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==Description==
==Description==
[[File:Bombus cryptarum - Solidago virgaurea - Keila2.jpg|thumb|left|[[European goldenrod]] is pollinated by ''[[Bombus cryptarum]]'']]
[[File:Bombus cryptarum - Solidago virgaurea - Keila2.jpg|thumb|left|[[European goldenrod]] is pollinated by ''[[Bombus cryptarum]]'']]
''Solidago'' species are perennials growing from woody [[caudex|caudices]] or [[rhizome]]s. Their stems range from [[decumbent]] (crawling) to ascending or erect, with a range of heights going from {{convert|5|cm|abbr=on}} to over a meter. Most species are unbranched, but some do display branching in the upper part of the plant. Both leaves and stems vary from [[glabrousness|glabrous]] (hairless) to various forms of [[pubescent (botany)|pubescence]] (strigose, strigillose, hispid, stipitate-glandular or villous). In some species, the basal leaves are shed before flowering. The [[leaf margin]]s are most commonly entire, but often display heavier [[serration]]. Some leaves may display trinerved [[Leaf#Venation (arrangement of the veins)|venation]] rather than the pinnate venation usual across Asteraceae.<ref name=fna/> The flower is also the state flower of Kentucky.
''Solidago'' species are perennials growing from woody [[caudex|caudices]] or [[rhizome]]s. Their stems range from [[decumbent]] (crawling) to ascending or erect, with a range of heights going from {{convert|5|cm|abbr=on}} to over a meter. Most species are unbranched, but some do display branching in the upper part of the plant. Both leaves and stems vary from [[glabrousness|glabrous]] (hairless) to various forms of [[pubescent (botany)|pubescence]] (strigose, strigillose, hispid, stipitate-glandular or villous). In some species, the basal leaves are shed before flowering. The [[leaf margin]]s are most commonly entire, but often display heavier [[serration]]. Some leaves may display trinerved [[Leaf#Venation (arrangement of the veins)|venation]] rather than the pinnate venation usual across Asteraceae.<ref name=fna/>


The [[flower head]]s are usually of the radiate type (typical daisy flower heads with distinct ray and disc [[floret]]s) but sometimes discoid (with only disc florets of mixed, sterile, male and types). Only ray florets are female, others are male, hermaphroditic or entire sterile. Head [[Bract|involucres]] are campanulate to cylindric or attenuate. [[Floret]] corollas are usually yellow, but white in the ray florets of a few species (such as ''[[Solidago bicolor]]''); they are typically hairless. Heads usually include between 2 and 35 disc florets, but in some species this may go up to 60. Filaments are inserted closer to the base of the corolla than its middle. Numerous heads are usually grouped in complex compound inflorescences where heads are arranged in multiple [[raceme]]s, [[panicle]]s, [[corymb]]s, or secund arrays (with florets all on the same side).<ref name=fna/>
The [[flower head]]s are usually of the radiate type (typical daisy flower heads with distinct ray and disc [[floret]]s) but sometimes discoid (with only disc florets of mixed, sterile, male and types). Only ray florets are female, others are male, hermaphroditic or entire sterile. Head [[Bract|involucres]] are campanulate to cylindric or attenuate. [[Floret]] corollas are usually yellow, but white in the ray florets of a few species (such as ''[[Solidago bicolor]]''); they are typically hairless. Heads usually include between 2 and 35 disc florets, but in some species this may go up to 60. Filaments are inserted closer to the base of the corolla than its middle. Numerous heads are usually grouped in complex compound inflorescences where heads are arranged in multiple [[raceme]]s, [[panicle]]s, [[corymb]]s, or secund arrays (with florets all on the same side).<ref name=fna/>
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Related Asteraceae genera, such as ''[[Chrysoma]]'', ''[[Euthamia]]'', and ''[[Oreochrysum]]'', have been included within ''Solidago'' at one point or another,<ref name="Anderson-1975">{{Cite journal|last1=Anderson|first1=Loran C.|last2=Creech|first2=Jessica B.|date=1975|title=Comparative Leaf Anatomy of ''Solidago'' and Related Asteraceae|jstor=2441956|journal=American Journal of Botany|volume=62|issue=5|pages=486–493|doi=10.2307/2441956}}</ref> but morphological evidence<ref name="Phytologia-1994">{{Cite journal|date=1994|title=Subtribal Classification of the Astereae (Asteraceae)|last1=Nesom|first1=Guy L.|url=http://biostor.org/reference/131828|journal=Phytologia|language=en|volume=76|issn=0031-9430}}</ref><ref name="Anderson-1975" /><ref name="Rhodora-1981">{{Cite journal|date=1981|title=The Taxonomy of the Genus ''Euthamia'' |url=http://biostor.org/reference/138608|journal=Rhodora|language=en|volume=83|issue=836|issn=0035-4902}}</ref> has suggested otherwise. In a study comparing morphological characters of ''Solidago'' and related subgroups, the authors consider the subjectivity of classifying a genus and how to define it within broader tendencies concerning the taxonomy of North American Asteraceae. Little to no differences were observed between ''Solidago'' and the subgroups in terms of karyotype. However, external morphological characters such as habit, or the general appearance of the plant and how a suite of traits contribute to its phenotype; pappus size; and the point of freeing of stamen filaments from the corolla tube, are useful classification schemes for ''Solidago'', since they are applied to differentiating between Asteraceae taxa. One school of Asteraceae taxonomy thought unites all taxa sharing similar floral head structure and subsequently ignores deviation from this morphology, while another places greater weight on these morphological deviations. The authors argue that the latter opinion should be applied. Since there is no theoretical foundation for relative taxonomic importance of traits, they assert that habit should be a central trait when defining taxa, and subsequently that all the subgroups considered in their study (''[[Brachychaeta]]'', ''Chrysoma'', ''Euthamia'', ''Oligoneuron'', and ''[[Petradoria]]'') should be segregated from ''Solidago''.<ref name="Kapoor-1966">{{Cite journal|last1=Kapoor|first1=B. M.|last2=Beaudry|first2=J. R.|date=1966-09-01|title=Studies on ''Solidago''. Vii. the Taxonomic Status of the Taxa ''Brachychaeta'', ''Brintonia'', ''Chrysoma'', ''Euthamia'', ''Oligoneuron'' and ''Petradoria'' in Relation to ''Solidago''|journal=Canadian Journal of Genetics and Cytology|volume=8|issue=3|pages=422–443|doi=10.1139/g66-053|issn=0008-4093}}</ref>
Related Asteraceae genera, such as ''[[Chrysoma]]'', ''[[Euthamia]]'', and ''[[Oreochrysum]]'', have been included within ''Solidago'' at one point or another,<ref name="Anderson-1975">{{Cite journal|last1=Anderson|first1=Loran C.|last2=Creech|first2=Jessica B.|date=1975|title=Comparative Leaf Anatomy of ''Solidago'' and Related Asteraceae|jstor=2441956|journal=American Journal of Botany|volume=62|issue=5|pages=486–493|doi=10.2307/2441956}}</ref> but morphological evidence<ref name="Phytologia-1994">{{Cite journal|date=1994|title=Subtribal Classification of the Astereae (Asteraceae)|last1=Nesom|first1=Guy L.|url=http://biostor.org/reference/131828|journal=Phytologia|language=en|volume=76|issn=0031-9430}}</ref><ref name="Anderson-1975" /><ref name="Rhodora-1981">{{Cite journal|date=1981|title=The Taxonomy of the Genus ''Euthamia'' |url=http://biostor.org/reference/138608|journal=Rhodora|language=en|volume=83|issue=836|issn=0035-4902}}</ref> has suggested otherwise. In a study comparing morphological characters of ''Solidago'' and related subgroups, the authors consider the subjectivity of classifying a genus and how to define it within broader tendencies concerning the taxonomy of North American Asteraceae. Little to no differences were observed between ''Solidago'' and the subgroups in terms of karyotype. However, external morphological characters such as habit, or the general appearance of the plant and how a suite of traits contribute to its phenotype; pappus size; and the point of freeing of stamen filaments from the corolla tube, are useful classification schemes for ''Solidago'', since they are applied to differentiating between Asteraceae taxa. One school of Asteraceae taxonomy thought unites all taxa sharing similar floral head structure and subsequently ignores deviation from this morphology, while another places greater weight on these morphological deviations. The authors argue that the latter opinion should be applied. Since there is no theoretical foundation for relative taxonomic importance of traits, they assert that habit should be a central trait when defining taxa, and subsequently that all the subgroups considered in their study (''[[Brachychaeta]]'', ''Chrysoma'', ''Euthamia'', ''Oligoneuron'', and ''[[Petradoria]]'') should be segregated from ''Solidago''.<ref name="Kapoor-1966">{{Cite journal|last1=Kapoor|first1=B. M.|last2=Beaudry|first2=J. R.|date=1966-09-01|title=Studies on ''Solidago''. Vii. the Taxonomic Status of the Taxa ''Brachychaeta'', ''Brintonia'', ''Chrysoma'', ''Euthamia'', ''Oligoneuron'' and ''Petradoria'' in Relation to ''Solidago''|journal=Canadian Journal of Genetics and Cytology|volume=8|issue=3|pages=422–443|doi=10.1139/g66-053|issn=0008-4093}}</ref>


Results from a leaf anatomy study comparing differences in mesophyll, [[Vascular bundle#Bundle-sheath cells|bundle sheath]] extensions, and midvein structure, among others in a suite of leaf traits,<ref name="Anderson-1975" /> are incongruent with those in an earlier study.<ref name="Kapoor-1966" /> Based on the lack of bundle sheath extensions, it is suggested that ''Chrysoma'', ''Euthamia'', ''[[Gundlachia (plant)|Gundlachia]]'', and ''Petradoria'' should be distinct taxa and outside of ''Solidago''.<ref name="Anderson-1975" /> However, ''Brachychaeta'', ''[[Brintonia]]'', ''Oligoneuron'', ''Oreochrysum'', and ''Aster'' should be considered as components of ''Solidago''. To summarize, the relation of ''Brachychaeta'' and ''Oligoneuron'' to ''Solidago'' is inconsistent based on these results.<ref name="Kapoor-1966" /><ref name="Anderson-1975" /> Both support the separation of ''Chrysoma'', ''Euthamia'', and ''Petradoria'' from ''Solidago''. A study reviews the taxonomic position of ''Oligoneuron'' relative to ''Solidago'', as based on taxonomic evidence, treats it as separate from ''Solidago'',<ref name="Phytologia-1994" /> similarly to Kapoor & Beaudry (1966). The first molecular phylogeny based on chloroplast DNA treats ''Brachychaeta'', ''Brintonia'', ''Oligoneuron'', and ''Oreochrysum'' as constituents of ''Solidago''.<ref name="Zhang-1996" /> Using consensus trees from ITS data, another study found support for ''Oligoneuron'' as part of ''Solidago'',<ref name="Beck-2004">{{Cite journal|last1=Beck|first1=James B.|last2=Nesom|first2=Guy L.|last3=Calie|first3=Patrick J.|last4=Baird|first4=Gary I.|last5=Small|first5=Randall L.|last6=Schilling|first6=Edward E.|date=2004|title=Is Subtribe Solidagininae (Asteraceae) Monophyletic?|jstor=4135444|journal=Taxon|volume=53|issue=3|pages=691–698|doi=10.2307/4135444}}</ref> and the findings of Zhang (1996). More recently, an analysis of combined ITS and ETS data provided additional support for the inclusion of ''Oligoneuron'' as part of ''Solidago''.<ref name="Schilling-2008" />
Results from a leaf anatomy study comparing differences in mesophyll, [[Vascular bundle#Bundle-sheath cells|bundle sheath]] extensions, and midvein structure, among others in a suite of leaf traits,<ref name="Anderson-1975" /> are incongruent with those in an earlier study.<ref name="Kapoor-1966" /> Based on the lack of bundle sheath extensions, it is suggested that ''Chrysoma'', ''Euthamia'', ''[[Gundlachia (plant)|Gundlachia]]'', and ''Petradoria'' should be distinct taxa and outside of ''Solidago''.<ref name="Anderson-1975" /> However, ''Brachychaeta'', ''[[Brintonia]]'', ''Oligoneuron'', ''Oreochrysum'', and ''Aster ptarmicoides'' should be considered as components of ''Solidago''. To summarize, the relation of ''Brachychaeta'' and ''Oligoneuron'' to ''Solidago'' is inconsistent based on these results.<ref name="Kapoor-1966" /><ref name="Anderson-1975" /> Both support the separation of ''Chrysoma'', ''Euthamia'', and ''Petradoria'' from ''Solidago''. A study reviews the taxonomic position of ''Oligoneuron'' relative to ''Solidago'', as based on taxonomic evidence, treats it as separate from ''Solidago'',<ref name="Phytologia-1994" /> similarly to Kapoor & Beaudry (1966). The first molecular phylogeny based on chloroplast DNA treats ''Brachychaeta'', ''Brintonia'', ''Oligoneuron'', and ''Oreochrysum'' as constituents of ''Solidago''.<ref name="Zhang-1996" /> Using consensus trees from ITS data, another study found support for ''Oligoneuron'' as part of ''Solidago'',<ref name="Beck-2004">{{Cite journal|last1=Beck|first1=James B.|last2=Nesom|first2=Guy L.|last3=Calie|first3=Patrick J.|last4=Baird|first4=Gary I.|last5=Small|first5=Randall L.|last6=Schilling|first6=Edward E.|date=2004|title=Is Subtribe Solidagininae (Asteraceae) Monophyletic?|jstor=4135444|journal=Taxon|volume=53|issue=3|pages=691–698|doi=10.2307/4135444}}</ref> and the findings of Zhang (1996). More recently, an analysis of combined ITS and ETS data provided additional support for the inclusion of ''Oligoneuron'' as part of ''Solidago''.<ref name="Schilling-2008" />


Until the 1980s, the genus ''Euthamia'' was largely considered to be a part of ''Solidago'' due to morphological similarities between species in both genera, and a history of synonymy of ''Solidago lanceolata'' and ''Euthamia graminifolia''.<ref name="Rhodora-1981" /> As mentioned, the lack of bundle sheath extensions in ''Euthamia'' compared to ''Solidago'',<ref name="Anderson-1975" /> and deviations in floral morphology<ref name="Kapoor-1966" /> present evidence for separation of these taxa. A taxonomy of ''Euthamia'' as a genus was presented, providing a detailed description of distinguishing external morphological characters, such as fibrous-roots, sessile leaves, and mostly corymbiform inflorescences.<ref name="Rhodora-1981" />
Until the 1980s, the genus ''Euthamia'' was largely considered to be a part of ''Solidago'' due to morphological similarities between species in both genera, and a history of synonymy of ''Solidago lanceolata'' and ''Euthamia graminifolia''.<ref name="Rhodora-1981" /> As mentioned, the lack of bundle sheath extensions in ''Euthamia'' compared to ''Solidago'',<ref name="Anderson-1975" /> and deviations in floral morphology<ref name="Kapoor-1966" /> present evidence for separation of these taxa. A taxonomy of ''Euthamia'' as a genus was presented, providing a detailed description of distinguishing external morphological characters, such as fibrous-roots, sessile leaves, and mostly corymbiform inflorescences.<ref name="Rhodora-1981" />
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Chromosome counts have proven to be a valuable character in ''Solidago'' taxonomy and in elucidating the cytogeographic history of the genus. Similar chromosome counts may indicate close evolutionary relationships, while different chromosome numbers may suggest distant relationships through reproductive isolation. Chromosome counts have been studied extensively in North America;<ref>{{Cite journal|last1=Cook|first1=Rachel E.|last2=Semple|first2=John C.|date=2008-11-13|title=Cytogeography of ''Solidago'' subsect. ''Glomeruliflorae'' (Asteraceae: Astereae)|journal=Botany|volume=86|issue=12|pages=1488–1496|doi=10.1139/B08-087|issn=1916-2790}}</ref><ref>{{Cite journal|last1=Semple|first1=John|last2=Watanabe|first2=Kuniaki|date=2013-03-02|title=A Review of Chromosome Numbers in Asteraceae with Hypotheses on Chromosomal Base Number Evolution|url=https://www.researchgate.net/publication/48460015}}</ref> all ''Solidago'' species have a base chromosome number of x=9, but the following ploidy levels have been observed: 2x, 3x, 4x, 6x, 8x, 10x, 12x, and 14x.
Chromosome counts have proven to be a valuable character in ''Solidago'' taxonomy and in elucidating the cytogeographic history of the genus. Similar chromosome counts may indicate close evolutionary relationships, while different chromosome numbers may suggest distant relationships through reproductive isolation. Chromosome counts have been studied extensively in North America;<ref>{{Cite journal|last1=Cook|first1=Rachel E.|last2=Semple|first2=John C.|date=2008-11-13|title=Cytogeography of ''Solidago'' subsect. ''Glomeruliflorae'' (Asteraceae: Astereae)|journal=Botany|volume=86|issue=12|pages=1488–1496|doi=10.1139/B08-087|issn=1916-2790}}</ref><ref>{{Cite journal|last1=Semple|first1=John|last2=Watanabe|first2=Kuniaki|date=2013-03-02|title=A Review of Chromosome Numbers in Asteraceae with Hypotheses on Chromosomal Base Number Evolution|url=https://www.researchgate.net/publication/48460015}}</ref> all ''Solidago'' species have a base chromosome number of x=9, but the following ploidy levels have been observed: 2x, 3x, 4x, 6x, 8x, 10x, 12x, and 14x.


Though negligible differences in karyotype among ''Solidago'' and related genera were found,<ref name="Kapoor-1966" /> ''Solidago'' taxa with multiple cytotypes are more common than those with one.<ref name="Semple-2016" /> Although chromosome count is a useful metric for differentiating among ''Solidago'' taxa, it may be problematic due to the frequent variation in ploidy levels. Cytogeographic patterns in the ''Solidago gigantea'' complex, with tetraploids occurring in eastern North America and hexaploids in Oregon and Washington, were observed.<ref>{{Cite journal|last1=Semple|first1=John C.|last2=Ringius|first2=Gordon S.|last3=Leeder|first3=Colleen|last4=Morton|first4=Gary|date=1984-07-01|title=Chromosome Numbers of Goldenrods, ''Euthamia'' and ''Solidago'' (Compositae: Astereae). II. Additional Counts with Comments on Cytogeography|journal=Brittonia|language=en|volume=36|issue=3|pages=280–292|doi=10.2307/2806528|issn=0007-196X|jstor=2806528|s2cid=186241866}}</ref> Cytogeographic patterns are also observed in the ''[[Solidago canadensis]]'' complex: hexaploids within ''S. canadensis'' have been observed east of the Great Plains and are treated as ''[[Solidago altissima]]'', and diploids and tetraploids occurring in the Great Plains are treated as ''Solidago gilvocanescens''. The taxonomic status of ''Solidago ptarmicoides'' created an extensive debate due to frequency hybridization of ''S. ptarmicoides'' with members of the ''Ptarmicoidei'' section of ''Solidago''.<ref name=fna/> It was asserted that ''S. ptarmicoides'' should be united with ''Solidago'' rather than the genus ''Aster'' due to external morphological features such as similar pappus length as well as the same chromosome base (x=9). Information about chromosome number is still a crucial part of current understanding and phylogenies of ''Solidago''.<ref name="Semple-2016" />
Though negligible differences in karyotype among ''Solidago'' and related genera were found,<ref name="Kapoor-1966" /> ''Solidago'' taxa with multiple cytotypes are more common than those with one.<ref name="Semple-2016" /> Although chromosome count is a useful metric for differentiating among ''Solidago'' taxa, it may be problematic due to the frequent variation in ploidy levels. Cytogeographic patterns in the ''Solidago gigantea'' complex, with tetraploids occurring in eastern North America and hexaploids in Oregon and Washington, were observed.<ref>{{Cite journal|last1=Semple|first1=John C.|last2=Ringius|first2=Gordon S.|last3=Leeder|first3=Colleen|last4=Morton|first4=Gary|date=1984-07-01|title=Chromosome Numbers of Goldenrods, ''Euthamia'' and ''Solidago'' (Compositae: Astereae). II. Additional Counts with Comments on Cytogeography|journal=Brittonia|language=en|volume=36|issue=3|pages=280–292|doi=10.2307/2806528|issn=0007-196X|jstor=2806528|bibcode=1984Britt..36..280S |s2cid=186241866}}</ref> Cytogeographic patterns are also observed in the ''[[Solidago canadensis]]'' complex: hexaploids within ''S. canadensis'' have been observed east of the Great Plains and are treated as ''[[Solidago altissima]]'', and diploids and tetraploids occurring in the Great Plains are treated as ''Solidago gilvocanescens''. The taxonomic status of ''Solidago ptarmicoides'' created an extensive debate due to frequency hybridization of ''S. ptarmicoides'' with members of the ''Ptarmicoidei'' section of ''Solidago''.<ref name=fna/> It was asserted that ''S. ptarmicoides'' should be united with ''Solidago'' rather than the genus ''Aster'' due to external morphological features such as similar pappus length as well as the same chromosome base (x=9). Information about chromosome number is still a crucial part of current understanding and phylogenies of ''Solidago''.<ref name="Semple-2016" />


== Ecology ==
== Ecology ==
Goldenrod is considered a [[keystone species]], and has been called the single most important plant for North American pollinator biodiversity.<ref>{{cite web |last1=Perkins |first1=Deborah |title=Goldenrods: Top Plant for Boosting Biodiversity |url=https://www.nrcm.org/blog/first-light-wildlife-habitats/goldenrods-top-plant-boosting-biodiversity/ |website=ncrm.org |date=23 September 2019 |publisher=Natural Resources Council of Maine}}</ref><ref>{{cite web |title=Goldenrod (Solidago) Is Trending! |url=https://www.nurturenativenature.com/post/goldenrod-solidago-is-trending |website=nurturenativenature.com|date=29 December 2020 }}</ref> Goldenrod species are used as a food source by the [[larva]]e of [[list of Lepidoptera that feed on goldenrods|many Lepidoptera species]]. As many as 104 species of butterflies and moths use it as a host plant for their larvae, and 42 species of bees are goldenrod specialists, visiting only goldenrod for food.<ref>{{cite web |title=Keystone Native Plants Eastern Temperate Forests - Ecoregion 8 |url=https://www.nwf.org/-/media/Documents/PDFs/Garden-for-Wildlife/Keystone-Plants/NWF-GFW-keystone-plant-list-ecoregion-8-eastern-temperate-forests.ashx?la=en&hash=1E180E2E5F2B06EB9ADF28882353B3BC7B3B247D |website=nwf.org |publisher=National Wildlife Federation}}</ref> Some lepidopteran larvae bore into plant tissues and form a bulbous tissue mass called a [[gall]] around it, upon which the larva then feeds. Various [[parasitoid wasp]]s find these galls and lay eggs in the larvae, penetrating the bulb with their [[ovipositor]]s. Woodpeckers are known to peck open the galls and eat the insects in the center.<ref>{{cite journal|title=Foraging patterns of Eastern gray squirrels (''Sciurus carolinensis'') on goldenrod gall insects, a potentially important winter food resource|author=Shealers, D. A.|pages=102–109|journal=The American Midland Naturalist|volume=142|issue=1|date=July 1999|doi=10.1674/0003-0031(1999)142[0102:FPOEGS]2.0.CO;2|s2cid=85741057 |issn=0003-0031|display-authors=etal}}</ref>
Goldenrod is considered a [[keystone species]], and has been called the single most important plant for North American pollinator biodiversity.<ref>{{cite web |last1=Perkins |first1=Deborah |title=Goldenrods: Top Plant for Boosting Biodiversity |url=https://www.nrcm.org/blog/first-light-wildlife-habitats/goldenrods-top-plant-boosting-biodiversity/ |website=ncrm.org |date=23 September 2019 |publisher=Natural Resources Council of Maine}}</ref><ref>{{cite web |title=Goldenrod (Solidago) Is Trending! |url=https://www.nurturenativenature.com/post/goldenrod-solidago-is-trending |website=nurturenativenature.com|date=29 December 2020 }}</ref> Goldenrod species are used as a food source by the [[larva]]e of many [[Lepidoptera]] species. As many as 104 species of butterflies and moths use it as a host plant for their larvae, and 42 species of bees are goldenrod specialists, visiting only goldenrod for food.<ref>{{cite web |title=Keystone Native Plants Eastern Temperate Forests - Ecoregion 8 |url=https://www.nwf.org/-/media/Documents/PDFs/Garden-for-Wildlife/Keystone-Plants/NWF-GFW-keystone-plant-list-ecoregion-8-eastern-temperate-forests.ashx?la=en&hash=1E180E2E5F2B06EB9ADF28882353B3BC7B3B247D |website=nwf.org |publisher=National Wildlife Federation}}</ref> Some lepidopteran larvae bore into plant tissues and form a bulbous tissue mass called a [[gall]] around it, upon which the larva then feeds. Various [[parasitoid wasp]]s find these galls and lay eggs in the larvae, penetrating the bulb with their [[ovipositor]]s. Woodpeckers are known to peck open the galls and eat the insects in the center.<ref>{{cite journal|title=Foraging patterns of Eastern gray squirrels (''Sciurus carolinensis'') on goldenrod gall insects, a potentially important winter food resource|author=Shealers, D. A.|pages=102–109|journal=The American Midland Naturalist|volume=142|issue=1|date=July 1999|doi=10.1674/0003-0031(1999)142[0102:FPOEGS]2.0.CO;2|s2cid=85741057 |issn=0003-0031|display-authors=etal}}</ref>


Goldenrods have become invasive species in many parts of the world outside their native range, including China, Japan, Europe and Africa.<ref>{{cite web |url=https://www.cabi.org/isc/datasheet/50599 |title=Solidago canadensis (Canadian goldenrod) |work=[[Invasive Species Compendium]] (ISC) |publisher=[[CAB International]]}}</ref><ref>{{cite web | url=https://www.cabi.org/isc/datasheet/50575 | title=Solidago gigantea (Giant goldenrod) }}</ref> ''Solidago canadensis'', which was introduced as a garden plant in Central Europe, has become common in the wild, and in [[Germany]] is considered an [[invasive species]] that displaces native vegetation from its natural habitat.
Goldenrods have become invasive species in many parts of the world outside their native range, including China, Japan, Europe and Africa.<ref>{{cite web |url=https://www.cabi.org/isc/datasheet/50599 |title=Solidago canadensis (Canadian goldenrod) |work=[[Invasive Species Compendium]] (ISC) |publisher=[[CAB International]]}}</ref><ref>{{cite web | url=https://www.cabi.org/isc/datasheet/50575 | title=Solidago gigantea (Giant goldenrod) }}</ref> ''Solidago canadensis'', which was introduced as a garden plant in Central Europe, has become common in the wild, and in [[Germany]] is considered an [[invasive species]] that displaces native vegetation from its natural habitat.
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Goldenrod often is inaccurately said to cause [[hay fever]] in humans.<ref name="Corporation2001"/> The pollen causing this allergic reaction is produced mainly by [[ragweed]] (''Ambrosia'' sp.), blooming at the same time as the goldenrod and pollinated by wind. Goldenrod [[pollen]] is too heavy and sticky to be blown far from the flowers, and is pollinated mainly by insects.<ref name="Corporation2001">{{cite book|author=Marshall Cavendish Corporation|title=Endangered Wildlife and Plants of the World: Fra-Igu|url=https://books.google.com/books?id=40jA0MOWejIC&pg=PA632|year=2001|publisher=Marshall Cavendish|isbn=978-0-7614-7199-8|pages=632–}}</ref> Frequent handling of goldenrod and other flowers, however, can cause allergic reactions, sometimes irritating enough to force [[floristry|florists]] to change occupation.<ref>{{cite journal|pmid=9534922|date=Feb 1998|author=de Jong, N. W.|title=Occupational allergy caused by flowers|volume=53|issue=2|pages=204–9|issn=0105-4538|journal=Allergy|doi=10.1111/j.1398-9995.1998.tb03872.x|s2cid=41094680|display-authors=etal}}</ref> Goldenrods are attractive sources of nectar for bees, flies, wasps, and butterflies. [[Honey]] from goldenrods often is dark and strong because of admixtures of other nectars. However, when [[honey flow]] is strong, a light (often water-clear), spicy-tasting [[monofloral honey]] is produced. While the bees are ripening the honey produced from goldenrods, it has a rank odour and taste; the finished honey is much milder.
Goldenrod often is inaccurately said to cause [[hay fever]] in humans.<ref name="Corporation2001"/> The pollen causing this allergic reaction is produced mainly by [[ragweed]] (''Ambrosia'' sp.), blooming at the same time as the goldenrod and pollinated by wind. Goldenrod [[pollen]] is too heavy and sticky to be blown far from the flowers, and is pollinated mainly by insects.<ref name="Corporation2001">{{cite book|author=Marshall Cavendish Corporation|title=Endangered Wildlife and Plants of the World: Fra-Igu|url=https://books.google.com/books?id=40jA0MOWejIC&pg=PA632|year=2001|publisher=Marshall Cavendish|isbn=978-0-7614-7199-8|pages=632–}}</ref> Frequent handling of goldenrod and other flowers, however, can cause allergic reactions, sometimes irritating enough to force [[floristry|florists]] to change occupation.<ref>{{cite journal|pmid=9534922|date=Feb 1998|author=de Jong, N. W.|title=Occupational allergy caused by flowers|volume=53|issue=2|pages=204–9|issn=0105-4538|journal=Allergy|doi=10.1111/j.1398-9995.1998.tb03872.x|s2cid=41094680|display-authors=etal}}</ref> Goldenrods are attractive sources of nectar for bees, flies, wasps, and butterflies. [[Honey]] from goldenrods often is dark and strong because of admixtures of other nectars. However, when [[honey flow]] is strong, a light (often water-clear), spicy-tasting [[monofloral honey]] is produced. While the bees are ripening the honey produced from goldenrods, it has a rank odour and taste; the finished honey is much milder.


Goldenrods are, in some places, considered a sign of good luck or good fortune.<ref name="Silverthorne2002"/> They are considered [[weed]]s by many in North America, but they are prized as garden plants in Europe, where British gardeners adopted goldenrod as a garden subject.{{citation needed|date=November 2022}} Goldenrod began to gain some acceptance in U.S. gardening (other than wildflower gardening) during the 1980s.{{citation needed|date=November 2022}}
Goldenrods are, in some places, considered a sign of good luck or good fortune.<ref name="Silverthorne2002"/> They are considered [[weed]]s by many in North America, but they are seen as invasive plants in Europe, where British gardeners adopted goldenrod as a garden subject.{{citation needed|date=November 2022}} Goldenrod began to gain some acceptance in U.S. gardening (other than wildflower gardening) during the 1980s.{{citation needed|date=November 2022}}


===Cultivated species===
===Cultivated species===
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===Industrial use===
===Industrial use===
{{more citations needed section|date=May 2022}}
{{more citations needed section|date=May 2022}}
Inventor [[Thomas Edison]] experimented with goldenrod to produce [[rubber]], which it contains naturally.<ref>{{cite magazine|url=http://content.time.com/time/subscriber/article/0,33009,881890,00.html|author=<!-- Staff writer(s); no by-line -->|title=Goldenrod Rubber|date=December 16, 1929|magazine=[[Time (magazine)|Time]]|access-date=June 6, 2017}}</ref> Edison created a fertilization and cultivation process to maximize the rubber content in each plant.<ref>{{Cite web |title=SL345/SS548: Fertilizer Experimentation, Data Analyses, and Interpretation for Developing Fertilization Recommendations—Examples with Vegetable Crop Research |url=https://edis.ifas.ufl.edu/publication/SS548 |access-date=2022-06-13 |website=edis.ifas.ufl.edu |language=en}}</ref> His experiments produced a {{convert|12|ft|m|adj=mid|-tall|abbr=on}} plant that yielded as much as 12% rubber. The tires on the [[Model T]] given to him by his friend [[Henry Ford]] were made from goldenrod. Like [[George Washington Carver]], [[Henry Ford]] was deeply interested in the regenerative properties of soil and the potential of alternative crops such as peanuts and soybeans to produce plastics, paint, fuel and other products.<ref>{{Cite web |last=Harris |first=Karen |title=George Washington Carver And Henry Ford Worked On Experimental Projects Together |url=https://historydaily.org/george-washington-carver-henry-ford-experiments |access-date=2022-06-13 |website=History Daily |language=en}}</ref> Ford had long believed that the world would eventually need a substitute for gasoline, and supported the production of ethanol (or grain alcohol) as an alternative fuel.<ref>{{Cite web |date=2012-11-25 |title=Henry Ford, Charles Kettering and the fuel of the future |url=https://environmentalhistory.org/people/henry-ford-charles-kettering-and-the-fuel-of-the-future/ |access-date=2022-06-13 |website=Environmental history |language=en-US}}</ref> In 1942, he would showcase a car with a lightweight plastic body made from soybeans. Ford and Carver began corresponding via letter in 1934, and their mutual admiration deepened after [[George Washington Carver]] made a visit to Michigan in 1937. As [[Douglas Brinkley]] writes in ''Wheels for the World'',<ref>{{Cite book |last=Brinkley |first=Douglas |url=https://cmc.marmot.org/Record/.b21749760 |title=Wheels for the world : Henry Ford, his company, and a century of progress, 1903-2003 / |date=2003 |publisher=Viking |isbn=978-0-670-03181-8}}</ref> his history of Ford, the automaker donated generously to the Tuskegee Institute, helping finance Carver's experiments, and Carver in turn spent a period of time helping to oversee crops at the Ford plantation in Ways, Georgia.
Inventor [[Thomas Edison]] experimented with goldenrod to produce [[rubber]], which it contains naturally.<ref>{{cite magazine|url=https://content.time.com/time/subscriber/article/0,33009,881890,00.html|author=<!-- Staff writer(s); no by-line -->|title=Goldenrod Rubber|date=December 16, 1929|magazine=[[Time (magazine)|Time]]|access-date=June 6, 2017}}</ref> Edison created a fertilization and cultivation process to maximize the rubber content in each plant.<ref>{{Cite web |title=SL345/SS548: Fertilizer Experimentation, Data Analyses, and Interpretation for Developing Fertilization Recommendations—Examples with Vegetable Crop Research |url=https://edis.ifas.ufl.edu/publication/SS548 |access-date=2022-06-13 |website=edis.ifas.ufl.edu |language=en}}</ref> His experiments produced a {{convert|12|ft|m|adj=mid|-tall|abbr=on}} plant that yielded as much as 12% rubber, and the new variant was named ''Solidago edisoni'',<ref>{{cite news |title=Phonograph exhibit hints at rubber invention |url=https://www.orlandosentinel.com/1992/10/04/phonograph-exhibit-hints-at-rubber-invention/ |access-date=19 December 2024 |publisher=The Orlando Sentinel |date=4 October 1992}}</ref><ref>{{cite book |last1=Thulesius |first1=Olav |title=Edison in Florida: the Green Laboratory |date=1997 |publisher=University Press of Florida |location=Gainesville |isbn=0-8130-1521-9 |pages=83-93}}</ref> also called ''Solidago edisoniana''.<ref>{{cite news |last1=Vargues |first1=Lisa |title=In Search of Thomas Edison's Botanical Treasures |url=https://www.nybg.org/blogs/science-talk/2013/10/in-search-of-thomas-edisons-botanical-treasures/ |access-date=19 December 2024 |publisher=The New York Botanical Garden |date=30 October 2013}}</ref> The tires on the [[Model T]] given to him by his friend [[Henry Ford]] were made from goldenrod. Like [[George Washington Carver]], [[Henry Ford]] was deeply interested in the regenerative properties of soil and the potential of alternative crops such as peanuts and soybeans to produce plastics, paint, fuel and other products.<ref>{{Cite web |last=Harris |first=Karen |title=George Washington Carver And Henry Ford Worked On Experimental Projects Together |url=https://historydaily.org/george-washington-carver-henry-ford-experiments |access-date=2022-06-13 |website=History Daily |language=en}}</ref>
Ford had long believed that the world would eventually need a substitute for gasoline, and supported the production of ethanol (or grain alcohol) as an alternative fuel.<ref>{{Cite web |date=2012-11-25 |title=Henry Ford, Charles Kettering and the fuel of the future |url=https://environmentalhistory.org/people/henry-ford-charles-kettering-and-the-fuel-of-the-future/ |access-date=2022-06-13 |website=Environmental history |language=en-US}}</ref> In 1942, he would showcase a car with a lightweight plastic body made from soybeans. Ford and Carver began corresponding via letter in 1934, and their mutual admiration deepened after [[George Washington Carver]] made a visit to Michigan in 1937. As [[Douglas Brinkley]] writes in ''Wheels for the World'',<ref>{{Cite book |last=Brinkley |first=Douglas |url=https://cmc.marmot.org/Record/.b21749760 |title=Wheels for the world : Henry Ford, his company, and a century of progress, 1903-2003 / |date=2003 |publisher=Viking |isbn=978-0-670-03181-8}}</ref> his history of Ford, the automaker donated generously to the Tuskegee Institute, helping finance Carver's experiments, and Carver in turn spent a period of time helping to oversee crops at the Ford plantation in Ways, Georgia.


By the time World War II began, Ford had made repeated journeys to Tuskegee to convince [[George Washington Carver]] to come to [[Dearborn, Michigan|Dearborn]] and help him develop a synthetic rubber to help compensate for wartime rubber shortages. Carver arrived on July 19, 1942, and set up a laboratory in an old water works building in Dearborn. He and Ford experimented with different crops, including sweet potatoes and dandelions, eventually devising a way to make the rubber substitute from goldenrod, a plant weed commercially viable.<ref>{{cite web|url=http://www.history.com/this-day-in-history/george-washington-carver-begins-experimental-project-with-henry-ford|title=George Washington Carver Begins Experimental Project with Henry Ford – Jul 19, 1942 |author=<!--Staff writer(s); no by-line.-->|publisher=[[History (U.S. TV channel)]]|access-date=20 May 2015}}</ref> Carver died in January 1943, Ford in April 1947, but the relationship between their two institutions continued to flourish: As recently as the late 1990s, Ford awarded grants of $4 million over two years to the George Washington Carver School at Tuskegee.<ref>{{Cite web |title=George Washington Carver |url=https://www.acs.org/content/acs/en/education/whatischemistry/landmarks/carver.html |access-date=2022-06-13 |website=American Chemical Society |language=en}}</ref>
By the time World War II began, Ford had made repeated journeys to Tuskegee to convince [[George Washington Carver]] to come to [[Dearborn, Michigan|Dearborn]] and help him develop a synthetic rubber to help compensate for wartime rubber shortages. Carver arrived on July 19, 1942, and set up a laboratory in an old water works building in Dearborn. He and Ford experimented with different crops, including sweet potatoes and dandelions, eventually devising a way to make the rubber substitute from goldenrod, a plant weed commercially viable.<ref>{{cite web|url=http://www.history.com/this-day-in-history/george-washington-carver-begins-experimental-project-with-henry-ford|title=George Washington Carver Begins Experimental Project with Henry Ford – Jul 19, 1942 |author=<!--Staff writer(s); no by-line.-->|publisher=[[History (U.S. TV channel)]]|access-date=20 May 2015}}</ref> Carver died in January 1943, Ford in April 1947, but the relationship between their two institutions continued to flourish: As recently as the late 1990s, Ford awarded grants of $4 million over two years to the George Washington Carver School at Tuskegee.<ref>{{Cite web |title=George Washington Carver |url=https://www.acs.org/content/acs/en/education/whatischemistry/landmarks/carver.html |access-date=2022-06-13 |website=American Chemical Society |language=en}}</ref>
Line 79: Line 81:


===Medicinal exploration===
===Medicinal exploration===
In various assessments by the European Medicines Agency with respect to ''[[Solidago virgaurea]]'', non-clinical data shows diuretic, anti-inflammatory, antioxidant, analgesic and spasmolytic, antibacterial, antifungal, anticancer and immunomodulatory activity. However, as no single ingredient is responsible for these effects, the whole herbal preparation of ''Solidago'' inflorescences must be considered as the active ingredient.<ref>European Medicines Agency, ''Aassessment Report on ''Solidago Virgaurea'' L., Herba'', European Medicines Agency Evaluation of Medicines for Human Use London, 4 September 2008 [https://www.ema.europa.eu/en/documents/herbal-report/assessment-report-solidago-virgaurea-l-herba_en.pdf Doc. Ref. EMEA/HMPC/285759/2007]</ref>
In various assessments by the European Medicines Agency with respect to ''[[Solidago virgaurea]]'', non-clinical data shows diuretic, anti-inflammatory, antioxidant, analgesic and spasmolytic, antibacterial, antifungal, anticancer and immunomodulatory activity. However, as no single ingredient is responsible for these effects, the whole herbal preparation of ''Solidago'' inflorescences must be considered as the active ingredient.<ref>European Medicines Agency, ''Assessment Report on ''Solidago Virgaurea'' L., Herba'', European Medicines Agency Evaluation of Medicines for Human Use London, 4 September 2008 [https://www.ema.europa.eu/en/documents/herbal-report/assessment-report-solidago-virgaurea-l-herba_en.pdf Doc. Ref. EMEA/HMPC/285759/2007]</ref>


==Cultural significance==
==Cultural significance==
Line 117: Line 119:
*''[[Solidago californica]]'' <small>Nutt.</small> - California goldenrod
*''[[Solidago californica]]'' <small>Nutt.</small> - California goldenrod
*''[[Solidago canadensis]]'' L. – Canada goldenrod, Canadian goldenrod, common goldenrod
*''[[Solidago canadensis]]'' L. – Canada goldenrod, Canadian goldenrod, common goldenrod
*''[[Solidago capulinensis]]'' <small>Cockerell & Andrews</small> L. – Capulin goldenrod
*''[[Solidago chilensis]]'' <small>Meyen</small>
*''[[Solidago chilensis]]'' <small>Meyen</small>
*''[[Solidago compacta]]'' <small>Turcz.</small>
*''[[Solidago compacta]]'' <small>Turcz.</small>
*''[[Solidago confinis]]'' <small>A.Gray</small>
*''[[Solidago confinis]]'' <small>A.Gray</small>
*''[[Solidago coreana]]'' <small>(Nakai) H.S.Pak</small>
*''[[Solidago coreana]]'' <small>(Nakai) H.S.Pak</small>
*''[[Solidago correllii]]'' <small>Semple</small> L. – Guadalupe Mountains goldenrod
*''[[Solidago curtisii]]'' <small>Torr. & A.Gray</small> &ndash; mountain decumbent goldenrod, Curtis' goldenrod
*''[[Solidago curtisii]]'' <small>Torr. & A.Gray</small> &ndash; mountain decumbent goldenrod, Curtis' goldenrod
*''[[Solidago dahurica]]'' <small>(Kitagawa) Kitagawa ex Juzepczuk</small>
*''[[Solidago dahurica]]'' <small>(Kitagawa) Kitagawa ex Juzepczuk</small>
Line 226: Line 230:


===Formerly included===
===Formerly included===
Numerous species formerly considered members of ''Solidago'' are now regarded as better suited to other genera, including ''[[Brintonia]], [[Duhaldea]], [[Euthamia]], [[Gundlachia (plant)|Gundlachia]], [[Inula]], [[Jacobaea]], [[Leptostelma]], [[Olearia]], [[Psiadia]], [[Senecio]], [[Sphagneticola]], [[Symphyotrichum]], [[Trixis]],'' and ''[[Xylothamia]]''.<ref name=hymenocallis/>
Numerous species formerly considered members of ''Solidago'' are now regarded as better suited to other genera, including ''[[Brintonia]]'', ''[[Duhaldea]]'', ''[[Euthamia]]'', ''[[Gundlachia (plant)|Gundlachia]]'', ''[[Inula]]'', ''[[Jacobaea]]'', ''[[Leptostelma]]'', ''[[Olearia]]'', ''[[Psiadia]]'', ''[[Senecio]]'', ''[[Sphagneticola]]'', ''[[Symphyotrichum]]'', and ''[[Trixis]]''.<ref name=hymenocallis/>


==References==
==References==

Latest revision as of 15:09, 19 December 2024

Solidago
Solidago virgaurea var. leiocarpa
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Clade: Asterids
Order: Asterales
Family: Asteraceae
Subfamily: Asteroideae
Tribe: Astereae
Subtribe: Solidagininae
Genus: Solidago
L. 1753 not Mill. 1754
Synonyms[1]
  • Actipsis Rafinesque
  • Aster Linnaeus subg. Solidago (Linnaeus) Kuntze
  • Leioligo Rafinesque

Solidago, commonly called goldenrods, is a genus of about 100[1] to 120[2] species of flowering plants in the family Asteraceae. Most are herbaceous perennial species found in open areas such as meadows, prairies, and savannas. They are mostly native to North America, including Mexico; a few species are native to South America and Eurasia.[1] Some American species have also been introduced into Europe and other parts of the world.

Description

[edit]
European goldenrod is pollinated by Bombus cryptarum

Solidago species are perennials growing from woody caudices or rhizomes. Their stems range from decumbent (crawling) to ascending or erect, with a range of heights going from 5 cm (2.0 in) to over a meter. Most species are unbranched, but some do display branching in the upper part of the plant. Both leaves and stems vary from glabrous (hairless) to various forms of pubescence (strigose, strigillose, hispid, stipitate-glandular or villous). In some species, the basal leaves are shed before flowering. The leaf margins are most commonly entire, but often display heavier serration. Some leaves may display trinerved venation rather than the pinnate venation usual across Asteraceae.[1]

The flower heads are usually of the radiate type (typical daisy flower heads with distinct ray and disc florets) but sometimes discoid (with only disc florets of mixed, sterile, male and types). Only ray florets are female, others are male, hermaphroditic or entire sterile. Head involucres are campanulate to cylindric or attenuate. Floret corollas are usually yellow, but white in the ray florets of a few species (such as Solidago bicolor); they are typically hairless. Heads usually include between 2 and 35 disc florets, but in some species this may go up to 60. Filaments are inserted closer to the base of the corolla than its middle. Numerous heads are usually grouped in complex compound inflorescences where heads are arranged in multiple racemes, panicles, corymbs, or secund arrays (with florets all on the same side).[1]

Solidago cypselae are narrowly obconic to cylindrical in shape, and they are sometimes somewhat compressed. They have eight to 10 ribs usually and are hairless or moderately hispid. The pappus is very big with barbellate bristles.[1]

Goldenrod and visiting Cerceris wasp

The many goldenrod species can be difficult to distinguish, due to their similar bright, golden-yellow flower heads that bloom in late summer. Propagation is by wind-disseminated seeds or by spreading underground rhizomes which can form colonies of vegetative clones of a single plant. They are mostly short-day plants and bloom in late summer and early fall. Some species produce abundant nectar when moisture is plentiful, or when the weather is warm and sunny.

The section Ptarmicoidei is sometimes treated as a separate genus Oligoneuron,[3] and is dropped by flat-topped to rounded corymbiform flowerheads.

Taxonomy

[edit]

Solidago is in the family Asteraceae (formerly known as Compositae), a diverse and widespread clade containing approximately 23,000 species and 12 tribes, which inhabit all continents except Antarctica. Within Asteraceae, Solidago is in the tribe Astereae and the subtribe Solidagininaeae.[4]

The genus Solidago is monophyletic as indicated by morphological characters[5] and molecular evidence.[6][7] All Solidago species are herbaceous perennials, growing from approximately 2 cm to 2.5 m tall. Yellow to white, pistillate ray flowers and yellow, perfect disc florets are characteristic of Solidago inflorescences, which have a wide range of shapes.[4] Molecular studies[8][6] using nuclear rDNA have hypothesized boundaries on the genus Solidago, but there have been difficulties in parsing out evolutionary relationships at the sub-genus scale and defining which should be included and separated from Solidago.

[edit]

Related Asteraceae genera, such as Chrysoma, Euthamia, and Oreochrysum, have been included within Solidago at one point or another,[9] but morphological evidence[10][9][11] has suggested otherwise. In a study comparing morphological characters of Solidago and related subgroups, the authors consider the subjectivity of classifying a genus and how to define it within broader tendencies concerning the taxonomy of North American Asteraceae. Little to no differences were observed between Solidago and the subgroups in terms of karyotype. However, external morphological characters such as habit, or the general appearance of the plant and how a suite of traits contribute to its phenotype; pappus size; and the point of freeing of stamen filaments from the corolla tube, are useful classification schemes for Solidago, since they are applied to differentiating between Asteraceae taxa. One school of Asteraceae taxonomy thought unites all taxa sharing similar floral head structure and subsequently ignores deviation from this morphology, while another places greater weight on these morphological deviations. The authors argue that the latter opinion should be applied. Since there is no theoretical foundation for relative taxonomic importance of traits, they assert that habit should be a central trait when defining taxa, and subsequently that all the subgroups considered in their study (Brachychaeta, Chrysoma, Euthamia, Oligoneuron, and Petradoria) should be segregated from Solidago.[12]

Results from a leaf anatomy study comparing differences in mesophyll, bundle sheath extensions, and midvein structure, among others in a suite of leaf traits,[9] are incongruent with those in an earlier study.[12] Based on the lack of bundle sheath extensions, it is suggested that Chrysoma, Euthamia, Gundlachia, and Petradoria should be distinct taxa and outside of Solidago.[9] However, Brachychaeta, Brintonia, Oligoneuron, Oreochrysum, and Aster ptarmicoides should be considered as components of Solidago. To summarize, the relation of Brachychaeta and Oligoneuron to Solidago is inconsistent based on these results.[12][9] Both support the separation of Chrysoma, Euthamia, and Petradoria from Solidago. A study reviews the taxonomic position of Oligoneuron relative to Solidago, as based on taxonomic evidence, treats it as separate from Solidago,[10] similarly to Kapoor & Beaudry (1966). The first molecular phylogeny based on chloroplast DNA treats Brachychaeta, Brintonia, Oligoneuron, and Oreochrysum as constituents of Solidago.[6] Using consensus trees from ITS data, another study found support for Oligoneuron as part of Solidago,[13] and the findings of Zhang (1996). More recently, an analysis of combined ITS and ETS data provided additional support for the inclusion of Oligoneuron as part of Solidago.[8]

Until the 1980s, the genus Euthamia was largely considered to be a part of Solidago due to morphological similarities between species in both genera, and a history of synonymy of Solidago lanceolata and Euthamia graminifolia.[11] As mentioned, the lack of bundle sheath extensions in Euthamia compared to Solidago,[9] and deviations in floral morphology[12] present evidence for separation of these taxa. A taxonomy of Euthamia as a genus was presented, providing a detailed description of distinguishing external morphological characters, such as fibrous-roots, sessile leaves, and mostly corymbiform inflorescences.[11]

Evolutionary relationships within Solidago

[edit]

Chromosome counts and advances in molecular systematics have enabled greater understanding of evolutionary relationships within Solidago. At the time a taxonomy of Solidago was published,[10] related taxa causing contention, such as Chrysoma, Euthamia, Oligoneuron, and Petradoria, were excluded from this genus. The number of Solidago species has remained relatively stable, around 120, with approximately 80 in North America.[7][10] Due to monophyletic support for the New World taxa[13][5] and taxonomic difficulties with Old World taxa, the taxonomy provided in the 1990s[10] only includes North American taxa and thus treats Solidago as non-monophyletic. Existing molecular-based phylogenies provide monophyletic support for Solidago[8][13][7][6] given its inclusion of Oligoneuron.

Chromosome counts have proven to be a valuable character in Solidago taxonomy and in elucidating the cytogeographic history of the genus. Similar chromosome counts may indicate close evolutionary relationships, while different chromosome numbers may suggest distant relationships through reproductive isolation. Chromosome counts have been studied extensively in North America;[14][15] all Solidago species have a base chromosome number of x=9, but the following ploidy levels have been observed: 2x, 3x, 4x, 6x, 8x, 10x, 12x, and 14x.

Though negligible differences in karyotype among Solidago and related genera were found,[12] Solidago taxa with multiple cytotypes are more common than those with one.[7] Although chromosome count is a useful metric for differentiating among Solidago taxa, it may be problematic due to the frequent variation in ploidy levels. Cytogeographic patterns in the Solidago gigantea complex, with tetraploids occurring in eastern North America and hexaploids in Oregon and Washington, were observed.[16] Cytogeographic patterns are also observed in the Solidago canadensis complex: hexaploids within S. canadensis have been observed east of the Great Plains and are treated as Solidago altissima, and diploids and tetraploids occurring in the Great Plains are treated as Solidago gilvocanescens. The taxonomic status of Solidago ptarmicoides created an extensive debate due to frequency hybridization of S. ptarmicoides with members of the Ptarmicoidei section of Solidago.[1] It was asserted that S. ptarmicoides should be united with Solidago rather than the genus Aster due to external morphological features such as similar pappus length as well as the same chromosome base (x=9). Information about chromosome number is still a crucial part of current understanding and phylogenies of Solidago.[7]

Ecology

[edit]

Goldenrod is considered a keystone species, and has been called the single most important plant for North American pollinator biodiversity.[17][18] Goldenrod species are used as a food source by the larvae of many Lepidoptera species. As many as 104 species of butterflies and moths use it as a host plant for their larvae, and 42 species of bees are goldenrod specialists, visiting only goldenrod for food.[19] Some lepidopteran larvae bore into plant tissues and form a bulbous tissue mass called a gall around it, upon which the larva then feeds. Various parasitoid wasps find these galls and lay eggs in the larvae, penetrating the bulb with their ovipositors. Woodpeckers are known to peck open the galls and eat the insects in the center.[20]

Goldenrods have become invasive species in many parts of the world outside their native range, including China, Japan, Europe and Africa.[21][22] Solidago canadensis, which was introduced as a garden plant in Central Europe, has become common in the wild, and in Germany is considered an invasive species that displaces native vegetation from its natural habitat.

Use and cultivation

[edit]

Young goldenrod leaves are edible.[23] Traditionally, Native Americans use the seeds of some species for food.[24] Herbal teas are sometimes made with goldenrod.[25]

Goldenrod often is inaccurately said to cause hay fever in humans.[26] The pollen causing this allergic reaction is produced mainly by ragweed (Ambrosia sp.), blooming at the same time as the goldenrod and pollinated by wind. Goldenrod pollen is too heavy and sticky to be blown far from the flowers, and is pollinated mainly by insects.[26] Frequent handling of goldenrod and other flowers, however, can cause allergic reactions, sometimes irritating enough to force florists to change occupation.[27] Goldenrods are attractive sources of nectar for bees, flies, wasps, and butterflies. Honey from goldenrods often is dark and strong because of admixtures of other nectars. However, when honey flow is strong, a light (often water-clear), spicy-tasting monofloral honey is produced. While the bees are ripening the honey produced from goldenrods, it has a rank odour and taste; the finished honey is much milder.

Goldenrods are, in some places, considered a sign of good luck or good fortune.[28] They are considered weeds by many in North America, but they are seen as invasive plants in Europe, where British gardeners adopted goldenrod as a garden subject.[citation needed] Goldenrod began to gain some acceptance in U.S. gardening (other than wildflower gardening) during the 1980s.[citation needed]

Cultivated species

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Cultivated goldenrods include S. bicolor, S. caesia, S. canadensis, S. cutleri, S. riddellii, S. rigida, S. shortii, and S. virgaurea.[29]

A number of cultivars have been selected, including several of hybrid origin. A putative hybrid with aster, known as ×Solidaster is less unruly, with pale yellow flowers, equally suitable for dried arrangements. Molecular and other evidence points to ×Solidaster (at least the cultivar 'Lemore') being a hybrid of Solidago ptarmicoides and Solidago canadensis, the former now in Solidago, but likely the "aster" in question.[8]

The cultivars 'Goldenmosa'[30] and S. × luteus 'Lemore'[31] have gained the Royal Horticultural Society's Award of Garden Merit.[32]

Industrial use

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Inventor Thomas Edison experimented with goldenrod to produce rubber, which it contains naturally.[33] Edison created a fertilization and cultivation process to maximize the rubber content in each plant.[34] His experiments produced a 12 ft-tall (3.7 m) plant that yielded as much as 12% rubber, and the new variant was named Solidago edisoni,[35][36] also called Solidago edisoniana.[37] The tires on the Model T given to him by his friend Henry Ford were made from goldenrod. Like George Washington Carver, Henry Ford was deeply interested in the regenerative properties of soil and the potential of alternative crops such as peanuts and soybeans to produce plastics, paint, fuel and other products.[38]

Ford had long believed that the world would eventually need a substitute for gasoline, and supported the production of ethanol (or grain alcohol) as an alternative fuel.[39] In 1942, he would showcase a car with a lightweight plastic body made from soybeans. Ford and Carver began corresponding via letter in 1934, and their mutual admiration deepened after George Washington Carver made a visit to Michigan in 1937. As Douglas Brinkley writes in Wheels for the World,[40] his history of Ford, the automaker donated generously to the Tuskegee Institute, helping finance Carver's experiments, and Carver in turn spent a period of time helping to oversee crops at the Ford plantation in Ways, Georgia.

By the time World War II began, Ford had made repeated journeys to Tuskegee to convince George Washington Carver to come to Dearborn and help him develop a synthetic rubber to help compensate for wartime rubber shortages. Carver arrived on July 19, 1942, and set up a laboratory in an old water works building in Dearborn. He and Ford experimented with different crops, including sweet potatoes and dandelions, eventually devising a way to make the rubber substitute from goldenrod, a plant weed commercially viable.[41] Carver died in January 1943, Ford in April 1947, but the relationship between their two institutions continued to flourish: As recently as the late 1990s, Ford awarded grants of $4 million over two years to the George Washington Carver School at Tuskegee.[42]

Extensive process development was conducted during World War II to commercialize goldenrod as a source of rubber.[43] The rubber is only contained in the leaves, not the stems or blooms.[44] Typical rubber content of the leaves is 7%. The resulting rubber is of low molecular weight, resulting in an excessively tacky compound with poor tensile properties.[45]

Traditional medicine

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Solidago virgaurea is used in a traditional kidney tonic by practitioners of herbal medicine to counter inflammation and irritation caused by bacterial infections or kidney stones.[46][47] Goldenrod is also used in some formulas for cleansing of the kidney or bladder during a healing fast, in conjunction with potassium broth and specific juices.[47] Some Native American cultures traditionally chew the leaves to relieve sore throats, and the roots to relieve toothaches.[28]

Medicinal exploration

[edit]

In various assessments by the European Medicines Agency with respect to Solidago virgaurea, non-clinical data shows diuretic, anti-inflammatory, antioxidant, analgesic and spasmolytic, antibacterial, antifungal, anticancer and immunomodulatory activity. However, as no single ingredient is responsible for these effects, the whole herbal preparation of Solidago inflorescences must be considered as the active ingredient.[48]

Cultural significance

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The goldenrod is the state flower of the U.S. states of Kentucky (adopted 1926) and Nebraska (adopted 1895). Solidago altissima, tall goldenrod, was named the state wildflower of South Carolina in 2003.[49] The sweet goldenrod (Solidago odora) is the state herb of Delaware.[50] Goldenrod was the state flower of Alabama, but it was later rejected in favor of the camellia.[51]

Diversity

[edit]
Solidago canadensis in Kerala
Solidago lepida
Solidago multiradiata
Solidago ptarmicoides
Solidago nemoralis
Solidago velutina ssp. sparsiflora
Solidago spectabilis
Gall formed in Solidago sp. by the fly Eurosta solidaginis
Solidago sp. with digger wasp Sphex ichneumoneus
Fruits of Solidago simplex

Accepted species

[edit]

Source[52][better source needed]

Natural hybrids

[edit]
  • Solidago × asperula Desf. (S. rugosa × S. sempervirens)[52]
  • Solidago × beaudryi Boivin (S. rugosa × S. uliginosa)[52]
  • Solidago × calcicola (Fernald) Fernald – limestone goldenrod[52]
  • Solidago × erskinei Boivin (S. canadensis × S. sempervirens)[52]
  • Solidago × niederederi[53][54][55][56] Khek[54][55][56] (S. canadensis × S. virgaurea)[53][55][56]
  • Solidago × ovata Friesner (S. sphacelata × S. ulmifolia)[52]
  • Solidago × ulmicaesia Friesner (S. caesia × S. ulmifolia)[52]

Formerly included

[edit]

Numerous species formerly considered members of Solidago are now regarded as better suited to other genera, including Brintonia, Duhaldea, Euthamia, Gundlachia, Inula, Jacobaea, Leptostelma, Olearia, Psiadia, Senecio, Sphagneticola, Symphyotrichum, and Trixis.[52]

References

[edit]
  1. ^ a b c d e f g "Solidago". Flora of North America.
  2. ^ Solidago. Flora of China.
  3. ^ "Solidago Linnaeus sect. Ptarmicoidei (House) Semple & Gandhi". Flora of North America.
  4. ^ a b The Families and Genera of Vascular Plants.
  5. ^ a b Hood, Jennifer L.A.; Semple, John C. (2003). "Pappus Variation in Solidago (Asteraceae: Astereae)". SIDA, Contributions to Botany. 20 (4): 1617–1630. JSTOR 41961022.
  6. ^ a b c d Zhang, Jie J. (1996). A Molecular Biosystematic Study on North American Solidago and Related Genera (Asteraceae: Astereae) Based on Chloroplast DNA RFLP Analysis [microform] (Thesis). University of Waterloo.
  7. ^ a b c d e Semple, John (2016-05-11). "An Intuitive Phylogeny and Summary of Chromosome Number Variation in the Goldenrod genus Solidago (Asteraceae: Astereae)". Phytoneuron. 2016–32: 1–9.
  8. ^ a b c d Schilling, E. E.; et al. (2008). "Molecular Analysis of Solidaster cv. Lemore, a Hybrid Goldenrod (Asteraceae)" (PDF). Journal of the Botanical Research Institute of Texas. 2: 7–18.
  9. ^ a b c d e f Anderson, Loran C.; Creech, Jessica B. (1975). "Comparative Leaf Anatomy of Solidago and Related Asteraceae". American Journal of Botany. 62 (5): 486–493. doi:10.2307/2441956. JSTOR 2441956.
  10. ^ a b c d e Nesom, Guy L. (1994). "Subtribal Classification of the Astereae (Asteraceae)". Phytologia. 76. ISSN 0031-9430.
  11. ^ a b c "The Taxonomy of the Genus Euthamia". Rhodora. 83 (836). 1981. ISSN 0035-4902.
  12. ^ a b c d e Kapoor, B. M.; Beaudry, J. R. (1966-09-01). "Studies on Solidago. Vii. the Taxonomic Status of the Taxa Brachychaeta, Brintonia, Chrysoma, Euthamia, Oligoneuron and Petradoria in Relation to Solidago". Canadian Journal of Genetics and Cytology. 8 (3): 422–443. doi:10.1139/g66-053. ISSN 0008-4093.
  13. ^ a b c Beck, James B.; Nesom, Guy L.; Calie, Patrick J.; Baird, Gary I.; Small, Randall L.; Schilling, Edward E. (2004). "Is Subtribe Solidagininae (Asteraceae) Monophyletic?". Taxon. 53 (3): 691–698. doi:10.2307/4135444. JSTOR 4135444.
  14. ^ Cook, Rachel E.; Semple, John C. (2008-11-13). "Cytogeography of Solidago subsect. Glomeruliflorae (Asteraceae: Astereae)". Botany. 86 (12): 1488–1496. doi:10.1139/B08-087. ISSN 1916-2790.
  15. ^ Semple, John; Watanabe, Kuniaki (2013-03-02). "A Review of Chromosome Numbers in Asteraceae with Hypotheses on Chromosomal Base Number Evolution". {{cite journal}}: Cite journal requires |journal= (help)
  16. ^ Semple, John C.; Ringius, Gordon S.; Leeder, Colleen; Morton, Gary (1984-07-01). "Chromosome Numbers of Goldenrods, Euthamia and Solidago (Compositae: Astereae). II. Additional Counts with Comments on Cytogeography". Brittonia. 36 (3): 280–292. Bibcode:1984Britt..36..280S. doi:10.2307/2806528. ISSN 0007-196X. JSTOR 2806528. S2CID 186241866.
  17. ^ Perkins, Deborah (23 September 2019). "Goldenrods: Top Plant for Boosting Biodiversity". ncrm.org. Natural Resources Council of Maine.
  18. ^ "Goldenrod (Solidago) Is Trending!". nurturenativenature.com. 29 December 2020.
  19. ^ "Keystone Native Plants Eastern Temperate Forests - Ecoregion 8". nwf.org. National Wildlife Federation.
  20. ^ Shealers, D. A.; et al. (July 1999). "Foraging patterns of Eastern gray squirrels (Sciurus carolinensis) on goldenrod gall insects, a potentially important winter food resource". The American Midland Naturalist. 142 (1): 102–109. doi:10.1674/0003-0031(1999)142[0102:FPOEGS]2.0.CO;2. ISSN 0003-0031. S2CID 85741057.
  21. ^ "Solidago canadensis (Canadian goldenrod)". Invasive Species Compendium (ISC). CAB International.
  22. ^ "Solidago gigantea (Giant goldenrod)".
  23. ^ Solidago missouriensis, Missouri goldenrod. Archived 2013-09-27 at the Wayback Machine Northern Rockies Natural History Guide. University of Montana, Missoula.
  24. ^ Solidago nemoralis. Native American Ethnobotany. University of Michigan, Dearborn.
  25. ^ Goldenrod. Complementary and Alternative Medicine Guide. University of Maryland Medical Center.
  26. ^ a b Marshall Cavendish Corporation (2001). Endangered Wildlife and Plants of the World: Fra-Igu. Marshall Cavendish. pp. 632–. ISBN 978-0-7614-7199-8.
  27. ^ de Jong, N. W.; et al. (Feb 1998). "Occupational allergy caused by flowers". Allergy. 53 (2): 204–9. doi:10.1111/j.1398-9995.1998.tb03872.x. ISSN 0105-4538. PMID 9534922. S2CID 41094680.
  28. ^ a b Silverthorne, E. (2002). Legends and Lore of Texas Wildflowers. Texas A&M University Press. pp. 61–. ISBN 978-1-58544-230-0. Retrieved 4 October 2010.
  29. ^ Jelitto, L.; Schacht, W. (1995). Hardy Herbaceous Perennials: A–K ; Vol. 2, L–Z. Timber Press. p. 629. ISBN 978-0-88192-159-5. Retrieved 4 October 2010.
  30. ^ "RHS Plant Selector - Solidago 'Goldenmosa'". Retrieved 10 June 2013.
  31. ^ "RHS Plant Selector - Solidago × luteus 'Lemore'". Retrieved 10 June 2013.
  32. ^ "AGM Plants - Ornamental" (PDF). Royal Horticultural Society. July 2017. p. 98. Retrieved 12 November 2018.
  33. ^ "Goldenrod Rubber". Time. December 16, 1929. Retrieved June 6, 2017.
  34. ^ "SL345/SS548: Fertilizer Experimentation, Data Analyses, and Interpretation for Developing Fertilization Recommendations—Examples with Vegetable Crop Research". edis.ifas.ufl.edu. Retrieved 2022-06-13.
  35. ^ "Phonograph exhibit hints at rubber invention". The Orlando Sentinel. 4 October 1992. Retrieved 19 December 2024.
  36. ^ Thulesius, Olav (1997). Edison in Florida: the Green Laboratory. Gainesville: University Press of Florida. pp. 83–93. ISBN 0-8130-1521-9.
  37. ^ Vargues, Lisa (30 October 2013). "In Search of Thomas Edison's Botanical Treasures". The New York Botanical Garden. Retrieved 19 December 2024.
  38. ^ Harris, Karen. "George Washington Carver And Henry Ford Worked On Experimental Projects Together". History Daily. Retrieved 2022-06-13.
  39. ^ "Henry Ford, Charles Kettering and the fuel of the future". Environmental history. 2012-11-25. Retrieved 2022-06-13.
  40. ^ Brinkley, Douglas (2003). Wheels for the world : Henry Ford, his company, and a century of progress, 1903-2003 /. Viking. ISBN 978-0-670-03181-8.
  41. ^ "George Washington Carver Begins Experimental Project with Henry Ford – Jul 19, 1942". History (U.S. TV channel). Retrieved 20 May 2015.
  42. ^ "George Washington Carver". American Chemical Society. Retrieved 2022-06-13.
  43. ^ "Extraction, Characterization, and Utilization of Goldenrod Rubber". US Department of Agriculture. 9 September 1944. Retrieved 27 Sep 2011.
  44. ^ Arias, Marina; Van Dijk, Peter J. (2019). "What Is Natural Rubber and Why Are We Searching for New Sources?". Frontiers for Young Minds. 7. doi:10.3389/frym.2019.00100.
  45. ^ "weakest rubber compounds: Topics by Science.gov". www.science.gov. Retrieved 2022-06-13.
  46. ^ Melzig, M. F. (November 2004). "Goldenrod – a Classical Exponent in the Urological Phytotherapy". Wiener Medizinische Wochenschrift. 154 (21–22): 523–527. doi:10.1007/s10354-004-0118-4. ISSN 0043-5341. PMID 15638071. S2CID 20348306.
  47. ^ a b Campion, K. (1995). Holistic Woman's Herbal – How to Achieve Health and Well-Being at Any Age. Barnes & Noble, Inc. 1995. pp. 65, 96. ISBN 978-0-7607-1030-2
  48. ^ European Medicines Agency, Assessment Report on Solidago Virgaurea L., Herba, European Medicines Agency Evaluation of Medicines for Human Use London, 4 September 2008 Doc. Ref. EMEA/HMPC/285759/2007
  49. ^ "Tall Goldenrod - South Carolina State Wildflower". www.sciway.net. Retrieved 2021-05-01.
  50. ^ State Seal, Song and Symbols of Delaware
  51. ^ Wilson, Sue (2016-05-07). "Remember when: Camellia wasn't always our state flower". The Andalusia Star-News. Retrieved 2022-06-13.
  52. ^ a b c d e f g h The Plant List, search for Solidago
  53. ^ a b "Updated Distribution of Solidago x niederederi in Poland". EPPO Reporting Service. 03–2018 (2018/065). European and Mediterranean Plant Protection Organization (EPPO). 2018-12-11. Retrieved 2021-02-22.
  54. ^ a b "Solidago × niederederi". Invasive Species Compendium (ISC). CABI (Centre for Agriculture and Bioscience International). 2019-11-19. Retrieved 2021-02-22.
  55. ^ a b c Skokanová, Katarína; Šingliarová, Barbora; Španiel, Stanislav; Hodálová, Iva; Mereďa, Pavol (2020). "Tracking the Expanding Distribution of Solidago ×niederederi (Asteraceae) in Europe and First Records from Three Countries Within the Carpathian Region". BioInvasions Records. 9 (4). Regional Euro-Asian Biological Invasions Centre Oy (REABIC): 670–684. doi:10.3391/bir.2020.9.4.02. ISSN 2242-1300.
  56. ^ a b c Pliszko, Artur; Łazarski, Grzegorz; Kalinowski, Paweł; Adamowski, Wojciech; Rutkowski, Lucjan; Puchałka, Radosław (2017-12-20). "An Updated distribution of Solidago × niederederi (Asteraceae) in Poland". Acta Musei Silesiae, Scientiae Naturales. 66 (3). Walter de Gruyter GmbH: 253–258. doi:10.1515/cszma-2017-0026. ISSN 2336-3207.
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