Difference between revisions of "Arctostaphylos"
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− | --><span class="statement" id="st-undefined" data-properties=""><b>Shrubs </b>or trees, either burled and resprouting after fire or not burled and killed by fire; bark usually promptly exfoliating, reddish, (thin), or, sometimes, persistent, gray, rough, shredded (A. morroensis, A. nissenana, A. nummularia, A. osoensis, A. pajaroensis, A. rudis, A. tomentosa). <b>Stems</b> prostrate to erect, glabrous or hairy, sometimes glandular. <b>Leaves</b> (usually spreading, sometimes erect, sometimes overlapping when petiole is short), usually isofacial, sometimes bifacial in stomatal distribution (stomata present only on abaxial surface) and usually in color or pubescence (A. andersonii, A. crustacea, A. edmundsii, A. insularis, A. morroensis, A. nummularia, A. pajaroensis, A. pumila, A. sensitiva, A. tomentosa, A. uva-ursi); petiole absent or present; blade ovate to elliptic, coriaceous, margins entire (serrulate in A. pacifica, rarely so in young plants or resprouts, sometimes ciliate), usually plane, rarely revolute, surfaces (smooth to papillate or scabrous), hairy or glabrous. <b>Inflorescences</b> racemes or panicles (panicle branches racemelike), 5–20(–50)-flowered, (partially developing with new stem growth and dormant (immature inflorescences) for 6–9 months, usually pendent, can be erect whenimmature, pendent in flower; bracts persistent, (deciduous after flowering in A. pringlei), tan or light brown, scalelike, sometimes keeled, deltate or ovate, (tips often marcescent), or hue as in leaves, leaflike, narrowly lanceolate and flat, buds usually clustered, bracts imbricate, sometimes buds spread apart on axis, bracts not imbricate); bracteoles absent. <b>Flowers</b> bisexual; sepals persistent, 5 (4 in A. nummularia, A. sensitiva), distinct, ovate to deltate; petals 5 (4 in A. nummularia, A. sensitiva), connate nearly their entire lengths, white to pink, corolla conic to urceolate; stamens (8–)10, included; filaments dilated, (usually hairy at base); anthers (dark red), with 2 (recurved), dorsal awns, dehiscent by terminal pores; ovary 2–10-locular; stigma capitate. <b>Drupes</b> red, reddish brown, or brown, globose or depressed-globose, (exocarp coriaceous, rarely thin), smooth, (mesocarp usually dry, mealy, rarely absent, endocarp multiple-seeded); pyrenes 1–10, connate or not. <b>Seeds</b> 1–10, distinct or connate along radial faces of stony endocarp into 2s or 3s, sometimes connate into single sphere, (triangular-ovoid). <b>x</b> = 13.</span><!-- | + | --><span class="statement" id="st-undefined" data-properties=""><b>Shrubs </b>or trees, either burled and resprouting after fire or not burled and killed by fire; bark usually promptly exfoliating, reddish, (thin), or, sometimes, persistent, gray, rough, shredded (<i>A. morroensis</i>, <i>A. nissenana</i>, <i>A. nummularia</i>, <i>A. osoensis</i>, <i>A. pajaroensis</i>, <i>A. rudis</i>, <i>A. tomentosa</i>). <b>Stems</b> prostrate to erect, glabrous or hairy, sometimes glandular. <b>Leaves</b> (usually spreading, sometimes erect, sometimes overlapping when petiole is short), usually isofacial, sometimes bifacial in stomatal distribution (stomata present only on abaxial surface) and usually in color or pubescence (<i>A. andersonii</i>, <i>A. crustacea</i>, <i>A. edmundsii</i>, <i>A. insularis</i>, <i>A. morroensis</i>, <i>A. nummularia</i>, <i>A. pajaroensis</i>, <i>A. pumila</i>, <i>A. sensitiva</i>, <i>A. tomentosa</i>, <i>A. uva-ursi</i>); petiole absent or present; blade ovate to elliptic, coriaceous, margins entire (serrulate in <i>A. pacifica</i>, rarely so in young plants or resprouts, sometimes ciliate), usually plane, rarely revolute, surfaces (smooth to papillate or scabrous), hairy or glabrous. <b>Inflorescences</b> racemes or panicles (panicle branches racemelike), 5–20(–50)-flowered, (partially developing with new stem growth and dormant (immature inflorescences) for 6–9 months, usually pendent, can be erect whenimmature, pendent in flower; bracts persistent, (deciduous after flowering in <i>A. pringlei</i>), tan or light brown, scalelike, sometimes keeled, deltate or ovate, (tips often marcescent), or hue as in leaves, leaflike, narrowly lanceolate and flat, buds usually clustered, bracts imbricate, sometimes buds spread apart on axis, bracts not imbricate); bracteoles absent. <b>Flowers</b> bisexual; sepals persistent, 5 (4 in <i>A. nummularia</i>, <i>A. sensitiva</i>), distinct, ovate to deltate; petals 5 (4 in <i>A. nummularia</i>, <i>A. sensitiva</i>), connate nearly their entire lengths, white to pink, corolla conic to urceolate; stamens (8–)10, included; filaments dilated, (usually hairy at base); anthers (dark red), with 2 (recurved), dorsal awns, dehiscent by terminal pores; ovary 2–10-locular; stigma capitate. <b>Drupes</b> red, reddish brown, or brown, globose or depressed-globose, (exocarp coriaceous, rarely thin), smooth, (mesocarp usually dry, mealy, rarely absent, endocarp multiple-seeded); pyrenes 1–10, connate or not. <b>Seeds</b> 1–10, distinct or connate along radial faces of stony endocarp into 2s or 3s, sometimes connate into single sphere, (triangular-ovoid). <b>x</b> = 13.</span><!-- |
-->{{Treatment/Body | -->{{Treatment/Body | ||
|distribution=North America;Mexico;Central America;Europe;Asia. | |distribution=North America;Mexico;Central America;Europe;Asia. | ||
|discussion=<p>Species 66 (62 in the flora).</p><!-- | |discussion=<p>Species 66 (62 in the flora).</p><!-- | ||
− | --><p>Arctostaphylos is richly diverse and taxonomically challenging. Unequivocal fossils appear as far back as the middle Miocene. Many pulses of diversification and decimation may have taken place in the genus since then; evidence suggests that there has been a rapid radiation in the last 1.5 million years. Some morphological features are not clearly differentiated among taxa and appear to be mosaically distributed.</p><!-- | + | --><p><i>Arctostaphylos</i> is richly diverse and taxonomically challenging. Unequivocal fossils appear as far back as the middle Miocene. Many pulses of diversification and decimation may have taken place in the genus since then; evidence suggests that there has been a rapid radiation in the last 1.5 million years. Some morphological features are not clearly differentiated among taxa and appear to be mosaically distributed.</p><!-- |
− | --><p>Multiple lines of evidence suggest that Arctostaphylos is a terminal branch within Arbutoideae. Arctous is treated here as a separate genus, as it is likely sister to Arctostaphylos. Only one species of Arctostaphylos, A. uva-ursi, is found outside of western North America, Mexico, and Guatemala. Taxa are concentrated within the California Floristic Province (southern Oregon to northern Baja California, Mexico) with the greatest diversity along the central California coast, where over half of the taxa are found. Along the immediate California coastline, most Arctostaphylos species are found within vegetation strongly influenced by summer fog, either within maritime chaparral, as a forest-edge species, or as part of a closed-cone conifer woodland and forest. Away from the coast, Arctostaphylos species are distributed to the desert edge in chaparral woodlands and forests.</p><!-- | + | --><p>Multiple lines of evidence suggest that <i>Arctostaphylos</i> is a terminal branch within Arbutoideae. <i>Arctous</i> is treated here as a separate genus, as it is likely sister to <i>Arctostaphylos</i>. Only one species of <i>Arctostaphylos</i>, <i>A. uva-ursi</i>, is found outside of western North America, Mexico, and Guatemala. Taxa are concentrated within the California Floristic Province (southern Oregon to northern Baja California, Mexico) with the greatest diversity along the central California coast, where over half of the taxa are found. Along the immediate California coastline, most <i>Arctostaphylos</i> species are found within vegetation strongly influenced by summer fog, either within maritime chaparral, as a forest-edge species, or as part of a closed-cone conifer woodland and forest. Away from the coast, <i>Arctostaphylos</i> species are distributed to the desert edge in chaparral woodlands and forests.</p><!-- |
− | --><p>The relationship of Arctostaphylos with poor soils correlates with a highly diverse mycorrhizal fungal community associated with these plants. Because conifers and other ectomycorrhizal trees share the ability to form mycorrhizae with a large percentage of the fungal species associated with Arctostaphylos, a long-term successional dynamic of shrub- and forest-dominated systems mediated by fire has arisen throughout the range of this genus. Habitats of Arctostaphylos species generally have nutrient-poor, usually acidic soils and relatively frequent fires. Fire has selected for different aspects of life history. Approximately one-third of the taxa have a burl—a swollen woody mass at the base of the main stem containing dormant buds (or in some species, also epicormic, forming at nodes where layering stems establish roots) from which plants can sprout after the canopy is killed by fire. The other taxa lack a burl and whole plants are killed by fire; for these species, replacement of populations is completely dependent on persistent soil seed banks.</p><!-- | + | --><p>The relationship of <i>Arctostaphylos</i> with poor soils correlates with a highly diverse mycorrhizal fungal community associated with these plants. Because conifers and other ectomycorrhizal trees share the ability to form mycorrhizae with a large percentage of the fungal species associated with <i>Arctostaphylos</i>, a long-term successional dynamic of shrub- and forest-dominated systems mediated by fire has arisen throughout the range of this genus. Habitats of <i>Arctostaphylos</i> species generally have nutrient-poor, usually acidic soils and relatively frequent fires. Fire has selected for different aspects of life history. Approximately one-third of the taxa have a burl—a swollen woody mass at the base of the main stem containing dormant buds (or in some species, also epicormic, forming at nodes where layering stems establish roots) from which plants can sprout after the canopy is killed by fire. The other taxa lack a burl and whole plants are killed by fire; for these species, replacement of populations is completely dependent on persistent soil seed banks.</p><!-- |
--><p>Because of the recent divergence, reproductive barriers are not strong among some species. Introgression and species of diploid hybrid origin may be frequent. Tetraploids are hypothesized to be of cross-clade hybridization followed by polyploidization. This makes identifying both diploid and tetraploid lineages difficult.</p><!-- | --><p>Because of the recent divergence, reproductive barriers are not strong among some species. Introgression and species of diploid hybrid origin may be frequent. Tetraploids are hypothesized to be of cross-clade hybridization followed by polyploidization. This makes identifying both diploid and tetraploid lineages difficult.</p><!-- | ||
− | --><p>In Arctostaphylos, one cannot overemphasize the importance of field observations for proper identification. Generally, one should carefully observe multiple individuals within a stand to determine whether individuals have burls and to determine the bark condition in older stems (described below). Other important characters include whether leaves are bifacial or isofacial, the indument patterns on young twigs, leaf shape and indument, and a number of features of the inflorescence, especially its indument, number of branches, size and shape of fruits, and whether stones within fruits are distinct or connate. Characters of the immature inflorescence (such as flowering bract size and shape and arrangement of bracts and buds) can be helpful. In post-fire habitats, plants can be readily observed sprouting from burls, but in older stands it is sometimes necessary to dig around the base of the plants to confirm the presence or absence of burls.</p><!-- | + | --><p>In <i>Arctostaphylos</i>, one cannot overemphasize the importance of field observations for proper identification. Generally, one should carefully observe multiple individuals within a stand to determine whether individuals have burls and to determine the bark condition in older stems (described below). Other important characters include whether leaves are bifacial or isofacial, the indument patterns on young twigs, leaf shape and indument, and a number of features of the inflorescence, especially its indument, number of branches, size and shape of fruits, and whether stones within fruits are distinct or connate. Characters of the immature inflorescence (such as flowering bract size and shape and arrangement of bracts and buds) can be helpful. In post-fire habitats, plants can be readily observed sprouting from burls, but in older stands it is sometimes necessary to dig around the base of the plants to confirm the presence or absence of burls.</p><!-- |
--><p>Older stems are most often smooth, exfoliating promptly after stem growth in the summer, to reveal reddish bark. In the foothills of the Sierra Nevada and along the California coast, some species bear bark that is usually grayish and becomes rough with persistent, flat, shredded pieces. The indument on twigs of the current year may vary widely with hairs of different lengths, types, or layers. Indument is found also on leaves, inflorescences, and fruits. Careful assessment is important; most frequently indument patterns are similar among these structures and variation from that pattern can be diagnostic.</p><!-- | --><p>Older stems are most often smooth, exfoliating promptly after stem growth in the summer, to reveal reddish bark. In the foothills of the Sierra Nevada and along the California coast, some species bear bark that is usually grayish and becomes rough with persistent, flat, shredded pieces. The indument on twigs of the current year may vary widely with hairs of different lengths, types, or layers. Indument is found also on leaves, inflorescences, and fruits. Careful assessment is important; most frequently indument patterns are similar among these structures and variation from that pattern can be diagnostic.</p><!-- | ||
− | --><p>Generally, two patterns of leaf morphology are found. In some species, leaves are bifacial; stomata are restricted to the abaxial surface. Stomata can be observed using a 10× hand lens and appear as white spots crowding the areas between leaf veinlets. When stomata are restricted abaxially, leaf surfaces typically differ in hue or indument patterns on adaxial versus abaxial surfaces. More frequently, leaves are isofacial; abaxial and adaxial surfaces are similar in hue and indument patterns, and stomata are found on both surfaces. There are exceptions to these general patterns, and it is important to examine both leaf surfaces under magnification. Arctostaphylos insularis, for example, has stomata restricted to the abaxial surface; otherwise, the leaf surfaces are similar in color and pubescence; A. pacifica has stomata on both leaf surfaces and the surfaces differ in hue.</p><!-- | + | --><p>Generally, two patterns of leaf morphology are found. In some species, leaves are bifacial; stomata are restricted to the abaxial surface. Stomata can be observed using a 10× hand lens and appear as white spots crowding the areas between leaf veinlets. When stomata are restricted abaxially, leaf surfaces typically differ in hue or indument patterns on adaxial versus abaxial surfaces. More frequently, leaves are isofacial; abaxial and adaxial surfaces are similar in hue and indument patterns, and stomata are found on both surfaces. There are exceptions to these general patterns, and it is important to examine both leaf surfaces under magnification. <i>Arctostaphylos insularis</i>, for example, has stomata restricted to the abaxial surface; otherwise, the leaf surfaces are similar in color and pubescence; <i>A. pacifica</i> has stomata on both leaf surfaces and the surfaces differ in hue.</p><!-- |
− | --><p>Arctostaphylos produces a single annual growth of stems immediately after flowering. New inflorescences develop at the ends of these stems during this growth period and do not fully mature. Immature inflorescences generally remain dormant four to six months; these are critical in identifying taxa. One species (A. pringlei) initiates inflorescences immediately prior to flowering and thus flowers on current year’s stems. Inflorescences range from relatively short racemes to larger, spreading panicles. Plants that produce racemes frequently have inflorescences with a single, relatively small branch—“racemelike” structures. Usually, examination of multiple inflorescences will provide insight into whether the plant has panicle inflorescences. These structures should be examined under a hand lens for patterns of indument along the axes, bracts, and pedicels of either the flower or the fruit.</p><!-- | + | --><p><i>Arctostaphylos</i> produces a single annual growth of stems immediately after flowering. New inflorescences develop at the ends of these stems during this growth period and do not fully mature. Immature inflorescences generally remain dormant four to six months; these are critical in identifying taxa. One species (<i>A. pringlei</i>) initiates inflorescences immediately prior to flowering and thus flowers on current year’s stems. Inflorescences range from relatively short racemes to larger, spreading panicles. Plants that produce racemes frequently have inflorescences with a single, relatively small branch—“racemelike” structures. Usually, examination of multiple inflorescences will provide insight into whether the plant has panicle inflorescences. These structures should be examined under a hand lens for patterns of indument along the axes, bracts, and pedicels of either the flower or the fruit.</p><!-- |
− | --><p>Although flower morphology varies among taxa, it is rarely important in identification. The pattern of indument on the ovary often is important. Frequently, the indument of the ovary is similar to that of mature fruit, but sometimes not; for example, Arctostaphylos canescens has densely hairy ovaries but the mature fruits are glabrescent. There are pairs of taxa for which ovary indument is the crucial distinguishing character; plant distribution can also be used in those cases.</p><!-- | + | --><p>Although flower morphology varies among taxa, it is rarely important in identification. The pattern of indument on the ovary often is important. Frequently, the indument of the ovary is similar to that of mature fruit, but sometimes not; for example, <i>Arctostaphylos canescens</i> has densely hairy ovaries but the mature fruits are glabrescent. There are pairs of taxa for which ovary indument is the crucial distinguishing character; plant distribution can also be used in those cases.</p><!-- |
− | --><p>Fruits are critical for identifying some taxa in Arctostaphylos. Fruits are usually present in a population because they are produced early in the spring, mature in the summer, and persist well into the fall and winter, often with some remaining into the next flowering season. Fruits can also be found in the litter during the latter part of the season. The fruits are a type of drupe, technically a nuculanium; the exocarp is dry at maturity, the mesocarp is dry and mealy or absent, and the fruit contains multiple hard stones. The stones are separate (distinct) in some taxa, each containing a single seed. In other taxa, stones may be connate along radial walls such that two or three stones are connate, while other stones in the same fruit remain distinct. Other species have fruits within which all radial surfaces of stones are connate, yielding a single structure, either globose or ellipsoid. With relatively few exceptions, fruits are of two general shapes: globose or nearly so, or depressed-globose and dimpled on both ends. Fruits also can be smooth and glabrous or hairy, sometimes viscid.</p> | + | --><p>Fruits are critical for identifying some taxa in <i>Arctostaphylos</i>. Fruits are usually present in a population because they are produced early in the spring, mature in the summer, and persist well into the fall and winter, often with some remaining into the next flowering season. Fruits can also be found in the litter during the latter part of the season. The fruits are a type of drupe, technically a nuculanium; the exocarp is dry at maturity, the mesocarp is dry and mealy or absent, and the fruit contains multiple hard stones. The stones are separate (distinct) in some taxa, each containing a single seed. In other taxa, stones may be connate along radial walls such that two or three stones are connate, while other stones in the same fruit remain distinct. Other species have fruits within which all radial surfaces of stones are connate, yielding a single structure, either globose or ellipsoid. With relatively few exceptions, fruits are of two general shapes: globose or nearly so, or depressed-globose and dimpled on both ends. Fruits also can be smooth and glabrous or hairy, sometimes viscid.</p> |
|tables= | |tables= | ||
|references={{Treatment/Reference | |references={{Treatment/Reference | ||
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|publication year= | |publication year= | ||
|special status= | |special status= | ||
− | |source xml=https:// | + | |source xml=https://bitbucket.org/aafc-mbb/fna-data-curation/src/2e0870ddd59836b60bcf96646a41e87ea5a5943a/coarse_grained_fna_xml/V8/V8_766.xml |
|subfamily=Ericaceae subfam. Arbutoideae | |subfamily=Ericaceae subfam. Arbutoideae | ||
|genus=Arctostaphylos | |genus=Arctostaphylos |
Latest revision as of 20:25, 9 February 2021
Shrubs or trees, either burled and resprouting after fire or not burled and killed by fire; bark usually promptly exfoliating, reddish, (thin), or, sometimes, persistent, gray, rough, shredded (A. morroensis, A. nissenana, A. nummularia, A. osoensis, A. pajaroensis, A. rudis, A. tomentosa). Stems prostrate to erect, glabrous or hairy, sometimes glandular. Leaves (usually spreading, sometimes erect, sometimes overlapping when petiole is short), usually isofacial, sometimes bifacial in stomatal distribution (stomata present only on abaxial surface) and usually in color or pubescence (A. andersonii, A. crustacea, A. edmundsii, A. insularis, A. morroensis, A. nummularia, A. pajaroensis, A. pumila, A. sensitiva, A. tomentosa, A. uva-ursi); petiole absent or present; blade ovate to elliptic, coriaceous, margins entire (serrulate in A. pacifica, rarely so in young plants or resprouts, sometimes ciliate), usually plane, rarely revolute, surfaces (smooth to papillate or scabrous), hairy or glabrous. Inflorescences racemes or panicles (panicle branches racemelike), 5–20(–50)-flowered, (partially developing with new stem growth and dormant (immature inflorescences) for 6–9 months, usually pendent, can be erect whenimmature, pendent in flower; bracts persistent, (deciduous after flowering in A. pringlei), tan or light brown, scalelike, sometimes keeled, deltate or ovate, (tips often marcescent), or hue as in leaves, leaflike, narrowly lanceolate and flat, buds usually clustered, bracts imbricate, sometimes buds spread apart on axis, bracts not imbricate); bracteoles absent. Flowers bisexual; sepals persistent, 5 (4 in A. nummularia, A. sensitiva), distinct, ovate to deltate; petals 5 (4 in A. nummularia, A. sensitiva), connate nearly their entire lengths, white to pink, corolla conic to urceolate; stamens (8–)10, included; filaments dilated, (usually hairy at base); anthers (dark red), with 2 (recurved), dorsal awns, dehiscent by terminal pores; ovary 2–10-locular; stigma capitate. Drupes red, reddish brown, or brown, globose or depressed-globose, (exocarp coriaceous, rarely thin), smooth, (mesocarp usually dry, mealy, rarely absent, endocarp multiple-seeded); pyrenes 1–10, connate or not. Seeds 1–10, distinct or connate along radial faces of stony endocarp into 2s or 3s, sometimes connate into single sphere, (triangular-ovoid). x = 13.
Distribution
North America, Mexico, Central America, Europe, Asia.
Discussion
Species 66 (62 in the flora).
Arctostaphylos is richly diverse and taxonomically challenging. Unequivocal fossils appear as far back as the middle Miocene. Many pulses of diversification and decimation may have taken place in the genus since then; evidence suggests that there has been a rapid radiation in the last 1.5 million years. Some morphological features are not clearly differentiated among taxa and appear to be mosaically distributed.
Multiple lines of evidence suggest that Arctostaphylos is a terminal branch within Arbutoideae. Arctous is treated here as a separate genus, as it is likely sister to Arctostaphylos. Only one species of Arctostaphylos, A. uva-ursi, is found outside of western North America, Mexico, and Guatemala. Taxa are concentrated within the California Floristic Province (southern Oregon to northern Baja California, Mexico) with the greatest diversity along the central California coast, where over half of the taxa are found. Along the immediate California coastline, most Arctostaphylos species are found within vegetation strongly influenced by summer fog, either within maritime chaparral, as a forest-edge species, or as part of a closed-cone conifer woodland and forest. Away from the coast, Arctostaphylos species are distributed to the desert edge in chaparral woodlands and forests.
The relationship of Arctostaphylos with poor soils correlates with a highly diverse mycorrhizal fungal community associated with these plants. Because conifers and other ectomycorrhizal trees share the ability to form mycorrhizae with a large percentage of the fungal species associated with Arctostaphylos, a long-term successional dynamic of shrub- and forest-dominated systems mediated by fire has arisen throughout the range of this genus. Habitats of Arctostaphylos species generally have nutrient-poor, usually acidic soils and relatively frequent fires. Fire has selected for different aspects of life history. Approximately one-third of the taxa have a burl—a swollen woody mass at the base of the main stem containing dormant buds (or in some species, also epicormic, forming at nodes where layering stems establish roots) from which plants can sprout after the canopy is killed by fire. The other taxa lack a burl and whole plants are killed by fire; for these species, replacement of populations is completely dependent on persistent soil seed banks.
Because of the recent divergence, reproductive barriers are not strong among some species. Introgression and species of diploid hybrid origin may be frequent. Tetraploids are hypothesized to be of cross-clade hybridization followed by polyploidization. This makes identifying both diploid and tetraploid lineages difficult.
In Arctostaphylos, one cannot overemphasize the importance of field observations for proper identification. Generally, one should carefully observe multiple individuals within a stand to determine whether individuals have burls and to determine the bark condition in older stems (described below). Other important characters include whether leaves are bifacial or isofacial, the indument patterns on young twigs, leaf shape and indument, and a number of features of the inflorescence, especially its indument, number of branches, size and shape of fruits, and whether stones within fruits are distinct or connate. Characters of the immature inflorescence (such as flowering bract size and shape and arrangement of bracts and buds) can be helpful. In post-fire habitats, plants can be readily observed sprouting from burls, but in older stands it is sometimes necessary to dig around the base of the plants to confirm the presence or absence of burls.
Older stems are most often smooth, exfoliating promptly after stem growth in the summer, to reveal reddish bark. In the foothills of the Sierra Nevada and along the California coast, some species bear bark that is usually grayish and becomes rough with persistent, flat, shredded pieces. The indument on twigs of the current year may vary widely with hairs of different lengths, types, or layers. Indument is found also on leaves, inflorescences, and fruits. Careful assessment is important; most frequently indument patterns are similar among these structures and variation from that pattern can be diagnostic.
Generally, two patterns of leaf morphology are found. In some species, leaves are bifacial; stomata are restricted to the abaxial surface. Stomata can be observed using a 10× hand lens and appear as white spots crowding the areas between leaf veinlets. When stomata are restricted abaxially, leaf surfaces typically differ in hue or indument patterns on adaxial versus abaxial surfaces. More frequently, leaves are isofacial; abaxial and adaxial surfaces are similar in hue and indument patterns, and stomata are found on both surfaces. There are exceptions to these general patterns, and it is important to examine both leaf surfaces under magnification. Arctostaphylos insularis, for example, has stomata restricted to the abaxial surface; otherwise, the leaf surfaces are similar in color and pubescence; A. pacifica has stomata on both leaf surfaces and the surfaces differ in hue.
Arctostaphylos produces a single annual growth of stems immediately after flowering. New inflorescences develop at the ends of these stems during this growth period and do not fully mature. Immature inflorescences generally remain dormant four to six months; these are critical in identifying taxa. One species (A. pringlei) initiates inflorescences immediately prior to flowering and thus flowers on current year’s stems. Inflorescences range from relatively short racemes to larger, spreading panicles. Plants that produce racemes frequently have inflorescences with a single, relatively small branch—“racemelike” structures. Usually, examination of multiple inflorescences will provide insight into whether the plant has panicle inflorescences. These structures should be examined under a hand lens for patterns of indument along the axes, bracts, and pedicels of either the flower or the fruit.
Although flower morphology varies among taxa, it is rarely important in identification. The pattern of indument on the ovary often is important. Frequently, the indument of the ovary is similar to that of mature fruit, but sometimes not; for example, Arctostaphylos canescens has densely hairy ovaries but the mature fruits are glabrescent. There are pairs of taxa for which ovary indument is the crucial distinguishing character; plant distribution can also be used in those cases.
Fruits are critical for identifying some taxa in Arctostaphylos. Fruits are usually present in a population because they are produced early in the spring, mature in the summer, and persist well into the fall and winter, often with some remaining into the next flowering season. Fruits can also be found in the litter during the latter part of the season. The fruits are a type of drupe, technically a nuculanium; the exocarp is dry at maturity, the mesocarp is dry and mealy or absent, and the fruit contains multiple hard stones. The stones are separate (distinct) in some taxa, each containing a single seed. In other taxa, stones may be connate along radial walls such that two or three stones are connate, while other stones in the same fruit remain distinct. Other species have fruits within which all radial surfaces of stones are connate, yielding a single structure, either globose or ellipsoid. With relatively few exceptions, fruits are of two general shapes: globose or nearly so, or depressed-globose and dimpled on both ends. Fruits also can be smooth and glabrous or hairy, sometimes viscid.
Selected References
Lower Taxa
Key
1 | Plants with burls present, sometimes epicormic, (sprouting after fire) | > 2 |
1 | Plants without burls, (not sprouting after fire) | > 17 |
2 | Leaves bifacial (stomata present only on abaxial surface (except A. ×campbelliae as a variant within A. crustacea subsp. crustacea), surfaces usually differing in hue and/or hairiness) | > 3 |
2 | Leaves isofacial (stomata present on both surfaces, sometimes fewer on adaxial surface, surfaces usually the same in hue and/or hairiness, except hue in A. pacifica) | > 5 |
3 | Bark of older stems persistent, gray, shredded. | Arctostaphylos tomentosa |
3 | Bark of older stems mostly persistent or exfoliating, reddish | > 4 |
4 | Plants prostrate, burl sometimes present, sometimes epicormic; fruits globose; leaf blades usually oblanceolate to obovate, sometimes narrowly elliptic; widespread in North America. | Arctostaphylos uva-ursi |
4 | Plants erect, burls present; fruits depressed-globose; leaf blades broadly elliptic or ovate; San Francisco Bay area to Channel Islands. | Arctostaphylos crustacea |
5 | Bark of older stems persistent, shredded, gray; (Nipomo, Burton mesas, Point Sal; San Luis Obispo and Santa Barbara counties, California) | Arctostaphylos rudis |
5 | Bark of older stems persistent or exfoliating, reddish | > 6 |
6 | Plants prostrate or mound-forming; inflorescences racemes, (simple or 1-branched); outer Coast Ranges, California, Nevada, Oregon, Washington | > 7 |
6 | Plants erect (or prostrate); inflorescences panicles; western North America | > 8 |
7 | Leaf margins serrulate; fruits reddish; San Mateo County, California. | Arctostaphylos pacifica |
7 | Leaf margins entire; fruits dark brown; Humboldt and Del Norte counties, California. | Arctostaphylos nevadensis |
8 | Twigs and/or inflorescence axes and bracts with glandular hairs | > 9 |
8 | Twigs, inflorescence axes, and bracts usually without glandular hairs (or minutely glandular in A. rainbowensis) | > 10 |
9 | Glandular hairs on twigs with golden glands, hairs relatively short; burls flat, obscure; widespread in high mountains of Pacific Northwest, Rocky Mountains, California. | Arctostaphylos patula |
9 | Glandular hairs on twigs with black or clear (rarely pink) glands, hairs various lengths; burls usually globose, prominent; coastal mountains from s Oregon to s California. | Arctostaphylos glandulosa |
10 | Leaf blades intensely gray-glaucous (sometimes slightly glaucous to strongly white-glaucous) | > 11 |
10 | Leaf blades green, greenish yellow, or greenish gray, not gray-glaucous | > 14 |
11 | Fruits globose, stones connate | > 12 |
11 | Fruits usually depressed-globose, stones mostly distinct | > 13 |
12 | Immature inflorescence axes 0.5-1.5 cm, short-hairy, eglandular. | Arctostaphylos parryana |
12 | Immature inflorescence axes 2-3 cm, usually glabrous or minutely glandular; (s Riverside and n San Diego counties). | Arctostaphylos rainbowensis |
13 | Fruits 12-16 mm diam., dark chocolate brown; (c, n Sierra Nevada, California). | Arctostaphylos mewukka |
13 | Fruits 6-10 mm diam., reddish brown. | Arctostaphylos glandulosa |
14 | Fruits globose; stones connate into single sphere. | Arctostaphylos parryana |
14 | Fruits depressed-globose (sometimes subglobose in A. patula); stones distinct to completely connate | > 15 |
15 | Immature inflorescences with some leaflike bracts (usually in proximal region). | Arctostaphylos glandulosa |
15 | Immature inflorescences with scalelike bracts | > 16 |
16 | Burls flat, obscure; high c Sierra Nevada. | Arctostaphylos patula |
16 | Burls globose, prominent; inner Coast Ranges and n Sierra Nevada, California. | Arctostaphylos manzanita |
17 | Leaf blades bifacial (stomata present only on abaxial surface, surfaces usually different in hue and/or pubescence) | > 18 |
17 | Leaf blades isofacial (stomata present on both surfaces, surfaces similar in hue and/or pubescence) | > 26 |
18 | Flowers 4-merous; fruits 3-4 mm diam | > 19 |
18 | Flowers 5-merous; fruits 5-15 mm diam | > 20 |
19 | Bark of older stems exfoliating, smooth, reddish; Marin, San Mateo, and Santa Cruz counties, California. | Arctostaphylos sensitiva |
19 | Bark of older stems persistent, shredded, gray; Mendocino and Sonoma counties, California. | Arctostaphylos nummularia |
20 | Abaxial leaf blade surfaces usually tomentose | > 21 |
20 | Abaxial leaf blade surfaces glabrous or sparsely hairy | > 22 |
21 | Leaf blades narrowly obovate to oblanceolate, 1-2 cm; plants prostrate or mound-forming; Monterey County, California. | Arctostaphylos pumila |
21 | Leaf blades oblong-ovate to oblong-elliptic, (base truncate or subcordate), 1.5-3 cm; plants erect or mound-forming; San Luis Obispo County, California. | Arctostaphylos morroensis |
22 | Plants usually prostrate or mound-forming | > 23 |
22 | Plants erect | > 24 |
23 | Leaf blades usually oblanceolate to obovate, sometimes narrowly elliptic, base cuneate. | Arctostaphylos uva-ursi |
23 | Leaf blades orbiculate to orbiculate-ovate, base truncate to ± lobed; (Monterey County, California). | Arctostaphylos edmundsii |
24 | Petioles 4-8 mm; leaf blades oblong-elliptic, base rounded; (Santa Cruz Island, California) | Arctostaphylos insularis |
24 | Petioles to 4 mm; leaf blades ovate to triangular-ovate or oblong, base auriculate-clasping | > 25 |
25 | Bark of older stems persistent, shredded, gray; leaf blades light green abaxially, blue-green adaxially; Monterey County, California. | Arctostaphylos pajaroensis |
25 | Bark of older stems persistent or exfoliating, shredding, reddish; leaf blades bright green; Santa Clara and Santa Cruz counties, California. | Arctostaphylos andersonii |
26 | Plants prostrate, mat-, or mound-forming, 0.1-0.5(-3) m | > 27 |
26 | Plants usually erect, sometimes mound-forming, 0.5-8 m | > 34 |
27 | Leaves: petiole to 2 mm, blade base auriculate-clasping; immature inflorescence bracts leaflike | > 28 |
27 | Leaves: petiole 1-12 mm, blade base rounded or obtuse to cuneate, not clasping; immature inflorescence bracts scalelike (partly or wholly leaflike in A. franciscana and A. nevadensis) | > 29 |
28 | Twigs, immature inflorescences, pedicels, and ovaries densely glandular- hairy; n San Mateo County, California. | Arctostaphylos imbricata |
28 | Twigs, immature inflorescences, pedicels, and ovaries not glandular-hairy; Monterey and San Luis Obispo counties, California. | Arctostaphylos cruzensis |
29 | Twigs, inflorescence axes, and bracts with glandular hairs; leaf blades glaucous; Klamath Mountains in n California. | Arctostaphylos klamathensis |
29 | Twigs, inflorescence axes, and bracts usually without glandular hairs (rarely minutely glandular-hairy in A. nevadensis); leaf blades green; Sonoma to San Luis Obispo counties, California, Oregon, Washington | > 30 |
30 | Inflorescences panicles, 3-5-branched; leaf blades usually 3-5 cm; (Sonoma County, California). | Arctostaphylos stanfordiana |
30 | Inflorescences racemes or 1-3(-5)-branched panicles; leaf blades usually 0.8-3 cm | > 31 |
31 | Fruits 3-6(-8) mm diam | > 32 |
31 | Fruits 6-8 mm diam | > 33 |
32 | Leaf blades narrow-elliptic to lanceolate-elliptic (rhombic), or widely elliptic, 0.8-3 × 0.4-1.5 cm; fruits 3-4 mm diam.; San Luis Obispo County. | Arctostaphylos hookeri |
32 | Leaf blades orbiculate-elliptic to elliptic, 1-2.5 × 1-1.5 cm; fruits 4-8 mm diam.; San Francisco County, California. | Arctostaphylos montana |
33 | Twigs gray-hairy; bracts 3-4 mm; serpentine soils in San Francisco, California. | Arctostaphylos franciscana |
33 | Twigs sparsely hairy; some bracts near base 5-10 mm; Washington to n Coast Range, Cascade Mountains, and Sierra Nevada in California. | Arctostaphylos nevadensis |
34 | Immature inflorescence bracts either predominantly scalelike (deltate to subulate or linear-lanceolate, wide-ovate, ovate, or awl-like) or fleshy (scoop-shaped) | > 35 |
34 | Immature inflorescences with bracts usually leaflike (narrowly lanceolate to ovate) | > 55 |
35 | Inflorescences mostly racemes, sometimes 1-2-branched | > 36 |
35 | Inflorescences panicles, (1-)3-8-branched | > 39 |
36 | Bark of older stems persistent, shredded, gray; (Nipomo and Burton mesas, Point Sal, San Luis Obispo and Santa Barbara counties, California) | Arctostaphylos rudis |
36 | Bark of older stems exfoliating, smooth, either reddish or dark red (with translucent, grayish patches) | > 37 |
37 | Twigs with glandular hairs, bark of older stems dark red with translucent, grayish patches (foothills of c Sierra Nevada near Ione, California). | Arctostaphylos myrtifolia |
37 | Twigs glabrous or tomentose, eglandular, bark of older stems reddish, without translucent, glaucous patches; widespread | > 38 |
38 | Immature inflorescence bracts stout, clublike, light green, recurving; widespread in Arizona, s California, Nevada, Texas, Utah, to Mexico; local in the interior of San Benito and Monterey counties, California. | Arctostaphylos pungens |
38 | Immature inflorescence bracts globose and cuplike, dark green, weakly spreading; along coast surrounding Monterey Bay, Monterey County, California. | Arctostaphylos hookeri |
39 | Leaf blades whitish, white-glaucous, gray-green, or gray-glaucous | > 40 |
39 | Leaf blades green, shiny or dull, not whitish or gray | > 44 |
40 | Fruits depressed-globose, 6-12 mm diam | > 41 |
40 | Fruits globose or subglobose, (10-)12-16 cm diam | > 42 |
41 | Immature inflorescence axes densely glandular, viscid; s Oregon, Sierra Nevada, Cascade Mountains, and n Coast Ranges, California. | Arctostaphylos viscida |
41 | Immature inflorescence axes sparsely hairy and sparsely glandular-hairy, not viscid; inner North Coast Ranges, southern Cascade foothills, northern Sierra Nevada foothills, California. | Arctostaphylos manzanita |
42 | Stones usually distinct, sometimes some stones connate; immature inflorescence bracts scalelike, deltate to linear-lanceolate, appressed to axis; fruits glabrous; w slope of nc Sierra Nevada | Arctostaphylos mewukka |
42 | Stones connate into single sphere, immature inflorescence bracts fleshy, scoop-shaped, spreading from axis; fruits glabrous or glandular-hairy; Coast Ranges of California | > 43 |
43 | Leaves: petiole 7-15 mm, blade base rounded, truncate, or slightly lobed; fruits viscid; Coast Ranges from Mount Diablo, Contra Costa to San Diego counties, California. | Arctostaphylos glauca |
43 | Leaves: petiole 1-4 mm, blade base auriculate; fruits glabrous; Gabilan Mountains, San Benito and Monterey counties, California. | Arctostaphylos gabilanensis |
44 | Twigs with glandular hairs or glands (hairs sparse to dense) | > 45 |
44 | Twigs without glandular hairs or sessile glands | > 50 |
45 | Immature inflorescences spreading or ascending to erect panicles, axes less than 1 mm diam., bracts tightly appressed (± equaling buds; buds scattered along inflorescence axis, appearing as round "beads"); n Coast Ranges, California | > 46 |
45 | Immature inflorescences pendent panicles, axes usually 1+ mm diam., bracts usually not fully appressed, (longer than buds, buds not scattered or appearing as "beads") | > 47 |
46 | Leaf blades 3-5 cm, bright green to slightly glaucous; flowers white to pink; young twigs usually glabrous (with glandular hairs in 1 subsp.). | Arctostaphylos stanfordiana |
46 | Leaf blades 1.5-3 cm, dull green; flowers white; young twigs finely glandular- hairy. | Arctostaphylos hispidula |
47 | Leaf blades widely ovate, round to oblong, orbiculate, or obovate, at least some leaves 3+ cm (usually 2-6 cm); interior mountains (300-3000 m) | > 48 |
47 | Leaf blades elliptic, ovate-elliptic, ovate, oblong-ovate, to orbiculate-ovate, 1.5-3 cm; Santa Cruz or Sonoma counties, California | > 49 |
48 | Twigs and immature inflorescence axes with dense, short, golden yellow, glandular hairs; leaf blades bright green, glabrous; widespread, upper montane habitats in Pacific Northwest, Rocky Mountains, Great Basin, California, and Baja California. | Arctostaphylos patula |
48 | Twigs and immature inflorescence axes with short, dark or clear glands on hairs; leaf blades dull green, puberulent, scabrous; Shasta and Tehama counties, California. | Arctostaphylos manzanita |
49 | Twigs sparsely long glandular-hairy above distinct layer of shorter, eglandular hairs; narrow endemic to shales on n Ben Lomond Mountain, Santa Cruz County, California. | Arctostaphylos ohloneana |
49 | Twigs densely glandular-hairy or finely tomentose with sessile glands beneath; serpentine, Sonoma County, California. | Arctostaphylos bakeri |
50 | Immature inflorescence axes mostly less than 1 mm diam | > 51 |
50 | Immature inflorescence axes 1+ mm diam | > 52 |
51 | Leaf blades 1-2.5 cm; immature inflorescence branches compact, ± spreading, pendent; bracts not appressed, (longer than buds); plants low-mounding; (Sonoma County, California) | Arctostaphylos densiflora |
51 | Leaf blades 3-5 cm; immature inflorescence branches widely spreading, ascending, or erect; bracts tightly appressed, (± equaling buds, buds scattered along inflorescence axis, appearing as round "beads"); plants erect. | Arctostaphylos stanfordiana |
52 | Leaf blades 1-2.5 cm. | Arctostaphylos montana |
52 | Leaf blades 2.5-5 cm | > 53 |
53 | Ovaries and fruits stipitate-glandular; plants shrubs or trees; volcanic mountains in s North Coast Range, California. | Arctostaphylos manzanita |
53 | Ovaries and fruits ± glabrous (not glandular, not densely hairy); plants either mound-forming, erect (sometimes prostrate) shrubs, or trees; various soils, widespread in n Coast Ranges, w slope of Sierra Nevada, and parts of Transverse Ranges, California | > 54 |
54 | Fruits globose; stones connate into single sphere; Transverse Ranges, s California | Arctostaphylos parryana |
54 | Fruit depressed-globose; stones distinct; n Coast Ranges and w slope of Sierra Nevada, California. | Arctostaphylos manzanita |
55 | Bark of older stems persistent, shredded, gray (can be red, smooth in some individuals of A. osoensis) | > 56 |
55 | Bark of older stems exfoliating, smooth, reddish | > 57 |
56 | Leaf bases cuneate to rounded, surfaces sparsely appressed-puberulent; narrow endemic of w Sierra Nevada foothills, California. | Arctostaphylos nissenana |
56 | Leaf bases lobed, clasping twigs, surfaces (shiny green), usually glabrous or sparsely short-hairy; hills e of Morro Bay, San Luis Obispo County, California. | Arctostaphylos osoensis |
57 | Leaf blade surfaces gray-canescent, feltlike, sometimes glabrescent | > 58 |
57 | Leaf blade surfaces not gray-canescent and feltlike, green or gray-green, glabrous or otherwise hairy | > 65 |
58 | Leaf bases lobed or auriculate-clasping; petioles to 4 mm | > 59 |
58 | Leaf bases cuneate, rounded, truncate, or ± lobed (not clasping); petioles 3-10 mm | > 61 |
59 | Ovaries and fruits glabrous; (e of Cuesta Pass, San Luis Obispo, California). | Arctostaphylos luciana |
59 | Ovaries and young fruits hairy (older fruits may be sparsely hairy) | > 60 |
60 | Ovaries and fruits eglandular white-hairy; Contra Costa County, California. | Arctostaphylos auriculata |
60 | Ovaries and fruits glandular-hairy; Santa Cruz County, California. | Arctostaphylos glutinosa |
61 | Ovaries usually glabrous, not glandular; corollas white | > 62 |
61 | Ovaries densely white-hairy, glandular or not; corollas white or pink | > 63 |
62 | Inflorescences simple or 1-2-branched, racemelike; pedicels 5-7 mm; Santa Cruz County, California. | Arctostaphylos silvicola |
62 | Inflorescences 2-4-branched panicles; pedicels 8-10 mm; San Luis Obispo and Monterey counties, California. | Arctostaphylos obispoensis |
63 | Immature inflorescences racemes (or 1-branched); twigs short-hairy (often minutely glandular) and long hispid-hairy; (Del Norte County, California, Curry and Josephine counties, Oregon) | Arctostaphylos nortensis |
63 | Immature inflorescences 2-5 branched panicles; twigs densely short-hairy, without hispid hairs | > 64 |
64 | Bracts leaflike, spreading; pedicels and ovaries eglandular, sometimes glandular. | Arctostaphylos canescens |
64 | Bracts scalelike, appressed, pedicels glandular; ovaries eglandular. | Arctostaphylos malloryi |
65 | Leaf bases auriculate-clasping or distinctly lobed, appearing to clasp twigs (except in A. hooveri) | > 66 |
65 | Leaf bases rounded, truncate, cuneate, or ± lobed (not auriculate) | > 73 |
66 | Immature inflorescence branches and bracts with eglandular hairs | > 67 |
66 | Immature inflorescence branches and bracts with gland-tipped hairs | > 70 |
67 | Pedicels hairy | > 68 |
67 | Pedicels usually glabrous | > 69 |
68 | Pedicels glandular-hairy; leaf blades green-glaucous; Contra Costa County, California. | Arctostaphylos pallida |
68 | Pedicels eglandular-hairy; leaf blades dark green; Santa Cruz Island, California. | Arctostaphylos viridissima |
69 | Ovaries glabrous; fruits 5-8 mm diam.; stones distinct; Santa Barbara County, California. | Arctostaphylos purissima |
69 | Ovaries hairy; fruits 8-12 mm diam.; stones mostly connate; San Luis Obispo County, California. | Arctostaphylos pechoensis |
70 | Fruits 10-15 mm diam., globose; stones connate into single sphere; (Santa Barbara County, California). | Arctostaphylos refugioensis |
70 | Fruits 6-10(-15) mm diam., depressed-globose; stones distinct | > 71 |
71 | Leaf blades light green, ovate, not boat-shaped with upturned tips, 2.5-4.5 cm; (San Mateo County, California). | Arctostaphylos montaraensis |
71 | Leaf blades dull gray-green, oblong to ovate, boat-shaped with upturned tips, 3-6 cm | > 72 |
72 | Petioles to 3 mm; leaf bases clasping twigs; n Santa Cruz Mountains, San Mateo County, California. | Arctostaphylos regismontana |
72 | Petioles 3-6 mm; leaf bases not clasping twigs; n Santa Lucia Mountains, Monterey County, California. | Arctostaphylos hooveri |
73 | Leaflike bracts bright pink, glandular-hairy, deciduous after flowering; (mountains of Arizona, s California, Nevada, Utah, and Baja California). | Arctostaphylos pringlei |
73 | Leaflike bracts green, glandular or eglandular, persistent after flowering | > 74 |
74 | Fruits globose or subglobose; stones partially or fully connate (distinct in A. catalinae) | > 75 |
74 | Fruits depressed-globose; stones usually distinct (sometimes partially connate in A. montereyensis) | > 76 |
75 | Fruits 6-8 mm diam.; ovaries densely glandular-hairy; leaf blade surfaces smooth, base rounded or truncate; San Diego County, California. | Arctostaphylos otayensis |
75 | Fruits 8-15 mm diam.; ovaries sparsely glandular-hairy; leaf blade surfaces papillate, scabridulous, base truncate or ± slightly lobed; Santa Catalina Island, California. | Arctostaphylos catalinae |
76 | Inflorescences racemes, simple (or 1-branched) | > 77 |
76 | Inflorescences 3-10-branched panicles | > 78 |
77 | Twigs, inflorescence axes, and bracts finely glandular-hairy, without long hairs; (Marin County, California). | Arctostaphylos virgata |
77 | Twigs, inflorescence axes, and bracts eglandular-hairy, with long hairs. | Arctostaphylos pilosula |
78 | Leaves overlapping; plants prostrate to erect shrubs, 0.1-2 m; (Santa Rosa Island, California). | Arctostaphylos confertiflora |
78 | Leaves not overlapping; plants erect shrubs or trees, 1-5 m | > 79 |
79 | Leaf blades lanceolate-ovate to narrowly oblong-ovate, dark green; immature inflorescences short-hairy, usually with long hairs, sometimes glandular; n California coast to Pacific Northwest, s British Columbia. | Arctostaphylos columbiana |
79 | Leaf blades orbiculate-ovate to orbiculate, light green, reddish hued, or slightly glaucous; immature inflorescences densely glandular-hairy; Monterey County, California. | Arctostaphylos montereyensis |