Fraxinus pennsylvanica

Marsh.

Green Ash

G4Apparently Secure Found in 17 roadless areas NatureServe Explorer →
G4Apparently SecureGlobal Rank
Critically endangeredIUCN
HighThreat Impact
Identity
Unique IDELEMENT_GLOBAL.2.144657
Element CodePDOLE040D0
Record TypeSPECIES
ClassificationSpecies
Classification StatusStandard
Name CategoryVascular Plant
IUCNCritically endangered
Endemicoccurs (regularly, as a native taxon) in multiple nations
KingdomPlantae
PhylumAnthophyta
ClassDicotyledoneae
OrderScrophulariales
FamilyOleaceae
GenusFraxinus
Other Common Names
Frêne rouge (FR) green ash (EN)
Concept Reference
Kartesz, J.T. 1994. A synonymized checklist of the vascular flora of the United States, Canada, and Greenland. 2nd edition. 2 vols. Timber Press, Portland, OR.
Taxonomic Comments
As treated here (following Kartesz 1994 and 1999 and many other recent authors), includes both the "red ash" (Fraxinus pennsylvanica, in a narrower sense, of many older works) and the "green ash" (Fraxinus lanceolata of older works). LEM 14Jun00.
Conservation Status
Rank Method Rank calculation - Biotics v2
Review Date2021-06-29
Change Date2021-06-29
Edition Date2021-06-29
Edition AuthorsTreher (2021)
Threat ImpactHigh
Range Extent>2,500,000 square km (greater than 1,000,000 square miles)
Number of Occurrences> 300
Rank Reasons
Fraxinus pennsylvanica occurs in Eastern North America from Florida and Texas north to Nova Scotia and Quebec; extending from the east, west to southeastern Alberta, Montana, Wyoming, Utah, and Texas. While the species is wide ranging and has many occurrences, it is suffering serious mortality due to the Emerald Ash Borer and has poor regeneration post infestation. Within six years of an invasion, the species can experience a nearly 100% decline with minimal regeneration. The Conservation Status of this species should be reviewed frequently to detect changes in the impact of the borer.
Range Extent Comments
Fraxinus pennsylvanica occurs in Eastern North America from Florida and Texas north to Nova Scotia and Quebec; extending from the east, west to southeastern Alberta, Montana, Wyoming, Utah, and Texas (Gleason and Cronquist 1991). It may also occur southward into Mexico (GBIF 2019; iNaturalist 2019; SEINet 2019).
Occurrences Comments
The number of occurrences is not known but is well over 300 based on specimen collections and photo based observations.
Threat Impact Comments
The primary threat to this species is mortality and reduced regeneration associated with the Emerald Ash Borer, a phloem-feeding beetle native to Asia. The invasive Emerald Ash Borer (EAB), Agrilus planipennis Fairmaire, 1888, was introduced in Detroit, Michigan from Asia in the 1990s (Haack et al. 2002) and has since caused rangewide declines in ash populations. The beetles feed on the leaves and lay their eggs in crevices of the bark. Larvae feed in the vascular structures during the summer, creating serpentine shaped galleries. They typically prepupae overwinter in the trees with pupation lasting from April-May, when adults emerge. Emerald Ash borers cause significant damage to the foliage of the tree and the vascular tissues. The tree will typically die within two years of the infestation (Poland and McCullough 2006). Within six years of an infestation, up to 99% mortality was observed in ash species (Knight et al. 2013, Klooster et al. 2014, McCullough et al. 2008, Steiner et al. 2019). Green ash appears to suffer the greatest mortality and least regeneration post-invasion (Robinett and McCullough 2019). Tree saplings with 2 or more cm dbh can be infested (McCullough et al. 2008, Aubin et al. 2015). While an infested tree may push out root sprouts for one to two years, the tree usually dies (Klooster et al. 2014). The mass mortality of reproductively mature plants that would replenish the seed bank and the relatively short persistence in the seed bank (2-3(7) years) (Klooster et al. 2014), causes concern about the species ability to regenerate post-infestation. Emerald Ash Borer has been reported in most states and provinces where this species occurs (Emerald Ash Borer Information Network 2020).
Several diseases afflict Fraxinus pennsylvanicus: 1.) Mycosphaerella fraxinicola, a leaf spot causing premature defoliation in young trees, 2.) Anthracnose (Gleosproium aridum) that also causes premature defoliation, especially in wet years, 3.) a petiole and twig distorting rust, Puccinia peridermiopora, 4.) Fomes fraxinophilus, the white-mottled heartwood rot, and 5.) root rot caused by Phymatotrichum omnivorum.
Ecology & Habitat

Description

Fraxinus pennsylvanica is a tree that grows to 25 m with flaky bark and pubecent to glabrous twigs and leaves. Leaf scars are straight to slightly concave on their upper margin. Leaflets are 5-9, ovate to oblong or elliptic, acute or acuminate, usually decurrent onto the short petiolule, and with serrate to subentire margins. The fruit is a linear to spathulate samara, 4-7.5 cm in length, with wings extending to the middle of the subterete body (Gleason and Cronquist 1991, Rhoads and Block 2000).

Diagnostic Characteristics

The samara of Fraxinus pennsylvanica is differentiated into a flat wing and a subterete or terete body, while the samaras of F. caroliniana, F. nigra, and F. quadrangulata are flat. The samara of F. pennsylvanica has a wing extending halfway or more down it's body versus a wing extending 1/3 to 1/2 the length of the subterete body on F. americana and F. profunda. Petiolules of the lower and middle leaflets on F. pennsylvanica usually have a wing extending from the blade nearly to the rachis, compared to the nearly wingless petiolules of F. americana and F. profunda (Gleason and Cronquist 1991, Rhoads and Block 2000).

Habitat

Fraxinus pennsylvanica is frequently found on moist, fertile soils of floodplains, riparian areas, and swamps including alluvial woods, lake margins, ravines, stream banks, and moist fields. It is typically found in seasonally wet habitats, but can tolerate drier, upland sites (Burns and Honkala 1990, Rhoads and Block 2000).

Ecology

The seed crop of this species provides food for a wide variety of wildlife (Burns and Honkala 1990).

Reproduction

This species flowers in the spring before the leaves emerge (Rhoads and Block 2000). Flowers may appear as early as March or April in Florida and from late April to early May in the northern part of its range. Fruits appear within a month after pollination and begin growth. Even if samaras reach their full size, the embryos are not mature until late September or early October (Burns and Honkala 1990).
Palustrine Habitats
FORESTED WETLANDRiparian
Other Nations (2)
CanadaN5
ProvinceRankNative
AlbertaS2Yes
New BrunswickS3Yes
ManitobaS4Yes
Nova ScotiaS1Yes
OntarioS4Yes
QuebecS3Yes
British ColumbiaSNANo
SaskatchewanS4Yes
Prince Edward IslandSNANo
United StatesN4
ProvinceRankNative
LouisianaSNRYes
New HampshireSNRYes
IllinoisSNRYes
KansasS5Yes
AlabamaSNRYes
New YorkS5Yes
MaineSNRYes
GeorgiaS5Yes
OhioSNRYes
ArkansasSNRYes
FloridaS4Yes
ColoradoSNRYes
VirginiaS5Yes
UtahSNRYes
New JerseyS4Yes
IndianaS4Yes
MissouriSNRYes
South CarolinaS5Yes
TennesseeSNRYes
MississippiSNRYes
MarylandSNRYes
MontanaS5Yes
District of ColumbiaS5Yes
DelawareS5Yes
North CarolinaS4Yes
MassachusettsSNRYes
WisconsinS3Yes
VermontS5Yes
KentuckyS5Yes
OklahomaSNRYes
IowaS5Yes
NebraskaSNRYes
ConnecticutSNRYes
MinnesotaSNRYes
PennsylvaniaS5Yes
MichiganSNRYes
WyomingS3Yes
North DakotaSNRYes
West VirginiaS2Yes
TexasSNRYes
South DakotaSNRYes
Threat Assessments
ThreatScopeSeverityTiming
8 - Invasive & other problematic species, genes & diseasesLarge (31-70%)Extreme or 71-100% pop. declineHigh (continuing)
8.1 - Invasive non-native/alien species/diseasesLarge (31-70%)Extreme or 71-100% pop. declineHigh (continuing)

Plant Characteristics
DurationPERENNIAL, Long-lived, DECIDUOUS
Economic Value (Genus)No
Roadless Areas (17)
Illinois (1)
AreaForestAcres
Burden FallsShawnee National Forest485
Michigan (1)
AreaForestAcres
FibreHiawatha National Forest7,432
North Dakota (4)
AreaForestAcres
Collar / Bennett - CottonwoodDakota Prairie Grasslands19,697
Long X DivideDakota Prairie Grasslands10,099
Tracy MountainDakota Prairie Grasslands9,756
WannaganDakota Prairie Grasslands6,026
Utah (7)
AreaForestAcres
418012Uinta National Forest25,758
418025Uinta National Forest32,698
Lewis PeakWasatch-Cache National Forest11,616
Mt. Logan NorthWasatch-Cache National Forest18,930
Mt. Logan SouthWasatch-Cache National Forest17,014
Mt. NaomiWasatch-Cache National Forest41,922
WellsvilleWasatch-Cache National Forest1,717
Virginia (2)
AreaForestAcres
Brushy MountainJefferson National Forest4,168
Oak KnobGeorge Washington National Forest10,882
Wyoming (2)
AreaForestAcres
Little GooseBighorn National Forest25,558
Piney CreekBighorn National Forest22,240
References (17)
  1. Burns, R. M., and B. H. Honkala, eds. 1990. Silvics of North America, vol. 2: Hardwoods. U.S. Department of Agriculture, Agriculture Handbook 654, Washington, DC. 877pp.
  2. Emerald Ash Borer Information Network. 2020. Available. Online: www.emeraldashborer.info/index.php (accessed 9 Apr 2020).
  3. Gleason, H.A., and A. Cronquist. 1991. Manual of vascular plants of northeastern United States and adjacent Canada. New York Botanical Garden, Bronx, New York. 910 pp.
  4. Global Biodiversity Information Facility (GBIF). 2019. GBIF data accessed through GeoCAT portal. Online. Available: http://geocat.kew.org/ (Accessed 2019).
  5. Haack, R., E. Jendek, H. Liu, K. Marchant, T. Petrice, T. Poland, and H. Ye. 2002. The emerald ash borer: a new exotic pest in North America. Newsletter of the Michigan Etymological Society 47(3-4):1-5.
  6. iNaturalist. Online. Available: http://www.inaturalist.org (accessed 2019).
  7. Kartesz, J.T. 1994. A synonymized checklist of the vascular flora of the United States, Canada, and Greenland. 2nd edition. 2 vols. Timber Press, Portland, OR.
  8. Klooster, W., D. Herms, K. Knight, C. Herms, D. McCullough, A. Smith, K. Gandhi, and J. Cardina. 2014. Ash (<i>Fraxinus</i> spp.) mortality, regeneration, and seed bank dynamics in mixed hardwood forests following invasion by emerald ash borer (<i>Agrilus planipennis</i>). Biological Invasions 16: 859-873.
  9. Knight, K., J. Brown, and R. Long. 2013. Factors affecting the survival of ash (<i>Fraxinus</i> spp.) trees infested by emerald ash borer (<i>Agrilus planipennis</i>). <i>Biological Invasions</i> 15: 371-383.
  10. Little, E.L., Jr. 1979. Checklist of United States trees (native and naturalized). Agriculture Handbook No. 541. U.S. Forest Service, Washington, D.C. 375 pp.
  11. McCullough, D.G., N.F. Schneeberger, and S.A. Katovich. 2008. Emerald ash borer pest alert. NA-PR-02-04. USDA Forest Service.
  12. Mceuen, A. B., and L. M. Curran. 2004. Seed Dispersal And Recruitment Limitation Across Spatial Scales In Temperate Forest Fragments. Ecology 85(2):507-518.
  13. <p>Aubin, I., F. Cardou, K. Ryall, D. Kreutzweiser, and T. Scarr. 2015. Ash regeneration capacity after emerald ash borer (EAB) outbreaks: Some early results. <i>The Forestry Chronicle</i> 91(3): 291-298.</p>
  14. Poland, T. M., and D. G. McCullough. 2006. Emerald Ash Borer: Invasion of the urban forest and and the threat to North America's ash resource. Journal of Forestry 104(3):118-124.
  15. Rhoads, A.F. and T.A. Block. 2000. The Plants of Pennsylvania: An Illustrated Manual. University of Pennsylvania Press: Philadelphia, Pennsylvania. 1061 pp.
  16. Southwest Environmental Information Network (SEINet). 2019. Collections Databases. Online. Available: http://swbiodiversity.org/seinet/collections/index.php (Accessed 2019).
  17. Steiner, K.C., L.E. Graboski, K.S. Knight, J.L. Koch, M.E. Mason. 2019. Genetic, spatial, and temporal aspects of decline and mortality in a Fraxinus provenance test following invasion by the emerald ash borer. Biological Invasions 21:3439–3450.