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RESEARCH ARTICLE

Effects of feeding fodder beet or kale in winter to dams and their heifer offspring on the heifer growth and production

R. R. Woods https://orcid.org/0000-0002-0625-9967 A * , D. E. Dalley https://orcid.org/0000-0003-3707-2051 A and J. P. Edwards https://orcid.org/0000-0003-4220-7408 A
+ Author Affiliations
- Author Affiliations

A DairyNZ Ltd, PO Box 85066, Lincoln University, Lincoln 7647, New Zealand.

* Correspondence to: Roshean.Woods@dairynz.co.nz

Handling Editor: Keith Pembleton

Animal Production Science 64, AN22474 https://doi.org/10.1071/AN22474
Submitted: 6 September 2022  Accepted: 26 March 2023  Published: 20 April 2023

© 2024 The Author(s) (or their employer(s)). Published by CSIRO Publishing

Abstract

Context

Fodder beet (FB) is a widely used winter feed in New Zealand’s southern regions due to its high yield, consistent quality, and environmental benefits. However, FB is low in crude protein, phosphorus and fibre, and a survey showed that many dairy farmers were concerned that feeding FB may have negative impacts on lifetime performance.

Aim

To determine whether winter feeding FB or kale (Ka) to dairy cows, and then their heifer offspring at 1 and 2 years old, affects the heifer performance from birth until the end of their first lactation.

Methods

In June–August 2017, pregnant dairy cows were fed FB or kale over winter and then 140 of the resultant heifer offspring were divided into four treatment groups at 9–11 months old according to their dam’s winter diet and offered either FB or kale, with pasture baleage. The groups were as follows (dam crop–heifer crop): FB–FB, FB–Ka, Ka–FB, Ka–Ka. The heifers’ subsequent performance (growth, stature, milk production, and reproduction) was measured to the end of their first lactation (May 2020), and blood mineral status was monitored from May 2018 to May 2019. This observational study has its limitations, but is useful for generating hypotheses to test in more controlled research.

Key results

Heifers grazing FB in winter (June–August) 2018 had lower blood plasma urea and phosphate concentrations than did heifers grazing kale, despite similar dietary crude protein contents. Treatments had no effect on milk production. However, the heifer liveweights were affected and there was an indication of poorer reproductive performance. The FB–FB heifer treatment group had a lower average liveweight than the FB–Ka heifers from 1 to 2.8 years old.

Conclusions

Although no impact on milk production for the first lactation was observed, the key results suggest possible negative impacts of feeding heifers FB during winter, particularly if their dam also wintered on FB.

Implications

The combined effects of FB dam and heifer winter diets on lifetime productivity warrant further investigation to help develop sustainable FB feeding systems. When feeding FB, we recommend that farmers test their crops and supplements to ensure that sufficient nutrition, in particular protein and phosphorus are provided.

Keywords: Beta vulgaris L, blood metabolites, Brassica oleracea L, cattle, cow, crude protein, dairy, lactation, phosphorus, reproduction, wintering.

Introduction

Fodder beet (FB, Beta vulgaris L.) is an attractive feed source for dairy systems due to its high yield, consistent quality, high palatability, and environmental benefits (Edwards et al. 2014a; Jonker et al. 2017; Yao et al. 2018; Dalley et al. 2020a). In the Canterbury, Otago and Southland regions in New Zealand, FB grazed in situ or lifted and fed often replaces grain and pasture silage as an early or late lactation feed supplement and replaces crops such as swedes and kale to feed during the period of low pasture growth over winter. A survey in 2018 showed that a large proportion (57%) of non-lactating cows were fed FB diets (containing an average of 66% FB) during winter (June–August) for an average of 8.9 weeks (Edwards et al. 2020). Typically, farmers aim to draft cows off crop paddocks and onto pasture-based pre-calving diets anywhere from 10 to 28 days prior to calving. The Edwards et al. (2020) survey also showed that 17% of 1-year-old and 27% of 2-year-old replacement heifers were fed FB diets during winter, containing an average of 74% and 66% FB respectively.

To meet animal requirements for metabolisable protein, dietary crude protein (CP) on a dry-matter (DM) basis of 12% for non-lactating cows, 14–18% for lactating cows, depending on stage of lactation, and 14–17% for heifer replacements is recommended (Kolver 2000; DairyNZ 2020). Lactating cow’s diets should contain >27–33% neutral detergent fibre (NDF), <38% soluble carbohydrate, 0.3–0.45% phosphorus (P), 0.6–0.8% calcium (Ca), 0.22–0.28% magnesium (Mg), >1% potassium (K), 0.23% sulfur (S) (Kolver 2000; DairyNZ 2020). The CP, NDF, P, Ca and gross energy concentrations of FB bulbs are low (Clark et al. 1987) compared with pasture or kale. When FB comprises a large proportion of the diet, it may not supply the recommended daily intake of these nutrients, as demonstrated in both non-lactating and lactating dairy cows (Waghorn et al. 2018, 2019). These imbalances can reduce animal production and impair animal health (Grace et al. 2010; Dittmer et al. 2017; Hammond et al. 2021). Nortjé et al. (2020) reported low plasma Ca and P concentrations for individual dairy cows wintered on FB and, while herd average plasma concentrations were in the normal range, hypocalcaemia and hypophosphatemia were common after calving on their case study farms. For pregnant cows grazing FB, understanding any in utero effects on offspring performance is important. Bryant and Pirat (2014) compared diets of kale and straw (12% CP), kale and oat baleage (13% CP), and FB and ryegrass baleage (11% CP) and saw a tendency for greater birth weights from the 13% CP kale diet, than from the other diets. Girth width was correlated with birth weight and was also greatest in the 13% CP diet. However, this variation at birth did not affect pre-weaning growth rates. In contrast to this, Moonsan et al. (2018) compared FB diets differing in CP content, i.e. low (7.5% CP, FB with maize silage) or moderate (13.4% CP, FB with lucerne silage), for 8 weeks prior to calving and found no effect of maternal diet on calf birth weight or stature. The authors suggested that dietary protein restriction in late gestation did not have any immediate negative effects on in utero calf development. Although, in this study, both treatments contained FB, making the effects of FB and CP difficult to distinguish. In a recent study with pregnant ewes, Hammond et al. (2021) reported lower bodyweights, lower growth rates and higher mortality rates of twin lambs born to ewes fed FB in mid-to-late gestation than of those born to ewes fed ryegrass. This indicates dietary impacts on offspring while in utero; however, the literature is inconsistent in relation to FB compared with other diets.

A survey of farmers and veterinarians about FB feeding practices in the 2016–2017 season identified that one of their greatest concerns was the unknown effects of feeding FB to heifer replacements on lifetime performance (metabolic health and growth, reproduction, and milk production) (D. Dalley, pers. comm.). Thus, the aim of this study was to determine whether winter feeding FB or kale to dairy cows, and then their heifer offspring at 1 and 2 years old, affected the heifer performance from birth until the end of their first lactation. Heifer growth, milk production, and reproduction were monitored to test the hypothesis that a system relying solely on FB feeding for wintering cows and heifer replacements (FB-FB treatment) would negatively affect performance of heifer replacements from birth until the end of their first lactation.

Materials and methods

Experimental design and site description

An opportunity arose as part of a winter-feeding trial in 2017 at the Southern Dairy Hub (Southland, New Zealand, 46°18′37.8″S, 168°18′46.1″E, 11 m asl) to conduct an observational winter grazing-systems study with 140 dairy heifers born in July–September 2017. This experimental design has its limitations but is useful for generating hypotheses to test in more controlled research since data on wintering systems are not readily available in New Zealand farm databases such as MINDA. Heifers were managed as a single group from birth until June 2018 (9–11 months old) when they were blocked for the pre-partum winter crop that their dams had grazed in 2017 (Dam17; fodder beet (FB) or kale (Ka)) and allocated to the crop diets that they were to graze in subsequent winters, June–August 2018 and June–August 2019 (Crop1819; fodder beet (FB) or kale (Ka)). This gave the following four treatments (Dam17–Crop1819): FB–FB, FB–Ka, Ka–FB, Ka–Ka (see Table 1 for more detail). Animals were allocated at random to their treatment groups and then balanced according to genetic merit (breeding worth), heifer age, and breed. At the time of allocation, herds were not specifically balanced for liveweight breeding values. Heifers in the treatments FB–FB and Ka–FB were wintered as a single group on FB and FB–Ka and Ka–Ka were wintered as a single group on kale. Post-winter 2018, heifers were managed as a single group grazed on pasture according to standard farm practice, then separated into their treatments again for winter 2019 (19–21 months old; Table 1). After calving, heifers were blocked for genetic merit and liveweight and allocated to four herds where their first-lactation performance was monitored. Heifer was considered the experimental unit for all measurements.

Table 1.Experimental design and timeline showing the number of animals at key time points (n), and animals removed noted as negative values.

TimelineDescriptionTreatments (Dam17–Crop1819)
FB–FBFB–KaKa–FBKa–Ka
Winter 2017Dams were wintered on FB or kale (Dam17) June–August 2017FBKa
Heifer replacements were born July–September 2017n = 83n = 61
Birth to winter 2018Heifers were managed as one group on a pasture diet
Four heifers culled for reasons unrelated to treatment13
Winter 2018Heifer replacements were wintered on FB or kale based on their treatment (Crop1819) June–August 2018FBKaFBKa
140 study animalsn = 40n = 42n = 30n = 28
Post winter 2018Heifers were managed as one group on a pasture diet September 2018 to May 2019, 14 heifers culled as not pregnant3623
Winter 2019Heifers were wintered on the same crop as they were in 2018 based on treatment, June–August 2019n = 37n = 36n = 28n = 25
Post winter 2019Nine heifers euthanised due to calving difficulties, or culled due to pregnancy loss45
Heifers calved July–September 2019 and were balanced between four milking herdsn = 33n = 31n = 28n = 25
Seven heifers culled1231
Seven heifers culled as empty3112
End of lactationHeifers remaining at end of lactation, May 2020n = 29n = 28n = 24n = 22

All procedures had prior approval of the Ruakura Animal Ethics Committee, Hamilton, New Zealand (RAEC #14453, #14518, and #14811).

Animals and feeding

Half of the dams were part of a previously published winter feeding study Dalley et al. (2020b), and the other half received a diet similar to the ‘target’ treatments in that study. In brief, FB dam diets ranged from an allocation of 9.1 kg DM/cow.day of FB with 4.5 kg DM/cow.day of pasture baleage to 11.9 kg DM/cow.day FB with 3 kg DM/cow.day of pasture baleage. Kale dam diets ranged from an allocation of 10.5 kg DM/cow.day kale with 4.5 kg DM/cow.day of pasture baleage to 14 kg DM/cow.day kale with 3 kg DM/cow.day pasture baleage. Animals were transitioned onto FB and kale crops, following industry good-practice management (Nichol et al. 2003; Gibbs 2014). For dams, transitioning onto their respective crop diets began on 31 May 2017, an average of 68 days (14 s.d.) pre-calving. Dams were on their full crop allocations for an average of 61 and 73 days for FB or kale respectively, and were drafted onto pasture and baleage 10–14 days before their expected calving date. Dam diet nutrient composition is presented in Table 2.

Table 2.Mean composition of total diets offered to mixed-age, pregnant dams during winter, June–August 2017.

ItemFBKaleSEDP-value
Nitrogen intake25230829.20.126
Crude protein (% DM)12.914.71.360.254
Neutral detergent fibre (% DM)23.9b32.4a1.130.002
Soluble sugars (% DM)40.6a18.2b1.40<0.001
Metabolisable energy (MJ/kg)12.9a11.5b0.190.002
Phosphorus (% DM)0.21b0.30a0.0130.002
Potassium (% DM)2.242.490.2450.364
Sulfur (% DM)0.17b0.61a0.046<0.001
Calcium (% DM)0.38b1.33a0.019<0.001
Magnesium (% DM)0.210.200.0190.559

Means with different letters (a, b) within a row are significantly different at the 5% level.

SED, standard error of the difference.

In winter 2018, heifers began transitioning onto their respective crop diets on 10 May 2018 for FB heifers and 1 June 2018 for kale heifers (reaching full allocation on 1 June 2018 and 4 June 2018 respectively). The FB heifers and kale heifers then spent 104 and 85 days respectively, at their full crop allocations.

In winter 2019, FB and kale heifers began transitioning onto their respective diets on 3 June 2019 and spent an average of 61 and 55 days at their full crop allocations respectively. Heifers were drafted off crop onto pasture and baleage on the basis of observations of changes in udder size. Average number of days off crop prior to calving was 14.6 and 12.9 days for FB and kale heifers respectively. Allocation (crop and baleage) and estimated utilisation (crop) of 2018 and 2019 heifer winter diets are presented in Table 3, and these parameters were combined with composition data of individual feed components (Table 4) to give the composition of key nutrients in the total diets (Table 5).

Table 3.Mean allocation and utilisation of fodder beet (FB) or kale diets fed in winters 2018 and 2019 to replacement dairy heifers born July–September 2017.

ItemRising 1-year-old heifersRising 2-year-old heifers
FBA 2018Kale 2018FBA 2019Kale 2019
Crop allocation (kg DM/cow/day)54.810.911.4
Utilisation of crop (%)91779480
Baleage allocation (kg DM/cow.day)3.33.23.43.4
Assumed utilisation of baleage (%)85858585
Dry-matter intake (kg DM/cow.day)7.46.513.112
Metabolisable energy intake (MJ/day)92 (88)B76169 (156)B132

AFB crops had an average of 80% bulb.

BMetabolisable energy of FB bulbs tend to be higher than what they feed at; this value calculated in parentheses assumes an ME of 13 MJ ME/kg DM for FB bulbs.

Table 4.Mean composition of fodder beet (FB) bulb and leaf, kale, and pasture baleage eaten by replacement dairy heifers (born July–September 2017) during winters 2018 and 2019.

ItemFB bulbFB leafKaleBaleageSEDP-value
n = 9n = 9n = 10n = 16
Dry matter (%)17.0b10.1c12.3bc46.1a6.83<0.001
Crude protein (% DM)9.2c21.8a14.5b13.4b1.81<0.001
Acid detergent fibre (% DM)8.2d15.1c21.5b29.5a1.34<0.001
Neutral detergent fibre (% DM)12.5c28.8b26.2b48.9a2.22<0.001
Organic matter (% DM)94.2a84.0c90.0b91.4b1.22<0.001
Ash (% DM)5.8c16.0a10.0b8.6b1.22<0.001
Digestibility of organic matter in dry matter (%)90.6a69.6c75.1b63.3d2.47<0.001
Soluble sugars (% DM)60.0a17.2c26.6b10.7d3.37<0.001
Metabolisable energy (MJ/kg)14.5a11.1c12.0b10.1d0.40<0.001
Nitrogen (% DM)1.45c3.46a2.30b2.09b0.287<0.001
Phosphorus (% DM)0.15b0.32a0.31a0.31a0.039<0.001
Potassium (% DM)1.12b2.21a2.39a2.17a0.4950.006
Sulfur (% DM)0.07c0.29b0.63a0.29b0.031<0.001
Calcium (% DM)0.15c0.95ab1.12a0.71b0.140<0.001
Magnesium (% DM)0.15b0.57a0.18b0.19b0.029<0.001
Sodium (% DM)0.46bc2.22a0.71b0.45c0.135<0.001

Means with the same letter (a–d) within a row are not significantly different at the 5% level.

SED, standard error of the difference.

Table 5.Mean composition of total winter diets offered to replacement dairy heifers (born July–September 2017) in June–August 2018 and 2019.

ItemFBAKaleASEDFB 2018BKale 2018BFB 2019BKale 2019BSEDP-value cropP-value yearP-value crop × year
Nitrogen intake (g N/cow.day)18520913.7152c145c217b274a19.30.090<0.0010.034
Crude protein (% DM)11.8b14.4a0.7213.414.410.314.31.010.0030.0440.055
Neutral detergent fibre (% DM)25.4b33.8a1.1328.2b33.2ab22.5c34.4a1.58<0.0010.0600.008
Soluble sugars (% DM)40.5a20.7b2.0632.6b22.8bc48.5a18.6c2.90<0.0010.013<0.001
Metabolisable energy (MJ/kg)12.7a11.4b0.1512.5a11.8b12.9a11.0c0.22<0.0010.2580.002
Phosphorus (% DM)0.22b0.32a0.0130.230.350.220.280.019<0.0010.0150.065
Potassium (% DM)1.51b2.43a0.2061.442.641.592.210.290<0.0010.5100.178
Sulfur (% DM)0.17b0.53a0.0190.19c0.47b0.14c0.59a0.027<0.0010.0970.001
Calcium (% DM)0.45b0.96a0.0510.51b0.90a0.38b1.03a0.072<0.0010.9330.026
Magnesium (% DM)0.22a0.18b0.0120.210.180.220.190.0170.0170.3800.847

SED, standard error of the difference.

AOverall crop means across both years with different letters (a, b) within a row are significantly different at the 5% level.

BCrop × Year means with the same letter (a–c) within a row are not significantly different at the 5% level.

Crop and supplement measurements

Crop and supplement samples were analysed by Hill Laboratories (Hamilton, New Zealand). In brief, the DM content of each feed was determined by drying at 105°C for a minimum of 24 h. In preparation for feed-quality and mineral analysis, separate samples were dried at 62°C overnight and ground to 1 mm before being analysed. Feed-quality parameters, nitrogen (N), CP, acid detergent fibre (ADF), NDF, digestibility of organic matter in dry matter (DOMD), soluble sugars, and ash, were estimated using near-infrared spectroscopy (MPA FT-NIR Analyser, Bruker Optics, Billericia, MA, USA). Organic matter was calculated as 100 – ash. Metabolisable energy (ME) was derived from DOMD using the following calculation ME = 0.16 × DOMD. Minerals P, K, S, Ca, Mg, and sodium (Na) were analysed by ICP–OES (iCAP™ 6500 or iCAP™ 7400, ThermoFisher Scientific, Waltham, MA USA,) following nitric acid–hydrogen peroxide digestion.

Growth and stature

Animals were weighed using Tru-Test™ scales (Datamars SA, Lamone, Switzerland) approximately every 3 months from October 2017 to May 2019, and daily during lactation using DeLaval AWS100 walk-over weigh scales (DeLaval, Tumba, Sweden). Scales were calibrated with a standard weight at each weighing for the Tru-Test™ scales, and DeLaval scales used during lactation were checked weekly. Stature measurements of wither height, body length and girth circumference were taken in May, August, and October 2018, then in June 2019 and June 2020. Body length was taken from the wither to the end of the tail head and the girth circumference was taken behind the front legs.

Animal performance during first lactation

At each milking, milk weight (kg) was recorded for each heifer by using DeLaval milk meters and DelPro™ Herd Management software (DelPro, DeLaval, Tumba, Sweden). Fortnightly milk samples for each heifer were collected at an afternoon and following morning milking from 26 August 2019 to 12 May 2020. These were analysed for milk composition (protein %, fat %, lactose % and somatic cell count (SCC)) with a Milkoscan milk analyser (Foss Electric Hillerød, Denmark) as part of the Livestock Improvement Corporation’s (LIC) herd-testing service. Heifers were milked once a day (OAD) from calving until 27 August 2019, then twice a day until 29 March 2020, followed by OAD until the end of lactation on 22 May 2020. The majority of heifers were milked through until the end of lactation, and the criteria for those dried off earlier was based on dry-off time body condition score (BCS) industry recommendations (DairyNZ 2020), or daily milk production of <5 L/cow.day. Production data for the full lactation for each cow were calculated using the daily milk meter-recorded milk weights, averaged by week, and the fortnightly milk composition data. The carry-forward last-value procedure was used to fill in the gaps for the weeks without milk composition data; these data were summed for the lactation to give the full lactation production. Body condition score (0–10 scale; Roche et al. 2009) of all heifers was recorded on 14 June 2019, and fortnightly from 11 July 2019 until the end of lactation.

For their first mating in October 2018, heifers were synchronised using a double prostaglandin (PG) injection program. Kamar® Heatmount® detectors (Kamar Products Inc. Zionsville, IN, USA) were used for heat detection for 5 days of artificial insemination (AI) mating. After this, bulls were used for natural mating (6 November to 20 December 2018). Pregnancy scan data from 6 February 2019 and calving records were used to determine pregnancy date and calving rates.

Mating from 2 November 2019 to 4 January 2020 (2.2–2.4 years old) used tail paint to identify animals to AI for 6 weeks and recorded matings allowed for calculation of 3- and 6-week submission rate. This was followed by 4 weeks of natural mating with bulls; these matings were recorded by checking tail paint weekly. Animals were pregnancy scanned on 21 January 2020, 4 March 2020, and 29 April 2020 and conception rate and pregnancy date and rate were determined, as were the intervals between planned start of mating (PSM) and submission, and conception.

Blood sampling

Blood was sampled from heifers between 9.00 am and 11.00 am, before their daily feed allocation on four occasions, pre-winter in May 2018, mid-winter in August 2018, pre-mating in October 2018, and pre-winter in May 2019. These were collected from the coccygeal blood vessels, using evacuated blood tubes containing lithium heparin (BD Vacutainer® Heparin Tube, Becton Dickinson Vacutainer Systems, Franklin Lakes, NJ, USA). Blood samples were kept on ice until they could be centrifuged at 1711g force at 4°C for 20 min for the extraction of plasma for subsequent analysis of urea, phosphate, Ca, Mg and aspartate aminotransferase (AST) concentrations by Gribbles Veterinary Pathology Ltd (Hamilton, New Zealand). In brief, blood metabolites were assayed using colorimetric techniques at 37°C, with a Hitachi Modular P800 analyser (Roche Diagnostics, Indianapolis, IN, USA). Roche reagent kits were used to measure plasma concentrations of urea (mmol/L; 2-oxoglutarate reaction in the presence of glutamate dehydrogenase and coenzyme NADH with ammonium following urea hydrolysis, rate of NADH oxidation is measured), phosphate (mmol/L; reaction with ammonium molybdate in sulphuric acid to form ammonium phosphomolybdate), Ca (mmol/L; 5-nitro-5′-methyl-BAPTA complex reaction with EDTA), Mg (mmol/L; xylidyl blue reaction), and AST (IU/L; AST is a catalyst for the reaction between α-ketoglutarate and L-aspartate, the oxaloacetate formed is then reacted with NADH and the rate of NADH oxidation is measured).

In August 2018 and October 2018, samples were also collected using evacuated blood tubes containing fluoride ethylenediaminetetraacetic acid (EDTA) (BD Vacutainer® Fluoride Tube, Becton Dickinson Vacutainer Systems, Franklin Lates, NJ, USA) for subsequent glucose analysis by Gribbles Veterinary Pathology Ltd (mmol/L; modified GOD-PAP method using 4-aminophenazone and phenol).

Statistical analyses

Sample size calculation determined that 30–40 heifers were required in each of the four combinations of dam crop and heifer crop to detect a 3.5% difference in liveweight and stature, with 80% power and a significance of 5%.

All analyses were performed using SAS 9.4 (2016, SAS Institute Inc., Cary, NC, USA). Dietary intakes of feed quality parameters and minerals were analysed using a one-way ANOVA for dam diets and a two-way ANOVA for heifer diets, with crop (FB, kale), year and their interaction included in the model as fixed effects.

Liveweight, stature, BCS, and blood data were analysed using a mixed-model approach to repeated measures ANOVA (Proc Mixed). The model for liveweight between October 2017 and May 2018 included dam crop (Dam17), time and their interaction as fixed effects. The models for liveweight from August 2018, as well as stature, BCS and blood data included Dam17, heifer crop within dam crop (Crop1819(Dam17)), time and their interactions as fixed effects and measurements from May 2018 as covariates. In addition, all models included breed group and genetic merit as covariates, and heifer ID as a random effect. The covariance pattern model used was compound symmetry. Daily liveweight gain (LWG) for each heifer was calculated for the periods from October 2017 to May 2018 (before the heifers themselves were on crop), from May 2018 to May 2019 (during and after the heifers’ first winter on crop), and May 2019 to May 2020 (during and after the heifers’ second winter on crop). The model for LWG during the first period included Dam17 as a fixed effect, and breed group, genetic merit, and liveweight in October 2017 as covariates. The model for the second period included Dam17, Crop1819(Dam17), time, and all their interactions as fixed effect, the same covariates as above and heifer as random effect.

Full lactation production data were analysed using two-way ANOVA, with Dam17 and Crop1819(Dam17) included as fixed effects, and breed group and genetic merit as covariates.

Binary outcomes for reproduction (3- and 6-week submission, conception and pregnancy rates, conception to first AI and final pregnancy rate) were analysed using binary logistic regression (Proc Glimmix), while time intervals between PSM and first submission or conception were subjected to survival analysis using a Cox proportional hazard model (Proc PHReg). In addition to Dam17 and Crop1819(Dam17), the model included the same covariates as above. A retrospective power analysis for reproductive performance determined that 60 heifers would have been required to detect a 7.5-day difference in the number of days from PSM to submission, with 80% power and a significance of 5%. Hence, because there were fewer than 60 heifers per treatment group, the significance of these results is not reported.

Tukey’s method was used for pairwise comparisons and significance was declared if P ≤ 0.05. Adjusted means are presented with their standard error of the difference (SED).

Results

Feed and crop

Dam diets with FB were lower in NDF, P, S and Ca, but had higher ME and soluble sugars, than did kale diets (P < 0.01; Table 2). Heifer FB winter diets (June to August) were lower in CP, NDF, P, K, S and Ca, and higher in ME and soluble sugars, than were kale diets (P < 0.05; Table 5).

Heifer growth and stature

Heifer liveweight was not affected by Dam17 (P = 0.513), but it was affected by heifer crop within dam crop (Crop1819(Dam17); P = 0.033), FB–FB heifers had a lower average liveweight than did FB–Ka. This was 8.3 kg lower in October 2018 (prior to mating), 14.8 kg lower in February 2019, and in February, April and May 2020, it was 13.6–23.1 kg lower (Fig. 1a). Liveweight gain between October 2017 and May 2018 (2–9 months of age) was 0.58–0.60 kg/day on average and was not affected by Dam17. Similarly, LWG between May 2018 and May 2019 (9–21 months of age; 0.61–0.64 kg/day), and June 2019 and May 2020 (0.20–0.24 kg/day) were not affected by Dam17 or Crop1819(Dam17). At 12 months old, heifers were on average 11.4 kg below (equivalent to 96% of) their target liveweight for their age. In October 2018, pre-mating, the FB–FB heifers were on average 13.5 kg below and the FB–Ka heifers were 6.8 kg above their target liveweights, equivalent to 96% and 102% of the targets respectively, while the Ka–FB and Ka–Ka heifers met their targets. In May 2019 (22 months old), heifers from all treatments were, on average, 24.7 kg below (or 95% of) their target liveweights. There were no significant differences among treatments for height, length, or girth measured between August 2018 and June 2020, except for girth in August 2018 where there was a treatment effect (P < 0.01; Fig. 1b).

Fig. 1.

Effect of pre-partum winter crop diet of dams in June–August 2017 (fodder beet (FB) versus kale (Ka)) and (from August 2018) the winter crop diet of their heifer replacement offspring (born July–September 2017) in 2018 (1 year old) and 2019 (2 years old) (FB vs Ka) on heifer (a) liveweights (kg) from October 2017, and (b) girth, height and length (m) from August 2018, through until the end of their first lactation (May 2020). Treatment groups are presented as ‘dam crop 2017’–‘heifer crop 2018 and 2019’ (FB–FB, FB–Ka, Ka–FB, Ka–Ka). Error bars are one standard error of the difference (SED). ** P < 0.01, * P < 0.05.


AN22474_F1.gif

Animal performance

During their first lactation, average BCS between June 2019 and May 2020 was higher for the heifers where the dam crop was FB (FB–FB, FB–Ka; 4.8) than for heifers where the dam crop was kale (Ka–FB, Ka–Ka; 4.7; P = 0.014; Fig. 2). There was no impact of Crop1819(Dam17) on BCS (P = 0.742).

Fig. 2.

Effect of pre-partum winter crop diet of dams in June–August 2017 fodder beet (FB) versus kale on their heifer offspring average body condition score in the season of their first lactation June 2019 to May 2020. Grey shading indicates 95% confidence interval.


AN22474_F2.gif

There were no significant differences among treatments in first-lactation milk production, i.e. milk yield (3571–3940 kg), fat content (4.9–5.0%), protein content (4.1%), fat yield (178–196 kg), protein yield (147–161 kg), lactose yield (179–197 kg), milk-solid yield (325–357 kg), fat:protein ratio (1.20–1.21), or somatic cell count (64 713–85 802 cells/mL). However, there was a trend (P < 0.1) for higher milk yield in the Ka–FB treatment, than in Ka–Ka, FB–Ka and FB–FB. Lactose content was lower for FB–FB (4.96%) than for FB–Ka (5.04%); although being statistically significant (P = 0.024), biologically these values were similar and did not result in an increased lactose yield.

For the second mating in November 2019 to January 2020 (2.2–2.4 years old), there was no effect of heifer crop if dam crop was kale (Ka–Ka, Ka–FB); however, if dam crop was FB (FB–FB, FB–Ka), there was an interesting trend for the FB–FB heifers to have lower submission, conception and pregnancy rates and longer intervals between PSM and first submission (Fig. 3a), and from PSM to conception (Fig. 3b), than for the FB–Ka heifers.

Fig. 3.

Survival curves for the interval between (a) planned start of mating and first submission, and (b) planned start of mating and conception for 2-year-old heifers (mating 2019) whose dams were wintered on either fodder beet (FB) or kale (Ka) in June–August 2017 and who were wintered on either FB or kale themselves in winters 2018 (1 year old) and 2019 (2 years old). Treatment groups are presented as ‘dam crop 2017’–‘heifer crop 2018 and 2019’ (FB–FB, FB–Ka, Ka–FB, Ka–Ka).


AN22474_F3.gif

Blood metabolites

In August 2018 (during their first winter), when heifer crop was FB (FB–FB and Ka–FB), heifers had lower blood plasma urea and phosphate, and higher blood plasma Mg and glucose, than did Ka–Ka and FB–Ka heifers (P < 0.001; Fig. 4). Blood plasma AST concentrations were higher for Ka–Ka heifers than FB–FB heifers in August 2018 (P = 0.003; Fig. 4e). In October 2018, (pre-mating) urea, Mg, AST and glucose were not significantly different, but the FB–FB heifers had higher phosphate concentrations than did FB–Ka heifers (Fig. 4). There were no significant differences in blood plasma Ca concentrations among treatments at any of the samplings (Fig. 4c).

Fig. 4.

Effect of dam crop in winter 2017 (fodder beet (FB) vs kale (Ka)) pre-partum and the winter crop of their heifer offspring (FB vs Ka) in 2018 on (a) blood plasma urea, (b) phosphate, (c) calcium, (d) magnesium, (e) aspartate aminotransferase, and (f) glucose concentrations of replacement dairy heifers. Treatment groups are presented as ‘dam crop 2017’–‘heifer crop 2018 and 2019’ (FB–FB, FB–Ka, Ka–FB, Ka–Ka). Error bars are one standard error of the difference (SED). *** P < 0.001, ** P < 0.01, * P < 0.05.


AN22474_F4.gif

Discussion

The authors acknowledge that this study follows a single cohort of animals from birth until the end of their first lactation; this has its limitations, therefore the results of this study need to be interpreted in this context. However, this observational winter grazing-systems study is useful for generating hypotheses to test in more controlled research since data on wintering systems are not readily available in New Zealand farm databases such as MINDA. Crop and supplements fed to heifers were accurately allocated; however, utilisation was not measured for supplements, this is less important for the differences in animal performance in this systems comparison but does create some limitations when trying to determine what might be contributing to these differences in terms of dietary intake.

Although milk production in first lactation was not affected by dam crop or heifer crop, the lower liveweight and numerical difference in reproductive performance of the FB–FB heifers, compared with FB–Ka heifers, suggest the possibility of cumulative effects of FB feeding, where the dam crop was FB. Previous studies have shown improved milk production for heifers who achieved liveweight targets at 12–21 months of age, compared with heifers not achieving targets (McNaughton and Lopdell 2013; Martín et al. 2020). In contrast, there were no differences in milk yield or milk-solid production among treatments in the current study, despite the FB–FB heifers not meeting their liveweight targets at planned start of mating and being, on average, 15 kg lighter at 18 months of age than the FB–Ka heifers (milk yields of 3777 and 3719 kg respectively). The observed differences in liveweight and FB–FB heifers not meeting their target liveweights pre-mating may explain the indication of poorer reproductive performance for the FB–FB heifers, than for the FB–Ka heifers, who met their target liveweights pre-mating.

The higher average BCS during the first lactation for heifers born to dams grazing FB, than for dams grazing kale, but no effect of heifer crop on BCS was an interesting observation, given the lack of difference in lactation milk production, although this difference was small. Several other studies have reported BCS gains to be similar for cows wintered on FB and kale diets (Edwards et al. 2014b; Dalley et al. 2020b); however, higher mean BCS for mixed-age cows wintered on FB, than on kale has been reported (Dalley et al. 2020b).

The lower blood plasma urea concentrations for heifers wintered on FB (FB–FB, Ka–FB) in August 2018, than for heifers wintered on kale (FB–Ka, Ka–Ka) occurred despite both the FB and kale winter diets in 2018 having similar diet CP contents (and N intakes; Table 5), both of which were below the industry-recommended 15–17% CP for 200–250 kg heifers (DairyNZ 2020). Hammond et al. (2021) reported lower plasma urea concentrations in twin-bearing ewes wintering on FB; however, this diet was lower in CP than their control diet where ewes were offered a ryegrass-dominant pasture. In contrast, research of Atkins et al. (2020) reported no difference in plasma urea concentration despite heifers fed diets containing FB having a lower dietary CP. These variable results suggest that the CP content of the diet may tell only part of the story and a more detailed analysis of dietary N components such as rumen degradable protein and rumen undegradable protein is required to explain the plasma urea results. Additionally, in the current study, the greater soluble sugars and metabolisable energy of the FB diets (Table 5) may have increased the efficiency of N capture by rumen microbes, and thus reduced plasma urea concentrations, as observed by Cosgrove et al. (2007). In winter 2019, the FB diet in the current study was below the industry-recommended 14% CP for 450 kg heifers (DairyNZ 2020), whereas the kale diets were sufficient.

The CP concentrations below industry recommendations in the FB diets in both winter 2018 and 2019 may have contributed to the lower liveweight but higher BCS, and subsequent indication of poorer reproductive performance of the FBFB heifers than of FB–Ka heifers. A study by McNaughton and Lopdell (2013) reported that heifers that were further from their pre-mating (15–17 months old) or pre-calving (18–21 months old) target liveweights produced less milk and had poorer reproductive performance as they were less likely to calve a first time, or to calve a second time.

The FB winter diets were low in P, which was reflected by lower blood plasma phosphate in August 2018 for FB–FB and Ka–FB heifers. Dietary P has been reported to be integral for skeletal growth; however, studies with dairy heifers have shown that different concentrations of dietary P (0.4% of DM vs 0.3% of DM) had no effect on bodyweight, external frame measurements, bone density or bone metabolism markers, reproductive efficiency, health and lactation performance (Esser et al. 2009; Bjelland et al. 2011). Similarly, dietary P (0.26%, 0.36% and 0.42% of DM) had no effect on bodyweight or body measurements of 8–10-month-old heifers (Zhang et al. 2016). By comparison, the 2018 and 2019 FB winter diets in the current study were only 0.22–0.23% P (Table 5), thus below these ranges reported in previous research. In addition to low dietary CP, this low dietary P may have also contributed to the lower liveweights observed, especially in the FB–FB treatment, although there were no significant differences in body measurements (Fig. 1b). Blood plasma phosphate concentrations in August 2018 in the current study (<2.1 mmol/L; Fig. 4b) were also lower than those reported in the overseas trials (2.4–2.8 mmol/L (Bjelland et al. 2011; Zhang et al. 2016)), indicating low circulating concentrations of P.

A surprising result was the higher blood plasma Mg in August 2018 when the heifers were wintered on FB (FB–FB, Ka–FB; Fig. 4d), despite similar dietary Mg concentrations between the FB and kale diets. The greater dry-matter intake of the FB diets may have contributed to this result. However, higher blood plasma Mg on FB supports that reported by Dalley et al. (2021) for mixed-age dairy cows wintered on FB. Dalley et al. (2021) attributed the higher Mg concentration in cows eating FB, than in those eating kale, to the increased soluble carbohydrates in the FB bulbs potentially lowering the ruminal pH and increasing the solubility of Mg for absorption. While not statistically different, the 2018 FB diet in the current experiment had numerically higher soluble sugar concentrations than the 2018 kale diet (Table 5). Another possibility for lower blood plasma Mg on the kale diet in winter 2018 is the higher K content of this diet potentially inhibiting Mg absorption for the FB–Ka and Ka–Ka heifers (Martens et al. 2018). Despite an effect of treatment (P = 0.023), Tukey comparisons showed that blood plasma Mg concentrations were not different among treatment groups in October 2018 when all heifers were managed as one group on the same diet. This result is expected because plasma Mg relies on the balance between absorption from the diet and excretion and is not actively mobilised from the body (Martens et al. 2018). However, it is possible that Mg may have been released if bone-P was being mobilised to compensate for the P-deficient FB diet (Table 5). Although diets high in Mg have been shown to reduce feed consumption and weight gain in young dairy calves (Gentry et al. 1978), this is not likely to have been the case in the current study since the concentrations of Mg offered (0.18–0.22% DM; Table 5) were not in excess of requirements and blood plasma concentrations were within the expected range of 0.74–1.4 mmol/L (Puls 1988).

The potential combined effects of dam and heifer winter diets on liveweight gain and indication of poorer reproduction seen in this observational study warrant further investigation in more controlled component experiments to tease out the interactions and identify the drivers behind these observations.

Conclusions

Although milk production was not affected by dam crop or heifer crop, results suggest differences in blood metabolites, heifer liveweights, and an indication of poorer reproductive performance. These could have implications for long-term animal performance and welfare and require further investigation in more controlled experiments. Consideration should be given to the diets of heifers in winter to ensure that they achieve minimum dietary requirements, particularly when feeding FB.

Data availability

The data that support this study will be shared upon reasonable request to the corresponding author.

Conflicts of interest

The authors declare no conflicts of interest.

Declaration of funding

This project was funded by the dairy farmers of New Zealand through DairyNZ Inc. (Hamilton, New Zealand), contract RDN1805.

Acknowledgements

We thank W. Ritchie and N. S. Hammond, C. Crack, H. McDonald for managing data collection, the farm team at the Southern Dairy Hub for animal management and B. Kuhn-Sherlock for statistical analysis.

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