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The Magazine of the Arnold Arboretum 


VOLUME 75 • NUMBER 1 • 2017 

Arnoldia (ISSN 0004-2633; USPS 866-100) 
is published quarterly by the Arnold Arboretum 
of Harvard University. Periodicals postage paid 
at Boston, Massachusetts. 

Subscriptions are $20.00 per calendar year 
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Arboretum, 125 Arborway, Boston, MA 02130- 
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e-mail arnoldia@arnarb.harvard.edu 

Arnold Arboretum members receive a subscrip¬ 
tion to Arnoldia as a membership benefit. To 
become a member or receive more information, 
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email wendy_krauss@harvard.edu 

Postmaster: Send address changes to 

Arnoldia Circulation Manager 
The Arnold Arboretum 
125 Arborway 
Boston, MA 02130-3500 

Nancy Rose, Editor 
Andy Winther, Designer 

Editorial Committee 
Anthony S. Aiello 
Peter Del Tredici 
Michael S. Dosmann 
William (Ned) Friedman 
Jon Hetman 
Julie Moir Messervy 

Copyright © 2017. The President and 
Fellows of Harvard College 


CONTENTS 

2 Plant Exudates and Amber: 

Their Origin and Uses 

Jorge A. Santiago-Blay and Joseph B. Lambert 

14 Other Order: Sound Walk for an Urban Wild 

Peter Del Tredici and Teri Rueb 

26 Floral Clocks, Carpet Beds, and the 
Ornamentation of Public Parks 

Phyllis Andersen 

36 Uncommon By Any Name: 

Acer pensylvanicum 

Jon Hetman 

Front cover: Plant parts, such as this flower, and 
animals trapped in amber can provide important sci¬ 
entific insights to the distant past. Photo courtesy of 
Patrick R. Craig. 

Inside Jront cover: Many public parks, including 
Boston's Public Garden, seen here, still create extensive 
annual bedding out displays, a practice first popularized 
in the Victorian era. Photo by Norman Eggert/Alamy 
Stock Photo. 

Inside back cover: Whether you call it striped maple, 
snalcebarlc maple, or moosewood, Acer pensylvanicum 
is an admirable native tree. Photo of Arnold Arboretum 
accession 137-2003-F by Jon Hetman. 

Back cover: A carpet of non-native lesser celandine 
(Ranunculus Jicaria ) blooms amid old stems of Helian- 
thus. Photo by Peter Del Tredici. 



The ARNOLD 
ARBORETUM 

of HARVARD UNIVERSITY 




ALL PHOTOGRAPHS BY JORGE A. SANTIAGO-BLAY UNLESS OTHERWISE NOTED 


Plant Exudates and Amber: Their Origin and Uses 

Jorge A. Santiago-Blay and Joseph B. Lambert 


P lants produce and export many different 
molecules out of their cellular and organ - 
ismal confines. Some of those chemicals 
become so abundant that we can see or smell 
them. The most visible materials oozed by 
many plants are called "exudates ." 

What are plant exudates? Generally, exudates 
are carbon-rich materials that many plants pro¬ 
duce and release externally. When exudates are 
produced, they are often sticky to human touch. 
Such plant chemicals can be the visible expres¬ 
sion of attack by bacteria, fungi, herbivores, or 



Prolific white, resinous exudation is seen on a tumor- 
like growth on the trunk of a white pine (Pinus strobus ) 
at the Arnold Arboretum. 


some other plant pathology. In other instances, 
such as in typical underground roots, exudate 
production appears to be part of the typical 
metabolism of healthy plants that helps stabi¬ 
lize the soil and foster interactions with other 
organisms around the roots. 

Different plant tissue types and organs can 
produce exudates. We have collected resins and 
gums from the above ground portions of plants, 
or shoots, as well as from the generally below 
ground portion of plants, or roots. Root exuda¬ 
tion has been known for decades and is respon- 



Resinous exudates on a conifer. 



Blobs of white resin on a relatively young shoot of a 
Japanese black pine (Pinus thunbergii, AA accession 
11371 - 0 ). 


REPRODUCED WITH PERMISSION OF AMERICAN SCIENTIST 






Plant Exudates and Amber 3 



A slab of Great Basin bristlecone pine (Pinus longaeva ) right out of the microwave oven showing extruded (and very 
hot!) resinous exudates. Microwave heating experiments were performed at the Laboratory of Tree-Ring Research, 
University of Arizona, Tucson. 


sible for many of the fascinating relationships 
in the interface of plant roots and soil microor¬ 
ganisms known as the rhizosphere. 

Collecting and Analyzing Plant Exudates 

After receiving collecting permission (if needed), 
we spend days walking the grounds of botani¬ 
cal gardens and arboreta, or do field work else¬ 
where. Exudates are easily collected directly 
from the trees with no harm to the plant and 
leaving no doubt about their botanical identity. 
Occasionally we use more forceful methods, 
such as carefully microwaving wood slabs to 
extract the exudates, then letting them reso¬ 
lidify. Once the material is collected, we place 
it in a small plastic zip-top bag. An additional, 
external bag is used to hold a paper label con¬ 
taining the collection data. If needed, we let the 
exudate dry slowly in an oven and, once dried, 
the materials are ready for subsequent analyses. 
In other instances, generous collaborators send 
us materials for chemical analyses. 

Carbon-13 solid state Nuclear Magnetic 
Resonance spectroscopy (ssNMR) is a state- 
of-the-art research tool that generates spectra 


(or chemical signatures) of materials, includ¬ 
ing plant exudates and amber or greatly 
fossilized plant resin. The analyses, which 
use a tiny amount (as little as 50 to 100 mil¬ 
ligrams, approximately the volume of a new 
eraser on a school pencil) of the exudate, are 
non-destructive. They are performed at North¬ 
western University (in Evanston, Illinois), one 
of a few research laboratories in the world 
with carbon-13 ssNMR capabilities. At times, 
we observe plants that evidently have produced 
exudates but the amounts are insufficient 
for our analyses. 

Solid exudates are pulverized manually and 
undergo two sets of carbon-13 ssNMR analyses: 
normal decoupling, which gathers signals for 
all carbon atoms, and interrupted decoupling, 
which, among others, obtains signals from car¬ 
bons lacking the attached hydrogens. Just like 
in spectra used in the health-allied sciences, 
different regions of the spectra provide valu¬ 
able information (see Figure 1 on page 4). In 
the case of NMR, the peaks represent different 
atoms and reflect their molecular environment. 
The height of the peaks largely represents rela- 




4 Arnoldia 75/1 • August 201 7 


(A) 



220 200 180 160 140 120 100 80 

fl (ppm) 


60 40 


20 


(B) 


Interrupted Decoupling - only carbons with strong C-H interactions analyzed 



I C=0 bonds as in carboxyls I C=C bonds as in alkenes [ as 111 

1 1 sugars 1 


C-C bonds as in alkanes 


— 1 - 

220 

- 1 - 

200 

- 1 - 

180 

- 1 - 

160 

- 1 - 

140 

- 1 -■- 1 - 

120 100 

(ppm) 

- 1 - 

80 

- 1 - 

60 

- 1 - 

40 

- 1 - 

20 

- 1 - 

0 



(C) 


Interrupted Decoupling - only carbons with strong C-H interactions analyzed 



| C=0 bonds as in | 
carboxyls 


C=C bonds as in alkenes 


C-O bonds 
as in 
sugars 


C-C bonds as in alkanes 


- 1 - 

220 

- 1 - 

200 

180 

160 

- 1 - 

140 

- 1 - 1 - 1 - 

120 100 

(ppm) 

- 1 - 

80 

- 1 - 

60 

- 1 - 

40 

- 1 - 

20 

- 1 - 

0 



Figure 1. Chemical identity of peaks on a C-13 ssNMR spectra. Panel (A) is a 
resin, panel (B) is a gum, and panel (C) is a kino (a type of phenolic, often found 
in Eucalyptus ). In all panels, the upper result uses interrupted decoupling, 
which eliminates peaks representing C-H single bonds. The lower result uses 
normal decoupling in which all carbon-to-atom bonds are represented. 


tive abundance of those atoms. 
The position of the peak along 
the horizontal axis (parts per mil¬ 
lion [ppm]) is the resonance fre¬ 
quency characteristic of the atom 
and its molecular neighborhood. 
This position is an indication 
of the chemical identity of the 
peak as compared to an external 
molecular reference. In carbon-13 
ssNMR, peaks in the 0-80 ppm 
region are singly bonded carbon 
atoms (-C-C-), or alkanes,- signals 
within the 80-100 ppm region are 
single bonded carbon atoms with 
electron-withdrawing neighbors, 
in particular, oxygen (C-O), as 
found in carbohydrates, such as 
sugars. Currently, we have ana¬ 
lyzed over 1,800 exudates of all 
types, including amber, represent¬ 
ing most of the major plant groups 
worldwide. However, a lot more 
samples still need to be acquired 
and analyzed. 

Types of Plant Exudates 

Using NMR, we have determined 
that there are three major types of 
plant exudates: resins, gums, and 
phenolics. Resins are made from 
terpene molecules. The basic 
molecular unit of terpenes is a 
five-carbon molecule, known as 
isoprene (see Figure 2 on page 6). 

When freshly produced, many 
resins are sticky and smell like 
Christmas trees or incense. Resins 
are insoluble in water and thus do 
not dissolve during rains. As time 
passes and the resins begin to 
"mature," many of their original 
chemical constituents evaporate. 
The materials remaining behind 
in the resin blob form chemical 
bonds, a process known as polym¬ 
erization, and the blob begins to 
harden. With the passage of mil¬ 
lennia, the resinous material 
becomes greatly polymerized and 




















JOSEPH O'BRIEN, USDA FOREST SERVICE, BUGWOOD. ORG 


Plant Exudates and Amber 5 


Not On the Collection List 


Not everything that looks like an exudate is an exudate. Some living organisms, 
particularly fungi, can resemble the kinds of plant exudates we collect. In other 
instances, the watery—and often foul smelling—material that decomposing 
portions of plants produce can also resemble exudates. As you may guess, 

we do not collect those! 




Clockwise: Some exudate mimics include a cedar-apple 
rust ( G ymn osp or an gi um juniperi-virginianae) fungal 
fruiting body on Juniperus virginiana; an unidenti¬ 
fied fungus growing on a Pinus hwangshanensis (AA 
accession 68-76-F)—note its superficial similarity to the 
yellowish color of some resins; a Polyporus fungus on 
Quercus palustris (AA accession 805-87-A); an exudate- 
resembling, foul smelling material resulting from 
decomposition by fungi and bacteria on a cut Cornus 
kousa (AA accession 524-49-D) branch. 

















CHIP CLARK, NATIONAL MUSEUM OF NATURAL HISTORY, SMITHSONIAN INSTITUTION CHIP CLARK, NATIONAL MUSEUM OF NATURAL HISTORY, SMITHSONIAN INSTITUTION 


6 Arnoldia 75/1 • August 201 7 



Close-up of resinous flow on the trunk of a pine ( Pinus ). 



Latex exudate emanating from a Euphorbia tirucalli stem. 



of resins. 

ChUOH 


H OH 

Figure 3. Model of a glucose, an example of a simple 
sugar molecule. Chemically linked sugar molecules 
make up carbohydrates. The carbon bound by two 
oxygen atoms (arrow) is known as anomeric carbon 
and is characteristic of sugars. Exudated carbohy¬ 
drates are known as gums. 

evolves into the robust gemstone called amber, 
produced only by specific plant species. Coni¬ 
fers such as pines [Pinus], firs [Abies], spruces 
[Picea], larches [Laiix], and some other familiar 
cone-bearing trees in northern latitudes tend to 
produce resinous exudates. Many angiosperms 
(flowering plants) also produce resins. 

The term “ latex" refers to milky-looking exu¬ 
dates produced by numerous flowering plants, 
including those in the euphorbia or spurge fam¬ 
ily (Euphorbiaceae). Latexes can be dangerous to 
touch, causing dermatitis or other damage, espe¬ 
cially to the eyes. Interestingly, all latexes we 
have examined thus far are resins in suspension. 

A second type of exudates is known as 
gums. Gums are large carbohydrates consist¬ 
ing of myriad sugar molecules linked together 
chemically (see Figure 3 above). Gums do not 


O v OH 


H 

i 

C 


\! 


H 












CHIP CLARK, NATIONAL MUSEUM OF NATURAL HISTORY, SMITHSONIAN INSTITUTION 


Plant Exudates and Amber 7 




Gum produced by a Yoshino cherry (Prunus x yedoensis ) 
growing near the Tidal Basin in Washington, D.C. 


Reddish phenolic exudates are visible on the trunk of 
this Eucalyptus sideroxylon. 


tend to smell because of their low volatility 
stemming from their high molecular weight. 
When freshly produced, many gums are spongy 
to touch because of their high water content. 
Thus, freshly produced gums dissolve easily 
during rains. If somehow gums manage to sur¬ 
vive and dry out, they can then be very hard to 
dissolve. However, as far as we are aware, gums 
are not known to survive millions of years as 
amber does. Gum exudates tend to be produced 
by flowering plants,- fruit trees in the genus 
Prunus , including cherries, plums, peaches, and 
almonds, commonly produce gums. 

The third major type of exudates is known 
as phenolics. Phenolics are chemically related 
to terpenes but form unsaturated ring com¬ 
pounds known as aromatics because of their 
often-pleasant odor. When freshly produced, 
phenolics tend to be watery and reddish brown, 
and lack the strong smell of resins. If they sur¬ 
vive dissolution, phenolics tend to form brittle 
solids. As with gums, we are not aware of phe- 
nolics that have survived deep time. Phenolics 


tend to be common in Eucalyptus and related 
plants. Combinations of these major types of 
exudates, such as gum resins, as well as several 
other minor kinds of exudates are also known. 

Uses of Plant Exudates 

In addition to their generally beautiful colors, 
pleasant aroma, and light weight, resins are 
water insoluble. These properties make resins, 
including amber, coveted natural products. 
Some uses of resins, including amber, include: 
ceremonial and artistic, as construction mate¬ 
rials, ingestive, and, of course, as objects of 
science because they provide windows into 
past worlds. 

Ceremonial and artistic uses 

Amber, that is, greatly polymerized resin, has 
been used for ceremonial purposes as well as for 
objects of trade, jewelry, sculptures, and many 
other items. Although highly valued in the mar¬ 
ket, amber varies greatly in color and translu- 
cency, from white to black and from translucent 




CHIP CLARK, NATIONAL MUSEUM OF 

PATRICK R. CRAIG PATRICK R. CRAIG NATURAL HISTORY, SMITHSONIAN INSTITUTION 


8 Amoldia 75/1 • August 201 7 



An assortment of typical yellowish amber specimens 
showing the wide range in color and translucency. 



A group of typical Baltic amber specimens shows 
varying color. 



Specimens of rare Dominican blue amber from the per¬ 
sonal collection of Patrick R. Craig. 



Earrings made from Columbian copal were treated in an 
autoclave, which applies heat and pressure, resulting in 
a color change from yellow to green. 



Retsina is a Greek wine traditionally flavored with 
pine resin. 


to opaque. Because of this variability, color and 
translucency on their own are generally not 
good diagnostic traits for identifying amber. 

On the other hand, copal (less polymerized 
resin) and modern resins are still used in some 
areas of Mexico and Central America for artis¬ 
tic and ceremonial purposes, prized because 


they smell of incense. Next time you encounter 
a pine, fir, or spruce tree, look carefully at its 
bark and you may be able to see some exudate 
blobs or “ teardrops ." Pick one of them up and 
smell it! Pine resin has been used in the prepa¬ 
ration of rosin, which is applied to the hairs 
of bows used to play string instruments such 


NSAA, WIKIMEDIA COMMONS PATRICK R. CRAIG 





Plant Exudates and Amber 9 



Is It Amber or Copal? 

Amber is greatly fossilized resin. This resinous fossilized material has been found in numer¬ 
ous localities worldwide. The oldest amber has been dated as early as the Carboniferous 
period, over 300 million years ago. Often, forests whose trees produced resins that eventu¬ 
ally became amber tended to be located close to sea level at the time of production. 

Partially polymerized resin is known as copal, a Nahuatl or Aztec word that means 
incense. At times, we have seen the term “semi-amber” used instead of copal. We recom¬ 
mend avoiding the term “semi-amber” because it suggests the material is older than it really 
is. Although it can be difficult to distinguish copal from resin, a straightforward preliminary 
way to distinguish between the two is by using a drop of organic chemical such as 95% etha¬ 
nol or acetone (the solvent used in most nail polish removers). Take a drop of the chemical 
and place it in a portion of the test sample that has little or no value to the owner. Then 
touch the wetted portion with the finger. If it feels sticky, the test sample likely is copal; 
if it does not feel sticky, likely it is amber. We have examined a number of alleged amber 
samples that turned out to be copal, some of which were in the collections of respectable 
museums. When finding “amber” specimens of potential scientific value, we recommend 
testing them by physicochemical means, such as nuclear magnetic resonance spectroscopy 
(NMR) or others, to gain more confidence on the specimen's true nature. 




ROBERT MAYER 


10 Arnoldia 75/1 • August 2017 


as the violin (rosin makes the hairs just sticky 
enough to grip the strings and create sound). 

Construction materials 

The metallic transatlantic cable that connected 
the Old and New Worlds telegraphically during 
the second half of the nineteenth century was 
insulated by gutta percha, the resinous exu¬ 
date of Palaquium gutta, a tropical Southeast 


Asian tree. The modern aviation and aerospace 
industry uses human-made, lightweight and 
strong, synthetic resins and phenolics in build¬ 
ing airplanes. 

Ingestive 

An old and interesting use of resins is in the 
preparation of retsina, a Greek wine that is 
flavored with a little bit of pine resin (typi¬ 
cally from Aleppo pine, Pinus hala- 
pensis). Gums are also sometimes 
eaten,- in places where the legumi¬ 
nous Acacia trees produce copious 
quantities of gums, these exudates 
are used as survival foods when 
other food is scarce. Although it has 
been alleged that amber has healing 
and other medicinal properties, we 
are not aware of scientific studies 
using a double-blind protocol that 
demonstrate any medicinal proper¬ 
ties of amber. 

Science 

For reasons that are not known, 
some forests in the past appear to 
have produced copious amounts of 
resins. Although these exudates may 
have attracted some organisms and 
repelled others, once small organ¬ 
isms such as insects landed on the 
sticky material it was difficult to 
detach from it. When subsequent 
resin flows covered the specimen 
it was protected from the action 
of decomposing organisms and the 
environment, allowing it to be pre¬ 
served for a longer time. Subsequent 
polymerization of the resin preserved 
a fraction of the resin-entombed 
organisms, which, when found, now 
have great value to scientists. Amber 
encased plant and animal specimens 
have contributed insights in a num¬ 
ber of scientific fields. 

Amber specimens that contain 
larger, rarely found organisms (e.g., 
scorpions, amphibians, lizards, birds) 
are of great interest and may com¬ 
mand great sums of money. How- 


Collecting Competition 

Interestingly, sometimes birds, such as the types of woodpeckers 
commonly called sapsuckers (genus Sphyrapicus), compete with 
us as they also feed on exudates and leave characteristic holes on 
the surface of some trees. Other birds and some insects are known 
to use exudates for nest construction. 



A yellow-bellied sapsucker (Sphyrapicus varius ) perches on a conifer branch 
that displays the typical holes created by this and other sapsucker species. 




PATRICK R. CRAIG PATRICK R. CRAIG 


Plant Exudates and Amber 11 



A drosophilid fly trapped in amber. 



Wood fibers encased in amber. 


ever, buyer beware, as there are unscrupulous 
sellers willing to make money from objects that 
are not genuine amber. 

Ongoing Research Goals 

Ultimately, we seek answers to questions 
because we are curious about nature. Some¬ 
times, our results can help answer a question. 
For example, along with several other col¬ 
leagues, including Dr. Lisa Niziolelc from the 
Field Museum of Natural History in Chicago, 
we answered the question: In what plant family 
was the tree that produced the blocks of resin 
found in a thirteenth century shipwreck exca¬ 
vated from the Java Sea? Our studies of many 
plant exudates have generated a large data¬ 
base of their NMR profiles. When we study a 
sample of unknown botanical provenance, that 
database allows us to compare the samples of 


unknown botanical origin, like the resin from 
the Java Sea wreck, with those in our database. 
With that information, we were able to suggest 
that the plant whose resins were harvested back 
in the thirteenth century was from the botani¬ 
cal family Dipterocarpaceae, and perhaps spe¬ 
cifically the genus Shorea. Having an idea of the 
botanical provenance of archeological artifacts 
enriches our knowledge of how our predeces¬ 
sors used plants. In this case, research tells us 
that aromatic resins were an important com¬ 
modity at the time and were often imported 
into China for use in Buddhist rituals as well 
as medicines, lacquers, and perfumes. We will 
continue to collect and analyze plant exudates 
from around the world, including amber and 
copal, as well as materials associated with 
anthropological artifacts, adding knowledge for 
future researchers to use. 

References 

Kosmowslca-Ceranowicz, B. 2015 Infrared spectra atlas 
of fossil resins, subfossil resins and selected 
imitations of amber. In: ATLAS, Infrared Spectra 
of the World’s Resins, Holotype Characteristics. 
pp. 3-213. Warszawa, Polska: Polska Akademia 
Nauk Muzeum Ziemi w Warszawie. 

Lambert, J. B., C. E. Shawl, G. O. Poinar, Jr., and 
J. A. Santiago-Blay. 1999. Classification of 
modern resins by solid nuclear magnetic 
resonance spectroscopy. Bioorganic Chemistry 
27: 409-433. 

Lambert, J. B., Y. Wu, and J. A. Santiago-Blay. 2005. 

Taxonomic and chemical relationships revealed 
by nuclear magnetic resonance spectra of 
plant exudates. Journal of Natural Products 68: 
635-648. 

Lambert, J. B., Y. Wu, and J. A. Santiago-Blay. 2002. 

Modern and ancient resins from Africa and 
the Americas. In: Archaeological Chemistry. 
Materials, Methods, and Meaning. Chapter 6, 
pp. 64-83. Symposium Series No. 831. K. A. 
Jakes (Editor). American Chemical Society. 
Washington, District of Columbia. 

Lambert, J. B., M. A. Kozminslci, C. A. Fahlstrom, and J. 

A. Santiago-Blay. 2007. Proton nuclear magnetic 
resonance characterization of resins from the 
family Pinaceae. Journal of Natural Products 
70(2): 188-195. 

Lambert, J. B., M. A. Kozminslci, and J. A. Santiago-Blay. 

2007. Distinctions among conifer exudates 
by proton magnetic resonance spectroscopy. 
Journal of Natural Products 70(8): 1283-1294. 















SUZANNE C. SHAFFER 


12 Arnoldia 75/1 • August 2017 


Lambert, J. B., Y. Wu, and M. A. Kozminski, and J. A. 

Santiago-Blay. 2007. Characterization of 
Eucalyptus and chemically related exudates 
by nuclear magnetic resonance spectroscopy. 
Australian Journal of Chemistry 60: 862-870. 

Lambert, J. B., J. A. Santiago-Blay, and K. B. Anderson. 

2008. Chemical signatures of fossilized resins 
and recent plant exudates. Mini Review. 
Angewandte Chemie (International Edition) 
47: 9608-9616. Also published in German, 
with the following bibliographic information: 
Chemischer Fingerabdruck von fossilen Harzen 
und rezenten Pflanzenexsudaten. Angewandte 
Chemie 120: 9750-9760. 

Lambert, J. B., E. R. Heclcenbach A. E. Hurtley, Y. Wu, 
and J. A. Santiago-Blay. 2009. Nuclear magnetic 
resonance spectroscopic characterization of 


legume exudates. Journal of Natural Products 
72:1028-1035. 

Lambert, J. B, E. A. Heckenbach, Y. Wu, and J. A. Santiago- 
Blay. 2010. Characterization of plant exudates 
by principal component and cluster analysis 
with nuclear magnetic resonance variables. 
Journal of Natural Products 73(10): 1643-1648. 

Lambert, J. B., C. Y.-H. Tsai, M. C. Shah, A. E. Hurtley, 
and J. A. Santiago-Blay. 2012. Distinguishing 
amber classes by proton magnetic resonance 
spectroscopy. Archaeometry 54(2): 332-348. 

Lambert, J. B., C. L. Johnson, E. W. Donnelly, E. A. 

Heckenbach, Y. Wu, and J. A. Santiago- 
Blay. 2013. Exudates from the asterids: 
characterization by nuclear magnetic resonance 
spectroscopy. Life: The Excitement of Biology 
1(1): 17-52. 



On the lookout even during vacation, author Jorge A. Santiago-Blay (left) noticed resinous exudates on several lodgepole pines 
(.Pinus contorta) in Yellowstone National Park, including one partially debarked, possibly by American bison (Bison bison ) (right). 
Note the copious exudate production (yellowish color) on the debarked portion of the trunk. 


SUZANNE C. SHAFFER 






Plant Exudates and Amber 13 


Lambert, J. B., E. W. Donnelly, E. A. Heckenbach, C. L. 

Johnson, M. A. Kozminski, Y. Wu, and J. A. 
Santiago-Blay. 2013. Molecular classification 
of the natural exudates of the rosids. 
Phytochemistry 94: 171-183. 

Lambert, J. B., A. J. Levy, ). A. Santiago-Blay, and Y. Wu. 

2013. NMR characterization of Indonesian 
amber. Life: The Excitement of Biology 1(3): 
136-155. 

Lambert, J. B., J. A. Santiago-Blay, Y. Wu, and A. J. 

Levy. 2014. Examination of amber and related 
materials by nuclear magnetic resonance 
spectroscopy. Magnetic Resonance in 
Chemistry (Special Issue on NMR in Cultural 
Heritage) 53: 2-8. 

Lambert, J. B., J. A. Santiago-Blay, R. Rodriguez Ramos, 
Y, Wu, and A. J. Levy. 2014. Fossilized, semi- 
fossilized, and modern resins from the Caribbean 
Basin and surrounding regions for possible pre- 
Columbian Trans-Caribbean cultural contacts. 
Life: The Excitement of Biology 2(4): 180—209. 

Lambert, J. B., C. L. Johnson, A. J. Levy, J. A. Santiago- 
Blay, and Y. Wu. 2015. Molecular classification 
of exudates horn the monocots, magnoliids, and 
basal eudicots. Life: The Excitement of Biology 
3(2): 083-117. 

Lambert, J. B., J. A. Santiago-Blay, Y. Wu, and A. Levy. 

2016. The structure of stantienite. Bulletin for 
the History of Chemistry 40(2): 86-94. 

Lambert, J. B., C. L. Johnson, T. M. Nguyen, Y. Wu, 
and J. A. Santiago-Blay. 2016. Ferns, cycads, 
Ginkgo, and Gnetophytes: Nuclear Magnetic 
Resonance characterization of exudates from 
exotic plant sources. Life: The Excitement of 
Biology 4(3): 215-232. https://blaypublishers. 
files.wordpress.com/2016/ll/lambert-et-al- 
2016-leb-43215-2321 .pdf 

Lambert, J. B. Y. Wu, and J. A. Santiago-Blay. 2016. High- 
resolution solid-state NMR spectroscopy of 
cultural organic materials. In: Webb, G. Modern 
Magnetic Resonance. Second Edition. Springer. 

Lambert, J. B., A. J. Levy, L. C. Niziolek, G. M. Fienman, P. 

J. Gayford, J. A. Santiago-Blay, and Y. Wu. 2017. 
The resinous cargo of a Java Sea shipwreck. 
Archaeometry. (A paper authored by M. 
Donahue describing this research was published 
in The Smithsonian Insider on May 15, 2017. 
http://insider, si. edu/2017/05/ resin-ship wreclc- 
hints-trade-routes-botany-ancient-asia/ .) 

Langenheim, J. H. 2003. Plant Resins: Chemistry, 
Evolution, Ecology, and Ethnohotany. Portland, 
Oregon: Timber Press. 

Mills, J. S. and R. White, R. 1994. The Organic Chemistry 
of Museum Objects. Second Edition. Oxford, 
England: Butterworth-Heineman. 


Nussinovich, A. 2010. Plant Gum Exudates of the 
World: Sources, Distribution, Properties, and 
Applications. Boca Raton, Florida: CRC Press. 

Rodriguez Ramos, R., J. Pagan Jimenez, J. A. Santiago- 
Blay, J. B. Lambert, and P. R. Craig. 2013. Some 
indigenous uses of plants in pre-Columbian 
Puerto Rico. Life: The Excitement of Biology 
1(1): 83-90. 

Santiago-Blay, J, A., R. L. Hoffman, J. B. Lambert, and Y. 

Wu. 2003. Cylindroiulus truncorum (Silvestri): 
a new milliped for Virginia (USA), with natural 
history observations (Julida: Julidae). Banisteria 
20: 62-66. 

Santiago-Blay, J. A. and J. B. Lambert. 2007. Amber's 
botanical origins uncovered. American Scientist 
95:150-157. (Reprinted with permission as Aux 
sources de l’ambre. Pour la Science [French 
version of Scientific American ] June 2007. 356: 
70-75. Abstracted by David M. Kondo in the 
Winter 2007 issue of Gems and Gemology 
43:395.) 

Santiago-Blay, J. A. and J. B. Lambert. 2010. Legumes and 
their exudates. Aridus (Bulletin of the Desert 
Legume Program of the Boyce Thompson 
Southwestern Arboretum and the University 
of Arizona) 22(1): 1, 4, 6. 

Santiago-Blay, J. A. and J. B. Lambert. 2010. Desert plants 
and their exudates. Desert Plants 26 (1): 1, 3-8. 

Santiago-Blay, J. A., J. B. Lambert, and P. P, Creasman. 2011. 

Expanded applications of dendrochronology 
collections: Collect and save exudates. Tree- 
Ring Research 67(1): 67-68. 

Vavra, N. 2015. Mineral names used for fossil resins, 
subfossil resins and similar materials. In: 
ATLAS. Infrared Spectra of the World’s Resins 
- Holotype Characteristics, pp. 215-280. 
Warszawa, Polska: Polska Akademia Naulc 
Muzeum Ziemi w Warszawie. 

Dedication 

Author Jorge A. Santiago-Blay dedicates this paper to 

his mother, Angeles Blay Salomons, who in the early 

1980s suggested to him that he pursue the study of “las 

resinitas” (the little resins) as she used to call exudates. 

Her memory always lives with him. 


Jorge A. Santiago-Blay is a Resident Research Associate 
in the Department of Paleobiology at the Smithsonian 
Institution's National Museum of Natural History in 
Washington, D.C, (blayi@si.edu). Joseph B. Lambert is 
Research Professor of Chemistry at Trinity University in 
San Antonio, Texas, and Clare Hamilton Hall Professor of 
Chemistry Emeritus, Northwestern University, Evanston, 
Illinois (ilambert@northwestern.edu). 



Other Order: Sound Walk for an Urban Wild 


Peter Del Tredici and Peri Rueb 


I n urban areas, vegetation that is not planted 
or maintained by people—including both 
native and non-native species—typically 
dominates many different habitats including 
river and stream banks, highway verges, vacant 
building lots, infrastructure edges, chain-link 
fence lines, and random pavement cracks. For 
most cities, the amount of spontaneous vegeta¬ 
tion they support varies inversely with their 
economic prosperity,- cities that have lost the 
most population and jobs show the highest lev¬ 
els of land abandonment and volunteer plant 
growth (Del Tredici 2010a, b ; Burkholder 2012). 

How city dwellers respond to the presence 
of spontaneous vegetation in their midst is 
influenced by personal preferences as well as 
by cultural norms. In many European cities, 
residents' feelings about spontaneous vegeta¬ 
tion is divided—some welcome it as a mani¬ 
festation of unrestrained urban nature while 
others see it as an indicator of dereliction that 
should be removed. Such responses have led to 
the categorization of urban residents as either 
"nature lovers" (a.lc.a. wilderness enthusiasts) 
or "neat freaks" (a.lc.a. urban devotees). Inter¬ 
estingly, the percentages of people in these cat¬ 
egories can vary dramatically from one city to 
the next in the same country (Keil 2005; Rink 
2005; Weber etal. 2014). 

In an effort to promote a wider appreciation 
and acceptance of "urban wilds," urban ecolo¬ 
gists have recently been attempting to calculate 
the value of the ecosystem services provided 
by spontaneous vegetation, especially in cit¬ 
ies where the population is shrinking and the 
amount of vacant land is expanding (Patalci et 
al. 2011; Burkholder 2012; Robinson and Lund- 
holm 2012). On the positive side, this vegeta¬ 
tion contributes to increasing the ecological 
functionality of the city in terms of storm 
water management, temperature reduction, 
carbon sequestration, soil development, and 


total biodiversity (Kowarilc and Korner 2005; 
Carroll 2011). Harder to quantify, but never¬ 
theless important, are the opportunities for 
social, cultural, educational, and nature expe¬ 
riences that spontaneous vegetation provides 
across the wide array of cultural contexts and 
sites that characterize most cities (Pfeiffer and 
Voelcs 2008; Daniel et al. 2012; Jorgensen and 
Keenan 2012). 

The aesthetics of spontaneous vegetation are 
usually considered negative given that much 
of it is perceived as ugly or messy (i.e., lack¬ 
ing ornamental characteristics or possessing 
an unkempt appearance), and its presence in 
the landscape is justifiably viewed as project¬ 
ing an image of neglect (Nassauer and Raskin 
2014). In the arena of public health, many people 
see spontaneous vegetation as providing habi¬ 
tat for animals that are vectors for a number 
of human pathogens and infectious diseases 
such as rats, mosquitoes, and ticks (Garvin et 
al. 2012; Gulachensilc et al. 2016). Similarly, the 
large size that spontaneous urban vegetation can 
reach in the absence of maintenance is viewed 
as providing cover for potential criminal activity 
and thus a threat to public safety. To the extent 
that urban landscapes dominated by spontane¬ 
ous urban vegetation are perceived as threaten¬ 
ing, they fit within a concept of a "wilderness" 
that is defined as land that exists outside the 
bounds of human control (Hofmeister 2010; 
Jorgensen and Keenan 2012; Desimini 2015). 

In this article we will explore the history of 
the "urban wilds" construct as it developed in 
Boston, Massachusetts, from its introduction 
in the mid-1970s through today, and present 
a case study of one such site, Bussey Brook 
Meadow at the Arnold Arboretum, to illustrate 
how multi-faceted urban wilds can be creatively 
interpreted for the general public utilizing 
GPS (global positioning system)-based cell 
phone technology. 


ALL PHOTOS BY PETER DEL TREDICI UNLESS OTHERWISE INDICATED 


Other Order: Sound Walk 15 



Urban vegetation takes hold in cracks in a neglected swath of asphalt pavement. 



Pretty wildflowers or invasive weeds? Chicory (Cichorium intybus ), yellow 
sweet clover (Melilotus officinalis ), and spotted knapweed (Centaurea stoebe 
subsp. micranthos ) bloom along a city street. 



Weedy trees take over an abandoned lot in Detroit. 


Urban Wilds in Boston 

In the United States, the idea that 
unmanaged "open space" in cities 
could perform valuable ecologi¬ 
cal services was foreshadowed by 
a movement in the 1970s that cat¬ 
egorized such sites as "urban wilds" 
(Tanner 1975; Desimini 2015). In 
1976, the Boston Redevelopment 
Authority (BRA), a city planning 
agency, officially adopted the term 
when it issued an inventory of Bos¬ 
ton's unimproved and unprotected 
natural areas under the title Boston 
Urban Wilds. The report—which 
was partially funded by a grant from 
the National Endowment for the 
Arts—was spearheaded by BRA land¬ 
scape architect Elliot Rhodeside. It 
identified 143 parcels of land (2,000 
total acres) of diverse sizes and own¬ 
erships that contained significant 
"natural resource value" but were 
threatened by on-going development 
pressure (BRA 1976). Most of the 
sites had histories of industrial, insti¬ 
tutional, or residential use, some 
dating back to the nineteenth cen¬ 
tury. Rhodeside left the BRA shortly 
after the report was published and 
the work of advocacy, fundraising, 
and protection for the Boston Urban 
Wilds project passed to a non-profit 
organization, the Boston Natural 
Areas Fund (BNAF), founded in 1977 
by Eugenie Beal (the head of the then 
newly formed Boston Conservation 
Commission) along with her future 
husband, John Blackwell. 

In its early days, BNAF was focused 
on trying to preserve and protect 
properties listed in the Urban Wilds 
report, but over time the emphasis of 
the organization shifted away from 
land acquisition to maintenance 
of already protected properties and 
coalition building with other non¬ 
profit organizations around issues of 
public advocacy. In 1988, the Boston 






16 Arnoldia 75/1 • August 2017 



Boston Urban Wilds , a 1976 report from the Boston 
Redevelopment Authority, identified 143 land parcels 
in Boston with potential value as preserved natural 
areas. This copy of the report is in the Arnold 
Arboretum library. 

Parks Department officially took over manage¬ 
ment of the Urban Wilds program which, as of 
2014, listed 39 properties in its inventory. The 
Parks Department currently provides mainte¬ 
nance and logistical support for those properties 
that are controlled by the city,- other proper¬ 
ties on the list receive varying levels of main¬ 
tenance depending on the resources allocated 
by the organization that controls it (Bird 2014). 

The original 1976 BRA report described 143 
sites that contained some significant "natural 
resource value," including geological features 
(68 sites), coastal or fresh water wetlands (20 
sites), shorelines (27 sites), or important veg¬ 
etation (28 sites). It was clearly a simpler time 
when the meaning of the words nature and 
natural were not contested and the dichotomy 
between native and exotic species had yet to 
emerge as the divisive issue it is today. In the 
1970s, urban wilds, regardless of their biological 


content or cultural history, were viewed as valu¬ 
able antidotes to blighted, barren cityscapes. 
By the late-1990s, the original concept of an 
urban wild became subsumed under the rubric 
of ecological restoration. This reconceptualiza¬ 
tion of urban nature—essentially attempting 
to affix a "native" label on it—represented a 
dramatic reversal of fortune for the non-native 
organisms that found themselves reclassified 
as invasive species. Older, less value-driven 
terms to describe these plants, including weed, 
pest, naturalized species, garden escapee, volun¬ 
teer, etc., fell by the wayside and with them an 
appreciation of their historic connection with 
the past land use of the site (Del Tredici 2010b). 

This privileging of native over non-native 
species has created problems for today's advo¬ 
cates of urban wilds because many of the sites 
they're striving to protect can no longer be 
"restored" to anything resembling their origi¬ 
nal ecological condition (Del Tredici 2010a, b; 
Carroll 2011). Similarly, the ways that some 
people use minimally maintained urban wilds, 
including drinking, doing drugs, having sex, 
painting graffiti, and camping out, has also 
caused problems for advocates because of com¬ 
plaints from abutting residents and other users. 
Like it or not, urban wilds are places where 
human behavior, like the plants and animals 
that occupy them, can sometimes be out of con¬ 
trol (Keil 2005; Thompson 2012). 

Bussey Brook Meadow 

Bussey Brook Meadow of the Arnold Arbore¬ 
tum of Harvard University was listed as an 
urban wild in the 1976 BRA report. This 25-acre 
wetland has a documented history of land use 
going back 350 years when, in 1662, one of the 
first roads leading southwest out of the city of 
Boston was constructed along its western edge. 
This road opened the land up to farmers who 
drained portions of the property and moved 
the stream, Bussey Brook, that ran through 
the middle of it to the periphery. A hundred 
and forty years later, in 1802, another road was 
built along its eastern edge, which eventually 
developed into a railroad line that is still in 
operation today. Once a stable earthen berm 
was constructed for the rail line in 1873, Bussey 








Other Order: Sound Walk 17 



Willows and cattails are among the moisture loving plants that thrive in Bussey Brook Meadow. 


Brook was effectively isolated from the larger, 
adjacent Stony Brook watershed that drains into 
the Charles River. Following this, the processes 
of fragmentation and filling of Bussey Brook 
Meadow accelerated dramatically, most notably 
with the installation in 1900 of a 9-foot-diame- 
ter, 3,600-foot-long high-level sewer line across 
the western edge of the property and the con¬ 
struction of an expanded Forest Hills train sta¬ 
tion to the north in 1909 (Arnold Arboretum). 

The Arnold Arboretum, through a land 
purchase from its Harvard University par¬ 
ent, acquired roughly half of the Bussey Brook 
Meadow parcel in 1919 and constructed Muddy 
Pond in the middle of the site, a wagon road 
following the track of the high-level sewer line, 
and a tree nursery on the site of former agricul¬ 
tural land. All of these activities over a period 
of seven years resulted in more wetland filling 
and disruption of surface drainage. In the 1950s, 


a privately owned eslcer on the site, composed 
mainly of sand and gravel, was excavated for 
construction purposes and replaced between 
1955 and 1965 with a 5-acre landfill consisting 
of construction debris from the demolition of 
several Boston public schools. In 1971, after an 
unfortunate incident in which two neighbor¬ 
hood children from a nearby public housing 
project drowned, Muddy Pond in the center of 
the Arboretum's portion of the wetland was 
filled in (Arnold Arboretum). 

In 1982, the northern end of Bussey Brook 
Meadow underwent a major transformation 
when an expansion of the Forest Hills train sta¬ 
tion was initiated in order to make room for 
the new Orange Line subway station. As part 
of this project, a pathway was built along the 
base of the landfill that linked the new subway 
station to the South Street gate of the Arbore¬ 
tum. In 1996, through the determined efforts of 







JAY CONNOR 


18 Arnoldia 75/1 • August 2017 


Eugenie Beal and John Blackwell and the two 
non-profit organizations they co-founded (the 
Boston Natural Areas Fund and the Arboretum 
Park Conservancy), the deeds to the variously 
owned parcels of Bussey Brook Meadow were 
bundled together and added to the Arnold Arbo¬ 
retum's 1882 indenture, thereby achieving per¬ 
manent protection for the entire 25-acre site. At 
the same time, grants from federal, state, and 
city agencies, together with funds generated by 
the Arboretum Park Conservancy, were used 
to construct granite entrance gates and upgrade 
the surface of the main pathway, now chris¬ 
tened Blackwell Path. 

In 2011, the Arboretum, in keeping with its 
scientific research mission, approved a plan 
that called for turning Bussey Brook Meadow 
into a site for long-term environmental moni¬ 
toring and research on urban ecology. While 
this meant that most of the land in Bussey 


Brook Meadow would be left alone to follow its 
own ecological trajectory, the Arboretum made 
a commitment to manage portions of the site 
that were heavily used by visitors, including 
mowing the edges of Blackwell Path regularly, 
removing hazard trees that threatened public 
safety, and mowing several meadow areas annu¬ 
ally to keep woody vegetation from taking over 
(Arnold Arboretum). 

Creating the Other Order Sound Walk 

Having developed a long-term strategy for the 
site, the Arboretum still had to contend with 
issues raised by discordant visitor perceptions of 
the land. Some saw Bussey Brook Meadow as a 
"natural" counterpoint to the well-maintained 
landscape of the Arnold Arboretum proper, 
while others saw it as a haven for invasive spe¬ 
cies that undermined the Arboretum's moral 
authority on matters of ecology. It was into this 



Bussey Brook Meadow with Blackwell Path running through it. 
















ARNOLD ARBORETUM ARCHIVES 


Other Order: Sound Walk 19 



The 9-foot-diameter sewer line being installed in Bussey Brook 
Meadow in August 1900. 



Blackwell Path in Bussey Brook Meadow in summer. 



A tree-of-heaven (Ailanthus altissima ) grove on the slopes of 
the landfill in Bussey Brook Meadow. Ring counts of downed 
trees indicated that they established themselves on the site 
in 1965 or 1966, shortly after dumping stopped. 


breech that the authors of this article stepped in 
2012 with a proposal to interpret Bussey Brook 
Meadow for the general public using a GPS- 
based sound walk designed for use with a cell 
phone. The purpose of the proposed app was 
to illuminate the complex cultural history of 
Bussey Brook Meadow, to reveal the complex 
ecological interactions that are currently taking 
place on the site, and to show some of the ways 
the site was being used by the general public. 
The ultimate goal of the project was to try and 
change how people thought and felt about the 
site—to help them see that it was not just a 
chaotic collection of weeds but a dynamic, orga¬ 
nized ecological system that reflected cultural 


values, past land-use history, and future eco¬ 
logical trajectories (Rueb and Del Tredici 2014). 

The Other Order app took two years to 
complete and involved a close collaboration 
between Del Tredici, who provided extensive 
verbal interpretation of the site in situ, and 
Rueb, who recorded this material and combined 
it with field recordings to create a soundscape 
designed for delivery via a downloadable mobile 
app. The app uses GPS to track visitors 7 move¬ 
ments and play the sounds at specific locations 
in Bussey Brook Meadow as they pass through 
them. In addition to Del Tredici's monologues 
on "cosmopolitan 77 vegetation, recordings 
included dozens of on-site conversations with 












20 Arnoldia 75/1 • August 201 7 



Non-native wetland plants growing in Bussey Brook Meadow: common reed (Phragmites australis ) in the background, 
yellow flag iris [Iris pseudacorus ) in the middle, and reed canarygrass [Phalaris arundinacea) in the foreground. These 
species have sorted themselves out across a moisture gradient to form a functional urban wetland. 


various experts, stakeholders, Arboretum staff, 
and park visitors including urban ecologists, 
park advocacy groups, multi-generation urban 
farmers, landscape architects, dog walkers, 
commuters, and transient residents. 

Over twenty hours of ambient field record¬ 
ings of the environment were also incorporated 
and used as inspiration for sound compositions 
evoking, for example, the material layers of the 
landfill, the interior sounds of the high level 
sewer pipeline, the leisure activity of past vis¬ 
itors mingled with those of the present, and 
the wildlife of the meadow. In some places one 
might find unexpected sounds such as light 
snoring tucked under a tree-of-heaven grove 
(Ailanthus altissima ) near a concrete over¬ 
hang, a flute mingling with sounds of laughter 


in a clearing in the center of the old Arboretum 
nursery, cows lowing and chickens clucking 
near the site of the former Bussey farmstead, 
and the sound of underwater gurgling as cap¬ 
tured with hydrophones dropped into Bussey 
Brook. All of these sounds reference actual and 
imagined ways in which the meadow has been 
inhabited over time and the various materi¬ 
als and organisms that make up the complex 
social, biological, and physical matrix that is 
Bussey Brook Meadow. 

Sound regions are arranged throughout the 
meadow in a manner that allows for a com¬ 
plete experience should visitors constrain their 
movements solely to Blackwell Path, which 
takes about twenty minutes to traverse at a lei¬ 
surely pace. However, additional sound regions 












Other Order: Sound Walk 21 



A wetland in Bussey Brook Meadow consisting of common reed (Phragmites australis ), yellow flag iris (Iris pseud- 
acorus ), and reed canarygrass (Phalaris arundinacea ). 


are spread throughout the meadow, rewarding 
the more adventurous and patient with sounds 
that may be accessed only by leaving the trail 
behind and following informal footpaths, trails, 
and tunnels through the dense vegetation. 

Blackwell Path is an egalitarian corridor that 
connects the elegant environs of the formal 
Arboretum with the urban hubbub of the Forest 
Hills subway station and surrounding neighbor¬ 
hoods. Intervening into this path system repre¬ 
sents a critique of conventional parks as much 
as an invitation to go off the beaten track and 
explore the wilds held within this "urban wild." 
Bussey Brook Meadow is a particularly complex 
social site as it sits somewhere between a man¬ 
aged botanical garden on the one hand, and an 
interstitial zone where commuters, neighbor¬ 
hood residents, and tourists from all over the 


world mix with transient populations who are 
often staying for extended periods of time or 
returning each year with the milder seasons to 
regular encampments. 

A central concern of the work is to commu¬ 
nicate a variety of perspectives on place as a 
means of critically engaging contested mean¬ 
ings, uses, and inhabitations of public sites. 
Voices in the work range from those of experts 
who tell us what to look for, what to hear, and 
what to value in this richly vegetated environ¬ 
ment, to those that offer meandering impres¬ 
sions, personal histories, random thoughts, and 
idiosyncratic perceptions of a place. Animals, 
wind, weather, and water are equal voices in 
this mix. Through this blending of voices, the 
work draws upon the cosmopolitan botany of 
the site as a central metaphor and a means for 




JON HETMAN 


22 Arnoldia 75/1 • August 201 7 



Peter Del Tredici and Teri Rueb recording conversations 
in Bussey Brook Meadow. 


asking probing questions about ownership, 
access, interpretation, and use of public parks 
and green spaces. 

Among the discoveries that stood out for 
the authors in developing the work and seeing 
its reception across various audiences was an 
awareness of the intensity of the experience as 
visitors were often torn between giving them¬ 
selves over to immersion in the layered sounds 
emanating from their headphones and relating 
them to the complex sights, sounds, and social 
activities of the site itself. Frequently groups 
of people would walk together, taking their 
headphones off at regular intervals to exchange 
impressions and ask each other if they heard the 
same thing, and if it was "in the headphones" or 
"real." A surprising number of people seemed 
willing to bushwhack through the Japanese 


lcnotweed and stinging nettles to find a sound 
buried deep in the meadow or high on top of an 
embankment. 

A challenge of sorts, Other Order could be 
approached as a kind of game where one tries 
to cover as much territory as possible, to visit 
each sound in its unique niche, or identify each 
of the plants and landmarks referenced in the 
sound composition and included in the project 
index. Related apps, including "Alpine Garden 
Misguide" by Jill Didur (2015), have success¬ 
fully used the game structure of an exotic plant 
hunt to engage critical perspectives on the colo¬ 
nial histories of botanical gardens and specimen 
collecting. As an educational and informative 
piece, the authors were happy to discover that 
Other Order was equally appealing to adults 
and children, though it is less accessible to 
audiences with physical disabilities that 
would limit their movement or ability to lis¬ 
ten through headphones. Finally, we found that 
visitors' appreciation of the botany of urban 
wilds was enhanced through the experience, 
but especially in the context of understanding 
plants in relation to their social entanglements 
with humans. 

At its core, the Other Order sound walk is 
an effort to combine scientific and cultural 
perspectives on urban ecology in a format that 
can reach broader publics in non-traditional 
settings. Bussey Brook Meadow is often mis¬ 
taken for a derelict parcel of public land—a 
park of sorts, but with an uneasy appearance 
when compared to the manicured landscape of 
the Arboretum grounds or with sections of the 
Olmsted-designed Emerald Necklace of Boston 
parks that bear the stamp of formal landscape 
design. As a public artwork, Other Order is 
aimed at drawing visitors into the site through 
a sonic overlay that reveals another kind 
of beauty—and another perspective on ecolog¬ 
ical environments that blend the biological, 
technological, cultural, and social elements. 
The contrasting aesthetics of urban wilds and 
more formal parks is brought into focus, reveal¬ 
ing a historical moment when each has under¬ 
gone dramatic shifts in purpose, perception, 
and public use. 



Other Order: Sound Walk 23 



fowl JirJfs gate 


Asti ton 


ARNOLD 

/'iRbi'crruM 


Via inmate 


(jj W.W 

b?/y >1—T iri 


STATION 1 


south 

strttt 

gut* 


A map of Bussey Brook Meadow showing the locations of the fifty-five sound regions that make up Other Order. 



Herb Nolan, a longtime Arboretum supporter, listening to Other Order. 


TERI RUEB 















NANCY ROSE 


24 Arnoldia 75/1 • August 201 7 



Other Order is available for free download from the App Store and Google Play Store. 
Visitors are encouraged to download the app in advance of their visit and wear head¬ 
phones in order to appreciate the stereo, binaural recordings as they blend with the 
actual environmental sounds of the meadow. The combination of stereo, binaural record¬ 
ings with the ambient sounds that surround visitors as they move through the meadow 
creates an uncanny sense of being simultaneously "here and now" and "there and then" 
in the site, further emphasizing the complex temporalities of the meadow, and complicat¬ 
ing the emplacement of visitors as situated actors within its operations. 



Urban vegetation provides autumn color along Blackwell Path in Bussey Brook Meadow. 





















Other Order: Sound Walk 25 


Acknowledgements 

The final work included over two and a half hours of 
edited sound recordings that were broken into roughly 
thirty-six different sound regions spread throughout the 
25-acre site. Spoken elements included excerpts from 
conversations with the following Arnold Arboretum staff 
members: Ned Friedman, Maggie Redfern, Jim Papargiris, 
Nima Samimi, Susan Hardy Brown, Ailene Ettinger, and 
Bob Mayer (Arboretum volunteer). From outside the 
Arboretum the following people were recorded: John Lee, 
Eugenie Beal, Nina Brown, Lucy Hutyra, Steve Decina, 
Matthew Battles, Kyle Parry, Anya Yermakova, and 
Richard, a longtime resident of Bussey Brook Meadow. 
And finally, thanks to Ernst Karel for help with sound 
recording. Funding for the development of Other Order 
was provided by a generous donation from Janine Luke in 
memory of Melvin Seiden. 

References 

Arnold Arboretum of Harvard University. Bussey Brook 
Meadow, https://www.arboretum.harvard.edu/ 
plants/featuredplants/bussey-broolomeadow/ 
(accessed March 20, 2017). 

Boston Redevelopment Authority (BRA). 1976. Boston 
Urban Wilds: A Natural Area Conservation 
Program. Boston: Boston Redevelopment 
Authority. 

Bird, C. J. 2014. Boston’s Urban Wilds: The Persistence 
of an Idea Over Time. Masters Thesis, 
City Planning, Massachusetts Institute of 
Technology, Cambridge Massachusetts. 

Burkholder, S. 2012. The new ecology of vacancy: 

rethinking land use in shrinking cities. 
Sustainability 4: 1154-1172. 

Carroll, S. P. 2011. Conciliation biology: the eco- 
evolutionary management of permanently 
invaded biotic systems. Evolutional 
Applications 4: 184-199. 

Daniel, T. C. et al. 2012. Contributions of cultural services 
to the ecosystem services agenda. Proceedings 
of the National Academy of Sciences 109: 
8812-8817. 

Del Tredici, P. 2010a. Wild Urban Plants of the Northeast: 

A Field Guide. Ithaca, New York: Cornell 
University Press. 

Del Tredici, P. 2010b. Spontaneous urban vegetation: 

reflections of change in a globalized world. 
Nature and Culture 5: 299-315. 

Desimini, J. 2015. Deciphering the urban wild: remnant 
and re-emergent. In: A. Berrizbeitia (Ed.), Urban 
Landscape, pp. 163-170. London: Routledge. 

Didur, J. 2015. Alpine Garden Misguide, mobile app 
available on iTunes, June 2015. 

Jorgensen, A. and R. Keenan (Eds.). 2012. Urban 
Wildscapes. London: Routledge. 


Garvin, E., C. Branas, S. Keddem, J. Sellman. 2012. More 
than just an eyesore: local insights and solutions 
on vacant land and urban health. Journal of 
Urban Health 90: 412-426. 

Gulachenski, A., B. M. Ghersi, A. E. Lesen, and M. J. 

Blum. 2016. Abandonment, ecological assembly 
and public health risks in counter-urbanizing 
cities. Sustainability 8: 491. 

Keil, A., 2005. Use and perception of post-industrial 
urban landscapes in the Ruhr. In: I. Kowarik and 
S. Korner (Eds.), Wild Urban Woodlands, pp. 
117-130. Berlin: Springer. 

Kowarik, I. and S. Korner (Eds.). 2005. Wild Urban 
Woodlands. Springer, Berlin. 

Hoimeister, S. 2009. Nature running wild: a social- 
ecological perspective on wilderness. Nature 
and Culture 4(3): 293-315. 

Nassauer, J. I. and J. Raskin. 2014. Urban vacancy and 
land use legacies: a frontier for urban ecological 
research, design, and planning. Landscape and 
Urban Planning 125: 245-253. 

Patalci, D. E. et al. 2011. Coupling biogeochemical cycles 
in urban environments: ecosystem services, 
green solutions and misconceptions. Frontiers 
in Ecology and the Environment 9: 27-36. 

Pfeiffer, J. M. and R. A. Voeks. 2008. Biological invasions 
and biocultural diversity: linking ecological and 
cultural systems. Environmental Conservation 
35:281-293 

Rink, D. 2005. Surrogate nature or wilderness? Social 
perceptions and notions of nature in an urban 
context. In: I. Kowarik and S. Korner (Eds.) Wild 
Urban Woodlands, pp. 67-80. Berlin: Springer. 

Robinson, S. L., and J. T. Lundholm. 2012. Ecosystem 
services provided by urban spontaneous 
vegetation. Urban Ecosystems 15: 545-557. 

Rueb, T. and P. Del Tredici. 2014. Other Order: A Bussey 
Brook Meadow Sound Walk, Version 1.1 (275 
MB). Mobile app commissioned by the Arnold 
Arboretum of Harvard University and available 
on iTunes and Google Play, October 2014. 

Tanner, O. 1975. Urban Wilds. New York: Time-Life, Inc. 

Thompson, C. W. 2012. Places to be wild in nature. 

In: A. Jorgensen and R. Keenan (Eds.), Urban 
Wildscapes, pp. 49-64. London: Routledge. 

Weber, F., Kowarik, I., and Saumel, I. 2014. A walk on the 
wild side: perceptions of roadside vegetation 
beyond trees. Urban Forestry and Urban 
Greening 13: 205-212. 


Peter Del Tredici is the former Director of Living 
Collections at the Arnold Arboretum and now a Retired 
Senior Research Scientist. Teri Rueb is a Professor in the 
Department of Media Study at the University at Buffalo 
— State University of New York. 



Floral Clocks, Carpet Beds, and the 
Ornamentation of Public Parks 

Phyllis Andersen 


HOT HOUSE AMO FLOWER BED? IN FClflE ET PARK, $Pfl|N£FICLI}. 



The geometric patterns and colorful flower and foliage plants typical of bedding out 
are seen in this postcard depicting part of Forest Park in Springfield, Massachusetts. 


M unicipal parks are the 
last territory of the 
decorative gardening 
tradition of bedding out: the 
practice of using brightly col¬ 
ored, low-growing flowering 
and foliage plants in ornamen¬ 
tal patterns in beds, mounds, 
pyramids, floral clocks, com¬ 
memorative plaques, and three- 
dimensional figures. Arranging 
plants to create decorative pat¬ 
terns is a convention of garden 
design from the eighteenth cen¬ 
tury, found from the parterres 
de broderie of Versailles to the 
boxwood fleur de lis of George 
Washington's Mount Vernon 
garden. But in the nineteenth 
century, perhaps as a reaction 
to the long reign of the picturesque model, 
which favored naturalistic design, bedding out 
jumped the walls of the aristocratic garden and 
found a home in public parks on both sides of 
the Atlantic. The bedding out practice elicited 
the admiration of the public and the sustained 
scorn of many landscape critics. 

A variety of names have been assigned to 
this practice: carpet bedding, mosaiculture, 
pattern gardening, "gardenesque." It is also 
called Victorian gardening, an homage to its 
popularity in nineteenth century Great Brit¬ 
ain, where advances in greenhouse technology 
and the introduction of tropical and subtropical 
species created a new way of displaying flow¬ 
ering plants. Bedding out, now the shorthand 
term, occupies a territory between art and 
craft. It is part of the history of ornamenta¬ 
tion as well as the history of gardening. Both 
embrace the power of serial imagery and the 
creator's virtuosity in creating original forms. 
Bedding out evoked heated discussion on the 
definition of taste: what is it, who has it, and 


who doesn't. Bedding out of brightly colored 
flowers in artificial situations became part of 
the larger discussion in which popular taste 
was defined as bad taste, the highbrow/lowbrow 
remnants of that discussion still being argued 
in gardening circles today. Bedding out was the 
territory of gardeners rather than landscape 
designers, anonymous individuals whose skills 
were admired but whose names are unknown. 
The great bedding out schemes in public parks 
in American cities were associated with civic 
pride, with a populist enthusiasm for both the 
intricate floral displays and the intensive labor 
that was needed to both create and maintain 
them. Horticulture, as well as city beautifica¬ 
tion, is inherently competitive. Supported by 
park commissioners and local officials, munici¬ 
pal gardeners were encouraged to expand their 
floral displays to accommodate the tastes of the 
people—"to show you care." 

Bedding out is temporary and labor inten¬ 
sive—a sink-hole of energy consumption. It is 
profoundly artificial, appealing most directly to 


COURTESY OF THE AUTHOR 



Floral Clocks, Carpet Beds 27 


CARPET BEDDING. 


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A color plate in Robert Thompson's The Gardener’s Assistant (1878 edition) shows 
carpet bedding patterns complete with lists of plants to be used. 


COURTESY OF UNIVERSITY OF WISCONSIN 








NANCY ROSE 


28 Arnoldia 75/1 • August 2017 



Brightly colored flowers and foliage along with exotic tropical 
plants are still a common feature in city parks, such as this 
streetside planting in Victoria, British Columbia. 


the senses rather than to the power of reflection 
or solitary contemplation. It is not a simula¬ 
crum of nature. It is antithetical to a prevail¬ 
ing notion of public parks based on a pastoral 
model, famously invoked in Frederick Law 
Olmsted and Calvin Vaux's design for Central 
Park in New York. It did not claim to bring the 
country into the city. The practice of bedding 
out produced no theoretical treatises, no literary 
or painterly allusions. It tapped into the public's 
love of spectacle and novelty, its appreciation 
of skilled labor well executed. Bedding out cap¬ 
tured the lure of the exotic by using newly dis¬ 
covered plants from South America and Africa, 
tropical and subtropical natives brought into a 
temperate climate. It had the repetitive power 
of a military parade, an analogy not lost on the 
British garden writer William Robinson, who 
observed "Gardeners were not so much plant 
stewards as drill sergeants." 

Critics of this type of floral display reached 
new heights of rhetorical disdain. William 


Robinson went on to call bedding out "pastry¬ 
making." The popular and widely published 
British writer Shirley Hibberd called ribbon 
beds (long meandering beds with alternating 
bands of floral color) "eels in misery." Land¬ 
scape architect Frederick Law Olmsted's antip¬ 
athy to floral display is well known. Writing 
in 1892 to his associates in Brookline, Massa¬ 
chusetts, about detached floral beds in London 
parks, he observed "I have hardly seen anything 
yet of that kind that did not seem to me child¬ 
ish, vulgar, flaunting, or impertinent, out of 
place and discordant with good general effect." 
In an article in a 1908 issue of Ladies Home 
Journal, the writer blamed municipal garden¬ 
ers for creating "veritable pimples on the face 
of Nature." 

The Roots of Bedding Out 

The evolutionary process that advanced the 
nineteenth century version of bedding out is 
traced to the writings of landscape designer 
and writer John Claudius Loudon (1783-1843) 
who, in the 1830s, introduced the word "gar- 
denesque" to the vocabulary of landscape. He 
encouraged his readers to think beyond the pic¬ 
turesque to what he defined as "scientific," col¬ 
lecting plants from all over the world to test 
their adaptability to different climates and grow¬ 
ing conditions (a close definition of arboreta and 
botanical gardens). The goal was not to imitate 
nature. While Loudon valued artifice and offered 
bedding designs in many of his publications, 
he did warn against the extremes of bedding out, 
the distorted beds and clashing colors. 

Loudon also recognized the limited educa¬ 
tional opportunities for gardeners whose only 
option was a long apprenticeship that isolated 
them from new plant introductions and plant¬ 
ing techniques. Loudon published Self Instruc¬ 
tion for Gardeners in 1815, the first of several 
publications in the nineteenth century that 
attempted to codify best practices for both 
estate gardening and later municipal park man¬ 
agement. With printing costs dropping, a num¬ 
ber of magazines were founded that addressed 
professional gardeners, giving them access to 
information on new bedding plants and propaga¬ 
tion techniques. They came to serve as pattern 
books for floral designs—fashion magazines for 




MISSOURI BOTANICAL GARDEN 


Floral Clocks, Carpet Beds 29 



With their bright colors and exotic, pouchlike flowers, 
South American calceolarias fit perfectly in the bed¬ 
ding out trend. Illustration of Calceolaria pisacomen- 
sis from Curtis’s Botanical Magazine (Volume 93, plate 
5677), 1867. 



ZONAL GERANIUM 

1, {PELARGONIUM ZOffALE) 1 & 1- HYBRIDS 
*, 1 * Njit, si:f* 

PL. A4 


Illustration by D. Bois of zonal pelargonium ( Pelargo¬ 
nium zonale ) and several hybrid selections (note the 
hybrids' larger petals and denser flower heads) in Edward 
Step's Favourite flowers of garden and greenhouse (Vol¬ 
ume 1, Plate 54), 1896-1897. 


aspiring enthusiasts. Florists’ Journal, Garden¬ 
ers’ Chronicle, and Gardener’s Magazine were 
available in Great Britain, and Magazine of Hor¬ 
ticulture, Gardener’s Monthly, Genesee Farmer 
and Gardener’s Journal informed gardeners in 
the United States. 

If principles of romanticism and aesthetic 
theory provided a structure for the pasto¬ 
ral park, advances in science and technology 
stimulated the expansion and complexity of 
bedding out. To underscore the artificiality of 
the bedding out system, the plant species used 
were often imports from South America, Africa, 
and the Mediterranean region. The botanical 
bounty collected by plant explorers, perhaps 
more appropriately called flower hunters, was 


given to botanic gardens and to commercial 
nurseries where species were hybridized to 
create showy selections with features such as 
compact growth, larger flowers, more brilliant 
colors, and variegated foliage. Plants were as 
much a product of the nursery trade as they 
were of plant collecting. Many global imports— 
begonias, calceolaria, echeveria, caladiums, 
cannas, coleus, and more—were commonly 
used in bedding out configurations. Sedums, 
sempervivums, and other succulents also had 
a brief period of popularity. Palms, yuccas, cro¬ 
tons, monkey puzzle trees, and banana plants, 
all valued for their exotic forms, were brought 
in to serve as backdrops for theatrical staging 
and to punctuate the flatness of planting beds. 


BIODIVERSITY HERITAGE LIBRARY 







COURTESY OF NIAGARA PARKS COURTESY OF THE AUTHOR 


Floral Clocks 


The association of plants with the passing of time has a very long history. Carl 
Linnaeus developed an idea for a flower clock in his 1751 treatise Philosophia 
Botanica. Based on his field observations, he proposed a Horologium Florae, a 
clock using forty-six flowers which opened and closed as the day progressed. But 
this more literal interpretation of flowers and time evolved into decorative objects: 
flower plantings with an imbedded clock mechanism. In the early twentieth 
century the floral clock was reinvented as a decorative object for parks, tourist 
sites, and international expositions. 




|4f 







A 1* 

1,1 

" 



First created in 1903, the floral clock in Edinburgh, Scotland, is still a popular attraction 
(postcard from the early twentieth century). 



The design for the 40-foot-wide floral clock in Ontario's Niagara Parks is changed yearly 
and requires 15,000 to 20,000 bedding plants. 













Floral Clocks, Carpet Beds 31 


No plant group was more subject to manipu¬ 
lation than the pelargoniums ( Pelargonium ), 
which are often called (erroneously, British 
gardeners would say) geraniums in the United 
States. Native to South Africa, pelargoniums 
are still ubiquitous garden plants: drought resis¬ 
tant, blooming throughout the summer, a plant 
that has become a symbol of cheerful welcome 
in window boxes and entry planters. Zonal pel¬ 
argoniums, introduced in the late eighteenth 
century, are characterized by alternating bands 
of dark and light green on their leaves and 
large, brilliantly colored flower heads. Contin¬ 
ual experimentation with hybridizing various 
Pelargonium species resulted in hundreds of 
upright, prostrate, variegated, and ivy-leafed 
cultivars. Instantly recognizable by the general 
public, the pelargonium is still among the most 
popular bedding plants in municipal parks. 

Growing and Designing With 
Bedding Plants 

By the mid-nineteenth century, glass houses, 
once a luxury of estate gardens, became acces¬ 
sible to municipalities and commercial nurs¬ 
eries. In Great Britain, the repeal of the glass 
tax in 1845 dropped the cost of the material 
and fueled experiments with mass production. 
In both the United States and Great Britain 
advances in cast and wrought iron construction 
developed for the glass pavilions of the Crystal 
Palaces in London, Syndenham, and New York 
City were adapted to smaller glass structures. 
Magazines for gardeners offered advice on ven¬ 
tilation, humidity control, and heating alterna¬ 
tives. Commercial nurseries created acres of 
glass houses for the mass production of bedding 
plants. Nurseryman and author Peter Hender¬ 
son (1822-1890) started with a small shop in 
New York City selling seeds. By the 1850s, his 
business skills and ability to predict the horti¬ 
cultural market allowed him to build extensive 
greenhouses near Jersey City, New Jersey. By his 
books, aimed at both the professional gardener 
and the amateur, and by his color catalogs, he 
developed a market for bedding plants, includ¬ 
ing his own introductions, most notably zinnias 
from Mexico and his hybrid 'Giant Butterfly' 
pansy. Henderson visited England in 1885 and 
noted that the carpet style beds "were interest¬ 


ing to the people in a way that no mixed border 
could ever be." He also noted the conspicuous 
lack of ornament in Central Park and Prospect 
Park, an omission he attributed to "a lack of 
taste in the management of our public parks." 

Color theory, the investigation of human 
color perception, guided gardeners in the design 
of beds and created the distinctive intense 
impact of color combinations, either gaudy or 
brilliant according to your taste. One of the 
first explorations of color perception was a 1743 
treatise by the French naturalist, Georges-Louis 
Buffon, followed by Johann Wolfgang von 
Goethe's Theory of Colours published in Eng¬ 
lish in 1840. But it was the work of Michel 
Eugene Chevreul (1786-1889), a French chem¬ 
ist employed by the Gobelins Tapestry Works 
whose work on color, first directed to the textile 
industry but also to horticulturists, gardeners, 
and artists, that proved the most influential. 



The 1900 autumn catalog from Peter Henderson and Company 
offered tulip bulbs for bedding out patterns. 


BIODIVERSITY HERITAGE LIBRARY 











BIBLIOTHEQUE NATIONALE DE FRANCE 


32 Arnoldia 75/1 • August 201 7 



Michel Eugene Chevreul's color circle was used by horticultur¬ 
ists and garden designers when creating bedding out displays. 


His book, The Principles of Harmony and Con¬ 
trast of Colours and Their Applications to the 
Arts, published in English in 1854, enhanced 
the gardener's understanding of how colors are 
modified when placed next to each other, in 
contrast to how the color is perceived when 
observed alone. Chevreul's Color Circle, a cir¬ 
cular chart organizing complimentary colors 
opposite each other, was a reference guide for 
gardeners well into the twentieth century. 

Bedding Out in City Parks 

The city of Chicago engaged some of the best 
landscape architects in the country to trans¬ 
form the flat terrain of the city into a sophis¬ 
ticated park system to rival those of Eastern 
cities. Frederick Law Olmsted and Calvert 
Vaux, H. W. S. Cleveland, and later Jens Jensen, 
with his passionate commitment to the prai¬ 
rie landscape, all left their imprint on the city. 


But parallel to their planning work, the city 
encouraged ornamental planting in the form 
of elaborate bedding out schemes. In the 1890s 
Chicago built a large glass conservatory in Lin¬ 
coln Park for the display of tropical plants, with 
extensive plant propagation areas for bedding 
plants. Earlier Chicago's South Park Commis¬ 
sioners supported ornamental plant attractions 
in Washington Park that included a twenty- 
foot-diameter globe, a sundial of echeverias, 
and wire structures covered in flowering plants 
depicting President Grant and Uncle Sam— 
what one writer called "floral masterpieces." 
In 1872 a Board of Botanical Directors was 
formed under the direction of H. H. Babcock, a 
prominent botanist and member of the Chicago 
Academy of Science. In a move antithetical to 
Olmsted, Cleveland, and Jensen's native plant 
perspective, the Board sent requests to botani¬ 
cal gardens and noted horticulturists all over 
the world and received seeds and bulbs from 
the United States, Europe, India, and Austra¬ 
lia. Many were eventually planted out in the 
Chicago parks. In 1891, the journalist Charles 
Pullen wrote extensively on the development of 
Chicago's park and parkway system, especially 
of Olmsted's plans. He carefully threaded his 
way through the controversies of natural and 
artificial but commented that "it is hoped that 
with the gradual evolution of the grander and 
simpler elements of the park landscape these 
features of curiosity will be given to more 
appropriate places, less antagonistic to the plea¬ 
sures obtained from natural scenery." 

Boston's Public Garden, still admired for its 
commitment to the bedding out tradition, rests 
on a set of artificial conditions that eliminated 
any call for a rural landscape model. The Gar¬ 
den was created out of brackish tidal flats as 
part of the landfill project that created Boston's 
Back Bay. The supporters of the Public Garden 
were men with strong horticultural interests 
as well as a dedication to civic improvement. 
William Doogue, the Irish-born horticultur¬ 
ist hired to bring architect George Meacham's 
original 1859 plan for the Public Garden to life, 
developed flower adornments for the Garden of 
great public appeal. He maintained a municipal 
greenhouse that produced thousands of plants 
for the extensive beds he created throughout the 



Floral Clocks, Carpet Beds 33 



A park with bedding out displays along Drexel Boulevard in Chicago. 



2800—Waih!njjt0n Park Chicago. 

A stereo view card with images of large floral sculptures in Chicago's Washington Park. 


CHICAGO HISTORY MUSEUM CHICAGO HISTORY MUSEUM 







































































34 Arnoldia 75/1 • August 201 7 


621:—Panorama, PuUlie Cardan, Boston, Mass. 



Early twentieth century postcard shows bedding out in Boston Public Garden. 



A Boston Public Garden floral carpet bed depicting the seal of the American 
Legion in 1930. 


Garden. A newspaper article in 1888 
described the summer scene: acan¬ 
thus, pyrethrum, beds of silverleaf 
geraniums and pansies, edged with 
lobelias and alternanthera. In the 
midst of this blaze of color, Doogue 
created a cactus bed, an exotic sight 
to Garden visitors. In one of the more 
memorable horticultural disputes of 
the nineteenth century, played out 
in the pages of Garden and Forest 
magazine in the 1880s, Mr. Doogue's 
plantings and their accompanying 
popularity with the public were con¬ 
demned by both signed and unsigned 
articles in the publication. Doogue 
and the supporters of his distinctive 
floral displays were pitted against an 
impenetrable fortress of opposition 
from the likes of landscape writer and 
architectural critic Mariana Griswold 
Van Rensselaer, Arnold Arboretum 
director Charles Sprague Sargent, 
and Frederick Law Olmsted. Doogue 
scoffed at their limited views, their 
isolated lives, and, most importantly, 
their lack of empathy for the taste of 
the general public. 

The bedding out tradition is seen 
as a historical remnant of the Vic¬ 
torian era, outside the canon of 
landscape design history: at best, 
charming and whimsical, at worst 
an affront to good taste and the sanc¬ 
tity of a natural landscape. It is seen 
as a vernacular tradition perpetuated 
by gardeners rather than professional 
landscape designers or landscape architects. In 
a postscript to the bedding out tradition, the 
Philadelphia Museum of Art sponsored an art 
installation in 2012 by the minimalist artist 
Sol LeWitt (1928-2007). The work was based 
on a proposal LeWitt made to the Fairmount 
Park Art Association in 1981. The resurrected 
Lines in Four Directions in Flowers was cre¬ 
ated from LeWitt's initial instructions: "To 
plant flowers of four different colors (white, 
yellow, red, and blue) in four equal rectangu¬ 
lar areas, in rows of four directions (vertical, 
horizontal, diagonal right and left) framed by 


evergreen hedges of about 2-foot height ... The 
type of plant, height, distance apart, and plant¬ 
ing details would be under the direction of a 
botanist and the maintenance by a gardener." 
It was a short term work, installed in 2012 and 
dismantled in 2015. It, perhaps unintentionally, 
reiterated the original power of bedding out: the 
appeal of geometric forms, the intervention of 
blocks of color in a green field, the fascination 
with observable change. 

Today, we still identify public parks with 
the core of civic life. The binary of ornamental 
versus pastoral is still rightfully argued, but, 


COURTESY OF THE AUTHOR COURTESY OF THE AUTHOR 










Floral Clocks, Carpet Beds 35 



Artist Sol LeWitt's work, Lines in Four Directions in Flowers , was installed in front of the Philadelphia Museum 
of Art from 2012 to 2015. 


more challenging, is the question: How do you 
translate planting techniques of mass appeal 
with contemporary values of sustainability 
and the still unspoken ideas of taste? In 1856, 
horticulturist and landscape designer Andrew 
Jackson Downing argued that the public park 
could modify artificial barriers of class, wealth, 
and fashion—a notion that is still valid and 
still contentious. Sophisticated observers may 
still feel a degree of discomfort at the use of 
bedding plants to spell out town names, patri¬ 
otic emblems, comic characters—the definition 
of kitsch being "the adaptation of one medium 
to another." But in the words of the art histo¬ 
rian Tomas Kullca, "If works of art were judged 
democratically—that is, according to how 
many people like them—kitsch would easily 
defeat all of its competitors." 


Further Reading 

Bluestone, D. 1991. Constructing Chicago. New Haven: 
Yale University Press. 

Chevreul, M. R. 1987. The Principles of Harmony and 
Contrast of Colors and Their Applications to 
the Arts. Revised edition with introduction 
and commentary by F. Birren. West Chester, 
Pennsylvania: Schiffer Publishing. 

Elliott, B. 1986. Victorian Gardens. London: Batsford. 

Musgrave, T. 2007. The Head Gardeners: Forgotten 
Heroes of Horticulture. London: Aurum Press. 

Wilkinson, A. 2007. The Passion for Pelargoniums: 

How They Found Their Place in the Garden. 
Gloucestershire: Sutton Publishing. 


Phyllis Andersen is a landscape historian and former 
director of the Institute for Cultural Landscape Studies 
of the Arnold Arboretum. 


COURTESY OF THE PMLADEPHIA MUSEUM OF ART 















Uncommon By Any Name: Acerpensylvanicum 

Jon Hetman 


O ne thing I found challenging when I first 
started working at the Arboretum was 
learning (and using) scientific names for 
plants instead of their common names. While 
perhaps easier to use than those tongue-twisting 
Latin binomials, common names prove prob¬ 
lematic for identification because they can refer 
to generic groupings (think of honeysuckle or 
rose) and can vary in usage from place to place 
(in the United States, a Tilia is called a linden,- 
in the United Kingdom, a lime). Nevertheless, 
common names can offer intriguing clues about 
plants and their formal, natural, and historical 
associations. Consider the diversity of refer¬ 
ences suggested by the many common names 
for Acer pensylvanicum —from striped maple to 
whistlewood—and you begin to appreciate how 
one plant can inspire many appellations. 

Native to North America from Nova Scotia 
to Wisconsin and south through the Appala¬ 
chians to northern Georgia, A. pensylvanicum 
is called striped maple or snalcebarlc maple 
because its smooth, olive-green bark bears 
bright green and white vertical striations. It 
shares this trait with more than a dozen other 
maples in Section Macrantha, though all the 
rest (including A. davidii, A. maximowiczii, 
and A. rufinerve) originate from Asia, making 
the snalcebarlc maples a great example of the 
eastern Asia/eastern North America disjunct 
pattern of biogeography. The considerable orna¬ 
mental interest provided by its bark makes 
A. pensylvanicum a real stand out, particularly 
in the winter landscape. 

In spring, the leaves of A. pensylvanicum 
unfold tinged with pink and mature to bright 
green. It bears large, serrately margined leaves 
that measure up to seven inches (18 centime¬ 
ters) across. Long-stallced and typically with 
three sharp-tipped lobes, the leaf shape suggests 
a third common name for the tree, goose-foot 
maple. In autumn, leaves turns a clear yellow. A 
primarily dioecious plant with male and female 
flowers on different plants, the tree bears long, 
pendent racemes of delicate, pale yellow-green 


flowers in early spring, which give way to grace¬ 
ful chains of pinkish samaras (winged seeds) 
that are extremely showy by summer's end. 

Not overly abundant in the wild, striped 
maples grow to only 30 to 40 feet (9 to 12 
meters) in height and spread, and are often 
multi-trunlced because of wildlife browsing. 
In addition to feeding on the tree's soft shoots 
and young foliage, deer and moose also rub 
the velvet on their antlers against the smooth 
trunks of A. pensylvanicum as they approach 
the rutting season, suggesting two additional 
common names—moose maple and moose- 
wood. When cultivated in the landscape with 
good soil, adequate moisture, and at least par¬ 
tial shade, moosewood can thrive as a striking 
specimen of intermediate size. While the spe¬ 
cies is not prone to any significant insect pest or 
disease problems, gardeners should protect its 
soft trunk from lawnmower injuries and other 
mishaps. The ease of its wood to yield to the 
knife once made it a popular choice for making 
whistles, and some still call it whistlewood. 

The Arboretum has cultivated A. pensyl¬ 
vanicum since 1874. Today, you may observe 
14 individuals of the species representing 
nine accessions, including two specimens of 
the cultivar 'Erythrocladum', selected for the 
coral pink to red color of its young winter twigs. 
Holdings of the species include individuals 
wild-collected by Senior Research Scientist 
Emeritus Peter Del Tredici in 1979 (in West 
Cornwall, Connecticut), Keeper of the Liv¬ 
ing Collections Michael Dosmann in 2008 
(in Franklin County, New York and Mt. Wachu- 
sett, Massachusetts), and Manager of Plant 
Records Kyle Port in 2013 (in Orland, Maine). 
Most grow on the east side of Meadow Road 
in the Azalea Border and along the edge of 
the Maple Collection, and on the west side of 
Meadow Road in the North Woods. Visit any 
time of year to appreciate this truly remarkable 
native, no matter what name you call it. 


Jon Hetman is Director of External Relations and 
Communications at the Arnold Arboretum. 








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