Description: A comprehensive dataset of non-native species (NNS) was assembled by combining the SInAS database of alien species occurrences (Seebens, 2021) with several other publicly available databases and NNS lists to examine NNS diversity globally (Bailey et al., 2020; Campbell et al., 2016; Carlton & Eldredge, 2009; Casties et al., 2016; Eldredge & Carlton, 2015; Hewitt et al., 2002, 2004; Lambert, 2002; Meyer, 2000; NEMESIS, 2017, 2020; Paulay et al., 2002; Richardson et al., 2020; Schwindt et al., 2020; Sturtevant et al., 2019; U.S. Geological Survey, 2017; Wonham & Carlton, 2005) to examine NNS diversity globally. The SInAS_AlienSpeciesDB_2.4.1 file was used as the base file for our dataset. Species without assignment of invaded country/region were removed from the dataset. Then, species assigned only as CASUAL and ABSENT in the columns degreeOfEstablishment (N) and occurrenceStatus (L), respectively, were also removed due to their undetermined non-native establishment status in those particular regions (Groom et al., 2019). Following, species from other publicly available databases and NNS lists that had not been listed for particular region/s in the SInAS database were added to the file. The species that were both native and NNS within a continent were retained in the dataset. Accordingly, the dataset consisted 36 822 species established outside of their native regions, out of which 36 326 came from Seebens (2021) and 496 species from other databases and NNS lists. Binominal scientific names, phylum, class, and family levels were assigned to each species based on the SInAS_AlienSpeciesDB_2.4.1_FullTaxaList file that was originally determined following Global Biodiversity Information Facility (GBIF). When a species was not automatically assigned to binominal scientific name and/or taxonomic level, an additional manual search of GBIF, World Register of Marine Species (WoRMS) and a general internet search engine was conducted in June and July 2022, and September 2023. Also, to examine NNS diversity among different habitats (i.e., terrestrial, freshwater, and marine), we assigned one or more habitats for each species based on the Step2_StandardTerms_GRIIS file; habitat data in the Step2_StandardTerms_GRIIS file originated from the Global Register of Introduced and Invasive Species (GRIIS). Again, if habitat(s) was(were) not automatically assigned to a species, an additional manual search of WoRMS and a general internet search engine was conducted from July to September 2022. We emphasize that due to the great number of species in our dataset and changing information availability over time, there is a possibility that we did not list all potential habitats for all species. Brackish habitats were defined as marine based on the Venice System (1958). Regions were assigned based on the geographic continental definitions (i.e., North America, South America, Europe, Africa, Asia, and Australia), with Pacific islands as a separate region due to their unclear/undefined continental affiliations (National Geographic Society, 2022). Finally, global estimated biodiversity (i.e., numbers of species per taxonomic group) of each particular phylum, class, and family was obtained from the GBIF in October 2022 (GBIF, 2022).

Description: Invasive alien species (IAS) cause myriad negative impacts, such as ecosystem disruption, human, animal and plant health issues, economic damage and species extinctions. There are many sources of emerging and future IAS, such as the poorly regulated international pet trade. However, we lack methodologies to predict the likely ecological impacts and invasion risks of such IAS which have little or no informative invasion history. This study develops the Relative Impact Potential (RIP) metric, a new measure of ecological impact that incorporates per capita functional responses (FRs) and proxies for numerical responses (NRs) associated with emerging invaders. Further, as propagule pressure is a determinant of invasion risk, we combine the new measure of Pet Propagule Pressure (PPP) with RIP to arrive at a second novel metric, Relative Invasion Risk (RIR). We present methods to calculate these metrics and to display the outputs on intuitive bi- and triplots. We apply RIP/RIR to assess the potential ecological impacts and invasion risks of four commonly traded pet turtles that represent emerging IAS: Trachemys scripta scripta, the yellow-bellied slider; T. s. troostii, the Cumberland slider; Sternotherus odoratus, the common musk turtle; and Kinosternon subrubrum, the Eastern mud turtle. The high maximum feeding rate and high attack rate of T. s. scripta, combined with its numerical response proxies of lifespan and fecundity, gave it the highest impact potential. It was also the second most readily available according to our UK surveys, indicating a high invasion risk. Despite having the lowest maximum feeding rate and attack rate, S. odoratus has a high invasion risk due to high availability and we highlight this species as requiring monitoring. The RIP/RIR metrics offer two universally applicable methods to assess potential impacts and risks associated with emerging and future invaders in the pet trade and other sources of future IAS. These metrics highlight T. s. scripta as having high impact and invasion risk, corroborating its position on the EU list of 49 IAS of Union Concern. This suggests our methodology and metrics have great potential to direct future IAS policy decisions and management. This, however, relies on collation and generation of new data on alien species functional responses, numerical responses and their proxies, and imaginative measures of propagule pressure.

Description: Environmental concerns and insecticide resistance threaten the sustained efficacy of mosquito control approaches which remain reliant on synthetic chemicals. Plant-based extracts may be an environmentally sustainable and effective alternative to contemporary mosquito control approaches; however, the efficacies of many possible plant-based extracts remain untested. The present study examines the effects of extracts from three floating and three submerged aquatic plants on larval mosquito Culex pipiens mortality, and development to pupal and adult stages. Physical impacts of floating plant species on mosquito mortality and development are also examined. Extracts of Lagarosiphon major and Lemna minuta were toxic, causing significantly increased mosquito mortality compared to plant-free controls. Effects of Azolla filiculoides, Crassula helmsii, Elodea canadensis and Lemna minor were statistically unclear, yet in some cases tended to increase pupal and larval numbers at high extract concentrations. Surface coverage of all floating Lemna species drove significant mosquito mortality through mechanical processes which likely impeded surface respiration by larval mosquitoes. In particular, high-density mats of L. minuta consistently caused total larval mortality. The present study thus suggests that targeted use of specific aquatic plants could assist in mosquito control protocols. However, as the chemical composition of botanic material will differ across spatial and temporal gradients, even for a singular species, localised assessment of the efficacy of plant-based extracts from within areas experiencing problematic mosquito control is required. The application of aquatic plants that are both toxic to larvae and are effective physical control agents presents an economic and effective method of mosquito control.