can segregate their use of the environment by dividing the temporal niche. Furthermore, being diurnal or nocturnal (or being cathemeral and enjoy both ‘worlds’) has strong implication on thermal biology and hence on metabolism and rates in which lizards take up resources and exchange them with the environment; 3. Diet: is a species insectivorous/carnivorous, as most lizards are? Or do they predominantly feed on plant matter (these guys seem to even take more leaves and plant parts with lower energy content)? Or do they in fact use both plants and animals (and then probably energy richer plant parts such as berries or sap)? This is directly related to the way a lizard affects its environment and may also influence its position across the sit and wait-active foraging continuum (no use waiting for plants); 4. Body size – while not an ecological trait per se size nonetheless strongly influences a host of ecological processes, from the degrees of metabolism and energy flow, to the types of available foods – and potential predators.
These four traits obviously interact, and some combinations may be more or less common than others: small, diurnal, terrestrial insectivore is after all the first picture to pop to mind when the term ‘lizard’ is introduced (except for the diehard gecko lovers among us, and well, there are a few of us with this infatuation). But are there tiny nocturnal herbivores? Or huge nocturnal lizards? How common is a marine iguana  (large, herbivorous, swimming diurnal beast) type lizard – do we remember it simply because it is exotic?

We used Archetypal Analysis to assign lizards to types – or archetypes. Archetypal Analysis is an unsupervised machine learning technique that seeks to find the number of clusters that create the smallest convex hull in an n-dimensional trait space, by using the extreme values rather than the centroid of the clusters. AA assigns, for each species, a vector of affinities to each archetype. Most species are probabilistically assigned to several archetypes, with the partial probabilities summing to one.
We found that the most common functional trait combinations are (1) diurnal, terrestrial, carnivores (20% of the species); (2) diurnal, scansorial, carnivores (16%); and (3) nocturnal, scansorial, carnivores (13%).
Lizards could be robustly classified into seven ecological “Archetypes”:

1. terrestrial (obviously, usually small, carnivorous, diurnal thing that are, well, active on the ground), think Ablepharus skinks, for example
2. Scansorial – small diurnal, carnivorous, scansorial species, such as Pristurus rupestris.
3. Nocturnal – small terrestrial, scansorial and carnivorous species that are, at least partially, active at night (i.e. they are either nocturnal or cathemeral). Like most geckos of course – say Hemidactylus
4. Herbivorous - relatively large, diurnal, terrestrial and scansorial species whose diet includes substantial amounts of plant matter (either as omnivores or herbivores). Saharo-Arabian Uromastyx for example fit the bill very nicely
5. Fossorial – lizards living at least partially underground, mainly small, carnivorous, with varied activity times. Many skinks, such as Ophiomorus represent this strategy
6. Large - very big (all species >200 g), mainly diurnal, terrestrial or scansorial species. You know, Varanus komodoensis and Komodo-dragon wannabes.
7. Semi-aquatic - dwelling in aquatic habitats, relatively large, and generally both carnivorous and diurnal, things like Uranoscodon superciliosus

We then partitioned the global spatial patterns of lizard richness into these seven archetypes, and found that each shows pretty distinct patterns. Turns out Australia is the main hotspot for the herbivorous, nocturnal, fossorial, and terrestrial strategies – and for lizards in general. The Amazon basin is the main hotspot for the semi-aquatic, and scansorial strategies, whereas the large strategy has pan-tropical hotspots, especially in both the Amazon Basin and Northern Australia, but also in Africa, SE Asia and Mexico.
Surprisingly, we found that functional diversity peaks in areas with medium species richness and slowly decreases toward the speciose areas. This unexpected richness-functional diversity unimodal association is also revealed within the scansorial, large, and semi-aquatic strategies. The richness patterns of terrestrial, nocturnal, herbivorous, and fossorial strategies increase with species richness, but globally functional richness peaks in areas with medium species richness.
Thus increases in richness do not necessarily stem from increased functional diversity. Species diversification within specific strategies often dominates richness patterns.  Our findings support the contention that it is important to consider different functional and ecological subgroups when studying richness patterns.

Author: Shai Meiri

Throughout the years, scientists have formulated various ecological "rules" describing how body size evolves as an adaptation to various climatic factors – the first and most famous of these being Bergmann's Rule which posits animals increase in size in cold habitats as an adaptation to minimize heat loss.
In our recent paper published in Global Ecology and Biogeography, we examined trends in body size of squamates, utilizing GARD's massive dataset of distributions and body sizes. We examined these trends both at the assemblage level (how median size of squamate assemblages changes from one area to the next, and how it's correlated with climatic conditions in those areas) and at the species level (how body size changes from one species to the next, and how it's correlated with the climatic conditions experienced by each species).

​​What we found is, for lack of a better term, a huge mess - the spatial patterns for squamates differ from the spatial patterns for lizards and snakes separately, and from continent to continent, and between different families. For each of the climatic variables we examined, we found positive relationships with size in roughly a third of the cases, negative relationships in roughly a third of the cases, and no relationships in about a third of the cases.

Author & photographer: Alex Slavenko

In a recent publication in Biological Journal of the Linnean Society, we present a comparative analysis exploring patterns and drivers of longevity of 1320 reptile species, spanning all orders.
In recent years, there have been many studies focusing on the effect of different ecological variables and life-history traits on the variation in longevity of specific taxonomic groups, focusing mostly on birds and mammals (with the only large- scale ectothermic study done on squamates by Scharf et al. 2015). In order to expand our knowledge on the effect of environmental and life-history variables on the variation in longevity of animals, we tested the effect of ecological variables (through various hypotheses) related to extrinsic mortality (e.g. predation) on the variation in longevity among and within lizards, snakes, turtles and crocodiles. We found that species living on islands, and in colder and more seasonal environments, live longer. Moreover, sampling more individuals increases the chances of finding older specimens, and should be corrected for when studying maximum longevity.

We hope these analyses will enable us to better understand the drivers of longevity in reptiles (and other taxa). We hope this paper will facilitate more large-scale comparative studies on the causes of the variation in longevity of tetrapods in general.

Author: Gavin Stark

In a recent publication in Global Ecology and Biogeograpy, I present a vast dataset of over 20 body size, ecological, thermal biology, geographic, phylogenetic and life history traits for global lizards.

I hope these data will facilitate more study into the biology of these most fascinating of creatures, and that the database publication will encourage others to add yet more data and to correct errors I surely have made when assembling them.

Author: Shai Meiri

In a recently published paper in Diversity and Distributions we try to illuminate aspects regarding the biology, and conservation of all narrow ranged lizard species, across the globe.

When exploring different attributes of small ranged species we found that most of them inhabit relatively inaccessible places in tropical climates worldwide. Furthermore, they are mostly small bodied species; many of them are active at night; and live in rocky habitats. Among the different lizard groups geckos and skinks dominate with many rare species.

 This work could help better focus conservation efforts by pointing at the species, and places, that are in the greatest need of protection. Many of the species, especially those which have not been observed for decades, may well be already extinct. However, to-date only six of the species studied have been officially recognized as such. In order to examine the true extent of such extinctions, and try to prevent future ones, the study provides invaluable information for directing future research and conservation efforts.

Authors: Shai Meiri and Uri Roll

In a recent publication in Global Ecology and Biogeography we explored the prevalence of nocturnality amongst Eurasian lizard species and tried to understand what drives these patterns.

Most animals – at least those that live above ground – are active either during the day or during the night. Being active at either time of day carries with it unique benefits and challenges, and thus particular adaptations. Because of this being nocturnal or diurnal is a trait that is pretty rigid amongst closely related species.

We found that nocturnal lizards have the highest species richness in the tropics and in deserts, and their richness decreases when they get closer to the North Pole. Nocturnal lizards are precluded altogether from the coldest regions inhabited by lizards – in high mountains and the highest latitudes.

Author: Enav Vidan

In a paper published in Nature Ecology and Evolution we present the first global maps of all reptiles - and thus complete the global distributions of all tetrapods. We further explore how the new reptile information changes how we think about global conservation priorities. As this is the first place where all of the GARD maps have been used and published, we use this opportunity to share some of the history of GARD itself, as well as the particular work that was carried out for this paper.

The beginnings of GARD
Planning for reptile conservation globally we first needed to map the distribution of all known species. About 8500 of them when we started in 2006, about 10,500 now recognized. This was a time when such global databases were being published for amphibians, birds, and mammals – some of us have been instrumental in assembling those databases, so we felt fairly confident we knew how it should be done.

We finally had at least some data for all the species or reptiles we thought one could map about two year ago. Then we met again to start the immensely important process of reviewing the distribution data to ensure errors were kept to the minimum (a process that is still ongoing).

Do unique reptilian biologies and ecologies demand particular conservation needs?
Or in other words do the major global conservation priorities designations adequately represent reptiles or do their unique distributions make them less protected. It turns out that many reptiles – predominantly lizards and turtles are left out of global priority regions and protected areas.

Ecoregions that increase in importance for conservation, when reptile data are added (dark blue - top decile ecoregions, light blue - top quartile ecoregions)​

Authors: Shai Meiri and Uri Roll

In a recent publication in the Journal of Biogeography we show that Insular lizards with variable clutch sizes follow the predictions of the island syndrome, while lizards with fixed clutches do not.

Author: Rachel Schwarz

In a 2017 publication in Global Ecology and Biogeography, we collated a novel quantitative volumetric dietary dataset for 308 lizard species worldwide from the field and literature. This novel dataset enabled us to test seven competing hypotheses posited to explain dietary niche breadth, focusing on those that are thought to either cause, or be influenced by, the latitudinal diversity gradient.

A major tenant explaining greater species richness in the tropics is interspecific competition. Dietary niche breadth has long been hypothesized to decrease from the poles toward the tropics, as the numbers of competitors increase. Geographical variation in niche breadth is also hypothesized to be linked to high ambient energy levels, water availability, productivity and climate stability – reflecting an increased number of available prey taxa. Range size and body size are also hypothesized to be strongly and positively associated with niche breadth. We sought to determine which of these factors is associated with geographical variation in niche breadth across broad spatial scales and thus potentially drive the latitudinal diversity gradient.

The synergistic effects of a narrow dietary niche and small range size augments the vulnerability of species to habitat loss and climate change. Based on our findings, the ‘competitionist’s paradigm’ seems to be the exception rather than the rule in explaining the latitudinal diversity gradient.

Author: Alison Gainsbury