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Making the most of native bees: hedgerow potential in agri-natural landscapes of

Mediterranean climate

Georgia D. PollardA
A
       School of Natural and Built Environments, University of South Australia, Adelaide, Mawson Lakes, 5095, Australia


Corresponding author. Email: georgia.pollard@me.com




Abstract

Although Australia has over 1,500 species of native bee, agriculture depends on the

introduced honeybee, Apis millfera for pollination. Pests and diseases that are likely

to reach Australia are currently decimating honeybee populations worldwide. Native

bees can meet pollination requirements if sufficient support is given. Hedgerows

when managed properly can provide valuable foraging habitat and a shift in

pollination dependency to native bee species is both practical and viable.



Introduction

Pollination is an essential ecosystem service. Honeybees, Apis millfera are the most

important managed pollinator in the world (Southwick and Southwick 1992) and can

enhance agricultural seed production and yield (Moradin and Winston 2006). In

Australia we depend on the introduced honeybee for honey and agricultural

pollination (Dollin et al. 2000). The honeybee is experiencing crisis in other parts of

the world because of pests such as the varroa mite, Varroa destructor, diseases like

Colony Collapse Disorder and insecticide use. Any one of these reaching Australia

will cause problems to industries dependant on honeybees, as in the US and Germany

(Cunningham et al. 2000). A solution entails changes in agricultural practise to

include use of native bees. Native bees require supportive foraging habitat, such as


                                                                                                                          1	
  
	
  
hedgerows. In this review, ‘hedgerow‘ is defined as, “a linear vegetation feature,

including field margins, windbreaks and roadsides” and ‘agri-natural landscapes’ as,

“land consisting of agricultural use and natural vegetation.” The potential for use and

management of native bees in agri-natural landscapes such as the Yorke Peninsula is

examined.



Native bee requirements

Australia has over 1,500 species of native bee, which have adapted to every type of

habitat available (Dollin et al. 2000). In South Australia there are many species of

mining bee, mainly Colletines and Halictines (Edwards 2010). All bees require

sources of pollen, nectar, floral oils, nest sites and nesting material to live (Westrich

1996; Hannon and Sisk 2009). Bee habitats can be separated into partial habitats of

either foraging or nesting habitat. They can be separate areas within a larger

landscape (Westrich 1996; Kleijn et al. 2006; Hopwood 2008; Smallbone and

Spooner 2008; Hannon and Sisk 2009).

        A study from Western USA found that the understorey vegetation is most

important when assessing whether the foraging habitat is resource rich or poor

(Hannon and Sisk 2009). Native plants are beneficial and tend to attract higher

abundance and variety of bee species (Kremen et al. 2002; Hopwood 2008; Edwards

2010), but flowering crops also make suitable foraging habitat (Heard 1999) when

insecticides do not affect bee numbers (Steffan-Dewenter and Tsharntke 1999;

Kremen et al. 2002; Moradin and Winston 2006; Hannon and Sisk 2009). The mining

species of native bee common to South Australia require nest sites that are open to the

sun but somewhat sheltered with vegetation cover not exceeding 50% (Edwards

2010). Both kinds of partial habitats can be provided in agri-natural landscapes under


                                                                                            2	
  
	
  
the right circumstances (Westrich 1996; Kremen et al. 2002; Kleijn et al. 2006;

Moradin and Winston 2006; Hopwood 2008; Hannon and Sisk 2009; Edwards 2010).



Hedgerow value

When comparing hedgerow value to remnant native vegetation there is some debate

(Westrich 1996). Although remnant vegetation may provide a wider variety of

resources, the avaliability of such vegetation must be considered. Ninety four percent

of Yorke Peninsulas native vegetation had been clear by 1989 (Malcolm and Wigan

1989). For mining bees, hedgerows do tend to be more heavily vegetated than is

suitable for nest sites but hedgerows can be valuable foraging habitat if the

understorey is rich in flowering shrubs and native ground cover (Westrich 1996;

Kremen et al. 2002; Hopwood 2008; Edwards 2010). Such hedgerows could link the

remnants left and help reduce the chance of regional extinction of surviving native

bee species (Westrich 1996). Hedgerows regulate surrounding air temperature, soil

water content and organic carbon (Bunce et al. 2009) as well as being beneficial to

other species such as birds and small mammals (Campi and MacNally 2001; Gelling

et al. 2007).



Viability of agricultural pollination by native bees

Bees provide pollination services in both natural and agricultural environments

(Heard 1999; Steffan-Dewenter and Tscharntke 1999; Kremen et al. 2002; Kleijn et

al. 2006; Moradin and Winston 2006; Hannon and Sisk 2009; Edwards 2010) and

enhance seed production and yield (Steffan-Dewwenter and Tsharntke 1999; Kremen

et al. 2002; Moradin and Winston 2006). The distance bees can fly for pollen

collection is positively correlated with body size (Steffan-Dewwenter and Tsharntke


                                                                                      3	
  
	
  
1999) unless nectar is available along the way (Westrich 1996). Native mining bees

have been reported travelling an average of 500 m for pollen, although one hive was

spotted in the centre of a canola field in South Australia (Edwards 2010). Having 30

% of uncultivated land within 750 m from field edges maximized crop yield and

profit (Moradin and Winston 2006).

         Full pollination requirements were met by just native bees on organically

managed farms near natural habitat in California, but they were insufficient on non-

organic farms, with extensive use of insecticides and lack of supplementary habitat

detrimental to the bees (Moradin and Winston 2006). Although the main crops grown

on the Yorke Peninsula are wheat and barley and so wind pollinated, other crops

grown there including canola, peas, lentils, beans, sunflowers and tomatoes would

benefit from bee pollination (Heard 1999; Steffan-Dewwenter and Tsharntke 1999;

Cunningham et al. 2000; Kremen et al. 2002; Moradin and Winston 2006).



Practical support of native bees in agri-natural landscapes

Recommendations on how to provide nesting habitat for native bees have been made

in a study from England (Kleijn et al. 2006), by widening field edges to 6 m or by

identifying small linear areas to be set aside from production for at least three years

with at least one such area per square kilometre (Edwards 2010). This land is suitable

as nesting habitat for mining bees.

         Supplementary foraging habitat needs to be available when crops are not

flowering (Kremen et al. 2002). Managed hedgerows along field edges and roadsides

close to fields, with understoreys of native shrubs and ground flora would provide

rich foraging habitat (Kremen et al. 2002; Hannon and Sisk 2009; Edwards 2010).

Fields retired from crop production but still being used as grazing land result in poor


                                                                                          4	
  
	
  
foraging habitat (Hannon and Sisk 2009) but I did not find studies on the impacts of

grazing on nest habitats of native mining bees.

         Extensive use of insecticides on fields adversely affects visiting bees.

Lessening their use and enhancing hedgerows can also increase abundance of other

beneficial insects (Kremen et al. 2002). To gain the full benefits from native bee

pollinators, the enhancement of foraging habitat and creation of nest habitats, as well

as minimised use of insecticides are recommended (Kremen et al. 2002; Hannon and

Sisk 2009; Edwards 2010).



Conclusion

Pests and diseases such as Colony Collapse Disorder or the varroa mite, reaching

Australia, are likely to have adverse effects our honeybee populations. A shift in

reliance on species of native bee for agricultural pollination is suggested as both

possible and viable (Cunningham et al. 2000) because bees have the potential to

compliment or meet the full pollination requirements of agricultural crops (Kremen et

al. 2002). Agriculture on the Yorke Peninsula can mitigate the risk of agricultural

pollination loss by changes to agricultural practise to encourage growth of native bee

species by implementing nesting and foraging habitats within hedgerows and field

edges.




References


                                                                                          5	
  
	
  
Bunce, R. G. H., Lassaletta, L., McCollin, D., and Sanchez, I. A. (2009). The effect of

       hedgerow loss on microclimate in the Mediterranean region: an investigation in

       Central Spain. Agroforestry Systems 78, 13-25. doi:10.1007/s10457-099-9224-z

Campi, M. J., and MacNally, R. (2001). Birds on edge: avian assemblages along

       forest-agricultural boundaries of central Victoria, Australia. Animal Conservation

       4, 121-132.

Cunningham, S. A., FitzGibbon, F., and Heard, T. A. (2000) The future of pollinators

       for Australian agriculture. Australian Journal of Agricultural Research 53, 893-

       900.

Dollin, A., Batley, M., Robinson, M., and Faulkner, B. (2000). Native bees of the

       Sydney region. Australian Native Bee Research Centre.

       http://www.aussiebee.com.au/fieldguide.html Accessed; April 2nd 2011.

Gelling, M., MacDonald, D. W., and Mathews, F. (2007). Are hedgerows the route to

       increased farmland small mammal density? Use of hedgerows in British pastoral

       habitats. Landscape Ecology 22, 1019-1032.

Edwards, M. (2010). Draft report – Assessment of native pollinators of crops in South

       Australia. (NRM: South Australia.)

Hannon, L. E., and Sisk, T. D. (2009). Hedgerows in an agri-cultural landscape:

       Potential habitat value for native bees. Biological Conservation 142, 2140-2154.

Heard, T. A. (1999). The role of stingless bees in crop pollination. Annual Review of

       Entomology 44, 186-206.

Hopwood, L. J. (2008). The contribution of roadside grassland restorations to native

       bee conservation. Biological Conservation 141, 2632-2640.




                                                                                          6	
  
	
  
Kleijn, D., Marshall, E. J. P., and West, T. M. (2006). Impacts of an agri-environment

       field margin prescription on the flora and fauna of arable farmland in different

       landscapes. Agriculture, Ecosystems & Environment 113, 36-44.

Kremen, C., Thorp, R. W., and Williams, N. M. (2002). Crop pollination from native

       bees at risk from agricultural intensification. Proceedings of the National

       Academy of Sciences of the United States of America 99, 16812-16816.

Malcolm, I., and Wigan, A. (1989). Report to Yorke Peninsula roadside vegetation

       steering group on roadside management plans for Yorke Peninsula.

Morandin, L. A., and Winston, M. L. (2006). Pollinators provide economic incentive

       to preserve natural land in agroecosystems. Agriculture, Ecosystems &

       Environment 116, 289-292.

Smallbone, L., and Spooner, P. G. (2008). Effects of road age on the structure of

       roadside vegetation in south-eastern Australia. Agriculture, Ecosystems &

       Environment 129, 57-64.

Steffan-Dewenter, I., and Tscharntke, T. (1999). Effects of habitat isolation on

       pollinator communities and seed set. Oecologia 121, 432-440.

Westrich, P. (1996). Habitat requirements of central European bees and the problems

       of partial habitats. The conservation of Bees 1-6.




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Native bees' hedgerow potential in agri-natural Mediterranean landscapes

  • 1. Making the most of native bees: hedgerow potential in agri-natural landscapes of Mediterranean climate Georgia D. PollardA A School of Natural and Built Environments, University of South Australia, Adelaide, Mawson Lakes, 5095, Australia Corresponding author. Email: georgia.pollard@me.com Abstract Although Australia has over 1,500 species of native bee, agriculture depends on the introduced honeybee, Apis millfera for pollination. Pests and diseases that are likely to reach Australia are currently decimating honeybee populations worldwide. Native bees can meet pollination requirements if sufficient support is given. Hedgerows when managed properly can provide valuable foraging habitat and a shift in pollination dependency to native bee species is both practical and viable. Introduction Pollination is an essential ecosystem service. Honeybees, Apis millfera are the most important managed pollinator in the world (Southwick and Southwick 1992) and can enhance agricultural seed production and yield (Moradin and Winston 2006). In Australia we depend on the introduced honeybee for honey and agricultural pollination (Dollin et al. 2000). The honeybee is experiencing crisis in other parts of the world because of pests such as the varroa mite, Varroa destructor, diseases like Colony Collapse Disorder and insecticide use. Any one of these reaching Australia will cause problems to industries dependant on honeybees, as in the US and Germany (Cunningham et al. 2000). A solution entails changes in agricultural practise to include use of native bees. Native bees require supportive foraging habitat, such as 1    
  • 2. hedgerows. In this review, ‘hedgerow‘ is defined as, “a linear vegetation feature, including field margins, windbreaks and roadsides” and ‘agri-natural landscapes’ as, “land consisting of agricultural use and natural vegetation.” The potential for use and management of native bees in agri-natural landscapes such as the Yorke Peninsula is examined. Native bee requirements Australia has over 1,500 species of native bee, which have adapted to every type of habitat available (Dollin et al. 2000). In South Australia there are many species of mining bee, mainly Colletines and Halictines (Edwards 2010). All bees require sources of pollen, nectar, floral oils, nest sites and nesting material to live (Westrich 1996; Hannon and Sisk 2009). Bee habitats can be separated into partial habitats of either foraging or nesting habitat. They can be separate areas within a larger landscape (Westrich 1996; Kleijn et al. 2006; Hopwood 2008; Smallbone and Spooner 2008; Hannon and Sisk 2009). A study from Western USA found that the understorey vegetation is most important when assessing whether the foraging habitat is resource rich or poor (Hannon and Sisk 2009). Native plants are beneficial and tend to attract higher abundance and variety of bee species (Kremen et al. 2002; Hopwood 2008; Edwards 2010), but flowering crops also make suitable foraging habitat (Heard 1999) when insecticides do not affect bee numbers (Steffan-Dewenter and Tsharntke 1999; Kremen et al. 2002; Moradin and Winston 2006; Hannon and Sisk 2009). The mining species of native bee common to South Australia require nest sites that are open to the sun but somewhat sheltered with vegetation cover not exceeding 50% (Edwards 2010). Both kinds of partial habitats can be provided in agri-natural landscapes under 2    
  • 3. the right circumstances (Westrich 1996; Kremen et al. 2002; Kleijn et al. 2006; Moradin and Winston 2006; Hopwood 2008; Hannon and Sisk 2009; Edwards 2010). Hedgerow value When comparing hedgerow value to remnant native vegetation there is some debate (Westrich 1996). Although remnant vegetation may provide a wider variety of resources, the avaliability of such vegetation must be considered. Ninety four percent of Yorke Peninsulas native vegetation had been clear by 1989 (Malcolm and Wigan 1989). For mining bees, hedgerows do tend to be more heavily vegetated than is suitable for nest sites but hedgerows can be valuable foraging habitat if the understorey is rich in flowering shrubs and native ground cover (Westrich 1996; Kremen et al. 2002; Hopwood 2008; Edwards 2010). Such hedgerows could link the remnants left and help reduce the chance of regional extinction of surviving native bee species (Westrich 1996). Hedgerows regulate surrounding air temperature, soil water content and organic carbon (Bunce et al. 2009) as well as being beneficial to other species such as birds and small mammals (Campi and MacNally 2001; Gelling et al. 2007). Viability of agricultural pollination by native bees Bees provide pollination services in both natural and agricultural environments (Heard 1999; Steffan-Dewenter and Tscharntke 1999; Kremen et al. 2002; Kleijn et al. 2006; Moradin and Winston 2006; Hannon and Sisk 2009; Edwards 2010) and enhance seed production and yield (Steffan-Dewwenter and Tsharntke 1999; Kremen et al. 2002; Moradin and Winston 2006). The distance bees can fly for pollen collection is positively correlated with body size (Steffan-Dewwenter and Tsharntke 3    
  • 4. 1999) unless nectar is available along the way (Westrich 1996). Native mining bees have been reported travelling an average of 500 m for pollen, although one hive was spotted in the centre of a canola field in South Australia (Edwards 2010). Having 30 % of uncultivated land within 750 m from field edges maximized crop yield and profit (Moradin and Winston 2006). Full pollination requirements were met by just native bees on organically managed farms near natural habitat in California, but they were insufficient on non- organic farms, with extensive use of insecticides and lack of supplementary habitat detrimental to the bees (Moradin and Winston 2006). Although the main crops grown on the Yorke Peninsula are wheat and barley and so wind pollinated, other crops grown there including canola, peas, lentils, beans, sunflowers and tomatoes would benefit from bee pollination (Heard 1999; Steffan-Dewwenter and Tsharntke 1999; Cunningham et al. 2000; Kremen et al. 2002; Moradin and Winston 2006). Practical support of native bees in agri-natural landscapes Recommendations on how to provide nesting habitat for native bees have been made in a study from England (Kleijn et al. 2006), by widening field edges to 6 m or by identifying small linear areas to be set aside from production for at least three years with at least one such area per square kilometre (Edwards 2010). This land is suitable as nesting habitat for mining bees. Supplementary foraging habitat needs to be available when crops are not flowering (Kremen et al. 2002). Managed hedgerows along field edges and roadsides close to fields, with understoreys of native shrubs and ground flora would provide rich foraging habitat (Kremen et al. 2002; Hannon and Sisk 2009; Edwards 2010). Fields retired from crop production but still being used as grazing land result in poor 4    
  • 5. foraging habitat (Hannon and Sisk 2009) but I did not find studies on the impacts of grazing on nest habitats of native mining bees. Extensive use of insecticides on fields adversely affects visiting bees. Lessening their use and enhancing hedgerows can also increase abundance of other beneficial insects (Kremen et al. 2002). To gain the full benefits from native bee pollinators, the enhancement of foraging habitat and creation of nest habitats, as well as minimised use of insecticides are recommended (Kremen et al. 2002; Hannon and Sisk 2009; Edwards 2010). Conclusion Pests and diseases such as Colony Collapse Disorder or the varroa mite, reaching Australia, are likely to have adverse effects our honeybee populations. A shift in reliance on species of native bee for agricultural pollination is suggested as both possible and viable (Cunningham et al. 2000) because bees have the potential to compliment or meet the full pollination requirements of agricultural crops (Kremen et al. 2002). Agriculture on the Yorke Peninsula can mitigate the risk of agricultural pollination loss by changes to agricultural practise to encourage growth of native bee species by implementing nesting and foraging habitats within hedgerows and field edges. References 5    
  • 6. Bunce, R. G. H., Lassaletta, L., McCollin, D., and Sanchez, I. A. (2009). The effect of hedgerow loss on microclimate in the Mediterranean region: an investigation in Central Spain. Agroforestry Systems 78, 13-25. doi:10.1007/s10457-099-9224-z Campi, M. J., and MacNally, R. (2001). Birds on edge: avian assemblages along forest-agricultural boundaries of central Victoria, Australia. Animal Conservation 4, 121-132. Cunningham, S. A., FitzGibbon, F., and Heard, T. A. (2000) The future of pollinators for Australian agriculture. Australian Journal of Agricultural Research 53, 893- 900. Dollin, A., Batley, M., Robinson, M., and Faulkner, B. (2000). Native bees of the Sydney region. Australian Native Bee Research Centre. http://www.aussiebee.com.au/fieldguide.html Accessed; April 2nd 2011. Gelling, M., MacDonald, D. W., and Mathews, F. (2007). Are hedgerows the route to increased farmland small mammal density? Use of hedgerows in British pastoral habitats. Landscape Ecology 22, 1019-1032. Edwards, M. (2010). Draft report – Assessment of native pollinators of crops in South Australia. (NRM: South Australia.) Hannon, L. E., and Sisk, T. D. (2009). Hedgerows in an agri-cultural landscape: Potential habitat value for native bees. Biological Conservation 142, 2140-2154. Heard, T. A. (1999). The role of stingless bees in crop pollination. Annual Review of Entomology 44, 186-206. Hopwood, L. J. (2008). The contribution of roadside grassland restorations to native bee conservation. Biological Conservation 141, 2632-2640. 6    
  • 7. Kleijn, D., Marshall, E. J. P., and West, T. M. (2006). Impacts of an agri-environment field margin prescription on the flora and fauna of arable farmland in different landscapes. Agriculture, Ecosystems & Environment 113, 36-44. Kremen, C., Thorp, R. W., and Williams, N. M. (2002). Crop pollination from native bees at risk from agricultural intensification. Proceedings of the National Academy of Sciences of the United States of America 99, 16812-16816. Malcolm, I., and Wigan, A. (1989). Report to Yorke Peninsula roadside vegetation steering group on roadside management plans for Yorke Peninsula. Morandin, L. A., and Winston, M. L. (2006). Pollinators provide economic incentive to preserve natural land in agroecosystems. Agriculture, Ecosystems & Environment 116, 289-292. Smallbone, L., and Spooner, P. G. (2008). Effects of road age on the structure of roadside vegetation in south-eastern Australia. Agriculture, Ecosystems & Environment 129, 57-64. Steffan-Dewenter, I., and Tscharntke, T. (1999). Effects of habitat isolation on pollinator communities and seed set. Oecologia 121, 432-440. Westrich, P. (1996). Habitat requirements of central European bees and the problems of partial habitats. The conservation of Bees 1-6. 7