Maya Saar

Maya Saar
University of Florida | UF · Department of Entomology and Nematology

Doctor of Philosophy

About

18
Publications
11,262
Reads
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96
Citations
Citations since 2017
16 Research Items
91 Citations
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Introduction
I study behavioral ecology of social insects (ants), integrating molecular and behavioral approaches. Currently a post-doc in UF (FL), USA.
Education
January 2022 - September 2023
University of Florida - Entomology & Nematology Department
Field of study
January 2020 - January 2022
University of Florida - Biology Department
Field of study
October 2018 - October 2019
Tel Aviv University
Field of study
  • Taxonomic revision of the harvester ant in Israel

Publications

Publications (18)
Article
Full-text available
The unique traits of eusocial insects, such as social behavior and reproductive division of labor, are controlled by their genetic system. To address how genes regulate social traits, we have developed mutant ants via delivery of CRISPR complex into young embryos during their syncytial stage. Here, we provide a protocol of CRISPR-mediated mutagenes...
Presentation
Full-text available
The recent discovery of Cataglyphis niger’s population structure in Israel, is an intriguing opportunity to investigate a supercolony structure in a non-invasive species. In 2.5 years, extensive collection of colonies in the wild, and 4 maze-solving experiments in the laboratory, enabled to obtain demography of colonies all year-round, no. of queen...
Article
Full-text available
We studied how food type and available landmarks affect spatial learning in the ant Cataglyphis niger while searching for food in a maze. We expected the ants to solve the maze faster with consecutive runs, when the preferred food type is offered, and in the presence of landmarks. Ants should also solve the maze more slowly following a mirror-route...
Article
Full-text available
Experience can lead to faster exploitation of food patches through spatial learning or other parallel processes. Past studies have indicated that hungry animals either search more intensively for food or learn better how to detect it. However, fewer studies have examined the contribution of non-spatial information on the presence of food nearby to...
Article
Full-text available
One neglected aspect of research on foraging behavior is that of the effect of obstacles that increase habitat complexity on foraging efficiency. Here, we explored how long it takes individually foraging desert ant workers (Cataglyphis niger) to reach a food reward in a maze, and examined whether maze complexity affects maze-solving time (the time...
Article
Full-text available
There is accumulating evidence that genetic diversity improves the behavioral performance and consequently the fitness in groups of social animals. We examined the behavioral performance of colonies of two co-occurring, congeneric harvester ant species (Messor arenarius and a non-described Messor sp.) in fitness-related behaviors, pertaining to for...
Poster
Full-text available
There is accumulating evidence that genetic diversity improves performance and consequently fitness in groups of social animals. We examined the performance of colonies of two co-occurring, congeneric harvester ant species (Messor arenarius and a un-described Messor sp.) in foraging, nest maintenance, and aggression bio-assays. We linked these beha...
Article
Full-text available
The co-occurrence of two similar species depends on their ability to occupy different ecological niches. Here we compared the consistency of different aspects of foraging behavior in two co-occurring harvester ant species (Messor ebeninus and Messor arenarius), under field conditions. The two species are active concomitantly and display a similar d...
Article
Full-text available
Central-place foragers need to explore their immediate habitat in order to reach food. We let colonies of the individually foraging desert ant Cataglyphis niger search for a food reward in a maze. We did so for three tests per day over two successive days and an additional test after a time interval of 4–20 days (seven tests in total). We examined...
Data
Data are avaiable as an excell file. (XLSX)
Data
A simple mathematical description of the maze used in the experiment. (DOCX)
Data
The effect of colony size and maze complexity on the slope of the three foraging response variables on day 1. (DOCX)
Poster
Full-text available
We let colonies of the individually foraging desert ant Cataglyphis niger forage and search for a food reward in a maze. We examined whether the colonies improved their performance following successive tests between days. Colonies improved in maze-solving and food-discovery time within and between days, indicating that colonies learnt and became mo...
Poster
Full-text available
We compared the consistency of different aspects of foraging behavior in two co-occurring harvester ant species (Messor ebeninus and Messor arenarius), under field conditions. We tested the food preference of colonies by presenting three non-native seed types. M. arenarius was more selective in its food choice. Colonies were then offered one type o...
Article
Full-text available
The nesting habits of ants play an important role in structuring ant populations. They vary from monodomy, a colony occupies a single nest, via polydomy, a colony occupies multiple adjacent nests, to supercoloniality, a colony spans over large territories comprising dozen to thousands nests without having any boundaries. The population structure of...

Questions

Questions (2)
Question
Hi, Did any one sequence the harvester ant Messor grandinidus (using mitochondrial or nuclear DNA primes)? This species' sequence doesn't appear on GenBank. I have found these beautiful ants in Israel for the first time and I would like to compare my sequence with other ants of this species, possibly found in North Africa (Tunisia is the type locality). Thank you for any assistance!
Question
Hi,
Looking for some info on how to perform repeated measures ANCOVA in R. Blogs are not very clear in this subject, offering many ways.
What would be the best way to test the effect of these 3 independent variables: colony size (continuous variable), food type (categorical) and landmarks (categorical) on 2 dependent variables; the same measurements but in different time points?
Thanks for any help

Network

Cited By

Projects

Projects (6)
Project
Applying novel molecular methods for future management and control in several pest ant species.
Project
Sampling in transects and sequencing Messor ants throughout Israel, towards unraveling new species and new classification of known ones.
Project
Testing the role of learning in intra species competition between N1 and N2 while N1 definition is the colonies have advantage of learning under Lotka-Volterra model, and, N2 is the colonies of ignorance. In this point, we remark that no one of the users of Lotka-Volterra model, aim to intra species competition, although the fact that this model suit for mission if we change from 'species' to 'competitors'. After all the logistic curve (Verhulst 1838) is the base of the model (Lotka 1932), and logistic equation including the intra species competition. Further look show clearly that (dN_1)/dt=r_1 N_1 ((K_1-N_1)/K_1 ) is equal statement to N_1= K_1/(1+(e^(-rt)) ) . (see more in ' Using Lotka-Volterra model for testing hypothesis') Find out what is the cost for ignorance for N2 in terms of resource. Calculate foraging model for learning Using Lotka-Volterra model for testing hypothesis: We find the previous model suitable for the goals of this study after enormous number of studies (Holt 1985, Arditi et al. 2016, ). The model where tested in large number of cases and now days is a part of evolutionary ecology fundamentals ( ). Many outers expressed this model in advanced mathematical methods ( ) but we found that the classical fit our study. Lotka-Volterra model was originally aim to inter species competition ( ), but we use it in our study for intra species competitors. In doing this, and, by using the term 'competitors' instead of 'species', the learning advantage cam to be the major difference between competitors, in same way that the genetic variance is the difference between similar species ( ). In our research, Lotka-Volterra model is experimental tool we use for extracting the value of learning. The model: (dN_1)/dt=r_1 N_1 ((K_1-N_1)/K_1 ) , (dN_2)/dt=r_2 N_2 ((K_2-N_2)/K_2 ). For 2 competitors N1 vs N2: Competitor 1. (dN_1)/dt=r_1 N_1 ((K_1-N_1-αN_2)/K_1 ). Competitor 2. (dN_2)/dt=r_2 N_2 ((K_2-N_2-βN_1)/K_2 ). α : The effect an individual of competitor 2 has on the population growth of competitor 1. β: The effect an individual of competitor 1 has on the population growth of competitor 2. In terms of resource use N1 = K1 and N2 = K2 under the assumption that resource use is limitation of population ( ). In this case we are able to state that resource use equal to population size, and. If we represent the gain of resource exploitation in G, the all equation may be expressed: (dG_1)/dt=r_1 G_1 ((K_1-G_1-αG_2)/K_1 ) And (dG_2)/dt=r_2 G_2 ((K_2-G_2-βG_1)/K_2 ) α : The effect of resource use of competitor 2 has on the resource use of competitor 1. β: The effect of resource use of competitor 1 has on the resource use of competitor 2. For example, if 4 individuals of competitor 2 namely: N2 are equal to 1 competitor of N1 in their resource use, hence, the ratio is 1/4 and α = 0.25. In this point we are deal with resource use directly and state: G2/G1 = 1/4, α = 0.25. In experiments level we wish to see strong signification between G and N. Lotka-Volterra model lead as well to: 0=r_1 N_1 ((K_1-N_1-αN_2)/K_1 ) then K_1-N_1-αN_2=0 then N_1=K_1-αN_2 isocline 0 of population growth of N1 or N1 = K1. Since we use Lotka-Volterra model for experiment deal with intra species competition we do not need to compute the N2 competitor since both of them from same species. We give in the experiment only one advantage to N1; knowledge and training of solving a maze that N2 do not have as state in hypothesis.