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580 results for “Eradication”

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edi56/100

Eradication via destratification: whole-lake mixing to selectively remove rainbow smelt, a cold-water invasive species.

Rainbow smelt (Osmerus mordax) are an invasive species associated with several negative changes to lake ecosystems in northern Wisconsin. We combined empirically based bioenergetics models with empirically based hydrodynamic models to assess lake destratification as a potential rainbow smelt eradication method. The dataset reported here is the otolith data from 20 age 1plus individuals.

openCC (other)Dec 2022View details →
edi44/100

Invasive rat eradication effects on seedling counts on Palmyra Atoll, 2004-2016

In order to investigate the impacts of rat eradication on plant communities on the Palmyra Atoll, Line Islands, Central Pacific Ocean ecosystem, a study was conducted surveying the native and non-native tree and palm seedling abundance before and after an eradication event which took place in June 2011. The common plant species examined were P. grandis and C. nucifera, while the less-common species were B. asiatica, C. subcordata, H. sonora, G. speciosa, N. oppositifolium, and C. inophyllum. Data for common plant species were collected in 2007, 2011, 2012, 2014, and 2016, and for less-common species in 2004, 2011, 2012, 2014, and 2016. Data were collected via survey methods; 55 transect sites were examined for the common species, and between 49 to 55 sites were examined depending on the year, for the less-common species.

openCC (other)Jun 2018View details →
zenodo40/100

Figure 12 in Taxonomy of Micronesian monitors (Reptilia: Squamata: Varanus): endemic status of new species argues for caution in pursuing eradication plans

Figure 12. Adult Varanus bennetti sp. nov., Losiep Island, Federated States of Micronesia (photo by James Reardon).

opencc-by-4.0May 2020View details →
zenodo40/100

Figure 5 in Taxonomy of Micronesian monitors (Reptilia: Squamata: Varanus): endemic status of new species argues for caution in pursuing eradication plans

Figure 5. (a) Dorsolateral and ventral aspects of the neotype (USNM 576258) of Varanus tsukamotoi. (b) Lateral profile of the head of the neotype (USNM 576258) of Varanus tsukamotoi.

opencc-by-4.0May 2020View details →
zenodo40/100

Figure 8 in Taxonomy of Micronesian monitors (Reptilia: Squamata: Varanus): endemic status of new species argues for caution in pursuing eradication plans

Figure 8. (a) Dorsolateral and ventral aspects of the holotype (USNM 507504) of Varanus bennetti sp. nov. (b) Lateral profile of the head of the holotype (USNM 507504) of Varanus bennetti sp. nov.

opencc-by-4.0May 2020View details →
zenodo40/100

Figure 11 in Taxonomy of Micronesian monitors (Reptilia: Squamata: Varanus): endemic status of new species argues for caution in pursuing eradication plans

Figure 11. Subadult Varanus bennetti sp. nov., Losiep Island, Federated States of Micronesia (photo by James Reardon).

opencc-by-4.0May 2020View details →
zenodo40/100

Figure 1 in Taxonomy of Micronesian monitors (Reptilia: Squamata: Varanus): endemic status of new species argues for caution in pursuing eradication plans

Figure 1. Map of the Pacific region showing the distribution of Varanus tsukamotoi (white dots), V. bennetti sp. nov. (red dots), V. lirungensis (yellow dot) and V. rainerguentheri (green dot).

opencc-by-4.0May 2020View details →
zenodo40/100

Figure 2 in Taxonomy of Micronesian monitors (Reptilia: Squamata: Varanus): endemic status of new species argues for caution in pursuing eradication plans

Figure 2. (a) Linear discriminant function analysis of scalational characters for V. bennetti sp. nov., V. lirungensis, V. rainerguentheri and V. tsukamotoi showing non-overlapping multivariate morpho-spaces for all species except V. bennetti sp. nov. and V. rainerguentheri. (b) Box-plot of relative tail length (proportion index 1) for examined individuals of V. bennetti sp. nov., V. lirungensis, V. rainerguentheri and V. tsukamotoi showing the exceptionally long tail of V. bennetti sp. nov.

opencc-by-4.0May 2020View details →
zenodo40/100

Figure 3 in Taxonomy of Micronesian monitors (Reptilia: Squamata: Varanus): endemic status of new species argues for caution in pursuing eradication plans

Figure 3. Strict consensus of the nine most-parsimonious trees resulting from the TNT analysis. Jackknife resampling values greater than 50% are shown above, and the numbers of synapomorphies shared by each clade are shown below the nodes in parentheses. Branch lengths represent the number of optimized character-state changes.

opencc-by-4.0May 2020View details →
zenodo40/100

A call to eradicate non-inclusive terms from science

<p>Source code and data associated with a commentary (Khan, 2021; eLife) that shows an increase of non-inclusive terms with racial connotations used in life-science literature and calls for action to make science inclusive for all.</p>

openother-openJan 2021View details →
dryad40/100

Gene drives for vertebrate pest control: realistic spatial modelling of eradication probabilities and times for island mouse populations

<p>Invasive alien species continue to threaten global biodiversity. CRISPR-based gene drives, which can theoretically spread through populations despite imparting a fitness cost, could be used to suppress or eradicate pest populations. We develop an individual-based, spatially explicit, stochastic model to simulate the ability of CRISPR-based homing and X-chromosome shredding drives to eradicate populations of invasive mice (Mus muculus) from islands. Using the model, we explore the interactive effect of the efficiency of the drive constructs and the spatial ecology of the target population on the outcome of a gene-drive release. We also consider the impact of polyandrous mating and sperm competition, which could compromise the efficacy of some gene-drive strategies. Our results show that both drive strategies could be used to eradicate large populations of mice. Whereas parameters related to drive efficiency and demography strongly influence drive performance, we find that sperm competition following polyandrous mating is unlikely to impact the outcome of an eradication effort substantially. Assumptions regarding the spatial ecology of mice influenced the probability of and time required for eradication, with short-range dispersal capabilities and limited mate-search areas producing `chase' dynamics across the island characterised by cycles of local extinction and recolonization by mice. We also show that highly efficient drives are not always optimal, when dispersal capabilities are low, rapid local population supression around the introduction sites can cause loss of the gene drive before it can spread to the entire island. We conclude that, although the design of efficient gene drives is undoubtedly critical, accurate data on the spatial ecology of target species is critical for predicting the result of a gene-drive release.</p>

opencc-zeroMay 2022View details →
zenodo40/100

Figure 7 in From Eradication to Containment: Invasion of French Polynesia by Bactrocera dorsalis (Hendel) (Diptera: Tephritidae) and Releases of Two Natural Enemies: A 17-Year Case Study

Figure 7. Annual percentage of individual guavas infested with fruit flies on Tahiti. Number of fruits incubated individually each year were: 172 in 2002, 348 in 2003, 539 in 2004, 607 in 2005, 98 in 2006, 4 in 2007, 237 in 2008, and 807 in 2009.

opencc-by-4.0Dec 2013View details →
zenodo40/100

Figure 6a–d in From Eradication to Containment: Invasion of French Polynesia by Bactrocera dorsalis (Hendel) (Diptera: Tephritidae) and Releases of Two Natural Enemies: A 17-Year Case Study

Figure 6a–d. Quarterly emergences on Tahiti of B. dorsalis and F. arisanus per kg fruit for guava (a), Tahitian chestnut (b), tropical almond (c), and mango (d). See under

opencc-by-4.0Dec 2013View details →
zenodo40/100

Figure 4 in From Eradication to Containment: Invasion of French Polynesia by Bactrocera dorsalis (Hendel) (Diptera: Tephritidae) and Releases of Two Natural Enemies: A 17-Year Case Study

Figure 4. Annual proportion of fruit fly (B. dorsalis, B. tryoni, B. kirki) and parasitoid (F. arisanus, D. longicaudata) emergences in guava, tropical almond, Tahitian chestnut, and mango fruits for selected years.

opencc-by-4.0Dec 2013View details →
zenodo40/100

Figure 3a, b in From Eradication to Containment: Invasion of French Polynesia by Bactrocera dorsalis (Hendel) (Diptera: Tephritidae) and Releases of Two Natural Enemies: A 17-Year Case Study

Figure 3a, b. Coconut husk block (a) and BactroMAT-ME (b) bait stations used for eradication of B. dorsalis. (Photos: L. Leblanc).

opencc-by-4.0Dec 2013View details →
zenodo40/100

Figure 1 in From Eradication to Containment: Invasion of French Polynesia by Bactrocera dorsalis (Hendel) (Diptera: Tephritidae) and Releases of Two Natural Enemies: A 17-Year Case Study

Figure 1. Monthly captures of B. dorsalis in methyl eugenol traps and quarterly percent parasitism on guava, Tahitian chestnut and tropical almond on Tahiti.

opencc-by-4.0Dec 2013View details →
zenodo40/100

Figure 5a–d in From Eradication to Containment: Invasion of French Polynesia by Bactrocera dorsalis (Hendel) (Diptera: Tephritidae) and Releases of Two Natural Enemies: A 17-Year Case Study

Figure 5a–d. Quarterly emergences on Tahiti of B. dorsalis and F. arisanus per fruit for guava (a), Tahitian chestnut (b), tropical almond (c), and mango (d). Numbers of fruits used for each host and each year (for guava, Tahitian chestnut, tropical almond and mango, respectively) were: 1998: 1634, 16238, 5314, 67; 1999: 264, 304, 993, 404; 2000: 37, 40, 154, 64; 2001: 52, 0, 20, 74; 2002: 492, 1204, 474, 268; 2003: 1531, 1539, 2685, 977; 2004: 2252, 1324, 810, 291; 2005: 1071, 904, 4373, 436; 2006: 1927, 3343, 3140, 1044; 2007: 1537, 1525, 4200, 1814; 2008: 3255, 2648, 5045, 2052; 2009: 1515, 1972, 5475, 549.

opencc-by-4.0Dec 2013View details →
zenodo40/100

Figure 2 in Eradication of African sacred ibis (Threskiornis aethiopicus) from South Florida, USA: a collaborative early detection and rapid response case study

Figure 2. Two African Sacred Ibis (Threskiornis aethiopicus) affixed with wing tags and GPS backpack transmitters in September of 2008 in order to employ the "scout" technique as part of a successful southern Florida, USA, eradication effort. Photo courtesy of USDA.

opencc-by-4.0Feb 2023View details →
zenodo40/100

Figure 1 in Eradication of African sacred ibis (Threskiornis aethiopicus) from South Florida, USA: a collaborative early detection and rapid response case study

Figure 1. Map of Florida (left) and southeastern Florida (right) where a successful eradication of African Sacred Ibis (Threskiornis aethiopicus) took place in 2008. Early detection at the Loxahatchee National Wildlife Refuge by a University researcher prompted a concerted effort to capture birds and employ the scout technique on two transmitter affixed birds. The scout method and reported species sightings resulted in identifying additional roost locations (4) where shooting operations took place.

opencc-by-4.0Feb 2023View details →
zenodo40/100

Figure 3 in Lessons learnt from large-scale eradication of Australian swamp stonecrop Crassula helmsii in a protected Natura 2000 site

Figure 3. Photo impressions of the large scale eradication of Crassula helmsii on the Island of Terschelling. A. The dominant infestation of C. helmsii in an artificial lake (location 5). B. Installing a mitigation fence in order to prevent entry by amphibians and reptiles (2.75 linear km). C. Drainage installation and steel road plates tracks. D. Excavation of 40 cm topsoil (Step 4 of the described eradication approach). E. Recolonization of characteristic native plant species in excavated area 2.5 years after the eradication of C. helmsii (March 2021). F. Guided tours in the study area to inform those concerned.

opencc-by-4.0Dec 2021View details →

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International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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OpenNeuro

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Last verified 2026-04-29Open record