On the public citation graph
Neonicotinoids Interfere with Specific Components of Navigation in Honeybees
0 signed · 382 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-9861(20000117)416:3<345::aid-cne6>3.0.co;2-topenalex-snapshot
Cytochemical evidence that acetylcholine is a neurotransmitter of neurons that make excitatory and inhibitory outputs in the locust ocellar visual system
inferredcites →https://doi.org/10.1002/anie.201302550openalex-snapshot
Nicotinic Acetylcholine Receptor Agonists: A Milestone for Modern Crop Protection
inferredcites →https://doi.org/10.1002/cne.10155openalex-snapshot
Synaptic organization of the mushroom body calyx in Drosophila melanogaster
inferredcites →https://doi.org/10.1002/cne.10867openalex-snapshot
Synaptic connections of cholinergic antennal lobe relay neurons innervating the lateral horn neuropile in the brain of Drosophila melanogaster
inferredcites →https://doi.org/10.1002/cne.23371openalex-snapshot
Choline acetyltransferase‐like immunoreactivity in a physiologically distinct subtype of olfactory nonspiking local interneurons in the cockroach (periplaneta americana)
inferredcites →https://doi.org/10.1002/cne.902860105openalex-snapshot
Histochemistry of acetylcholinesterase and immunocytochemistry of an acetylcholine receptor‐like antigen in the brain of the honeybee
inferredcites →https://doi.org/10.1002/cne.903350202openalex-snapshot
Immunohistochemical localization of a ligand‐binding and a structural subunit of nicotinic acetylcholine receptors in the central nervous system of Drosophila melanogaster
inferredcites →https://doi.org/10.1002/ps.2780330208openalex-snapshot
Actions of imidacloprid and a related nitromethylene on cholinergic receptors of an identified insect motor neurone
inferredcites →https://doi.org/10.1002/ps.331openalex-snapshot
Toxicity and nicotinic acetylcholine receptor interaction of imidacloprid and its metabolites in Apis mellifera (Hymenoptera: Apidae)
inferredcites →https://doi.org/10.1002/ps.631openalex-snapshot
Learning performances of honeybees ( Apis mellifera L) are differentially affected by imidacloprid according to the season
inferredcites →https://doi.org/10.1007/978-94-007-2099-2openalex-snapshot
Honeybee Neurobiology and Behavior
inferredcites →https://doi.org/10.1007/978-94-007-2099-2_13openalex-snapshot
Neurotransmitter Systems in the Honey Bee Brain: Functions in Learning and Memory
inferredcites →https://doi.org/10.1007/978-94-007-2099-2_9openalex-snapshot
Navigation and Communication in Honey Bees
inferredcites →https://doi.org/10.1007/bf00218999openalex-snapshot
Choline acetyltransferase-like immunoreactivity in the brain of Drosophila melanogaster
inferredcites →https://doi.org/10.1007/bf00318481openalex-snapshot
Distribution of acetylcholinesterase activity in the deutocerebrum of the sphinx moth Manduca sexta
inferredcites →https://doi.org/10.1007/s00244-007-9071-8openalex-snapshot
Effects of Sublethal Doses of Acetamiprid and Thiamethoxam on the Behavior of the Honeybee (Apis mellifera)
inferredcites →https://doi.org/10.1007/s00359-005-0007-3openalex-snapshot
Acetylcholine, GABA and glutamate induce ionic currents in cultured antennal lobe neurons of the honeybee, Apis mellifera
inferredcites →https://doi.org/10.1007/s00359-006-0136-3openalex-snapshot
Spatial memory, navigation and dance behaviour in Apis mellifera
inferredcites →https://doi.org/10.1007/s10158-005-0013-8openalex-snapshot
The actions of the neonicotinoid imidacloprid on cholinergic neurons of Drosophila melanogaster
inferredcites →https://doi.org/10.1007/s10158-007-0062-2openalex-snapshot
Study of nicotinic acetylcholine receptors on cultured antennal lobe neurones from adult honeybee brains
inferredcites →https://doi.org/10.1007/s10646-010-0566-0openalex-snapshot
A meta-analysis of experiments testing the effects of a neonicotinoid insecticide (imidacloprid) on honey bees
inferredcites →https://doi.org/10.1007/s10646-011-0594-4openalex-snapshot
Honeybee tracking with microchips: a new methodology to measure the effects of pesticides
inferredcites →https://doi.org/10.1007/s10646-012-0863-xopenalex-snapshot
Neonicotinoids in bees: a review on concentrations, side-effects and risk assessment
inferredcites →https://doi.org/10.1007/s13592-012-0134-0openalex-snapshot
Neural effects of insecticides in the honey bee
inferredcites →https://doi.org/10.1016/j.cub.2011.02.039openalex-snapshot
A Common Frame of Reference for Learned and Communicated Vectors in Honeybee Navigation
inferredcites →https://doi.org/10.1016/j.gene.2004.09.010openalex-snapshot
Apisα2, Apisα7-1 and Apisα7-2: three new neuronal nicotinic acetylcholine receptor α-subunits in the honeybee brain
inferredcites →https://doi.org/10.1016/j.neubiorev.2012.04.003openalex-snapshot
Insights from honeybee (Apis mellifera) and fly (Drosophila melanogaster) nicotinic acetylcholine receptors: From genes to behavioral functions
inferredcites →https://doi.org/10.1016/j.nlm.2006.02.003openalex-snapshot
Involvement of α-bungarotoxin-sensitive nicotinic receptors in long-term memory formation in the honeybee (Apis mellifera)
inferredcites →https://doi.org/10.1016/j.tree.2008.12.007openalex-snapshot
The honeybee waggle dance: can we follow the steps?
inferredcites →https://doi.org/10.1016/s0304-3940(01)02400-4openalex-snapshot
The insecticide imidacloprid is a partial agonist of the nicotinic receptor of honeybee Kenyon cells
inferredcites →https://doi.org/10.1038/nature03526openalex-snapshot
The flight paths of honeybees recruited by the waggle dance
inferredcites →https://doi.org/10.1038/nature11585openalex-snapshot
Combined pesticide exposure severely affects individual- and colony-level traits in bees
inferredcites →https://doi.org/10.1038/ncomms2648openalex-snapshot
Cholinergic pesticides cause mushroom body neuronal inactivation in honeybees
inferredcites →https://doi.org/10.1038/nrn3357openalex-snapshot
The honeybee as a model for understanding the basis of cognition
inferredcites →https://doi.org/10.1046/j.1365-2583.2003.00409.xopenalex-snapshot
Identification and localization of the nicotinic acetylcholine receptor alpha3 mRNA in the brain of the honeybee, Apis mellifera
inferredcites →https://doi.org/10.1073/pnas.0408550102openalex-snapshot
Honey bees navigate according to a map-like spatial memory
inferredcites →https://doi.org/10.1073/pnas.1201734109openalex-snapshot
General anesthesia alters time perception by phase shifting the circadian clock
inferredcites →https://doi.org/10.1101/gr.4549206openalex-snapshot
The nicotinic acetylcholine receptor gene family of the honey bee, Apis mellifera
inferredcites →https://doi.org/10.1111/j.1471-4159.2006.04084.xopenalex-snapshot
Neonicotinoid insecticides display partial and super agonist actions on native insect nicotinic acetylcholine receptors
inferredcites →https://doi.org/10.1126/science.1215025openalex-snapshot
Neonicotinoid Pesticide Reduces Bumble Bee Colony Growth and Queen Production
inferredcites →https://doi.org/10.1126/science.1215039openalex-snapshot
A Common Pesticide Decreases Foraging Success and Survival in Honey Bees
inferredcites →https://doi.org/10.1146/annurev.pharmtox.45.120403.095930openalex-snapshot
NEONICOTINOID INSECTICIDE TOXICOLOGY: Mechanisms of Selective Action
inferredcites →https://doi.org/10.1371/journal.pone.0030023openalex-snapshot
RFID Tracking of Sublethal Effects of Two Neonicotinoid Insecticides on the Foraging Behavior of Apis mellifera
inferredcites →https://doi.org/10.1897/08-110.1openalex-snapshot
Subchronic exposure of honeybees to sublethal doses of pesticides: Effects on behavior
inferredcites →https://doi.org/10.3389/fphys.2013.00037openalex-snapshot
A common pesticide decreases foraging success and survival in honey bees: questioning the ecological relevance
inferredcites →https://doi.org/10.3389/fphys.2013.00062openalex-snapshot
Ecological relevance in honeybee pesticide risk assessment: developing context-dependent scenarios to manage uncertainty
inferredcites →https://doi.org/10.4159/harvard.9780674418776openalex-snapshot
The Dance Language and Orientation of Bees
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4685684openalex-extracted
Effects of the Exposure to Thiamethoxam and Pyraclostrobin in the Development of Sensory Structures in Newly Emerged Bees of Scaptotrigona Postica
inferred← citeshttps://doi.org/10.1002/9781119415961.ch19openalex-snapshot
ECOSYSTEM HEALTH AS THE BASIS FOR HUMAN HEALTH
inferred← citeshttps://doi.org/10.1002/eap.2442openalex-snapshot
Inferring pesticide toxicity to honey bees from a field‐based feeding study using a colony model and Bayesian inference
inferred← citeshttps://doi.org/10.1002/ece3.5143openalex-snapshot
Pesticide exposure affects flight dynamics and reduces flight endurance in bumblebees
inferred← citeshttps://doi.org/10.1002/ece3.74363openalex-snapshot
The Future of Native Bees in Australia Under Environmental and Anthropogenic Change
inferred← citeshttps://doi.org/10.1002/ece3.8480openalex-snapshot
Searching beyond the streetlight: Neonicotinoid exposure alters the neurogenomic state of worker honey bees
inferred← citeshttps://doi.org/10.1002/etc.2800openalex-snapshot
Fate and effects of clothianidin in fields using conservation practices
inferred← citeshttps://doi.org/10.1002/etc.3581openalex-snapshot
Colony impact of pesticide-induced sublethal effects on honeybee workers: A simulation study using BEEHAVE
inferred← citeshttps://doi.org/10.1002/jmr.3008openalex-snapshot
Modeling disruption of Apis mellifera (honey bee) odorant‐binding protein function with high‐affinity binders
inferred← citeshttps://doi.org/10.1002/ps.4547openalex-snapshot
Performance of honey bee colonies under a long‐lasting dietary exposure to sublethal concentrations of the neonicotinoid insecticide thiacloprid
inferred← citeshttps://doi.org/10.1002/ps.5124openalex-snapshot
Chronic toxicity of clothianidin, imidacloprid, chlorpyrifos, and dimethoate to Apis mellifera L. larvae reared in vitro
inferred← citeshttps://doi.org/10.1002/ps.5411openalex-snapshot
Impact of acute oral exposure to thiamethoxam on the homing, flight, learning acquisition and short‐term retention of Apis cerana
inferred← citeshttps://doi.org/10.1002/ps.7162openalex-snapshot
Assessment of acute and chronic toxicity of cyantraniliprole and sulfoxaflor on honey bee ( Apis mellifera ) larvae
inferred← citeshttps://doi.org/10.1007/698_2024_1182openalex-snapshot
What We Know About Aquatic and Semi-Aquatic Mammals’ Ecotoxicity of Pesticides
inferred← citeshttps://doi.org/10.1007/978-3-030-50530-1_2openalex-snapshot
Pesticide Impacts on the Environment and Humans
inferred← citeshttps://doi.org/10.1007/978-3-031-81669-7_9openalex-snapshot
Ecotoxicological Impacts of Pesticide
inferred← citeshttps://doi.org/10.1007/978-3-319-60637-8_3openalex-snapshot
Predicting Both Obvious and Obscure Effects of Pesticides on Bees
inferred← citeshttps://doi.org/10.1007/978-3-319-78497-7_1openalex-snapshot
Introductory Chapter: An Interweaving to Be Formalized, the Biosphere Faced with the Relationship Between the Human and the Non-human
inferred← citeshttps://doi.org/10.1007/s00040-018-0660-5openalex-snapshot
Applications of RFID technology on the study of bees
inferred← citeshttps://doi.org/10.1007/s00114-026-02086-3openalex-snapshot
Unraveling pesticide impacts on pollinators: a global challenge for sustainable crop protection
inferred← citeshttps://doi.org/10.1007/s00248-022-01986-xopenalex-snapshot
Geographical and Seasonal Analysis of the Honeybee Microbiome
inferred← citeshttps://doi.org/10.1007/s00359-015-0987-6openalex-snapshot
The memory structure of navigation in honeybees
inferred← citeshttps://doi.org/10.1007/s00359-023-01619-9openalex-snapshot
Navigation and dance communication in honeybees: a cognitive perspective
inferred← citeshttps://doi.org/10.1007/s00359-025-01735-8openalex-snapshot
Flupyradifurone, imidacloprid and clothianidin disrupt the auditory processing in the locust CNS
inferred← citeshttps://doi.org/10.1007/s00894-016-2993-1openalex-snapshot
Quantum chemical study on the stability of honeybee queen pheromone against atmospheric factors
inferred← citeshttps://doi.org/10.1007/s10343-021-00572-4openalex-snapshot
Entwicklungen des Insektizid-Einsatzes in Winterraps (Brassica napus L.) infolge des Anwendungsverbotes neonicotinoider Beizen
inferred← citeshttps://doi.org/10.1007/s10646-014-1283-xopenalex-snapshot
Exposure to neonicotinoids influences the motor function of adult worker honeybees
inferred← citeshttps://doi.org/10.1007/s10646-015-1537-2openalex-snapshot
Sublethal imidacloprid effects on honey bee flower choices when foraging
inferred← citeshttps://doi.org/10.1007/s10646-016-1669-zopenalex-snapshot
The neonicotinoid pesticide, imidacloprid, affects Bombus impatiens (bumblebee) sonication behavior when consumed at doses below the LD50
inferred← citeshttps://doi.org/10.1007/s10646-017-1826-zopenalex-snapshot
Residual ground-water levels of the neonicotinoid thiacloprid perturb chemosensing of Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1007/s10646-018-1925-5openalex-snapshot
Sublethal effects of clothianidin and Nosema spp. on the longevity and foraging activity of free flying honey bees
inferred← citeshttps://doi.org/10.1007/s10646-018-1937-1openalex-snapshot
A long-term field study on the effects of dietary exposure of clothianidin to varroosis-weakened honey bee colonies
inferred← citeshttps://doi.org/10.1007/s10646-018-1976-7openalex-snapshot
Imidacloprid alters ant sociobehavioral traits at environmentally relevant concentrations
inferred← citeshttps://doi.org/10.1007/s10646-019-02070-wopenalex-snapshot
Oral acute toxicity and impact of neonicotinoids on Apis mellifera L. and Scaptotrigona postica Latreille (Hymenoptera: Apidae)
inferred← citeshttps://doi.org/10.1007/s10646-019-02145-8openalex-snapshot
Honeybee survival and flight capacity are compromised by insecticides used for controlling melon pests in Brazil
inferred← citeshttps://doi.org/10.1007/s10646-023-02699-8openalex-snapshot
The survival and flight capacity of commercial honeybees and endangered stingless bees are impaired by common agrochemicals
inferred← citeshttps://doi.org/10.1007/s10886-016-0672-4openalex-snapshot
Measurements of Chlorpyrifos Levels in Forager Bees and Comparison with Levels that Disrupt Honey Bee Odor-Mediated Learning Under Laboratory Conditions
inferred← citeshttps://doi.org/10.1007/s11252-020-00956-wopenalex-snapshot
Bee community response to local and landscape factors along an urban-rural gradient
inferred← citeshttps://doi.org/10.1007/s11356-014-3471-xopenalex-snapshot
Effects of neonicotinoids and fipronil on non-target invertebrates
inferred← citeshttps://doi.org/10.1007/s11356-017-0341-3openalex-snapshot
An update of the Worldwide Integrated Assessment (WIA) on systemic insecticides. Part 2: impacts on organisms and ecosystems
inferred← citeshttps://doi.org/10.1007/s11356-017-0498-9openalex-snapshot
QSAR modeling in ecotoxicological risk assessment: application to the prediction of acute contact toxicity of pesticides on bees (Apis mellifera L.)
inferred← citeshttps://doi.org/10.1007/s11356-020-08530-9openalex-snapshot
The effects of field-realistic doses of imidacloprid on Melipona quadrifasciata (Apidae: Meliponini) workers
inferred← citeshttps://doi.org/10.1007/s11356-020-12147-3openalex-snapshot
Supplying honey bees with waterers: a precautionary measure to reduce exposure to pesticides
inferred← citeshttps://doi.org/10.1007/s11356-022-22977-yopenalex-snapshot
Effect of repeated intakes of a neonicotinoid insecticide on the foraging behaviours of Apis mellifera in field trials
inferred← citeshttps://doi.org/10.1007/s11356-024-34363-xopenalex-snapshot
Ornamental plants as vectors of pesticide exposure and potential threat to biodiversity and human health
inferred← citeshttps://doi.org/10.1007/s13592-016-0429-7openalex-snapshot
Modulation of pesticide response in honeybees
inferred← citeshttps://doi.org/10.1007/s13592-016-0479-xopenalex-snapshot
Chronic exposure of honeybees, Apis mellifera (Hymenoptera: Apidae), to a pesticide mixture in realistic field exposure rates
inferred← citeshttps://doi.org/10.1007/s13592-017-0497-3openalex-snapshot
Landscape and pesticide effects on honey bees: forager survival and expression of acetylcholinesterase and brain oxidative genes
inferred← citeshttps://doi.org/10.1007/s13592-019-00669-wopenalex-snapshot
Effects of sublethal acetamiprid doses on the lifespan and memory-related characteristics of honey bee (Apis mellifera) workers
inferred← citeshttps://doi.org/10.1007/s13592-019-00672-1openalex-snapshot
Sublethal exposure to clothianidin during the larval stage causes long-term impairment of hygienic and foraging behaviours of honey bees
inferred← citeshttps://doi.org/10.1007/s13592-019-00726-4openalex-snapshot
Synergistic toxicity and physiological impact of thiamethoxam alone or in binary mixtures with three commonly used insecticides on honeybee
inferred← citeshttps://doi.org/10.1007/s13592-020-00787-wopenalex-snapshot
Effects of residual doses of neonicotinoid (imidacloprid) on metabolic rate of queen honey bees Apis mellifera (Hymenoptera: Apidae)
inferred← citeshttps://doi.org/10.1007/s13592-022-00909-6openalex-snapshot
Is acetamiprid really not that harmful to bumblebees (Apidae: Bombus spp.)?
inferred← citeshttps://doi.org/10.1007/s13592-022-00929-2openalex-snapshot
Oxidative stress and apoptosis in Asian honey bees (A. cerana) exposed to multiple pesticides in intensive agricultural landscape
inferred← citeshttps://doi.org/10.1007/s13592-023-01040-wopenalex-snapshot
The effects of anthropogenic toxins on honey bee learning: Research trends and significance
inferred← citeshttps://doi.org/10.1007/s13592-025-01180-1openalex-snapshot
Glyphosate-based herbicide increases the number of foraging trips but does not affect the homing of Bombus terrestris
inferred← citeshttps://doi.org/10.1007/s13592-026-01273-5openalex-snapshot
Toxicity of neonicotinoid insecticides to honey bees: a network meta-analysis
inferred← citeshttps://doi.org/10.1007/s13592-026-01306-zopenalex-snapshot
The mitochondrial axis of honey bee resilience: integrating energy, behavior, and environmental adaptation
inferred← citeshttps://doi.org/10.1007/s13593-018-0513-7openalex-snapshot
Vine and citrus mealybug pest control based on synthetic chemicals. A review
inferred← citeshttps://doi.org/10.1007/s13744-018-0651-2openalex-snapshot
Effect of Sub-lethal Doses of Imidacloprid on Learning and Memory Formation of Indigenous Arabian Bee (Apis mellifera jemenitica Ruttner) Adult Foragers
inferred← citeshttps://doi.org/10.1007/s40726-020-00142-8openalex-snapshot
A Review of Sub-lethal Neonicotinoid Insecticides Exposure and Effects on Pollinators
inferred← citeshttps://doi.org/10.1007/s41348-016-0041-0openalex-snapshot
Sublethal exposure to neonicotinoids and related side effects on insect pollinators: honeybees, bumblebees, and solitary bees
inferred← citeshttps://doi.org/10.1007/s42690-020-00114-xopenalex-snapshot
Pesticides use, practice and its effect on honeybee in Ethiopia: a review
inferred← citeshttps://doi.org/10.1016/b978-0-443-14082-2.00012-0openalex-snapshot
The rise of systemic insecticides and their environmental repercussions
inferred← citeshttps://doi.org/10.1016/b978-0-443-33596-9.00018-0openalex-snapshot
Pesticides and pollinators: impacts of agrochemical intensification on pollination services, biodiversity, and agricultural sustainability
inferred← citeshttps://doi.org/10.1016/bs.aecr.2015.10.007openalex-snapshot
Protecting an Ecosystem Service
inferred← citeshttps://doi.org/10.1016/bs.aiip.2023.01.004openalex-snapshot
How do neonicotinoids affect social bees? Linking proximate mechanisms to ecological impacts
inferred← citeshttps://doi.org/10.1016/bs.ant.2019.11.005openalex-snapshot
Neurotoxicity of Neonicotinoids
inferred← citeshttps://doi.org/10.1016/j.aspen.2020.03.011openalex-snapshot
Honeybees (Apis mellifera) modulate dance communication in response to pollution by imidacloprid
inferred← citeshttps://doi.org/10.1016/j.aspen.2021.03.012openalex-snapshot
Effects of sequential exposures of sub-lethal doses of amitraz and thiacloprid on learning and memory of honey bee foragers, Apis mellifera
inferred← citeshttps://doi.org/10.1016/j.biocon.2019.108356openalex-snapshot
Bees and pesticide regulation: Lessons from the neonicotinoid experience
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.02.105openalex-snapshot
The impact of four widely used neonicotinoid insecticides on Tetragonisca angustula (Latreille) (Hymenoptera: Apidae)
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.02.129openalex-snapshot
Hazard of a neonicotinoid insecticide on the homing flight of the honeybee depends on climatic conditions and Varroa infestation
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.128518openalex-snapshot
Short-term lab assessments and microcolonies are insufficient for the risk assessment of insecticides for bees
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.128572openalex-snapshot
Acute contact with imidacloprid in soil affects the nesting and survival success of a solitary wild bee, Osmia lignaria (Hymenoptera: Megachilidae)
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.130134openalex-snapshot
Pesticide risk assessment in honeybees: Toward the use of behavioral and reproductive performances as assessment endpoints
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.132461openalex-snapshot
A food-ingested sublethal concentration of thiamethoxam has harmful effects on the stingless bee Melipona scutellaris
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2023.139595openalex-snapshot
Effects of thiamethoxam on brain structure of Bombus terrestris (Hymenoptera: Apidae) workers
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2024.144057openalex-snapshot
Neonicotinoid pesticides in African agriculture: What do we know and what should be the focus for future research?
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2025.144335openalex-snapshot
Romance in peril: A common pesticide impairs mating behaviours and male fertility of solitary bees (Osmia bicornis)
inferred← citeshttps://doi.org/10.1016/j.cois.2016.08.009openalex-snapshot
Synapsin-based approaches to brain plasticity in adult social insects
inferred← citeshttps://doi.org/10.1016/j.compag.2024.108966openalex-snapshot
Honeybee pollen but not nectar foraging greatly reduced by neonicotinoids: Insights from AI and simulation
inferred← citeshttps://doi.org/10.1016/j.cropro.2014.12.010openalex-snapshot
The effects of insecticide dose and herbivore density on tri-trophic effects of thiamethoxam in a system involving wheat, aphids, and ladybeetles
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2016.06.038openalex-snapshot
Secondary biomarkers of insecticide-induced stress of honey bee colonies and their relevance for overwintering strength
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2017.08.047openalex-snapshot
Assessment of acute sublethal effects of clothianidin on motor function of honeybee workers using video-tracking analysis
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2019.05.007openalex-snapshot
The neonicotinoid clothianidin impairs memory processing in honey bees
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.110367openalex-snapshot
Thiamethoxam impairs honey bee visual learning, alters decision times, and increases abnormal behaviors
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.110809openalex-snapshot
Superparasitism by a parasitoid wasp: The absence of sublethal effects from the neonicotinoid insecticide imidacloprid enlightens the specificity of the cholinergic pathway involved
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.110998openalex-snapshot
Ecotoxicity of neonicotinoids and diamides on population growth performance of Zygogramma bicolorata (Coleoptera: Chrysomelidae)
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.119403openalex-snapshot
Indirect effects of insecticides on honey bee queens and their eggs via workers exposed to sublethal doses
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2026.120413openalex-snapshot
Holistic assessment of acute exposure to Bacillus velezensis on honey bee behaviour and flight performance
inferred← citeshttps://doi.org/10.1016/j.eja.2021.126350openalex-snapshot
Farmers’ perspectives of future management of winter oilseed rape (Brassica napus L.): A case study from north-eastern Germany
inferred← citeshttps://doi.org/10.1016/j.enceco.2025.12.009openalex-snapshot
Neonicotinoid pesticides dinotefuran increase honeybee body temperature and accelerate honeybee (Apis mellifera) translocation of contaminants into hives to enhance ecotoxicity risk
inferred← citeshttps://doi.org/10.1016/j.enceco.2026.06.014openalex-snapshot
Timing matters: Nighttime pesticide application reduces honeybee exposure and acute mortality
inferred← citeshttps://doi.org/10.1016/j.envadv.2021.100051openalex-snapshot
Sublethal neonicotinoid exposure attenuates the effects of electromagnetic fields on honey bee flight and learning
inferred← citeshttps://doi.org/10.1016/j.envint.2026.110424openalex-snapshot
A moment of heat, a lifetime exposure? Integrating effects of temperature and heatwaves into toxicokinetic modelling of a neonicotinoid in aquatic invertebrates
inferred← citeshttps://doi.org/10.1016/j.envpol.2017.04.003openalex-snapshot
Exposure of honey bees ( Apis mellifera ) to different classes of insecticides exhibit distinct molecular effect patterns at concentrations that mimic environmental contamination
inferred← citeshttps://doi.org/10.1016/j.envpol.2020.114011openalex-snapshot
Toxicogenomics provides insights to toxicity pathways of neonicotinoids to aquatic insect, Chironomus dilutus
inferred← citeshttps://doi.org/10.1016/j.envpol.2020.115297openalex-snapshot
The neonicotinoid thiacloprid causes transcriptional alteration of genes associated with mitochondria at environmental concentrations in honey bees
inferred← citeshttps://doi.org/10.1016/j.envpol.2021.117720openalex-snapshot
A common fungicide, Pristine®, impairs olfactory associative learning performance in honey bees (Apis mellifera)
inferred← citeshttps://doi.org/10.1016/j.envpol.2023.121451openalex-snapshot
Pesticide residues in nectar and pollen of melon crops: Risk to pollinators and effects of a specific pesticide mixture on Bombus terrestris (Hymenoptera: Apidae) micro-colonies
inferred← citeshttps://doi.org/10.1016/j.envpol.2026.127855openalex-snapshot
Chlorfenapyr-based insecticide causes multiple side effects on workers of the stingless bee Partamona helleri (Friese, 1900) (hymenoptera: Apidae)
inferred← citeshttps://doi.org/10.1016/j.etap.2021.103792openalex-snapshot
Effects of glyphosate exposure on honeybees
inferred← citeshttps://doi.org/10.1016/j.heliyon.2025.e43023openalex-snapshot
The sterol biosynthesis inhibiting fungicide difenoconazole can reduce the impact of the neonicotinoid acetamiprid on honeybee behavior
inferred← citeshttps://doi.org/10.1016/j.ibmb.2026.104502openalex-snapshot
Rethinking insecticide toxicology for the 21st century
inferred← citeshttps://doi.org/10.1016/j.isci.2020.101827openalex-snapshot
The Neonicotinoid Insecticide Imidacloprid Disrupts Bumblebee Foraging Rhythms and Sleep
inferred← citeshttps://doi.org/10.1016/j.jare.2021.08.007openalex-snapshot
First insights into the honey bee (Apis mellifera) brain lipidome and its neonicotinoid-induced alterations associated with reduced self-grooming behavior
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2019.06.013openalex-snapshot
Biopesticide spinosad induces transcriptional alterations in genes associated with energy production in honey bees (Apis mellifera) at sublethal concentrations
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.131179openalex-snapshot
Atrazine exposure can dysregulate the immune system and increase the susceptibility against pathogens in honeybees in a dose-dependent manner
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.137186openalex-snapshot
Estimation and evaluation of usage, loss and ecological risk of neonicotinoid pesticides in a large catchment
inferred← citeshttps://doi.org/10.1016/j.jip.2018.10.005openalex-snapshot
Synergistic effects of pathogen and pesticide exposure on honey bee (Apis mellifera) survival and immunity
inferred← citeshttps://doi.org/10.1016/j.jneumeth.2019.108455openalex-snapshot
Towards image-based animal tracking in natural environments using a freely moving camera
inferred← citeshttps://doi.org/10.1016/j.jrurstud.2019.07.004openalex-snapshot
Enhancing knowledge among smallholders on pollinators and supporting field margins for sustainable food security
inferred← citeshttps://doi.org/10.1016/j.neuro.2019.02.012openalex-snapshot
Neural conduction, visual motion detection, and insect flight behaviour are disrupted by low doses of imidacloprid and its metabolites
inferred← citeshttps://doi.org/10.1016/j.pestbp.2018.08.003openalex-snapshot
Metabolomic analysis of honey bee, Apis mellifera L. response to thiacloprid
inferred← citeshttps://doi.org/10.1016/j.pestbp.2022.105219openalex-snapshot
Review on effects of some insecticides on honey bee health
inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105483openalex-snapshot
Acute and chronic effects of sublethal neonicotinoid thiacloprid to Asian honey bee (Apis cerana cerana)
inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105594openalex-snapshot
S-dinotefuran affects the social behavior of honeybees (Apis mellifera)and increases their risk in the colony
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2015.08.131openalex-snapshot
Influence of pesticide use in fruit orchards during blooming on honeybee mortality in 4 experimental apiaries
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.01.113openalex-snapshot
Weight of evidence evaluation of a network of adverse outcome pathways linking activation of the nicotinic acetylcholine receptor in honey bees to colony death
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2019.01.154openalex-snapshot
Effects of radiofrequency electromagnetic radiation (RF-EMF) on honey bee queen development and mating success
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2019.02.202openalex-snapshot
Acute exposure of common yabby (Cherax destructor) to the neonicotinoid pesticide
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2019.04.402openalex-snapshot
Long-term dynamics of honey bee colonies following exposure to chemical stress
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.146642openalex-snapshot
Nicotinic receptor targeting in physiological and environmental vulnerability: A whole of biosphere perspective
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.156857openalex-snapshot
Lethal, sublethal, and combined effects of pesticides on bees: A meta-analysis and new risk assessment tools
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.163820openalex-snapshot
Thiacloprid impairs honeybee worker learning and memory with inducing neuronal apoptosis and downregulating memory-related genes
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.177166openalex-snapshot
Insecticide exposure alters flight-dependent gene-expression in honey bees, Apis mellifera
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.178262openalex-snapshot
A neonicotinoid pesticide causes tissue-specific gene expression changes in bumble bees
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2025.178460openalex-snapshot
Sub-lethal pesticide exposure interferes with honey bee memory of learnt colours
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2025.179388openalex-snapshot
Detoxification response in honey bee larvae exposed to agricultural intensification
inferred← citeshttps://doi.org/10.1016/j.trac.2021.116506openalex-snapshot
Presence and distribution of pesticides in apicultural products: A critical appraisal
inferred← citeshttps://doi.org/10.1016/j.tree.2016.12.009openalex-snapshot
Why Bees Are So Vulnerable to Environmental Stressors
inferred← citeshttps://doi.org/10.1021/acs.est.1c05692openalex-snapshot
Toxicological Effect and Molecular Mechanism of the Chiral Neonicotinoid Dinotefuran in Honeybees
inferred← citeshttps://doi.org/10.1021/acs.est.4c13656openalex-snapshot
Reduced Honeybee Pollen Foraging under Neonicotinoid Exposure: Exploring Reproducible Individual and Colony Level Effects in the Field Using AI and Simulation
inferred← citeshttps://doi.org/10.1021/acs.est.5b01287openalex-snapshot
Ecological and Landscape Drivers of Neonicotinoid Insecticide Detections and Concentrations in Canada’s Prairie Wetlands
inferred← citeshttps://doi.org/10.1021/acs.est.6b00678openalex-snapshot
Molecular Effects of Neonicotinoids in Honey Bees ( Apis mellifera )
inferred← citeshttps://doi.org/10.1021/acs.est.6b02658openalex-snapshot
Honey Bees’ Behavior Is Impaired by Chronic Exposure to the Neonicotinoid Thiacloprid in the Field
inferred← citeshttps://doi.org/10.1021/acs.est.6b04791openalex-snapshot
The Neonicotinoid Insecticide Thiacloprid Impacts upon Bumblebee Colony Development under Field Conditions
inferred← citeshttps://doi.org/10.1021/acs.est.8b01801openalex-snapshot
Global Transcriptomic Effects of Environmentally Relevant Concentrations of the Neonicotinoids Clothianidin, Imidacloprid, and Thiamethoxam in the Brain of Honey Bees (Apis mellifera)
inferred← citeshttps://doi.org/10.1021/acs.est.9b02452openalex-snapshot
Traces of a Neonicotinoid Induce Precocious Foraging and Reduce Foraging Performance in Honey Bees
inferred← citeshttps://doi.org/10.1021/acs.jafc.6c02215openalex-snapshot
Elucidating Neonicotinoid Exposure Risks: A Structure-Informed Review of Trends, Hazards, and a Sustainable Development Framework
inferred← citeshttps://doi.org/10.1021/acsearthspacechem.1c00059openalex-snapshot
Probing Matrix Effects on the Heterogeneous Photochemistry of Neonicotinoid Pesticides, Dinotefuran and Nitenpyram
inferred← citeshttps://doi.org/10.1038/nature14414openalex-snapshot
Bees prefer foods containing neonicotinoid pesticides
inferred← citeshttps://doi.org/10.1038/nature16167openalex-snapshot
Neonicotinoid pesticide exposure impairs crop pollination services provided by bumblebees
inferred← citeshttps://doi.org/10.1038/ncomms5359openalex-snapshot
Pesticide risk assessment in free-ranging bees is weather and landscape dependent
inferred← citeshttps://doi.org/10.1038/s41467-018-07914-3openalex-snapshot
Field-level clothianidin exposure affects bumblebees but generally not their pathogens
inferred← citeshttps://doi.org/10.1038/s41598-017-01039-1openalex-snapshot
A sublethal dose of a neonicotinoid insecticide disrupts visual processing and collision avoidance behaviour in Locusta migratoria
inferred← citeshttps://doi.org/10.1038/s41598-017-01361-8openalex-snapshot
A common neonicotinoid pesticide, thiamethoxam, impairs honey bee flight ability
inferred← citeshttps://doi.org/10.1038/s41598-017-17553-1openalex-snapshot
Continuous Radar Tracking Illustrates the Development of Multi-destination Routes of Bumblebees
inferred← citeshttps://doi.org/10.1038/s41598-019-38963-3openalex-snapshot
Natural biocide disrupts nestmate recognition in honeybees
inferred← citeshttps://doi.org/10.1038/s41598-019-39383-zopenalex-snapshot
Late effect of larval co-exposure to the insecticide clothianidin and fungicide pyraclostrobin in Africanized Apis mellifera
inferred← citeshttps://doi.org/10.1038/s41598-019-44581-wopenalex-snapshot
Extremely low neonicotinoid doses alter navigation of pest insects along pheromone plumes
inferred← citeshttps://doi.org/10.1038/s41598-020-65425-yopenalex-snapshot
Chronic within-hive video recordings detect altered nursing behaviour and retarded larval development of neonicotinoid treated honey bees
inferred← citeshttps://doi.org/10.1038/s41598-020-72041-3openalex-snapshot
Neonicotinoids disrupt circadian rhythms and sleep in honey bees
inferred← citeshttps://doi.org/10.1038/s41598-020-79660-wopenalex-snapshot
Honeybee colonies compensate for pesticide-induced effects on royal jelly composition and brood survival with increased brood production
inferred← citeshttps://doi.org/10.1038/s41598-020-80620-7openalex-snapshot
Thiamethoxam exposure deregulates short ORF gene expression in the honey bee and compromises immune response to bacteria
inferred← citeshttps://doi.org/10.1038/s41598-025-17599-6openalex-snapshot
Impact of acetamiprid on fatty acid composition of the central nervous system in honey bees
inferred← citeshttps://doi.org/10.1038/s41598-026-35416-6openalex-snapshot
Young honey bees Apis mellifera learn to avoid pollen contaminated with glyphosate or imidacloprid
inferred← citeshttps://doi.org/10.1038/s42003-021-02336-2openalex-snapshot
Long-term field-realistic exposure to a next-generation pesticide, flupyradifurone, impairs honey bee behaviour and survival
inferred← citeshttps://doi.org/10.1038/s42003-026-09669-wopenalex-snapshot
Bee swimming is adaptive but disrupted by insecticide
inferred← citeshttps://doi.org/10.1038/srep10989openalex-snapshot
A neonicotinoid impairs olfactory learning in Asian honey bees (Apis cerana) exposed as larvae or as adults
inferred← citeshttps://doi.org/10.1038/srep15322openalex-snapshot
Low doses of neonicotinoid pesticides in food rewards impair short-term olfactory memory in foraging-age honeybees
inferred← citeshttps://doi.org/10.1038/srep16508openalex-snapshot
Bumblebee learning and memory is impaired by chronic exposure to a neonicotinoid pesticide
inferred← citeshttps://doi.org/10.1038/srep29608openalex-snapshot
Neonicotinoid-contaminated pollinator strips adjacent to cropland reduce honey bee nutritional status
inferred← citeshttps://doi.org/10.1038/srep38110openalex-snapshot
Neonicotinoid-induced impairment of odour coding in the honeybee
inferred← citeshttps://doi.org/10.1038/srep38957openalex-snapshot
Effect of acute pesticide exposure on bee spatial working memory using an analogue of the radial-arm maze
inferred← citeshttps://doi.org/10.1038/srep42756openalex-snapshot
Sublethal doses of imidacloprid disrupt sexual communication and host finding in a parasitoid wasp
inferred← citeshttps://doi.org/10.1071/en15064openalex-snapshot
Distributions of neonicotinoid insecticides in the Commonwealth of Massachusetts: a temporal and spatial variation analysis for pollen and honey samples
inferred← citeshttps://doi.org/10.1073/pnas.2313442121openalex-snapshot
Mapping seasonal migration in a songbird hybrid zone -- heritability, genetic correlations, and genomic patterns linked to speciation
inferred← citeshttps://doi.org/10.1080/00218839.2018.1494889openalex-snapshot
Chemical residues in beebread, honey, pollen and wax samples collected from bee hives placed on canola crops in Western Australia
inferred← citeshttps://doi.org/10.1080/00218839.2019.1675337openalex-snapshot
Chronic exposure to a neonicotinoid pesticide and a synthetic pyrethroid in full-sized honey bee colonies
inferred← citeshttps://doi.org/10.1080/00218839.2020.1825044openalex-snapshot
Influence of neonicotinoids on pollinators: A review
inferred← citeshttps://doi.org/10.1080/00218839.2021.1908739openalex-snapshot
Neonicotinoid-contaminated diet causes behavior changes in forager honey bees (Apis mellifera) that may reduce colony survival during late fall
inferred← citeshttps://doi.org/10.1080/00218839.2022.2146343openalex-snapshot
Does diatomaceous earth (DE) cause mortality on Apis mellifera and Bombus terrestris ?
inferred← citeshttps://doi.org/10.1080/00779962.2024.2425452openalex-snapshot
An amitraz-based miticide does not appear to affect the bacterial microbiota of Apis mellifera (Apidae: Hymenoptera, Linnaeus, 1758) or Varroa destructor (Acari: Varroidae, Anderson & Trueman, 2000)
inferred← citeshttps://doi.org/10.1080/03601234.2017.1369320openalex-snapshot
The transfer of active ingredients of insecticides and fungicides from an orchard to beehives
inferred← citeshttps://doi.org/10.1080/23311932.2021.1872192openalex-snapshot
Honeybee keeping constraints and future prospects
inferred← citeshttps://doi.org/10.1093/conphys/coae002openalex-snapshot
Divergent impacts of the neonicotinoid insecticide, clothianidin, on flight performance metrics in two species of migratory butterflies
inferred← citeshttps://doi.org/10.1093/ee/nvab059openalex-snapshot
Neonicotinoid Pesticides Cause Mass Fatalities of Native Bumble Bees: A Case Study From Wilsonville, Oregon, United States
inferred← citeshttps://doi.org/10.1093/femsec/fiaf080openalex-snapshot
Friend or foe? Concentration of a commensal microbe induces distinct responses in developing honey bees exposed to field-realistic pesticide concentrations
inferred← citeshttps://doi.org/10.1093/jee/toad032openalex-snapshot
Potential risk to pollinators from neonicotinoid applications to host trees for management of spotted lanternfly,Lycorma delicatula(Hemiptera: Fulgoridae)
inferred← citeshttps://doi.org/10.1093/jee/toae227openalex-snapshot
Identifying and modeling the impact of neonicotinoid exposure on honey bee colony profit
inferred← citeshttps://doi.org/10.1093/jee/tov287openalex-snapshot
Uptake of Neonicotinoid Insecticides by Water-Foraging Honey Bees (Hymenoptera: Apidae) Through Guttation Fluid of Winter Oilseed Rape
inferred← citeshttps://doi.org/10.1093/jee/tox111openalex-snapshot
Agricultural Landscape and Pesticide Effects on Honey Bee (Hymenoptera: Apidae) Biological Traits
inferred← citeshttps://doi.org/10.1093/jee/tox262openalex-snapshot
Sublethal Effects of the Neonicotinoid Insecticide Thiamethoxam on the Transcriptome of the Honey Bees (Hymenoptera: Apidae)
inferred← citeshttps://doi.org/10.1093/jisesa/ieab095openalex-snapshot
Honey Bees (Hymenoptera: Apidae) Decrease Foraging But Not Recruitment After Neonicotinoid Exposure
inferred← citeshttps://doi.org/10.1096/fj.14-267179openalex-snapshot
Chronic exposure to neonicotinoids increases neuronal vulnerability to mitochondrial dysfunction in the bumblebee ( Bombus terrestris )
inferred← citeshttps://doi.org/10.1098/rsbl.2019.0359openalex-snapshot
Modality-specific impairment of learning by a neonicotinoid pesticide
inferred← citeshttps://doi.org/10.1098/rsbl.2020.0559openalex-snapshot
Landscape-level toxicant exposure mediates infection impacts on wildlife populations
inferred← citeshttps://doi.org/10.1098/rsbl.2025.0749openalex-snapshot
Volatilized prallethrin impairs the homing ability of bumblebees
inferred← citeshttps://doi.org/10.1098/rsbl.2026.0087openalex-snapshot
Using sound to detect Formica rufa behavioural changes to a common pesticide
inferred← citeshttps://doi.org/10.1098/rspb.2015.1738openalex-snapshot
Interaction betweenVarroa destructorand imidacloprid reduces flight capacity of honeybees
inferred← citeshttps://doi.org/10.1098/rspb.2015.1821openalex-snapshot
A restatement of recent advances in the natural science evidence base concerning neonicotinoid insecticides and insect pollinators
inferred← citeshttps://doi.org/10.1098/rspb.2015.2110openalex-snapshot
Reconciling laboratory and field assessments of neonicotinoid toxicity to honeybees
inferred← citeshttps://doi.org/10.1098/rspb.2016.2149openalex-snapshot
Covert deformed wing virus infections have long-term deleterious effects on honeybee foraging and survival
inferred← citeshttps://doi.org/10.1098/rspb.2019.2442openalex-snapshot
Insecticide exposure during brood or early-adult development reduces brain growth and impairs adult learning in bumblebees
inferred← citeshttps://doi.org/10.1098/rspb.2022.0253openalex-snapshot
Field-realistic concentrations of a neonicotinoid insecticide influence socially regulated brood development in a bumblebee
inferred← citeshttps://doi.org/10.1098/rspb.2024.0040openalex-snapshot
Synergistic negative effects between a fungicide and high temperatures on homing behaviours in honeybees
inferred← citeshttps://doi.org/10.1101/105700openalex-snapshot
First indication of acetylcholine-based communication in honeybee haemocytes and its modulation by a neonicotinoid insecticide
showing the first 200 of 333 · page through all 333
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.