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Review

Lessons from the Varietal Evolution of Durum Wheat in Italy

by
Martina Ludovica Careddu
*,
Francesco Giunta
and
Rosella Motzo
Department of Agricultural Science, University of Sassari, 07100 Sassari, Italy
*
Author to whom correspondence should be addressed.
Agronomy 2024, 14(1), 87; https://doi.org/10.3390/agronomy14010087
Submission received: 15 November 2023 / Revised: 12 December 2023 / Accepted: 21 December 2023 / Published: 29 December 2023
(This article belongs to the Special Issue In Memory of the 200th Anniversary of Gregor Mendel: Genetics and the Father of Genetics)
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Abstract

:
The leading role of Italy in the cultivation of durum wheat stimulated intense breeding activities in the country from the beginning of the 20th century, much earlier than in any other country involved in durum wheat production. Older, genetically more heterogeneous landraces were replaced with new, highly productive, superior quality varieties, and this led to an inevitable reduction in the overall genetic diversity among new cultivars, which makes the genetic variability preserved in old cultivars particularly valuable and important. The aim of this paper was to assist future breeding programs by providing a detailed description of the history of durum wheat breeding in Italy and of the changes in yield, quality, and related traits that subsequently occurred, starting from the most diffuse landraces present between 1900 and 1920 up until the present day. The parallel evolution of breeding techniques, breeding goals, and agricultural systems in this period is also described, and some future breeding goals suggested. In the current context of climate change and of rapidly mutating pathogen populations, preserving the yield level through the continuous introduction of new cultivars by exploiting the reservoir of largely unused genetic variation stored in old cultivars and landraces could be as important as increasing grain yield and quality.

1. Introduction

Durum wheat (Triticum turgidum subsp. durum (Desf.) Husn) is grown on around 17 million ha worldwide, primarily in the Mediterranean Basin, Canada, and the United States (Eurostat). Its global production for 2020 was assessed to be 33.6 million tons, and approximately half of this came from the Mediterranean Basin [1]. Within Europe, Italy is the front-runner in durum wheat production, with a cultivation area averaging 1.23 million ha (EUROSTAT, average for the last three years), equivalent to 53% of the EU’s surface area dedicated to durum wheat and 57% of the EU’s overall production [2].
The first ever durum wheat breeding program was launched in Italy back in the early 1900s, an unsurprising fact considering the economic significance of the pasta industry and the country’s leading position in Europe in terms of durum wheat production [3]. The nation’s careful and prolonged breeding work has generated a valuable germplasm that is widely cultivated both nationally and internationally [4].
The aim of this review is three-fold: (i) to describe the rich and interesting history of durum wheat breeding in Italy, highlighting the strong interplay between breeding and the evolution of agricultural systems; (ii) to analyze the effects of breeding on grain yield, yield-related traits, and grain quality; and (iii) to propose future avenues and directions for breeders to pursue.

2. Varietal Evolution

2.1. Landraces and Local Populations (1800–1920)

Before Mendel’s discoveries in the 19th century on the principles of genetic inheritance and before Strampelli’s work at the turn of the century on genetic improvement (initially on bread wheat and subsequently on durum), durum wheat cultivation in Italy was mostly based on indigenous landraces that had evolved and adapted to the agroecosystem of Southern Italy (primarily the islands of Sicily and Sardinia). They came about through natural selection and/or unconscious selection by farmers [5]. In 1927, Emanuele De Cillis, in his book “I Grani d’Italia”, described the most widespread landraces of wheat at that time [6] (Table 1).
Most of these landraces belonged to the mediterraneum type [7,8,9] (Figure 1), characterized by tall plants (up to 180 cm) with early vigor, prone to lodging, late flowering, and with high grain filling rates. After the war between Italy and the Ottoman Empire in 1912, North African (Libyan in particular), Syrian, and Palestinian landraces (e.g., “Aziziah” and “Eiti”) arrived in Italy, thus contributing to the maintenance of a large genetic base. Many of them belonged to the so-called syriacum type, which is characterized by profuse tillering, shorter plants (below 120 cm), and earlier anthesis than the mediterraneum type due to the different climatic conditions of their respective areas of origin [8,9].
These landraces formed an important part of a self-supporting rural economy based on complex agricultural systems, where animals provided labor and manure for fertilization, and rotations with legumes provided animal feed whilst increasing soil nitrogen content. Fallowing was also common, particularly on the islands.

2.2. First Period: Genealogical Selection from Local and Exotic Populations (1920–1950)

In the 30 years spanning 1920 to 1950, Italy was the first country within the Mediterranean basin to begin ‘conscious’ breeding—primarily focused on the genealogical selection of pure lines derived from previously cultivated local varieties. The only exception was “Garigliano”, a pure line ‘created’ by Strampelli, who, for the first time, used controlled hybridization to create genetic variability. These more uniform new cultivars gradually replaced the original landraces in Italy, whereas other countries continued to grow durum landraces until the so-called “Green Revolution” in the late 1960s [10].
The most successful cultivar of this period was “Senatore Cappelli” (from here on referred to as “Cappelli”), released by Strampelli in 1915, and subsequently cultivated across up to 60% of the area dedicated to durum wheat in Italy. Cultivation of the “Cappelli” variety also spread to other Mediterranean countries, namely Spain and Turkey. Although it is generally assumed that “Cappelli” originated from the North African population “Jean Rhetifah”, recent studies highlighted a genetic distance between “Cappelli” and “Jean Rhetifah” [11,12,13] and instead confirmed its genetic similarity to the Tunisian “Bidi”.
“Cappelli” was appreciated for its high grain yield (2.6 t ha−1 on a plot basis according to Strampelli), being 33% higher than that of preceding landraces according to Maliani [14] due to its adaptability, high number of kernels per spike and spikelet, and excellent semolina quality [15]. It was not the only cultivar developed during those years, and Strampelli was not the only active breeder, the others being De Cillis, Conti, Barbieri, and Casale (Table 2).
Despite its undisputed success, “Cappelli”—a typical component of the mediterraneum group and hence tall and late—faced challenges such as rust and lodging susceptibility, which were long-”ignored”, partly because its low sowing density and low soil fertility requirement did not exacerbate the lodging problem. Moreover the distribution of nitrogen fertilizers was quite limited (4.0 kg ha−1 of N2, 7.8 of P2O5 and 0.5 of K2O, referring to the total agricultural area of about 21 million ha) [16]—low compared with contemporary fertilization rates.
During this period, the area dedicated to durum wheat cultivation in Italy also experienced significant variation in the surface area (from 1.2 million ha in the 1926–1930 period to 1.3 million ha in the 1946–1950 period, ISTAT data) and geographic distribution. Initially restrained to the islands and South and Central Italy, in the late 1940s, durum wheat cultivation expanded to other regions within Central Italy, namely Tuscany, Marche, and Umbria [17].
With the “Battle for Wheat”, the average yield raised from the 0.9 t ha−1 of the 1920s to 1.2 t ha−1 in the latter half of the 1930s. However, during the 1940s, yields dropped to 1920s levels due to the impact of the war. This suggests that the agronomic component may have been more decisive than the genetic component in determining yields during that period [18]. After the war, the insufficiency of durum wheat production in Italy in both quantitative and qualitative terms also occurred because it was primarily concentrated in the southern regions, often on infertile and resource-limited soils. The limited yields did not encourage the necessary investment. Thus, to ensure an adequate supply, milling and pasta industries blended locally grown durum wheat with durum wheat from other parts of the world, such as the United States, Canada, and Argentina (e.g., “Candeal-Taganrog”, a selection from the original Russian population). These imports exhibited characteristics such as a yellowish color and a high gluten strength [19].

2.3. Second Period: Intra- and Inter-Specific Hybridization and Mutagenesis (1950–1973)

Between the 1950s and 1960s, the genetic improvement in durum wheat in Italy was governed by the crossbreeding of lines from the mediterraneum group, mainly from North Africa (like “Cappelli”), and the syriacum group (“Aziziah”, “Eiti”, “Sinai”, “Tripolino”) with the aim of generating variability for subsequent selection. Nazareno Strampelli had already proposed this breeding technique, creating the “Garigliano” cultivar as early as 1927 through the crossbreeding of “Cappelli” with “Tripolino” [20].
Many of the new cultivars released during this period (“Capeiti 8”, “Patrizio 6” [21], “Casale 92”, “Sincape 9”, “Grifoni 235”) were based on “Cappelli” (Table 3), meaning that this cultivar appears in the pedigree of almost all durum wheat cultivars bred in Italy and elsewhere [22].
The crossbreeding between the mediterraneum and syriacum types reduced plant height to less than 120 cm and thus the lodging incidence and brought anthesis forward [23]. This marked the beginning of a gradual genetic improvement to enhance earliness, making Italian varieties generally earlier than those grown in other Mediterranean areas [24].
The best results were obtained with “Capeiti 8” and “Patrizio 6”, which outperformed “Cappelli” in yield [16], earliness, and lodging resistance, bringing about the decline of “Cappelli” by the mid-1960s [8]. The reduction in plant height, initially appreciated solely for its positive effect on lodging, also led to an initial, significant increase in the harvest index (HI), a dominant theme in durum wheat genetic improvement, from about 0.32 in “Cappelli” to about 0.40 in “Capeiti 8” [25,26].
On the other hand, both the milling and pasta-making qualities of “Capeiti 8” and “Patrizio 6” were considerably worse than those of “Cappelli” [27], in part because of the expansion of durum wheat cultivation into less suitable areas compared with those where “Cappelli” was grown [28]. In addition to a lower grain weight [23,25,26], the new cultivars exhibited deficiencies in the plasticity of dough [17], as well as greater lipoxidase activity [8], negatively impacting the amber coloration of semolina.
Durum breeding was very intense in Italy in the following years up until 1973. “Capeiti 8” was widely used as a parent for intra-specific crosses, producing cultivars including “Maristella”, “Nuragus” and “Ichnusa” [29] (Table 3) in Sardinia and “Hymera” and “Trinakria” in Sicily [30]. “Maristella” and “Trinakria” were known for their good quality, although not as good as that of Cappelli. “Appulo”, selected by Dionigi in Apulia, was the most successful cultivar of this group. After being registered in the Varietal Register in 1973, the following year it ranked among the top four most widely cultivated Italian cultivars together with “Capeiti 8”, “Patrizio”, and “Cappelli” (ISTAT). Using results from about 200 field trials, Rivoira [31] estimated a 12% increase in yield with the transition from “Cappelli” to “Capeiti 8” and another 7% increase from “Capeiti 8” to “Appulo”, “Maristella”, and “Isa”.
Inter-specific hybridization with other Triticum species, like T. dicoccum, T. turgidum, and T. sphaerococcum, was also common during this period to improve resistance to pathogens, cold, and lodging and to increase spike fertility. These efforts resulted in the creation of varieties such as “Lambro” and “Belfuggito”, characterized by high yields and cold resistance but not widely cultivated [32].
In the same years, mutagenesis was applied to durum breeding by the groups led by D’Amato and Scarascia-Mugnozza at the CNEN (National Committee for Nuclear Energy, now ENEA) to obtain the cultivars making up the Castel group: “Castelporziano” and “Castelfusano” (a “Cappelli” mutant), “Casteldelmonte” (a “Grifoni” mutant), and “Castelnuovo” (a “Garigliano” mutant) [26,33,34]. “Castelporziano” was more lodging-resistant than “Cappelli”, thanks to a single partially dominant gene capable of reducing height by 34% [35].
During this period, the cultivated area for durum wheat in Italy increased from 1.4 to 1.6 million ha due to its expansion across the south as well as in more northern regions such as Marche, Umbria, Lombardy, Veneto, and Emilia Romagna. Altogether, the more favorable pedoclimatic conditions of these regions, the improved cultivars, and the increase in nitrogen fertilization made the reduction in plant height possible and boosted national grain yields from 1.12 to 1.9 t ha−1 (ISTAT).

2.4. Final Period: Semi-Dwarf Cultivars (1974–Today)

The last period of durum breeding began with the production of the first semi-dwarf cultivars, which continue to be grown today. The success of dwarfing genes, responsible for a reduction in height and an increase HI and ear fertility at similar biomass levels, arose from a strong synergy between breeding and management: these new cultivars were able to exploit the high nitrogen rates made available by the contemporary replacement of animal waste with industrially produced ammonia as the primary source of nitrogen; their lower competitiveness towards weeds was compensated for through the use of herbicides; and they were better suited to the increasing levels of mechanization in farming practices. Interestingly, the scheme followed by Norman Borlaug, the father of the Green Revolution, was practically the same as Strampelli’s and benefited from the preceding diffusion of Strampelli’s varieties all over the world. What was different was the organization level (Borlaug worked at CIMMYT [36]) and the reference agro-ecosystems, which were not yet prepared to exploit the potential of semi-dwarf cultivars at the time of Strampelli.
The semi-dwarf Rht-B1b allele, the central protagonist of the 1960s Green Revolution of bread wheat, appeared for the first time in commercial durum wheat cultivars in the 1970s as the outcome of the breeding work carried out by Vallega and Zitelli, ENEA (Italian National Agency for New Technologies, Energy, and Sustainable Economic Development), the Experimental Institute for Cereal Research and the Experimental-Agricultural Regional Center in Sardegna. These first semi-dwarf cultivars were “Valgerardo”, “Valnova”, “Creso”, and “Karel” [37] (Table 4). The Japanese bread wheat “Norin 10” was the donor of Rht alleles, and durum wheats from Central and North America were the donors of various resistances to pathogens. “Creso” originated from a cross between a segregating population from CIMMYT (Centro Internacional de Mejoramiento de Maiz Y Trigo, Mexico) with Cp B 144, a Cappelli mutant. Registered in 1974, “Creso” spread across Italy quickly, especially in the central and northern regions due to its lateness, gradually replacing “Capeiti 8” and “Appulo”. Its diffusion reached a peak in 1987, when it was responsible for 43% of national durum wheat production (ISTAT). It was one of the most longeval durum wheat cultivars, remaining within the top 10 Italian cultivars until 2005, i.e., for about 30 years.
The take up of “Val” group varieties (“Valgerardo”, “Valnova”, “Valforte”, etc.) was limited, primarily due to their inadequate commercialization rather than to genuine genetic inferiority [19]. These cultivars did not spread as widely as “Creso”, in spite of being earlier than the latter and hence more suited to southern regions. During this period, the cultivar “Karel” (“Mex” × “198” × “Maristella”), established in Sardinia at the CRAS (Centro Regionale Agrario Sperimentale) by Deidda in 1979, exhibited higher production levels and greater production stability compared with “Creso”, albeit with smaller kernels and a medium–low pasta-making quality. Results from a three-year varietal comparison trial conducted across 33 locations in central and southern Italy [38] found the earliness of Karel to be similar to that of “Appulo”, “Maristella” and “Trinakria”, but it outperformed other dwarf and semi-dwarf cultivars in production levels (averaging 4.5 t ha−1 over three years and across all locations), along with “Valforte” (4.3 t ha−1) and “Valgerardo” (4.1 t ha−1).
The productivity enhancements achieved with these new cultivars compared with “Capeiti 8” varied from 21 to 33% [38]. Besides the height variations, studies reported a higher ratio of useful to total tillering and greater synchrony in the development of secondary tillers compared with that for primary tillers [31]. Overall, these new durum wheat cultivars achieved production levels comparable to those of bread wheat, while maintaining the high technological quality required by the pasta industry.
The rapid evolution of durum breeding led, in 1974, to the foundation of the National Network for Comparison of Durum Wheat Varieties, coordinated by the Research Unit for the Quality Enhancement of Cereals (CREA) in Rome, which aimed to orient farmers in their cultivar choice. This network is still active and organizes 50–60 variety comparison trials each year across six areas encompassing the different environmental conditions of Italy, with the scope of comparing new cultivars against the most cultivated ones. The parameters evaluated include data on heading date, plant height, grain yield and yield components, quality, and other agronomic traits, providing a useful historical dataset with which to analyze the evolution of durum wheat productivity.
New legal regulations accompanied the entering of semi-dwarf wheats into the panorama of durum wheat cultivars, such as the Italian decree n. 580/67, which encouraged the use of durum for “pasta pureness”; regulation (EEC) n. 1143/76, which established a community support system for various types of cereals, including durum wheat; the Italian decree n. 1096/71 “Discipline of seed activity”, which established Variety Registers, the registration of cultivars, and the official certification of seeds as preliminary conditions for their commerce.
The success of the recently established varieties and the enactment of these new legal regulations spurred increased investments in durum wheat improvement and ultimately led to a decline in the contribution of public breeders to varietal development, which were progressively substituted by private seed companies (Table 4). This change made the marketing and commercialization activities carried out by seed companies crucial to the success of a cultivar, which did not always mirror its actual agronomic value. As a result of this intense breeding work, the entire available gene pool for tetraploid wheats underwent recombination, and a plethora of highly productive new cultivars incorporating novel germplasm, primarily sourced from CIMMYT, were registered on the national register [39,40,41,42].
Breeding techniques still mostly rely on the conventional schemes adopted for autogamous species, i.e., the creation of genetic variability through controlled hybridization and the subsequent selection of pure lines. Marker-assisted selection has been a useful aid since 1990, particularly for the so-called “breeding by design” (involving the assembling of specific alleles necessary to obtain a previously defined “ideotype”), although it is mostly effective when “qualitative” traits controlled by just a single or few genes are involved (e.g., disease resistances, grain quality, or development traits).
The adoption of new cultivars did not keep pace with the rhythm of appearance of new cultivars, as demonstrated by the dynamics of seed certification (Table 5). For example, “Duilio”, one of the most used cultivars until 2010, reached its maximum diffusion in 1993, despite being registered nearly a decade earlier in 1984; “Simeto”, registered four years later in 1988, reached its maximum diffusion (at 33%, expressed as the percentage of the seed used considering the top ten cultivars) in 1996. Among the cultivars registered in the 1990s, “Colosseo”, “Iride”, “Ciccio”, and “Claudio” were the most diffuse. Apart from “Colosseo” (which became moderately widespread in the same year as its registration and reached its maximum diffusion just three years later at 10%,), “Ciccio”, “Iride”, and “Claudio” only appeared 3–6 years after their respective registrations. “Iride” was the most widespread, peaking at 13.2% in 2008, i.e., 12 years after being registered.
In 2017, four years after being registered in the Varietal Register, “Antalis” ascended to the fourth position among the most produced seeds. This success reached its zenith in 2020 when “Antalis” claimed the top spot as the most produced cultivar. “Simeto”, “Iride”, and “Claudio”, each with a registration history spanning over two decades in the Varietal Register, consistently maintained prominent positions among the most diffused cultivars until 2020. Overall, the varietal landscape seems to be heading towards greater diversification, considering that the top ten cultivars for seed production represented a whopping 84% of the total seeds produced in 1992, compared with only 58% in 2010 and 46% in 2018 [43].
The great diffusion of “Antalis” was justified by its greater productivity in the varietal comparisons carried out from 2015 to 2021, together with “Ramirez”, “Monastir”, “Claudio”, and “Kanakis.
The steady rise in the number of cultivars being registered is testament to this intense breeding activity: 58 cultivars in 1981 [31], 134 in 2002, 174 in 2011, and an enormous 327 in 2022; thus, there has been an average of 14 new cultivars per year over the last decade. Alongside the new varieties, several older varieties are still present, including “Cappelli”, “Castelporziano”, “Appulo”, “Valnova”, and “Creso”, all registered before 1975, as well as a group of 25 older constitutions registered as “varietà da conservazione”, including some of the pure lines diffused earlier on (“Bidì”, “Tripolino”, “Ruscia”, “Capeiti”, etc.). Cultivars imported from other countries, mainly France, appeared in the Italian Register as early as 1995, and their presence has increased in recent years. Indeed, one of the most diffuse cultivars in the last decade, “Antalis”, was developed in France.
Grain yields showed a continuous and almost linear increase from the introduction of semi-dwarf cultivars until 2020, an increase that already began as early as in the second half of the 1960s (Figure 2). Although lower than the 96% average increase recorded between 1926–1930 and 1976–1980, when semi-dwarf cultivars were first cultivated, the 76% average increase observed from 1976–1980 to 2016–2020 is still relevant. On the other hand, it cannot be attributed to varietal evolution only, because ISTAT data refer to farm or ‘actual’ yields, and hence they reflect the combined effects of management, environment, cultivar, and geographic distribution. Sowing rates of 350–400 viable seeds m−2 and fertilization rates of 100–180 kg of nitrogen ha−1 are common for modern cultivars, compared with 200 seeds m−2 and 40–60 kg of nitrogen ha−1 for the old cultivars.
The cultivation area assigned to durum wheat continued to grow after the appearance of semi-dwarf cultivars in parallel with the increase in yields, reaching a peak of 1.8 million ha in the 1986–1990 period. A progressive decline in the area invested in durum wheat cultivation in Italy was observed after 1990, despite the MacSharry Reform (1765/92), which introduced an additional payment to durum wheat producers, compensating them for income loss due to the alignment of the price of durum wheat with those of other cereals. Unfortunately, the MacSharry Reform also led to a deterioration in farming practices, which was responsible for the deterioration in the quality of European durum wheat [44]. Starting from 1995, pressures by seed producer lobbies led the Ministry of Agriculture to impose the use of 100% certified seeds to access the additional aid for durum wheat production areas, thus increasing the seed renewal rate from 30% in the early 1990s to over 70% [45].
The reduction in the area dedicated to durum wheat cultivation after 2005 primarily affected regions traditionally suited for durum wheat cultivation, such as South Italy and the islands. Several factors contributed to this decrease, including the significant price volatility of durum wheat, with extended periods of low profitability often failing to cover production costs. The introduction of decoupling from the new European Union regulations, which no longer tied premium payments to crop selection, also had a significant impact. Puglia became the top-ranking region, providing 27% of the national surface dedicated to durum wheat, followed by Sicily (21%), Basilicata (9%), Marche (8%), and Emilia Romagna (6%) (mean for the 2016–2020 data, ISTAT). This decrease in the cultivated area resulted in a decrease in the national production of durum wheat, exacerbating the incapacity of Italy to meet the needs of the processing industry [46]. Consequently, Italy is compelled to import durum wheat (2.318.604 t in 2021, according to ISTAT).

3. Evolution of Grain Yield and Related Traits

Grain yield is a complex, low-heritable trait that is affected by a number of physiological mechanisms. Although empirical selection for grain yield has been effective in the past, improving plant types through physiological breeding [47] may prove to be the more effective approach nowadays, when the relative rates of yield increase are declining [48]. The premise for designing improved plant types is knowledge about well-characterized genetic resources to use in crossing strategies. An understanding of the changes in the grain yield and related traits resulting from durum wheat breeding in Italy and a characterization of the genotypes involved can, therefore, help physiological breeding.

3.1. Grain Yield

Evaluating the effect of breeding on grain yield is a difficult task because of the strong interaction between genotype, environmental conditions, and management.
Even when cultivars from different eras of breeding are grown side-by-side and, as a consequence, subjected to the same environment, evaluation of the genotypic component can be biased by management, since old durum wheat cultivars cannot be grown at the same plant population density and with the same rates of nitrogen fertilization commonly adopted for modern semi-dwarf cultivars due to their susceptibility to lodging. Moreover, both the biotic and abiotic environment may change over the time span of comparison, so that adaptation to these changes is also included in the apparent “breeding progress” [48,49]. Giunta et al. [50] compared cultivars from different eras of breeding in Sardinia with their pertaining sowing rates, two sowing dates (normal and late), and two nitrogen rates, one suitable for old and the other suitable for modern cultivars. A 37% increase in yield potential was calculated for a comparison of old cultivars (pure lines grown until 1950) with an intermediate group including cultivars obtained by crossing mediterraneum and syriacum germplasm, plus an additional 19% considering the introduction of Rht genes, corresponding to a mean increase of 23.9 kg ha−1 year−1. The greater productivity of modern cultivars was expressed at both N rates and sowing dates, although modern cultivars benefited more from the higher nitrogen supply. Similar results were obtained by De Vita et al. [51], who estimated an genetic yield gain of 19.9 kg ha−1 year−1 for cultivars covering the same historical period as Giunta et al. [50], grown under different fertilization rates and with vs. without irrigation in South Italy. Grain yield variation between cultivars ranged from 3.26 to 5.43 t ha−1, i.e., the same range observed by Giunta et al. [50] between old and modern cultivars. In both experiments, the genetic gain was most clearly associated with a higher kernel number m−2 [50,51].
These comparisons, although informative, mainly reflect the effect of Rht introgression, but they cannot quantify the effects of breeding on the grain yield of the semi-dwarf cultivars released in the last 50 years. To the best of our knowledge, no side-by-side comparison of durum wheat semi-dwarf cultivars released after 1974 exists in the present literature.
Historical data available from the National Network for Comparison of Durum Wheat Varieties have been used, and the breeding effect was isolated from other sources of variation (environment, geographical distribution, management, etc.) by means of the “check cultivars” included in all trials. Until the late 1980s, approximately 50% of the increase in agricultural yield was attributed to breeding, and the remaining 50% to agronomic management practices [52]. However, both processes significantly contributed, and the overall benefits were enhanced by positive interactions between genetic improvement and agronomic management. The combined effectiveness of these two approaches led to more substantial improvements compared to what could have been achieved by each process individually [53].
Bianchi and Mariani (1993) [54], using data from the trials conducted between 1974 and 1992, for which the check cultivars were “Appulo”, “Capeiti 8”, and “Trinakria”, quantified an average yield increase of 1.4 t ha−1 during the considered period, equivalent to an annual increment of approximately 0.07 t ha−1. It is worth noting that the maximum recorded yields exceeded 5.5 t ha−1 during this period. Bias was introduced into the evaluation of their genetic progress by the tall stature of the check cultivars that tended to lodge when grown at high planting densities and with high doses of nitrogen fertilizers. The cultivars that contributed the most to this genetic improvement included “Duilio” and “Simeto” [54].
A similar approach was subsequently used by Salis [55] with the 153 cultivars compared between 1990 and 2010 in 39 field trials, involving 25 cultivars from each of the two Sardinian fields belonging to the national evaluation network. The check cultivars in this period were the semi-dwarf cultivars “Creso”, “Duilio”, and “Simeto”. The analysis allowed for the identification of the most productive cultivars released before the 1980s and in different five-year periods, spanning from 1981–1985 to 2001–2005. A continuous increase in grain yield in the considered period was highlighted (Figure 3). “Duetto”, the best among the cultivars released between 2001 and 2005, produced an average 23% (more than 8 t ha−1) more than the check cultivars. Although the check cultivars were semi-dwarf varieties in this case, an overestimation of genetic progress may have arisen from the generally observed ‘decay’ in productivity of a given cultivar (the check cultivars in this case), often deriving from a progressive increase in susceptibility to insects and diseases [49].
The record yield of 10.56 t ha−1 recorded with the cultivar “Fiore” was assumed to represent the potential yield for this type of environment, but the cultivar “Iride” also produced more than 10 t ha−1 in the same year (2005). Similar potential yields have been reported for bread wheat grown in the UK [48], confirming that the two wheat species share a comparable yield potential. Comparing this potential yield with the attainable water-limited yields (assumed to be equal to the average field yields) and the farm or actual yields, as reported in the ISTAT database (Figure 4), reveals large differences. While the gap between the potential and attainable yield can mostly be attributed to the notable variability in the amounts and patterns of rainfall in Mediterranean environments, the gap between attainable and farm yields highlights the importance of actions aimed at supporting farmers’ activities (infrastructure, education, extension services, etc.).

3.2. Plant Height, Lodging Resistance, HI

The gradual reduction in plant height associated with an increase in the harvest index has been a primary breeding objective, affecting lodging susceptibility, sink capacity, and biomass partitioning [56,57]. The initial reduction in plant height, of about 30 cm, was obtained by crossing the mediterraneum with the syriacum germplasm (cultivars released between 1950 and 1970, or the so-called ‘intermediate cultivars’), followed by a further reduction of about 20 cm attained by the introduction of the Rht1 gene [50]. These events caused a height decrease of approximately 0.51 cm year−1 for cultivars grown between 1900 and 2000 [57]. This progressive reduction in height also occurred in other countries such as Spain [1] and Argentina [58].
The strong correlation between decrease in plant height and increase in harvest index (HI) led to a notable increase in HI, even before the introgression of Rht genes. Starting from average values of 0.25–0.28 for the old cultivars, the HI of the intermediate cultivars was 10% higher, rising a further 4% in the modern, semi-dwarf cultivars released at the end of 20th century, reaching a maximum value of around 0.40 [50,59]. The resulting estimated average increase in HI was 0.19 ± 0.017% per year, comparable to the 0.2% increase per year calculated by Brancourt-Hulmel et al. (2003) [60] in bread wheat cultivars released in France between 1946 and 1992.
The reasons why the decrease in plant height translated into an increase in HI are that total biomass was almost unaffected [50,57] and that the reduced stem growth rates allowed for more resources to be allocated to the developing ear, resulting in a greater number of fertile florets and grains per ear [48] and, ultimately, in an estimated increase of 35–41 kernels m−2 year−1 [50,57]. Kernel weight was almost unaffected by the year of release of durum wheat cultivars, or showed just a slight decrease, but grain yield, being closely associated to kernel number m−2, increased by 20–24 kg ha−1 year−1 [50,57].
Following the increase in wheat yield, over 70% of commercial wheat worldwide now contains Rht1 (located on the B genome of bread and durum wheat) or Rht2 (on the D genome of bread wheat) [61]. One of the pleiotropic effects of Rht1 and Rht2 is to reduce plant height by decreasing cell size and reducing cell elongation due to insensitivity to endogenous gibberellins. This results in a shorter coleoptile length and smaller leaf areas in seedlings, undesirable traits in semi-arid and arid environments, where they lead to poor emergence and reduced early growth if sowing conditions are unfavorable [61,62]. A gibberellin-sensitive dwarfing gene (Rht14) was identified in the old durum wheat cultivar “Castelporziano”, and it was proposed that it could be used to cope with this problem [62]. Rht14 exerts no negative effects on coleoptile length and seedling establishment, although it negatively affects kernel weight and some quality traits [62].
Lodging incidence also changed as a consequence of the reduction in plant height. Not only does lodging reduce grain yield due to inefficient radiation use but it also worsens grain quality [63]. Lodging depends on plant height [64] and may be caused by stem buckling [65] or by the failure of the root–soil complex. Breeding has not significantly altered stem or anchorage strength [66]; hence, the improved resistance to lodging of modern cultivars comes from the reduction in plant height. Reducing plant height through the introgression of the syriacum germplasm was less efficient at reducing lodging than the introgression of Rht genes, because while the lodging incidence of intermediate cultivars was still lower than that of old cultivars, it remained higher than that of semi-dwarf ones [50].

3.3. Leaf and Canopy Traits

Breeding for grain yield and earliness indirectly affected a number of leaf and canopy traits involved in carbon assimilation and transpiration. In particular, the progressive reduction in plant height increased canopy’s aerodynamic resistance, ultimately resulting in a higher canopy temperature of the modern Italian durum wheat cultivars compared with old ones [67]. This result was confirmed, although only for the grain filling period, in a larger set including landraces and modern cultivars from the whole Mediterranean basin [1]. At the leaf level, breeding acted in the opposite direction by decreasing the stomatal resistance of modern cultivars [67]. The combination of a lower canopy temperature and a higher stomatal resistance in older cultivars may be advantageous for the crop’s water requirements and water use efficiency, especially during grain filling [1].
Modern cultivars also produce smaller and thicker flag leaves than older cultivars [67], similarly to what was noted in UK bread wheat [68], likely as a consequence of the presence of semi-dwarfing alleles at Rht-B1 [69,70]. Overall, these changes should be considered positive for photosynthesis, because a lower flag leaf area may help to improve light capture by lower leaves, and the thickness was associated with a greater photosynthetic machinery density, as shown by the parallel increase in the nitrogen content per unit of leaf surface [67]. It should be noted that the change in this latter trait had already occurred in the cultivars obtained by crossing the mediterraneum germplasm with the syriacum germplasm before the introgression of “Norin 10” genes. Consistent with this observations, the photosynthetic efficiency of the flag leaf, often correlated with Rubisco activity, is one of the factors associated with grain yield in modern wheat cultivars [71,72,73].
No effect of breeding was observed on the green area index or the leaf area index [74], but senescence began later relative to anthesis date and developed at a faster rate in the modern than in the old cultivars. The earlier anthesis in modern cultivars is one of the reasons for their later onset of senescence, because it shifts the anthesis–maturity period to less stressful conditions. As a result, modern cultivars maintain their greenness over a greater proportion of their anthesis-to-maturity period [67].
It is interesting that, in both bread wheat and durum wheat, the morphological changes in the flag leaf seen with this ‘breeding progress’ (e.g., smaller, more erect, higher N per unit area, and higher chlorophyll concentration) were not unlike those reported for winter wheat progress in the United Kingdom [52].

3.4. Phenology

The timing of phenological events is one of the most critical factors for crop adaptation and yield in a specific environment [75,76], and an optimal window for flowering can be defined for each environment. In Mediterranean environments, this optimal window is bound by spring frost, on one side, and by terminal water and temperature stress on the other. The lateness of old cultivars with respect to this optimal window led to an advance in the anthesis date as a consequence of breeding [50]. In contrast with what was observed in bread wheat [77], in durum wheat, the advance in the anthesis date was attained before the introgression of Rht genes, thanks to crosses with the syriacum germplasm [50], while the subsequent introgression of Rht genes appears to have delayed flowering time with respect to intermediate cultivars [78].
The genetic regulation of flowering time in wheat is determined by the interplay of at least 20 genes scattered across the whole genome [79]. These genes have been classified according to whether they respond to vernalization or to photoperiod or whether they confer earliness per se [80,81,82]. Understanding which of these genes were involved in the change in anthesis date in the shift from old to modern cultivars and which ones are governing the development of modern cultivars may be useful to improve the adaptation and yield potential even further [83]. According to Motzo and Giunta (2007) [78], the lateness of old cultivars was due to their greater photoperiod sensitivity and cold requirements, whereas the greater earliness, per se, was the reason for the earlier flowering time of the intermediate group of cultivars. Rht genes reduced photoperiod sensitivity but decreased earliness per se. This residual earliness per se is fundamental to modern cultivars to preserve and increase the length of the terminal spikelet–anthesis period because the longer this period, the greater the ear fertility [84]. Interestingly, some quantitative cold requirements are still present in modern Italian cultivars, although they are generally classified as spring types [78], partly because the traditional autumn sowings ensure the cold requirement is met [78]. In any case, the lower cold requirement of modern cultivars compared with old ones has the drawback of increasing their inter-annual variability in anthesis date by increasing the role of temperature in the control of their development [85].
The reduced duration of the vegetative phase of modern cultivars [57] moved the grain filling period to less stressful conditions and lengthened its duration whenever the terminal drought caused the simultaneous senescence of all cultivars, contributing to the increase in HI. Therefore, the above-mentioned relative constancy of grain weight was the result of an almost full compensation between rate and duration of grain filling, as shown by the negative correlation between the maximum rate of grain filling (that ranged between 2.4 and 3.3 mg d−1) and the year of cultivar release of six Italian cultivars constituted between 1910 and 1996 [86]. The high rate of grain filling of old cultivars confers tolerance to terminal drought [87], i.e., the ability to maintain high grain weights despite the high temperatures and short grain filling period caused by their lateness [88].

3.5. Nitrogen Uptake and Use-Efficiency

In contrast with what was observed in bread wheat [89], durum wheat breeding induced an increase in total nitrogen uptake, necessary to sustain the increases in yield and harvest index [50]. Grains have a higher nitrogen concentration than straw, and the greater proportion of dry matter allocated to grains as a consequence of the increase in HI was, therefore, the reason for the increase in total N uptake, despite the parallel reduction in grain protein percentage [90]. This is why similar time trends were observed between HI and NHI, with the latter increasing from 0.71 in old cultivars to 0.80 in semi-dwarf ones [50].
Although substantial progress has been made, wheat is the least efficient major crop in terms of nitrogen use, with its nitrogen use efficiency (NUE, grain yield vs. total available N in the soil) being around 25% lower than those of maize and rice [91]. From an agronomic point of view, fertilizer use efficiency (fertilizer recovered in total biomass as a fraction of fertilizer applied) is a useful index to consider and is estimated to be only 33% in wheat [92].
A recent study by Lupini et al. (2021) [93], comparing NUE and tolerance to water and nitrogen stress in old and modern durum wheat varieties, found that modern cultivars outperformed old ones under conventional nitrogen and water regimes, whereas old varieties were better able to cope with both water and nitrogen stress, particularly at the stem elongation and milk-ripening stages of development, when nitrate and ammonium transporter gene expression in the root was the highest. NUE, in this paper, was calculated as total biomass production per unit of N taken up to avoid the penalization conferred to old cultivars from their low HIs [94]. These findings confirm recent discoveries suggesting the possible indirect selection of wheat varieties with better NUE values through the choice of high-yielding varieties [11,95]. In particular, Taranto et al. [11] showed that major well-known genes and/or QTLs (quantitative trait loci) influencing traits such as plant height (RHT), earliness (VRN, PPD), and grain quality could explain the differences between old and modern durum wheat varieties and are often located in the same genomic regions where genes related to nitrogen metabolism are found.

3.6. Grain and Semolina Quality

Durum wheat quality is evaluated according to the final product obtained. Before the 20th century, no distinction was made between bread and durum wheat, and durum was used for both bread and pasta production. It was De Cillis (1942) [6,18] who first demonstrated that pasta made using vitreous grains, which have a higher protein content, has a better cooking quality than pasta made from starchy grains with a lower protein content. Nowadays, durum wheat is mainly used for pasta production, although in the south of Italy, it is traditionally used for breadmaking too. In both cases, protein percentage and gluten strength are the traits defining the quality of durum wheat, with grain protein percentage contributing the most (40%) to the EUQuality Index for durum wheat (European Commission Regulation No. 2237/2003, 23 December 2003).
One of the trade-offs for an increase in grain yield obtained with breeding is the decrease in grain protein percentage, estimated at 0.14–0.19% year−1 [57,96]. This has led to an average difference in protein percentage of about 1–1.5% between landraces and modern Italian cultivars [50,97], with protein content of old cultivars ranging between 11.9 and 14% against a variation in the range of 10.5–12% for modern cultivars in a five-year field trial which compared 14 old against 14 modern cultivars [85]. This superiority of old cultivars in protein percentage persists even when they are grown in soils characterized by lower fertility and with lower fertilization rates than modern ones [85]. As stated above, this difference cannot be attributed to a lower capacity of modern cultivars to take up nitrogen, nor to a reduced NHI, but rather to the decrease in the amount of nitrogen allocated to each grain caused by the higher number of grains m−2 set up by modern cultivars, responsible for their high grain yields [85].
Gluten strength describes the continuity and strength of the protein network associated with gluten viscosity and elasticity. Strong and tenacious gluten is needed when pasta is the final product, whereas strong but extensible gluten is needed in the case of breadmaking. Given similar protein percentages, gluten strength depends on the types of glutenin and gliadin proteins present (genetically determined) and on their ratio [98], and it can be quantified via the Gluten Index (0–100%) [99,100]. Breeding activity on durum wheat was mainly directed at ameliorating pasta-making quality and compensated for the above-mentioned decrease in protein percentage by improving gluten strength through the incorporation of favorable combinations of alleles for both high (HMW-GS) and low (LMW-GS) molecular weight glutenin subunits and by an increase in the expression of B-type LMW-GS [101]. As a consequence, the glutenin–gliadin ratio increased, the Gluten Index increased from 6–32% in landraces to 55–87% in modern cultivars, and the technological quality of dough in general improved [51,97,101,102,103]. Similar results were obtained in Spain [96]. The higher gluten strength of modern cultivars, combined with their lower protein percentage, resulted in a lower or similar spaghetti cooking quality [102,104] depending on the pasta drying temperature—low (<60 °C), high (60–80 °C), or ultra-high (80–100 °C)—with consequent changes in the relative importance of the quantity vs. the quality of proteins. While the quality of pasta dried at low temperatures is governed by both protein quantity and quality, the quality of pasta dried at high and ultra-high drying temperatures is governed by protein quantity only [105].
The successful breeding work on gluten strength had the negative side effect of decreasing the large genetic variability in gluten characteristics present in the landraces to the very low levels retained in modern cultivars [10]. This means that landraces provide potential sources of genetic variation for gluten characteristics [106], particularly when bread is the final product in mind [3,97].
Durum wheat bread is characterized by a higher protein content, greater yellowness, and a longer shelf-life than common bread. It remains highly traditional in the Mediterranean region, particularly in Italy [107,108,109]. However, bread made with durum wheat cannot achieve the same volume as bread made with bread wheat, because although its gluten is more tenacious, it is less strong and elastic as a consequence of the absence of the glutenin D-genome, which confers extensibility to bread wheat [110,111,112]. Substituting the glutenin alleles of durum wheat was a less effective breeding strategy than transferring bread wheat chromosome 1D, responsible for gluten and dough strength, and/or chromosome 5D, responsible for kernel softness [108,112,113,114,115]. The improved gluten extensibility and superior baking quality obtained by Canadian breeders by crossing durum with emmer wheat (T. dicoccum, tetraploid) improved the breadmaking quality of durum wheat without sacrificing its strong gluten and pasta-cooking quality [116,117].
The importance of pasta color for the market led breeders to try to enhance the carotenoid contents of durum kernels and semolina through the introgression of a yellow pigment gene (Yp) [118]. In contrast with De Vita et al. (2007) [57], who did not find any difference in color between old and modern cultivars, several studies ascertained modern cultivars to have a higher yellow index than old cultivars [96,119]

4. Future Prospects: Lessons from the Past

4.1. Grain Yield

Increasing biomass production seems to be the most promising strategy for increasing grain yield [120] given the limited scope for increasing HI above the actual potential 50% due to the negative consequences of further reductions in plant height on grain yield [121]. It was suggested that the optimal plant height to maximize yield often falls between 0.7 and 1.0 m. Greater biomass already appears to be contributing to genetic yield progress in modern bread wheat cultivars released since about 1990 (e.g., [52,122]).
Biomass can be increased by lengthening the growth cycle. Antedate sowings can lengthen the growing season if phenology is also changed through the introduction of some cold requirement and/or with an increase in photoperiodic sensitivity to avoid excessively early anthesis. Crop simulations reveal that an early sowing system combined with slower-developing wheat genotypes could exploit a longer growing season and increase grain yield in spite of the recent climate changes [123]. In semi-arid and arid environments, advancing sowing date would also require an increased sowing depth to guarantee sufficient humidity for seed germination. Gibberellin-sensitive Rht genes, such as Rht14 in the old “Castelporziano” cultivar, are needed in this case, because their longer coleoptiles are associated with good seedling emergence.

4.2. Phenology: Is the Advance in Anthesis Date Still Desirable?

Between 2011 and 2020, the average surface temperature increased by 1.1 °C compared with the average temperature of the late 19th century (before the industrial revolution), and it is now warmer than any other period in the last 100,000 years [124]. The earliness of most durum wheat cultivars, partly due to limited or absent vernalization sensitivity, could already represent a problem today, but even more so in the future. The increasing temperatures associated with climate change may cause an excessive advance in anthesis date and a shortening of the whole growing period (the time from sowing to maturity), becoming the main yield-reduction factor [125]. Both modelling and field data have demonstrated that the combination of a delayed anthesis and a higher rate of grain filling compared with current cultivars is an effective adaptation strategy in warmer climates, because it increases both grain and protein yield, provided that nitrogen supply is not limiting [126]. This combination of traits is present in many old cultivars [86,88]. The positive effect of a delayed anthesis on grain yield is likely the consequence of the lengthening of the sowing–anthesis period that, by allowing for a greater biomass at anthesis, may result in an increased grain set [127].

4.3. Grain Quality: Are Grain Yield and Grain Protein Content Mutually Exclusive?

Durum wheat grain protein content and grain yield are often negatively correlated [85,128]. The comparison between old (lower grain yields and higher grain protein percentages) and modern (the opposite combination) cultivars has identified in an imbalance between the increase in total nitrogen uptake and the increase in grain number m−2 (the main determinant of grain yield), the reason for this trade-off associated with breeding. In modern cultivars, a rather limited source of nitrogen is diluted by high grain numbers [129]. Grain nitrogen comes partly from the N absorbed before anthesis, which is remobilized to the grains from senescing organs and partly from post-anthesis N uptake. It seems that the good capacity to absorb N after anthesis endows a cultivar with the ability to make the most of favorable weather conditions in the spring by combining a high grain N content with a high grain yield [130,131]. Traits that improve the post-anthesis N uptake are a high potential grain weight [132] and prolonged root activity after anthesis [131].
Breeding for gluten strength in durum wheat focused on the pasta-making quality so that only part of the genetic diversity of durum wheat has been captured by the modern varieties generated through breeding over the last century, and the modern germplasm is characterized by a drastically limited variation at the loci and in the allelic combinations controlling gluten strength [10]. Landraces and old cultivars represent, therefore, a potential source of genetic variability, and could be used to identify the best gluten composition and the appropriate gluten strength, particularly for final products other than pasta, such as bread [3,101,106,133].
A wide range of micro-nutrients (iron and zinc primarily) has been observed in durum landraces [134,135], making them potentially useful for improving the nutritional value of modern cultivars, which are instead characterized by a rather limited range of micro-nutrients [136].
The volatile organic compounds responsible for bread aroma, a very complex and important trait for breadmaking, are different in old vs. modern cultivars, once again offering new opportunities for future breeding with this quality in mind [106].

5. Conclusions

The effective process of genetic improvement, by replacing older and genetically heterogeneous varieties with new highly productive and superior quality varieties, inevitably involved a reduction in the overall genetic diversity [10]. In the current context of climate change and rapidly mutating pathogen populations, preserving the yield level through the continuous introduction of new cultivars, exploiting the reservoir of largely unused genetic variation stored in old cultivars and landraces, could be as important as increasing grain yield and quality [137]. The accurate phenotyping of agronomic and physiological traits and the study of the relationships between agronomic performance and genetic structure will be fundamental for exploiting the genetic variability present in old constitutions. In the future of durum wheat improvement, the synergistic integration of conventional and molecular approaches emerges as a promising perspective. The conventional approach, based on hybridization and selection of pure lines, can be enhanced using molecular markers to facilitate the identification of the parents needed to generate the desired genetic variability, and to accelerate the development timelines of new varieties by a more effective selection within the segregating progenies. New genetic variability could be used thanks to genome sequences, TILLING mutant collections, genomic selection and editing, although plants containing genes mutated through editing cannot still be grown in Europe [138].
The emerging interest towards mixed systems as a way to increase sustainability by improving the carbon balance and carbon sequestration could restore the value of straw in the future, eventually leading breeders to increase plant height.

Author Contributions

Conceptualization, M.L.C. and R.M.; methodology, F.G.; data curation, M.L.C.; writing—original draft preparation, M.L.C.; writing—review and editing, M.L.C., R.M. and F.G.; supervision, R.M. All authors have read and agreed to the published version of the manuscript.

Funding

This study was carried out within the Agritech National Research Center (Spoke 7) and received funding from the European Union Next-GenerationEU (PIANO NAZIONALE DI RIPRESA E RESILIENZA (PNRR)—MISSIONE 4 COMPONENTE 2, INVESTIMENTO 1.4—D.D. 1032 17/06/2022, CN00000022). The research was funded by the FAR (Fondo di Ateneo per la Ricerca 2020) of the University of Sassari. This manuscript reflects only the authors’ views and opinions, neither the European Union nor the European Commission can be considered responsible for them.

Data Availability Statement

Publicly available datasets were analyzed in this study.

Conflicts of Interest

The authors declare no conflicts of interest.

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Figure 1. Schematic representation of durum wheat from the syriacum typicum(blue) and mediterraneum typicum (black) groups (modified from Ali Dib et al. [9]).
Figure 1. Schematic representation of durum wheat from the syriacum typicum(blue) and mediterraneum typicum (black) groups (modified from Ali Dib et al. [9]).
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Figure 2. Evolution of the surface area (red crosses) and grain yield (circles) according to ISTAT data. Data are means of five-year periods.
Figure 2. Evolution of the surface area (red crosses) and grain yield (circles) according to ISTAT data. Data are means of five-year periods.
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Figure 3. Productivity indices (yield expressed as a percentage of the controls) of the best cultivars within each five-year period of constitution and average grain yield for the trials in which they were present (modified from Salis [55]).
Figure 3. Productivity indices (yield expressed as a percentage of the controls) of the best cultivars within each five-year period of constitution and average grain yield for the trials in which they were present (modified from Salis [55]).
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Figure 4. Potential, attainable, and farm yields for two Sardinian sites in absolute values and as percentages (numbers inside the bars). Potential yield was considered to be equal to the record yield in the 20 years of experimental trials, i.e., 10.56 t ha−1, attainable yields were field means, and farm yields were obtained by ISTAT (modified from Salis [55]).
Figure 4. Potential, attainable, and farm yields for two Sardinian sites in absolute values and as percentages (numbers inside the bars). Potential yield was considered to be equal to the record yield in the 20 years of experimental trials, i.e., 10.56 t ha−1, attainable yields were field means, and farm yields were obtained by ISTAT (modified from Salis [55]).
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Table 1. The main landraces of durum wheat cultivated in Italy until the 1920s.
Table 1. The main landraces of durum wheat cultivated in Italy until the 1920s.
NameDistributionAverage Productivity (tons/ha)Rust Resistance
Late autumn-sown landraces
RossiaCalabria, Basilicata1.2medium
BiancucciaSicilia1.1high
SicilianuSardegna1medium
Saragolla siciliana Campania1.1medium
Trigu arrubbiuSardegna1.3medium
Biancale o Trigu biancuSardegna0.9medium
Autumn-sown landraces, medium earliness
Saragolla o Duro di PugliaCampania,
Puglia,
Basilicata, Abruzzo, Molise, Lazio		0.8–1.6high
RealforteSicilia1.2–1.4high
SammartinaraSicilia1low
RusselloSicilia1.2high
ScorzoneraSicilia1.1high
Trigu murruSardegna1.1–1.2high
Autumn-sown landraces, early
RusciaSicilia1low
GiganteSicilia1.1medium
Spring-sown landraces
TriminiaSicilia, Puglia1.2–1.3medium
RusticanuSardeqna0.8high
Table 2. Durum wheat cultivars based on single pure lines developed in Italy between the 1920s and 1950s through genealogical selection from landraces (exception “Garigliano”).
Table 2. Durum wheat cultivars based on single pure lines developed in Italy between the 1920s and 1950s through genealogical selection from landraces (exception “Garigliano”).
BreederCultivarOrigin
Strampelli (1866–1941) CappelliNorth African population Jean Rhetifah
Aziziah 17–45Aziziah, Lybian population but of Palestinian origin and hence “syriacum type”
TripolinoSynonimous of Aziziah, according to De Cillis
Duro di PugliaSynonimous of Saragolla, according to De Cillis
DaunoGroup of cultivars originated from an unknow cross
GariglianoTripolino x Cappelli
U. De Cillis (1901–1984) Timilia S.1Homonimous local population
Russello S.97Homonimous local population
Conti (1889–1966)Aziziah 301 e 302Aziziah, Lybian population but of Palestinian origin, “syriacum type”
Russello 329Homonimous local population
Russello S.G. 7Homonimous local population (1)
Triminia 284Homonimous local population
Barbieri (1911–1975)BiancaleTrigu biancu
Casale (1902–1972)Eiti6“Eiti”, North-African population, but “syriacum type”
Table 3. Durum wheat cultivars selected in Italy between the 1950s and the first half of the 1970s from segregating populations obtained through inter- and intra-specific hybridization.
Table 3. Durum wheat cultivars selected in Italy between the 1950s and the first half of the 1970s from segregating populations obtained through inter- and intra-specific hybridization.
Cultivar CrossBreeder
Capeiti 8Eiti 6 × CappelliCasale (1955)
Patrizio 6 Eiti 6 × CappelliCasale (1955)
Casale 92 Aziziah × CappelliCasale
Sincape 9Sinai × Cappelli De Cillis U. (1963)
Grifoni 235 o B52 Spontaneous crossbreeding Cappelli × unknown wheat (Grifoni 1955), possibly Aziziah (D’Amato, 1989).Grifoni (1955)
ForlaniVilla Glori × T.turgidumMaliani (1968)
C. Jucci Forlani × RusselloMaliani
CaltelporzianoCappelli mutantScarascia Mugnozza (1968)
CasteldelmonteGrifoni mutantScarascia Mugnozza (1968)
IchnusaBiancale × Capeiti 8Barbieri e Deidda(1968)
NuraghusBiancale × Patrizio Barbieri e Deidda(1968)
MaristellaDauno III × Capeiti 8Barbieri e Deidda(1968)
TrinakriaB14 × Capeiti 8 Ballatore (1970)
HymeraB14 × Capeiti 8 Ballatore (1970)
Appulo(Cappelli × Grifoni 235) × Capeiti 8 Dionigi (1973)
Table 4. Main semi-dwarf cultivars released between 1974 and 2000.
Table 4. Main semi-dwarf cultivars released between 1974 and 2000.
CultivarYear of RegistrationPedegreeBreederType of Institution
Creso1974Cpb 144 × [(Yt54-N10-B) Cp2 63 Tc1]ENEA RomaPublic
Valgerardo1975(Yt54-N10-B) BY2 LD 390, II 14587/(Cappelli × Yuma)Ist. Sperimentale Cerealicoltura RomaPublic
Valnova1975Cappelli × {[Sel F2(Yt54-N10-B)BY2] LD 390, II 14587} × (S.Cappelli × Yuma)Ist. Sperimentale Cerealicoltura RomaPublic
Karel1979Mex × 198 × MaristellaCRAS CagliariPublic
Appio1982Cappelli × Gaviota × YumaFederconsorzi RomaPrivate
Arcangelo1983Creso × AppuloGranital Srl, RomaPrivate
Tresor1984Amber durum × S-22-80ISEA AnconaPrivate
Duilio1984Cappelli × (Anhinga × Flamingo)Federconsorzi RomaPrivate
Adamello1985Valforte × sel Turchia 7116Ist. Sperimentale Cerealicoltura RomaPublic
Lira1985Mandon × FD 1104Società Produttori Sementi BolognaPrivate
Messapia1985(Mex × Crane “S”) × TitoIst. Migl. Gen. BariPublic
Grazia1985M 6800127 × ValsesaMaliani Genetica RecanatiPrivate
Vitron1987Turquia 77 × (Jori “S” × Anhinga “S” × Flamingo “S”)Ramon Battle Vernis MadridPrivate
Plinio1988Linea D 50 × Trigo CandealFederconsorzi RomaPrivate
Simeto1988Capeiti 8 × ValnovaStaz. sperim. granicoltura, CaltagironePublic
Neodur1990(184-7 × Valdur) × EdmoreGae Masse Francia
Ofanto1990Adamello × AppuloIst. Sperim. Cerealicoltura FoggiaPublic
Flavio1992Latino × CappelliFederconsorzi RomaPrivate
Gianni1992Incroci di genotipi turchi e varietà italianeMosconi Giovanni AnconaPrivate
Radioso1992Creso × IsaProseme FoggiaPrivate
Parsifal1992INRA 92-1 × D81028Venturoli Sementi BolognaPrivate
Italo1993Incroci di genotipi turchi e varietà italianeMosconi Giovanni AnconaPrivate
Colosseo1995Mutante Mexa × CresoEurogen (Proseme)Private
Giemme1995Duilio × GraziaMaliani Genetica RecanatiPrivate
Iride1996Altar84 × Ares SibSocietà Produttori Sementi SPA (BO)/ENEA Private
Svevo1996Sel. Cimmyt × Zenit sibSocietà Produttori Sementi SPA (BO)/ENEA Private
Rusticano1996Linea CIMMYT F2-ce/16 0 n.09Società Produttori Sementi SPA (BO)/ENEA Private
Ciccio1996(Appulo × Valnova) × (Valforte × Patrizio)Eurogen (Proseme)Private
Claudio1998(Sel. Cimmyt × Durango) × (ISI 938 × Grazia)Sinagro ISEA Falconara MarittimaPrivate
Table 5. The percentage of seed production for the top ten cultivars over the total production of the top ten cultivars between 1992 and 2010 in Italy (ISTAT data).
Table 5. The percentage of seed production for the top ten cultivars over the total production of the top ten cultivars between 1992 and 2010 in Italy (ISTAT data).
Year of
Registration		Cultivar1992199319941995199619971998199920002001200220032004200520062007200820092010
1973Appulo4.510.82.33.83.13.02.62.42.0
1974Creso16.113.49.37.97.58.69.18.67.97.87.46.25.94.7
1982Appio11.910.87.75.93.83.73.2
1983Arcangelo1.02.54.44.65.25.87.48.09.010.17.57.76.96.8
1984Duilio15.615.911.79.110.213.613.315.013.912.312.311.310.39.68.47.47.15.43.4
1985Grazia13.310.78.57.16.26.15.44.23.62.82.8
1988Simeto14.419.428.532.132.626.622.620.419.219.319.318.819.817.721.419.316.015.59.6
1990Neodur2.93.73.01.21.21.41.8
1990Ofanto4.76.311.213.311.08.07.35.44.32.63.1
1992Radioso 2.7
1995Colosseo 2.26.310.39.67.95.55.75.25.44.2
1996Ciccio 3.36.98.39.18.47.05.46.25.24.43.3
1996Iride 2.44.96.48.210.112.213.213.012.9
1996Rusticano 2.42.92.4
1996Svevo 1.82.01.72.23.4
1996San Carlo 2.32.12.22.42.2
1998Claudio 1.12.13.24.04.75.04.96.17.0
1999Orobel 0.3 2.42.52.22.43.2
2002Levante 2.84.54.65.35.7
2003Anco Marzio 2.4
2004Saragolla 1.93.75.78.7
2004Latinur 0.31.63.33.7
Total top ten 84.393.586.685.183.083.183.079.677.073.767.166.968.566.858.661.761.663.057.7
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Careddu, M.L.; Giunta, F.; Motzo, R. Lessons from the Varietal Evolution of Durum Wheat in Italy. Agronomy 2024, 14, 87. https://doi.org/10.3390/agronomy14010087

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Careddu ML, Giunta F, Motzo R. Lessons from the Varietal Evolution of Durum Wheat in Italy. Agronomy. 2024; 14(1):87. https://doi.org/10.3390/agronomy14010087

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Careddu, Martina Ludovica, Francesco Giunta, and Rosella Motzo. 2024. "Lessons from the Varietal Evolution of Durum Wheat in Italy" Agronomy 14, no. 1: 87. https://doi.org/10.3390/agronomy14010087

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