Although astrobiology studies how life functions and evolves, ecology is still largely overlooked in astrobiology research. Here we present an argument for astroecology, a merger of ecology and astrobiology, a self-aware scientific endeavour. Ecology is rarely mentioned in influential documents like the NASA Astrobiology Strategy (2015), and terms such as ‘niche’ can end up being used in a less precise fashion. As ecology deals with sequential levels of organization, we suggest astrobiologically-relevant problems for each of these levels. Organismal ecology provides ecological niche modelling, which can aid in evaluating the probability that Earth-like life would survive in extraterrestrial environments. Population ecology provides a gamut of models on the consequences of dispersal, and if lithopanspermia can be validated as a form of space dispersal for life, then metabiospheres and similar astrobiological models could be developed to understand such complex structure and dynamics. From community ecology, the discussion of habitability should include the concept of true vacant habitats (a misnomer, perhaps better called ‘will-dwells’) and contributions from the blossoming field of microbial ecology. Understanding ecosystems by focusing on abiotic properties is also key to extrapolating from analogue environments on Earth to extraterrestrial ones. Energy sources and their distribution are relevant for ecological gradients, such as the biodiversity latitudinal gradient – would tropics be species-rich in other inhabited planets? Finally, biosphere ecology deals with integration and feedback between living and non-living systems, which can generate stabilized near-optimal planetary conditions (Gaia); but would this work for other inhabited planets? Are there ‘strong’ (like Earth) and ‘weak’ (perhaps like Mars) biospheres? We hope to show ecology can contribute relevant ideas to the interdisciplinary field of astrobiology, helping conceptualize further levels of integration. We encourage new partnerships and for astrobiologists to take ecology into account when studying the origin, evolution and distribution of life in the universe.

The extent to which weed species vary in their ability to acquire and use different forms of nitrogen (N) (inorganic and organic) has not been investigated but could have important implications for weed survival and weed–crop competition in agroecosystems. We conducted a controlled environment experiment using stable isotopes to determine the uptake and partitioning of organic and inorganic N (amino acids, ammonium, and nitrate) by seven common weed and non-weed species. All species took up inorganic and organic N, including as intact amino acids. Concentrations of 15N derived from both ammonium and amino acids in shoot tissues were higher in large crabgrass [Digitaria sanguinalis (L.) Scop.] and barnyardgrass [Echinochloa crus-galli (L.) P. Beauv] than in common lambsquarters (Chenopodium album L.), redroot pigweed (Amaranthus retroflexus L.), and sorghum-sudangrass [Sorghum bicolor (L.) Moench × Sorghum bicolor (L.) ssp. drummondii (Nees ex Steud.) de Wet & Harlan]. In contrast, the concentration of 15N derived from nitrate was higher in wild mustard (Sinapis arvensis L.) shoots than in wild oat (Avena fatua L.) shoots. Root concentration of 15N derived from ammonium was lower in sorghum-sudangrass compared with other species, except for A. retroflexus and A. fatua, while root concentration of 15N derived from nitrate was lower in A. retroflexus compared with other species, except for C. album and S. arvensis. Discriminant analysis classified species based on their uptake and partitioning of all three labeled N forms. These results suggest that common agricultural weeds can access and use organic N and differentially take up inorganic N forms. Additional research is needed to determine whether species-specific differences in organic and inorganic N uptake influence the intensity of competition for soil N.

Snakes are sensitive to both environmental and climate gradients. To design conservation plans, a scientific understanding of snake habitats in light of environmental and climatic variables is an essential prerequisite. For venomous snakes, denoting favourable habitats should also be relevant for snakebite management. We have considered 18 spatial variables to portray the range of terrestrial venomous snake distribution in Bangladesh. Our results indicate that the distribution of 29 studied venomous snakes in this country is primarily driven by climatic and environmental variables. We found that especially low elevation and flood risk constrain the distribution of those terrestrial snakes, i.e. regular floods in central Bangladesh push venomous snakes towards the edges of the country. Moreover, none of these species occupies the whole of its anticipated climatically favourable area. Projections into the future indicated that 11 studied species, Amphiesma platyceps, Boiga siamensis, Chrysopelea ornata, Pseudoxenodon macrops, Rhabdophis himalayanus, Rhabdophis subminiatus, Bungarus lividus, Ophiophagus hannah, Daboia russelii, Ovophis monticola and Trimeresurus popeiorum will lose their entire climatically suitable area within the country. Therefore, we suggest establishing more protected areas in the hilly ecosystems in the eastern part and in the mangrove forests in the south-western corner of Bangladesh to mitigate future extinction risks, such as climate change, sea-level rise and increase in flood severity. Conserving village forests and croplands, which are subject to rapid change, will also need to be addressed equally, as these are inhabited by almost one-third of the studied species. The occurrence of the cobras and kraits in village forests and cropland dominant habitats demands more attention to minimise snakebite related mortality and morbidity.

The Hawaiian archipelago was formerly home to one of the most species-rich land snail faunas (> 752 species), with levels of endemism > 99%. Many native Hawaiian land snail species are now extinct, and the remaining fauna is vulnerable. Unfortunately, lack of information on critical habitat requirements for Hawaiian land snails limits the development of effective conservation strategies. The purpose of this study was to examine the plant host preferences of native arboreal land snails in Puʻu Kukui Watershed, West Maui, Hawaiʻi, and compare these patterns to those from similar studies on the islands of Oʻahu and Hawaiʻi. Concordant with studies on other islands, we found that four species from three diverse families of snails in Puʻu Kukui Watershed had preferences for a few species of understorey plants. These were not the most abundant canopy or mid canopy species, indicating that forests without key understorey plants may not support the few remaining lineages of native snails. Preference for Broussaisia arguta among various island endemic snails across all studies indicates that this species is important for restoration to improve snail habitat. As studies examining host plant preferences are often incongruent with studies examining snail feeding, we suggest that we are in the infancy of defining what constitutes critical habitat for most Hawaiian arboreal snails. However, our results indicate that preserving diverse native plant assemblages, particularly understorey plant species, which facilitate key interactions, is critical to the goal of conserving the remaining threatened snail fauna.

Parasites have the power to impose significant regulatory pressures on host populations, making evolutionary patterns of host switching by parasites salient to a range of contemporary ecological issues. However, relatively little is known about the colonization of new hosts by parasitic, commensal and mutualistic eukaryotes of metazoans. As ubiquitous symbionts of coelomate animals, Blastocystis spp. represent excellent candidate organisms for the study of evolutionary patterns of host switching by protists. Here, we apply a big-data phylogenetic approach using archival sequence data to assess the relative roles of several host-associated traits in shaping the evolutionary history of the Blastocystis species-complex within an ecological framework. Patterns of host usage were principally determined by geographic location and shared environments of hosts, suggesting that weight of exposure (i.e. propagule pressure) represents the primary force for colonization of new hosts within the Blastocystis species-complex. While Blastocystis lineages showed a propensity to recolonize the same host taxa, these taxa were often evolutionarily unrelated, suggesting that historical contingency and retention of previous adaptions by the parasite were more important to host switching than host phylogeny. Ultimately, our findings highlight the ability of ecological theory (i.e. ‘ecological fitting’) to explain host switching and host specificity within the Blastocystis species-complex.

Common practices for invasive species control and management include physical, chemical, and biological approaches. The first two approaches have clear limitations and may lead to unintended (negative) consequences, unless carefully planned and implemented. For example, physical removal rarely completely eradicates the targeted invasive species and can cause disturbances that facilitate new invasions by nonnative species from nearby habitats. Chemical treatments can harm native, and especially rare, species through unanticipated side effects. Biological methods may be classified as biocontrol and the ecological approach. Similar to physical and chemical methods, biocontrol also has limitations and sometimes leads to unintended consequences. Therefore, a relatively safer and more practical choice may be the ecological approach, which has two major components: (1) restoration of native species and (2) biomass manipulation of the restored community, such as selective grazing or prescribed burning (to achieve and maintain viable population sizes). Restoration requires well-planned and implemented planting designs that consider alpha-, beta-, and gamma-diversity and the abundance of native and invasive component species at local, landscape, and regional levels. Given the extensive destruction or degradation of natural habitats around the world, restoration could be most effective for enhancing ecosystem resilience and resistance to biotic invasions. At the same time, ecosystems in human-dominated landscapes, especially those newly restored, require close monitoring and careful intervention (e.g., through biomass manipulation), especially when successional trajectories are not moving as intended. Biomass management frequently uses prescribed burning, grazing, harvesting, and thinning to maintain overall ecosystem health and sustainability. Thus, the resulting optimal, balanced, and relatively stable ecological conditions could more effectively limit the spread and establishment of invasive species. Here we review the literature (especially within the last decade) on ecological approaches that involve biodiversity, biomass, and productivity, three key community/ecosystem variables that reciprocally influence one another. We focus on the common and most feasible ecological practices that can aid in resisting new invasions and/or suppressing the dominance of existing invasive species. We contend that, because of the strong influences from neighboring areas (i.e., as exotic species pools), local restoration and management efforts in the future need to consider the regional context and projected climate changes.

‘Where is everybody?’ remarked Enrico Fermi, leading to the famous, and as yet unanswered ‘Fermi's Paradox’ as this remark has come to be known. While there are a number of possible solutions that vary from the distances are too great; the cost prohibitive or civilizations naturally decline or eliminate themselves before interstellar travel becomes possible, none of these are intellectually satisfying. More recently, Manasvi Lingam and Abraham Loeb suggested that for those planets orbiting red dwarfs, atmospheric erosion may be a partial solution to this ‘paradox’. Such planets may experience greater exposure to stellar winds and/or extreme ultraviolet and X-radiation (henceforth abbreviated to EUV). While this proposition is undeniably reasonable, it is likely incomplete. A more fundamental limitation on the development of biological complexity is imposed by plate tectonics: time. On asynchronously rotating planets, the habitable area for any species is defined by latitudinal bands that encompass the globe. Conversely, on synchronous rotators, the comparative habitable area is limited to broadly concentric regions surrounding the Sub-Stellar Point (SSP). Given that terrestrial mammals and from them humans evolved in tropical or subtropical regions, the geographical area subtended with these conditions is likely to be smaller and transected by suitable landmasses for shorter periods than on asynchronously rotating worlds. Habitable subaerial regions for individual species are therefore more limited in area. This leads to a greater limitation on the temporal intervals over which biological complexity can evolve.

The gastropod shell influences important aspects of the hermit crab's life; however, the shells are commonly a limited resource. Therefore, different hermit crab species that coexist in intertidal areas are commonly involved in intraspecific and interspecific competition for shells. We assess if differences in shell preference, exploitation ability, or competition by interference can explain the partitioning of shells between the coexisting species Calcinus californiensis and Clibanarius albidigitus. Clibanarius preferred shells of Nerita funiculata among the six gastropod shells tested, while Calcinus did not establish a hierarchy in shell preference. Therefore, the preference for gastropod shell species does not seem to diminish the competition for shells in the wild. Clibanarius identified and attended to chemical cues signalling potential sites of available shells (chemical cues of dead gastropods); Calcinus did not respond to these cues (competition by exploitation). However, Calcinus was more successful in obtaining a new shell by interspecific shell fighting than Clibanarius. Consequently, the use of better quality shells (intact shells) by Calcinus in the wild can be explained by its greater fighting ability compared with Clibanarius. The bias in shell distributions through dominance by shell fighting, more than by exploitation ability, has also been suggested for other hermit crab species of these genera.

Hutchinson's (1957) definition of an ecological niche as a multidimensional hypervolume determined by a number of physical and biotic variables is adopted. The number of niche dimensions is very great, but as a working hypothesis it is assumed that a few are sufficient to characterize the niche of a parasite species to a high degree of accuracy. They are host species, microhabitat(s), macrohabitat(s), geographical range, sex and age of host, season, food and hyperparasites. Methods to measure niche width, in particular specificity indices, are discussed, and some examples of niche restriction are described. Proximate and ultimate causes of niche restriction are discussed, mainly using marine parasites as examples. Among proximate causes of one niche dimension, host specificity, are ecological factors restricting exposure to infection to certain host species; host-specific chemical factors that induce hatching, direct infective stages to a host and bring about settlement of a parasite; factors that lead to mortality in or on the wrong host; morphological adaptations that guarantee survival in or on the ‘correct’ host; and availability of suitable hosts. Many factors are likely to be responsible for microhabitat specificity, but have been little studied, except for some physiological and morphological adaptations to particular microhabitats. Macrohabitats and geographical range may be determined by the distribution of intermediate hosts and certain food items, and by a variety of chemical and physical factors. Hosts of different sexes may differ in feeding habits and the composition of the skin, and thus acquire parasites differentially. Hosts of different age may be differentially infected due to accumulation of parasites with age, loss of parasites due to developing resistance (or immunity), and different size and feeding habits. Among ultimate causes of niche restriction and segregation are avoidance of competition, predation and hyperparasites; facilitation of mating; reinforcement of reproductive barriers; and adaptations to environmental complexity. Few studies permit a decision on which factor or factors are responsible in particular cases. Interspecific competition may play a greater role in helminth communities of some host groups than of others, but it seems that, overall, its role has been exaggerated at least for marine parasites. Some ‘classical’ examples of microhabitat segregation explained by interspecific competition can also be explained by reinforcement of reproductive barriers. There is evidence for the importance of facilitation of mating in microhabitat restriction, and the availability of many vacant niches indicates that competition, overall, is not of great importance.

Cover crops represent a potentially important biological filter during weed community assembly in agroecosystems. This filtering could be considered directional if different cover-crop species result in weed communities with predictably different species composition. We examined the following four questions related to the potential filtering effects of cover crops in a field experiment involving five cover crops grown in monoculture and mixture: (1) Do cover crops differ in their effect on weed community composition? (2) Is competition more intense between cover crops and weeds that are in the same family or functional group? (3) Is competition more intense across weed functional types in a cover-crop mixture compared with cover crops grown in monocultures? (4) Within a cover-crop mixture, is a higher seeding rate associated with more effective biotic filtering of the weed community? We found some evidence that cover crops differentially filtered weed communities and that at least some of these filtering effects were due to differential biomass production across cover-crop species. Monocultures of buckwheat and sorghum–sudangrass reduced the number of weed species relative to the no-cover-crop control by an average of 36 and 59% (buckwheat) and 25 and 40% (sorghum–sudangrass) in 2011 and 2012, respectively. We found little evidence that competition intensity was dependent upon the family or functional classification of the cover crop or weeds, or that cover-crop mixtures were stronger assembly filters than the most effective monocultures. Although our results do not suggest that annual cover crops exert strong directional filtering during weed community assembly, our methodological framework for detecting such effects could be applied to similar future studies that incorporate a greater number of cover-crop species and are conducted under a greater range of cover-cropping conditions.

Two core questions in plant community ecology are to what extent the distributions of species are structured by local environmental conditions, and whether taxa differ in this regard. We compared the distributions of trees, Melastomataceae and ferns on soil and topographic gradients in a Costa Rican lowland rain forest (trees and ferns 983 plots, Melastomataceae 277 plots). To test whether these plant groups differed in the prevalence or type of habitat specialization, we calculated species’ environmental optima and tolerances on each gradient. Habitat specialization was defined as a significantly biased optimum, or a narrow tolerance, relative to values obtained under spatially restricted randomizations of species occurrences. Within plant groups, we also asked whether the dispersion of species optima differed from random expectation on each gradient. Fern optima were over-dispersed on multiple gradients, implying considerable interspecific habitat partitioning, and tree optima were over-dispersed in relation to topographic position. Habitat specialization was more prevalent in the two predominantly understorey groups than in trees (75% of Melastomataceae species, 81–87% of ferns, 57–58% of trees). Species optima of Melastomataceae and ferns also tended towards lower landscape positions than did those of trees, perhaps reflecting a higher proportion of drought-sensitive species in these two groups.