The mid-domain effect: It’s not just about space

Ecologists and biogeographers have long sought to understand how and why diversity varies across space. Up until the late 20th century, the dominant role of environmental gradients and historical processes in driving geographical species richness patterns went largely undisputed. However, almost 20 years ago, Colwell & Hurtt (1994) proposed a radical reappraisal of ecological gradient theory that called into question decades of empirical and theoretical research. That controversial idea was later termed the ‘the mid-domain effect’: the simple proposition that in the absence of environmental gradients, the random placement of species ranges within a bounded domain will give rise to greatest range overlap, and thus richness, at the center of the domain (Colwell & Lees, 2000) (Fig. 1a). The implication of this line of reasoning is that the conventional null model of equal species richness regardless of latitude, elevation or depth should be replaced by one where richness peaks at some midpoint in geographical space. Our intention here is to draw attention to a neglected, yet important manifestation of the mid-domain effect, namely the application of mid-domain models (also referred to as geometric constraint models) to non-spatial domains. If individual species have ranges that exist not just in geographical space but also in environmental factors, such as temperature, rainfall, pH, productivity or disturbance, shouldn’t we also expect mid-domain richness peaks along non-spatial gradients? A mid-domain model applied to non-spatial gradients predicts the maximum potential richness for every value of an environmental factor. As with spatial mid-domain models, realized richness would probably be less, but the limits to richness are still predicted to be hump-shaped. Indeed, hump-shaped relationships emerge with remarkably high frequency across various non-spatial gradients. For instance, two of ecology’s most fundamental, albeit controversial theories – the productivity–diversity relationship and the intermediate disturbance hypothesis – predict mid-domain peaks in species richness. However, the potential of non-spatial mid-domain models has gone largely ignored

Is the notion that species interactions are stronger and more specialized in the tropics a zombie idea?

A short review of a controversial topic

Alpine plants are on the move: Quantifying distribution shifts of Australian alpine plants through time

Aim Alpine plant species’ distributions are thought to have been shifting to higher elevations in response to climate change. By moving upslope, species can occupy cooler and more suitable environments as climate change warms their current ranges. Despite evidence of upslope migration in the northern hemisphere, there is limited evidence for elevational shifts in southern hemisphere plants. Our study aimed to determine if alpine plants in Australia have migrated upslope in the last 2 to 6 decades. Location Kosciuszko National Park, NSW, Australia. Methods We collated historic occurrence data for 36 Australian alpine plant species from herbarium specimens and historic field observations and combined these historic data with modern occurrence data collected in the field. Results Eleven of the thirty-six species had shifted upslope in mean elevation and four species showed downslope elevational shifts. The rate of change for upslope shifts varied between 4 and 10 m per year and the rate of change for most downslope shifts was between 4 and 8 m per year, with one species shifting downslope at a high rate of 18 m per year. Additionally, some species showed shifts upward in their upper range edge and/or upward or downward shifts in their lower range edge. Five species also showed range contractions in the difference between their lower and upper range edges over time, while two showed range expansions. We found no significant differences in elevational shifts through time among herbaceous dicotyledons, herbaceous monocotyledons and shrubs. Main Conclusions Plant elevational shifts are occurring rapidly in the Australian alpine zone. This may allow species to persist under climate change. However, if current warming trends continue, several species within the Australian alpine zone will likely run out of suitable habitat within a century

Southern hemisphere plants show more delays than advances in flowering phenology

Shifts in flowering phenology have been studied in detail in the northern hemisphere and are a key plant response to climate change. However, there are relatively fewer data on species' phenological shifts in the southern hemisphere. We combined historic field data, data from herbarium specimens dating back to 1842 and modern field data for 37 Australian species to determine whether species were flowering earlier in the year than they had in the past. We also combined our results with data compiled in the southern and northern hemispheres, respectively, to determine whether southern hemisphere species are showing fewer advances in flowering phenology through time. Across our study species, we found that 12 species had undergone significant shifts in flowering time, with four species advancing their flowering and eight species delaying their flowering. The remaining 25 species showed no significant shifts in their flowering phenology. These findings are important because delays or lack of shifts in flowering phenology can lead to mismatches in trophic interactions between plants and pollinators or seed dispersers, which can have substantial impacts on ecosystem functioning and primary productivity. Combining our field results with data compiled from the literature showed that only 58.5% of southern hemisphere species were advancing their flowering time, compared with 81.6% of species that were advancing their flowering time in the northern hemisphere. Our study provides further evidence that it is not adequate for ecologists to assume that southern hemisphere ecosystems will respond to future climate change in the same way as ecosystems north of the Equator. Synthesis. Field data and data from the literature indicate that southern hemisphere species are showing fewer advances in their flowering phenology through time, especially in comparison to northern hemisphere species

The Relation Between Activity and Environment in Compact Groups of Galaxies

We present the results of the classification of spectral activity types for 193 galaxies from a new sample of 49 compact groups of galaxies in the southern hemisphere (SCGs). This sample was selected in automated fashion from a digitized galaxy catalogue, covering an area of ~5200 sq deg, around the South Galactic Pole. It is complete up to m ~14.5 in b_j for the brightest galaxy of the group. The spectral analysis of the SCG galaxies confirms the results previously obtained for a smaller sample of Hickson's compact groups (HCG). We confirm the luminosity-activity and morphology-activity relations, as well as the predominance of AGNs (41% of SCGs galaxies). We verified also that the number of early-type non-emission-line galaxies increases with the number of members in the group. The SCGs contain more star-forming galaxies (SFGs) and less non-emission-line galaxies than HCGs, which suggests that they probe a wider range of physical properties. The SFGs are composed in majority of HII Nucleus Galaxies, which have less intense star formation than starburst galaxies. The star formation activity in SCGs is, consequently, remarkably low. The SFGs show also evidence for nuclear activity. If these results are further confirmed, 70% of the galaxies in SCGs would then have an active nucleus, making these systems remarkably rich in AGNs. Curiously, however, this characteristic of CGs generally excludes Seyfert 1 galaxies.(Abridged)Comment: 53 pages, Latex, 9 encapsulated postscript figures, Accepted for publication in The Astronomical Journa

Taller plants have lower rates of molecular evolution

Rates of molecular evolution have a central role in our understanding of many aspects of species' biology. However, the causes of variation in rates of molecular evolution remain poorly understood, particularly in plants. Here we show that height account

Untangling direct species associations from indirect mediator species effects with graphical models

Ecologists often investigate co‐occurrence patterns in multi‐species data in order to gain insight into the ecological causes of observed co‐occurrences. Apart from direct associations between the two species of interest, they may co‐occur because of indirect effects, where both species respond to another variable, whether environmental or biotic (e.g. a mediator species). A wide variety of methods are now available for modelling how environmental filtering drives species distributions. In contrast, methods for studying other causes of co‐occurence are much more limited. “Graphical” methods, which can be used to study how mediator species impact co‐occurrence patterns, have recently been proposed for use in ecology. However, available methods are limited to presence/absence data or methods assuming multivariate normality, which is problematic when analysing abundances. We propose Gaussian copula graphical models (GCGMs) for studying the effect of mediator species on co‐occurence patterns. GCGMs are a flexible type of graphical model which naturally accommodates all data types, for example binary (presence/absence), counts, as well as ordinal data and biomass, in a unified framework. Simulations demonstrate that GCGMs can be applied to a much broader range of data types than the methods currently used in ecology, and perform as well as or better than existing methods in many settings. We apply GCGMs to counts of hunting spiders, in order to visualise associations between species. We also analyse abundance data of New Zealand native forest cover (on an ordinal scale) to show how GCGMs can be used analyse large and complex datasets. In these data, we were able to reproduce known species relationships as well as generate new ecological hypotheses about species associations.F.K.C.H. is supported by an ANU cross‐disciplinary research grant. D.I.W. was supported by an Australian Research Council Future Fellowship (FT120100501). G.C.P. was supported by the Australia Postgraduate Award and ARC Discovery Project scheme (DP180103543). A.T.M. is supported by an Australia Research Council Discovery Grant (DP180100836). F.J.T. is supported from the Marsden Fast‐Start Fund and the Royal Society of New Zealand

Putting plant resistance traits on the map: a test of the idea that plants are better defended at lower latitudes

It has long been believed that plant species from the tropics have higher levels of traits associated with resistance to herbivores than do species from higher latitudes. A meta-analysis recently showed that the published literature does not support this theory. However, the idea has never been tested using data gathered with consistent methods from a wide range of latitudes. We quantified the relationship between latitude and a broad range of chemical and physical traits across 301 species from 75 sites world-wide. Six putative resistance traits, including tannins, the concentration of lipids (an indicator of oils, waxes and resins), and leaf toughness were greater in highlatitude species. Six traits, including cyanide production and the presence of spines, were unrelated to latitude. Only ash content (an indicator of inorganic substances such as calcium oxalates and phytoliths) and the properties of species with delayed greening were higher in the tropics. Our results do not support the hypothesis that tropical plants have higher levels of resistance traits than do plants from higher latitudes. If anything, plants have higher resistance toward the poles. The greater resistance traits of high-latitude species might be explained by the greater cost of losing a given amount of leaf tissue in low-productivity environments.EEA Santa CruzFil: Moles, Angela T. The University of New South Wales. School of Biological, Earth and Environmental Sciences. Evolution & Ecology Research Centre; Australia.Fil: Moles, Angela T. Victoria University of Wellington. School of Biological Sciences; Nueva ZelandiaFil: Moles, Angela T. Australian National University. Research School of Biology; Australia.Fil: Moles, Angela T. Macquarie University. Department of Biological Sciences; Australia.Fil: Wallis, Ian R. Australian National University. Research School of Biology; Australia.Fil: Foley, William J. Australian National University. Research School of Biology; Australia.Fil: Warton, David I. The University of New South Wales. School of Mathematics and Statistics and Evolution & Ecology Research Centre; Australia.Fil: Stegen, James C. University of North Carolina. Department of Biology; Estados UnidosFil: Bisigato, Alejandro J. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Nacional Patagónico; Argentina.Fil: Cella-Pizarro, Lucrecia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Nacional Patagónico; Argentina.Fil: Clark, Connie J. Woods Hole Research Center; Estados UnidosFil: Cohen, Philippe S. Stanford University. Jasper Ridge Biological Preserve; Estados UnidosFil: Cornwell, William K. University of British Columbia. Biodiversity Research Centre; Canadá.Fil: Peri, Pablo Luis. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Santa Cruz; Argentina.Fil: Peri, Pablo Luis. Universidad Nacional de la Patagonia Austral; Argentina.Fil: Peri, Pablo Luis. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina.Fil: Prior, Lynda D. University of Tasmania. School of Plant Science; Australia

Phenotypic differentiation among native, expansive and introduced populations influences invasion success

Aim: Humans influence species distributions by modifying the environment and by dispersing species beyond their natural ranges. Populations of species that have established in disjunct regions of the world may exhibit trait differentiation from native populations due to founder effects and adaptations to selection pressures in each distributional region. We compared multiple native, expansive and introduced populations of a single species across the world, considering the influence of environmental stressors and transgenerational effects. Location: United States Gulf and Atlantic coasts, United States interior, European Atlantic and Mediterranean coasts, east coast of Australia. Taxon: Baccharis halimifolia L. (eastern baccharis). Methods: We monitored seed germination, seedling emergence, survival and early growth in a common garden experiment, conducted with over 18,200 seeds from 80 populations. We also evaluated the influence of environmental stress and maternal traits on progeny performance. Results: Introduced European Atlantic populations had faster germination and early growth than native populations. However, this was not the case for the more recently naturalized European Mediterranean populations. Introduced Australian populations grew faster than native populations in non-saline environments but had lower survival in saline conditions commonly encountered in the native range. Similarly, expansive inland US populations germinated faster than coastal native populations in non-saline environments but grew and germinated more slowly in saline environments. Maternal inflorescence and plant size were positively related with seed germination and seedling survival, whereas flower abundance was positively correlated with seedling early growth and survival. However, maternal traits explained a much lower fraction of the total variation in early demographic stages of B. halimifolia than did distributional range. Main conclusions: Phenotypic differentiation could allow B. halimifolia to adapt to different biotic and abiotic selection pressures found in each distributional range, potentially contributing to its success in introduced and expansive ranges