Walter Jacob Eyerdam

Maqui ( Aristotelia chilensis ) is a small tree endemic to Patagonia. It is currently being actively domesticated for its edible berries, which have high polyphenol content and anti-oxidant capability. However, little is known about its population structure and evolutionary history, information which is useful for the design of effective conservation and domestication strategies. Based on information from other species, we hypothesize that genetic diversity in maqui is higher in northern population and decrease to the South, associated with past migration patterns and as a result has well-structured populations. To explore the genetic diversity of 14 populations (183 samples) of this species, that represent the geographic distribution of the species in Chile we used 13 polymorphic microsatellite markers. Clusters based on Bayesian genetic and spatial structure analyses were used to reconstruct patterns of phylogeographic and demographic history. We found that maqui populations are well-structured, with a substantial reduction of genetic diversity from north to south. The lowest diversity was found in areas that were once covered by ice during the quaternary glaciation. In conclusion, three main genetic groups were revealed by Structure analysis, and genetic diversity reduction from its northern limit in central Chile to the Patagonian region was found, suggesting that an active recolonization process took place during the last few millennia following the last glacial period. These results will help to define accessions from different regions and contribute to support conservation and domestication initiatives.

Understanding how, and from where, invasive species were introduced is critical for revealing the invasive mechanism, explaining the invasion success, and providing crucial insights for effective management. Here, we combined a phylogeographic approach with ecological niche modeling comparisons to elucidate the introduction mode and source of Nicotiana glauca , a native South American species that is now invasive worldwide. We tested three different scenarios based on the invasion source—random native, restricted native, and bridgehead invasive—considering genetic diversity and climatic niche comparisons among native and invaded areas. We found three genetic lineages geographically and climatically differentiated within the native range. Only one of these genetic groups contained the invasive haplotypes, but showed no climatic niche overlap with any invaded area. Conversely, one invaded area located in western South America, with more genetic diversity than other invaded areas but less than the native range, showed climatic niche overlap with almost all other invaded areas worldwide. These findings indicate that N. glauca first likely invaded the southernmost areas beyond its native range, forming a bridgehead invasive source, from which the species subsequently invaded other regions around the world. Invasiveness would have been fostered by changes in the environmental preferences of the species in the bridgehead area, towards drier, colder and less seasonal climates, becoming the actual source of invasion to areas climatically similar throughout the world. The fine scale resolution analyses combining genetic and climatic approaches within the native range were essential to illuminating the introduction scenario of this invasive species.

Epiarenic (sand-growing) Tillandsia vegetation in the hyperarid and arid region of the Chilean-Peruvian Atacama Desert represents an extreme case of adaptation in plant species-poor ecosystems. The involved species exist at the limit of terrestrial life and form mono/oligo-specific and very characteristic structures within the landscape. Covering thousands of square kilometers they represent the major carbon sink in the hyperarid Atacama core. The various Tillandsia species and respective vegetation may have evolved and adapted independently to this extreme environment. The most abundant vicariant diploid species are T. landbeckii in Chile and T. purpurea in Peru. Spatio-temporally varying distribution range overlaps may have caused potentially adaptive gene flow between different species leading to present day gene pools. Using species distribution modelling we explored the idea that from Last Glacial Maximum (LGM) onwards both species shifted their distribution ranges, which resulted in the formation of varying suture zones from Peru towards northern Chile. We further explored genetic data from a Tillandsia loma vegetation in Southern Peru with three sympatrically growing species exemplifying inter-species gene flow crossing even ploidy levels. This mechanism highlights a strategy to evolve and adapt more rapidly to environmental changes in extreme arid and hyperarid habitats and provides an opportunity for Tillandsia populations to efficiently conserve new genotypes via subsequent clonal propagation.

Predicting the likelihood that non-native species will be introduced into new areas remains one of conservation’s greatest challenges and, consequently, it is necessary to adopt adequate management measures to mitigate the effects of future biological invasions. At present, not much information is available on the areas in which non-native aquatic plant species could establish themselves in the Iberian Peninsula. Species distribution models were used to predict the potential invasion risk of (1) non-native aquatic plant species already established in the peninsula (32 species) and (2) those with the potential to invade the peninsula (40 species). The results revealed that the Iberian Peninsula contains a number of areas capable of hosting non-native aquatic plant species. Areas under anthropogenic pressure are at the greatest risk of invasion, and the variable most related to invasion risk is temperature. The results of this work were used to create the Invasion Risk Atlas for Alien Aquatic Plants in the Iberian Peninsula, a novel online resource that provides information about the potential distribution of non-native aquatic plant species. The atlas and this article are intended to serve as reference tools for the development of public policies, management regimes, and control strategies aimed at the prevention, mitigation, and eradication of non-native aquatic plant species.

Risk analysis plays a crucial role in regulating and managing alien and invasive species but can be time-consuming and costly. Alternatively, combining invasion and impact history with species distribution models offers a cost-effective and time-efficient approach to assess invasion risk and identify species for which a comprehensive risk analysis should take precedence. We conducted such an assessment for six traded alien fern species, determining their invasion risk in countries where they are traded. Four of the species (Dicksonia antarctica, Dryopteris erythrosora, Lygodium japonicum, and Phlebodium aureum) showed limited global distributions, while Adiantum raddianum and Sphaeropteris cooperi had broader distributions. A. raddianum, however, was the only species found to pose a high invasion risk in two known trade countries – the USA and Australia – and requires a complete risk analysis to determine the appropriate regulatory responses. Dicksonia antarctica, Phlebodium aureum (for New Zealand), and Dryopteris erythrosora (for the USA) posed a medium risk of invasion due to the lack of evidence of impacts, and a complete risk analysis is thus deemed less crucial for these species in these countries. For other species, suitable environments were not predicted in the countries where they are traded, thus the risk of invasion is low, and a complete risk analysis is not required. For species in countries where suitable environments are predicted but no trade information or presence data are available, risk assessments are recommended to better determine the risk posed. Despite the relatively limited potential global distribution of the studied ferns relative to other major plant invaders (e.g., Pinus spp. and Acacia spp.), their history of invasion, documented impacts in pristine environments, and high propagule pressure from trade warrants concern, possibly necessitating legislative and regulatory measures in environmentally suitable regions.

Climate suitability analyses based on ecological niche modeling provide a powerful tool for biological control practitioners to assess the likelihood of establishment of different candidate agents prior to their introduction in the field. These same analyses could also be performed to understand why some agents establish more easily than others. The release of three strains of Aphalara itadori (Shinji) (Hemiptera: Pysllidae), each from a different source locality in Japan, for the biological control of invasive knotweed species, Reynoutria spp. Houtt. (Caryophyllales: Polygonaceae), provides an important opportunity to compare the utility of climate suitability analyses for identifying potential climate‐based limitations for successful biological control introductions. Here, we predict climate suitability envelopes for three target species of knotweed in Europe and two target species of knotweed in North America and compare these suitability estimates for each of these species to the source localities of each A. itadori strain. We find that source locality of one strain, the Kyushu strain, has little‐to‐no suitability compared to other locations in Japan based on knotweed records from Europe, supporting an earlier study based on North American Japanese knotweed records. The source locality of a second strain, the Murakami strain, was predicted to have medium‐to‐high suitability based on records of knotweeds from North America. In contrast, European records of Reynoutria × bohemica Chrtek & Chrtková and Reynoutria sachalinensis (F. Schmidt) Nakai predicted no suitability for this locality compared to other locations in Japan, while European records for Reynoutria japonica Houtt. predicted low suitability. The source locality of the final strain, the Hokkaido strain, was predicted as having medium‐to‐high suitability based on knotweed records of all examined species from both North America and Europe.

The physiology of insects is directly influenced by environmental temperature, and thermal tolerance is therefore intrinsically linked to their thermal niche and distribution. Understanding the mechanisms that limit insect thermal tolerance is crucial to predicting biogeography and range shifts. Recent studies on locusts and flies suggest that the critical thermal minimum (CTmin) follows from a loss of CNS function via a spreading depolarization. We hypothesized that other insect taxa share this phenomenon. Here we investigate whether spreading depolarization events occur in butterflies exposed to cold. Supporting our hypothesis, we find that exposure to stressful cold induced spreading depolarization in all 12 species tested. This reinforces the idea that spreading depolarization is a common mechanism underlying the insect CTmin. Furthermore, our results highlight how CNS function is tuned to match species’ environments. Further research into the physiology underlying spreading depolarization will likely elucidate key mechanisms determining insect thermal tolerance and ecology.

Premise: Cacti are characteristic elements of the Neotropical flora and of major interest for biogeographic, evolutionary, and ecological studies. Here we test global biogeographic boundaries for Neotropical Cactaceae using specimen‐based occurrences coupled with data from visual observations, as a means to tackle the known collection biases in the family.MethodsSpecies richness and record density were assessed for preserved specimens and human observations and a bioregional scheme tailored to Cactaceae was produced using the interactive web application Infomap Bioregions based on data from 261,272 point records cleaned through automated and manual steps.Key ResultsWe find that areas in Mexico and southwestern USA, Eastern Brazil and along the Andean region have the greatest density of records and the highest species richness. Human observations complement information from preserved specimens substantially, especially along the Andes. We propose 24 cacti bioregions, among which the most species‐rich are: northern Mexico/southwestern USA, central Mexico, southern central Mexico, Central America, Mexican Pacific coast, central and southern Andes, northwestern Mexico/extreme southwestern USA, southwestern Bolivia, northeastern Brazil, Mexico/Baja California.ConclusionsThe bioregionalization proposed shows biogeographical boundaries specific to cacti, and can thereby aid further evolutionary, biogeographic, and ecological studies by providing a validated framework for further analyses. This classification builds upon, and is distinctive from, other expert‐derived regionalization schemes for other taxa. Our results showcase how observation data, including citizen‐science records, can complement traditional specimen‐based data for biogeographic research, particularly for taxa with specific specimen collection and preservation challenges and those that are threatened or internationally protected.This article is protected by copyright. All rights reserved.

Endemic to the Neotropics, Monnina is the second largest genus of Polygalaceae, yet little is known about its phylogenetic history, biogeography, and morphological character evolution. To address these knowledge gaps, we conducted Bayesian and maximum likelihood (ML) analyses of nuclear ITS and plastid trnL–F regions to test the monophyly of Monnina s.l. We used this phylogenetic framework to (i) infer divergence time estimates of lineages within the genus and reconstruct their historical biogeography; (ii) reconstruct the evolution of morphological characters of putative ecological and evolutionary importance in Monnina; and (iii) test for correlations between our phylogenetic hypothesis and environmental data. Our results reveal that Monnina is monophyletic with an indehiscent, 1–2-seeded fruit as a synapomorphy for the genus. We identify six clades within Monnina based on our combined phylogenetic results: Clades A, B, and D are primarily distributed in southern and eastern South America, Clades C and E are primarily Central Andean, and Clade F is chiefly distributed in the Northern Andes and Central America. The ancestor of the Monnina stem lineage dispersed from Australia/Africa to South America during the late Eocene to early Oligocene. The divergences of major lineages within the genus began in the early Miocene. We inferred the most recent common ancestor of Monnina to be an herbaceous plant with one-seeded samaroid fruits. The origins of fleshy fruits and shrubby habits are phylogenetically correlated within Monnina, and their concerted convergent evolution may have promoted increased net diversification rates in the two most species-rich subclades of the genus.

(no abstract available)