Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Mechanistic Models: Compartment Models in Individual and Population Analysis01:23

Mechanistic Models: Compartment Models in Individual and Population Analysis

Mechanistic models are utilized in individual analysis using single-source data, but imperfections arise due to data collection errors, preventing perfect prediction of observed data. The mathematical equation involves known values (Xi), observed concentrations (Ci), measurement errors (εi), model parameters (ϕj), and the related function (ƒi) for i number of values. Different least-squares metrics quantify differences between predicted and observed values. The ordinary least squares (OLS)...
Toxicity Testing in Animals01:23

Toxicity Testing in Animals

Toxicity tests in animals are grounded on two main assumptions: first, the effects observed in laboratory animals can be extrapolated to humans, especially when adjusted for body surface area; second, high-dose exposure in animals is essential to identify potential human hazards from lower doses. This is based on the quantal dose-response concept, which faces the challenge of extrapolating results from relatively few test animals to much larger human populations. For example, a 0.01% incidence...
Pharmacodynamic Models: Additive and Proportional Drug Effect Model01:09

Pharmacodynamic Models: Additive and Proportional Drug Effect Model

Drug response models describe how pharmacological agents interact with biological systems to produce measurable effects. Baseline responses are inherent physiological activities without a drug significantly influencing the observed pharmacological outcomes. Depending on the drug response model employed, these baseline responses may combine with the drug's effect in either an additive or proportional manner.Additive Drug Response ModelIn the additive model, the drug effect is independent of the...
Model Approaches for Pharmacokinetic Data: Distributed Parameter Models01:06

Model Approaches for Pharmacokinetic Data: Distributed Parameter Models

Pharmacokinetic models are mathematical constructs that represent and predict the time course of drug concentrations in the body, providing meaningful pharmacokinetic parameters. These models are categorized into compartment, physiological, and distributed parameter models.
The distributed parameter models are specifically designed to account for variations and differences in some drug classes. This model is particularly useful for assessing regional concentrations of anticancer or...
Model Approaches for Pharmacokinetic Data: Compartment Models01:14

Model Approaches for Pharmacokinetic Data: Compartment Models

Compartmental analysis is a widely adopted approach to characterizing drug pharmacokinetics. It uses compartment models that conceptualize the body as a collection of reversibly communicating compartments, each representing a group of tissues exhibiting similar drug distribution characteristics. The movement rate of the drug between these compartments is typically described by first-order kinetics.
Two primary types of compartment models are recognized: mammillary and catenary. The more...
Pharmacodynamic Models: Logarithmic Concentration–Effect Model01:15

Pharmacodynamic Models: Logarithmic Concentration–Effect Model

The log-linear model is a pharmacological framework used to describe the relationship between drug concentration and its effect. This model is particularly relevant when the observed effects range between 20% and 80% of the drug’s maximum effect (Emax), where a near-linear relationship is observed between the log of drug concentration and the measured effect. However, the log-linear model does not predict the maximum possible effect (Emax) or the effect at zero drug concentration, limiting its...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Quaternary ammonium compounds in paired indoor dust and human urine: suspect screening and exposure associations.

Environmental pollution (Barking, Essex : 1987)·2026
Same author

Uncovering correlates of decline and critical refuges for a threatened terrestrial mammal.

Conservation biology : the journal of the Society for Conservation Biology·2026
Same author

Seasonal Divergence between Microbiomes on Microplastics and Natural Particles Increases with Rising Water Temperatures in Urban Rivers.

Environmental science & technology·2026
Same author

Environmentally Safe and Just Pharmacy: A Framework and Action Plan for Operating within the Earth System Boundary for Novel Entities.

Environmental science & technology·2026
Same author

ICMPE turns pearl: Celebrating 30 years of achievements.

Marine pollution bulletin·2026
Same author

A tailored MoS<sub>2</sub> membrane with strong DNA-binding capability enhances aquatic biota detection through environmental DNA metabarcoding.

National science review·2026
Same journal

Correction to "Marine Scrubbers vs Low-Sulfur Fuels: A Comprehensive Well-To-Wake Life Cycle Assessment Supported by Measurements Aboard an Ocean-Going Vessel".

Environmental science & technology·2026
Same journal

Emissions and Cost Trade-Offs of Time-Matched Clean Electricity Procurement under Interannual Weather Variability: A Case Study of Hydrogen Production.

Environmental science & technology·2026
Same journal

Divergent Thermal Feedbacks of Urbanization and Greening Modulate the Urban Heat Island in 21st-Century China.

Environmental science & technology·2026
Same journal

Friction-Mediated Transfer of Low Molecular Weight Chemicals from Consumer Mats to Fabrics: Insights for Dermal Exposure.

Environmental science & technology·2026
Same journal

Molecular Drivers of Contrasting Photoreactivity in Extracellular versus Intracellular Organic Matter from Chlorophyta and Cyanobacteria.

Environmental science & technology·2026
Same journal

Effective Precipitate Cleaning with a Reversible Flow Cell Sustains Stable Energy Intensity for Oceanic CO<sub>2</sub> Removal.

Environmental science & technology·2026
See all related articles

Related Experiment Video

Updated: Jun 27, 2026

Using Caenorhabditis elegans for Studying Trans- and Multi-Generational Effects of Toxicants
08:58

Using Caenorhabditis elegans for Studying Trans- and Multi-Generational Effects of Toxicants

Published on: July 29, 2019

A Bayesian mixture model for estimating intergeneration chronic toxicity.

Jonathan R Rhodes1, Eric P M Grist, Kevin W H Kwok

  • 1Wealth from Oceans Flagship, CSIRO, GPO Box 1538, Hobart, TAS 7001, Australia.

Environmental Science & Technology
|November 27, 2008
PubMed
Summary
This summary is machine-generated.

This study used a Bayesian mixture model to analyze copper (Cu) exposure effects across three generations of copepods. Results show Cu negatively impacts reproduction, but adaptation may occur with a potential cost.

More Related Videos

Evaluating Toxicity of Chemicals using a Zebrafish Vibration Startle Response Screening System
06:25

Evaluating Toxicity of Chemicals using a Zebrafish Vibration Startle Response Screening System

Published on: January 12, 2024

Related Experiment Videos

Last Updated: Jun 27, 2026

Using Caenorhabditis elegans for Studying Trans- and Multi-Generational Effects of Toxicants
08:58

Using Caenorhabditis elegans for Studying Trans- and Multi-Generational Effects of Toxicants

Published on: July 29, 2019

Evaluating Toxicity of Chemicals using a Zebrafish Vibration Startle Response Screening System
06:25

Evaluating Toxicity of Chemicals using a Zebrafish Vibration Startle Response Screening System

Published on: January 12, 2024

Area of Science:

  • Environmental toxicology
  • Aquatic ecotoxicology
  • Population dynamics

Background:

  • Assessing multigenerational toxic effects is vital for understanding long-term chemical pollution impacts in aquatic ecosystems.
  • Standard statistical methods often struggle with complex, multi-generational experimental data.
  • There is a need for advanced statistical approaches to analyze intergenerational toxicity data.

Purpose of the Study:

  • To apply a Bayesian mixture model with random-effects to evaluate intergenerational copper (Cu) exposure on the reproductive output of Tigriopus japonicus.
  • To analyze reproductive data across three generations to understand the subtle effects of Cu exposure.
  • To compare the robustness of Bayesian models against standard statistical methods for ecotoxicological data.

Main Methods:

  • Utilized a Bayesian mixture model with random-effects to analyze three generations of Tigriopus japonicus reproductive data.
  • Specified nonstandard statistical distributions and accounted for correlations within the experimental data.
  • Investigated the impact of Cu exposure on ovisac maturation rate and nauplii production.

Main Results:

  • Intergenerational Cu exposure negatively affected current generation reproductive output.
  • Both current and parent generation Cu exposures demonstrated detrimental effects on reproduction.
  • Evidence suggests potential adaptation to parental Cu exposure, but with a reproductive cost when Cu concentrations differed.

Conclusions:

  • Bayesian mixture and random-effects models offer a robust framework for analyzing complex multigenerational ecotoxicological data.
  • The developed model provides more reliable inferences than traditional statistical methods.
  • This approach enhances the understanding of chemical toxicity and adaptive responses in aquatic populations.