Insect pollinators and their relative abundance on black cumin (Nigella sativa L.) At Dera Ismail Khan

Similar documents
Incidence of different insect visitors and their relative abundance associated with coriander (Coriandrum sativum) in district Charsadda

Study the abundance of insect pollinators/visitors in rapeseed-mustard (Brassica juncea L.)

POLLINATORS VISITING SESAME (SESAMUM INDICUM L.) SEED CROP WITH REFERENCE TO FORAGING ACTIVITY OF SOME BEE SPECIES

POLLINATORS VISITING CARROT (DAUCUS CAROTA L.) SEED CROP

Sesame (Sesamum Indicum L.) Crop Insect Pollinators with Special Reference to the Foraging Activity of Different Species of Honeybees

Oilseed rape pollen dispersal by insect pollinators in agricultural landscape

Insect Visitors and Abundance of Four Species of Apis on Sunflower Helianthus annuus L. in Pakistan

Impact of Honeybee and Other Insect Pollinators on the Seed Setting and Yield Production of Black Cumin Nigella sativa L.

INSECT POLLINATORS' DIVERSITY OF RAPESEED (Brassica campestris var. toria) IN CHITWAN, NEPAL

Diversity and abundance of insect pollinators on Allium cepa L.

Flower-visiting insect pollinators of mustard (Brassica napus) in Jammu Region

In seed crop of onion (Allium cepa L.), the

Who visits the tropical biofuel crop Jatropha curcas L. flowers?

Effect of different modes of pollination on seed set of mustard (Brassica juncea L.) sown on different sowing dates

Received: 21st April-2012 Revised: 28 th April-2012 Accepted: 02 nd May-2012 Research article

Flower Species as a Supplemental Source of Pollen for Honey Bees (Apis mellifera) in Late Summer Cropping Systems

In-hive pollen transfer between bees enhances cross-pollination of plants

Where in the world does your food come from?

Flower Visitor Interaction and Fruit production of Grewia asiatica L.

Impact of Pollinators in Rangelands. months. Insects are vital to humans, and without them, humans would disappear, too. Insects

Nectar Sugar Concentration as a Measure of Pollination of Alfalfa (Medicago sativa L.)

FORAGING PATTERN OF INSECT POLLINATORS IN PENTAS LANCEOLATA (FORSSK.) DEFLERS AND CATHARANTHUS ROSEUS (L.) G. DON IN THRISSUR DISTRICT, KERALA, INDIA

THE STUDY OF POLLEN BIOLOGY OF Bauhinia variegata L. AT AGRA (U.P.)

Pollination of Pumpkin and Winter Squash - Thanks to Bumble Bees! Dr. Kimberly Stoner Connecticut Agricultural Experiment Station New Haven

Research Article. Purti 1 *, Rinku 1 and Anuradha 2

The Influence of Nectar Sugar Production on Insect Visitors to Flowers of Brassica rapa L. M.A. Taylor and A.R. Davis

Materials and Methods. Usman H Dukku α, Zecarias Russom σ & Albert G Domo ρ

Pollination mechanism in CorŸ

Protecting Pollinating Insects

COMPARISON OF FORAGING ACTIVITY BETWEEN MASON BEE OSMIA ORIENTALIS

Community Involvement in Research Monitoring Pollinator Populations using Public Participation in Scientific Research

Fermented Beer-based Bait Attracted Insects Taxa in Songculan Lagoon, Songculan, Dauis, Bohol, Philippines

Pollination, the Grand Interaction Among Flowers, Bees, Growers and Beekeepers

POPULATION DYNAMICS OF CHILLI THRIPS, Scirtothrips dorsalis HOOD IN RELATION TO WEATHER PARAMETERS BAROT, B.V., PATEL, J.J.* AND SHAIKH, A. A.

Pollinators. Pam Brown University of Florida/IFAS Extension, Retired

POLLINATION STATION. Wild Discover Zone

G.J.B.B., VOL.7 (2) 2018: ISSN

Passion Fruit Pests and Their Control

Habitat Enhancements to Support Bees: Agriculture to Urban Research. Neal Williams Department of Entomology

FLORAL MORPHS AND MODE OF POLLINATION IN OXALIS CORNICULATA L., FROM PAKISTAN

Session Seven Flowering, fruit set and yield

U.S. Fish & Wildlife Service. Attracting Pollinators to Your Garden

Bees. By: Jourdan Wu, Olakunle Olawonyi, Adina Gibson, Elizabeth Peterson. Image drawn by Adina Gibson using Sketchpad 5.1

There are approximately 25,000 species of Bee in the World There are almost 4000 species of Bee in North America There are approximately 1000

Pollinator Adaptations

Pollinator Conservation

Teacher Packs in Experimental Science. Bio Pack 4. Agents of pollination

Protecting Pollinators in Home Lawns and Landscapes

The Importance of Bees

What factors limit fruit production in the lowbush blueberry, Vaccinium angustifolium? Melissa Fulton and Linley Jesson University of New Brunswick

Beneficial Insects. PJ Liesch UW-Madison: Insect Diagnostic Lab

STUDIES ON FLOWER BIOLOGY AND POLLINATION IN MUSTARD (BRASSICA JUNCEA L.)

Exposure of pollinating insects to neonicotinoids by guttation on straw cereals after seed-treated sugar beet (November 2017)

Chapter 24-Flowering Plant and Animal Coevolution

Some changes in germination and morphological traits of black seed under different soil types and common bean densities

Foliar spray of benzoic acids on pollinators behavior and plant fitness benefits

Your future flies on the wings of pollinators: Things you should know about pollinators and pollination

Genetic Divergence Studies for the Quantitative Traits of Paddy under Coastal Saline Ecosystem

ABSTRACT. Apiculture is a science-based industry using bees as. micromanipulators to harvest n~ectar and pollen from plant sources to

GardenBuzz Project Report Trent Lyle Savannah Highsmith Eric Sutton Kennan Wood

LAyOUT OF ExPERIMENTAL SITES

Annie S. White, PhD, ASLA. How Native Cultivars Affect Plant/Pollinator Interactions

Study of Genetic Divergence in Pea (Pisum sativum L.) based on Agro-Morphic Traits

Day of Science and Service May 8, 2014

Lesson Adapted from Food, Land, People

Rearing Honeybee Queens in, Apis Mellifera L. Colonies During the Activity Season of Oriental Wasps Vespa Orientalis L

Pea Patch Pollination Game

An assessment of Vicia faba and Trifolium pratense as forage crops for Bombus hortorum

INFLUENCE OF ELEVATION ON HONEYBEES Apis mellifera ITS IMPACT ON FRUIT SET AND QUALITY OF WATERMELON

Pollination for Berry Production

BEES AND POLLINATION. Journeyman Class Staci Siler Special thanks to: Bill Grayson

Entomological Analysis of the Popular Press News Article: Scientists Finally Figure Out How Bees Fly

How Does Pollination Work?

AP Biology Summer 2017

Morphometric and Wings Venation Analysis of Honey Bee Species in Dehradun, Uttarakhand

Elementary Science: Pollination

FLOWERS AND POLLINATION. This activity introduces the relationship between flower structures and pollination.

BENEFICIAL INSECTS GOING BUGGY

Potential Pollinators of Gossypium hirsutum L.

Plants can be either herbaceous or woody.

Life Cycle Duration of Philosamia ricinii (L.)

NATURE S. Insect Pollinators, Plants, and. The pedigree of honey Does not concern the bee; A clover, anytime, to her Is aristocracy.

Seasonal incidence of major insect pests of okra in the north eastern hill region of India

28 3 Insects Slide 1 of 44

Population Dynamics of Sugarcane Plassey Borer Chilo tumidicostalis Hmpson (Lepidoptera: Pyralidae)

Bees: The most important pollinators

Key Words: conservation biology, insectary plants, cover crops, nectar, pollen, syrphids, biological control

Research Article Several New Aspects of the Foraging Behavior of Osmia cornifrons in an Apple Orchard

Black grass bug adult Nabids Twice-stabbed stink bug Other bugs

FINAL REPORT TO MICHIGAN DEPARTMENT OF AGRICULTURE AND RURAL DEVELOPMENT HORT FUND PROJECT FY 2015

Pollination Best Practices in Southern Highbush Blueberry in Florida 1

Honey Bees QUB Green Champions 9 th April

Onion Pollination as Affected by Different Levels of Pollinator Activity

Seasonal Variations in Hornet s Spp. and Efficiency of Different Traps as a Tool for Control

Honey Bees. QUB CCRCB 11 th January

Lesson: Why a Butterfly Garden? Seeking Pollinator Certification for a Butterfly Garden

Land, water and bees don t take us for granted: Bees and their pollinating partners

Parts of a Flower. A lesson from the New Jersey Agricultural Society Learning Through Gardening Program

Pollen fertility Vs Spikelet fertility in F2 of a CMS based hybrids in rice (Oryza sativa L.) under Aerobic condition

Genetic variability, Heritability and Genetic Advance for Yield, Yield Related Components of Brinjal [Solanum melongena (L.

Transcription:

2017; 5(5): 1252-1258 E-ISSN: 2320-7078 P-ISSN: 2349-6800 JEZS 2017; 5(5): 1252-1258 2017 JEZS Received: 12-07-2017 Accepted: 13-08-2017 Muhammad Abrar Department of Entomology, The University of Agriculture Sajjad Ahmad Department of Entomology, The University of Agriculture Saboor Naeem Department Of Agriculture, Hazara University, Dhodial, Mansehra, Pakistan Spogmay Naeem Khyber Medical College, Insect pollinators and their relative abundance on black cumin (Nigella sativa L.) At Dera Ismail Khan Muhammad Abrar, Sajjad Ahmad, Saboor Naeem and Spogmay Naeem Abstract The current study was conducted at Agriculture Research Institute Ratha Kulachi, Dera Ismail Khan, to study the population dynamics of insect pollinators on Black Cumin during 2014. A 100m 2 plot was selected for research purpose. The Insects were observed twice a day i.e. from 9:30-10:30 am and 2:30-3:30 pm from the beginning of flowering stage up to the crop maturity i.e. 7 February to7 March. Nine species of pollinators belonging to class Insecta were recorded, in which four were Dipterous (Syrphid fly) that is Episyrphus balteatus De., Melanostoma orientale Wied., Eupeodes bucculatus Rond. and Eristalis tenax L. Three belonging to order Hymenoptera (two were honey bees i.e. Apis dorsata Fabr. and Apis florea Fabra., while one was small carpenter bee i.e. Ceratina spp Latr.) and two belonging to order Lepidoptera i.e. Cabbage Butterfly (Pieris brassicae L.) and Monarch Butterfly (Danaus chrysippus L.). Apis florea was recorded very high with a percent value of 36.79% as compare to other species, followed by Pieris brassicae and Apis dorsata with values of 14.5% and 12.5% respectively, while Eristalis tenax and Danaus chrysippus were reported to have the lowest population of similar values of 3.53%. The population of Apis florea, Apis dorsata, Ceratina spp, Pieris brassicae and Melanostoma orientale were more with values of 57%, 54.7%, 60%, 51.30% and 52% respectively at 2:30-3:30 pm than morning. On the other hand the population of Danaus chrysippus was equal at both the time intervals during the research period. Keywords: Black cumin, flowering stage, Insect pollinators, Population dynamics Correspondence Sajjad Ahmad Department of Entomology, The University of Agriculture Introduction Black cumin (Nigella sativa L.) belongs to family Ranunculaceae and originated from South West Asia and now grown in many countries of the world like Egypt, India, Pakistan, Saudi Arabia, Syria and Turkey [1]. Nigella sativa L. is an important medicinal plant and use in the cure of many diseases. It is also used in bakery food products as a flavouring agent. It is a rich source of proteins, amino acids, carbohydrates, calcium, potassium, sodium, and iron [2]. In the Muslim world it has earned a valuable and significant medicinal value due to the hadith of Hazrat Muhammad (SAW), One day he said: "Black cumin is a remedy for all diseases except death" [3]. Plants were used in every era for the cure of different diseases and day by day its medicinal importance is increasing. Similarly, Nigella sativa has a key role in the control of different diseases such as throat infections and liver cancer. The seed and oil of Black cumin was tested as treatment for different patients by the doctors for the control of numerous diseases. Positive results were obtained by scientists and thus regarded it as a significant medicinal plant for the cure of many diseases [4]. Every plant species need pollination and fertilization to produce seeds and fruits and pollinators play a key role in pollination. In plants the process of pollination starts from flowering stage in which pollen transfer from the anther to the stigma by different means. It was claimed and proved experimentally by researchers that 80% of pollination takes place by insects in which 80% is done by honey bees [5]. Many insect pollinators visit flowers and generate the process of pollination. Honeybees as compared to other are the best pollinators, their visit time per minute was recorded more than other insects, and their presence in the nearby area of the crop during the flowering stage is helpful for pollination [6]. Pakistan is an agricultural country and along with cash crops, fruits, and vegetables the need and use of medicinal plants is also raising up now a days. On the other hand the growers do not give importance to insect pollinators because they have no knowledge and information ~ 1252 ~

about the pollinators and pollination and their impact on yield and quality. Therefore to identify insect pollinators and to know their abundance at different time intervals the present study was conducted. Materials and methods The current study was conducted at Agriculture Research Institute Ratha Kulachi Dera Ismail Khan to study the population dynamics of insect pollinators on Black cumin at morning i.e. 9:30-10:30 am and afternoon i.e. 2:30-3:30 pm during 2014. A 100 m 2 plot was prepared to conduct a research. Data Collection The data was recorded twice a day that is from 9:30-10:30am and 2:30-3:30pm from the beginning of flowering stage up to the crop maturity. Black cumin plants during each observation were given a time of 40 minutes from different angles in the experimental plot. The species and number of insect pollinators visited were carefully noted. The relative abundance of insect pollinators was determined by using the formula; Number of individuals visit flowers Relative abundance of species = 100 Total number of pollinators Collection of insect pollinators visiting Black cumin flowers At the flowers blooming stage various species of insect pollinators were collected for further study. Hand net was used for the collection of insect pollinators. The collected specimens with the help of available literature were identified up to the species level, properly labelled, preserved and were submitted to the research laboratory of the Entomology department, The University of Agriculture, Peshawar. For identification of specimens belonging to the families of Syrphidae [7], Apidae [8] and Pieridae [9] different keys were used. Results and discussion Various insect pollinator species recorded on Black cumin The data showed that nine different pollinators were observed during the flowering season of Black cumin. The pollinators are listed and classified in Table 1. Out of these nine species four were Dipterous, three Hymenopterous and two pollinators were Lepidopterous. Four species of order Diptera contain syrphid flies (Episyrphus balteatus De., Melanostoma orientale Wied., Eupeodes bucculatus Rond. and Eristalis tenax L.) while three Hymenopterans in which two were honey bees (Apis dorsata Fabr., Apis florea Fabra.) and one was small carpenter bee (Ceratina spp Latr.). The other two Lepidopterous species wee cabbage butterfly (Pieris brassicae L.) and monarch butterfly (Danaus chrysippus L.) on Black cumin. Munawar et al., (2009) [10] also found honey bees, syrphid fleis and butterflies in pollination activities on Black cumin. Mukherjee et al., (2013) [11] recorded honey bees and butterflies as pollinating agents on Black cumin. Kant et al., (2013) [12] observed that honey bees played an important role in pollination of Black cumin and some other miner seed spice crops. Zaitoun et al., (2008) [13] studied different species of honey bees from flowering stage up to mature stage of on Black cumin. Table 1: Various species of insect pollinators recorded on Black cumin. Common name Technical name Order/ Family 1- Syrphid fly 1 Episyrphus balteatus De. Diptera (Syrphidae) 2- Syrphid fly 2 Melanostoma orientale Wied. Diptera (Syrphidae) 3- Syrphid fly 3 Eupeodes bucculatus Rond. Diptera (Syrphidae) 4- Syrphid fly 4 Eristalis tenax L. Diptera (Syrphidae) 5- Gaint Honey bee Apis dorsata Fabr. Hymenoptera (Apidae) 6- Small Honey bee Apis florrea Fabr. Hymenoptera (Apidae) 7- Small carpenter bee Ceratina spp Latr. Hymenoptera (Apidae) 8- Cabbage Butterfly Pieris brassicae L. Lepidoptera (Pieridae) 9- Monarch Butterfly Danaus chrysippus L. Lepidoptera (Pieridae) Relative abundance (%) of insect pollinator of same species at 9:30-10:30am and 2:30-3:30pm on Black cumin Fig.1 shows the relative abundance (%) of insect pollinator species recorded at 9:30-10:30am and 2:30-3:30pm on Black cumin. According to the figure 1 the bars indicate that the relative abundance of E. balteatus was recorded more (60.80%) at 9:30-10:30am but less (39.13%) at 2:30-3:30pm, while in M. orientale it was less (48.00%) at 9:30-10:30am but more (52%) at 2:30-3:30pm. The relative abundance of both E. bucculatus and E. tenax was more (53% and 53.30%) at 9:30-10:30am and less (47% and 46.66%) at 2:30-3:30pm respectively, while the bars of A. florea and A. dorsata shows that it was reported less (43% and 45.20%) in both species at 9:30-10:30am but more (57% and 54.7%) at 2:30-3:30pm respectively. On the other hand the bars of Ceratina spp also indicate same result i.e. less (40%) at 9:30-10:30am but more (60%) at 2:30-3:30pm respectively. The relative abundance of P. brassicae was less at 9:30-10:30am (48.60%) and more at 2:30-3:30pm (51.30%). D. chrysippus shows same (50%, 50%) relative abundance at both 9:30-10:30am and 2:30-3:30pm respectively. ~ 1253 ~ Fig 1: Relative abundance (%) of insect pollinator of same species at 9:30-10:30am and 2:30-3:30pm on Black cumin.

Average Relative abundance (%) of insect pollinators on Black cumin Fig.2 indicates the data about the average relative abundance of nine different insect pollinator species recorded on Black cumin. In all of these nine species the average relative abundance of E. balteatus, M. orientale, E. bucculatus and E. tenax were 4.9%, 5.89%, 4.0% and 3.53% respectively. On other hand A. florea, A. dorsata and Ceratina spp were 36.79%, 12.5% and 10.61% respectively while 14.5% and 3.53% was of P. brassicae and D. chrysippus respectively observed on Black cumin. On over all bases among these pollinators the relative abundance of A. florea was recorded very high as compare to other species and followed by P. brassicae, A. dorsata, Ceratina spp, M. orientale, E. balteatus, and E. bucculatus in descending order whiles E. tenax and D. chrysippus was reported same and low relative abundance in all insect pollinators. Fig 2: Average Relative abundance (%) of different insect pollinators on Black cumin. Population dynamics of insect pollinators at 9:30-10:30am and 2:30-3:30pm on Black cumin. Episyrphus balteatus De. Fig.3 shows the population dynamics of E. balteatus. According to the fig.3 the population was started from 7 th February which was increased on 14 th February and reached to its peak on 21 st February. The population trend declined on 28 th February and reached to lowest level on 7 March at both 9:30-10:30am and 2:30-3:30pm. The population dynamics was reported maximum at 9:30-10:30 as compared to 2:30-3:30pm. Fig 3: Population dynamics of Episyrphus balteatus on Black cumin. Melanostoma orientale Wied. Fig. 4 indicates the population dynamics of M. orientale. The figure shows that the population of M. orientale was started from 7 th February, which increased on 14 th Feb and on 21 st February it was reached to its peak at the morning. The population was then declined on 28 th February and on 7 th March it reached to its lowest level at 9:30-10:30am. On 7 th February at 2:30-3:30pm, the population was very low and remains in same condition on 14 th February, but it has achieved its peak on 21 st February and was remained same on 28 th February and 7 March. In overall, the population dynamics was noted higher at 2:30-3:30pm as compared to 9:30-10:30am. ~ 1254 ~

Fig 4: Population dynamics of Melanostoma orientale on Black cumin. Eupeodes bucculatus Rond. Fig.5 shows the population dynamics of E. bacculatus. At 9:30-10:30am the population was founded minimum on 7 th February, which increased on 14 th February and reached to maximum on 21 st February. The number of insect pollinators declined on 28 th February. The decreasing trend tends to continued as the population density reached to its minimum on 7 th March. At 2:30-3:30pm the population was on its lowest level on 7 th and14 th February. The population increased on 21 st February and remained same till the observations lasted i.e. 28 th February and 7 th March. The population dynamics was noticed minimum at 2:30-3:30pm as compared to 9:30-10:30am. Fig 5: Population dynamics of Eupeodes bucculatus on Black cumin. Eristalis tenax L. Fig.6 indicates the population dynamics of E. tenax. According to the Figure the population was minimum on 7 th February at both the time intervals i.e. 9:30-10:30am and 2:30-3:30pm, while in the morning on 14 th February it was increased and reached to peak on 21 st February, while on 28 th February and 7 th March the population again came down to a minimum value. On the other hand the number of pollinator at the afternoon on 14 th February remained same to that on 7 th February, while on 21 st and 28 th February the values of population of E.tenax as pollinator were also same as shown in figure 6, but decreased to least on 7 th March. The population dynamics was observed maximum at 9:30-10:30am as compared to 2:30-3:30pm. Fig 6: Population dynamics of Eristalis tenax on Black cumin. ~ 1255 ~

Apis florea Fabr. The population dynamics of A. florea is given in figure 7 and tells us that the population of this small bee was started from 7 th February and was recorded minimum during the observations at both the time intervals (morning and afternoon) but on 14 th February it was increased at both the observation times. The number of pollinator continued to increase and gained its peak on 21 st of February during 9:30-10:30am and 2:30-3:30pm separately. The values of the population then decreased at both the time intervals on 28 th February. The figures of population of the pollinator went down further during the morning and afternoon on 7 th March. At 2:30-3:30pm the population dynamics was reported maximum as compared to 9:30-10:30am. Fig 7: Population dynamics of Apis florea on Black cumin. Apis dorsata Fabr Fig.8 indicates the population dynamics of A. dorsata. According to the figure 8 at 9:30-10:30am and 2:30-3:30pm on 7 th February minimum population of the pollinators were reported. On 14 th February at both the time intervals the number of pollinators increased very little. The figures of population achieved its highest point on 21 st February at the morning and afternoon. The population decreased on 28 th of February during both the observation periods, the decreasing trend tends to continued on 7 th March also, at morning and afternoon as shown in figure 8. The population of A.dorsata was higher at the afternoon than the morning. Fig 8: Population dynamics of Apis dorsata on Black cumin. Ceratina spp Latr Fig.9 shows the population dynamics of Ceratina spp. The data infers that the population of Ceratina spp was recorded from 7 th February at 9:30-10:30am and 2:30-3:30pm. The figure shows increase of population at the mornings of 14 th and 21 st February, while on 14 th of February during 2:30-3:30pm a high increasing jump in population can be noticed which is followed by a little increase of pollinator s number on 21 st February. The figure 9 indicates decrease in population on 28 th February and least population on 7 th March at the morning. At afternoon a big decreasing jump can be observed on 28 th of February, while on 7 th March the population further decreased at 2:30-3:30pm. At 2:30-3:30pm the population dynamics was reported maximum as compared to 9:30-10:30am. ~ 1256 ~

Fig 9: Population dynamics of Ceratina spp on Black cumin. Pieris brassicae L. Fig.10 indicates the population dynamics of P. brassicae. The population was reported lowest at the morning on 7 th February as compared to the mornings of other observation dates. The population figure raised on 14 th February and then attained its peak on 21 st February during morning. The population was decreased on 28 th February, and continued to decrease up to 7 th March as shown in figure 10. At the afternoon i.e. 2:30-3:30pm the value of population was recorded lowest on 7 th February. The population increased gradually on 14 th and 21 st February and reached to its maximum value on 28 th February, which is then declined greatly on 7 th March. The population dynamics was noticed minimum at 9:30-10:30am as compared to 2:30-3:30pm. Fig 10: Population dynamics of Pieris brassicae on Black cumin. Danaus chrysippus L. Fig.11 shows the population dynamics of D. chrysippus. According to the figure 11 the population was started from 7 th February and reported minimum during 9:30-10:30am and 2:30-3:30pm both. The number of D.chrysippus remained same during 9:30-10:30am on 14 th and 21 st February. The population came back to its lowest density during the morning of 28 th February and then again increased on 7 th March. At 2:30-3:30pm on14th February the pollinator number was similar to that of 7 th February, while on 21 st February during same time interval the number of pollinator gained its peak. The population decreased on 28 th February and continued to decline on 7 th March at the afternoon. In overall, the population dynamics was noted higher at 2:30-3:30pm as compared to 9:30-10:30am. Fig 11: Population dynamics of Danaus chrysippus on Black cumin. ~ 1257 ~

Results of Ali and Ali (1989) [14] show concurrence with our findings, as they noticed Apis florea prevalence up to some extent. Munawar et al., (2009) [10] examined role of pollinators in the production of Nigella saiva and found different species at two time intervals in which honeybees were found densely. Kant et al., (2013) [12] also recorded Apis florea and Apis melifera abundantly at two time intervals. Zaitoun et al., (2008) [13] worked on the effect on yield by pollinating bees and reported honeybees more in number on Black cumin. Our results are at par with the conclusions made by Douka and Fohouo (2013) [15] from their research. They found that a single honey bee of specie Apis mellifera in a minute visits 27.98 flowers. Meena et al., in 2015 did research in Rajasthan on pollinators of seed spices from the initial flowering stages till crop harvest. They concluded that Apis florea have the highest percentage among other pollinators, followed by Apis dorsata and Apis mellifera [16]. Conclusion and recommendations The current experimental work indicated that Apis florea, Pieris brassicae and Apis dorsata were the major pollinators of Black cumin in Dera Ismail Khan. Insects pollinators belongs to family Syrphidae of order Diptera also played its role in pollination. Most of the pollinators were having higher population in the afternoon than morning Number of population of pollinators were highest on 21 st February followed by 28 th February both in the morning and afternoon. Farmers and nursery owners are advised not to apply insecticide during the last days of February when Black cumin plants are at their peak blossoming stage as it would adversely affect the pollinators. Farmers should concern honeybee keepers in order to place bee colonies in their field, so that pollination is enhanced. All those practices should be adopted that could make the environment favourable for Honeybees, Butterflies and Syrphid flies as these are the most prevalent pollinators of Black cumin in Dera Ismail Khan. Iftikhar F, Mahmood R. Pollination by Honeybees increased seed setting and yield in black seed (Nigella sativa L.). Int. J. Agr Bio. 2009; 11(5):611-615. 11. Mukherjee S, Mandal A, Gupta S, Datta AK. Pollination events in Nigella sativa L. Int. J. Res. 2013; 4(3):342-344. 12. Kant K, Singh B, Meena SR, Ranjan JK, Mishra BK, Solanki RK et al. Relative abundances and foraging behavior of honeybee species on minor seed spice crops. Int. J. seed spic. 2013; 3(2):51-54. 13. Zaitoun S, Al-Ghazawi AA, Samarah N, Alqudah A. Comparative study in seed yield and flower attractivity to Bee visitors between Nigella sativa L. and Nigella damascene L. grown under semiarid conditions. Ita. J. Agr. 2008; 2:125-130. 14. Ali T, Ali SI. Pollination biology of Calotropis procera subsp. hamiltonii (Asclepiadaceae). Phyton-Horn (Austria) 1989; 29(2):175-188. 15. Douka C, Fohouo FHT. Foraging and pollination behavior of Apis mellifera adansonii L. (Hymenoptera, Apidae) on Phaseolus vulgaris (Fabaceae) flowers at Maroua, Cameroon. Inter. Res. J. Plant Sci. 2013; 4(2):45-54. 16. Meena NK, Singh B, Kant K, Meena RD, Solanki RK. Role of insect pollinators in pollination of seed spices a review. Int. J. Seed Spices. 2015; 5(1):1-17. References 1. Donmez A, Mutlu B. A New Species of Nigella (Ranunculaceae) from Turkey. Bot J. Lin Soc. 2004; 146:251-255. 2. Amin GR. Popular Medicinal Plants of Iran, Ministry of Health Publications, Tehran, Iran. 1991; 1:118-119. 3. Al- Bukhari M. Hadith 11, Kitab-Ul-Tab (Book of Medicine) Sahih al-bukhari, 5688, 7. 4. Rajsekhar S, Kuldeep B. Pharmacognosy and pharmacology of Nigella sativa. Int res J. Pharm. 2011; 2(11):36-39. 5. Robinson WE, Morse RA. The value of honeybees as pollinators of US crops. Americ Bee J. 1989; 129(1):477-487. 6. Panda P, Rath LK, Padhi J, Panigrahi D. Relative abundance and foraging behaviour of common bee species on Niger in phulbani district, Orissa, India. Ind Bee j. 1995; 57:10-14. 7. Brunetti Diptera E, Pipunculidae, Syrphidae, Conopidae, Oestridae. In: Shipley, A. E., (ed.), the fauna of British India, including Ceylon and Burma. Taylor and Francis. London. 1923; 3:1-424. 8. Bingham CT. Fauna of British India (Hymenoptera). London. Taylor and Francis. 1897; 1:1-564. 9. Bingham CT. Fauna of British India. Butterflies. Papilionidae, Pieridae and Lycaenidae. Taylor and Francis. 1907, 2. 10. Munawar MS, Sarwar G, Raja S, Waghchoure ES, ~ 1258 ~