Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-14T11:13:33.795Z Has data issue: false hasContentIssue false

Research on subsoil biopores and their functions in organically managed soils: A review

Published online by Cambridge University Press:  15 January 2014

Timo Kautz*
Affiliation:
Institute of Organic Agriculture, University of Bonn, Katzenburgweg 3, 53115 Bonn, Germany.
*
Corresponding author: [email protected]
Rights & Permissions [Opens in a new window]

Abstract

The living soil is the basis for crop production in organic agriculture. Biopores are voids in the soil which were formed by the activity of soil life. The first scientific studies on biopores were published in the 1870s–90s by Victor Hensen who stated that earthworms were opening channels to the subsoil and coating them with humus, thus creating a beneficial environment for root growth. His work was originally widely recognized, but then research on biopores was neglected for many decades and was only revitalized with the rise of ecological concerns in the 1960s. In recent times, biopores have attracted the attention of agronomists with a focus on organic agriculture. New visualization techniques, such as X-ray micro computed tomography, in-situ endoscopy and nuclear magnetic resonance imaging have been applied. Biopores contribute to air transport through the soil, increase water infiltration, reduce water runoff and soil erosion, serve as preferential pathways for root elongation and can facilitate the acquisition of water and nutrients from the subsoil. The relevance of biopores for nutrient acquisition can be pronounced particularly in organic production systems, where crops are more dependent on nutrient acquisition from the solid soil phase than under conditions of conventional agriculture. Organic land-use strategies should aim to increase number, stability and quality of biopores. The biopore density can be increased by the share of dicotyledons in the crop rotation and by cultivating perennial crops with taproot systems. Moreover, density and—in particular—the quality of biopores, e.g., the nutrient contents of pore walls, can be influenced by anecic earthworms which can be promoted by adapted tillage practices.

Type
Review Article
Copyright
Copyright © Cambridge University Press 2014 

Introduction

Biopores are voids in the soil which were formed by biological activity. In general, biopores can have diameters from <30 μm (these are for instance the pores created by enchytraeids or root hairs) up to >5 mmReference Yunusa and Newton 1 . Typically the term biopores refers to tubular shaped, continuous pores formed by plant roots and burrowing soil animals such as earthworms (Fig. 1). In most agricultural soils, the largest biopores are the burrows of anecic earthworms. For instance, the channels created by Lumbricus terrestris L. have an average diameter of 9.4 mmReference Joschko, Diestel and Larink 2 . Larger voids, such as the channels created by moles, have been attributed to biopores as wellReference Beven and Germann 3 , but they do not cover large areas in agricultural soils and are therefore not included in this review. Despite studies on biopores often focusing on earthworm burrows and other coarse pores, over 80% of the biopores per unit area can have a diameter of less than 1 mmReference Wuest 4 . Biopores are present throughout the soil profile, from the surface to several meters in depth. In arable soils, tillage frequently destroys biopore systems in the plough horizon, but not in the subsoil. Biopores >30 μm in diameter provide channels for new root growth and water and air conductionReference Yunusa and Newton 1 . In the subsoil—which is generally assumed to be relatively compact and poor in nutrients—biopores are supposed to have a special relevance for root growthReference Ehlers, Köpke, Hesse and Böhm 5 (Fig. 2) and serve as hot spots for nutrient acquisition of crop rootsReference Kautz, Amelung, Ewert, Gaiser, Horn, Jahn, Javaux, Kemna, Kuzyakov, Munch, Pätzold, Peth, Scherer, Schloter, Schneider, Vanderborght, Vetterlein, Walter, Wiesenberg and Köpke 6 . In organic farming systems, facilitation of root growth and nutrient uptake can have particular relevance since the availability of nutrients is generally limitedReference Köpke 7 . For instance, synthetic mineral fertilizers are not permitted in organic agriculture in the European Union (Council Regulation (EC) No. 834/2007). Instead, organic farming strategies aim to close nutrient cycles as much as possibleReference Mäder, Fliessbach, Dubois, Gunst, Fried and Niggli 8 and to mobilize nutrients from the solid phase. Thus, extensive and active root systems can contribute to nutrient acquisition.

Figure 1. Biopores in 45 cm soil depth (top view). The picture covers approximately 50×50 cm.

Figure 2. Biopore (longitudinal section). Soil depth approximately 50–80 cm.

Starting from the 19th century, studies on biopores were inspired by advances in the field of ecological sciences. In turn, research on biopores contributed to a deeper understanding of soil ecological processes, providing a background of knowledge for organic management of soils. Against this background, this article reviews research on biopores from its beginnings to date, summarizes the current state of knowledge about the functions of biopores in agricultural soils and outlines possible consequences for organic management.

Biopores Through the Ages: Ecology and Biopore Research

Biopores as objects of research do not appear in the literature until the second half of the 19th century. One apparent reason for the long inobservance of biopores is that they were hardly recognized before soil was studied extensively, i.e., before trenches or pits were arranged and biopores were dissected. In fact, soil was seldom studied below a depth of a few centimeters until soil science as a natural science was established by V. V. Dokuchaev in the 1870s and 80s. Prior to this, however, it was a crop scientist named Hugo Thiel who first studied root growth in a clover field as part of his dissertation researchReference Thiel 9 . In 1865, Thiel observed that roots were proliferating through previously existing channels especially in the subsoil. ThielReference Thiel 9 already noted that these channels (‘canales’) were made by roots or soil animals. He counted 5–20 channels on 900 cm2 in 2 m soil depth. However, to commence in-depth research on biopores it was necessary to research more about their functions. In other words, it was necessary to study how soil organisms (explicitly roots and earthworms) interact with each other and with their abiotic environment (mineral and organic particles, air and water). Thus, research on biopores required, by definition, ecological thinking. The first researcher who published studies on the properties of biopores was, using current science nomenclature, an ecologist—Victor Hensen, a marine biologist who is known as ‘the father of quantitative plankton ecology’Reference Taylor, Sears and Merriman 10 . In 1877, HensenReference Hensen 11 reported on the burrowing activity of earthworms in his garden. He concluded that earthworms were opening channels to the subsoil and that they were coating them with humus, thus creating a beneficial environment for root growth. Moreover, HensenReference Hensen 11 made the first remarks on the dynamics of the biopore properties over time, reporting that the walls of fresh pores were covered with dark humps made up of earthworm excreta, whereas the walls of older pores, no longer colonized by worms, were uniformly covered with dark soil originating from earthworms. He also mentioned pores completely filled with dark soil that he assumed to ‘diffuse’ into the surrounding soil and to weather over time, until only unfertile soil remains. HensenReference Hensen 12 clearly pointed to the relevance of earthworm channels for roots as a fertile environment with a low penetration resistance, stating, ‘More beneficial conditions for the growth of plant roots may hardly be found …’. In a following publication, HensenReference Hensen 13 provided detailed drawings of roots growing through biopores. Although he did not use the term ‘biopore’ and was focused on pores that were clearly earthworm channels, he also reported on fresh roots following the void created by a decomposing old root. Moreover, one of his drawings shows a pore ‘not yet’ coated with excrement, but containing a plant root. This pore may have been a pore originating from roots or a pore not colonized by an earthworm for a long time.

Hensen's first publication was cited by Charles DarwinReference Darwin 14 in his influential book The Formation of Vegetable Mould Through the Action of Worms, published in 1881. Interestingly, Darwin noted that some of his own observations ‘have been rendered almost superfluous’ by the ‘admirable’ paper by HensenReference Hensen 11 . Hensen's work was widely recognized, especially by agricultural scientists and practical farmers, and encouraged some of them to undertake their own studies on earthworm activity and biopores and to discuss the role of biopores for crop production. For instance, Albert Schultz-LupitzReference Schultz-Lupitz 15 postulated the guiding principle of crop production that crop farmers can stimulate root development by supporting the prosperity of subterranean animals such as earthworms. Furthermore, Ewald Wollny was inspired by Hensen's publications and conference contributions. Wollny had a special interest in soil physics and—different from the more agrochemical-oriented mainstream of his time—highlighted the importance of soil structure for the performance of crops. In column experiments, WollnyReference Wollny 16 documented that incubation with earthworms increased the permeability of soil for air and water.

Moreover, the role of biopores as pathways for preferential water flow was already described by the end of the 19th century. In 1881, Lawes et al.Reference Lawes, Gilbert, Warington and Station 17 noted that after heavy rainfalls, some water drained off through open ‘channels’ before the soil became saturated. However, this finding was not quantified and did not result in further investigations for many years.

After the first ‘wave’ of biopore research at the end of the 19th century, studies on biopores became rare during the following decades. In the early 20th century, many technical advances in agriculture were made, including the fabrication of mineral nitrogen (N) fertilizer based on the Haber–Bosch process. During this era many agronomists emphasized the question of how crops can be supplied with optimum amounts of nutrients rather than studying natural resources and their functions. Moreover, since the early 1940s major advances were made in development and application of chemical pesticides, which was also described as the beginning of the ‘organic pesticide era’Reference Glass and Thurston 18 . In contrast to the documentation of obvious yield increases resulting from mineral fertilization and pesticide application, it was more difficult to quantify the effect of earthworm activity and biopores on crop growth, holding all other factors influencing plant growth constant; thus only a few reliable studies were published during that eraReference Hopp and Slater 19 .

The interest in biopores was revitalized in the 1960s. By that time, ecologists expressed major concerns about the application of chemicals in agro-ecosystems. Rachel Carson's book Silent Spring Reference Carsons 20 (1962), systematically criticizing the widespread use of pesticides from an ecological point of view, is often regarded as the beginning of the modern environmental movementsReference Lytle 21 , followed by an increased ecological awareness in the 1960s and 1970s. Certainly, it must be seen in this historical context that research on natural soil functions and their relevance for crop production was boosted in that time. Among other aspects of soil fertility, interest in biopores increased for soil scientists, agronomists and soil ecologists.

By this time, ecology was increasingly recognized as a distinct independent academic discipline. This nascent field of study was advanced through the seminal textbook Fundamentals of Ecology by Eugene P. Odum in 1953Reference Odum 22 , which also helped to establish the concept of ecosystems. The ecosystem concept, which postulates the presence of open sub-systems within the biosphere that are defined by the interactions between organisms and their abiotic environment, had been originally developed by Tansley in 1935Reference Tansley 23 . The application of this concept to soil allowed the understanding of soil as a complex network of activity by soil animals, microorganisms and roots, and their interaction with water, gasses, mineral and organic particles. Biopores evidently are implied as specific areas of interest as a living space for soil organisms within this network.

With this new system-oriented view, pores created by soil animals or plant roots were now understood as a functional unit. Newly developed methods, such as the microscopic investigation of soil peelsReference Bouma and Hole 24 , Reference Van der Plas, Slager and Jongerius 25 , also allowed quantification of pores on a much smaller scale. However, while large earthworm burrows can be identified with comparative ease by their characteristic coatings and typical dark-colored surface, the origin of pores with smaller diameters often remained unclear. In 1964, SlagerReference Slager and Jongerius 26 overcame this methodological problem by combining investigation of pores from different origins and being the first to use the word ‘biopore’ as a superordinate concept for pores generated by animals or roots.

Also in the 1960s and 1970s, much progress was made in characterizing the chemical properties of the surroundings of biopores. For instance, GraffReference Graff 27 studied the downward transport of nutrients by earthworms and quantified the enrichment of N, phosphorus (P), potassium (K) and calcium (Ca) in the pore wall. Furthermore, earthworm channels were shown to have beneficial effects on biomass and nutrient contents of crops in pot experimentsReference Rhee 28 and field studiesReference Graff 29 . GraffReference Graff 30 , referring to the history of agriculture, appreciated the pioneering role of Victor Hensen for research on earthworms and biopores. As researchers became more interested in the 2 mm zone around earthworm burrows as a place of increased concentrations of nutrients and soil organic matter, it was denoted as the ‘drilosphere’ by BouchéReference Bouché, Kilbertius, Reisinger, Mourey and Cancela da Fonseca 31 . The role of biopores in soil hydrology also received increasing attention, as well as initial suggestions for supporting the formation of biopores through agronomic measures. For instance, EhlersReference Ehlers 32 highlighted the relevance of biopores for water infiltration and demonstrated the possibility of increasing the number of biopores per unit area by a reduction of tillage intensity.

Advances in computer applications made during the 1980s allowed the use of computer models to predict the influence of biopores on root and shoot growth of cropsReference Dexter 33 . A model developed by Jakobsen and DexterReference Jakobsen and Dexter 34 predicted that biopores made significant contributions to root penetration, but resulted in reduced water availability during the grain-filling period due to increased early water useReference Jakobsen and Dexter 35 . In the 1990s the newly developed concept of ecosystem engineers again drew attention to biopores. Ecosystem engineers are organisms that ‘modulate the availability of resources to other organisms by causing physical state changes in biotic or abiotic materials’Reference Jones, Lawton and Shachak 36 . In this context, researchers focused on earthworms and roots as ecosystem engineers that both create biopores with subsequent new living spaces for soil organismsReference Lavelle, Bignell, Lepage, Wolters and Roger 37 . Furthermore microbiological methods such as enzyme assays became widespread during the 1990s, allowing more detailed understanding of the biochemistry of biopore wallsReference Stehouwer, Dick and Traina 38 .

In recent times, biopores have attracted the attention of agronomists who focus on their relevance for crop performance. For instance, biopores and their implications for root growth and water percolation were studied in hard-setting clay soils which severely restrict penetration by crop rootsReference Carter, Mele and Steed 39 , Reference Pankhurst, Pierret, Hawke and Kirby 40 . In addition, researchers oriented toward organic or sustainable agriculture focus on the biopores’ functions, such as improving the water supply to crops or providing hot spots for nutrient acquisition contributing to plant nutritionReference Putten, Anderson, Bardgett, Behan-Pelletier, Bignell, Brown, Brown, Brussaard, Hunt, Ineson and Wall 41 . When the topsoil is dry or poor in nutrients, organic farming or low input systems can particularly benefit from bioporesReference Kautz, Amelung, Ewert, Gaiser, Horn, Jahn, Javaux, Kemna, Kuzyakov, Munch, Pätzold, Peth, Scherer, Schloter, Schneider, Vanderborght, Vetterlein, Walter, Wiesenberg and Köpke 6 . This is an example of a management strategy in organic agriculture that incorporates recent ecological knowledgeReference Drinkwater and Francis 42 . Developing strategies for creating, maintaining and using biopores is inherent to organic agricultural production, as well as in conventional systems that utilize conservation management practices such as no-tillage and cover cropping. Nevertheless, many questions on biopores and their effects on soil fertility and root growth remain unanswered. Future fields of research include the quantification of root–soil contact in biopores, nutrient uptake from the drilosphere and the temporal dynamics of biopore networks as a consequence of root growth, earthworm activity and abiotic factors. Presumably, future studies on biopores will increasingly rely on new visualization techniques, such as X-ray micro computed tomography which can create three-dimensional X-ray imagesReference Peth 43 . For visualization of root growth in biopores new approaches have recently been described and will probably contribute to our understanding of nutrient acquisition from biopores. In-situ endoscopyReference Athmann, Kautz, Pude and Köpke 44 , Reference Kautz and Köpke 45 (Fig. 3) allows direct observation of roots growing in biopores, and nuclear magnetic resonance imaging allows the measurement of both root dynamics and earthworm activity in undisturbed soil coresReference Nagel, Kastenholz, Jahnke, van Dusschoten, Aach, Mühlich, Truhn, Scharr, Terjung, Walter and Schurr 46 . Recently, the effect of biopores was integrated into a crop model solution, demonstrating the importance of biopores for root growth, water and nutrient uptake of spring wheat on soils with pronounced subsoil clay accumulationReference Gaiser, Perkons, Kupper, Kautz, Uteau-Puschmann, Ewert, Enders and Krauss 47 . However, more research is needed to check the applicability of this result for other crops and soil types.

Figure 3. Endoscopic views into biopores: (a) biopore coated with earthworm feces; (b) biopore containing two vertical roots of Brassica napus and an older, decomposing root from a previous crop.

Functions of Biopores in Agricultural Soils: Current State of Research

Gas exchange, water infiltration and water percolation

Biopores contribute to the transport of airReference Dziejowski, Rimmer and Steenhuis 48 as well as water and solutesReference Edwards, Shipitalo, Owens and Norton 49 through the soil. The transport of oxygen from the soil surface to deeper soil layers through the soil matrix primarily occurs by gaseous diffusionReference Craul 50 . Oxygen concentration of soil air generally decreases with increasing depth as a consequence of length and tortuosity of the diffusion pathwayReference Craul 50 , Reference Lal and Shukla 51 . In contrast, vertical continuous biopores provide straight paths of diffusion in the soil. Furthermore, there is evidence for convection through large continuous bioporesReference Hillel 52 . Hence, the oxygen concentration inside these biopores remains relatively stable throughout the soil profileReference Glinski and Lipiec 53 .

Large-sized biopores drain rapidly and become air-filled after rainfall eventsReference Hillel 52 . Under wet conditions the air permeability of a clay soil was found to be greater vertically than in the horizontal direction, which can be explained by the presence of vertically oriented bioporesReference Berisso, Schjønning, Keller, Lamandé, Simojoki, Iversen, Alakukku and Forkman 54 . As a result, elevated oxygen concentrations in biopores may have an effect on microbial activity and nutrient uptake by roots limited by a lack of oxygen in a dense subsoilReference Sierra and Renault 55 , Reference Stępniewski and Przywara 56 .

Biopores with diameters larger than 0.3–0.5 mm support non-equilibrium water flowReference Jarvis 57 . After rainfall events, water is transported downwards predominantly through large continuous pores. A single pore of 3 mm diameter can contribute more to water infiltration rate than the infiltration through the soil matrix in a 30 cm diameter areaReference Smettem and Collis-George 58 . Macropore flow can be substantially enhanced after cultivation of alfalfa (Medicago sativa L.), a taprooted crop which can increase the number of continuous soil poresReference Angers and Caron 59 . Positive correlations were found between the number of pores having diameters ⩾2.0 mm per area unit and both hydraulic conductivity and air-filled porosityReference Yunusa, Mele, Rab, Schefe and Beverly 60 . In a sandy loam from an organic dairy farm the number of earthworm burrows and consequently hydraulic conductivity was found to be higher than in a similar soil under conventional managementReference Schjønning, Munkholm, Moldrup and Jacobsen 61 . Increased water infiltration rates can have beneficial effects on soil fertility on arable land because they (1) reduce the risk of water ponding on flat terrain and (2) reduce water runoff and potential soil erosion on sloping terrainReference Horn, Domżżał, Słowińska-Jurkiewicz and van Ouwerkerk 62 . In addition to water infiltration at the soil surface, biopores also contribute to water percolation deeper in the soil profileReference Pitkänen and Nuutinen 63 . Under saturated or near saturated conditions, large earthworm burrows (>6 mm in diameter) in the subsoil act as preferential flow paths for water even when not continuous from the topsoilReference Pitkänen and Nuutinen 63 .

Since biopores allow water and solutes to be transported rapidly into deeper soil layers, they potentially have unwanted effects on nutrient leaching, as shown for the transport of nitrate through root channelsReference Li and Ghodrati 64 . Generally, slow percolation of water through the soil matrix allows P adsorption, whereas water and solutes transported through large biopores bypass the adsorptive capacity of the soilReference Heathwaite and Dils 65 . Thus, preferential flow through biopores can increase leaching of dissolved PReference Djodjic, Börling and Bergström 66 . However, the largest leaching losses of P in macropore flow were reported from soils with excessive topsoil P contents due to over-fertilizationReference Jarvis 57 . In conventional agriculture, preferential flow through biopores could also contribute to the transport of agrochemicals and potential contamination of natural groundwater bodiesReference Dadfar, Allaire, Bochove, Denault, Thériault and Charles 67 .

Root growth

The distribution of roots in soil is a main determinant in the ability of crops to acquire nutrients because the concentration of soluble nutrients in the liquid soil phase is typically lowReference Lammerts van Bueren, Struik and Jacobsen 68 . For this reason, soil structural features facilitating root growth are of particular interest in organically managed soils. The early observation that roots preferentially expand through bioporesReference Hensen 13 has been confirmed by numerous studiesReference Ehlers, Köpke, Hesse and Böhm 5 , Reference Köpke 69 , Reference Nakamoto 70 . Several reasons for this preference have been identified. First and foremost, roots follow biopores because they provide zones of reduced mechanical resistanceReference Logsdon and Linden 71 . This is of particular relevance because mechanical resistance has been identified as a major limitation to soil exploration by rootsReference Hoad, Russell, Lucas and Bingham 72 , Reference Unger and Kaspar 73 . Root elongation is particularly slowed when stresses are exerted in an axial direction, which occurs when roots are growing through the bulk soilReference Bengough 74 . When growing through severely compacted soil zones, roots can potentially be deflected and buckleReference Whiteley, Hewitt and Dexter 75 , which further delays root extension to deeper soil layers. Additionally, biopores are attractive for roots because they provide higher oxygen concentrations in the gaseous phase and higher nutrient concentrations in the solid phase (i.e., the pore wall) as compared to the surrounding soilReference Stewart, Moran and Wood 76 . Because of elevated oxygen concentrations, root respiration and root growth in biopores can occur at greater depths as compared to the bulk soilReference McMahon and Christy 77 .

The importance of biopores for root elongation varies with soil properties. Whereas in comparatively compact subsoils, roots have been reported to grow predominantly in bioporesReference Ehlers, Köpke, Hesse and Böhm 5 , Reference Köpke 69 , the share of roots in biopores did not exceed 25% in a Haplic LuvisolReference Kautz, Perkons, Athmann, Pude and Köpke 78 . In the latter study, the percentage of roots growing in biopores was lower in the C horizon than in the denser Bt horizon. This result indicates that roots growing along biopores can eventually bypass compacted soil layers and re-enter the bulk soil in less compacted soil layers. Accordingly, root growth through biopores can facilitate the exploration of water and nutrients stored in the deep bulk soil. Soil strength and the angle of the biopores are crucial for the likelihood that a root re-enters the bulk soil from a bioporeReference Bengough, Kroon and Visser 79 . In a study by Hirth et al.Reference Hirth, McKenzie and Tisdall 80 most roots of Lolium perenne L. were able to leave artificial biopores with an inclination of 40°, whereas the roots predominantly remained in vertical pores.

Acquisition of water and nutrients

The facilitation of root growth by biopores can increase the accessibility of water resources for crops. Gaiser et al.Reference Gaiser, Perkons, Küpper, Puschmann, Peth, Kautz, Pfeifer, Ewert, Horn and Köpke 81 demonstrated that the extraction of water from > 95 cm soil depth by spring wheat during a dry spell was increased when it was grown in field plots where the biopore density in the subsoil was increased by previous cultivation of perennial lucerne.

Biopores can facilitate the acquisition of nutrients from the subsoil via (1) increasing the root-length density in the bulk soil or (2) uptake of nutrients from the pore wall. The relevance of both processes largely depends on topsoil conditions. Low nutrient concentrationsReference Kuhlmann, Barraclough and Weir 82 , Reference Kuhlmann and Baumgärtel 83 and droughtReference Fleige, Grimme, Renger and Strebel 84 have been shown to increase the percentage of nutrients taken up from the subsoil. Because the frequency of drought in some areas is expected to increase under global climate changeReference Calanca 85 , subsoil processes related to biopores could be of increasing importance in the future, particularly in organic production systems with a rather low nutrient availability in the topsoil.

The contribution of biopores to nutrient acquisition is not yet quantified. Nutrient acquisition from the bulk soil can only be increased by biopores if the soil conditions allow re-entry of roots growing through biopores into the bulk soil. At least for earthworm burrows, the properties of biopore walls can be considered to be favorable for nutrient uptake. Most importantly, the coatings of biopores typically can contain more nutrients than the surrounding soil, which has been reported particularly for nitrateReference Parkin and Berry 86 , Reference Vinther, Eiland, Lind and Elsgaard 87 , ammoniumReference Devliegher and Verstraete 88 , phosphate and KReference Graff 27 , Reference Pankhurst, Pierret, Hawke and Kirby 40 . Total carbon and organic carbon are enriched in the pore wall as wellReference Mele, Yunusa, Kingston and Rab 89 , Reference Tiunov and Scheu 90 .

The walls of earthworm burrows have been identified as a hot spot of microbiological activity, as indicated by increased basal respiration, dehydrogenase activity and phosphatase activityReference Stehouwer, Dick and Traina 38 , Reference Tiunov and Scheu 90 , Reference Jégou, Schrader, Diestel and Cluzeau 91 . Therefore, earthworm coatings potentially provide not only the nutrients deposited by feces and mucus of earthworms, but also nutrients mobilized from the solid phase by microbial activity. In addition, root activity can enhance weathering in the pore wallReference Eich-Greatorex and Strand 92 . However, lack of root–soil contact in biopores much larger than the root's diameter, as well as clumping of roots in biopores, have been reported to be a major drawback of biopore benefits for crop performanceReference Passioura 93 , Reference Stirzaker, Passioura and Wilms 94 . On the other hand, under field conditions about 85% of winter barley or oilseed rape roots growing in biopores with a diameter of >5 mm did contact the pore wall—barley roots established the contact mainly by thin vertical roots, whereas rapeseed typically established the contact via lateral roots emerging from thick vertical main roots, growing centrally through the poreReference Athmann, Kautz, Pude and Köpke 44 . White and KirkegaardReference White and Kirkegaard 95 reported that wheat roots growing without direct contact to the pore wall frequently had root hairs contacting and entering the wall. Although precise quantification of nutrient uptake from biopores is still lacking, it is plausible that biopores contribute to the nutrient acquisition of crops, especially if they are coated with nutrient-rich earthworm excreta.

Managing Large-sized Biopores in the Subsoil

Biopore density can be influenced by the share of dicotyledons in the crop rotation because the roots of dicots generally have a higher proportion of thicker roots which are more capable of penetrating dense soil because they exert large radial pressuresReference Materechera, Alston, Kirby and Dexter 96 , Reference Oades 97 . Hence, they are assumed to create more stable biopores than the roots of monocotsReference Materechera, Alston, Kirby and Dexter 98 . Moreover, perennial root systems have the ability to create comparatively stable, continuous pore systemsReference Benjamin, Mikha, Nielsen, Vigil, Calderon and Henry 99 . Taprooted ley crops commonly grown in organic crop rotations in temperate climates, such as grass–clover or lucerne, were repeatedly shown to increase macroporosityReference Kautz, Stumm, Kösters and Köpke 100 Reference Riley, Pommeresche, Eltun, Hansen and Korsaeth 103 .

Likewise, catch crops with taproot systems can be used to create biopores. In this context, forage radish (Raphanus sativus var. longipinnatus) seems to be an appropriate crop because it is known to have a particular high penetration capability as compared with other catch crops such as oilseed rape or ryeReference Chen and Weil 104 . Root growth and yield of soybeans were greater following a combination of forage radish and rye as cover crops than following no fodder crop, probably because remaining root channels had provided soybean roots with low resistance paths to subsoil waterReference Williams and Weil 105 . Furthermore, forage radish grown as a cover crop was reported to benefit root penetration of following maize in compacted soilReference Chen and Weil 106 .

Density and—in particular—the quality of biopores, e.g., the nutrient contents of pore walls, can be also influenced by the activity of anecic earthworms. Anecic earthworms can create new pores even in compacted soil layersReference Joschko, Diestel and Larink 2 . Moreover, anecic earthworms reuse existing burrows, which was reported for both juvenile individualsReference Nuutinen and Karaca 107 and mature individuals of L. terrestris L.Reference Butt, Nuutinen and Sirén 108 , Reference Nuutinen and Butt 109 . Specimens of L. terrestris can enter narrow pores and widen them because they can exert high radial pressuresReference Keudel and Schrader 110 . Such widening can increase the stability of pores because wider pores are less prone to compression than the narrower poresReference Schäffer, Stauber, Mueller, Müller and Schulin 111 . Furthermore, earthworms deposit fine-textured material in the pore wallReference Curry, Byrne and Schmidt 112 which results in increased packing density and stability of the pore wall. The populations of anecic earthworms can be increased by reducing the frequency and intensity of tillageReference Curry, Byrne and Schmidt 112 , Reference Emmerling 113 . Thus, any measures to increase the duration of soil rest are considered beneficial for promoting earthworm populations. Tillage also destroys the openings of vertical biopores to the surface and therefore diminishes the effectiveness of these pores in promoting water infiltration and gas exchange with the atmosphere. It has to be taken into account, that even after longer periods of soil rest, earthworm abundances will decrease drastically after the first tillage event. Nonetheless, the effects on subsoil structure generated during the period of increased population size and activity may remain, because biopores may be stable for decadesReference Beven and Germann 3 , Reference Hagedorn and Bundt 114 . Moreover, the time of tillage can have an effect on earthworm populations. For example, the abundance of L. terrestris was reported to be higher after spring cultivation as compared to autumn cultivationReference Nuutinen 115 , probably due to the longer presence of crop residues on the soil surface. Furthermore, food quality parameters (such as C/N-ratioReference Schönholzer, Kohli, Hahn, Daniel, Goez and Zeyer 116 , Reference Shipitalo, Protz and Tomlin 117 , polyphenol concentrationReference Hendriksen 118 and textureReference Wright 119 ) were found to influence earthworm populations.

Other strategies for increasing earthworm populations in arable fields include the reduction of tillage depth and implementation of conservation tillage—or even no-till practicesReference Chan 120 . These measures have considerable effects on anecic earthworms; however, in organic agriculture they can be difficult to establish under Central European climates because of the importance of tillage for nutrient mobilization and weed suppression.

Conclusions

Based on the current state of research it can be assumed that a high biopore density will mostly result in beneficial effects on root growth and crop performance. The relevance of these effects can be particularly pronounced in organic production systems, where crops largely rely on nutrient acquisition from the solid soil phase with particular benefit from increased root-length density and the presence of hot spots for nutrient acquisition in the subsoil. Organic land-use strategies should take into account the consequences of cultivation on formation and maintenance of biopores and aim to increase number, stability and quality of biopores.

Managing biopores to facilitate access to water and nutrients follows the fundamental principle of organic farming. Crop production should be based on the living soil and on ecological processes. Moreover, a high density of biopores could facilitate the acquisition of water and nutrients particularly under conditions of drought, thus contributing to increased cropping system stability, another overall aim of organic agriculture. In 1943, Howard, one of the pioneers of organic agricultural research, stated that organic farmers should manage their soils after ‘nature's methods of soil management’Reference Howard 121 . In this spirit, promoting the formation of biopores is a classic organic element of soil management.

References

1 Yunusa, I.M. and Newton, P. 2003. Plants for amelioration of subsoil constraints and hydrological control: The primer-plant concept. Plant and Soil 257(2):261281.Google Scholar
2 Joschko, M., Diestel, H., and Larink, O. 1989. Assessment of earthworm burrowing efficiency in compacted soil with a combination of morphological and soil physical measurements. Biology and Fertility of Soils 8(3):191196.Google Scholar
3 Beven, K. and Germann, P. 1982. Macropores and water flow in soils. Water Resources Research 18(5):13111325.Google Scholar
4 Wuest, S.B. 2001. Soil biopore estimation: Effects of tillage, nitrogen and photographic resolution. Soil and Tillage Research 62:111116.CrossRefGoogle Scholar
5 Ehlers, W., Köpke, U., Hesse, F., and Böhm, W. 1983. Penetration resistance and root growth of oats in tilled and untilled loess soil. Soil and Tillage Research 3:261275.Google Scholar
6 Kautz, T., Amelung, W., Ewert, F., Gaiser, T., Horn, R., Jahn, R., Javaux, M., Kemna, A., Kuzyakov, Y., Munch, J.-C., Pätzold, S., Peth, S., Scherer, H.W., Schloter, M., Schneider, H., Vanderborght, J., Vetterlein, D., Walter, A., Wiesenberg, G.L.B., and Köpke, U. 2013. Nutrient acquisition from arable subsoils in temperate climates: A review. Soil Biology and Biochemistry 57:10031022.Google Scholar
7 Köpke, U. 1995. Nutrient management in organic farming systems: The case of nitrogen. Biological Agriculture and Horticulture 11(1–4):1529.Google Scholar
8 Mäder, P., Fliessbach, A., Dubois, D., Gunst, L., Fried, P., and Niggli, U. 2002. Soil fertility and biodiversity in organic farming. Science 296(5573):16941697.CrossRefGoogle ScholarPubMed
9 Thiel, H. 1865. De radicum plantarum quarundam ab agricolis praecipue cultarum directione et extensione. Dissertation, University of Bonn.Google Scholar
10 Taylor, F. 1980. Phytoplankton ecology before 1900: Supplementary notes to the ‘Depths of the Ocean’. In Sears, M. and Merriman, D. (eds). Oceanography: The Past. Springer, New York. p. 509521.CrossRefGoogle Scholar
11 Hensen, V. 1877. Die Thätigkeit des Regenwurms (Lumbricus terrestris L.) für die Fruchtbarkeit des Erdbodens. Zeitschrift für wissenschaftliche Zoologie 28:354364.Google Scholar
12 Hensen, V. 1882. Über die Fruchtbarkeit des Erdbodens in ihrer Abhängigkeit von den Leistungen der in der Erdrinde lebenden Würmer. Landwirtschaftliche Jahrbücher 11:661698.Google Scholar
13 Hensen, V. 1892. Die Wurzeln in den tieferen Bodenschichten. Jahrbuch der Deutschen Landwirtschafts-Gesellschaft 7:8496.Google Scholar
14 Darwin, C. 1881. The Formation of Vegetable Mould, Through the Action of Worms, with Observations on their Habits. John Murray, London.CrossRefGoogle Scholar
15 Schultz-Lupitz, A. 1891. Über die Bewurzelung der landwirtschaftlichen Kulturgewächse und deren Bedeutung für den praktischen Ackerbau. Jahrbuch der Deutschen Landwirtschafts-Gesellschaft 6:7894.Google Scholar
16 Wollny, E. 1890. Untersuchungen über die Beeinflussung der Fruchtbarkeit der Ackerkrume durch die Tätigkeit der Regenwürmer. Forschungen auf dem Gebiete der Agrikultur-Physik 13:381394.Google Scholar
17 Lawes, J.B., Gilbert, J.H., Warington, R. and Station, R.E. 1881. On the Amount and Composition of the Rain and Drainage-Waters Collected at Rothamsted. William Clowes and Sons, London.Google Scholar
18 Glass, E.H. and Thurston, H.D. 1978. Traditional and modern crop protection in perspective. Bioscience 28:109115.Google Scholar
19 Hopp, H. and Slater, C.S. 1948. Influence of earthworms on soil productivity. Soil Science 66(6):421428.CrossRefGoogle Scholar
20 Carsons, R. 1962. Silent Spring. Houghton Mifflin, Boston.Google Scholar
21 Lytle, M.H. 2007. The Gentle Subversive: Rachel Carson, and the Rise of the Environmental Movement. Oxford University Press, New York.CrossRefGoogle Scholar
22 Odum, E. 1953. Fundamentals of Ecology. Saunders, Philadelphia.Google Scholar
23 Tansley, A.G. 1935. The use and abuse of vegetational concepts and terms. Ecology 16(3):284307.Google Scholar
24 Bouma, J. and Hole, F. 1965. Soil-peels and a method for estimating biopore size distribution in soils. Soil Science Society of America Journal 29(4):483485.Google Scholar
25 Van der Plas, L. and Slager, S. 1964. A method to study the distribution of biopores in soils. In Jongerius, A. (ed.). Soil Micromorphology Proceedings of the Second International Working-Meeting on Soil Micromorphology Arnhem, The Netherlands, September 22–25, 1964. Elsevier, Amsterdam. p. 411419.Google Scholar
26 Slager, S. 1964. A study of the distribution of biopores in some sandy soils in The Netherlands. In Jongerius, A. (ed.). Soil Micromorphology Proceedings of the Second International Working-Meeting on Soil Micromorphology Arnhem, The Netherlands, September 22–25, 1964. Elsevier, Amsterdam. p. 421427.Google Scholar
27 Graff, O. 1967. Über die Verlagerung von Nährelementen in den Unterboden durch Regenwurmtätigkeit. Landwirtschaftliche Forschung 20:117127.Google Scholar
28 Rhee, J.A. 1965. Earthworm activity and plant growth in artificial cultures. Plant and Soil 22(1):4548.CrossRefGoogle Scholar
29 Graff, O. 1971. Beeinflussen Regenwurmröhren die Pflanzenernährung? Landbauforschung Völkenrode 21:103108.Google Scholar
30 Graff, O. 1979. Die Regenwurmfrage im 18. und 19. Jahrhundert und die Bedeutung Victor Hensens.(La question du ver de terre au XVIII et au XIX siècle et l'importance de Victor Hensens). Zeitschrift für Agrargeschichte und Agrarsoziologie 27(2):232243.Google Scholar
31 Bouché, M. 1975. Action de la faune sur les états de la matière organique dans les écosystèmes. In Kilbertius, G., Reisinger, O., Mourey, A., and Cancela da Fonseca, J.A. (eds). Humification et biodégradation. Pierron, Sarreguemines. p. 157168.Google Scholar
32 Ehlers, W. 1975. Observations on earthworm channels and infiltration on tilled and untilled loess soil. Soil Science 119(3):242249.CrossRefGoogle Scholar
33 Dexter, A. 1986. Model experiments on the behaviour of roots at the interface between a tilled seed-bed and a compacted sub-soil. Plant and Soil 95(1):149161.CrossRefGoogle Scholar
34 Jakobsen, B. and Dexter, A. 1987. Effect of soil structure on wheat root growth, water uptake and grain yield. A computer simulation model. Soil and Tillage Research 10(4):331345.CrossRefGoogle Scholar
35 Jakobsen, B.E. and Dexter, A.R. 1988. Influence of biopores on root growth, water uptake and grain yield of wheat (Triticum aestivum) based on predictions from a computer model. Biology and Fertility of Soils 6(4):315321.Google Scholar
36 Jones, C.G., Lawton, J.H., and Shachak, M. 1994. Organisms as ecosystem engineers. Oikos 69:373386.CrossRefGoogle Scholar
37 Lavelle, P., Bignell, D., Lepage, M., Wolters, V., and Roger, P. 1997. Soil function in a changing world: The role of invertebrate ecosystem engineers. European Journal of Soil Biology 33(4):159193.Google Scholar
38 Stehouwer, R.C., Dick, W.A., and Traina, S.J. 1993. Characteristics of earthworm burrow lining affecting atrazine sorption. Journal of Environmental Quality 22:181185.Google Scholar
39 Carter, M.R., Mele, P.M., and Steed, G.R. 1994. The effects of direct drilling and stubble retention on water and bromide movement and earthworm species in a duplex soil. Soil Science 157(4):224231.Google Scholar
40 Pankhurst, C.E., Pierret, A., Hawke, B.G., and Kirby, J.M. 2002. Microbiological and chemical properties of soil associated with macropores at different depths in a red-duplex soil in NSW Australia. Plant and Soil 238:1120.CrossRefGoogle Scholar
41 Putten, W., Anderson, J., Bardgett, R.D., Behan-Pelletier, V., Bignell, D., Brown, G., Brown, V., Brussaard, L., Hunt, H., and Ineson, P. 2004. The sustainable delivery of goods and services provided by soil biota. In Wall, D.H. (ed.). Sustaining Biodiversity and Ecosystem Services in Soils and Sediments. Island Press, Washington, DC. p. 1543.Google Scholar
42 Drinkwater, L.E. 2009. Ecological knowledge: Foundation for sustainable organic agriculture. In Francis, C. (ed.). Organic Farming: The Ecological System. Agronomy Monograph 54. p. 1947.Google Scholar
43 Peth, S. 2010. Applications of microtomography in soils and sediments. Developments in Soil Science 34:73101.Google Scholar
44 Athmann, M., Kautz, T., Pude, R., and Köpke, U. 2013. Root growth in biopores—evaluation with in situ endoscopy. Plant and Soil 371:179190.Google Scholar
45 Kautz, T. and Köpke, U. 2010. In situ endoscopy: New insights to root growth in biopores. Plant Biosystems 144(2):440442.Google Scholar
46 Nagel, K.A., Kastenholz, B., Jahnke, S., van Dusschoten, D., Aach, T., Mühlich, M., Truhn, D., Scharr, H., Terjung, S., Walter, A., and Schurr, U. 2009. Temperature responses of roots: Impact on growth, root system architecture and implications for phenotyping. Functional Plant Biology 36(11):947959.CrossRefGoogle ScholarPubMed
47 Gaiser, T., Perkons, U., Kupper, P.M., Kautz, T., Uteau-Puschmann, D., Ewert, F., Enders, A., and Krauss, G. 2013. Modeling biopore effects on root growth and biomass production on soils with pronounced sub-soil clay accumulation. Ecological Modelling 256:615.Google Scholar
48 Dziejowski, J.E., Rimmer, A., and Steenhuis, T.S. 1997. Preferential movement of oxygen in soils? Soil Science Society of America Journal 61(6):16071610.CrossRefGoogle Scholar
49 Edwards, W.M., Shipitalo, M.J., Owens, L.B., and Norton, L.D. 1990. Effect of Lumbricus terrestris L. burrows on hydrology of continuous no-till corn fields. Geoderma 46(1–3):7384.Google Scholar
50 Craul, P.J. 1992. Urban Soils in Landscape Designs. John Wiley, New York.Google Scholar
51 Lal, R. and Shukla, A. 2004. Principles of Soil Physics. CRC, Boca Raton.Google Scholar
52 Hillel, D. 1998. Environmental Soil Physics. Academic Press, San Diego.Google Scholar
53 Glinski, J. and Lipiec, J. 1990. Soil Physical Conditions and Plant Growth. CRC, Boca Raton.Google Scholar
54 Berisso, F.E., Schjønning, P., Keller, T., Lamandé, M., Simojoki, A., Iversen, B.V., Alakukku, L., and Forkman, J. 2013. Gas transport and subsoil pore characteristics: Anisotropy and long-term effects of compaction. Geoderma 195–196:184191.Google Scholar
55 Sierra, J. and Renault, P. 1998. Temporal pattern of oxygen concentration in a hydromorphic soil. Soil Science Society of America Journal 62(5):13981405.CrossRefGoogle Scholar
56 Stępniewski, W. and Przywara, G. 1992. The influence of soil oxygen availability on yield and nutrient uptake (N, P, K, Ca, Mg, Na) by winter rye (Secale cereale). Plant and Soil 143(2):267274.Google Scholar
57 Jarvis, N. 2007. A review of non-equilibrium water flow and solute transport in soil macropores: Principles, controlling factors and consequences for water quality. European Journal of Soil Science 58(3):523546.Google Scholar
58 Smettem, K. and Collis-George, N. 1985. The influence of cylindrical macropores on steady-state infiltration in a soil under pasture. Journal of Hydrology 79(1):107114.CrossRefGoogle Scholar
59 Angers, D.A. and Caron, J. 1998. Plant-induced changes in soil structure: processes and feedbacks. Biogeochemistry 42(1):5572.Google Scholar
60 Yunusa, I., Mele, P., Rab, M., Schefe, C., and Beverly, C. 2002. Priming of soil structural and hydrological properties by native woody species, annual crops, and a permanent pasture. Soil Research 40(2):207219.CrossRefGoogle Scholar
61 Schjønning, P., Munkholm, L.J., Moldrup, P., and Jacobsen, O.H. 2002. Modelling soil pore characteristics from measurements of air exchange: The long-term effects of fertilization and crop rotation. European Journal of Soil Science 53(2):331339.Google Scholar
62 Horn, R., Domżżał, H., Słowińska-Jurkiewicz, A., and van Ouwerkerk, C. 1995. Soil compaction processes and their effects on the structure of arable soils and the environment. Soil and Tillage Research 35(1–2):2336.CrossRefGoogle Scholar
63 Pitkänen, J. and Nuutinen, V. 1998. Earthworm contribution to infiltration and surface runoff after 15 years of different soil management. Applied Soil Ecology 9:411415.Google Scholar
64 Li, Y. and Ghodrati, M. 1994. Preferential transport of nitrate through soil columns containing root channels. Soil Science Society of America Journal 58(3):653659.Google Scholar
65 Heathwaite, A.L. and Dils, R.M. 2000. Characterising phosphorus loss in surface and subsurface hydrological pathways. Science of The Total Environment 251/252:523538.Google Scholar
66 Djodjic, F., Börling, K., and Bergström, L. 2004. Phosphorus leaching in relation to soil type and soil phosphorus content. Journal of Environmental Quality 33(2):678684.Google Scholar
67 Dadfar, H., Allaire, S.E., Bochove, E.v., Denault, J.-T., Thériault, G., and Charles, A. 2010. Likelihood of burrow flow in Canadian agricultural lands. Journal of Hydrology 386(1–4):142159.Google Scholar
68 Lammerts van Bueren, E.T., Struik, P.C., and Jacobsen, E. 2002. Ecological concepts in organic farming and their consequences for an organic crop ideotype. NJAS—Wageningen Journal of Life Sciences 50(1):126.CrossRefGoogle Scholar
69 Köpke, U. 1981. A comparison of methods for measuring root growth of field crops [oats, Avena sativa L.]. Zeitschrift fuer Acker und Pflanzenbau 150:3949.Google Scholar
70 Nakamoto, T. 1997. The distribution of maize roots as influenced by artificial vertical macropores. Japanese Journal of Crop Science 66(2):331332.Google Scholar
71 Logsdon, S.D. and Linden, D.R. 1992. Interactions of earthworms with soil physical conditions influencing plant growth. Soil Science 154(4):330337.Google Scholar
72 Hoad, S., Russell, G., Lucas, M., and Bingham, I. 2001. The management of wheat, barley, and oat root systems. Advances in Agronomy 74:193246.Google Scholar
73 Unger, P.W. and Kaspar, T.C. 1994. Soil compaction and root growth: A review. Agronomy Journal 86(5):759766.Google Scholar
74 Bengough, A.G. 2012. Root elongation is restricted by axial but not by radial pressures: So what happens in field soil? Plant and Soil 360(1–2):1518.Google Scholar
75 Whiteley, G.M., Hewitt, J.S., and Dexter, A.R. 1982. The buckling of plant roots. Physiologia Plantarum 54(3):333342.CrossRefGoogle Scholar
76 Stewart, J.B., Moran, C.J., and Wood, J.T. 1999. Macropore sheath: Quantification of plant root and soil macropore association. Plant and Soil 211:5967.Google Scholar
77 McMahon, M.J. and Christy, A.D. 2000. Root growth, calcite precipitation, and gas and water movement in fractures and macropores: A review with field observations. Ohio Journal of Science 100:8893.Google Scholar
78 Kautz, T., Perkons, U., Athmann, M., Pude, R., and Köpke, U. 2013. Barley roots are not constrained to large-sized biopores in the subsoil of a deep Haplic Luvisol. Biology and Fertility of Soils 49:959963.Google Scholar
79 Bengough, A. 2003. Root growth and function in relation to soil structure, composition, and strength. In Kroon, H. and Visser, E.J.W. (eds). Root Ecology. Springer, Berlin. p. 151172.Google Scholar
80 Hirth, J.R., McKenzie, B.M., and Tisdall, J.M. 2005. Ability of seedling roots of Lolium perenne L. to penetrate soil from artificial biopores is modified by soil bulk density, biopore angle and biopore relief. Plant and Soil 272(1):327336.Google Scholar
81 Gaiser, T., Perkons, U., Küpper, P.M., Puschmann, D.U., Peth, S., Kautz, T., Pfeifer, J., Ewert, F., Horn, R., and Köpke, U. 2012. Evidence of improved water uptake from subsoil by spring wheat following lucerne in a temperate humid climate. Field Crops Research 126:5662.Google Scholar
82 Kuhlmann, H., Barraclough, P., and Weir, A. 1989. Utilization of mineral nitrogen in the subsoil by winter wheat. Zeitschrift für Pflanzenernährung und Bodenkunde 152(3):291295.Google Scholar
83 Kuhlmann, H. and Baumgärtel, G. 1991. Potential importance of the subsoil for the P and Mg nutrition of wheat. Plant and Soil 137(2):259266.Google Scholar
84 Fleige, H., Grimme, H., Renger, M., and Strebel, O. 1983. Zur Erfassung der Nährstoffanlieferung durch Diffusion im effektiven Wurzelraum. Mitteilungen der Deutschen Bodenkundlichen Gesellschaft 38:381386.Google Scholar
85 Calanca, P. 2007. Climate change and drought occurrence in the Alpine region: How severe are becoming the extremes? Global and Planetary Change 57(1):151160.Google Scholar
86 Parkin, T.B. and Berry, E.C. 1999. Microbial nitrogen transformations in earthworm burrows. Soil Biology and Biochemistry 31:17651771.Google Scholar
87 Vinther, F.P., Eiland, F., Lind, A.-M., and Elsgaard, L. 1999. Microbial biomass and numbers of denitrifiers related to macropore channels in agricultural and forest soils. Soil Biology and Biochemistry 31:603611.Google Scholar
88 Devliegher, W. and Verstraete, W. 1997. Microorganisms and physico-chemical conditions in the drilosphere of Lumbricus terrestris . Soil Biology and Biochemistry 29:17211729.CrossRefGoogle Scholar
89 Mele, P.M., Yunusa, I.A.M., Kingston, K.B., and Rab, M.A. 2003. Response of soil fertility indices to a short phase of Australian woody species, continuous annual crop rotations or a permanent pasture. Soil and Tillage Research 72(1):2130.Google Scholar
90 Tiunov, A.V. and Scheu, S. 1999. Microbial respiration, biomass, biovolume and nutrient status in burrow walls of Lumbricus terrestris L. (Lumbricidae). Soil Biology and Biochemistry 31:20392048.CrossRefGoogle Scholar
91 Jégou, D., Schrader, S., Diestel, H., and Cluzeau, D. 2001. Morphological, physical and biochemical characteristics of burrow walls formed by earthworms. Applied Soil Ecology 17:165174.Google Scholar
92 Eich-Greatorex, S. and Strand, L.T. 2006. Soil chemical properties in the vicinity of pores with and without roots. Soil Science Society of America Journal 70(3):778785.Google Scholar
93 Passioura, J.B. 2002. Soil conditions and plant growth. Plant, Cell and Environment 25(2):311318.Google Scholar
94 Stirzaker, R., Passioura, J., and Wilms, Y. 1996. Soil structure and plant growth: Impact of bulk density and biopores. Plant and Soil 185(1):151162.Google Scholar
95 White, R.G. and Kirkegaard, J.A. 2010. The distribution and abundance of wheat roots in a dense, structured subsoil–implications for water uptake. Plant, Cell and Environment 33(2):133148.Google Scholar
96 Materechera, S., Alston, A., Kirby, J., and Dexter, A. 1992. Influence of root diameter on the penetration of seminal roots into a compacted subsoil. Plant and Soil 144(2):297303.Google Scholar
97 Oades, J.M. 1993. The role of biology in the formation, stabilization and degradation of soil structure. Geoderma 56(1–4):377400.Google Scholar
98 Materechera, S., Alston, A., Kirby, J., and Dexter, A. 1993. Field evaluation of laboratory techniques for predicting the ability of roots to penetrate strong soil and of the influence of roots on water sorptivity. Plant and Soil 149(2):149158.Google Scholar
99 Benjamin, J., Mikha, M., Nielsen, D., Vigil, M., Calderon, F., and Henry, W. 2007. Cropping intensity effects on physical properties of a no-till silt loam. Soil Science Society of America Journal 71(4):11601165.Google Scholar
100 Kautz, T., Stumm, C., Kösters, R., and Köpke, U. 2010. Effects of perennial fodder crops on soil structure in agricultural headlands. Journal of Plant Nutrition and Soil Science 173(4):490501.Google Scholar
101 Lesturgez, G., Poss, R., Hartmann, C., Bourdon, E., Noble, A., and Ratana-Anupap, S. 2004. Roots of Stylosanthes hamata create macropores in the compact layer of a sandy soil. Plant and Soil 260(1–2):101109.Google Scholar
102 McCallum, M., Kirkegaard, J., Green, T., Cresswell, H., Davies, S., Angus, J., and Peoples, M. 2004. Improved subsoil macroporosity following perennial pastures. Animal Production Science 44(3):299307.Google Scholar
103 Riley, H., Pommeresche, R., Eltun, R., Hansen, S., and Korsaeth, A. 2008. Soil structure, organic matter and earthworm activity in a comparison of cropping systems with contrasting tillage, rotations, fertilizer levels and manure use. Agriculture, Ecosystems and Environment 124(3–4):275284.Google Scholar
104 Chen, G. and Weil, R.R. 2011. Root growth and yield of maize as affected by soil compaction and cover crops. Soil and Tillage Research 117:1727.Google Scholar
105 Williams, S.M. and Weil, R.R. 2004. Crop cover root channels may alleviate soil compaction effects on soybean crop. Soil Science Society of America Journal 68:14031409.Google Scholar
106 Chen, G. and Weil, R.R. 2010. Penetration of cover crop roots through compacted soils. Plant and Soil 331:3143.CrossRefGoogle Scholar
107 Nuutinen, V. 2011. The meek shall inherit the burrow: Feedback in earthworm soil modification. In Karaca, A. (ed.). Biology of Earthworms. Soil Biology 24. Springer, Berlin. p. 123140.Google Scholar
108 Butt, K.R., Nuutinen, V., and Sirén, T. 2003. Resource distribution and surface activity of adult Lumbricus terrestris L. in an experimental system: The 7th international symposium on earthworm ecology, Cardiff, Wales, 2002. Pedobiologia 47:548553.Google Scholar
109 Nuutinen, V. and Butt, K.R. 2005. Homing ability widens the sphere of influence of the earthworm Lumbricus terrestris L. Soil Biology and Biochemistry 37:805807.Google Scholar
110 Keudel, M. and Schrader, S. 1999. Axial and radial pressure exerted by earthworms of different ecological groups. Biology and Fertility of Soils 29:262269.Google Scholar
111 Schäffer, B., Stauber, M., Mueller, T.L., Müller, R., and Schulin, R. 2008. Soil and macro-pores under uniaxial compression. I. Mechanical stability of repacked soil and deformation of different types of macro-pores. Geoderma 146:183191.Google Scholar
112 Curry, J.P., Byrne, D., and Schmidt, O. 2002. Intensive cultivation can drastically reduce earthworm populations in arable land. European Journal of Soil Biology 38(2):127130.Google Scholar
113 Emmerling, C. 2001. Response of earthworm communities to different types of soil tillage. Applied Soil Ecology 17(1):9196.Google Scholar
114 Hagedorn, F. and Bundt, M. 2002. The age of preferential flow paths. Geoderma 108:119132.Google Scholar
115 Nuutinen, V. 1992. Earthworm community response to tillage and residue management on different soil types in southern Finland. Soil and Tillage Research 23(3):221239.Google Scholar
116 Schönholzer, F., Kohli, L., Hahn, D., Daniel, O., Goez, C., and Zeyer, J. 1998. Effects of decomposition of leaves on bacterial biomass and on palatability to Lumbricus terrestris L. Soil Biology and Biochemistry 30(13):18051813.Google Scholar
117 Shipitalo, M.J., Protz, R., and Tomlin, A.D. 1988. Effect of diet on the feeding and casting activity of Lumbricus terrestris and L. rubellus in laboratory culture. Soil Biology and Biochemistry 20(2):233237.Google Scholar
118 Hendriksen, N.B. 1990. Leaf litter selection by detritivore and geophagous earthworms. Biology and Fertility of Soils 10(1):1721.Google Scholar
119 Wright, M.A. 1972. Factors’ governing ingestion by the earthworm Lumbricus terrestris (L.), with special reference to apple leaves. Annals of Applied Biology 70(2):175188.Google Scholar
120 Chan, K.Y. 2001. An overview of some tillage impacts on earthworm population abundance and diversity—implications for functioning in soils. Soil and Tillage Research 57(4):179191.Google Scholar
121 Howard, A. 1943. An Agricultural Testament. Oxford University Press, Oxford.Google Scholar
Figure 0

Figure 1. Biopores in 45 cm soil depth (top view). The picture covers approximately 50×50 cm.

Figure 1

Figure 2. Biopore (longitudinal section). Soil depth approximately 50–80 cm.

Figure 2

Figure 3. Endoscopic views into biopores: (a) biopore coated with earthworm feces; (b) biopore containing two vertical roots of Brassica napus and an older, decomposing root from a previous crop.