Black walnut tree named ‘Beineke 7’

Abstract

A new and distinct cultivar of black walnut tree (Juglans nigra L.) is distinctly characterized by extremely rapid growth rate, very strong central stem tendency, and excellent straightness, thereby producing good timber qualities. The new variety of black walnut tree (Juglans nigra L.) was discovered by the applicant near South Raub, Tippecanoe Country, Ind. in a black walnut planting of seedling progeny from a previously selected tree for outstanding timber producing potential. This selection has been designated as BW503, a seedling progeny of patented Purdue-1 (U.S. Plant Pat. No. 4,543) in records maintained by the applicant on the performance of the selection and grafts made from the selection will be known henceforth as ‘Beineke 7.’

Description

Latin name of the genus and species: Juglans nigra L.

BACKGROUND OF THE INVENTION

This new variety of black walnut tree (Juglans nigra L.) was discovered by the applicant near South Raub, Tippecanoe Country, Ind. in a black walnut planting of seedling progeny from previously selected trees for outstanding timber producing potential. This selection has been designated as BW503, a seedling progeny of Purdue 1 (U.S. Plant Pat. No. 4,543) in records maintained by the applicant on the performance of the selection and grafts made from the selection and will be known henceforth as ‘Beineke 7.’ The male parent is unknown, as is generally the case with black walnut trees (Beineke, 1989).

SUMMARY OF THE INVENTION

A new and distinct cultivar of black walnut tree (Juglans nigra L.) which is distinctly characterized by extremely rapid growth rate, very strong central stem tendency, and excellent straightness, thereby producing excellent timber qualities at 9 years. The new variety has poor nut bearing qualities. Nut crops are erratic, that is unpredictable. Beneke 7 was 9 years old when described at a location near South Raub, Ind.

After the original clone was selected, and assigned an identity number of BW503 the aforesaid tree was reproduced by collecting scions from it and grafting these onto common black walnut rootstocks at American Forestry Technologies, Inc., West Point, Ind. These asexual reproductions ran true to the original tree and to each other in all respects.

Color values used were from the Munsell Color Chart for Plant Tissues. However, color is too dependent on weather conditions and fertilization to be consistent or distinctive. For example, leaves can be made a deeper green by applying nitrogen. Walnut tree leaves turn yellow as the season progresses, especially if there is a lack of rainfall. As black walnut meats dry, they become darker. Simply being on the ground for a week causes the outer shell to darken. Bark color involves many shades of gray through brown and black.

Beineke 7 is hardy in USDA zones 4, 5, 6, 7, and 8.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a photograph showing the timber form of ‘Beineke 7.’

FIG. 2 is a photograph showing the leaves of ‘Beineke 7.’

FIG. 3 is a photograph showing the nuts of ‘Beineke 7.’

BOTANICAL DESCRIPTION OF THE PLANT

The botanical details of this new and distinct variety of walnut tree are as follows:

Tree:

Size.—Large, 43 ft. at 9 years old, crown diameter of 12 ft.

Vigor.—Vigorous.

Growth rate.—Very rapid, faster than Purdue 1 (U.S. Plant Pat. No. 4,543). 18% larger in diameter than the average of patented Purdue 1 (U.S. Plant Pat. No. 4,543) grafts, planted the same year on the same site. Diameter growth rate (at 4½ feet above the ground) averages 0.678 inches per year, over 9 years about 6.1 inches.

Form.—Excellent timber form, as good as Purdue 1 — 51% straighter than average of the entire planting. Beineke 7 averages 1. Stem form was obtained by subjectively rating the straightness of the main stem on a scale of 1 to 5 with 1 representing a perfectly straight stem; 2, slight crook or deviation of the central stem; 3, about average straightness; 4, several severe crooks or a single fork; and 5, a very crooked, forked and/or leaning central stem. The trees of the present invention are grown in plantations, not open fields (not natural stands). In plantations, trees are upright and have no distinctive or characteristic crown shape because all branches are seeking to grow upwards.

Branches: Diameter depends on age and size of tree, varies from ½″ to 12″, bark color varies from grays to browns.

Leaves:

Compound leaves.—Size — Much shorter than average; average length — 13.63″.

Leaflets.—Size — Average; average length — 3.93″; average width — 2.8″; average number of leaflets — 20.0 — lanceolate; acutely pointed; rounded.

Thickness.—Thin; Texture — smooth; Margin — serrated.

Color.—Topside — dark green, 2.5 G 4/4 on the Munsell Color Chart for Plant Tissues; Underside — light green (5GY5/4 on the Munsell Color Chart for Plant Tissues), base — rounded; petioles — short.

Anthracnose resistance.—Fair.

Nut:

Size.—Small; average length — 1.20″; average diameter in suture plane — 1.13″; average diameter cheek to cheek — 1.27″.

Uniformity of size.—Not much variation.

Form.—Round, see FIG. 3.

Blossom end.—Rounded.

Basal end.—Rounded.

Thickness of shell.—Thick.

Ridges.—Rounded off; not sharp.

Color.—Mottled, 5 YR 3/2 and 2/5 YR 3/4 on the Munsell Color Chart for Plant Tissues.

Flowering habit:

Flowers typically in May.

Age at which trees start producing catkins.—Early, it takes about 4-5 years to flower but the flower number varies with the age of the tree.

Number of catkins produced.—Few.

Age at which tree starts producing pistillate flowers.—Early, 4-5 years.

Number of pistillate flowers produced by young trees.—Few.

Lateral shoots producing pistillate flowers.—None.

Number of pistillate flowers per inflorescence.—2 to 3, but flower numbers vary with the age of the tree.

Nut crop:

Bearing.—Erratic.

Productivity.—Light.

Ripening period.—September-October.

Evenness of maturity (period between first and last nuts are ready for harvest).—Even.

Quality.—Good.

Distribution of nuts on tree.—Throughout.

GENETIC METHOD OF IDENTIFICATION

DNA “fingerprint” for identification of ‘Beineke 7:’

DNA was isolated from the leaves of ‘Beineke 7.’ For purposes of DNA fingerprinting, nine highly polymorphic loci from a suite of microsatellites developed by Woeste et al. (2002) were chosen. Microsatellites sizes were checked against previously published standards and verified by a second independent analysis. The “fingerprint” is the collection of microsatellite allele sizes at each locus for ‘Beineke 7.’

DNA was isolated from the leaves of 10 black walnut trees obtained from Walter Beineke using CTAB extraction buffer (50 mM TRIS-HCL, pH 8.0, 20 mM ETDA, pH 8.0, 0.7 M NaCl, 0.4 M LiCl, 2% SDS, 2% TAB, nd 1% PVP). After isolation the DNA from each tree was quantified and diluted with nanopure distilled water to a final concentration of 5 ng/&mgr;L. The samples were stored in 96-well plates at 20° C.

For purposes of DNA fingerprinting, nine highly polymorphic loci from a suite of microsatellites developed by Woeste et al. (2002) were chosen. Amplification of each locus was performed with an MJ Research Tetrad Thermocycler (Waltham, Mass.) using 10 &mgr;L reactions in 96-well plates. The PCR reaction mix contained 2 &mgr;L of the aforementioned black walnut DNA, 5 &mgr;L Sigma Taq ReadyMix (Sigma Aldrich, St. Louis, Mo.), 0.4 &mgr;L of a 20 pmol mixture of forward and reverse fluorescence labeled primer, and 3 &mgr;L PCR grade water supplied with the Sigma ReadyMix. PCR amplification was for 30 cycles of 94° C. for 20 sec, 55° C. for 30 sec, and 72° C. for 1 min. All primers were annealed at 55° C. The products were then held at 4° C. until aliquots could be loaded into 6% Long Ranger (polyacrylamide) denaturing gels (BMA, Rockland, Me.). For each individual 0.5 &mgr;L PCR product was added to 0.75 &mgr;L blue dextran and 0.25 &mgr;L of CXR 350 bp Ladder Standard (Promega, Fitchburg Center, Wis.) in a new 96-well 1 late. The samples were denatured for 2 min at 95° C. and loaded onto a CAL96 96-well laminated membrane comb (The Gel Company, San Francisco, Calif.). Electrophoresis was at 3,000 V, 60 mA, 200 Watts, 50° C. for 2 hours using an ABI 377 (Perkin Elmer) with 36 cm plates and 0.2 mm spacers. The resulting data was analyzed using ABI's GeneScan 3.1.2 and Genotyper 2.5 (Perkin Elmer). Microsatellite sizes were checked against previously published standards and verified by a second independent analysis. The “fingerprint” is the collection of microsatellite allele sizes at each locus for each tree.

Locus Forward WGA2 GACGACGAAGGTGTACGGAT (SEQ ID NO:1) WGA6 CCATGAAACTTCATGCGTTG (SEQ ID NO:2) WGA24 TCCCCCTGAAATCTTCTCCT (SEQ ID NO:3) WGA32 CTCGGTAAGCCACACCAATT (SEQ ID NO:4) WGA33 TGGTCTGCGAAGACACTGTC (SEQ ID NO:5) WGA86 ATGCCTCATCTCCATTCTGG (SEQ ID NO:6) WGA89 ACCCATCTTTCACGTGTGTG (SEQ ID NO:7) WGA90 CTTGTAATCGCCCTCTGCTC (SEQ ID NO:8) WGA97 GGAGAGGAAAGGAATCCAAA (SEQ ID NO:9) Reverse WGA2 GTACGGCTCTCCTTGCAGTC (SEQ ID NO:10) WGA6 CATCCCAAGCGAAGGTTG (SEQ ID NO:11) WGA24 TTCTCGTGGTGCTTGTTGAG (SEQ ID NO:12) WGA32 ACGGGCAGTGTATGCATGTA (SEQ ID NO:13) WGA33 GGTTCGTCGTTTGTTGACCT (SEQ ID NO:14) WGA86 TGAGTGGCAATCACAAGGAA (SEQ ID NO:15) WGA89 TGCCTAATTAGCAATTTCCA (SEQ ID NO:16) WGA90 TACCTGCAACCCGTTACACA (SEQ ID NO:17) WGA97 TTGAACAAAAGGCCGTTTTC (SEQ ID NO:18)

The best interpretation of the current data indicates that the probability that any other black walnut tree would have the collection of microsatellite allele sizes listed is less that 1 in 10−17.

Sizes (bp) of microsatellites at 9 loci used to fingerprint ‘Beineke 7’ (2 alleles at each locus).

WGA2 WGA6 WGA24 WGA32 WGA90 150 150 142 144 228 234 221 221 150 154 WGA86 WGA97 WGA33 WGA89 232 238 153 159 242 242 187 197

DOCUMENTS CITED

Beineke, Walter F. (1989) Twenty years of black walnut genetic improvement at Purdue University North J. Appl. For. 6:68-71.

Woeste, K., Burns, R., Rhodes, O., and Michler, C. (2002) Thirty polymorphic nuclear microsatellite loci from black walnut. Journal of Heredity, 93(1): 58-60.

18 1 20 DNA Artificial Sequence Description of Artificial Sequence Primer 1 gacgacgaag gtgtacggat 20 2 20 DNA Artificial Sequence Description of Artificial Sequence Primer 2 ccatgaaact tcatgcgttg 20 3 20 DNA Artificial Sequence Description of Artificial Sequence Primer 3 tccccctgaa atcttctcct 20 4 20 DNA Artificial Sequence Description of Artificial Sequence Primer 4 ctcggtaagc cacaccaatt 20 5 20 DNA Artificial Sequence Description of Artificial Sequence Primer 5 tggtctgcga agacactgtc 20 6 20 DNA Artificial Sequence Description of Artificial Sequence Primer 6 atgcctcatc tccattctgg 20 7 20 DNA Artificial Sequence Description of Artificial Sequence Primer 7 acccatcttt cacgtgtgtg 20 8 20 DNA Artificial Sequence Description of Artificial Sequence Primer 8 cttgtaatcg ccctctgctc 20 9 20 DNA Artificial Sequence Description of Artificial Sequence Primer 9 ggagaggaaa ggaatccaaa 20 10 20 DNA Artificial Sequence Description of Artificial Sequence Primer 10 gtacggctct ccttgcagtc 20 11 18 DNA Artificial Sequence Description of Artificial Sequence Primer 11 catcccaagc gaaggttg 18 12 20 DNA Artificial Sequence Description of Artificial Sequence Primer 12 ttctcgtggt gcttgttgag 20 13 20 DNA Artificial Sequence Description of Artificial Sequence Primer 13 acgggcagtg tatgcatgta 20 14 20 DNA Artificial Sequence Description of Artificial Sequence Primer 14 ggttcgtcgt ttgttgacct 20 15 20 DNA Artificial Sequence Description of Artificial Sequence Primer 15 tgagtggcaa tcacaaggaa 20 16 20 DNA Artificial Sequence Description of Artificial Sequence Primer 16 tgcctaatta gcaatttcca 20 17 20 DNA Artificial Sequence Description of Artificial Sequence Primer 17 tacctgcaac ccgttacaca 20 18 20 DNA Artificial Sequence Description of Artificial Sequence Primer 18 ttgaacaaaa ggccgttttc 20

Claims

1. A new and distinct variety of black walnut tree named ‘Beineke 7’ substantially as illustrated and described, which has excellent timber quality, is fast growing, has strong central stem tendency, no sweep, and no crooks.