The global increase in migration over the past few decades [1] has drawn the attention of ethnobotanists to the effects of these events on ethnobotanical knowledge and related traditional healing practices among migrant communities [24]. Over the past few years, numerous cross-cultural studies among migrants of ethnic groups have been conducted e.g. in the United States [58], in Cuba [3, 9] and in Europe [1021] to provide a better understanding of the dynamics of medicinal plant use by migrants engaged in international or national migration processes. In the course of these studies, it became obvious that the dynamic social interaction between migrants and host societies is strongly influenced by changing natural and social environments, e.g. changing health conditions and different healthcare systems to which the newcomers are exposed [2, 22].

This study focuses on the traditional knowledge of medicinal plants of Tyroleans living in the Austrian province (Bundesland) of Tyrol, and Tyroleans and their descendants who emigrated to Australia (from the 1950s), Brazil (between 1933 and 1938) and Peru (in 1859 and 1868). Throughout the history of Austrian migration there have been significant regional differences in Austria. Although the migration patterns of the federal state of Tyrol are statistically similar to those of Burgenland, Vienna and Lower Austria, the Tyrolean emigration projects are well known [23]. The immigration countries for the research project were selected to represent i) different social milieus and structures of settlement, ii) different economic conditions, iii) different environmental conditions iv) different periods of immigration and v) sizeable Tyrolean emigrant populations. Traditional knowledge (TK) is a “cumulative body of knowledge, practice and belief, evolving by adaptive processes and handed down through generations by cultural transmission, about the relationship of living beings (including humans) with one another and with their environment” [24] in rural, semi-urban and urban communities. These adaptive processes tend to be experimental, dynamic and closely related to a way of life in a particular geographic area. This includes the processes whereby knowledge is generated, stored, applied and transmitted to others within specific social-ecological contexts [25]. The term “traditional” refers to cultural and historical continuity in a group’s resource use practice and includes the transmission of knowledge on health practices based on ethnobotanical knowledge [24]. The impact of migration events on cultural-related health practices are many and complex and may severely challenge beliefs, values, knowledge, technology, exchange systems and the use of natural resources since the application of traditional knowledge most often depends on continued access to specific land and resources [26, 27]. Previous studies state that ethnobotanical knowledge changes as it is transferred and appropriated by people in order to adapt to new surroundings and changing environments [3, 4, 9, 2729]. The new context might contribute to the creation of new knowledge and practices in the area of arrival as migrants exchange knowledge, cultural traditions and medicinal plants with the local population [22, 30]. Therefore, the level of the migrants’ knowledge can turn out to be even higher or more diverse than the knowledge they initially had before emigration. Migration is actually one of the main drivers by which plants and associated ethnobotanical knowledge are, and have been, dispersed across the globe [3]. Some of the traditional knowledge of medicinal plants taken with them might continue to be applied if there is access to the desired plant resource or the natural conditions for the designated plant are available [31]. Therefore, depending on the specific context and conditions of migration, the following two processes take place: (1) adaptation to the new flora of the host country by substituting and/or incorporating plants into health practices and (2) continued use of plants that grow in both host and home environments or acquisition of the desired plant from the migrants’ home countries through importation and cultivation [3, 4].

This study aims to explore the transformations in migrant Tyroleans’ knowledge of medicinal plants that have occurred during their migration history. Ethnobotanical studies [3235] undertaken in Tyrol in Austria have shown that people in Tyrol still have traditional knowledge about the medicinal use of plants. So far most studies undertaken on long-distance or international migration have examined the impacts of migration on medicinal plant knowledge of groups of people who have moved from the tropics to temperate countries [4]. The focus of this study is on a subject that has not received much attention until now: the long-distance migration of groups of people from a temperate area to temperate, subtropical and tropical areas of the world at different times.

The data collected from Tyroleans and Tyrolean migrants and their descendants in four different areas of the world will be presented and discussed regarding 1) the traditional knowledge of medicinal plants and their uses, 2) knowledge distribution and variation, and 3) the continuation and adaptation of traditional medicinal plant knowledge over time. Quantitative comparisons of the knowledge generated within the various field sites should provide a better understanding of the complexities and dynamics of medicinal plant knowledge within the context of long-distance migration. Based on the results obtained, the study’s findings will be explored regarding the cultural and environmental forces that have shaped knowledge of medicinal plants among migrants with a Tyrolean cultural background.


Ethnogeography and biogeography of research sites

Austria Tyrol

Tyrol is the third largest federal state in Austria covering an area of 12,640 km2 and a population of 704,472 [36] (Figure 1). It is situated in the Alps (465 m to 3,798 m above sea level) and is characterised by a temperate inner alpine climate with subcontinental influences. Valleys with narrow and remote side valleys shaped by high mountain ranges form its landscape. The main structure of settlement consists of villages, a few small cities (up to 20,000 inhabitants) and the region’s capital, Innsbruck, which has a population of 118,035 [36]. Besides small and medium-sized industries (textiles, glass, metal processing and food production), tourism provides the main source of income. The alpine landscape is predominantly characterised by spruce forests and alpine pastures. Farmers’ gardens in mountainous alpine areas are a typical element of land use within the mosaic of agroecosystems managed by farmers [37]. Since farming systems have undergone a process of change over the last few decades they are now seen as economically less important, but still play a major role in Tyrolean’s view of themselves and the maintenance of the countryside. Until the 1950s, the predominantly peasant community had to rely on medicinal plants as they lived in remote areas where there was a lack of medical care. Owing to limited means and poor transportation, doctors were only called out in serious cases and therefore people had to rely on their own or local experts’ knowledge of medicinal plants growing in their surroundings [33]. This knowledge has changed significantly due to changes in people’s socioeconomic situations and improvements in national healthcare facilities due to ongoing industrialisation and globalisation [35]. Austria has a compulsory state-funded healthcare system along with the option of private healthcare which provides a large, high-quality network of doctors and hospitals all over the country. Overall health in Austria is among the best in developed countries. Life expectancy at birth is 78 for men and 83 for women. The major causes of mortality are diseases of the circulatory system (50%) and neoplasms (23%) which are patterns of disease similar to those in other developed countries [38]. Medicinal plants for self-medication are now no longer essential, but offer people a popular alternative to conventional health practices such as the use of pharmaceuticals, healthcare professionals and medical facilities. Medicinal plants in Europe, their extracts, active components and finished products have been described in many national pharmacopoeias that have ultimately led to a unified European Pharmacopoeia (EP), setting the standards in Europe for the use of these products as drugs. The study sites in Tyrol were chosen to represent the areas from where most of the migrants who moved to Australia, Brazil and Peru came. Most of the migrants living in Treze Tílias today came from Wildschönau (47 270″N, 12°30″O), which is in the Upper Inn Valley area. [38]. Many of those living in Pozuzo today came from Silz (47°160″N, 10°5560″E) in the Lower Inn Valley. Both sites are in Western Tyrol. We also carried out field research in Eastern Tyrol/Lienz (46 4947″N, 12°4611″E) from where some of the migrants to Australia came.

Figure 1
figure 1

Research sites.

Australia New South Wales, Queensland, South Australia and Victoria

After the Second World War, Austria’s poor economic situation provided a strong incentive for emigration. However, many of those who wanted to emigrate did not have the financial means to do so [39]. The Assisted Passage Scheme (APS) was the only opportunity for some Tyrolean applicants to relocate to a new country [40]. The APS agreement was signed between the Australian Government and the Provisional Government in Austria in 1952 and allowed Austrians to apply for immigration. Immigrants could travel to Australia for a nominal sum of ten British pounds, provided they signed a contract to work for two years in a job allocated to them by the Australian Government [39]. Many Austrian migrants wanted to improve their living standards and between 1952 and 1961 almost 17,000 Austrians took advantage of this opportunity. Most of the migrants were in their early twenties when they read newspaper advertisements offering them a new start in Australia. A small number of unassisted immigrants who paid for the journey themselves also moved to Australia. It is not clear how many Tyroleans migrated since 1948 as no statistical records are kept for specific Austrian provinces (Bundesländer). The National Archives of Australia [41] holds 173 migration records of Austrians born in Tyrol who migrated to Australia between 1948 and 1967. After 1967 migration records were only ordered alphabetically, with the country of departure no longer indicated, making it impossible to determine the exact number of Tyroleans who migrated. From 1959 the pattern of Austrian migration became more individualistic and the number of migrants decreased. However, in 2008 the estimated resident population of Austrians born in Austria is 20,828 [42]. Before the 1970s most Austrians settled in New South Wales (36%), followed by Queensland (11.6%) and South Australia (10%). The interviewees live in the greater metropolitan area of Sydney (33°53S, 51°12 O) in New South Wales, on the Gold Coast (27°59S, 153°22O) in Queensland, in Adelaide (34°550″S, 138°360″E) in South Australia and in the greater metropolitan area of Melbourne (37°50S, 145°00O) and in Beechworth (36 210″S, 146°410″E) in Victoria (Figure 1).

Austrian migrants in Australia have not formed separate communities and mainly live dispersed throughout the urban and peri-urban areas of Australia. Having learnt English, the Austrian migrants became assimilated fairly quickly and participated in creating the identity of what is now a multicultural Australian society, together with numerous migrants from other European countries in the 1950s. Like other ethnic groups who migrated to Australia, Austrian migrants set up Austrian national clubs in the main cities where Austrian culture is still celebrated today, predominantly by older members, through various club activities. Many of the respondents regularly travel to Austria and maintain contact with their Austrian relatives and friends through the modern convenience of internet applications (email and Skype, for example).

Depending on the research site, climatic conditions range from a temperate climate in the south and east (South Australia and Victoria) to subtropical (New South Wales) and tropical conditions in the north (Queensland). Many species of plants in Australia are found nowhere else on earth (more than 80% are endemic to the country), except where they have been introduced by humans. The high diversity of flora includes large numbers of species in ecologically significant genera such as Acacia, Eucalyptus, Melaleuca, Grevillea and Allocasuarina [43]. The Australian population generally has a good health record, with life expectancy one of the highest among developed countries (M: 79; F: 84) [44]. However there are some groups with a poor health status, notably Aboriginal people and Torres Strait Islanders who now only make up 2% of the population. Otherwise the pattern of disease is similar to that of other developed countries. Some of the common health concerns in Australia are skin cancer, heat strokes, obesity, diabetes, dengue fever and other chronic diseases common in developed countries [44]. Healthcare in Australia follows Western traditions with technical and scientific skills used to prevent, examine and treat illness. The Australian government provides help with medical expenses and hospital care through a scheme called Medicare which is Australia’s public healthcare system designed to give access to free or low cost medical, optometric and hospital care [44]. Besides the dominant healthcare system of biomedicine, western herbal medicine is the most widely used form of complementary healthcare. European herbal medicine was introduced to Australia by the first European settlers and has remained influenced by European rather than indigenous medical practices [45]. It is provided professionally by qualified herbalists and naturopaths and largely uses plants native to Europe. Indigenous herbal medicine, although still used to some extent by aboriginal Australians, has no broad usage in mainstream Australian society at present [45, 46]. The herbal medicine market in Australia has experienced rapid growth in the past ten years with herbal products being available from supermarkets, pharmacies, health food stores and by mail order.

Brazil Treze Tílias

Treze Tílias (27°00″S, 51°240″W) is a municipality in Santa Catarina covering an area of 185.205 km2 in Southern Brazil (796 m above sea level) (Figure 1) with a population of 6,341, of whom 4,715 in urban areas and 1,626 in rural areas [47]. The population now consists mainly of descendants of people of Italian, German, Austrian and Japanese origin with just 0.13% of the population comprising indigenous people of the region. 74% of the population live in the centre of the settlement, while the remainder live as farmers in the surrounding rural area. The landscape is characterised by hills and determined by temperate climatic conditions. The natural vegetation is composed of mixed Araucárian (Araucaria angustifolia) forests. Agricultural activities are important in the region, with corn as the dominant crop. Other agricultural goods are soya, grapes, mate tea, manioc, wheat, black bean, oranges and rice. Between September 1933 and January 1938, 789 Austrians – of whom 560 were Tyrolean –moved to Treze Tílias. Over 300 of the migrants came from the Lower Inn Valley in Tyrol [48, 49]. The foundation of the “Tyrolean Brazil” goes back to a migration project initiated by the Austrian Minister of Agriculture, Andreas Thaler, and was funded by the Austrian Government. The project was designed to allow émigré Austrians to maintain their customs and traditions. A location was chosen that was said to be free of other populations and a long way from the next city in order to avoid “cultural assimilation” [50]. Farmers predominantly were allowed to take part in the project because they were thought to be used to hard work and able to live in harsh living conditions [51]. These preconditions were seen as the best qualifications for establishing an Austrian colony in Brazil. When migrants arrived in the Treze Tílias area, the infrastructure was barely developed and migrants had more or less to build the settlement themselves (Figure 2). In the early years, migrants practised subsistence farming and lived scattered throughout the municipality. The outbreak of the Second World War halted immigration from Austria but official contact with Austria was re-established after the end of the Second World War. Ethnic tourism was introduced, supported by the Tyrolean government, and led to an improvement in the economic situation [49, 52, 53]. A telenovela filmed in Treze Tílias and broadcast on public television across Brazil in 1991 made “Tyrolean Brazil” famous. Today, Treze Tílias is considered a tourist location predominantly for Brazilians. A range of restaurants offer typical Austrian-Tyrolean food, Tyrolean dances, music and other traditions for tourists.

Figure 2
figure 2

A Tyrolean-style farmer’s house in Treze Tílias (Photo: Elisabeth Kuhn).

In 2004 life expectancy in Santa Catarina was 73 (M: 69; F: 77) and the area had Brazil’s lowest infant mortality rate and was equipped with modern healthcare facilities (two hospitals) [47]. Since there was no hospital or pharmacy in Treze Tílias before the arrival of the Austrians, medical care was provided by four Austrian nuns who also migrated to Treze Tílias to take care of the migrants’ education and health needs [54]. Although modern medical facilities are now the predominant form of healthcare in Treze Tílias, medicinal plants are still recognised as being valuable for healing purposes. Local pharmacies therefore offer a wide range of medicinal plants in the form of herbal teas coming from all over Brazil. This attitude is reflected in the habit of many informants of consulting a medicinal plants expert who is a woman of Italian origin. Several medicinal plants such as Matricaria chamomilla, Calendula officinalis, Rosmarinus officinalis, Ocimum. basilicum and Origanum vulgare were introduced and adapted by immigrants of mainly Italian, German and Austrian origin [55, 56]. Brandão’s surveys [55, 57] reflect that Brazilian flora offers one of the world’s richest sources of medicinal plants due to its biodiversity. The accelerated expansion of pharmaceutical production in Brazil since the Second World War has led to medicinal plants and botanical products native to the country being replaced by synthetic products and foreign plants within the Brazil’s Official Pharmacopoeia. Today, Brazil remains an important supplier of botanical raw material for the international pharmaceutical market.

Peru Pozuzo

Pozuzo (10°40″S, 75°320″W) is a district in the Department of Oxapampa in the Central Andean region (750 m above sea level) of Pasco in Peru (Figure 1). Pozuzo has a tropical climate. 170 Tyrolean and German immigrants founded the capital of Pozuzo (Pozuzo Centro) in 1859, when they eventually arrived at their destination after a long and exhausting two-year journey from Lima (Figure 3). A second group arrived in 1868. Due to the difficult travelling conditions, the number of people in both groups dropped. The Peruvian state planned to connect the Pacific Ocean to the Atlantic with a direct route and invited Germans and Tyroleans to colonise the land leading up to the Amazon, but this plan was dropped due to the construction of the Panama Canal [58]. The planned road to Pozuzo for 1858 was therefore not built until 1974 which meant that until that time the closest towns could only be reached following a three-day walk. Their isolation meant the migrants endured mainly subsistence living and were therefore able to preserve their costumes and language [5860]. After the road was built, Peruvian settlers moved to Pozuzo, improvements were made to education and the infrastructure, and cattle’s breeding was established. Increased migration from other parts of Peru led to decreased use of the German “Tiroles” dialect and more intermarrying between “colonists” and Peruvians. Contact with Tyrol was re-established from the 1930s and intensified from the 1970s, which included ongoing financial assistance from Tyrol and Germany [61]. The district of Pozuzo now has a population of 7,760, of whom just 1,038 live in urban areas [62]. About one third of them are descendents of Tyrolean and German colonists [63]. Farming (mainly cattle) is still hugely important for generating income for the people of Pozuzo. The overall health status of the Peruvian population is poor compared with other countries in Latin America. Child mortality rates are high within highland communities and life expectancy in 2009 was 74 for women and 77 for men [64]. In rural areas and small towns like Pozuzo, healthcare services are limited, while in major cities healthcare is more widely available and considered adequate. Thus a large proportion of Peruvians have inadequate access to health services. A “Basic Health-for-All Programme” was introduced into the Peruvian healthcare system by the MINSA (Ministerio de Salud). The programme was aimed at strengthening the health services available to all Peruvian citizens and providing them with access to publicly-run health services.

Figure 3
figure 3

View of Pozuzo (Photo: Ruth Haselmair).

Since Pozuzian people are quite isolated due to the lack of transport, the first settlers had no medical health care system until the 1940s when the first medical doctor opened his practice in Pozuzo. Before that settlers relied on the use of local medical plants which they learned about from the local indigenous people. A regular clinic was only established in Pozuzo the 1970s and a fully developed clinic, built with the financial support of Austrian donors, was only established in 2004 [61]. Biomedical facilities are provided in the local clinic and the local pharmacies mainly offer pharmaceutical products. Medicinal plants and products are mainly collected in the rainforest or grown in people’s gardens (Figure 4). Although local medicinal plants are still used in household remedies, they have to compete with the exponential increase in modern biomedical facilities. A local indigenous healer with indigenous medical knowledge lives in the area and is consulted by some of the habitants. There are few regions in the world where biological diversity is greater than in the Peruvian Amazon. According to estimates, 8% of the total number of the world’s plant species are found in the region around Pozuzo [65]. For centuries, indigenous peoples have been using plants for healing purposes. Only 1% has been validated so far from a pharmacological or phytochemical point of view and despite its unique plant diversity, few pharmaceutical ingredients have reached the markets in industrialised countries [66].

Figure 4
figure 4

Dried flowers of “Macela” (Achyrocline satureioides) collected by a Tyrolean informant (Photo: Elisabeth Kuhn).


The fieldwork was conducted simultaneously by the first, second and third author in April 2008 in the following Tyrol (T) areas in Austria: Wildschönau in the Lower Inn Valley, Silz in the Upper Inn Valley and Eastern Tyrol. Five respondents were interviewed in each district. Field research was undertaken between June 2008 and December 2008 in Australia (A) in the federal states of New South Wales (Sydney), Queensland (Brisbane and the Gold Coast), South Australia (Adelaide) and Victoria (Beechworth and Melbourne), in Brazil (B) (Treze Tílias) and in Peru (P) (Pozuzo). Prior to field research, initial contact for a first sample was made through people involved in Tyrolean emigration in order to arrange logistics and the organisation of field research in all study areas. The first sample was complemented by snowball sampling. Eligibility criteria for the sample included a minimum age of 18, being of Tyrolean descent (first, second or third generation) and permanently resident in the area of migration. In all, 65 people (A: 20; T, B and P: 15) aged from 26 to 95 (average age: T: 55, stdev 18.5; A: 53, stdev 18.06; B: 63, stdev 18.39; P: 48, stdev 11.87) were interviewed. Endeavours were made to keep the sample gender evenly distributed (A: 55% male / 45% female; B: 47% male / 53% female; P: 53% male / 47% female; T: 47% male / 53% female). In Australia two respondents were interviewed in English, in Brazil nine interviews were conducted in Portuguese and in Peru 14 interviews were held in Spanish. All other interviews were in German. Informants in Australia were all born in Austria, in Brazil informants were first, second and third generation and in Peru all respondents were at least third generation.

Data acquisition

Prior to the interviews all informants received formal letters explaining the content of the project and assuring them that any data would be used confidentially. Oral informed consent was obtained from the informants for publication of the collected data and any accompanying images. Successive free lists were accomplished with informants to reveal the local plant names of the area’s plants used for medicinal purposes to provide data for further analysis [67, 68]. The free-listing question was “Please list all the medicinal plants you know”. After the first listing they were asked: “Is there anything else that comes to mind?” Interviewees will frequently forget to mention a certain taxon because free lists tend only to reflect terms in a respondent’s active vocabulary or they intentionally omit items they know. Therefore an attempt was made to maximise free-list output by repeating the free-listing question. Finally, the free-list items already mentioned were read out and the informants asked again for further quotes. After the free lists were made, the specific medicinal use of each plant given was requested by asking “When and how do you use the plant?”

Then socio-demographic data (name, address, sex, age, place of birth, mother tongue, year of migration, parentage) were recorded. Interview notes were written on prepared forms and all interviews were audio recorded (Olympus Digital Voice Recorder DS-30). After the free lists, informants were asked if they would show their gardens at home, if they had one, so that the plants listed could be documented by taking photographs. The collected socio-demographic data, interview data and related plant data were stored on an MS Access database.

Plant identification

Although it is obligatory in any botanical research to collect voucher specimens and deposit them in an internationally accessible herbarium, as well as have them professionally identified [6971] no voucher specimens were taken owing to the organisational difficulties of obtaining plant collection permits for the research sites. As an alternative, detailed photographs were taken of the medicinal plants (the entire plant, stems, bark, leaves, inflorescences, infructescences and exudates) cited in the free list or the product packages of medicinal plants already processed (e.g. tea bags, homeopathic products), including their scientific names. Plant photographs were identified by Rodolfo Vásquez M. (researcher at the Jardín Botánico de Missouri, Oxapampa, Pasco, Peru), Fernando Witting Schaus (forestry engineer at the Universidad Nacional Agraria La Molina, Lima, Peru), Osmar do Santos Ribas (curator of the Museu Botânico Municipal herbarium, Curitiba, Brazil) and Prof. Dr. Valdely Ferreira Kinupp (curator of the Instituto Federal de Educação, Ciência e Tecnologia do Amazonas herbarium, Manaus, Brazil) and by specialists from the Plant Identification and Botanical Information Service at the National Herbarium of New South Wales. For plants that were mentioned but could not be photographed because they were not available, were only used in the country of origin or for which data could not be acquired in the growing season, scientific plant names were generated through their local name by literature review [65, 66, 7283] as well as by the use of specific websites [84, 85]. There is awareness of the fact that the credibility of plant identification through a comparison of literature is in some doubt since confusion of local names with official names when looking them up in botanical literature can lead to errors in plant identification [71]. All scientific plant names were checked through the Missouri Botanical Garden database [86]. Field research was supplemented by taking detailed pictures of medicinal plants or products containing the plants mentioned in the free lists and found in botanical gardens, pharmacies, markets and herb shops.

Data analysis

As a first step, the free lists were revised for spelling and language. If plant names were given in German as well as in the local language, the name in the local language was chosen for free list analysis. A citation of a medicinal plant in the free list was considered as one single item. Each item corresponds to a specific plant taxon (genus or species level). The free lists were analysed in relation to the items listed and the respondent’s characteristics using ANTHROPAC 4.0 for Windows [67, 87]. Calculations were made of (1) the percentage of people who mentioned each item (Resp%), (2) the frequency of mentions per item (F), (3) the average rank of the order in which each item was mentioned (Av rank) and (4) the salience(s) which accounts for frequency and the average rank of items mentioned in the respondent’s list. S is calculated by the formula S = {∑[(Li – Ri + 1) / Li}/N, where S is the salience of an individual item, Li is the length of an individual list and Ri is the rank of the item in that list. Scores range from 1 (maximal salience: first item on every list) to 0. The minimum, maximum and average number of items listed per field site was determined in relation to the respondents [32, 67, 87]. The analysis of free lists revealed the theoretical knowledge of the plant taxa mentioned. However no evaluations of the plant taxon’s practical importance or significance can be drawn from this since it is possible that a plant taxon scores high in cultural value if people in a culture can name the plant taxon, but low in practical value if people rarely use the plant taxon [88]. After free-list analyses for each field site, the aggregated free lists were compared between field sites using the scientific plant names generated.

Agreement indices based on free-listing interviews

One important tool for measuring the distribution of knowledge of medicinal plants is the cultural consensus analysis [67, 89]. However, consensus analysis can only be conducted with categorical-type response data (true-false, multiple choice or fill-in-the-blank-question formats). Free-list data cannot be used for consensus analysis since more than one answer for each free-list question is given in free lists [90]. Therefore the proportion of agreement (PA) index [91] based on quantitative data was used. PA measures agreement on the respective domain among respondents through the ratio of the shared items of two respondents to all items listed by two respondents [91]. For example informant 1 listed seven medicinal plants and informant 2 mentioned four. Of these, two plants were mentioned by both respondents and so the PA of the pair of informants is calculated as 2/9. Adding the individual percentages of agreement of one respondent with every other respondent and dividing this sum by the number of respondents produces the overall agreement (OA) of one respondent with every other respondent. Finally, adding together each respondent’s OA and dividing this sum by the number of respondents produces the overall agreement of a free list (OAF). PA is basically similar to consensus analysis, since both indices calculate agreement through the proportion of identical answers between individuals. However for consensus analysis, all respondents are asked the same number of questions while in free-list data collection all respondents list different numbers of items. In consensus analysis all questions are considered for analysis, whereas for PA only those items listed by both respondents are considered for analysis. The items listed by other respondents are left out of the analysis. Hence while in consensus analysis respondents are compared through “matches”, the proportion of agreement (PA) index compares respondents through “positive matches” [92]. An additional difference between consensus analysis and PA is that for PA, the answer does not need to be corrected for guessing, since guessing is not an issue in free listing. PA can be used to measure the extent of agreement among informants and the extent of individuals’ cultural knowledge [91]. Consequently informants who agree with all other informants to a greater percentage can be assumed to have more cultural competence [93]. However, the PA index cannot be used to investigate what information is common knowledge among individuals in a cultural context. In order to reveal a kind of cultural agreement about the items people list and the people who list them, free-list analysis (frequency, average rank and Smith’s salience) [89] is an adequate method.

The single-mentioned (SM) items index was developed by the authors and consists of the ratio of single-mentioned items per field site to the total number of items listed per field site. “Single-mentioned items” are defined as items that are listed in one field site only once. It can be contested that these items belong to the cultural domain of medicinal plants. In contrast, when an item was listed at least twice in an investigation area, minimum agreement is evident about the extent to which this item belongs to the domain. The ratio of single-mentioned items to the total number of items listed in one field site therefore compares the number of contested items to the number of items that definitely belong to the domain investigated. The higher this ratio, the more single-mentioned items are listed in the field site and the higher the disagreement between interviewees about which items belong to the domain. Hence, the single-mentioned items index indicates the level of agreement among respondents in one field site.

Cultural importance of plant use value, relative frequency of citation, informant agreement ratio

Different indices were selected to reveal the cultural importance of medicinal plant use and then compared to provide a better understanding of the pattern of medicinal plant knowledge among Tyroleans and Tyrolean migrants and their descendants. The indication of claimed uses remained mostly generic and indefinite (e.g. “cleansing, digestive, soothing, relaxing”) which is common in ethnobotany and can be regarded as indicative of genuine information [94].

The number of use reports (UR) provides basic information on the intra-cultural importance of the different plant taxa [95]. Each plant taxon use (tu) mentioned by an informant (i) in the use category (u) is considered a “single-use report”. Phillips and Gentry [96] developed the use value (UV) index, a quantitative method that demonstrates the relative importance of plant taxa known locally. It is calculated using the following formula:

U V = U i / N

Uiis the number of different uses mentioned by each informant (i) and N is the total number of informants for each study site interviewed for the survey.

To measure the agreement among informants concerning which plants to use for specific use categories, Trotter and Logan’s “informant agreement ratio” (IAR), which is widely used in comparative ethnobotanical studies [9799] was applied.

The citations of plant uses were grouped into 22 use categories (u) following the economic botany data collection standard [100] as follows: circulatory system disorders, digestive system disorders, endocrine system disorders, genitourinary system disorders, immune system disorders, infections, inflammation, injuries, menstruation/pregnancy/birth/puerperium/menopausal, mental disorders, metabolic system disorders, muscular-skeletal system disorders, nervous system disorders, nutritional disorders, pain, poisonings, respiratory system disorders, sensory system disorders, skin/subcutaneous cellular tissue disorders and unspecified medicinal disorders. The categories ‘cancer’ and ‘others’ were added to the categories of the economic botany data collection standard. Ailments mentioned for the categories are listed in Table 1.

Table 1 The 22 categories of use comprising the ailments mentioned by informants in the research areas

The IAR for each use category in the four countries of investigation were calculated using the following formula:

I A R = n ur n t / n ur 1.

The informant agreement ratio compares the number of mentions in each use category (nur) and the total number of taxa (nt) used in each use category. The values for the factor range from 0 to 1: a higher value indicates agreement among informants and a well-defined medicinal plant tradition [98] since a high value indicates that relatively few taxa are used by most of the people. It is assumed that medicinal use categories with most use records show the most prevalent and common health problems that are treated by the use of medicinal plants.

Inductive statistics

Correlation analyses (Spearman Rank Coefficient) were performed between socio-demographic variables (age, sex) and the length of free lists and PA. Mann–Whitney tests were conducted using the length of free lists, the proportion of agreement (PA) and use value (UV) as dependent variables and the countries of investigation as independent variables. Inductive statistics were conducted in SPSS16. A one-tailed paired t-test was used to determine whether the average value of the informant agreement ratio (IAR) of Tyrolean migrants and their descendants was not significantly greater than that for people living in Tyrol. Several use categories with undefined IAR were not included in the calculation of the p value for the paired t-test. Furthermore, use categories that were not applicable in a studied group of the four countries were not included in the analyses [99]. Therefore the categories included were circulatory system disorders, digestive system disorders, genitourinary system disorders, infections, injuries, nervous system disorders, nutritional disorders, respiratory system disorders, sensory system disorders and skin/subcutaneous cellular tissue disorders. A critical point of the study is the small number of informants, therefore the results of the quantitative analysis are not as reliable from a statistical point of view as they might be and can be regarded as a pilot methodology for providing possible indications for further studies involving a larger number of informants.


Table 2 provides descriptive statistics of free lists and plant use on medicinal plants in all areas of investigation. Table 3 lists the 15 most salient medicinal plant taxa for each country by vernacular names (as reported by informants), scientific name (genus and species level), along with their botanical families, claimed uses, basic values (respondent percentage, frequency of mention, number of use reports, number of different uses), indices (salience, use value) and their ranking based on the indices. Table 4 shows Informant’s agreement percentages (%) in free lists in all countries. Table 5 illustrates medicinal plant use indices according to use categories (number of taxa in each category, number of use reports, number of use reports percentages, informant agreement ratio) in the different research areas. Table 1 illustrates the 22 categories of use comprising the ailments mentioned by informants in the research areas.

Table 2 Descriptive statistics of free lists and plant use on medicinal plant taxa in Tyrol (n = 15), Australia (n = 20), Brazil (n = 16) and Peru (n = 15)*
Table 3 Evaluation of the 15 most salient plant taxa mentioned in free lists, following the Smith’s salience (S) value and their stated uses in Tyrol, Australia, Brazil and Peru
Table 4 Informant’s agreement percentages (%) in free lists (n = 65) in all areas of investigation
Table 5 Medicinal plant use indices according to use categories in the different research areas

All respondents (n = 65) were able to answer the free-list question and 1.139 citations were recorded in total (Table 2). There is no significant correlation (Spearman) between the sex or age of respondents and the length of free lists in any of the countries investigated. We recorded 1.286 use citations for 744 different uses belonging to 22 different categories of use. The length of the free list in Tyrol differs significantly from the migrants’ countries (A: p < 0.001; B: p < 0.001, P: p = 0.026). Other than Tyrol, knowledge of medicinal plants was most developed in Peru. The length of free list differs significantly from Australia (p = 0.002) and Brazil (p = 0.029) as indicated by the Mann–Whitney test. In Australia and Brazil the length of the free list is similar (p = 0.366). Use values are significantly different between Tyrol and Australia (p < 0.001) but not between Tyrol and Brazil (p = 0.127) and Tyrol and Peru (p = 0.853).


In Tyrol the 15 informants interviewed cited 486 items in the free-list question for medicinal plants (Table 2). The listed items correspond to 164 botanical taxa (Table 2) of which 100 were identified to species and 64 to genus level – belonging to 58 families. The shortest free list consisted of ten items, while the longest had 79 items listed (Table 2). On average the Tyrolean respondents listed 32 medicinal plant taxa per interview. In Tyrol 13 medicinal plant taxa were listed by at least half the respondents (Table 3). The plant taxa quoting the highest salience index was U. dioica (s = 0.608). This plant is reported to be used for tea preparation, in tinctures and as a vegetable to provide vitamins and iron and support blood cleansing. Use values ranged between 0.07 and 0.53 (mean = 0.1244, stdev = 0.0885, 95% CI: 0.1107 – 0.1380). Sambucus nigra had the highest use value, but this extensively used species would be underestimated if the frequency and salience value alone were used as indices for measuring the plant’s importance. It is still very popular to use the flowers to prepare syrup for cold drinks in summer and infusions (colds, fever, sore throat, influenza, bladder infection, immune system) and its berries are processed into jellies and aspics. For external application, the leaves are used as packing to reduce fever. The plant is regarded as a “universal remedy” and is also used in the preparation of a traditional Tyrolean dish called Holunder Kiachlen (flowers dipped in a pancake-like dough, fried in oil and served topped with powdered sugar). A. montana is used as a tincture for external application in the form of liniments to treat sprains, bruises, muscle aches, rheumatism and injuries (Table 5). Some of the informants still collect the flower buds of the protected plant that grows at high altitudes and prepare tinctures of it. Informants also report using it in the form of ointments and homeopathic globules. In Tyrol 552 different use reports, assigned into 18 medicinal categories, were recorded (Table 5). The most relevant categories were nutritional disorders (19%) and respiratory system disorders (18%) as listed in Table 5. Most plant taxa listed in the nutritional disorders category were used as a condiment or kitchen herb. Rosmarinus officinalis and Taraxacum officinalis were the most cited plants in this category. Ailments with the most mentions in the respiratory system disorders category were coughs followed by sore throats (Table 5). The most cited plants in this category were Plantago lanceolata and Salvia officinalis. The highest agreement values were obtained for ailments related to menstruation/pregnancy/birth/puerperium/ menopausal disorders (IAR = 0.667) with Alchemilla sp. as the most common plant taxon, followed by respiratory system disorders, where the most cited plant taxon was Salvia officinalis (Table 5).

Sydney, Gold Coast, Melbourne/Australia

In Australia respondents (n = 20) listed 193 items altogether. The listed items correspond to 87 different botanical taxa (Table 2) - of which 58 were identified to species level and 29 to genus level – belonging to 41 different families. The shortest free list was completed with three items, while the longest list had 31 items. On average, the Australian respondents listed ten items per interview (Table 2). Table 3 lists the most salient plant species. The first three are also listed by half the respondents. Use values ranged from 0.05 to 0.3 (mean = 0.0770, stdev = 0.0533, 95% CI 0.0657 – 0.0884). Matricaria chamomilla has the highest use value. The popular plant is only bought in teabags in the supermarket and used to cure colds and stomach aches and is preferably used as a calmative and for general wellbeing. Arncia montana is not cultivated in Australia and is therefore only available as a homeopathic product. The tincture is sourced from Germany and France and processed by local companies. One Tyrolean women reported bringing in the tincture from Tyrol after visiting her family there. In Australia 200 use reports for 16 medicinal categories were recorded (Table 5). The most relevant category was nutritional disorders (16%) wherein most plant taxa were used as spices, with the most relevant plants in the category being Allium sativum and Petroselinum crispum (Table 3). The respiratory system disorders category was frequently mentioned in Australia (16%) (Table 5). Colds and sore throats were the most mentioned ailments of respiratory system disorders, with Matricaria camomilla and Salvia officinalis the plants most often cited for treating claimed ailments in this category (Table 5). This might be due to the fact that long winters in Tyrol cause many ailments of the respiratory system and although migrants in Australia no longer face lengthy winters, they still remember related uses from their childhood in their home country. All plant taxa named in this category in Australia (Abies sp., Allium sativum, Althaea spp. Matricaria chamomilla, Mentha. x piperita, Picea abies, Pinus mugo, Plantago lanceolato, Salvia offiicinalis, Sambucus nigra, Tilia spp., Tussilago. farfara, Verascum spp.) were also named in Tyrol, except for Backhousia citriodora, Eucalyptus spp., Zingiber officinale. These three plant taxa grow in Australia but not in Austria and have been integrated into the medicinal plant knowledge of Tyroleans in Australia.

There was full agreement on the use of Arnica montana in the muscular disorders category (IAR = 1) in Australia (Table 5). This category was followed by circulatory system disorders (IAR = 0.6) with Urtica dioica as the most cited plant. The number of use reports and use values (p < 0.001) are lower and differ significantly from the other countries of investigation. This might be due to the fact that most Tyrolean migrants live in urban or semi-urban areas with no access to a garden in which they could cultivate the required herbs. It is interesting to note that in the rare cases where people did have a garden, they were very proud of having Urtica dioica or Sambucus nigra (Figure 5) growing in their garden. Both plants are common and widespread in Tyrol.

Figure 5
figure 5

Sambucus nigra in the garden of a Tyrolean informant in Australia (Photo: Heidemarie Pirker).

Treze Tílias /Brazil

In Brazil the respondents (n = 15) listed 157 items altogether and these items correspond to 84 different botanical taxa (Table 2), of which 70 were identified to species level and 14 to genus level, belonging to 57 different families. The shortest free list was completed with four items, while the longest list had 20 items listed (Table 2). On average, ten items were listed per interview (Table 2). The most salient plant taxa mentioned by over half the respondents are listed in Table 3. These taxa also had the highest use values (UV) (Table 5). UV ranged from 0.07 to 0.4 (mean = 0.969, stdev = 0.0623, 95% C 0.0837 – 0.1102). Aloe spp. is widely distributed in this area and grows in almost every garden. It is seen as a “universal remedy” among informants. The plant is claimed to cure injuries, burns, wounds, stomach ulcers and digestive problems, as well as prevent cancer. There are many different recipes for its preparation: pulp from the inner leaves is eaten fresh or frozen, and mixed with honey by some informants. Matricaria chamomilla grows in almost every garden and is hardly ever bought in a shop. Achyrocline satureioides (Figure 4) uses are similar to the uses of M. chamomilla (Table 3) although A. satureioides is cited more often in use as a bath additive and for the preparation of tea for young children (Figure 4). While M. chamomilla can be seen as a ”universal plant”, the distribution of A. satureioides is more likely to be limited to South America and has substituted some of the uses attributed to M. chamomilla in Tyrol. In Brazil 180 use reports for 18 categories were recorded (Table 5). The gastrointestinal disorders category was the most prevalent in Treze Tílias (35%), with stomach disorders the most frequently mentioned ailments. Some of the plants cited and used by Tyrolean migrants and their descendents help support digestion after a “heavy meal”, which is quite common in Treze Tílias. After the indulgence of “savoury roast pork”, “goulash” or the beloved “churrasco”, a tea made from the leaves of Pneumus boldus, Cynara cardunculus or Mentha spp. is an essential conclusion to the meal. Serious trouble with digestion might even require tea from Artemisia absinthium and the fresh pulp of Aloe spp. (Figure 6) helps overcome digestive discomforts.

Figure 6
figure 6

Aloe spp. in the garden of a Tyrolean informant in Treze Tílias (Photo: Elisabeth Kuhn).

Figure 7
figure 7

“Santa Maria” (Piper spp.) in the garden of a Tyrolean descendant in Pozuzo (Photo: Ruth Haselmair).

Agreement on the use of medicinal plants was highest for the metabolic system disorders category (IAR = 1), with Urera spp. as the cited plant, followed by injuries (IAR = 0.6) and gastrointestinal disorders (IAR = 0.548), both categories having Aloe spp. as the most cited plant taxon (Table 5). During interviews, respondents in Brazil reported that some migrants tried to bring plants traditionally used for healing purposes in Tyrol with them. Not all of them suited the growing conditions in Treze Tílias. One informant remembered that she brought Allium schoenoprasum and Ribes rubrum to grow in her garden, but the latter could not be cultivated in Treze Tílias due to the growing conditions there. The migrants themselves grow plants such as Matricaria chamomilla, Aloe spp., Calendula officinalis, Urtica dioica and many more in their own gardens for use as home remedies for ailments.


In Peru respondents (n = 15) listed 303 items altogether. These items correspond to 134 different botanical taxa (Table 2) – 92 were identified to species level and 36 to genus level –belonging to 57 families, while 6 remain unidentified. The shortest free list was completed with six items, while the longest list was completed with 52 items (Table 2). On average, Peruvian respondents listed 20 items (Table 2). The most salient plant taxa, the first six mentioned in Peru by more than half the respondents, are listed in Table 3.

Use values (UV) ranged between 0.07 and 0.47 (mean = 0.1185, stdev = 0.08115, 95% CI 0.1046 – 0.1323. Cissus gongylodes reached the highest UV (Table 3). In Peru 354 use reports for 22 categories were recorded (Table 5). The most relevant medicinal category was gastrointestinal system disorders (27%), with stomach disorders the most frequently mentioned ailment. Plant species mentioned most often in this category were Psidium guajava, Croton lechleri and Verbena litoralis. Agreement on the use of medicinal plants was highest in the cancer category (IAR = 0.571), with U. guianensis the most cited plant, followed by skin/subcutaneous cellular tissue disorders (IAR = 0.457) with C. lechleri the most cited plant species (Table 5).

Agreement between informants and an overall comparison

Table 4 shows the percentages of proportion of agreement (PA), single-mentioned (SM) plant taxa among informants in all research areas, other plant taxa mentioned in only one country and plant taxa cited in both the migrants’ country and in Tyrol. The highest proportion of agreement (PA) in free lists was calculated for Tyrol (17%), followed by Peru (12.2%), Australia (11.9%) and Brazil (11.2%). The proportion of agreement differs significantly between informants in Australia and Tyrol (p = 0.001), Brazil and Tyrol (p = 0.001) and Peru and Tyrol (p = 0.001) and is similar between informants among the migrant countries as indicated by the Mann–Whitney test. There are no significant correlations between the sex or age of respondents and the proportion of agreement.

The proportion of single-mentioned botanical taxa was lowest for informants in Tyrol (53% of all taxa listed in Tyrol), followed by Peru (62%), Australia (62%) and Brazil (63%). The number of plant taxa listed only in Tyrol is 91 (20.1%), 92 (20.3%) in Peru, 35 (7.7%) in Brazil and 20 (4.4%) in Australia.

Of all the botanical taxa listed, five (1.1%) were listed in all four investigation countries (Allium sativum, Artemisia absinthium, Brassica oleracea, Matricaria spp. and Plantago spp.). In Australia and Tyrol together, 199 different plant taxa were listed. Of these, 52 (26%) were listed in both regions, while 33 (17%) were listed in Australia only and 114 plant taxa (57%) were listed in Tyrol only. In Treze Tílias and Tyrol, 210 different plant taxa were listed. Of these, 33 plant species (16%) were listed in both regions, while 46 plant species (22%) were listed in Treze Tílias only and 131 plant species (62%) were listed only in Tyrol. In Pozuzo and Tyrol, 278 different plant taxa were listed in total. Of these, 16 plant species (5.7%) were listed in both regions, while 109 plant species (39%) were listed in Pozuzo only and 153 plant species (55%) were listed in Tyrol only.

It is assumed that the use categories with the highest number of mentions were the most common and important among Tyroleans and the migrants. In no investigation area did the use category with the highest number of use mentions match the ones informants agreed on most. For the categories included in the statistics, the average informant agreement ratio (IAR) in Tyrol is significantly higher than in Australia (p = 0.089) and Brazil (p = 0.238) but not Peru (p = 0.019).


The knowledge held by Tyroleans and Tyrolean migrants and their descendants about medicinal plants as it is today is presented approximately 50 years after emigration to Australia, 80 years after emigration to Brazil and 150 years after emigration to Peru. The different timescales offer insights into how transformation processes on traditional knowledge progressively occurred in the host cultures. Tyrolean migrants and their descendants experienced different societal and environmental influences in the course of their migration history. All respondents in all four investigation areas claimed to know and use medicinal plants to treat basic ailments in their day-to-day lives. Although the tendency has been observed in studies for older informants to have greater knowledge of medicinal plants, these findings are not supported by this research [101, 102]. Results in research carried out on gender differences within knowledge distribution concerning ethnobotanical knowledge are inconsistent [101104]. Our findings show that men and women have similar knowledge of medicinal plants in all the countries investigated.

As described before in ethnobotanical studies on this subject [4], processes of continuation and adaptation of medicinal plant knowledge both took place during the migration of people from Tyrol. The length of free lists, number of plant taxa cited, number of use citations, use values (UV) and the proportion of agreement (PA) are highest in Tyrol and the number of single-mentioned (SM) items lowest. These results relate to a well-established tradition of medicinal plant knowledge in the country of departure and indicate that knowledge and use of medicinal plants is most pronounced there. Therefore migration clearly had a corrosive effect on the traditional knowledge of medicinal plants and their applications among migrants as compared to informants living in Tyrol. Reduced ethnomedicinal knowledge among migrant groups compared with their country of origin has been reported before [9, 15, 21]. Kirsch [26] recognises that local knowledge may be lost when it depends on continued access to specific land and resources. If some resources are unavailable for migrants they will no longer teach their descendants specific knowledge linked to these resources. However, culturally salient species continue to be important after migration [30] and their uses tend to be more resilient towards changes if they are relevant elements of global knowledge [16, 22, 24]. Cosmopolitan plants (e.g. Matricaria chamomilla, Hypericum perforatum, Plantago spp., Urtica spp.) are most likely to be used continuously and this can be explained by the fact that they are regarded as medicinally very effective and are also often easy to access. The plants listed in all four areas of investigation for medicinal purposes (Allium sativum, Artemisia absinthium, Brassica oleracea, Matricaria spp. and Plantago spp.) could be considered such species and therefore used continuously.

Due to the fact that all Tyrolean respondents living in Australia were born and brought up in Tyrol and therefore still remember the medicinal plants and may have experienced their use during childhood consensus on the knowledge of medicinal plant taxa (26%) is highest between Tyrol and Australia. Further, all informants in Australia still return to Austria on a regular basis and therefore probably stay in closer contact with the traditions of their country of birth as compared to the other research areas. The dispersed settlement of Tyrolean emigrants, the increasing influence of urbanisation with mostly no access to a garden and well-established healthcare facilities made the continuation strategy with some new incorporated plants the most obvious one to establish among migrants in Australia. It is striking that out of the 87 medicinal plants named in free listing in Australia, only four (Eucalyptus spp., Melaleuca alternifolia, Xanthorrhoea spp. and Acacia spp.) are native to Australia. Although Australian Indigenous people had and still have extensive knowledge of medicinal and native Australian plants, other than Eucalyptus spp. and M. alternifolia they have failed to enter existing herbal pharmacopoeias [45]. Strict import and quarantine regulations on flowers, plants and plant-related materials have been implemented to protect Australia’s unique nature, hampering the import of plants and plant-related material, and therefore the private import of medicinal plants or products to Australia (e.g. herbal tea mixtures or homespun remedies) is negligible. Nevertheless, many herbs in the traditional Tyrolean pharmacopoeia can be obtained from herbalists, naturopaths and health care shops. This mode of acquisition is probably the most dominant here compared to the other areas investigated, where informants mostly source medicinal plants from their own garden and through collection in the wild. Tyroleans in Australia are not in close contact with one other and live more individual lives, so the absence of a network that supports the exchange of knowledge of medicinal herbs might also have a detrimental effect on the use of traditional Tyrolean medicinal herbs, with only a small amount of knowledge of traditional medicinal herbs being passed on to the next generation.

Compared with Latino migrants in New York who continue to import, trade and use herbs to serve their ethnic community in special shops such as botánicas in New York [5, 7] or in Amsterdam, where a store specialising in medicinal plants from Suriname offers fresh, dried and frozen medicinal plants from Suriname to the immigrant community [19], this study’s findings show that Tyrolean migrants in both Brazil and Peru adapted to the new flora and related health practices in the host country. Migrant groups’ knowledge of medicinal plants in Brazil and Peru has changed more than it has in Australia. The shared knowledge among Tyroleans in Brazil differs a great deal from the shared knowledge about medicinal plants in Tyrol. Migrants in Brazil faced the influence of migrants from different continents, which led to a mixture of continuation and adaptation processes, although it is difficult to track down the origin of a plant because of an absence of information about the geographic distribution of species growing in both the country of origin and the host country.

Nowadays Tyrolean migrants and their descendants in Treze Tílias have knowledge of medicinal plants known in Brazil and Tyrol. Some plants which were not mentioned during free listing in Tyrol obtained a high score in the Smith’s salience index in the free lists in Brazil, such as Aloe spp., Achyrocline satureioides or Baccharis articulata and Baccharis trimera. These plants can be regarded as substituting plants from the Tyrolean pharmacopoeia that were not easily accessible in Brazil. Individual imports of plants and plant products from Austria are negligible since permission is required from the Ministry of Agriculture before they can be imported into the country.

In Peru and Tyrol no plant taxon listed in both countries was mentioned by more than a third of respondents. Therefore it can be assumed that Tyrolean migrants in Peru substituted and replaced most of the traditional medical plants from Tyrol. When Tyrolean migrants finally arrived in the remote area of Pozuzo in Peru, they faced a situation in which they had to build a completely new settlement. Therefore people had to rely on the knowledge of indigenous groups on how to use plants from the rich local flora of the tropical rainforest as they were also confronted by completely different illnesses (e.g. malaria, typhus and yellow fever) than those found in their home country. This explains the fact that the percentage of plants only named in Peru was highest and that consensus on medicinal plants with informants in Tyrol was lowest. Out of the ten most salient plants listed by informants in Pozuzo, only Plantago spp. is also found among the most salient plants in Tyrol. After three generations the medicinal knowledge of traditional Tyrolean plants has been exchanged almost completely. Many plants from Tyrol have been forgotten over the years as they do not grow in tropical conditions and they were substituted by other plants. New plants for medicating diseases which were unknown until then also became incorporated. Therefore, the circumstances of long-lasting isolation led to the adaptation strategy in Peru. Medical healthcare facilities have now improved and are geared towards conventional medicine, while the use of medicinal plants is starting to play a secondary role as globalisation, increasing industrialisation and the accelerating destruction of botanically rich native ecosystems are challenging the continuation of traditional medicinal health practices. Nevertheless there are still Pozuzian people who collect medicinal plants or cultivate them in their gardens (Figure 7). Use values (p = 0.853) come close to Tyrolean informants, which indicates that there is a strong tradition still alive around the use of medicinal plants. Since people in Pozuzo have begun to recognise the value of the tropical rainforest, with Peru’s flora providing one of the world’s richest sources for plant-based medicines [65, 105] and they are very important commercially, there is now increasing interest in specific medicinal plants. One example that has come to light in recent years is “Uña de gato” (Uncaria guianensis) which is a powerful medicinal plant thought to provide relief for inflammation and rheumatic diseases [65]. The woody vine that takes its name from the hook-like thorns that grow along it resembling a cat’s claw has a long history of use among the indigenous people of the Amazonian Rainforest [106]. Since “Uña de gato” seems to have positive effects in the curing of cancer, the plant is “booming” on the international pharmaceutical trade market ever since, resulting in it being well known in Pozuzo.


Tyrolean migrants did not simply adapt to a new medical culture when they migrated to another country. Instead the use of traditional medicinal plants continued concurrently and progressively, some practices were abandoned and new elements were integrated into the medicinal plant knowledge system. We conclude that the main processes that happened in knowledge transformation in all countries were to abandon specific medicinal plants and related practices from the original pharmacopoeia if the plants were neither available nor cultivated in the country of arrival. The social ties between the relatively low numbers of migrants and their country of origin were not constant and strong enough to offer greater scope for the importation of important plants from the home flora. In conclusion, it can be stated that the choice of medicinal plant use decades after Tyroleans’ migration to Australia, Brazil and Peru was greatly influenced by the existing environmental and social conditions in the country of arrival, the predominant healthcare system, the degree of contact with the local population (e.g. social networks) and the home country and the opportunities for acquiring plants through importation. Overall, our findings indicate that the medicinal plant tradition in Tyrol and Pozuzo is more clearly defined than among the Tyroleans and their descendants interviewed in Australia and Treze Tílias, although the knowledge in Peru has undergone major transformational shifts compared to Australia and Brazil where the various influences from other migration processes may have had a more dispersing influence on the field of medicinal plants along with an eroding effect on the degree of knowledge.