USPP14271P3 - Mahaleb rootstock named ‘UCMH 56’ - Google Patents

Mahaleb rootstock named ‘UCMH 56’ Download PDF

Info

Publication number
USPP14271P3
USPP14271P3 US10/028,772 US2877201V USPP14271P3 US PP14271 P3 USPP14271 P3 US PP14271P3 US 2877201 V US2877201 V US 2877201V US PP14271 P3 USPP14271 P3 US PP14271P3
Authority
US
United States
Prior art keywords
mahaleb
cultivar
rootstock
standard
ucmh
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US10/028,772
Other versions
US20030126654P1 (en
Inventor
Stephen M. Southwick
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
University of California
Original Assignee
University of California
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by University of California filed Critical University of California
Priority to US10/028,772 priority Critical patent/USPP14271P3/en
Assigned to REGENTS OF THE UNIVERSITY OF CALIFORNIA, THE reassignment REGENTS OF THE UNIVERSITY OF CALIFORNIA, THE ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SOUTHWICK, STEPHEN M.
Publication of US20030126654P1 publication Critical patent/US20030126654P1/en
Application granted granted Critical
Publication of USPP14271P3 publication Critical patent/USPP14271P3/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01HNEW PLANTS OR NON-TRANSGENIC PROCESSES FOR OBTAINING THEM; PLANT REPRODUCTION BY TISSUE CULTURE TECHNIQUES
    • A01H6/00Angiosperms, i.e. flowering plants, characterised by their botanic taxonomy
    • A01H6/74Rosaceae, e.g. strawberry, apple, almonds, pear, rose, blackberries or raspberries
    • A01H6/7427Prunus, e.g. almonds
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A40/00Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
    • Y02A40/10Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in agriculture

Definitions

  • Botanical/commercial classification Prunus mahaleb /Mahaleb Rootstock.
  • Mahaleb rootstocks i.e., Prunus mahaleb rootstocks
  • Prunus mahaleb rootstocks are widely used during both sweet and sour cherry production throughout the world. It has been the common practice to form such rootstock plants from seed following the random outcrossing of parent plants. Accordingly, cherry production encountered when using such plants as an understock has tended to be somewhat variable due to differences in the genotype of the understock. Such variation often has led to reduced field performance on some cherry trees on a random and unpredictable basis.
  • Mahaleb rootstocks in the past have generally been found to be incapable of vegetative propagation on a reliable basis, such as through the use of softwood and hardwood cuttings. Also, such rootstocks in the past have been susceptible to root and crown fungal diseases generally known as Phytophthora spp.
  • Prunus mahaleb rootstocks that possess characteristics that overcome shortcomings of the Mahaleb rootstock presently being used during cherry production. More specifically, it was my goal to provide cherry rootstocks that could be vegetatively propagated in an expeditious and reliable manner so that cherry growers can eliminate crop variation that can be traced to lack of uniformity in the rootstock. Also, it was a goal of my research to provide new Mahaleb rootstocks that inherently display needed resistance to disease and thereby make possible a satisfactory cherry crop on a more consistent basis combined with a reduction in the need to replant because of tree loss that is traceable to disease.
  • the original tree of the new Prunus mahaleb cultivar of the present invention was discovered through detailed evaluation and selection while growing in a cultivated area at the Experimental Orchards at the University of California located at Davis, Calif., U.S.A.
  • the exact parentage of the new cultivar is unknown.
  • the seeds used to form the planting where the discovery took place came from a random collection of wild Prunus mahaleb germplasm that had been collected from around the world.
  • the large number of seedlings present in the planting were carefully studied and evaluated and a single plant possessing the combination of characteristics of the new cultivar of the present invention was selected and was preserved. Had this plant not been discovered and preserved, it would have been lost to civilization.
  • Prunus mahaleb cultivars resulting from the same research are ‘UCMH 55’ (U.S. Plant patent application Ser. No. 10/028,771, filed concurrently herewith), and ‘UCMH 59’ (U.S. Plant patent application Ser. No. 10/029,284, filed concurrently herewith).
  • the new cultivar of the present invention well meets the needs of cherry producers for use as an improved rootstock.
  • Cherry scion characteristics are no longer influenced by variation in the Mahaleb rootstock resulting from the random outcrossing of parental plants.
  • the disease resistance made possible by the new cultivar is a major advantage for cherry producers.
  • the new cultivar of the present invention has been repeatedly reproduced through the use of softwood, semi-hardwood, and hardwood cuttings at Davis, Calif., U.S.A. Such propagation has confirmed that the characteristics of the new cultivar are stable and are firmly fixed and are transmitted to subsequent generations on a reliable basis.
  • the new cultivar of the present invention initially was designated ‘UC MAHALEB 156-5’, and subsequently has been named ‘UCMH 56’.
  • FIG. 1 shows a tree of approximately 5 to 7 years of age during December.
  • the tree is a mother plant that was being used to make propagules for additional testing and evaluation. Most of the leaves had dropped by the end of the preceding October.
  • FIG. 2 shows a specimen of a current season's shoot with leaves collected during mid-October. Such shoot was suitable for use to make a hardwood or semi-hardwood cutting.
  • FIG. 3 shows specimens of typical branches with buds of the new cultivar during the winter. Dimensions in inches and centimeters are included at the left.
  • FIG. 4 shows specimens of typical stones of the new cultivar during the winter. Dimensions in centimeters and inches are included.
  • FIG. 5 shows the DNA fingerprint of the new cultivar of the present invention as well as that of the ‘UCMH 55’ and ‘UCMH 59’ cultivars for comparative purposes.
  • Three microsatellite markers were used during the DNA determinations (i.e., PMS30, PMS40 and PMS15).
  • Data with respect to the plants of the new cultivar of the present invention is designated “156-5”.
  • Data with respect to the plants of the ‘UCMH 55’ cultivar is designated “155-1”
  • data with respect to the ‘UCMH 59’ cultivar is designated “159-5”.
  • FIG. 6 shows typical inflorescences of the new cultivar.
  • the pellets were air dried and resolved in 50 ⁇ l TE buffer. Quantification of DNA was performed with ethidium bromide agarose gel plates. PCR was carried out under the following conditions: 100-150 ng of template DNA, 250 nM of each primer, 200 ⁇ M of dNTPs, 0.5 U of Taq Polymerase, and 1.5 mM of MgCl 2 . The reaction was run for 45 cycles (denaturing at 94° C. for 1 minute, annealing at 60° C. for 1 minute, with a two minute extension at 72° C.), followed by a single extension at 72° C. for 60 minutes.
  • the amplification products were detected on 5.5 percent polyacrylamide gels using a Li-Cor IR 2 4200 DNA sequencer (Li-Cor, Nebr., U.S.A.).
  • the three microsatellite markers clearly distinguished the three cultivars. Both repeats of each rootstock showed identical fingerprints.
  • the marker PMS30 produced two bands for rootstock ‘UCHM 55’ at 132 bp (base pair) and 159 bp, two bands for ‘UCMH 56’ at 132 bp and 168 bp, and one band for ‘UCMH 59’ at 142 bp.
  • Marker PMS40 produced two bands for ‘UCMH 55’ at 92 bp and 111 bp, and one band for ‘UCMH 56’ at 92 bp, and two bands for ‘UCMH 59’ at 92 bp and 129 bp.
  • Marker PMS15 produced two bands for ‘UCMH 55’ at 118 bp and 128 bp, two bands for ‘UCMH 56’ at 112 bp and 123 bp, and two bands for ‘UCMH 59’ at 105 bp and 115 bp.
  • FIG. 6 shows a typical inflorescence
  • Wood The wood is fine to intermediate and commonly ranges from less than 1 cm to 3 cm in diameter.
  • Plant growth form Straight in the upper canopy and pendulous in the lower canopy with one leaf per node in a spiral pattern around the shoot, and laterals arise at approximately 90 degrees from the point of origin on the main scaffold and are branched at approximately 75 to 90 degrees.
  • Spurs Commonly 1 to 4 spurs are present per 85 cm of previous season shoot that measure approximately 1 to 5 cm in length. The coloration is Chickadee gray (47 A 1) underlaid with Burnt umber (15 A 12).
  • Internode length On mixed shoots approximately 1 to 4 cm in length and increasing in length basipetally, and approximately 2 mm to 2.5 cm in length between reproductive nodes.
  • Lenticels Prominent, densely distributed, and under magnification are raised.
  • the size on subsidiary shoots commonly ranges from 2 to 5 mm in length with approximately 15 lenticles being present per square inch.
  • the coloration is Parchment (12 B 3).
  • Axillary buds Vegetative buds are borne in the axils of every leaf along the shoot, and are single. The buds are imbricate and sessile. The bud tips are pointed and the bud pose is adpressed on dormant new wood. The bud support is small.
  • Length Approximately 3 to 5 cm in length and approximately 2.5 to 3.5 cm in width on the upper canopy and on the lower canopy.
  • Width Approximately 2.5 to 3.5 cm on the upper canopy and on the lower canopy.
  • Form. Oval-elliptic to oval with an acuminate tip and a truncate base on the upper canopy and on the lower canopy
  • Petiole. Commonly with glands that are dark Russet brown (14 I 12) in coloration at the leaf-petiole juncture, approximately 1 to 1.5 cm in length, and Russet Green (20 K 1)in coloration. Such glands commonly are less than 1 mm in length and less than 0.5 mm in width.
  • the paniculate inflorescence has 5 to 10 flowers and commonly 3 to 5 flowers with a peduncle including the rachis of approximately 1 to 1.5 cm in length and a pedicel of approximately 0.7 to 1.2 cm in length.
  • the peduncles and pedicels are Cossak green (23 L 11) in coloration.
  • Petal size Approximately 7 mm in length and approximately 6 mm in width at the widest point.
  • Pistil. Approximately 6 to 7 mm in length with the stigma and style being Marguerite Yellow (10 C 1) in coloration.
  • Stamen Commonly approximately 10 to 14 per flower, and approximately 5 to 7 mm in length.
  • Skin color Dark purple-mahogany (56 A 12) to near black (48 A 12).
  • Fruit juice color Dark purple-mahogany (56 A 12) to near black (48 A 12).
  • Fruit stalk Short, and approximately 0.7 to 1.5 cm when pedicel alone is measured. Very small bracts may persist and leaves commonly are absent on the stalk.
  • Stone shape Substantially spherical (as illustrated in FIG. 4 ).
  • Stone size Very small and approximately 3 to 4 mm in diameter.
  • Seed color Oyster white (10 B 1).
  • the new cultivar has shown over a 90 percent survival rate in field trials at sites that are heavily infested with Phytophthora spp. and stem pitting virus. At the same sites, approximately 50 percent of the standard Mahaleb plants died.
  • Vegetative propagation The new cultivar asexually reproduces well through the rooting of softwood and hardwood cuttings. The use of softwood cuttings is preferred.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Natural Medicines & Medicinal Plants (AREA)
  • Physiology (AREA)
  • Botany (AREA)
  • Developmental Biology & Embryology (AREA)
  • Environmental Sciences (AREA)
  • Breeding Of Plants And Reproduction By Means Of Culturing (AREA)

Abstract

A new and distinct cultivar of Prunus mahaleb is provided. The new cultivar is particularly well suited for serving as an understock during cherry production. A number of advantages are provided when compared to the standard Mahaleb rootstock. The cultivar is readily amenable to vegetative propagation (e.g., by the use of softwood cuttings), and exhibits improved resistance to Phytophthora spp. When used with a ‘Bing’ cherry scion, increased yields and yield efficiency have been observed without reduced fruit size. Improved precocity in bearing is displayed when compared to the standard Mahaleb rootstock. The new cultivar when grown without use as an understock forms a smaller tree than the ‘UCMH 55’ cultivar and the standard Mahaleb rootstock. Few suckers are produced.

Description

Botanical/commercial classification: Prunus mahaleb/Mahaleb Rootstock.
Varietal denomination: cv. ‘UCMH 56’.
SUMMARY OF THE INVENTION
Mahaleb rootstocks (i.e., Prunus mahaleb rootstocks) are widely used during both sweet and sour cherry production throughout the world. It has been the common practice to form such rootstock plants from seed following the random outcrossing of parent plants. Accordingly, cherry production encountered when using such plants as an understock has tended to be somewhat variable due to differences in the genotype of the understock. Such variation often has led to reduced field performance on some cherry trees on a random and unpredictable basis. Mahaleb rootstocks in the past have generally been found to be incapable of vegetative propagation on a reliable basis, such as through the use of softwood and hardwood cuttings. Also, such rootstocks in the past have been susceptible to root and crown fungal diseases generally known as Phytophthora spp.
SUMMARY OF THE NEW CULTIVAR
It was an object of my research to provide Prunus mahaleb rootstocks that possess characteristics that overcome shortcomings of the Mahaleb rootstock presently being used during cherry production. More specifically, it was my goal to provide cherry rootstocks that could be vegetatively propagated in an expeditious and reliable manner so that cherry growers can eliminate crop variation that can be traced to lack of uniformity in the rootstock. Also, it was a goal of my research to provide new Mahaleb rootstocks that inherently display needed resistance to disease and thereby make possible a satisfactory cherry crop on a more consistent basis combined with a reduction in the need to replant because of tree loss that is traceable to disease.
The original tree of the new Prunus mahaleb cultivar of the present invention was discovered through detailed evaluation and selection while growing in a cultivated area at the Experimental Orchards at the University of California located at Davis, Calif., U.S.A. The exact parentage of the new cultivar is unknown. The seeds used to form the planting where the discovery took place came from a random collection of wild Prunus mahaleb germplasm that had been collected from around the world. The large number of seedlings present in the planting were carefully studied and evaluated and a single plant possessing the combination of characteristics of the new cultivar of the present invention was selected and was preserved. Had this plant not been discovered and preserved, it would have been lost to mankind.
Other Prunus mahaleb cultivars resulting from the same research are ‘UCMH 55’ (U.S. Plant patent application Ser. No. 10/028,771, filed concurrently herewith), and ‘UCMH 59’ (U.S. Plant patent application Ser. No. 10/029,284, filed concurrently herewith).
It was found that the new Prunus mahaleb cultivar of the present invention exhibits the following combination of characteristics:
(a) readily is amenable to vegetative propagation,
(b) performs well as an understock for cherry production,
(c) forms a smaller tree than the ‘UCMH 55’ cultivar and the standard Mahaleb rootstock,
(d) displays improved resistance to Phytophthora spp.
(e) makes possible increased ‘Bing’ sweet cherry scion yield and yield efficiency when compared to the standard Mahaleb rootstock without reduced fruit size,
(f) demonstrates improved precocity in bearing when compared to the standard Mahaleb rootstock, and
(g) produces few suckers.
In view of the above combination of characteristics, the new cultivar of the present invention well meets the needs of cherry producers for use as an improved rootstock. Cherry scion characteristics are no longer influenced by variation in the Mahaleb rootstock resulting from the random outcrossing of parental plants. Also, the disease resistance made possible by the new cultivar is a major advantage for cherry producers.
The new cultivar of the present invention has been repeatedly reproduced through the use of softwood, semi-hardwood, and hardwood cuttings at Davis, Calif., U.S.A. Such propagation has confirmed that the characteristics of the new cultivar are stable and are firmly fixed and are transmitted to subsequent generations on a reliable basis.
The new cultivar of the present invention initially was designated ‘UC MAHALEB 156-5’, and subsequently has been named ‘UCMH 56’.
BRIEF DESCRIPTION OF THE PHOTOGRAPHS
The accompanying photographs show specimens of the plant and plant parts, and also provide DNA information concerning the new cultivar of the present invention. Color is shown as nearly true as is possible to make the same in color illustrations of this character. The trees of the new cultivar were grown at the Experimental Orchards of the University of California located at Davis, Calif., U.S.A.
FIG. 1 shows a tree of approximately 5 to 7 years of age during December. The tree is a mother plant that was being used to make propagules for additional testing and evaluation. Most of the leaves had dropped by the end of the preceding October.
FIG. 2 shows a specimen of a current season's shoot with leaves collected during mid-October. Such shoot was suitable for use to make a hardwood or semi-hardwood cutting.
FIG. 3 shows specimens of typical branches with buds of the new cultivar during the winter. Dimensions in inches and centimeters are included at the left.
FIG. 4 shows specimens of typical stones of the new cultivar during the winter. Dimensions in centimeters and inches are included.
FIG. 5 shows the DNA fingerprint of the new cultivar of the present invention as well as that of the ‘UCMH 55’ and ‘UCMH 59’ cultivars for comparative purposes. Three microsatellite markers were used during the DNA determinations (i.e., PMS30, PMS40 and PMS15). Data with respect to the plants of the new cultivar of the present invention is designated “156-5”. Data with respect to the plants of the ‘UCMH 55’ cultivar is designated “155-1”, and data with respect to the ‘UCMH 59’ cultivar is designated “159-5”.
FIG. 6 shows typical inflorescences of the new cultivar.
The primer Sequences (SEQ ID NOS: 1-6) used in this determination are as follows:
PMS 30 Forward CTG TCG AAA TGC CTA TGC
Reverse ATG AAT GCT GTG TAC ATG AGGC
PMS 40 Forward TCA CTT TCG TCC ATT TTC CC
Reverse TCA TTT TGG TCT TTG AGC TCG
PMS 15 Forward TCC GCT TCT CTG TGA GTG TG
Reverse CGA TAG TTT CCT TCC CAG ACC.
When preparing the DNA fingerprints, a total of six leaf samples were randomly collected from two different but replicate trees. Accordingly, each genotype was sampled and replicated twice. The two samples are distinguished during the presentation of data by the final digit shown in FIG. 5 (i. e., by “−1” or by “−2”). DNA was extracted using Dneasy Plant Kit from Qiagene, Inc. (Valencia, Calif., U.S.A.) following the manufacturer's protocol. The extracted DNA was purified by adding {fraction (1/10)} volume 3M sodium acetate and 2 volumes 100 percent ethanol and subsequent storage at −20° C. for an hour. The samples were centrifuged at 13,000 rpm for 15 minutes and the pellets were washed two times with 70 percent ethanol. The pellets were air dried and resolved in 50 μl TE buffer. Quantification of DNA was performed with ethidium bromide agarose gel plates. PCR was carried out under the following conditions: 100-150 ng of template DNA, 250 nM of each primer, 200 μM of dNTPs, 0.5 U of Taq Polymerase, and 1.5 mM of MgCl2. The reaction was run for 45 cycles (denaturing at 94° C. for 1 minute, annealing at 60° C. for 1 minute, with a two minute extension at 72° C.), followed by a single extension at 72° C. for 60 minutes. The amplification products were detected on 5.5 percent polyacrylamide gels using a Li-Cor IR2 4200 DNA sequencer (Li-Cor, Nebr., U.S.A.). The three microsatellite markers clearly distinguished the three cultivars. Both repeats of each rootstock showed identical fingerprints. The marker PMS30 produced two bands for rootstock ‘UCHM 55’ at 132 bp (base pair) and 159 bp, two bands for ‘UCMH 56’ at 132 bp and 168 bp, and one band for ‘UCMH 59’ at 142 bp. Marker PMS40 produced two bands for ‘UCMH 55’ at 92 bp and 111 bp, and one band for ‘UCMH 56’ at 92 bp, and two bands for ‘UCMH 59’ at 92 bp and 129 bp. Marker PMS15 produced two bands for ‘UCMH 55’ at 118 bp and 128 bp, two bands for ‘UCMH 56’ at 112 bp and 123 bp, and two bands for ‘UCMH 59’ at 105 bp and 115 bp.
FIG. 6 shows a typical inflorescence.
DETAILED DESCRIPTION
The following is a detailed description of the new cultivar. The tree was grown at the Experimental Orchards of the University of California at Davis, Calif., U.S.A. Color designations are presented with reference to the “Dictionary of Color” by Maerz and Paul, First Edition (1930).
Tree:
Size.—Smaller than the ‘UCMH 55’ and ‘UCMH 59’ cultivars. An eight year-old tree of the ‘UCMH 56’ cultivar that has undergone some pruning commonly will display a height of approximately 4 meters and a width of approximately 3 meters. Trunk girth at 30 cm above the soil line commonly will possess a cross-sectional area of approximately 400 cm2.
Growth.—Highly branched, the upper canopy is very upright, and two-year-old wood in the lower canopy is pendulous.
Wood.—The wood is fine to intermediate and commonly ranges from less than 1 cm to 3 cm in diameter.
Bark.—Possesses a rough raised surface and an Iron Grey (24 A 2) coloration.
Branches:
Shoot growth form.—Straight in the upper canopy and pendulous in the lower canopy with one leaf per node in a spiral pattern around the shoot, and laterals arise at approximately 90 degrees from the point of origin on the main scaffold and are branched at approximately 75 to 90 degrees.
Size.—Both current and previous season wood is fine to intermediate and varies in diameter less than 1 cm.
Spurs.—Commonly 1 to 4 spurs are present per 85 cm of previous season shoot that measure approximately 1 to 5 cm in length. The coloration is Chickadee gray (47 A 1) underlaid with Burnt umber (15 A 12).
Internode length.—On mixed shoots approximately 1 to 4 cm in length and increasing in length basipetally, and approximately 2 mm to 2.5 cm in length between reproductive nodes.
Shoot bark.—Smooth in texture, and the coloration is Burnt umber (15 A 12), and Arabian brown (14 A 11) to Madura (14 I 8).
Main scaffold bark.—Platinum (45 A 3) in coloration with an underlay of Rubient (55 L 8).
Lenticels.—Prominent, densely distributed, and under magnification are raised. The size on subsidiary shoots commonly ranges from 2 to 5 mm in length with approximately 15 lenticles being present per square inch. The coloration is Parchment (12 B 3).
Axillary buds.—Vegetative buds are borne in the axils of every leaf along the shoot, and are single. The buds are imbricate and sessile. The bud tips are pointed and the bud pose is adpressed on dormant new wood. The bud support is small.
Leaves:
Bearing.—Simple, spiraled around the shoot, and petiolate.
Pose.—Curved outward and downward, and often curve under slightly at the apex.
Length.—Approximately 3 to 5 cm in length and approximately 2.5 to 3.5 cm in width on the upper canopy and on the lower canopy.
Width.—Approximately 2.5 to 3.5 cm on the upper canopy and on the lower canopy.
Form.—Oval-elliptic to oval with an acuminate tip and a truncate base on the upper canopy and on the lower canopy
Margins.—Crenate and glandular between rounded teeth.
Surfaces.—Glabrous on the dorsal and ventral surfaces with short stiff hairs along the midrib of the ventral surface that are visible with magnification.
Petiole.—Commonly with glands that are dark Russet brown (14 I 12) in coloration at the leaf-petiole juncture, approximately 1 to 1.5 cm in length, and Russet Green (20 K 1)in coloration. Such glands commonly are less than 1 mm in length and less than 0.5 mm in width.
Venation.—Pinnate, with the midrib and other venation being Russet green (20 K 1) in coloration.
Color.—21 L 6 (Parrot Green) to 21 L 9 on the upper surface and Piquant green (20 K 6) on the under surface.
Leaf drop.—On Dec. 11, 2000 there was approximately 1 to 5 percent leaf fall.
Flowers:
Bloom time.—Full bloom on Apr. 4, 2002.
Floral buds.—Approximately 2 mm in length and approximately 1 mm in width, and Burmese ruby (7 H 6) in colorattion.
Type.—Primarily inflorescent in panicles, but occasionally found as singles.
Form.—The paniculate inflorescence has 5 to 10 flowers and commonly 3 to 5 flowers with a peduncle including the rachis of approximately 1 to 1.5 cm in length and a pedicel of approximately 0.7 to 1.2 cm in length. The peduncles and pedicels are Cossak green (23 L 11) in coloration.
Bearing.—Directly on previous season's laterals in mixed shoots of 50 to 90 cm in length on average without spurs. Inflorescences are single at each node and whorled along the upper one-half of one year-old wood up to the apex of the previous season's growth. Five to ten lateral shoot buds are proximal to the reproductive portion and commonly 12 to 15 floral buds are present within the reproductive portion. Axillary buds on one year-old wood break after the floral buds and grow out to vegetative laterals during fruit development. The current season portion of the shoot is vegetative and few of the axillary buds on this portion break in the current year.
Pollination required.—Any Mahaleb rootstock that is producing flowers which overlap with the bloom period.
Color.—White.
Petal number.—Five.
Petal size.—Approximately 7 mm in length and approximately 6 mm in width at the widest point.
Carpel.—Single.
Pistil.—Approximately 6 to 7 mm in length with the stigma and style being Marguerite Yellow (10 C 1) in coloration.
Stamen.—Commonly approximately 10 to 14 per flower, and approximately 5 to 7 mm in length.
Anthers.—Sulphur Yellow (10 J 1) in coloration when indehiscent.
Filaments.—Marguerite Yellow (10 C 1) in coloration.
Pollen.—Sulpur Yellow (10 J 1) in coloration.
Scent.—Mildly fragrant and similar to that of almond flowers.
Fruit:
Chilling requirement.—Approximatley 750 to 1,000 hours less than or equal to 45° F.
Bearing.—Drupe.
Fruit shape.—Substantially round.
Fruit size.—Approximately 0.8 to 1.2 cm in diameter.
Maturity date.—Late June to early July.
Skin color.—Dark purple-mahogany (56 A 12) to near black (48 A 12).
Fresh color.—Dark purple-mahogany (56 A 12) to near black (48 A 12).
Flesh firmness.—Soft when fully ripe and juicy.
Fruit juice color.—Dark purple-mahogany (56 A 12) to near black (48 A 12).
Cracking susceptibility.—None observed during observations to date.
Eating quality.—Astringent and bitter taste renders unsuitable for eating.
Fruit drop.—Susceptibility is low (approximately 10 to 40 percent).
Fruit stalk.—Short, and approximately 0.7 to 1.5 cm when pedicel alone is measured. Very small bracts may persist and leaves commonly are absent on the stalk.
Leaves on fruit stalk.—None, however, very small bracts occasionally persist that are Paradise green (22 L 11) in coloration.
Susceptibility to pre-harvest fruit drop.—Low (approximately 10 to 40 percent).
Stone shape.—Substantially spherical (as illustrated in FIG. 4).
Stone size.—Very small and approximately 3 to 4 mm in diameter.
Seed color.—Oyster white (10 B 1).
Disease resistance: The new cultivar has shown over a 90 percent survival rate in field trials at sites that are heavily infested with Phytophthora spp. and stem pitting virus. At the same sites, approximately 50 percent of the standard Mahaleb plants died.
Vegetative propagation: The new cultivar asexually reproduces well through the rooting of softwood and hardwood cuttings. The use of softwood cuttings is preferred.
Use as a scion rootstock: Field testing has been conducted using a scion of ‘Bing’ cherry following budding. Full bloom appeared slightly earlier than when utilizing a standard Mahaleb rootstock. This may lead to earlier ripening fruit or suggest a lower chill requirement for the rootstock compared to standard Mahaleb. The new cultivar has been found to yield a slightly smaller scion tree than that formed on the standard Mahaleb rootstock; however, the resulting tree nevertheless is considered to be vigorous. Precocious flowering and cropping are facilitated when using the new cultivar as a rootstock. For instance, flower and fruit production can begin easily in the 4th or 5th growing season with the flowers opening earlier in the season. ‘Bing’ cherry yield was approximately 1.6 times that of comparable trees where the rootstock was standard Mahaleb. There also was a higher yield efficiency when using the new cultivar as a rootstock. Accordingly, the new variety has been found to provide greater productivity per unit of land occupied. The fruit size has been found to be comparable to that formed with standard Mahaleb rootstock even with the higher yield per tree. To date the new cultivar produced low numbers of root and crown suckers.
6 1 18 DNA Artificial Sequence PMS 30 forward primer 1 ctgtcgaaat gcctatgc 18 2 22 DNA Artificial Sequence PMS 30 reverse primer 2 atgaatgctg tgtacatgag gc 22 3 20 DNA Artificial Sequence PMS 40 forward primer 3 tcactttcgt ccattttccc 20 4 21 DNA Artificial Sequence PMS 40 reverse primer 4 tcattttggt ctttgagctc g 21 5 20 DNA Artificial Sequence PMS 15 forward primer 5 tccgcttctc tgtgagtgtg 20 6 21 DNA Artificial Sequence PMS 15 reverse primer 6 cgatagtttc cttcccagac c 21

Claims (1)

I claim:
1. A new and distinct cultivar of Prunus mahaleb plant that exhibits the following combination of characteristics:
(a) readily is amenable to vegetative propagation,
(b) performs well as an understock for cherry production,
(c) forms a smaller tree than the ‘UCMH 55’ cultivar and the standard Mahaleb rootstock,
(d) displays improved resistance to Phytophthora spp.,
(e) makes possible increased ‘Bing’ sweet cherry scion yield and yield efficiency without reduced fruit size when compared to the standard Mahaleb rootstock,
(f) demonstrates improved precocity in bearing when compared to the standard Mahaleb rootstock, and
(g) produces few suckers;
substantially as illustrated and described.
US10/028,772 2001-12-28 2001-12-28 Mahaleb rootstock named ‘UCMH 56’ Expired - Lifetime USPP14271P3 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US10/028,772 USPP14271P3 (en) 2001-12-28 2001-12-28 Mahaleb rootstock named ‘UCMH 56’

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US10/028,772 USPP14271P3 (en) 2001-12-28 2001-12-28 Mahaleb rootstock named ‘UCMH 56’

Publications (2)

Publication Number Publication Date
US20030126654P1 US20030126654P1 (en) 2003-07-03
USPP14271P3 true USPP14271P3 (en) 2003-11-04

Family

ID=21845325

Family Applications (1)

Application Number Title Priority Date Filing Date
US10/028,772 Expired - Lifetime USPP14271P3 (en) 2001-12-28 2001-12-28 Mahaleb rootstock named ‘UCMH 56’

Country Status (1)

Country Link
US (1) USPP14271P3 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USPP15723P3 (en) * 2002-01-11 2005-04-19 Krymsk Breeding Station Prunus plant named ‘VSL-2’

Also Published As

Publication number Publication date
US20030126654P1 (en) 2003-07-03

Similar Documents

Publication Publication Date Title
USPP17742P3 (en) Peach tree—named ‘White County’ cultivar
USPP17911P3 (en) Peach tree—named ‘White Rock’ cultivar
USPP22464P3 (en) Peach tree named ‘White Diamond’
USPP14271P3 (en) Mahaleb rootstock named ‘UCMH 56’
USPP26920P3 (en) Peach tree named ‘Souvenirs’
USPP14359P3 (en) Mahaleb rootstock named ‘UCMH 59’
USPP24410P3 (en) Distylium plant named ‘PIIDIST-I’
USPP14321P3 (en) Mahaleb rootstock named ‘UCMH 55’
US20110119797P1 (en) Peach tree, 'Burpeachtwentythree'
USPP16068P2 (en) Peach tree ‘Sweet Henry’
USPP35017P2 (en) Peach tree named ‘Whitewater’
USPP26367P3 (en) Nectarine tree named ‘Amoore Sweet’
USPP34612P2 (en) Strawberry plant named ‘QBC-1’
USPP21723P2 (en) Interspecific tree named ‘NEWROOT-1’
US20210243927P1 (en) Peach Tree Named 'A-858P'
USPP28932P2 (en) Morus plant named ‘Trader’
USPP13526P2 (en) Interspecific tree named ‘Yuba Gold’
USPP13503P2 (en) Interspecific tree named ‘Spicezee’
USPP15291P2 (en) Nectarine tree named ‘Honey Diva’
USPP19920P2 (en) Cherry tree named ‘Royal Hazel’
USPP20745P3 (en) Grape plant named ‘A-2640’
USPP16590P2 (en) Interspecific tree named ‘Flavor Finale’
USPP15557P2 (en) Peach tree named ‘Klamath’
USPP15399P3 (en) Cherry tree named ‘Royal Kay’
USPP16599P2 (en) Interspecific tree named ‘Autumn Sprite’

Legal Events

Date Code Title Description
AS Assignment

Owner name: REGENTS OF THE UNIVERSITY OF CALIFORNIA, THE, CALI

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:SOUTHWICK, STEPHEN M.;REEL/FRAME:012574/0934

Effective date: 20020126