scholarly journals Effect of Abscisic Acid (ABA) Combined with Two Different Beekeeping Nutritional Strategies to Confront Overwintering: Studies on Honey Bees’ Population Dynamics and Nosemosis

Insects ◽  
2019 ◽  
Vol 10 (10) ◽  
pp. 329 ◽  
Author(s):  
Nicolás Szawarski ◽  
Agustín Saez ◽  
Enzo Domínguez ◽  
Rachel Dickson ◽  
Ángela De Matteis ◽  
...  

In temperate climates, beekeeping operations suffer colony losses and colony depopulation of Apis mellifera during overwintering, which are associated with biotic and abiotic stressors that impact bees’ health. In this work, we evaluate the impacts of abscisic acid (ABA) dietary supplementation on honey bee colonies kept in Langstroth hives. The effects of ABA were evaluated in combination with two different beekeeping nutritional strategies to confront overwintering: “honey management” and “syrup management”. Specifically, we evaluated strength parameters of honey bee colonies (adult bee and brood population) and the population dynamics of Nosema (prevalence and intensity) associated with both nutritional systems and ABA supplementation during the whole study (late autumn-winter-early spring). The entire experiment was designed and performed with a local group of beekeepers, “Azahares del sudeste”, who showed interest in answering problems associated with the management of honey bee colonies during the winter. The results indicated that the ABA supplementation had positive effects on the population dynamics of the A. mellifera colonies during overwintering and on the nosemosis at colony level (prevalence) in both nutritional strategies evaluated.

2021 ◽  
Author(s):  
◽  
Tammy Leigh Waters

<p>The honey bee Apis mellifera is experiencing colony losses across the world, this is not the first time in history colony losses have been reported. New molecular detection methods such as real-time PCR allow the detection and analysis of pathogens present in colonies, quickly and reliably.  Of the pathogens that the honey bee is host to, trypanosomes are one of the least understood and trypanosome interactions within the honey bee host remain largely unknown. Using the bumble bee as a model for this host-parasite relationship. The trypanosome C. bombi is known to cause a reduced ability to gain nutrients from food and an overall decrease in efficiency of queens in founding colonies in spring. These negative correlations are significant enough in the bumble bee to warrant investigation into trypanosomes in the honey bee.  The trypanosome C. mellificae was first described in the honey bee in 1967. A screening study in 2009 included a test for and detected the trypanosome in modern honey bee samples. In 2013 C. mellificae was identified as a contributory factor to overwintering colony losses when co-infected with N. ceranae. Following studies detected trypanosomes and led to the characterisation of a new species, L. passim in 2013. Lotmaria passim was first detected in New Zealand in 2014 however no subsequent studies had been undertaken to identify the distribution and dynamics of trypanosomes in New Zealand honey bee colonies.  My goal in this study was to identify the presence of trypanosomes in New Zealand. In an overview study of 47 honey bee colonies from across New Zealand, 46 were positive for the L. passim species. Identified by sequencing of the GAPDH gene. A yearlong study of 15 colonies revealed that the infection rate of L. passim was consistent throughout the year and very low genetic variation was detected. Lotmaria passim was detected in all parts of New Zealand sampled in this study and often in high levels. A positive correlation was detected when L. passim was present in addition to N. apis. There was no detection of C. mellificae in my study. The lack of detection of C. mellificae may suggest that the species is not present, or that it is in such low levels it cannot yet be detected.  In parallel to this trypanosome study two Nosema spp. and DWV were also examined. Nosema apis was found to be more prevalent than N. ceranae, which was not present in any South Island samples. A strong positive correlation was detected between the two Nosema spp. DWV showed a high level of variation likely a reflection of differing Varroa management practices in apiaries in this study.  This study of trypanosomes is the first of its kind in New Zealand identifying the presence and population dynamics of L. passim. This in conjunction with data on Nosema spp. and DWV will be of value to the New Zealand apiculture industry and contribute to global honey bee health studies.</p>


2021 ◽  
Author(s):  
◽  
Tammy Leigh Waters

<p>The honey bee Apis mellifera is experiencing colony losses across the world, this is not the first time in history colony losses have been reported. New molecular detection methods such as real-time PCR allow the detection and analysis of pathogens present in colonies, quickly and reliably.  Of the pathogens that the honey bee is host to, trypanosomes are one of the least understood and trypanosome interactions within the honey bee host remain largely unknown. Using the bumble bee as a model for this host-parasite relationship. The trypanosome C. bombi is known to cause a reduced ability to gain nutrients from food and an overall decrease in efficiency of queens in founding colonies in spring. These negative correlations are significant enough in the bumble bee to warrant investigation into trypanosomes in the honey bee.  The trypanosome C. mellificae was first described in the honey bee in 1967. A screening study in 2009 included a test for and detected the trypanosome in modern honey bee samples. In 2013 C. mellificae was identified as a contributory factor to overwintering colony losses when co-infected with N. ceranae. Following studies detected trypanosomes and led to the characterisation of a new species, L. passim in 2013. Lotmaria passim was first detected in New Zealand in 2014 however no subsequent studies had been undertaken to identify the distribution and dynamics of trypanosomes in New Zealand honey bee colonies.  My goal in this study was to identify the presence of trypanosomes in New Zealand. In an overview study of 47 honey bee colonies from across New Zealand, 46 were positive for the L. passim species. Identified by sequencing of the GAPDH gene. A yearlong study of 15 colonies revealed that the infection rate of L. passim was consistent throughout the year and very low genetic variation was detected. Lotmaria passim was detected in all parts of New Zealand sampled in this study and often in high levels. A positive correlation was detected when L. passim was present in addition to N. apis. There was no detection of C. mellificae in my study. The lack of detection of C. mellificae may suggest that the species is not present, or that it is in such low levels it cannot yet be detected.  In parallel to this trypanosome study two Nosema spp. and DWV were also examined. Nosema apis was found to be more prevalent than N. ceranae, which was not present in any South Island samples. A strong positive correlation was detected between the two Nosema spp. DWV showed a high level of variation likely a reflection of differing Varroa management practices in apiaries in this study.  This study of trypanosomes is the first of its kind in New Zealand identifying the presence and population dynamics of L. passim. This in conjunction with data on Nosema spp. and DWV will be of value to the New Zealand apiculture industry and contribute to global honey bee health studies.</p>


2018 ◽  
pp. 83-87
Author(s):  
Marianna Takács ◽  
János Oláh

An apiary trial was conducted in 2016 August to October in Szabolcs-Szatmár-Bereg County, Nyírmada to evaluate the influence of queen’s age on the Varroa destructor-burden in the treatment colonies. Sixty colonies of bees belonging to the subspecies Apis mellifera carnica pannonica in Hunor loading hives (with 10 frames in the brood chamber/deep super) were used. The colonies were treated with amitraz and the organophosphate pesticide coumaphos active ingredients. The amitraz treatment includes 6 weeks. The coumaphos treatment with Destructor 3.2% can be used for both diagnosis and treatment of Varroasis. For diagnosis, one treatment is sufficient. For control, two treatments at an interval of seven days are required. The colonies were grouped by the age of the queen: 20 colonies with one-year-old, 20 colonies with two-year-old and 20 colonies with three-year-old queen. The mite mortality of different groups was compared. The number of fallen mites was counted at the white bottom boards. The examination of spring growth of honey bee colonies has become necessary due to the judgement of efficiency of closing treatment. The data was recorded seven times between 16th March 2017 and 19th May 2017. Data on fallen mites were subjected to one-way analysis of variance (ANOVA) and Post-Hoc Tukey-test. Statistical analysis was performed using the software of IBM SPSS (version 21.). During the first two weeks after treatments, the number of fallen mites was significantly higher in the older queen’s colonies (Year 2014). The total mite mortality after amitraz treatment in the younger queen’s colonies was lower (P<0.05) compared to the three-year-old queen’s colonies. According to Takács and Oláh (2016) although the mitemortality tendency, after the coumaphos (closing) treatment in colonies which have Year 2014 queen showed the highest rate, considering the mite-burden the colonies belongs to the average infected category. The colonial maintenance ability of three-year-old queen cannot be judged based on the influencing effect on the mite-burden. The importance of the replacement of the queen was judged by the combined effect of several factors. During the spring-growth study (16th March–19th May) was experienced in the three-year-old queen’s colonies the number of brood frames significantly lower compared to the one- and two-year-old queen’s colonies. In the study of 17th April and 19th May each of the three queen-year-groups were varied. Therefore in the beekeeping season at different times were determined the colonial maintenance ability of queens by more factors: efficiency of closing treatment in early spring, the spring-growth of bee colonies, the time of population shift (in current study, this time was identical in each queen-year), honey production (from black locust).


2018 ◽  
Author(s):  
Richard Odemer ◽  
Peter Rosenkranz

ABSTRACTIn the last decade, the use of neonicotinoid insecticides increased significantly in the agricultural landscape and meanwhile considered a risk to honey bees. Besides the exposure to pesticides, colonies are treated frequently with various acaricides that beekeepers are forced to use against the parasitic mite Varroa destructor. Here we have analyzed the impact of a chronic exposure to sublethal concentrations of the common neonicotinoid thiacloprid (T) and the widely used acaricide τ-fluvalinate (synthetic pyrethroid, F) - applied alone or in combination - to honey bee colonies under field conditions. The population dynamics of bees and brood were assessed in all colonies according to the Liebefeld method. Four groups (T, F, F+T, control) with 8-9 colonies each were analyzed in two independent replications, each lasting from spring/summer until spring of the consecutive year. In late autumn, all colonies were treated with oxalic acid against Varroosis. We could not find a negative impact of the chronic neonicotinoid exposure on the population dynamics or overwintering success of the colonies, irrespective of whether applied alone or in combination with τ-fluvalinate. This is in contrast to some results obtained from individually treated bees under laboratory conditions and confirms again an effective buffering capacity of the honey bee colony as a superorganism. Yet, the underlying mechanisms for this social resilience remain to be fully understood.


Diversity ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 403
Author(s):  
Aleš Gregorc

In recent decades, independent national and international research programs have revealed possible reasons for the death of managed honey bee colonies worldwide. Such losses are not due to a single factor, but instead are due to highly complex interactions between various internal and external influences, including pests, pathogens, honey bee stock diversity, and environmental change. Reduced honey bee vitality and nutrition, exposure to agrochemicals, and quality of colony management contribute to reduced colony survival in beekeeping operations. Our Special Issue (SI) on ‘’Monitoring of Honey Bee Colony Losses’’ aims to address specific challenges facing honey bee researchers and beekeepers. This SI includes four reviews, with one being a meta-analysis that identifies gaps in the current and future directions for research into honey bee colonies mortalities. Other review articles include studies regarding the impact of numerous factors on honey bee mortality, including external abiotic factors (e.g., winter conditions and colony management) as well as biotic factors such as attacks by Vespa velutina and Varroa destructor.


PLoS ONE ◽  
2013 ◽  
Vol 8 (5) ◽  
pp. e59084 ◽  
Author(s):  
David S. Khoury ◽  
Andrew B. Barron ◽  
Mary R. Myerscough

2020 ◽  
Vol 10 (1) ◽  
pp. 123-137
Author(s):  
O. V. Lisohurska ◽  
D. V. Lisohurska ◽  
V. M. Sokolyuk ◽  
S. V. Furman ◽  
M. M. Kryvyi ◽  
...  

Over the last decades, the number of honey bee colonies in the world has been declining. A honey bee is the most important pollinator in agriculture. According to estimates, such a situation can threaten the food security of humanity. The purpose was to investigate the specific aspects of the managed honey bee population in Zhytomyr region. The population dynamics, number, and density were determined. For this purpose the statistics of the State Statistics Committee of Ukraine on the number of bee colonies by categories of producers in Ukraine and Zhytomyr region were used. It was established that in Zhytomyr region over the past quarter century, the population of honey bee (Apis mellifera L.) has increased by 2 times up to 193.4 thousand colonies. During the same period, the number of bee colonies in Ukraine has increased by 1.4 times. At present, Zhytomyr region is a leader in the state in the development of the beekeeping industry. Eight percent of all honey bee colonies in the country are concentrated here. In the Zhytomyr region, the density of honey bee population is one of the highest in Ukraine. 82 colonies are concentrated here on one conditional pasture area (1256 hectares), with 7 colonies per 100 hectares of land. In Ukraine, these indicators are 52 and 4 respectively. The distribution of bee colonies in the region is uneven. The vast majority of colonies (58.5%) are concentrated in the Polissia. There are from 1 to 18 colonies per 100 hectares of land in each of the units in the region, on the conditional pasture area from 16 to 224. The results of these studies are relevant for the commodity apiaries for the rational use of honey flow and to make a well-considered decision on the prospect of increasing the number of bee colonies. Further work will be aimed at the investigation into the melliferous base and the calculation of the feed balance of the beekeeping industry in Zhytomyr region.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Szymon Smoliński ◽  
Aleksandra Langowska ◽  
Adam Glazaczow

AbstractVarroa destructor is the main pest of the honey bee Apis mellifera, causing colony losses. We investigated the effect of temperature on the autumn abundance of V. destructor in bee colonies over 1991–2020 in Central Europe. We tested the hypothesis that temperature can affect autumn mite populations with different time-lags modulating the bee abundance and brood availability. We showed that raised spring (March–May) and autumn (October) temperatures reinforce autumn V. destructor infestation in the bee colonies. The critical temperature signals embrace periods of bee activity, i.e., just after the first cleansing flights and just before the last observed bee flights, but no direct effects of phenological changes on V. destructor abundance were found. These effects were potentially associated with increased bee reproduction in the specific periods of the year and not with the extended period of activity or accelerated spring onset. We found significant effects of autumn bee abundance, autumn capped brood abundance, and the number of colonies merged on autumn mite infestation. We also observed differences in V. destructor abundance between bees derived from different subspecies. We indicated that climatic effects, through influence on the bee abundance and brood availability, are one of the main drivers regulating V. destructor abundance.


1993 ◽  
Vol 39 (4) ◽  
pp. 231-237
Author(s):  
Jerry J. Bromenshenk ◽  
Gloria DeGrandi-Hoffman

2012 ◽  
Vol 56 (1) ◽  
pp. 147-158 ◽  
Author(s):  
Cecilia Costa ◽  
Ralph Büchler ◽  
Stefan Berg ◽  
Malgorzata Bienkowska ◽  
Maria Bouga ◽  
...  

A Europe-Wide Experiment for Assessing the Impact of Genotype-Environment Interactions on the Vitality and Performance of Honey Bee Colonies: Experimental Design and Trait EvaluationAn international experiment to estimate the importance of genotype-environment interactions on vitality and performance of honey bees and on colony losses was run between July 2009 and March 2012. Altogether 621 bee colonies, involving 16 different genetic origins of European honey bees, were tested in 21 locations spread in 11 countries. The genetic strains belonged to the subspeciesA. m. carnica, A. m. ligustica, A. m. macedonica, A. m. mellifera, A. m. siciliana.At each location, the local strain of bees was tested together with at least two "foreign" origins, with a minimum starting number of 10 colonies per origin. The common test protocol for all the colonies took into account colony survival, bee population in spring, summer and autumn, honey production, pollen collection, swarming, gentleness, hygienic behaviour,Varroa destructorinfestation,Nosemaspp. infection and viruses. Data collection was performed according to uniform methods. No chemical treatments against Varroa or other diseases were applied during the experiment. This article describes the details of the experiment set-up and the work protocol.


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