1
FARMSCAPING:HEDGEROWAND ROADSIDE
PLANTINGS
FOR BIOINTENSIVE PEST MANAGEMENT
Robert L.
Bugg
InformationGroup
Sustainable
Agriculture Research
and
Education Program
University
of
California
Davis,
CA 95616-8533
John
H.
Anderson
Yolo
County
Resource
Conservation
District
221 West Court StreetNo. 5
ABSTRACT
Farmscaping is the conscious and integrated modificationof agricultural settings,em¬
phasizing management of field margins,hedgerows, windbreaks, and specific vegetation planted along roadsides, ditches, and adjoiningwildlands. The ultimate aim of farmscaping is
toachieve moresustainable farmingsystems. Biologically-intensiveorbiointensive pestman¬
agementrelies primarilyonbiological and cultural controls and host plant resistance. Taken together, these could be thoughtof as "agroecosystem resistance" to pests. Hedgerows and
otherborderplantings can have important impacts on biointensive integrated pest manage¬
ment;properly designed and managed hedgerows and vegetationally-diverse field borders can
assist inboth biological and cultural control of arthropod pests of agriculture. Untilnow, the bulk of the researchonthissubject has been conductedinEngland andEurope. Most priorstudies
sufferfrom lackoftruereplication and insufficient spatial scale. Moreover, in the vastmajor¬
ity ofcases, the hedgerows employed have notbeenplanned with arthropods in mind. Based
on ourmany yearsof practical and research experience, we have developed a design fora
bio-diversehedgerow comprising native and introduced shrubs, perennialgrasses,and herbaceous perennial and annual broadleafplants known to attract and sustain beneficial arthropods and other desirable wildlife. The estimated costof establishment per 1/2-mile strip is $1,378.00.
Roadside plantings ofnative perennialgrasses and associatedspecies have been usedin Iowa and other midwesternstates tosuppress weeds, reduce the need for herbiciding and other
maintenance tools, and restore wildlife. In California, conventional managementof agricul¬
tural roadsides leads todominationby noxious weeds. Availability of seed forvarious native grasses is increasing,asis public interest in their restoration. Agricultural roadsides typically contain severaltopographiczones orniches withvaryingenvironmental conditionsand man¬
agementrequirements. Growth form, height, and environmentaloptima and tolerances of the various speciesdictate the niches towhich theymaybe assigned. Complexes ofnativegrasses
can be established using either herbicide-intensive ornon-herbicidal techniques, which are summarized here. Once the grasses areestablished, herbicidesareseldomneeded.
Farmscaping is the conscious and integrated modification ofagricultural settings, em¬
phasizing management of field margins, hedgerows, windbreaks, and specific vegetation
planted alongroadsides, ditches,and adjoining wildlands. Theproximal goals of farmscaping
maybe toprovidehabitat for wildlife, enhance the esthetics of the farm, provide natural
weed controlthrough competition, andestablish arthropod pestcontrol through enhancement
of naturalenemyactivity. Plants maybeemployed that have specialentomological associa¬ tions. The ultimate aim of farmscaping is to achieve more sustainable farming systems. Biointensive pest managementrelies primarilyon biological and cultural controlsand host plant resistance (Frisbie and Smith, 1989). Taken together, these could be thought of as
"agroecosystem resistance" topests. Hedgerows and other border plantings canhave important impacts on biointensive integrated pest management; properly designed and managed hedgerows and vegetationally-diverse field borders canassist inbothbiological and cultural
control ofarthropod pestsof agriculture. Until now,the bulk ofthe research onthis subject has
been conducted inEngland and Europe. Mostpriorstudies suffer fromlackoftruereplication and insufficientspatial scale. Moreover, inthe vast majority ofcases, the hedgerows employed havenotbeen planned with arthropods inmind. Based on our manyyears of practical and re¬ searchexperience,we havedeveloped a design fora biodiverse hedgerow comprising native andintroducedshrubs, perennialgrasses,and herbaceousperennial and annualbroadleafplants knownto attractand sustainbeneficial arthropods and otherdesirable wildlife.
Roadside plantings of native perennialgrassesand associated species havebeen used in
Iowaand othermidwesternstates tosuppress weeds, reduce the need forherbiciding and other
maintenance tools, and restore wildlife. InCalifornia, conventional managementof agricul¬ turalroadsidesleadstodominationby noxious weeds. Availability ofseed for various native grassesis increasing, as is public interest intheir restoration. Agricultural roadsides typically contain several topographic zones or nicheswith varyingenvironmental conditions and man¬
agementrequirements. Growth form, height, and environmental optima and tolerances of the variousspeciesdictate the niches towhichtheymaybe assigned. Complexes of nativegrasses
canbeestablished using either herbicide-intensive or non-herbicidal techniques, which are
summarized here. Once the grasses areestablished, herbicidesareseldom needed.
Here we will discuss the theory and practiceofhedgerow and roadside plantings in California.
Hedgerows
Thegoldenageof windbreaks in theUrdted States occurred during the 1930s and 1940s,
when, to staveoff wind erosionoftopsoil, the U.S.D.A. Soil Conservation Service (S.C.S.) su¬
pervised the planting of thousands of acres in shelterbelts throughout the Midwest (Van
Eimern, 1967). Yet the broad and tall windbreaks planted by the S.C.S. are merely hedgerows
ofspecial types. The tradition of fostering hedgerows extendsmuch furtherback than the Dust
BowlDays. From time immemorial, hedgerows have played key roles in agriculture. In an¬ cient Europeand the British Isles, hedgerows comprising trees, shrubs,and perennial grasses demarcated propertylines, sheltered farmlands and dwellings from winds, and provided food (game animals, hazelnut, walnut, quince), fodder (acorns), and coppicingtree specieswere re¬
peatedly harvested for bothstructural and fuel wood (Pott, 1989). Moreover, research has re¬
peatedly shown thathedgerows and windbreakscan play importantroles in agriculturalpest
management, both negative and positive (see reviewsby Van Eimern, 1964, Van Emden, 1965, Altieri and Letourneau, 1982).
Perennialvegetation harborssomearthropods that donot venture much into surround¬
ingarable crops("hard-edgespecies" inthe usageof Duelli et al., 1990). For example, Bishop andRiechert (1990)showed that there were few species incommonbetweenthe spiderfauna of
vegetable gardens and that ofa nearby wooded area. Similar results were obtained by Maelfaitand De Keer(1990) in comparingthe spider faunaeof intensively-grazed pastureland and itsborderareas. On the other hand certain"soft-edge species" mayshow increased abun¬
dance inthe arable landsadjoining perennialvegetation,suchashedgerows. Therecanbeneg¬
On the negative side, hedgerows might includeplants thatserve as reservoirs
for
in¬ sect-borne viruses,or as overwintering sites for boll weevil (Slosseretal., 1984), and poplarsand cottonwoods{Populusspp.) arerequired alternatehost for variousrootaphids {Pemphigus
spp.) thatattack beets and lettuce (Davidsonand Lyon, 1986). In
South Africa,
windbreaks of
silky oak {Grevillea robusta)can predisposeforproblems with citrus
thrips
{Scirtothrips
au-rantii) (Grout and Richards, 1990). Windbreakscanalsopredispose forlocalinfestations
of
aphids (Homoptera: Aphididae) and thrips (Thysanoptera; Thripidae) because
the
winged
colonizingforms settle insheltered areas (Lewis,1965a, 1965b).
Onthe positiveside, hedgerowscan harbor importantbeneficial arthropods.
Much of
the relevantresearch has beendone in England and Germany. Ground beetles (Carabidae:Coleoptera)mayoccupyhedgerowsduring winter, thendisperseto adjoining
field
cropswith
the advent ofspring,aswassuggested forPlatynus dorsalts inanunreplicated study ofan inten¬ sively-run farm nearKiel, Germany (Knauerand Stachow, 1987). InEngland,
willows
{Salix
spp.) andanalder {Alnusglutinosa) canharbor predatory truebugs (Hemiptera:
Anthocoridae,
Miridae) that later disperse to orchards and attackcodling moth {Cydia pomonella) or pear
psylla {Psylla pyricola) (Solomon, 1981; Gangeand Llewellyn, 1989). Wind shelter (Lewis,
1965a;Pollard, 1971) and flowers(Bowdenand Dean, 1971) provided byhedgerows canbecru¬
cial to hoverflies (Diptera: Syrphidae) which attack aphid pests ofcrops. Nectarsources in hedgerows arealso importantto parasiticwasps (Van Emden, 1962). In California, perennial
grasses (whichcanbecontained in hedgerows)canprovide sitesforaestival-hibernal diapause
by convergentlady beetle {Hippodamia convergens, Coleoptera: Coccinellidae) (Hagen, 1962,
1974). In South Africa, facultatively-pollinivorous predatory mites {Euseius addoensis a
d-doensis) can be particularlyabundant in citrus (Citrus sinensis) sheltered bywindbreaks of pollen-producing Montereypine (Pinus radiata) (Grout and Richards, 1990). Anagrus epos, a
key parasite ofgrape leafhopper (Erythroneura elegantula) and westerngrape leafhopper
(Erythroneura variabilis) can be harbored onoverwintering eggs of leafhoppers that infest
and Nakata, 1965, 1973) orcultivated plants (e.g., prune leafhopper, Edwardsiana prunicola,
onFrench prunes[Kidoetal., 1984, Pickettetal., 1990]). Frenchprunes are now being planted
alongside Californiavineyardsto enhancebiological control.
Relatively few of thedust-bowl-erashelterbelts and the prehistoric hedgerows re¬ main,duetothe push in the U.S. andin Europe during the 1960s and 70sto plantarablecrops
fencerowtofencerow inorderto"feed the world." Moreover,the trend towards "cleanfarming"
hasentailed indiscriminate herbicidingordisking ofnon-croppedground in ordertoavoidweed
problems. These agriculturaltrendshave led to a greatloss of wild, and often native, vegeta¬ tion thatonce persisted in roadsides and along sloughs. As a result, biodiversity has been
greatly reducedon farmlands. The erosionof foreign markets hassomewhatlessened the col¬
lectiveurge to farm marginal lands, and there is increased awareness of the need topreserve and restore native vegetationand wildlife habitat.
Hedgerows, those valuable and venerable features of the farmscape, can makea major
contributiontowardsimproving this situation. Thishasbeen clearly shownby 10yearsofexpe¬
rienceat Hedgerow Farms (owned byJ.H. Anderson). This site nearWinters, Yolo County,
California) features roadside and hedgerow plantings that bya conservative estimate com¬
prise 14 native and 9 introduced speciesof native perennialgrasses, 9 native and 6 introduced
genera of shrubs, and 6 nativeand 5introduced treespecies. Many ofthese plants have
clear
as¬sociations withbeneficial insects and otherdesirable wildlife. Eighty-eightspecies of birds
have been observed atthe site(Table 1), reflecting the richnessof the habitats provided. We believethat the knowledge developedat HedgerowFarms can now be applied in designing
multispecies hedgerows to attractbeneficial insectsand otherdesirable wildlife, and topro¬ mote biologically-intensiveintegrated pestmanagement.
Californiaagriculture has longused both exoticand native trees for windbreaks, inar¬ eas where windsare a persistentproblem. Coastal and desert areas have especially benefited fromwind shelterprovided by Arizona cypress {Cupressusglabra), athel {Tamarix aphylla), blue gum{Eucalyptusglobulus), Lombardy poplar(Populusnigi-avar. italica), Montereycypress
{Cupressus macrocarpa), and Siberian elm (Ulmus pumila). However, these species wereusu¬
allyemployed in single-species windbreaks, and without regard to their value (or lack thereof) tobeneficial arthropodsor otherdesirable wildlife. These facts have almost cer¬
tainly lessenedanypositive contribution that these windbreaks could have made to biologi¬ cally-intensive integratedpestmanagement. Basedonourlong experience and ourreviewof the
relevantliterature, we conclude thathedgerow and windbreak compositioncanbe improved
and diversified, withaneye to enhancing activityby beneficial arthropods. Anancillary ben¬ efit will beprovision of habitat fora diversity of desirable wildlife species, including am¬ phibians, reptiles, birds, and mammals. Therural landscape will be beautified through addi¬ tionof esthetically-pleasing nativegrasses and shrubs. Webelieve that by such approaches, restorationecology and production agriculturecan dovetail.
Hedgerow Designand Implementation
Ourobjective is toestablish multispecies hedgerows to enhance biological controland desirable wildlifespecies, through provision of shelter, overwinteringhabitat, nesting sites, and food.
Hedgerow Species Composition
Weare testingnew hedgerow designs. Wind isnota majorproblem in Yolo County,so we focus mainlyonshrubs, perennial grasses, and herbaceous perennials and annuals, rather
thanon trees,so as to minimize the shading of adjacent farmlands. Weemphasize a rangeof
native Californianshrubs easilygrownin Yolo County, and knownto attract largenumbers of beneficial insects: blue elderberry {Sambucus caerulea), coyote brush (Baccharis pilularis) (Kido et al., 1981; Bugg and Heidler, 1981), California coffeeberry {Rhatnnus californica),
California lilacs {Ceanothus spp.) (Bugg and Heidler, 1981), California wild buckwheat
{Eriogonum fasciculatum) (Swisher, 1979), holly-leaved cherry (Prunus ilicifolia), toyon
{Heteromeles arbutifolia), and various native willows {Salix spp.). Wealso use exotic species
known forentomological associations: soapbarktree {Quillaja saponaria) (Bugg, 1987), sweet fennel {Foeniculum vulgarevar.dulce) (Maingayetal., 1991), and toothpickammi {Ammi
vis-naga)(Buggand Wilson,1989). See Appendix 1 fora discussionof beneficial
insect/plant
asso¬ciations thatwehave observed. Outofconcern forother wildlife, weinclude the low-mainte¬ nancefruit-producingpersimmon{Diospyroskaki) andpomegranate {Punica granatum), which arebothuseda sourcesof winter foodby native bird species. The understoriesof the hedgerows
will beassigned tomixtures ofnativeCalifornianperennialgrasses: bluewildrye{Elymus glau-cus), California brome {Bromuscarinatus),slenderwheatgrass {Agropyron trachycaulum var.
majus), creepingwildrye {Leymus triticoides), meadowbarley {Hordeum brachyanther um)
and
purpleneedle grass {Stipa pulchra). Our extensive experience shows that
several
of these
grasses haveexcellent seedling vigor, establish rapidly, and will thereaftersuppress
the
inva¬sive annual weeds that dominateconventionally-managed fencerowsandroadsides. Perennial grassesare well knownas the major siteforaestival-hibernal diapause
of
convergentlady bee¬
tle {Hippodamia convergens) (Hagen, 1962, 1974). Once the hedgerow isreasonably weed free,
we willestablish ablend ofinsectaryplants (Harmony Farm Supply, Sebastopol, California).
Together,the hedgerow plants would supplyaccessiblenectar, pollen, and alternate
hosts
and
prey through mostof theyear (see Figures 1 and 2,basedon our ownobservations
and
Munz,1973).
HedgerowDesign andImplementation
Ourapproach is tousestandard farming implements and practicesto
install hedgerow
shrubsamid stands of nativeperennialgrasses. Hedgerowswill be4.58m (180")wide, andwill
eachcomprise 3, 1.52-m (60") beds,separated by irrigation furrows.All beds
will be seeded
tonative grasses;thecentral bed will containshrubsas well. Seedof the
perennial
grasseswill
be
drilled to a depthof 1.27cmduring October. Theouteredgesofeach of theouterbeds will beseeded tocreepingwildrye, becauseourobservationsshow that itcanrecover
rapidly from
in¬advertent diskingorherbicide application. The remainder ofeachof the two outerbeds and the entire central bed will be seeded with appropriate mixesof the other species. Sections will
berandomlyassigned tomixturesofblue wildrye, California brome,meadow
barley, and
slen¬ derwheatgrass (by-weight 1:1:1:1 blend of seeds)orof meadowbarleyandpurple
needlegrass(1:1). Grass isseeded using a Truaxnativegrassseed drill. Shrubsand herbaceous
perennials
(1-year-old liners)will beplanted during NovemberthroughMarch into thecentral bed
amid
a matrixofperennialgrasses.After grasses areestablished (year 2) andweedsaresuppressed, astrip will be disked outand replaced with a seeded commercial insectary mixture, and native Lomatium spp., Perideridia spp.,Achillea borealis, andAsclepiasfascicularis.
Theschedule ofoperationsand approximatecosts for hedgerowestablishmentare pre¬ sented inTable2. Theestimated costof establishment per1/2 -mile (0.8km) strip is $1,378.00.
Roadside Plantings
Roadsideplantings of native perennialgrasses andassociated species have been used in Iowa and othermidwesternstates tosuppress weeds, reduce the needfor herbiciding and other
maintenance tools, and restore wildlife. In California, conventional managementof agricul¬ tural roadsides leads to domination by invasive annual weeds, including wild oat {Avena
fatua), ripgutbrome {Bromus rigidus), and yellow starthistle (Ceiitaurea solstitialis).
Established stands of many native grasses can preemptcolonzation by these weeds. Availability of seed for various nativegrasses is increasing, as is public interest in their
restoration. Agricultural roadsides typically containseveral topographiczones orniches with
varyingenvironmental conditionsand managementrequirements. Growthform,height, and en¬
vironmental optima and tolerancesof the various species dictate the niches in which they are
suitable (Figure 3,adapted from Bugg etal., 1991). Complexes of nativegrasses canbe estab¬
lished using eitherherbicide-intensive ornon-herbicidal techniques, whicharesummarized in
Table 3 (adapted from Buggetal., 1992). Once thegrasses areestablished, herbicides aresel¬
Literature Cited
Altieri, M.A., and D.K. Letourneau. 1982. Vegetationmanagement andbiological control in
agroecosystems. Crop Protection1:405-430.
Bishop, L., and S.E. Riechert. 1990. Spidercolonizationofagroecosystems:Source and mode.
EnvironmentalEntomology 19:1738-1745.
Bowden, J. , and G.J.W. Dean. 1977. The distribution of flying insects in and near a tall
hedgerow. Journal ofApplied Ecology 14:343-354.
Bugg, R.L. 1987. Observations on insects associated with a nectar-bearing Chilean tree, Quillaja saponaria. Pan-Pacific Entomologist 63:60-64.
Bugg, R.L. 1990. Farmscaping with insectaryplants. Permaculture Activist6(2):1, 6-7.
Bugg,R.L. 1991. Farmscaping With InsectaryPlants. Sustainable Agriculture Research and
EducationProgram, UniversityofCalifornia, Davis. Mimeographed handout. 7pp. Bugg, R. L., D. Amme,J.H. Anderson, W.T. Lanini,andW.S.Halverson. 1992. Establishing na¬
tive perennial grasses in California. Sustainable Agriculture News (a newsletterof the University of California Sustainable AgricultureResearch and Education Program, Davis, Calif.)4 (3):In press.
Bugg,R.L., J.H. Anderson,J.W.Menke, K.Crompton, and W.T.Lanini. 1991.
Perennial
grassesas roadside covercrops to reduce agricultural weeds. Components (a newsletter of the
University of CaliforniaSustainable Agriculture Research and Education Program,
Davis,
Calif.) 2(1):14-16.
Bugg, R.L., and N.F.Heidler 1981. Pest Management with California Native
Landscape
Plants. University of California Appropriate Technology Program, Research Leaflet Series #8-78-28. 8 pp.Bugg,R.L.,and L.T. Wilson. 1989. Ammi visnaga (L.) Lamarck (Apiaceae): associated
benefi¬
cial insects and implications for biological control, with emphasis on the bell-pepper agroecosystem. Biological Agricultureand Horticulture6:241-268.Davidson, R.H.,and W.F. Lyon. 1987. Insectpests of farm, garden, and orchard. John Wiley
and Sons, NewYork, N.Y.
Doutt, R.L., and Nakata, J. 1965. Overwintering refuge of Anagrus epos (Hymenoptera:
Mymaridae). Journal ofEconomicEntomology 58:586.
Doutt,R.L., and Nakata, J. 1973. The Rubus leafhopperand its egg parasitoid:an endemic
bi-oticsystemuseful ingrapepestmanagement. EnvironmentalEntomology 2:381-386.
Duelli, P., Studer,M., Marchand, 1., and S.Jakob. 1990. Population movementsofarthropods betweennatural and cultivated areas. Biological Conservation54:193-207.
Frisbie, R.E., andJ.W. Smith, Jr. 1989. Biologically intensive integrated pestmanagement:The Future. Pp. 151-164 in: Menn, J. J., and A.L. Steinhauer, Editors. Progress and Perspectives
for the21stCentury. EntomologicalSociety of America, Centennial National Symposium. Entomological Society of America, Lanham, Maryland.
Gange, A.C.,and M. Llewelyn. 1989. Factors affecting colongisationby theblack-kneed capsid (Blepharidopterus angulatus (Hemiptera: Miridae) from alder windbreaks. Annals of Applied Biologyl14:221-230.
Grout, T.G.,and G.l. Richards. 1990. The influenceof windbreak species on citrus thrips (Thysanoptera:Thripidae) populations and theirdamage to SouthAfrican citrusorchards.
Journal of theEntomological Society of South Africa 53:151-157.
Hagen, K.S. 1962. Biology and ecology of predaceous Coccinellidae. Annual Review of Entomology7:289-326.
Hagen, K.S. 1974. The significanceof predaceous Coccinellidae inbiological and integrated controlofinsects. Entomophaga 7:25-44.
Kido, H., D.L. Flaherty, C.E. Kennett, N.F. McCalley, and D.F.Bosch. 1981. Seeking therea¬
sons fordifferences in orangetortrix infestations. California Agriculture 35(7,8): 27-28.
Kido, H., D.L. Flaherty, D.F. Bosch, and K.A. Valero. 1984. French prunetrees asoverwinter¬ ing sites for the grape leafhopper egg parasite. American Journal of Enology and Viticulture 35:156-160.
Knauer, N., and U. Stachow. 1987. Activitaten vonLaufkafern (Carabidae Col.) in einem
in-tensiv wirtschaftendenAckerbaubetrieb - - ein Beitrag zur Agrarokosystemanalyse. Journal ofAgronomyand Crop Science 159:131-145.
Lewis, T. 1965a. Theeffectsof an artificial windbreakonthe aerial distribution of flying in¬
sects. Annals of Applied Biology55:503-512.
Lewis, T. 1965b. Theeffect ofanartificial windbreakonthedistribution ofaphids ina lettuce crop. Annals of Applied Biology55:513-518.
Maelfait, J.-P.,and R. De Keer. 1990. The borderzoneofanintensively grazed pastureasa cor¬ ridor forspiders Araneae. Biological Conservation 54:223-238.
Maingay, H., R.L. Bugg, R.W. Carlson, and N.A. Davidson. 1991. Predatory and parasitic
wasps(Hymenoptera) feeding at flowersofsweetfennel {Foeniculutn vulgare Miller var.
dulce Battandier &: Trabut, Apiaceae) and spearmint {Mentha spicataL., Lamiaceae) in
Massachusetts. Biological Agriculture and Horticulture 7:363-383.
Munz, P.A. (in collaboration with D. D. Keck). 1973. A California Flora and Supplement. Universityof California Press,Berkeley.
Pickett, C.H., L.T. Wilson,and D.L.Flaherty. 1990. Theroleof refuges incrop protection, with
reference toplantings ofFrenchprune trees inagrape agroecosystem. Chp. 10, pp. 151-165
in: N. J. Bostonian, L. T. Wilson, and T. J. Dennehy (eds.) Monitoring and Integrated Management ofArthropod Pests of Small Fruit Crops. InterceptLtd., Andover,Hampshire, England.
Pollard, E. 1971. Hedges. VI. Habitat diversityand crop pests: a study of Brcuicoryne
Frass/-cae and itssyrphid predators. Journal ofApplied Ecology8:751-780.
Pott, R. 1989. Historische und aktuelle Formen der Bewirtshaftung von Hecken in
Nordwestdeutschland. ForstwissenshaftlichesCentralblatt 108:111-112.
Slosser,J.E.; R.J. Fewin, J.R. Price, L.J. Meinke, and J.R. Bryson. 1984. Potential of shelterbelt
managementfor boll weevil (Coleoptera:Curculionidae) control in the Texasrolling plains.
Solomon, M.G. 1981. Windbreaks as a sourceof orchard pestsand predators. Pp. 273-283 in:
Thresh, J.M. (ed.)pests,pathogens and Vegetation. Pitman, London.
Swisher, R.G. 1979. ASurveyof the Insect FaunaonEriogonumfasciculatumin the San Gabriel
Mountains,Sauthern California. M.S. thesis. Dept. of Biology, Calif. State Univ., Los
Angeles.
Van Eimern, J. (Chairman). 1964. Windbreaks and Shelterbelts. World Meteorological AssociationTechnicalNoteNo.59. 188 pp.
Van Emden, H.F. 1962. Observations of the effectof flowers onthe activity of parasitic Hymenoptera. Entomologist's Monthly Magazine 98:265-270.
Van Emden, H.F. 1965. The role of uncultivated land in the biology ofcrop pestsandbeneficial insects. Scientific Horticulture 17:121-136.
Table 1. Birds observed at
Hedgerow Farms
(Yolo County
Roads
27
and
88,
be¬
tween Winters and
Esparto,
Yolo
County,
California) (R. Jones
and J.H.
Anderson,
personal
communications).
Order: Common Names
CICONIIFORMES: AMERICAN BITTERN, GREAT EGRET, SNOWY EGRET, GREEN
HERON, GREAT BLUEHERON
ANSERIFORMES:MALLARD, CINNAMON TEAL
FALCONIFORMES: TURKEY VULTURE, BLACK-SHOULDEREDKITE, NORTHERN
HARRIER, GOLDEN EAGLE, RED-TAILED HAWK, SWAINSON'S HAWK,
ROUGH-LEGGEDHAWK,AMERICANKESTREL, MERLIN, PRAIRIEFALCON
GALLIFORMES:RING-NECKEDPHEASANT, CALIFORNIA QUAIL
CHARADRIFORMES: KILLDEER, LONGBILLEDCURLEW
COLUMBIFORMES:MOURNINGDOVE, ROCK DOVE
STRIGIFORMES:GREAT HORNED OWL,COMMON BARN OWL, BURROWING OWL
APODIFORMES:ANNA'S HUMMINGBIRD, BLACK-CHINNEDHUMMINGBIRD,
PICCIFORMES: NORTHERN FLICKER, REDBREASTED SAPSUCKER, NUTTAL'S
WOODPECKER,DOWNY WOODPECKER, ACORN WOODPECKER
PASSERIFORMES:WESTERN KINGBIRD, ASH-THROATED FLYCATCHER, BLACK
PHOEBE, SAY'S PHOEBE, HORNED LARK, BARN SWALLOW, CLIFF SWALLOW,
NORTHERN ROUGH-WINGED SWALLOW, SCRUBJAY, YELLOW-BILLEDMAGPIE,
COMMON RAVEN, AMERICAN CROW, PLAIN TITMOUSE, BUSH-TIT,REDBREASTED
NUTHATCH, BEWICK'S WREN, HOUSE WREN, RUBY CROWNED KINGLET, HERMIT
THRUSH, SWAINSON'S THRUSH, AMERICAN ROBIN, WESTERN BLUEBIRD,
MOUNTAIN BLUEBIRD, NORTHERN MOCKINGBIRD, AMERICAN PIPIT, CEDAR
WAXWING, LOGGERHEADSHRIKE, EUROPEAN STARLING, WARBLING VIREO,
YELLOW-RUMPEDWARBLER, YELLOWWARBLER, WILSON'S WARBLER,
ORANGE-CROWNED WARBLER, BLACK-THROATED GREY WARBLER, TOWNSENDS
WARBLER, HERMITWARBLER, WESTERN TANAGER, BLACK-HEADED GROSBEAK, CALIFORNIA BROWN TOWHEE, RUFOUS-SIDEDTOWHEE, SAVANNAH SPARROW,
SONG SPARROW, DARK-EYEDJUNCO, WHITE-CROWNED SPARROW,
GOLDEN-CROWNED SPARROW, FOX SPARROW, WESTERN MEADOWLARK, RED-WINGED
BLACKBIRD, BREWER'S BLACKBIRD, BROWN-HEADED COWBIRD, NORTHERN
ORIOLE, AMERICAN GOLDFINCH, LESSER GOLDFINCH, HOUSE FINCH, PURPLE
Table 2. Establishmentschedule for
hedgerows.
Operation
Time Period Cost/Acre(1/2-mile
long strip).
1. Till soil and form 60"-beds
September-October
90.00 2. Preirrigate
orwait
for
early
rains
togermi¬
nate weedsSeptember
20-October 20
0.00-50.003. Eliminate
early-ger¬
minated weeds with
herbicides, flamer, or shallow
tillage
(Steps
2
and 3may not
be
neces¬sary
if weed
seed bank
is
depleted,
orweed
com¬plex is
notoverly
com¬petitive).
October 40.00
4.
Using the Truax
na¬ tive grassseed
drill,
seed the native grass mixture into the 3bedsOctober-November 300.00
5. Plant
woody
vegeta¬tion at
approximately
10' centers in centerbed.
Costs include include
those for the
plants, fer¬
tilizer tabs,
protective
devices (milkcarton,
stakes, weed nets).
By
this
planting
arrange¬ ment, a 1/2mile-long
hedgerow
would
com¬prise
about
264
plants
at $1.00 per.If plants
arearranged in islands
or groups,reduce
plant
number to 132.
November-March 528.00
6. Broadleaf weed con¬
trol; herbicides with shields toprotect
woody
vegetation.
7.
Vegetation
control
around individual
woody
plants.
February-May
40.008. Furrow
irrigation
every
2-4
weeks for
the
first year.
June-January
150.009. Summer spot
weed
control,
using
herbicide
or hoe.
June
-September
40.0010. Drill orbroadcast mixes offorb seeds into outerbeds:
toothpick
ammi, fennel yarrow,
blazing
star,bee
phacelia,
etc.September-October
100.001 7
Table 2. Weed
California native
et al., in press.
-control
procedures
for enhancing
establishment
of
perennial
grassesin
rights-of-way.
Adapted
from Bugg
Objective
Year Months Herbicide Procedure^ Alternative Procedure Reduce weed plant population and seed reservoir prior to seedbed prepara¬ tion 1-2 years before seeding. February - March, April-May. Application of glyphosate (Roundup®)orthe"'softresidual"herbicide oryzalin (Surflan®) to suppressexistinggrowthand seed production.
Establishsummerfallow bydisk¬
ing weeds before seed has ma¬
tured. This reduces the weedseed bank; the practicecanbeused for one ormoreyearspriortoseeding a site with native perennial grasses. In thefinalyear, it can
simultaneouslyprepare a seed bed for fall seeding of native
perennial grasses. Disking also
perpetuates the disturbedcondi¬
tions underwhichweeds prosper. Onsomesites, scraping isbetter,
because it will remove muchof
theweed seed reservoir. Mowing
before seed hasmatured canalso
beeffective againstsome species ofweeds, but others, suchas an¬
nual ryegrass and introducedan¬
nual wild barleys canproduce seed heads low tothe ground fol-lowingmowing Reduce weed popu-1ation af¬ terseedbed prepara¬ tion Septem- ber- Novem-ber
Afterwinter-annual weeds have
germinated and sprouted inre¬
sponse to rain or preirrigation,
apply glyphosate or paraquat (GramoxoneExtra®). This is af¬
terseed-bed preparationbutprior
toseeding nativegrasses.
F1a me-k i 11 emerged weed
seedlings after rains orpreirriga¬
tion, butprior toseeding native perennialgrasses. Very shallow
tillage (e.g., disking or spike-tooth harrowing) can also beef¬ fective. Shallowness isessential
to avoidbringingmore weedseed
1 8 Reduce weed popu-1 ation af¬ ter seeding but before emergence 0 f native grass seedlings Septem- ber-Novem ber Chlorsulfuron
(Telar®)^applica¬
tion tosoil following seeding of
nativegrasses,toreduce germina-tion of introduced annual broadleaf and grassweeds. This gives exellent control ofannual
ryegrass. Chlorsulfuron is the only broadleaf selective herbi¬
cide that givesgood suppression ofasteraceous (composite) weeds,
such as yellow starthistle or
pricklylettuce. It does notdeter germination of blue wildrye,
California brome, or purple
needlegrass,but does affect seed
of meadowbarley and possibly others yet to be tested. Chlorsulfuron cannotbeused ad¬
jacent to agricultural land with¬
out an intervening buffer zone.
LowratesofSimazinecanbe used tosuppresswildoat.
After seeding but before emer¬ gence ofnative grasses,flaming will kill cool-season annuals.
Timing is critical, because any
emerged native grasses will be
killed, as well. Reduce weed com¬ petition and densi¬ ties during establish¬ mentof na-tive grasses 1 February-April 2,4-D, dicamba
(Banvel®)^,
ortriclopyr (Garlon 4®) tocontrol
broadleaf weeds following
early-establishment phase of native
grasses(i.e., after native grasses
have reached the 3-leaf stage).
Triclopyris not very effective againstasteraceous weeds.
Mowing, haying, orgrazing by livestock canremove the
taller-growing and (often) more-palat¬ able winter annuals duringlate
winter and early spring. This im¬
proves the competitiveposture of the nativeperennialgrasses.
Reduce weed com¬ petition, densities, and seed production duringfirst season of native grass growth March-mid April
Wickapplication of glyphosate
to selectively kill annual rye¬
grass, ripgutbrome, wild oats, and otherweedy annual grasses
that are overtopping lower-grow¬
ing native grasses. After April,
natives are usually high enough
tobesusceptible;also, weeds will
have gonetoseed.
High mowing (6" minimum) can be used to removeseed heads of
winter-annual grasses, and thus
reduce seed bank of theseweeds in
subsequentyears. Most native
grasses produce seed later, and
can recoverfromhigh mowing at this time.
1 9 Reduce weed plant densities and seed production duringfirst season of native grass growth April-June
Dicamba can be applied for om-trol ofbroadleaf weeds. Dicamba
works betteragainst older yellow
star thistle plants thandoes
2,4-D.
Ifstands ofnatives arevigorous and producingseed, mowing or
grazing of native
perennial
grassesshouldbeavoided during this period, to allow seedmatu¬
ration. On the otherhand, ifin¬
troducedgrasses aredominantand havesetseed,haycanbemade by
mowing,raking,andbaling. The haycanbefedtolivestock. Thus,
the weed seed and excessive
residue will beremoved, andna¬
tive stands canbeaugmentedby furtherseedingsduringthesubse¬ quent autumn. Reduce warm-sea¬ songrasses. May-Septem¬ ber
Spot-spraying glyphosate for
warm-season annual and peren¬ nial grasses (Bermuda, Johnson, barnyard grasses); dust onthe
plants reduces efficacyof herbi¬
cide: underdusty conditions, in¬ crease useofadjuvants.
Mechanical control of weeds
through (hoeing, weed whipping, mowing, digging) to remove, or
prevent reseedingby, patches of
warm-season annual and peren¬
nial weeds. Inhibit germina¬ tionofwin¬ ter-annual weedseeds 2 Septem- ber- Novem-ber
Apply chlorsulfuron,granular
tri-fluralin (treflan®), oryzalin
(surflan®), and/orlow rates of simazine (Princep®) toprevent germination of annual weeds.
Theseherbicides willnotdamage
established standsof blue
wildrye, California brome. Purpleneedlegrass,meadow bar¬ ley, the wheatgrasses, and the
fescuesarenotaffected by
chlor-sulfuron once established.
Chlorsulfuronwill inhibit germi¬
nationofbroadleafweeds and an¬
nualryegrass. Low-rate applica¬ tionof simazineinhibits wild oat
germinationduringsecond year.
Selective control of remaining weedinfes¬ tations 2 February-Septem¬ ber
Glyphosateused inspot-spraying
as for first year. Dicamba canbe
used for serious infestations of
yellow starthistle, prickly let¬
tuce, and otherbroadleaf weeds.
Mowingasmentionedfor the first
yearof establishment. Spotuseof
hoe or weed whip to remove
patches annual and perennial
weeds. Maintenan ce of ma¬ ture stands 0 f native grasses 3 February-Septem¬ ber
Glyphosate used inselectivespot spraying.
Mowingasmentioned for the first
yearof establishment. Spotuseof
hoe or weed whip to remove
patches annual and perennial
weeds.
^Standard safety precautions should be observed inall use
of
herbicides.
Restricted
herbicides
mustbeused inaccordance withcounty,state,and federal regulations. For information regard¬ ingpermitsand usage, contact countyagriculturalcommissioners'offices.
^Chlorsulfuroncanhavesevereeffectsonsensitivenon-targetspecies,and it should beavoided
where runoffordriftonto sensitive sites islikely
. Specifically,itcannotbe used in oron the
banks ofirrigation ditches and canals,
^2,4-D
and dicannba arerestricted-useherbicides, and shouldbe usedonly withcare. Donotuse dicamba where downward orlateral movementofwaterwillbring it intocontact with desir¬ableplants. Also avoid applicationortakesteps tominimize driftontosensitive plants when temperature exceeds85®F(30®C),
Figure
1.
Flowering
Periods
of
Native
Insectary
Trees
and
Shrubs
Salix tasiolepis (Arroyo WiUow)
Salix lasiamdra (Ytllow Willow)
Ceanothus euneatus (A California
Lilac)
Bacckaris viminea (Mule Fat)
Salix goodingii ssp, variabilis
(Gooding's
Willow)
Salix laevigata (Red Willow)Prunus ilicifolla (Holly-Leaf Cherry)
Rhamnus californlca (California
Coffeeberry)
Sambucus caerulea (Blue Elderberry)
Heteromeles arbutifolia (Toyon)
Eriogonum fasciculatum
(California
Buckwheat)
Figure
2.
Flowering
Periods
of
Wild Insectary Forbs
Jan Feb
1
MarApr
1
May
June July Aug Sep Oct Nov DecStellaria media (Chickweed)
<
^ ^1 f __
4..^
J
L
Euphorbia maculata (Prostrate Spurge) ...1... I- 1 ;
Polygonum aviculare (Common Knotweed) 1
=3:
Ammi visnaga (Toothpick Ammi) : { 1
Daucus carota (Wild Carrot) •
.Jfc
L:;y
,Foeniculum vulgare var, dulce (Sweet Fennel)
.J
>=
A < Asclepias fascicularis (Milkweed)Xanthium spinosum (Spiny Clotbur)
'
<
i i
—
23
Figure 3
Suggested
Roadside
Native
Prairie
Complexes
Native Prairie
Complex
#1
Pavement
edge: Pine
bluegrass (Poa
scahrella
Roadside berm: Red fescue
{Festuca
rubra)
and
California
brome
{Bromus
carinatus).
Inner ditchbank: Meadow
barley
(Hordeum
hrachy
anther um).
Ditch bed: Meadow
barley.
Outer ditchbank: Blue
wildrye.
Fieldside berm and field
edge:
Creeping
wildrye.
Native PrairieComplex
#2
Pavement
edge:
Pine
bluegrass
and
Idaho
fescue {Festuca
idahoen-sis).
Roadside berm: Pine
bluegrass,
Idaho
fescue,
purple
needlegrass
{Stipa
pulchra),
and
squirreltail
{Sitanion
jubatum).
Inner ditchbank: Meadow
barley,
Idaho fescue,
purple
needlegrass,
nodding
stipa
{Stipa
cernua),
California
oniongrass
{Melica
califor-nica).
Ditch bed: Meadow
barley,
purple
needlegrass,
and
spikerush
{Eleocharis
spp.).
24
Fieldside berm: Blue
wildrye, California brome, and
creeping
wildrye.
25
Appendix 1:
Beneficial Insects
and
their
Associations
with
Trees,
Shrubs,
Cover
Crops,
and
Weeds
(Adapted
from
Bugg,
1990)
Beneficial insects include parasites and predators. Parasites are usually more re¬ stricted as to which insects theywill attack. Some predators may be fairly
specialized,
as well, but many are generalists - - feeding opportunistically on various
insects
and
mites. Generalist predators may be especially importantin field andvegetable
crops, becausethey can persist in the absence of pests, may arrive in the cropfirst,
and
may act to preempt or slow down pest outbreaks. Some importantbeneficial insects
have
special plant associations.BIgeyed Bugs {Geocorisspp., Lygaeldae) are
opportunistic
predators
on awide
range of insects and mites, and are. They will also feed on nectar.
They
areespecially
important from May to mid July when they are arecommonly
found
onmelon,
okra,
pepper, and squash plants. These predators can be
abundant
in
stands
of
commonknotweed {Polygonum avicuiare) along field margins. They can also
build
upin
cool-season cover crops, like berseem clover {Trifolium alexandrium) , and subterranean
clovers, {Trifolium subterraneum), and disperse to adjoining
vegetable
cropswhen
the
clovers die early summer.Hoverflies (Syrphldae) often resemble stinging wasps or bees. Manyare
important
predators of aphids. Adult hoverflies are principally flower
visitors, feeding
onnectar
and pollen. The larvae are maggots, and these attack aphids.
Wind
shelter
is
veryim¬
portant to syrphids. Nectar is probably important as an
"energy
food"
tosustain the
hoverflies. Dietary pollen is important for reproduction. Flowering
buckwheat
(Fagopyrum esculentum), commonly used as acover crop, is
attractive
tosyrphid
flies.
Among weeds common in California, adult syrphids have been
shown
tobe
attracted to
corn spurry {Spergula arvensis) . Allograptaspp.,
Sphaerophoria
spp.,and
Paragus
tibialisv^ere observed at flowers of common knotweed. Toothpick ammi {Ammi visnaga) attracted Scaeva pyrastri, Eupeodes voiucris, Metasyrphus, Melanostoma. In summer,
we observed Allograpta obliqua, Sphaerophoriaspp., and Paragus
tibialis. Among
plants
suitable forwindbreaks or hedgerows, syrphids are heavily drawn to such native plants
as California lilacs, {Ceanothus spp.); coyote brush { Baccharis
pilularis),
holly-leaved
cherry {Prunusilicifolia) , and wild buckwheats {Eriogonumspp.).
The
soapbark tree
{Quillaja saponaria) was shown to attract Scaeva
pyrastri,
Metasyrphus,
and
Melanostoma.
Lady Beetles (Coccinellldae) are important predators of
aphids
and
other
soft-bodied insects. Convergent lady beetle {Hippodamiaconvergens) is important in
field,
vegetable, and orchard crops; ash-gray lady beetle {Olla
v-nigrum) is
mainly impor¬
tant in tree crops. In the late spring, aphids usually disappear fromCalifornian
grasslands and most crops, so, out ofdesperation, convergenet
lady
beetle feeds
onpollen
and nectar. This species is extremely abundant on flowering
soapbark
treefrom
mid
June through late June. Nectar and pollen are important in building upfat
reservesin
the beetles. Convergent lady beetle will seek bunchgrasses and form great masses of beetles that may remain dormant through the summer and early winter.If bunchgrasses
are not available on agricultural field margins, convergent lady beetle may
fly
topro-26
viding cover crops that harbor aphlds or other alternate prey. A Mixture of hairy vetch ( Vicia vHlosa), and rye {Secale cereale) works well in the cool season, and hemp
ses-bania, {Sesbania exaltata) may prove useful during the summer. Shrubs and trees can also harbor aphids that sustain lady beetles. Black locust {Robinia pseudoacacea) ,
saltbush {Atriplex spp.), and California coffee berry ,{Rhamnus californica) appear promising in this regard.
Minute Pirate Bug (Or/us fr/sf/co/or, Anthocoridae) These tiny bugs are
important predators of corn earworm. They mainly attack the eggs of these and other
moths. Theyare common in the silks of corn, and can also build up on flowering cover crops, shrubs, and weeds. Particularly potent sources are hairy vetch and 'Lana' vetch, toothpick ammi, buckwheat, and wild buckwheats.
Green Lacewings (Chrysopidae) are predatory in the larval stages, and for some
species in the adult stage. In other species, adults feed only on nectar, pollen, and hon-eydew. Comanche lacewing {Chrysoperia comanche) is extremely abundant on flowering soapbark tree from mid June through mid July, and on and bottle tree {Brachychiton populneum) from mid June into October.
Brown Lacewings (Hemeroblidae) are predatory in the adult and larval stages, and
have been shown to be important predators of artichoke plume moth in California.
Adults also feed on nectar, pollen, and honeydew, and are extremely abundant on flow¬ ering soapbark tree late at night, during June, and at bottle tree flowers from June into
October.
Parasitic Wasps (Braconidae, Chaicidoidea, and ichneumonidae) are im¬
portant in biological control of insect pests, and may rely on honeydew or pollen and
nectar in the adult stages. In Massachusetts, flowering sweet fennel {Foeniculum
vul-gare war. dulce) planted amid an organic market garden attracted 48 species of
Ichneumonidae. Fennel is probably also important for parasitic wasps in California, as
has been shown for common knotweed and toothpick ammi. Twenty species of
Ichneumonidae were observed taking extraflorat nectarfrom faba bean {Vicia faba) from late September through late October. For unknown reasons, few ichneumonids visit buckwheat or wild buckwheats.
Predatory Wasps include both social (Vespidae) and solitary species {Eumenidae and Sphecidae). The Vespidae include paper wasps and yellowjackets, which attack many
species of caterpillars. Eumenidae are also prey mainly on caterpillars. Solitary wasps
of the Sphecidae, as a group, attack wide ranges of insects, including caterpillars,
crickets, and weevils. All thesewasps require nesting sites. Many solitary species are
diggerwasps that nest in sandy areas. Some social wasps also nest in the ground, others
undereaves of buildings or in trees. Social and solitary wasps rely heavily on nectar, and commonly visit flowers and extrafloral nectaries. In Massachusetts, sweet fennel planted amid an organic market garden flowered throughout the 12 weeks of sampling. Hymenoptera collected from sweetfennel at two sites included four species of Sphecidae (solitary wasps) and four of Vespidae (social wasps). Flowering spearmint {Mentha spicata) attracted six species ofSphecidae, two of Eumenidae, and two of Vespidae. Cover
crops thatattract many predatory wasps include buckwheat, cowpea {Vigna unguicuiata
ssp. unguicuiata), and white and yellow sweetclovers {Melilotus alba and M. officinalis) .
In Massachusetts, eighteen types of wasps were obtained from buckwheat, and eleven
from annual white sweetclover. In Georgia, buckwheat attracted 9 types of Sphecidae, 2 types of Eumenidae, and onetype of Vespidae, whereas extrafloral nectar of cowpea at¬ tracted 10types of Sphecidae, 6 of Vespidae, and 4 of Pompilidae.
Tachinid Flies (Tachinidae) include numerous species that parasitize
stink
bugs,
squash bugs, and the caterpillar stages of various
moths and
butterflies.
Many
of these
flies are relianton nectar and pollen during the adult stage. Seven types oftachinidwere collected from toothpick ammi. Buckwheat, wild buckwheat, California coffeeberry , coyotebrush, other Baccharisspp., toyon
{Heteromeles
arbutifolia), and white
sweet-clover are also heavily visited.
Softwinged Flower Beetle {Collops vittatus) is a brightly-colored
insect,
with
wing covers striped with bright red and metallic blue-green. Adults
feed
on manypests,
and are commonly found running rapidly over thefoliage ofvegetable crops,
searching
for eggs of moths. Larvae are pink and crawl about on the soil surface,feeding
onother
insects. Adults are often encountered feeding atthe extrafloral nectaries of cowpeas or