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Article

Plant Species as Potential Forage for Honey Bees in the Al-Baha Mountain Region in Southwestern Saudi Arabia

by
Ahmad A. Al-Ghamdi
1 and
Nageeb A. Al-Sagheer
2,3,*
1
College of Food and Agriculture Sciences, King Saud University, Riyadh 11451, Saudi Arabia
2
Biology Department, Faculty of Science and Arts in Qilwah, Albaha University (BU), Qilwah 65565, Saudi Arabia
3
Agricultural Research and Extension Authority (AREA), Dhamar 87148, Yemen
*
Author to whom correspondence should be addressed.
Plants 2023, 12(6), 1402; https://doi.org/10.3390/plants12061402
Submission received: 3 February 2023 / Revised: 10 March 2023 / Accepted: 15 March 2023 / Published: 22 March 2023
(This article belongs to the Special Issue Plants: Sources of Diversity in Propolis and Honey Properties)

Abstract

:
The contribution of bee forages in the form of nectar, pollen, and propolis to beekeeping development depends on plant species diversity. The data concerning the increase in honey production in southwestern Saudi Arabia, which was unexpected with the deterioration of the vegetation cover, becomes a concrete background for this study, which planned to list the bee plant species contributing as sources of nectar, pollen, and propolis. The sampling method followed a purposive random sampling approach, and 20 × 20 m plots were considered with a total of 450 sample plots. Bee forage plants were identified based on flower morphology and honey bees’ actions during floral visits at active foraging hours. A checklist of bee forages containing 268 plants species belonging to 62 families was documented. The number of pollen source plants (122) was more than nectar (92) and propolis (10) source plants. Regarding seasonal distribution, spring and winter were relatively good seasons for honey bees in terms of pollen, nectar, and propolis availability. Generally, this study is an essential step towards understanding, conserving, and rehabilitating plant species providing nectar, forage, and propolis to honey bees in Al-Baha Region of Saudi Arabia.

1. Introduction

Al-Baha is one of the regions in the Kingdom of Saudi Arabia characterized by arid and semi-arid climatic types. This region has relatively great potential for beekeeping with its rich vegetation and diverse environmental conditions. Vegetation diversity is regarded as one of the most important comparative features distinguishing this region from others; wild plants can be found in the deserts, villages, oases, plains, valleys, and mountains of Al-Baha’s landscapes [1]. As a result of its rich floral resource, beekeeping in Al-Baha is one of the most popular and socially accepted livelihood activities in both the Sarawat mountainous and the Tehama coastal areas, which constitute the main apicultural landscapes in the region [2]. A recent study conducted by Al-Ghamdi et al. [3] also reported the existence of enormous honey bee floral resources in the region. However, most of the plant habitats are vulnerable to deterioration and vegetation degradation amid anthropogenic activities, habitat loss, over-exploitation, invasive plant species, and climate change [4].
Honey bee colonies contribute greatly to human well-being by contributing to the provision of ecosystem services and completing plants’ life cycles [5,6,7]. Although it is known that the ecosystem contributes positively to the sustainable development of life [8,9], there are no studies confirming the shared contribution of bees to achieve sustainable development goals through the ecosystem. Numerous research endeavors have demonstrated the importance of insect pollinators in achieving multiple sustainable development goals by regulating natural cycles, biological control, pollination, seed dispersal, and even as a biological inspiration [5,10,11]. The role of bees in pollinating plants has been emphasized as a direct contribution to food security and biodiversity. Therefore, sustainable development of honey bee resources and forage starts by identifying and documenting the honey bee plants to assure honey bees’ services.
There has been a constant demand for honey bee services since ancient times; however, the honey production sub-sector, which relied on limited floral resources could not fulfill the long-standing demand for honey and related products and byproducts while the country continued importing from abroad. Saudi Arabia currently imports more than 15,000 metric tons of table honey each year. Australia, Turkey, Mexico, Argentina, Pakistan, United States, Germany, and Yemen are the largest honey-producing countries, in order of volume imported to the country. However, this trend shall be changed and the country shall focus on boosting its apicultural production and declare self-dependency by advocating beekeeping development and apicultural resource development endeavors [2]. In doing so, rehabilitation and restoration of apicultural landscapes through reforestation and plantation activities while emphasizing local honey bee floral genetic resources shall draw the attention of development agents. However, so far, information about the high-value nectar and pollen sources, which include indigenous and locally available plant genetic material, is not largely available; when it is available, it is only limited to a few species [3]. Logically, it is worth identifying and documenting the honey bee plant species and creating an area-specific checklist to make use of the resources in times of development needs as part of the beekeeping development effort. The current list of honey bee flora of Al-Baha might not be the most comprehensive of all bee plant species, but it can at least be a foundation list of available honey bee flora for the government-community partnership and non-governmental organizations (NGOs) interested in rehabilitating the honey bee floral resource of this region.
Coupled with the mapping of botanical communities of bee plants in the region, the list can be an excellent developmental aid that contributes to improving the beekeeping conditions and increasing the average output production per colony. Therefore, this study offers a way for future restoration and rehabilitation works to boost the apicultural sub-sector and hence contributes to achieving some of the nation’s development goals, such as Vision 2030. In line with this, the current study is aimed at documenting honey bee flora in arid and semi-arid areas by enlisting bee-plant species in the Al-Baha Region of Saudi Arabia, respective to the different seasons.

2. Results

Pollen sources were found to be greater in number than the nectar and propolis source plants with recorded numbers of species being 122, 92, and 10, respectively. Similarly, plant family numbers were higher for pollen sources than the nectar and propolis, with 31, 14, and 3 plant family classes, respectively. In the current study, about 62 families were recorded as a source of nectar, pollen, and both nectar and pollen source plants. Asteraceae has the highest number of individual plant species with 35 in total, and all of which are considered as sources of nectar, pollen, or both. The Fabaceae family followed the Asteraceae in bee plant documentation in the region, while the Lamiaceae, Malvaceae, and the Amaranthaceae were found to contribute significantly, in this order of importance, to honey bee resources in the form of nectar and pollen. Euphorbiaceae, Plantaginaceae, Boraginaceae, Brassicaceae, and Acanthaceae were also among the top ten plant families holding major shares in the contribution of honey bee resources in the region. These ratings were based on the number of individual plant species contributing to the bee forage resource in the region. (Table 1 and Table 2).
Season-wiseanalysis of the distribution of bee plant species found that spring is the most valuable (p < 0.05) flowering season for the bees, followed by winter, autumn, and summer with 170, 128, 96, and 89 flowering plants, respectively. Spring and winter are more precious flowering seasons (p < 0.05) than autumn and summer for beekeepers in Al-Baha region, and the number of bee plants secreting nectar was 54 and 50, respectively (Table 3).
The variations in the distribution of flowering and not-flowering status of plant species were found to be significant (p < 0.05) in spring and winter, while only slight variations were seen between summer and autumn (Figure 1).
The percentages of plants that did not flower in summer and autumn were observed to be 64.16% and 68.28%, respectively (Table 3). The diversity index showed that the flowering plant species in spring (H′ = 2.22) and winter (H′ = 2.16) were more diverse than the autumn (H′ = 1.99) and summer (H′ = 1.94).
On the other hand, spring and winter were found to be the most valuable seasons with a high percentage of plants that flower at 63.43% and 45.48%, respectively (Table 4).
Results from the contingency analysis of the Chi-square test revealed that flowering plants behaved significantly (p < 0.05) differently distributed across all the seasons. A higher number of flowering plants were found to be significant in spring and winter with a value of p < 0.05. There is a significant (p < 0.05) clustering in the number of flowering plants in spring and winter compared with summer and autumn, as shown in the correspondence analysis (Figure 1).
Results of the current study show that wild plant species constitute 84.70%, followed by regional endemic (10.45%), near-endemic (2.99%), and endemic plants (1.87%) of the bee flora of the region. Many bee-forage plants like Ziziphus spina-christi, Vechilia species Senegalia asak, and Senegalia hamulosa are designated as rare and endangered. Some plant species are rare, such as Blepharis edulis and Hypoestes forskaolii, and are considered valuable honey sources with high rates (Figure 2), (Table 2).

3. Discussion

The current study is aimed at documenting honey bee flora in arid and semi-arid areas by enlisting honey bee plant species in Al-Baha Region of Saudi Arabia, respective of the different seasons. The existing flora in the current study area benefits the honey bees by providing forage resources, namely nectar, pollen, and propolis; ultimately, they were found to be the main rewards offered by flowers to honey bees. Meanwhile, pollen sources outweighed the nectar and propolis sources in the number of plant species. In agreement with the current study, plants certainly provide pollen more than nectar [12]. Based on the honey bee’s requirement for forage, adult bees mostly consume more nectar than pollen, whereas larvae need more volume of both pollen and nectar (bee bread) [13,14,15,16]. This fact has been proven in the current study, as well as a sustainable mutualism association between the bee and plant species, where bees benefit the plants through pollination while they obtain their basic nutrients from the pollen. Honey bees do not gather the forage resource for their survival only, but for their broods also [17,18,19], which guarantees the continuation of their species.
Similar to the current study, Al-Ghamdi et al. [3] mentioned that bee plants are important in strengthening bee colonies, and mentioned the total number of bee plants found in the Al-Baha Region is 204 plant species under 58 families dominated by nine main honey source plants. The distribution and availability of pollen source plants could be attributed to the fact that the genetic constitution of plants often produces pollen grain for sexual multiplication, and bees benefit from the process of pollination whilst collecting pollen. Understanding the floral resource (nectar, pollen, and propolis) and their flowering season is critically important for the improvement of the management of carrying capacity in their habitats [20]. Similar studies have implied that the flowering calendar varies among species and locations. However, listing and classifying plants based on their potential benefit to honey bees is essential to help support beekeeping [21].
Similar results were reported by Al-Namazi et al. [22]. They found that the plant diversity in southwest Saudi Arabia was about 319 plant species from 75 families and 228 genera, among which only two species are endemic; 14 are endemic to the Arabian Peninsula, five are regional-endemic only found in East Africa and the Arabian Peninsula, and 39 are rare and endangered. The significant number of rare and endangered plant species could raise an alarm to initiate effective remedial measures for the preservation and conservation of the existing flora. Shada Mountain, the highest landscape in the lowlands of Al-Baha Region of southwestern Saudi Arabia, is the most important plant area and was found to have 495 plant species belonging to 314 genera and 76 families, including 19 endemic species and 43 endangered species, accounting for 22% of Saudi Arabia’s total flora [23].
Furthermore, the outcomes of this study showed that about 268 plant species under 62 families were recorded in the study area. They are there for providing bee floral rewards, pollen, nectar, and propolis either in a combined or separate manner in that order of importance of contribution to the wellbeing of honey bees. Similar floral richness to the current study related to different geographic, edaphic, and environmental factors was also reported by Al-Aklabi et al. [24]. The fact is that the research location has varied geographical and climate elements that could explain the variance in the diversity of flowering plants throughout time. The most plant families observed in the region were the Asteraceae, Fabaceae, Lamiaceae, and Malvaceae. These families were found to have the highest number of species in Saudi Arabia, likely due to their long-developed stress and drought tolerance abilities. Similarly, Amaranthaceae, Euphorbiaceae, Plantaginaceae, Boraginaceae, Brassicaceae, and Acanthaceae are known for their adaptation to arid and semi-arid regions, thus holding major shares in the honey bee resource contribution in the current region, which is mainly characterized by dry climates. Similar findings were reported by Kuppler et al. [25] and Zurbuchen and Müller [26].
In our study, spring and winter were relatively good seasons for honey bees in terms of pollen, nectar, and propolis availability. This might be due the relatively conducive plant growing weather conditions in winter and spring. The region’s erratic foggy weather in winter and early spring and relatively moderate temperature and rainfall records were reported by National Center for Metrology [27]. Autumn season is frequently coupled with heavy rain and fog, which is still considered favorable for most plants in highland locations and foothills. The impact of environmental conditions on species diversity and richness was reported by Slezák et al. [28] and Al Zandi et al. [29].

4. Materials and Methods

4.1. Study Sites

The study was conducted in the Al-Baha Region, southwestern Saudi Arabia starting from 2019 to the end of 2021. The ecological area consists of four regions, namely, the Tehama coastal area, the Tehama Foothills, the high-altitude area, and the eastern foothills [24]. The average temperature in the summer ranged between 20–30 °C and 8–20 °C in the winter. Rainfall varies among geographical areas. In the highlands, it ranged from 300 to 550 mm/year, while it was less than 150 mm/year in the Tehama Region. The humidity ranged from 40% to 58% from November to May [27]. The region is known for its erratic foggy weather in winter and early spring while the plant populations thrive well as relatively moderate temperature and rainfall records are common in these seasons. In May, the environmental and geographical characteristics create a favorable ecological niche for diversifying the life forms of plant species. Al-Baha Region has been described in many studies as one of the best ecological landscapes for harboring vast floral and faunal diversity in Saudi Arabia [3,22,27,28]. The sampled sites were mapped using ArcGIS software (Figure 3).

4.2. Sampling and Bee Plant Identification

The study concentrated on surveying the bee plant species distributed throughout the region for three consecutive years, from Jan 2019 to Dec 2021. A sampling model was used in many studies on enumerating plant diversity [24,30,31]. The survey covered an area of 180,000 m2 using a 20 × 20 m quadrat laid purposively to exhaustively include the most possible plant diversity. A total of 450 plots were considered. In areas with homogeneous plant cover, samples were taken randomly, leading to the use of purposive random sampling technique. Plant specimens were collected from the field and immediately pressed to get dried and finally glued on herbarium sheets; then, all specimens were archived and placed in the herbarium of Al-Baha University based on the scientific methods of identification following Collenette [32].
The plant species valuable to bees were identified based on flower avaliability, bees’ action during foraging hours on the flowers, presence of pollen in the corbiculae, and the old regional beekeepers’ experience (who observe how the bees take resources from the flowers: when the bees send their proboscis to a flower, it implies that the plant is a nectar source. It is a pollen source if the bees uptake the pollen powder in their body and collect it in the pollen basket. It is also clear when bees collect the propolis and can be observed by the researchers [33]). After data collection, we classified the bee plants into different groups according to the type of collected forages as follows: nectar (N) source, pollen (P) source, and both pollen and nectar source plants. The latter group was marked according to the main dominance source as follows: N + P (the main source of the forage was nectar and some pollen was observed) or P + N (the main source of the forage was pollen and some nectar was observed). Careful observations were made on the bees’ actions while collecting resources for bee forage source plant categorization. The propolis (Po) source plants were determined by the observations made on bees’ visits to vegetative parts of plants collecting the plant secretions from leaves, stems, fruits, and branches (Supplementary Data: images showing bees on the forage plants). Observations on honey bee visits were conducted during foraging hours respective of the different seasons: every two hours from 5:30 AM to 6:30 PM in spring, summer and autumn, and every one hour from 9:00 AM to 5:00 PM in winter. In most parts of the region, the cold stresses of the winter season are common during early morning and late afternoon. Data were filtered and managed using Microsoft Office Excel 2013. The responses of nominal variables like the seasonal distribution of flowering plants in spring, summer, autumn, and winter were tested using Chi-square (χ2) tests of contingency analysis, followed by correspondence analysis to show the relationship between the variables. Shannon’s diversity index (H′) of flowering plants in different seasons was applied to test the species richness among the flowering seasons using Multivariate Statistical Package (MVSP) version 3.22 [34].
Shannon’s diversity index [35]
H = i = 1 s p i L n ( p i )
where pi is the proportion of individuals of species in its species.
All statistical analysis was performed in JMP statistical software version 5 to analyze the variation among variables [36].

5. Conclusions

Al-Baha Region is found to be a potential place for beekeeping practices and producing honey in local as well as international markets. The high demand by many local consumers is an indicator of its high preference. The plant diversity and environmental factors could be the secret behind the quantity and quality of the Al-Baha honey. The conservation of honey bee plant species is critical due to the increase in genetic loss of important honey bee plant species from naturally existing forests. The narrow population of these economic plant species cast a shadow on the purchasing process of honey products and increased price rate. All the bee forage plants under danger and deterioration can be propagated and conserved using in situ and ex situ techniques. Apart from this, variation of plants in blooming seasons may support the continuous flow of honey throughout the year. For sustainable and continuous honey production, urgent action has to be taken to protect the bee forage plant populations in arid and semi-arid areas of Al-Baha, as the floral diversity is dwindling due to harsh ecosystem components. Furthermore, the current research outcome exposes the increasing demand to conserve the floral diversity through the anticipation of think tanks from all related sectors, including scientists in collaboration with government and non-government agencies. Moreover, awareness creates endeavors in conservation for the local inhabitants of the Kingdom of Saudi Arabia.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/plants12061402/s1.

Author Contributions

Conceptualization, N.A.A.-S.; methodology, N.A.A.-S.; software, N.A.A.-S.; validation, N.A.A.-S.; formal analysis, N.A.A.-S.; investigation, N.A.A.-S.; resources, N.A.A.-S.; data curation, N.A.A.-S.; writing—original draft preparation, N.A.A.-S.; writing—review and editing, N.A.A.-S. and A.A.A.-G.; supervision, A.A.A.-G.; project administration, A.A.A.-G.; funding acquisition, A.A.A.-G. All authors have read and agreed to the published version of the manuscript.

Funding

This work was funded by the National Plan for Science, Technology and Innovation (MAARIFAH), King Abdulaziz City for Science and Technology, Kingdom of Saudi Arabia, Award Number (13-AGR2118-02).

Data Availability Statement

All data generated or analyzed during this study are included in this published article and its Supplementary Information Files.

Acknowledgments

Authors are grateful to the National Plan for Science, Technology and Innovation (MAARIFAH), King Abdulaziz City for Science and Technology, Kingdom of Saudi Arabia, Award Number (13-AGR2118-02).

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Correspondence analysis of the distribution of flowering honey bee plants across the different seasons. × = Seasons; Plants 12 01402 i001 = Flowering status; Sp = Spring; Wi = Winter; Au = Autumn; Su = Summer. The category “Yes” is quite near to “Winter” and “Spring” while “No” is related to “Autumn” and “Summer”, implying that flowering honey bee plants occur more during winter and spring and less in summer and autumn.
Figure 1. Correspondence analysis of the distribution of flowering honey bee plants across the different seasons. × = Seasons; Plants 12 01402 i001 = Flowering status; Sp = Spring; Wi = Winter; Au = Autumn; Su = Summer. The category “Yes” is quite near to “Winter” and “Spring” while “No” is related to “Autumn” and “Summer”, implying that flowering honey bee plants occur more during winter and spring and less in summer and autumn.
Plants 12 01402 g001
Figure 2. Percentage of endemism among bee plant species in Al-Baha region, southwestern Saudi Arabia.
Figure 2. Percentage of endemism among bee plant species in Al-Baha region, southwestern Saudi Arabia.
Plants 12 01402 g002
Figure 3. Map of the study area and locations of sample sites.
Figure 3. Map of the study area and locations of sample sites.
Plants 12 01402 g003
Table 1. Number of plant species and families benefiting the bees in Al-Baha region, southwestern Saudi Arabia.
Table 1. Number of plant species and families benefiting the bees in Al-Baha region, southwestern Saudi Arabia.
NN + PP + NPProN + P + Pro
No.%No.%No.%No.%No.%No.%
Number of plants92 25.110929.8287.71223110352
Number of Families1415.42931.91213.233.334.12.73.31.42.2
N (Nectar), P (Pollen), Pro (Propolis).
Table 2. Checklist of the bee forage plants from Al Baha, Southwestern Saudi Arabia. Nectar (N), Pollen (P), and Propolis (Pro).
Table 2. Checklist of the bee forage plants from Al Baha, Southwestern Saudi Arabia. Nectar (N), Pollen (P), and Propolis (Pro).
Botanical NameFamilySource of
Forage
Flowering CalendarEndemism
  • Anisotes trisulcus (Forssk.) Nees Barleria bispinosa
Acanthaceae JussNJan, Feb, Mar, Apr and MayRegional endemic
2.
Barleria bispinosa (Forssk.) Vahl
N + P Jan, Feb, Mar and DecNear-endemic
3.
Barlria prionitis L.
N + PJan, Feb, Mar, Apr and MayWild spread
4.
Blepharis edulis (Forssk.) Pers
NJan, Feb, Mar, Apr and MayWild spread
5.
Hypoestes forskaolii (Vahl) R. Br. Justicia flava
NJan, Feb, Mar and AprWild spread
6.
Justicia flava (Forssk.) Vahl
N + PJan, Feb and MarWild spread
7.
Justicia odora (Forssk.) Lam. Leucas alba
N + Pflowering calendar; Jan, Feb, Mar and DecWild spread
8.
Sesuvium portulacastrum L.
Aizoaceae MartinovN + PAug and SeptWild spread
9.
Trianthema portulacastrum L.
N + PAug and SeptWild spread
10.
Achyranthes aspera L.
Amaranthaceae Juss.PMar, Apr and MayWild spread
11.
Aerva javanica (Burm.f.) Juss. ex Schult.
PJan, Feb, Mar, Apr, May, Nov and DecWild spread
12.
Amaranthus blitum L. (=Amaranthus viridis All.)
PSept, Oct and NovWild spread
13.
Chenopodiastrum murale (L.) S. Fuentes, Uotila & Borsch (=Chenopodium murale L.)
NDec and JanWild spread
14.
Chenopodium album L.
NDec and JanWild spread
15.
Digera muricata (L.) Mart.
NJan, Feb and Mar.Wild spread
16.
Dysphania ambrosioides (L.) Mosyakin & Clemants (=Chenopodium ambrosioides L.)
NOct, Nov and DecWild spread
17.
Oxybasis glauca (L.) S. Fuentes, Uotila & Borsch (=Chenopodium glaucum L.)
NMay, June and JulyWild spread
18.
Psilotrichum gnaphalobryum (Hochst.) Schinz
NDec and JanWild spread
19.
Salsola kali L.
NNov and DecWild spread
20.
Salsola tragus L.
PMar, Apr, May, and JuneWild spread
21.
Crinum album (Forssk.) Herb
Amaranthaceae Juss.PFeb and MarEndemic
22.
Searsia retinorrhoea (Steud. ex Oliv.) Moffett
Anacardiaceae R.Br.NAug, Sept, Oct and Nov
23.
Ammi majus L.
Apiaceae Lindl.N + PApr, May and June
24.
Conium maculatum L.
N + PAug and Sept
25.
Foeniculum vulgare Mill
N + PApr, Dec, Jan, Feb and Mar.
26.
Calotropis procera (Aiton) W. T. Aiton
Apocynaceae Juss.N + P + PrFeb, Mar and NovWild spread
27.
Carissa spinarum L.
NApr. May, June, July, Aug. and Sept.Wild spread
28.
Leptadenia pyrotechnica (Forssk.)
NNov. and Dec.Wild spread
29.
Cynanchum viminale (L.) L. (=Sarcostemma viminale (L.) R. Br.
NApr. May, June, July, Aug. and Sept.Wild spread
30.
Phoenix caespitosa Chiov.
Arecaceae Bercht. & J.PreslNNov. and Dec.Wild spread
31.
Phoenix dactylifera L.
NFeb. Mar. and Apr.Wild spread
32.
Asparagus africanus Lam.
Asparagaceae JussN + PFeb. Apr. May, Nov. and DecWild spread
33.
Aloe castellorum J. R. I. Wood
Asphodelaceae JussN + PFeb, Mar, Apr, May, June, July and AugNear-endemic
34.
Aloe pseudorubroviolacea Lavranos & Collen.
N + PApr and MayEndemic
35.
Aloe shadensis Lavranos & Collen.
N + PApr and MayEndemic
36.
Aloe saudiarabica T. A. McCoy
N + PMar, Apr and MayEndemic
37.
Asphodelus fistulosus L.
PMay and JuneWild spread
38.
Asphodelus tenuifolius Cav.
PJan, Feb, Mar, Apr and MayWild spread
39.
Achillea arabica Kotschy (=Achillea biebersteinii Afanasiev)
Asteraceae Bercht. & J.PreslPMar. and Apr.Wild spread
40.
Ambrosia maritima L.
NAug, Sept, Oct and NovWild spread
41.
Baccharoides schimperi (DC.) Isawumi, El-Ghazaly & B. Nord. (=Vernonia schimperi DC.)
NMay and JuneWild spread
42.
Bidens pilosa L.
N + PSept, Oct, Nov and DecWild spread
43.
Calendula arvensis L.
N + PJan, Feb, Mar and Apr.Wild spread
44.
Carduus pycnocephalus L.
N + PMar, Apr and MayWild spread
45.
Centaurea sinaica DC.
N + PJan, Feb, Mar, Apr, May and DecWild spread
46.
Centaurea schimperi DC.
N + PJan, Feb, Mar, Apr, Nov and DecWild spread
47.
Cichorium bottae Deflers
N + PDec and JanNear-endemic
48.
Cichorium intybus L.
N + PMay, June, July and Aug
49.
Erigeron incanus Vahl (=Conyza incana (Vahl) Willd.)
N + PNov, Dec and JanWild spread
50.
Eschenbachia gouanii (L.) G. L. Nesom (=Conyza hochstetterii Sch.Bip. ex A.Rich.)
N + PJan and FebWild spread
51.
Eschenbachia stricta (Willd.) Raizada. (=synonym Conyza stricta Wall.)
N + PNov, Dec and JanWild spread
52.
Crepis foetida L.
PApr and MayWild spread
53.
Crepis rueppellii Sch.Bip.
PJan and Feb.Regional endemic
54.
Echinops polyceras Boiss
NApr, May, June and JulyWild spread
55.
Felicia abyssinica Sch.Bip. ex A. Rich.
N + PDec, Jan, Feb, Mar, Apr and MayRegional endemic
56.
Felicia dentata (A.Rich.) Dandy
N + PDec, Jan, Feb, Mar, Apr, May and JuneRegional endemic
57.
Flaveria trinervia (Spreng.) C. Mohr
P + NApr, May, June, July, Dec and Jan.Wild spread
58.
Helichrysum glumaceum DC.
N + PNov, Dec, Jan, Feb, Mar, Apr and MayWild spread
59.
Lactuca serriola L
P + NJuly, Aug and Sept.Wild spread
60.
Onopordum heteracanthum C. A. Mey
NApr, May and JuneWild spread
61.
Picris asplenioides subsp. asplenioides (=Picris radicata Less.)
N + PMay and JuneWild spread
62.
Pluchea dioscorides (L.) DC.
N + ProNov, Dec, Jan, Feb, Mar and AprWild spread
63.
Psiadia punctulata Vatke
N + PNov, Dec, Jan, Feb and Mar.Wild spread
64.
Pulicaria undulata (L.) C.A.Mey.
N + PDec, Jan, Feb, Mar, Apr, May and JuneWild spread
65.
Pulicaria petiolaris Jaub. & Spach
P + NDec, Jan and FebWild spread
66.
Pulicaria schimperi DC
P + NDec, Jan and FebWild spread
67.
Ramaliella musilii (Velen.) Zaika, Sukhor. & N.Kilian (=Scorzonera musilii Velen)
N + PMar, Apr, May and JuneWild spread
68.
Sonchus oleraceus L.
PJan, Feb, Mar, Apr, May and JuneWild spread
69.
Osteospermum vaillantii (Decne.) Norl
N + PJan, Feb, Mar, Apr and MayWild spread
70.
Tagetes minuta L.
N + PApr and MayWild spread
71.
Verbesina encelioides (Cav.) Benth. & Hook.f. ex A.Gray
N + PJan, Feb, Mar, Apr and MayWild spread
72.
Orbivestus cinerascens (Sch.Bip.) H.Rob. (=Vernonia cinerascens Sch.Bip.)
N + PAug and Sept.Wild spread
73.
Veronica anagallis-aquatica L.
N + PDec, Jan and FebWild spread
74.
Cordia africana Lam.
Boraginaceae Juss.NJun, July and AugWild spread
75.
Cordia monoica Roxb.
NJun, July and AugWild spread
76.
Echium rauwolfii Delile
N + PJan, Feb, Mar, Apr and MayWild spread
77.
Echium sp
N + PJan, Feb and MarWild spread
78.
Ehretia obtusifolia Hochst. ex A.DC
NAug, Sept and OctWild spread
79.
Heliotropium arbainense Fresen
N + PJan, Feb, Mar, Apr, Aug, Sept and OctWild spread
80.
Heliotropium longiflorum (A.DC.) Jaub. & Spach
N + PJuly, Aug, Sept and OctWild spread
81.
Heliotropium pterocarpum (DC.) Hochst. & Steud. ex Bunge
NAug, Sept, Oct, Nov, Dec, Jan, Feb and MarWild spread
82.
Coincya tournefortii (Gouan) Alcaraz, T.E.Díaz, Rivas Mart. & Sánchez-Gómez (=Brassica tournefortii Gouan)
Brassicaceae BurnettP + NFeb, Mar and AprWild spread
83.
Crambe orientalis L.
N + PNov, Dec, Jan and FebWild spread
84.
Eruca vesicaria (L.) Cav. (=Eruca sativa Mill.)
N + PNov, Dec, Jan, Feb, Mar and Apr.Wild spread
85.
Nasturtium officinale W.T.Aiton
PNov, Dec, Jan, Feb, and MarWild spread
86.
Rapistrum rugosum (L.) All.
PAug, Sept, Oct. Nov and DecWild spread
87.
Sinapis alba L.
N + PDec, Jan, Feb and MarWild spread
88.
Sisymbrium irio L.
P + NJan, Feb and MarWild spread
89.
Sisymbrium orientale L
P + NJan, Feb and MarWild spread
90.
Commiphora gileadensis (L.) C.Chr.
Burseraceae KunthPJan, Feb, Mar and AprRegional endemic
91.
Commiphora kataf (Forssk.) Engl.
PNov, Dec, Jan and FebRegional endemic
92.
Commiphora kua (R.Br. ex Royle) Vollesen
PNov, Dec, Jan and FebRegional endemic
93.
Commiphora myrrha (T.Nees) Engl.
POct, Nov and DecRegional endemic
94.
Opuntia ficus-indica (L.) Mill
Cactaceae JussN + PMay and JuneWild spread
95.
Cylindropuntia imbricata subsp. rosea (DC.) M.A.Baker
N + PMay and JuneWild spread
96.
Celtis africana Burm.f.
Cannabaceae MartinovPFeb and MarWild spread
97.
Boscia integrifolia J.St.-Hil.
Capparaceae JussNAug and SeptWild spread
98.
Capparis cartilaginea Decne
PApr, May, June, July and AugWild spread
99.
Capparis decidua (Forssk.) Edgew
POct and NovWild spread
100.
Capparis tomentosa Lam
PMar and AprWild spread
101.
Maerua crassifolia Forssk
P + NJuly and AugWild spread
102.
Maerua oblongifolia (Forssk.) A.Rich
P + NMay, June and JulyWild spread
103.
Polycarpaea repens (Forssk.) Asch. & Schweinf
Caryophyllaceae JussPJan, Feb and MarWild spread
104.
Gymnosporia parviflora (Vahl) Chiov. (=Maytenus parviflora (Vahl) Sebsebe)
Celastraceae R.Br.N + PSept, Oct and NovWild spread
105.
Cleome pallida Kotschy (=Dipterygium glaucum Decne.)
Cleomaceae Airy ShawP + NMar and AprWild spread
106.
Cleome ramosissima Parl. ex Webb
P + NNov and DecRegional endemic
107.
Cleome gynandra L.
NAug, Sept and OctWild spread
108.
Combretum pisoniiflorum (Klotzsch) Engl. (=Combretum molle R.Br. ex G.Don)
Combretaceae R.BrP + NMar, Apr and MayWild spread
109.
Combretum aculeatum Vent
N + PFeb and Mar and AprWild spread
110.
Commelina albescens Hassk
Commelinaceae MirbPJan, Jan, Fab and MarWild spread
111.
Commelina Africana L.
PJan, Jan, Fab and MarWild spread
112.
Commelina africana subsp. Africana
PJan, Jan, Fab and MarWild spread
113.
Convolvulus arvensis L.
Convolvulaceae JussNJune, July, Aug and Sept.Wild spread
114.
Convolvulus asyrensis Kotschy
NJan, Feb and MarEndemic
115.
Ipomoea obscura (L.) Ker Gawl.
NOct and NovWild spread
116.
Crassula schimperi Fisch. & C.A.Mey
Crassulaceae J.St.-Hil.PJan and FebWild spread
117.
Citrullus colocynthis (L.) Schrad
Cucurbitaceae JussPJan, Feb, Jun and OctWild spread
118.
Juniperus procera Hochst. ex Endl
Cupressaceae GrayProResin secretion Jan, Feb, Mar and Apr.Regional Endemic
119.
Diospyros mespiliformis Hochst. ex A.DC.
Ebenaceae GürkeNApr, Aug and SeptWild spread
120.
Euclea racemosa L
N + POct and NovWild spread
121.
Erica arborea L.
Ericaceae DurandeN + PMar, Apr and MayWild spread
122.
Euphorbia balbisii Boiss. (=Euphorbia serpens Balb. ex Boiss.)
Euphorbiaceae JussNDec, Jan, Feb and MarWild spread
123.
Euphorbia cuneata Vahl
NJuly and AugWild spread
124.
Euphorbia falcata L.
NDec and JanWild spread
125.
Euphorbia inarticulata Schweinf
NDec, Nov, Jan, Feb, Mar and AprNear-endemic
126.
Euphorbia parciramulosa Schweinf.
NMar and Aprendemic
127.
Euphorbia schimperiana var. schimperiana Scheele
NJuly and AugWild spread
128.
Jatropha glauca Vahl
NAug, Sept and Oct.Region Endemic
129.
Jatropha pelargoniifolia Courbon
NMar and AprRegion Endemic
130.
Ricinus communis L.
NJan, Feb, Mar, Apr, May and JuneRegion Endemic
131.
Argyrolobium arabicum (Decne.) Jaub. & Spach
Fabaceae LindlNDec, Jan, Feb and Mar.Wild spread
132.
Astragalus atropilosulus subsp. atropilosulus (=Astragalus atropilosulus subsp. abyssinicus (Hochst.)) Gillett
PDec, Jan, Feb, Mar, Apr and MayRegion Endemic
133.
Astragalus vogelii subsp. fatmensis (Hochst. ex Chiov.) Maire (=Astragalus fatmensis Hochst. ex Chiov)
PDec, Jan, Feb and MarWild spread
134.
Crotalaria emarginella Vatke
PJan Feb, Mar, Apr, Sept and Oct.Region Endemic
135.
Delonix elata (L.) Gamble
PJan, Feb, Mar and AprRegion Endemic
136.
Dorycnopsis abyssinica (A.Rich.) V.N.Tikhom. & D.D.Sokoloff (=Vermifrux abyssinica (A.Rich.) J.B.Gillett)
P + NJan, Feb and MarWild spread
137.
Faidherbia albida (Delile) A.Chev
PApr, May, Sept and OctWild spread
138.
Lotus quinatus (Forssk.) Gillent
NJan, Feb, Mar, Apr and MayWild spread
139.
Medicago laciniata (L.) Mill
NNov, Dec, Jan, Feb and Mar.Wild spread
140.
Medicago minima (L.) Bartal
NMar and AprWild spread
141.
Medicago polymorpha L
NDec, Jan, Feb and MarWild spread
142.
Melilotus indicus (L.) All.
NDec, Jan, Feb and MarWild spread
143.
Onobrychis ptolemaica (Delile) DC.
NJan, Feb, Mar and AprWild spread
144.
Rhynchosia malacophylla (Spreng.)
NJuly and AugWild spread
145.
Senegalia asak (Forssk.) Kyal. & Boatwr. (=Acacia asak (Forssk.) Willd
N + PApr, May, June, July, Aug and Sept.Wild spread
146.
Senegalia hamulosa (Benth.) Boatwr. (=Acacia hamulosa Benth.)
N + PApr, May, June, July and AugWild spread
147.
Senna alexandrina Mill
PApr, May and NovWild spread
148.
Senna italica Mill
PApr, May and NovWild spread
149.
Tephrosia nubica (Boiss.) Baker
NNov and Dec.Wild spread
150.
Trifolium arvense L.
N + PMar, Apr and MayWild spread
151.
Trifolium campestre Schreb
N + PMar and Apr.Wild spread
152.
Trifolium retusum L.
NMar, Apr and MayWild spread
153.
Vachellia etbaica (Schweinf.) Kyal. & Boatwr. (=Acacia etbaica Schweinf)
N + PApr, May, June, July, Aug and sept.Wild spread
154.
Vachellia flava (Forssk.) Kyal. & Boatwr. (=Acacia ehrenbergiana Heyne)
N + PFeb, Mar, Apr, May, June, July and Aug.Wild spread
155.
Vachellia gerrardii (Benth.) P.J.H.Hurter (=Acacia gerrardii Benth)
NMay, June, July, Aug, sept and Oct.Wild spread
156.
Vachellia johnwoodii (Boulos) Ragup.، Seigler، Ebinger & Maslin (=Acacia johnwoodii Boulos)
N + PJuly, Aug, sept, Oct, Nov, Dec, Jan and FebWild spread
157.
Vachellia oerfota (Forssk.) Kyal. & Boatwr = (Acacia oerfota)
Nsept and Oct.Wild spread
158.
Vachellia origena (Hunde) Kyal. & Boatwr. (=Acacia origena Hunde)
NApr, May and JuneWild spread
159.
Vachellia tortilis (Forssk.) Galasso & Banfi (=Acacia tortilis (Forssk.) Heyne)
NJan, Feb, Mar, Apr, Oct, Nov and Dec.Wild spread
160.
Erodium cicutarium (L.) L’Hér
Geraniaceae JussNDec, Jan and FebWild spread
161.
Erodium malacoides (L.) L’Hér
NDec, Jan and FebWild spread
162.
Erodium neuradifolium Delile ex Godr
NDec, Jan and FebWild spread
163.
Geranium molle L.
N + PApr and MayWild spread
164.
Pelargonium multibracteatum Hochst. ex A.Rich.
N + PMay and JuneRegional Endemic
165.
Gladiolus dalenii Van Geel
Iridaceae JussN + PJan, Feb and MarWild spread
166.
Isodon ternifolius (D.Don) Kudô (=Plectranthus ternifolius D.Don)
Lamiaceae MartinovNFeb, Mar, Apr and May and JulyWild spread
167.
Lavandula atriplicifolia Benth
NMay, June, Sept and OctWild spread
168.
Lavandula citriodora A.G.Mill.
NMay, June, Sept, Oct and NovNear-endemic
169.
Lavandula coronopifolia Poir
NDec and JanWild spread
170.
Lavandula dentata L.
NNov, Dec, Jan, Feb, Mar, Apr and MayWild spread
171.
Leucas alba (Forssk.) Sebald
N + PApr, May, July, Aug and Sept.Near-endemic
172.
Leucas glabrata (Vahl) Sm.
NSept, Oct, Nov, Dec, Jan, Feb, Mar, Apr and MayWild spread
173.
Mentha longifolia L.
NOct, Nov, Dec, Mar, Apr and MayWild spread
174.
Micromeria imbricata (Forssk.) C.Chr.
NDec, Nov, Jan, Feb and Mar.Wild spread
175.
Nepeta deflersiana Schweinf. ex Hedge
NJan, Feb, Mar, Apr, May and JuneNear-endemic
176.
Ocimum filamentosum Forssk.
N + PMar, Apr, May and JuneWild spread
177.
Ocimum forskoelei Benth.
N + PJan and JulyWild spread
178.
Otostegia fruticosa (Forssk.) Schweinf. ex Penzig
NJan, Feb, June, Sept, Oct and NovWild spread
179.
Premna resinosa (Hochst.) Schauer
NMar, Apr, May and JuneWild spread
180.
Coleus arabicus Benth. (=Plectranthus asirensis J.R.I.Wood)
NJan, Feb and Mar.Wild spread
181.
Salvia aegyptiaca L.
NApr, May and June.Wild spread
182.
Salvia dianthera Roth (=Meriandra bengalensis (J.Koenig ex Roxb.) Benth.)
NJan, Feb, Mar, Apr and MayWild spread
183.
Salvia merjamie Forssk.
NMar and AprRegional Endemic
184.
Teucrium yemense Deflers
N + PFeb, Mar, Apr and MayRegional Endemic
185.
Lawsonia inermis L.
Lythraceae J.St.-Hil.PNov, Dec and JanWild spread
186.
Corchorus olitorius L.
Malvaceae JussPNov, Dec, Jan and FebWild spread
187.
Grewia erythraea Schweinf
P + NMay and Oct.Wild spread
188.
Grewia tembensis Fresen
P + NApr, May, Sept and Oct.Wild spread
189.
Grewia tenax (Forssk.) Fiori
P + NAug, Sept, Oct and NovWild spread
190.
Grewia trichocarpa Hochst. ex A.Rich.
P + NMay, Sept and OctRegional Endemic
191.
Grewia mollis Juss. (=Grewia velutina Franch.)
P + NAug and Sept.Wild spread
192.
Grewia villosa Willd
P + NSept and OctWild spread
193.
Hibiscus aponeurus Sprague & Hutch
N + PAug, Sept, Oct, Nov and DecRegional Endemic
194.
Hibiscus deflersii Schweinf. ex Cufod
N + PDec, Apr and MayRegional Endemic
195.
Hibiscus micranthus L.f.
N + PApr and Sept.Wild spread
196.
Hibiscus vitifolius L.
PJan and FebWild spread
197.
Malva parviflora L.
PNov and Sept.Wild spread
198.
Triumfetta heterocarpa Sprague & Hutch.
PNov, Dec, Jan and FebWild spread
199.
Glinus lotoides L.
Molluginaceae BartlNDec and JanWild spread
200.
Moringa peregrina (Forssk.) Fiori
Moringaceae MartinovPApr and MayWild spread
201.
Ficus carica L.
Moraceae GaudichProResin secretion Mar, Apr, May and JuneWild spread
202.
Ficus glumosa Delile
ProResin secretion Sept, Oct, Nov and DecWild spread
203.
Ficus ingens (Miq.) Miq
ProResin secretion Oct, Nov, Dec and JanWild spread
204.
Ficus palmata Forssk
ProResin secretion Mar, Apr, May and JuneWild spread
205.
Ficus salicifolia Vahl (=Ficus cordata subsp. salicifolia (Vahl) C.C.Berg)
ProResin secretion Nov, Dec and JanWild spread
206.
Ficus sycomorus L.
ProResin secretion Nov, Dec, Jan and FebWild spread
207.
Ficus vasta Forssk
ProMar, Apr and MayRegional Endemic
208.
Boerhavia elegans Choisy
Nyctaginaceae JussNMay and JuneWild spread
209.
Boerhavia diffusa L.
N + PFeb, Mar and AprWild spread
210.
Ochna inermis (Forssk.) Schweinf
Ochnaceae DC.N + PMar, Apr, May, June, July and Aug.Wild spread
211.
Jasminum grandiflorum L.
Oleaceae Hoffmanns. & LinkNDec and JanWild spread
212.
Olea europaea L.
P + NMay and JuneWild spread
213.
Buchnera hispida Buch.-Ham. ex D.Don
Orobanchaceae VentNSept and OctWild spread
214.
Oxalis corniculata L
Oxalidaceae R.Br.N + PJuly, Aug, Sept, Nov and DecWild spread
215.
Argemone mexicana L.
Papaveraceae JussP + NFeb, Mar and Apr.Wild spread
216.
Argemone ochroleuca Sweet
P + NJan, Feb and Mar.Wild spread
217.
Glaucium corniculatum (L.) Curtis
PFeb and Mar.Wild spread
218.
Papaver decaisnei Hochst. & Steud. ex Elkan
PFeb and MarWild spread
219.
Papaver dubium L.
PFeb and MarWild spread
220.
Papaver laevigatum M.Bieb. (=Papaver dubium subsp. laevigatum (M.Bieb.) Kadereit)
PFeb and MarWild spread
221.
Flueggea virosa (Roxb. ex Willd.) Royle
Phyllanthaceae MartinovPSept and OctWild spread
222.
Anarrhinum forskaohlii (J.F.Gmel.) Cufod
Plantaginaceae JussNJan, Feb, Mar and AprWild spread
223.
Bacopa monnieri (L.) Wettst
PNov and DecWild spread
224.
Plantago afra L.
PFeb and MarWild spread
225.
Plantago albicans L. (=Plantago ciliata Boiss.)
PMar and AprWild spread
226.
Plantago cylindrica Forssk
PFeb and MarWild spread
227.
Plantago lanceolata L.
PMar and AprWild spread
228.
Schweinfurthia pterosperma (A.Rich.) A.Braun
PFeb and MarWild spread
229.
Scoparia dulcis L.
PJan and FebWild spread
230.
Cenchrus ciliaris L.
Poaceae BarnhartPNov, Dec and JanWild spread
231.
Cynodon dactylon (L.) Pers.
PApr, May and JuneWild spread
232.
Polygala abyssinica R.Br. ex Fresen
Polygalaceae Hoffmanns. & LinkPMay and JuneWild spread
233.
Polygala erioptera DC.
PMar and AprWild spread
234.
Polygala sinaica var. glabrescens (Zohary) Boulos (=Polygala negevensis Danin)
PNov, Dec and JanWild spread
235.
Polygala senensis Klotzsch
PAug and SeptRegional Endemic
236.
Rumex nervosus Vahl
Polygonaceae Juss.N + PJan, Feb, Mar and AprWild spread
237.
Portulaca grandiflora Hook
Portulacaceae JussPNov and DecWild spread
238.
Portulaca kermesina N.E.Br.
PNov, Dec and JanWild spread
239.
Portulaca oleracea L.
P + NFeb, May and JuneWild spread
240.
Clematis hirsuta Guill. & Perr
Ranunculaceae JussN + PFeb, May and AprWild spread
241.
Caylusea hexagyna (Forssk.) M.L.Green
Resedaceae MartinovP + NDec, Nov, Jan, Feb, Mar, Apr and MayWild spread
242.
Ochradenus baccatus Delile
P + NApr, May and JuneWild spread
243.
Rhamnus staddo A.Rich
Rhamnaceae JussP + NApr and MayRegional Endemic
244.
Sageretia thea (Osbeck) M.C.Johnst
NJan, July and AugWild spread
245.
Ziziphus mucronata Willd
NSept and OctWild spread
246.
Ziziphus spina-christi (L.) Desf.
NJuly, Aug, Sept and OctWild spread
247.
Rosa abyssinica R.Br. ex Lindl
Rosaceae JussN + PApr and MayWild spread
248.
Rubus creticus Tourn. ex L.
N + PMay, June and JulyWild spread
249.
Pavetta gardeniifolia var. gardeniifolia Hochst. ex A.Rich.(=Pavetta longiflora.)
Rubiaceae JussNMar, Apr, May and JuneWild spread
250.
Psydrax schimperianus (A.Rich.) Bridson
NApr and MayWild spread
251.
Pyrostria phyllanthoidea (Baill.) Bridson
NApr and MayRegional Endemic
252.
Ruta chalepensis L.
Rutaceae JussNJan, Feb, Mar, Apr and MayWild spread
253.
Dodonaea viscosa subsp. angustifolia (L.f.) J.G.West
Sapindaceae JussPJan, Feb and MarWild spread
254.
Mimusops laurifolia (Forssk.) Friis
PJune and JulyRegional Endemic
255.
Buddleja polystachya Fresen
Scrophulariaceae PMar, Apr and MayWild spread
256.
Lycium shawii Roem. & Schult
Solanaceae JussPOct and NovWild spread
257.
Solanum glabratum Dunal
NNov, Dec and JanWild spread
258.
Solanum incanum L.
P + NApr, May, Sept, Oct, Nov, Dec and JanWild spread
259.
Solanum schimperianum Hochst (=Solanum schimperianum subvar. cordifolium Bitter)
P + NSept, Oct, Nov and DecRegional Endemic
260.
Solanum villosum Mill
P+NOct, Nov, Dec, Feb, May and JuneWild spread
261.
Withania somnifera (L.) Dunal
N + PDec, Jan, Feb, May and JuneWild spread
262.
Nuxia oppositifolia (Hochst.) Benth
Stilbaceae KunthNMay, June and Sept.Wild spread
263.
Tamarix aphylla (L.) H.Karst
Tamaricaceae LinkPMay and JuneWild spread
264.
Tamarix nilotica (Ehrenb.) Bunge
PJan, Feb, Sept and OctWild spread
265.
Lantana rugosa Thunb
Verbenaceae J.St.N + PFeb, Mar, Aug and SeptWild spread
266.
Zygophyllum bruguieri (DC.) Christenh. & Byng (=Fagonia bruguieri DC.)
Zygophyllaceae R.Br.NMar, May and JuneWild spread
267.
Zygophyllum indicum (Burm.f.) Christenh. & Byng (=Fagonia indica Burm.f.)
NNov and DecWild spread
268.
Zygophyllum simplex L. (=Tetraena simplex (L.) Beier & Thulin)
NDec and JanWild spread
269.
Tribulus parvispinus C.Presl
N + PApr and MayWild spread
270.
Tribulus terrestris L.
N + PMay, June, Oct and NovWild spread
271.
Tribulus macropterus Boiss
N + PFeb, Mar, Apr, May and JuneWild spread
Table 3. Nectar and Pollen flow during different seasons in Al-Baha region, Southwestern Saudi Arabia.
Table 3. Nectar and Pollen flow during different seasons in Al-Baha region, Southwestern Saudi Arabia.
Source CategoriesNN + PP + NPProN + P + ProTotal
Seasons (Months) No.%No.%No.%No.%No.%No.%
Spring (III, IV, V)54 31.85130.01810.64124.14 2.421.2170
Summer (VI, VII, VIII)3640.42730.3910.11213.522.233.489
Autumn (IX, X, XI)3233.32324.01111.52425.533.133.196
Winter (XII, I, II)5039.13628.1129.424 18.832.332.3128
N (Nectar), P (Pollen), Pro (Propolis).
Table 4. Contingency analysis of flowering honey bee plants by seasons in Al-Baha region, southwestern Saudi Arabia.
Table 4. Contingency analysis of flowering honey bee plants by seasons in Al-Baha region, southwestern Saudi Arabia.
SeasonsYesNoTest
No. (%)No. (%)DFX2-Valuep-Value
Autumn (Fall)
Spring96 (19.32)172 (29.91)
Summer170 (34.21)98 (17.04)
Winter85 (17.10)183 (31.83)374.590.0001
No.: number of species; DF: degree of freedom; Yes: those species flower in the particular season; No: those species do not flower in the particular season.
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Al-Ghamdi, A.A.; Al-Sagheer, N.A. Plant Species as Potential Forage for Honey Bees in the Al-Baha Mountain Region in Southwestern Saudi Arabia. Plants 2023, 12, 1402. https://doi.org/10.3390/plants12061402

AMA Style

Al-Ghamdi AA, Al-Sagheer NA. Plant Species as Potential Forage for Honey Bees in the Al-Baha Mountain Region in Southwestern Saudi Arabia. Plants. 2023; 12(6):1402. https://doi.org/10.3390/plants12061402

Chicago/Turabian Style

Al-Ghamdi, Ahmad A., and Nageeb A. Al-Sagheer. 2023. "Plant Species as Potential Forage for Honey Bees in the Al-Baha Mountain Region in Southwestern Saudi Arabia" Plants 12, no. 6: 1402. https://doi.org/10.3390/plants12061402

APA Style

Al-Ghamdi, A. A., & Al-Sagheer, N. A. (2023). Plant Species as Potential Forage for Honey Bees in the Al-Baha Mountain Region in Southwestern Saudi Arabia. Plants, 12(6), 1402. https://doi.org/10.3390/plants12061402

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