zondag 27 december 2020

How humans have changed natural environments

How humans have changed natural environments

On The Science Show with Robyn Williams

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Wherever you look the effect of human influence is seen in the natural environment. David Mabberley describes the impact, such as the Australian Aborigines’ use of fire and the use of bison by native North Americans which is thought to have extended the prairies. In Africa, human pressure on the environment including poaching is seeing the decline of pachyderms such as elephants, rhinoceros, or hippopotamus, and other animals, and plants reliant on them for dispersal. In Britain, there is no original vegetation left other than the odd mountain top or sea cliff.

Painting by Numbers The life and art of Ferdinand Bauer

Author: David Mabberley

Published by NewSouth Books

Speaker

David Mabberley

Former Director Royal Botanic Garden Sydney

Presenter

Robyn Williams

Producer

David Fisher

Duration: 7min 53sec

Broadcast: Sat 5 Dec 2020, 12:01pm


Robyn Williams: We end with another book and another author in this year of Captain Cook. Remember him? Dr David Mabberley takes us back to those European beginnings in Australia.


David Mabberley: When Lieutenant James Cook came to Australia in 1770, he and his naturalist super-cargo, Joseph Banks, were surprised by the relative openness of the vegetation at Botany Bay, as was their natural history artist Sydney Parkinson who wrote, 'The trees, quite free from underwood, appeared like plantations in a gentleman's park.' Everywhere Cook and other European commentators wrote of smoke from fires set by Aboriginal people. These observations are but a small part of the huge corpus of literature and illustrations brought together by Bill Gammage to make the compelling case for the ancient very heavy fire management and therefore enormous botanical modification of eastern Australia by Aboriginal people, long before European settlement.


The first Australians had modified, largely by fire it would seem, the Australian landscape, such that they could coexist in an apparently sustainable way with the plants and animals here. In many parts of the country, the highly modified vegetation known as a fire climax, dominated by those of the original tree species adapted to fire regimes due to lightning, expanded symbiotically with the clever new bipeds, at the expense of less fire tolerant species.


With the opening up of the vegetation and their increasing prominence, grasses, adapted to tolerance of grazing marsupials palatable to humans, were therefore maintained in the landscape because their usual ecological successors, trees, would have been nibbled away as seedlings.


The human/fire/grass/grazing-animal system is not unique to Australia, but by the time of the first Dutch and British arrivals here, the first Australians had had tens of thousands of years to reach such a kind of mutualistic equilibrium. But it would be foolish to have some kind of rosy Rousseau-esque view of that first human infiltration of the continent. As it was to be with later European conquest, there is likely to have been a number of casualties in terms of animal and plant extinctions. It is still hotly debated as to how much of the original megafauna, for example, was helped on its way, but the story in other parts of the world suggest that the arrival of the first humans had, as usual, a devastating effect.


Humans are good at ecosystem modification, sometimes with disastrous consequences for them and the rest of the environment. In terms of the well-known collapse of civilisations like the Maya, but the speed with which this modification happened in the distant past is shown by the example of Europe. With the withdrawal of the ice sheets at the end of the last glaciation, the tundra vegetation was grazed by animals, including mammoths, and we know what happened to them! In an urbanising Africa and Asia today, we are now witnessing the similar end of the pachyderms, besides many, many other animals and associated plants reliant on them for disbursal.


In Europe, as it warmed, there came a forest maximum. But if you travelled to, say, Britain today, there is no original forest, in fact no original vegetation left at all, save perhaps on a few mountaintops and sea cliffs. The whole North European landscape is an artefact of just 10,000 years of human activity, and such landscapes were those over much of eastern and other coastal Australia in 1770. What is surprising in Europe is that the richest habitats today include grasslands with orchids and other small plants that must've been very rare in the forest maximum and are maintained by the incisors of introduced animals, particularly sheep. Take away the sheep, and a species-poor secondary scruffy woodland appears.


Similarly, native North Americans extended the prairies through their management of bison. The eastern United States was in fact less wooded than it is today, and firewood was a precious resource, so that the locals on seeing Europeans arrive by ship drew the reasonable conclusion that the settlers must've run out of firewood at home, the only good reason to move away.


Similarly, in the upper Blue Mountains where I live, the forest surrounded settlements, now called Blackheath and Mount Victoria, were visited by Governor Macquarie in 1815. He named them Hounslow Heath and One Tree Hill. You do not give such names to heavily forested places.


The botanical revelation that comprised the European recording of Australia's plants from 1606 until the arrival here of Charles Darwin in 1836 was the result of a combination of pursuits with different motives. The initial search for riches comparable with those in South America yielded little, Terra Australis turning out to be a largely arid continent with no crops suited to European agriculture, while the immense mineral wealth of Australia remained largely hidden.


Then came the concern about rival spheres of influence of European powers in the Pacific, especially Britain and France, the real reason for major expeditions being dispatched and land claimed. Incidental to establishing such presences was the collecting of natural productions, usually with a hope that these would be resources to allow colonies to survive without financial support from their European masters.


Charles Darwin visited Australia in 1836 and later in his monumental book, Variation of Animals and Plants under Domestication, effectively the evidence for much of his theory of natural selection in the hastily drawn up Origin of Species, he wrote of the potentially economic plants in Australia: 'It has often been remarked that we do not owe a single useful plant to Australia or the Cape of Good Hope or to New Zealand. Their plants have not been improved and consequently cannot compete with those which have been cultivated and improved during thousands of years in Europe.'


Similarly blinkered, shortly afterwards Thomas Livingstone Mitchell misinterpreted Aboriginal grain harvesting for hay making, when in fact there was what has now been posited as an Aboriginal grain belt right across the interior of the country, with grindstones argued to have been made up to 25,000 years ago.


It is true that internationally traded edible Australian commodities comprise products from species encountered by Europeans after Darwin's visit and that he was echoing opinions considered irrefutable. In fact, at first the most useful species commercially were the timbers, most of which were then still to be described scientifically. Such included red cedar, Toona ciliata, especially from the Hunter Valley, hoop pine, Araucaria cunninghamii, from the Brisbane area, and many eucalypts, Sydney blue gum, Eucalyptus saligna, being said to be the most generally useful of all the Australian woods.


Robyn Williams: Dr David Mabberley, former director of our oldest scientific institution, the Royal Botanic Garden, Sydney. His books are superb. The Florilegium is available any day now.

zondag 7 juni 2020

Economic Botany 2003, Ancient techniques of linen production of flax (Linum usitatissimum)

Economic Botany 2003

Renee Ruhaak, Marijke Langeveld
qryEconomicBotanyBlog
Ancient techniques of linen production of flax (Linum usitatissimum)
The aim of this paper is to give an overview of the techniques which were used in making linen.
Ancient techniques of linen production of flax (Linum usitatissimum)
Flax ( Linum usitatissimum) is one of the oldest plants of which textile is being made.
European cloth made from flax, likely to be made of cultivated plants, of 8000 up to 9000 years old has been found.
cloth made from flax, likely to be made of cultivated plants, of 8000 up to 9000 years old has
been found.
Book 1: (Kalkman, C. Planten voor dagelijks gebruik, KNNV Utrecht, 2003)
Besides linen, flax is used for a high variety of other purposes, as its name says; Linum usitatissimum means ‘most useful flax’.
Both stalks and seed are exploited for human use.
From the fibres of the flax plant, paper is made, which is nowadays used in products as money billets and cigarette paper.
Longer fibres can be used as isolation material and the spinned thread is good for the stitching of wounds.
From the seed of Linen, oil is extracted (linseed oil) and that can be used as basis for paint (it is a quick drying oil) and to make linoleum.
The seed can be eaten and both oil and seed have a medicinal value. (1)
In the past, two types of L. usitatissimum have been cultivated; one which produces much good seed and a type that gives long, strong fibres.
The seed-producing plants are smaller and more branched than the plants for the production of fibres, which can become about 1 m. high and do not branch much.
From fibre plants, harvesting of seed is important too to get offspring.
Other than ramie, (Boehmeria nivea), which is a fibre plant giving soft, water resistant fibres, flax has the greatest tensile strength of any natural fibre, and is 20% stronger when wet.(1)
Spinning flax into thread is facilitated by properties inherent to the fibre, including its length (two to three feet when will prepared).
The cloth linen is very soft and it can be woven into a rather
thin textile. It is a very durable textile which can be washed at high temperatures without shrinking.
A typical character is that flax is hard to spin evenly.
This makes linen not as smooth as cotton which is made from hair and not fibres.
Although flax has many advantages as a fibre crop, its overwhelming disadvantage is the amount of labor, skilled and otherwise, required from sowing to harvest.(9)
website https://www.nps.gov/jame/learn/historyculture/flax-production-in-the-seventeenth-century.htm
At the end of this paper we will discuss the future perspectives of linen.

FIGURE:Morphology of Linum usitatissimum. Flax is a small annual plant with lanceolate leaves. The fruit does not open.

dinsdag 14 april 2020

Economic Botany Course in 2010

I am looking for all the participants from the Economic Botany Course in 2010



title Author
2010? Auke Haanstra/ Hiemstra?
Banana & Plantain (Musa L.) Susana Arias Guerrero
Jackfruit (Artocarpus heterophyllus) Bhanumas Chantarasuwan
Medicinal use of Cannabis sativa Constantijn Mennes
Mesoamerican “Copals” Ainslie Harrison
MUSANGA CECROPIOIDES - umbrella tree Sabine van Onselen
Sacred trees, A short overview on several trees from the Moraceae family Britt Myren


23 years of Economic Botany in Leiden

woensdag 18 december 2019

Bananas– The war on wilt, Origin of edibility



Bananas– The war on wilt, Origin of edibility; Rody Blom, Saskia Bollerman, Janna Horjus, Koen Rurenga
At the origin of edible bananas are wild species that typically produce fruits full of seeds.
Even though only a handful of species have been domesticated, the banana's wild relatives comprise more than 75 species that are native to the humid tropical forests that extend from India to the Pacific.
We now know that edibility in the bananas and plantains depends primarily on the occurrence of parthenocarpy, which is the development of the fruit without pollination of the female flower (Perrier, 2009, 2011)
and always coupled with more or less female sterility, causing a tendency for the fruit to be seedless (Dodds, 1943).
The potential to produce parthenocarpic fruits has been traced to genes present in Musa acuminata (Simmonds, 1953).
But since these plants were still fertile, they continued mating with other fertile banana plants.
Domestication for edibility most likely started with farmers transplanting the offshoots (suckers) of plants that were edible by virtue of having less seeds and more pulp.
latter could be plants from the same or different (sub)species.
Sterility is most likely due to a combination of structural and genetic factors (Sardos et al. 2016).
The structural factors are linked to hybridization between distant relatives as inherited mismatched chromosomes made it difficult for the progeny to produce fertile ovules and pollen.
But scientists also believe that farmers preferentially propagating the plants that produced fruits with the least seeds might have selected for genes that contribute to sterility (Sardos et al., 2016).
Triploidy made further sexual reproduction extremely unlikely.
Although sterility and parthenocarpy are important factors that contribute to the desirability of banana fruits, sterility has impeded progress in breeding programs.
Through natural somatic (vegetative) mutation, hybridization, and selection over many thousands of years, considerable genetic variability has arisen within the cultivated bananas, giving rise to more than 1000 varieties (Nelson, 2002).
Figure 2. Evolution of the cultivated bananas, modified from Simmonds (1995) by Nayar (2010)



Bananas– The war on wilt, The Genus Musa



Bananas– The war on wilt, The Genus Musa ; Rody Blom, Saskia Bollerman, Janna Horjus, Koen Rurenga
The genus Musa was initially divided in two species: M. paradisiaca for plantains and M. sapientum for the common banana by Linnaeus, respectively.
However, it was soon discovered that both were falsely identified as separate species and in fact both were hybridized variants of M. paradisiaca and M. balbisiana.
Eventually, M. x paradisiaca was accepted as the general name for the hybrid species (Valmayor et al., 2000)
At the moment the genus comprises four different sections, with each their own characteristics.
Two with 11 chromosome pairs and two with 10 chromosome pairs.
Two with 11 chromosome pairs and two with 10 chromosome pairs. Section Eumusa Baker may be called the group of the true bananas.
It contains the two commonest and most widely ranging species in the genus, M. acuminata and M. balbisiana and with them all the cultivated forms that we believe to have been derived from them.
Bananas and plantains are starchy berries produced by hybrids and/or sports of Musa acuminata and Musa balbisiana.
Rare genome contributions from another species may have occurred but are not yet well documented (Simmonds, 1986).
M. balbisiana combines with almost anything, which is very interesting in view of its wide range, well-defined nature as a species, and relatively narrow variation (Cheesman, 1947).
Musa balbisiana accessions displayed resistance to Xanthomonas wilt in a greenhouse trial (Tripathi et al., 2008).
Musa acuminata is a wild species of banana best known for being at the origin of the vast majority of edible bananas, by itself or through hybridization with Musa balbisiana.
Four subspecies (banksii, zebrina, malaccensis and burmannica) have been confirmed to be involved in the domestication of the banana (Perrier, 2009).

Bananas– The war on wilt, Taxonomy



Bananas– The war on wilt, Taxonomy  ;Rody Blom, Saskia Bollerman, Janna Horjus, Koen Rurenga
Bananas belong to the genus Musa of the Musaceae in the order Zingiberales (Stover and Simmonds, 1987).
Musaceae includes 2 genera, Ensete and Musa.
The family has not been revised after the classical work of Cheesman (1947–1950) and Simmonds (1953, 1962), although several species have been subsequently described (Nayar, 2010).

Bananas– The war on wilt, Morphology



Bananas– The war on wilt, Morphology ;Rody Blom, Saskia Bollerman, Janna Horjus, Koen Rurenga
Bananas are the very variable fruits derived from crossed species within the genus Musa, therefore a general morphological description of the genus Musa is included.
The banana plant is a large, perennial, monocarpic (fruiting once, then dying), monocotyledonous herb 2-9 m in height that arises from large, subterranean rhizomes (Nelson et al., 2006). The roots are adventitious,
spreading 4-5 m laterally, descending to 75 cm, but mainly in the top 15 cm,
forming a dense mat (Moore, 1992). Suckers spring up around the main plant forming a clump or "stool'', the eldest sucker replacing the main plant when it fruits and dies, and this process of succession continues indefinitely (Morton, 1987).
Leaves are produced by a single apical meristem, which typically forms only a low short stem or pseudobulb (McClatchey, 2000).
Smooth, oblong or elliptic, fleshy-stalked leaves, numbering 4 or 5 to 15, are arranged spirally. They may be entirely green, green with maroon splotches, or green on the upper side and red purple beneath (Morton 1987).
The petioles of the leaves are long and expanded below into long, sheathing and stem-encircling leaf-bases forming a pseudostem (Cheesman, 1947).
New leaves originating from the corm grow up continuously through the centre of the pseudostem with their laminas tightly rolled.
The emerging leaf unfolds a large oblong blade, 150-400 cm x 70-100 cm, with a pronounced supporting midrib and well-marked, pinnately arranged, parallel veins (Moore, 1992).
One terminal inflorescence rises from each corm, its axis (peduncle) extending through the centre of the pseudostem and bending down when exserted (Moore, 1992).
The spike, at first, is a large, long-oval, tapering, purple-clad bud.
As it opens, it is seen that the slim, nectar-rich, tubular, toothed, white flowers are clustered in whorled double rows along the floral stalk, each cluster covered by a thick, waxy bract, purple outside, deep-red within.
Normally, the bract will lift from the first hand in 3 to 10 days. If the plant is weak, opening may not occur until 10 or 15 days (Morton, 1987).
The bracts open in sequence (about 1 per day) from base to top while the peduncle elongates.
They often become reflexed when the flowers develop and they are shed when the fruits start to develop, but this differs between species.
Female flowers develop in the proximal 5-15 rows, male flowers at the distal end of the inflorescence, in the middle sometimes neuter flowers are present (Moore,
Figure 1. Basic morphology of the banana plant
1992).


The flowers contain 5 stamens and an inferior, trilocular ovary.
The perianth (according to the usual interpretation) usually consists of two parts: a compound tepal (calyx) essentially tubular, but split to the base on the adaxial side, 5-toothed at the apex (Cheesman, 1947).
In about one day after the opening of the flower clusters, the male flowers and their bracts are usually shed,
leaving most of the upper stalk naked except at the very tip where there usually remains an unopened bud containing the last-formed of the male flowers.
However, there are some mutants such as 'Dwarf Cavendish' with persistent male flowers and bracts which wither and remain, filling the space between the fruits and the terminal bud (Morton, 1987).
The fruits are variable in size, shape and colour. They are generally elongate-cylindrical, straight to strongly curved, 3-40 cm long and 2-8 cm in diameter.
The fruit apex is important in variety identification; it may be tapered, rounded or blunt (Nelson, 2002).
The endocarp, ivory-white to yellow or pink, may be firm, even gummy with latex when unripe, turning tender and slippery, or soft and mellow or rather dry and mealy or starchy when ripe.
The flavour may be mild and sweet or subacid with a distinct apple tone.
The common cultivated types are generally seedless with only vestiges of ovules visible as brown specks (Morton, 1987).
Seeds are often present in wild Musa species.
When seeds are present, they vary among species in shape and morphology.
Seeds of Musa balbisiana are dark brown, ovoid, about 4 mm long with a conspicuous white, powdery endosperm (Nelson, 2002).