Milk protein hydrolysates, content in cow’s milk, hydrolysis process used and their related bioactivity.
\r\n\tOver the years, the concept of maintenance became more comprehensive, reducing fault occurrence and increasing industrial system availability. Besides, reliability, safety, and criticality requirements were associated with the system or equipment under analysis. Maintenance strategies or schemes can be classified as corrective (run-to-break), preventive (time-based), and predictive (condition-based maintenance). Corrective maintenance is only performed after an occurrence of a fault. Therefore, it involves unexpected breakdowns, high costs, changes in the production chain, and it could lead to catastrophic events. Preventive maintenance and interventions occur based on a scheduled maintenance plan or the equipment's mean time between failures. Although it is more effective than corrective maintenance, unexpected failure may still occur by preventing most failures. Additionally, the process cost is still high, especially the costs associated with labor, inventory, and unnecessary replacement of equipment or components.
\r\n\tOn the other hand, predictive maintenance analyses the equipment condition so that a possible fault can still be identified at an early stage. Predictive maintenance aims to identify a machine anomaly so that it does not result in a fault. Such maintenance involves advanced monitoring, processing, and signal analysis techniques, which are generally performed non-invasively and, in many cases, in real-time. In the case of machines or processes, these techniques can be developed based on vibration, temperature, acoustic emission, or electrical current signal monitoring. It should be noted that monitoring such signals or parameters to verify the operating condition is called condition monitoring. Condition monitoring aims to observe the machine's current operational condition and predict its future condition, keeping it under a systematic analysis during its remaining life. In this sense, a fault condition can be detected and identified from systematic machine condition monitoring. A diagnosis procedure can be established, whereby properly investigating the fault symptoms and prognosis.
\r\n\t
\r\n\tThis book will aim to merge all these ideas in a single volume, aggregate new maintenance experiences, apply new techniques and approaches, and report field experiences to establish new maintenance processes and management paradigms.
\r\n\t
The overall composition of milk depends on a range of factors including genetics (species and breed), physiological state (age and stage of lactation) and environment (food and climate) [1–5]. While water is the main constituent of milk, comprising ~87% of the total volume, the remainder is composed of carbohydrates, fats and proteins in varying volumes across different species [6–8]. Among the numerous nutritional benefits of milk, milk proteins have gathered enormous attention for being a ‘complete’ protein as they provide all nine essential amino acids (leucine, isoleucine, valine, phenylalanine, tryptophan, histidine, threonine, methionine, lysine) required by humans [9]. The proteins in milk are categorised into major proteins that include casein and whey fractions [1] and minor proteins that include lactoferrin, lactoperoxidases, lipases, lactase [6, 10] and miscellaneous proteins (cytokines, immunoglobulins, etc.) [11].
\nThe process of breaking down milk proteins to shorter peptide sequences is termed ‘hydrolysis’. This process happens naturally in the gastrointestinal tract and can be simulated in the laboratory or on an industrial scale. During the normal transit through the gastrointestinal tract, milk proteins are exposed to proteinases such as pepsin, trypsin and chymotrypsin which break them down into smaller peptides. These peptides are further digested by brush border peptidases present at the surface of intestinal epithelial cells where they produce amino acids; however, some oligopeptides still remain intact [12]. In laboratory or at an industrial scale, milk hydrolysates are released either by treatment of milk proteins with food grade enzymes or through fermentation with bacteria, which is described in detail in the following sections.
\nThe shorter peptide sequences often possess bioactive properties beyond their nutritional contribution along with eradicating any protein-specific allergenicity [13, 14]. Processing and enriching for food grade bioactive peptides is a goal for the functional food industry. A functional food can be described as:
\nOnce the hydrolysates are released, they can potentially have bioactive properties which can exert their effects in receptive cells, including those present in the gastrointestinal tract [16]. The bioactivities of the resulting hydrolysates are variable depending on a range of factors, including the enzyme used, the processing conditions and the final size of the peptide sequence following hydrolysis [17]. The degree of hydrolysis (DH) is defined as the percentage of cleaved peptide bonds, i.e. the number of hydrolysed bonds per total number of peptide bonds in the protein [18]. This affects the size and amino acid composition of the peptides, which subsequently determines the biological activity of the peptide. Hence, DH is an important consideration from the perspective of functional food research [19].
\nThe enzymatic hydrolysis process is conducted under mild conditions (pH 6–8, temperature 40–60°C) to minimise side reactions and to retain the amino acid composition similar to the starting material [17]. Enzymatic hydrolysis improves the solubility and heat stability of peptides, which is of benefit to the food industry. However, consumption of certain enzymes leads to allergic or toxic responses; hence, consumer safety is an important factor and requires the regulation of enzymes used for hydrolysis [20]. Enzymes that obtain ‘generally recognised as safe’ (GRAS) status and special approval of ‘food grade’ quality are legally considered as safe [20]. The food grade enzymes generally used to hydrolyse milk proteins into hydrolysates include pepsin, trypsin and chymotrypsin [21, 22]. In addition, food grade proteolytic enzymes, derived from microorganisms, can also be used to generate hydrolysates [23]. Proteolytic enzymes are of two types, depending upon their hydrolysing mechanism: endopeptidases which hydrolyse peptide bonds within protein molecules and exoproteases which hydrolyse N or C terminal peptide bonds. Post enzymatic hydrolysis, the hydrolysates usually need an additional treatment. The most common procedures include ultrafiltration, heat treatment and/or activated carbon treatment to control molecular size and elimination of bitterness in the hydrolysates [17].
\nFermentation of milk proteins with proteolytic starter culture is another method of bulk production of hydrolysates. Safety measures should be considered with regard to toxicity and pathogenicity associated with the microorganisms used for fermentation. Food grade microorganisms with no related toxigenic and pathogenic response in humans are widely used. During microbial fermentation, milk proteins are subjected to ‘splitting’ as they are broken down by the proteolytic system of microorganisms [24]. Bacterial cultures of
The
After the generation of milk hydrolysates, their bioactivity profile needs to be determined. In laboratory or at an industrial scale, the primary screening for the bioactivity is performed on
Although cell- and tissue-based model systems are an alternative to animal experiments, they do not reflect the
To date, the bioactivities of a wide variety of hydrolysates have been characterised using
~ | \nEH | \nBifidogenic | \n[51, 52] | \n|
\n | \n | EH | \nAntimicrobial | \n[62] | \n
\n | \n | EH | \n↑Mucin | \n[72, 77] | \n
\n | \n | EH | \n↑IgG, ↑IgA | \n[88] | \n
\n | \n | EH, Fermentation, PS | \nImmunomodulation | \n[37, 38, 92, 93, 99] | \n
α-S1 casein | \n9.1 | \nEH | \nAntimicrobial | \n[62] | \n
\n | \n | EH, Fermentation | \n↑IgG, ↑IgA | \n[86, 87] | \n
α-S2 casein | \n2.4 | \nEH | \nAntimicrobial | \n[62] | \n
\n | \n | EH, Fermentation | \n↑IgG, ↑IgA | \n[86, 87] | \n
β-Casein | \n8.5 | \nEH | \n↑Mucin | \n[74, 75] | \n
\n | \n | EH, Fermentation | \n↑IgG, ↑IgA | \n[86, 87] | \n
k-Casein | \n3.0 | \nEH | \nAntimicrobial | \n[64] | \n
\n | \n | EH | \nImmunomodulation | \n[94, 100, 101] | \n
~ | \nFermentation | \nBifidogenic | \n[53] | \n|
\n | \n | EH | \nAntimicrobial | \n[60] | \n
\n | \n | EH | \n↑Mucin | \n[78, 79] | \n
\n | \n | EH | \n↑IgG, ↑IgA | \n[89] | \n
\n | \n | EH | \nImmunomodulation | \n[89] | \n
α-Lactalbumin | \n1.1 | \nEH | \nAntimicrobial | \n[60, 65] | \n
\n | \n | EH | \n↑Mucin | \n[73, 80] | \n
β-Lactoglobulin | \n2.8 | \nEH, Fermentation | \nBifidogenic | \n[54] | \n
\n | \n | EH | \nAntimicrobial | \n[60] | \n
\n | \n | EH | \n↑Mucin | \n[76] | \n
Lactoferrin, lactoperoxidase, lysozyme, proteose-peptone, glycomacropeptide | \n~3% | \nEH | \nBifidogenic | \n[55, 56, 58] | \n
\n | \n | EH, PS | \nAntimicrobial | \n[67, 68, 69] | \n
\n | \n | EH, PS | \n↑IgG, ↑IgA, ↑IgM | \n[90] | \n
Milk protein hydrolysates, content in cow’s milk, hydrolysis process used and their related bioactivity.
EH, enzyme hydrolysis; PS, peptide synthesis
The World Health Organisation now recommends breastfeeding for up to 6 months, as breast milk has a major positive impact on the health and growth of the infant [41]. One of the most important benefits of breastfeeding the newborn is the colonisation of the gut by ‘healthy’ microbiota. ‘Healthy’ gut microbiota confers nutritive, metabolic and protective functions that affect intestinal physiology, immunity and whole-body metabolism. The establishment of a ‘healthy’ microflora in the gut during early life is crucial for the healthy development of a balanced immune regulatory network in the gut, a feature which affects the overall health of the individual [42]. Beneficial gut microorganisms aid gut health by releasing growth substrates from milk [43], improving vaccine responses [44] and decreasing gut permeability [45, 46]. After birth, the gut is colonised with bacteria from four main phyla namely
Milk hydrolysates show bifidogenic activity, i.e. they support the growth of Gram-positive anaerobic bacteria namely
Antimicrobial milk peptides prevent attachment and invasion of pathogens by either directly interacting with the pathogen and killing them or changing the host environment, leading to the inhibition of growth of microorganisms [59, 60]. The direct interaction of antimicrobial milk hydrolysates with microorganisms is specific, as they show affinity towards polarised bacterial membranes rather than dipolar membranes of eukaryotic cells [50]. There is growing evidence that the antimicrobial property of milk hydrolysates is related to the formation of α-helical structure of the peptides. The modifications of peptide’s secondary and tertiary structures by phosphorylation of specific amino acid or chemical modification of C or N terminal dramatically affects the antimicrobial activity [50, 61]. Another mode of action for antimicrobial peptides is by aggregating in the cytoplasmic membrane, disrupting the membrane permeability of bacteria, and causing cell death [13, 30]. On the contrary, the indirect antimicrobial activity of milk hydrolysates is achieved by decreasing the host intestinal pH and thus limiting the growth of pathogenic microorganisms. This mechanism is also known as ‘colonisation resistance’ [57].
\nThe antimicrobial effects of milk hydrolysates have been listed in Table 1. Casein is a major source of antimicrobial peptides, and hydrolysates of α-S1 casein exert protective effects against
The intestinal epithelial cell layer of the gastrointestinal tract lies at the border between the gut-associated lymphoid tissue (GALT), which is the most abundant accumulation of lymphocytes in the body, and the intestinal lumen which contains a high number of dietary antigens and a varied commensal microbiota [70]. The intestinal epithelial cell layer is covered by a mucus gel, which functions as a protective layer for the gastrointestinal system. This barrier function includes the prevention of entry of pathogenic microorganisms, toxins and allergens. The mucus gel is composed of glycoproteins called mucins, with up to 20 mucin genes identified. Mucin genes are expressed by specific cells (goblet cells and enterocytes) and categorised as gel-forming secretory mucins (
Milk hydrolysates can influence the expression and secretion of mucins, as outlined in Table 1. The modulation of mucin production by milk hydrolysates may assist in the development of dietary strategies to enhance and protect the mucus layer. In rats, jejunal
The intestinal mucosa exists in a non-pathological state of continuous ‘physiological inflammation’. This low level of inflammation is required to prime the GALT for potential pathogenic bacteria [82]. The mucosal immune system features immune cells including neutrophils, monocyte/macrophages, dendritic cells, mast cells, B and T cells. The crosstalk between intestinal epithelial cells, gut microbiota and local immune cells is essential to maintain intestinal homeostasis, whereas, dysregulation leads to chronic intestinal inflammation [83]. Much of the experimental data come from model organisms such as mice and rats; however, a number of studies have been carried out in humans. Several examples of anti-inflammatory activity exhibited by a variety of milk hydrolysates across a range of experimental models are listed elsewhere [59, 60, 82, 84].
\nSeveral milk protein hydrolysates enhance immune cell function by increasing secretion of immunoglobulins, as outlined in Table 1. Immunoglobulins are glycoprotein molecules that specifically recognise antigens from bacteria or viruses and aid in their destruction through a highly complex and specific immune response [85]. Hydrolysates of αs1-casein, αs2-casein and β-casein stimulated the immune system through the enhancement of immunoglobulin G (IgG) and IgA concentrations [86, 87]. Casein hydrolysates conferred protective effects against pathogenic microorganisms in mice challenged with bacterial endotoxin, LPS, by increasing intestinal and faecal IgA and anti-LPS IgA levels [88]. Similar modulation of immune response was recorded in mice against
Immune cells, such as monocytes and macrophages, play an important role in inflammatory responses and tissue repair and remodelling by either interacting directly with microorganisms during infections and/or secretion of cytokines that mediate biological effects [91]. Milk hydrolysates can modulate the gastrointestinal immune system by modulating proliferation and maturation of localised immune cells; the immunomodulatory activities of milk hydrolysates are outlined in Table 1. Casein peptides induced innate host immune responses in humans, by stimulating the proliferation of lymphocytes and macrophages, [92] and in mice, by activating monocytes and macrophages [93]. On the contrary, rennin-digested κ-casein fragments inhibited the proliferation of mouse spleen lymphocyte and rabbit Peyer’s patch cells [94]. The mechanisms of this κ-casein fragment include acting either as an anti-IL-1 antibody or suppressing IL-2 receptor expression on CD4+ T-cells [95]. Functionally, the phagocytic activity of inflamed murine macrophages was increased by
Particular milk hydrolysates modulate the MAP kinase and NF-κβ pathways that consequently control the secretion of several cytokines that can induce inflammatory responses and strengthen the host defence mechanisms [97]. Mice supplemented with
The potential health benefits of milk hydrolysates are a subject of growing commercial interest from a health-promoting functional-food perspective. Several commercial products are currently available in the market, and this trend is likely to continue. There are three major areas where developments can be made. The generation of milk hydrolysates is the first area of development. The generation and processing of food grade milk hydrolysates should be carefully designed to yield hydrolysates with diverse bioactivities. Novel technologies can be developed, focussing on the process of enrichment of the hydrolysates with active peptides from milk proteins. The second area of development is the research technologies used to evaluate the bioactivity of milk hydrolysates. The investigation of biochemical properties using newly developed modern analytical technologies is required to understand the cross reactivity between milk hydrolysates and the carrier food matrix. Third, robust platforms should be developed to study the molecular mechanisms by which the bioactives exert their activities. This area is the most challenging research area as the outcome from these studies forms the basis of tailored dietary formulations.
\nThe Quaternary is characterized worldwide by important climate oscillations, with extremes represented by glacial and interglacial periods resulting from temperature variations that caused marked changes in sea level (e.g., [1]). In coastal areas, transgressive-regressive events have generated a sequence of erosion forms (coastal terraces and paleocliffs) and beach deposits that, for different reasons, have been protected from degradation processes and are therefore an important testimony of climate changes that have occurred in most recent geologic time [2].
In 1941, Milankovitch developed a planetary theory that attributes Quaternary glacial and interglacial cycles to modifications of orbital parameters such as eccentricity (100 Ka), obliquity (41Ka), and precession of the equinoxes (19 Ka).
Since the beginning of the Pleistocene, climatic oscillations would have followed periodic cycles of about 40 Ky that seem to conform the variation cycle of the earth axis. The amplitude of the cycles tended to increase 1.5 My ago, and from 600 Ka the glacial cycles have occurred at intervals of between 80 and 120 Ky (e.g., [3, 4]). This duration of the recent cycles is similar to the period of variation of the eccentricity of the earth orbit, of 100 Ky.
The different glacial and interglacial events occurred during the Quaternary were differentiated through the marine isotope stages (MIS). These MIS represent alternate cold and warm periods established on the basis of δ180 of benthic foraminifers, obtained from cores of the sea bottom [5]. Emialiani [6] divided the last million years in successive isotopic stages on the basis of the δ180/δ160 relationship. Each isotopic stage represents a glacial period (designated with an odd number) or interglacial (designated with an even number), and reveal the advance and retreat of the ice during the last glaciations.
Globally, the MIS 11 encompasses from 424 to 374 ka. It was a long warm period that reached a global mean sea level of 6 to 13 m above the present one between 410 and 400 ka [2]. Some authors (e.g., [7, 8, 9]) consider the MIS 11 as an analogous of the Holocene both in climatic conditions and orbital forcing. According to Ashton et al. [10] the climatic conditions in marine isotopic and ice sheet records include at least two large warm episodes with an intermediate cooling phase. The warm conditions of this interglacial were reflected in different marine and terrestrial communities (e.g., [9, 11, 12]).
MIS 9 encompasses from ca. 330 up to 310 ka and sea level was 3 ± 3 m below the present one [13]. In the Northern Hemisphere, at Henderson Island (24°22’S/128°20’W), the highest sea level recorded in MIS 9 is between 334 ± 4 and 324 ± 3 ka in agreement with the maximum sun insulation of 333 ka [14]. In the western Mediterranean (Spain) the sea surface temperature (SST) and the salinity recorded in this interglacial were similar to those of MIS 7 and MIS 5e [15], whereas other authors (e.g., [16]) suggested that according to paleontological evidence, this interglacial was warmer than MIS 7 and the Holocene, and similar to MIS 5e.
MIS 7 encompasses from ca. 245 up to 190 ka [17] with three temperature maximums [18]. Isotopic data of some deep sea cores suggest that the sea level would not have reached the level of the present cero [19, 20], although other authors suggest values around −18 m [17]. SST of this interglacial was higher than the present one [21, 22, 23]. In the European coasts, the marine deposits of MIS 7 record the appearance of the “Senegalese” marine fauna from the African coast, confirming this stage as warm in the Northern Hemisphere (e.g., [24, 25, 26]). Similar conditions are observed in the Southern Hemisphere: the SST of the southern Argentine Patagonia (42°–43°S) is proposed to be similar or slightly warmer than today on the basis of the record of warm water mollusks (e.g., [27, 28]).
MIS 5 in the substage e, is one of the most studied episodes, and best represented worldwide. It encompasses from ca. 130 ± 2 to 119 ± 2 ka [29] and the SST was approximately 2°C higher than the present one (e.g., [30, 31]). Comparing with other interglacials, MIS 5e has the best records of SST [18]. Evidence of warm water benthic mollusks, and changes in their geographic distribution was found in MIS 5e (e.g., [5, 26, 27, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48]).
MIS 1 encompasses the last 11.7 ka [49], when the last glaciation is considered to be ended [50]. There is an increase of the SST and humidity worldwide (e.g., [4, 51, 52, 53, 54, 55, 56]) with some records in the Southern Hemisphere (e.g., [37, 49, 50, 57, 58, 59]). This phenomenon is reflected worldwide in the biotic communities with changes in composition, abundance, diversity and distribution (e.g., [60, 61, 62]).
In the Argentine Patagonian region, the stages MIS 11 to MIS 1 are represented, as well as ingressions older then MIS 11, but with poor records and fossil content [32].
Along the Argentine coast, broad extensions of the littoral of the Buenos Aires Province (BAP) and north Patagonia were affected by accumulation and erosion processes produced by sea level oscillations during Quaternary transgressions (e.g., [63, 64]).
Northern Patagonia has been divided into two regions according to their province. The first groups three areas of the south of the BAP (A-C) and record the presence of the interglacials ≥ MIS 9, MIS 5e and MIS 1 [5, 65, 66], and the other one belongs to region D, and records the presence of the interglacials ≥ MIS 9, MIS 7, MIS 5e, and MIS 1 (Figure 1).
(A) Map of study, and (B) four areas in the northern Patagonia in Argentina.
In region A, from Peninsula Verde to Otero Island, the transgressive deposits have been assigned to the Sangamon (? Late Pleistocene), which are represented in the area of the Colorado River delta by paleocliffs associated with coast lines up to 10 m height [67]. These marine deposits are assigned to the oldest interglacials because of their geomorphological, altimetric and cementation similarity [68]. Among them, there are scarce, thin, and isolated deposits on the continent which are assigned to ≥ MIS 9 [68, 69]. The terminal area of the delta is formed by the marine deposits of the MIS 1 ingression, which are beach ridges or intertidal environments [68].
In region B, which extends from the Otero Island to near the Jabalí Island, Weiler [70] correlated the Pleistocene and Holocene marine deposits of the central area with three transgressive events of the Late Pleistocene and Holocene, and related them to environments of barriers and coastal lagoons of the transgression of the Sangamon interglacial (with a minimum age of 43 Ka), the interstadial transgression of the middle Wisconsin (38.5 to 25 Ka), and the postglacial transgression of the MIS 1 (middle Holocene, between 5 and 5.2 Ka). More recently, Schnack et al. [71] related the oldest deposits of the area described by Weiler [43] with the Interglacial MIS 5e, considering the radiocarbon datings as minimum ages.
In region C, from the Jabalí Island up to Villa 7 de Marzo, Fucks et al. [68] reinterpreted the stratigraphic sequences, assigning a minimum of four transgressive cycles. Beach ridges, as well as beach strand plains and tidal plains, with maximum altitudes of 6 m a.s.l. and very clear morphologies are present from the coast to the present day continent, particularly in Isla Jabalí. Above them, at altitudes of 8 to 10 m a.s.l. that increase gradually to over 30 m a.s.l., clear ridges could be probably related to MIS 5e. These could have been originated in two ≥ 9 transgressive events.
In region D, north of San Matías Gulf from near the El Cóndor beach up to Las Grutas beach, there are records of the interglacials MIS 7, MIS 5e and MIS 1 plus a fourth one, 60 m height, that probably corresponds to an interglacial ≥ MIS 9. According to Fucks et al. [72] the deposits of interglacials MIS 7 and MIS 5e correspond to Baliza San Matias and San Antonio formations, respectively, and those of Holocene age have no designation.
The main geomorphological features are littoral ridges formed by high energy conditions, although, deposits corresponding to intertidal environments, coastal lagoons, spit sand cliffs forms have been described mainly for the Holocene transgressive event as well (e.g.,[5, 68, 72, 73, 74, 75]).
All these deposits contain marine mollusks, particularly gastropods and bivalves (Figure 2) (Table 1) [5, 35, 36, 37, 65, 82].
(A) Profile of Holocene deposit with
Province | Área | Coordinates (Lat-long) | Sites | Ages (14C and ESR) | Altitude (m.a.m.s.l) | Cites |
---|---|---|---|---|---|---|
South of Buenos Aires | Delta del río Colorado | 39°20′S;62°04′W–39°55′S;62°08′W | P. Verde (39°21′S;62°5.9′W) | 2170 ± 86 ka | 5–2.5 | [76] |
Pta Laberinto – rio Colorado Viejo (39°30′S–39°50′S) | 6.63 ± 0.12 ka–0.409 ± 0.10 ka | 10–7.5 7.5 and 2 | [74] | |||
Sur del río Colorado viejo (39°53′S; 62°10′W) | 9.46 ± 0.12 ka–0.407 ± 0.10 ka | 5–2.5 | [74] | |||
Bahía Anegada | 39°55′S;62°08′W–40°28′S;62°11′W | Pleistocene deposits (40°03′S–40°26′S) | 43 ka, 38.55 ka, 25 ka | 40–25 | [70, 77] | |
43 ka, 38.8 ka, 31 ka | 10–7 | [75] | ||||
Canal Villalonga (40°1’S; 62°19’W) | 5.98 ± 0.10 ka–3.69 ± 0.10 ka | 4–2.5 | ||||
Los Pocitos (42°25′S; 62°25′W) | 4.4 ± 0.08 and 4.5 ± 0.09 ka | 3 | [72, 74, 78] | |||
Isla Jabalí – Villa 7 de marzo | 40°36′S;62°11′W–41°1′S;62°45′W | Oeste de isla Jabalí (40°40′S;62°30′W) | 30.78 ± 1.65 ka–28.4 ± 0.80 ka | 3–9.5 | [75, 79] | |
Isla Jabalí (40°34′S;62°13′W) | 5. 37 ± 0.11 ka-2.17 ± 0.11 | 4–5 | [37] | |||
Faro Segunda Barranca (40°46′S;62°16′W) | 102–108 ka 94.5, 79 and 72.7 ka 28 a 40 ka | 8–10 | [80, 81] | |||
Northern of Rio Negro | Norte del golfo San Matías | 40°51′S;65°7′W–41°02′S; 62°49′W | Caleta Falsa correlation with localities: south of Piedras Coloradas | ≥230 and ≥169 ka | 8–12 | [80, 81] |
Baliza San Matias (40°42′S; 64°51′W) | 97.3–83 ka | 8 | [73] | |||
La Rinconada (40°41′S;65°9′W) | 107–91 ka | 10 | ||||
Las Grutas (40°48′S;65°4′W) | 70.3–66.8 ka | 10 | ||||
La Conchilla (40°49’S/64°52’O) | 2.43 ± 0.60 ka | 1.50 | [5] |
Absolute dating available from the study área.
A total of 84 localities were studied in two areas, 31 Pleistocene, 29 Holocene, and 24 modern ones. In these localities 7385 valves and shells of mollusks were collected. Each coastal deposit to be studied is identified on topographic maps. At each level of the site, a volumetric sample of 1 dm3. In contrast, at modern beach sites the sample is taken in a quadrant 1 m x 1 m along transects perpendicular to the coast line.
Each fraction of biogenic content recovered from the sieves (2.80, 1.40 and 0.080 mm) was identified, measured with digital caliper, and labeled. Species were identified through catalogs and specific literature.
Valves and shells found in the marine deposits are considered as assemblages representing the accumulation of non-contemporary individuals in a single set, and occurs because the time of generation of these individuals is faster than the burial rates. In this context, it has to be taken into account the changes produced during the transition of the animal remains from the biosphere to the lithospere, which is studied through a discipline called taphonomy (etymologically derived from the Greek taphos, tomb, and nom, law). Taphonomy was defined by Efremov [83] as the science that studies the laws of burial, and accepted that taphonomic processes lead to the loss of information and are the cause of gaps in the fossil record. Currently this concept has been reversed since numerous studies (e.g., [84, 85, 86, 87]) support the idea that the faunal associations of both current and fossil valves provide relevant information on living communities, or paleocommunities, being able in both cases to reconstruct the environments or paleoenvironments from the analysis of the faunal associations and thus interpret environmental and climatic changes.
The studied mollusks form transported faunal associations, which, according to different authors, preserve compositional fidelity concerning taxonomy and relative abundance of the communities that inhabited each environment within the considered period, and represent the accumulations of non-contemporary individuals as a whole.
The four areas identified in northern Patagonian according to their geomorphology (A-D), in which 84 sites were studied, yielded 78 species (42 bivalves and 36 gastropods). Eleven of them are micromollusks:
Bivalves | Salinity | Life habit | Depth (m) | Substrate | Trophic type | Distribution area |
---|---|---|---|---|---|---|
E | I | 0–200 | S | D | 23°S–53.5°S | |
E | I | 5–1850 | S | D | 22.93°S–55.5°S | |
E | I | 20–75 | S | D | 22.93°S–39°S* | |
E | I | 10–75 | S | Sf | 10°S–42°S | |
P–E | Ep | 0–50 | H | Sf | 68°N–55.5°S | |
P–E | Ep | 0–25 | H | Sf | 34°S–42°S | |
E | Ep | 0–30 | H | Sf | 34°S–55.5°S | |
E | Ep | 10–120 | M | Sf | 21°S–42.58°S | |
P–E | Ce | 0–3 | H | Sf | 35°N–35°S* | |
E | Ce | 0–120 | H | Sf | 35.3°N–34°S* | |
P–E | Ce | 0–80 | H | C | 37°N–42°S | |
P–E | Ce | 0–70 | H | C | 22°S–42°S | |
P–E | Ce | 0–50 | H | C | 21.4°S–35°S | |
E | Ce | 0–40 | H | Sf | Cosmopolitan | |
E | I | 36–102 | S | Sf | 21°S–42.58°S | |
E | I | 25–77 | S | Sf | 21°S–42°S | |
E | I | 17–70 | S | Sf | 23°S–39°S* | |
E | I | 0–11 | S | Sf | 35°N–42°S | |
P–E | I | 0–25 | S | Sf | 34°S–42°S | |
P–E | I | 0–25 | S | Sf | 23°S–42°S | |
P–E | I | 0–11 | S | Sf | 39°N–41°S | |
E | I | 0–20 | S | Sf | 23°S–41°S | |
E | I | 10–18 | S | Sf | 23°S–39°S* | |
E | I | 18–70 | S | D | 29°S–39°S* | |
E | I | 13–55 | S | D | 23°S–43°S | |
E | I | 0–50 | S | D | 35°N–23°S* | |
P | I | 0–10 | S | Sf | 42°N–54°S | |
E | I | 0–55 | S | Sf | 21°S–42°S | |
P–E | I | 0.3–5 | S | Sf | 18°N–39°S* | |
E | I | 10–100 | S | Sf | 22°S–38.7°S* | |
E | I | 0–20 | S | Sf | 19°S–43°S | |
E | I | 50–70 | S | Sf | 34°S–55.5°S | |
E | I | 5–50 | S | Sf | 34°S–54°S | |
E | I | 25–75 | S | Sf | 23°S–48°S | |
E | I | 15–90 | S | Sf | 23°S–43°S | |
E | I | 11–67 | S | Sf | 19°S–43°S | |
E | I | 10–27 | S | Sf | 6°S–42°S | |
E | I | 15–150 | R | Sf | 34°S–43°S | |
E | I | 50–86 | S | Sf | 38.3°S–41°S | |
E | I | ? | S | Sf | 35°S–40.5°S | |
E | I | 50–86 | S | Sf | 22°S–42.58°S |
Ecological requeriments and distribution of bivalves.
Taxa found in the studied area.
The references of species are found on MolluscanBase eds(2021).
Ep, epifaunal; I, infaunal; Ce, cemented; H, hard; S, soft; C, carnivorous; D, detritivorous; He, herbivore; Sf, suspension feeder; O, oligohaline (3–8‰); M, mesohaline (8–18‰); P, polyhaline (18–30‰); E, euhaline (>30–35‰).
Gastropods | Salinity | Life habit | Depth (m) | Substrate | Trophic type | Distribution area |
---|---|---|---|---|---|---|
E | Ep | 0–200 | H | He | 38.5°S–55.5°S | |
E | Ep | 0–15 | H | He | 11°N–45°S | |
E | Ep | 0 | H | He | 48°S–55°S | |
E | Ep | 0–55 | H | He | 23°S– | |
E | Ep | 0–60 | S | He | 40.37°S–41.67°S | |
E | Ep | 13–86 | S | He | 30°S–44.21°S | |
E | Ep | 0–57 | H | He | 23°S–54°S | |
E | Ep | 0–9 | H | He | 38°S–55°S | |
E | Ep | 0–46 | H | Sf | 25°S–45.8°S | |
E | Ep | 30–50 | H | Sf | 38°S–41.03°S | |
E | Ep | 0–66 | H | Sf | 35°S–55.8°S | |
E | I | 0–113 | S | C | 22.4°S–42.58°S | |
O, P, M | Ep | 0–60 | M | He | 24°S–41°S | |
E | Ep | 0–101 | M | He | 23.37°S–44.27°S | |
E | Ep | 30 | M | He | 23°S–41°S | |
E | Ep | 0–50 | H | C | 32°S–40°S | |
E | Ep | 0–58 | H | C | 36.42°S–54.98°S | |
E | Ep | 28–28 | H | C | 32°S–41°S | |
E | Ep | 10–90 | S | C | 23°S–42°S | |
E | Ep | 0–250 | S | C | 23°S–52°S | |
E | Ep | 40–75 | S | C | 20° S–52°S | |
E | Ep | 10–200 | M | C | 35°S–55.2°S | |
E | Ep | 10–80 | S | C | 22.93°S–42°S | |
E | Ep | 15–57 | S | C | 23.69°S–43°S | |
E | Ep | 5–50 | S | C | 19°S–42°S | |
E | Ep | 0–22 | S | C | 23°S–42.5°S | |
E | Ep | 0–30 | S | C | 23°S–40.6°S | |
E | Ep | 0–50 | S | C | 35°N–42°S | |
E | Ep | 5–66 | S | C | 23°S–42.58°S | |
E | Ep | 0–6 | S | C | 35°S–46°S | |
E | Ep | 15–45 | S | C | 24°S–42°S | |
E | Ep | 10–65 | S | C | 30°S–54°S | |
E | Ec | 0–20 | S | C | 35°N–54°S | |
E | Ec | 18–57 | S | C | 35°S–41°S | |
E | Ec | 30–65 | S | C | 39°S–41°S | |
E | Ec | 30–65 | S | C | 40°S–46°S | |
E | Ep | 0 | H | He | 32°S–55.22°S |
Ecological requeriments and distribution of gastropods.
The references of species are found on MolluscanBase eds(2021).
Ep, epifaunal; I, infaunal; Ce, cemented; Ec, ectoparasite; H, hard; S, soft; M, mixed; C, carnivorous; D, detritivorous; He, herbivore; Sf, suspension feeder; O, oligohaline (3–8‰); M, mesohaline (8–18‰); P, polyhaline (18–30‰); E, euhaline (>30–35‰).
Seventy species were identified in areas A-C (37 bivalves and 33 gastropods), and 45 species in region D (19 bivalves and 24 gastropods), with a similarity of 51.3% in bivalve species and 48.5% in gastropods.
In areas A-C, all the studied sites assigned to the interglacial ≥ MIS 9, are paleobeaches and littoral ridges; i.e., high energy environments in which the marine fauna is euryhaline (salinity > 30–35 gr/l) and of sandy substrate. Warm water species prevailed in bivalve associations (50–67%) compared to the other interglacials recorded in the area. However, no bivalve or gastropod of warm lineage that constitutes itself a paleoindicator was found.
Interglacial MIS 5e is represented in all the studied sites mostly by littoral ridges in which most associations are euryhaline, of sandy substrate and subordinate rocky substrate. Most species are epifaunal except in region A, prevailing filter feeders and carnivores. The proportion of warm water species in this interglacial is lower than in the previous one (44–50%) being outstanding the record of the warm lineage bivalve
Interglacial MIS 1 was recorded in the whole study area, with two types of deposits in areas A-C: littoral ridges (high energy environments) and tidal plains (low energy environments). In the first ones, the malacofaunal associations are mostly euryhaline, of sandy substrates. In the second ones instead, the associations vary in salinity from oligohaline to mesohaline-polyhaline (salinity between 3 and 30 gr/l), of fine sand substrate, mostly epifaunal and filter feeders prevailing infaunal and carnivores in region A. This latter would be related to the modern geomorphological features of low energy environments (wide tidal plains, tidal channels and non-functional fluvial courses), that resulted in the formation of islands which can be seen in all the southern coast of the Buenos Aires Province. This interglacial MIS 1 is recognized in area D in littoral ridges, being the malacofaunal associations mostly euryhaline, of sandy substrate with rocky subordinate. In the associations of MIS 1 there is 45 to 50% of warm water species in areas A-C, unlike areas D in which this proportion is only 18% of the total bivalves.
In modern beaches of the south of BAP, but not in the northern sector of Bahía Anegada there are sandy beaches together with mud-sandy ones, and malacofaunal associations correspond to marine parameters of high energy, euryhaline of sandy substrate with scattered rocky substrate, mainly in area C. Instead, the modern beaches of area D are larger often exceeding hundreds of meters wide. There are two types of beaches regarding the granulometry: a low intertidal sector of fine to medium sand with high distal sectors of gravels, organogenic in composition, and a low intertidal sector and high distal one of fine-medium sand. Both are associated with high energy environments where the malacological associations are mostly euryhaline, of sandy substrate, with less proportion of fauna of scattered rocky substrate. There is one exception, the modern beach of Villa 7 de Marzo which has a particular feature, fine sand substrate with abundance of two bivalves
In area D, all the analyzed sites of MIS 7 correspond to paleobeaches. They are currently represented by coastal platforms, of high energy, with mostly euryhaline malacofaunal associations of sandy substrate and subordinated rocky substrate. Respect to the indicators of sea water temperature, these associations are formed only by 20% of warm water bivalves, although it is recorded the gastropod
In MIS 5e there is a slightly higher proportion of associations of warm waters (27%) with respect to the previous interglacial, being conspicuous the presence of
In MIS 1 the associations of warm water are in lesser proportion than those of MIS 5e (18%), being outstanding the record of
Paleoecological features of all regions (A–D) in interglacial MIS 5e.
Paleoecological features of all regions (A–D) in interglacial MIS 1.
Paleoecological features of all regions (A–D) in modern beaches.
Paleoecological features of region D in interglacial MIS 7.
These two interglacials recorded in area D were not recorded in the northeast of BAP. In areas A-C, a total of nine species of mollusks were recorded in the Interglacial ≥ MIS 9, and among them, there is 50–67% of warm water species of bivalves, being this the oldest record of marine mollusks for the BAP. In MIS 7 analyzed in area D, a total of 11 species was recorded with 20% of warm water bivalves. Most recorded species in both interglacials still inhabit the modern coasts of Argentina, except for the gastropod
Both interglacials (≥MIS 9 and MIS 7) revealed the presence of warm water mollusks which are not recorded in the marine deposits of the northeast of BAP where these deposits have not been preserved [124]. The record of these interglacials in the BAP is a novelty in the analysis of gastropods and bivalves. Whereas Aguirre et al. [27, 28] reported that in the coasts of southern Patagonia, in areas such as Bahía Vera-Camarones (44.2° to 45°S) and Bahía Bustamente-Caleta Olivia (44.9°–45.3°S, Chubut Province, Argentina), the environmental conditions (substrate, depth, and energy conditions) during the late Pleistocene (MIS 7 and MIS 5e) suggest SST similar to those of the modern littoral and even slightly higher than present, recording faunas of warm to temperate waters.
In the marine deposits of this interglacial in area D, 44 molluskan species (25 bivalves and 19 gastropods) were recorded. These deposits are represented by littoral ridges and tidal plains along the south of the BAP coast, and by littoral ridges along area D, with scarce content of calcium carbonate, favoring the record of mollusks. In area C the associations of MIS 5e and MIS 1 have respectively 34 and 33 species. This similarity was also found in area D, in which 22 species were recognized for MIS 5e and 23 for MIS 1. Unlike area D, the mollusks of MIS 5e of the northeast of the BAP are characterized by less abundance and diversity of species related to those of the Holocene MIS 1 [32]. This could be due to a less representation of the Interglacial MIS 5e, and because most valves and shells of Pleistocene deposits are dissolved and/or crystallized, preventing the species identification.
Between 50 and 44% of warm water species of bivalves recorded in the Interglacial MIS 5e of area D, are represented in areas A-C, whereas this relationship is only 27% of the species from area D. Warm water mollusks were recognized in the study area, among the most prominent species of this interglacial, in areas A-C, is the bivalve
The warm species of Pleistocene. (A)
Another warm lineage species found in area D, is the bivalve
A total of 58 species (31 bivalves and 27 gastropods) was recorded in the marine malacofauna of the Interglacial MIS 1 of northern Patagonia (areas A-D), which differs from the northeast of BAP where Aguirre [89] reported a total of 62 species (25 bivalves and 37 gastropods). Concerning the molluscan composition, in the northeast of BAP, gastropods are more abundant than bivalves both in number of species and of individuals. As a comparison, among the regions studied, area A recorded 51 species (29 bivalves and 22 gastropods), and area B 49 species (25 bivalves and 24 gastropods), being in both regions, bivalves more numerous than gastropods. Whereas in area C, 34 species (17 bivalves and 17 gastropods) were recorded, unlike area D where 42 species (20 bivalves and 22 gastropods) were recorded, being in this latter the number of gastropods slightly higher than bivalves.
The marine deposits of MIS 1 in areas A-C are formed by tidal plains and littoral ridges. Tidal plains yielded mainly
The marine deposits and their malacofauna in the northeast and south (areas A-C) of the BAP are similar in the two types of deposits of the Interglacial MIS 1. The tidal plains are represented in regions A-C and are related to the development of the Colorado River and Bahía Anegada. The most common species are
Warm water vs. cold water during the quaternary in all regions (A–D).
In the last 400.000 years there were variations in the molluskan paleocommunities of north Patagonia (southern BAP and north of Río Negro Province). The marine malacofauna of this area is composed by two associations, the first one is formed by Holocene sites with abundance of
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On September, 29th 2006 he has won a post PhD fellowship from the university of Bologna (from October 2006 to October 2008), at the competitive examination he was ranked first in the industrial engineering area. He extensively served as referee for several international journals. He is author/coauthor of more than 100 research papers. He has been involved in some projects supported by MURST and European Community. His research interests include pattern recognition, bioinformatics, and biometric systems (fingerprint classification and recognition, signature verification, face recognition).",institutionString:null,institution:null},{id:"496",title:"Dr.",name:"Carlos",middleName:null,surname:"Leon",slug:"carlos-leon",fullName:"Carlos Leon",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Seville",country:{name:"Spain"}}},{id:"512",title:"Dr.",name:"Dayang",middleName:null,surname:"Jawawi",slug:"dayang-jawawi",fullName:"Dayang Jawawi",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Technology Malaysia",country:{name:"Malaysia"}}},{id:"528",title:"Dr.",name:"Kresimir",middleName:null,surname:"Delac",slug:"kresimir-delac",fullName:"Kresimir Delac",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/528/images/system/528.jpg",biography:"K. 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From 1985 to 1986, he was a Research Fellow in the Research Institute for Electronic Equipment, ZZU AD, Plovdiv, Bulgaria. In 1986, he joined the Department of Control Systems, Technical University of Sofia at the Plovdiv campus, where he is presently a Full Professor. He has held long-term visiting Professor/Scholar positions at various institutions in South Korea, Turkey, Mexico, Greece, Belgium, UK, and Germany. And he has coauthored one book and authored or coauthored more than 80 research papers in conference proceedings and journals. 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Aalborg University has Two Satellite Campuses, one in Copenhagen (Aalborg University Copenhagen) and the other in Esbjerg (Aalborg University Esbjerg).\n· He is a member of prestigious IEEE (Institute of Electrical and Electronics Engineers), and IAENG (International Association of Engineers) organizations. \n· He is the chief Editor of the Journal of Software Engineering.\n· He is the member of the Editorial Board of International Journal of Computer Science and Software Technology (IJCSST) and International Journal of Computer Engineering and Information Technology. \n· He is also the Editor of Communication in Computer and Information Science CCIS-20 by Springer.\n· Reviewer For Many Conferences\nHe is the lead person in making collaboration agreements between Aalborg University and many universities of Pakistan, for which the MOU’s (Memorandum of Understanding) have been signed.\nProfessor Akbar is working in Academia since 1990, he started his career as a Lab demonstrator/TA at the University of Sussex. After finishing his P. hD degree in 1992, he served in the Industry as a Scientific Officer and continued his academic career as a visiting scholar for a number of educational institutions. In 1996 he joined National University of Science & Technology Pakistan (NUST) as an Associate Professor; NUST is one of the top few universities in Pakistan. In 1999 he joined an International Company Lineo Inc, Canada as Manager Compiler Group, where he headed the group for developing Compiler Tool Chain and Porting of Operating Systems for the BLACKfin processor. The processor development was a joint venture by Intel and Analog Devices. In 2002 Lineo Inc., was taken over by another company, so he joined Aalborg University Denmark as an Assistant Professor.\nProfessor Akbar has truly a multi-disciplined career and he continued his legacy and making progress in many areas of his interests both in teaching and research. He has contributed in stochastic estimation of control area especially, in the Multiple Target Tracking and Interactive Multiple Model (IMM) research, Ball & Beam Control Problem, Robotics, Levitation Control. He has contributed in developing Algorithms for Fingerprint Matching, Computer Vision and Face Recognition. He has been supervising Pattern Recognition, Formal Languages and Distributed Processing projects for several years. He has reviewed many books on Management, Computer Science. Currently, he is an active and permanent reviewer for many international conferences and symposia and the program committee member for many international conferences.\nIn teaching he has taught the core computer science subjects like, Digital Design, Real Time Embedded System Programming, Operating Systems, Software Engineering, Data Structures, Databases, Compiler Construction. 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Many of these genes contribute to immunity. Particularly, MHC‐encoded class I and class II molecules, which are typically highly polymorphic and polygenic, are central in defining the specificity of the adaptive immune response. Among the diversity of genes associated with disease resistance, MHC genes are particularly interesting as they are associated with resistance and susceptibility to a wide range of diseases, some of which produce important economic losses in livestock. Enzootic bovine leukosis is an infectious disease caused by the retrovirus bovine leukemia virus (BLV), with an important economic impact, mainly in dairy herds. In this chapter, MHC‐associated genetic resistance to BLV is revised. Certain alleles of the bovine MHC (BoLA) class II locus have been found strongly associated with resistance to viral dissemination. Genetic selection of resistant animals emerges as a natural strategy for the control of infectious diseases, especially when there is no other alternative of control or prevention, as vaccines. Founded on this knowledge, a BLV control program based on selection of genetically resistant cattle was designed. The proof of concept indicates that this strategy is feasible to implement in dairy herds.",book:{id:"5405",slug:"trends-and-advances-in-veterinary-genetics",title:"Trends and Advances in Veterinary Genetics",fullTitle:"Trends and Advances in Veterinary Genetics"},signatures:"Silvina Elena Gutiérrez, Eduardo Néstor Esteban, Claudia María\nLützelschwab and Marcela Alicia Juliarena",authors:[{id:"188776",title:"Dr.",name:"Silvina Elena",middleName:null,surname:"Gutiérrez",slug:"silvina-elena-gutierrez",fullName:"Silvina Elena Gutiérrez"},{id:"189290",title:"Dr.",name:"Marcela Alicia",middleName:null,surname:"Juliarena",slug:"marcela-alicia-juliarena",fullName:"Marcela Alicia Juliarena"},{id:"189291",title:"Dr.",name:"Eduardo Néstor",middleName:null,surname:"Esteban",slug:"eduardo-nestor-esteban",fullName:"Eduardo Néstor Esteban"},{id:"189293",title:"Dr.",name:"Claudia María",middleName:null,surname:"Lützelschwab",slug:"claudia-maria-lutzelschwab",fullName:"Claudia María Lützelschwab"}]},{id:"52940",doi:"10.5772/65848",title:"Beyond Fifty Shades: The Genetics of Horse Colors",slug:"beyond-fifty-shades-the-genetics-of-horse-colors",totalDownloads:3218,totalCrossrefCites:2,totalDimensionsCites:4,abstract:"Since the dawn of horse domestication, coat colors have always fascinated humankind. In the last century, knowledge of genetics and development of scientific tools have become powerful enough so that the effects of many DNA mutations could be critically studied. Coat color nomenclature varies according to countries and breed associations; in addition, many factors can modify the color of the coat, such as sun exposure, age, sex, and nutritional status of the animal. Nevertheless, horses are capable of producing only two pigments. Several genes have been indicated as putative to coat color modification, altering the basic color by dilution, redistribution, or lacking of pigments.",book:{id:"5405",slug:"trends-and-advances-in-veterinary-genetics",title:"Trends and Advances in Veterinary Genetics",fullTitle:"Trends and Advances in Veterinary Genetics"},signatures:"Adriana Pires Neves, Eduardo Brum Schwengber, Fabiola Freire\nAlbrecht, José Victor Isola and Liana de Salles van der Linden",authors:[{id:"188768",title:"Associate Prof.",name:"Adriana",middleName:null,surname:"Pires Neves",slug:"adriana-pires-neves",fullName:"Adriana Pires Neves"},{id:"188993",title:"Dr.",name:"Eduardo",middleName:null,surname:"Brun Schwengber",slug:"eduardo-brun-schwengber",fullName:"Eduardo Brun Schwengber"},{id:"188994",title:"Mrs.",name:"Fabiola",middleName:null,surname:"Freire Albrecht",slug:"fabiola-freire-albrecht",fullName:"Fabiola Freire Albrecht"},{id:"188996",title:"Ph.D. Student",name:"Liana",middleName:null,surname:"de Salles van der Linden",slug:"liana-de-salles-van-der-linden",fullName:"Liana de Salles van der Linden"},{id:"188997",title:"Mr.",name:"José Victor",middleName:null,surname:"Vieira Isola",slug:"jose-victor-vieira-isola",fullName:"José Victor Vieira Isola"}]},{id:"59305",doi:"10.5772/intechopen.74008",title:"Avian Coccidiosis, New Strategies of Treatment",slug:"avian-coccidiosis-new-strategies-of-treatment",totalDownloads:3686,totalCrossrefCites:2,totalDimensionsCites:4,abstract:"The control of avian coccidiosis since the 1940s has been associated with the use of ionophores and chemical drugs. Recently, a significant interest in natural sources has developed due to the pressure to poultry industry to produce drug-free birds. Consequently, the search of products derived from plants and other natural sources has increased in the last years. Today, many commercial products containing essential oils, extracts, and other compounds are available. The use of these compounds of natural origin is related to an increased immune response, a body weight gain, destruction of oocyst, among other benefits. The main inconvenience of these products is the act on some species of Eimeria, but not all. This genetic variability found in the parasite makes the use of products difficult to control and treat coccidiosis. In this chapter, several proposals of treatment are presented based on the use of natural products, considering the new strategies of treatment with minimal consequences to birds.",book:{id:"5543",slug:"farm-animals-diseases-recent-omic-trends-and-new-strategies-of-treatment",title:"Farm Animals Diseases, Recent Omic Trends and New Strategies of Treatment",fullTitle:"Farm Animals Diseases, Recent Omic Trends and New Strategies of Treatment"},signatures:"Rosa Estela Quiroz-Castañeda",authors:[{id:"187735",title:"Dr.",name:"Rosa Estela",middleName:null,surname:"Quiroz Castañeda",slug:"rosa-estela-quiroz-castaneda",fullName:"Rosa Estela Quiroz Castañeda"}]},{id:"58461",doi:"10.5772/intechopen.72638",title:"Natural Compounds as an Alternative to Control Farm Diseases: Avian Coccidiosis",slug:"natural-compounds-as-an-alternative-to-control-farm-diseases-avian-coccidiosis",totalDownloads:2078,totalCrossrefCites:1,totalDimensionsCites:3,abstract:"Coccidiosis is one of the most aggressive and expensive parasite diseases in poultry industry worldwide. Currently, the most used control techniques are chemoprophylaxis and anticoccidial feed additives. Although there is a great variety of commercial anticoccidial drugs and vaccines in the market, there is also a significant resistance to use them in animals with human as final consumer. To date, none available product offers effective protection toward coccidiosis; however, the search for novel strategies to control this disease continues, and natural products have arisen as a potential way to cope with avian coccidiosis. In this chapter, we highlight recent advances in natural compounds, their anticoccidial properties, and mechanisms.",book:{id:"5543",slug:"farm-animals-diseases-recent-omic-trends-and-new-strategies-of-treatment",title:"Farm Animals Diseases, Recent Omic Trends and New Strategies of Treatment",fullTitle:"Farm Animals Diseases, Recent Omic Trends and New Strategies of Treatment"},signatures:"Mayra E. Cobaxin-Cárdenas",authors:[{id:"223051",title:"Dr.",name:"Mayra E.",middleName:null,surname:"Cobaxin-Cárdenas",slug:"mayra-e.-cobaxin-cardenas",fullName:"Mayra E. Cobaxin-Cárdenas"}]},{id:"58679",doi:"10.5772/intechopen.72636",title:"Genome-Based Vaccinology Applied to Bovine Babesiosis",slug:"genome-based-vaccinology-applied-to-bovine-babesiosis",totalDownloads:1161,totalCrossrefCites:1,totalDimensionsCites:3,abstract:"Genomics approaches in veterinary research have been a very useful tool to identify candidates with potential to be used in prevention of animal diseases. In Babesia, genome information analysis has elucidated a wide variety of protein families and some members are described in this chapter. Here, we present some of the most recent studies about B. bovis and B. bigemina genomes where some proteins have been identified with potential to prevent infections by these parasites.",book:{id:"5543",slug:"farm-animals-diseases-recent-omic-trends-and-new-strategies-of-treatment",title:"Farm Animals Diseases, Recent Omic Trends and New Strategies of Treatment",fullTitle:"Farm Animals Diseases, Recent Omic Trends and New Strategies of Treatment"},signatures:"Juan Mosqueda, Diego Josimar Hernández-Silva and Mario\nHidalgo-Ruiz",authors:[{id:"220191",title:"Dr.",name:"Juan",middleName:null,surname:"Mosqueda",slug:"juan-mosqueda",fullName:"Juan Mosqueda"}]}],mostDownloadedChaptersLast30Days:[{id:"59305",title:"Avian Coccidiosis, New Strategies of Treatment",slug:"avian-coccidiosis-new-strategies-of-treatment",totalDownloads:3686,totalCrossrefCites:2,totalDimensionsCites:4,abstract:"The control of avian coccidiosis since the 1940s has been associated with the use of ionophores and chemical drugs. Recently, a significant interest in natural sources has developed due to the pressure to poultry industry to produce drug-free birds. Consequently, the search of products derived from plants and other natural sources has increased in the last years. Today, many commercial products containing essential oils, extracts, and other compounds are available. The use of these compounds of natural origin is related to an increased immune response, a body weight gain, destruction of oocyst, among other benefits. The main inconvenience of these products is the act on some species of Eimeria, but not all. This genetic variability found in the parasite makes the use of products difficult to control and treat coccidiosis. In this chapter, several proposals of treatment are presented based on the use of natural products, considering the new strategies of treatment with minimal consequences to birds.",book:{id:"5543",slug:"farm-animals-diseases-recent-omic-trends-and-new-strategies-of-treatment",title:"Farm Animals Diseases, Recent Omic Trends and New Strategies of Treatment",fullTitle:"Farm Animals Diseases, Recent Omic Trends and New Strategies of Treatment"},signatures:"Rosa Estela Quiroz-Castañeda",authors:[{id:"187735",title:"Dr.",name:"Rosa Estela",middleName:null,surname:"Quiroz Castañeda",slug:"rosa-estela-quiroz-castaneda",fullName:"Rosa Estela Quiroz Castañeda"}]},{id:"58604",title:"Genomics of Apicomplexa",slug:"genomics-of-apicomplexa",totalDownloads:1181,totalCrossrefCites:2,totalDimensionsCites:2,abstract:"Apicomplexa is a eukaryotic phylum of intracellular parasites with more than 6000 species. Some of these single-celled parasites are important pathogens of livestock. At present, 128 genomes of phylum Apicomplexa have been reported in the GenBank database, of which 17 genomes belong to five genera that are pathogens of farm animals: Babesia, Theileria, Eimeria, Neospora and Sarcocystis. These 17 genomes are Babesia bigemina (five chromosomes), Babesia divergens (514 contigs) and Babesia bovis (four chromosomes and one apicoplast); Theileria parva (four chromosomes and one apicoplast), Theileria annulata (four chromosomes), Theileria orientalis (four chromosomes and one apicoplast) and Theileria equi (four chromosomes and one apicoplast); Eimeria brunetti (24,647 contigs), Eimeria necatrix (4667 contigs), Eimeria tenella (12,727 contigs), Eimeria acervulina (4947 contigs), Eimeria maxima (4570 contigs), Eimeria mitis (65,610 contigs) and Eimeria praecox (53,359 contigs); Neospora caninum (14 chromosomes); and Sarcocystis neurona strains SN1 (2862 contigs) and SN3 (3191 contigs). The study of these genomes allows us to understand their mechanisms of pathogenicity and identify genes that encode proteins as a possible vaccine antigen.",book:{id:"5543",slug:"farm-animals-diseases-recent-omic-trends-and-new-strategies-of-treatment",title:"Farm Animals Diseases, Recent Omic Trends and New Strategies of Treatment",fullTitle:"Farm Animals Diseases, Recent Omic Trends and New Strategies of Treatment"},signatures:"Fernando Martínez-Ocampo",authors:[{id:"195818",title:"Dr.",name:"Fernando",middleName:null,surname:"Martinez",slug:"fernando-martinez",fullName:"Fernando Martinez"}]},{id:"59436",title:"Pathogenomics and Molecular Advances in Pathogen Identification",slug:"pathogenomics-and-molecular-advances-in-pathogen-identification",totalDownloads:1642,totalCrossrefCites:2,totalDimensionsCites:2,abstract:"Today exists a spread spectrum of tools to be used in pathogen identification. Traditional staining and microscopic methods as well as modern molecular methods are presented in this chapter. Pathogen identification is only the beginning to obtain information related to pathogenicity of the microorganism in the near future. Once the pathogen is identified, genome-sequencing methods will provide a significant amount of information that can be elucidated only through bioinformatics methods. In this point, pathogenomics is a powerful tool to identify potential virulence factors, pathogenicity islands, and many other genes that could be used as therapeutic targets or in vaccine development. In this chapter, we present an update of the molecular advances used to identify pathogens and to obtain information of their diversity. We also review the most recent studies on pathogenomics with a special attention on pathogens of veterinary importance.",book:{id:"5543",slug:"farm-animals-diseases-recent-omic-trends-and-new-strategies-of-treatment",title:"Farm Animals Diseases, Recent Omic Trends and New Strategies of Treatment",fullTitle:"Farm Animals Diseases, Recent Omic Trends and New Strategies of Treatment"},signatures:"Rosa Estela Quiroz-Castañeda",authors:[{id:"187735",title:"Dr.",name:"Rosa Estela",middleName:null,surname:"Quiroz Castañeda",slug:"rosa-estela-quiroz-castaneda",fullName:"Rosa Estela Quiroz Castañeda"}]},{id:"61222",title:"The Use of Genetically Modified Organisms for Repopulation of Species of Commercial Importance in Aquatic Environment: Effects on Genetic Pool, Risks to Protected Areas and Policies for Their Proper Management",slug:"the-use-of-genetically-modified-organisms-for-repopulation-of-species-of-commercial-importance-in-aq",totalDownloads:1073,totalCrossrefCites:1,totalDimensionsCites:1,abstract:"In recent years, the reproduction of organisms through genetic engineering has been presented as an option for the repopulation of fish stocks of species that are at the limit or have passed their maximum sustainable exploitation. However, are the potential effects on genetic diversity known? The possible mutations? The risks to protected ecosystems? or Are there adequate policies and regulations for its management? This chapter aims to review the biological and population effects of the use of these organisms and the potential impacts they can cause to natural protected areas, as well as if there are adequate regulations or policies for their use. Finally, the authors give indicators for the sustainable integrated management of genetically modified organisms.",book:{id:"6647",slug:"animal-genetics-approaches-and-limitations",title:"Animal Genetics",fullTitle:"Animal Genetics - Approaches and Limitations"},signatures:"Maurilio Lara-Flores and Evelia Rivera-Arriaga",authors:null},{id:"58730",title:"Metagenomics and Diagnosis of Zoonotic Diseases",slug:"metagenomics-and-diagnosis-of-zoonotic-diseases",totalDownloads:1800,totalCrossrefCites:0,totalDimensionsCites:0,abstract:"Zoonotic diseases represent a public health problem worldwide, since approximately 60% of human pathogens have a zoonotic origin. A variety of methodologies have been developed to diagnose zoonosis, including culture-dependent and immunological-based methods, which allow the identification of a huge range of pathogens. However, some of them are not detected easily with these approaches. Additionally, molecular tests have been developed, and they are designed to identify a single pathogen or mixtures of them. In this context, metagenomics comes as an alternative to get genome sequences of different microorganisms, which comprise a microbial community. Metagenomics have been used to characterize microbiomes and viromes, which are not cultivable under laboratory conditions. This methodology could be a powerful tool in the diagnosis of zoonotic diseases because it allows not only identification of genus and species, but also detection of some proteins in specific conditions on specific tissues, through structural and functional metagenomics, respectively.",book:{id:"5543",slug:"farm-animals-diseases-recent-omic-trends-and-new-strategies-of-treatment",title:"Farm Animals Diseases, Recent Omic Trends and New Strategies of Treatment",fullTitle:"Farm Animals Diseases, Recent Omic Trends and New Strategies of Treatment"},signatures:"Laura Inés Cuervo-Soto, Silvio Alejandro López-Pazos and Ramón\nAlberto Batista-García",authors:[{id:"201362",title:"Dr.",name:"Ramón Alberto",middleName:null,surname:"Batista-García",slug:"ramon-alberto-batista-garcia",fullName:"Ramón Alberto Batista-García"}]}],onlineFirstChaptersFilter:{topicId:"303",limit:6,offset:0},onlineFirstChaptersCollection:[],onlineFirstChaptersTotal:0},preDownload:{success:null,errors:{}},subscriptionForm:{success:null,errors:{}},aboutIntechopen:{},privacyPolicy:{},peerReviewing:{},howOpenAccessPublishingWithIntechopenWorks:{},sponsorshipBooks:{sponsorshipBooks:[],offset:8,limit:8,total:0},allSeries:{pteSeriesList:[{id:"14",title:"Artificial Intelligence",numberOfPublishedBooks:9,numberOfPublishedChapters:89,numberOfOpenTopics:6,numberOfUpcomingTopics:0,issn:"2633-1403",doi:"10.5772/intechopen.79920",isOpenForSubmission:!0},{id:"7",title:"Biomedical Engineering",numberOfPublishedBooks:12,numberOfPublishedChapters:104,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2631-5343",doi:"10.5772/intechopen.71985",isOpenForSubmission:!0}],lsSeriesList:[{id:"11",title:"Biochemistry",numberOfPublishedBooks:32,numberOfPublishedChapters:318,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2632-0983",doi:"10.5772/intechopen.72877",isOpenForSubmission:!0},{id:"25",title:"Environmental Sciences",numberOfPublishedBooks:1,numberOfPublishedChapters:12,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2754-6713",doi:"10.5772/intechopen.100362",isOpenForSubmission:!0},{id:"10",title:"Physiology",numberOfPublishedBooks:11,numberOfPublishedChapters:141,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-8261",doi:"10.5772/intechopen.72796",isOpenForSubmission:!0}],hsSeriesList:[{id:"3",title:"Dentistry",numberOfPublishedBooks:8,numberOfPublishedChapters:129,numberOfOpenTopics:2,numberOfUpcomingTopics:0,issn:"2631-6218",doi:"10.5772/intechopen.71199",isOpenForSubmission:!0},{id:"6",title:"Infectious Diseases",numberOfPublishedBooks:13,numberOfPublishedChapters:113,numberOfOpenTopics:3,numberOfUpcomingTopics:1,issn:"2631-6188",doi:"10.5772/intechopen.71852",isOpenForSubmission:!0},{id:"13",title:"Veterinary Medicine and Science",numberOfPublishedBooks:11,numberOfPublishedChapters:105,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2632-0517",doi:"10.5772/intechopen.73681",isOpenForSubmission:!0}],sshSeriesList:[{id:"22",title:"Business, Management and Economics",numberOfPublishedBooks:1,numberOfPublishedChapters:19,numberOfOpenTopics:2,numberOfUpcomingTopics:1,issn:"2753-894X",doi:"10.5772/intechopen.100359",isOpenForSubmission:!0},{id:"23",title:"Education and Human Development",numberOfPublishedBooks:0,numberOfPublishedChapters:5,numberOfOpenTopics:1,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100360",isOpenForSubmission:!0},{id:"24",title:"Sustainable Development",numberOfPublishedBooks:0,numberOfPublishedChapters:15,numberOfOpenTopics:5,numberOfUpcomingTopics:0,issn:null,doi:"10.5772/intechopen.100361",isOpenForSubmission:!0}],testimonialsList:[{id:"13",text:"The collaboration with and support of the technical staff of IntechOpen is fantastic. The whole process of submitting an article and editing of the submitted article goes extremely smooth and fast, the number of reads and downloads of chapters is high, and the contributions are also frequently cited.",author:{id:"55578",name:"Antonio",surname:"Jurado-Navas",institutionString:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRisIQAS/Profile_Picture_1626166543950",slug:"antonio-jurado-navas",institution:{id:"720",name:"University of Malaga",country:{id:null,name:"Spain"}}}},{id:"6",text:"It is great to work with the IntechOpen to produce a worthwhile collection of research that also becomes a great educational resource and guide for future research endeavors.",author:{id:"259298",name:"Edward",surname:"Narayan",institutionString:null,profilePictureURL:"https://mts.intechopen.com/storage/users/259298/images/system/259298.jpeg",slug:"edward-narayan",institution:{id:"3",name:"University of Queensland",country:{id:null,name:"Australia"}}}}]},series:{item:{id:"13",title:"Veterinary Medicine and Science",doi:"10.5772/intechopen.73681",issn:"2632-0517",scope:"Paralleling similar advances in the medical field, astounding advances occurred in Veterinary Medicine and Science in recent decades. These advances have helped foster better support for animal health, more humane animal production, and a better understanding of the physiology of endangered species to improve the assisted reproductive technologies or the pathogenesis of certain diseases, where animals can be used as models for human diseases (like cancer, degenerative diseases or fertility), and even as a guarantee of public health. Bridging Human, Animal, and Environmental health, the holistic and integrative “One Health” concept intimately associates the developments within those fields, projecting its advancements into practice. This book series aims to tackle various animal-related medicine and sciences fields, providing thematic volumes consisting of high-quality significant research directed to researchers and postgraduates. It aims to give us a glimpse into the new accomplishments in the Veterinary Medicine and Science field. 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She is also a frequent referee for various journals.",institutionString:null,institution:{name:"University of Évora",institutionURL:null,country:{name:"Portugal"}}},editorTwo:null,editorThree:null},subseries:{paginationCount:3,paginationItems:[{id:"19",title:"Animal Science",coverUrl:"https://cdn.intechopen.com/series_topics/covers/19.jpg",isOpenForSubmission:!0,editor:{id:"259298",title:"Dr.",name:"Edward",middleName:null,surname:"Narayan",slug:"edward-narayan",fullName:"Edward Narayan",profilePictureURL:"https://mts.intechopen.com/storage/users/259298/images/system/259298.jpeg",biography:"Dr. Edward Narayan graduated with Ph.D. degree in Biology from the University of the South Pacific and pioneered non-invasive reproductive and stress endocrinology tools for amphibians - the novel development and validation of non-invasive enzyme immunoassays for the evaluation of reproductive hormonal cycle and stress hormone responses to environmental stressors. \nDr. Narayan leads the Stress Lab (Comparative Physiology and Endocrinology) at the University of Queensland. A dynamic career research platform which is based on the thematic areas of comparative vertebrate physiology, stress endocrinology, reproductive endocrinology, animal health and welfare, and conservation biology. \nEdward has supervised 40 research students and published over 60 peer reviewed research.",institutionString:null,institution:{name:"University of Queensland",institutionURL:null,country:{name:"Australia"}}},editorTwo:null,editorThree:null},{id:"20",title:"Animal Nutrition",coverUrl:"https://cdn.intechopen.com/series_topics/covers/20.jpg",isOpenForSubmission:!0,editor:{id:"175967",title:"Dr.",name:"Manuel",middleName:null,surname:"Gonzalez Ronquillo",slug:"manuel-gonzalez-ronquillo",fullName:"Manuel Gonzalez Ronquillo",profilePictureURL:"https://mts.intechopen.com/storage/users/175967/images/system/175967.png",biography:"Dr. Manuel González Ronquillo obtained his doctorate degree from the University of Zaragoza, Spain, in 2001. He is a research professor at the Faculty of Veterinary Medicine and Animal Husbandry, Autonomous University of the State of Mexico. He is also a level-2 researcher. He received a Fulbright-Garcia Robles fellowship for a postdoctoral stay at the US Dairy Forage Research Center, Madison, Wisconsin, USA in 2008–2009. He received grants from Alianza del Pacifico for a stay at the University of Magallanes, Chile, in 2014, and from Consejo Nacional de Ciencia y Tecnología (CONACyT) to work in the Food and Agriculture Organization’s Animal Production and Health Division (AGA), Rome, Italy, in 2014–2015. He has collaborated with researchers from different countries and published ninety-eight journal articles. He teaches various degree courses in zootechnics, sheep production, and agricultural sciences and natural resources.\n\nDr. Ronquillo’s research focuses on the evaluation of sustainable animal diets (StAnD), using native resources of the region, decreasing carbon footprint, and applying meta-analysis and mathematical models for a better understanding of animal production.",institutionString:null,institution:{name:"Universidad Autónoma del Estado de México",institutionURL:null,country:{name:"Mexico"}}},editorTwo:null,editorThree:null},{id:"28",title:"Animal Reproductive Biology and Technology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/28.jpg",isOpenForSubmission:!0,editor:{id:"177225",title:"Prof.",name:"Rosa Maria Lino Neto",middleName:null,surname:"Pereira",slug:"rosa-maria-lino-neto-pereira",fullName:"Rosa Maria Lino Neto Pereira",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bS9wkQAC/Profile_Picture_1624519982291",biography:"Rosa Maria Lino Neto Pereira (DVM, MsC, PhD and) is currently a researcher at the Genetic Resources and Biotechnology Unit of the National Institute of Agrarian and Veterinarian Research (INIAV, Portugal). 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Portugal",institution:null},editorTwo:null,editorThree:null}]},overviewPageOFChapters:{paginationCount:13,paginationItems:[{id:"82285",title:"Parvovirus Vectors: The Future of Gene Therapy",doi:"10.5772/intechopen.105085",signatures:"Megha Gupta",slug:"parvovirus-vectors-the-future-of-gene-therapy",totalDownloads:4,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Recent Advances in Canine Medicine",coverURL:"https://cdn.intechopen.com/books/images_new/11580.jpg",subseries:{id:"19",title:"Animal Science"}}},{id:"81793",title:"Canine parvovirus-2: An Emerging Threat to Young Pets",doi:"10.5772/intechopen.104846",signatures:"Mithilesh Singh, Rajendran Manikandan, Ujjwal Kumar De, Vishal Chander, Babul Rudra Paul, Saravanan Ramakrishnan and Darshini Maramreddy",slug:"canine-parvovirus-2-an-emerging-threat-to-young-pets",totalDownloads:16,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Recent Advances in Canine Medicine",coverURL:"https://cdn.intechopen.com/books/images_new/11580.jpg",subseries:{id:"19",title:"Animal Science"}}},{id:"81271",title:"The Diversity of Parvovirus Telomeres",doi:"10.5772/intechopen.102684",signatures:"Marianne Laugel, Emilie Lecomte, Eduard Ayuso, Oumeya Adjali, Mathieu Mével and Magalie Penaud-Budloo",slug:"the-diversity-of-parvovirus-telomeres",totalDownloads:38,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Recent Advances in Canine Medicine",coverURL:"https://cdn.intechopen.com/books/images_new/11580.jpg",subseries:{id:"19",title:"Animal Science"}}},{id:"79209",title:"Virtual Physiology: A Tool for the 21st Century",doi:"10.5772/intechopen.99671",signatures:"Carmen Nóbrega, Maria Aires Pereira, Catarina Coelho, Isabel Brás, Ana Cristina Mega, Carla Santos, Fernando Esteves, Rita Cruz, Ana I. 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She obtained her Ph.D. in Veterinary Sciences from the University of Trás-os-Montes e Alto Douro, Portugal. After almost 32 years of teaching at the University of Trás-os-Montes and Alto Douro, she recently moved to the University of Évora, Department of Veterinary Medicine, where she teaches in the field of Animal Reproduction and Clinics. Her primary research areas include the molecular markers of the endometrial cycle and the embryo–maternal interaction, including oxidative stress and the reproductive physiology and disorders of sexual development, besides the molecular determinants of male and female fertility. She often supervises students preparing their master's or doctoral theses. She is also a frequent referee for various journals.",institutionString:null,institution:{name:"University of Évora",institutionURL:null,country:{name:"Portugal"}}}]},{type:"book",id:"7144",title:"Veterinary Anatomy and Physiology",subtitle:null,coverURL:"https://cdn.intechopen.com/books/images_new/7144.jpg",slug:"veterinary-anatomy-and-physiology",publishedDate:"March 13th 2019",editedByType:"Edited by",bookSignature:"Catrin Sian Rutland and Valentina Kubale",hash:"75cdacb570e0e6d15a5f6e69640d87c9",volumeInSeries:2,fullTitle:"Veterinary Anatomy and Physiology",editors:[{id:"202192",title:"Dr.",name:"Catrin",middleName:null,surname:"Rutland",slug:"catrin-rutland",fullName:"Catrin Rutland",profilePictureURL:"https://mts.intechopen.com/storage/users/202192/images/system/202192.png",biography:"Catrin Rutland is an Associate Professor of Anatomy and Developmental Genetics at the University of Nottingham, UK. She obtained a BSc from the University of Derby, England, a master’s degree from Technische Universität München, Germany, and a Ph.D. from the University of Nottingham. She undertook a post-doctoral research fellowship in the School of Medicine before accepting tenure in Veterinary Medicine and Science. Dr. Rutland also obtained an MMedSci (Medical Education) and a Postgraduate Certificate in Higher Education (PGCHE). She is the author of more than sixty peer-reviewed journal articles, twelve books/book chapters, and more than 100 research abstracts in cardiovascular biology and oncology. She is a board member of the European Association of Veterinary Anatomists, Fellow of the Anatomical Society, and Senior Fellow of the Higher Education Academy. Dr. Rutland has also written popular science books for the public. https://orcid.org/0000-0002-2009-4898. www.nottingham.ac.uk/vet/people/catrin.rutland",institutionString:null,institution:{name:"University of Nottingham",institutionURL:null,country:{name:"United Kingdom"}}}]},{type:"book",id:"8524",title:"Lactation in Farm Animals",subtitle:"Biology, Physiological Basis, Nutritional Requirements, and Modelization",coverURL:"https://cdn.intechopen.com/books/images_new/8524.jpg",slug:"lactation-in-farm-animals-biology-physiological-basis-nutritional-requirements-and-modelization",publishedDate:"January 22nd 2020",editedByType:"Edited by",bookSignature:"Naceur M'Hamdi",hash:"2aa2a9a0ec13040bbf0455e34625504e",volumeInSeries:3,fullTitle:"Lactation in Farm Animals - Biology, Physiological Basis, Nutritional Requirements, and Modelization",editors:[{id:"73376",title:"Dr.",name:"Naceur",middleName:null,surname:"M'Hamdi",slug:"naceur-m'hamdi",fullName:"Naceur M'Hamdi",profilePictureURL:"https://mts.intechopen.com/storage/users/73376/images/system/73376.jpg",biography:"Naceur M’HAMDI is Associate Professor at the National Agronomic Institute of Tunisia, University of Carthage. He is also Member of the Laboratory of genetic, animal and feed resource and member of Animal science Department of INAT. He graduated from Higher School of Agriculture of Mateur, University of Carthage, in 2002 and completed his masters in 2006. Dr. M’HAMDI completed his PhD thesis in Genetic welfare indicators of dairy cattle at Higher Institute of Agronomy of Chott-Meriem, University of Sousse, in 2011. 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